CN103122585B - Oiling agent of large tow PAN (Polyacrylonitrile)-based carbon fiber precursors - Google Patents
Oiling agent of large tow PAN (Polyacrylonitrile)-based carbon fiber precursors Download PDFInfo
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- CN103122585B CN103122585B CN201110369956.5A CN201110369956A CN103122585B CN 103122585 B CN103122585 B CN 103122585B CN 201110369956 A CN201110369956 A CN 201110369956A CN 103122585 B CN103122585 B CN 103122585B
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- dimethyl silicone
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Abstract
The invention relates to an oiling agent of large tow PAN (Polyacrylonitrile)-based carbon fiber precursors, which mainly aims at solving the problem in the prior art that an oiling agent for carbon fiber precursors is poor in antistatic property, and thus the possibility of low full-package rate is high. The technical scheme for solving the problem well is that an oiling agent for the large tow PAN based carbon fiber precursors is a mixture of V and W at the mixed weight ratio of 3:(1-3), wherein the V comprises the following components in parts by weight: 5 to 20 parts of amino modified polydimethylsiloxane A, 40 to 60 parts of amino modified polydimethylsiloxane B, 10 to 30 parts of polyether modified polydimethylsiloxane, and 5 to 20 parts of an emulsifying agent; and the W is an epoxy adduct of an amide compound which is obtained from reaction of diethylenetriamine and stearic acid. The oiling agent can be applied to industrial production of the large tow PAN-based carbon fiber precursors.
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 the performance of its excellence.Large tow polyacrylonitrile-based carbon fibre (hereinafter referred to as large tow PAN base carbon fibre) is the one of function admirable in numerous carbon fiber, is the critical material needed for strategic missile, satellite, aerospace craft, large aircraft etc.Along with the develop rapidly of sky way, the demand of large tow (being greater than 24K) PAN base carbon fibre obtains swift and violent raising.
Industrially prepare PAN base carbon fibre using following procedures: to the spinning process carrying out one-step method or two-step method spinning as PAN polymer and obtain carbon fibre precursor; Be that in the oxidation 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, in order to prevent between filament heating bonding, fiber and the friction of mechanical surface, causing fibre pick, fracture of wire and surface damage, needing use PAN base carbon fiber protofilament finish.
Chinese patent ZL200580044949.0 embodiment 2 discloses a kind of carbon fibre precursor finish, and it is made up of the amino-modified silicone oil of 100 weight portions and the alkylphenol polyoxyethylene of 30 weight portions and 8.8 weight portion KM902 (SHIN-ETSU HANTOTAI's chemical industry (strain) system).This finish antistatic behaviour is poor, easily causes the problem that full-rolling rate is low.
Summary of the invention
Technical problem to be solved by this invention is that to there is antistatic behaviour in carbon fibre precursor finish in prior art poor, easily cause the problem that full-rolling rate is low, there is provided a kind of large tow PAN base carbon fiber protofilament finish newly, this finish has the advantage that in use procedure, finish antistatic behaviour is good, full-rolling rate is high.
As follows for solving the problems of the technologies described above the technical solution used in the present invention: a kind of large tow PAN base carbon fiber protofilament finish is the mixture of V and W, the mixed weight ratio of V and W is V: W=3: 1 ~ 3; V comprises following component with weight parts:
A) 5 ~ 20 parts of amino modified dimethyl silicone polymer A;
B) 40 ~ 60 parts of amino modified dimethyl silicone polymer B;
C) 10 ~ 30 parts of polyether-modified dimethyl silicone polymers;
D) 5 ~ 20 parts of emulsifying agents;
The wherein said viscosity of amino modified dimethyl silicone polymer A 25 DEG C time 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 are 4.0 ~ 10.0; At least one in the material group be made up of fatty alcohol-polyoxyethylene ether, aliphatic acid polyethenoxy ether, polyoxyethylene alkylphenol ether taken from by described emulsifying agent, its ethoxymer distribution is 3 ~ 8, and the carbon number in its fatty alcohol, aliphatic acid or alkylphenol is 12 ~ 16;
W is the epoxy radicals addition product that diethylenetriamine and stearic acid react the amide compound obtained, the synthetic method of the epoxy radicals addition product of described amide compound is: take p-methyl benzenesulfonic acid as catalyst, 1mol diethylenetriamine and 2mol stearic acid are reacted 5 hours at 200 ~ 220 DEG C, obtain amide compound, then carry out the epoxy radicals addition product W that addition reaction obtains amide compound with 10mol oxirane.
Amino modified dimethyl silicone polymer A described in technique scheme and amino modified dimethyl silicone polymer B is that a part of side chain that end has a dimethyl-silicon of methyl is replaced by the amino that following chemical formula (I) represents the compound obtained; Described polyether-modified dimethyl silicone polymer is that a part of side chain that end has a dimethyl-silicon of methyl is replaced by the polyether-based that following chemical formula (II) represents the compound obtained:
-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 the viscosity 25 DEG C time is 60mm
2/ s ~ 150mm
2/ s, amino equivalent is 4500 ~ 6000; Described amino modified dimethyl silicone polymer B preferable range is the viscosity 25 DEG C time is 1000mm
2/ s ~ 3000mm
2/ s, amino equivalent is 1500 ~ 2000; Described emulsifying agent preferred fat alcohol polyoxyethylene ether; Described emulsifier preferable range is 10 ~ 15 parts.
Finish of the present invention can also comprise other components well known to those skilled in the art.Such as in order to give finish, there is bactericidal effect, being conducive to long term storage and not corrupt, bactericide can be comprised in finish of the present invention, such as benzalkonium bromide, nipalgin etc.; Finish of the present invention uses with the form of aqueous dispersion, and in order to easy to use, this finish can also comprise water.
The preparation method of described PAN base carbon fiber protofilament finish for: the amino modified dimethyl silicone polymer A in component V described in finish of the present invention, amino modified dimethyl silicone polymer B, polyether-modified dimethyl silicone polymer and emulsifying agent and bactericide etc. are stirred.When V comprises water, then progressively water is added under stirring after preferably first being mixed by its active principle, be beneficial to obtained evenly emulsion, the maximum adding quantity of water makes the concentration of finish emulsion be not less than working concentration, and the emulsion working concentration of finish of the present invention is generally 0.5-3.0 % by weight.Added water by component W described in finish of the present invention, then heat stirring and dissolving, obtained the same with component V emulsion concentration, finally component V emulsion under agitation mixed with component W emulsion, the mixing ratio of V and W is V: W=3: 1-3.
The use step of finish of the present invention is as follows:
(1) concentration of finish emulsion in finishing bathtray adjusted and maintain 0.5 ~ 3.0 % by weight
Directly can use when finish of the present invention is the emulsion form of 0.5-3.0 % by weight, otherwise need the water under agitation adding amount of calculation, water used preferably uses deionized water.
(2) 30-50 DEG C, under condition of normal pressure, be impregnated into the carbon fibre precursor through densification in the finish emulsion in step (1) and oil to carbon fibre precursor.
One skilled in the art will appreciate that the precursor processed through above-mentioned steps (1) and (2), can carbon fiber be obtained through super-dry, pre-oxidation, carbonization and other processes successively.
Key problem in technology of the present invention is the epoxy radicals addition product employing antistatic excellent amide compound in oil formula, improve the antistatic behaviour (namely the ratio resistance of carbon fibre precursor declines) of tow, improve full-rolling rate, experimental result shows, the ratio resistance of comparative example is 3 × 10
9Ω cm, full-rolling rate is only 65%, and ratio resistance of the present invention decline about 1 order of magnitude, full-rolling rate is greater than 73%, achieves good technique effect, can be used in the industrial production of large tow PAN base carbon fiber protofilament.
Below by embodiment, the present invention is further elaborated.
Detailed description of the invention
[embodiment 1 ~ 10]
In embodiment 1, emulsifying agent adopts laurate polyoxyethylene ether surface active agent; In example 2, emulsifying agent adopts nonylphenol polyoxyethylenes 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.
The evaluation of antistatic property.With the YG321 fiber ratio resistance instrument that Co., Ltd of Changzhou Textile Machinery Plant No.2 produces, employing oil content is the PAN base carbon fiber protofilament of the 36K of 1 % by weight, and measure the ratio resistance of fiber by the method for GB/T14342-93, evaluation result is in table 3.
The spinnability of PAN base carbon fiber protofilament is represented with full-rolling rate.The test condition of full-rolling rate is, the PAN base carbon fiber protofilament of 500 tons/year is adopted to produce evaluating apparatus, be the PAN base carbon fiber protofilament of the 36K of 1 % by weight with oil content, reel with the winding speed of 200 ms/min, reach 30 kilograms for full volume with PAN base carbon fiber protofilament winding weight.In winding process, there is fracture of wire namely obtain rolling up less than curled hair, fracture of wire does not occur in winding process and then obtains full curled hair volume, the computing formula of full-rolling rate is: full-rolling rate=[full curled hair volume number/(less than curled hair volume number+full curled hair volume number)] × 100%.Evaluation result is in table 3.
[comparative example 1]
In comparative example 1, adopt the oil formula that Chinese patent ZL200580044949.0 embodiment 2 provides.Wherein, amino modified silicon 100 weight portion, emulsifying agent (Nonyl pheno base ether (6)) 30 weight portions, KM902 (SHIN-ETSU HANTOTAI's chemical industry (strain) system) 8.8 weight portions, the 1.2 parts of emulsifying agents added in order to emulsification KM902, the percetage by weight that emulsification dosage accounts for finish total surfactant is 22 % by weight; Amino-modified silicone oil kinematic viscosity at 25 DEG C is 3500mm
2/ s, amino equivalent is 2000.
Except adopting the finish of comparative example 1, the evaluation of antistatic property and the test of full-rolling rate, with embodiment 1 ~ 10, the results are shown in Table 3.
Ratio resistance data as can be seen from table 3, the antistatic property of large tow PAN base carbon fiber protofilament finish of the present invention has clear improvement than prior art.
Full-rolling rate data as can be seen from table 3, the tow full-rolling rate of large tow PAN base carbon fiber protofilament finish of the present invention is significantly improved than prior art, has good spinnability.
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
| Carbon fibre precursor ratio resistance, Ω cm | Full-rolling rate % | |
| Embodiment 1 | 8×10 8 | 75 |
| Embodiment 2 | 8×10 8 | 76 |
| Embodiment 3 | 8×10 8 | 73 |
| Embodiment 4 | 6×10 8 | 80 |
| Embodiment 5 | 5×10 8 | 85 |
| Embodiment 6 | 3×10 8 | 90 |
| Embodiment 7 | 3×10 8 | 93 |
| Embodiment 8 | 1×10 8 | 98 |
| Embodiment 9 | 9×10 7 | 95 |
| Embodiment 10 | 7×10 7 | 94 |
| Comparative example 1 | 3×10 9 | 65 |
Claims (1)
1. a large tow PAN base carbon fiber protofilament finish, composed as follows:
A) 15 parts of amino modified dimethyl silicone polymer A;
B) 55 parts of amino modified dimethyl silicone polymer B;
C) 15 parts of polyether-modified dimethyl silicone polymers;
D) 15 parts of emulsifying agents;
E) the W component of 90 parts;
The wherein said viscosity of amino modified dimethyl silicone polymer A 25 DEG C time is 200mm
2/ s, amino equivalent is 4000; Amino modified dimethyl silicone polymer B is 1300mm the viscosity of 25 DEG C
2/ s, amino equivalent is 1700; Described polyether-modified dimethyl silicone polymer is 530mm the viscosity of 25 DEG C
2/ s, HLB are 5; Described emulsifying agent is C13 alcohol polyoxyethylene (6) ether; W is the epoxy radicals addition product that diethylenetriamine and stearic acid react the amide compound obtained, the synthetic method of the epoxy radicals addition product of described amide compound is: take p-methyl benzenesulfonic acid as catalyst, 1mol diethylenetriamine and 2mol stearic acid are reacted 5 hours at 200 ~ 220 DEG C, obtain amide compound, then carry out the epoxy radicals addition product W that addition reaction obtains amide compound with 10mol oxirane;
The YG321 fiber ratio resistance instrument that the evaluation of antistatic property adopts Co., Ltd of Changzhou Textile Machinery Plant No.2 to produce, adopt oil content to be the PAN base carbon fiber protofilament of the 36K of 1 % by weight, the ratio resistance recording fiber by the method for GB/T14342-93 is 9 × 10
7Ω cm;
The spinnability of PAN base carbon fiber protofilament is represented with full-rolling rate, the test condition of full-rolling rate is, the PAN base carbon fiber protofilament of 500 tons/year is adopted to produce evaluating apparatus, it is the PAN base carbon fiber protofilament of the 36K of 1 % by weight with oil content, reel with the winding speed of 200 ms/min, 30 kilograms are reached for full volume with PAN base carbon fiber protofilament winding weight, in winding process, there is fracture of wire namely obtain rolling up less than curled hair, in winding process, there is not fracture of wire then obtain full curled hair volume, the computing formula of full-rolling rate is: full-rolling rate=[full curled hair volume number/(less than curled hair volume number+full curled hair volume number)] × 100%, the measured value of full-rolling rate is 95%.
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|---|---|---|---|
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|---|---|---|---|
| CN201110369956.5A CN103122585B (en) | 2011-11-18 | 2011-11-18 | Oiling agent of large tow PAN (Polyacrylonitrile)-based carbon fiber precursors |
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| CN103122585B true CN103122585B (en) | 2015-01-07 |
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| CN104452270A (en) * | 2014-12-19 | 2015-03-25 | 四川创越炭材料有限公司 | Spinning finish for asphalt carbon fiber |
| 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 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| CN101876096A (en) * | 2009-11-26 | 2010-11-03 | 中复神鹰碳纤维有限责任公司 | Production method of proto-filament oiling agent in carbon fiber production process |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| CN101876096A (en) * | 2009-11-26 | 2010-11-03 | 中复神鹰碳纤维有限责任公司 | Production method of proto-filament oiling agent in carbon fiber production process |
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| JP特开2008-63705A 2008.03.21 * |
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