CN1323754C - Catalyst for synthesizing dimethyl carbonate and its preparing process - Google Patents
Catalyst for synthesizing dimethyl carbonate and its preparing process Download PDFInfo
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- CN1323754C CN1323754C CNB2005100177799A CN200510017779A CN1323754C CN 1323754 C CN1323754 C CN 1323754C CN B2005100177799 A CNB2005100177799 A CN B2005100177799A CN 200510017779 A CN200510017779 A CN 200510017779A CN 1323754 C CN1323754 C CN 1323754C
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Abstract
The present invention discloses a catalyst used for synthesizing dimethyl carbonate and a preparation method thereof. The catalyst is prepared from 0.1 to 5 wt% of main catalyzing component, 0.1 to 6 wt% of auxiliary catalyzing component, 0.1 to 10 wt% of chlorine carrier and balance of carriers, wherein the main catalyzing components are platinum-group metal halides, the auxiliary catalyzing component is the metal chloride of Fe, Cu, Co, Mo, W, La, Ce, Na, K, Ca, and the like, and the chlorine carrier is IIIA group metal chloride. The catalyst has good stability, the activity can be maintained for 300h under the condition that chlorine ions are not replenished, and the high activity can be maintained for a long time under the condition of replenishing the chlorine ions.
Description
Technical field
The invention belongs to petrochemical industry, relate to a kind of Catalysts and its preparation method that is used for Synthesis of dimethyl carbonate (DMC), particularly be used for the Catalysts and its preparation method that carbon monoxide and methyl nitrite carry out gas-phase oxidation/carbonylation prepared in reaction dimethyl carbonate.
Background technology
Dimethyl carbonate has important industrial use, is the environment-friendly chemical products that are subjected to domestic and international extensive concern in recent years.Owing to contain CH in its molecule
3-, CH
3O-, CH
3O-CO-,-multiple functional groups such as CO-, have good reactivity, and this compound is nontoxic, non-corrosiveness.Therefore, it can substitute chemicals such as hypertoxic phosgene, dimethyl suflfate, as important carbonylation agent and methylating agent; On the other hand, be the meticulous specialty chemicals that multiple high added value can be developed, be prepared to raw material with DMC, at medicine, agricultural chemicals, a lot of fields such as synthetic fuel, foodstuff flavouring agent, electronic chemical product obtain extensive use; The 3rd, its dimethyl carbonate is made fuel additive, can improve the antiknock value of engine fuel greatly.Because the oxygen content of dimethyl carbonate is higher than the methyl tertiary butyl ether(MTBE) that generally adopts at present, the capability of antidetonance is better.The recent findings methyl tertiary butyl ether(MTBE) is seriously polluted to underground water, has limited its use in the area that the U.S. has, and dimethyl carbonate is the sorrow of nonpollution environment then, is the substitute products of potential methyl tertiary butyl ether(MTBE).Along with the improvement of dimethyl carbonate manufacturing process and the decline of production cost, can be converted into the carbon monoxide that methyl alcohol and oil plant produce dimethyl carbonate by this method and join in the gasoline and go, both can improve gasoline output, can improve gasoline quality again.
Carry out in the technical process of gas-phase oxidation/carbonylation prepared in reaction dimethyl carbonate at carbon monoxide and methyl nitrite, the step of most critical is exactly the oxidative carbonylation process, and its core technology is exactly the catalyst of function admirable.Carry out the catalyst that gas-phase oxidation/carbonylation prepared in reaction dimethyl carbonate is used about carbon monoxide and methyl nitrite, disclose many patents.From disclosed patented technology, all there is a common shortcoming, i.e. the poor stability of catalyst activity, the life-span is short, best situation is under the condition of continuous supplementation hydrogen chloride, and activity of such catalysts can maintain more than 80% of initial activity in 500 hours.And most of catalyst only can be kept 10～20 hours under the situation of not taking the necessary measures.The example that does not also have at present the activity stabilized longer time.As: United States Patent (USP) 5162563 discloses a kind of catalyst: do carrier with active carbon, main component is a platinum-group metal halides, content 0.1%～10%; Optimum content: 0.5%～2%; Aiding catalytic component is the chloride of iron, copper, bismuth, the mol ratio of its tenor and main component: 1: 50, optimum was 1: 10; United States Patent (USP) 5498744 discloses a kind of catalyst: do carrier with active carbon or aluminium oxide, main component is a kind of amido complex compound [Pd (N (R1, R2 of palladium bichloride, R3)) n] X2, secondary component is Cu, Fe, the halide of V and Mo, improver are Li, Na and K; United States Patent (USP) 5688984 discloses a kind of carrier that is used for the synthetic catalyst of dimethyl carbonate, lithium aluminate with spinel structure, utilize the catalyst of this preparing carriers to have higher activity and selectivity, the selectivity to carbon monoxide and methyl nitrite reaches more than 95 respectively.By adding different aiding catalytic components and selecting different carriers for use, raising that all can be in various degree activity of such catalysts, selectivity and life-span, be very limited but improve, life of catalyst is still shorter.Learn from the data of patent report, even in course of reaction, constantly replenish HCl, activity of such catalysts generally all between 100 hour stage of reaction in decline 20%～30%, this has just limited the commercial Application of these catalyst.
Summary of the invention
The present invention be directed to catalyst in the prior art and can not keep high activity and the bad shortcoming of stability for a long time, and a kind of catalyst that carbon monoxide and methyl nitrite carry out gas-phase oxidation/carbonylation reaction Synthesis of dimethyl carbonate that is used for of function admirable is provided, this catalyst has stability preferably, under the condition of not replenishing chlorion, can keep the active 300h of surpassing, suitably replenishing under the condition of chlorion, catalyst can keep high activity for a long time.
The catalyst of Synthesis of dimethyl carbonate provided by the invention, form by the main catalytic component of 0.1～5 weight %, the aiding catalytic component of 0.1～6 weight %, Cl-carrier and the balance carriers of 0.1～10 weight %, wherein main catalytic component is a platinum-group metal halides, preferred palladium bichloride, preferred 0.3～2 weight % of this component shared weight percentage in catalyst; Aiding catalytic component can be the chloride of metals such as Fe, Cu, Co, Mo, W, La, Ce, Na, K or Ca, preferred copper chloride, preferred 0.5～4.4 weight % of this component shared weight percentage in catalyst; Cl-carrier is an IIIA family metal chloride, preferred aluminium chloride, preferred 0.5～4 weight % of this component shared weight percentage in catalyst, the weight percentage of above-mentioned main catalytic component, aiding catalytic component and Cl-carrier all account for the percentage of total catalyst weight in its contained metallic element weight; Carrier is the natural materials of active carbon, aluminium oxide, molecular sieve, various siliceous and aluminium, preferred active carbon (comprising coal mass active carbon and various wood activated charcoal), aluminium oxide, alumina silicate or molecular sieve.
The present invention also provides a kind of preparation method of Synthesis of dimethyl carbonate catalyst system therefor, and its preparation method comprises the steps:
1) use hydrochloric acid solution as maceration extract, wherein the concentration of hydrochloric acid solution is 10%～35%, and optimum is 15%～30%;
2) main catalytic component and aiding catalytic component are dissolved in the Cl-carrier said ratio are mixed with maceration extract in the hydrochloric acid solution, at room temperature adopt the carrier 5 hours of saturated infusion process dipping proportioning weight, make active constituent loading on carrier;
3) with 2) carrier of the carrying active component that obtains dried 8 hours under 80 ℃ of conditions, under 130 ℃ of conditions dry 8 hours, catalyst of the present invention.
Catalyst of the present invention can be used for the reaction of CO gas-phase oxidative carbonylation to be produced in the technical process of dimethyl carbonate, and the reaction condition of this technical process is: 60 ℃～150 ℃ of reaction temperatures; Reaction pressure is 0～1.0Mpa; Air speed is 500h
-1～20000h
-1It is respectively that CO 5%～40% that raw material is formed; CH
3ONO5%～50%; NO 0～10%; CH
3OH 0～20%; CO
2And/or N
250%～90%, in the raw material cumulative volume.
Catalyst of the present invention to the source of used CO without limits, can be producing synthesis gas from coal, oil plant catalytic cracking flue gas, steel mill's converter gas or steel mill's blast furnace gas etc. in use.
Catalyst compared with prior art of the present invention has stability preferably, can keep the active 300h of surpassing under the condition of not replenishing chlorion, is suitably replenishing under the condition of chlorion, and catalyst can keep high activity for a long time.
The specific embodiment
In order to further specify the present invention, provide some embodiments of the present invention below, but these embodiment do not limit the scope of the invention.
Space-time yield in embodiment and the Comparative Examples (STY) Y (g/l.hr) is calculated as follows:
M in the formula
DMCBe the gram number of the DMC of generation, V
CatBe the catalyst loading amount, rise that t is the reaction time, hour.
Selectivity S is calculated as follows:
N represents the mass percent of each product in the fluid product in the formula, and product comprises dimethyl carbonate (DMC), dimethyl oxalate (DMO), methyl formate (MF), dimethoxymethane (FDA).
Embodiment 1
With 1.7g PdCl
2, 5.4g CuCl
2.2H
2O and 10gAlCl
3Be dissolved in 40ml concentration and be in 30% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 1% Pd, 2.0% Cu, 2% Al and 10.9% Cl through X-ray fluorescence analysis catalyst.
Embodiment 2
With 1.7g PdCl
2, 5.8g FeCl
3And 10gAlCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 82.5g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put that 130 ℃ of dryings obtained catalyst in 8 hours in the baking oven, contain 1% Pd, 2.0% Fe, 2.0% Al and 12.5% Cl through X-ray fluorescence analysis catalyst.
Embodiment 3
With 1.7g PdCl2,3.5g LaCl
3With 10g AlCl
3Be dissolved in 150ml concentration and be in 15% the hydrochloric acid solution., other step is the same, makes catalyst, contains 1% Pd, 2.0% La and 10.2% Cl through X-ray fluorescence analysis catalyst.
Embodiment 4
With 1.7g PdCl2,3.5g CeCl
3With 10g AlCl
3Be dissolved in 150ml concentration and be in 10% the hydrochloric acid solution.Intermediate steps is the same, obtains catalyst, contains 1% Pd, 2.0% Ce and 10.2% Cl through X-ray fluorescence analysis catalyst 4.
Comparative Examples 1
With 1.7g PdCl2 and 5.8g CuCl
2Be dissolved in 40ml concentration and be in 30% the hydrochloric acid solution.Intermediate steps is the same, obtains catalyst, contains 1% Pd, 2.0% Cu and 2.92% Cl through X-ray fluorescence analysis catalyst.
Comparative Examples 2
With 1.7g PdCl2 and 5.8gFeCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.Intermediate steps is the same, obtains catalyst, contains 1% Pd, 2.0% Fe and 4.5% Cl through X-ray fluorescence analysis catalyst.
Comparative Examples 3
With 1.7g PdCl2 and 3.5g LaCl
3Be dissolved in 150ml concentration and be in 15% the hydrochloric acid solution.Intermediate steps is the same, obtains catalyst, contains 1% Pd, 2.0% La and 2.38% Cl through X-ray fluorescence analysis catalyst.
Comparative Examples 4
With 1.7g PdCl2 and 3.5g CeCl
3Be dissolved in 150ml concentration and be in 10% the hydrochloric acid solution.Intermediate steps is the same, obtains catalyst, contains 1.0% Pd, 2.0% Ce and 2.38% Cl through X-ray fluorescence analysis catalyst.
Embodiment 5
With 1.7g PdCl
2, 3.8g KCl and 10gAlCl
3Be dissolved in 40ml concentration and be in 30% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 1% Pd, 2.0% K, 2% Al and 10.9% Cl through X-ray fluorescence analysis catalyst.
Embodiment 6
With 1.7g PdCl
2, 3.8g CaCl
2And 10gAlCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 1% Pd, 2.0% Ca, 2% Al and 10.9% Cl through X-ray fluorescence analysis catalyst.
Embodiment 7
With 1.7g PdCl
2, 5.4g CuCl
2.2H
2O and 10gAlCl
3Be dissolved in 150ml concentration and be in 15% the hydrochloric acid solution.This solution is slowly poured in the r-alumina support that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 1% Pd, 2.0% Cu, 2% Al and 10.9% Cl through X-ray fluorescence analysis catalyst.
Embodiment 8
With 1.7g PdCl
2, 5.4g CuCl
2.2H
2O and 10gAlCl
3Be dissolved in 155ml concentration and be in 12% the hydrochloric acid solution.This solution is slowly poured in the NaY molecular sieve carrier that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 1% Pd, 2.0% Cu, 2% Al and 10.9% Cl through X-ray fluorescence analysis catalyst.
Embodiment 9
With 2.1g H
1PtCl
6, 5.4g CuCl
2.2H
2O and 10gAlCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 1% Pt, 2.0% Cu, 2% Al and 10.9% Cl through X-ray fluorescence analysis catalyst.
Embodiment 10
With 0.9g PdCl
2, 5.4g CuCl
2.2H
2O and 10gAlCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 0.5% Pd, 2.0% Cu, 2% Al and 10.7% Cl through X-ray fluorescence analysis catalyst.
Embodiment 11
With 3.4g PdCl
2, 5.4g CuCl
2.2H
2O and 10gAlCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 2.0% Pd, 2.0% Cu, 2% Al and 11.1% Cl through X-ray fluorescence analysis catalyst.
Embodiment 12
With 1.7g PdCl
2, 1.8g CuCl
2.2H
2O and 10gAlCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 0.5% Pd, 0.7% Cu, 2% Al and 10.6% Cl through X-ray fluorescence analysis catalyst.
Embodiment 13
With 1.7g PdCl
2, 10.8g CuCl
2.2H
2O and 10gAlCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 0.5% Pd, 4.0% Cu, 2% Al and 11.2% Cl through X-ray fluorescence analysis catalyst.
Embodiment 14
With 1.7g PdCl
2, 5.4g CuCl
2.2H
2O and 5gAlCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 0.5% Pd, 4.0% Cu, 1% Al and 8.7% Cl through X-ray fluorescence analysis catalyst.
Embodiment 15
With 1.7g PdCl
2, 5.4g CuCl
2.2H
2O and 20gAlCl
3Be dissolved in 110ml concentration and be in 20% the hydrochloric acid solution.This solution is slowly poured in the active carbon that the 85g granularity is 0.5～2mm, constantly stir and make solution and active carbon even contact, flooded the back 80 ℃ of oven dry 8 hours, put in the baking oven 130 ℃ of dryings 8 hours, obtain catalyst, contain 0.5% Pd, 4.0% Cu, 4% Al and 21.7% Cl through X-ray fluorescence analysis catalyst.
Embodiment 10
Above-mentioned catalyst is respectively charged in the tubular reactor, with the constant temperature oil bath heating, the long 40cm of reactor, internal diameter 0.8.cm, catalyst loading amount 5ml, catalyst layer are respectively charged into equal-volume and equigranular quartz sand up and down.Reaction gas is formed (volume): CO 20%, CH
3ONO 24%, and all the other are N
2, air speed 2000h
-1, 120 ℃ of reaction temperatures, reaction pressure are normal pressure, sample divider places ice-water bath to collect fluid product.Fluid product carries out chromatography, and calculates the space-time yield STY and the selectivity S of dimethyl carbonate.
Table 1
| Routine number | Space-time yield (STY), g/l.h | Selectivity S, % | ||||||
| 10h | 50h | 100h | 500h | 10h | 50h | 100h | 500h | |
| Embodiment 1 embodiment 2 embodiment 3 embodiment 4 Comparative Examples 1 Comparative Examples 2 Comparative Examples 3 Comparative Examples 4 embodiment 5 embodiment 6 embodiment 7 embodiment 8 embodiment 9 embodiment 10 embodiment 11 embodiment 12 embodiment 13 embodiment 14 embodiment 15 | 484 434 421 474 452 421 425 412 435 402 479 451 497 341 658 434 414 478 403 | 485 452 433 455 390 352 361 372 408 388 457 413 474 347 677 438 426 475 400 | 432 420 418 431 208 188 172 192 365 315 424 382 420 286 582 378 343 218 329 | 358 344 322 308 35 21 33 31 271 245 327 298 368 230 513 321 293 142 285 | 94 94 93 93 93 94 93 93 94 95 95 90 95 92 94 90 91 94 94 | 94 93 91 92 88 84 84 88 91 93 95 87 94 92 94 90 90 83 94 | 91 89 89 90 68 59 57 58 85 88 91 85 92 89 89 85 86 53 92 | 88 82 83 84 11 8 10 9 80 82 90 80 87 87 85 82 84 28 89 |
As can be seen from the above table, activity of such catalysts of the present invention, stability and selectivity all are better than relevant patent, can keep the active 300h of surpassing under the condition of not replenishing chlorion, suitably replenish under the condition of chlorion, catalyst can keep high activity for a long time.
Claims (4)
1. the catalyst of a Synthesis of dimethyl carbonate, it is characterized in that: by the main catalytic component of 0.1～5 weight %, 0.1 the aiding catalytic component of～6 weight %, 0.1 the Cl-carrier of～10 weight % and balance carriers are formed, wherein main catalytic component is a platinum-group metal halides, aiding catalytic component is Fe, Cu, Co, Mo, W, La, Ce, Na, the metal chloride of K or Ca, Cl-carrier is an IIIA family metal chloride, carrier is siliceous and natural materials aluminium, active carbon, aluminium oxide or molecular sieve, described main catalytic component, the weight percentage of aiding catalytic component and Cl-carrier all accounts for the percentage of total catalyst weight in its contained metallic element weight.
2. catalyst according to claim 1 is characterized in that: described main catalytic component is a palladium bichloride, and aiding catalytic component is a copper chloride, and Cl-carrier is an aluminium chloride, and carrier is active carbon, aluminium oxide, alumina silicate or molecular sieve.
3. catalyst according to claim 1 is characterized in that: the content of described main catalytic component is 0.3～2 weight %, and the content of aiding catalytic component is 0.5～4.4 weight %, and the content of Cl-carrier is 0.5～4 weight %, and surplus is a carrier.
4. the described Preparation of catalysts method of claim 1, it is characterized in that: this preparation method comprises the steps:
1) use hydrochloric acid solution as maceration extract, wherein the concentration of hydrochloric acid solution is 5%～35%;
2) be mixed with maceration extract in the hydrochloric acid solution being dissolved in Cl-carrier, at room temperature adopt the carrier 5 hours of saturated infusion process dipping proportioning weight, make active constituent loading on carrier by the main catalytic component of the described proportioning of claim 1 and aiding catalytic component;
3) with 2) carrier of the carrying active component that obtains dried 8 hours under 80 ℃ of conditions, under 130 ℃ of conditions dry 8 hours, catalyst.
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| CN101519602B (en) * | 2008-02-28 | 2013-04-24 | 中国石油化工股份有限公司 | Material for trapping the unsaturated hydrocarbon in hydrocarbon raw materials |
| US9249082B2 (en) | 2010-02-09 | 2016-02-02 | King Abdulaziz City for Science and Technology (KACST) | Synthesis of dimethyl carbonate from carbon dioxide and methanol |
| CN101966460B (en) * | 2010-09-21 | 2013-06-19 | 中山大学 | Supported catalyst for synthesis of dimethyl carbonate, preparation method and using method thereof |
| CN102614900B (en) * | 2012-03-08 | 2014-08-20 | 天津大学 | Mesoporous carbon-loaded catalyst for synthesizing diethyl carbonate by gas phase oxidation carbonyl of ethanol and preparation method thereof |
| CN107866220B (en) * | 2016-09-26 | 2020-01-03 | 中国石油化工股份有限公司 | Catalyst applied to synthesis of 1, 4-diacetoxybutane |
| CN106693965B (en) * | 2016-11-21 | 2019-07-30 | 中国科学院福建物质结构研究所 | A kind of Pd/MgTiO3The sol-gel process for preparing of catalyst and its application |
| CN107376954B (en) * | 2017-08-02 | 2021-02-02 | 宁波中科远东催化工程技术有限公司 | Catalyst for CO gas phase coupling synthesis of dimethyl carbonate, preparation method and application thereof |
| CN110563585B (en) * | 2019-10-11 | 2021-02-09 | 山东德普化工科技有限公司 | Preparation method of dimethyl carbonate |
| CN111085220A (en) * | 2019-12-27 | 2020-05-01 | 宁波中科远东催化工程技术有限公司 | Catalyst, preparation method thereof and dimethyl carbonate synthesis method |
| CN111760580A (en) * | 2020-07-10 | 2020-10-13 | 上海诺哈尔化工技术有限公司 | Catalyst for synthesizing dimethyl carbonate and preparation method and application thereof |
| CN115463675A (en) * | 2022-10-26 | 2022-12-13 | 高化学（江苏）化工新材料有限责任公司 | Novel catalyst for synthesizing dimethyl carbonate and preparation method thereof |
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