CN103013563B - A kind of method of lightweight C 5 fraction Hydrogenation ethylene cracking material - Google Patents
A kind of method of lightweight C 5 fraction Hydrogenation ethylene cracking material Download PDFInfo
- Publication number
- CN103013563B CN103013563B CN201110290488.2A CN201110290488A CN103013563B CN 103013563 B CN103013563 B CN 103013563B CN 201110290488 A CN201110290488 A CN 201110290488A CN 103013563 B CN103013563 B CN 103013563B
- Authority
- CN
- China
- Prior art keywords
- hydrogenation
- lightweight
- fraction
- raw material
- ethylene cracking
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
A method for lightweight C 5 fraction Hydrogenation ethylene cracking material, is carried out hydrogenation reaction by hydrogenation catalyst fixed bed in the presence of hydrogen gas by the lightweight C 5 fraction raw material of hydrogenation and is converted into stable hydrocarbon to make the unsaturated hydrocarbons in lightweight C 5 fraction raw material.Hydrogenation products part is common by hydrogenation catalyst fixed bed after returning and mixing with raw material as solvent, and the latter is 1 with the former charged material weight ratio: (6 ~ 10).First desulfurization is carried out by sweetening agent fixed bed before mixing with raw material as the hydrogenation products of solvent.Sweetening agent is the modified particles shaped activated carbon of load active ingredient, and active ingredient is CuO and Co
2o
3, in sweetening agent, the content of active ingredient is 1 ~ 5wt%, and the atomicity of Cu and Co ratio is 1: (0.2 ~ 0.8).The present invention can carry out hydrogenation to the lightweight C 5 fraction material that active sulfide content is 0.02wt about ‰, and sweetening agent and hydrogenation catalyst all can ensure long-term operation.
Description
Technical field
The present invention relates to a kind of method of hydrotreating of the C 5 fraction containing unsaturated hydrocarbons, particularly also contain the C 5 fraction of active sulfide through the method for hydrogenation reaction for the preparation of the raw material of cracking ethylene preparation by containing unsaturated hydrocarbons.
Background technology
The traditional raw material of industrial preparing ethylene by steam cracking is petroleum naphtha, and along with petroleum resources are day by day short, what oil refining process produced is main component with C4 ~ C6, and lighter hydrocarbons resource is also more come the more to be used.Relative to petroleum naphtha, lighter hydrocarbons are comparatively light due to component, therefore can obtain higher ethene and propene yield.But, containing higher unsaturated hydrocarbons in this light hydrocarbon materials, mainly comprise the alkynes of alkene, diolefine and small amount, under the hot environment of pyrolyzer, unsaturated hydrocarbons by being polymerized, the reaction such as cyclisation or condensation thus cause producing a large amount of cokings, therefore these light hydrocarbon materials elder generation must just can be used as the raw material of preparing ethylene by steam cracking after hydrogenation reaction makes unsaturated hydrocarbons be converted into stable hydrocarbon.As " C4 hydrogenation of olefins produces the technical study of feed ethylene " (" petrochemical technology and application ", 22nd volume the 5th phase, in September, 2004) literary composition describes and how the C4 fraction that catalytic cracking unit produces prepared ethylene cracking material after hydrogenation, and article has also systematically carried out the investigation of technique and catalyst stability.
The a considerable amount of C 5 fraction of byproduct in process of naphtha steam cracking ethene, the comprehensive utilization of current C 5 fraction most worthy produces the higher m-pentadiene of wherein economic worth, isoprene and dicyclopentadiene three kinds of diolefins by separation of extractive distillation.Before C 5 fraction separation of extractive distillation diolefin, first a part must be contained carbon five feed separation of carbon four lighter hydrocarbons out, this part material accounts for about the 20wt% of C 5 fraction total amount, industrially usually this material is called lightweight C 5 fraction.Lightweight C 5 fraction is also a kind of lighter hydrocarbons that can be used as preparing ethylene by steam cracking, wherein same containing higher unsaturated hydrocarbons, also must through hydrogenation reaction to remove unsaturated hydrocarbons before cracking.
The loaded catalyst that the desirable catalyzer of hydrogenation reaction of unsaturated hydrocarbon is is active ingredient with palladium metal or metallic nickel, classical as Pd/Al
2o
3catalyzer, Ni/ diatomite catalyzer etc.But day by day serious along with petroleum resources in poor quality trend, oil refining adopts the proportion of high sulfur content crude oil obviously to increase, a considerable amount of active sulfide is enriched in the light hydrocarbon materials that above-mentioned oil refining process produces, as thiomethyl alcohol, sulfur alcohol, dithiocarbonic anhydride and dimethyl sulfide etc., and palladium metal or metallic nickel very responsive to active sulfide, when the content of active sulfide in hydrogenation material is more than 0.003wt ‰, Pd/Al
2o
3, Ni/ diatomite one class hydrogenation catalyst is just easy to poisoning and loses activity.
The technical study of feed ethylene " the C4 hydrogenation of olefins produce " literary composition describe adopt the catalyzer of sulfide type to tackle common metal active constituent easily more poisoning by active sulfide the problem of inactivation, but this catalyzer is obviously not ideal enough for the Hydrogenation of diolefin, as described herein, when containing 1 of seldom amount in C4 fraction, during 3-divinyl, whole hydrogenation process must divide two sections to carry out, and is first the hydrogenation carrying out monoolefine after monoolefine again by di-olefins.First paragraph hydrogenation reaction is in order to avoid the autohemagglutination of diolefin, and hydrogenation process must control to carry out under the reaction conditions that intensity is very low.And the content of diolefin and alkynes is usually up to about 35wt% in lightweight C 5 fraction, the catalyzer of this sulfide type is not obviously suitable for the hydrogenation of lightweight C 5 fraction.
Having there is the desulfurization technology of multiple maturation in prior art, carries out desulfurization process as adopted gac as sweetening agent to the material of sulfur compound.Active carbon desulfurization mainly relies on the active group of activated carbon surface to realize the katalysis that sulfide and oxygen react, and be converted into elemental sulfur after sulfide reaction and be tightly held by activated carbon, therefore gac has catalysis and adsorption concurrently in sweetening process.Normal activated carbon is for H
2s mono-class inorganic sulfur has higher removal efficiency, and to organosulfur, particularly the effect that removes of lower boiling organosulfur is relatively poor.Prior art generally makes load iron in gac, copper, nickel, cobalt, chromium or the metallic compound such as basic metal, alkaline-earth metal carry out modification to gac by pickling process, to improve its catalytic adsorption performance to organosulfur.As " TheInfluenceoftheAdditionofCobalt, Nickel, MangancseandVanadiumtoActiveCarbononTheirEfficientlyinSO
2removalfromStackGases. " [" Fuel " 1992,71 (11)] literary composition describes Co
2+, V
5+, Ni
2+and Mn
4+introduce the result of study for active carbon desulfurization improved performance after gac Deng metal ion, the modified activated carbon of a certain amount of CuO of " research of modified activated carbon sorbent desulfurization performance " (" application chemical industry " 05 phase in 2010) one literary composition prompting load its to be desulphurizing activatedly significantly improved.
But, the desulfurization treatment temp that usual modified activated carbon is suitable is about 50 DEG C, and as previously mentioned, just very easily 1 of autohemagglutination is there is containing under relatively large room temperature in lightweight C 5 fraction, diolefin and the alkynes such as 3-divinyl, isoprene, cyclopentadiene and 2-butyne, the oligopolymer that polymerization produces can gather on modified activated carbon, covers the catalytic active site of modified active carbon surface and the micropore of blocking gac, and modified activated carbon is by the catalysis lost very soon sulfide and adsorption function.
Summary of the invention
The invention provides a kind of method of lightweight C 5 fraction Hydrogenation ethylene cracking material, hydrogenation reaction adopts active higher Ni/ diatomite catalyzer, the present invention coordinates conventional active carbon desulfurization technology, devise a kind of new hydrogenation technique flow process, technical problem to be solved still can carry out hydrogenation smoothly when active sulfide content is higher in raw material, and hydrogenation catalyst can keep hydrogenation activity for a long time.
Below the concrete technical scheme of the present invention:
A kind of method of lightweight C 5 fraction Hydrogenation ethylene cracking material, the method comprises by the lightweight C 5 fraction raw material of hydrogenation in the presence of hydrogen gas, carries out hydrogenation reaction be converted into stable hydrocarbon to make the unsaturated hydrocarbons in lightweight C 5 fraction raw material by hydrogenation catalyst fixed bed.The product section of hydrogenation reaction is common by hydrogenation catalyst fixed bed after returning and mixing with by the lightweight C 5 fraction raw material of hydrogenation as solvent, is 1: (6 ~ 10) by the lightweight C 5 fraction raw material of hydrogenation and the charged material weight ratio of the hydrogenation reaction product as solvent.
The present invention is different from prior art, and the hydrogenation products as solvent first carries out desulfurization by sweetening agent fixed bed before mixing with the lightweight C 5 fraction raw material by hydrogenation.The processing condition of desulfurization are: volume liquid hourly space velocity is 3.0 ~ 16.0hr
-1, system pressure is 0.2 ~ 0.6MPaG, and feeding temperature is 5 ~ 60 DEG C, and sweetening agent is the modified particles shaped activated carbon of load active ingredient, and its particle diameter is 3 ~ 6mm, and active ingredient is CuO and Co
2o
3, in sweetening agent, the content of active ingredient is 1 ~ 5wt%, and the atomicity of Cu and Co ratio is 1: (0.2 ~ 0.8).
Volume liquid hourly space velocity in above-mentioned desulfurization process conditions is preferably 4.0 ~ 12.0hr
-1; System pressure is preferably 0.3 ~ 0.5MPaG; Feeding temperature is preferably 10 ~ 40 DEG C; The granular active carbon of sweetening agent preferably selects ature of coal granular active carbon.
Above-mentioned hydrogenation reaction can adopt conventional processing condition, is generally: volume liquid hourly space velocity is 4.0 ~ 20.0hr
-1, system pressure is 1.0 ~ 4.0MPaG, and it is 20 ~ 100 DEG C that feeding temperature controls, by the lightweight C 5 fraction raw material of hydrogenation with the total amount of wherein unsaturated hydrocarbons, hydrogen be (2 ~ 5) by the molar ratio of the lightweight C 5 fraction raw material of hydrogenation: 1.The hydrogenation catalyst of recommendation of the present invention is to be taken Ni as active constituent and take diatomite as the loaded catalyst of carrier, and in catalyzer, the content of Ni is 30 ~ 50wt%.
In the processing condition of above-mentioned hydrogenation reaction, volume liquid hourly space velocity is preferably 6.0 ~ 12.0hr
-1; System pressure is preferably 1.5 ~ 3.0MPa; Feeding temperature is preferably 30 ~ 60 DEG C; Hydrogen be preferably (3 ~ 4) by the molar ratio of the lightweight C 5 fraction raw material of hydrogenation: 1; 1 is preferably: (7 ~ 9) by the lightweight C 5 fraction raw material of hydrogenation and the charged material weight ratio of the hydrogenation reaction product as solvent.
In technical scheme provided by the invention, the Ni/ diatomite catalyzer of employing is classical hydrogenation of unsaturated hydrocarbons catalyzer, this to be a kind of with Ni be active constituent and take diatomite as the loaded catalyst of carrier.Catalyzer can adopt conventional pickling process to be prepared, and first diatomite is configured as particle and obtains carrier, is then loaded on carrier by Ni by the solution impregnation containing Ni salt, then drying, high-temperature roasting, reduction treatment and the obtained finished catalyst that sieves.
The preparation of sweetening agent also adopts conventional method; as commercially available ature of coal granulated active carbon can be adopted as carrier; steeping fluid is mixed with water miscible Cu salt and Co salt (as cupric nitrate, Jing Ti/Bao Pian COBALT NITRATE CRYSTALS/FLAKES); loaded on gac by the salt of equi-volume impregnating by Cu, Co, then drying, roasting and the obtained sweetening agent finished product that sieves.
Because hydrogenation process is thermopositive reaction, usually need by being removed reaction heat to control the temperature of beds to adding solvent in the raw material of hydrogenation.The present invention adopts the alkane of C4 ~ C6 to be suitable in theory, and directly adopts hydrogenation products as solvent obviously economical rationality the most, and this is also industrial conventional operational means.The present invention make use of this point just, and its key problem in technology changes the traditional habit of raw material being carried out to desulfurization process before hydrogenation, desulfurization process is placed on after hydrogenation reaction and carries out for this part hydrogenation products returned as solvent.Owing to substantially not containing unsaturated hydrocarbons in hydrogenation products, the catalytic active site that avoiding problems the modified active carbon surface occurred because of gathering of oligopolymer in sweetening process is capped with the duct of gac blocked, and sweetening agent can keep higher sulfur removal rate for a long time.
On the other hand, through the hydrogenation products of desulfurization process as solvent after being mixed by required processing requirement by the raw material of hydrogenation, enter active sulfide content in the material of hydrogenation catalyst fixed bed and significantly reduce.The active sulfide generally contained in lightweight C 5 fraction Hydrogenation ethylene cracking material is 0.02wt about ‰, conveniently required solvent adding amount, enter active sulfide content in the material of hydrogenation catalyst fixed bed can guarantee to be reduced to 0.003wt less than ‰, this guarantees the ground steady running of hydrogenation catalyst energy long period.
Compared with prior art advantage of the present invention is very remarkable, can carry out hydrogenation to the lightweight C 5 fraction material that active sulfide content is 0.02wt about ‰, and sweetening agent and hydrogenation catalyst all can ensure long-term operation.Continuous operation 500 hours back end hydrogenation beds hydrogenation activities still can remain unchanged substantially, and sweetening agent also still maintains higher sulfur removal rate, and the actual service life of hydrogenation catalyst and sweetening agent can reach more than 8000 hours.
Lightweight C 5 fraction material carbon four unsaturated hydrocarbons wherein after hydrogenation is converted into butane, and chain carbon five and straight chain carbon five unsaturated hydrocarbons are separately converted to iso-pentane and Skellysolve A.Result of practical application shows, hydrogenation products is used for producing ethene with steam cracking process, and yield of ethene reaches about 35%, and propene yield reaches about 18%.
Below by specific embodiment, the invention will be further described, and in an embodiment, the definition of the saturation exponent of volume liquid hourly space velocity, unsaturated hydrocarbons is respectively:
Note: hydrogenation material is the mixture comprising the hydrogenation products as solvent and the lightweight C 5 fraction raw material by hydrogenation.
Embodiment
The lightweight C 5 fraction feed composition that embodiment adopts sees the following form:
[embodiment 1 ~ 10]
Hydrogenation reaction is carried out in stainless steel tubular reactor, and reactor is the very little stainless steel tubular reactor for φ 25mm × 1000mm of one ruler.Load 100mL hydrogenation catalyst in reaction tubes and form fixed bed, hydrogenation catalyst is to be taken Ni as active constituent and take diatomite as the loaded catalyst of carrier, and in catalyzer, the weight percentage of Ni is 30 ~ 50%, reactor bottom filling inert ceramic balls.Need before charging to activate live catalyst with hydrogen.
The desulfurization process of hydrogenation products is carry out in the stainless steel tubular reactor of φ 25mm × 1000mm at one ruler cun.Load 200mL sweetening agent in the reactor and form fixed bed.Sweetening agent is the modified particles shaped activated carbon of load active ingredient, and its particle diameter is 3 ~ 6mm, and active ingredient is CuO and Co
2o
3, in sweetening agent, the content of active ingredient is 1 ~ 5wt%, and the atomicity of Cu and Co ratio is 1: (0.2 ~ 0.8).Sweetening agent first carries out processed before runtime, and the high temperature nitrogen of available 250 DEG C purges bed, and nitrogen flow is set as 1000NmL/min, and purge time is 12 hours, and it is for subsequent use to be down to room temperature after process terminates.The hydrogenation products pump that earlier experiments prepares is sent into reactor and is carried out desulfurization process from bottom.
Lightweight C 5 fraction raw material mixes in required ratio with the hydrogenation products through desulfurization process, hydrogenator is sent into the speed of setting by top with pump after preheating, hydrogen enters in reactor by gas distributor, enters hydrogenation catalyst bed layer and carry out hydrogenation reaction after the mixture of lightweight C 5 fraction raw material and the hydrogenation products through desulfurization process and hydrogen mix.Hydrogenation products is by entering a gas-liquid separator bottom hydrogenator, liquid phase material enters product storage tank.The unreacting hydrogen separated by gas-liquid separator is emptying enter wet gas meter metering after variable valve decompression after, or Returning reacting system after compression.
A part of hydrogenation products in product storage tank sends into desulphurization reactor, sends into the material allocation system of hydrogenation reaction after desulfurization process as solvent, and whole device so starts normal running and runs.
The hydrogenation reaction that each embodiment is concrete and desulfurization treatment process condition are respectively in table 1 and table 2.
Table 1.
* carbon five i.e. lightweight C 5 fraction raw material, and with the total amount of wherein unsaturated hydrocarbons;
* carbon five i.e. lightweight C 5 fraction raw material;
* * solvent is hydrogenation products.
Table 2.
Get the hydrogenation products that hydrogenation reaction has carried out 72 hours and 500 hours respectively, carry out compositional analysis by vapor-phase chromatography and calculate saturation exponent.And get the material that hydrogenation reaction carried out 72 hours and entered hydrogenator for 500 hours respectively, namely as solvent hydrogenation products with by the mixture of the lightweight C 5 fraction raw material of hydrogenation, measure active sulfide content by chromatogram-atomic emission spectrum method.The results are shown in Table 3.
Table 3.
Claims (11)
1. the method for a lightweight C 5 fraction Hydrogenation ethylene cracking material, the method comprises is carried out hydrogenation reaction by hydrogenation catalyst fixed bed in the presence of hydrogen gas by the lightweight C 5 fraction raw material of hydrogenation and is converted into stable hydrocarbon to make the unsaturated hydrocarbons in lightweight C 5 fraction raw material, the product section of hydrogenation reaction is common by hydrogenation catalyst fixed bed after returning and mixing with by the lightweight C 5 fraction raw material of hydrogenation as solvent, be 1 by the lightweight C 5 fraction raw material of hydrogenation and the charged material weight ratio of the hydrogenation reaction product as solvent: (6 ~ 10), is characterized in that:
Hydrogenation products as solvent first carries out desulfurization by sweetening agent fixed bed before mixing with the lightweight C 5 fraction raw material by hydrogenation, and the processing condition of desulfurization are: volume liquid hourly space velocity is 3.0 ~ 16.0hr
-1, system pressure is 0.2 ~ 0.6MPaG, and feeding temperature is 5 ~ 60 DEG C, and sweetening agent is the modified particles shaped activated carbon of load active ingredient, and its particle diameter is 3 ~ 6mm, and active ingredient is CuO and Co
2o
3, in sweetening agent, the content of active ingredient is 1 ~ 5wt%, and the atomicity of Cu and Co ratio is 1: (0.2 ~ 0.8).
2. the method for lightweight C 5 fraction Hydrogenation ethylene cracking material according to claim 1, is characterized in that the volume liquid hourly space velocity in described desulfurization process conditions is 4.0 ~ 12.0hr
-1.
3. the method for lightweight C 5 fraction Hydrogenation ethylene cracking material according to claim 1, is characterized in that the system pressure in described desulfurization process conditions is 0.3 ~ 0.5MPaG.
4. the method for lightweight C 5 fraction Hydrogenation ethylene cracking material according to claim 1, is characterized in that the feeding temperature in described desulfurization process conditions is 10 ~ 40 DEG C.
5. the method for lightweight C 5 fraction Hydrogenation ethylene cracking material according to claim 1, is characterized in that described granular active carbon is ature of coal granular active carbon.
6. the method for lightweight C 5 fraction Hydrogenation ethylene cracking material according to claim 1, is characterized in that the processing condition of described hydrogenation reaction are: volume liquid hourly space velocity is 4.0 ~ 20.0hr
-1system pressure is 1.0 ~ 4.0MPaG, feeding temperature is 20 ~ 100 DEG C, by the lightweight C 5 fraction raw material of hydrogenation with the total amount of wherein unsaturated hydrocarbons, hydrogen be (2 ~ 5) by the molar ratio of the lightweight C 5 fraction raw material of hydrogenation: 1, hydrogenation catalyst is to be taken Ni as active constituent and take diatomite as the loaded catalyst of carrier, and in catalyzer, the content of Ni is 30 ~ 50wt%.
7. the method for lightweight C 5 fraction Hydrogenation ethylene cracking material according to claim 6, is characterized in that described volume liquid hourly space velocity is 6.0 ~ 12.0hr
-1.
8. the method for lightweight C 5 fraction Hydrogenation ethylene cracking material according to claim 6, is characterized in that described system pressure is 1.5 ~ 3.0MPa.
9. the method for lightweight C 5 fraction Hydrogenation ethylene cracking material according to claim 6, is characterized in that described feeding temperature is 30 ~ 60 DEG C.
10. the method for lightweight C 5 fraction Hydrogenation ethylene cracking material according to claim 6, it is characterized in that described hydrogen with by the molar ratio of the lightweight C 5 fraction raw material of hydrogenation for (3 ~ 4): 1.
The method of 11. lightweight C 5 fraction Hydrogenation ethylene cracking materials according to claim 1 or 6, is characterized in that described is 1 by the lightweight C 5 fraction raw material of hydrogenation and the charged material weight ratio of the hydrogenation reaction product as solvent: (7 ~ 9).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201110290488.2A CN103013563B (en) | 2011-09-28 | 2011-09-28 | A kind of method of lightweight C 5 fraction Hydrogenation ethylene cracking material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201110290488.2A CN103013563B (en) | 2011-09-28 | 2011-09-28 | A kind of method of lightweight C 5 fraction Hydrogenation ethylene cracking material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103013563A CN103013563A (en) | 2013-04-03 |
| CN103013563B true CN103013563B (en) | 2016-01-27 |
Family
ID=47962685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201110290488.2A Expired - Fee Related CN103013563B (en) | 2011-09-28 | 2011-09-28 | A kind of method of lightweight C 5 fraction Hydrogenation ethylene cracking material |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN103013563B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115785991B (en) * | 2022-12-09 | 2023-08-08 | 武汉科林化工集团有限公司 | Cracking carbon five hydrofining process |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4064152A (en) * | 1975-06-16 | 1977-12-20 | Union Oil Company Of California | Thermally stable nickel-alumina catalysts useful for methanation |
| CN1699309A (en) * | 2004-05-20 | 2005-11-23 | 中国石化上海石油化工股份有限公司 | Process for preparing pentane from light C5 distillate |
-
2011
- 2011-09-28 CN CN201110290488.2A patent/CN103013563B/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4064152A (en) * | 1975-06-16 | 1977-12-20 | Union Oil Company Of California | Thermally stable nickel-alumina catalysts useful for methanation |
| CN1699309A (en) * | 2004-05-20 | 2005-11-23 | 中国石化上海石油化工股份有限公司 | Process for preparing pentane from light C5 distillate |
Non-Patent Citations (1)
| Title |
|---|
| 陈红萍，周坤.固体脱硫剂的应用研究及展望.《燃料与化工》.2010,第41卷(第2期),第6-9、28页. * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN103013563A (en) | 2013-04-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TW200418790A (en) | Process for the selective hydrogenation of alkynes | |
| CN105985800B (en) | A kind of alkylation of solid acid catalysis | |
| CN103459565B (en) | The manufacture method of hydrocarbon feed | |
| CN103045304A (en) | Hydrogenation method for carbon four fraction rich in alkyne and diene | |
| CN104557408A (en) | A selective hydrogenation method for a light C5 fraction | |
| CN103013563B (en) | A kind of method of lightweight C 5 fraction Hydrogenation ethylene cracking material | |
| CN103013562B (en) | Lightweight C 5 fraction Hydrogenation is for the method for ethylene cracking material | |
| CN105732263B (en) | Selective hydrogenation method for trace acetylene in methanol-to-olefin device | |
| CN103012038A (en) | Method for preparing pentane by hydrogenating light C5 fractions | |
| CN103013565B (en) | Lightweight C 5 fraction Hydrogenation ethylene cracking material | |
| CN109465022A (en) | Low-carbon hydrocarbon aromatization catalyst and preparation and application suitable for Fischer-Tropsch synthesis oil | |
| CN103120947B (en) | Catalyst for preparing mononuclear aromatics by using polycyclic aromatic hydrocarbon | |
| CN103013561B (en) | By lightweight C 5 fraction Hydrogenation ethylene cracking material | |
| CN103012040A (en) | Method for preparing pentane by hydrogenating light C5 fractions | |
| CN103012032A (en) | Method for preparing pentane by hydrogenating light C5 fractions | |
| CN103012041A (en) | Method for preparing pentane by hydrogenating light C5 fractions | |
| CN103013564B (en) | The method of lightweight C 5 fraction Hydrogenation ethylene cracking material | |
| CN105732271B (en) | Front hydrogenation method of trace acetylene in methanol-to-olefin device | |
| CN102775264A (en) | Preparation of pentane through hydrogenation of lightweight C5 fraction | |
| CN102773107A (en) | Regeneration method for metallic Ni hydrogenation catalyst | |
| CN103012039A (en) | Method for preparing pentane by hydrogenating light C5 fractions | |
| CN101805239A (en) | By the selection hydrofining of acetylene being contained the aromatic fraction of acetylene | |
| CN102776021A (en) | Preparation method for raw material used for cracking production of ethylene through hydrogenation of lightweight C5 fraction | |
| CN104177211B (en) | A kind of method of hydrotreating of C 4 fraction | |
| CN112844405B (en) | Catalyst for selective hydrogenation of light hydrocarbon cracking carbon-enriched fraction |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160127 Termination date: 20210928 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |