CN105457619A - Preparation method of calcium-loaded silica gel catalyst - Google Patents

Preparation method of calcium-loaded silica gel catalyst Download PDF

Info

Publication number
CN105457619A
CN105457619A CN201510776724.XA CN201510776724A CN105457619A CN 105457619 A CN105457619 A CN 105457619A CN 201510776724 A CN201510776724 A CN 201510776724A CN 105457619 A CN105457619 A CN 105457619A
Authority
CN
China
Prior art keywords
calcium
preparation
sodium metasilicate
silica gel
gel catalyst
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.)
Pending
Application number
CN201510776724.XA
Other languages
Chinese (zh)
Inventor
贾东新
焦德华
何玲丽
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
WUXI PUAIDE ENVIRONMENTAL PROTECTION TECHNOLOGY Co Ltd
Original Assignee
WUXI PUAIDE ENVIRONMENTAL PROTECTION TECHNOLOGY Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by WUXI PUAIDE ENVIRONMENTAL PROTECTION TECHNOLOGY Co Ltd filed Critical WUXI PUAIDE ENVIRONMENTAL PROTECTION TECHNOLOGY Co Ltd
Priority to CN201510776724.XA priority Critical patent/CN105457619A/en
Publication of CN105457619A publication Critical patent/CN105457619A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/02Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the alkali- or alkaline earth metals or beryllium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/08Silica

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Catalysts (AREA)

Abstract

The present invention discloses a preparation method of calcium-loaded silica gel catalyst, which is obtained by reaction of sodium metasilicate and a calcium source in an organic phase environment. Compared with the prior art, the calcium-loaded silica gel catalyst has the catalytic calcium dispersedly immobilized on a silica gel carrier to expand the area of contact with the reaction substrate materials. Compared with the prior art, the calcium-loaded silica gel catalyst has higher catalytic efficiency, requires more moderate catalytic conditions, and is in favor of industrial production. At the same time, the method of the present invention is completed under the condition of pure organic phase; and by contrast, the obtained calcium-loaded silica gel catalyst has higher catalytic efficiency than the one obtained in general water content conditions.

Description

The preparation method of a kind of year calcium silica-gel catalyst
Technical field
The invention belongs to catalyst field, be specifically related to the preparation method of a kind of year calcium silica-gel catalyst.
Background technology
The low-carbon alkene such as ethene, propylene is raw material the most basic in petrochemical industry.For ethene, about there are the petrochemicals of 75% by ethylene production, it is mainly used to produce the multiple important Organic chemical products such as polyethylene, polyvinyl chloride, ethylene oxide/ethylene glycol, dichloroethanes, styrene, polystyrene, ethanol, vinyl acetate, in fact, ethylene yield has become the mark of a measurement national oil chemical engineering industry development level.
Statistics display, from nineteen ninety by 2003, China's ethene equivalent consumption figure increases by 12% every year, after this growth rate is more surprising, within 2003, China's ethene equivalent consumption figure is 1,350 ten thousand tons, within 2005, this numeral just reaches 1,876 ten thousand tons, has increased nearly 40% on foot between 2 years, and Chinese Market for Ethylene has become the country that global growth rate is the fastest, the growth duration is the longest.
In the technique of preparing ethylene, propylene and other functionalized olefin, the effect of catalyst has great impact for the productive rate of product and qualification rate.Calcium series catalysts is a kind of conventional catalyst in industrial production, but comparatively active because of it, and reducing power is comparatively strong, and therefore reaction condition is comparatively harsh.Improving calcium series catalysts catalytic efficiency in the industrial production, is a current large study hotspot.
Summary of the invention
The technical problem to be solved in the present invention is to provide the preparation method of a kind of year calcium silica-gel catalyst, not high to solve the catalytic efficiency of prior art existence, the problems such as catalytic condition is harsh.
For solving the problems of the technologies described above, the technical solution used in the present invention is as follows:
A preparation method for year calcium silica-gel catalyst, it comprises the steps:
(1) sodium metasilicate is dissolved in organic solvent, under the condition of nitrogen protection, in organic solvent, passes into hydrogen chloride gas, at 30 ~ 60 DEG C, react 3 ~ 6h;
(2) keep nitrogen protection condition, in the mixed system of step (1) gained, add calcium source, at 40 ~ 45 DEG C, react 1 ~ 3h;
(3) in the mixed system of gained in step (2), add precipitating reagent, fully mix, after colloidal sol is complete, get gel;
(4) by after the gel detergent of gained in step (3), drying, roast, obtain carrying calcium silica-gel catalyst.
Wherein, described sodium metasilicate is anhydrous sodium metasilicate.
Wherein, in above-mentioned preparation method, in step (1) ~ (3), agents useful for same is all through anhydrous process.
Wherein, in above-mentioned preparation method, in step (1) and (2), reaction is all placed on shaking table to be carried out.
In step (1), described organic solvent is methyl-sulfoxide.
In step (1), the weight ratio of sodium metasilicate and organic solvent is 1:50 ~ 200.
In step (1), the mol ratio of sodium metasilicate and hydrogen chloride is 1:1.5 ~ 3.5.
In step (2), described calcium source is calcium chloride, calcium phosphate or calcium carbonate.
In step (2), in sodium metasilicate and calcium source, the mol ratio of calcium is 30 ~ 55:1.
In step (3), described precipitating reagent is polyacrylamide or ferric sulfate; Wherein, the mass ratio of precipitating reagent and sodium metasilicate is 1:600 ~ 750.
In step (4), the method for washing is for using deionized water rinsing 2 ~ 3 times, and dry method is for using sodium sulfite dry, and the method for roast is roasting 1 ~ 1.5h at 600 ~ 700 DEG C.
What above-mentioned preparation method prepared carries calcium silica-gel catalyst also within protection scope of the present invention.
Above-mentioned year calcium silica-gel catalyst in the application of catalyst field also within protection scope of the present invention.
Beneficial effect: compared with prior art, the present invention has following advantage:
Year calcium silica-gel catalyst in the present invention, is fixed on silica-gel carrier by the calcium dispersion playing catalytic action, expands itself and the contact area of reacting bed material.Compared with prior art, the catalytic efficiency of this year calcium silica-gel catalyst is higher, and required catalytic condition milder, is conducive to industrial production.Meanwhile, the inventive method completes under pure organic phase condition, and through contrast, more general aqueous conditions, it is higher that gained carries calcium silica-gel catalyst catalytic efficiency.
Detailed description of the invention
According to following embodiment, the present invention may be better understood.But those skilled in the art will readily understand, the content described by embodiment only for illustration of the present invention, and should can not limit the present invention described in detail in claims yet.
The preparation of embodiment 1 catalyst
Preparation method:
(1) anhydrous sodium metasilicate is dissolved in methyl-sulfoxide, under the condition of nitrogen protection, in methyl-sulfoxide, passes into hydrogen chloride gas, on shaking table, react 4h at 45 DEG C;
(2) keep nitrogen protection condition, in the mixed system of step (1) gained, add calcium chloride, on shaking table, react 1h at 40 DEG C;
(3) in the mixed system of gained in step (2), add polyacrylamide, fully mix, after colloidal sol is complete, get gel;
(4) by the gel of gained in step (3) with after deionized water rinsing 2 ~ 3 times, dry with sodium sulfite, finally after roasting 1h, obtain carrying a calcium silica-gel catalyst at 700 DEG C.
In step (1) ~ (3), agents useful for same is all through anhydrous process.
In step (1), the weight ratio of anhydrous sodium metasilicate and organic solvent is 1:120.
In step (1), the mol ratio of anhydrous sodium metasilicate and hydrogen chloride is 1:2.7.
In step (2), in anhydrous sodium metasilicate and calcium chloride, the mol ratio of calcium is 35:1.
In step (3), the mass ratio of polyacrylamide and anhydrous sodium metasilicate is 1:650.
Comparative example 1
Preparation method is with embodiment 1, and difference is, sodium metasilicate used is metasilicate pentahydrate sodium.
Comparative example 2
Preparation method is with embodiment 1, and difference is, methyl-sulfoxide is replaced with water.
Embodiment 2
The reaction of calcium silica-gel catalyst for the synthesis of 9-hydroxyphenyl fluorene-9 methyl formate is carried by what prepare in embodiment 1, comparative example 1 and comparative example 2.Under the same conditions, according to the conversion of reaction rate, if the catalytic efficiency carrying calcium silica-gel catalyst in embodiment 1 is 1, the catalytic efficiency in comparative example 1 is 0.82, and the catalytic efficiency in comparative example 2 is 0.73.

Claims (8)

1. carry a preparation method for calcium silica-gel catalyst, it is characterized in that, comprise the steps:
(1) sodium metasilicate is dissolved in organic solvent, under the condition of nitrogen protection, in organic solvent, passes into hydrogen chloride gas, at 30 ~ 60 DEG C, react 3 ~ 6h;
(2) keep nitrogen protection condition, in the mixed system of step (1) gained, add calcium source, at 40 ~ 45 DEG C, react 1 ~ 3h;
(3) in the mixed system of gained in step (2), add precipitating reagent, fully mix, after colloidal sol is complete, get gel;
(4) by after the gel detergent of gained in step (3), drying, roast, obtain carrying calcium silica-gel catalyst.
2. preparation method according to claim 1, is characterized in that, in step (1), described organic solvent is methyl-sulfoxide.
3. preparation method according to claim 1, is characterized in that, in step (1), the weight ratio of sodium metasilicate and organic solvent is 1:50 ~ 200.
4. preparation method according to claim 1, is characterized in that, in step (1), the mol ratio of sodium metasilicate and hydrogen chloride is 1:1.5 ~ 3.5.
5. preparation method according to claim 1, is characterized in that, in step (2), described calcium source is calcium chloride, calcium phosphate or calcium carbonate.
6. preparation method according to claim 1, is characterized in that, in step (2), in sodium metasilicate and calcium source, the mol ratio of calcium is 30 ~ 55:1.
7. preparation method according to claim 1, is characterized in that, in step (3), described precipitating reagent is polyacrylamide or ferric sulfate; Wherein, the mass ratio of precipitating reagent and sodium metasilicate is 1:600 ~ 750.
8. preparation method according to claim 1, is characterized in that, in step (4), the method for washing is for using deionized water rinsing 2 ~ 3 times, and dry method is for using sodium sulfite dry, and the method for roast is roasting 1 ~ 1.5h at 600 ~ 700 DEG C.
CN201510776724.XA 2015-11-13 2015-11-13 Preparation method of calcium-loaded silica gel catalyst Pending CN105457619A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510776724.XA CN105457619A (en) 2015-11-13 2015-11-13 Preparation method of calcium-loaded silica gel catalyst

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510776724.XA CN105457619A (en) 2015-11-13 2015-11-13 Preparation method of calcium-loaded silica gel catalyst

Publications (1)

Publication Number Publication Date
CN105457619A true CN105457619A (en) 2016-04-06

Family

ID=55596034

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510776724.XA Pending CN105457619A (en) 2015-11-13 2015-11-13 Preparation method of calcium-loaded silica gel catalyst

Country Status (1)

Country Link
CN (1) CN105457619A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006193708A (en) * 2004-12-15 2006-07-27 Kaneka Corp Fluorene skeleton-containing (meth)acrylic polymer and method for producing the same
CN103633268A (en) * 2012-08-22 2014-03-12 海洋王照明科技股份有限公司 Preparation method of silicon dioxide composite separators
CN104190396A (en) * 2014-08-28 2014-12-10 无锡普爱德环保科技有限公司 Preparation method of lithium-loaded silica gel catalyst

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006193708A (en) * 2004-12-15 2006-07-27 Kaneka Corp Fluorene skeleton-containing (meth)acrylic polymer and method for producing the same
CN103633268A (en) * 2012-08-22 2014-03-12 海洋王照明科技股份有限公司 Preparation method of silicon dioxide composite separators
CN104190396A (en) * 2014-08-28 2014-12-10 无锡普爱德环保科技有限公司 Preparation method of lithium-loaded silica gel catalyst

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
文海,等: "9-羟基芴-9-甲酸和醇酯化反应的无水氯化钙催化剂", 《内蒙古林学院学报(自然科学版)》 *
朱旭,等: "用无水氯化钙作催化剂的研究", 《内蒙古石油化工》 *
朱洪法: "《催化剂载体制备及应用技术》", 31 October 2014, 石油工业出版社 *
陆鼎一: "《化学故事新编》", 31 July 2007, 苏州大学出版社 *

Similar Documents

Publication Publication Date Title
CN104525237A (en) Nitrogen-doped active carbon catalyzer and application thereof in chloroethylene synthesis
CN104190396B (en) A kind of preparation method carrying lithium silica-gel catalyst
JP6719527B2 (en) Method for preparing azoxystrobin intermediate
CN105348071B (en) One class is based on the preparation method and applications of the discrete type metal organic nanotube that tetraphenyl ethylene derivative is constructed
CN103570493A (en) Method for synthesizing 1,2-orthodiol through immobilized type heteropolyacid phase-transfer catalytic oxidation
CN103182322B (en) A kind of method processing deactivated titanium silicon molecular sieve
CN106916109B (en) A method of it protonating pyrazoles ionic liquid and utilizes its catalytically synthesizing cyclic carbonate ester
CN109746042B (en) Catalyst for synthesizing 3-methoxy methyl acrylate and solid-supported and using method
CN100453540C (en) Process for preparing cyclic alkyl carbonate
CN106732770B (en) In a mild condition by CO2It is converted into the catalyst and method of cyclic carbonate
CN103910363B (en) A kind of method of HTS modification and application thereof
CN102442992A (en) Method for synthesizing glycerol carbonate with biodiesel based crude glycerine and dimethyl carbonate
TR200003096T2 (en) Improved process for producing pure carboxylic acids.
CN105457619A (en) Preparation method of calcium-loaded silica gel catalyst
CN105289567A (en) Calcium-loaded silica gel catalyst and applications thereof
CN105457634A (en) Copper-based catalyst and application thereof
CN105289607A (en) Preparation method of copper based catalyst
CN105665022A (en) Dual-function catalyst for preparing cyclic carbonates through cycloaddition of CO2 and epoxy compound and preparation method thereof
CN105457639A (en) Preparation method of composite catalyst
CN106366026A (en) Preparation method of sulfhydryl compound
CN103880780B (en) A kind of method that propylene liquid phase epoxidation prepares expoxy propane
CN105251481A (en) Preparation method of dechlorination catalyst
CN105251495A (en) Composite catalyst and application thereof
CN102942548B (en) Delta-dodecalactone synthesis method
CN105289618A (en) Hydrogenation catalyst, and applications thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20160406