CN102558559A - Method of synthetizing small molecule hydroxyl silicone oil through using continuation method - Google Patents

Method of synthetizing small molecule hydroxyl silicone oil through using continuation method Download PDF

Info

Publication number
CN102558559A
CN102558559A CN2011104545808A CN201110454580A CN102558559A CN 102558559 A CN102558559 A CN 102558559A CN 2011104545808 A CN2011104545808 A CN 2011104545808A CN 201110454580 A CN201110454580 A CN 201110454580A CN 102558559 A CN102558559 A CN 102558559A
Authority
CN
China
Prior art keywords
silicone oil
hydroxyl silicone
grams
product
fixed bed
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
Application number
CN2011104545808A
Other languages
Chinese (zh)
Other versions
CN102558559B (en
Inventor
肖赣湘
孙秀珍
廖桂根
贺志江
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.)
Jiangxi Bluestar Xinghuo Silicone Co Ltd
Original Assignee
JIANGXI XINGHUO ORGANIC SILICON PLANT LANXING CHEMICAL NEW MATERIAL 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 JIANGXI XINGHUO ORGANIC SILICON PLANT LANXING CHEMICAL NEW MATERIAL CO Ltd filed Critical JIANGXI XINGHUO ORGANIC SILICON PLANT LANXING CHEMICAL NEW MATERIAL CO Ltd
Priority to CN201110454580.8A priority Critical patent/CN102558559B/en
Publication of CN102558559A publication Critical patent/CN102558559A/en
Application granted granted Critical
Publication of CN102558559B publication Critical patent/CN102558559B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention relates to a method of synthetizing small molecule hydroxyl silicone oil through using a continuation method. The method comprises the steps as follows: adding the1,000 g of hexamethyl cyclotrisiloxane, 1,400 g of acetone and 120 g of water into a 3,000 ml four-mouth bottle with the stirring function, heating and keeping the temperature to 40 DEG C to 60 DEG C, melting and mixing uniformly; adopting a peristaltic pump to continuously pass through two fixed beds added with 100 g of strongly acidic styrene cation exchange resin, wherein the strongly acidic styrene cation exchange resin comprises a macroporous type and a gel type, and has the following grades: 732, D001, KY-2 and KY-23; obtaining a small molecule hydroxyl silicone oil crude product after the each fixed bed reaction temperature is 40 DEG C to 60 DEG C and the retention time is controlled to 30-70 seconds; and obtaining small molecule hydroxyl silicone oil after the crude product is subject to normal pressure desolvation, decompression and removal of low component. The method has the advantages of continuation production, high reproducibility and high product yield; and moreover, the product is colorless transparent liquid from the appearance, the viscosity is 15-30 mm2/s, and the hydroxyl content is in the range of 6-10%.

Description

A kind of method of continuous processing synthesizing small molecular hydroxy silicon oil
Technical field
The present invention relates to a kind of method of synthesizing small molecular hydroxy silicon oil, especially a kind of method of continuous processing synthesizing small molecular hydroxy silicon oil.
Background technology
Micromolecular hydroxyl silicone oil is the material that has the reactive group hydroxyl, is Zylox ideal constitution controller.The method for preparing micromolecular hydroxyl silicone oil has multiple, and suitability for industrialized production is used more be D4 (DMC) and acetic anhydride at present, but product has the acetic acid taste.
Summary of the invention
The present invention provides a kind of method of continuous processing synthesizing small molecular hydroxy silicon oil, with the by product D that obtains in the production of organosilicon methyl cyclosiloxane 3Be raw material, make hydroxy silicon oil, the digestion by product, the added value of raising by product, yield is high, and product can be used by oneself or export trade.
A kind of method of continuous processing synthesizing small molecular hydroxy silicon oil; Hexamethyl cyclotrisiloxane 1000 grams, acetone 1400 grams, water 120 grams are joined in the 3000ml four-hole bottle of band stirring; Heating up also keeps 40-60 ℃, dissolve mix after, adopt peristaltic pump continuously through 2 fixed beds that are added with 100 gram strongly acidic styrene type cation exchange resins; 40-60 ℃ of each fixed bed reaction temperature, the residence time are controlled at 30-70 second; Obtain the thick product of micromolecular hydroxyl silicone oil, reducing pressure behind the thick frequent pressure-off solvent of product removes low component again, obtains micromolecular hydroxyl silicone oil.
Wherein strongly acidic styrene type cation exchange resin comprises macroporous type and gel-type, comprises the following trade mark: 732, and D001, KY-2, KY-23.
The inventive method is raw material with the hexamethyl cyclotrisiloxane, and technology can serialization production, good reproducibility; Product yield is high, and stability in storage is better, and the shelf lives can reach more than 6 months, and product appearance is a colourless transparent liquid, and viscosity is at 15-30mm 2/ s, hydroxy radical content is between 6-10%; Technology does not have " three wastes " pollution in the production process, and solvent and low-boiling-point substance can be recycled, but industrialized production.
After stability was embodied in 6 months shelf liveves, product appearance is colourless transparent liquid, and was not stratified, after 6 months shelf liveves hydroxy radical content measure with the shelf lives before compare to descend and be no more than 5%.
Embodiment
Embodiment 1:
A kind of method of continuous processing synthesizing small molecular hydroxy silicon oil joins hexamethyl cyclotrisiloxane 1000 gram, acetone 1400 grams, water 120 grams in the 3000ml four-hole bottle that band stirs, and heats up and keeps 50 ℃; Dissolve mix after, adopt peristaltic pump continuously through the fixed bed of 100 gram D001 strong-acid ion exchange resins and the fixed bed of 100 gram KY-23 strong-acid ion exchange resins, 50 ℃ of each fixed bed reaction temperature, the residence time were controlled at 50 seconds; Obtain the thick product of micromolecular hydroxyl silicone oil; Reduce pressure again behind the thick frequent pressure-off solvent of product and remove low component, obtain micromolecular hydroxyl silicone oil, viscosity 22CS; Hydroxy radical content 9%, yield 94.6%.
After stability was embodied in 6 months shelf liveves, product appearance is colourless transparent liquid, and was not stratified, after 6 months shelf liveves hydroxy radical content measure with the shelf lives before compare to descend and be no more than 2%.
Embodiment 2:
A kind of method of continuous processing synthesizing small molecular hydroxy silicon oil joins hexamethyl cyclotrisiloxane 1000 gram, acetone 1400 grams, water 120 grams in the 3000ml four-hole bottle that band stirs, and heats up and keeps 40 ℃; Dissolve mix after, adopt the peristaltic pump fixed bed through being added with 100 grams, 732 ion exchange resin and the fixed bed of 100 gram KY-2 ion exchange resin continuously, 40 ℃ of each fixed bed reaction temperature, the residence time were controlled at 30 seconds; Obtain the thick product of micromolecular hydroxyl silicone oil; Reduce pressure again behind the thick frequent pressure-off solvent of product and remove low component, obtain micromolecular hydroxyl silicone oil, viscosity 24CS; Hydroxy radical content 8%, yield 90.1%.
After stability was embodied in 6 months shelf liveves, product appearance is colourless transparent liquid, and was not stratified, after 6 months shelf liveves hydroxy radical content measure with the shelf lives before compare to descend and be no more than 5%.
Embodiment 3:
A kind of method of continuous processing synthesizing small molecular hydroxy silicon oil joins hexamethyl cyclotrisiloxane 1000 gram, acetone 1400 grams, water 120 grams in the 3000ml four-hole bottle that band stirs, and heats up and keeps 60 ℃; Dissolve mix after, adopt peristaltic pump to be added with the fixed bed of 100 gram D001 strong-acid ion exchange resins and the fixed bed of 100 gram KY-2 ion exchange resin through 2 continuously, 60 ℃ of each fixed bed reaction temperature, the residence time were controlled at 70 seconds; Obtain the thick product of micromolecular hydroxyl silicone oil; Reduce pressure again behind the thick frequent pressure-off solvent of product and remove low component, obtain micromolecular hydroxyl silicone oil, viscosity 20CS; Hydroxy radical content 9%, yield 93.9%.
After stability was embodied in 6 months shelf liveves, product appearance is colourless transparent liquid, and was not stratified, after 6 months shelf liveves hydroxy radical content measure with the shelf lives before compare to descend and be no more than 5%.
Embodiment 4:
A kind of method of continuous processing synthesizing small molecular hydroxy silicon oil joins hexamethyl cyclotrisiloxane 1000 gram, acetone 1400 grams, water 120 grams in the 3000ml four-hole bottle that band stirs, and heats up and keeps 35 ℃; Dissolve mix after, adopt peristaltic pump continuously through 1 fixed bed that is added with 100 grams, 732 ion exchange resin, 38 ℃ of each fixed bed reaction temperature, the residence time were controlled at 27 seconds; Obtain the thick product of micromolecular hydroxyl silicone oil; Reduce pressure again behind the thick frequent pressure-off solvent of product and remove low component, obtain micromolecular hydroxyl silicone oil, viscosity 13CS; Hydroxy radical content 5%, yield 70.7%.
After stability was embodied in 6 months shelf liveves, product appearance is colourless transparent liquid, and was not stratified, after 6 months shelf liveves hydroxy radical content measure with the shelf lives before compare to descend and be no more than 8%.
Embodiment 5:
A kind of method of continuous processing synthesizing small molecular hydroxy silicon oil joins hexamethyl cyclotrisiloxane 1000 gram, acetone 1400 grams, water 120 grams in the 3000ml four-hole bottle that band stirs, and heats up and keeps 65 ℃; Dissolve mix after, adopt peristaltic pump continuously through 1 fixed bed that is added with 100 gram KY-23 strong-acid ion exchange resins, 65 ℃ of each fixed bed reaction temperature, the residence time were controlled at 75 seconds; Obtain the thick product of micromolecular hydroxyl silicone oil; Reduce pressure again behind the thick frequent pressure-off solvent of product and remove low component, obtain micromolecular hydroxyl silicone oil, viscosity 10CS; Hydroxy radical content 11%, yield 72.8%.
After stability was embodied in 6 months shelf liveves, product appearance is colourless transparent liquid, and was not stratified, after 6 months shelf liveves hydroxy radical content measure with the shelf lives before compare to descend and be no more than 10%.

Claims (3)

1. the method for a continuous processing synthesizing small molecular hydroxy silicon oil; It is characterized by: hexamethyl cyclotrisiloxane 1000 grams, acetone 1400 grams, water 120 grams are joined in the 3000ml four-hole bottle of band stirring; Heating up also keeps 40-60 ℃, dissolve mix after, adopt peristaltic pump continuously through 2 fixed beds that are added with 100 gram strongly acidic styrene type cation exchange resins; 40-60 ℃ of each fixed bed reaction temperature, the residence time were controlled at 50 ± 20 seconds; Obtain the thick product of micromolecular hydroxyl silicone oil, reducing pressure behind the thick frequent pressure-off solvent of product removes low component again, obtains micromolecular hydroxyl silicone oil.
2. the method for a kind of continuous processing synthesizing small molecular hydroxy silicon oil as claimed in claim 1 is characterized by: strongly acidic styrene type cation exchange resin comprises macroporous type and gel-type, and the following trade mark is arranged: 732, and D001, KY-2, KY-23.
3. the method for a kind of continuous processing synthesizing small molecular hydroxy silicon oil as claimed in claim 1; It is characterized by: hexamethyl cyclotrisiloxane 1000 grams, acetone 1400 grams, water 120 grams are joined in the 3000ml four-hole bottle of band stirring; Heating up also keeps 50 ℃, dissolve mix after, adopt peristaltic pump continuously through the fixed bed of 100 gram D001 strong-acid ion exchange resins and the fixed bed of 100 gram KY-23 strong-acid ion exchange resins; 50 ℃ of each fixed bed reaction temperature, the residence time were controlled at 50 seconds; Obtain the thick product of micromolecular hydroxyl silicone oil, reducing pressure behind the thick frequent pressure-off solvent of product removes low component again, obtains micromolecular hydroxyl silicone oil.
CN201110454580.8A 2011-12-30 2011-12-30 Method of synthetizing small molecule hydroxyl silicone oil through using continuation method Active CN102558559B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201110454580.8A CN102558559B (en) 2011-12-30 2011-12-30 Method of synthetizing small molecule hydroxyl silicone oil through using continuation method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201110454580.8A CN102558559B (en) 2011-12-30 2011-12-30 Method of synthetizing small molecule hydroxyl silicone oil through using continuation method

Publications (2)

Publication Number Publication Date
CN102558559A true CN102558559A (en) 2012-07-11
CN102558559B CN102558559B (en) 2014-03-05

Family

ID=46405266

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201110454580.8A Active CN102558559B (en) 2011-12-30 2011-12-30 Method of synthetizing small molecule hydroxyl silicone oil through using continuation method

Country Status (1)

Country Link
CN (1) CN102558559B (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102898646A (en) * 2012-09-06 2013-01-30 江苏梅兰化工有限公司 Continuous production process for silicone oil
CN105754102A (en) * 2016-04-27 2016-07-13 广州道林合成材料有限公司 Hydroxyl silicone oil and continuous preparation method thereof
CN107722276A (en) * 2017-10-18 2018-02-23 广州道林合成材料有限公司 Silicone oil and its continuous preparation method
CN108440757A (en) * 2018-03-29 2018-08-24 李卓瑾 A kind of constitution controller and production technology
CN110527482A (en) * 2019-09-17 2019-12-03 陕西杨凌磐基新材料科技有限公司 Railway ballastless track special dual-component filleting waterproof gasket cement and preparation method thereof
CN110606953A (en) * 2019-09-26 2019-12-24 唐山三友硅业有限责任公司 Low-viscosity hydroxyl-terminated vinyl methyl silicone oil and continuous preparation method thereof
CN111234192A (en) * 2020-03-26 2020-06-05 山东福司特新材料科技有限公司 Preparation method of organic silicon modified saturated polyester resin with high weather resistance
CN112119111A (en) * 2018-05-17 2020-12-22 赢创运营有限公司 Linear polydimethylsiloxane-polyoxyalkylene block copolymers of the ABA structure type
CN112625241A (en) * 2020-10-12 2021-04-09 湖北兴瑞硅材料有限公司 Synthesis method of low-viscosity hydroxyl silicone oil

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3853932A (en) * 1973-12-28 1974-12-10 Gen Electric Process for producing silanol end-stopped polymers of low molecular weight
CN101225170A (en) * 2008-01-26 2008-07-23 中国船舶重工集团公司第七二五研究所 Method for synthesizing short-chain hydroxyl silicone oil
CN101570601A (en) * 2008-04-30 2009-11-04 中国石油天然气股份有限公司 Method for preparing low-molecular-weight hydroxyl silicone oil
CN101735258A (en) * 2009-12-18 2010-06-16 嘉兴学院 Method for preparing micromolecular hydroxyl silicone oil
DE102010000993A1 (en) * 2010-01-19 2011-07-21 Evonik Goldschmidt GmbH, 45127 Novel polysiloxanes with quaternary ammonium groups, process for their preparation and their use in cleansing and conditioning formulations

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3853932A (en) * 1973-12-28 1974-12-10 Gen Electric Process for producing silanol end-stopped polymers of low molecular weight
CN101225170A (en) * 2008-01-26 2008-07-23 中国船舶重工集团公司第七二五研究所 Method for synthesizing short-chain hydroxyl silicone oil
CN101570601A (en) * 2008-04-30 2009-11-04 中国石油天然气股份有限公司 Method for preparing low-molecular-weight hydroxyl silicone oil
CN101735258A (en) * 2009-12-18 2010-06-16 嘉兴学院 Method for preparing micromolecular hydroxyl silicone oil
DE102010000993A1 (en) * 2010-01-19 2011-07-21 Evonik Goldschmidt GmbH, 45127 Novel polysiloxanes with quaternary ammonium groups, process for their preparation and their use in cleansing and conditioning formulations

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
李美江等: "低粘度羟基封端聚甲基苯基硅氧烷的合成研究", 《化工生产与技术》 *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102898646B (en) * 2012-09-06 2015-01-28 江苏梅兰化工有限公司 Continuous production process for silicone oil
CN102898646A (en) * 2012-09-06 2013-01-30 江苏梅兰化工有限公司 Continuous production process for silicone oil
CN105754102A (en) * 2016-04-27 2016-07-13 广州道林合成材料有限公司 Hydroxyl silicone oil and continuous preparation method thereof
WO2017185874A1 (en) * 2016-04-27 2017-11-02 广州道林合成材料有限公司 Hydroxyl silicone oil and continuous method for preparing same
CN105754102B (en) * 2016-04-27 2018-08-21 广州道林合成材料有限公司 A kind of hydroxy silicon oil and its continuous preparation method
CN107722276B (en) * 2017-10-18 2020-08-07 广州福泽新材料有限公司 Silicone oil and continuous preparation method thereof
CN107722276A (en) * 2017-10-18 2018-02-23 广州道林合成材料有限公司 Silicone oil and its continuous preparation method
CN108440757A (en) * 2018-03-29 2018-08-24 李卓瑾 A kind of constitution controller and production technology
CN112119111A (en) * 2018-05-17 2020-12-22 赢创运营有限公司 Linear polydimethylsiloxane-polyoxyalkylene block copolymers of the ABA structure type
CN110527482A (en) * 2019-09-17 2019-12-03 陕西杨凌磐基新材料科技有限公司 Railway ballastless track special dual-component filleting waterproof gasket cement and preparation method thereof
CN110527482B (en) * 2019-09-17 2021-06-29 陕西杨凌磐基新材料科技有限公司 Special two-component caulking waterproof sealant for railway ballastless track and preparation method thereof
CN110606953A (en) * 2019-09-26 2019-12-24 唐山三友硅业有限责任公司 Low-viscosity hydroxyl-terminated vinyl methyl silicone oil and continuous preparation method thereof
CN111234192A (en) * 2020-03-26 2020-06-05 山东福司特新材料科技有限公司 Preparation method of organic silicon modified saturated polyester resin with high weather resistance
CN112625241A (en) * 2020-10-12 2021-04-09 湖北兴瑞硅材料有限公司 Synthesis method of low-viscosity hydroxyl silicone oil

Also Published As

Publication number Publication date
CN102558559B (en) 2014-03-05

Similar Documents

Publication Publication Date Title
CN102558559B (en) Method of synthetizing small molecule hydroxyl silicone oil through using continuation method
CN102295658B (en) Refining method of disodium phosphocreatine
CN103613501A (en) Method for preparing tributyl citrate by taking macroporous strong-acid cation exchange resin as catalyst
CN102503845A (en) Preparation method of DL-lysine aspirin salt and application thereof
CN103420881A (en) Novel method for preparing medicinal despun hydroxyl methionine calcium
CN103183602B (en) The crystallization method of 2,2-dipropyl propanedioic acid
CN103193636A (en) Method for synthetizing 2,3-butanediol ester
CN102838455A (en) Method for extracting high-content resveratrol from polygonum cuspidatum
CN103922925B (en) A kind of production technique of Fenofibric Acid
CN104745660B (en) Method for preparing trehalose through enzymatic synthesis
CN103012536A (en) Sodium fusidate crystallization method
CN103804174A (en) Organic acid refining method
CN103819478B (en) The preparation method of my Ge Lieting intermediate 2-methyl-pyrazolo [1,5-A] pyrimidine-6-carboxylic acid
CN107814709A (en) A kind of high-quality glycolic purifying technique
CN102010345A (en) Method for preparing D-phenylalanine through dynamic kinetic resolution
CN103922901B (en) The process for purification of polidocanol
CN103571891B (en) Method for extracting resveratrol from polygonum cuspidatum
CN103030658B (en) The industrialized preparing process of diisopinocampheylchloroborane
CN101768190B (en) Improvement method for refining and extracting technique in production process of fosphenytoin sodium intermediate
CN104557515A (en) Method for extracting and separating L-lactic acid from ammonium lactate fermentation material liquid
CN102040673B (en) Refining and purification method of enoxaparin
CN103923959B (en) A kind of D Tagatose production methods based on enzymatic isomerization reaction and continuous chromatography separation coupling in situ
CN103172532B (en) A kind of preparation method of ethylenediaminetetraacidic acidic calcium disodium salt
CN104262415A (en) Efficient production method of D-arabinose
CN104327128A (en) Preparation method of glucosamine hydrochloride

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
CP03 Change of name, title or address
CP03 Change of name, title or address

Address after: 330300 Yangjialing, Yongxiu County, Jiujiang City, Jiangxi Province

Patentee after: JIANGXI BLUESTAR XINGHUO ORGANIC SILICONE Co.,Ltd.

Address before: 330319 Spark Industrial Park, Yongxiu County, Jiujiang City, Jiangxi Province

Patentee before: Jiangxi Star-Fire Silicone Factory of Bluestar New Chemical Materials Co.,Ltd.