CN103031622B - Large-tow PAN (polyacrylonitrile) base carbon fiber protofilament oil agent - Google Patents
Large-tow PAN (polyacrylonitrile) base carbon fiber protofilament oil agent Download PDFInfo
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- CN103031622B CN103031622B CN201110300633.0A CN201110300633A CN103031622B CN 103031622 B CN103031622 B CN 103031622B CN 201110300633 A CN201110300633 A CN 201110300633A CN 103031622 B CN103031622 B CN 103031622B
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- silicone polymer
- carbon fiber
- dimethyl silicone
- modified dimethyl
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Abstract
The invention provides a large-tow PAN (polyacrylonitrile) base carbon fiber protofilament oil agent, which mainly solves the problem that in the prior art, the consumption of emulsifying agents in the oil agent used for the carbon fiber protofilament is high, so the heat resistance of the oil agent in the use process is poor. The large-tow PAN base carbon fiber protofilament oil agent is adopted and comprises the following ingredients through being metered in parts by weight: a, 5 to 20 parts of amino modified polydimethylsiloxane A; b, 40 to 60 parts of amino modified polydimethylsiloxane B; c, 10 to 30 parts of polyether modified polydimethylsiloxane; and d, 5 to 20 parts of emulsifying agents. Through the technical scheme, the problem is perfectly solved, and the large-tow PAN base carbon fiber protofilament oil agent can be used for the industrial production of large-tow PAN base carbon fiber protofilaments.
Description
Technical field
The present invention relates to a kind of large tow PAN base carbon fiber protofilament finish.
Background technology
Carbon fiber, as the fortifying fibre of composite of new generation, is used widely at space flight, aviation and automobile, building, light industry etc. with its excellent performance.Little tow polyacrylonitrile-based carbon fibre (hereinafter to be referred as little tow PAN base carbon fibre) is the good one of numerous carbon fiber performances, is the required critical materials such as strategic missile, satellite, aerospace craft, large aircraft.Along with the develop rapidly of sky way, the demand of large tow (being greater than 24K) PAN base carbon fibre has obtained swift and violent raising.
Industrially prepare PAN base carbon fibre using following operation: the spinning process that obtains carbon fibre precursor to carrying out one-step method or two-step method spinning as PAN polymer; Be that in the oxidisability atmosphere of 200～400 DEG C, precursor carries out pre-oxidation in temperature, obtain preoxided thread; And be this preoxided thread of carbonization in 400～2000 DEG C of inert gases in temperature, change into the carbonation process of carbon fiber.In above-mentioned spinning technique, the friction of, fiber bonding in order to prevent from generating heat between filament and mechanical surface, causes fibre pick, fracture of wire and surface damage, need to use PAN base carbon fiber protofilament finish.
Chinese patent ZL200580044949.0 embodiment 2 discloses a kind of carbon fibre precursor finish, and the alkylphenol polyoxyethylene of its amino-modified silicone oil by 100 weight portions and 30 weight portions and 8.8 weight portion KM902 (SHIN-ETSU HANTOTAI's chemical industry (strain) system) form.Wherein alkylphenol polyoxyethylene is non-ionic surface active agent, can play the effect of emulsifying agent, and its large usage quantity in use can cause the problem of finish poor heat resistance.
Summary of the invention
Technical problem to be solved by this invention is in prior art, to exist carbon fibre precursor large with emulsifier in finish, causes the in use problem of poor heat resistance of finish, and a kind of new large tow PAN base carbon fiber protofilament finish is provided.It is few that this finish has emulsifier, the advantage of finish good heat resistance in use procedure.
In order to solve the problems of the technologies described above, the technical solution used in the present invention is as follows: a kind of large tow PAN base carbon fiber protofilament finish, comprises following component in parts by weight:
A) the amino modified dimethyl silicone polymer A of 5-20 part;
B) the amino modified dimethyl silicone polymer B of 40-60 part;
C) the polyether-modified dimethyl silicone polymer of 10-30 part;
D) 5-20 part emulsifying agent;
The viscosity of wherein said amino modified dimethyl silicone polymer A in the time of 25 DEG C is 50mm
2/ s～250mm
2/ s, amino equivalent is 4000～8000; Amino modified dimethyl silicone polymer B is 500mm the viscosity of 25 DEG C
2/ s～4000mm
2/ s, amino equivalent is 1000～3000; Described polyether-modified dimethyl silicone polymer is 400mm the viscosity of 25 DEG C
2/ s～1000mm
2/ s, HLB is 4.0～10.0; Described emulsifying agent is taken from least one in the material group being made up of fatty alcohol-polyoxyethylene ether, aliphatic acid polyethenoxy ether, polyoxyethylene alkylphenol ether, its ethoxymer distribution is 3～8, and the carbon number in its fatty alcohol, aliphatic acid or alkylphenol is 12～16.
In technique scheme, described amino modified dimethyl silicone polymer A and amino modified dimethyl silicone polymer B are that the amino that a part of side chain of the end dimethyl-silicon with methyl is represented by following chemical formula (I) replaces the compound obtaining; Described polyether-modified dimethyl silicone polymer is that the polyether-based that a part of side chain of the end dimethyl-silicon with methyl is represented by following chemical formula (II) replaces the compound obtaining:
-CH
2-CH
2-NH-CH
2-CH
2-NH
2(I)
The preferred HLB value of polyether-modified dimethyl silicone polymer described in technique scheme is 4-5; Described amino modified dimethyl silicone polymer A preferable range is that the viscosity in the time of 25 DEG C is 60mm
2/ s～150mm
2/ s, amino equivalent is 4500～6000; Described amino modified dimethyl silicone polymer B preferable range is that the viscosity in the time of 25 DEG C is 1000mm
2/ s～3000mm
2/ s, amino equivalent is 1500～2000; Described emulsifying agent preferred fat alcohol polyoxyethylene ether; Described emulsifier is taking parts by weight preferable range as 10-15 part.
Finish of the present invention can also comprise other components well known to those skilled in the art.For example there is bactericidal effect in order to give finish, be conducive to long term storage and not corrupt, in finish of the present invention, can comprise bactericide, such as benzalkonium bromide, nipalgin etc.; There is better antistatic effect in order to give finish, finish of the present invention can also comprise conventional antistatic additive, such as anionic antistatic agents such as alkyl phosphoric acid ester ammonium salt, alkyl phosphate diethanolamine salt, alkyl phosphate triethanolamine salts, the cationic antistatic additive such as octadecyl dimethyl ethoxy quaternary ammonium nitrate, betaine type amphoteric antistatic additive; Finish of the present invention uses with the form of aqueous dispersion, and for easy to use, this finish can also comprise water.
The preparation method of described PAN base carbon fiber protofilament finish is: the amino modified dimethyl silicone polymer A described in finish of the present invention, amino modified dimethyl silicone polymer B, polyether-modified dimethyl silicone polymer and emulsifying agent and bactericide and antistatic additive etc. are stirred.In the time that formula comprises water, then under stirring after preferably first other components being mixed, progressively add water, be beneficial to make more uniform emulsion, the maximum adding quantity of water is to make the concentration of finish emulsion be not less than working concentration, and the emulsion working concentration of finish of the present invention is generally 0.5-3.0wt%.
The use step of finish of the present invention is as follows:
(1) by the concentration adjustment of finish emulsion in finishing bathtray and maintain 0.5～3.0wt%
In the time of emulsion form that finish of the present invention is 0.5-3.0wt%, can directly use, otherwise need under agitation add the water of amount of calculation, water used is preferably used deionized water.
(2) under 30-50 DEG C, condition of normal pressure, with being impregnated in the finish emulsion in step (1) and oiling to carbon fibre precursor through the carbon fibre precursor of densification.
One skilled in the art will appreciate that through the precursor of above-mentioned steps (1) and (2) processing, can obtain carbon fiber through super-dry, pre-oxidation, carbonization and other processes successively.
Key problem in technology of the present invention is to have used in oil formula two kinds of different amino modified dimethyl silicone polymers of amino equivalent, dwindle emulsification gradient, reduce the consumption of emulsifying agent, thereby improve the heat resistance of finish, heat-resisting residual mass fraction improves more than 20% than prior art, has obtained good technique effect.
Below by embodiment, the present invention is further elaborated.
Detailed description of the invention
[embodiment 1～10]
Amino modified component dimethyl silicone polymer A, amino modified dimethyl silicone polymer B, polyether-modified dimethyl silicone polymer and emulsifying agent are uniformly mixed to 30 minutes in required ratio in the composite still of finish, taking the finish that 1g is uniformly mixed is placed in aluminium crucible, and process 5h in 105 DEG C of baking ovens, be over dry state.The above-mentioned over dry finish of accurate weighing 15mg-20mg, is placed in the aluminium crucible of TGA (thermogravimetric analysis), surveys its heat-resisting residual mass fraction.First under moving air state, be heated to 240 DEG C, and keep 60min, record heat-resisting residual mass fraction r1; And then switch atmosphere (switching to nitrogen by air), in nitrogen atmosphere, be heated to 450 DEG C, and keep 30s, record heat-resisting residual mass fraction r2.Total heat-resisting residual mass fraction r=r1 × r2.
Amino modified component dimethyl silicone polymer A, amino modified dimethyl silicone polymer B, polyether-modified dimethyl silicone polymer and emulsifying agent are uniformly mixed in 100ml beaker in required ratio, then in stirring, progressively add normal temperature deionization pure water, be mixed with the emulsion of 10.0wt% concentration, static placement 72hr, the stability of observing emulsion.Emulsion stability is not stratified, is judged as, and emulsion has lamination, is judged as bad.
In embodiment 1, emulsifying agent adopts laurate polyoxyethylene ether surface active agent; In embodiment 2, emulsifying agent adopts nonyl phenol polyoxyethylene ether surface active agent; In embodiment 3-10, emulsifying agent adopts fatty alcohol-polyoxyethylene ether surfactant.
The concrete component of each embodiment is in table 1, and the content of each component is in table 2, and evaluation result is in table 3.Can be found out by evaluation result, large tow PAN base carbon fiber protofilament finish of the present invention has clear improvement than the stability of emulsion of prior art and heat resistance, and its heat-resisting residual mass fraction improves more than 20% than prior art.
[comparative example 1]
In comparative example 11, the oil formula that adopts Chinese patent ZL200580044949.0 embodiment 2 to provide.Wherein, amino modified silicon 100 weight portions, emulsifying agent (Nonyl pheno base ether (6)) 30 weight portions, KM902 (SHIN-ETSU HANTOTAI's chemical industry (strain) system) 8.8 weight portions, 1.2 parts of emulsifying agents that add for emulsification KM902, the percetage by weight that emulsification dosage accounts for finish total surfactant is 22wt%; Amino-modified silicone oil kinematic viscosity at 25 DEG C is 3500mm
2/ s, amino equivalent is 2000.
The character of the key component of table 1 finish of the present invention
The composition of table 2 finish of the present invention
The evaluation of table 3 oil performance
Claims (5)
1. a large tow PAN base carbon fiber protofilament finish, composed as follows in parts by weight:
A) the amino modified dimethyl silicone polymer A of 5-20 part;
B) the amino modified dimethyl silicone polymer B of 40-60 part;
C) the polyether-modified dimethyl silicone polymer of 10-30 part;
D) 5-20 part emulsifying agent;
The viscosity of wherein said amino modified dimethyl silicone polymer A in the time of 25 DEG C is 60mm
2/ s～150mm
2/ s, amino equivalent is 4500～6000; Amino modified dimethyl silicone polymer B is 1000mm the viscosity of 25 DEG C
2/ s～3000mm
2/ s, amino equivalent is 1500～2000; Described polyether-modified dimethyl silicone polymer is 400mm the viscosity of 25 DEG C
2/ s～1000mm
2/ s, HLB is 4.0～10.0; Described emulsifying agent is taken from least one in the material group being made up of fatty alcohol-polyoxyethylene ether, aliphatic acid polyethenoxy ether, polyoxyethylene alkylphenol ether, its ethoxymer distribution is 3～8, and the carbon number in its fatty alcohol, aliphatic acid or alkylphenol is 12～16.
2. large tow PAN base carbon fiber protofilament finish according to claim 1, is characterized in that described amino modified dimethyl silicone polymer A and amino modified dimethyl silicone polymer B are that a part of side chain of the end dimethyl-silicon with methyl is replaced the compound obtaining by the amino of following represented by formula I; Described polyether-modified dimethyl silicone polymer is that the polyether-based that a part of side chain of the end dimethyl-silicon with methyl is represented by following Formulae II replaces the compound obtaining:
-CH
2-CH
2-NH-CH
2-CH
2-NH
2 (I)、
3. large tow PAN base carbon fiber protofilament finish according to claim 1, the HLB value that it is characterized in that described polyether-modified dimethyl silicone polymer is 4-5.
4. large tow PAN base carbon fiber protofilament finish according to claim 1, is characterized in that described emulsifying agent is fatty alcohol-polyoxyethylene ether.
5. large tow PAN base carbon fiber protofilament finish according to claim 1, is characterized in that described emulsifying agent is taking parts by weight consumption as 10-15 part.
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| CN201110300633.0A CN103031622B (en) | 2011-09-29 | 2011-09-29 | Large-tow PAN (polyacrylonitrile) base carbon fiber protofilament oil agent |
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|---|---|---|---|
| CN201110300633.0A CN103031622B (en) | 2011-09-29 | 2011-09-29 | Large-tow PAN (polyacrylonitrile) base carbon fiber protofilament oil agent |
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| CN103031622B true CN103031622B (en) | 2014-11-26 |
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| CN106544760B (en) * | 2015-09-18 | 2019-03-12 | 中国石油天然气股份有限公司 | A kind of carbon fibre precursor is oil solution dedicated and preparation method thereof |
| CN108774568B (en) * | 2018-05-25 | 2021-05-14 | 清华大学天津高端装备研究院 | Semisynthetic aluminum alloy processing liquid and preparation method thereof |
| CN110725025B (en) * | 2019-09-26 | 2022-01-25 | 江苏恒神股份有限公司 | Oiling agent for carbon fiber precursor |
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|---|---|---|---|---|
| CN101091010A (en) * | 2004-12-27 | 2007-12-19 | 东丽株式会社 | Oil agent for carbon fiber precursor fiber, carbon fiber and method for producing carbon fiber |
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| CN101091010A (en) * | 2004-12-27 | 2007-12-19 | 东丽株式会社 | Oil agent for carbon fiber precursor fiber, carbon fiber and method for producing carbon fiber |
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