CN105778050A - Epoxy resin curing agent - Google Patents

Epoxy resin curing agent Download PDF

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Publication number
CN105778050A
CN105778050A CN201610180453.6A CN201610180453A CN105778050A CN 105778050 A CN105778050 A CN 105778050A CN 201610180453 A CN201610180453 A CN 201610180453A CN 105778050 A CN105778050 A CN 105778050A
Authority
CN
China
Prior art keywords
parts
curing agent
epoxy resin
ether
weight
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
CN201610180453.6A
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Chinese (zh)
Inventor
王悦康
潘晓鑫
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.)
NANTONG CITY FULAITE CHEMICAL CO Ltd
Original Assignee
NANTONG CITY FULAITE CHEMICAL 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 NANTONG CITY FULAITE CHEMICAL CO Ltd filed Critical NANTONG CITY FULAITE CHEMICAL CO Ltd
Priority to CN201610180453.6A priority Critical patent/CN105778050A/en
Publication of CN105778050A publication Critical patent/CN105778050A/en
Pending legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • C08G59/4207Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof aliphatic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • C08G59/4215Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof cycloaliphatic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • C08G59/4223Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof aromatic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/02Fibres or whiskers
    • C08K7/04Fibres or whiskers inorganic
    • C08K7/10Silicon-containing compounds
    • C08K7/12Asbestos
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2227Oxides; Hydroxides of metals of aluminium

Abstract

The invention discloses an epoxy resin curing agent. The epoxy resin curing agent is prepared from the following components in parts by weight: 40-60 parts of acid-anhydride mixture, 20-25 parts of aluminum oxide, 15-30 parts of isoprene, 10-25 parts of n-butyl alcohol-water glyceryl ether, 8-15 parts of asbestos fiber and 10-15 parts of diluent. The epoxy resin curing agent provided by the invention has high curing reaction speed, and the complete curing time of epoxy resin can be shortened.

Description

Epoxy curing agent
Technical field
The disclosure relates generally to technical field of coatings, is specifically related to epoxy resin, particularly relates to ring Epoxy resins firming agent.
Background technology
Epoxy resin is a kind of amorphous thick liquid, and heating, in plasticity, does not has obvious fusing point, It is heated deliquescing, gradually fusing and stickness, water insoluble, itself will not harden, therefore it is almost There is no single use value.Epoxy curing agent is and epoxy resin generation chemical reaction, Form netted space polymers, composite aggregate envelope among reticulate body, make line style tree Fat becomes the additive of tough and tensile build solid.After epoxy resin adds a certain amount of firming agent, The most gradually solidify.
Owing to having good mechanical strength and insulating properties, epoxy resin after epoxy resin cure It is widely used in the manufacture of electronic product as bonding agent, needs epoxy as on circuit board Resin carries out adhesive curing together to some electrical equipments.But due to epoxy resin at normal temperatures (28 DEG C) are long for hardening time, typically just can be fully cured at 8-12 hour, have a strong impact on work Make efficiency.
Summary of the invention
In view of drawbacks described above of the prior art or deficiency, it is desirable to provide one to reduce at normal temperatures The epoxy curing agent of the hardening time of epoxy resin.
The epoxy curing agent that the present invention provides, including each component of following parts by weight: acid Acid anhydride mixture 40-60 part, aluminium oxide 20-25 part, isoprene 15-30 part, n-butyl alcohol water Glycerin ether 10-25 part, asbestos fibre 8-15 part and diluent 10-15 part.
The epoxy curing agent curing reaction speed that the present invention provides is fast, it is possible to decrease epoxy resin The completely crued time was to 5.2 hours.
Detailed description of the invention
Embodiment 1
Epoxy curing agent in the present embodiment, including each component of following parts by weight:
Acid anhydride mixture 40 parts
Aluminium oxide 20 parts
Isoprene 15 parts
N-butyl alcohol water glycerin ether 10 parts
Asbestos fibre 8 parts
Diluent 10 parts
Wherein, acid anhydride mixture includes hexahydrophthalic anhydride 5 parts, maleic anhydride 15 Part and trimellitic anhydride 20 parts.Diluent includes polypropylene glycol diglycidyl ether 3 parts, ring Ethylene Oxide butyl ether 3 parts and Ethylene glycol diglycidyl ether 4 parts.
Embodiment 2
Epoxy curing agent in the present embodiment, including each component of following parts by weight:
Acid anhydride mixture 45 parts
Aluminium oxide 21 parts
Isoprene 18 parts
N-butyl alcohol water glycerin ether 12 parts
Asbestos fibre 10 parts
Diluent 11 parts
Wherein, acid anhydride mixture includes hexahydrophthalic anhydride 6 parts, maleic anhydride 17 Part and trimellitic anhydride 22 parts.Diluent includes polypropylene glycol diglycidyl ether 3 parts, ring Ethylene Oxide butyl ether 3 parts and Ethylene glycol diglycidyl ether 5 parts.
Embodiment 3
Epoxy curing agent in the present embodiment, including each component of following parts by weight:
Acid anhydride mixture 50 parts
Aluminium oxide 22 parts
Isoprene 19 parts
N-butyl alcohol water glycerin ether 16 parts
Asbestos fibre 11 parts
Diluent 12 parts
Wherein, acid anhydride mixture includes hexahydrophthalic anhydride 8 parts, maleic anhydride 18 Part and trimellitic anhydride 24 parts.Diluent includes polypropylene glycol diglycidyl ether 3 parts, ring Ethylene Oxide butyl ether 4 parts and Ethylene glycol diglycidyl ether 5 parts.
Embodiment 4
Epoxy curing agent in the present embodiment, including each component of following parts by weight:
Acid anhydride mixture 55 parts
Aluminium oxide 24 parts
Isoprene 25 parts
N-butyl alcohol water glycerin ether 20 parts
Asbestos fibre 13 parts
Diluent 14 parts
Wherein, acid anhydride mixture includes hexahydrophthalic anhydride 9 parts, maleic anhydride 20 Part and trimellitic anhydride 26 parts.Diluent includes polypropylene glycol diglycidyl ether 4 parts, ring Ethylene Oxide butyl ether 4 parts and Ethylene glycol diglycidyl ether 6 parts.
Embodiment 5
Epoxy curing agent in the present embodiment, including each component of following parts by weight:
Acid anhydride mixture 60 parts
Aluminium oxide 25 parts
Isoprene 30 parts
N-butyl alcohol water glycerin ether 25 parts
Asbestos fibre 15 parts
Diluent 15 parts
Wherein, acid anhydride mixture includes hexahydrophthalic anhydride 10 parts, maleic anhydride 20 parts and trimellitic anhydride 30 parts.Diluent include polypropylene glycol diglycidyl ether 4 parts, Epoxy propane butyl ether 5 parts and Ethylene glycol diglycidyl ether 6 parts.
Same process is used to prepare the epoxy curing agent in above-mentioned 5 embodiments, And correspondence lays the 1-5 experimental group respectively, also include a matched group.Each experimental group with Matched group to solidifying the epoxy resin of same components respectively, and is added up under equivalent environment Go out 6 group epoxy resin and reach the completely crued time.Find through test, in 1-5 group Be fully cured in required time respectively less than matched group be fully cured required time 10.8h, Wherein the required time that is fully cured of the 3rd group is the shortest, specially 5.2h.
Above description is only the preferred embodiment of the application and saying institute's application technology principle Bright.It will be appreciated by those skilled in the art that invention scope involved in the application, do not limit In the technical scheme of the particular combination of above-mentioned technical characteristic, also should contain simultaneously without departing from In the case of described inventive concept, above-mentioned technical characteristic or its equivalent feature carry out combination in any And other technical scheme formed.Such as features described above and (but not limited to) disclosed herein The technical characteristic with similar functions is replaced mutually and the technical scheme that formed.

Claims (4)

1. an epoxy curing agent, it is characterised in that include each group of following parts by weight Point:
Acid anhydride mixture 40-60 part
Aluminium oxide 20-25 part
Isoprene 15-30 part
N-butyl alcohol water glycerin ether 10-25 part
Asbestos fibre 8-15 part
Diluent 10-15 part.
Epoxy curing agent the most according to claim 1, it is characterised in that include as Each component of lower parts by weight:
Acid anhydride mixture 45-55 part
Aluminium oxide 21-23 part
Isoprene 17-20 part
N-butyl alcohol water glycerin ether 15-20 part
Asbestos fibre 10-13 part
Diluent 12-13 part.
Epoxy curing agent the most according to claim 1, it is characterised in that described acid Acid anhydride mixture includes hexahydrophthalic anhydride, maleic anhydride and trimellitic anhydride, and Ratio of weight and number is 1~2:3~4:4~5.
Epoxy curing agent the most according to claim 1, it is characterised in that described dilute Release agent and include that polypropylene glycol diglycidyl ether, epoxy propane butyl ether and ethylene glycol bisthioglycolate shrink are sweet Oil ether, and parts by weight ratio is 1~2:1~2:2~3.
CN201610180453.6A 2016-03-25 2016-03-25 Epoxy resin curing agent Pending CN105778050A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610180453.6A CN105778050A (en) 2016-03-25 2016-03-25 Epoxy resin curing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610180453.6A CN105778050A (en) 2016-03-25 2016-03-25 Epoxy resin curing agent

Publications (1)

Publication Number Publication Date
CN105778050A true CN105778050A (en) 2016-07-20

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610180453.6A Pending CN105778050A (en) 2016-03-25 2016-03-25 Epoxy resin curing agent

Country Status (1)

Country Link
CN (1) CN105778050A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106584941A (en) * 2016-12-06 2017-04-26 太仓大唐化纤厂 Industrial fiber cloth and curing agent for same
CN107298755A (en) * 2017-08-16 2017-10-27 吴丹 A kind of epoxy curing agent
CN107353782A (en) * 2017-08-22 2017-11-17 马鞍山中粮生物化学有限公司 A kind of chemistry painting industry special curing agent and preparation method thereof
CN107446118A (en) * 2017-08-16 2017-12-08 吴丹 A kind of fast epoxy curing agent of curing reaction speed
CN107746456A (en) * 2017-09-19 2018-03-02 合肥惠科金扬科技有限公司 A kind of AMOLED display screens epoxy curing agent
CN108178828A (en) * 2017-12-27 2018-06-19 上海华谊树脂有限公司 Epoxy resin cured product and composition epoxy resin

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102850725A (en) * 2012-07-23 2013-01-02 北京赛诺膜技术有限公司 Epoxy potting material for microfiltration or ultrafiltration membrane filling and preparation method thereof
CN102964567A (en) * 2012-12-11 2013-03-13 南通市福来特化工有限公司 Epoxy resin curing agent
CN103146150A (en) * 2013-03-27 2013-06-12 南通市福来特化工有限公司 Novel epoxy resin curing agent
CN103665323A (en) * 2013-11-14 2014-03-26 昆山珍实复合材料有限公司 Novel latent curing agent of epoxy resin

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102850725A (en) * 2012-07-23 2013-01-02 北京赛诺膜技术有限公司 Epoxy potting material for microfiltration or ultrafiltration membrane filling and preparation method thereof
CN102964567A (en) * 2012-12-11 2013-03-13 南通市福来特化工有限公司 Epoxy resin curing agent
CN103146150A (en) * 2013-03-27 2013-06-12 南通市福来特化工有限公司 Novel epoxy resin curing agent
CN103665323A (en) * 2013-11-14 2014-03-26 昆山珍实复合材料有限公司 Novel latent curing agent of epoxy resin

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106584941A (en) * 2016-12-06 2017-04-26 太仓大唐化纤厂 Industrial fiber cloth and curing agent for same
CN107298755A (en) * 2017-08-16 2017-10-27 吴丹 A kind of epoxy curing agent
CN107446118A (en) * 2017-08-16 2017-12-08 吴丹 A kind of fast epoxy curing agent of curing reaction speed
CN107353782A (en) * 2017-08-22 2017-11-17 马鞍山中粮生物化学有限公司 A kind of chemistry painting industry special curing agent and preparation method thereof
CN107746456A (en) * 2017-09-19 2018-03-02 合肥惠科金扬科技有限公司 A kind of AMOLED display screens epoxy curing agent
CN108178828A (en) * 2017-12-27 2018-06-19 上海华谊树脂有限公司 Epoxy resin cured product and composition epoxy resin

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PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
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Application publication date: 20160720