JP2001279581A - Fabric softening composition - Google Patents
Fabric softening compositionInfo
- Publication number
- JP2001279581A JP2001279581A JP2000093777A JP2000093777A JP2001279581A JP 2001279581 A JP2001279581 A JP 2001279581A JP 2000093777 A JP2000093777 A JP 2000093777A JP 2000093777 A JP2000093777 A JP 2000093777A JP 2001279581 A JP2001279581 A JP 2001279581A
- Authority
- JP
- Japan
- Prior art keywords
- group
- composition
- polyoxyalkylene
- carbon atoms
- modified polysiloxane
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 26
- 239000004744 fabric Substances 0.000 title abstract description 29
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 10
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- 239000004902 Softening Agent Substances 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- -1 polysiloxane Polymers 0.000 abstract description 43
- 229920001296 polysiloxane Polymers 0.000 abstract description 31
- 239000004753 textile Substances 0.000 abstract description 4
- 238000004383 yellowing Methods 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 238000012360 testing method Methods 0.000 description 15
- 239000000835 fiber Substances 0.000 description 14
- 229920000742 Cotton Polymers 0.000 description 10
- 206010040880 Skin irritation Diseases 0.000 description 10
- 238000010521 absorption reaction Methods 0.000 description 10
- 230000036556 skin irritation Effects 0.000 description 10
- 231100000475 skin irritation Toxicity 0.000 description 10
- 239000007788 liquid Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 239000004205 dimethyl polysiloxane Substances 0.000 description 7
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 7
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 7
- 125000003342 alkenyl group Chemical group 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 235000002639 sodium chloride Nutrition 0.000 description 6
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000005215 alkyl ethers Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 206010061218 Inflammation Diseases 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000004054 inflammatory process Effects 0.000 description 2
- 238000010409 ironing Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000001153 anti-wrinkle effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 235000011148 calcium chloride Nutrition 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229920002678 cellulose Chemical class 0.000 description 1
- 239000001913 cellulose Chemical class 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 235000011147 magnesium chloride Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Chemical class 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Chemical class 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Silicon Polymers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は布帛の柔軟処理用組
成物に関し、詳しくは、布帛に優れた柔軟性や吸水性を
付与し、かつ、皮膚刺激の少ない布帛の柔軟処理用組成
物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a composition for softening a fabric, and more particularly to a composition for softening a fabric, which imparts excellent flexibility and water absorption to the fabric and has little skin irritation.
【0002】[0002]
【従来の技術】衣料および繊維製品は、着用・使用と洗
濯・乾燥を繰り返すうちに繊維処理剤が洗い落とされた
り、繊維が本来保有している柔らかさ・嵩高さ・しっか
り感等の風合いが損なわれたり、繊維同士の摩擦力が上
昇して損傷が促進されることによって風合いが低下する
ので、これを防止するために従来から柔軟処理剤が使用
されている。家庭で用いられる柔軟処理剤としては、洗
濯後の濯ぎ時に使用される柔軟仕上剤が一般的であり、
このような柔軟仕上剤として、1分子中に2個の長鎖ア
ルキル基を有する第4級アンモニウム塩や各種のアミン
または高分子化合物等の有機系柔軟基材を主成分とする
水性組成物が知られている。一方、オルガノポリシロキ
サン系化合物は、繊維に吸着すると繊維間や繊維表面の
摩擦を軽減して、優れた柔軟性,平滑性,滑らかさ,感
触の良い肌触り,絹のような感触,ふんわり感,弾力
性,乾燥時の非油性感,帯電防止性,防皺性等の良好な
風合いを付与し、加えて、再湿潤時間の低減,縮み防
止,皺除去,へたり防止,ごわつき防止,乾燥時間の短
縮,アイロンかけを容易にする等の効果が発現すること
から、柔軟処理剤の基材として使用されたり、各種の有
機系柔軟基材と組み合わせて使用されている。しかしな
がら、ポリジメチルシロキサンに代表されるような非親
水性のポリシロキサンを用いた場合は、水分散性が悪い
ため水性組成物に配合し難い上に吸水性が乏しく、さら
に繊維に吸着し難いので柔軟性付与効果が低いといった
問題点があり、アミノ基やアミド基等の窒素原子を有す
るポリシロキサンを用いた場合には、繊維が黄変した
り、ぬめり感が強すぎたり、皮膚刺激性がある等の問題
点があった。アルキル変性ポリシロキサン、エポキシ変
性ポリシロキサン、カルボキシ変性ポリシロキサン等の
有機変性ポリシロキサンを用いた場合には、吸水性や柔
軟性が不十分で良好な風合いが得られないという問題点
があった。また、ポリオキシアルキレン変性ポリシロキ
サンとしては、従来、ジメチルシロキサン単位の重合度
が100程度の低重合度の共重合体が使用されている
が、この場合は吸水性が良好であるものの、柔軟性が不
十分で優れた風合いが得られないという問題点があっ
た。さらに、炭素原子数6以上の長鎖アルキル基を有す
るポリオキシアルキレン変性ポリシロキサンも知られて
いるが(特開平1−162878号公報参照)、このよ
うなポリシロキサンにより処理された繊維は親水性が低
く、ごわついた風合いを有するといった欠点があった。2. Description of the Related Art Clothes and textiles are washed, worn, used, washed and dried repeatedly, and the fiber treatment agent is washed away, or the texture, such as the softness, bulkiness, and firmness, inherent to the fibers, is possessed. Since the texture is reduced by being damaged or by increasing the frictional force between the fibers to promote the damage, a softening agent is conventionally used to prevent this. As a softening agent used at home, a softening agent used at the time of rinsing after washing is generally used,
As such a soft finish, an aqueous composition mainly composed of an organic soft base material such as a quaternary ammonium salt having two long-chain alkyl groups in one molecule or various amines or polymer compounds is used. Are known. On the other hand, when the organopolysiloxane compound is adsorbed on the fiber, the friction between the fiber and the fiber surface is reduced, so that excellent flexibility, smoothness, smoothness, good touch, silky feel, softness, Gives good texture such as elasticity, non-oiliness during drying, antistatic property, anti-wrinkle property, etc. In addition, reduction of rewetting time, prevention of shrinkage, removal of wrinkles, prevention of settling, prevention of stiffness, drying time It has been used as a base material of a softening agent, or used in combination with various organic soft base materials, because it has effects such as shortening of ironing and facilitation of ironing. However, when a non-hydrophilic polysiloxane represented by polydimethylsiloxane is used, it is difficult to mix in an aqueous composition because of poor water dispersibility, has poor water absorption, and is difficult to be adsorbed to fibers. There is a problem that the flexibility-imparting effect is low, and when a polysiloxane having a nitrogen atom such as an amino group or an amide group is used, the fibers may turn yellow, the slimy feeling may be too strong, or the skin may be irritating. There were some problems. When an organically modified polysiloxane such as an alkyl-modified polysiloxane, an epoxy-modified polysiloxane, and a carboxy-modified polysiloxane is used, there is a problem that water absorption and flexibility are insufficient and a good hand cannot be obtained. As the polyoxyalkylene-modified polysiloxane, a copolymer having a low degree of polymerization of about 100 dimethylsiloxane units is conventionally used. In this case, although the water absorption is good, the flexibility is low. However, there was a problem that the texture was insufficient and an excellent texture could not be obtained. Further, a polyoxyalkylene-modified polysiloxane having a long-chain alkyl group having 6 or more carbon atoms is also known (see Japanese Patent Application Laid-Open No. 1-162878). However, fibers treated with such a polysiloxane are hydrophilic. However, there were drawbacks such as a low texture and a rough texture.
【0003】[0003]
【発明が解決しようとする課題】本発明者らは上記問題
点を解決するために鋭意検討した結果、重合度の高いポ
リオキシアルキレン変性ポリシロキサンを使用すること
により、各種繊維に優れた風合いを付与できることを見
出し、本発明に到達した。即ち、本発明の目的は、皮膚
刺激性や黄変の問題が無く、繊維製品に優れた柔軟性や
肌触り等の風合いと吸水性を付与し得る布帛の柔軟処理
用組成物を提供することにある。The inventors of the present invention have conducted intensive studies to solve the above-mentioned problems. As a result, by using a polyoxyalkylene-modified polysiloxane having a high degree of polymerization, an excellent texture can be imparted to various fibers. They have found that they can be applied, and have reached the present invention. That is, an object of the present invention is to provide a composition for softening a fabric which can impart a texture and a water absorbing property such as excellent softness and feel to textiles without problems of skin irritation and yellowing. is there.
【0004】[0004]
【課題を解決するための手段】本発明は、平均構造式
(1):The present invention provides an average structural formula (1):
【化2】 [式中、Pは式:−(R3)cO(C2H4O)a(C3H6O)bR4
{R3は炭素原子数1〜10のアルキレン基であり、R4
は水素原子,炭素原子数1〜6の1価炭化水素基,式:
−OCR5または−COOR5(R5は炭素原子数1〜6
の1価炭化水素基である。)で示される基である。aお
よびbはそれぞれ0〜50の数であり、かつ、(a+
b)は1以上であり、cは0または1である。}で表さ
れる基であり、R1は炭素原子数1〜5の1価炭化水素
基,水素原子,水酸基またはアルコキシ基であり、全R
1の内90モル%以上がメチル基であり、R2は上記R1
またはPで示される基である。xは150〜2000の
数であり、yは1〜50の数である。]で示され、ポリ
オキシアルキレン鎖部分の重量割合が全重量の50%未
満であるポリオキシアルキレン変性ポリシロキサンを配
合してなることを特徴とする布帛の柔軟処理用組成物に
関する。Embedded image Wherein, P is the formula :-( R 3) c O (C 2 H 4 O) a (C 3 H 6 O) b R 4
{R 3 is an alkylene group having 1 to 10 carbon atoms, R 4
Is a hydrogen atom, a monovalent hydrocarbon group having 1 to 6 carbon atoms, a formula:
—OCR 5 or —COOR 5 (R 5 is 1 to 6 carbon atoms)
Is a monovalent hydrocarbon group. ). a and b are each a number from 0 to 50, and (a +
b) is 1 or more, and c is 0 or 1. Wherein R 1 is a monovalent hydrocarbon group having 1 to 5 carbon atoms, a hydrogen atom, a hydroxyl group or an alkoxy group;
90 mol% or more of 1 is a methyl group, R 2 is R 1 above
Or a group represented by P. x is a number from 150 to 2000, and y is a number from 1 to 50. And a weight ratio of the polyoxyalkylene chain portion is less than 50% of the total weight of the polyoxyalkylene-modified polysiloxane.
【0005】[0005]
【発明の実施の形態】本発明組成物に使用される上記平
均構造式(1)で示されるポリオキシアルキレン変性ポ
リシロキサン中、Pは式:−(R3)cO(C2H4O)a(C3
H6O)bR4で表される基である。式中、R3は炭素原子
数1〜10のアルキレン基であり、エチレン基,プロピ
レン基,ブチレン基が例示されるが、これらの中でもプ
ロピレン基が好ましい。R4は水素原子,炭素原子数1
〜6の1価炭化水素基,式:−OCR5または−COO
R5(R5はメチル基,エチル基,イソプロピル基のよう
な炭素原子数1〜6の1価炭化水素基である。)で示さ
れる基であり、メチル基,エチル基,プロピル基等のア
ルキル基、フェニル基等のアリール基、ビニル基,アリ
ル基,ヘキセニル基等のアルケニル基、式:−OCCH
3,式:−COOCH3で示される基が例示されるが、こ
れらの中でも水素原子またはメチル基であることが好ま
しい。aおよびbはそれぞれ0〜50の数であり、か
つ、(a+b)は1以上であるが、aが5〜40の範囲
であり、bが0〜30の範囲であるものが好ましい。ま
た、ポリオキシアルキレン鎖中のオキシエチレン基の比
率は、a/(a+b)=0.4〜1.0の範囲であること
が好ましい。cは0または1であり、通常は1である
が、cが0であり、かつ、R4がアルケニル基であるポ
リオキシアルキレン鎖が少量存在していてもよい。尚、
1分子中のポリオキシアルキレン鎖は、同一でも異なっ
ていてもよい。R1は炭素原子数1〜5の1価炭化水素
基,水素原子,水酸基またはアルコキシ基であり、1価
炭化水素基としては、メチル基,エチル基,プロピル基
等のアルキル基;ビニル基,アリル基等のアルケニル基
のような非置換の1価炭化水素基の他、アミノ基,カル
ボキシル基,エポキシ基等で置換された炭素原子数1〜
5のアルキル基が挙げられる。アルコキシ基としてはメ
トキシ基,エトキシ基,イソプロポキシ基が例示され
る。但し、全R1の90モル%以上がメチル基であるこ
とが必要であり、すべてのR1がメチル基であることが
好ましい。R2は上記R1で示される基またはPで示され
るポリオキシアルキレン鎖であり、中でもメチル基が好
ましい。xは150〜2000の数であり、300〜2
000の範囲が好ましく、420〜2000の範囲がよ
り好ましく、450〜1000の範囲がさらに好まし
い。yは1〜50の数であり、5〜20の範囲であるこ
とが好ましい。また、上記平均構造式(1)において、
Pで示されるポリオキシアルキレン鎖部分の重量割合
は、該ポリオキシアルキレン変性シロキサン全重量の5
0%未満であり、25〜40%の範囲であることが好ま
しい。これは、50%未満であると適度な親水性が得ら
れるためである。このポリオキシアルキレン変性ポリシ
ロキサンの25℃における粘度は3000mm2/s以
上であることが好ましく、5000mm2/s以上であ
ることがより好ましい。BEST MODE FOR CARRYING OUT THE INVENTION In the polyoxyalkylene-modified polysiloxane represented by the above average structural formula (1) used in the composition of the present invention, P has the formula:-(R 3 ) c O (C 2 H 4 O) ) a (C 3
H 6 O) b R 4 . In the formula, R 3 is an alkylene group having 1 to 10 carbon atoms, and examples thereof include an ethylene group, a propylene group, and a butylene group. Of these, a propylene group is preferable. R 4 is a hydrogen atom, having 1 carbon atom
To 6 monovalent hydrocarbon groups, formula: —OCR 5 or —COO
R 5 (R 5 is a monovalent hydrocarbon group having 1 to 6 carbon atoms such as a methyl group, an ethyl group, and an isopropyl group), such as a methyl group, an ethyl group, and a propyl group. Aryl group such as alkyl group and phenyl group, alkenyl group such as vinyl group, allyl group and hexenyl group, formula: -OCCH
3, the formula: is -COOCH groups represented by 3 are illustrated, it is preferable among these is a hydrogen atom or a methyl group also. a and b are each a number from 0 to 50, and (a + b) is 1 or more, and it is preferable that a is in the range of 5 to 40 and b is in the range of 0 to 30. Further, the ratio of oxyethylene groups in the polyoxyalkylene chain is preferably in the range of a / (a + b) = 0.4 to 1.0. c is 0 or 1, usually 1. However, a small amount of a polyoxyalkylene chain in which c is 0 and R 4 is an alkenyl group may be present. still,
The polyoxyalkylene chains in one molecule may be the same or different. R 1 is a monovalent hydrocarbon group having 1 to 5 carbon atoms, a hydrogen atom, a hydroxyl group or an alkoxy group. Examples of the monovalent hydrocarbon group include an alkyl group such as a methyl group, an ethyl group and a propyl group; a vinyl group; In addition to an unsubstituted monovalent hydrocarbon group such as an alkenyl group such as an allyl group, an amino group, a carboxyl group, an epoxy group, and the like,
And 5 alkyl groups. Examples of the alkoxy group include a methoxy group, an ethoxy group, and an isopropoxy group. However, more than 90 mole% of the total R 1 is required to be methyl group, it is preferable that all of R 1 is a methyl group. R 2 is a group represented by R 1 or a polyoxyalkylene chain represented by P, and among them, a methyl group is preferable. x is a number from 150 to 2000;
000 is preferable, 420-2000 is more preferable, and 450-1000 is more preferable. y is a number from 1 to 50, and preferably ranges from 5 to 20. In the above average structural formula (1),
The weight ratio of the polyoxyalkylene chain represented by P is 5% of the total weight of the polyoxyalkylene-modified siloxane.
It is less than 0% and preferably in the range of 25 to 40%. This is because if it is less than 50%, appropriate hydrophilicity can be obtained. The viscosity at 25 ° C. of the polyoxyalkylene-modified polysiloxane is preferably not less than 3000 mm 2 / s, more preferably not less than 5000 mm 2 / s.
【0006】上記平均構造式(1)で示されるポリオキ
シアルキレン変性ポリシロキサンは、例えば、少なくと
も一つのケイ素原子結合水素原子を有する直鎖状のポリ
シロキサンと、構造式:CH2=CH(CH2)nO(C2H4
O)a(C3H6O)bR4(式中、nは0〜8の整数であり、
R4,aおよびbは前記と同じである。)で表されるよ
うなアルケニル基含有ポリエーテル化合物とを、白金を
代表とする遷移金属系化合物を触媒として用いて無溶媒
または溶媒中で反応させることにより製造することがで
きる。ここで使用されるケイ素原子結合水素原子を有す
る直鎖状のポリシロキサンは、環状もしくは鎖状のケイ
素原子結合水素原子含有シロキサンと環状のジメチルシ
ロキサンとを、活性白土等の固体酸性触媒や塩酸,硫
酸,トリフロロ酢酸およびトリフルオロメタンスルホン
酸等の酸性化合物を触媒として用いて公知の方法により
製造することができる。アルケニル基含有ポリエーテル
化合物は各種構造のものが市販されており、容易に入手
することができる。尚、このポリエーテル化合物とし
て、構造の異なる2種類以上を組み合わせた混合物を使
用してもよい。 反応に使用される溶媒としては、エタ
ノール,イソプロパノールおよびこれらとトルエンとの
混合物が好ましい。また、ポリシロキサン中のケイ素原
子結合水素原子に対するポリエーテル化合物中のアルケ
ニル基のモル比は、通常、0.7〜3.0の範囲であ
り、0.9〜2.0の範囲が好ましい。The polyoxyalkylene-modified polysiloxane represented by the above average structural formula (1) includes, for example, a linear polysiloxane having at least one silicon-bonded hydrogen atom and a structural formula: CH 2 CHCH (CH 2 ) n O (C 2 H 4
O) a (C 3 H 6 O) b R 4 (where n is an integer of 0 to 8,
R 4 , a and b are the same as described above. The alkenyl group-containing polyether compound represented by the formula (1) can be produced by using a transition metal compound represented by platinum as a catalyst without a solvent or in a solvent. The linear polysiloxane having a silicon-bonded hydrogen atom used herein is obtained by converting a cyclic or chain silicon-bonded hydrogen-containing siloxane and a cyclic dimethylsiloxane into a solid acidic catalyst such as activated clay, hydrochloric acid, It can be produced by a known method using an acidic compound such as sulfuric acid, trifluoroacetic acid and trifluoromethanesulfonic acid as a catalyst. Alkenyl group-containing polyether compounds having various structures are commercially available and can be easily obtained. As the polyether compound, a mixture of two or more kinds having different structures may be used. As the solvent used in the reaction, ethanol, isopropanol and a mixture of these with toluene are preferred. The molar ratio of the alkenyl group in the polyether compound to the silicon-bonded hydrogen atoms in the polysiloxane is usually in the range of 0.7 to 3.0, preferably in the range of 0.9 to 2.0.
【0007】このような平均構造式(1)で示されるポ
リオキシアルキレン変性ポリシロキサンとしては、下記
式で表されるシロキサンが例示される。The polyoxyalkylene-modified polysiloxane represented by the average structural formula (1) is exemplified by a siloxane represented by the following formula.
【化3】 Embedded image
【化4】 Embedded image
【0008】このようなポリオキシアルキレン変性ポリ
シロキサンは、側鎖のポリオキシアルキレン鎖が長く、
ポリシロキサン主鎖の重合度が大きいものほど粘度が高
くなるので、製造時の作業性改善および水性組成物への
配合を容易にするために、各種の有機溶剤または水に溶
解させて使用するのが好ましい。使用される有機溶剤と
しては、エタノール,ジプロピレングリコール,ブチル
カルビトールが挙げられる。また、界面活性剤を使用し
て水中に乳化してから使用することも可能である。本発
明組成物に使用されるポリオキシアルキレン変性ポリシ
ロキサンは、ポリジメチルシロキサンに比べて親水性な
ので、該ポリジメチルシロキサンよりも容易に溶解、乳
化できるという利点を有する。また、上記ポリオキシア
ルキレン変性ポリシロキサンの配合量は、通常、0.0
5重量%以上であり、経済性の点からは15重量%を越
えない量が好ましく、より好ましくは0.1〜10重量
%の範囲である。Such a polyoxyalkylene-modified polysiloxane has a long side chain polyoxyalkylene chain,
The higher the degree of polymerization of the polysiloxane main chain, the higher the viscosity.Therefore, in order to improve the workability during production and facilitate the incorporation into an aqueous composition, the polysiloxane is preferably used after being dissolved in various organic solvents or water. Is preferred. Examples of the organic solvent used include ethanol, dipropylene glycol, and butyl carbitol. It is also possible to emulsify in water using a surfactant before use. Since the polyoxyalkylene-modified polysiloxane used in the composition of the present invention is more hydrophilic than polydimethylsiloxane, it has an advantage that it can be more easily dissolved and emulsified than polydimethylsiloxane. The amount of the polyoxyalkylene-modified polysiloxane is usually 0.0%.
The amount is 5% by weight or more, and from the viewpoint of economy, the amount is preferably not more than 15% by weight, more preferably 0.1 to 10% by weight.
【0009】本発明組成物には、必要に応じて、炭素原
子数8〜30の長鎖アルキル基または長鎖アルキルエス
テル基を1個または2個有するアミン化合物やその中和
塩,4級アンモニウム塩,4級化イミダゾリニウム系化
合物,ポリアンモニウム化合物,ポリアミン塩およびポ
リアルキレンイミン塩等の有機系柔軟剤を配合すること
ができる。さらに本発明の効果を妨げない範囲であれ
ば、この他の任意成分としてジメチルポリシロキサン以
外の、柔軟剤に添加配合される公知の成分を添加しても
よい。このような成分としては、高級アルコールのエチ
レンオキサイド付加物,牛脂アルキルアミンのエチレン
オキサイド付加物等の非イオン性界面活性剤;ステアリ
ン酸,オレイン酸等の高級脂肪酸;2―エチルヘキサン
酸とグリセリンまたはペンタエリスリトールとの部分エ
ステル化物等の非イオン性界面活性剤;食塩,塩化アン
モニウム,塩化カルシウム,塩化マグネシウム,塩化カ
リウム等の水溶性塩;エチレングリコール,プロピレン
グリコール,ヘキシレングリコール等の溶剤;尿素,殺
菌剤,酸化防止剤,染料,顔料,高級アルコール,液状
炭化水素および液状エステル等の油性物質;セルロース
誘導体,紫外線吸収剤,蛍光増白剤,香料が挙げられ
る。The composition of the present invention may contain, if necessary, an amine compound having one or two long-chain alkyl groups or long-chain alkyl ester groups having 8 to 30 carbon atoms, a neutralized salt thereof, and a quaternary ammonium salt. Organic softeners such as salts, quaternized imidazolinium-based compounds, polyammonium compounds, polyamine salts and polyalkyleneimine salts can be blended. Further, as long as the effects of the present invention are not impaired, known components other than dimethylpolysiloxane which are added to and blended with the softener may be added as other optional components. Examples of such components include nonionic surfactants such as ethylene oxide adducts of higher alcohols and ethylene oxide adducts of tallowalkylamine; higher fatty acids such as stearic acid and oleic acid; 2-ethylhexanoic acid and glycerin or Nonionic surfactants such as partially esterified products with pentaerythritol; water-soluble salts such as sodium chloride, ammonium chloride, calcium chloride, magnesium chloride, and potassium chloride; solvents such as ethylene glycol, propylene glycol, and hexylene glycol; Oily substances such as bactericides, antioxidants, dyes, pigments, higher alcohols, liquid hydrocarbons and liquid esters; cellulose derivatives, ultraviolet absorbers, fluorescent brighteners, and fragrances.
【0010】本発明組成物が適用される布帛としては、
麻,綿,ウール,シルク等の天然繊維;ポリアミド系,
ポリエステル系,ポリアクリル系,ポリビニルアルコー
ル系,ポリ塩化ビニリデン系,ポリオレフィン系,ポリ
ウレタン系またはポリテトラフロロエチレン系等の合成
繊維;再生繊維,半合成繊維,ガラス繊維およびこれら
繊維の混紡や交織製の製品や不織布が挙げられる。本発
明組成物を用いて布帛を処理する際には、上記ポリオキ
シアルキレン変性ポリシロキサンが0.005〜1.0
重量%になるような量付着させることが必要である。The fabric to which the composition of the present invention is applied includes:
Natural fibers such as hemp, cotton, wool and silk; polyamides,
Synthetic fibers such as polyester, polyacryl, polyvinyl alcohol, polyvinylidene chloride, polyolefin, polyurethane or polytetrafluoroethylene; regenerated fibers, semi-synthetic fibers, glass fibers, and blended or mixed fabrics of these fibers Products and nonwoven fabrics. When treating a fabric with the composition of the present invention, the polyoxyalkylene-modified polysiloxane is used in an amount of 0.005 to 1.0.
It is necessary to apply the amount so as to obtain the weight%.
【0011】以上のような本発明の柔軟処理用組成物
は、各種衣料や繊維製品に優れた柔軟性,親水性,帯電
防止性を付与して風合いを著しく向上させるという特徴
を有する。特に、これまでポリオキシアルキレン変性ポ
リシロキサンの欠点であった柔軟性等の良好な風合い
を、ジメチルポリシロキサンや長鎖アルキル基含有シロ
キサンの不存在下で付与できるという利点を有する。こ
のような本発明組成物は、家庭で洗濯後の濯ぎ時に使用
される家庭用柔軟仕上剤として最も有効であるが、この
他にも、衣料洗濯用の液体洗浄剤に配合したり、アイロ
ンがけ助剤やタンブル乾燥器用シートのコーティング組
成物中に添加した場合にも同様の効果が期待できる。The composition for softening treatment of the present invention as described above is characterized by imparting excellent flexibility, hydrophilicity and antistatic properties to various kinds of clothing and textiles, thereby significantly improving the feel. In particular, there is an advantage that good texture such as flexibility, which has been a drawback of the polyoxyalkylene-modified polysiloxane, can be imparted in the absence of dimethylpolysiloxane or siloxane containing a long-chain alkyl group. Such a composition of the present invention is most effective as a household softener used in rinsing after washing at home. In addition, the composition of the present invention can be added to a liquid detergent for clothes washing or ironed. Similar effects can be expected when they are added to the coating composition of an auxiliary agent or a sheet for a tumble dryer.
【0012】[0012]
【実施例】次に、本発明を実施例に基づいて詳細に説明
する。尚、ポリオキシアルキレン変性ポリシロキサンと
しては、表1に示した平均構造を有するシロキサンを使
用した。Next, the present invention will be described in detail with reference to examples. As the polyoxyalkylene-modified polysiloxane, a siloxane having an average structure shown in Table 1 was used.
【0013】[0013]
【表1】 [Table 1]
【0014】[0014]
【実施例1】表1に示したポリオキシアルキレン変性ポ
リシロキサンA4〜A14のそれぞれ5gを、ポリオキ
シエチレンアルキルエーテル0.5gを使用して94.
5gの水中に乳化分散したものを柔軟処理用試験液とし
た。一方、全自動洗濯機[松下電器(株)製]を使用し
て、市販の木綿タオル、綿Tシャツおよびアクリルジャ
ージを、市販の家庭用衣料洗剤を用いて50℃で2回繰
り返し洗濯した後、常温の水道水で充分濯ぎ、脱水後乾
燥したものを試験布とした。次に、上記全自動洗濯機漕
内に30Lの水道水を溜め、上記で調製した柔軟処理用
試験液10gを添加した後、上記の試験布1kgを投入
して3分間標準速度で攪拌した。次いで30秒間脱水し
て、その後、室温で48時間乾燥した。このように処理
した試験布について、柔軟性,滑らかさ,ふっくらさ,
吸水性および皮膚刺激性を次の方法で測定した。これら
の結果を表2に示した。表2の結果から明らかのよう
に、本発明組成物で処理した布帛は、皮膚刺激性がな
く、吸水性と共に柔軟性等の風合いにも非常に優れてい
た。 <柔軟性、滑らかさ、ふっくらさ>男女5名づつ計10
名のパネラーが、柔軟処理用試験液で処理した試験布
(木綿タオル、アクリルジャージ)と、柔軟処理用試験
液を添加せずに同様に処理した試験布(無処理布)とを
手で触り、これらを下記の基準に従って測定した。評価
としては、最も回答人数の多かったものを採用した。 ◎:無処理布に比べて処理布の方が非常に優れていた。 ○:無処理布に比べて処理布の方が良好であった。 △:処理布と無処理布はほぼ同じであった。 ×:無処理布に比べて処理布の方が明らかに劣ってい
た。 <吸水性> 処理した試験布(木綿タオル)に水を数滴落とし、その
後の水の状態を下記の基準に従って測定した。 ◎:試験布に滴下直後にしみ込んだ。 ○:すぐにはしみ込まず、滴下してから60秒以内にし
み込んだ。 ×:滴下後60秒経過してもしみ込まなかった。 <皮膚刺激性>健康な男女10名づつ計20名を被験者
とし、処理した綿Tシャツを24時間着用した後の皮膚
の様子を目視で観察した。炎症が起きた人はいなかった
場合を皮膚刺激性なしとし、炎症が起きた人がいた場合
を皮膚刺激性ありとした。EXAMPLE 1 5 g of each of the polyoxyalkylene-modified polysiloxanes A4 to A14 shown in Table 1 was used, and 0.5 g of polyoxyethylene alkyl ether was used.
What was emulsified and dispersed in 5 g of water was used as a test liquid for softening treatment. On the other hand, using a fully automatic washing machine [manufactured by Matsushita Electric Industrial Co., Ltd.], a commercially available cotton towel, cotton T-shirt and acrylic jersey were repeatedly washed twice at 50 ° C. using a commercially available household detergent. The test cloth was thoroughly rinsed with tap water at room temperature, dehydrated and dried. Next, 30 L of tap water was pooled in the fully automatic washing machine tank, 10 g of the test liquid for softening treatment prepared above was added, and then 1 kg of the test cloth was charged and stirred at a standard speed for 3 minutes. Then, it was dehydrated for 30 seconds, and then dried at room temperature for 48 hours. About the test cloth treated in this way, flexibility, smoothness, plumpness,
Water absorption and skin irritation were measured by the following methods. Table 2 shows the results. As is clear from the results in Table 2, the fabric treated with the composition of the present invention did not have skin irritation, and was extremely excellent in texture such as flexibility as well as water absorption. <Flexibility, smoothness, and plumpness> 5 men and women, 10 each
The name paneler touches the test cloth (cotton towel, acrylic jersey) treated with the test liquid for softening treatment and the test cloth (non-treated cloth) treated in the same manner without adding the test liquid for softening treatment. These were measured according to the following criteria. As the evaluation, the one with the largest number of respondents was adopted. ◎: The treated cloth was much better than the non-treated cloth. :: The treated cloth was better than the untreated cloth. Δ: The treated cloth and the non-treated cloth were almost the same. X: The treated cloth was clearly inferior to the untreated cloth. <Water Absorption> Several drops of water were dropped on the treated test cloth (cotton towel), and the state of the water thereafter was measured according to the following criteria. A: Immediately after dripping on the test cloth. :: Not soaked immediately, but soaked within 60 seconds after dripping. C: No impregnation occurred 60 seconds after the dropping. <Skin irritation> A total of 20 subjects, 10 healthy men and women, were examined, and the appearance of the skin after wearing the treated cotton T-shirt for 24 hours was visually observed. No skin irritation occurred when no inflammation occurred, and skin irritation occurred when any inflammation occurred.
【0015】[0015]
【比較例1】表1に示したポリオキシアルキレン変性ポ
リシロキサンA1〜A3のそれぞれ5gを、ポリオキシ
エチレンアルキルエーテル0.5gを使用して94.5
gの水中に乳化分散したものを柔軟処理用試験液とし
た。得られた試験液を使用して、市販の木綿タオル、綿
Tシャツおよびアクリルジャージを、実施例1と同様に
して処理した。処理後の試験布について、柔軟性,滑ら
かさ,ふっくらさ,吸水性および皮膚刺激性を実施例1
と同様の方法で測定した。これらの結果を表2に示し
た。Comparative Example 1 5 g of each of the polyoxyalkylene-modified polysiloxanes A1 to A3 shown in Table 1 and 94.5 using 0.5 g of polyoxyethylene alkyl ether.
g emulsified and dispersed in water was used as a test liquid for softening treatment. Using the obtained test solution, a commercially available cotton towel, cotton T-shirt and acrylic jersey were treated in the same manner as in Example 1. After treatment, the test cloth was evaluated for flexibility, smoothness, plumpness, water absorption and skin irritation.
The measurement was performed in the same manner as described above. Table 2 shows the results.
【0016】[0016]
【比較例2】重合度410のポリジメチルシロキサンD
1および重合度600のポリジメチルシロキサンD2の
それぞれ5gを、ポリオキシエチレンアルキルエーテル
0.5gを使用して94.5gの水中に乳化分散したも
のを柔軟処理用試験液とした。得られた試験液を使用し
て、市販の木綿タオル、綿Tシャツおよびアクリルジャ
ージを、実施例1と同様にして処理した。処理後の試験
布について、柔軟性,滑らかさ,ふっくらさ,吸水性お
よび皮膚刺激性を実施例1と同様の方法で測定した。こ
れらの結果を表2に示した。Comparative Example 2 Polydimethylsiloxane D having a Degree of Polymerization of 410
A test liquid for softening treatment was prepared by emulsifying and dispersing 5 g of each of 1 and polydimethylsiloxane D2 having a polymerization degree of 600 in 94.5 g of water using 0.5 g of polyoxyethylene alkyl ether. Using the obtained test solution, a commercially available cotton towel, cotton T-shirt and acrylic jersey were treated in the same manner as in Example 1. With respect to the test cloth after the treatment, flexibility, smoothness, plumpness, water absorption and skin irritation were measured in the same manner as in Example 1. Table 2 shows the results.
【0017】[0017]
【表2】 [Table 2]
【0018】[0018]
【発明の効果】本発明の布帛の柔軟処理用組成物は、高
重合度のポリオキシアルキレン変性ポリシロキサンを配
合しているので、皮膚刺激や黄変がなく、各種繊維製品
に優れた柔軟性,滑り性等の風合いと吸水性を付与する
という特徴を有する。The composition for softening fabrics of the present invention contains a polyoxyalkylene-modified polysiloxane having a high degree of polymerization, so that it does not cause skin irritation or yellowing and has excellent flexibility for various fiber products. It is characterized by imparting texture such as slipperiness and water absorption.
Claims (5)
{R3は炭素原子数1〜10のアルキレン基であり、R4
は水素原子,炭素原子数1〜6の1価炭化水素基,式:
−OCR5または−COOR5(R5は炭素原子数1〜6
の1価炭化水素基である。)で示される基である。aお
よびbはそれぞれ0〜50の数であり、かつ、(a+
b)は1以上であり、cは0または1である。}で表さ
れる基であり、R1は炭素原子数1〜5の1価炭化水素
基,水素原子,水酸基またはアルコキシ基であり、全R
1の内90モル%以上がメチル基であり、R2は上記R1
またはPで示される基である。xは150〜2000の
数であり、yは1〜50の数である。]で示され、ポリ
オキシアルキレン鎖部分の重量割合が全重量の50%未
満であるポリオキシアルキレン変性ポリシロキサンを配
合してなることを特徴とする布帛の柔軟処理用組成物。An average structural formula (1): Wherein, P is the formula :-( R 3) c O (C 2 H 4 O) a (C 3 H 6 O) b R 4
{R 3 is an alkylene group having 1 to 10 carbon atoms, R 4
Is a hydrogen atom, a monovalent hydrocarbon group having 1 to 6 carbon atoms, a formula:
—OCR 5 or —COOR 5 (R 5 is 1 to 6 carbon atoms)
Is a monovalent hydrocarbon group. ). a and b are each a number from 0 to 50, and (a +
b) is 1 or more, and c is 0 or 1. Wherein R 1 is a monovalent hydrocarbon group having 1 to 5 carbon atoms, a hydrogen atom, a hydroxyl group or an alkoxy group;
90 mol% or more of 1 is a methyl group, R 2 is R 1 above
Or a group represented by P. x is a number from 150 to 2000, and y is a number from 1 to 50. Wherein the proportion by weight of the polyoxyalkylene chain portion is less than 50% of the total weight of the composition.
を特徴とする請求項1に記載の柔軟処理用組成物。2. The composition for softening treatment according to claim 1, wherein x ranges from 300 to 2,000.
を特徴とする請求項1に記載の柔軟処理用組成物。3. The composition for softening treatment according to claim 1, wherein x is in the range of 420 to 2,000.
を特徴とする請求項1に記載の柔軟処理用組成物。4. The composition for softening treatment according to claim 1, wherein x ranges from 450 to 1,000.
いずれか1項に記載の柔軟処理用組成物。5. The composition for softening treatment according to claim 1, which is a softening agent for household use.
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JP2000093777A JP3703679B2 (en) | 2000-03-30 | 2000-03-30 | Composition for softening fabric |
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JP2000093777A JP3703679B2 (en) | 2000-03-30 | 2000-03-30 | Composition for softening fabric |
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JP2001279581A true JP2001279581A (en) | 2001-10-10 |
JP3703679B2 JP3703679B2 (en) | 2005-10-05 |
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ID=18608914
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001336071A (en) * | 2000-05-30 | 2001-12-07 | Dow Corning Toray Silicone Co Ltd | Softener composition for fabric |
WO2008059978A1 (en) | 2006-11-13 | 2008-05-22 | Kao Corporation | Fiber product-treating agent |
JP2016011471A (en) * | 2014-06-27 | 2016-01-21 | 花王株式会社 | Textile treatment composition |
-
2000
- 2000-03-30 JP JP2000093777A patent/JP3703679B2/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001336071A (en) * | 2000-05-30 | 2001-12-07 | Dow Corning Toray Silicone Co Ltd | Softener composition for fabric |
WO2008059978A1 (en) | 2006-11-13 | 2008-05-22 | Kao Corporation | Fiber product-treating agent |
US8038730B2 (en) | 2006-11-13 | 2011-10-18 | Kao Corporation | Fiber product treating agent |
JP2016011471A (en) * | 2014-06-27 | 2016-01-21 | 花王株式会社 | Textile treatment composition |
Also Published As
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JP3703679B2 (en) | 2005-10-05 |
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