JPS6247990B2 - - Google Patents
Info
- Publication number
- JPS6247990B2 JPS6247990B2 JP6180282A JP6180282A JPS6247990B2 JP S6247990 B2 JPS6247990 B2 JP S6247990B2 JP 6180282 A JP6180282 A JP 6180282A JP 6180282 A JP6180282 A JP 6180282A JP S6247990 B2 JPS6247990 B2 JP S6247990B2
- Authority
- JP
- Japan
- Prior art keywords
- component
- metal
- spinning
- wet conditions
- present
- 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.)
- Expired
Links
- 229910052751 metal Inorganic materials 0.000 claims description 36
- 239000002184 metal Substances 0.000 claims description 36
- 238000009987 spinning Methods 0.000 claims description 24
- -1 alkali metal salt Chemical class 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 13
- 239000003795 chemical substances by application Substances 0.000 claims description 12
- 239000001993 wax Substances 0.000 claims description 11
- 229910019142 PO4 Inorganic materials 0.000 claims description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims description 7
- 238000009499 grossing Methods 0.000 claims description 7
- 239000004480 active ingredient Substances 0.000 claims description 6
- 229920002164 Polyalkylene glycol copolymer Polymers 0.000 claims description 4
- 150000001413 amino acids Chemical class 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 239000003921 oil Substances 0.000 description 20
- 238000005299 abrasion Methods 0.000 description 15
- 229920001296 polysiloxane Polymers 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 238000009941 weaving Methods 0.000 description 13
- 230000000694 effects Effects 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000012209 synthetic fiber Substances 0.000 description 9
- 229920002994 synthetic fiber Polymers 0.000 description 9
- 235000014676 Phragmites communis Nutrition 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 235000021317 phosphate Nutrition 0.000 description 6
- 244000273256 Phragmites communis Species 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 125000000217 alkyl group Polymers 0.000 description 3
- 235000001014 amino acid Nutrition 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- OQILCOQZDHPEAZ-UHFFFAOYSA-N octyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCC OQILCOQZDHPEAZ-UHFFFAOYSA-N 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 235000019809 paraffin wax Nutrition 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- AVBJHQDHVYGQLS-AWEZNQCLSA-N (2s)-2-(dodecanoylamino)pentanedioic acid Chemical compound CCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O AVBJHQDHVYGQLS-AWEZNQCLSA-N 0.000 description 1
- BBOPKBHSDDSVFS-UHFFFAOYSA-N 1-chloro-4-ethoxy-2-fluorobenzene Chemical compound CCOC1=CC=C(Cl)C(F)=C1 BBOPKBHSDDSVFS-UHFFFAOYSA-N 0.000 description 1
- YTPNTTUPPCGZPJ-UHFFFAOYSA-N 11-methyldodecyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCCCCCCC(C)C YTPNTTUPPCGZPJ-UHFFFAOYSA-N 0.000 description 1
- SRBSSROHORQGBO-UHFFFAOYSA-N 11-methyldodecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCC(C)C SRBSSROHORQGBO-UHFFFAOYSA-N 0.000 description 1
- BHPUZXHJBNPVQQ-UHFFFAOYSA-N 2-(dodecanoylamino)-3-hydroxybutanoic acid Chemical class CCCCCCCCCCCC(=O)NC(C(C)O)C(O)=O BHPUZXHJBNPVQQ-UHFFFAOYSA-N 0.000 description 1
- PFSGUIFKRGNSHV-UHFFFAOYSA-N 2-(dodecanoylamino)-4-methylsulfanylbutanoic acid Chemical class CCCCCCCCCCCC(=O)NC(C(O)=O)CCSC PFSGUIFKRGNSHV-UHFFFAOYSA-N 0.000 description 1
- BZXMNFQDWOCVMU-UHFFFAOYSA-N 2-[dodecanoyl(methyl)amino]acetic acid;sodium Chemical compound [Na].CCCCCCCCCCCC(=O)N(C)CC(O)=O BZXMNFQDWOCVMU-UHFFFAOYSA-N 0.000 description 1
- 241001589086 Bellapiscis medius Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- JWGGSJFIGIGFSQ-UHFFFAOYSA-N N-dodecanoylglycine Chemical class CCCCCCCCCCCC(=O)NCC(O)=O JWGGSJFIGIGFSQ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical class [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 1
- TVACALAUIQMRDF-UHFFFAOYSA-N dodecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(O)=O TVACALAUIQMRDF-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 239000004209 oxidized polyethylene wax Substances 0.000 description 1
- 235000013873 oxidized polyethylene wax Nutrition 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- JEMLSRUODAIULV-UHFFFAOYSA-M potassium;2-[dodecanoyl(methyl)amino]acetate Chemical compound [K+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O JEMLSRUODAIULV-UHFFFAOYSA-M 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 108700004121 sarkosyl Proteins 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- VLKIFCBXANYYCK-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]acetate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CC([O-])=O VLKIFCBXANYYCK-GMFCBQQYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- QEIJVPZRDAHCHE-UHFFFAOYSA-N tridecyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCC QEIJVPZRDAHCHE-UHFFFAOYSA-N 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
本発明は、湿時における金属の摩耗防止に優れ
た配合組成物に関し、更に詳しくは、本発明は最
小量の配合量で、耐熱性に優れ且つ湿時の耐金属
摩耗性が改善された合成繊維の紡糸油剤に関する
ものである。
従来より合成繊維糸条を製造するに際し、湿時
の耐金属摩耗性を向上させて糸の損傷をできるだ
け防止しようということは、ウオータージエツト
ルームによる無糊糸の製繊性を向上させるといつ
た考え方から検討され、比較的分子量の低い一塩
基酸のエステルやワツクス類やシリコン類などが
検討されている。これらの例は、例えば特開昭50
−101694号公報、特開昭53−45498号公報にみら
れる如く、糸と金属の間の動摩擦を下げるため比
較的分子量の低いエステル類などを多量に含有す
る組成物では、湿時の糸/金属間の単糸切れの防
止効果が認められ、また水不溶性のワツクス類や
シリコン類も同じような効果が認められる。
しかし、実際の使用に当つては、ワツクス類を
多量に使用すれば延伸ローラー上あるいはガイド
類にスカム様のものが堆積して糸導を非常に汚染
するばかりでなく、なおその上にウオータージエ
ツトによる製織時にも、筬、綜絖などにスカムが
付着して製織稼動率を大巾に低下させてしまうこ
とが多い。また水不溶性のシリコンなどを多量に
配合すると、得られた糸条の染色性を非常に阻害
したり、染色工程で布にシリコンが再付着して実
用上問題になる場合が多い。
更に、一塩性酸のエステルの配合は比較的分子
量の低いものを主成分とした場合には、繊維と金
属の間の摩擦を低下させて湿時における単糸切れ
による毛羽やもつれを改良する面からは好ましい
方向ではあるが、その防止効果も限度がある。す
なわち一般に低分子量のものは、耐熱性が不良で
昨今使用し難い場合が多く、逆に耐熱性を向上さ
せて且つ繊維と金属との摩擦を下げるために、エ
ステル系化合物の分子量を上げていく方法では思
つた程繊維と金属間の摩擦を下げることは難かし
く、なおその上に湿時の耐金属の摩耗性は逆に不
良化していく方向にある。
最近、繊維の製造において、生産能率の向上と
いうことで、より高速化及び高温側での製糸条件
が採用される一方、製織工程の合理化という面か
らは合成繊維糸条を無糊でウオータージエツトル
ームを用い製織することが行なわれているが、こ
の場合、製糸工程でのスカムの発生がきわめて少
なく、なおその上に湿時における糸と金属間の摩
耗性を低下させて単糸毛羽を防ぐといつたことに
よりもつと積極的に湿時の耐金属摩耗性(筬の摩
耗防止)の働きをあわせてもつた糸条が望まれ、
それに適した紡糸油剤が強く望まれている。
本発明者はかゝる現状に鑑み紡糸及び延伸工程
でのトラブルが少なく、かつウオータージエツト
ルームによる製織時においても耐金属摩耗性にす
ぐれた合成繊維糸条を得るべく、鋭意検討の結
果、紡止工程において、特殊な紡糸油剤配合物を
採用することにより所期の目的を達成する本発明
に到達した。
即ち、本発明は公知の平滑剤、乳化剤、集束剤
などからなる通常の紡糸油剤に対して、従来のよ
うな水不溶性の限定された平滑剤やワツクスやシ
リコン類を用いる方法とは全く異なり、特に平滑
剤及び/又はポリアルキレングリコール共重体を
含む油剤において、炭素数12〜18のアルキルホス
フエート類のアルカリ金属塩(A成分)、アミノ
酸のN−アシル誘導体のアルカリ金属塩(B成
分)、変性シリコン類(C成分)、及びワツクス類
(D成分)の4者が必須成分として配合されその
際A+B+C+Dが常に全有効成分中で4%〜10
%(重量)を占めると共に重量%でA+B>C+
Dで、かつ、C+Dは全有効成分中で4%(重
量)以下の割合で配合された組成物からなる湿時
の耐金属摩耗が改善された油剤である。
本発明の目的は、A成分、B成分、C成分そし
てD成分の4者が共存するとき始めて達成される
のであつて、前4者のいづれが欠けても所期の効
果が得られないといつた驚くべきシネルギー効果
が発揮されることである。この事実はこれまで全
く知られていないし、他方これまでに知られてい
る湿時の耐金属摩耗性を向上させるというエステ
ル系の平滑剤あるいは水不溶性のワツクス類やシ
リコン類とは全く異なつた機作によるものでもつ
と積極的に湿時の金属表面に油膜を形成させて保
護膜を金属表面に生成させるものである。もう一
つ重要なことは、本発明では、シネルギー効果か
ら各成分の配合率を夫々最低の範囲におされなが
ら湿時の耐金属摩耗性を大巾に向上させるといつ
たもので当然のことながら、製糸工程は云うに及
ばず、製織工程において、無糊でウオータージエ
ツトが用いられてもスカム付着などはきわめて低
減するものである。
更に大きな特徴は平滑剤や乳化剤あるいはポリ
アルキレングリコール共重合体などからなる通常
公知の紡糸油剤に適用でき、本発明の4者を配合
することによつて本発明の効果を大きく発現させ
ることができることである。
本発明における各成分についてさらに詳述する
と、A成分としては炭素数が12〜18の直鎖あるい
は側鎖の飽和あるいは不飽和のアルキル基を有す
る通常公知のアルキルホスフエートのアルカリ金
属塩例えばナトリウム、カリウム、リチウムから
なる。ここで、通常制電剤としてよく用いられる
ポリオキシエチレン変性のアルキルホスフエート
類は耐金属摩耗性は小さく、本発明から全く除外
される。例えばエチレンオキシドが1モル付加し
たPOE(1)ラウリルホスフエート系のものでも該
ホスフエートを50%以上含有するものは本発明か
ら除外されるというきびしい制限がある。
本発明のアルキルホスフエートの金属塩の中で
も好ましくは分岐のない直鎖のアルキル基を有す
るものがよく、ラウリル、セチル、パルミチルス
テアリルなどが好ましい。一方A成分に併用され
るB成分としては、アミノ酸のN−アシル誘導体
のアルカリ金属塩からなり、一般式(1)及び一般式
(2)に示される化合物からなる。
〔但し、Rは炭素数8〜22のアルキル基、アルケ
ニル基、フルオロアルキル基を示し、nは1又は
2の正の整数、Zは−CO−、−CO2−を示し、M
はカリウム、ナトリウム、リチウムを示し、
R′は水素原又はメチル基を示す。〕
もつと具体的には、N−ラウロイルザルコシン
ソーダ、N−ラウロイルザルコシンのカリウム
塩、N−オレオイルザルコシのナトリウム塩、N
−ステアロイルザルコシンのオタリウム塩、N−
ラウロイルグルタミン酸のジナトリウム塩あるい
はジカリウム塩、N−オクタノイルアスパラギン
酸やN−パーフルオロオクタンスルホニルグルタ
ミン酸などのナトリウム塩あるいはカリウム塩、
N−ラウロイルグリシン、N−ラウロイルメチオ
ニン、N−ラウロイルスレオニンなどのナトリウ
ム塩あるいはカリウム塩などが好適に用いられ
る。
さらにA成分、B成分に併用されるC成分は変
性シリコン類が用いられる。この例としてはフエ
ニル変性シリコン、エポキシ変性シリコン、ポリ
オキシアルキレン変性シリコン、脂肪酸変性シリ
コンなどが挙げられるが、これらの変性シリコン
類は通常非イオン活性剤で乳化されたものが市販
で入手可能である。さらに、A成分、B成分、C
成分に併用されるD成分としては、水不溶性の各
種の公知のワツクス類が用いられる。この例とし
ては、パラフインワツクス、酸化ミクロクリスタ
リンワツクス、カルナウバロウ、密ロウ、酸化ポ
リエチレンワツクスなどの天然及び合成ワツクス
が挙げられ、なかでも融点が30℃以上140℃以下
のパラフインワツクスなどが好ましい。これらの
ワツクス類も通常非イオン系の乳化剤によつて水
中に分散したものが入手できるので水性エマルジ
ヨンとして適用される。
前記4成分を夫々組合せることによつて、本発
明の所期の効果を得るためには、A、B、C及び
Dの各成分が常に必須であり、その中の1成分が
欠けても十分にその効果を発現できないし、各成
分比のバランスがくづれても最小の添加量で湿時
の耐金属摩耗効果を著るしく向上せしめることが
できなくなる。もちろん、本発明の範囲を越えて
A+B+C+Dの和が10%を越える製糸工程さら
にはウオータージエツトでの製織工程でロールや
ガイドさらには筬や綜絖へのスカムの付着といつ
たトラブルが増大するので好ましくない。
さらに重要なことは、ホスフエート類やアミノ
酸のN−アシル化合物のアルカリ金属塩は、一般
にイオン交換性があり、とくにウオータージエツ
トで製織する場合には水の硬化が大きくなるとイ
オン交換によつて得られる水不溶性のスカムが筬
や綜絖に付着して稼動率の低下の直接的な原因と
なるとも云われている。したがつて、本発明に用
いられる配合組成物が筬や綜絖などの湿時の摩耗
に防止効果があるとしても、必要量以上の配合は
当然さけるべきで最小量におさえることが好まし
いことは云うまでもない。
したがつて、本発明においては通常A+B+C
+Dの和は4%以上10%(重量)以下におさえら
れる。しかも、A+B>C+D即ちアニオン成分
は常にワツクス類とシリコン類の和よりも多く、
かつ、C+Dは4%以下で用いられる。
このCあるいはD成分は通常水不溶成分である
が、適当な乳化剤を用いて分散することにより通
常公知の紡糸油中に4.0%以上混合することもで
きるが、製糸工程や、製織工程でのスカムの堆積
という面から好ましくは3.0%以下用いるのが良
い。
かくして製糸・製織工程にスカムトラブルなし
に湿潤状態において非常にすぐれた耐金属摩耗防
止効果を発揮することができる。
本発明の湿時における耐金属摩耗防止の組成物
は通常公知の紡糸油剤に配合して用いられ、公知
の紡糸油剤を何等限定するものではない。例えば
通常公知の紡糸油剤として知られている平滑剤及
び/又は、ポリアルキレングリコール共重合体か
らなる公知の紡糸油剤さらにくわしくは、鉱物
油、オクチル−パルミテート、イソトリデシルラ
ウレート、オレイルオレート、イソトリデシルパ
ルミテート、イソトリデシルステアレートなどの
一塩基酸のエステル系化合物を主成分として通常
公知の乳化剤でエマルジヨン化された紡糸油剤及
び/又は特公昭41−13564号公報や英国特許
833450号または、米国特許3338830号明細書に開
示されているような仮撚加工用の油剤としてよく
知られている、ポリアルキレングリコール類やエ
チレンオキシドとプロピレンオキシド基からなる
水不溶性あるいは水可溶性のランダムまたはブロ
ツコのポリエーテル類を主体とする公知の紡糸油
剤であつても、本発明の組成物を配合することに
よつて湿時の優れた耐金属摩耗性を発揮すること
ができる。
本発明の対象となる合成繊維としては、ポリエ
ステル、ポリアミド等の熱可塑性合成繊維よりな
り、常法によつて溶融紡糸して得られる合成繊維
マルチフイラメントからなり、特にポリエチレン
テレフタレート系のポリエステル繊維に適用する
と非常にすぐれた効果を示す。
以上のようにして得られた油剤組成物は、合成
繊維用として適用されるが、かゝる合成繊維マル
チフイラメントへの本発明の紡糸油剤の付与方法
は、溶融紡糸された未延伸糸に通常公知のローラ
ーオイリング、スプレーオイリングなどによつて
付与することができる。
以上のようにして、本発明によれば、合成繊維
マルチフイラメントの製造工程において紡糸及び
延伸性を何等阻害することなく、さらには無糊の
ウオータージエツトによる製織においても特にす
ぐれた製織性を与え、安定した湿時における耐金
属摩耗防止効果が得られる。
次に実施例を示すが、何等これに限定されるも
のではなく、実施例中の「部」は重量%を示す。
また、実施例中の湿時の耐金属摩耗については、
夫々以下に示す方法によつて測定、評価を行つ
た。
〔〕 湿潤時の耐金属摩耗性の測定評価法
湿潤時の糸及び金属の間の摩耗性については
以下の方法を用いて評価を行つた。
糸条に付与する初期張力を10g(標準)とし
て測定条件の強度ということで夫々20g、30g
と変え、糸速10m/分で走行させながら、金属
より摩擦体に接触する前に走行糸を0.6秒間水
に浸漬しあと摩擦体に接触させた。そして金属
摩擦体は種々の材質で検討した。
摩擦体(1) 直径5cmのクロムメツキの梨地ピ
ン、粗度11S
摩擦体(2) ステンレススチル棒
なお金属摩擦体は、糸の走行方向の前後に、
毎分50〜300回に変速して摺動できるようにし
て30分から数時間糸を走行させた後に金属表面
の摩耗痕を級判定して評価した。5級(良)→
1級(不良)でランク付けした。
実施例1〜3、比較例1〜6
第一表に示す組成の各油剤を夫々40〜50℃に昇
温均一化し、40〜50℃の温水中に撹拌しながら注
加し、濃度10%の夫々のエマルジヨンを作成し、
ローラー式給油方法によつて1000m/分の速さで
巻取られつゝあるポリエチレンテレフタレート未
延伸糸(149デニール/24フイラメント)に油剤
としての有効成分の付着率が1.0%の夫々を付与
せしめた。
該未延伸糸をドローツイスターを使用し、予熱
ピン温度90℃、熱セツト180℃で3.1倍に延伸し、
50デニールの延伸糸を得た。各延伸糸について該
評価法にしたがつて湿時における耐金属摩耗性を
測定した。
The present invention relates to a compounded composition that is excellent in preventing wear of metals in wet conditions. This invention relates to a fiber spinning oil. Conventionally, when producing synthetic fiber yarn, it is important to improve the metal abrasion resistance in wet conditions and prevent damage to the yarn as much as possible. Based on this idea, monobasic acid esters, waxes, and silicones with relatively low molecular weights are being considered. Examples of these include, for example,
101694 and Japanese Patent Application Laid-Open No. 53-45498, compositions containing a large amount of relatively low molecular weight esters to reduce dynamic friction between the thread and the metal, when wet, The effect of preventing single filament breakage between metals has been observed, and water-insoluble waxes and silicones have also been observed to have a similar effect. However, in actual use, if a large amount of wax is used, not only will scum build up on the drawing rollers or guides, contaminating the yarn guide very much, but also cause water leakage on top of it. Even during weaving using ets, scum often adheres to the reeds, heddles, etc., greatly reducing the weaving operating rate. Furthermore, if a large amount of water-insoluble silicone is added, the dyeability of the resulting yarn will be severely inhibited, or the silicone will re-adhere to the cloth during the dyeing process, which often causes practical problems. Furthermore, when the ester of monohydrochloric acid is mainly composed of one with a relatively low molecular weight, it reduces the friction between the fiber and the metal and improves fuzz and tangles caused by single filament breakage when wet. Although this is a preferable direction from a perspective, there are limits to its preventive effect. In other words, in general, compounds with low molecular weights have poor heat resistance and are difficult to use these days.On the other hand, in order to improve heat resistance and reduce friction between fibers and metals, the molecular weight of ester compounds is increased. With this method, it is difficult to reduce the friction between the fibers and the metal as much as expected, and what's more, the wear resistance of the metal in wet conditions is actually becoming worse. Recently, in fiber manufacturing, higher speed and higher temperature spinning conditions have been adopted in order to improve production efficiency, while synthetic fiber threads have been water jetted without glue in order to streamline the weaving process. Weaving is carried out using a loom, but in this case, the generation of scum during the spinning process is extremely small, and in addition, it reduces the abrasion between the thread and metal in wet conditions and prevents single thread fuzz. For this reason, it is desirable to have a yarn that also has the function of actively resisting metal abrasion in wet conditions (preventing reed abrasion).
A spinning oil suitable for this purpose is strongly desired. In view of the current situation, the inventors of the present invention have made extensive studies in order to obtain a synthetic fiber yarn that causes fewer troubles during the spinning and drawing processes and has excellent metal abrasion resistance even during weaving using a water jet loom. The present invention has been achieved in which the desired objective is achieved by employing a special spinning oil formulation in the spinning process. That is, the present invention is completely different from the conventional method of using a limited amount of water-insoluble smoothing agents, waxes, and silicones in contrast to the conventional spinning oil consisting of known smoothing agents, emulsifiers, sizing agents, etc. In particular, in oils containing a smoothing agent and/or a polyalkylene glycol copolymer, an alkali metal salt of an alkyl phosphate having 12 to 18 carbon atoms (component A), an alkali metal salt of an N-acyl derivative of an amino acid (component B), Modified silicones (component C) and waxes (component D) are blended as essential ingredients, and A+B+C+D always accounts for 4% to 10% of the total active ingredients.
% (weight) and in weight % A+B>C+
In D, C+D is an oil agent with improved metal wear resistance in wet conditions, which is composed of a composition containing 4% (by weight) or less of all active ingredients. The purpose of the present invention can only be achieved when the four components A, B, C, and D coexist, and even if any of the former four components is missing, the desired effect cannot be obtained. An amazing synergistic effect is exhibited. This fact has not been known at all, and on the other hand, it has a completely different mechanism from the previously known ester-based smoothing agents, water-insoluble waxes, and silicones that improve metal wear resistance in wet conditions. This method actively forms an oil film on the wet metal surface to form a protective film on the metal surface. Another important point is that in the present invention, the metal abrasion resistance in wet conditions is greatly improved while keeping the blending ratio of each component within the minimum range due to the synergy effect. However, in the weaving process, not to mention the yarn spinning process, even if waterjet is used without glue, scum adhesion is extremely reduced. Another major feature is that it can be applied to commonly known spinning oils made of smoothing agents, emulsifiers, polyalkylene glycol copolymers, etc., and the effects of the present invention can be greatly expressed by blending the four components of the present invention. It is. To explain each component in the present invention in more detail, component A includes an alkali metal salt of a commonly known alkyl phosphate having a linear or side chain saturated or unsaturated alkyl group having 12 to 18 carbon atoms, such as sodium; Consists of potassium and lithium. Here, polyoxyethylene-modified alkyl phosphates, which are commonly used as antistatic agents, have low metal wear resistance and are completely excluded from the present invention. For example, even POE(1) lauryl phosphate to which 1 mole of ethylene oxide has been added is subject to severe restrictions, such as those containing 50% or more of the phosphate are excluded from the present invention. Among the metal salts of alkyl phosphates of the present invention, those having an unbranched straight chain alkyl group are preferred, and lauryl, cetyl, palmitylstearyl and the like are preferred. On the other hand, component B used in combination with component A consists of an alkali metal salt of an N-acyl derivative of an amino acid, and has the general formula (1) and the general formula
Consists of the compound shown in (2). [However, R represents an alkyl group, alkenyl group, or fluoroalkyl group having 8 to 22 carbon atoms, n is a positive integer of 1 or 2, Z represents -CO-, -CO 2 -, M
represents potassium, sodium, and lithium;
R' represents a hydrogen atom or a methyl group. ] Specifically, N-lauroylsarcosine sodium, N-lauroylsarcosine potassium salt, N-oleoylsarcosine sodium salt, N-lauroylsarcosine sodium salt,
- Otarium salt of stearoylsarcosine, N-
Disodium salt or dipotassium salt of lauroylglutamic acid, sodium salt or potassium salt of N-octanoyl aspartic acid or N-perfluorooctanesulfonylglutamic acid,
Sodium salts or potassium salts of N-lauroylglycine, N-lauroylmethionine, N-lauroylthreonine, etc. are preferably used. Furthermore, modified silicones are used as component C, which is used in combination with component A and component B. Examples include phenyl-modified silicone, epoxy-modified silicone, polyoxyalkylene-modified silicone, fatty acid-modified silicone, etc. These modified silicones are usually commercially available emulsified with nonionic activators. . Furthermore, A component, B component, C
Various known water-insoluble waxes can be used as component D to be used in combination. Examples of this include natural and synthetic waxes such as paraffin wax, oxidized microcrystalline wax, carnauba wax, beeswax, and oxidized polyethylene wax, among which paraffin waxes with a melting point of 30°C or higher and 140°C or lower are included. preferable. These waxes are usually available as dispersed in water using a nonionic emulsifier and are therefore applied as an aqueous emulsion. In order to obtain the desired effect of the present invention by combining the above four components, each component A, B, C, and D is always essential, and even if one of them is missing, The effect cannot be sufficiently expressed, and even if the ratio of each component is unbalanced, the metal wear resistance effect in wet conditions cannot be significantly improved even with the minimum amount added. Of course, beyond the scope of the present invention, troubles such as scum adhesion to rolls, guides, reeds and heddles will increase in yarn spinning processes where the sum of A+B+C+D exceeds 10%, and in weaving processes using water jets. Undesirable. More importantly, phosphates and alkali metal salts of N-acyl compounds of amino acids generally have ion-exchange properties, and especially when weaving with a water jet, the hardening of the water increases the amount of ion exchange that can be obtained. It is also said that the water-insoluble scum deposited on the reeds and healds is a direct cause of reduced operating efficiency. Therefore, even if the blended composition used in the present invention has the effect of preventing wear of reeds, healds, etc. in wet conditions, it is natural to avoid blending more than the necessary amount, and it is preferable to keep the amount to a minimum. Not even. Therefore, in the present invention, usually A+B+C
The sum of +D is kept within 4% or more and 10% (weight) or less. Moreover, A+B>C+D, that is, the anion component is always greater than the sum of waxes and silicones.
Moreover, C+D is used at 4% or less. This C or D component is usually a water-insoluble component, but it can be mixed in a commonly known spinning oil at a concentration of 4.0% or more by dispersing it with an appropriate emulsifier, but it is difficult to prevent scum from forming during the spinning process or weaving process. From the viewpoint of deposition, it is preferable to use 3.0% or less. In this way, it is possible to exhibit excellent metal abrasion prevention effects in wet conditions without causing scum trouble in the spinning and weaving processes. The composition for preventing metal abrasion in wet conditions of the present invention is usually used by being mixed with a known spinning oil, and the known spinning oil is not limited in any way. For example, known spinning oils such as smoothing agents and/or polyalkylene glycol copolymers commonly known as spinning oils, and more specifically mineral oils, octyl palmitate, isotridecyl laurate, oleyl oleate, and Spinning oils and/or emulsions containing ester compounds of monobasic acids such as tridecyl palmitate and isotridecyl stearate with commonly known emulsifiers and/or Japanese Patent Publication No. 13564/1989 and British patents.
833450 or U.S. Pat. No. 3,338,830, water-insoluble or water-soluble random or Even a known spinning oil mainly composed of Brodzko's polyethers can exhibit excellent metal abrasion resistance in wet conditions by incorporating the composition of the present invention. The synthetic fibers to which the present invention is applied are made of thermoplastic synthetic fibers such as polyester and polyamide, and are made of synthetic fiber multifilaments obtained by melt-spinning by conventional methods, and are particularly applicable to polyethylene terephthalate-based polyester fibers. It shows very good effects. The oil composition obtained as described above is applied to synthetic fibers, but the method for applying the spinning oil of the present invention to such synthetic fiber multifilament is usually applied to melt-spun undrawn yarn. It can be applied by known roller oiling, spray oiling, etc. As described above, according to the present invention, the spinning and drawing properties are not hindered in any way during the manufacturing process of synthetic fiber multifilament, and furthermore, particularly excellent weaving properties are provided even in weaving using glue-free waterjet. , stable metal abrasion prevention effect in wet conditions can be obtained. Examples are shown next, but the invention is not limited thereto, and "parts" in the examples indicate weight %.
In addition, regarding the metal wear resistance in wet conditions in the examples,
Measurement and evaluation were performed using the methods shown below. []Measurement and evaluation method of metal abrasion resistance when wet The abrasion resistance between the thread and metal when wet was evaluated using the following method. The initial tension applied to the yarn is 10g (standard), and the strength under the measurement conditions is 20g and 30g, respectively.
While running at a yarn speed of 10 m/min, the running yarn was immersed in water for 0.6 seconds before it came into contact with the friction body than the metal, and then was brought into contact with the friction body. We also investigated various materials for the metal friction body. Friction body (1) 5cm diameter chrome-plated satin pin, roughness 11S Friction body (2) Stainless steel rod The metal friction body should be placed at the front and back in the thread running direction.
The thread was allowed to slide at speeds of 50 to 300 times per minute, and the yarn was allowed to run for 30 minutes to several hours, and then the wear marks on the metal surface were graded and evaluated. Grade 5 (good) →
Ranked as grade 1 (poor). Examples 1 to 3, Comparative Examples 1 to 6 Each oil agent having the composition shown in Table 1 was heated uniformly to 40 to 50°C, and poured into warm water at 40 to 50°C with stirring, and the concentration was 10%. Create an emulsion of each of
An undrawn polyethylene terephthalate yarn (149 denier/24 filaments) that was being wound at a speed of 1000 m/min by a roller oiling method was coated with an active ingredient as an oil agent at a deposition rate of 1.0%. . The undrawn yarn was stretched 3.1 times using a draw twister at a preheating pin temperature of 90°C and a heat setting of 180°C.
A drawn yarn of 50 denier was obtained. The metal abrasion resistance in wet conditions was measured for each drawn yarn according to the evaluation method.
【表】【table】
【表】
第一表をみてもわかるように本発明の組成物の
湿時における耐金属摩耗性が非常にすぐれている
のがわかる。但し、比較例7は湿時の耐金属摩耗
性は良好であるが、紡糸時のローラースカムが増
大し、操業性が不良であり、またさらにウオータ
ージエツトルームによる無糊製織時に筬及び綜絖
のスカム堆積がいちじるしく稼動率を低下すると
共に織布上はスカムが付着し、織物の品位を害す
るため本発明の範囲からは除外される。
実施例5〜、比較例8〜10
実施例−1と同じようにポリエチレンテレフタ
レートを紡糸し、表2に示す組成の各油剤を1.0
%付着させ、同じような方法で湿時における耐金
属摩耗性を測定した。[Table] As can be seen from Table 1, the composition of the present invention has excellent metal abrasion resistance in wet conditions. However, although Comparative Example 7 has good metal abrasion resistance in wet conditions, roller scum increases during spinning and operability is poor, and furthermore, the reeds and heddles deteriorate during glueless weaving using a water jet loom. Scum accumulation significantly lowers the operating rate and scum adheres to the fabric, impairing the quality of the fabric, and is therefore excluded from the scope of the present invention. Examples 5 to 10, Comparative Examples 8 to 10 Polyethylene terephthalate was spun in the same manner as in Example 1, and each oil agent having the composition shown in Table 2 was added to 1.0%
%, and metal wear resistance in wet conditions was measured in a similar manner.
【表】【table】
【表】
表2の結果をみてもわかるように本発明の4成
分の存在は非常にすぐれた湿時の耐金属摩耗性を
示した。[Table] As can be seen from the results in Table 2, the presence of the four components of the present invention showed very excellent wet metal wear resistance.
Claims (1)
共重合体を含む紡糸油剤において、有効成分に対
し炭素数12〜18のアルキルホスフエート類のアル
カリ金属塩(A成分)、アミノ酸のN−アシル誘
導体のアルカリ金属塩(B成分)、変性シリマン
類(C成分)及びワツクス類(D成分)の4者を
必須成分として配合され、その際A+B+C+D
が常に有効成分中で4.0%以上10%以下(重量)
を占めると共にA+B>C+Dで、且つC+Dは
全有効成分中で、4%(重量)以下の割合で配合
された組成物からなる、湿時の耐金属摩耗が改善
された組成物。1. In a spinning oil containing a smoothing agent and/or a polyalkylene glycol copolymer, an alkali metal salt of an alkyl phosphate having 12 to 18 carbon atoms (component A) and an alkali metal of an N-acyl derivative of an amino acid are added to the active ingredients. It is formulated with four essential components: salt (component B), modified silimanes (component C), and waxes (component D), in which case A+B+C+D
is always between 4.0% and 10% (by weight) of the active ingredients.
A composition with improved metal wear resistance in wet conditions, comprising a composition in which A+B>C+D, and C+D is contained in a proportion of 4% (weight) or less of all active ingredients.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6180282A JPS58180675A (en) | 1982-04-15 | 1982-04-15 | Composition improved in wet metal wear resistance |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6180282A JPS58180675A (en) | 1982-04-15 | 1982-04-15 | Composition improved in wet metal wear resistance |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58180675A JPS58180675A (en) | 1983-10-22 |
| JPS6247990B2 true JPS6247990B2 (en) | 1987-10-12 |
Family
ID=13181581
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6180282A Granted JPS58180675A (en) | 1982-04-15 | 1982-04-15 | Composition improved in wet metal wear resistance |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58180675A (en) |
-
1982
- 1982-04-15 JP JP6180282A patent/JPS58180675A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58180675A (en) | 1983-10-22 |
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