JP2008045266A - Fiber scouring agent composition - Google Patents
Fiber scouring agent composition Download PDFInfo
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- JP2008045266A JP2008045266A JP2007232470A JP2007232470A JP2008045266A JP 2008045266 A JP2008045266 A JP 2008045266A JP 2007232470 A JP2007232470 A JP 2007232470A JP 2007232470 A JP2007232470 A JP 2007232470A JP 2008045266 A JP2008045266 A JP 2008045266A
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- 238000009991 scouring Methods 0.000 title claims abstract description 58
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 40
- 239000000203 mixture Substances 0.000 title claims abstract description 31
- 239000000835 fiber Substances 0.000 title claims description 11
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 13
- 150000003839 salts Chemical class 0.000 claims abstract description 8
- 125000006353 oxyethylene group Chemical group 0.000 claims abstract description 5
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 4
- 150000004671 saturated fatty acids Chemical class 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 18
- -1 oxypropylene group Chemical group 0.000 claims description 10
- 239000013543 active substance Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 150000005215 alkyl ethers Chemical class 0.000 claims description 4
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 3
- 125000003158 alcohol group Chemical group 0.000 claims description 2
- 230000001105 regulatory effect Effects 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 5
- 230000035699 permeability Effects 0.000 abstract description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- 239000004744 fabric Substances 0.000 description 21
- 239000003513 alkali Substances 0.000 description 16
- 229920000742 Cotton Polymers 0.000 description 13
- 238000012360 testing method Methods 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 7
- 239000002738 chelating agent Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 7
- 238000000926 separation method Methods 0.000 description 7
- 239000006260 foam Substances 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000005187 foaming Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 238000004061 bleaching Methods 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- 239000012209 synthetic fiber Substances 0.000 description 3
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- 102100021809 Chorionic somatomammotropin hormone 1 Human genes 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- 101000895818 Homo sapiens Chorionic somatomammotropin hormone 1 Proteins 0.000 description 2
- 101000956228 Homo sapiens Chorionic somatomammotropin hormone 2 Proteins 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000006065 biodegradation reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229920000847 nonoxynol Polymers 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- YLQLIQIAXYRMDL-UHFFFAOYSA-N propylheptyl alcohol Chemical compound CCCCCC(CO)CCC YLQLIQIAXYRMDL-UHFFFAOYSA-N 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- 238000009941 weaving Methods 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 238000000944 Soxhlet extraction Methods 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 231100000209 biodegradability test Toxicity 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
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- Detergent Compositions (AREA)
Abstract
Description
本発明は、繊維用精練剤組成物に関し、より詳細には原綿等の天然繊維及びポリエステル等の合成繊維及びこれらの混紡繊維製品等の漂白、染色、仕上げ等の後工程の効果を高めるために、天然繊維由来の一次夾雑物、合成繊維の製織段階で使用されたサイジング剤、糊剤等の二次夾雑物等を除去するために実施される「精練」工程に用いられる精練剤組成物に関する。 The present invention relates to a fiber scouring agent composition, and more specifically, to enhance the effects of post-processes such as bleaching, dyeing and finishing of natural fibers such as raw cotton and synthetic fibers such as polyester and blended fiber products thereof. The present invention relates to a scouring agent composition used in a “scouring” process carried out to remove primary impurities derived from natural fibers, sizing agents used in the weaving stage of synthetic fibers, secondary impurities such as glues, etc. .
原綿をはじめとする天然繊維には、綿ロウ、たんぱく質等の一次夾雑物が付着し、ポリエステル繊維等の合成繊維の生機には、製織時に使用されるサイジング油剤、糊剤等の二次夾雑物が付着している。これら夾雑物を「精練」工程で充分に除去しないと、後の漂白、染色、仕上げ工程でトラブルが生じ、多大な不利益を被る。加工工程が簡素化、高速化していく昨今では、より高機能で使いやすく、また最近の環境問題から生分解性の高い精練剤への要求が高まっている。 Primary contaminants such as cotton wax and protein adhere to natural fibers such as raw cotton, and secondary contaminants such as sizing oils and glues used during weaving are used on the raw machinery of synthetic fibers such as polyester fibers. Is attached. If these impurities are not sufficiently removed in the “scouring” step, troubles occur in the subsequent bleaching, dyeing and finishing steps, resulting in a great disadvantage. In recent years when the processing process has been simplified and speeded up, there is an increasing demand for a scouring agent that is more functional and easy to use, and that is highly biodegradable due to recent environmental problems.
このような背景の中、最近では安価な海外生機の輸入が増加し、以前より日本市場で出回っている組成の明確な生機、油剤や糊剤ではなく、組成不明の油剤、糊剤が使用されている海外生機、難精練生機が増大しており、従来の様な精練剤や精練条件では対処しきれなくなっている。中でも、綿織物をはじめとする繊維製品の、高温、高アルカリ条件下で実施される精練工程では、最近の現場工程の簡略化や自動供給システムといったハード面から高濃度ストックタンクを採用するケースが多く、それに伴いアルカリ濃度が70〜100g/Lと非常に高く設定され、従来の非イオン活性剤主体の精練剤ではアルカリ浴中で分離を起こし、性能が発現しないという問題が生じている。その上、機械の高速化から高アルカリ条件でも繊維へより素早く浸透し、より低泡性で精練性にも優れるといった高機能薬剤への要求が高まっている。 Against this backdrop, imports of cheap overseas raw machinery have increased recently, and oil agents and pastes with unknown composition have been used instead of raw machinery, oil agents and pastes with a clear composition that have been on the Japanese market. The number of overseas and difficult scouring machines is increasing, and the conventional scouring agents and scouring conditions cannot cope with them. In particular, in the scouring process of textile products such as cotton fabrics that are carried out under high temperature and high alkali conditions, there are many cases in which high concentration stock tanks are adopted from the viewpoint of hardware such as the recent simplification of on-site processes and automatic supply systems. As a result, the alkali concentration is set to a very high value of 70 to 100 g / L, and the conventional nonionic active agent-based scouring agent causes separation in an alkaline bath, causing a problem that the performance does not appear. In addition, there is an increasing demand for highly functional drugs that can penetrate fibers more quickly even under high alkaline conditions due to higher machine speeds, and have lower foaming properties and excellent scouring properties.
従来の精練剤は、アニオン活性剤やPOEのリン酸エステルもしくはスルホン酸エステル等のアニオン成分等を混合することにより、ある程度の耐アルカリ性能を実現しているが、より高い濃度の耐アルカリ性能を持ちながら、低温安定性、浸透性、精練性能を全て満たす精練剤組成物は未だ得られていない(特許文献1〜4)。 Conventional scouring agents achieve a certain level of alkali resistance by mixing anionic components such as anionic activators and phosphoric acid esters or sulfonic acid esters of POE. A scouring agent composition that satisfies all of the low-temperature stability, permeability, and scouring performance while possessing it has not yet been obtained (Patent Documents 1 to 4).
一方で、精練剤組成物には、環境問題に対応するノニルフェノールフリーや、PRTR法該当物質を使用しないという要望もある。
本発明は、上記に鑑みてなされたものであり、従来より高い濃度の耐アルカリ性能を持ちながら、低温安定性、浸透性、精練性能等の要求を全て満たす繊維用精練剤組成物を提供することを目的とする。 The present invention has been made in view of the above, and provides a fiber scouring agent composition that satisfies all requirements for low temperature stability, permeability, scouring performance, etc. while having a higher concentration of alkali resistance than conventional ones. For the purpose.
本発明の繊維用精練剤組成物は、上記の課題を解決するために、
(A)下記一般式(1)で表され、多分散度(Mw/Mn)が1.01〜1.20である非イオン界面活性剤に由来し、下記一般式(2)で表されるリン酸エステル及び/又はその塩、
(B)下記一般式(3)で表されるポリオキシアルキレンアルキルエーテル型非イオン活性剤、及び
(C)炭素数8〜22の飽和脂肪酸又は不飽和脂肪酸、及び/又はその塩
を含有してなるものとする。
(A) It is represented by the following general formula (1), derived from a nonionic surfactant having a polydispersity (Mw / Mn) of 1.01 to 1.20, and represented by the following general formula (2). Phosphate esters and / or salts thereof,
(B) a polyoxyalkylene alkyl ether type nonionic active agent represented by the following general formula (3), and (C) a saturated or unsaturated fatty acid having 8 to 22 carbon atoms and / or a salt thereof. Shall be.
式(1),(2)中、R1はn−ペンチル基、R2はn−プロピル基を示し、POはオキシプロピレン基、EOはオキシエチレン基を示し、m,nは、m=0〜2、n=1〜8の数字を示す。POとEOの付加形態はランダム付加、ブロック付加又はこれらの混合付加である。また、式(2)中のXは、OH又はR−O−[(PO)m−(EO)n]を示す。 In the formulas (1) and (2), R 1 represents an n-pentyl group, R 2 represents an n-propyl group, PO represents an oxypropylene group, EO represents an oxyethylene group, and m and n are m = 0. -2, the number of n = 1-8 is shown. The addition form of PO and EO is random addition, block addition, or a mixed addition thereof. Moreover, X in Formula (2) shows OH or R-O-[(PO) m- (EO) n].
R3−O−[(PO)p−(EO)q]−H …(3)
式(3)中、R3は炭素数が8〜20の直鎖或いは分岐のアルコール残基を示し、POはオキシプロピレン基、EOはオキシエチレン基を示し、p,qは、p=0〜2、q=1〜8の数字を示す。POとEOの付加形態は、ランダム付加、ブロック付加又はこれらの混合付加である。但し、PRTR法により規制されるC12〜15のエトキシレートを除く。
R 3 -O - [(PO) p- (EO) q] -H ... (3)
In the formula (3), R 3 represents a linear or branched alcohol residue having 8 to 20 carbon atoms, PO represents an oxypropylene group, EO represents an oxyethylene group, and p and q represent p = 0 to 0. 2, q = 1 to 8 is shown. The addition form of PO and EO is random addition, block addition, or a mixed addition thereof. However, C12-15 ethoxylates regulated by the PRTR method are excluded.
本発明の精練剤組成物は、成分(A)を含有することにより、従来の精練剤より高アルカリ条件下においても安定かつ顕著な浸透力と精練性を発揮する。 By containing the component (A), the scouring agent composition of the present invention exhibits stable and remarkable penetrating power and scourability even under higher alkaline conditions than conventional scouring agents.
また、成分(B)を用いることで、浸透性、精練布の再湿潤性が従来よりも顕著に向上し、それに伴い精練性も向上する。また、生分解性が高いため排水の環境への負荷が少なく、使用者が安心して処理できる精練剤を提供できる。 Moreover, by using the component (B), the permeability and the rewetting property of the scouring cloth are remarkably improved as compared with the conventional one, and the scouring property is also improved accordingly. In addition, since the biodegradability is high, it is possible to provide a scouring agent that is less burdened on the environment of waste water and can be treated with peace of mind by the user.
さらに、成分(C)を配合することで低泡化し、また耐アルカリ性能を向上させることができる。 Furthermore, by blending the component (C), it is possible to reduce the foam and improve the alkali resistance.
本発明で用いる(A)成分は、上記の通り、一般式(2)で表されるリン酸エステル及び/又はその塩であって、一般式(1)におけるR1及びR2は、R1がn−ペンチル基、R2がn−プロピル基であり、かつ多分散度(Mw/Mn)が1.01〜1.20である非イオン界面活性剤から得られるものである。 As described above, the component (A) used in the present invention is a phosphate ester represented by the general formula (2) and / or a salt thereof, and R 1 and R 2 in the general formula (1) are R 1. Is an n-pentyl group, R 2 is an n-propyl group, and is obtained from a nonionic surfactant having a polydispersity (Mw / Mn) of 1.01-1.20.
この非イオン界面活性剤は、原料アルコールとして2−プロピル−1−ヘプタノールを用いることにより得られる。 This nonionic surfactant is obtained by using 2-propyl-1-heptanol as a raw material alcohol.
このような(A)成分を含有することで、従来使用されている多分散度(Mw/Mn)が1.25で同様の構造(炭素数が10の分岐型のイソデシル残基)を持つアニオン成分よりも、精練剤の耐アルカリ性能が飛躍的に向上する。これに伴い、高アルカリ下で製品分離を起こすことなく、優れた精練性と耐アルカリ浸透力を並行して発現することができ、本発明の目的を達成することが可能となる。 By containing such a component (A), a conventionally used anion having a polydispersity (Mw / Mn) of 1.25 and a similar structure (branched isodecyl residue having 10 carbon atoms) is used. Compared to ingredients, the alkali resistance of scouring agents is dramatically improved. Accordingly, excellent scouring properties and alkali penetration resistance can be expressed in parallel without causing product separation under high alkali, and the object of the present invention can be achieved.
リン酸エステルの塩としては、ナトリウム塩、カリウム塩、アミン塩等が使用可能であるが、特にトリエタノールアミン塩が、製品高濃度化、低温安定性(流動良)の面から好ましい。 As the phosphate ester salt, sodium salt, potassium salt, amine salt and the like can be used, and triethanolamine salt is particularly preferable from the viewpoints of high product concentration and low temperature stability (good flow).
成分(B)は、上記の通り一般式(3)で表されるポリオキシアルキレンアルキルエーテル型非イオン界面活性剤であり、多分散度(Mw/Mn)が1.01〜1.20である直鎖或いは分岐のポリオキシアルキレンアルキルエーテル型非イオン活性剤であることが好ましい。多分散度(Mw/Mn)が1.01未満の場合、脱脂力をはじめとする精練効果が低下する傾向にあり、また1.21以上であると要求される浸透力や再湿潤性が発現し難くなる傾向にある。 The component (B) is a polyoxyalkylene alkyl ether type nonionic surfactant represented by the general formula (3) as described above, and has a polydispersity (Mw / Mn) of 1.01 to 1.20. A linear or branched polyoxyalkylene alkyl ether type nonionic activator is preferred. When the polydispersity (Mw / Mn) is less than 1.01, the scouring effect including degreasing power tends to be reduced, and the penetration force and rewetability required to be 1.21 or more are exhibited. It tends to be difficult.
成分(B)としては、中でも、2−プロピル−1−ヘプタノールを原料アルコールとしたC10の分岐型非イオン界面活性剤が好ましい。C10の分岐型非イオン界面活性剤を中心とした1種類以上の非イオン界面活性剤を配合し、加えて炭素数8〜20の非イオン界面活性剤を広範囲に配合することで、良好な浸透性と再湿潤性等の精練全般の性能を確保しながら、水への易溶解性、他成分との相溶性、可溶化性等を落とすことなく各種性能を付与できる。 As the component (B), a C10 branched nonionic surfactant using 2-propyl-1-heptanol as a raw material alcohol is preferable. By blending one or more types of nonionic surfactants, mainly C10 branched nonionic surfactants, in addition, a wide range of C8-20 nonionic surfactants can be blended in a wide range. Various performances can be imparted without degrading easy solubility in water, compatibility with other components, solubilization, and the like, while ensuring the performance of scouring in general, such as property and rewetting.
但し、昨今の環境ホルモン問題からC9のノニルフェノールエトキシレートが敬遠され、また最近施行された化学物質排出把握管理促進法(PRTR法)でC12〜15のエトキシレートの排出報告義務が発生したことから、このような構造を持つ非イオン界面活性剤は本発明では使用しない。 However, because of the recent environmental hormone problem, C9 nonylphenol ethoxylate was shunned, and the recently enacted chemical substance emission grasp management promotion law (PRTR law) has caused an obligation to report C12-15 ethoxylate emissions. Nonionic surfactants having such a structure are not used in the present invention.
さらに成分(C)は、炭素数8〜22の飽和脂肪酸及び不飽和又はその塩である。塩は、ナトリウム塩、カリウム塩、アミン塩等であり、特に限定されないがアミン塩が好ましい。 Furthermore, a component (C) is a C8-22 saturated fatty acid and unsaturated or its salt. The salt is a sodium salt, potassium salt, amine salt or the like, and is not particularly limited, but an amine salt is preferable.
成分(C)は、成分(A)や(B)に由来する泡の消泡に寄与し、これを使用することにより、低泡性能を向上させることが可能となる。 Component (C) contributes to the defoaming of bubbles derived from components (A) and (B), and by using this, it is possible to improve the low bubble performance.
上記成分(A)〜(C)の配合比率は、成分(A)のアニオン活性剤と成分(B)の非イオン活性剤の重量比が、(A)/(B)=1/9〜3/7であることが好ましく、成分(A)と成分(C)の重量比として、両者の合計量10部中で成分(A)が8部以上10部未満であることが好ましい。 The mixing ratio of the components (A) to (C) is such that the weight ratio of the anionic active agent of the component (A) and the nonionic active agent of the component (B) is (A) / (B) = 1/9 to 3 The weight ratio of the component (A) to the component (C) is preferably / 7, and the component (A) is preferably 8 parts or more and less than 10 parts in a total amount of 10 parts of both.
本発明の組成物において、より一層の低泡化を図る必要がある場合には、成分(D)として消泡剤を含有させることができる。 In the composition of the present invention, when it is necessary to further reduce the foam, an antifoaming agent can be contained as the component (D).
その場合の成分(D)としては、2−エチルヘキサノール、オレイルアルコール、イソステアリルアルコール等の高級アルコール系消泡剤やグリコールエーテル系自己乳化型シリコンのような相溶性に害を及ぼさないシリコン系消泡剤を配合すればよい。 In this case, as component (D), a silicon alcohol that does not adversely affect compatibility, such as higher alcohol antifoaming agents such as 2-ethylhexanol, oleyl alcohol, isostearyl alcohol, and glycol ether self-emulsifying silicon. What is necessary is just to mix | blend a foaming agent.
また、低温時の製品安定性をより安定に保持し高濃度化を図る為に、溶剤としてイソプロピルアルコール、メタノール、ブチルセロソルブ等を配合することもできる。 In addition, isopropyl alcohol, methanol, butyl cellosolve, or the like can be added as a solvent in order to maintain product stability at a low temperature more stably and to increase the concentration.
本発明において精練剤組成物は、有効成分(固形分)の重量%として、成分(A)を5〜25重量%、好ましくは10〜25重量%、より好ましくは15〜20重量%、成分(B)を30〜70重量%、好ましくは40〜60重量%、成分(C)を10重量%以下、好ましくは5〜8重量%、成分(D)は0〜10重量%、好ましくは2〜10重量%配合する。 In the present invention, the scouring agent composition contains 5 to 25% by weight, preferably 10 to 25% by weight, more preferably 15 to 20% by weight of the component (A) as the weight% of the active ingredient (solid content). B) is 30 to 70% by weight, preferably 40 to 60% by weight, component (C) is 10% by weight or less, preferably 5 to 8% by weight, and component (D) is 0 to 10% by weight, preferably 2 to 2%. Mix 10% by weight.
また、成分(A)、(B)、(C)、(D)の総量は、50〜95重量%であることが好ましく、より好ましくは55〜90重量%であるように配合し、残部の10〜45重量%は通常は水を使用する。 The total amount of components (A), (B), (C) and (D) is preferably 50 to 95% by weight, more preferably 55 to 90% by weight, and the balance 10 to 45% by weight usually uses water.
これらの配合比における精練剤組成物で精練した生機は、白度も高く、その後の漂白、染色、仕上工程をトラブルなく経ることができ、非常に高品質な仕上がりになる。 The raw machine scoured with the scouring agent composition at these blending ratios has high whiteness, and can undergo subsequent bleaching, dyeing, and finishing processes without any trouble, resulting in a very high quality finish.
本発明の精練剤組成物には、本発明の目的を損なわない範囲内で、他の添加物、例えばEDTA4Na(EDTA:エチレンジアミンテトラアセティックアシッド)のようなキレート剤等を含有させることもできる。 The scouring agent composition of the present invention may contain other additives such as a chelating agent such as EDTA4Na (EDTA: ethylenediaminetetraacetic acid) within the range not impairing the object of the present invention.
以下、本発明の実施例について説明するが、本発明は以下の実施例に限定されるものではない。 Examples of the present invention will be described below, but the present invention is not limited to the following examples.
1.綿織物、ポリエステル/綿混紡織物(以下、T/C織物という)、ポリエステル織物の精練性能試験(残脂率、再湿潤性)
以下の通り、綿織物、T/C織物、ポリエステル織物につき、精練性能試験(残脂率、再湿潤性の評価)を行った。精練剤組成物の組成を表1,2に示す。なお、表における多分散度は非イオン界面活性剤の多分散度を示す。
1. Cotton fabrics, polyester / cotton blended fabrics (hereinafter referred to as T / C fabrics), and polyester fabric scouring performance tests (residual fat ratio, rewetting)
A scouring performance test (evaluation of residual oil rate and rewetability) was performed on cotton fabric, T / C fabric, and polyester fabric as follows. The composition of the scouring agent composition is shown in Tables 1 and 2. In addition, the polydispersity in a table | surface shows the polydispersity of a nonionic surfactant.
[供試布] (a)綿織物 100%生機
[処理条件]
精練剤(有効成分) 1.5g/L
NaOH(固) 20.0g/L
サイゾール(登録商標、以下同様)LM(第一工業製薬(株)製キレート剤) 0.5g/L
酸化糊抜剤 8.0g/L
*機種 ミニ・カラー(テクサム技研(株)製)
*浴比 1:20
*温度・時間 95℃×30分→湯洗2分→水洗×1分→乾燥
(95℃で30分間処理した後、約50℃の湯で2分間洗浄し、次いで常温の水で1分間洗浄し、乾燥した。以下においても時間が異なる以外は同様である。)
[Test cloth] (a) 100% cotton fabric [processing conditions]
Scouring agent (active ingredient) 1.5g / L
NaOH (solid) 20.0 g / L
Saisol (registered trademark, the same shall apply hereinafter) LM (Daiichi Kogyo Seiyaku Co., Ltd. chelating agent) 0.5 g / L
Oxidizing paste remover 8.0g / L
* Model Mini color (Texam Giken Co., Ltd.)
* Bath ratio 1:20
* Temperature / Time 95 ° C x 30 minutes → Washing 2 minutes → Washing x 1 minute → Dry (After treating at 95 ° C for 30 minutes, wash with hot water at about 50 ° C for 2 minutes, then wash with room temperature water for 1 minute (The same applies to the following except that the time is different.)
[供試布] (b)T/C(70/30)織物生機
[処理条件]
精練剤(有効成分) 1.0g/L
NaOH(固) 10.0g/L
サイゾールLM(第一工業製薬(株)製キレート剤) 0.5g/L
酸化糊抜剤 4.0g/L
*機種 ミニ・カラー(テクサム技研(株)製)
*浴比 1:20
*温度・時間 90℃×30分→湯洗(50℃)2分→水洗×1分→乾燥
[Test cloth] (b) T / C (70/30) woven fabric machine [Treatment conditions]
Scouring agent (active ingredient) 1.0 g / L
NaOH (solid) 10.0 g / L
Saisol LM (Daiichi Kogyo Seiyaku Co., Ltd. chelating agent) 0.5g / L
Oxidizing paste remover 4.0g / L
* Model Mini color (Texam Giken Co., Ltd.)
* Bath ratio 1:20
* Temperature / Time 90 ° C x 30 minutes → Washing (50 ° C) 2 minutes → Washing x 1 minute → Dry
[供試布] (c)ポリエステル100%織物生機
[処理条件]
精練剤(有効成分) 1.0g/L
NaOH(固) 1.0g/L
サイゾールFX−20(第一工業製薬(株)製キレート剤) 0.5g/L
*機種 ミニ・カラー(テクサム技研(株)製)
*浴比 1:10
*温度・時間 90℃×10分→湯洗(50℃)2分→水洗×1分→乾燥
[Test cloth] (c) 100% polyester fabric raw material [Treatment conditions]
Scouring agent (active ingredient) 1.0 g / L
NaOH (solid) 1.0 g / L
Saisol FX-20 (Daiichi Kogyo Seiyaku Co., Ltd. chelating agent) 0.5g / L
* Model Mini color (Texam Giken Co., Ltd.)
* Bath ratio 1:10
* Temperature / Time 90 ℃ × 10min → Wash (50 ℃) 2min → Wash × 1min → Dry
[供試布] (d)ナイロン織物生機
[処理条件]
精練剤(有効成分) 1.0g/L
NaOH(固) 1.0g/L
サイゾールFX−20(第一工業製薬(株)製キレート剤) 0.5g/L
*機種 ミニ・カラー(テクサム技研(株)製)
*浴比 1:10
*温度時間 90℃×10分→湯洗(50℃)2分→水洗×1分→乾燥
[Test cloth] (d) Nylon fabric raw machine [Processing conditions]
Scouring agent (active ingredient) 1.0 g / L
NaOH (solid) 1.0 g / L
Saisol FX-20 (Daiichi Kogyo Seiyaku Co., Ltd. chelating agent) 0.5g / L
* Model Mini color (Texam Giken Co., Ltd.)
* Bath ratio 1:10
* Temperature time 90 ℃ × 10min → Washing (50 ℃) 2min → Washing × 1min → Drying
上記各処理により得られた処理布につき、以下の方法で残脂率及び再湿潤性を調べた。結果を表3に示す。
残脂率(%):ソックスレー抽出処理(溶媒:ジエチルエーテル)前後の生地重量から次式により算出した;
Residual fat ratio (%): calculated from the weight of the dough before and after Soxhlet extraction treatment (solvent: diethyl ether) by the following formula;
再湿潤性(cm):幅4cm×12cmの試験布に染料水を5分間浸漬し、吸上げた長さを測定する吸上げ法により評価した。なお、この評価は(a)綿、(b)T/C織物についてのみ実施した。 Rewetting property (cm): Dye water was immersed in a test cloth having a width of 4 cm × 12 cm for 5 minutes, and evaluation was performed by a sucking method in which the sucked length was measured. This evaluation was carried out only for (a) cotton and (b) T / C fabric.
2.耐アルカリ浸透性
実施例1,2,3,5及び比較例1〜4の精練剤組成物を用い、次の浴組成で処理した処理布につき、下記の評価方法で耐アルカリ性、アルカリ浸透性を調べた。結果を表4に示す。
2. Alkali permeation resistance Using the scouring agent compositions of Examples 1, 2, 3, and 5 and Comparative Examples 1 to 4, the treated cloth treated with the following bath composition was subjected to alkali resistance and alkali permeation by the following evaluation methods. Examined. The results are shown in Table 4.
[浴組成]
精練剤(有効成分) 1.5g/L
NaOH(固) Xg/L
サイゾールLM 0.5g/L(第一工業製薬(株)製キレート剤)
ラクトーゲンLS 15.0g/L(洛東化成(株)製酸化糊抜剤)
[評価方法]
*耐アルカリ性:NaOH 60g/L〜100g/Lまでの溶液を作製し、精練剤の分離の有無を確認した。評価は常温5時間放置後、○〜×(○:分離なし、×:分離あり)で目視評価した。
[Bath composition]
Scouring agent (active ingredient) 1.5g / L
NaOH (solid) Xg / L
Saisol LM 0.5g / L (Daiichi Kogyo Seiyaku Co., Ltd. chelating agent)
Lactogen LS 15.0g / L (Oxidizing paste remover manufactured by Nitto Kasei Co., Ltd.)
[Evaluation methods]
* Alkali resistance: Solutions of NaOH from 60 g / L to 100 g / L were prepared, and the presence or absence of separation of the scouring agent was confirmed. The evaluation was visually evaluated by ○ to × (○: no separation, x: with separation) after standing at room temperature for 5 hours.
*アルカリ浸透性:NaOH(固)=60g/L濃度で、綿キャンバスディスク法(2cm角の綿キャンバス生機を測定浴に浮かせ、浸透時間と浸漬時間を測定する。)により行った。なお、「浸透時間」はキャンバスが染みる迄の時間を示し、「沈降時間」はキャンバスがビーカーの底に沈み始める時間を示す。 * Alkali permeability: at a concentration of NaOH (solid) = 60 g / L, by a cotton canvas disc method (a 2 cm square cotton canvas was floated in a measurement bath and the permeation time and immersion time were measured). The “penetration time” indicates the time until the canvas is stained, and the “settling time” indicates the time when the canvas starts to sink to the bottom of the beaker.
3.起泡性・消泡性試験
実施例1,2及び比較例2,4の精練剤組成物を用い、次の浴組成で処理した処理布につき、下記の評価方法で起泡性・消泡性を調べた。結果を表5に示す。
3. Foaming and defoaming tests Using the scouring agent compositions of Examples 1 and 2 and Comparative Examples 2 and 4, treated cloths treated with the following bath composition were foamed and defoamed by the following evaluation methods. I investigated. The results are shown in Table 5.
[浴組成]
精練剤(有効成分) 1.5g/L
NaOH(固) 60.0g/L
サイゾールLM(第一工業製薬(株)製キレート剤) 0.5g/L
ラクトーゲンLS(洛東化成(株)製酸化糊抜剤) 15.0g/L
*測定浴 200cc
[測定方法]
JIS−2518(空気導入法)に準拠し、以下の方法で評価した。
*起泡性…1リットルメスシリンダーに試験浴200mlを入れ、空気導入ポンプで1000ml/10秒で空気を導入し、泡が1リットルの目盛までに至る時間を測定した。
[Bath composition]
Scouring agent (active ingredient) 1.5g / L
NaOH (solid) 60.0 g / L
Saisol LM (Daiichi Kogyo Seiyaku Co., Ltd. chelating agent) 0.5g / L
Lactogen LS (Oxidizing agent remover manufactured by Nitto Kasei Co., Ltd.) 15.0 g / L
* Measurement bath 200cc
[Measuring method]
Based on JIS-2518 (air introduction method), the following method evaluated.
* Foaming property: 200 ml of a test bath was placed in a 1 liter graduated cylinder, air was introduced at 1000 ml / 10 seconds with an air introduction pump, and the time until the foam reached the scale of 1 liter was measured.
*消泡性…泡が1リットルの目盛まで到達後、空気導入を停止し、30秒毎の泡残存量を測定した。 * Defoaming property: After the foam reached the scale of 1 liter, the introduction of air was stopped, and the remaining amount of foam was measured every 30 seconds.
4.低温安定性
精練剤組成物を調製し、常温と低温(−5℃恒温槽:24時間放置後)で製品の状態を目視で確認し、○〜×(○:流動性があり、粘度約800mPa・s以下、×:流動性がなく、粘度約1000mPa・s以上)で評価した。結果を表6に示す。
4). Low temperature stability A scouring agent composition was prepared, and the state of the product was visually confirmed at room temperature and low temperature (-5 ° C. constant temperature bath: after standing for 24 hours), ○ to × (○: fluidity, viscosity of about 800 mPa)・ S or less, x: no fluidity, viscosity of about 1000 mPa · s or more). The results are shown in Table 6.
5.生分解性評価
化審法分解度試験に基づき、BOD法による生分解性試験を実施した。一般には、生分解率が60%以上とすれば良好と判断されるが、本試験では、生分解率が80%以上のものを◎、70〜79%のものを○、60〜69%のものを△、59%以下のものを×とした。結果を表7に示す。
5. Biodegradability evaluation Based on the Chemical Substances Control Law Degradability Test, a biodegradability test was conducted by the BOD method. In general, it is judged that the biodegradation rate is 60% or more, but in this test, the biodegradation rate is 80% or more, ◎, 70-79% ○, 60-69%. Those with Δ and those with 59% or less were marked with ×. The results are shown in Table 7.
上記結果から分かるように、本発明の精練剤組成物は、成分(A)を含有することにより、従来の精練剤がNaOH60g/L前後で分離を起こしていたのに対し、NaOH 80〜100g/Lまで濃度アップしても分離を起こさず高アルカリ条件下においても安定で、且つ顕著な浸透力と精練性を発揮する。 As can be seen from the above results, the scouring agent composition of the present invention contains component (A), so that the conventional scouring agent caused separation around NaOH 60 g / L, whereas NaOH 80 to 100 g / L. Even if the concentration is increased to L, separation does not occur, it is stable even under highly alkaline conditions, and it exhibits remarkable penetrating power and scouring properties.
また、成分(B)を用いることで、綿キャンバス法におけるキャンバス生機の浸透性、精練布の再湿潤性が従来よりもはるかに向上し、それに伴い精練性が良くなった。これは、精練後の生地の再湿潤性をみれば明らかである。残脂率も従来以上に低く、脱脂力がアップした。また、C9のノニルフェノールエトキシレートや化学物質排出把握管理促進法(PRTR法)該当物質であるC12〜15のエトキシレートを含まない非イオン界面活性剤で構成しているため、環境にも優しく、生分解性がより高いため排水への負荷が少なく、使用者が安心して処理できる。 Further, by using the component (B), the penetrability of the canvas raw machine and the rewetability of the scouring cloth in the cotton canvas method are much improved than before, and the scouring property is improved accordingly. This is apparent from the rewetability of the dough after scouring. The residual fat rate was also lower than before and the degreasing power was improved. In addition, because it is composed of nonionic surfactants that do not contain C9 nonylphenol ethoxylate and C12-15 ethoxylate, which is a chemical substance emission control management promotion method (PRTR method), Because it is more degradable, there is less load on the waste water and the user can handle it with peace of mind.
また、成分(C)を配合することで低泡化及び耐アルカリ性能の向上が図れる。 Moreover, a foam reduction and the improvement of alkali-proof performance can be aimed at by mix | blending a component (C).
加えて成分(D)のグリコール類を配合することで、高濃度にも関わらず減粘可能であり、また成分(C)では不十分な消泡性能を、高級アルコール系、自己乳化型シリコン系等の消泡剤を含有することにより、低泡性能を付与することができる。 In addition, by blending the component (D) glycols, the viscosity can be reduced despite the high concentration, and the component (C) has insufficient defoaming performance, higher alcohol type, self-emulsifying silicone type By containing an antifoaming agent such as, it is possible to impart low foaming performance.
本発明の精練剤組成物はアルカリ高濃度での製品安定性が良いことから、原綿の精練等の高アルカリ条件をはじめ、ポリエステル、その他混紡生機等あらゆる条件下で精練剤の安定性を気にすることなく精練することが可能となる。また、高濃度アルカリストックタンクで、貯蔵、自動供給ができるという特長や、高速に流れる生地に素早く浸透し、高い精練効果が得られるという特長も有する。さらに、生分解性が良好であり、ノニルフェノールフリー、PRTR非該当物質であることから、法規制に則した環境に優しい精練剤であり、河川を汚染しないメリットがある。 Since the scouring agent composition of the present invention has good product stability at a high alkali concentration, the stability of the scouring agent is considered under all conditions such as high alkali conditions such as scouring raw cotton, polyester, and other blended spinning machines. It becomes possible to refine without doing. In addition, it has the advantage that it can be stored and automatically supplied in a high concentration alkali stock tank, and it can quickly penetrate into dough flowing at high speed to obtain a high scouring effect. Furthermore, it is a biodegradable, nonylphenol-free, PRTR non-corresponding substance, so it is an environmentally friendly scouring agent that complies with laws and regulations and has the advantage of not polluting rivers.
Claims (1)
(B)下記一般式(3)で表されるポリオキシアルキレンアルキルエーテル型非イオン活性剤、及び
(C)炭素数8〜22の飽和脂肪酸又は不飽和脂肪酸、及び/又はその塩
を含有してなることを特徴とする繊維用精練剤組成物。
R3−O−[(PO)p−(EO)q]−H …(3)
(式(3)中、R3は炭素数が8〜20の直鎖或いは分岐のアルコール残基を示し、POはオキシプロピレン基、EOはオキシエチレン基を示し、p,qは、p=0〜2、q=1〜8の数字を示す。POとEOの付加形態はランダム付加、ブロック付加又はこれらの混合付加である。但し、PRTR法により規制されるC12〜15のエトキシレートを除く。) (A) It is represented by the following general formula (1), derived from a nonionic surfactant having a polydispersity (Mw / Mn) of 1.01 to 1.20, and represented by the following general formula (2). Phosphate esters and / or salts thereof,
(B) a polyoxyalkylene alkyl ether type nonionic active agent represented by the following general formula (3), and (C) a saturated or unsaturated fatty acid having 8 to 22 carbon atoms and / or a salt thereof. A fiber scouring agent composition characterized by comprising:
R 3 -O - [(PO) p- (EO) q] -H ... (3)
(In Formula (3), R 3 represents a linear or branched alcohol residue having 8 to 20 carbon atoms, PO represents an oxypropylene group, EO represents an oxyethylene group, and p and q represent p = 0. -2, q = 1 to 8. The addition form of PO and EO is random addition, block addition, or mixed addition of these, except for C12-15 ethoxylates regulated by the PRTR method. )
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Cited By (3)
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---|---|---|---|---|
KR101223340B1 (en) | 2009-12-31 | 2013-01-16 | 주식회사 효성 | Non-silicon based spandex spinning oil composition and spandex fiber prepared by using the same |
CN102995468A (en) * | 2012-11-26 | 2013-03-27 | 浙江安诺其助剂有限公司 | Polyester fabric dyeing degreaser and preparation method thereof |
CN116043555A (en) * | 2023-01-05 | 2023-05-02 | 江苏新瑞贝科技股份有限公司 | Bio-based super-soft pretreatment scouring agent and preparation method and application thereof |
Families Citing this family (1)
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CN106498723A (en) * | 2016-10-14 | 2017-03-15 | 无锡市华诚印染剂厂 | A kind of low alveolitoid water solublity refining agent |
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JPH09324364A (en) * | 1996-06-07 | 1997-12-16 | Kao Corp | Scouring agent composition for fiber |
JPH11131091A (en) * | 1997-09-01 | 1999-05-18 | Kao Corp | Scouring agent composition for fiber |
JP2001003263A (en) * | 1999-06-21 | 2001-01-09 | Sanyo Chem Ind Ltd | Scouring agent for fiber |
JP4087393B2 (en) * | 2005-05-31 | 2008-05-21 | 第一工業製薬株式会社 | Fiber scouring agent composition |
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JPH09324364A (en) * | 1996-06-07 | 1997-12-16 | Kao Corp | Scouring agent composition for fiber |
JPH11131091A (en) * | 1997-09-01 | 1999-05-18 | Kao Corp | Scouring agent composition for fiber |
JP2001003263A (en) * | 1999-06-21 | 2001-01-09 | Sanyo Chem Ind Ltd | Scouring agent for fiber |
JP4087393B2 (en) * | 2005-05-31 | 2008-05-21 | 第一工業製薬株式会社 | Fiber scouring agent composition |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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KR101223340B1 (en) | 2009-12-31 | 2013-01-16 | 주식회사 효성 | Non-silicon based spandex spinning oil composition and spandex fiber prepared by using the same |
CN102995468A (en) * | 2012-11-26 | 2013-03-27 | 浙江安诺其助剂有限公司 | Polyester fabric dyeing degreaser and preparation method thereof |
CN116043555A (en) * | 2023-01-05 | 2023-05-02 | 江苏新瑞贝科技股份有限公司 | Bio-based super-soft pretreatment scouring agent and preparation method and application thereof |
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