Tuesday, November 18, 2008

Desalter Operation Optimization

  • By Adhi Budhiarto - Rabigh, KSA
Desalter is used to eliminate salts, water, sediment, and suspended solid. We need to have desalter for some reasons, as follows :
  1. To avoid corrosion (effected by salts) – it is usually main target of desalter operation.
  2. To avoid fouling and coking (effected by salts, sediment, and suspended solid).
  3. To avoid erosion inside piping/equipment (effected by sediment).
  4. To avoid high energy consumption (effected by salts, water, sediment, and suspended solid).
  5. To avoid catalyst poisoning (effected by salts).
  6. To avoid high cost of chemical used for handling fouling and corrosion (effected by salts, sediment, and suspended solid).
As my experience, there are some factors influencing emulsion stability of liquid inside of the desalter, as follows :
  1. Crude density ,Emulsion between crude and water can be broken by density by following Stoke formulae : V = K*(rhow-rhoo)*G*d^2/no (which are : V = water droplet fall down velocity ; K = constant; rhow = water density; rhoo = oil density; G = gravity acceleration; d = water droplet diameter; no = oil bulk viscosity). Eventhough crude density gives big impact to the emulsion stability, but it is not a operating variable.
  2. . Crude inlet temperature , Crude viscosity dereases with increasing temperature, so that water droplet can be easier to be separated. Higher desalter temperature can also increase water droplet combination efficiency by : a) Increasing the dilution of natural emulsion stabilizer, such as naphthenic acid. b) Increasing crashing frequency between water droplets.c) Accelerating the diffusion of demulsifier into oil-water interface.Higher desalter temperature can also influence crude density. Crude density decreases with increasing temperature, so that it can increase efficiency (see Stroke formulae). Yet, there is a maximum limitation for desalter temperature. Too high desalter temperature can evaporate light ends which can make turbulence. This turbulence can increase can decrease desalter efficiency.
  3. Electrical grid of desalter (if the type of desalter is bielectric) , electrical grid operation is usually trouble-free (eventhough there is a possibility of short circuit). Problems can be anticipated by having voltage and ampere indicators. In normal operation, these indicators should not be fluctuated.
  4. Wash water injection rate, Wash water injection rate should be moderate, not too low or too high. Too low wash water injection rate can decrease desalter efficiency, because water droplets in emulsion established by mixing valve can be too far to combine each other in the electrical field. Yet, too high wash water injection rate can make emulsion to be too conductive which can increase electrical current and decrease voltage, so that it can decrease driving force for polarizing droplets, combining each other in electrical field, and decreasing desalter efficiency. Wash water injection rate varies depending on crude properties, usually 4 to 6 % volume of crude (for crude having high specific gravity, wash water injection rate can be increased to 6 – 9 % volume of crude). The influence of water droplet population/density in the process of water droplet combination in electrical field can be described by formulae as follows : F = K*E^2*a^6/d^4 (which are : F = pulling force among droplets in electrical field; K = constant; E = voltage gradient among grids; a = radius of nearest water droplets; d = distance among droplets in electrical field). If wash water injection rate is low, the water droplet population/density is also low. If the distance among droplets in electrical field is wider, the driving force for polarizing droplets in electrical field will decrease, so that desalter efficiency will also decrease.
  5. pH of Wash water injection , Optimum pH of wash water injection is between 5.5 to 7.5. If pH is less than 5.5, it will cause corrosion in desalter. If pH is over then 7.5, it will stabilize emulsion, much oil will breakthrough as effluent water. In high pH environment, naphthenic acid contained in crude will be ionized and make sodium soap or potassium naphthenate which is a powerful emulsifier. If water in emulsion contains calcium and magnesium carbonate or sulfate, high pH of wash water can make sludge in desalter and scale in effluent water piping or downstream heat exchanger. For this reason wash water is sometimes injected by acid to control wash water pH.
  6. dP of mixing valve, Energy of water-oil mixing is controlled by pressure drop of mixing valve. This pressure drop is used to disperse wash water to be small droplets into the oil. If pressure drop is too low, the efficiency will be low. If pressure drop is too big, emulsion which is made will be too stable to be broken. Generally, crude having high specific gravity will need pressure drop 5-12 psi and crude having low specific gravity will need pressure drop 10-20 psi.
  7. Interface level of desalter, Interface level of desalter is usually based on experience. For howe-desalter, water level should be maintained to be 6-12” under inlet distributor header. For Petreco low-velocity desalter, water level should be maintained to be 6” above header. For Petreco Cylectric and bilectric desalter, water level should be maintained to be 12-24” under lower electrical grid.
  8. Desalter pressure, Desalter operating pressure is usually between 50 to 250 psig depending on discharge pressure of feed pump and desalter location in the preheater system. Desalter operating pressure should be enough to avoid crude evaporation within normal operation temperature. Howe suggested to have desalter operating pressure at least 20 psi above vapor pressure of oil-water compound at desalter normal operating pressure. High evaporation can cause vapor space in the upper side of desalter which can automatically cut electric current supply to electrical grid.
  9. Demulsifier, The objective of introducing demulsifier is to decrease oil content of desalter effluent water and to decrease salts and solids. By having demulsifier, pressure drop of mixing valve can be set higher, so that salt removal efficiency can be increased. The usual type of demulsifier is alkoxylated alkyl-phenol/formaldehyde resin. Demulsifier can increase desalter performance in some ways as follows :
  • Surface active components will replace emulsifying agent in oil-water interface which results in the combination of water droplets.
  • W etting agent makes the solid particle surface wet, so that the solid can be removed from oil phase or from oil-water interface and it will disperse into water phase. This will decrease solid contained in desalted crude and results in water droplet combination.
  • Floculant combines droplets and particles to make bigger droplets. Floculant also decreases emulsion layer volume at oil-water interface.
  • Some demulsifier components help breaking the oil out from wash water, so that cleaner effluent water will be produced.
  • Some demulsifier components help removing water from oil.

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Thursday, September 4, 2008

Job Vacancy at PT Pertamina UP II

Job vacancy at PT Pertamina

PERTAMINA is a State Owned oil & gas company (National Oil Company), established on December 10, 1957 under the name PT PERMINA. In 1961 the company changed its name to PN PERMINA and after the merger with PN PERTAMIN in 1968 it became PN PERTAMINA. With the enactment of Law 8 of 1971 the company became PERTAMINA. This name persisted until after PERTAMINA changed its legal status to PT PERTAMINA (PERSERO) on October 9, 2003. PERTAMINA’s scope of business incorporates the upstream and downstream sectors. The upstream sector covers oil, gas and geothermal energy exploration and production both domestically and overseas. The foregoing is pursued through own operations and through partnerships in the form of joint operations with JOBs (Joint Operating Bodies), TACs (Technical Assistance Contracts) and JOCs (Joint Operating Contracts), whereas the downstream sector includes processing, marketing, trading and shipping. Commodities produced range from Fuel (BBM) and Non Fuel (Non BBM), LPG, LNG, petrochemicals to Lube Base oil.
Dalam rangka memenuhi kebutuhan pekerja di lingkungan Daerah Operasi Unit Pengolahan (UP) II Dumai, PT PERTAMINA (PERSERO) membutuhkan 52 orang lulusan Diploma 3/sederajat untuk dipekerjakan sebagai Teknisi Operator dan Pemeliharaan Kilang dengan kriteria sebagai berikut :

PERSYARATAN :

1. Jenis kelamin laki-laki .
2. Status belum menikah bagi pelamar dari luar Pertamina, kecuali bagi pelamar dari pekerja outsourcing Pertamina.
3. Pendidikan terakhir D3 jurusan : Teknik Kimia (TK), Analis Kimia (AK), Teknik Listrik Arus Kuat (TLA), Teknik Mesin (TM), Teknik Instrumen/Elektronika (TI/E), Teknik Lingkungan (TL), Teknik Pengolahan Migas (TPM).
4. Bagi pelamar dari pekerja outsourcing Pertamina, minimal pengalaman kerja 3 tahun di Pertamina UP II Dumai.
5. IPK minimal 2.75 bagi pelamar dari luar Pertamina atau 2,50 bagi pelamar dari pekerja outsourcing Pertamina.
6. Usia maksimal 24 tahun per 01/01/2008 bagi pelamar dari luar Pertamina, atau maksimal 32 tahun per 01/01/2008 bagi pelamar dari pekerja outsourcing Pertamina.
7. Tinggi badan minimal 160 cm.
8. Tercatat sebagai pencari kerja di Kantor Dinas Tenaga Kerja (Disnaker) setempat.
9. Bebas narkoba.
10. Berbadan sehat, tidak buta warna dan diutamakan tidak berkaca mata/contact lens.
11. Bersedia ditempatkan di seluruh wilayah operasi PT PERTAMINA (PERSERO).
12. Lulus seluruh tahapan seleksi.

Bagi pelamar yang memenuhi kriteria tersebut di atas, dapat mengajukan Surat Lamaran dengan melampirkan dokumen :

a. Daftar Riwayat Hidup.
b. Copy ijazah D3 yang telah dilegalisir.
c. Copy transkrip nilai yang telah dilegalisir oleh pejabat berwenang.
d. Copy akte kelahiran/surat kenal lahir dari instansi berwenang.
e. Surat Keterangan Catatan Kepolisian (SKCK) dari Kepolisian setempat.
f. Surat Pernyataan Diri Bebas Narkoba di atas materai Rp.6.000,-
g. Copy KTP/SIM yang masih berlaku.
h. Copy Kartu Pencari Kerja (Kartu Kuning/Hijau) yang masih berlaku
i. 3 (tiga) lembar pas foto terbaru ukuran 4 x 6 (berwarna).
j. Alamat untuk surat panggilan (harap dicantumkan alamat terakhir, kode pos, nomor telpon/HP yang dapat dihubungi.

Lamaran harus dikirimkan melalui Pos dalam amplop tertutup dan ditujukan kepada : TIM REKRUTASI PO BOX 2000 DUMAI (RIAU)

Pada sudut kiri atas amplop lamaran, cantumkan kode jurusan bagi pelamar dari luar Pertamina, atau “OS” bagi pelamar dari pekerja outsourcing Pertamina.
Lamaran selambat-lambatnya diterima tanggal: 30 September 2008 (stempel pos).
Hanya pelamar yang memenuhi kriteria di atas yang akan dipanggil untuk mengikuti tes/seleksi dan tidak dikenakan biaya apapun (tanpa biaya).

Lamaran yang disampaikan sebelum pengumuman ini tidak akan diproses, dan surat lamaran yang telah dikirim tidak akan dikembalikan.

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Monday, July 21, 2008

Process Engineer : Job Description

Job Description of A Process Engineer A Process Engineer develops and optimize economical industrial processes to make the huge range of products on which modern society depends. A Process Engineer may work in small, medium and large businesses. The work is concerned with chemical and biochemical processes in which raw materials undergo change, and involves scaling up processes from the laboratory into the processing plant. Responsibilities involve designing equipment, understanding the reactions taking place, installing control systems, and starting, running and upgrading the processes. Environmental protection and health and safety aspects are also significant concerns.
Work is project-orientated and you may be working on a number of projects, all at various different stages, at any given time. Several process engineering companies act as consultancies.

Typical work activities include:

  • assessing processes for their relevance, and assessing the adequacy of engineering equipment;
  • reviewing existing data (also lab analysis) to see if more research and information need to be collated;
  • designing, installing and commissioning new production units, monitoring modifications and upgrades, and troubleshooting existing processes;
  • applying the principles of mass, momentum and heat transfer to process and equipment design, including conceptual, scheme and detail design;
  • conducting process development experiments to scale in a laboratory;
  • preparing reports, flow diagrams and charts;
  • assessing the availability of raw materials and the safety and environmental impact of the plant;
  • managing the cost and time constraints of projects;
  • selecting, managing and working with sub-contractors;
  • supporting the conversion of small-scale processes into commercially viable large-scale operations;
  • assuming responsibility for risk assessment, including hazard and operability (HAZOP) studies, for the health and safety of both company staff and the wider community;
  • working closely with chemical engineers to monitor and improve the efficiency, output and safety of a plant;
  • ensuring the process works at the optimum level, to the right rate and quality of output, in order to meet supply needs;
  • making observations and taking measurements directly, as well as collecting and interpreting data from the other technical and operating staff involved;
  • assuming responsibility for environmental monitoring and ongoing performance of processes and process plant;
  • ensuring that all aspects of an operation or process meet specified regulations;
  • working closely with other specialists, including: scientists responsible for the quality control of raw materials, intermediates and finished products; engineers responsible for plant maintenance; commercial colleagues on product specifications and production schedules; and the operating crew.

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Thursday, July 3, 2008

DCS Foxboro I/A Series : Solaris vs Windows

DCS Foxboro I/A Series : Solaris vs Windows When it comes to the significant points:
  1. Windows high point - Microsoft OS is the most used OS in the world and many great people are trained on it and the tools that are based on it.
  2. Windows low point - Microsoft OS is the most used OS in the world and many evil people are trained on it and the tools that are based on it.
  3. Unix low point - Not many people are familiar with Unix so it is tough to hire an experienced Unix person.
  4. Unix high point - Not many people are familiar with Unix so it is not attacked or played with. Hackers will leave you alone.
From a Foxboro AW point of view both computers work well as CP hosts and as long as you keep all of your control in the CP's both hosts would give you good service. There are slight differences but nothing to get really excited about. I would never recommend control of a process in the AW whether Unix or Win based. Supervisory control is OK as long as your CP takes control when the AW fails. Some of the differences as I see them (if anyone knows differently please let me know - my experience is still mostly with 51 series):
  1. You can easily do tape backup/restore of the Solaris boxes. Windows it's fairly straightforward to do backups but full restores are not possible - need to re-install windows, re-install I/A, re-commit and then restore custom files.
  2. On Solaris, you can use ICC from any workstation to any control station no matter which workstation you are working on and which host. On windows boxes you can only use ICC for a given control station from it's host AW. If you use IACC this does not appear to be an issue.
  3. All Solaris workstations are servers. It is easy to open a remote DM/FV from any workstation to any other workstation. Telnet, ftp, rmount, rcp, rlogin, rsh, nfs all just work. SSH can be made to work. XP boxes are not really servers. FTP works pretty well. Telnet under the Nutcracker suite has some issues. If you remotely access an XP box it's a shared screen. The P91 boxes running Win2003Server largely offset these issues.
  4. The nutcracker shell on Widows workstations gives an approximation of a Unix shell to try to preserve compatibility of many Foxboro and user software and scripts under Windows. All the user friendliness of Unix and all the reliability of Windows.
  5. I've had problems with AHD on windows WPs. Not sure if this can be made to work. We had off-platform AIM* and Solaris AWs - Windows WP could not retrieve AHD. My understanding is that Windows WPs can't retrieve AHD from any other workstation.
  6. Commits and QFs on a Windows box are more of a hassle than on a Solaris box. With Solaris you can do them remotely, and often don't need a reboot at all. Windows you can't do remotely. You have to reboot with I/A off, do the commit/QF, and reboot again with I/A on. If memory serves, some require extra reboots.
  7. Multiple monitors on Solaris are very simple - each has it's own desktop. Multiple monitors on Windows are actually a single desktop across two windows. Managing things so they stay on one monitor or the other can be a pain - like warnings and install menues which often pop up centered on the desktop spanning monitors.
  8. If you shut down a Foxboro Windows box using the traditional Start -> Shut Down sequence you will hang the box. You have to use CTRL-ALT-DEL -> Shut Down.
  9. In Solaris, switching to the appropriate environment can give you full administrative access to the workstation. If you want to secure the box from Operators using Windows you can boot to FV only, but then you have to reboot to FV+Windows to get full administrative access to the workstation.
  10. Because Foxboro has to qualify all the Microsoft patches, the patch levels of I/A boxes will be well behind current. This is true of Solaris also, but your MIS department is likely to be far more concerned about Windows patch levels on boxes connected to their network than about Solaris patch levels on Sun boxes connected to their network.
  11. Anti-virus software is available on the Windows boxes - this may be a pro or a con depending on your point of view. Managing updates for this software is not automatic. After the initial license there will be an ongoing license cost. If your MIS department already has a McAfee Corporate license this may be easy, although the version running on the I/A boxes (Enterprise 7 I think, maybe 8) may not match the Corporate version.
  12. I've had problems with frequent shell windows popping up and closing too quickly to see what they said on the windows boxes. Appears to be related to the OPC server and/or AIM*. I've seen this on both off-platform AIM*/OPC server boxes and on P91 I/A servers.
  13. A failed process can be easily restarted on an UNIX box. A failed process on a Windows box is far more likely to require a reboot of the workstation. Having said this, I rarely see failed processes on either platform any more. XP and Win2003 appear to be far more stable than NT.
  14. If you run a mixed system with both Solaris and Windows, maintaining graphics across the system is not trivial. Most of us have some version of a copy script that lets you change a graphic on your workstation and copy it to all other appropriate workstations. With the new FV, all changes must be done on the Windows platform.
  15. Changed files can easily be copied to other Windows workstations but need to be changed to .g files to copy to Solaris boxes where they have to be changed back to .fdf files under Solaris. This can still be scripted but it is more complicated.
  16. If you are using a V7.x system, telnets to F boxes across the switches seem to be extremely slow sometimes. I haven't seen this problem with the Windows boxes (and it may be fixed now for the Solaris boxes).
If you guys would just quit requesting windows. Foxboro could focus their development effort on something we wanted. Here are a couple more vs.
  1. Windows documentation for MKS/NutCracker is largely non-existant. You will need to go to the internet to get & understand them. Unix provides cryptic man pages for the various commands. You will need to go to the internet to understand them.
  2. Windows hardware costs less. Whether it's a keyboard, kvm switch, monitor, or cables PC hardware generally costs less than the equivalent Sun hardware. Typically not a lot, but if you have a large installation it can add up.
  3. Microsoft offers some "administrative windows scripting" languages that you can download, but they are not certified by Invensys and from my limited experience tend to be lacking. Think Microsoft's version of applescript. (Zune vs Ipod?) Doubtless these are improving, and seem to get updated on a fairly regular basis. Also there are the Microsoft Services for Unix or SFU. I would be very afraid to run these with the MKS/NutCracker installed, but hey, it's your plant. Unix system administration can become very automated, but you have to be willing to invest a lot of time up front to learn to do it. If you want to see what Microsoft thinks of scripting read this. (It's short, and hilarious if you do any shell scripting at all.) http://www.microsoft.com/technet/scriptcenter/topics/beginner/firststeps.mspx
  4. Windows has the registry. A one stop shop that can render your computer useless. UNIX doesn't.
  5. Windows has services that must run as a specific user, with a specific password. Unix has daemons that must run as root, but you are able to change the root password.
  6. Windows has any development language you like. Unix has any development language you like as long as it's not VB.
  7. When installing other programs either purchased or self written, Unix does not suffer fools gladly. Windows will gladly fool you. It can introduce subtle errors to other programs making it nearly impossible to determine the root cause of failure. DLLs are like Unix's shared libraries, but for some reason windows programmers are less disciplined about stomping on previous versions of DLLs.
  8. Unix does not ask for confirmation of rm -r /*. Windows will ask you "Are you sure?" so often you will hit OK regardless of the question like format C:
Refference : http://www.freelists.org/list/foxboro

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AIM Historian : Using cfgpts to get configuration information from your historian

Using cfgpts to get configuration information from your historian You can find the cfgpts and in /opt/fox/hstorian/bin/ on the 51 series AP or AW. Documentation for this tool is in the same directory in cfgpts.doc. To get a list of configured points in your historian: # cd /opt/fox/hstorian/bin # cfgpts -Rv hist01 ID=ANALOG1:TT405.PNT, PD=KILN 3 TEMP, DB=0.100000, SR=10, RC=216; ID=ANALOG1:TIC405.SPT, PD=KILN 3 TEMP CONTROLLER, DB=1.000000, SR=10, RC=216; ID=ANALOG1:TIC405.PNT, PD=KILN 3 TEMP CONTROLLER, DB=0.100000, SR=10, RC=216; ID=AVALOG1:TIC405.OUT, PD=KILN 3 TEMP CONTROLLER, DB=0.100000, SR=10, RC=216; etc.... The R option gets the points from the historian hist01 which have not been marked as deleted, and the v option (for verbose) displays full configuration information for each point. The output is in the form: ID (Point ID), PD (Point description), DB (Dead-band), SR (Sample rate), RC (Sample file size in blocks of 100 samples); Fields are separated with a comma and records are separated with a semi-colon. To get a summary of the data in the historian: # cfgpts -sq { Total Collection Points = 1000 Total Sample Files = 999 Total File space (apx.) = 657 MBytes (if AP20 database), Total File space (apx.) = 785 MBytes (if AP50 database), Combined Sample Rate = 13637 Samples/minute. } The s option is for statistics, and the q option suppresses display of the configuration records. Extracting the historian data points To get a list of just the configured points, you can use grep to select only those lines that start with "ID" (avoiding error messages and statistics), and nawk to print only the point name: # cfgpts -Rv hist01 | grep "^ID" | nawk -F"[=,]" '{print $2}' ANALOG1:TT405.PNT ANALOG1:TIC405.SPT ANALOG1:TIC405.PNT AVALOG1:TIC405.OUT etc... Dissecting this: cfgpts -Rv hist01 generates a list of non-deleted points in the historian which is piped to grep: | grep "^ID" filters for those lines starting with ID, the output of which is piped to nawk: | nawk -F"[=,]" '{print $2}' define the field separators for this command as "=" and "," and print the second field. Modifying the command to save the results to a file gives: # cfgpts -Rv hist01 | grep "^ID" | nawk -F"[=,]" '{print $2}' > hist01.txt Validate the historian data points To validate the collection points in the historian we can use the file (histpoints.txt) from the above example and Foxboro's omget tool (/opt/fox/bin/tools/omget) which returns the current value of a point if it is valid, or returns an error message if the point is invalid. Please note, with a large list of points this can take quite some time to run, especially if there are a large number of bad points. From the command line in the C shell: # foreach item ( `cat hist01.txt` ) ? /opt/fox/bin/tools/omget $item ? sleep 1 ? end ANALOG1:TT405.PNT (f): 878 ANALOG1:TIC405.SPT (f): 880 /opt/fox/bin/tools/omget: object [ANALOG1:TIC405.PNT] OM error [ -60 ]. /opt/fox/bin/tools/omg: object [AVALOG1:TIC405.OUT] does not exist. etc... In the above example, the OM error 60 is the result of an bad parameter type for the valid block (no PNT parameter in a PID block), and the "does not exist" error is the result of a compound:block that can't be located. We can refine this to take the bad points and save them to a file: # rm hist01.bad # foreach item ( `cat hist01.txt` ) ? /opt/fox/bin/tools/omget $item | grep "object" | nawk -F"[\\[\\]]" '{print $2}' >> hist01.bad ? sleep 1 ? end # In the examples above, note the back-quotes rather than quotes in ( `cat hist01.txt` ) which executes the enclosed command. The grep on "object" just selects the error lines. The nawk command sets the field separators to "[" and "]" for this command to enable us to print just the object between the brackets. The list of bad points is then appended to hist01.bad. Because we are appending a line at a time to the file hist01.bad, we delete any previous copies prior to starting the verification. The "sleep 1" reduces the load on the nodebus. Dealing with the bad points There are a number of causes for bad points in the historian database. The ones I see most include spelling mistakes in compound and block names, use of an improper parameter type, and the moving or deletion of the original block. If your verification of the historian's database turns up just a few bad points it is probably easiest to fix or delete them through the normal collection point configurator. If you have lots of bad points I find it is easiest to delete them all with cfgpts and add back the correct ones as I figure out what they should have been. Deleting the points we have determined to be bad is quite simple. WARNING -- Caution should be taken when using the cfgpts to add and delete points!!! Using the file hist01.bad generated in the last example we need to build a list of points to remove in the format recognized by cfgpts, which means "ID=" before the point name and a ";" at the end of each line. We can use sed to make these edits (without overwriting the original file) and send the result to cfgpts. The listing of points removed can be displayed or alternately sent to a file. The historian should be turned off before adding or deleting points. Also, it is good practice to get a backup listing of the historian's database: # histonoff hist01 OFF # cfgpts -Rv hist01 > hist01.backup # sed 's/^.*$/ID=&;/' hist01.bad | cfgpts -Dv hist01 > hist01.removed # histonoff hist01 ON # Check the file hist01.removed for errors encountered during the deletion. If all went smoothly, you will have a list of the points deleted. To reverse this action in the event of an error (ie. CP was off while you were generating bad points list), you can undo the deletion by: # histonoff hist01 OFF # cfgpts -Av hist01 hist01.added # histonoff hist01 ON # Building a list of points for addition Sometimes there is a need to add a large group of points to the historian. If the information to be added can be expressed easily such as "MEAS, SPT and OUT parameters on all PIDX blocks in 36CP03 at a scan rate of 10 seconds and a dead-band of 0.5% of scale retaining 60 hours of data" then it is easy to build an input file for cfgpts to add the points. To do exactly this, we can use the iccprt tool to extract the information and format it for cfgpts with awk and sed. First the use iccprt to extract the parameter level information from a station: # cd /opt/fox/ciocfg/api # iccprt -p -o 36CP03.txt 36CP03 # The "-p" tells iccprt to extract parameters, "-o 36CP03.txt" says output to a file named 36CP03.txt, and the final 36CP03 is the station letterbug. This generates a file that can be used to build an addition file for cfgpts. First, sed can be used to change the "END" after each block in the text file to something that can be used as a record separator: sed 's/^END//' 36CP03.txt Next, the parameter identifier tags can be stripped out and replaced with a space: sed 's/^.*= / /' Next, awk (or nawk in this case to handle longer records) can be used to list just the fields we want. For the PIDX block, field 1 is the compound and block, 2 is the type (PIDX), 3 is the description, 8 is HSCI1, 9 is LSCI1, 21 is HSCO1 and 22 is LSCO1: nawk 'BEGIN {FS="\n"; RS=""} {print $1, $2, $3, $8, $9, $21, $22}' Finally grep can be used to list only the PIDX records: grep PIDX Putting it all together, on a command line: # sed 's/^END//' 36CP03.txt | sed 's/^.*= / /' | nawk 'BEGIN {FS="\n"; RS=""} {print $1, $2, $3, $8, $9, $21, $22}' | grep PIDX ANALOG2:TIC3601 PIDX REACTOR 1 JACKET TEMP CONTROLLER 200.0 0.0 100.0 0.0 ANALOG2:TIC3601 PIDX REACTOR 2 JACKET TEMP CONTROLLER 200.0 0.0 100.0 0.0 ANALOG2:TIC3601 PIDX REACTOR 1 CORE TEMP CONTROLLER 500.0 0.0 100.0 0.0 ANALOG2:TIC3601 PIDX REACTOR 2 CORE TEMP CONTROLLER 500.0 0.0 100.0 0.0 # This gives a list in the format NAME TYPE DESCRIPTION HSCI1 LSCI1 HSCO1 LSCO1 which is useful as a reference but can't be used as an input to cfgpts yet. The nawk portion of the command can also be used for formatting the output, and then sed can be used to strip extra information: # sed 's/^END//' 36CP03.txt | sed 's/^.*= / /' | nawk 'BEGIN {FS="\n"; RS=""} {print $2 "ID="$1".MEAS, PD="$3", DB="($8-$9)*0.005", SR=10, RC=216;"}' | grep PIDX | sed 's/^ PIDX//' | sed 's/= /=/g' ID=ANALOG2:TIC3601, PD=REACTOR 1 JACKET TEMP CONTROLLER, DB=1, SR=10, RC=216; ID=ANALOG2:TIC3601, PD=REACTOR 2 JACKET TEMP CONTROLLER, DB=1, SR=10, RC=216; ID=ANALOG2:TIC3601, PD=REACTOR 1 CORE TEMP CONTROLLER, DB=1, SR=10, RC=216; ID=ANALOG2:TIC3601, PD=REACTOR 2 CORE TEMP CONTROLLER, DB=1, SR=10, RC=216; # This gives a properly formatted list for cfgpts, but only for the MEAS parameter. The print portion of the nawk statement can be expanded to add the SPT and OUT parameters. The output can be directed to a file and then used with cfgpts to add the points to the historian: # sed 's/^END//' 36CP03.txt | sed 's/^.*= / /' | nawk 'BEGIN {FS="\n"; RS=""} {print $2 "ID="$1".MEAS, PD="$3", DB="($8-$9)*0.005", SR=10, RC=216;"; print $2 "ID="$1".SPT, PD="$3", DB="($8-$9)*0.005", SR=10, RC=216;"; print $2 "ID="$1".OUT, PD="$3", DB="($21-$22)*0.005", SR=10, RC=216;"; }' | grep PIDX | sed 's/^ PIDX//' | sed 's/= /=/g' > 36CP03.histadd # cp 36CP03.histadd /opt/fox/hstorian/bin/ # cd /opt/fox/hstorian/bin # histonoff hist01 OFF # cfgpts -Av <>hist01.add # histonoff hist01 ON # Foxboro and I/A Series are registered trademarks of The Foxboro Company Reff : AIM*Historian IA Series, Invensys

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Rules of Thumb For Delayed Cokers

Rules of Thumb For Delayed Cokers

  1. Setiap pengurangan 8 psi coke drum pressure akan mengurangi coke yield 1.0 wt% on feed.
  2. Setiap pengurangan 8 psi coke drum pressure akan menaikkan liquid yield 1.3 vol% on feed.
  1. Setiap kenaikan 10 degF coke drum vapor line temperature akan menurunkan coke yield 0.8 wt% on feed.
  2. Setiap kenaikan 10 degF coke drum vapor line temperature akan menaikkan gas dan distillate 1.1 vol% on feed.
  3. Setiap penurunan 1 wt% VCM memerlukan kenaikan –7 sampai 9 degF coke drum vapor line temperature.
  4. Penurunan recycle 10% on feed akan mengurangi coke yield 1.2 wt% on feed.
  5. Penurunan 10% virgin gas oil content of coker feed akan mengurangi coke yield 1.5 wt% on feed.
  6. Penurunan coke yield 1.0 wt% on feed akan menaikkan liquid yiled 1.5 vol% on feed.
  7. Penurunan 6 jam cycle time akan mengurangi coke VCM 1.0 wt%.
  8. Kenaikan heater tube spacing dari dua ke tiga kali diameter tube akan mengurangi 25% peak heat flux
  9. Coking heater mass velocity criteria (lb/ft2second) :
  • Kurang dari 80==> disaster
  • 100 s/d 150 ==> marginal
  • 200 s/d 250 ==> reasonable run lengths
  • 300 plus ==> good design practice

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Thermal Cracking Process

Thermal Cracking Process ( Proses Perengkahan Termal) Proses perengkahan thermal (thermal Cracking) adalah suatu proses pemecahan rantai hydrocarbon dari senyawa rantai panjang menjadi hydrocarbon dengan rantai yang lebih kecil melalui bantuan panas. Suatu proses perengkahan thermal bertujuan untuk mendapatkan fraksi minyak bumi dengan boiling range yang lebih rendah dari feed (umpannya). Dalam proses ini dihasilkan: gas, gasoline (naphtha), gas oil (diesel), residue atau coke. Feednya dapat berupa gas oil atau residue.
Setelah mengalami pemanasan awal dan ditampung dalam akumulator, proses pemanasan selanjutnya dilakukan dalam suatu furnace (dapur) sampai mencapai temperatur rengkahnya. Keluar dari furnace, minyak yang sudah pada suhu rengkah tadi dimasukkan dalam suatu soaker, yaitu suatu alat berbentuk drum tegak yang berguna untuk memperpanjang reaksi perengkahan yang terjadi. Selanjutnya hasil perengkahan dimasukkan kedalam suatu menara / kolom pemisah (fractionator) dimana berikutnya akan dipisahkan masing-masing fraksi yang dikehendaki. Ada juga bagian yang dikembalikan lagi untuk direngkah lebih lanjut yang disebut recycle stock. Selain menghasilkan produk BBM (bahan bakar minyak) dan gas, dalam proses perengkahan thermal juga dihasilkan cokes. Cokes yang diharapkan hanya terbentuk di dalam chamber (coke drum) dapat pula terbentuk di dinding tubes heater/furnace dan transfer line (pipa transfer). Cokes tersebut terbentuk sedikit demi sedikit dan pada akhirnya akan terakumulasi. Jika akumulasi sudah dianggap mengganggu jalannya operasi, maka unit perengkahan thermal tersebut harus dihentikan untuk proses penghilangan akumulasi cokes atau SAD (Steam Air Decoking). Untuk memperkirakan apakah akumulasi cokes sudah berlebihan dan mengganggu operasi atau belum biasanya dilihat dari tanda-tanda sbb :
  1. Penurunan tekanan antara inlet dan outlet furnace sampai tingkat maksimum tertentu.
  2. Tekanan soaker/reaction chamber yang makin tinggi sampai tingkat maksimum tertentu.
  3. Temperatur tube metal (tube skin) makin naik.
Pembersihan akumulasi cokes tersebut disamping secara proses (SAD), dapat juga dilakukan secara mekanis menggunakan pompa bertekanan tinggi (aquadyne/hammelmann). I. UNIT VISBREAKING Adapun alat utama dari unit ini adalah sebagai berikut : 1. FLASH CHAMBER Fungsi utama flash chamber adalah memisahkan residue dari recycle untuk menghindari coking dalam heater/furnace. Agar residue tidak overcracking, maka dapat dilakukan quenching dari inlet flash chamber agar tempeaturnya menjadi kurang lebih 450 degC saja. Kadang-kadang hal ini dihilangkan jika sudah dilengkapi dengan sistem washing di top column dari flash chamber, karena dianggap cukup membantu mendinginkan bottom temperature. Sistem washing ini mempunyai keuntungan antara lain :
  • Mencuci atau menahan residue yang akan ikut keatas bersama uap.
  • Residue tidak terlalu melekat dengan coke terutama sepanjang dinding chamber.
Bahan pencuci biasanya adalah sidecut yang dingin dari fractionator. Untuk mengurangi residence time dari residue didalam flash chamber, dibuat suatu bentuk leher yang memanjang pada bagian bottom dengan menjaga level kurang lebih 50%. Typical bottom temperature didalam first stage flash chamber adalah 425 degC dengan overhead temperature 390 degC. Sedangkansecond stage flash chamber bottom suhunya 400 degC dan overheadnya 296 degC. 2. REACTION CHAMBER Reaction Chamber membantu fungsi furnace agar tidak terlalu besar. Dalam reaction chamber proses perengkahan terjadi tanpa harus menambah panasan. Temperatur keluar furnace kira-kira 480 degC dan keluar reaction chamber akan turun menjadi kurang lebih 465 degC. Tekanan reaction chamber dijaga kurang lebih 16.2 kg/cm2g untuk menjaga agar semua material masih dalam fase liquid hingga pembentukan coke minimum. Reaction chamber juga membantu berfungsi sebagai surge chamber yang dapat menahan fluktuasi operasi. 3. PROCESS VARIABLE Seperti dijelaskan didepan bahwa visbreaker ini menghasilkan light dan haeavy fraction. Yang diutamakan sebenarnya bukan light fractionnya tetapi heavy heavy fractionnya diinginkan seminimum mungkin tetapi masih memenuhi spec fuel oil. Variabel-variabel utamanya adalah :
  • Charge stock properties
  • Cracking temperature
  • Residence time
Secara umum dapat dikatakan bahwa kenaikan baik temperatur maupun residence time maka visbreaking severity akan naik. Kenaikan dari severity of cracking akan menaikkan produksi gas dan gasoline dan mengurangi viscosity dari cracked residu. Feed stock dengan harga K rendah, hasil gas dan gasoline makin rendah, tetapi makin tinggi viscosity residuenya dan makin tinggi BS&W pada cracking temperature dan residence time tertentu. II. DELAYED COKING Proses delayed coking dikembangkan dalam rangka me-minimize residue yang dihasilkan dari pengolahan minyak mentah melalui thermal cracking yang lebih severe. Jadi pada dasarnya proses delayed coking adalah juga proses thermal cracking yang dilakukan pada temperatur yang relatif sangat tinggi. Sebagai feed untuk unit ini kebanyakan adalah vacuum residue (short residue) . Pada operasi sebelum adanya delayed coking unit, operasi thermal cracking dijaga sedemikian rupa sehingga tidak akan terbentuk coke dalam heater/furnace. Namun dengan berkembangnya teknologi dan semakin meningkatnya kebutuhan oil product, telah dapat dikembangkan suatu proses dimana pada pemanasan residue sampai temeperatur yang tinggi didalam heater/furnace tetapi coke tetap tidak terbentuk didalam heater/furnace tubes. Hal ini dilakukan dengan memberikan velocity yang tinggi (residence time yang minimum) di dalam heater dan menambah drum/chamber di outlet heater untuk tempat terjadinya coking, sehinga proses ini kemudian disebut "Delayed coking". Dari segi reaksi kimiawi sebenarnya tidak berbeda dengan reaksi didalam proses thermal cracking yang lain, hanya disini sebagai salah satu produk akhir adalah carbon (coke). Coke dalam kenyataannya masih mengandung sejumlah volatile matter (VM) atau Hydrocarbon (HC) dengan boiling point tinggi. Untuk menghilangkan atau mengurangi kandungan volatile matter didalamnya, coke dipanasi lebih lanjut sampai 2000 - 2300 degF didalam suatu tanur/kiln yang berputar (Unit Calciner). Telah banyak kilang-kilang didunia yang memiliki unit delayed coking baik dengan tujuan untuk memproduksi calcined coke maupun dalam rangka maximizing oil products. Produk yang lain seperti unsaturated LPG, naphtha, gas oil kemudian diproses lebih lanjut untuk mendapatkan produk akhir yang on-spec. Selanjutnya naphtha diolah lebih lanjut di NHDT (Naphtha Hydrotreater), gas oil di proses di Hydrocracker. 1. DISKRIPSI PROSES Umpan vacuum residue yang berasal dari bottom vacuum column pertama-tama dimasukkan kedalam fractionator pada tray ke 2 sampai ke 4 dari bawah. Tujuannya adalah :
  • Untuk mendinginkan uap hydrocarbon yang datang dari coke chamber ke fractionator untuk mencegah terbentuknya coke didalamnya dan sekaligus untuk mengkondensasikan sebagian heavy oil yang akan di-recycle.
  • Adanya lighter material didalam vacuum residue feed sudah dapat stripped out.
  • Untuk preheating feed.
Fresh feed yang telah bercampur dengan heavy oil yang condenser di bottom factionator dipompakan kedalam coker heater yang kemudian masuk kedalam salah satu dari dua coke chamber (drum). Untuk mengontrol velocity dan mencegah terbentuknya deposit coke didalam tube diinjeksikan steam kedalam tube heater. Sejumlah tertentu dari material yang tidak menguap dalam fluida yang keluar dari heater akan tinggal didalam coke drum dan oleh karena adanya efek temperatur dan residence time akan menyebabkan terbentuknya coke. Uap yang keluar dari puncak coke drum akan dialirkan ke bottom fractionator. Dalam uap yang keluar dari coke drum, mengandung steam danhasil cracking yang terdiri dari gas, naphtha, gas oil. Uap akan mengalir ke top column melalui quench tray, kemudian produk gas oil akan ditarik dari tray diatas feed tray. Sebagaimana dalam crude fractionator, dalam delayed coker fractionator juga dilengkapidengan sistem hot dan cold reflux dengan maksud selain untuk memperbaiki distilasi juga untuk memanfaatkan panas yang didapat dalam column sehingga dapat digunakan untuk preheating dll. Akibatnya yang juga merupakan suatu keuntungan, bahwa beban overhead condensor akan lebih kecil. Untuk menarik naphtha biasa dilakukan pada 8-10 tray diatas gas oil draw-off. 2. OPERASI PENGAMBILAN COKE. Bila coke drum yang in-service (coking) telah penuh dengan coke, aliran feed kemudian dipindahkan (switch) ke drum yang telah kosong dengan mengoperasikan three way valve (switching valve), sementara itu drum yang telah penuh dengan coke diisolate untuk operasi pengambilan/pembongkaran coke. Mula-mula dialirkan steam untuk menghilangkan uap hydrocarbons yang masih ada didalam drum, kemudian didinginkan dengan mengisi air secara pelan-pelan sesuai dengan cooling rate yang dianjurkan agar tidak mengalami shock cooling. Pelaksanaan pengambilan/ pembongkaran coke (decoking), dimulai dengan membuka coke chamber, kemudian dengan mechanical drill atau hydraulic system yang menggunakan air bertekanan tinggi. Dengan sistem mechanical & water jet sedikit demi sedikit coke yang mengisi hampir seluruh coke drum akan terpotong masuk kedalam coke pit atau gerobag yang memang telah disediakan untuk selanjutnya diangkut ke storage. 3. SIFAT FISIS DAN PENGGUNAAN COKE Kebanyakan coke dihasilkan sebagai bahan yang keras, porous, bentuknya tidak teratur dengan ukuran dari 20 inch sampai kecil seperti debu. Coke type ini dikenal sebagai sponge coke. Penggunaan dari coke jenis ini adalah untuk :
  • Pembuatan electrode untuk digunakan dalam electrical furnace dalam pabrik Titanium oxide, baja.
  • Pembuatan anode untuk cell electrolytic dipabrik alumina.
  • Digunakan sebagai sumber carbon didalam pembuatan elemen phosphor, calcium carbide, silica carbide.
  • Pembuatan graphite.
Typical analysis dari Petroleum sponge coke adalah sebagai berikut : Wt % Wt % (Dari Delayed Coker) (Setelah Calcining) Air 2 – 4 nil Volatile matter 7 – 10 2 - 3 Fixed carbon 85 – 91 95 Kandungan sulfur 0.5 – 1.0 1 – 2 Kandungan sulfur didalam petroleum coke yang dihasilkan adalah bervariasi tergantung pada sulfur yang ada didalam feed stock. Biasanya antara 0.3- 1.5 wt % tapi kadang-kadang juga bisa mencapai 6%. Selain sponge coke, dikenal pula jenis coke lain yang disebut needle coke. Needle coke dihasilkan dari feed stock yang mengandung aromatic yang sangat tinggi. Needle coke ini lebih disenangi daripada sponge coke untuk digunakan sebagai electrode karena ia mempunyai electrical resistively dan coeficient thermal expansion yang lebih rendah sehingga tidak mudah berubah bentuk dan tidak boros pemakaiannya. 4. OPERASI DELAYED COKER Sebagaimana telah disinggung dalam decoking, coke drum diisi dan dikosongkan atas dasar suatu time cycle tertentu, sedang fraksinator dioperasikan secara kontinyu untuk memproduksi LPG, coker naphtha dan coker gas oil. Paling sedikit harus ada dua coke drum, namun ada pula yang lebih seperti di UP II Dumai yang mempunyai empat coke drum dengan pembagian : dua diisi / in operation (coking) dan dua yang lain dikosongkan (decoking) Typical waktu pengoperasian dari coke drum adalah sbb : Operasi Waktu (jam) Pengisian dengan coke 24 Memindah (switch) dan steaming out 03 Pendinginan (cooling down) 03 Drain 02 Buka tutup dan decoking 05 Tutup kembali dan test 02 Pemasangan kembali 07 Spare time 02 48 Operating variable dalam delayed coker antara lain adalah :
  • Temperatur outlet heater
  • Tekanan fractionating tower
  • Temperatur uap ex coke drum yang masuk fractionator
  • Free carbon content dalam feed.
Semakin tinggi temperatur yang keluar heater akan menaikkan proses cracking dan reaksi coking sehingga akan menaikkan pula jumlah gas dan coker naptha yang dihasilkan dan sebaliknya produksi coker gas oil yang berkurang. Menaikkan tekanan di fractionator mempunyai pengaruh yang sama dengan menaikkan temperatur outlet heater, karena dengan kenaikan tekanan di fractionator akan menambah jumlah vapor yang terkondensasi termasuk gas oil yang akan dikembalikan sehingga di-recycle bersama feed ke heater. Temperatur dari uap hydrocarbon ex coke drum yang semakin tinggi akan menaikkan end point dari produk coker gas oil sehingga jumlah gas oil yang direcycle menjadi berkurang akibatnya produksi coke akan berkurang pula. Dalam operasi delayed coker secara umum dapat dinyatakan bahwa semakin banyak gas oil yang direcycle akan menaikkan cracking yang selanjutnya akan menghasilkan gas, coker naphtha, dan coke yang lebih banyak dan menurunnya produksi coker gas oil. Refferences :
  1. “How to predict coker yield”; Castiglioni,B.P.; Hydrocarbon Processing, September 1983.
  2. UOP Operating Manual , “Delayed Coking Unit”

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Wednesday, June 11, 2008

Oil Refining : Platforming Process

INTRODUCTION Motor gasoline (Mogas) production starts with the distillation of crude oil. One of the products out of that process is a fraction of low octane gasoline, normally referred to as naphtha, typically boiling in the range 100 - 160 0C. Other gasoline fractions are produced as a result of secondary processes like catalytic cracking, isomerisation, alkylation and platforming. Petrol is then produced by blending a variety of these gasoline components of different qualities to meet a series of product specifications.
One very important property of Mogas is the octane number, which influences "knocking" or "pinking" behaviour in the engine of cars. Traditionally lead compounds have been added to petrol to improve the octane number. Over the past years, in many countries legislation has been implemented aimed at reducing the emission of lead from exhausts of motor vechiles and this, calls for other means of raising the octane number. The role of a platformer is to pave the way for this by a process which reforms the molecules in low octane naphtha to produce a high octane gasoline component. This is achieved by employing a catalyst with platinum as its active compound; hence the name Platformer. For many refinery catalyst applications, a promoter is used, and in the platforming process, it is a chloride promoter which stimulates the 'acidity' of the catalyst and thereby the isomerisation reactions. Often, a bimetallic catalyst is used, i.e. in addition to the platinum, a second metal, for instance Rhenium is present on the catalyst. The main advantage is a higher stability under reforming conditions. The disadvantage is that the catalyst becomes more sensitive towards poisons, process upsets and more susceptible to non-optimum regenerations. The main reactions of platforming process are as follows:
  • Dehydrogenation of naphthenes, yielding aromatics and hydrogen
  • Dehydro-isomerisation of alkyl cyclopentanes to aromatic and hydrogen
  • Isomerisation of paraffins and aromatics
  • Dehydrocyclisation of paraffins to aromatics and hydrogen
  • Hydrocracking of paraffins and naphthenes to ligher, saturated paraffins at the expense of hydrogen
The process literally re-shapes the molecules of the feed in a reaction in the presence of a platinum catalyst. Normally it is the hydrocarbon in the C6-C10 parafins that get converted to aromatics. The above reactions takes place concurrently and to a large extent also sequentially. The majority of these reactions, involve the conversion of paraffins and naphtenes and result in an increase in octane number and a nett production of hydrogen. Characteristic of the total effect of these reactions is the high endothermicity, which requires the continuous supply of process heat to maintain reaction temperature in the catalyst beds. That is why the process is typically done in four reactors in series with furnaces in between, in order to remain sufficiently high reactor temperatures. The reactions takes place at the surface of the catalyst and are very much dependent, amongst other factors, on the right combination of interactions between platinum, its modifiers or activators, the halogen and the catalyst carrier. During operating life of the catalyst, the absolute and relative reaction rates are influenced negatively by disturbing factors like gradual coke deposition, poisons and deterioration of physical characteristic of the catalyst (surface area decline). The process of platforming: The feedstock of the platformer is drawn from the refinery's distillation units. This is first treated by passing the feedstock together with hydrogen over a catayst, in a process called 'hydrotreating, to convert the sulphur and nitrogen compunds to hydrogen sulphide and ammonia, in order to prevent poisoning of the expensive platformer catalyst. After hydrotreating, ,the reactor effluent moves on through a stabiliser column to remove the gases formed (hydrogen sulphide, ammonia and fuel gas). In a second column, the C5 and some of the C6 is removed in a separate fraction called 'tops'. The reason to remove C5/C6 is that this component will crack in the platformer to produce fuel gas, while C6 gets converted into benzene, which can only be allowed in limited amount into the mogas because of its toxicity. From the bottom of the splitter column, the naphtha stream is produced, which is the feed for the Platforming section. At the heart of the Platformer process are the four reactors, each linked to furnaces to sustain a suffiently high reaction temperature, about 500 0C at the inlet of the reactors. Over time, coke will build up on the catalyst surface area, which reduces the catalyst activity. The catalyst can be easily regenerated however, by burning the coke off with air. After coke burning, the catalyst needs to be reconditioned by a combined treatment of air and HCl under high temperature. This regeneration step is called 'oxy-chlorination'. After this step the catalyst is dryed with hot nitrogen and subsequently brought in its active condition by reducing the surface with hot hydrogen. The refinery will therefore regulary have to take out one of the reactors to undergo this regeneration process. This type of process is therefore called semi-regen platforming. During the regeneration process, the refinery will suffer production loss, which is the reason why UOP developed a major process enhancement by making the regeneration possible continuously, in a Continous Catalytic Reformer, CCR. In the CCR unit, the reactors are cleverly stacked, so that the catalyst can flow under gravity. From the bottom of the reactor stack, the 'spent' catalyst is 'lifted' by nitrogen to the top of the regenerator stack. In the regenerator, the above mentioned different steps, coke burning, oxychlorination and drying are done in different sections, segregated via a complex system of valves, purge-flows and screens. From the bottom of the regenerator stack, catalyst is lifted by hydrogen to the top of the reactor stack, in a special area called the reduction zone. In the reduction zone, the catalyst passes a heat exchanger in which it is heated up against hot feed. Under hot conditions it is brought in contact with hydrogen, which performs a reduction of the catalyst surface, thereby restoring its activity. In such a continuous regeneration process, a constant catalyst activity can be maintained without unit shutdown for a typical runlength of 3 - 6 years. After 300 - 400 cycles of reaction/regeneration, the surface area of the catalyst will have dropped to a level (120 - 130 m2/g) that it becomes more difficult to maintain catalyst activity and at such a time normally the catalyst will be replaced by a fresh batch. The batch of 'spent' catalyst is then sent for platinum reclaim to recover the valuable precious metals. For economic reasons, the design capacities of Platformer units vary from 1000 - 4500 t/d; operating pressures can vary over a wide range, units with from 3.5 barg up to 30 barg can be found, whereby the latest generation CCR's are typically at the lower pressure range. A lower pressure enhances the endothermic reactions, which gives less cracking reactions and thereby a higher liquid yield. However, at a lower reactor operating pressure, the hydrogen partial pressure will be lower as well, which favours coke formation. The reason why semi regen platformers will not operate at a too low pressure, otherwise the cycle length between regenerations becomes to short. A second disadvantage of operating at a lower pressure is that a larger compressor will be required to boost the pressure of the hydrogen up to the normal pressure of the hydrogen system (about 20 barg). Typical design reformate octane numbers are in the 95-104 range. The reactor temperature is in a region of 450-530 0C. At the outlet of the last reactor the product is still well above 400 0C. It is cooled down against cold feed in massive heat exchanger, either a so called 'Texas Tower' or a Packinox plate-pack heat exchanger. The special design of those heat exchangers ensures that minimum heat loss occurs in order to minimise the fuel consumption of the furnaces. After passing the feed/effluent exchanger, the reaction products are cooled in air/water coolers and routed to a product separator, where the hydrogen is the main gaseous product. Part of the hydrogen produced is recycled back (via a compressor) to the feed, in order to maintain a high enough hydrogen partial pressure in the reactors. The remainder of the gases are compressed and brought in contact again with the liquid from the product separator. This is step is called 'recontacting' and is done in order to recover as much as possible hydrocarbons from the hydrogen produced. The reactor product, now in liquid form, goes on to the platformer stabiliser which removes Liquid Petroleum Gas ( LPG) and other gases to leave a liquid high octane gasoline component called platformate, ready for blending into the refinery mogas pool. Summarising, the Platformer unit produces about 85% liquid platformate, 10% hydrogen and 5% LPG. The Continuous Catalytic Reforming unit or better known as CCR Platformer is licensed by UOP, Universal Oil Products, based in USA. More recently, other technology vendors have copied the concept, one of the main competitors for UOP in this field is IFP from France. Main Equipment in a CCR Platformer: A CCR typically contains a feed/effluent heat exchanger (Texas Tower or Packinox), 4 furnaces, 4 reactors, a regenerator, overhead recontacting section, net gas compressor, recycle gas compressor and a stabiliser column.

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Database & System Improvement

INTRODUCTION Database adalah kumpulan dari item data yang saling berhubungan satu dengan yang lainnya yang diorganisasikan berdasarkan sebuah skema atau struktur tertentu, tersimpan di hardware komputer dan dengan software untuk melakukan manipulasi untuk kegunaan tertentu baik untuk waktu sekarang maupun untuk waktu yang akan datang.
Dalam perkembangannya database telah mengalami beberapa perubahan system : a. Flat File system, dimana data dengan katagori yang sama ditulis pada sebuah flat file menggunakan sistem baris dan kolom. File yang menyimpan data disebut Table, sedangkan baris(row) disebut Record dan kolom disebut field. Kelemahan sistem ini adalah pada proses pencarian data yang rumit, karena harus mencari data baris per baris. Jika jumlah data yang sudah tersimpan banyak pencarian data akan membutuhkan waktu yang lama. Selain itu juga sering terjadi kelebihan data. b. Hierarchical storage system. Pada sistem ini data disimpan meniru struktur pohon. Pada sistem ini hubungan antara data induk dan data anak (parent-child relationship) mulai dikenal. Kelemahan sistem ini sulit menangani hubungan many to many pada database, dimana harus dibuatkan file-file yang berisi informasi yang sama untuk mendukung many to many relationship. Akibatnya pengelolaan datanya menjadi sangat merepotkan. c. RDBMS (Relational Data Base Management System). Sistem ini diperkenalkan oleh Dr. Edgar F. Codd pada tahun 1970. Codd memperkenalkan prinsip-prinsip relational model pada sistem database. Dalam hal ini dilakukan penambahan item relasi yang berfungsi untuk menyimpan informasi hubungan antar table yang satu dengan yang lain. Dengan demikian sebuah item data tunggal dapat disimpan hanya pada satu tempat. RDBMS (Relational Data Base Management System). RDBMS merupakan sekumpulan data yang disimpan sedemikian rupa sehingga mudah diambil informasinya bagi pengguna, dan data tersebut saling berhubungan. RDBMS merupakan suatu paket perangkat lunak yang kompleks digunakan untuk memanipulasi database. Ada tiga prinsip dalam RDBMS :
  1. Data definition, mendefinisikan jenis data yang akan dibuat (dapat berupa angka atau huruf), cara relasi data, validasi data dan lainnya.
  2. Data Manipulation, data yang telah dibuat dan didefinisikan tersebut akan dilakukan beberapa pengerjaan, seperti menyaring data, melakukan proses query, dsb
  3. Data Control, bagian ini berkenaan dengan cara mengendalikan data, seperti siapa saja yang bisa melihat isi data, bagaimana data bisa digunakan oleh banyak user, dsb.
Semua operasi input dan output yang berhubungan dengan database harus menggunakan DBMS. Bila pemakai akan mengakses database, DBMS menyediakan penghubung (interface) antara pemakai dengan database. Hubungan pemakai dengan database dapat dilakukan dengan dua cara :
  1. Secara interaktif menggunakan bahasa pertanyaan (query language).
  2. Dengan menggunakan program aplikasi.

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Comparing DIPA vs MDEA

PERBANDINGAN DIPA dan MDEA DARI ASPEK TEKNIS Untuk membandingkan efektifitas DIPA dengan MDEA dalam melaksanakan fungsinya sebagai solvent pelarut acid gas terdapat beberapa variabel pembanding penting yang dapat dijadikan bahan pertimbangan yaitu sbb:
a. Potensi Degradasi. DIPA diklasifikasikan sebagai secondary alkanoamine yang dengan mudah dapat bereaksi dengan CO2 menghasilkan senyawa carbamat .Ion carbamat yang terbentuk dapat bereaksi lebih lanjut menghasilkan produk degradasi lainnya yaitu oxazolidone yang tidak dapat diregenerasi di regenerator. Berbeda halnya dengan senyawa MDEA (tertiary amine) yang relatif tidak berekasi dengan CO2 membentuk senyawa carbamat karena tertiary amine tidak mempunyai atom hidrogen radikal yang terikat dengan atom nitrogen sehingga potensi degradasi tertiary amine oleh CO2 sangat kecil. DIPA : HO-CH-CH2-N-CH2-CH-OH CH3 H CH3 MDEA : HO-CH2-CH2-N-CH2-CH2-OH CH3 Namun hal ini akan menambah kandungan CO2 di treated gas sehingga dikhawatirkan akan mempengaruhi performance katalis reformer. Hal ini telah dikonfirmasikan dengan pihak Kujang United Catalyst selaku Vendor katalis reformer UP-VI dan dari hasil korespondensi tersebut dinyatakan bahwa CO2 tidak mempunyai pengaruh terhadap kinerja katalis, maka tidak ada limitasi kandungan CO2 menuju reformer sehubungan dengan sifat gas CO2 yang merupakan inert. b. Selektivitas terhadap H2S. Tingkat selektivitas H2S dapat dilihat dari kecepatan reaksi Amine terutama dengan H2S dan CO2. Pada senyawa DIPA (Amine Sekunder) reaksi Amine dengan H2S hampir sama cepatnya dengan CO2 sehingga tingkat selektivitasnya terhadap H2S menjadi kecil. Tetapi pada senyawa MDEA (Tertiary Amine) reaksi dengan H2S jauh lebih cepat dibandingkan dengan reaksinya dengan CO2 sehingga selektivitasnya terhadap H2S lebih besar. Untuk H2S treating seperti di Kilang UP-VI, penggunaan MDEA akan lebih menguntungkan. c. Maximum H2S Loading. Maximum loading didefinisikan sebagai nilai tertinggi ratio jumlah mol H2S dengan jumlah mole amine yang masih bisa digunakan di sistem tanpa mengakibatkan terjadinya permasalahan korosi pada kondisi normal. Maximum loading sering pula dikatakan sebagai maximum acid gas loading. MDEA mempunyai H2S rich amine loading yang lebih tinggi (0.5 mole H2S/mole MDEA) dibandingkan dengan DIPA (0,3 mole H2S/mole MDEA). Dari nilai ini terlihat bahwa batas maximum limitasi H2S yang menuju ke sistem tanpa mengakibatkan terjadinya permasalahan korosi untuk MDEA lebih baik. d. Kebutuhan Energi. Energi yang diperlukan untuk memecah ikatan kimia antara secondary amine (DIPA) dengan acid gas lebih tinggi dibandingkan dengan tertiary amine (MDEA). Dengan demikian, MDEA akan membutuhkan steam stripping di regenerator yang lebih rendah dibandingkan DIPA sehingga akan menurunkan utilities cost yang dikeluarkan. e. Base strength. Base strength didefinisikan sebagai kekuatan sifat basa dari solven. Semakin tinggi sifat basa berarti akan memberikan performance yang lebih baik dalam acid gas removal karena yang ingin diabsobsi adalah gas H2S yang bersifat asam. Jika dilihat dari nilai base strength ini, primary dan secondary amine (termasuk didalamnya DIPA) mempunyai nilai yang lebih tinggi dibandingkan dengan tertiary amine (MDEA). f. Hydrocarbon Solubility. Menunjukkan besarnya jumlah Hydrocarbon yang terlarut dalam larutan Amine. Semakin tinggi kelarutan Hydrocarbon pada Amine maka semakin besar pula Amine Losses yang terjadi. Jika dibandingkan dengan primary dan secondary amine (termasuk didalamnya DIPA), tertiary amine (MDEA) mempunyai kelarutan hydrocarbon yang paling besar sehingga memperbesar potensi amine losses. g. Solvent Viscosity. Semakin tinggi viskositas suatu solvent, maka tendensi terjadinya foaming akan semakin tinggi pula. Pada konsentrasi yang sama, DIPA memiliki viskositas yang lebih tinggi dibanding MDEA sehingga potensi foaming yang dimilikinya lebih besar.

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Amine Solution : MEA , DEA , DGA , MDEA , TEA , DIPA

INTRODUCTION Pemilihan jenis absorbent (amine solution) dalam hal ini amine tergantung dari tujuan proses dan karakteristik dari tipe absorbent, antara lain selektivity untuk H2S, CO2, COS, pengendalian kandungan air di umpan gas, pengontrolan kandungan air di sirkulasi absorbent, cost, suplai absorbent, thermal stability, dll. Pemilihan absorbent juga ditentukan oleh kondisi operasi seperti tekanan dan temperature dari umpan gas, komposisinya, dan purity dari produk gas yang diinginkan serta penghilangan secara simultan gas H2S dan CO2 atau hanya selektif H2S dihilangkan.
Reaksi kimia yang terjadi untuk penyerapan H2S oleh amine sebagai berikut :
  • Overall Reaction : H2S + Amine ==> [Amine]H+ + HS-
  • Protonation of Amine : H+ + RR’NH ==> RR’NH2+ ……...… 1.1
  • Dissociation of Water : H2O ==> H+ + OH- …………………. 1.2
  • Dissociation of H2S : H2S ==> H+ + HS- ………………….... 1.3
  • Dissociation of HS- : HS- ==> H+ + S2- ……….………....... 1.4
Jenis-jenis amine yang digunakan :
  1. MEA (monoethanolamine), secara umum digunakan pada konsentrasi 10 -20 %wt dalam air. Acid gas loading terbatas 0.3 – 0.4 mol acid gas per mol amine. MEA dibandingkan dengan amine yang lain lebih korosif, terlebih lagi bila konsentrasi >20%wt, juga membutuhkan heat of reaction dengan H2S & CO2 sangat tinggi (sekitar 30% lebih tinggi dibandingkan DEA). Vapor pressure yang tinggi dari MEA mengakibatkan mudah kehilangan larutan di absorber dan stripper yang signifikan akibat vaporisasi yang tinggi.
  2. DEA (diethanolamine) , secara umum digunakan pada konsentrasi 25 – 35 %wt dalam air. Acid gas loading juga terbatas pada 0.3 – 0.4 mol acid gas per mol amine. DEA dibandingkan dengan MEA kurang korosif.
  3. DGA (diglycolamine atau 2 2-aminoethoxy ethanol), secara umum digunakan pada konsentrasi 40 – 60 % wt dalam air. Acid gas loading terbatas 0.3 – 0.4 mol acid gas per mol amine. Sifatnya similar dengan MEA tetapi mempunyai vapor pressure yang lebih rendah sehingga diperlukan konsentrasi yang lebih tinggi. Tingkat degradasi DGA juga tinggi.
  4. MDEA (methyldiethanolamine), secara umum digunakan pada konsentrasi 30 -50 %wt. Acid gas loading tinggi 0.7 – 0.8 mol acid gas per mol amine. Karena acid gas loading yang tinggi maka dapat mengurangi jumlah (flowrate) dari sirkulasi larutan amine (hal ini juga berarti mengurangi konsumsi energi pompa). MDEA juga tidak mudah terdegradasi baik secara thermal maupun chemical, dan mempunyai heat of reaction dengan H2S yang rendah.
  5. TEA (triethanolamine), merupakan tersier amine dan larutan amine yang pertama kali dikomersialkan untuk digunakan dalam gas sweetening. TEA tidak bisa menghasilkan produk gas dengan spesifikasi H2S rendah.
  6. DIPA (diisopropanolamine), digunakan pada proses ADIP dan Sulfinol (keduanya lisensi Shell International Petroleum Company-SIPM). DIPA tidak bisa menghasilkan produk gas dengan spesifikasi H2S rendah dan sekarang SIPM sudah menggantikan DIPA dengan MDEA.

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Oil Refining : Hydrotreating Process

INTRODUCTION

The objective of the Hydrotreating prococess is to remove suplur as well as other unwanted compunds, e.g. unsaturated hydrocarbons, nitrogen from refinery process streams. Until the end of World War 2, there was little incentive for the oil industry to pay significant attention to improving product quality by hydrogen treatment. However, soon after the war the production of high sulphur crudes increased significantly, which gave a more stringent demand on the product blending flexibility of refineries, and the marketing specifications for the products became tighter, largely due to environmental considerations.
Furthermore, the catalyst used in the Platforming process can only handle sulfur in the very low ppm level, so hydrotreating of naphtha became a must. The necessity for hydrotreating of middle distillates (kerosene/gasoil) originates from pressure to reduce sulfur emissions into the environment. Overall, this situation resulted in an increased necessity for high sulphur removal capability in many refineries.Furthermore, the catalyst used in the Platforming process can only handle sulfur in the very low ppm level, so hydrotreating of naphtha became a must. The necessity for hydrotreating of middle distillates (kerosene/gasoil) originates from pressure to reduce sulfur emissions into the environment. Overall, this situation resulted in an increased necessity for high sulphur removal capability in many refineries. Hydrodesulphursiation has been extensively used commercially for treating naphtha as Feedstock for catalytic reformers to meet the very stringent sulphuir specification of less than 1 ppm wt to protect the platinum catalyst. It has also been widely used for removal of sulphur compounds from kerosine and gasoils to make them suitable as blending components. In cases where products are from catalytic or thermal crackers, hydrogen treatment is used to improve product quality specifications like colour, smoke point, cetane index, etc. For Hydrotreating, two basic processes are applied, the liquid phase (or trickle flow) process for kerosine and heavier straight-run and cracked distillates up to vacumn gas oil and the vapour phase process for light straight-run and cracked fractions. Both processes use the same basic configuration: the feedstock is mixed with hydrogen- rich make up gas and recycle gas. The mixture is heated by heat exchange with reactor effluent and by a furnace and enters a reactor loaded with catalyst. In the reactor, the sulphur amd nitrogen compounds present in the feedstock are converted into hydrogen sulphide and ammonia respectively. The olefins present are saturated with hydrogen to become di-olefins and part of the aromatics will be hydrogenated. If all aromatics needs to be hydrogenated, a higher pressure is needed in the reactor compared to the conventional operating mode. The reactor operates at temperatures in the range of 300-380 0C and at a pressure of 10-20 bar for naphta and kero, as compared with 30-50 bar for gasoil, with excess hydrogen supplied. The temperature should not exceed 380 0C, as above this temperature cracking reactions can occur, which deteriorates the colour of the final product. The reaction products leave the reactor and, after having been cooled to a low temperature, typically 40-50 0C, enter a liquid/gas separation stage. The hydrogen-rich gas from the high pressure separation is recycled to combine with the feedstock, and the low pressure off- gas stream rich in hydrogen sulphide is sent to a gas-treating unit, where hydrogen sulphide is removed. The clean gas is then suitable as fuel for the refinery furnaces. The liquid stream is the product from hydotreating. It is normally sent to a stripping column where H2S and other undesirable components are removed, and finally, in cases where steam is used for stripping, the product is sent to a vacumn drier for removal of water. Some refiners use a salt dryer in stead of a vacuum drier to remove the water. The catalyst used is normally cobalt, molybdenum and nickel finely distributed on alumina extrudates. It slowly becomes choked by coke and must be renewed at regular intervals (typically 2-3 years). It can be regenerated (by burning off the coke) and reused typically once or twice before the breakdown of the support's porous structure unacceptably reduces its activity. Catayst regeneration is, nowadays, mainly carried out ex- situ by specialised firms. Other catalysts have also been developed for applications where denitrification is the predominant reaction required or where high stauration of olefins is necessary. A more recent development is the application of Hydrotreating for pretreatment of feedstcok for the catalytic cracking process. By utilisation of a suitable hydrogenation- promoting catalyst for conversion of aromatics and nitrogen in potential feedstocks, and selection of severe operating conditions, hydrogen is taken up by the aromatic molecules. The increased hydrogen content of the feedstock obtained by this treatment leads to significant conversion advantages in subsequent catalytic cracking, and higher yield of light products can be achieved. Hydrotreatment can also be used for kerosine smoke point improvement (SPI). It closely resembles the conventional Hydrotreating Process however an aromatic hydrogenation catalyst consisting of noble metals on a special carrier is used. The reactor operates at pressure range of 50-70 bar and temperatures of 260-320 0C. To restrict temperature rise due to the highly exothermic aromatics conversion reactions, quench oil is applied between the catalysts beds. The catalyst used is very sensitive to traces of sulphur and nitrogen in the feedstock and therefore pretreatment is normally applied in a conventional hydrotreater before kerosine is introduced into the SPI unit. The main objective of Smoke Point Improvement is improvement in burning characteristics as the kerosine aromatics are converted to naphthenes. Hydrotreatment is also used for production of feedstocks for isomersiation unit from pyrolysis gasoline (pygas) which is one of the byproducts of steam cracking of hydrocarbon fractions such as naphtha and gasoil. A hyrotreater and a hydrodesulphuriser are basically the same process but a hydotreater termed is used for treating kerosene or lighter feedstock, while a hydodesulhuriser mainly refers to gasoil treating. The hydrotreatment process is used in every major refinery and is therefore also termed as the work horse of the refinery as it is the hydrotreater unit that ensures several significant product quality specifications. In most countries the Diesel produced is hydrodesulhurised before its sold. Sulphur specifications are getting more and more stringent. In Asia, countries such as Thailand, Singapore and Hong Kong already have a 0.05%S specification and large hydrodesulphurisation units are required to meet such specs. The by-products obtained from HDT/HDS are light ends formed from a small amounts of cracking and these products are used in the refinery fuelgas pool. The other main by-product is Hydrogen Sulphide which is oxidized to sulphur and sold to the chemical industry for further processing. In combination with temperature, the pressure level (or rather the partial pressure of hydrogen) generally determines the types of components that can be removed and also determines the working life of the catalyst. At higher (partial) pressures, the desulphurisation process is 'easier', however, the unit becomes more expensive for instance due to larger compressors and heavier reactors. Also, at higher pressure, the hydrogen consumption of the unit increases, which can be a signficant cost factor for the refinery. The minimum pressure required typically goes up with the required severity of the unit, i.e. the heavier the feedstock, or the lower levels of sulphur in product required. Source : Hardeep Hundal, original editing by Jeroen Buren Adapted for The Chemical Engineers’ Resource Page by Chris Haslego

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Tuesday, June 10, 2008

History of Refinery Process

INTRODUCTION Petroleum refining has evolved continuously in response to changing consumer demand for better and different products. The original requirement was to produce kerosene as a cheaper and better source of light than whale oil. The development of the internal combustion engine led to the production of gasoline and diesel fuels. The evolution of the airplane created a need first for high-octane aviation gasoline and then for jet fuel, a sophisticated form of the original product, kerosene. Present-day refineries produce a variety of products including many required as feedstock for the petrochemical industry.
  1. Distillation Processes. The first refinery, opened in 1861, produced kerosene by simple atmospheric distillation. Its by-products included tar and naphtha. It was soon discovered that high-quality lubricating oils could be produced by distilling petroleum under vacuum. However, for the next 30 years kerosene was the product consumers wanted. Two significant events changed this situation: (1) invention of the electric light decreased the demand for kerosene, and (2) invention of the internal combustion engine created a demand for diesel fuel and gasoline (naphtha).
  2. Thermal Cracking Processes. With the advent of mass production and World War I, the number of gasoline-powered vehicles increased dramatically and the demand for gasoline grew accordingly. However, distillation processes produced only a certain amount of gasoline from crude oil. In 1913, the thermal cracking process was developed, which subjected heavy fuels to both pressure and intense heat, physically breaking the large molecules into smaller ones to produce additional gasoline and distillate fuels. Visbreaking, another form of thermal cracking, was developed in the late 1930's to produce more desirable and valuable products.
  3. Catalytic Processes. Higher-compression gasoline engines required higher-octane gasoline with better antiknock characteristics. The introduction of catalytic cracking and polymerization processes in the mid- to late 1930's met the demand by providing improved gasoline yields and higher octane numbers. Alkylation, another catalytic process developed in the early 1940's, produced more high-octane aviation gasoline and petrochemical feedstock for explosives and synthetic rubber. Subsequently, catalytic isomerization was developed to convert hydrocarbons to produce increased quantities of alkylation feedstock. Improved catalysts and process methods such as hydrocracking and reforming were developed throughout the 1960's to increase gasoline yields and improve antiknock characteristics. These catalytic processes also produced hydrocarbon molecules with a double bond (alkenes) and formed the basis of the modern petrochemical industry.
  4. Treatment Processes. Throughout the history of refining, various treatment methods have been used to remove nonhydrocarbons, impurities, and other constituents that adversely affect the properties of finished products or reduce the efficiency of the conversion processes. Treating can involve chemical reaction and/or physical separation. Typical examples of treating are chemical sweetening, acid treating, clay contacting, caustic washing, hydrotreating, drying, solvent extraction, and solvent dewaxing. Sweetening compounds and acids desulfurize crude oil before processing and treat products during and after processing.
Following the Second World War, various reforming processes improved gasoline quality and yield and produced higher-quality products. Some of these involved the use of catalysts and/or hydrogen to change molecules and remove sulfur. A number of the more commonly used treating and reforming processes are described in this chapter of the manual. History of Refining : Year/Process Name/Purpose/Product 1862 Atmospheric distillation Produce kerosene Naphtha, tar, etc. 1870 Vacuum distillation Lubricants (original) Asphalt, residual Cracking feedstocks (1930's) Coker feedstocks 1913 Thermal cracking Increase gasoline Residual, bunker fuel 1916 Sweetening reduce sulfur & odor Sulfur 1930 Thermal reforming Improve octane number Residual 1932 Hydrogenation Remove sulfur Sulfur 1932 Coking Produce gasoline basestocks Coke 1933 Solvent extraction Improve lubricant viscosity index Aromatics 1935 Solvent dewaxing Improve pour point Waxes 1935 Cat. polymerization Improve gasoline yield Petrochemical & octane number feedstocks 1937 Catalytic cracking Higher octane gasoline Petrochemical feedstocks 1939 Visbreaking reduce viscosity Increased distillate,tar 1940 Alkylation Increase gasoline octane & yield High-octane aviation gasoline 1940 Isomerization Produce alkylation feedstock Naphtha 1942 Fluid catalytic cracking Increase gasoline yield & octane Petrochemical feedstocks 1950 Deasphalting Increase cracking feedstock Asphalt 1952 Catalytic reforming Convert low-quality naphtha Aromatics 1954 Hydrodesulfurization Remove sulfur Sulfur 1956 Inhibitor sweetening Remove mercaptan Disulfides 1957 Catalytic isomerization Convert to molecules with high Alkylation feedstocks octane number 1960 Hydrocracking Improve quality and reduce Alkylation feedstocks sulfur 1974 Catalytic dewaxing Improve pour point Wax 1975 Residual hydrocracking Increase gasoline yield from Heavy residuals residual Reff : OSHA Technical Manual , Section IV Chapter 2 , 2003

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Introduction to Petroleum Refinery Operations

INTRODUCTION. A petroleum refinery is a manufacturing operation where crude petroleum, the raw material, is converted into usable finished products. In other words, it is the manufacturing phase of the oil industry. This chapter presents a general introduction to overall refinery operations as a forerunner to the detailed information on specific processes and products which follows, and the technologies that are applied to pressure relief operations. Other chapters cover the major operations and processes used in refining, and discuss the critical properties and end uses of the products. However, it should be emphasized that a refinery is only one of the major phases of the petroleum industry; others being exploration, production, transportation, and marketing, and a variety of feedstock chemicals that supply the raw materials for various product lines. Research and engineering might also be listed, but they are, in reality, a necessary and integral part of each of the phases.
REFINERY OPERATIONS The function of the refinery is to convert crude oil into the finished products required by the market in the most efficient, and hence most profitable manner. The methods employed necessarily vary widely from one refinery to another, depending on the crude processed, the nature and location of the market, the type of equipment available, and many other factors. However, for simplification, it may be considered that all refining processes fall into one of four basic categories. The first category is fractionation or distillation. This method of physically separating a mixture of compounds was the earliest process used in petroleum refining, and today is still one of the most important. However, since it is not generally possible to separate the complex petroleum mixtures into individual compounds, such mixtures are segregated into fractions or "cuts", each of which is characterized by a carefully controlled boiling range. These cuts are then further processed or utilized in the refinery operations. The second basic type of process, essentially chemical in nature, consists of converting or chemically transforming certain of these "cuts" into products of higher commercial value. There are many ways of doing this, but all consist fundamentally of altering the molecular structure of the components. In the case of a heavy oil, the molecules may be cracked to form lighter, more valuable products, as for instance in catalytic cracking and coking. On the other hand, gaseous products may be polymerized or otherwise combined to form liquid products which may be blended into gasoline. With certain processes, e.g. catalytic reforming, both cracking and polymerization take place concurrently with the more desirable de-hydrogenation, hydrogenation, and isomerization reactions. The net result of all these transformations is the production of mixtures containing new arrays of hydrocarbons of higher value than the starting materials. Nearly all the fractions produced by the processes mentioned above contain certain objectionable constituents or impurities. The third basic category is, therefore, treating. This group of processes includes the removal of the unwanted components, or their conversion to innocuous or less undesirable compounds. Removal of the impurities is sometimes accomplished by physical treating, as exemplified by the process for manufacturing kerosene, wherein sulfur and certain undesirable hydrocarbons are removed by extraction with liquid sulfur dioxide. Alternatively, the removal may be carried out by converting the unwanted compounds to a form more readily removed as is done in the hydrodesulfurization of diesel fuel. Here the sulfur compounds are cracked and hydrogenated. The sulfur is converted to hydrogen sulfide which can be readily separated from the heavier diesel oil by fractionation. An example of the conversion of undesirable components to innocuous compounds which remain in the product is found in the gasoline sweetening processes. There the mercaptans present give the product a foul, objectionable odor. The sweetening process Introductionto Petroleum Refinery Operations merely transforms the mercaptans to organic disulfides which are less objectionable. Although sulfur is perhaps the commonest and most troublesome of the impurities found in petroleum, it is certainly not the only one. Substances such as nickel, vanadium, and nitrogen may also be present in the crude oil. These impurities are undesirable because of the difficulty they cause during processing in the refinery or because of some detrimental effect during consumer use of the product. Furthermore, presence of certain hydrocarbons or certain types of hydrocarbons may lower the quality of a specific product. It was mentioned that aromatics are removed from kerosene by SO, extraction. The aromatics have undesirable burning characteristics and hence the product quality is improved if these "impurities" are removed. Lube oil treating process such as dewaxing, deasphalting, and phenol treating also fall into this category. The fourth basic category is blending of the finished cuts into commercially saleable products such as motor gasoline, kerosene, lubricating oils, and bunker fuel oil, according to their specifications. These four basic categories encompass the fundamental operation of a refinery. All other activities are carried out to implement them. The specifications for a given product are established to insure a satisfactory level of product performance. Specifications can be altered from time to time, but a product normally must meet the then existing product specifications. Various crudes on the other hand yield fractions with significantly different properties. At first glance, it might appear reasonable to select crudes to best match the product needs of each refinery. Many times, however, this is not economical as the money saved in eliminating various conversion and treating processes is offset by other factors. These might include crude availability, price, and transportation or specialty product requirements. A refinery is a sophisticated multi-component process operated in overall balance. The balance is set by economic considerations with the major variables being crude oil, process costs, and final products. It is thus easier to see why (1) no two refineries are exactly alike, (2) various conversion and purification processes are required, and (3) crude selection is important. TYPES OF REFINERIES Each refinery is designed to manufacture products as economically as possible based on the best knowledge available with regard to end product needs, future expansion plans, crude availability and other pertinent factors. A basic modern refinery which does not produce lubricating oils or chemicals is commonly referred to as a fuel products refinery. It is designed to produce primarily motor gasoline, distillate fuels (diesel oil, jet fuel, and heating oil), and bunker (residual) fuel oil. The fuel products refineries can be considered basic and minimum as regards refinery product and processing requirements. Hydroskimming and conversion are the two major variations of this type refinery. There is a wide range of conversion levels. The term maximum conversion type has no precise definition but is often used to describe a level of conversion ,where there is no net fuel oil manufacture. A fuel products refinery with specialities may manufacture lubricating oils, asphalts, greases, solvents, waxes and chemical feed stocks in addition to the primary fuel products. The number and diversity of products will naturally vary from one refinery to another. Refineries produce chemical feed stocks for sale to the chemical affiliates and do not have responsibility for the manufacture of chemical products directly. Both operations may be carried out at the same physical location but the corporate product responsibilities are usually separate. FUEL PRODUCTS REFINERY Hydroskimmer A hydroskimming refinery lends itself to locations where the market demands for the major fuel products (gasoline, gas oil, and residual fuel oil) approximate the quantities of these products obtainable by distillation from the available crudes. A typical hydroskimming refinery would include the following:
  1. Atmospheric Pipestill
  2. Powerforming (Catalytic Naphtha Reforming)
  3. Light Ends Recovery -Fractionation
  4. Treating and Blending
The atmospheric pipestill performs the initial distillation of crude oil into gas, naphtha, distillates, and residuum. The naphtha may be separated into gasoline blending stock, solvents, and Powerformer feed. The distillates include kerosene, jet fuel, heating oil and diesel oil. The residuum is blended for use as bunker fuel oil. The Powerforming unit is required to upgrade virgin naphtha to produce high octane gasoline. Powerforming is a fixed bed catalytic reforming process employing a regenerable platinum catalyst. In the process, a series of reactions takes place. The most important of these is aromatization; other reactions include isomerization, cracking, hydrogenation, and polymerization. The desired product is of approximately the same boiling range as the feed, but the molecules have been rearranged or reformed into higher octane compounds. Light ends recovery and fractionating equipment is necessary after the Powerformer and on the pipestill overhead stream to separate the effluent mixtures into the desired boiling range cuts. Hydrofining is used to reduce sulfur and/or other impurities and to improve odor, color, and stability of the pipestill fractions. Hydrofining is a fixed-bed catalytic process using a regenerable cobalt molybdate catalyst in a hydrogen atmosphere. The hydrogen is produced by the Powerformer with supplemental hydrogen manufactured if necessary. The difficulty of hydrofining (desulfurization) increases with increase in the hydrocarbon boiling point. Naphthas are generally desulfurized up to 99+ % by hydrofining while the maximum desulfurization of distillates is usually 90 %. The components produced by the process sequence outlined above are blended as required to meet final product rates and qualities. Conversion The hydroskimming type refinery is used where the gasoline demand is substantially lower and hence the final product demand is close to that yielded by single stage distillation. In areas where the demand for gasoline is relatively high, conversion processing is required. The minimum processes for a fuel products refinery designed would typically include:
  1. Atmospheric and Vacuum Crude Distillation
  2. Catalytic Gas Oil Cracking
  3. Powerforming
  4. Light Ends Recovery -Fractionation
  5. Treating and Blending
The atmospheric P/Sresiduum can be fed to a vacuum pipestill. The vacuum tower enables the refiner to cut deeper into the crude, at the same time avoiding high temperatures (above about 750 OF) which cause thermal cracking with resultant deposition of coke and tarry residues in the equipment. The vacuum gas oil produced by vacuum distillation is fed to a catalytic crackmg unit for conversion into high octane gasoline blending stock. Byproducts are gas, distillate, cycle gas oil, and fractionator bottoms. The process uses a fluidized catalyst system. The catalyst is circulated continuously between the reactor where cracking takes place and the regenerator where the coke deposited on the catalyst is burned off. The major competing process is hydrocracking which offers greater conversion and flexibility but usually requires a higher investment. Hydrocracking is a fixed bed catalytic process which cracks and hydrogenates hydrocarbon feeds. The process consumes large quantities of hydrogen and a hydrogen plant is usually necessary to support the operation. Practically any stock can be hydrocracked, including refractory feeds which resist conversion by other processes. In general, the very heavy residuum from the vacuum pipestill does not make good quality feed for catalytic cracking. In the refinery shown it is blended into residual fuel oil. Many times, however, the market for large volumes of residual fuel oil does not exist. When this is the case, additional conversion units are added to further process the vacuum pipestill bottoms. In other words, the higher the conversion of the refinery the more lighter fractions are produced. The relative levels of conversion vary from refinery to refinery. A typical maximum conversion type refinery is shown in Figure 3. The higher conversion levels are obtained by ad&tional processing of the bottoms and/or light ends. To increase conversion of the bottoms the amount and/or severity of processing is increased. The resulting fuel oil levels may decrease to zero. Included here in addition to the basic components of a conversion refinery may be fluid coking, delayed coking, and/or visbreaking. These processes are basically thermal cracking processes for reducing the volume and viscosity of the vacuum residuum while producing appreciable quantities of lighter products. Each of the three processes is commercially used with selection based on particular needs at a given refinery. Some of the various characteristics include: 1. Coking-Delayed Coking and Fluid Coking are the two major variations of this process. Fluid coking produces less coke as compared with delayed coking and hence yields a better product distribution. That is, for a given product slate less crude is converted into coke. The coke produced by fluid coking, however, is of little value as it consists of fine hard particles in contrast to large pieces for delayed coke. This difference in size and texture is important to electrode manufacturers who historically have used delayed coke. 2. Visbreaking is the least expensive of the cracking processes but is limited to the lowest conversion of perhaps 20 to 25% of the feed to 680 "F material. To obtain light ends conversion, alkylation and polymerization are used to increase the relative amounts of liquid fuel products manufactured. Alkylation converts olefins, (propylene, butylenes, amylenes, etc.), into high octane gasoline by reacting them with isobutane. Polymerization involves reaction of propylene and/or butylenes to produce an unsaturated hydrocarbon mixture in the motor gasoline boiling range. An old variation of the conversion type is a catalytic combination unit. Development of this scheme was necessitated by the rising cost of refinery construction after World War I1 and by the great demand for capital for postwar expansion. The scheme reduced the investment and operating costs for refining equipment. The basic feature of the combination unit lies in the integration of the fractionation facilities of the reduced crude distillation and catalytic cracking sections. A FUEL PRODUCTS REFINERY WITH SPECIALTIES A fuel products refinery with specialties may manufacture products such as lubricating oils, asphalts, greases, solvents, waxes and chemical feed stocks in addition to the primary fuel products. The number and diversity of products will naturally vary from one refinery to another, but for purposes of discussion a fuel products refinery with specialties may include many of the following processes. 1. Two-Stage Crude Distillation (Atmospheric and Vacuum) -The vacuum stage can be used alternately to produce heavy gas oil for catalytic cracking feed or raw lube distillate cuts for lubricating oil manufacture. 2. Virgin Naphtha Catalytic Reforming (Powerforming) -This technique is used for the production of high octane motor gasoline, or as a source of aromatic compounds. 3. Light Ends Recovery, Fractionation, and Conversion -Propylenes and butylenes may be recovered for feed to a polymerization plant for production of high octane gasoline; or chemicals. Butylenes and isobutane may be desired for use in an alkylation plant where they are combined to make aviation gasoline and motor gasoline blendstocks. Propanes and butanes may be recovered in essentially pure form for sale as liquefied petroleum gases. It may be profitable to recover ethylene for chemical production. Certain of the light ends components, particularly ethylene, propylene, and butadiene are so in demand that processes such as steam cracking are employed specifically for their 4. Fuel Products Treating a. Sweetening -This is a process for improving odor of gasolines, kerosenes, and heating oils. The foul smelling mercaptans are converted into bisulfides whose odor is much less objectionable. Among the types in use are copper chloride, hypochlorite, Merox, Mercapfining, and air inhibitor sweetening. b. Hydroprocessing -The nomenclature system with regard to hydrogen processing is quite confusing with an array of labels involving trade names, terms such as mild, medium, and severe, high and low pressure. Choice of terminology varies widely from company to company. A wide variety of petroleum fractions may be treated at elevated temperature and pressure with hydrogen in the presence of a catalyst to reduce sulfur, improve stability, odor, combustion characteristics, appearance, and to convert heavy fractions to lighter more valuable products. The most severe form of hydroprocessing as discussed previously is hydrocracking. For fuel products treating, however, two less severe hydroprocessing operations are used, hydrofining and hydrotreating. Hydrofining usually involves only minor molecular changes of the feed with hydrogen consumption in the range of about 100 to 1,0oO cu.ft./bbl. Typical applications include desulfurization of a wide range of feeds (naphtha, light and heavy distillates, and certain residua) and occasional pretreatment of cat cracker feeds. Hydrotreating essentially involves no reduction in molecular size with hydrogen consumption less than about 100 cu. ft./bbl. Primary application is to remove small amounts of impurities with typical uses including naphtha and kerosene hydrosweetening. c. SO, Extraction -This is a method of solvent extraction with liquid SO, to remove aromatic hydrocarbons and cyclic sulfur compounds. It is used to improve the burning qualities of kerosene and diesel fuels, and to reduce sulfur. This process has practically been supplanted by other solvent extraction or by hydrotreating. 5. Fluid catalytic Cracking. 6. Hydrocracking. 7. Residuum Conversion -Included here may be fluid coking, delayed coking, visbreaking, and residuum hydroprocessing. 8. Solvent Deasphalting -This is the solvent extraction of virgin residuum to remove asphaltenes or other tarry constituents. The deasphalted oil may be further processed into lubricating oils and greases, or used as cat cracking feed. 9. Lubricating Oil Manufacture -This will usually consist of the following processes: &. Solvent Deasphalting. Phenol Treating -An extraction process for removal of aromatic asphaltic and sulfur compounds from the lube cut. Solvent Dewaxing -Waxy lube is diluted with a solvent such as propane or methyl ethyl ketone (MEK), and cooled to crystallize the wax which is then removed by filtration. 10. Grease Manufacture -Selected lube oil fractions 2::: blended with various metallic soaps to produce high viscosity lubricating greases. 11. Wax Manufacture -A waxy distillate cut frox i(ude or the wax byproduct from lube oil dewaxing is first deoiled. Resulting low oil content wax is hydrofined for color improvement and fractionated into appropriate melting point grades. 12. Asphalt Manufacture -Saleable asphalts are produced from the residua of selected crudes. The residuum itself may be sold as straight reduced cuts to make it easier to handle, producing the so called cut-back asphalts. Another variation is air blown or oxidized asphalts for improved tenacity, greater resistance to weathering, and decreased brittleness. Emulsified asphalts are made for application at relatively low temperatures. 13. Chemical and Other Specialty Manufacture -A wide variety of products may be derived from petroleum feed stocks, including such diverse materials as alcohols, butyl rubber, sulfur, additives, and resins. Other specialties such as solvent naphthas, white oils, Isopars, Varsol, may also be produced. As indicated previously the respective chemical affiliate usually has responsibility for products broadly classified as petrochemicals. There are many other processes used in refineries not mentioned here. The list above is intended only to emphasize the wide diversity of processing which is common to petroleum refining and to introduce in a very general way some of the more important of these processes. Also it must be emphasized that only fundamental principles of refinery operations have been discussed and modem manufacturing techniques vary widely from company to company.

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Monday, June 9, 2008

CO2 Removal : DEA , ACT-1, MDEA & Piperazine

CO2 Removal : DEA , ACT-1, MDEA & Piperazine Carbon Dioxide (CO2) gas must be removed and recovered from ammonia process gas to make it fit for the synthesis reaction and later used for urea production. The removal of CO2 gas in ammonia plant is considered as a key stage in ammonia production. Organic amines (Primary, Secondary & Tertiary) have the ability to perform alone, or in combination with an inorganic salt the CO2 removal from gas mixture. The analysis of these organic amines in the scrubbing solution is usually performed by a recommended traditional procedure supplied by manufacturer, where the concentration of the concerned amine is determined by spectrophotometric or potentiometric methods.
These methods suffer from many disadvantages like interference with degraded amine products & carbon dioxide. Furthermore, these methods are not accurate and are unsuited to distinguish between different amines. The method gives the specific determination of each amine like (DEA, ACT-1, MDEA & Piperazine). The method is simple, accurate and allows the determination of amines even in CO2 loaded solution. Profitability and reliability in ammonia plants depends heavily on the efficiency of the CO2 removal from process gas. New technologies have dramatically improved the absorption rate efficiency, reduced CO2 slip to a few parts per million by volume, lowered energy requirements for CO2 regeneration and minimised corrosion in plant equipment. In addition, emerging technologies now apply non-toxic scrubbing solutions. Primary and secondary Organic amines, Monoethanol amine (MEA) and Diethanolamine (DEA) are currently employed alone and or in combination with hot potassium carbonate solution to catalyse the CO2 removal Process[1]. They achieve this catalysis by increasing the absorption rate of the chemical reaction between CO2 gas and the solution. Tertiary amines, Methyldiethanol amine (MDEA) on the other hand do not have a hydrogen atom attached to the nitrogen. The CO2 reaction can only occur after the CO2 dissolves in the water to from a bicarbonate ion. The bicarbonate formation is slow and only occurs in the liquid phase. Thus to effectively use MDEA for bulk CO2 removal, the liquid phase residence time should be high so that the CO2 reaction occurs efficiently. The disadvantage of using MDEA alone was solved by addition of an activator, namely Piperazine a cyclic amine, which has revolutionised the technology for CO2 removal. CO2 absorption by pure MDEA is quite slow but Piperazine enhances the absorption rate. The variation of the activator concentration can shift the thermodynamic behaviour in terms of process economics, reliability, energy consumption, corrosion control etc. Unlike MEA and DEA, the inability of tertiary amine to react with CO2 to form amides and subsequently amine carbamate may be the reason why these are less corrosive. Amines are usually prone to foaming but such tendency is not pronounced with MDEA solution. A mild dose of antifoam agent controls containment-induced foaming. Activating Agent in CO2 Removal :
  1. Diethanolamine (DEA) is a secondary amine : HO-CH2-CH2
  2. ACT-1 used in Ammonia -2 is a ploy alkyl amine. It is a proprietary chemical supplied by UOP Incorporated, USA
  3. Methyl Diethanol amine (MDEA) a tertiary amine : HO-CH2-CH2 NCH3 MDEA HO-CH2-CH2
  4. Piperazine is a cyclic amine which as an activator in scrubbing solution.
Each scrubbing solution has its own amine to promote the efficiency of the CO2 removal. Licensors supplied method to test their solution. Hence, Lab has been adopting three methods to quantify the amine content in its scrubbing solutions. Many times the inaccuracy was obvious. Samples of the same solution at different stages of the same system gave different results on the same amine. Specification check results on new chemical consignment lead to dispute with suppliers. Several check samples were done during CO2 slip to ascertain the amine content. Apart from involving three different methods there were many problems associated with these determinations.

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Wednesday, May 28, 2008

Temperature Control : Tuning a PID

Tuning a temperature controller involves setting the proportional, integral, and derivative values to get the best possible control for a particular process. If the controller does not include an autotune algorithm, or if the autotune algorithm does not provide adequate control for the particular application, then the unit must be tuned using trial and error. There are other tuning procedures which can also be used, but they all use a similar trial and error method.
Note that if the controller uses a mechanical relay (rather than a solid state relay), a longer cycle time (20 seconds) should be used when starting out.
  1. Cycle time - Also known as duty cycle; the total length of time for the controller to complete one on/off cycle. Example: with a 20 second cycle time, an on time of 10 seconds and an off time of 10 seconds represents a 50 percent power output. The controller will cycle on and off while within the proportional band.
  2. Proportional band - A temperature band expressed in % of full scale or degrees within which the controller‘s proportioning action takes place. The wider the proportional band, the greater the area around the setpoint in which the proportional action takes place. This is sometimes referred to as gain, which is the reciprocal of proportional band.
  3. Integral, also known as reset, is a function which adjusts the proportional bandwidth with respect to the setpoint to compensate for offset (droop) from setpoint; that is, it adjusts the controlled temperature to setpoint after the system stabilizes.
  4. Derivative, also known as rate, senses the rate of rise or fall of system temperature and automatically adjusts the proportional band to minimize overshoot or undershoot.
A PID (three mode) controller is capable of exceptional control stability when properly tuned and used. The operator can achieve the fastest response time and smallest overshoot by following these instructions carefully. The information for tuning this three mode controller may be different from other controller tuning procedures. Normally a SELF TUNE feature will eliminate the need to use this manual tuning procedure for the primary output; however, adjustments to the SELF TUNE values may be made if desired. A. TUNING OUTPUTS FOR HEATING CONTROL
  1. Enable the OUTPUT(S) and start the process.
  2. The process should be run at a setpoint that will allow the temperature to stabilize with heat input required.
  3. With RATE and RESET turned OFF, the temperature will stabilize with a steady state deviation, or droop, between the setpoint and the actual temperature. Carefully note whether or not there are regular cycles or oscillations in this temperature by observing the measurement on the display. (An oscillation may be as long as 30 minutes.)The tuning procedure is easier to follow if you use a recorder to monitor the process temperature.
  4. If there are no regular oscillations in the temperature, divide the PB by 2 (see Figure 1). Allow the process to stabilize and check for temperature oscillations. If there are still no oscillations, divide the PB by 2 again. Repeat until cycles or oscillations are obtained. Proceed to Step 5.
  5. If oscillations are observed immediately, multiply the PB by
  6. Observe the resulting temperature for several minutes. If the oscillations continue, increase the PB by factors of 2 until the oscillations stop.
  7. The PB is now very near its critical setting. Carefully increase or decrease the PB setting until cycles or oscillations just appear in the temperature recording.
  8. If no oscillations occur in the process temperature even at the minimum PB setting of 1%, skip Steps 6 through 11 below and proceed to paragraph B.
  9. Read the steady-state deviation, or droop, between setpoint and actual temperature with the “critical” PB setting you have achieved. (Because the temperature is cycling a bit, use the average temperature.)
  10. Measure the oscillation time, in minutes, between neighboring peaks or valleys (see Figure 2). This is most easily accomplished with a chart recorder, but a measurement can be read at one minute intervals to obtain the timing.
  11. Now, increase the PB setting until the temperature deviation, or droop, increases 65%. The desired final temperature deviation can be calculated by multiplying the initial temperature deviation achieved with the CRITICAL PB setting by 1.65 (see Figure 3) or by use of the convenient Nomogram I (see Figure 4). Try several trial¬and-error settings of the PB control until the desired final temperature deviation is achieved.
  12. You have now completed all the measurements necessary to obtain optimum performance from the Controller. Only two more adjustments are required - RATE and RESET.
  13. Using the oscillation time measured in Step 7, calculate the value for RESET in repeats per minutes as follows: RESET = (8/5) x (1 /To) Where To = Oscillation Time in Minutes.
  14. Again using the oscillation time measured , calculate the value for RATE in minutes as follows : RESET = To / 10 Where TO = Oscillation Time
  15. If overshoot occurred, it can be eliminated by decreasing the RESET time. When changes are made in the RESET value, a corresponding change should also be made in the RATE adjustment so that the RATE value is equal to : RATE = 1 / (6 x Reset Value )i.e., if reset = 2 R/M, theRATE = 0.08 min.
  16. Several setpoint changes and consequent RESET and RATE time adjustments may be required to obtain the proper balance between “RESPONSE TIME” to a system upset and “SETTLING TIME.” In general, fast response is accompanied by larger overshoot and consequently shorter time for the process to “SETTLE OUT.” Conversely, if the response is slower, the process tends to slide into the final value with little or no overshoot. The requirements of the system dictate which action is desired.
  17. When satisfactory tuning has been achieved, the cycle time should be increased to save contactor life (applies to units with time proportioning outputs only (TPRI)). Increase the cycle time as much as possible without causing oscillations in the measurement due to load cycling.

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