CN1614134A - Nomex fibre surface modifying method - Google Patents
Nomex fibre surface modifying method Download PDFInfo
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- CN1614134A CN1614134A CN 200310103287 CN200310103287A CN1614134A CN 1614134 A CN1614134 A CN 1614134A CN 200310103287 CN200310103287 CN 200310103287 CN 200310103287 A CN200310103287 A CN 200310103287A CN 1614134 A CN1614134 A CN 1614134A
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- aromatic polyamide
- polyamide fibre
- surface modifier
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- 239000000835 fiber Substances 0.000 title claims abstract description 333
- 238000000034 method Methods 0.000 title claims abstract description 46
- 229920000784 Nomex Polymers 0.000 title description 4
- 239000004763 nomex Substances 0.000 title description 4
- 238000012986 modification Methods 0.000 claims abstract description 90
- 230000004048 modification Effects 0.000 claims abstract description 90
- 229920003235 aromatic polyamide Polymers 0.000 claims abstract description 64
- 239000004760 aramid Substances 0.000 claims description 62
- 239000003607 modifier Substances 0.000 claims description 47
- 239000004593 Epoxy Substances 0.000 claims description 26
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 22
- 229920000647 polyepoxide Polymers 0.000 claims description 22
- 238000006243 chemical reaction Methods 0.000 claims description 21
- 239000012948 isocyanate Substances 0.000 claims description 19
- JESXATFQYMPTNL-UHFFFAOYSA-N 2-ethenylphenol Chemical compound OC1=CC=CC=C1C=C JESXATFQYMPTNL-UHFFFAOYSA-N 0.000 claims description 18
- -1 aliphatic isocyanates Chemical class 0.000 claims description 18
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical group CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 14
- RGIBXDHONMXTLI-UHFFFAOYSA-N chavicol Chemical compound OC1=CC=C(CC=C)C=C1 RGIBXDHONMXTLI-UHFFFAOYSA-N 0.000 claims description 12
- 229940018564 m-phenylenediamine Drugs 0.000 claims description 12
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 10
- 239000008367 deionised water Substances 0.000 claims description 10
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 10
- 230000035484 reaction time Effects 0.000 claims description 9
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical group NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 7
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims description 7
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 6
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 6
- IAZKGRRJAULWNS-UHFFFAOYSA-N Chavicol Natural products OC1=CC=C(CCC=C)C=C1 IAZKGRRJAULWNS-UHFFFAOYSA-N 0.000 claims description 6
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 6
- 125000003368 amide group Chemical group 0.000 claims description 6
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 6
- 238000012545 processing Methods 0.000 claims description 6
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 5
- QXGBIHFUXMYJEF-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.N=C=O.C(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound N=C=O.N=C=O.N=C=O.N=C=O.C(C1=CC=CC=C1)C1=CC=CC=C1 QXGBIHFUXMYJEF-UHFFFAOYSA-N 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- 150000002513 isocyanates Chemical class 0.000 claims description 5
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 claims description 4
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- QIRNGVVZBINFMX-UHFFFAOYSA-N 2-allylphenol Chemical compound OC1=CC=CC=C1CC=C QIRNGVVZBINFMX-UHFFFAOYSA-N 0.000 claims description 3
- LZYPBIRCWAPCOY-UHFFFAOYSA-N 2-ethenylbut-3-en-1-ol Chemical compound OCC(C=C)C=C LZYPBIRCWAPCOY-UHFFFAOYSA-N 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 3
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims description 3
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 claims description 3
- 150000007824 aliphatic compounds Chemical class 0.000 claims description 3
- 150000001491 aromatic compounds Chemical class 0.000 claims description 3
- SIIVGPQREKVCOP-UHFFFAOYSA-N but-1-en-1-ol Chemical compound CCC=CO SIIVGPQREKVCOP-UHFFFAOYSA-N 0.000 claims description 3
- QVYARBLCAHCSFJ-UHFFFAOYSA-N butane-1,1-diamine Chemical compound CCCC(N)N QVYARBLCAHCSFJ-UHFFFAOYSA-N 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 claims description 3
- 150000002085 enols Chemical class 0.000 claims description 3
- LHTVMBMETNGEAN-UHFFFAOYSA-N pent-1-en-1-ol Chemical compound CCCC=CO LHTVMBMETNGEAN-UHFFFAOYSA-N 0.000 claims description 3
- KJOMYNHMBRNCNY-UHFFFAOYSA-N pentane-1,1-diamine Chemical compound CCCCC(N)N KJOMYNHMBRNCNY-UHFFFAOYSA-N 0.000 claims description 3
- 229920000768 polyamine Polymers 0.000 claims description 3
- ASUAYTHWZCLXAN-UHFFFAOYSA-N prenol Chemical compound CC(C)=CCO ASUAYTHWZCLXAN-UHFFFAOYSA-N 0.000 claims description 3
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 3
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 66
- 238000010521 absorption reaction Methods 0.000 abstract description 47
- 229920005989 resin Polymers 0.000 abstract description 13
- 239000011347 resin Substances 0.000 abstract description 13
- 239000011159 matrix material Substances 0.000 abstract description 4
- 238000005516 engineering process Methods 0.000 abstract description 3
- 239000003822 epoxy resin Substances 0.000 description 20
- 229920003368 Kevlar® 29 Polymers 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 11
- 230000002708 enhancing effect Effects 0.000 description 10
- 230000014759 maintenance of location Effects 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 8
- 229910021641 deionized water Inorganic materials 0.000 description 8
- 238000002715 modification method Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000002131 composite material Substances 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- 238000005303 weighing Methods 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229920000271 Kevlar® Polymers 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 150000002118 epoxides Chemical group 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000004761 kevlar Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000009958 sewing Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000005495 cold plasma Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920003369 Kevlar® 49 Polymers 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical group NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- 239000004835 fabric adhesive Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000005213 imbibition Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 125000002462 isocyano group Chemical group *[N+]#[C-] 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000011089 mechanical engineering Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
本发明涉及一种聚芳酰胺纤维的表面改性方法。更具体地说，本发明中的改性技术在于改性后的聚芳酰胺纤维的吸水性能及吸水后纤维的强度得到明显的改善，吸水率下降50％～80％，吸水后强度提高20％～30％，纤维和树脂基体间的结合强度也提高10％～20％。
The invention relates to a method for surface modification of polyaramid fibers. More specifically, the modification technology in the present invention is that the water absorption performance of the modified polyaramid fiber and the strength of the fiber after water absorption are significantly improved, the water absorption rate is reduced by 50% to 80%, and the strength after water absorption is increased by 20%. ~30%, the bonding strength between fiber and resin matrix is also increased by 10%~20%.
Description
Technical field
The present invention relates to a kind of surface modifying method of aromatic polyamide fibre.
Background technology
Aromatic polyamide fibre is widely used in the reinforcing material of composite, the sewing thread of various members, weaving and bullet resistant material.After sewing, the mechanical property of composite-material laminates has had significant improvement, but owing to contain amide group in the aromatic polyamide fibre, very easily suction, thus cause the performance of composite and sewing parts to descend significantly.In addition, because the highly crystalline of aromatic polyamide fibre self is therefore very poor with the wettability of most of resin matrixes, thereby after making composite, the interface performance of material is very poor.These shortcomings of aromatic polyamide fibre have influenced its application greatly.Therefore, how to improve the water absorbing properties and the interface performance of aromatic polyamide fibre, be subjected to great concern.
Commonly used in the aromatic polyamide fibre have Kevlar, a Nomex fiber.Kevlar fiber wherein commonly used is developed successfully the sixties by E.I.Du Pont Company, and it is a kind of aromatic polyamide fibre of high-strength light, and its construction unit is:
The researcher carried out a lot of the trial aromatic polyamide fibre was carried out surface treatment both at home and abroad so far, and purpose is for water absorbing properties that improves fiber and interface performance.Its processing method roughly can be divided into two classes, and a class is a physical modification, and a class is a chemical modification.
In the physical method modification, the more a kind of method that adopts both at home and abroad is the plasma surface modification method at present.[Wertheimer M.R., Sheveibev H.P. such as M.R.Wertheimer; J.Appl.Polym.Sci., 1981,26:2087] and R.E.Alfred[Allred D.E.et al.; Molecular Characterization of Composite Interface, 1983:333] handle the aromatic polyamide fibre surface with the cold plasma under inert gas and the reactant gas condition, all improved the interlaminar strength of aromatic polyamide fibre laminated board effectively.Chinese Academy of Sciences's Lanzhou materialization and the researcher of National Space Industry Corporation also once modification was carried out on the aromatic polyamide fibre surface with the air cold plasma, introduce active group at fiber surface, improve the nitrogen content and the oxygen content on surface, the bombardment of plasma has simultaneously also improved the roughness of fiber surface, can improve the bond strength between fiber and resin matrix.[Liu Xujun, Li Tongsheng, Yao Jialiang etc.; " surface treatment is to the influence of kevlar fabric adhesive property and frictional behaviour ", mechanical engineering material, 2000, the 3rd phase, P38-42] but decline significantly that the shortcoming of this method maximum is bombardment brings in various degree damage to cause to handle the intensity of back fiber to fiber surface, loss of strength even reach 70% more than.Plasma modification method cost is very high in addition, and instrument is very expensive, only is suitable for can't carrying out large batch of industrial production in the test of laboratory small lot.Another shortcoming of using plasma modification method is the uniform treatment that can't guarantee fiber surface when the batch fiber is carried out modification, and the treatment effect poor repeatability.
E.U.Okoroafor, people such as P.R.Huddleston and R.Hill once adopted at aromatic polyamide fibre surface-coated one deck organo-silicon coupling agent, in the hope of the fiber after the raising coating and the bond strength of interlaminar resin, but the aromatic polyamide fibre surface differs too big with the structure of organo-silicon coupling agent, its result makes the bonding strength of fiber and interlaminar resin descend 40% to 70% on the contrary, visual effects is not satisfactory, and this method also can't be improved the water absorbing properties of aromatic polyamide fibre.【E.U.Okoroafor，P.R.Huddleston，R.Hill.；“Alternative?Means?for?Evaluating?Fibre-matrix?Adhesion?in?Composites”，Journal?ofMaterials?Science，31(1996)3057-3064】
Also have other physical treatment method in addition, for example adopt ionic fluid, aura irradiation and flame treatment method etc.These methods are intended to improve the roughness of fiber surface, to improve the interface bond strength of fiber and resin, but they exist common shortcoming to be, in the time of modification the intensity of fiber itself is brought very large destruction, reduced the serviceability of fiber, and these processing method costs are very high, the treatment conditions strictness, be not suitable for industrialized mass, can't guarantee the uniform treatment of fiber surface during to the batch fiber treatment, the poor repeatability of treatment effect.
In chemical treatment method, previously, people such as Marom once were immersed in aromatic polyamide fibre and handled in the bromine water, though this method of modifying can improve the roughness of fiber surface, improve the interface performance of fiber and interlaminar resin, but brought great loss but for the intensity of fiber itself.【M.Breznick，J.Banbaji，H.Guttmann?and?G.Marom；Polym.Commun，28，55-56(1987)】
Afterwards, people such as A.G.Andreopoulos adopt acetic anhydride, the metering system isoxazolecarboxylic acid, the multiple finishing agents such as mixed solution of sulfuric acid nitric acid carry out surface treatment to aromatic polyamide fibre, make the interface bond strength between fiber and polyester matrix obtain raising to a certain degree, but the still damage that can't avoid these finishing agents that fiber self is caused, the carrying of fibrous fracture after the processing have descended and 20%～70% have not waited.【A.G.Andreopoulos；“A?New?Coupling?Agent?for?Aramid?Fibers”，Journalof?Applied?Polymer?Science.，Vol.38，1053-1064(1989)】
In addition, the chemical method of having reported also comprises " hydrogen ion method " " chlorosulfonic acid reducing process " " surface grafting method " " nitroreduction method " etc.
The hydrogen ion method mainly is fiber surface to be carried out hydrogen ion in advance activate the chemism that improves the surface, grafting epoxide group on the fiber surface of activation then, and two key groups etc. are to improve the bond strength of fiber and interlaminar resin.But this method treatment conditions harshness, the extraneous atmosphere during to temperature and reaction all has than higher requirement, is not suitable for mass industrialized production.【Takayanaki?M.et?al.；“N-Substituted?Poly(P-Phenylene?Terephthalamide)”，J.Polym.Chem.，1981，19：1133】
S.R.Wu, people such as G.S.Shu and S.S.Shyu once utilized chlorosulfonic acid under-10 ℃ condition the Kevlar fiber to be carried out surface treatment, the fiber after the processing with the bond strength of resin matrix on raising has been arranged, but fiber self loss of strength is very big.In addition, the treatment conditions of this method are also very high to the requirement of temperature and concentration, are not suitable for large-scale industrialization production.【S.R.Wu，G.S.Shu，S.S.Shyu.；“Kevlar?Fiber-Epoxy?Adhesion?and?Its?Effect?on?Composite?Mechanicaland?Fracture?Properties?by?Plasma?and?Chemical?Treatment”，Journal?of?Applied?Polymer?Science，Vol.62，1347-1360(1996)】
The surface grafting method is by fiber surface being carried out in advance certain activation processing (comprising plasma preliminary treatment and the preliminary treatment of active hydrogen ion etc.), then direct graft polymers or in the method for surperficial direct growth polymer molecule thereon.But behind the polymer, though the water absorption rate of fiber has reduced, the adhesion of fibre bundle very easily takes place in the fiber after this method is handled, and causes the compliance of fiber seriously to descend, even lumps on the fibre grafting, can't continue to use.
The restore nitrification method also is to introduce active group with effective combination that improves the fiber/resin interface by chemical method on the aromatic polyamide fibre surface.Yet this chemical method operation is complicated, and violent reaction condition has also brought great damage for fiber itself.【Wu?Y.L.，Tesoro?C.；J.Appl.Polym.Sci.，1986，31：1041】
In above all chemical method modifications, mostly be the bond strength of having considered how to improve fiber and interlaminar resin, and to the problem of the water absorption rate that how to reduce fiber self, reported method is few at present, does not more have this respect systematic research.
Summary of the invention
Goal of the invention
The surface modifying method that the purpose of this invention is to provide a kind of aromatic polyamide fibre, the intensity of the water absorbing properties of the aromatic polyamide fibre after the modification and suction back fiber is significantly improved, water absorption rate descends 50%～80%, suction back intensity increases by 20%～30%, and the bond strength of fiber and interlaminar resin has increased by 10%～20%.It is complicated that this method of modifying has overcome the operation of method of modifying in the past, the condition harshness, and performance is inhomogeneous and cost is high, shortcoming such as can't produce in batches, has that operation is simple, is suitable for large batch of industrial characteristics.
Specifically, purpose of the present invention
1. the surface modifying method of an aromatic polyamide fibre is characterized in that:
(1) described aromatic polyamide fibre is immersed in the first kind surface modifier, described aromatic polyamide fibre is carried out surface modification, contain isocyanate groups in the described first kind surface modifier, the number of described isocyanate groups is more than or equal to 2, be preferably 2-10, more preferably 2-6 is preferably 2-4, and described first kind surface modifier can be selected from aliphatic isocyanates or aromatic isocyanate, and the fiber surface after the processing contains isocyanate groups;
(2) spend deionised water, the isocyanate groups of fiber surface is converted into amino, obtain the aromatic polyamide fibre after the modification.
2. as the surface modifying method of 1 described aromatic polyamide fibre, it is characterized in that: the reaction temperature of step (1) is 0 ℃-120 ℃, be preferably 25 ℃-110 ℃, more preferably 40 ℃-100 ℃, be preferably 50 ℃-95 ℃, the reaction time is 0.1-10 hour, is preferably 0.3-8 hour, more preferably 0.5-5 hour, be preferably 1-3 hour.
3. as the surface modifying method of 1 or 2 described aromatic polyamide fibres, it is characterized in that: described first kind surface modifier is selected from 2,4 toluene diisocyanate, 1,3-phenylene diisocyanate, 2, the 6-toluene di-isocyanate(TDI), '-diphenylmethane diisocyanate, terephthalylidene vulcabond, hexamethylene diisocyanate, isophorone diisocyanate, dicyclohexyl methyl hydride diisocyanate, xyxylene vulcabond between tetramethyl, hexamethylene diisocyanate, naphthalene-1, the 5-vulcabond, 2,4,6-toluene triisocyanate, 1,2, the own triisocyanate of 6-, the diphenyl-methane tetraisocyanate, 1,2,5, the own tetraisocyanate of 6-.
4. the surface modifying method of an aromatic polyamide fibre, it is characterized in that: described surface modifying method comprises the steps:
(1) described aromatic polyamide fibre is immersed in the first kind surface modifier, described aromatic polyamide fibre is carried out surface modification, contain isocyanate groups in the described first kind surface modifier, the number of described isocyanate groups is more than or equal to 2, be preferably 2-10, more preferably 2-6 is preferably 2-4, and described first kind surface modifier can be selected from aliphatic isocyanates or aromatic isocyanate, and the fiber surface after the processing contains isocyanate groups;
(2) aromatic polyamide fibre that above-mentioned steps (1) is obtained immerses in the second class surface modifier, and described aromatic polyamide fibre is carried out surface modification, contain in the described second class surface modifier can with the group of isocyanate reaction.
5. as the surface modifying method of 4 described aromatic polyamide fibres, it is characterized in that: the reaction condition of step (1) is: reaction temperature is 0 ℃-120 ℃, be preferably 25 ℃-110 ℃, more preferably 40 ℃-100 ℃, be preferably 50 ℃-95 ℃, the reaction time is 0.1-10 hour, is preferably 0.3-8 hour, more preferably 0.5-5 hour, be preferably 1-3 hour; The reaction condition of step (2) is: reaction temperature is 0 ℃-150 ℃, is preferably 25 ℃-130 ℃, more preferably 40 ℃-110 ℃, be preferably 50 ℃-100 ℃, the reaction time is 0.1-10 hour, is preferably 0.3-8 hour, more preferably 0.5-5 hour, be preferably 1-3 hour.
6. as the surface modifying method of 4 described aromatic polyamide fibres, it is characterized in that: described first kind surface modifier is selected from 2,4 toluene diisocyanate, 1,3-phenylene diisocyanate, 2, the 6-toluene di-isocyanate(TDI), '-diphenylmethane diisocyanate, terephthalylidene vulcabond, hexamethylene diisocyanate, isophorone diisocyanate, dicyclohexyl methyl hydride diisocyanate, xyxylene vulcabond between tetramethyl, hexamethylene diisocyanate, naphthalene-1, the 5-vulcabond, 2,4,6-toluene triisocyanate, 1,2, the own triisocyanate of 6-, the diphenyl-methane tetraisocyanate, 1,2,5, the own tetraisocyanate of 6-.
7. as the surface modifying method of each described aromatic polyamide fibre among the 4-6, it is characterized in that: can be selected from amino, hydroxyl, aldehyde radical with the group of isocyanate reaction, carboxyl, amide groups, urethano, epoxy radicals in the described second class surface modifier.
8. as the surface modifying method of each described aromatic polyamide fibre among the 4-6, it is characterized in that: the described second class surface modifier is selected from especially: enol class surface modifier A, saturated and unsaturated polyamines class surface modifier B, hydroxyl epoxies surface modifier C, and described surface modifier A, B, C can be an aliphatic compound, also can be aromatic compound.
9. as the surface modifying method of 8 described aromatic polyamide fibres, it is characterized in that:
Described surface modifier A is selected from propenyl, butenol, and isobutene alcohol, prenol, positive pentenol, a vinylphenol, to vinylphenol, adjacent vinylphenol, a chavicol, chavicol, o-allyl phenol, 3-methylol-1,4-pentadiene.
Described surface modifier B is selected from Diethylenetriamine, three second tetramines, tetren, p-phenylenediamine (PPD), ethylenediamine, the third two press, butanediamine, pentanediamine, hexamethylene diamine, hexa, a triphenylamine, two (4-aminophenyl) amine, 5-allyl m-phenylene diamine (MPD), 5-vinyl m-phenylene diamine (MPD), 3,5-diaminourea (2,3) glycidoxy benzene.
Described surface modifier C is selected from epoxy prapanol, epoxy butanols, epoxy isobutanol, epoxy amylalcohol.
Technical scheme
Surface modifying method to aromatic polyamide fibre provided by the invention is as follows:
First kind surface modifying method:
With the first kind surface modifier aromatic polyamide fibre is carried out surface modification: earlier fiber and first kind surface conditioning agent are reacted, its objective is the group introducing fiber surface that reactivity is bigger, to improve the reactivity of aromatic polyamide fibre.Reaction temperature is 0 ℃-120 ℃, is preferably 25 ℃-110 ℃, more preferably 40 ℃-100 ℃, be preferably 50 ℃-95 ℃, and the reaction time is 0.1-10 hour, is preferably 0.3-8 hour, more preferably 0.5-5 hour, is preferably 1-3 hour.Being characterized as of this first kind surface modifier contains isocyanate groups, the isocyano number that contains in this surface modifier structure is to be not less than 2 integer, is preferably 2-10, more preferably 2-6, being preferably 2-4, can be aliphatic or aromatic isocyanate.This surface conditioning agent can be selected from: 2,4 toluene diisocyanate, 1, the 3-phenylene diisocyanate, 2, the 6-toluene di-isocyanate(TDI), '-diphenylmethane diisocyanate, terephthalylidene vulcabond, hexamethylene diisocyanate, isophorone diisocyanate, dicyclohexyl methyl hydride diisocyanate, xyxylene vulcabond between tetramethyl, hexamethylene diisocyanate, naphthalene-1,5-vulcabond, 2,4,6-toluene triisocyanate, 1,2, the own triisocyanate of 6-, diphenyl-methane tetraisocyanate, 1,2,5, the own tetraisocyanate of 6-.Wherein, be preferably 2,4 toluene diisocyanate, its structural formula is:
On structure, have two isocyanate groups in the ortho position of methyl and the contraposition, one of them isocyanate group can react with the active hydrogen on the aromatic polyamide fibre, with the grafting of another one isocyanate group to the main chain of fiber.Under certain condition, with aromatic polyamide fibre and vulcabond mixing and reaction, through the deionized water washing, remaining isocyanate group is hydrolyzed to amino on the fiber, obtains a kind of aromatic polyamide fibre of modification.On the aromatic polyamide fibre of modification, original water imbibition amide group is replaced by amino, and the fiber appearance has also been wrapped up the aromatic series carbochain simultaneously, has reduced the water absorption rate of fiber.
After modification aspect the intensity of fiber and since in the grafting of fiber appearance the phenyl ring group of rigidity, so the intensity of fiber also is maintained after the modification.
On boundary strength, because the isocyanate group hydrolysis in the grafting obtains amino, amino can participate in the curing of resin matrix, must improve the bond strength of fiber and resin greatly.
The second class surface modifying method:
(1) aromatic polyamide fibre is immersed in the first kind surface modifier, described aromatic polyamide fibre is carried out surface modification.Reaction temperature is 0 ℃-120 ℃, is preferably 25 ℃-110 ℃, more preferably 40 ℃-100 ℃, be preferably 50 ℃-95 ℃, and the reaction time is 0.1-10 hour, is preferably 0.3-8 hour, more preferably 0.5-5 hour, is preferably 1-3 hour;
(2) carry out the surface modification second time with the fiber of the second class surface modifier after to above-mentioned modification.Reaction temperature is 0 ℃-150 ℃, is preferably 25 ℃-130 ℃, more preferably 40 ℃-110 ℃, be preferably 50 ℃-100 ℃, and the reaction time is 0.1-10 hour, is preferably 0.3-8 hour, more preferably 0.5-5 hour, is preferably 1-3 hour.
The second class surface modifier that is adopted in the second class surface modifying method be selected from contain can with the organic substance of isocyanate groups reaction, be preferably the organic substance that contains active hydrogen.The group that wherein contains active hydrogen is preferably amino, hydroxyl, aldehyde radical, carboxyl, amide groups, urethano, epoxy radicals etc.More preferably, this contains one or more groups that also contain in the organic substance of active hydrogen in the two keys of epoxy, arylamine, fatty amine or C=C.Wherein, the particularly preferred second class surface modifier is:
(a) enols used, it is characterized in that containing two keys and hydroxyl, the number of two keys and hydroxyl all is to be not less than 1 integer, is preferably 1-10, more preferably 1-5 is preferably 1-3, can be aliphatic or aromatic series enol.Specifically can be propenyl, butenol, isobutene alcohol, prenol, positive pentenol, between vinylphenol, to vinylphenol, adjacent vinylphenol, a chavicol, chavicol, o-allyl phenol, 3-methylol-1,4-pentadiene or the like is preferably propenyl, and its structural formula is:
CH
2＝CH-CH
2-OH
(b) polyamine compounds can be primary amine or secondary amine or tertiary amine, wherein the quantity of primary amine and secondary amine group and greater than 2, be preferably 2-10, more preferably 2-8 is preferably 3-5, this surface modifier can belong to aliphatic or aromatic series, also can contain two keys or epoxide group simultaneously.Specifically can be Diethylenetriamine, three second tetramines, tetren, p-phenylenediamine (PPD), ethylenediamine, the third two press, butanediamine, pentanediamine, hexamethylene diamine, hexa, a triphenylamine, two (4-aminophenyl) amine, 5-allyl m-phenylene diamine (MPD), 5-vinyl m-phenylene diamine (MPD), 3,5-diaminourea (2,3) glycidoxy benzene.Be preferably Diethylenetriamine, its structural formula is:
(c) contain the compound of epoxide group and hydroxyl, the number of epoxide group and hydroxyl is and is not less than 1 integer, is preferably 1-10, and more preferably 1-5 is preferably 1-3, can be aliphatic or aromatic compound.Specifically can be epoxy prapanol, epoxy butanols, epoxy isobutanol, epoxy amylalcohol.Be preferably epoxy prapanol, its structural formula is:
When adopting the second class method of modifying, since wherein (a) and (b), (c) three class modifier all contain can with the group of isocyanate reaction, thereby be easy to and grafting on isocyanate groups react, thereby epoxy, arylamine, fatty amine or C=C grafting to aromatic polyamide fibre, are obtained the aromatic polyamide fibre after the modification.
On the aromatic polyamide fibre of modification, original bibulous amide group is by epoxy radicals, amino, and ethylene linkage replaces, and the fiber appearance has also been wrapped up aliphatic or aromatic series carbochain simultaneously, has reduced the water absorption rate of fiber.
After modification aspect the intensity of fiber and since in the grafting of fiber appearance the phenyl ring group of rigidity, therefore the intensity of fiber also is maintained after modification.
On boundary strength, owing to epoxy on the fibre grafting after the modification, amino, ethylene linkage can participate in the curing of resin matrix, also must improve the bond strength of fiber and resin greatly.
The test that intensity after high temperature water absorbing properties and the suction keeps performance
Aromatic polyamide fibre is selected the Kevlar29 fiber for use, carries out the high temperature poach and tests and measure its water absorption rate, measures Strength Changes through the Kevlar29 fiber after the high temperature suction by intensity experiment.Through measuring, we find:
(1) the Kevlar29 fiber has higher water absorption rate when 95 ℃ high temperature poach; After 10 hours poach time, suction reaches capacity substantially, as Fig. 1;
(2) intensity of fiber sharply descends along with the prolongation of poach time under the high temperature, the intensity decreases of poach Kevlar29 fiber after 10 hours 20%, poach after 10 hours intensity decreases slow down, fibre strength is with a toll of about 40%, as Fig. 2 after 55 hours;
We can see from figure, and on the water absorption rate curve, water absorption rate reached capacity at the 10th hour, should be made as evaluation point; On intensity curve, 10 hours and 55 hours is two more representational points, therefore also is made as evaluation point.In subsequent experimental, 10 hours measured value is chosen in the water absorption rate assessment, and high temperature suction back strength assessment is chosen 10 hours and 55 hours two time points.
The high temperature water absorbing properties of fiber after the modification and unmodified fibers and these two aspects of strength retention after the suction are tested, and method of testing is:
Load weighted fiber is placed in the deionized water, at 95 ℃ of following poach.At the 10th hour fiber is taken out, remove remained on surface liquid, air-dry through cold wind, treat weighing after the constant weight, measure the water absorption rate of fiber this moment, the computing formula of water absorption rate is:
Water absorption rate=[(M
2-M
1)/M
1] * 100%
M1: fibre weight before the suction
M2: suction back fibre weight
The measurement of fibre strength comprises the fibre strength of fibre strength after the modification, 95 ℃ of following poach 10 hours and 55 hours.
Fiber after the modification is removed surperficial residual liquid, clean repeatedly twice with acetone and deionized water, dry up through cold wind, treat to measure the maximum breaking load of fibre single thread and write down measured value after the constant weight, get the evaluation criterion of the mean value of 100 samples at least as fibre strength.
Fiber after the modification is placed in the deionized water, at 95 ℃ of following poach.The 10th hour and the 55th hour fiber is taken out, remove surperficial residual liquid, dry up through cold wind, treat to measure after the constant weight intensity of fibre single thread, measuring method is the same.
Experiment measuring shows, aspect the bond strength at water absorption rate, strength retention and interface, has increased significantly than unmodified Kevlar29 fiber through the fiber after the used method of modifying processing of the present invention.The intensity of the water absorbing properties of the aromatic polyamide fibre after the method for modifying modification among employing the present invention and suction back fiber is significantly improved, water absorption rate descends 50%～80%, the intensity of fiber has good maintenance after the modification, strength ratio unmodified fibers through high temperature suction back fiber can increase by 20%～30%, and the bond strength of fiber and interlaminar resin has increased by 10%～20%.
From in appearance, the fiber surface after the modification becomes coarse, and coarse surface more helps the combination with resin system.On structure, increased dissimilar functional groups with the fiber surface after this method processing, these functional groups can both participate in the curing of resin system, further improve the bond strength of fiber and resin.
Description of drawings
Fig. 1 be the untreatment fiber water absorption rate over time;
Fig. 2 is the variation of untreatment fiber intensity with the poach time.
The specific embodiment
Used aromatic polyamide fibre is the Kevlar29 fiber in the specific embodiment, but to those skilled in the art, the Kevlar29 fiber is as the representative in the aromatic polyamide fibre, have and similar structure of other Nomex and character, the aromatic polyamide fibre that is easy to spread to other by the Kevlar29 fiber among the embodiment is (as Kevlar49, the Nomex fiber), also can handle with same surface modifying method.
First kind surface-modification method
Embodiment 1
The Kevlar29 fiber of even clip 80 centimeter length, 1500 dawn.Air-dry under the room temperature, weigh.
Take by weighing a certain amount of 2,4 toluene diisocyanate and pour in the beaker, consumption is heated to 70 ℃ complete submergence fibre weight being as the criterion with solution.After treating temperature constant, fiber is put into beaker under nature, and make it be immersed in the 2,4 toluene diisocyanate fully, reacted 1 hour, take out fiber, clean twice repeatedly with deionized water and anhydrous propanone successively, cold wind dries up, after treating constant weight, measure the intensity of fiber after the modification, the bond strength after the modification between fiber and epoxy resin, and after the modification fiber in water absorption rate and 95 ℃ poach the fibre strength 10 hour and 55 hour after of 95 ℃ of poach after 10 hours.
Embodiment 2
Described according to embodiment 1, temperature is brought up to 80 ℃, all the other operations are constant.
Embodiment 3
Described according to embodiment 1, temperature is brought up to 90 ℃, all the other operations are constant.
With embodiment 1,2, the water absorption rate data of fiber and suction back fibre strength data compare with unmodified fibers after 3 modifications that obtain.Water absorption rate relatively includes table 1.
The fiber water absorption rate relatively after 95 ℃ of high temperature of table 1 absorbed water 10 hours
| Treatment temperature | Unmodified fibers | ????70℃ | ????80℃ | ????90℃ |
| 10 hours water absorption rate of 95 ℃ of suctions | ??3.50％ | ????0.75％ | ????0.81％ | ????1.10％ |
| The rate of descent of fiber water absorption rate after the modification | ??- | ????78.5％ | ????76.8％ | ????68.6％ |
The intensity of fiber and suction back strength ratio include table 2 after the modification.
The intensity of fiber and 95 ℃ of high temperature suction back fibre strengths are relatively after table 2 modification
| Treatment temperature | Unmodified fibers | ??70℃ | ??80℃ | ??90℃ |
| Handle the back fiber *Intensity (cN) | ????31.1 | ??29.3 | ??28.8 | ??29.1 |
| The conservation rate of fibre strength is 94.5% | The conservation rate of fibre strength is 92.9% | The conservation rate of fibre strength is 93.6% | ||
| 95 ℃ the suction 10 hours after fibre strength (cN) | ????25.0 | ??25.7 | ??26.7 | ??24.6 |
| Raising rate than unmodified fibers intensity is 2.8% | Raising rate than unmodified fibers intensity is 6.7% | Raising rate than unmodified fibers intensity is-1.6% | ||
| 95 ℃ the suction 55 hours after fibre strength (cN) | ????20.1 | ??21.7 | ??22.5 | ??21.5 |
| Raising rate than unmodified fibers intensity is 8.7% | Raising rate than unmodified fibers intensity is 12.7% | Raising rate than unmodified fibers intensity is 7.3% |
* fibre strength refers to the breaking load of single fiber, down together.
Bond strength after the modification between fiber and epoxy resin interface relatively includes table 3.
Bond strength after table 3 modification between fiber and epoxy resin interface relatively
| Treatment temperature | Unmodified fibers | ????70℃ | ????80℃ | ????90℃ |
| Bond strength between fiber and epoxy resin interface *????(cN) | ??34.4 | ????41.3 | ????39.3 | ????39.1 |
| The raising rate of bond strength | ??- | ????20％ | ????14.3％ | ????13.7％ |
* the monofilament withdrawal force on the bond strength single fiber that refers to extract measuring every millimeter in epoxy resin-base by monofilament, down with.
From table 1, can see in 2,3, the fiber after handling through method of modifying of the present invention, along with the difference of treatment temperature, its water absorption rate has substantial degradation than unmodified fibers, and rate of descent is 68%～78%.
Also having on strength retention preferably of fiber shows after the modification under different temperatures, and strength retention is 93%～95%.
Fiber after the modification has had certain lifting in the strength ratio unmodified fibers of 95 ℃ of high temperature suctions after 10 hours, and intensity has improved 3%～7%.
Fiber after the modification has had certain lifting in the strength ratio unmodified fibers of 95 ℃ of high temperature suctions after 55 hours, and intensity has improved 7%～13%.
Fiber and the bond strength between epoxy resin interface after the modification have had certain lifting than unmodified fibers, and enhancing rate is 14%～20%.
The second class surface-modification method: the Kevlar29 fiber after handling through first kind surface-modification method is carried out surface modification
Embodiment 4
The Kevlar29 fiber of even clip 80 centimeter length, 1500 dawn.Air-dry under the room temperature, weigh.
Take by weighing a certain amount of 2,4 toluene diisocyanate and pour in the beaker, consumption is heated to 70 ℃ complete submergence fibre weight being as the criterion with solution.After treating temperature constant, fiber is put into beaker under nature, and it is immersed in the 2,4 toluene diisocyanate fully, reacted 1 hour, take out fiber, remove the reactant liquor of remained on surface with benzinum.In the propenyl that the rapid input of fiber under moisture state is 55 ℃, the consumption of propenyl reacted 1 hour complete submergence fibre weight being as the criterion, and took out fiber, cleaned twice repeatedly with anhydrous propanone and deionized water, and cold wind dries up.After treating constant weight, measure the intensity of fiber after the modification, the bond strength after the modification between fiber and epoxy resin, and after the modification fiber in the water absorption rate of 95 ℃ of poach after 10 hours and the intensity of the fiber of 95 ℃ of poach after 10 hours and 55 hours.
Embodiment 5
Described according to embodiment 4, the propenyl temperature is brought up to 70 ℃, 75 ℃, 80 ℃, 85 ℃, 90 ℃ of five different temperature are carried out modification respectively, and other operations are constant.
The water absorption rate data of fiber and suction back fibre strength data compare with unmodified fibers after the modification that embodiment 4,5 is obtained.Water absorption rate relatively includes table 4.
The fiber water absorption rate relatively after 95 ℃ of high temperature of table 4 absorbed water 10 hours
| Treatment temperature | Unmodified fibers | 55℃ | 70℃ | 75℃ | 80℃ | 85℃ | 90℃ |
| 10 hours water absorption rate of 95 ℃ of suctions | ??3.50％ | 2.79％ | 1.89％ | 1.54％ | 2.41％ | 2.45％ | 1.64％ |
| The rate of descent of fiber water absorption rate after the modification | ??- | 20.3％ | 46.0％ | 56.0％ | 31.1％ | 30％ | 53.1％ |
The intensity of fiber and suction back strength ratio include table 5 after the modification.
The intensity of fiber and 95 ℃ of high temperature suction back fibre strengths are relatively after table 5 modification
| Treatment temperature | Unmodified fibers | ??55℃ | ??70℃ | ??75℃ | ??80℃ | ??85℃ | ??90℃ |
| Handle back fibre strength (cN) | ??31.1 | ??25.6 | ??26.0 | ??29.6 | ??29.2 | ??29.1 | ??27.1 |
| The conservation rate of fibre strength is 82.6% | The conservation rate of fibre strength is 83.9% | The conservation rate of fibre strength is 95.4% | The conservation rate of fibre strength is 94.2% | The conservation rate of fibre strength is 93.7% | The conservation rate of fibre strength is 87.3% | ||
| 95 ℃ the suction 10 hours after fibre strength (cN) | ??25.0 | ??23.4 | ??22.9 | ??28.9 | ??28.2 | ??31.3 | ??23.1 |
| Raising rate than unmodified fibers intensity is-6% | Raising rate than unmodified fibers intensity is-8% | Raising rate than unmodified fibers intensity is 16% | Raising rate than unmodified fibers intensity is 13% | Raising rate than unmodified fibers intensity is 25% | Raising rate than unmodified fibers intensity is-8% | ||
| 95 ℃ the suction 55 hours after fibre strength (cN) | ??20.1 | ??22.0 | ??18.6 | ??26.6 | ??24.9 | ??27.3 | ??20.6 |
| Raising rate than unmodified fibers intensity is 10% | Raising rate than unmodified fibers intensity is-7% | Raising rate than unmodified fibers intensity is 33% | Raising rate than unmodified fibers intensity is 25% | Raising rate than unmodified fibers intensity is 37% | Raising rate than unmodified fibers intensity is 3% |
Bond strength after the modification between fiber and epoxy resin interface relatively includes table 6.
Bond strength after table 6 modification between fiber and epoxy resin interface relatively
| Treatment temperature | Unmodified fibers | ??55℃ | ??70℃ | ??75℃ | ??80℃ | ??85℃ | ??90℃ |
| Bond strength between fiber and epoxy resin interface (cN) | ??34.4 | ??35.2 | ??38.2 | ??39.0 | ??37.1 | ??35.1 | ??34.6 |
| The raising rate of bond strength | ??- | ??2.4％ | ??11.1％ | ??13.4％ | ??7.9％ | ??2.1％ | ??0.6％ |
From table 4, can see in 5,6, the fiber after handling through method of modifying of the present invention, along with the difference of treatment temperature, its water absorption rate has significantly than unmodified fibers and reduces, and reduction rate is 20%～56%.
Also having on strength retention preferably of fiber shows after the modification under different temperatures, and strength retention is 94%～95% preferably.
Fiber after the modification has greatly improved in the strength ratio unmodified fibers of 95 ℃ of high temperature suctions after 10 hours, and enhancing rate is 13%～25% preferably.
Fiber after the modification has greatly improved in the strength ratio unmodified fibers of 95 ℃ of high temperature suctions after 55 hours, and enhancing rate is 25%～37% preferably.
Fiber and the bond strength between epoxy resin interface after the modification have had certain lifting than unmodified fibers, and enhancing rate is 11%～13% preferably.
Embodiment 6
The Kevlar29 fiber of even clip 80 centimeter length, 1500 dawn.Air-dry under the room temperature, weigh.
Take by weighing a certain amount of 2,4 toluene diisocyanate and pour in the beaker, consumption is heated to 70 ℃ complete submergence fibre weight being as the criterion with solution.After treating temperature constant, fiber is put into beaker under nature, and it is immersed in the 2,4 toluene diisocyanate fully, reacted 1 hour, take out fiber,, remove the reactant liquor of remained on surface with cleaning in the benzinum.In the Diethylenetriamine that the rapid input of fiber under moisture state is 70 ℃, the consumption of Diethylenetriamine is complete submergence fibre weight being as the criterion, reacted 1 hour, take out fiber, clean twice repeatedly with anhydrous propanone and deionized water, cold wind dries up, after treating constant weight, measure the intensity of fiber after the modification, the bond strength after the modification between fiber and epoxy resin, and after the modification fiber in the water absorption rate of 95 ℃ of poach after 10 hours and the intensity of the fiber of 95 ℃ of poach after 10 hours and 55 hours.
Embodiment 7
Described in embodiment 6, the temperature of Diethylenetriamine solution is brought up to 80 ℃, 90 ℃, under two kinds of temperature, experimentize respectively, other operations are constant.
The water absorption rate data of fiber and suction back fibre strength data compare with last modified fibre after the modification that embodiment 6,7 is obtained.Water absorption rate relatively includes table 7.
The fiber water absorption rate relatively after 95 ℃ of high temperature of table 7 absorbed water 10 hours
| Treatment temperature | Unmodified fibers | ????70℃ | ????80℃ | ????90℃ |
| 10 hours water absorption rate of 95 ℃ of suctions | ????3.50％ | ????1.82％ | ????2.09％ | ????1.93％ |
| The rate of descent of fiber water absorption rate after the modification | ????- | ????48％ | ????40.3％ | ????44.9％ |
The intensity of fiber and suction back strength ratio include table 8 after the modification.
The intensity of fiber and 95 ℃ of high temperature suction back fibre strengths are relatively after table 8 modification
| Treatment temperature | Unmodified fibers | ??70℃ | ??80℃ | ??90℃ |
| Handle back fibre strength (cN) | ????31.1 | ??29.0 | ??29.3 | ??29.9 |
| The conservation rate of fibre strength is 93.5% | The conservation rate of fibre strength is 94.5% | The conservation rate of fibre strength is 96.6% | ||
| 95 ℃ the suction 10 hours after fibre strength (cN) | ????25.0 | ??28.1 | ??29.1 | ??26.0 |
| Raising rate than unmodified fibers intensity is 11.2% | Raising rate than unmodified fibers intensity is 16.3% | Raising rate than unmodified fibers intensity is 4.1% | ||
| 95 ℃ the suction 55 hours after fibre strength (cN) | ????20.1 | ??22.1 | ??24.2 | ??23.1 |
| Raising rate than unmodified fibers intensity is 10.5% | Raising rate than unmodified fibers intensity is 20.8% | Raising rate than unmodified fibers intensity is 15.3% |
Bond strength after the modification between fiber and epoxy resin interface relatively includes table 9
Bond strength after table 9 modification between fiber and epoxy resin interface relatively
| Treatment temperature | Unmodified fibers | ????70℃ | ????80℃ | ????90℃ |
| Bond strength between fiber and epoxy resin interface (cN) | ??34.4 | ????40.2 | ????40.0 | ????39.9 |
| The raising rate of bond strength | ??- | ????16.8％ | ????16.3％ | ????16.0％ |
From table 7, can see in 8,9, the fiber after handling through method of modifying of the present invention, along with the difference of treatment temperature, its water absorption rate has bigger reduction than unmodified fibers, and reduction rate is 40%～48%.
Also having on strength retention preferably of fiber shows after the modification under different temperatures, and strength retention is 94%～97%.
Fiber after the modification has had certain lifting in the strength ratio unmodified fibers of 95 ℃ of high temperature suctions after 10 hours, and enhancing rate is 4%～16%.
Fiber after the modification has had certain lifting in the strength ratio unmodified fibers of 95 ℃ of high temperature suctions after 55 hours, and enhancing rate is 11%～15%.
Fiber and the bond strength between epoxy resin interface after the modification have had certain lifting than unmodified fibers, and enhancing rate is 16%～17%.
Embodiment 8
The Kevlar29 fiber of even clip 80 centimeter length, 1500 dawn.Air-dry under the room temperature, weigh.
Take by weighing a certain amount of 2,4 toluene diisocyanate and pour in the beaker, consumption is heated to 70 ℃ complete submergence fibre weight being as the criterion with solution.After treating temperature constant, fiber is put into beaker under nature, and it is immersed in the 2,4 toluene diisocyanate fully, reacted 1 hour, take out fiber, remove the reactant liquor of remained on surface with benzinum.In the epoxy prapanol that the rapid input of fiber under moisture state is 70 ℃, the consumption of epoxy prapanol is complete submergence fibre weight being as the criterion, reacted 1 hour, take out fiber, clean twice repeatedly with anhydrous propanone and deionized water, cold wind dries up, after treating constant weight, measure the intensity of fiber after the modification, the bond strength after the modification between fiber and epoxy resin, and after the modification fiber in the water absorption rate of 95 ℃ of poach after 10 hours and the intensity of the fiber of 95 ℃ of poach after 10 hours and 55 hours.
Embodiment 9
Described according to embodiment 8, the epoxy prapanol solution temperature is brought up to 80 ℃, 85 ℃, under two kinds of temperature, experimentize respectively, other operations are constant.
The water absorption rate data of fiber and suction back fibre strength data compare with unmodified fibers after the modification that embodiment 8,9 is obtained.Water absorption rate relatively includes table 10.
The fiber water absorption rate relatively after 95 ℃ of high temperature of table 10 absorbed water 10 hours
| Treatment temperature | Unmodified fibers | ????70℃ | ????80℃ | ????85℃ |
| 10 hours water absorption rate of 95 ℃ of suctions | ??3.50％ | ????1.49％ | ????1.19％ | ????1.31％ |
| The rate of descent of fiber water absorption rate after the modification | ??- | ????57.4％ | ????66.0％ | ????62.5％ |
The intensity of fiber and suction back strength ratio include table 11 (videing infra) after the modification.
Bond strength after the modification between fiber and epoxy resin interface relatively includes table 12 (videing infra).
The intensity of fiber and 95 ℃ of high temperature suction back fibre strengths are relatively after table 11 modification
| Treatment temperature | Unmodified fibers | 70℃ | 80℃ | 85℃ |
| Handle back fibre strength (cN) | ????31.1 | 32.1 | 32.2 | 31.3 |
| The conservation rate of fibre strength is 103.6% | The conservation rate of fibre strength is 103.8% | The conservation rate of fibre strength is 101.0% | ||
| 95 ℃ the suction 10 hours after fibre strength (cN) | ????25.0 | 27.9 | 27.0 | 26.1 |
| Raising rate than unmodified fibers intensity is 11.3% | Raising rate than unmodified fibers intensity is 8.0% | Raising rate than unmodified fibers intensity is 4.5% | ||
| 95 ℃ the suction 55 hours after fibre strength (cN) | ????20.1 | 25.0 | 23.5 | 23.6 |
| Raising rate than unmodified fibers intensity is 24.8% | Raising rate than unmodified fibers intensity is 17.5% | Raising rate than unmodified fibers intensity is 17.8% |
Bond strength after table 12 modification between fiber and epoxy resin interface relatively
| Treatment temperature | Unmodified fibers | ????70℃ | ????80℃ | ????90℃ |
| Bond strength between fiber and epoxy resin interface (cN) | ??34.4 | ????41.9 | ????42.0 | ????41.1 |
| The raising rate of bond strength | ??- | ????21.7％ | ????22.0％ | ????19.4％ |
From table 10, can see in 11,12, the fiber after handling through method of modifying of the present invention, along with the difference of treatment temperature, its water absorption rate has bigger reduction than unmodified fibers, and reduction rate is 57%～66%.
Also having on strength retention preferably of fiber shows after the modification under different temperatures, and intensity does not only reduce, and has a certain upgrade on the contrary, and strength retention is 101%～104%.
Fiber after the modification has had certain lifting in the strength ratio unmodified fibers of 95 ℃ of high temperature suctions after 10 hours, and enhancing rate is 5%～11%.
Fiber after the modification has had bigger lifting in the strength ratio unmodified fibers of 95 ℃ of high temperature suctions after 55 hours, and enhancing rate is 18%～25%.
Fiber and the bond strength between epoxy resin interface after the modification have had certain lifting than unmodified fibers, and enhancing rate is 19%～22%.
Though the present invention is described in detail with reference to technology contents and embodiment, but should describe only for purposes of illustration, to those skilled in the art, it all is conspicuous under the situation that does not deviate from scope of the present invention the present invention being carried out various variations and changes, and can not be defined as the described content of specification to the present invention.
Claims (9)
1. the surface modifying method of an aromatic polyamide fibre, it is characterized in that: described method of modifying comprises the steps:
(1) described aromatic polyamide fibre is immersed first kind surface modifier and carry out surface modification, contain isocyanate groups in the described first kind surface modifier, the number of described isocyanate groups is more than or equal to 2, be preferably 2-10, and described first kind surface modifier can be selected from aliphatic isocyanates or aromatic isocyanate, and the fiber surface after the processing contains isocyanate groups;
(2) spend deionised water, the isocyanate groups of fiber surface is converted into amino, obtain the aromatic polyamide fibre after the modification.
2. the surface modifying method of aromatic polyamide fibre as claimed in claim 1, it is characterized in that: the reaction temperature of step (1) is 0 ℃-120 ℃, and the reaction time is 0.1-10 hour.
3. the surface modifying method of aromatic polyamide fibre as claimed in claim 1 or 2, it is characterized in that: described first kind surface modifier is selected from 2,4 toluene diisocyanate, 1,3-phenylene diisocyanate, 2, the 6-toluene di-isocyanate(TDI), '-diphenylmethane diisocyanate, terephthalylidene vulcabond, hexamethylene diisocyanate, isophorone diisocyanate, dicyclohexyl methyl hydride diisocyanate, xyxylene vulcabond between tetramethyl, hexamethylene diisocyanate, naphthalene-1, the 5-vulcabond, 2,4,6-toluene triisocyanate, 1,2, the own triisocyanate of 6-, the diphenyl-methane tetraisocyanate, 1,2,5, the own tetraisocyanate of 6-.
4. the surface modifying method of an aromatic polyamide fibre, it is characterized in that: described surface modifying method comprises the steps:
(1) described aromatic polyamide fibre is immersed first kind surface modifier and carry out surface modification, contain isocyanate groups in the described first kind surface modifier, the number of described isocyanate groups is more than or equal to 2, be preferably 2-10, and described first kind surface modifier can be selected from aliphatic isocyanates or aromatic isocyanate, and the fiber surface after the processing contains isocyanate groups;
(2) aromatic polyamide fibre that above-mentioned steps (1) is obtained immerses in the second class surface modifier, and described aromatic polyamide fibre is carried out surface modification, contain in the described second class surface modifier can with the group of isocyanate reaction.
5. the surface modifying method of aromatic polyamide fibre as claimed in claim 4, it is characterized in that: the reaction condition of step (1) is: reaction temperature is that reaction temperature is 0 ℃-120 ℃, and the reaction time is 0.1-10 hour; The reaction condition of step (2) is: reaction temperature is 0 ℃-150 ℃, and the reaction time is 0.1-10 hour.
6. the surface modifying method of aromatic polyamide fibre as claimed in claim 4, it is characterized in that: described first kind surface modifier is selected from 2,4 toluene diisocyanate, 1,3-phenylene diisocyanate, 2, the 6-toluene di-isocyanate(TDI), '-diphenylmethane diisocyanate, terephthalylidene vulcabond, hexamethylene diisocyanate, isophorone diisocyanate, dicyclohexyl methyl hydride diisocyanate, xyxylene vulcabond between tetramethyl, hexamethylene diisocyanate, naphthalene-1, the 5-vulcabond, 2,4,6-toluene triisocyanate, 1,2, the own triisocyanate of 6-, the diphenyl-methane tetraisocyanate, 1,2,5, the own tetraisocyanate of 6-.
7. as the surface modifying method of each described aromatic polyamide fibre among the claim 4-6, it is characterized in that: can be selected from amino, hydroxyl, aldehyde radical with the group of isocyanate reaction in the described second class surface modifier, carboxyl, amide groups, urethano, epoxy radicals.
8. as the surface modifying method of each described aromatic polyamide fibre among the claim 4-7, it is characterized in that: the described second class surface modifier is selected from: enol class surface modifier A, saturated and unsaturated polyamines class surface modifier B, hydroxyl epoxies surface modifier C, and described surface modifier A, B, C can be an aliphatic compound, also can be aromatic compound.
9. the surface modifying method of aromatic polyamide fibre as claimed in claim 8 is characterized in that:
Described surface modifier A is selected from propenyl, butenol, and isobutene alcohol, prenol, positive pentenol, a vinylphenol, to vinylphenol, adjacent vinylphenol, a chavicol, chavicol, o-allyl phenol, 3-methylol-1,4-pentadiene.
Described surface modifier B is selected from Diethylenetriamine, three second tetramines, tetren, p-phenylenediamine (PPD), ethylenediamine, the third two press, butanediamine, pentanediamine, hexamethylene diamine, hexa, a triphenylamine, two (4-aminophenyl) amine, 5-allyl m-phenylene diamine (MPD), 5-vinyl m-phenylene diamine (MPD), 3,5-diaminourea (2,3) glycidoxy benzene.
Described surface modifier C is selected from epoxy prapanol, epoxy butanols, epoxy isobutanol, epoxy amylalcohol.
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| CN 200310103287 CN1261638C (en) | 2003-11-05 | 2003-11-05 | Surface Modification Method of Polyaramid Fiber |
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN101787647A (en) * | 2010-02-10 | 2010-07-28 | 中蓝晨光化工研究院有限公司 | Surface treatment method of aramid fiber III |
| CN101203488B (en) * | 2005-07-22 | 2011-12-14 | 三井化学株式会社 | Process for production of isocyanate, isocyanate produced by the process, and use of the isocyanate |
| CN102734288A (en) * | 2011-04-14 | 2012-10-17 | 马格纳斯泰尔汽车技术两合公司 | Node element made of fiber-reinforced plastic, method for producing the same and use thereof |
| CN105670229A (en) * | 2016-04-07 | 2016-06-15 | 主义 | Technology for preparing epoxy-resin-polymer grouting liquid |
| CN105803789A (en) * | 2016-03-29 | 2016-07-27 | 深圳市新纶科技股份有限公司 | Surface modification aramid fiber and preparation method thereof |
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- 2003-11-05 CN CN 200310103287 patent/CN1261638C/en not_active Expired - Fee Related
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101203488B (en) * | 2005-07-22 | 2011-12-14 | 三井化学株式会社 | Process for production of isocyanate, isocyanate produced by the process, and use of the isocyanate |
| US8183407B2 (en) | 2005-07-22 | 2012-05-22 | Mitsui Chemicals, Inc. | Process for production of isocyanate, isocyanate produced by the process, and use of the isocyanate |
| CN101787647A (en) * | 2010-02-10 | 2010-07-28 | 中蓝晨光化工研究院有限公司 | Surface treatment method of aramid fiber III |
| CN102734288A (en) * | 2011-04-14 | 2012-10-17 | 马格纳斯泰尔汽车技术两合公司 | Node element made of fiber-reinforced plastic, method for producing the same and use thereof |
| CN105803789A (en) * | 2016-03-29 | 2016-07-27 | 深圳市新纶科技股份有限公司 | Surface modification aramid fiber and preparation method thereof |
| CN105803789B (en) * | 2016-03-29 | 2018-01-02 | 深圳市新纶科技股份有限公司 | A kind of surface modification of aramid fiber and preparation method thereof |
| CN105670229A (en) * | 2016-04-07 | 2016-06-15 | 主义 | Technology for preparing epoxy-resin-polymer grouting liquid |
| CN105906260A (en) * | 2016-04-07 | 2016-08-31 | 主义 | Preparation method of epoxy resin polymer concrete |
| CN105670229B (en) * | 2016-04-07 | 2019-02-05 | 主义 | A kind of preparation process of epoxide resin polymer grouting liquid |
| CN107903508A (en) * | 2017-12-15 | 2018-04-13 | 会通新材料股份有限公司 | A kind of aramid fiber reinforced polypropylene micro foaming composite material and preparation method thereof |
| CN107903508B (en) * | 2017-12-15 | 2021-02-26 | 会通新材料股份有限公司 | Aramid fiber reinforced polypropylene micro-foaming composite material and preparation method thereof |
| CN108440977A (en) * | 2018-03-12 | 2018-08-24 | 长安大学 | Modified pitch, modifying agent and preparation method for high-modulus Rut resistance concrete |
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