JPH01104882A - Low foamable refining penetrant composition - Google Patents
Low foamable refining penetrant compositionInfo
- Publication number
- JPH01104882A JPH01104882A JP25462987A JP25462987A JPH01104882A JP H01104882 A JPH01104882 A JP H01104882A JP 25462987 A JP25462987 A JP 25462987A JP 25462987 A JP25462987 A JP 25462987A JP H01104882 A JPH01104882 A JP H01104882A
- Authority
- JP
- Japan
- Prior art keywords
- foaming
- group
- low
- power
- ethylene oxide
- 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 25
- 238000007670 refining Methods 0.000 title 1
- 238000005187 foaming Methods 0.000 claims abstract description 40
- 238000009991 scouring Methods 0.000 claims abstract description 19
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 15
- 238000002156 mixing Methods 0.000 claims abstract description 9
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract description 16
- -1 alkyl phosphate Chemical compound 0.000 abstract description 15
- 230000000149 penetrating effect Effects 0.000 abstract description 8
- 229910019142 PO4 Inorganic materials 0.000 abstract description 6
- 239000010452 phosphate Substances 0.000 abstract description 6
- 238000004043 dyeing Methods 0.000 abstract description 4
- 230000001804 emulsifying effect Effects 0.000 abstract description 4
- 150000002148 esters Chemical class 0.000 abstract description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 2
- 238000007730 finishing process Methods 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 description 27
- 238000000034 method Methods 0.000 description 25
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- 230000035515 penetration Effects 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 230000003254 anti-foaming effect Effects 0.000 description 5
- 238000004061 bleaching Methods 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 4
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 2
- BYLSIPUARIZAHZ-UHFFFAOYSA-N 2,4,6-tris(1-phenylethyl)phenol Chemical compound C=1C(C(C)C=2C=CC=CC=2)=C(O)C(C(C)C=2C=CC=CC=2)=CC=1C(C)C1=CC=CC=C1 BYLSIPUARIZAHZ-UHFFFAOYSA-N 0.000 description 2
- CJWNFAKWHDOUKL-UHFFFAOYSA-N 2-(2-phenylpropan-2-yl)phenol Chemical compound C=1C=CC=C(O)C=1C(C)(C)C1=CC=CC=C1 CJWNFAKWHDOUKL-UHFFFAOYSA-N 0.000 description 2
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000012644 addition polymerization Methods 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 238000009981 jet dyeing Methods 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 2
- 150000005691 triesters Chemical class 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N (3S)-octan-3-ol Natural products CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical group CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000004712 monophosphates Chemical class 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 235000019795 sodium metasilicate Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は低起泡性で、しかも湿潤浸透力、洗浄力に優れ
た繊維の染色加工工程で使用される低起泡性精練浸透剤
組成物に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention provides a low-foaming scouring penetrant composition for use in fiber dyeing processes that has low foaming properties and has excellent wet penetration power and detergency. relating to things.
[従来の技術]
界面活性剤は種々の用途で使用されているが、従来公知
の界面活性剤の多くは起泡力が高く、そのため工業的諸
用途においては使用中及び使用後に種々の障害を起こし
ていることが多い、これは工業的用途では通常大規模で
機械力を重視した方式が採られるため、発泡は処理工程
のスピードアップにとって阻害要因になるなどに起因し
ている。[Prior Art] Surfactants are used for various purposes, but many of the conventionally known surfactants have a high foaming power, and therefore, in various industrial applications, they pose various problems during and after use. This is due to the fact that in industrial applications, large-scale, mechanically-intensive methods are usually used, and foaming becomes an impediment to speeding up the processing process.
例えば、繊維工業における精練、漂白及び染色工程では
界面活性剤が精練浸透剤、均染剤などとして用いられて
いるが、工程の合理化、高能率化のため起泡力が低く、
浸透力、洗浄力の高いものが要求されている。特に、納
期の短縮化、多品種少I生産化に対応して時間短縮、低
浴比化などの長所を有する液流染色機が急速に普及して
いるが、液流染色機ではジェッI・ノズルより液を布に
噴射し、その力などで布を循環させるために非常に発泡
し易い条件になっており、起泡力の高い従来の界面活性
剤では使用できない、また、廃水処理の面からも界面活
性剤の発泡は大きな問題になっている。For example, surfactants are used as scouring penetrants, leveling agents, etc. in the scouring, bleaching, and dyeing processes in the textile industry, but their foaming power is low due to rationalization and high efficiency of the process.
Products with high penetration and cleaning power are required. In particular, liquid jet dyeing machines are rapidly becoming popular due to their advantages such as shortened delivery times, high-mix, low-volume production, and other advantages such as time reduction and low bath ratio. The liquid is sprayed onto the cloth from a nozzle, and the force of the liquid is used to circulate the cloth, creating conditions that make it extremely easy to foam, making it impossible to use conventional surfactants with high foaming power, and making it difficult to treat wastewater. Foaming of surfactants has become a major problem.
従来、界面活性剤の発泡を抑制する方法として種々の方
法が試みられているが、大別すれば次の3方法になる:
■消泡剤の添加によって発泡を抑制する方法;■界面活
性剤を起泡性の少ない特別な構造にする方法;
■2種以上の界面活性剤を調合することによって発泡を
少なくする方法。Conventionally, various methods have been tried to suppress the foaming of surfactants, but they can be roughly divided into the following three methods: ■ A method of suppressing foaming by adding an antifoaming agent; ■ A method of suppressing foaming by adding a surfactant. A method of creating a special structure with less foaming; ■ A method of reducing foaming by blending two or more types of surfactants.
[発明が解決しようとする問題点1
以上の方法のうち、第1の方法は効果的な場合もあるが
、消泡剤の多くは水不溶性であるため浮遊物を生じ、そ
の付着によるトラブルが発生し易い、第2の方法につい
ては種々の構造のものが提案されており、例えばポリオ
キシエチレンポリオキシプロピレンエーテル、ポリオキ
シエチレンポリオキシプロビレンアルキルフェニルエー
テルなどが知られているが、充分に低起泡性である場合
は洗浄力、浸透力、乳化力などの性能が比較的劣ってい
ることなどから、利用できる分野が限られている欠点が
ある。第3の方法において比軸的効果の大きいものは界
面活性能の大きい界面活性剤と消泡作用のある界面活性
剤とを混合する方法であるが、従来知られているこの種
の配合物では充分低起泡性で且つ界面活性能の優れたも
のは得られていなかった。[Problem to be solved by the invention 1 Among the above methods, the first method is effective in some cases, but since most antifoaming agents are water-insoluble, they produce floating substances, which can cause problems due to their adhesion. Regarding the second method, which is more likely to occur, various structures have been proposed, such as polyoxyethylene polyoxypropylene ether, polyoxyethylene polyoxypropylene alkylphenyl ether, etc., but Low-foaming products have relatively poor performance in terms of detergency, penetration, emulsification, etc., and therefore have the disadvantage that the fields in which they can be used are limited. In the third method, a method with a large specific axial effect is a method of mixing a surfactant with a large surfactant ability and a surfactant with an antifoaming effect, but conventionally known formulations of this type A product with sufficiently low foaming properties and excellent surface activity has not been obtained.
従って、本発明の目的は低起泡性であり、しがも、浸透
力、洗浄力、乳化力に優れた精練浸透剤組成物を得るこ
とにある。Therefore, an object of the present invention is to obtain a scouring penetrant composition that has low foaming properties and is also excellent in penetrating power, detergent power, and emulsifying power.
[問題点を解決するための手段]
本発明者らはこれらの欠点をなくし、低起泡力で浸透力
、洗浄力、乳化力に優れた低起泡性精練浸透剤組成物を
得るべく鋭意研究した結果、ポリオキシアルキレン系エ
ーテル型非イオン界面活性剤に、特定のリン酸エステル
のエチレンオキシド付加物を配合した場合、充分に低起
泡性であり且つ界面活性剤としての有用な性質がポリオ
キシアルキレン系エーテル型非イオン界面活性剤単独の
場合とほとんど変わらないことを見出し、本発明を完成
するに至った。[Means for Solving the Problems] The present inventors have worked diligently to eliminate these drawbacks and obtain a low-foaming scouring penetrant composition that has low foaming power and excellent penetration, detergency, and emulsifying power. As a result of research, it was found that when an ethylene oxide adduct of a specific phosphate ester is blended with a polyoxyalkylene ether type nonionic surfactant, the polyoxyalkylene ether has sufficiently low foaming properties and has useful properties as a surfactant. The present inventors have discovered that there is almost no difference from the case of using an oxyalkylene ether type nonionic surfactant alone, and have completed the present invention.
即ち、本発明は少なくとも (a)下記の一般式(1)
RO(A O)nH(式中、Rは炭素数6個以上のアル
キル基、アルケニル基、シクロアルキル基またはアルキ
ルフェニル基を表し、Aは1種または2種以上のアルキ
レン基を表し、nは正の数である)で示される水溶性非
イオン界面活性剤、及び(b)下記の一般式(2)
%式%)
(式中、Rは炭素数6以上のアルキル基、アルケニル基
、シクロアルキル基またはアルキルフェニル基を表し、
各々のR基は同一であっても、異なっていでもよく、n
は1〜10である)で示される化合物を含有してなり、
水溶性非イオン界面活性剤(a)及び化合物(b)の重
量混合比(a):(b)= 10 :90〜80 :2
0である低起泡性M棟浸透剤組成物に係る。That is, the present invention provides at least (a) the following general formula (1)
RO(A O)nH (wherein, R represents an alkyl group, alkenyl group, cycloalkyl group, or alkylphenyl group having 6 or more carbon atoms, A represents one or more alkylene groups, and n is (a positive number), and (b) the following general formula (2) (% formula %) (wherein R is an alkyl group having 6 or more carbon atoms, an alkenyl group, a cyclo represents an alkyl group or an alkylphenyl group,
Each R group may be the same or different, n
is 1 to 10),
Weight mixing ratio of water-soluble nonionic surfactant (a) and compound (b) (a):(b)=10:90-80:2
It relates to a low-foaming M-ridge penetrant composition having a low foaming property of 0.
[作 用]
本発明者らは先に低起泡性界面活性剤組成物に関し、ジ
アルキル(またはアルケニル)リン酸エステルのエチレ
ンオキシド付活物を必須の構成成分とする界面活性剤を
提案しているが、当該化合物について更に詳細に検討し
た結果、一般のポリオキシアルキレン系エーテル型非イ
オン界面活性剤と特定の割合で配合することにより、発
泡が極めて少なく、しかも広い温度範囲にわたって良好
な界面活性能を有し、精練浸透剤として極めて良好であ
ることを見出した。このような現象に対する機構は必ず
しも明確ではないが、ジアルキル(またはアルケニル)
リン酸エステルのエチレンオキシド付加物が良好な界面
活性能を有すると共に一般の非イオン界面活性剤に対し
て消泡作用を有するなめど考えられる。[Function] The present inventors have previously proposed a surfactant containing an ethylene oxide activated product of a dialkyl (or alkenyl) phosphate ester as an essential component for a low-foaming surfactant composition. However, as a result of a more detailed study of the compound, it was found that by blending it with a general polyoxyalkylene ether type nonionic surfactant in a specific ratio, foaming is extremely low and it has good surfactant properties over a wide temperature range. It has been found that it has a very good properties as a scouring penetrant. Although the mechanism for this phenomenon is not always clear, dialkyl (or alkenyl)
It is thought that the ethylene oxide adduct of phosphoric acid ester has good surfactant ability and also has an antifoaming effect against common nonionic surfactants.
本発明において一般式(1)で示される水溶性非イオン
界面活性剤(エーテル型非イオン界面活性剤)(a)と
しては、アルコール類、フェノール類に1種または2種
以上のアルキレンオキシドを付加した型のポリオキシア
ルキレンアルキルエーテル、ポリオキシアルキレンアル
キルフェニルエーテル等があるが、用いられるアルキレ
ンオキシドのうち、少なくとも1種はエチレンオキシド
であることが好ましく、付加方法はランダムまたはブロ
ックのいずれの方法によるものでもよい、−最大(1)
で示される界面活性剤の具体例としてはヘキサノール、
2−エチルヘキサノール、オクタツール、デカノール、
ドデカノール、トリデカノール、テトラデカノール、ヘ
キサデカノー、ル、オレイルアルコールなどのアルコー
ル類や、フェニルフェノール、オクチルフェノール、ノ
ニルフェノール、ドデシルフェノール、クミルフェノー
ル、スチレン化フェノールなどのフェノール類にエチレ
ンオキシド、プロピレンオキシド、ブチレンオキシドな
どから選ばれたアルキレンオキシドの1種または2種以
上を付加した型の化合物を挙げることができる。In the present invention, the water-soluble nonionic surfactant (ether type nonionic surfactant) (a) represented by the general formula (1) is an alcohol or phenol to which one or more alkylene oxides are added. There are polyoxyalkylene alkyl ethers, polyoxyalkylene alkyl phenyl ethers, etc., but at least one of the alkylene oxides used is preferably ethylene oxide, and the addition method is either random or block. May be - maximum (1)
Specific examples of surfactants represented by are hexanol,
2-ethylhexanol, octatool, decanol,
Alcohols such as dodecanol, tridecanol, tetradecanol, hexadecanol, oleyl alcohol, phenols such as phenylphenol, octylphenol, nonylphenol, dodecylphenol, cumylphenol, styrenated phenol, ethylene oxide, propylene oxide, butylene oxide, etc. Examples include compounds to which one or more alkylene oxides selected from the following are added.
本発明に用いられる一般式(2)で示される化合物(b
)は種々の方法で合成しうるが、例えばアルコール類ま
たはフェノール類と無水リン酸を反応させて得られるリ
ン酸ジエステルに公知の方法でエチレンオキシドを付加
する方法が挙げられる。Compound (b) represented by general formula (2) used in the present invention
) can be synthesized by various methods, such as adding ethylene oxide to a phosphoric acid diester obtained by reacting alcohols or phenols with phosphoric anhydride using a known method.
なお、リン酸ジエステルの合成時には一最にモノエステ
ル及びトリエステルが副生ずる。これらの化合物は必ず
しも除去する必要はないが、トリエステルは浸透力や洗
浄力などの界面活性能はほとんどなく、モノエステルの
エチレンオキシド付加物もジエステルのエチレンオキシ
ド付加物よりはこれらの界面活性能が劣るので、モノリ
ン酸エステル及びトリリン酸エステルはできるだけ生成
しないようにすることが好ましい、また、この場合のエ
チレンオキシドの付加モル数については、用いるアルコ
ール及びフェノールとの関連で最適値が異なるが、1〜
10モル、好ましくは1〜5モルが良好であり、これよ
り多いと消泡力が低下し、浸透力や洗浄力が低下する。In addition, during the synthesis of phosphoric acid diester, monoester and triester are produced as by-products. Although these compounds do not necessarily need to be removed, triesters have almost no surface-active properties such as penetrating power or detergency, and ethylene oxide adducts of monoesters are also inferior to ethylene oxide adducts of diesters in these surface-active properties. Therefore, it is preferable to suppress the formation of monophosphate and triphosphate as much as possible.Also, in this case, the optimum number of moles of ethylene oxide to be added differs depending on the alcohol and phenol used, but it is 1 to 1.
10 moles, preferably 1 to 5 moles, is good; if the amount is more than this, the antifoaming power will decrease, and the penetration power and detergency will decrease.
用いるアルコール及びフェノールの炭素数は4〜22個
のものがよく、その具体例としては、ヘキサノール、2
−エチルヘキサノール、オクタツール、デカノール、ド
デカノール、トリデカノール、テトラデカノール、ヘキ
サデカノール、オレイルアルコールなどのアルコール類
や、フェニルフェノール、オクチルフェノール、ノニル
フェノール、ドデシルフェノール、クミルフェノール、
スチレン化フェノールなどのフェノール類等が挙げられ
る。The alcohol and phenol used preferably have 4 to 22 carbon atoms, and specific examples thereof include hexanol, 2
- Alcohols such as ethylhexanol, octatool, decanol, dodecanol, tridecanol, tetradecanol, hexadecanol, oleyl alcohol, phenylphenol, octylphenol, nonylphenol, dodecylphenol, cumylphenol,
Examples include phenols such as styrenated phenol.
本発明に用いられる一般式(1)で表される水溶性非イ
オン界面活性剤(a)と−最大(2)で表される化合物
(b)の重量混合比[(a):(b)]は10:90〜
80 :20の範囲内、好ましくは30ニア0〜80
:20の範囲内で任意に変化させることができるが、そ
れぞれの構造、使用上要求される起泡性の度合など諸性
能に対する要求により個々に調整することが望ましい、
なお、−最大(2)で表される化合物(b)の配合率が
20重量%未満では低起泡性という目的が達せられず、
また、90重旦%を超えると一般式(1)で表される水
溶性非イオン界面活性剤(エーテル型非イオン界面活性
剤)の特性が発揮できない。The weight mixing ratio of the water-soluble nonionic surfactant (a) represented by the general formula (1) used in the present invention and the compound (b) represented by -maximum (2) [(a):(b) ] is from 10:90
80: within the range of 20, preferably 30 near 0 to 80
: It can be arbitrarily changed within the range of 20, but it is desirable to adjust it individually depending on the structure and performance requirements such as the degree of foaming required for use.
In addition, if the compounding ratio of compound (b) represented by -maximum (2) is less than 20% by weight, the purpose of low foaming property cannot be achieved,
Moreover, if it exceeds 90% by weight, the characteristics of the water-soluble nonionic surfactant (ether type nonionic surfactant) represented by the general formula (1) cannot be exhibited.
本発明の低起性精練浸透剤組成物は発泡が問題となる繊
維の染色加工工程等広範な用途に使用できるが、特に、
湿潤浸透力、洗浄力、乳化力が要求され且つ特に低起泡
性が要求される液流染色機に適している。また、本発明
の低起泡性精練浸透剤組成物は酸、アルカリ、塩類等と
併用できることは勿論、本発明の目的を損なわない限り
他の界面活性剤と併用してもよい0本発明の低起泡性精
練浸透剤組成物の使用量は使用工程や目的などによって
異なるが、概ね0.005〜5重量%程度を水に溶解し
て使用する。The low-origin scouring penetrant composition of the present invention can be used in a wide range of applications such as fiber dyeing processes where foaming is a problem, but in particular,
It is suitable for jet dyeing machines which require wet penetration power, detergency power, emulsification power, and especially low foaming property. In addition, the low foaming scouring penetrant composition of the present invention can of course be used in combination with acids, alkalis, salts, etc., and may also be used in combination with other surfactants as long as the purpose of the present invention is not impaired. The amount of the low-foaming scouring penetrant composition to be used varies depending on the process and purpose of use, but approximately 0.005 to 5% by weight is dissolved in water and used.
[実 施 例]
次に、実施例により本発明を更に詳細に説明するが、本
発明は必ずしも以下の実施例に限定されるものではない
ことを理解されたい。[Examples] Next, the present invention will be explained in more detail with reference to Examples, but it should be understood that the present invention is not necessarily limited to the following Examples.
以下の実施例及び比較例において、以下の第1表に記載
する水溶性非イオン界面活性剤を用いた。In the following Examples and Comparative Examples, water-soluble nonionic surfactants listed in Table 1 below were used.
第1表中、RはC+Z〜14第2級アル第2ルアルコー
ル二羞ノ31ユ9痣@遣JU」2−エチルヘキサノール
またはドデカノールと五酸化ニリンを90℃で反応させ
た後、加水分解し、アルキルリン酸エステルを得た。こ
れにエチレンオキシドを60〜90℃で付加重合し、第
2表に示したような種々のアルキルリン酸エステルのエ
チレンオキシド付加物を合成した。なお、第2表中、ア
ルキルリン酸エステルの組成は中和滴定法により、≠な
、エチレンオキシドの平均付加モル数は’H−NMR法
などによりそれぞれ求めた。In Table 1, R is C+Z~14 secondary alcohol 2-alcohol, Then, an alkyl phosphate ester was obtained. This was subjected to addition polymerization with ethylene oxide at 60 to 90°C to synthesize various ethylene oxide adducts of alkyl phosphate esters as shown in Table 2. In Table 2, the composition of the alkyl phosphate ester was determined by the neutralization titration method, and the average number of moles of ethylene oxide added was determined by the 'H-NMR method.
較例のための組成物6の合成例
組成物4のアルキルリン酸エステルエチレンオキシド付
加物に、更にエチレンオキシドを90℃で付加重合し、
合計11.0モル付加物の組成物6を得た。Synthesis Example of Composition 6 for Comparative Example Addition polymerization of ethylene oxide to the alkyl phosphate ester ethylene oxide adduct of Composition 4 at 90°C,
Composition 6 was obtained with a total of 11.0 moles of adduct.
のための゛の る ゞ
従来公知の消泡効果のある界面活性剤として第3表の各
界面活性剤を用いた。Each surfactant in Table 3 was used as a conventionally known surfactant having an antifoaming effect.
箸工点
第3表中、TMPはトリメチロールプロパン残基を表す
。In Table 3, TMP represents trimethylolpropane residue.
施例1〜11、比較例1〜13
本発明の低起泡性精練浸透剤組成物及び比較例の界面活
性剤について起泡力、浸透力及び表面張力を測定した。Examples 1 to 11, Comparative Examples 1 to 13 Foaming power, penetrating power, and surface tension were measured for the low foaming scouring penetrant composition of the present invention and the surfactant of the comparative example.
結果を第4表に示す。The results are shown in Table 4.
なお、起泡力はロスマイルス法により、浸透力はキャン
パスディスク法によりそれぞれ測定した。Note that the foaming power was measured by the Ross Miles method, and the penetrating power was measured by the campus disk method.
また、表面張力は協和化学(株)製、協和CBVP式表
面張力計を用いて測定した。Moreover, the surface tension was measured using a Kyowa CBVP type surface tension meter manufactured by Kyowa Kagaku Co., Ltd.
第4表から分かるように、本発明の界面活性剤組成物は
洗浄力、浸透力等の界面活性能に優れた従来の非イオン
界面活性剤(比較例1〜3及び8〜10)に比べて著し
く低起泡性であるにもかかわらず、浸透力は同程度であ
り、表面張力低下能はむしろ浸れている。また、従来公
知の消泡効果の良好な界面活性剤を配合した組成物(比
較例5〜7.11〜13)と比較すると、起泡性は実用
の範囲で差がなく、表面張力低下能及び浸透力は明らか
に優れている。As can be seen from Table 4, the surfactant composition of the present invention has superior surfactant properties such as detergency and penetrating power compared to conventional nonionic surfactants (Comparative Examples 1 to 3 and 8 to 10). Despite having significantly lower foaming properties, their penetrating powers are comparable and their ability to lower surface tension is even better. Furthermore, when compared with conventionally known compositions containing surfactants with good antifoaming effects (Comparative Examples 5 to 7, 11 to 13), there is no difference in foaming properties within a practical range, and the ability to lower surface tension is and the penetration power is clearly superior.
来1sxiλ二18−よ1IffiNl生ごじ目と綿ブ
ロード生機を下記の条件で一浴精練漂白し、精練漂白性
を調べた。結果を第5表に示す。1sxiλ218-1IffiNl Nagojime and broad cotton greige were scoured and bleached in a single bath under the following conditions, and the scouring and bleaching properties were examined. The results are shown in Table 5.
く精練漂白条件〉
浴比: 1:20
温度= 85℃
時間二 30分間
配合: 35%過酸化水素、 0.3重量%メタケイ
酸ナトリウム 0.311に量%界面活性剤組成物
0.04重量%
く評価〉
精練漂白性の評価は吸水高さ及びハンター白皮により行
なった。まず、吸水高さについては精練漂白処理を終え
た布地から幅2cm、長さ20cmの試験布をとり、染
料を溶解した水溶液に試験布の一端を浸漬し、30秒後
の染料水の吸上げ高さ(c@)を測定した。また、ハン
ター白皮は日本重色工業(株)製デジタルカラースタジ
オCS−101D型により測定した。Scouring and bleaching conditions〉 Bath ratio: 1:20 Temperature = 85°C Time: 2 30 minutes Blending: 35% hydrogen peroxide, 0.3% by weight sodium metasilicate, 0.311% surfactant composition
0.04% by weight Evaluation> The scouring and bleaching properties were evaluated based on water absorption height and hunter's white skin. First, for the water absorption height, take a test cloth 2 cm wide and 20 cm long from the fabric that has been scoured and bleached, immerse one end of the test cloth in an aqueous solution containing the dye, and after 30 seconds absorb the dye water. The height (c@) was measured. In addition, Hunter's white skin was measured using Digital Color Studio Model CS-101D manufactured by Nihon Heavy Industries Co., Ltd.
本発明の低起泡性精練浸透剤組成物は従来広く使用され
ている比較的1〜3の界面活性剤と同等の精練漂白性が
得られており、比較例5〜7の低起泡性界面活性剤組成
物と比べると明らかに優れている。The low-foaming scouring penetrant composition of the present invention has a scouring and bleaching property comparable to that of comparatively 1 to 3 surfactants that have been widely used in the past, and has a low foaming property of Comparative Examples 5 to 7. It is clearly superior to surfactant compositions.
[発明の効果]
本発明の効果は低起泡性であり、しかも浸透力、洗浄力
、乳化カー力優れた低起泡性精練浸透剤組成物を得たこ
とにある。[Effects of the Invention] The effects of the present invention are that a low-foaming scouring penetrant composition has been obtained which is low-foaming and has excellent penetration power, detergency, and emulsifying power.
特許出願人 旭電化工業株式会社Patent applicant: Asahi Denka Kogyo Co., Ltd.
Claims (1)
基、シクロアルキル基またはアルキルフェニル基を表し
、Aは1種または2種以上のアルキレン基を表し、nは
正の数である) で示される水溶性非イオン界面活性剤、及び(b)下記
の一般式(2) ▲数式、化学式、表等があります▼ (式中、Rは炭素数6以上のアルキル基、アルケニル基
、シクロアルキル基またはアルキルフェニル基を表し、
各々のR基は同一であっても、異なつていてもよく、n
は1〜10である) で示される化合物 を含有してなり、水溶性非イオン界面活性剤(a)及び
化合物(b)の重量混合比(a):(b)=10:90
〜80:20である低起泡性精練浸透剤組成物。[Scope of Claims] At least (a) the following general formula (1) RO(AO)_nH (wherein R represents an alkyl group, alkenyl group, cycloalkyl group, or alkylphenyl group having 6 or more carbon atoms, A represents one or more alkylene groups, n is a positive number) and (b) the following general formula (2) ▲ Numerical formula, chemical formula, table etc.▼ (In the formula, R represents an alkyl group, alkenyl group, cycloalkyl group, or alkylphenyl group having 6 or more carbon atoms,
Each R group may be the same or different, n
is 1 to 10), and the weight mixing ratio of water-soluble nonionic surfactant (a) and compound (b) is (a):(b)=10:90
-80:20 low foaming scouring penetrant composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25462987A JPH0711107B2 (en) | 1987-10-12 | 1987-10-12 | Low foaming scouring penetrant composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25462987A JPH0711107B2 (en) | 1987-10-12 | 1987-10-12 | Low foaming scouring penetrant composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01104882A true JPH01104882A (en) | 1989-04-21 |
JPH0711107B2 JPH0711107B2 (en) | 1995-02-08 |
Family
ID=17267675
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25462987A Expired - Lifetime JPH0711107B2 (en) | 1987-10-12 | 1987-10-12 | Low foaming scouring penetrant composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0711107B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05106158A (en) * | 1991-10-11 | 1993-04-27 | Dai Ichi Kogyo Seiyaku Co Ltd | Scouring agent for yarn |
JPH0693558A (en) * | 1992-09-08 | 1994-04-05 | Sanyo Chem Ind Ltd | Scouring agent composition |
CN103290689A (en) * | 2013-07-02 | 2013-09-11 | 江苏省海安石油化工厂 | Low-foaming penetrating agent |
CN104313914A (en) * | 2014-10-25 | 2015-01-28 | 合肥市安山涂层织物有限公司 | Organic silicon penetrating agent for leather |
-
1987
- 1987-10-12 JP JP25462987A patent/JPH0711107B2/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05106158A (en) * | 1991-10-11 | 1993-04-27 | Dai Ichi Kogyo Seiyaku Co Ltd | Scouring agent for yarn |
JPH0693558A (en) * | 1992-09-08 | 1994-04-05 | Sanyo Chem Ind Ltd | Scouring agent composition |
CN103290689A (en) * | 2013-07-02 | 2013-09-11 | 江苏省海安石油化工厂 | Low-foaming penetrating agent |
CN104313914A (en) * | 2014-10-25 | 2015-01-28 | 合肥市安山涂层织物有限公司 | Organic silicon penetrating agent for leather |
Also Published As
Publication number | Publication date |
---|---|
JPH0711107B2 (en) | 1995-02-08 |
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