CN106883330A - A kind of high viscosity pastes the preparation method of resin - Google Patents

A kind of high viscosity pastes the preparation method of resin Download PDF

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Publication number
CN106883330A
CN106883330A CN201510955427.1A CN201510955427A CN106883330A CN 106883330 A CN106883330 A CN 106883330A CN 201510955427 A CN201510955427 A CN 201510955427A CN 106883330 A CN106883330 A CN 106883330A
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CN
China
Prior art keywords
latex
vcm
added
polymeric kettle
resin
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
CN201510955427.1A
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Chinese (zh)
Inventor
刘金刚
田爱娟
李永胜
李益成
张东洲
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Tianjin Botian Chemical Co Ltd
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Tianjin Botian Chemical Co Ltd
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Application filed by Tianjin Botian Chemical Co Ltd filed Critical Tianjin Botian Chemical Co Ltd
Priority to CN201510955427.1A priority Critical patent/CN106883330A/en
Publication of CN106883330A publication Critical patent/CN106883330A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F114/00Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
    • C08F114/02Monomers containing chlorine
    • C08F114/04Monomers containing two carbon atoms
    • C08F114/06Vinyl chloride
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/12Polymerisation in non-solvents
    • C08F2/16Aqueous medium
    • C08F2/22Emulsion polymerisation
    • C08F2/24Emulsion polymerisation with the aid of emulsifying agents
    • C08F2/26Emulsion polymerisation with the aid of emulsifying agents anionic

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

A kind of high viscosity pastes the preparation method of resin, is produced using emulsion polymerization, in the composition of raw materials ratio of following weight portion:100~700 parts of VCM, 100~700 parts of deionized water, 1~12 part of potassium peroxydisulfate, 1~12 part of sodium hydrogensulfite, 1~8 part of sodium lauryl sulfate, 1~6 part of ammonium hydrogen carbonate, monomer and auxiliary agent are added into polymeric kettle, evacuated, deoxidation, under stirring, it is warming up to 50~63 DEG C, polymerisation is carried out at this temperature, and 0.83MPa pressure begins to decline, when pressure drops to 0.4MPa, reaction terminates, the method have the characteristics that:High viscosity paste resin can be prepared using emulsion method.The purpose of control paste resin viscosity is reached by the adjustment to technique.Require that paste resin viscosity is high and is easy to deaeration using the imitative rubber safety and industrial gloves of this kind of paste production of resins.

Description

A kind of high viscosity pastes the preparation method of resin
Technical field
It is specifically a kind of that high viscosity paste is prepared using emulsion method the invention belongs to macromolecule chemical industry technical field The production method of resin.
Background technology
China is the production base of world's safety and industrial gloves, and the sector is larger to pasting the consumption of resin, and at present only The P737 for having Sweden can be used alone, but price is higher, and domestic rouge and powder can partly substitute P737, but There is the lacklustre phenomenon of gloves, thus most producers using more than 3 kinds of paste resin be used in mixed way come Reach requirement.Annual the sector should be more than 100,000 tons to the consumption of resin, the imitative rubber labour protection of non-liner More than 20,000 tons, imitative rubber safety and industrial gloves requirement paste resin viscosity is high at present and is easy to deaeration for gloves consumption, Product is glossy.The sector has new processing producer to go into operation every year, imitates at the demand of rubber safety and industrial gloves In the trend for rising.
The content of the invention
It is an object of the invention to provide the preparation method that a kind of high viscosity pastes resin, the obtained particle diameter for pasting resin It is required that at 5.0 μm~20.0 μm, high viscosity paste resin is prepared on this basis.
The object of the present invention is achieved like this:Its technical scheme includes following chemical composition, composition and its formula:
A kind of high viscosity pastes the preparation method of resin, it is characterised in that using emulsion polymerization production, by following The composition of raw materials ratio of weight portion:100~700 parts of VCM, 100~700 parts of deionized water, over cure 1~12 part of sour potassium, 1~12 part of sodium hydrogensulfite, 1~8 part of sodium lauryl sulfate, 1~6 part of ammonium hydrogen carbonate, Monomer and auxiliary agent are added into polymeric kettle, evacuated, deoxidation under stirring, is warming up to 50~63 DEG C, Polymerisation is carried out at this temperature, and 0.83MPa pressure begins to decline, when pressure drops to 0.4MPa, instead Should terminate, detailed process is as follows:
(1) in the state of stirring, lauryl alcohol sulfuric acid is added by deionized water addition polymeric kettle in proportion Sodium, sodium hydrogensulfite, ammonium hydrogen carbonate;
(2) then polymeric kettle vacuumize, deoxidation, by formula add VCM, by polymerization kettle temperature raising extremely 50~63 DEG C, sodium lauryl sulfate is continuously added in the course of the polymerization process;
(3) the good potassium persulfate solution of water dissolves is added continuously in polymeric kettle, is kept stirring for state, entered Row polymerisation, control is reacted at 50~63 DEG C, when 0.83MPa pressure begins to decline, when pressure drops to 0.4MPa When, reaction terminates;
(4) after reaction terminates, unreacted VCM is first recycled to gas holder, latex is delivered into latex Storage tank;
(5) using the VCM in vaporizing extract process removal latex:Extracted out from latex storage tank by delivery pump Latex, by steam direct heating after, into stripper, residual monomer and a small amount of moisture content are by tower in latex Removing is vacuumized, the vinyl chloride being stripped out is recycled to gas holder, passed through the latex after gas with delivery pump Filter is sent to drying section;
(6) dry
Stripped latex is dried treatment using spray drying process, it is desirable to water content≤0.4%;
(7) particle diameter of dried material is at 5.0~20.0 μm;
(8) and then weighed, packed.
The method have the characteristics that:
1. high viscosity paste resin can be prepared using emulsion method.
2. the purpose of control paste resin viscosity is reached by the adjustment to technique.
3. require that paste resin viscosity is high and is easy to deaeration using the imitative rubber safety and industrial gloves of this kind of paste production of resins.
Specific implementation 1
(1) over cure of the VCM of 12Kg, the deionized water of 12Kg, 10g is added by above-mentioned formula Sour potassium, the sodium hydrogensulfite of 10g, the sodium lauryl sulfate of 140g, the ammonium hydrogen carbonate of 5g.
(2) then polymeric kettle vacuumize, deoxidation, by formula add VCM, by polymerization kettle temperature raising extremely 50~63 DEG C, sodium lauryl sulfate is continuously added in the course of the polymerization process;
(3) the good potassium persulfate solution of water dissolves is added continuously in polymeric kettle, is kept stirring for state, entered Row polymerisation, control is reacted at 52.0 DEG C, when 0.81MPa pressure begins to decline, when pressure drops to 0.4MPa When, reaction terminates;
(4) after reaction terminates, unreacted VCM is first recycled to gas holder, latex is delivered into latex Storage tank;
(5) using the VCM in air- extraction removal latex:Extracted out from latex storage tank by delivery pump Latex, by steam direct heating after, into stripper, residual monomer and a small amount of moisture content are by tower in latex Removing is vacuumized, the vinyl chloride being stripped out is recycled to gas holder, passed through the latex after gas with delivery pump Filter is sent to drying section;
(6) dry
Stripped latex is dried treatment using spray drying process, it is desirable to water content≤0.4%;
(7) particle diameter of dried material is at 5.0~20.0 μm;
(8) and then weighed, packed.
(9) material test data is average degree of polymerization:1250;Average grain diameter:13μm;Paste resin viscosity: 42000mpa.s。
Specific implementation 2
(1) over cure of the VCM of 13Kg, the deionized water of 12Kg, 10g is added by above-mentioned formula Sour potassium, the sodium hydrogensulfite of 10g, the sodium lauryl sulfate of 140g, the ammonium hydrogen carbonate of 5g.
(2) then polymeric kettle vacuumize, deoxidation, by formula add VCM, by polymerization kettle temperature raising extremely 50~63 DEG C, sodium lauryl sulfate is continuously added in the course of the polymerization process;
(3) the good potassium persulfate solution of water dissolves is added continuously in polymeric kettle, is kept stirring for state, entered Row polymerisation, control is reacted at 50.0 DEG C, when 0.80MPa pressure begins to decline, when pressure drops to 0.4MPa When, reaction terminates;
(4) after reaction terminates, unreacted VCM is first recycled to gas holder, latex is delivered into latex Storage tank;
(5) using the VCM in gas hair removal latex:Extracted out from latex storage tank by delivery pump Latex, by steam direct heating after, into stripper, residual monomer and a small amount of moisture content are by tower in latex Removing is vacuumized, the vinyl chloride being stripped out is recycled to gas holder, passed through the latex after gas with delivery pump Filter is sent to drying section;
(6) dry
Stripped latex is dried treatment using spray drying process, it is desirable to water content≤0.4%;
(7) particle diameter of dried material is at 5.0~20.0 μm;
(8) and then weighed, packed.
(9) material test data is average degree of polymerization:1350;Average grain diameter:10μm;Paste resin Viscosity:38000mpa.s.

Claims (1)

1. a kind of high viscosity pastes the preparation method of resin, it is characterised in that using emulsion polymerization production, press The composition of raw materials ratio of following weight portion:100~700 parts of VCM, 100~700 parts of deionized water, 1~12 part of potassium peroxydisulfate, 1~12 part of sodium hydrogensulfite, 1~8 part of sodium lauryl sulfate, ammonium hydrogen carbonate 1~6 Part, monomer and auxiliary agent are added into polymeric kettle, evacuated, deoxidation under stirring, is warming up to 50~63 DEG C, Polymerisation is carried out at this temperature, and 0.83MPa pressure begins to decline, when pressure drops to 0.4MPa, instead Should terminate, detailed process is as follows:
(1) in the state of stirring, lauryl alcohol sulfuric acid is added by deionized water addition polymeric kettle in proportion Sodium, sodium hydrogensulfite, ammonium hydrogen carbonate;
(2) then polymeric kettle vacuumize, deoxidation, by formula add VCM, by polymerization kettle temperature raising extremely 50~63 DEG C, sodium lauryl sulfate is continuously added in the course of the polymerization process;
(3) the good potassium persulfate solution of water dissolves is added continuously in polymeric kettle, is kept stirring for state, entered Row polymerisation, control is reacted at 50~63 DEG C, when 0.83MPa pressure begins to decline, when pressure drops to 0.4MPa When, reaction terminates;
(4) after reaction terminates, unreacted VCM is first recycled to gas holder, latex is delivered into latex Storage tank;
(5) using the VCM in vaporizing extract process removal latex:Extracted out from latex storage tank by delivery pump Latex, by steam direct heating after, into stripper, residual monomer and a small amount of moisture content are by tower in latex Removing is vacuumized, the vinyl chloride being stripped out is recycled to gas holder, passed through the latex after gas with delivery pump Filter is sent to drying section;
(6) dry
Stripped latex is dried treatment using spray drying process, it is desirable to water content≤0.4%;
(7) particle diameter of dried material is at 5.0~20.0 μm;
(8) and then weighed, packed.
CN201510955427.1A 2015-12-16 2015-12-16 A kind of high viscosity pastes the preparation method of resin Pending CN106883330A (en)

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Application Number Priority Date Filing Date Title
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109957055A (en) * 2019-04-05 2019-07-02 唐山三友氯碱有限责任公司 It is used to prepare the production method of the PVC paste resin of safety and industrial gloves dipping layer

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101735355A (en) * 2008-11-06 2010-06-16 上海氯碱化工股份有限公司 Production method of high-viscosity PVC paste resin
CN103059182A (en) * 2012-12-13 2013-04-24 安徽天辰化工股份有限公司 High viscosity polyvinyl chloride paste resin PE1311 and preparation method thereof
CN104072649A (en) * 2014-06-27 2014-10-01 唐山三友氯碱有限责任公司 Method for producing polyvinyl chloride paste resin
CN104387508A (en) * 2014-12-15 2015-03-04 天津渤天化工有限责任公司 Method for preparing paste resin with medium viscosity
CN104403031A (en) * 2014-12-15 2015-03-11 天津渤天化工有限责任公司 Paste resin glove material with middle viscosity
CN104403032A (en) * 2014-12-15 2015-03-11 天津渤天化工有限责任公司 Low-viscosity paste resin glove material
CN104497178A (en) * 2014-12-15 2015-04-08 天津渤天化工有限责任公司 Method for preparing low-viscosity paste resin

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101735355A (en) * 2008-11-06 2010-06-16 上海氯碱化工股份有限公司 Production method of high-viscosity PVC paste resin
CN103059182A (en) * 2012-12-13 2013-04-24 安徽天辰化工股份有限公司 High viscosity polyvinyl chloride paste resin PE1311 and preparation method thereof
CN104072649A (en) * 2014-06-27 2014-10-01 唐山三友氯碱有限责任公司 Method for producing polyvinyl chloride paste resin
CN104387508A (en) * 2014-12-15 2015-03-04 天津渤天化工有限责任公司 Method for preparing paste resin with medium viscosity
CN104403031A (en) * 2014-12-15 2015-03-11 天津渤天化工有限责任公司 Paste resin glove material with middle viscosity
CN104403032A (en) * 2014-12-15 2015-03-11 天津渤天化工有限责任公司 Low-viscosity paste resin glove material
CN104497178A (en) * 2014-12-15 2015-04-08 天津渤天化工有限责任公司 Method for preparing low-viscosity paste resin

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109957055A (en) * 2019-04-05 2019-07-02 唐山三友氯碱有限责任公司 It is used to prepare the production method of the PVC paste resin of safety and industrial gloves dipping layer

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Application publication date: 20170623