JPH0299669A - Textile treating agent - Google Patents
Textile treating agentInfo
- Publication number
- JPH0299669A JPH0299669A JP24752188A JP24752188A JPH0299669A JP H0299669 A JPH0299669 A JP H0299669A JP 24752188 A JP24752188 A JP 24752188A JP 24752188 A JP24752188 A JP 24752188A JP H0299669 A JPH0299669 A JP H0299669A
- Authority
- JP
- Japan
- Prior art keywords
- copolymer
- treatment agent
- water
- maleic acid
- neutralized
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000004753 textile Substances 0.000 title abstract description 5
- 239000000835 fiber Substances 0.000 claims abstract description 35
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 33
- 229920001577 copolymer Polymers 0.000 claims abstract description 31
- 239000000178 monomer Substances 0.000 claims abstract description 29
- 229920000058 polyacrylate Polymers 0.000 claims abstract description 16
- 239000011976 maleic acid Substances 0.000 claims abstract description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 14
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 11
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims abstract description 11
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims abstract description 11
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 9
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000470 constituent Substances 0.000 claims abstract description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 7
- 238000002156 mixing Methods 0.000 abstract description 7
- 229920002994 synthetic fiber Polymers 0.000 abstract description 6
- 239000012209 synthetic fiber Substances 0.000 abstract description 5
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 239000000203 mixture Substances 0.000 abstract description 3
- LZDDXRWBWZUFHD-ODZAUARKSA-N (z)-but-2-enedioic acid;2-methylprop-1-ene Chemical compound CC(C)=C.OC(=O)\C=C/C(O)=O LZDDXRWBWZUFHD-ODZAUARKSA-N 0.000 abstract 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 abstract 1
- 238000007598 dipping method Methods 0.000 abstract 1
- -1 e.g. Polymers 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 description 9
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000009941 weaving Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- DTCCVIYSGXONHU-CJHDCQNGSA-N (z)-2-(2-phenylethenyl)but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)\C=CC1=CC=CC=C1 DTCCVIYSGXONHU-CJHDCQNGSA-N 0.000 description 1
- NBJZEUQTGLSUOB-UHFFFAOYSA-N 1-chloro-4-isocyanato-2-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC(N=C=O)=CC=C1Cl NBJZEUQTGLSUOB-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- BBGGWHMVXARXRU-UHFFFAOYSA-N 2-methylprop-1-ene 5-phenylpenta-2,4-dienoic acid Chemical compound C(=CC1=CC=CC=C1)C=CC(=O)O.CC(C)=C BBGGWHMVXARXRU-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- FEIQOMCWGDNMHM-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid Chemical compound OC(=O)C=CC=CC1=CC=CC=C1 FEIQOMCWGDNMHM-UHFFFAOYSA-N 0.000 description 1
- USSIQXCVUWKGNF-UHFFFAOYSA-N 6-(dimethylamino)-4,4-diphenylheptan-3-one Chemical group C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 USSIQXCVUWKGNF-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
この発明は繊維処理剤に関し、詳しくは繊維−二すぐれ
た強度と伸度を付与すると共に、剥落量の低減された繊
維処理剤に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a fiber treatment agent, and more particularly to a fiber treatment agent that imparts superior strength and elongation to fibers and reduces the amount of flaking. be.
[従来の技術および発明が解決しようとする課題]綿糸
を織成して織物を製造する!二当たっては、通常、織成
工程における糸切れを防止するため、綿糸を特定の処理
剤を用いて処理することが行われる。この処理によって
綿糸に強度゛を付与し糸切れを防止する。[Prior art and problems to be solved by the invention] Weaving cotton threads to produce textiles! In order to prevent yarn breakage during the weaving process, the cotton yarn is usually treated with a specific treatment agent. This treatment gives strength to the cotton yarn and prevents it from breaking.
一方、合成繊維の場合、織成して織物を製造するに当た
って、主として織物を収束する目的で特定の処理剤が用
いられる。On the other hand, in the case of synthetic fibers, when weaving them into fabrics, a specific processing agent is used mainly for the purpose of converging the fabrics.
このような繊維処理剤として、水溶性アクリル系ポリマ
ーとポリビニルアルコールとからなるものが知られてい
る(CMCr水溶性高分子の応用と市場J 1984.
11.24発行、P2O)。As such a fiber treatment agent, one consisting of a water-soluble acrylic polymer and polyvinyl alcohol is known (CMCr Water-Soluble Polymer Applications and Markets J 1984).
Published 11.24, P2O).
この繊維処理剤は、綿糸における強度等の付与、合成繊
維における収束性についてはほぼ満足すべき水準にある
ものの、そのためには処理剤を加温して処理しなければ
ならないという不都合があった。また、いずれの場合に
おいても、処理後の処理剤の剥落量(通常、落糊量と称
される)が多く、これにともない特に綿糸の場合は落綿
を生じるという問題があった。Although this fiber treatment agent is at a nearly satisfactory level in terms of imparting strength, etc. to cotton threads and convergence to synthetic fibers, it has the disadvantage that the treatment agent must be heated for this purpose. Furthermore, in any case, there is a problem in that the amount of the treatment agent that comes off after treatment (usually referred to as the amount of size removed) is large, and this causes the problem that cotton yarn, especially in the case of cotton yarn, causes cotton to fall off.
この発明は、このような従来の欠点を解消し、繊維に強
度と伸度を付与すると共に、剥落量が低減され、しかも
繊維の処理に際して特に加温する必要のない繊維処理剤
を提供することを目的とする。The present invention solves these conventional drawbacks and provides a fiber treatment agent that imparts strength and elongation to fibers, reduces the amount of peeling, and does not require special heating during treatment of fibers. With the goal.
[課題を解決するための手段]
発明者はAij記目的を達成するために、水溶性アクリ
ル系ポリマーに配合する成分について種々検討を重ねた
結果、特定の共重合体の中和処理物を用いることによっ
て、繊維に強度と伸度を付与することができ、まt;、
処理剤の剥落量も少なく、さらに繊維の処理を室温下で
行うことのできる繊維処理剤が得られるということを見
い出し、この知見に基づいてこの発明をなすに至った。[Means for Solving the Problems] In order to achieve the object described in Aij, the inventor conducted various studies on the components to be added to the water-soluble acrylic polymer, and as a result, used a neutralized product of a specific copolymer. By doing so, it is possible to impart strength and elongation to the fibers, and;
The present inventors have discovered that a fiber treatment agent can be obtained that has a small amount of peeling of the treatment agent and can further treat fibers at room temperature, and based on this knowledge, the present invention has been completed.
−4゛なわち、この発明によれば、下記1および2の発
明が提供される。-4゛That is, according to this invention, the following inventions 1 and 2 are provided.
1、インブチレン、スチレンおよびアクリル酸系モノマ
ーかも選ばれた少なくとも1種のモノマーとマレイン酸
系モノマーとを構成単位とする共重合体の中和処理物な
らびに水溶性アクリル系ポリマーからなる繊維処理剤。1. A fiber treatment agent consisting of a neutralized copolymer containing a maleic acid monomer and at least one monomer selected from inbutylene, styrene, and an acrylic acid monomer, and a water-soluble acrylic polymer. .
2、インブチレン、スチレンおよびアクリル酸系モノマ
ーから選ばれた少なくとも1種のモノマーとマレイン酸
系モアマーとを構成単位とする共重合体の中和処理物、
水溶性アクリル系ポリマーならびにポリビニルアルコー
ルからなる繊維処理剤。2. Neutralized copolymer comprising at least one monomer selected from inbutylene, styrene, and acrylic acid monomers and a maleic acid moamer,
A fiber treatment agent made of water-soluble acrylic polymer and polyvinyl alcohol.
この発明の繊維処理剤が適用される繊維には特に制限は
なく、天然繊維、人造繊維、再生繊維、半合成繊維また
は合成繊維に対して有効である。There is no particular restriction on the fibers to which the fiber treatment agent of the present invention is applied, and it is effective for natural fibers, artificial fibers, regenerated fibers, semi-synthetic fibers, and synthetic fibers.
この発明の繊維処理剤を構成する共重合体の中和処理物
としては、イソブチレン、スチレンおよびアクリル酸系
モノマーから選ばれた少なくとも1種のモノマーとマレ
イン酸系モノマーとを構成単位とする共重合体であり、
この中に存在するカルボキシル基をアルカリで中和処理
したものが用いられる。The neutralized copolymer constituting the fiber treatment agent of this invention is a copolymer containing at least one monomer selected from isobutylene, styrene, and acrylic acid monomers and a maleic acid monomer as a constituent unit. It is a combination,
The carboxyl groups present therein are neutralized with an alkali and used.
アクリル酸系モノマーとしては、アクリル酸、メタクリ
ル酸またはこれらのエステルが挙げられ、マレイン酸系
モノマーとしては、マレイン酸または無水マレイン酸を
挙げることができる。Examples of the acrylic acid monomer include acrylic acid, methacrylic acid, or esters thereof, and examples of the maleic acid monomer include maleic acid or maleic anhydride.
具体的には、インブチレン−マレイン酸系モノマー共重
合体、スチレン−マレイン酸系モノマー共重合体、アク
リル酸系モノマー−マレイン酸系モノマー共重合体、イ
ンブチレン−スチレン−マレイン酸系モノマー共重合体
、インブチレン−アクリル酸系モノマー−マレイン酸系
モノマー共重合体、スチレン−アクリル酸系モノマー−
マレイン酸系モノマー共重合体、イソブチレン−スチレ
ン−アクリル酸系モノマー−マレイン酸系モノマー共重
合体などの二元、三元または四元共重合体を挙げること
ができる。Specifically, inbutylene-maleic acid monomer copolymer, styrene-maleic acid monomer copolymer, acrylic acid monomer-maleic acid monomer copolymer, inbutylene-styrene-maleic acid monomer copolymer Coalescence, inbutylene-acrylic acid monomer-maleic acid monomer copolymer, styrene-acrylic acid monomer-
Examples include binary, ternary, or quaternary copolymers such as a maleic acid monomer copolymer and an isobutylene-styrene-acrylic acid monomer-maleic acid monomer copolymer.
これらの共重合体中のマレイン酸系モノマーから選ばれ
た七ノで一単位とそれ以外の七ツマー単位とのモル比は
、通常1:o、9ないし1:5の範囲内である。また、
この共重合体としては粘度平均分子量500〜400,
000.好ましくは1.000〜200,000の範囲
のものが適当である。The molar ratio of the heptadone unit selected from the maleic acid monomer and the other heptad units in these copolymers is usually within the range of 1:o, 9 to 1:5. Also,
This copolymer has a viscosity average molecular weight of 500 to 400,
000. Preferably, a range of 1.000 to 200,000 is suitable.
このような共重合体は、たとえば次のようにして製造す
ることができる。Such a copolymer can be produced, for example, as follows.
すなわち、まずインブチレンを用いる場合は、イソブチ
レンを除く各七ツマー成分の所要量を反応容器中に仕込
み、冷却下に十分に脱気したのちインブチレンを加える
。次いで重合開始剤を加え、かきまぜながら加熱反応さ
せる。この際の反応温度としては、30〜200°C1
好ましくは50〜150℃が用いられる。また、この際
に用いられる重合開始剤としては、過酸化ベンゾイル、
過酸化ラウロイル、クメンヒドロパーオキシド、第三級
ブチルヒドロパーオキシド、ジクミルパーオキシド、ア
ゾヒスイソブチロニトリルなどが好適である。That is, when using inbutylene, the required amounts of each of the 7-mer components except isobutylene are charged into a reaction vessel, sufficiently degassed while cooling, and then inbutylene is added. Next, a polymerization initiator is added, and the mixture is heated and reacted while stirring. The reaction temperature at this time is 30 to 200°C1
Preferably a temperature of 50 to 150°C is used. In addition, the polymerization initiators used at this time include benzoyl peroxide,
Preferred are lauroyl peroxide, cumene hydroperoxide, tertiary butyl hydroperoxide, dicumyl peroxide, azohisisobutyronitrile, and the like.
この反応は、所望に応じエチルベンゼン、クメン、
n−7’チルベンゼン、アセトニトリル、ニトロメタン
、ニトロエタン、メチルエチルケトン、アセトン、N、
N−ジメチルホルムアミド、ジメラルスルホキシドなど
の溶媒中で行うことができる。反応時間は、モノマーの
種類、混合比、溶媒の有無、反応温度などにより変わる
が、通常、0.5〜20時間の範囲である。This reaction can be performed using ethylbenzene, cumene,
n-7' thylbenzene, acetonitrile, nitromethane, nitroethane, methyl ethyl ketone, acetone, N,
This can be carried out in a solvent such as N-dimethylformamide or dimeral sulfoxide. The reaction time varies depending on the type of monomer, the mixing ratio, the presence or absence of a solvent, the reaction temperature, etc., but is usually in the range of 0.5 to 20 hours.
次に、このようにして得た共重合体を中和処理するにあ
たっては、この共重合体に水酸化ナトリウム、水酸化カ
リウム、水酸化アンモニウム、炭酸ナトリウム、アンモ
ニアの水溶液を加え、20〜150’O,好ましくは5
0〜100°Cにおいて、0.5〜10時間かきまぜる
ことによって行われる。中和剤どしては、上記の無機塩
基だけでなく酢酸ナトリウム、尿素、チオ尿素、有機ア
ミン類のような有機塩基を用いることもできる。中和度
としては、中和処理前に存在する酸性基の数に基づき、
0.1〜1.0程度が適当である。Next, to neutralize the copolymer thus obtained, an aqueous solution of sodium hydroxide, potassium hydroxide, ammonium hydroxide, sodium carbonate, and ammonia is added to the copolymer, O, preferably 5
This is done by stirring at 0-100°C for 0.5-10 hours. As the neutralizing agent, not only the above-mentioned inorganic bases but also organic bases such as sodium acetate, urea, thiourea, and organic amines can be used. The degree of neutralization is based on the number of acidic groups present before neutralization.
Approximately 0.1 to 1.0 is appropriate.
この発明の繊維処理剤を構成する他の成分としては水溶
性アクリル系ポリマーが用いられる。A water-soluble acrylic polymer is used as the other component constituting the fiber treatment agent of this invention.
この水溶性アクリル系ポリマーとしては、ポリアクリル
酸塩、ポリメタクリル酸塩、ポリアクリル酸エステルの
部分ケン化物、ポリメタクリル酸エステルの部分ケン化
物、ポリアクリルアミドなどを挙げることができる。Examples of the water-soluble acrylic polymer include polyacrylates, polymethacrylates, partially saponified polyacrylic esters, partially saponified polymethacrylic esters, and polyacrylamide.
これら水溶性アクリル系ポリマーは粘度平均分子量が1
.000〜5,000,000、好ましくは5,000
−1,000,000のものが用いられるが、この分子
量は特に制限的ではない。These water-soluble acrylic polymers have a viscosity average molecular weight of 1
.. 000 to 5,000,000, preferably 5,000
-1,000,000 is used, but this molecular weight is not particularly limited.
これら水溶性アクリル系ポリマーの配合割合についても
特に制限はなく、広範囲にわたって配合しうる。すなわ
ち、前記共重合体の中和処理物100重量部に対し、5
〜200,000重量部、好ましくは10〜100,0
00重量部である。There are no particular restrictions on the blending ratio of these water-soluble acrylic polymers, and they can be blended over a wide range. That is, for 100 parts by weight of the neutralized copolymer, 5 parts by weight
~200,000 parts by weight, preferably 10-100,0
00 parts by weight.
この発明は、前記共重合体の中和処理物および前記水溶
性アクリル系ポリマーからなる繊維処理剤を提供するが
、さらに、前記共重合体の中和処理物、前記水溶性アク
リル系ポリマーおよびポリビニルアルコールからなる繊
維処理剤をも提供する。The present invention provides a fiber treatment agent comprising a neutralized product of the copolymer and the water-soluble acrylic polymer; A fiber treatment agent comprising alcohol is also provided.
ここで用いるポリビニルアルコールとしては、通常のポ
リ酢酸ビニルをアルカリ、酸またはアンモニア水などで
ケン化して得られるものでよく、その重合度としては1
00〜5 、OOO1好ましくは200〜3,000の
ものである。The polyvinyl alcohol used here may be one obtained by saponifying ordinary polyvinyl acetate with an alkali, acid, or aqueous ammonia, and its degree of polymerization is 1.
00-5, OOO1 preferably 200-3,000.
このポリビニルアルコールの配合割合も広範囲にわたり
、前記共重合体の中和処理物100重量部に対し、5〜
200,000重量部、好ましくは10−100,00
0重量部である。The blending ratio of this polyvinyl alcohol also ranges widely, from 5 to 5 parts by weight per 100 parts by weight of the neutralized copolymer.
200,000 parts by weight, preferably 10-100,00 parts by weight
It is 0 parts by weight.
この発明においては、いずれの発明においても所望に応
じ可塑剤として、多価アルコールまたはそのエステル、
たとえば、グリセリン、エチレングリコール、ジエチレ
ングリコール、トリエチレングリコールなどを配合する
ことができる。これらの配合量としては、全重量に基づ
き0.1〜5重量%が適当である。また、分散剤として
アニオン系または、ノニオン系界面活性剤を添加するこ
ともできる。In this invention, polyhydric alcohol or its ester,
For example, glycerin, ethylene glycol, diethylene glycol, triethylene glycol, etc. can be blended. The appropriate amount of these compounds is 0.1 to 5% by weight based on the total weight. Furthermore, an anionic or nonionic surfactant may be added as a dispersant.
この発明の繊維処理剤は、前記共重合体の中和処理物の
水溶液に、水溶性アクリル系ポリマーを配合し、必要に
応じてさらに水を加え、室温で撹拌混合して調製するこ
とができる。また、必要によりポリビニルアルコールを
、さらに所望により可塑剤を配合して調製される。The fiber treatment agent of the present invention can be prepared by blending a water-soluble acrylic polymer into an aqueous solution of the neutralized copolymer, adding water if necessary, and stirring and mixing at room temperature. . Further, it is prepared by adding polyvinyl alcohol if necessary and further adding a plasticizer if desired.
このようにして調製した濃度2〜20重量%の溶液を処
理浴として、この中に所望の繊維を浸漬するか、または
処理浴中のローラーに繊維を通過させ処理液を繊維に絞
り込ませたのち、乾燥することにより適用することがで
きる。The solution prepared in this manner with a concentration of 2 to 20% by weight is used as a treatment bath, and the desired fibers are immersed in this solution, or the fibers are passed through a roller in the treatment bath to squeeze the treatment liquid onto the fibers. , can be applied by drying.
[実施例]
以下、実施例および比較例を挙げて、この発明をさらに
詳しく説明する。[Examples] The present invention will be described in more detail below with reference to Examples and Comparative Examples.
実施例1〜7および比較例
内容積1区のオートクレーブに、インブチレンを用いる
場合はインブチレンを除く成分を所定量仕込み、−10
℃に冷却するとともに、容器内を十分に脱気しI;。次
いで、イソブチレンの所定量と溶媒としてアセトニトリ
ル460mQ、触媒として過酸化ベンゾイル0.6gを
加え、400rpmでかきまぜながら、110”Oにお
いて2時間重合反応を行わせたのち、反応混合物を水中
に投入して共重合体を沈殿物として得た。このようにし
て得られた共重合体の粘度平均分子量、インブチレン量
、スチレン量、アクリル酸メチル量およびマレイン酸量
をモル比で法衣に示す。Examples 1 to 7 and Comparative Examples When using inbutylene, a predetermined amount of components other than inbutylene was charged into an autoclave with an internal volume of 1, and -10
While cooling to ℃, thoroughly degas the inside of the container. Next, a predetermined amount of isobutylene, 460 mQ of acetonitrile as a solvent, and 0.6 g of benzoyl peroxide as a catalyst were added, and the polymerization reaction was carried out at 110"O for 2 hours while stirring at 400 rpm, and then the reaction mixture was poured into water. A copolymer was obtained as a precipitate.The viscosity average molecular weight, amount of inbutylene, amount of styrene, amount of methyl acrylate, and amount of maleic acid of the copolymer thus obtained are shown in molar ratios on the vest.
次に、この共重合体に水酸化ナトリウム水溶液を添加し
、濃度を20重量%に調整したのち、90°Cにおいて
6時間中和反応を行わせた。次いで、この共重合体の中
和処理物の水溶液に、水溶性アクリル系ポリマーおよび
水を加えて繊維処理剤を調製した。Next, an aqueous sodium hydroxide solution was added to this copolymer to adjust the concentration to 20% by weight, followed by a neutralization reaction at 90°C for 6 hours. Next, a water-soluble acrylic polymer and water were added to an aqueous solution of the neutralized copolymer to prepare a fiber treatment agent.
また、実施例7においては、ポリビニルアルコールを添
加した繊維処理剤をも調製した。In Example 7, a fiber treatment agent containing polyvinyl alcohol was also prepared.
この処理剤を30°Cに保ち、総本数1,000本(荒
巻ビーム4本)の綿糸405を、処理剤中を絞りローラ
ー2基により2 、4 kg/ cm”の絞り圧下で2
0m/分の速度で通し、乾燥ローラーにて113°Cの
温度で乾燥して処理系を得た。This treatment agent was kept at 30°C, and a total of 1,000 cotton threads 405 (4 Aramaki beams) were squeezed through the treatment agent under a squeezing pressure of 2.4 kg/cm'' using two squeezing rollers.
It was passed through at a speed of 0 m/min and dried with a drying roller at a temperature of 113°C to obtain a treatment system.
このようにして得た処理系50cmに切断したものを試
料として用い、引張試験機(東洋ボールドウィン株式会
社製)によりその引張強度および伸度を測定した。また
、処理剤剥落・落綿量も測定し lこ 。The treatment system thus obtained was cut into 50 cm pieces and used as a sample, and its tensile strength and elongation were measured using a tensile tester (manufactured by Toyo Baldwin Co., Ltd.). In addition, the amount of peeling and cotton removal of the treatment agent was also measured.
結果を表に示す。The results are shown in the table.
[発明の効果1
この発明によれば、繊維にすぐれた強度と伸度を付与す
ると共に、剥落量の低減された繊維処理剤が提供される
。また、この繊維処理剤は特に加温する必要がなく、室
温で処理することによって充分な繊維処理剤としての機
能を発揮するものである。このため、繊維工業分野にお
いてきわめて有用である。[Advantageous Effects of the Invention 1] According to the present invention, a fiber treatment agent is provided that imparts excellent strength and elongation to fibers and reduces the amount of peeling. Further, this fiber treatment agent does not require particular heating, and can sufficiently function as a fiber treatment agent when treated at room temperature. Therefore, it is extremely useful in the textile industry.
Claims (1)
ーから選ばれた少なくとも1種のモノマーとマレイン酸
系モノマーとを構成単位とする共重合体の中和処理物な
らびに水溶性アクリル系ポリマーからなる繊維処理剤。 2 イソブチレン、スチレンおよびアクリル酸系モノマ
ーから選ばれた少なくとも1種のモノマーとマレイン酸
系モノマーとを構成単位とする共重合体の中和処理物、
水溶性アクリル系ポリマーならびにポリビニルアルコー
ルからなる繊維処理剤。[Scope of Claims] 1. Neutralized copolymers containing at least one monomer selected from isobutylene, styrene, and acrylic acid monomers and maleic acid monomers as constituent units, and water-soluble acrylic polymers. A fiber treatment agent. 2. A neutralized product of a copolymer having a maleic acid monomer and at least one monomer selected from isobutylene, styrene, and acrylic acid monomers,
A fiber treatment agent made of water-soluble acrylic polymer and polyvinyl alcohol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24752188A JPH0299669A (en) | 1988-10-03 | 1988-10-03 | Textile treating agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24752188A JPH0299669A (en) | 1988-10-03 | 1988-10-03 | Textile treating agent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0299669A true JPH0299669A (en) | 1990-04-11 |
Family
ID=17164728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24752188A Pending JPH0299669A (en) | 1988-10-03 | 1988-10-03 | Textile treating agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0299669A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017089073A (en) * | 2015-11-17 | 2017-05-25 | 東洋紡Stc株式会社 | Functional fiber product and manufacturing method therefor |
-
1988
- 1988-10-03 JP JP24752188A patent/JPH0299669A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017089073A (en) * | 2015-11-17 | 2017-05-25 | 東洋紡Stc株式会社 | Functional fiber product and manufacturing method therefor |
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