JP2018127727A - 弾性繊維用処理剤及び弾性繊維 - Google Patents
弾性繊維用処理剤及び弾性繊維 Download PDFInfo
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- JP2018127727A JP2018127727A JP2017020013A JP2017020013A JP2018127727A JP 2018127727 A JP2018127727 A JP 2018127727A JP 2017020013 A JP2017020013 A JP 2017020013A JP 2017020013 A JP2017020013 A JP 2017020013A JP 2018127727 A JP2018127727 A JP 2018127727A
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- Prior art keywords
- salt
- phosphate
- hexyl
- amine
- elastic fiber
- 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.)
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- 210000004177 elastic tissue Anatomy 0.000 title claims abstract description 70
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 60
- -1 ester salt Chemical class 0.000 claims abstract description 226
- 238000009499 grossing Methods 0.000 claims abstract description 11
- 229910019142 PO4 Inorganic materials 0.000 claims description 57
- 239000010452 phosphate Substances 0.000 claims description 57
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 29
- 125000002947 alkylene group Chemical group 0.000 claims description 13
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 150000002148 esters Chemical class 0.000 claims description 12
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 9
- 238000012545 processing Methods 0.000 claims description 7
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 4
- 150000003512 tertiary amines Chemical class 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 3
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 229960002261 magnesium phosphate Drugs 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 150000003335 secondary amines Chemical group 0.000 claims description 2
- 239000004753 textile Substances 0.000 claims 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 48
- 235000021317 phosphate Nutrition 0.000 description 46
- 150000003839 salts Chemical class 0.000 description 13
- 239000003921 oil Substances 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- 229920001451 polypropylene glycol Polymers 0.000 description 11
- 239000002994 raw material Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 239000004814 polyurethane Substances 0.000 description 9
- 229920002635 polyurethane Polymers 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 238000004804 winding Methods 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 235000005956 Cosmos caudatus Nutrition 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 229940031098 ethanolamine Drugs 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N monoethanolamine hydrochloride Natural products NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 5
- 239000000347 magnesium hydroxide Substances 0.000 description 5
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- ISWBTWLQPHYWFQ-UHFFFAOYSA-N C(CCCCCCC)NCCCCCCCC.P(=O)(OCCCCCCCC)(O)O Chemical compound C(CCCCCCC)NCCCCCCCC.P(=O)(OCCCCCCCC)(O)O ISWBTWLQPHYWFQ-UHFFFAOYSA-N 0.000 description 4
- 239000000314 lubricant Substances 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 230000003472 neutralizing effect Effects 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- NMKDMCDDHMCCHT-UHFFFAOYSA-N 1-decoxydecane;phosphoric acid Chemical compound OP(O)(O)=O.CCCCCCCCCCOCCCCCCCCCC NMKDMCDDHMCCHT-UHFFFAOYSA-N 0.000 description 3
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 3
- XULHFMYCBKQGEE-MRXNPFEDSA-N 2-Hexyl-1-decanol Natural products CCCCCCCC[C@H](CO)CCCCCC XULHFMYCBKQGEE-MRXNPFEDSA-N 0.000 description 3
- XULHFMYCBKQGEE-UHFFFAOYSA-N 2-hexyl-1-Decanol Chemical compound CCCCCCCCC(CO)CCCCCC XULHFMYCBKQGEE-UHFFFAOYSA-N 0.000 description 3
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 3
- RXCWRQVJIBFOHH-UHFFFAOYSA-N C(CCC)N(CCO)CCCC.P(=O)(O)(O)O.C(C)C(COCC(CCCC)CC)CCCC Chemical compound C(CCC)N(CCO)CCCC.P(=O)(O)(O)O.C(C)C(COCC(CCCC)CC)CCCC RXCWRQVJIBFOHH-UHFFFAOYSA-N 0.000 description 3
- MKLNXTUOLSPEOG-UHFFFAOYSA-L P(=O)(OC(CC(C)C)CC(C)C)([O-])[O-].[Mg+2] Chemical compound P(=O)(OC(CC(C)C)CC(C)C)([O-])[O-].[Mg+2] MKLNXTUOLSPEOG-UHFFFAOYSA-L 0.000 description 3
- QEDGVMSZCNAIFT-UHFFFAOYSA-L [Mg+2].P(=O)(OCC(CCCCCCCC)CCCCCC)([O-])[O-] Chemical compound [Mg+2].P(=O)(OCC(CCCCCCCC)CCCCCC)([O-])[O-] QEDGVMSZCNAIFT-UHFFFAOYSA-L 0.000 description 3
- UYJOKFKIGLUREI-UHFFFAOYSA-H [Mg+2].P(=O)([O-])([O-])[O-].C(C)C(COCC(CCCC)CC)CCCC.P(=O)([O-])([O-])[O-].[Mg+2].[Mg+2] Chemical compound [Mg+2].P(=O)([O-])([O-])[O-].C(C)C(COCC(CCCC)CC)CCCC.P(=O)([O-])([O-])[O-].[Mg+2].[Mg+2] UYJOKFKIGLUREI-UHFFFAOYSA-H 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
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- 230000000052 comparative effect Effects 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
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- 238000006386 neutralization reaction Methods 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- IWSZDQRGNFLMJS-UHFFFAOYSA-N 2-(dibutylamino)ethanol Chemical class CCCCN(CCO)CCCC IWSZDQRGNFLMJS-UHFFFAOYSA-N 0.000 description 2
- NKFNBVMJTSYZDV-UHFFFAOYSA-N 2-[dodecyl(2-hydroxyethyl)amino]ethanol Chemical class CCCCCCCCCCCCN(CCO)CCO NKFNBVMJTSYZDV-UHFFFAOYSA-N 0.000 description 2
- CCSZFGAULWOMJD-UHFFFAOYSA-N 2-[dodecyl(2-hydroxyethyl)amino]ethanol;2-ethylhexyl dihydrogen phosphate Chemical compound CCCCC(CC)COP(O)(O)=O.CCCCCCCCCCCCN(CCO)CCO CCSZFGAULWOMJD-UHFFFAOYSA-N 0.000 description 2
- YFWQPSUBPWTQGT-UHFFFAOYSA-N 2-[dodecyl(2-hydroxyethyl)amino]ethanol;octyl dihydrogen phosphate Chemical compound CCCCCCCCOP(O)(O)=O.CCCCCCCCCCCCN(CCO)CCO YFWQPSUBPWTQGT-UHFFFAOYSA-N 0.000 description 2
- XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 2
- QKGOGFRALUIHCW-UHFFFAOYSA-N 2-propylheptyl dihydrogen phosphate Chemical compound CCCCCC(CCC)COP(O)(O)=O QKGOGFRALUIHCW-UHFFFAOYSA-N 0.000 description 2
- ZIBTVWZOICJAQT-UHFFFAOYSA-N C(CCC)N(CCO)CCCC.P(=O)(O)(O)O Chemical compound C(CCC)N(CCO)CCCC.P(=O)(O)(O)O ZIBTVWZOICJAQT-UHFFFAOYSA-N 0.000 description 2
- KOPWDVGLRYMZCC-UHFFFAOYSA-N C(CCC)N(CCO)CCCC.P(=O)(OC(CC(C)C)CC(C)C)(O)O Chemical compound C(CCC)N(CCO)CCCC.P(=O)(OC(CC(C)C)CC(C)C)(O)O KOPWDVGLRYMZCC-UHFFFAOYSA-N 0.000 description 2
- NUCXPRMDXLESBQ-UHFFFAOYSA-N C(CCC)N(CCO)CCCC.P(=O)(OCC(CCCCCC)CCCC)(O)O Chemical compound C(CCC)N(CCO)CCCC.P(=O)(OCC(CCCCCC)CCCC)(O)O NUCXPRMDXLESBQ-UHFFFAOYSA-N 0.000 description 2
- HRQXVOAEVCLHTQ-UHFFFAOYSA-N C(CCC)N(CCO)CCCC.P(=O)(OCCCCCCCCCCC(C)C)(O)O Chemical compound C(CCC)N(CCO)CCCC.P(=O)(OCCCCCCCCCCC(C)C)(O)O HRQXVOAEVCLHTQ-UHFFFAOYSA-N 0.000 description 2
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- BKQXQFGEZJCKJX-UHFFFAOYSA-N C(CCCCCCC)NCCCCCCCC.P(=O)(OCC(CCCCC)CCC)(O)O Chemical compound C(CCCCCCC)NCCCCCCCC.P(=O)(OCC(CCCCC)CCC)(O)O BKQXQFGEZJCKJX-UHFFFAOYSA-N 0.000 description 2
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- FUOAEGIXILDOEB-UHFFFAOYSA-L [Mg+2].P(=O)(OCCCCCC)([O-])[O-] Chemical compound [Mg+2].P(=O)(OCCCCCC)([O-])[O-] FUOAEGIXILDOEB-UHFFFAOYSA-L 0.000 description 1
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- 125000004122 cyclic group Chemical group 0.000 description 1
- SCIGVHCNNXTQDB-UHFFFAOYSA-N decyl dihydrogen phosphate Chemical compound CCCCCCCCCCOP(O)(O)=O SCIGVHCNNXTQDB-UHFFFAOYSA-N 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
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- FARYTWBWLZAXNK-WAYWQWQTSA-N ethyl (z)-3-(methylamino)but-2-enoate Chemical compound CCOC(=O)\C=C(\C)NC FARYTWBWLZAXNK-WAYWQWQTSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- UJQJZAHIRTUBHP-UHFFFAOYSA-N hexadecyl dihydrogen phosphate octan-1-amine Chemical compound CCCCCCCCN.CCCCCCCCCCCCCCCCOP(O)(O)=O UJQJZAHIRTUBHP-UHFFFAOYSA-N 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000004137 magnesium phosphate Substances 0.000 description 1
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- LTZZKILZCADVRM-UHFFFAOYSA-L magnesium;decyl phosphate Chemical compound [Mg+2].CCCCCCCCCCOP([O-])([O-])=O LTZZKILZCADVRM-UHFFFAOYSA-L 0.000 description 1
- YPEFBMUHVPWWMN-UHFFFAOYSA-L magnesium;dodecyl phosphate Chemical compound [Mg+2].CCCCCCCCCCCCOP([O-])([O-])=O YPEFBMUHVPWWMN-UHFFFAOYSA-L 0.000 description 1
- ARVCLLSAMSKMHO-UHFFFAOYSA-L magnesium;hexadecyl phosphate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCOP([O-])([O-])=O ARVCLLSAMSKMHO-UHFFFAOYSA-L 0.000 description 1
- VMDYXCZMLYOOOR-UHFFFAOYSA-L magnesium;octadecyl phosphate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCCOP([O-])([O-])=O VMDYXCZMLYOOOR-UHFFFAOYSA-L 0.000 description 1
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Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Treatment Of Fibers During Manufacturing Processes (AREA)
Abstract
Description
リン酸エステルアミン塩:脂肪族アルコール及び脂肪族アルコール1モルに対し炭素数2〜4のアルキレンオキサイドを1〜10モルの割合で付加させた化合物から選ばれる少なくとも一つと、五酸化二リン又はオキシハロゲン化リンとを反応させて得られるリン酸エステルのアミン塩
リン酸エステル塩(P−1)の調製
1Lフラスコに2,6−ジメチル−4−ヘプタノールを432g加え、撹拌しながら50〜70℃で五酸化二リン284gを徐々に添加した後、70〜80℃で4時間熟成反応させた。室温に冷却後、水酸化マグネシウムを73g加えて中和した後、脱水処理を行いリン酸エステル塩(P−1)を得た。
2Lフラスコに2−エチル−1−ヘキサノールのエチレンオキサイド2モル付加物を654g加え、撹拌しながら50〜70℃で五酸化二リン284gを徐々に添加した後、70〜80℃で4時間熟成反応させた。室温に冷却後、水酸化マグネシウムを73g加えて中和した後、脱水処理を行いリン酸エステル塩(P−2)を得た。
3Lフラスコに11−メチル−1−ドデカノールを600g加え、撹拌しながら50〜70℃で五酸化二リン284gを徐々に添加した後、70〜80℃で4時間熟成反応させた。これにステアリン酸マグネシウムを591g加えて塩交換により、リン酸エステル塩(P−3)を得た。
2Lフラスコに2−ヘキシル−1−デカノールを726g加え、撹拌しながら50〜70℃で五酸化二リン284gを徐々に添加した後、70〜80℃で4時間熟成反応させた。室温に冷却後、水酸化マグネシウムを73g加えて中和した後、脱水処理を行いリン酸エステル塩(P−4)を得た。
1Lフラスコにオキシ塩化リンを145g加えて、撹拌しながら10〜20℃で2−オクチル−1−ドデカノール270gを徐々に滴下した後、30℃で減圧状態にして塩化水素を除去しながら4時間反応を続けて中間体を得た。その後、2Lフラスコにキシレン300g、メチルイソブチルケトン300g、純水600gを加えて撹拌しながら60〜70℃で前記中間体を全量徐々に滴下し、加水分解反応を行った後、120℃に昇温して1時間反応させた。これを分液漏斗に移し、有機層を分取し、この有機層からキシレンとメチルイソブチルケトンを留去し、水酸化マグネシウム58gを加えて中和した後、脱水処理を行いリン酸エステル塩(P−5)を得た。
2Lフラスコに11−メチル−1−ドデカノールを600g加え、撹拌しながら50〜70℃で五酸化二リン284gを徐々に添加した後、70〜80℃で4時間熟成反応させた。室温に冷却後、ジメチルドデシルアミンを266g加えて中和し、リン酸エステル塩(P−6)を得た。
2Lフラスコに2−ヘキシル−1−デカノールのエチレンオキサイド2モル付加物を990g加え、撹拌しながら50〜70℃で五酸化二リン284gを徐々に添加した後、70〜80℃で4時間熟成反応させた。室温に冷却後、ジブチルエタノールアミンを216g加えて中和し、リン酸エステル塩(P−7)を得た。
2Lフラスコに2−オクチル−1−ドデカノールを810g加え、撹拌しながら50〜70℃で五酸化二リン284gを徐々に添加した後、70〜80℃で4時間熟成反応させた。室温に冷却後、ドデシルジエタノールアミンを341g加えて中和し、リン酸エステル塩(P−8)を得た。
アルコールの種類:原料として用いたアルコールの種類
EO付加モル数:アルコール1モルに対するエチレンオキサイドの付加モル数
P−1:2,6−ジメチル−4−ヘプチルリン酸エステルマグネシウム塩
P−2:ポリオキシエチレン2モル付加2−エチル−1−ヘキシルエーテルリン酸エステルマグネシウム塩
P−3:11−メチル−1−ドデシルリン酸エステルマグネシウム塩
P−4:2−ヘキシル−1−デシルリン酸エステルマグネシウム塩
P−5:2−オクチル−1−ドデシルリン酸エステルマグネシウム塩
P−6:11−メチル−1−ドデシルリン酸エステルジメチルドデシルアミン塩
P−7:ポリオキシエチレン2モル付加2−エチル−1−ヘキシルエーテルリン酸エステルジブチルエタノールアミン塩
P−8:2−オクチル−1−ドデシルリン酸エステルドデシルジエタノールアミン塩
実施例1
表2に記載した平滑剤(L−1)34部と平滑剤(L−2)60部と、表1に記載したリン酸エステル塩(P−1)1部とリン酸エステル塩(P−6)3部と、ゲルベアルコール(G−1)2部をよく混合して均一にし、実施例1の弾性繊維用処理剤を調製した。
実施例1と同様にして、平滑剤、リン酸エステル塩、加える場合のゲルベアルコールを混合することにより、実施例2〜5、比較例1及び2の弾性繊維用処理剤を調製した。
粘度:30℃における動粘度(mm2/s)
L−1:信越化学工業社製の商品名KF−96−10cs
L−2:出光興産社製の商品名ダイアナフレシア W8
L−3:SK Lubricants社製の商品名YUBASE 3
L−1〜L−3:表2に記載した平滑剤
P−1〜P−8:表1に記載したリン酸エステル塩
G−1:2−ヘキシル−1−デカノール(日産化学社製の商品名ファインオキソコール1600)
先ず、分子量2900のテトラメチレンエーテルグリコール、ビス−(p−イソシアネートフェニル)−メタン及びエチレンジアミンからなるポリウレタンのN,N−ジメチルアセトアミド溶液(35重量%)を重合し、ポリマー溶液(A)とした。
・低温安定性の評価
試験区分2で調製した各例の弾性繊維用処理剤を5℃で1週間静置したものについて目視観察し、以下の基準で低温安定性を評価して、結果を表4にまとめて示した。
◎:沈殿、分離が無く、調製時と同様に均一な状態を保っていた。
○:若干の沈殿が生じたが、25℃に5時間静置することで調製時と同様に均一な状態に復元した。
×:沈殿、分離が生じ、25℃に5時間静置しても均一な状態に復元しなかった。
二つのフリーローラー間に直径1cmで表面粗度2Sのクロムメッキ梨地ピンを配置し、このクロムメッキ梨地ピンに対し、前記のパッケージから引き出したポリウレタン系弾性繊維の接触角度が90度となるようにした。このクロムメッキ梨地ピンの下部1cmの位置に静電電位測定器(春日電機社製の商品名KSD−0103)を配置し、25℃で60%RHの条件下、50m/分の速度で送り出し、100m/分の速度で巻き取ったときの発生電気を測定して、次の基準で評価し、結果を表4にまとめて示した。
○:発生電気が100ボルト未満(安定に操業できる)
×:発生電気が100ボルト以上(整経工程で糸の寄りつきが起こり、操業に問題が起きる)
片側に第1駆動ローラーとこれに常時接する第1遊離ローラーとで送り出し部を構成し、また相対側に第2駆動ローラーとこれに常時接する第2遊離ローラーとで巻き取り部を構成して、該送り出し部に対し該巻き取り部を水平方向で20cm離して設置した。第1駆動ローラーに前記のパッケージを装着し、糸巻の厚さが2mmになるまで解舒して、第2駆動ローラーに巻き取った。第1駆動ローラーからのポリウレタン系弾性繊維の送り出し速度を50m/分で固定する一方、第2駆動ローラーへのポリウレタン系弾性繊維の巻き取り速度を50m/分より徐々に上げて、ポリウレタン系弾性繊維をパッケージから強制解舒した。この強制解舒時において、送り出し部分と巻き取り部分との間でポリウレタン系弾性繊維の踊りがなくなる時点での巻き取り速度V(m/分)を測定し、下記の数1から解舒性(%)を求め、次の基準で評価し、結果を表4にまとめて示した。
○:解舒性が120%未満(全く問題なく、安定に解舒できる)
×:解舒性が120%以上(糸の引き出しに抵抗があり、糸切れもあって、操業に問題がある)
Claims (8)
- 平滑剤とリン酸エステル塩とを含有して成る弾性繊維用処理剤であって、該リン酸エステル塩が下記のリン酸エステルマグネシウム塩と下記のリン酸エステルアミン塩とから成るものであることを特徴とする弾性繊維用処理剤。
リン酸エステルマグネシウム塩:脂肪族アルコール及び脂肪族アルコール1モルに対し炭素数2〜4のアルキレンオキサイドを1〜10モルの割合で付加させた化合物から選ばれる少なくとも一つと、五酸化二リン又はオキシハロゲン化リンとを反応させて得られるリン酸エステルのマグネシウム塩
リン酸エステルアミン塩:脂肪族アルコール及び脂肪族アルコール1モルに対し炭素数2〜4のアルキレンオキサイドを1〜10モルの割合で付加させた化合物から選ばれる少なくとも一つと、五酸化二リン又はオキシハロゲン化リンとを反応させて得られるリン酸エステルのアミン塩 - 脂肪族アルコールが、分岐アルコールである請求項1記載の弾性繊維用処理剤。
- リン酸エステルアミン塩のアミンが、2級アミン又は3級アミンである請求項1又は2記載の弾性繊維用処理剤。
- リン酸エステルアミン塩のアミンが、3級アミンである請求項1又は2記載の弾性繊維用処理剤。
- リン酸エステル塩が、リン酸エステルマグネシウム塩/リン酸エステルアミン塩=10/90〜90/10(質量比)の割合から成るものである請求項1〜4のいずれか一つの項記載の弾性繊維用処理剤。
- 更にゲルベアルコールを含有する請求項1〜5のいずれか一つの項記載の弾性繊維用処理剤。
- 平滑剤、リン酸エステル塩及びゲルベアルコールの合計量中にゲルベアルコールを0.01〜15質量%の割合で含有する請求項6記載の弾性繊維用処理剤。
- 請求項1〜7のいずれか一つの項記載の弾性繊維用処理剤が付着していることを特徴とする弾性繊維。
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