CN105237741A - Curing agent composition - Google Patents

Curing agent composition Download PDF

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Publication number
CN105237741A
CN105237741A CN201510783023.9A CN201510783023A CN105237741A CN 105237741 A CN105237741 A CN 105237741A CN 201510783023 A CN201510783023 A CN 201510783023A CN 105237741 A CN105237741 A CN 105237741A
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China
Prior art keywords
curing agent
agent composition
curing
agent
present
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Pending
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CN201510783023.9A
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Chinese (zh)
Inventor
华玉叶
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Individual
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Individual
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Priority to CN201510783023.9A priority Critical patent/CN105237741A/en
Publication of CN105237741A publication Critical patent/CN105237741A/en
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Abstract

The invention discloses a curing agent composition. The curing agent composition has the beneficial effect that the Tg value of the curing agent composition is increased under the premise that the usage amount is not changed by compounding two different types of curing agents.

Description

A kind of curing agent composition
Technical field
The present invention relates to a kind of curing agent composition.
Background technology
Solidifying agent has another name called stiffening agent, ripening agent or set agent, is that a class is promoted or controls material or the mixture of curing reaction.Resin solidification is through the chemical reactions such as condensation, closed loop, addition or catalysis, makes thermosetting resin that irreversible change procedure occur, and solidification has come by adding solidification (being cross-linked) agent.Solidifying agent is absolutely necessary additive, is to make caking agent, coating, mould material all to need to add solidifying agent, otherwise epoxy resin can not solidify.
Curing reaction belongs to chemical reaction, and affect very large by solidification value, increase in temperature, speed of response is accelerated, and gel time shortens; The logarithmic value of gel time is with solidification value rising linearly downtrending substantially.But solidification value is too high, condensate performance is often made to decline, so there is the upper limit of solidification value; The temperature making curing speed and condensate performance compromise must be selected, as suitable solidification value.Solidifying agent can be divided into four classes by solidification value: low temperature curing agent solidification value is below room temperature; Toughess at room temperature solidification value is room temperature ~ 50 DEG C; Intermediate temperature setting agent is 50 ~ 100 DEG C; High-temperature curing agent solidification value is more than 100 DEG C.The solidifying agent kind belonging to low temperature curing type is little, has poly-coloured glaze alcohol type, polyisocyanic acid ester type etc.; T-31 modified amine, the YH-82 modified amine of domestic development operation all can be solidified below 0 DEG C.The kind belonging to room temperature curing type is a lot: aliphatic polyamine, alicyclic polyamine; Versamid and aromatic amine etc.Belong to some alicyclic polyamine of intermediate temperature setting type, tertiary amine, narrow azole and boron trifluoride complex etc.What belong to high temperature modification solidifying agent has aromatic polyamine, acid anhydrides, resole, aminoresin, Dyhard RU 100 and hydrazides etc.
For hot setting system, solidification value is generally divided into two benches, low-temperature curing is adopted before gel, after reaching gel state or the state slightly higher than gel state, heat carries out after fixing (post-cure) again, and relative leading portion is cured as Procuring (pre-cure).
But existing solidifying agent, most solidification value is not high, or can provide higher solidification value, but cost is high.
Summary of the invention
The object of the invention is to propose a kind of curing agent composition, it is composite by two kinds of dissimilar solidifying agent, under the prerequisite that consumption is constant, improves its Tg value.
For reaching this object, the present invention by the following technical solutions:
A kind of curing agent composition, it comprises following component:
(1)
(2)
The mass ratio of two kinds of components described in described composition is 3:1-1:3, and preferred 2:1-1:2, has preferred 2:1 further.
Embodiment
The present invention is described pharmaceutical composition of the present invention by following embodiment.
Embodiment 1
I. the synthesis of formula 1 compound
Described in formula 1, compound is known compound, and those skilled in the art can obtain in commercially available purchase, also can synthesize and prepare.Its typical but non-limiting synthesis example is as follows:
First, in reaction vessel, add with the ratio being 1mol maleic anhydride relative to 1.6mol dimethyladamantane or ethyl diamantane, and the internal temperature of reaction vessel is remained on about 160 DEG C.Then, in this reaction vessel, the solution being dissolved in a small amount of dimethyladamantane or ethyl diamantane as the such as ditertiary butyl peroxide 5.5mmol of free radical generating agent is dripped with 3 hours.About 3 hours from dropping end terminate reaction, obtain reaction product.By to the underpressure distillation of gained reaction product, thus obtain corresponding target compound.Wherein, suitably can change the feed ratio, temperature of reaction, the reaction times that illustrate herein uprises to make target compound yield, also can use the free radical generating agent of other kind.
II. the synthesis of formula 2 compound
Described compound is known compound, and those skilled in the art can obtain in commercially available purchase, also can synthesize and prepare.Its typical but non-limiting synthesis example is as follows:
7.5ml formaldehyde solution (35%) added in 1 hour in 5,6,7, the 8-tetrahydro-s-naphthalidine of the 25g in the 74ml acidic medium of maintenance 60 DEG C, wherein this acidic medium is made up of 29ml propan-2-ol, 36ml water and the 9ml vitriol oil.This mixture is heated 3.5 hours further, then cools, neutralization, and by this product and water together grind into powder.Convert the soft solid obtained to vitriol, use washing with acetone, filter, the amine regeneration using ammonia solution to make to dissociate, and make the powder washing the pinkish obtained with water, then dry, produce amber solid, it is 80-120 DEG C of fusing.
By the component I for preparing and II, obtain described anti-curing agent composition according to 2:1 is composite.
At 180 DEG C, use standard cure circulation, by above-mentioned curing agent composition and epoxy resin MY721 (commercially available in Huntsman, UK) stoichiometrically equivalent reaction.Measured the Tg of resulting polymers by DMA, its Tg is 289 DEG C.
Comparative example 1
Component I, not containing component I I, all the other conditions are constant, and its Tg is 146 DEG C.
Comparative example 2
Only containing component I I, not containing component I, all the other conditions are constant, and its Tg is 211 DEG C.
Above-described embodiment and comparative example explanation, curing agent composition of the present invention, it is composite by two kinds of dissimilar activess, under same amount prerequisite, composite Tg effect will be better than far away being used alone of two kinds of components, proves to create synergistic effect between two kinds of solidifying agent that the present invention adopts.
Applicant states, the present invention illustrates curing agent composition of the present invention by above-described embodiment, but the present invention is not limited to above-mentioned special formulation, does not namely mean that the present invention must rely on above-mentioned detailed component and formula could be implemented.Person of ordinary skill in the field should understand, any improvement in the present invention, to equivalence replacement and the interpolation of ancillary component, the concrete way choice etc. of each raw material of product of the present invention, all drops within protection scope of the present invention and open scope.

Claims (3)

1. a curing agent composition, it comprises following component:
The mass ratio of two kinds of components described in described composition is 3:1-1:3.
2. curing agent composition as claimed in claim 1, it is characterized in that, the mass ratio of described two kinds of components is 2:1-1:2.
3. curing agent composition as claimed in claim 1, it is characterized in that, the mass ratio of described two kinds of components is 2:1.
CN201510783023.9A 2015-11-14 2015-11-14 Curing agent composition Pending CN105237741A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510783023.9A CN105237741A (en) 2015-11-14 2015-11-14 Curing agent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510783023.9A CN105237741A (en) 2015-11-14 2015-11-14 Curing agent composition

Publications (1)

Publication Number Publication Date
CN105237741A true CN105237741A (en) 2016-01-13

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510783023.9A Pending CN105237741A (en) 2015-11-14 2015-11-14 Curing agent composition

Country Status (1)

Country Link
CN (1) CN105237741A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102226033A (en) * 2011-05-03 2011-10-26 广东生益科技股份有限公司 Epoxy resin composition as well as prepreg and metal-foil-clad laminated board manufactured by using same
CN102884101A (en) * 2010-03-24 2013-01-16 赫克塞尔复合材料有限公司 Novel curing agents
CN104755526A (en) * 2012-11-01 2015-07-01 三菱瓦斯化学株式会社 Epoxy resin curing agent

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102884101A (en) * 2010-03-24 2013-01-16 赫克塞尔复合材料有限公司 Novel curing agents
CN102226033A (en) * 2011-05-03 2011-10-26 广东生益科技股份有限公司 Epoxy resin composition as well as prepreg and metal-foil-clad laminated board manufactured by using same
CN104755526A (en) * 2012-11-01 2015-07-01 三菱瓦斯化学株式会社 Epoxy resin curing agent

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Application publication date: 20160113