CN1204038C - CO isothermal sulfur resistant conversion process - Google Patents

CO isothermal sulfur resistant conversion process Download PDF

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Publication number
CN1204038C
CN1204038C CN 01142861 CN01142861A CN1204038C CN 1204038 C CN1204038 C CN 1204038C CN 01142861 CN01142861 CN 01142861 CN 01142861 A CN01142861 A CN 01142861A CN 1204038 C CN1204038 C CN 1204038C
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gas
reactor
reaction
isothermal
conversion process
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CN1429764A (en
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李欣
张新堂
毛鹏生
孙海燕
纵秋云
田兆明
陈依萍
白志敏
郭建学
余汉涛
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China Petroleum and Chemical Corp
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Qilu Petrochemical Co of Sinopec
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Abstract

The present invention relates to an isothermal sulfur resistant conversion process by using reaction of carbon monoxide and steam to generate hydrogen and carbon dioxide. The process can be used for preparing ammonia synthesis gas, hydrogen, city gas, OXO synthesis gas, etc. The process adopts water, steam and/or other circulatory mediators for shifting out heat of reaction, and the reaction temperature can be controlled by regulating the pressure and/or the flow capacity of circulatory mediators. By adopting the method, the bed temperature of a reactor is controlled near an isothermal level, and the present invention also has the advantages of simple operation and stable control. The low-temperature conversion activity of the catalyst can be fully exerted, and the life time of the catalyst can also be obviously prolonged. The process invented by the method has obvious energy conservation effects, and the CO content of an exit port can be reduced to a sufficient low level under the condition of not substantial increase of the catalyst dosage. The process can be used for moderate-temperature sulfur resistant conversion, can also be used for low-temperature sulfur resistant conversion, and is especially suitable for the sulfur resistant conversion with a high CO content.

Description

A kind of CO isothermal sulfur-tolerant conversion process
Technical field
The present invention relates to a kind of isothermal sulfur-tolerant conversion process that carbon monoxide and steam reaction are produced hydrogen and carbonic acid gas that is used for.
Background technology
The CO transformationreation plays an important role in synthetic ammonia, oxo-synthesis gas and town gas engineering, and the energy consumption of conversion section is occupied suitable ratio in whole energy consumption, in recent years, the conversion type of furnace, conversion process are optimized, transform, when reducing steam consumption, the high and low position heat energy of fully recycling transformation system will be one of energy-saving and cost-reducing important channel of synthesis ammonia plant.
In traditional CO sulfur resistant conversion process, reaction is carried out in the common response device, is in adiabatic condition, has following drawback: move because the most of catalyzer in the beds is in higher temperature, its life-span must be affected; Temperature of reactor is difficult to control, occurs fluctuation easily; Catalyst vulcanization process complexity, and be easy to generate the sulfuration overtemperature; Need extra start up boilers, so as to catalyzer heat up, sulfuration etc.; Owing to be subjected to the influence of thermal insulation warming, reactor outlet CO concentration is subjected to the equilibrated restriction, is difficult to the level that reaches lower; Be subjected to the restriction of factors such as catalyst shape, type of feed, gas distribution is inhomogeneous; The shift converter volume is big, the flow process complexity.
Summary of the invention
The objective of the invention is to overcome the deficiencies in the prior art part, a kind of new CO sulfur resistant conversion process is provided.Compared with prior art, this technology has characteristics such as temperature operation is steady, control is simple, easy to operate, and flow process is short, and outlet CO minimum content is low.
In order to achieve the above object, technology of the present invention mainly is made up of reactor assembly and heat recuperation-temperature controlling system.
Reactor assembly of the present invention can be an independently reactor, also can adopt a plurality of reactors in series, the in parallel use.Catalyzer both can be seated in a series of tube banks of shell and tube reactor, also can directly be seated in the tower tank reactor of built-in heat exchange coil.The purpose that adopts this special reaction device structure is the heat that produces in the CO transformationreation process in order to remove fast, thereby reaches isothermal purpose.The heat-transfer medium that is used to remove reaction heat of the present invention mainly is a water, promptly so-called saturation water-steam system.Certainly, also can adopt other similar material, its objective is in reaction process and remove reaction heat fast.
Isothermal sulfur-tolerant conversion process of the present invention, unstripped gas is at first through the gas heater heating, enter isothermal sulfur-tolerant conversion reactor (the tower tank reactor of shell and tube reactor or built-in coil pipe) then, the process gas of leaving reactor enters into next workshop section (purification section) through after the heat exchange.The steam that produces in the shell and tube reactor reaction process enters and obtains circulation or recovery in the water-steam drum that is located at outside the reactor; Coil pipe in tower tank reactor heat-transfer medium cycling element and the heat exchange unit outer with being located at reactor is connected, and heat-transfer medium is removed the reaction heat that produces in the reaction process.
For shell and tube reactor, catalyst loading is used for fluming water-steam and/or other heat-transfer medium between pipe in a series of tube banks of shell and tube reactor.When reaction process was stablized, the water level of bottom also tended towards stability between the pipe of reactor, and produced in a large number when hot when reaction, and the water of bottom inlet becomes water vapor fast, formation gas-liquid two-phase flow body in reactor assembly.Because the carburetion of saturation water, make the heat that produces in the reaction process to remove by the mode of steam.The band that leaves reactor press steam through pipe-line transportation in the drum of reactor outside, part is as heat recuperation, another part comes back to shift-converter after by condensation.Therefore, can reach isothermal purpose by the temperature that the internal circulating load or the pressure of steam regulation-saturation water system are regulated beds.Reduce as saturated water amount, can suitably be complemented in the saturator, little to the temperature effect of reactor assembly.There is not strict restriction for size, quantity and the length of tubulation, can be according to producing decisions such as load, process gas composition, but must be able to satisfy the requirement of catalyzer.In addition, the heat-transfer effect of tubulation will be got well, so that reaction heat in time can be delivered between pipe.
In the technology of the present invention, catalyzer also can directly be seated in the tower tank reactor, at this moment, is provided with an amount of heat exchange coil in the beds of reactor, and this coil pipe is embedded in the beds fully, and mobile is a heat-conducting medium in the pipe.Heat-conducting medium can be any mobile material, but the fluidic thermal capacitance should be enough big, so that can utilize effective flow just reaction heat in time can be shifted out beds in the unit time.As adopting this catalyst loading pattern, then above-mentioned drum part should correspondingly change heat-transfer medium cycling element and heat exchange unit into.The heat-transfer medium cycling element comprises heat-transfer medium and impels its round-robin handling equipment that in heat exchange unit, the contained reaction heat of heat-transfer medium is removed.
In the isothermal sulfur-tolerant conversion process of the present invention, reactor can be one section shift-converter, also can increase to the 2-3 section according to actual needs.
Isothermal sulfur-tolerant conversion process of the present invention, can be different the raw gas that produces of gas-making process as raw material.Typical process feed gas comprises: the synthetic gas that the residual oil partial oxidation process produces; The synthetic gas that coal water slurry gasification technology produces; The synthetic gas that the coal gasification method produces etc.Wherein, be particularly suitable for handling the higher synthetic gas of CO content, for example the high CO synthetic gas of producing by coal dust gasification.Under normal operational condition, butt CO forms can reach 75% even higher.For the lower low temperature shift process of CO content, the present invention is particularly suitable also, and the minimum outlet of shift converter this moment CO content can reach 1%.
In the technology of the present invention, the reactor operating temperature range is controlled at 180~450 ℃, pressure range between 1~10Mpa, and process gas sulphur content>0.01%V/V, water to steam ratio are 0.4~1.8.
Outstanding feature of the present invention is:
(1) adopt vapor pressure, heat-conducting medium flow to come the conditioned reaction temperature, production control and operate simple and flexible more;
(2) catalyzer is in comparatively in the demulcent isothermal reaction process, can prolong catalyzer work-ing life.
(3) catalyst vulcanization is simple, rapidly and do not have overheated danger, is difficult for producing the sulfuration overtemperature;
(4) the used vapour heat directly heats up to catalyzer, does not need extra start up boilers;
(5) can eliminate the restriction of the balance factor of the generation by thermal insulation to outlet CO minimum concentration, under identical condition, outlet CO content is starkly lower than traditional sulfur resistant conversion process.
Description of drawings
Fig. 1 is traditional sulfur resistant conversion process general flow chart.
Fig. 2 is an isothermal sulfur-tolerant conversion process sketch of the present invention.
Fig. 3 is the sketch of catalyst loading pattern 1 of the present invention.
Fig. 4 is the sketch of catalyst loading pattern 2 of the present invention.
General flow chart of the present invention as shown in Figure 2.Fluid in the pipeline 1 is the raw gas from gas making workshop section, and this coal gas passes through impurity such as washing tower 2 laggard one-step removal carbon blacks, and water/dry gas is adjusted to suitable level, and phlegma wherein enters the ground hyposulculus through pipeline 22.The process gas that goes out washing tower 2 obtains heating in gas heater 6 behind the outlet line 3 of washing tower 2 and pipeline 5, enter isothermal reactor 8 through the process gas of preheating through pipeline 7.Transformationreation is carried out in the tubulation tube bank that the isothermal sulfur-tolerant conversion catalyzer is housed.In case of necessity, this process gas can enter another unit such as temperature shift reaction such as grade.In isothermal reactor 8, the process gas and the water-steam between pipe of restraining by tubulation carry out the noncontact heat exchange, and reaction heat is restrained through tubulation and taken away by heat-transfer medium.
Portion water between reactor tube is vaporized owing to having absorbed a large amount of reaction heat, and pressure raises and enters respectively in the water- steam drum 10,16 that is located at separately outside the reactor through pipeline 9,15.In described drum 10,16, band presses steam to be transported to suitable steam pipe system through steam-pipe 11,17 respectively, so that further utilize.What of reaction heat vapor pressure in the drum 10 depend primarily on, and also is subjected to the restriction of its flow simultaneously.Saturation water in the drum 10,16 is back between the pipe of reactor by pipeline 12,18 respectively, and the process gas that goes out reactor 8 enters in the reactor 14 through piping 13, enters next workshop section through piping 19 then.The thermal source of gas heater 6 is carried by pipeline 20 and 21.
When the transformationreation temperature raises, can control by flow or the pressure of regulating water-steam.When owing to a large amount of delivery of steam when pipe network makes that the water yield reduces, it is additional pass through pipeline 23 (24 etc.).
Can come reactor assembly input N by pipeline 4 2Or in system, add steam.Particularly use latter stage, be necessary by normally carrying out that the mode of replenishing steam guarantees to react when catalyzer.In reactor assembly, feed N 2Mainly be to be used for purposes such as purging.
The process gas that gas heater 6 is mainly used in entering first shift converter heats, and is minimum with water of condensation content in the process gas that guarantees to enter reactor.The thermal source of gas heater 6 can be a steam, also can be the process gas of heat.
Fig. 3 is a catalyst loading pattern 1 of the present invention.In the suitable reactor of a volume, a series of tube banks that distributing equably, the quantity of tube bank and length are determined by factors such as conversion load and reaction conditionss.Catalyst loading is in tubulation, and mobile is the water-steam mixture two phase flow in the space between pipe.When reaction process was stablized, the water level of bottom also tended towards stability between reactor tube, and produced in a large number when hot when reaction, and unnecessary heat can be vaporized rapidly because of the water between pipe and is pulled away.Thereby the bottom between reactor tube, should keep the suitably water of height, so that the heat that produces in the reaction process in time can be removed.As mentioned above, can and or 24 replenish suitable water by pipeline 23.
Fig. 4 is a catalyst loading pattern 2 of the present invention.Reactor among the figure is similar to the reactor that is adopted in traditional sulfur resistant conversion process.Different is that one or one group of coil pipe that supplies heat exchange to use have been placed by portion within it.This coil pipe is embedded in the beds fully, and circulation is heat-conducting medium in the pipe.As adopt catalyst loading pattern shown in Figure 4, corresponding heat-transfer medium cycling element and the heat exchange unit of changing into of the drum part among Fig. 2.This cycling element comprises heat-transfer medium and impels its round-robin handling equipment that in described heat exchange unit, the contained reaction heat of heat-transfer medium is removed.
Embodiment
For characteristics of the present invention are described better, be described further below in conjunction with embodiment, but the present invention is not limited to following embodiment.
Embodiment 1
At pressure 4.0MPa, dry gas air speed 3000hr -1, water/dry gas ratio is 1.2, inlet gas is formed (butt) and is: CO 45.5%, CO 22.5%, H 2S 3000ppm, CH 40.4%, surplus is H 2Condition under, the situations such as reactor outlet CO of isothermal sulfur-tolerant conversion process are investigated.And compare with traditional sulfur resistant conversion process, the results are shown in table 1.Tradition conversion appreciation condition is an adiabatic reactor, and conversion conditions such as catalyst loading are identical with isothermal process of the present invention.
Traditional sulfur resistant conversion process of table 1 and isothermal sulfur-tolerant conversion process are relatively
Sequence number The tradition sulfur resistant conversion process Isothermal sulfur-tolerant conversion process
Temperature in (℃) Temperature out (℃) CO interconversion rate (%) Temperature of reaction (℃) CO interconversion rate (%)
1 180 313 91.1 180 91.9
2 250 408 96.4 250 96.7
3 285 438 94.2 285 95.6
4 300 449 91.8 300 94.5
5 450 495 88.5 450 91.3
Embodiment 2
Under identical entry condition, the active comparing result of 1000 hours front and back of catalyzer operation is listed in table 2.The activity rating condition is: pressure 4.0MPa, dry gas air speed 3000hr -1, water/dry gas 1.2, inlet gas is formed (butt): CO 45.5%, CO 22.5%, H 2S 3000ppm, CH 40.4%, surplus is H 2Tradition conversion appreciation condition is an adiabatic reactor, and conversion conditions such as catalyst loading are identical with isothermal process of the present invention.
Catalyst life relatively under the identical entry condition of table 2
Temperature in (℃) Hot(test)-spot temperature (℃) Temperature out (℃) CO interconversion rate (%)
Raw catalyst After 1000 hours
Traditional technology 285 435 408 94.2 90.5
Isothermal process 285 286.5 285 95.6 95.1
Embodiment 3
Under identical entry condition, the active comparing result of catalyzer under high CO condition listed in table 3.The activity rating condition is: pressure 4.0MPa, dry gas air speed 3000hr -1, water/dry gas 1.2.Inlet gas is formed (butt): CO 65.5%, CO 23.5%, H 2S 3000ppm, CH 40.4%, surplus is H 2Tradition conversion appreciation condition is an adiabatic reactor, and conversion conditions such as catalyst loading are identical with isothermal process of the present invention.
The contrast of table 3 under high CO entry condition
Sequence number The tradition sulfur resistant conversion process Isothermal sulfur-tolerant conversion process
Temperature in (℃) Temperature out (℃) CO interconversion rate (%) Temperature of reaction (℃) CO interconversion rate (%)
1 250 452 91.2 250 95.9
2 285 468 89.4 285 94.8
3 300 489 87.1 300 93.7
Embodiment 4
Under identical entry condition, the active comparing result of catalyzer under low inlet CO content condition sees Table 4.The activity rating condition is: catalyzer loading amount 100 grams, pressure 4.0MPa, dry gas air speed 3000hr -1, water/dry gas 1.2.Inlet gas is formed (butt): CO 1%, CO 238%, H 2S 3000ppm, CH 40.4%, surplus is H 2
The contrast of table 4 under low CO entry condition
Sequence number The tradition sulfur resistant conversion process Isothermal sulfur-tolerant conversion process
Temperature in (℃) Temperature out (℃) CO interconversion rate (%) Temperature of reaction (℃) CO interconversion rate (%)
1 250 254 69.1 250 69.9
2 285 291 67.9 285 68.6
3 300 307 66.7 300 66.8
Embodiment 5
Under the identical entry condition, isothermal process of the present invention and the traditional technology comprehensive contrast situation on large-scale plant is listed in table 5.Pressure 4.0MPa, total dry gas volumetric flow rate: 110000m 3/ hour, water/dry gas 1: 2,285 ℃ of temperature ins.Inlet gas is formed (butt): CO 45.5%, CO 22.5%, H 2S 3000ppm, CH 40.4%, surplus is H 2Tradition conversion appreciation condition is an adiabatic reactor, and conversion conditions such as catalyst loading are identical with isothermal process of the present invention.Catalyst loading in this example is in shell and tube reactor.
Two kinds of technology contrasts on large-scale plant of table 5
The catalyzer loading amount, m 3 The CO outlet, % Temperature out, ℃ The CO transformation efficiency, %
Traditional technology 10 20.859 364.89 44.80928
15 16.3455 391.16 55.07375
20 13.5745 409.34 61.77965
25 8.347 427.15 75.36429
30 6.3155 433.61 81.00397
35 4.352 439.32 86.66357
40 4.1565 444.68 87.23876
45 3.7825 447.14 88.34516
50 3.5955 449.76 88.90135
Isothermal process 10 19.1425 285.0 48.62125
15 15.808 285.2 56.34943
20 12.376 285.4 64.78252
25 11.3295 286.0 67.45741
30 8.957 285.8 73.71191
35 6.435 285.4 80.66627
40 4.407 285.1 86.50214
45 2.964 285.0 90.79456
50. 2.171 284.8 93.20509
Embodiment 6
Conversion condition: reaction pressure 8.25MPa, total dry gas volumetric flow rate: 65000m 3/ hour, water/dry gas 1.3, inlet gas is formed (butt): CO 46%, CO 20.1%, H 2S 3000ppm, CH 40.4%, surplus is H 2Catalyst loading in this example is in the tower tank reactor, and the inlet transformation temperature is 285 ℃.Reaction result is listed in table 6.
Table 6 catalyst loading is in the isothermal transform effect of tower tank reactor
The catalyzer loading amount, m 3 The CO outlet, % Temperature out, ℃ The CO transformation efficiency, %
Isothermal process 10 16.79 286.0 57.07
20 10.85 285.2 72.35
30 7.85 285.4 80.71
40 3.86 286.0 92.59
50 1.91 285.8 98.76

Claims (8)

1, a kind of carbon monoxide and steam reaction are produced the isothermal sulfur-tolerant conversion process of hydrogen and carbonic acid gas, comprising:
(1) catalyst loading is in the tube bank of shell and tube reactor;
(2) unstripped gas at first passes through gas heater, enters shell and tube reactor then, and the process gas of leaving reactor enters into purification section through after the heat exchange;
(3) steam that produces in the reaction process enters to be located at and obtains circulation or recovery in the outer water-steam drum of reactor.
2, isothermal sulfur-tolerant conversion process according to claim 1 is characterized in that described shell and tube reactor working pressure is between 1~10.0Mpa, and temperature of reaction is between 180~450 ℃.
3, isothermal sulfur-tolerant conversion process according to claim 1 is characterized in that in the described unstripped gas that CO contents on dry basis scope is 1~75%.
4, isothermal sulfur-tolerant conversion process according to claim 1 is characterized in that described unstripped gas comprises: the synthetic gas that coal water slurry gasification technology produces, the synthetic gas that the coal gasification method produces, the synthetic gas that the residual oil partial oxidation process produces.
5, a kind of carbon monoxide and steam reaction are produced the isothermal sulfur-tolerant conversion process of hydrogen and carbonic acid gas, comprising:
(1) catalyst loading is in the beds of the tower tank reactor of built-in coil pipe;
(2) unstripped gas at first passes through gas heater, enters the tower tank reactor then, and the process gas of leaving reactor enters into purification section through after the heat exchange;
(3) heat-transfer medium cycling element and the heat exchange unit outer with being located at reactor of the coil pipe in the tower tank reactor is connected, and heat-transfer medium is removed the reaction heat that produces in the reaction process.
6, isothermal sulfur-tolerant conversion process according to claim 5 is characterized in that described tower tank reactor working pressure is between 1~10.0Mpa, and temperature of reaction is between 180~450 ℃.
7, isothermal sulfur-tolerant conversion process according to claim 5 is characterized in that in the described unstripped gas that CO contents on dry basis scope is 1~75%.
8, isothermal sulfur-tolerant conversion process according to claim 5 is characterized in that described unstripped gas comprises: the synthetic gas that coal water slurry gasification technology produces, the synthetic gas that the coal gasification method produces, the synthetic gas that the residual oil partial oxidation process produces.
CN 01142861 2001-12-30 2001-12-30 CO isothermal sulfur resistant conversion process Expired - Lifetime CN1204038C (en)

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CN100336715C (en) * 2005-06-07 2007-09-12 昆明理工大学 Process for preparing hydrogen by part changing of yellow phosphorus tail gas
CN101157442B (en) * 2007-04-27 2010-07-21 中国石化集团宁波工程有限公司 Waste heat reclaiming process for CO transformation
CN101050390B (en) * 2007-04-27 2011-04-27 中国石化集团宁波工程有限公司 CO conversion technique matched to coal gasification
CN101704513B (en) * 2009-08-13 2011-11-16 上海国际化建工程咨询公司 Shunting-type isothermal sulfur-tolerant conversion process and equipment thereof
CN101955154A (en) * 2010-10-25 2011-01-26 付元波 Isothermal conversion process method for high-concentration carbon monoxide conversion
CN102001623B (en) * 2010-11-01 2012-08-29 中国五环工程有限公司 Process method for converting entrained-bed coal gasification high-concentration carbon monoxide
CN103508416B (en) * 2012-06-27 2015-05-20 中国石油化工股份有限公司 CO (Carbonic Oxide) sulfur-tolerant shift catalytic reaction process
CN102976270A (en) * 2012-09-18 2013-03-20 东华工程科技股份有限公司 Novel CO isothermal conversion method
CN103449365B (en) * 2013-04-28 2015-09-30 山东齐鲁科力化工研究院有限公司 Process for converting high-concentration CO-tolerant sulfur and device thereof
CN103641067A (en) * 2013-12-05 2014-03-19 天脊煤化工集团股份有限公司 Carbon monoxide isothermal-transformation process method
CN103881765B (en) * 2014-03-24 2015-07-08 中石化宁波工程有限公司 Split circulating CO transformation process
CN105561889A (en) * 2014-10-23 2016-05-11 新煤化工设计院(上海)有限公司 Radial flow by-product steam isothermal shift converter
CN112142003B (en) * 2019-06-27 2022-05-17 中石化南京化工研究院有限公司 Carbon monoxide conversion process

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