CN112871190A - Chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether and preparation method and application thereof - Google Patents
Chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether and preparation method and application thereof Download PDFInfo
- Publication number
- CN112871190A CN112871190A CN202110045444.7A CN202110045444A CN112871190A CN 112871190 A CN112871190 A CN 112871190A CN 202110045444 A CN202110045444 A CN 202110045444A CN 112871190 A CN112871190 A CN 112871190A
- Authority
- CN
- China
- Prior art keywords
- acid
- catalyst
- reaction
- metal organic
- monomethyl ether
- 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.)
- Granted
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J27/188—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J27/188—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
- B01J27/19—Molybdenum
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/1691—Coordination polymers, e.g. metal-organic frameworks [MOF]
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
- B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
- B01J31/223—At least two oxygen atoms present in one at least bidentate or bridging ligand
- B01J31/2239—Bridging ligands, e.g. OAc in Cr2(OAc)4, Pt4(OAc)8 or dicarboxylate ligands
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/09—Preparation of ethers by dehydration of compounds containing hydroxy groups
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/60—Complexes comprising metals of Group VI (VIA or VIB) as the central metal
- B01J2531/62—Chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
The invention relates to a chromium-based metal organic framework solid acid catalyst for catalytic synthesis of hydroquinone monomethyl ether, and a preparation method and application thereof, and belongs to the technical field of solid acid catalysis. The method takes sulfonic acid functionalized terephthalate as a ligand, and encapsulates heteropoly acid in situ in the process of synthesizing a metal organic framework, and the two different modes of introducing an acid center can synergistically enhance the acidity of the catalyst; meanwhile, the in-situ encapsulation technology can effectively reduce the risk of heteropolyacid loss, so that the catalyst can keep extremely high stability. Tests prove that the yield of the catalyst in the preparation of hydroquinone monomethyl ether by a hydroquinone methylation reaction can reach 75.7%; after the operation is carried out for 200 hours, the activity is only slightly reduced, the stability of the catalyst is greatly improved compared with that of a molecular sieve modified by sulfuric acid and phosphotungstic acid in the prior art, and the catalyst has potential application prospect.
Description
Technical Field
The invention relates to a chromium-based metal organic framework solid acid catalyst for catalytic synthesis of hydroquinone monomethyl ether, and a preparation method and application thereof, and belongs to the technical field of solid acid catalysis.
Background
Hydroquinone monomethyl ether, also called hydroquinone monomethyl ether, p-hydroxyanisole and p-methoxyphenol, is a high-efficiency polymerization inhibitor of acrylic compounds, can also be used as an antioxidant of edible oil or animal oil, and can also be used as a stabilizer of photosensitive materials, polyester, intermediate dyes, agricultural chemicals and medicines. Hydroquinone monomethyl ether is also a lubricant additive for high temperature gas turbine engine oils, and a synthetic intermediate.
Hydroquinone monomethyl ether is prepared by using hydroquinone as a raw material and dimethyl sulfate, methanol, dimethyl carbonate and the like as methylating agents and reacting under the catalysis of an acid catalyst. The methanol is used as a methylation reagent, so that the environmental pollution caused by other highly toxic reagents can be effectively avoided, and the yield of the target product hydroquinone monomethyl ether is greatly improved. Early catalysts are generally homogeneous liquid acids, such as sulfuric acid and heteropoly acid, and the catalysts have serious pollution of three wastes, a plurality of byproducts, difficult purification and poor product quality. US4294991 proposes to use sulfated polystyrene resin as a catalyst and benzoquinone as a cocatalyst, wherein the sulfated polystyrene catalyst can eliminate the alkali neutralization step after the reaction, and the catalyst can be recovered by simple filtration, thereby greatly simplifying the process steps and reducing the possibility of environmental pollution; meanwhile, benzoquinone is used as a cocatalyst, so that the yield of the catalytic reaction can be obviously improved. The following auxiliary actions of many scholars on benzoquinone are summarized as follows: the benzoquinone firstly reacts with hydroquinone to form the quinohydroquinone, then the quinoquinone is subjected to carbonyl addition with methanol to form an unstable intermediate, the unstable intermediate is converted into hydroquinone monomethyl ether in the presence of a strong acid catalyst, and the benzoquinone is regenerated at the same time, the reaction speed of the method is far higher than that of the original reaction path, and the regeneration of the dimethyl ether is effectively inhibited.
Based on the advantages of solid acid catalysts, new solid acids are continuously applied to the synthesis of hydroquinone monomethyl ether. Ganapati et al developed Clay-Supported Heteropolyacids ("Synthesis of Hydroquinone monomer Ether from Hydroquinone and methane over heteropolysaccharides Supported on Clay Clay: Kinetics", Ind. Eng. chem. Res.2005,44, 7969-7977); the southern group developed a sulfonic acid modified molecular sieve (CN 109420519A); the catalytic performance of the solid acid catalyst still needs to be further improved.
Metal-organic frameworks (MOFs) are porous crystalline materials formed by self-assembly of metal ions or metal clusters and organic ligands, have various advantages of high specific surface area and pore volume, adjustable pore structure, capability of functional modification and the like, and have been widely applied in the fields of gas adsorption separation, gas storage, reaction catalysis and the like in recent years. The metal sites and organic ligands of the MOFs material can be used as potential catalytic active centers; due to the abundant pore structure of MOFs materials, nanometer metal active components can be dispersed in pore channels to introduce a new catalytic active center, and the MOFs as a novel solid catalyst shows wide development prospect in the field of catalytic application.
Disclosure of Invention
Based on the prior art, the invention firstly develops a chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether, and the material takes sulfonic acid functionalized terephthalate as a ligand and is self-assembled with metal chromium ion coordination to form a framework structure with large specific surface area; meanwhile, heteropoly acid is loaded in situ in the self-assembly process, and the heteropoly acid is encapsulated in a mesoporous cage of a metal organic framework so as to strengthen the acidity of the catalyst. The novel metal organic framework solid acid catalyst developed by the invention has high conversion rate and selectivity when used for catalytically synthesizing hydroquinone monomethyl ether, and has extremely high stability.
One of the purposes of the invention is to provide a chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether, wherein the metal organic framework material is a sulfonic acid functionalized chromium-based metal organic framework material coated with heteropoly acid, the heteropoly acid is one or more of phosphotungstic acid, phosphomolybdic acid, silicotungstic acid and silicomolybdic acid, and the content of the heteropoly acid accounts for 3wt% -15wt% of the total mass of the catalytic material.
Further, the heteropoly acid is preferably phosphotungstic acid and phosphomolybdic acid, and the content of the heteropoly acid is preferably 4wt% -8wt% of the total mass of the catalytic material.
The invention also aims to provide a preparation method of the chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether, which comprises the following specific steps:
respectively dissolving monosodium 2-sulfoterephthalate and chromium nitrate in deionized water, mixing the two solutions, continuously stirring, adding heteropoly acid after uniform mixing, ultrasonically mixing for 40-60min, transferring the obtained mixture into a stainless steel reaction kettle with a polytetrafluoroethylene lining, carrying out hydrothermal reaction at the temperature of 200-250 ℃ for 6-12h, naturally cooling to room temperature after the reaction is finished, centrifugally collecting solids, washing and drying to obtain the sulfonic acid functionalized chromium-based metal organic framework material coated with heteropoly acid.
Furthermore, the molar ratio of the raw material 2-sulfoterephthalic acid monosodium, the chromic nitrate and the heteropoly acid is 1:0.3-3: 0.01-0.03.
Further, the temperature of the hydrothermal reaction is preferably 220 ℃, and the reaction time is preferably 6-10 h.
The invention also aims to provide the application of the catalyst in catalytic synthesis of hydroquinone monomethyl ether.
The specific method of the application is as follows: filling a catalyst into a fixed bed reactor, pumping reaction raw materials of hydroquinone, methanol and an auxiliary agent of benzoquinone into the reactor for etherification reaction, and preparing hydroquinone monomethyl ether.
Furthermore, the mol ratio of the hydroquinone, the methanol and the benzoquinone added in the reaction process is 1:10-60: 0.05-0.3.
Furthermore, the temperature in the reaction process is 30-70 ℃, and the reaction time is 1-8 h.
The method takes sulfonic acid functionalized terephthalate as a ligand, and encapsulates heteropoly acid in situ in the process of synthesizing a metal organic framework, and the two different modes of introducing an acid center can synergistically enhance the acidity of the catalyst; meanwhile, the in-situ encapsulation technology can effectively reduce the risk of heteropolyacid loss, so that the catalyst can keep extremely high stability.
Tests prove that the sulfonic acid functionalized chromium-based metal organic framework material coated with the heteropoly acid has higher conversion rate and selectivity in the preparation of hydroquinone monomethyl ether by a hydroquinone methylation reaction, and the yield can reach 75.7%; after the operation is carried out for 200 hours, the activity is only slightly reduced, the stability of the catalyst is greatly improved compared with that of a molecular sieve modified by sulfuric acid and phosphotungstic acid in the prior art, and the catalyst has considerable prospect.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Example 1
Respectively dissolving monosodium 2-sulfoterephthalate and chromic nitrate in deionized water, mixing the two solutions, continuously stirring, adding phosphotungstic acid after uniformly mixing, and ultrasonically mixing for 40min, wherein the molar ratio of monosodium 2-sulfoterephthalate, chromic nitrate and phosphotungstic acid is 1:1: 0.03; transferring the obtained mixture into a stainless steel reaction kettle with a polytetrafluoroethylene lining, carrying out hydrothermal reaction for 10h at 220 ℃, naturally cooling to room temperature after the reaction is finished, centrifugally collecting solids, washing, and drying at 110 ℃ to obtain a sulfonic acid functionalized chromium-based metal organic framework material coated with phosphotungstic acid; the content of phosphotungstic acid accounts for 7.8 wt% of the total mass of the catalytic material.
Example 2
Respectively dissolving monosodium 2-sulfoterephthalate and chromic nitrate in deionized water, mixing the two solutions, continuously stirring, adding phosphotungstic acid after uniformly mixing, and ultrasonically mixing for 50min, wherein the molar ratio of monosodium 2-sulfoterephthalate, chromic nitrate and phosphotungstic acid is 1:0.8: 0.026; transferring the obtained mixture into a stainless steel reaction kettle with a polytetrafluoroethylene lining, carrying out hydrothermal reaction for 8 hours at 220 ℃, naturally cooling to room temperature after the reaction is finished, centrifugally collecting solids, washing, and drying at 100 ℃ to obtain a sulfonic acid functionalized chromium-based metal organic framework material coated with phosphotungstic acid; the content of phosphotungstic acid accounts for 7.0 wt% of the total mass of the catalytic material.
Example 3
Respectively dissolving monosodium 2-sulfoterephthalate and chromium nitrate in deionized water, mixing the two solutions, continuously stirring, adding phosphomolybdic acid after uniformly mixing, and ultrasonically mixing for 50min, wherein the molar ratio of monosodium 2-sulfoterephthalate, chromium nitrate and phosphomolybdic acid is 1:1.4: 0.03; transferring the obtained mixture into a stainless steel reaction kettle with a polytetrafluoroethylene lining, carrying out hydrothermal reaction for 10 hours at 220 ℃, naturally cooling to room temperature after the reaction is finished, centrifugally collecting solids, washing, and drying at 100 ℃ to obtain a sulfonic acid functionalized chromium-based metal organic framework material coated with phosphomolybdic acid; the content of the phosphomolybdic acid accounts for 6.4 wt% of the total mass of the catalytic material.
Example 4
The catalysts prepared in examples 1 to 3 were used in a reaction for preparing hydroquinone monomethyl ether (HQMME) by a hydroquinone methylation reaction. The specific implementation process is as follows:
filling a catalyst into a fixed bed reactor, pumping reaction raw materials of hydroquinone, methanol and an auxiliary agent of benzoquinone into the reactor for etherification reaction, wherein the molar ratio of the hydroquinone, the methanol and the benzoquinone is 1:30:0.15, and the temperature in the reaction process is 50 ℃; performing component analysis on the product after the reaction is performed for 8 hours, and calculating the conversion rate and selectivity of hydroquinone monomethyl ether; for comparison, a molecular sieve modified by sulfuric acid and phosphotungstic acid is prepared, and the activity of the solid acid catalyst is tested under the same reaction condition; meanwhile, in order to test the stability of the catalyst, the reaction was continued for 200 hours, and the components of the resulting product were also analyzed, and all the results are shown in table 1.
TABLE 1 analysis of the activity and stability of the catalyst for the preparation of hydroquinone monomethyl ether by the methylation of hydroquinone
As is apparent from Table 1, the sulfonic acid functionalized chromium-based metal organic framework material coated with the heteropoly acid has higher conversion rate and selectivity in the preparation of hydroquinone monomethyl ether by hydroquinone methylation reaction, and the yield can reach 75.7%; after the catalyst is operated for 200 hours, the activity is only slightly reduced, the yield can also reach 72.9 percent, and the yield is improved by 11.0 percent compared with the molecular sieve modified by sulfuric acid and phosphotungstic acid in the prior art, which shows that the catalyst has extremely high stability.
In addition, it should be understood that although the present description is described in terms of embodiments with photocatalysis, not every embodiment may contain only a single embodiment, and such description is for clarity only, and those skilled in the art will be able to make the description as a whole, and the embodiments in each example may be appropriately combined to form other embodiments as will be appreciated by those skilled in the art.
Claims (9)
1. The chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether is characterized in that the metal organic framework material is a sulfonic acid functionalized chromium-based metal organic framework material coated with heteropoly acid, the heteropoly acid is one or more of phosphotungstic acid, phosphomolybdic acid, silicotungstic acid and silicomolybdic acid, and the content of the heteropoly acid accounts for 3-15 wt% of the total mass of the catalyst material.
2. The catalyst according to claim 1, wherein the heteropoly acid is preferably phosphotungstic acid or phosphomolybdic acid, and the content of the heteropoly acid is preferably 4-8 wt% of the total mass of the catalytic material.
3. The preparation method of the catalyst according to claim 1, characterized by comprising the following steps:
respectively dissolving monosodium 2-sulfoterephthalate and chromium nitrate in deionized water, mixing the two solutions, continuously stirring, adding heteropoly acid after uniform mixing, ultrasonically mixing for 40-60min, transferring the obtained mixture into a stainless steel reaction kettle with a polytetrafluoroethylene lining, carrying out hydrothermal reaction at the temperature of 200-250 ℃ for 6-12h, naturally cooling to room temperature after the reaction is finished, centrifugally collecting solids, washing and drying to obtain the sulfonic acid functionalized chromium-based metal organic framework material coated with heteropoly acid.
4. The production method according to claim 3, wherein the molar ratio of the starting material, monosodium 2-sulfoterephthalate, chromium nitrate and heteropoly acid is 1:0.3-3: 0.01-0.03.
5. The method according to claim 3, wherein the hydrothermal reaction is carried out at a temperature of 220 ℃ for a time of 6-10 hours.
6. Use of a catalyst according to any one of claims 1-2 for the catalytic synthesis of hydroquinone monomethyl ether.
7. The application of claim 6, wherein the specific method of the application is as follows: filling a catalyst into a fixed bed reactor, pumping reaction raw materials of hydroquinone, methanol and an auxiliary agent of benzoquinone into the reactor for etherification reaction, and preparing hydroquinone monomethyl ether.
8. The use according to claim 7, wherein the molar ratio of hydroquinone, methanol and benzoquinone added during the reaction is 1:10-60: 0.05-0.3.
9. The use according to claim 7, wherein the temperature of the reaction process is 30-70 ℃ and the reaction time is 1-8 h.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110045444.7A CN112871190B (en) | 2021-01-13 | 2021-01-13 | Chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether and preparation method and application thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110045444.7A CN112871190B (en) | 2021-01-13 | 2021-01-13 | Chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether and preparation method and application thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN112871190A true CN112871190A (en) | 2021-06-01 |
| CN112871190B CN112871190B (en) | 2021-08-20 |
Family
ID=76045869
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202110045444.7A Active CN112871190B (en) | 2021-01-13 | 2021-01-13 | Chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether and preparation method and application thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN112871190B (en) |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4469897A (en) * | 1980-11-13 | 1984-09-04 | Anic S.P.A. | Process for preparing monoalkylethers of hydroquinone and its derivatives |
| CN104338556A (en) * | 2013-07-25 | 2015-02-11 | 中国科学院大连化学物理研究所 | Method for directly synthesizing mesoporous material coated heteropolyacid functionalized MOF material |
| CN104857988A (en) * | 2015-05-07 | 2015-08-26 | 盐城工学院 | Heteropolyacid-modified Zr-MOF catalyst as well as preparation method and application thereof |
| CN105344378A (en) * | 2015-10-13 | 2016-02-24 | 华南理工大学 | Phosphotungstic acid-metal organic skeleton used for catalyzing hydrolysis of cellulose, and preparation method and application thereof |
-
2021
- 2021-01-13 CN CN202110045444.7A patent/CN112871190B/en active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4469897A (en) * | 1980-11-13 | 1984-09-04 | Anic S.P.A. | Process for preparing monoalkylethers of hydroquinone and its derivatives |
| CN104338556A (en) * | 2013-07-25 | 2015-02-11 | 中国科学院大连化学物理研究所 | Method for directly synthesizing mesoporous material coated heteropolyacid functionalized MOF material |
| CN104857988A (en) * | 2015-05-07 | 2015-08-26 | 盐城工学院 | Heteropolyacid-modified Zr-MOF catalyst as well as preparation method and application thereof |
| CN105344378A (en) * | 2015-10-13 | 2016-02-24 | 华南理工大学 | Phosphotungstic acid-metal organic skeleton used for catalyzing hydrolysis of cellulose, and preparation method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN112871190B (en) | 2021-08-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN107056649B (en) | A kind of preparation method and applications for the metal-organic framework materials loading schiff bases complex | |
| CN108262073B (en) | Metal organic framework supported phosphotungstic acid catalyst, preparation method and application of catalyst in catalytic synthesis of adipic acid | |
| CN108558598B (en) | Method for preparing cyclohexanol by catalyzing hydrolysis reaction of cyclohexyl compounds with acidic swelling polyion liquid | |
| CN111116934B (en) | Preparation of MOFs derivative with hollow structure and application of MOFs derivative in catalyzing olefin epoxidation | |
| CN112206808A (en) | Catalyst for synthesizing isobutyl isobutyrate and preparation method and application thereof | |
| CN102259025B (en) | Catalyst for preparing cyclohexanol by hydration of cyclohexene as well as preparation method and application method thereof | |
| CN107245065B (en) | method for preparing valerolactone by catalytic hydrogenation of ethyl levulinate | |
| CN112844481A (en) | Zirconium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether and preparation method and application thereof | |
| CN112871190B (en) | Chromium-based metal organic framework solid acid catalyst for synthesizing hydroquinone monomethyl ether and preparation method and application thereof | |
| CN103769215B (en) | A kind of nature-changed cation resin catalyst and its preparation method and application | |
| CN110102343B (en) | Composite acid catalyst and method for preparing 5-hydroxymethylfurfural by catalyzing saccharides through composite acid catalyst | |
| CN112830912A (en) | Method for continuously preparing 2, 5-furan dicarboxaldehyde oxime by solid acid catalysis | |
| CN106378189B (en) | Catalyst and its preparation method and application for synthesizing polymethoxy dimethyl ether | |
| CN110483678B (en) | Catalyst for preparing isosorbide by dehydrating sorbitol and preparation method and application thereof | |
| CN115286665B (en) | Method for preparing fructose by glucose isomerization | |
| CN111250166A (en) | Heteropolyacid-supported sulfonic acid catalyst, and preparation method and application thereof | |
| CN111389445A (en) | Composite solid acid catalyst for preparing 2,2, 4-trimethyl-1, 3-pentanediol diisobutyrate and preparation method thereof | |
| US11938465B2 (en) | Coordination zirconium phosphotungstate catalyst and its application in catalytic hydrogenation of furfural | |
| CN102909041B (en) | Method for synthesizing methyl sec-butyl ether | |
| CN113333022A (en) | Preparation method and application of bifunctional solid acid catalyst | |
| CN1275689C (en) | Catalyzer synthesized from ethyl lactate and hydrogen in use for 1, 2 propylene glycol, and preparation method | |
| CN115626869B (en) | Method for preparing 3-hydroxy propanal by hydration of acrolein | |
| CN116351412B (en) | Supported bimetallic catalyst for antioxidant 44PD synthesis and catalytic method thereof | |
| CN114797827B (en) | Palladium catalyst for synthesizing D-biotin intermediate, and preparation method and application thereof | |
| CN114656442B (en) | Method for preparing caprolactone from 5-hydroxymethyl furoic acid |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |