CN101680158A - 液体织物调理剂组合物和使用方法 - Google Patents
液体织物调理剂组合物和使用方法 Download PDFInfo
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- CN101680158A CN101680158A CN200880018588A CN200880018588A CN101680158A CN 101680158 A CN101680158 A CN 101680158A CN 200880018588 A CN200880018588 A CN 200880018588A CN 200880018588 A CN200880018588 A CN 200880018588A CN 101680158 A CN101680158 A CN 101680158A
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- Prior art keywords
- fabric
- agent
- quaternary ammonium
- conditioning
- composition
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- 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
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
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- 229920002647 polyamide Polymers 0.000 description 1
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- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
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- PHXATPHONSXBIL-UHFFFAOYSA-N xi-gamma-Undecalactone Chemical group CCCCCCCC1CCC(=O)O1 PHXATPHONSXBIL-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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- C11D1/62—Quaternary ammonium compounds
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- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
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- C11D3/30—Amines; Substituted amines ; Quaternized amines
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
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- C11D3/32—Amides; Substituted amides
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- C11D3/32—Amides; Substituted amides
- C11D3/323—Amides; Substituted amides urea or derivatives thereof
-
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- C11D3/3707—Polyethers, e.g. polyalkyleneoxides
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- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
- C11D3/3742—Nitrogen containing silicones
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- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
- D06L1/12—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using aqueous solvents
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- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
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- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
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- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
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Abstract
本发明提供织物的调理方法,包括让织物与含氨基官能化硅酮和季铵的液态组合物接触,并在200华氏度或更高下干燥所述织物。本发明还提供织物的调理方法,包括在具有大于10的洗涤pH值的清洁剂中洗涤织物,让织物与含氨基官能化硅酮和季铵的液态组合物接触,并在小于200华氏度下干燥所述织物。本发明进一步提供织物的调理方法,其中将柔软性、抗静电和抗皱性能赋予该织物,经调理的织物在工业和公共设施条件中抗泛黄,洗涤pH值大于9和/或织物温度是200华氏度或更大。
Description
发明领域
本发明涉及在工业和公共设施用织物护理条件下处理纺织品以赋予柔软性同时减少泛黄的方法。更具体地说,本发明涉及用含氨基官能化硅酮和季铵的织物调理组合物处理纺织品的方法。
发明背景
使用含主要量的水、次要量的织物软化剂和少量的任选成分例如芳香剂、着色剂、防腐剂和稳定剂的织物软化组合物当今在消费和居住领域中已变得普遍。此类组合物是水悬浮液或乳液,适宜地将它们添加到居民洗涤机的漂洗浴中以改进经洗涤织物的手感。
然而,找到在工业和公共设施环境中出现的苛刻条件中仍有效但对织物不造成负面影响的类似作用的液态织物软化组合物是完全不同的情况。即,在工业领域中,织物软化剂一般引起织物的过早泛黄。术语“工业和公共设施”是指操作位于服务性行业中,包括但不限于旅馆、汽车旅店、医院、疗养院、饭店、健身俱乐部等。由于许多因素,与消费或居住领域相比,织物在工业和公共设施环境中暴露于相当大苛刻的条件下。在工业和公共设施领域中,亚麻布中出现的污物水平比居住或消费领域中的高得多。因而,工业和公共设施环境中使用的清洁剂与消费领域中不太碱性的那些相比更具碱性。居住领域中的洗涤循环具有接近中性的pH值,而工业和公共设施领域中的洗涤循环具有大于大约9的pH值。
造成消费者洗涤和工业和公共设施环境中的洗涤之间操作条件方面的总体差异的另一种因素是在工业和公共设施领域中必须在比消费者市场所容许的更短时间内处理高容量的洗涤物。在此类操作中的干燥器以比消费或居住市场中出现的那些高得多的温度操作。据预期,工业或商业干燥器在提供通常在大约180华氏度至大约270华氏度的织物温度的水平下操作,而消费或居住用干燥器通常在大约120-大约160华氏度的最大织物温度下操作。应当理解,消费或居住用干燥器的温度通常根据正干燥的物品而改变。虽然如此,居住用干燥器不具有在工业和公共设施领域中出现的高温下操作的能力。工业和公共设施用干燥器在大约180华氏度至大约270华氏度,更优选大约220华氏度至大约260华氏度,最优选大约240华氏度至大约260华氏度的最大织物温度的范围内操作。
许多不同类型的织物软化剂用于为居住或消费市场设计的市售织物柔软剂。它们包括季铵。含季铵的织物柔软剂在接近中性pH值的洗剂中非常好地工作并降低居住市场的干燥器温度条件。含季铵化合物的软化剂赋予洗涤物柔软性并且在居住和消费领域中是非泛黄的。这些品质是纺织品例如纤维和织物(纺织和无纺)的性能的高度希望的组合。柔软性是指由用户经由它们的触觉认知为柔软的质量。这种触觉可认知的柔软性可以具有,但不限于,回弹力、挠性、蓬松性、滑爽度和光滑度和主观描述例如″感觉如同丝绸或法兰绒″的特性。
相反,申请人发现季铵化合物当在工业和公共设施领域中出现的苛刻条件中使用时引起织物不可接受的泛黄。公共设施和工业领域中的大多数亚麻布是白色的。如可以预期的那样,此种泛黄在白色亚麻布的情况下明显得多。泛黄充其量给与亚麻布不清洁或令人讨厌的外观。因而,使用引起泛黄的季铵织物调理剂可以提供美好的感觉,但是缩短亚麻布的总寿命,因为必须在到达其使用寿命之前摈弃亚麻布。在着色亚麻布的情况下,泛黄是不太明显的,但是季铵化合物随着时间引起颜色的暗淡。容易领会的是,希望提供不引起经重复洗涤和干燥的织物的显著泛黄或暗淡的织物调理剂。此外,通常希望经干燥的白色洗涤物保留白色,甚至在多个干燥循环之后仍如此。即,希望织物在织物调理组合物存在下在重复的干燥循环之后不泛黄或暗淡。
申请人发现,在工业和公共设施领域的较高碱性和较高温度条件中,将氨基硅酮或氨基官能化硅酮添加到含季铵的织物调理组合物中不改变某些织物调理性能。申请人惊奇地发现,织物调理组合物中组分的这种组合使洗涤物在工业和公共设施条件中显示减少的泛黄或暗淡,而不会不利地影响软化性能。
包括抗皱剂以提供抗皱性能是本领域中已知的。示例性抗皱剂可以包括含硅氧烷或硅酮的化合物。虽然在织物调理组合物中包括硅酮以帮助抗皱是本领域中已知的,但是此前还不知道添加含氨基官能团的硅酮以便用于高温干燥器例如工业和公共设施环境中使用的高温干燥器。此外,也不知道将氨基官能化硅酮添加到织物调理组合物中以减少织物通常在工业和公共设施领域中经历的由于极端条件而引起的泛黄。也不知道将硅酮包括在织物调理组合物中以减少当使用高碱性清洁剂时织物的泛黄。
经由各种方法递送织物调理或织物软化组合物。液态软化剂在居住市场中是常用的,干燥器片也是这样。又一种递送方法是经由固体块。虽然所有递送方法有效将软化剂递送给织物,但是据信液体递送方法导致软化剂在织物上的更高的沉积水平。在较高的软化剂水平下,存在提高的发生泛黄的机率。
发明概述
本发明涉及在工业或公共设施洗涤操作的漂清循环期间调理织物的组合物和方法。本发明的组合物于是用来赋予经洗涤织物当触摸时光滑、柔顺和似绒毛(即柔软)的质地或手感此外还赋予织物降低的获取和/或保留静电荷的倾向(即静电控制),和减少通常称为泛黄的褪色,特别是当在高碱性清洁剂中洗涤和/或在自动干燥器中在工业和公共设施条件下干燥织物时。
本发明涉及用于工业和公共设施织物护理操作的含胺官能化硅酮化合物和季铵化合物的液态织物护理组合物或织物调理剂。本发明进一步涉及织物的处理方法,包括在工业和公共设施织物护理操作中用含胺官能化硅酮化合物和季铵化合物的组合物调理该织物。
令人惊奇地,本发明方法赋予至少相当于商业或居住软化剂的柔软性并提供不泛黄和/或具有降低的在多个洗涤/干燥循环内使经处理的纺织品褪色的倾向的附加利益。本发明提供处理经历了工业和公共设施领域的高热干燥器的纺织品的方法,该方法包括用含氨基官能化硅酮和季铵的组合物处理该纺织品。
然而,本发明组合物的调理益处不限于软化和减少的泛黄。本发明的益处可以包括抗静电性能以及抗皱性能。所述织物调理剂组合物可以包括以下物质中的至少一种:抗静电剂、抗皱剂、改进的吸收性、染料转印抑制/颜色保护剂、除气/气味捕获剂、污物阻挡/污物释放剂、易干燥、紫外光防护剂、香料、消毒剂、杀菌剂、防水剂、驱虫剂、抗起球剂、酸化剂、除霉剂、酶、淀粉、漂白剂、光学增白剂、抗过敏剂和它们的混合物。
附图简述
图1示出了为本发明的对照样品和三种组合物的b*值对循环#绘图的图解。
发明详述
织物调理剂组合物
季铵组分
本发明的织物调理剂组合物的组分是称为季铵化合物的一般类型的织物软化剂组分。示例性季铵化合物包括烷基化的季铵化合物、环或环状季铵化合物、芳族季铵化合物、二季铵化合物、烷氧基化的季铵化合物、酰氨基胺季铵化合物、酯季铵化合物和其混合物。
示例性的烷基化季铵化合物包括具有含6-24个碳原子的烷基的铵化合物。示例性的烷基化季铵化合物包括单烷基三甲基季铵化合物、单甲基三烷基季铵化合物和二烷基二甲基季铵化合物。烷基化的季铵化合物的实例可以品名AdogenTM、和商购。烷基可以是脂族和饱和或不饱和或直链或支链的C8-C22基团或C8-C18基团或C12-C22基团,烷基,苄基,烷基醚丙基,氢化牛脂基,椰油基,硬脂基,棕榈基和大豆基。示例性的环或环状季铵化合物包括咪唑啉鎓季铵化合物并可以品名获得。示例性的咪唑啉鎓季铵化合物包括甲基-1-氢化牛脂酰氨基乙基-2-氢化牛脂咪唑啉鎓-甲基硫酸盐,甲基-1-牛脂酰氨基乙基-2-牛脂咪唑啉鎓-甲基硫酸盐,甲基-1-油烯基酰氨基乙基-2-油烯基咪唑啉鎓-甲基硫酸盐和1-亚乙基双(2-牛脂基,1-甲基,咪唑啉鎓-甲基硫酸盐)。示例性的芳族季铵化合物包括结构中具有至少一个苯环的那些化合物。示例性的芳族季铵化合物包括二甲基烷基苄基季铵化合物、单甲基二烷基苄基季铵化合物、三甲基苄基季铵化合物和三烷基苄基季铵化合物。烷基可以含有约6-约24个碳原子,可以含有约10-约18个碳原子,可以是硬脂基或氢化牛脂基。示例性的芳族季铵化合物可以品名和获得。芳族季铵化合物可以包括多个苄基。二季铵化合物包括具有至少两个季铵基的那些化合物。示例性的二季铵化合物是N-牛脂五甲基丙烷二氯化二铵并可以品名Adogen 477得到。示例性的烷氧基化季铵化合物包括甲基二烷氧基烷基季铵化合物、三烷氧基烷基季铵化合物、三烷氧基甲基季铵化合物、二甲基烷氧基烷基季铵化合物和三甲基烷氧基季铵化合物。烷基可以含有约6-约24个碳原子,烷氧基可以含有约1-约50个烷氧基单元,其中每一烷氧基单元含有约2-约3个碳原子。示例性的烷氧基化季铵化合物可以品名和获得。示例性酰氨基胺季铵化合物包括二酰氨基胺季铵化合物。示例性二酰氨基胺季铵化合物可以品名(可从Stepan获得)或(可从EvonikIndustries获得)获得。可以根据本发明使用的示例性的酰氨基胺季铵化合物是甲基-双(牛脂酰氨乙基)-2-羟乙基铵甲基硫酸盐、甲基双(油烯基酰氨基乙基)-2-羟乙基铵甲基硫酸盐和甲基双(氢化牛脂酰氨基乙基)-2-羟乙基铵甲基硫酸盐。示例性的酯季化合物可以品名StephantexTM获得。
季铵化合物可以包括任何平衡离子,这种平衡离子允许所述组分使用时赋予根据本发明的织物软化性能。示例性的平衡离子包括氯离子、甲基硫酸根、乙基硫酸根和硫酸根。
在本发明的某些液态漂洗添加组合物中,活性季铵组分的量可以按重量计为总组合物的大约2%-大约35%,大约4%-大约27%,和总组合物的大约6%-大约25%。
本文所使用的术语“活性”是指存在于组合物中的组分的量。如本领域技术人员将认可的那样,本发明的许多组分作为乳液销售并且制造商将为买方提供包括活性成分百分率的数据。仅作为举例,如果最终组合物的100%由乳液X组成并且如果乳液X含有60%活性组分X,则我们将说最终组合物含有60%活性组分X。
硅酮组分
本发明的织物调理组合物的另一种组分是硅酮化合物。本发明的硅酮可以是直链或支化的结构化硅酮聚合物。本发明的硅酮可以是单一聚合物或聚合物的混合物。适合的硅酮可以从Wacker Chemical获得并且包括但不限于是高分子量聚硅氧烷的FC 201和是预交联硅酮橡胶的FC 205。
本发明的织物调理组合物的另一种组分是氨基官能化硅酮。氨基官能化硅酮在本文也称作氨基官能化硅酮。本发明的氨基官能化硅酮可以是直链或支化的结构化氨基官能化硅酮聚合物。本发明的氨基官能化硅酮可以是单一聚合物或聚合物的混合物,包括其中聚合物之一不包含氨基官能团,例如聚二甲基硅氧烷聚合物的聚合物混合物。适合的氨基官能化硅酮可以从Wacker获得并且包括FC 203,它是含聚醚基的氨基官能化硅酮。
通常按大约0.2wt%至大约12wt%的水平将活性氨基官能化硅酮化合物结合到本发明组合物中。更优选,按大约0.5wt%-大约10wt%的水平包括氨基官能化硅酮组分。最优选,按大约1wt%-大约6wt%的水平包括氨基官能化硅酮组分。
本发明可以呈许多形式中的任一种。它可以呈可稀释织物调理剂的形式,该可稀释织物调理剂可以是液体、表面活性剂结构化的液体、颗粒、喷雾干燥的或干共混的粉末、片剂、糊剂、模塑固体或本领域技术人员已知的任何其它织物调理剂形式。″可稀释的织物调理″组合物对于本公开内容的目的定义为旨在通过用水或非水溶剂按大于100∶1的比例稀释来使用的产物,以制备适合于处理纺织品并赋予它们一种或多种调理益处的液体。水溶性片材或小袋也预期为本发明的潜在形式。它们可以在各种名称下销售并用于许多目的。对于所有情况,然而,这些组合物旨在通过用水或非水溶剂按大于100∶1的比例稀释来使用,以形成适合于处理织物的液体。
本发明的尤其优选的形式包括调理剂产品,特别是为液体或粉末,打算在洗涤循环或最终漂洗期间应用为织物软化剂。对于本公开内容的目的,术语′织物软化剂″、″织物调理剂″或″织物调理剂″应当理解为是指添加到洗涤过程的洗涤或漂清循环中以专门或主要用于提供一种或多种调理益处的工业产品。
它也可以呈织物软化剂的形式,这种织物软化剂旨在应用于制品而无需显著稀释和作为本领域技术人员已知的任何形式销售作为将此种织物柔软剂递送至工业和公共设施市场的潜在介质。直接应用于织物的喷涂物,例如气溶胶或泵喷涂物也认为在本公开内容的范围内。然而,这些实例是出于说明性目的而提供的并不打算限制本发明的范围。
可以根据本发明加工的织物包括可以在工业干燥器中加工以除去水的任何纺织品或织物材料。在工业洗涤操作的情况下,织物通常称为洗涤物。虽然在调理″织物″的范围中表征本发明,但是应当理解可以类似地处理包括织物的物品或制品。另外,应当理解,物品例如毛巾、片材和服装通常称为洗涤物并且是织物的类型。通过本发明方法的处理受益的纺织品的示例是(i)天然纤维例如棉、亚麻、丝绸和羊毛;(ii)合成纤维例如聚酯、聚酰胺、聚丙烯腈、聚乙烯、聚丙烯和聚氨酯;和(iii)无机纤维例如玻璃纤维和碳纤维。优选地,通过本发明方法处理的纺织品是由上述纤维材料或其混纺物中的任一种制备的织物。最优选地,纺织品是含棉织物例如棉或棉-聚酯混纺物。可以通过织物处理组合物处理的其它洗涤物品包括运动鞋、附件、填塞动物、刷子、毡、帽子、手套、外衣、帆布、帐篷和窗帘。然而,由于工业干燥器施加的苛刻条件,可用于根据本发明调理的洗涤物品必须经得起工业干燥器中出现的高温条件。
其中可以使用根据本发明的织物软化剂组合物的干燥器包括使用热和/或搅动和/或空气流从洗涤物除去水的任何类型的干燥器。示例性干燥器包括翻滚型干燥器,其中洗涤物提供在转鼓内,该转鼓使洗涤物在干燥器的操作期间翻滚。翻滚型干燥器常用于工业和公共设施领域洗涤操作中。
本发明的组合物尤其可用于工业和公共设施环境中出现的苛刻条件。术语“工业和公共设施”是指操作位于服务性行业中,包括但不限于旅馆、汽车旅店、饭店、健身俱乐部、保健场所等。在此类操作中的干燥器以比消费或居住市场中出现的那些高得多的温度操作。据预期,工业或商业干燥器在通常提供在大约180华氏度至大约270华氏度的最大织物温度下操作,并且消费或居住用干燥器通常在大约120-大约160华氏度的最大织物温度下操作。工业和公共设施用干燥器在大约180华氏度至大约270华氏度,更优选大约220华氏度至大约260华氏度,最优选大约240华氏度至大约260华氏度的范围内操作。
最大织物温度是通过将温度监测条放入潮湿枕头套中获得的。温度监测条作为可以从Paper Thermometer Co,Inc.获得的Thermolabel销售。然后将该枕头套放入装入了潮湿洗涤物的翻滚干燥器中。一旦装入物干燥,就从该枕头套取出温度监测条并且最大记录温度是最大织物温度。
通常希望经干燥的洗涤物保留白色,甚至在多个干燥循环之后仍如此。即,希望织物在织物调理组合物存在下在重复的干燥循环之后不泛黄。白色保留性可以根据b*测量,例如,Hunter Lab仪器。一般而言,希望用本发明组合物处理并在高温下干燥的织物在15个洗涤、软化和干燥循环之后显示较低的Δb(较少黄色)。Δb*=b*最终-b*初始。
通常希望使用本发明的织物调理组合物在干燥器中处理的织物具有柔软性优先选择,该柔软性优先选择至少与市售液态织物软化剂显示的柔软性优先选择相当。柔软性优先选择源自通过用根据本发明的织物处理组合物或用市售液态织物软化剂处理的织物(例如毛巾)的一一对比的小组试验。一般而言,希望得自所述织物处理组合物的柔软性优先选择优于市售液态织物软化剂显示的柔软性优先选择。
可以将相容的助剂添加到这里的组合物中用于它们已知的目的。这些助剂包括,但不限于,粘度控制剂、芳香剂、乳化剂、防腐剂、抗氧化剂、杀细菌剂、杀真菌剂、着色剂、染料、荧光染料、增白剂、不透明剂、冻融控制剂、污物释放剂和收缩控制剂,及其它提供熨烫容易性的试剂(例如,淀粉等)。如果使用,这些助剂以它们正常的水平添加,一般而言,每种占优选的液态组合物的至多大约5wt%。
织物调理组合物(当它包括抗静电剂时)可以产生与没有经历处理的织物相比时的静电降低。已经注意到,与市售液态软化剂相比,使用根据本发明的织物调理组合物处理的织物显示更恒定的静电降低百分率。
织物调理组合物可以包括抗静电剂例如洗涤物干燥工业中常用的那些以提供抗静电性能。示例性的抗静电剂包括软化剂范围中所提及的那些季化合物。因此,包括季基的调理剂的使用利益是它们还可以提供抗静电性能。
织物调理组合物可以包括气味捕获剂。一般而言,气味捕获剂认为通过捕获或包围提供气味的某些分子而发挥作用。示例性的气味捕获剂包括环糊精,和蓖麻醇酸锌。
织物调理组合物可以包括纤维保护剂,它涂覆织物的纤维以降低或防止纤维的崩解和/或降解。示例性的纤维保护剂包括纤维素质聚合物。
织物调理组合物可以包括用于涂覆织物的纤维的颜色保护剂以降低染料从织物逃逸到水中的倾向。示例性的颜色保护剂包括季铵化合物和表面活性剂。示例性的季铵颜色保护剂包括二-(nortallow羧乙基)羟乙基甲基铵甲基硫酸盐,它可以品名Varisoft WE 21CP从Evonik-Goldschmidt Corporation获得。示例性的表面活性剂颜色保护剂可以品名Varisoft CCS-1从Evonik-Goldschmidt Corporation获得。示例性的阳离子聚合物颜色保护剂可以品名Tinofix CL从CIBA获得。其它颜色保护剂可以品名Color Care Additive DFC9、ThiotanTR、Nylofixan P-Liquid、Polymer VRN、Cartaretin F-4和CartaretinF-23从Clariant;以品名EXP 3973Polymer从Alco和以品名Coltide从Croda获得。
织物调理组合物可以包括污物释放剂,它们可以提供用于涂覆织物的纤维以降低污物附着纤维的倾向。示例性的污物释放剂包括聚合物例如可以品名Repel-O-Tex SRP6和Repel-O-Tex PF594从Rhodia;以品名TexaCare 100和TexaCare 240从Clariant和以品名SokalanHP22从BASF获得的那些。
织物调理组合物可以包括为织物赋予发荧光化合物的光学增白剂。一般而言,发荧光化合物具有提供带蓝色色调的倾向,该带蓝色色调可以认知为对织物赋予亮色。示例性的光学增白剂包括二苯乙烯衍生物、联苯衍生物和香豆素衍生物。示例性的联苯衍生物是二苯乙烯基联苯二磺酸钠盐。示例性的二苯乙烯衍生物包括氰尿酰氯/二氨基二苯乙烯二磺酸钠盐。示例性的香豆素衍生物包括二乙基氨基香豆素。示例性的光学增白剂可以品名Tinopal 5BM-GX、Tinopal CBS-CL、Tinopal CBS-X和Tinopal AMS-GX从CIBA获得。然而,应当指出,当在提高的干燥器温度下在不添加光学增白剂的情况下使用本发明组合物时,观察到泛黄的总体减少。
织物调理组合物可以包括UV保护剂以为织物提供增强的UV保护。在服装的情况下,据信通过对服装施用UV保护剂,可以降低紫外辐射对提供在该服装下方的皮肤的有害影响。随着服装在重量上变得更轻,UV光具有更大的穿透服装的倾向并且在该服装下方的皮肤可能变得晒黑。示例性的UV保护剂包括得自CIBA的Tinosorb FD。
织物调理组合物可以包括抗起球剂,它作用在纤维的从纤维伸出或离开的部分上。抗起球剂可以作为酶例如纤维素酶获得。示例性的纤维素酶抗起球剂可以品名Puradex从Genencor和以品名Endolase和Carezyme从Novozyme获得。
织物调理组合物可以包括防水剂,它们可以施用于织物上以增强防水性能。示例性的防水剂包括全氟丙烯酸酯共聚物、烃蜡和聚硅氧烷。
织物调理组合物可以包括杀菌剂和/或消毒剂。示例性的消毒和/或杀菌剂包括过酸或过氧酸。其它示例性的消毒和/或杀菌剂包括季铵化合物例如烷基二甲基苄基氯化铵、烷基二甲基乙基苄基氯化铵、辛基癸基二甲基氯化铵、二辛基二甲基氯化铵和二癸基二甲基氯化铵。
织物调理组合物可以包括酸化剂,它们中和可能存在于织物上的残留碱。酸化剂可以用来控制织物的pH值。酸化剂可以包括酸类例如饱和脂肪酸、二元羧酸和三元羧酸。酸化剂可以包括无机酸类例如盐酸、硫酸、磷酸和HFS酸等。
织物调理组合物可以包括驱虫剂例如驱蚊剂和驱/阻床虱剂。示例性的驱虫剂是DEET。示例性的阻床虱剂包括氯菊酯、萘、Xylol和氨。另外,织物调理组合物可以包括杀死霉菌的防霉剂和降低某些织物上存在的过敏症可能性和/或提供防细菌性能的抗过敏剂。
粘度控制剂性质上可以是有机或无机。有机粘度调节剂的实例是脂肪酸和酯、脂肪醇和水混容性溶剂例如短链醇。无机粘度控制剂的实例是水溶性的可电离盐。可以使用各种各样的可电离盐。适合的盐的实例是元素周期表第IA和IIA族金属的卤化物,例如氯化钙、氯化镁、氯化钠、溴化钾和氯化锂。氯化钙是优选的。这些可电离盐在将成分混合以制备本文的液体组合物和稍后以获得所需粘度的过程中是尤其有用的。所使用的可电离盐的量取决于这些组合物中使用的活性成分的量并且可以根据配剂师的意愿加以调节。用来控制组合物粘度的盐的典型水平按重量计是大约20-大约6,000份/百万份(ppm),优选大约20-大约4,000ppm组合物。
还可以作为表面活性剂浓度助剂或加强其效果的无机粘度/可分散性控制剂包括水溶性、可电离盐,它们也可以任选地结合到本发明组合物中。可以使用各种各样的可电离盐。适合的盐的实例是元素周期表第IA和IIA族金属的卤化物,例如氯化钙、氯化镁、氯化钠、溴化钾和氯化锂。这些可电离盐在将成分混合以制备本文的组合物和稍后以获得所需粘度的过程中是尤其有用的。所使用的可电离盐的量取决于这些组合物中使用的活性成分的量并且可以根据配剂师的意愿加以调节。用来控制组合物粘度的盐的典型水平按重量计是大约20-大约20,000份/百万份(ppm),优选大约20-大约11,000ppm组合物。
可以将稳定剂添加到本发明的织物调理组合物中。稳定剂例如过氧化氢用于使防腐剂例如Kathon CG/ICP的长期保存限期稳定性稳定。稳定剂可以包括在本发明组合物中以控制防腐剂的降解并且可以为大约0.05wt%至大约0.1wt%。可以按大约0.05wt%至大约0.15wt%将防腐剂例如可以从Rohm and Haas获得的Kathon CG/ICP添加到本发明组合物中。可用于本发明组合物的,可以要求或可以不要求使用稳定剂的其它防腐剂包括但不限于可以从Dow获得的Ucaricide、可以从Rohm&Haas获得的Neolone M-10和同样可以从Rohm&Haas获得的Korolone B119。
织物调理组合物还可以包括芳香剂。虽然前香料可以单独地使用和简单地与基本的织物软化成分(最值得注意的是表面活性剂)混合,但是它们也可以令人希望地结合到三组分配方中,这种配方组合(a)结合一种或多种合成纤维软化剂的非加香织物软化基料,(b)根据本发明的一种或多种前芳香P-酮酯和(c)完全配制的香料。后者提供合乎需要的包装内和使用中(洗涤时间)的香料,而前香料为洗涤的纺织品纤维提供长期香味。
在配制本发明的织物调理组合物时,可以使用天然或合成来源的许多已知的有气味成分制备完全配制的香料。天然原料物质的范围可以不但涵盖容易挥发性,而且涵盖中等挥发性和略微挥发性组分并且合成物的范围可以包括实际上各类芳香物的代表,如将从以下示例性汇编易见的那些:天然产物,例如树苔净油(tree moss absolute)、罗勒油、柑橘果油(例如香柠檬油、橘子油等)、mastix absolute、香桃木油、玫瑰草油、广藿香油、巴拉圭橙叶油、苦艾油,醇例如金合欢醇、香叶醇、沉香醇、橙花醇、苯乙醇、左旋香茅醇、肉桂醇,醛例如柠檬醛、HelionalTM、α-己基-肉桂醛、羟基香茅醛、LilialTM(对叔丁基-α-甲基二氢肉桂醛)、甲基壬基乙醛,酮例如烯丙基紫罗酮、α-紫罗酮、β-紫罗酮、isoraldein(异甲基-α-紫罗酮)、甲基紫罗酮,酯例如苯氧乙酸烯丙酯、水杨酸苄酯、丙酸肉桂酯、香茅醇乙酸酯、citronellyl ethoxolate、乙酸癸酯、乙酸二甲基苄基甲醇酯、丁酸二甲基苄基甲醇酯、乙酰乙酸乙酯、乙酰基乙酸乙酯、异丁酸己烯基酯、乙酸里哪酯、二氢茉莉酮酸甲酯、乙酸苏合香酯、乙酸香根酯等,内酯例如γ-十一烷酸内酯,香料中通常使用的各种组分,例如麝香酮、吲哚、对孟烷-8-硫醇-3-酮和甲基-丁子香酚。同样,可以将本领域中已知的任何常规芳香缩醛或缩酮添加到本发明组合物中作为常规配制的芳香剂的任选组分。此类常规芳香缩醛和缩酮包括众所周知的甲基和乙基缩醛和缩酮,以及基于苯甲醛的缩醛或缩酮,含苯乙基结构部分的那些。优选将前芳香材料与常规香料分别地添加到本发明织物调理剂组合物中。
所述组合物的对保存稳定性优选的pH值范围为大约3-大约8。pH值取决于本发明组合物的特定组分。如果季铵组分是酯季铵,则优选的pH值略低,因为酯键可能在较高的pH值下破裂。因而,优选本发明的包括酯季铵的组合物具有大约3-大约6,更优选大约4-大约5的pH值。酰氨基胺季铵容许略高的pH值并因而本发明的包括酰氨基胺季铵的组合物将很可能具有大约3-大约8的pH值。因为许多阳离子聚合物可以在高pH值下分解,特别是当它们含有胺结构部分时,所以希望保持所述组合物的pH值在用来将所选聚合物季化的胺基的pKa以下,在该pKa以下,这种情况发生的倾向大大地降低。这种反应可以使产物随着时间损失有效性并产生不希望的产物气味。因而,应该理想地使用比该pKa小1-2个pH值单位的合理的安全裕度以驱使这种反应的平衡强烈地促进聚合物稳定性。虽然产物的优选的pH值将取决于为配方选择的具体的阳离子聚合物,但是这些值通常应该小于大约6至大约8.5。调理浴pH值,特别是在粉末软化剂和组合清洁剂/软化剂产品的情况下,通常可以是不太重要的,因为聚合物分解的动力学通常是缓慢的,并且一个调理循环的时间通常不足以允许这种反应对产物的性能或气味具有显著的影响。较低的pH值还可以帮助较高粘度的产物的配制。
优选的实施方案包含:含本发明织物调理组合物的液态漂洗水组合物。
本发明实施方案
在本发明的某些液态漂洗添加组合物中,季铵组分的量可以按重量计为总组合物的大约2%-大约35%,大约4%-大约27%,和总组合物的大约6%-大约25%。
此种组合物中氨基官能化硅酮的含量可以按重量计为这种浓缩物的大约0.05%-大约40%;大约0.1%-大约20%;和大约0.5%-大约15%。
载体是选自水和水与短链C1-C4一元醇的混合物的液体。使用的水可以是蒸馏水、去离子水和/或自来水。水和至多大约10%,优选小于大约5%短链醇例如乙醇、丙醇、异丙醇或丁醇和其混合物的混合物也可用作载液。主要由水组成的载体是合乎需要的。添加的游离水,优选呈去离子水形式,可以按至多大约95wt%,更优选至多大约80wt%,最优选至多大约60wt%的量存在于本发明组合物中。术语“添加的游离水”是指添加到本发明组合物中的不属于存在于其它各成分中的任何水的水。
一些短链醇存在于市售季铵化合物产品中。这些产品可以用于制备本发明的优选的水性组合物。短链醇通常以重量计按占水性组合物大约0.5%-大约10%的水平存在于这些产品中。
可以通过许多方法制备本发明的组合物。在以下非限制性实施例中公开了一些适宜和令人满意的方法。
实施例
除非另有说明,所有洗涤和漂洗程序在35磅Milnor洗涤机中使用5grain水进行。
以下毛巾、遵循擦洗程序和洗涤/漂洗/干燥以便低和高碱性洗涤:
擦洗从Institutional Textiles购买的各自具有0.5kg近似重量的新白色棉毛圈毛巾以从织物除去在制造期间使用的任何加工助剂。在351b.Milnor洗涤机中进行擦洗并根据以下程序完成。
擦洗规程
步骤一:
(a)在130华氏度下进行第一次大约12加仑的低水水平的洗涤20分钟。将70克可以从Ecolab of St.Paul,MN获得的L2000XP清洁剂用于这种第一次低水水平的洗涤。从洗涤盆沥干水。
(b)在120华氏度下使用70g L2000XP清洁剂进行第二次大约12加仑的低水水平的洗涤10分钟。从该洗涤盆沥干洗涤水。
(c)进行第一次大约15加仑的高水水平的漂洗3分钟。水漂洗水温度是120华氏度。从洗涤盆沥干水。
(d)在90华氏度下进行第二次大约15加仑的高水水平的漂洗3分钟并沥干水。
(e)在90华氏度下进行第三次大约15加仑的高水水平的漂洗3分钟并沥干水。
(f)在90华氏度下进行第四次大约15加仑的高水水平的漂洗3分钟并沥干水。
(g)进行5分钟抽取,其中旋转洗涤盆以除去过量水分。
步骤二:
重复步骤一的分步(a)和(b),但不添加L2000XP清洁剂。
重复步骤一的分步(c)至(g)-漂洗至抽取。
步骤三:
将湿毛巾放入Huebsch干燥器(Stack 30 Pound(300L)容量)中并基于高设置干燥毛巾50-60分钟以致织物温度达到大约200华氏度。如果擦洗更大加载量的毛巾,则增加时间。在步骤三完成之后,毛巾没有残留游离水。
洗涤/调理/干燥循环
用与居住或消费市场中找到的那些类似的低碱性清洁剂洗涤一批经擦洗毛巾。低碱性清洁剂规程提供在下面。用与工业和公共设施领域中找到的那些类似的高碱性清洁剂洗涤第二批经擦洗的毛巾。高碱性清洁剂规程提供在下面。在取得白度和柔软性结果之前让样品经历洗涤/调理/干燥循环(每个规程中的步骤一和二)的至少10个循环。在35磅洗涤机中进行这两个规程。
虽然在本文中使用术语“低碱性清洁剂”、“中pH值清洁剂”和“高碱性清洁剂”,但是它们仅对比目的。对本发明来说,“高碱性pH值清洁剂”具有大于大约9,大于大约10,或大于大约11或更高的洗涤pH值。洗涤pH值是指洗涤浴的pH值。
低碱性清洁剂(洗涤pH值8):
步骤一:
(a)在130华氏度下用104g可以从位于St.Paul MN的Ecolab获得的Flexylite清洁剂进行大约12加仑的低水水平的洗涤步骤7分钟。
(b)在130华氏度下用100mL可以从位于St.Paul,MN的Ecolab获得的Laundri Destainer氯漂液(大约100ppm有效氯)进行大约12加仑的低水水平的漂白步骤7分钟。
(c)在110华氏度下进行大约15加仑的高水水平的漂洗步骤2分钟。
(d)在100华氏度下进行大约15加仑的高水水平的漂洗步骤2分钟。
(e)在100华氏度下用32g织物调理剂进行大约12加仑的低水水平的调理步骤5分钟。织物调理剂的组成提供在下表1至8中。
(f)进行标准最终抽取(旋转)5分钟。
步骤二:
干燥毛巾50-60分钟直到干燥。在干燥步骤期间的织物温度在200华氏度或更高的高温下。
以下毛巾,遵循擦洗程序和洗涤/漂洗/干燥以便中范围pH值洗
涤:
擦洗从Institutional Textiles购买的各自具有0.5kg近似重量的新白色棉毛圈毛巾以从织物除去在制造期间使用的任何加工助剂。在351b.Unimac洗涤机中进行擦洗并根据以下程序完成。
擦洗规程
步骤一:
(a)在140华氏度下进行第一次大约12加仑的低水水平的洗涤15分钟。对于这第一次低水水平的洗涤使用100克50%NaOH溶液。从洗涤盆沥干水。
(b)进行第一次大约15加仑的高水水平的漂洗2分钟。水漂洗水温度是120华氏度。从洗涤盆沥干水。
(c)进行一分钟抽取,其中以400RPM旋转洗涤盆以除去过量水分。
(d)在110华氏度下进行第二次大约15加仑的高水水平的漂洗2分钟并沥干水。
(e)进行5分钟抽取,其中以400RPM旋转洗涤盆以除去过量水分。
步骤二:
(a)在130华氏度下使用70g L2000XP清洁剂进行第一次大约12加仑的低水水平的洗涤20分钟。从该洗涤盆沥干洗涤水。
(b)在120华氏度下使用70g L2000XP清洁剂进行第二次大约12加仑的低水水平洗涤10分钟。从该洗涤盆沥干洗涤水。
(c)进行第一次大约15加仑的高水水平的漂洗3分钟。水漂洗水温度是120华氏度。从洗涤盆沥干水。
(d)在90华氏度下进行第二次大约15加仑的高水水平的漂洗3分钟并沥干水。
(e)在90华氏度下进行第三次大约15加仑的高水水平的漂洗3分钟并沥干水。
(f)在90华氏度下进行第四次大约15加仑的高水水平的漂洗3分钟并沥干水。
(g)进行5分钟抽取,其中以400RPM旋转洗涤盆以除去过量水分。
步骤三:
重复步骤二的分步(a)至(g),同时外加L2000XP清洁剂。
重复步骤一的分步(a)至(e),但不添加50%NaOH进一步漂洗亚麻布。
步骤四:
将湿毛巾放入Huebsch干燥器(Stack 30Pound(300L)容量)中并基于高设置干燥毛巾50-60分钟以致织物温度达到大约200华氏度。如果擦洗更大加载量的毛巾,则增加时间。在步骤三完成之后,毛巾没有残留游离水。
中pH值清洁剂规程(洗涤pH值9.7):
步骤一:
(a)将Ecolab Formula 1胶囊加入分配器中以产生浓缩产品在5grain水中的10%溶液。
(b)用530g 10%Formula 1溶液(可以从位于St.Paul,MN的Ecolab获得的浓缩产品)在120华氏度下进行大约12加仑的低水水平的洗涤步骤15分钟。
(c)进行第一次大约15加仑的高水水平的漂洗2分钟。水漂洗水温度是120华氏度。从洗涤盆沥干水。
(d)进行一分钟抽取,其中以400RPM旋转洗涤盆以除去过量水分。
(e)在110华氏度下进行第二次大约15加仑的高水水平的漂洗2分钟并沥干水。
(f)进行5分钟抽取,其中400RPM旋转洗涤盆以除去过量水分。
步骤二:
干燥毛巾60分钟直到干燥。在干燥步骤期间的织物温度在200华氏度的高温下。
高碱性清洁剂规程(洗涤pH值11.3):
步骤一:
(a)在130华氏度下用50g可以从位于St.Paul,MN的Ecolab获得的无着色剂的L2000XP清洁剂进行大约12加仑的低水水平的洗涤步骤7分钟。在可供选择的规程中,使用70g清洁剂。
(b)在130华氏度下用50mL可以从位于St.Paul,MN的Ecolab获得的Laundri Destainer氯漂液(大约50ppm有效氯)进行大约12加仑的低水水平的漂白步骤7分钟。在可供选择的规程中,使用100mL漂液。
(c)在110华氏度下进行大约15加仑的高水水平的漂洗步骤2分钟。
(d)在100华氏度下进行大约15加仑的高水水平的漂洗步骤2分钟。
(e)在100华氏度下进行大约15加仑的高水水平的漂洗步骤2分钟。
f)在100华氏度下用55g织物调理剂进行大约12加仑的低水水平的调理步骤5分钟。在可供选择的规程中,使用64g织物调理剂。织物调理剂的组成提供在下表1至6中。
(g)进行标准最终抽取(旋转)5分钟。
步骤二:
以高热干燥毛巾50-60分钟直到干燥。在干燥步骤期间的织物温度在小于180华氏度的低温或200华氏度或更高的高温下。
柔软性
通过来自受训专家的评价小组的评级确定柔软性。通过七个受训专家的评价小组评价每种组的两个毛巾的柔软性。小组成员被要求将柔软性分0-7级进行排列,其中0是非常粗糙,中等是3.5,7是非常柔软。将每一条件下的小组成员的排列平均。
吸光度
通过将4”×7”试验样本的1厘米浸入着色染料溶液测定吸光度并允许静置6分钟。在6分钟之后,在着色染料的最高点标记样本。然后从该1cm浸渍点到更高线测量样本(毫米)。每一试验样本重复三次并报道平均值。
白度测定
使用具有如下标准化设置的Hunter Lab Colorquest XE分光光度计取得初始白度读数:模式=RSIN,视域=大,口尺寸=1.00”,UV滤光片=420nm。HunterLab测量设置包括:选择:CIELAB,光源:D65,观察者:10度。对十个经擦洗毛巾各读数两次。将20个读数平均。
在洗涤、调理和干燥循环(步骤一和二)完成之后,在Hunter Lab仪器上对每一毛巾取得读数(L、a、b*、WI、YI)。对总共10-15个洗涤、调理和干燥循环重复这种程序。将b*对循环数绘图。这示出了在每一累进洗涤/调理/干燥循环中毛巾的黄度,越正的b*值意味着越黄色的毛巾。典型地,Ab*=b*最终-b*初始值是对每一变量计算的以对初始平均读数的差值提公因子。结果在图1中示出。结果表明随着洗涤/调理/干燥循环的增加,使用本发明组合物(组合物A、B和C)的样品与对照样品(织物调理剂组合物I)相比具有更少黄色(更白)。
视觉白度数据
七个个体的受训试验评价小组被要求在两个样品之间选择更白的毛巾。结果显示为选择样品作为更白毛巾的个体数。
表1
碱性织物调理剂组合物I
原材料 | wt% |
去离子水 | 75.521 |
聚二牛脂酰基甲基硫酸盐90%(Accosoft 501酰氨基胺季铵) | 23 |
氯化钙78%薄片二水合物 | 0.3 |
防腐剂 | 0.15 |
香料 | 1 |
表2
碱性织物调理剂组合物II
原材料 | wt% |
去离子水 | 75.521 |
StephantexTM(酯季铵) | 23.0 |
氯化钙78%薄片二水合物 | 0.3 |
防腐剂 | 0.15 |
香料 | 1 |
表3
织物调理剂A=酰氨基胺季铵化合物加上氨基官能化硅酮化合物
织物调理剂A wt%
碱性织物调理剂I | 90.9 |
Wacker FC 201(氨基官能化硅酮) | 9.1 |
表4
织物调理剂B=酰氨基胺季铵化合物加上含聚醚基的氨基官能化硅酮
织物调理剂B wt%
碱性织物调理剂I | 90.9 |
Wacker FC 203 | 9.1 |
表5
织物调理剂C=酰氨基胺季铵化合物加上硅酮橡胶
织物调理剂C wt%
碱性织物调理剂I | 90.9 |
Wacker FC 205 | 9.1 |
表6
织物调理剂D=酯季铵化合物加上氨基官能化硅酮化合物
织物调理剂D wt%
碱性织物调理剂II | 90.9 |
Wacker FC 201 | 9.1 |
以下表7概括了依据低碱性清洁剂规程,使用有和没有氨基官能化硅酮的酰氨基胺季铵(碱性调理剂I)织物调理剂(组合物A)并在工业环境中将经历的高温下干燥的洗涤毛巾的数据。
表7
清洁剂 | 调理剂 | 干燥器温度(华氏度) | 硅酮 | Δb值 | 视觉白度(选择样品为最白的个体#) |
低碱性 | 碱性调理剂I(对照样品) | 高-245F | 无 | 0.41 | 6 |
低碱性 | 调理剂A | 高-245F | 有 | -0.02 | 16 |
低碱性 | 碱性调理剂I(对照样品) | 高-200F | 无 | -0.09 | -- |
低碱性 | 调理剂A | 高-200F | 有 | -0.92 | -- |
以下表8概括了依据高碱性清洁剂规程使用有和没有氨基官能化硅酮的酰氨基胺季铵(碱性调理剂I)织物调理剂(组合物A)并在低和高温下干燥的洗涤毛巾的数据。使用在工业环境中的高碱性清洁剂。对于表8所示的样品,使用无着色剂的清洁剂。市售清洁剂包括可能改变结果的蓝色着色剂。即使当使用高碱性清洁剂并在较低或消费者干燥器条件(较低温度)下干燥时,也看到实践本发明时的利益。当根据本发明处理(含硅酮的调理剂)时,样品还是更吸收性的。
表8
清洁剂 | 调理剂 | 规程条件(g清洁剂/ml漂液/g调理剂) | 干燥器条件(华氏度) | 硅酮 | Δb-值 | 柔软性保留 | 吸光度 |
高碱性 | 碱性调理剂I(对照样品) | 70g/100ml/64g | 低-150F | 无 | -0.04 | -- | -- |
高碱性 | 调理剂A | 70g/100ml/64g | 低-150F | 有 | -0.94 | -- | -- |
高碱性 | 碱性调理剂I(对照样品) | 50g/50ml/55g | 高-200F | 无 | -0.68 | 5.2 | 2.5 |
高碱性 | 调理剂A | 50g/50ml/55g | 高-200F | 有 | -1.00 | 5.6 | 5.1 |
高碱性 | 碱性调理剂I(对照样品) | 50g/50ml/55g | 高-240F | 无 | 0.12 | 5.3 | 2.7 |
高碱性 | 调理剂A | 50g/50ml/55g | 高-240F | 有 | -0.57 | 6.2 | 5.1 |
高碱性 | 碱性调理剂I(对照样品) | 70g/100ml/64g | 高-245F | 无 | 0.94 | -- | -- |
高碱性 | 调理剂A | 70g/100ml/64g | 高-245F | 有 | 0.29 | -- | -- |
表8所选重复样品的视觉白度数据
清洁剂 | 调理剂 | 规程条件(g清洁剂/ml漂液/g调理剂) | 干燥器条件(华氏度) | 硅酮 | Δb值 | 视觉白度(选择样品为最白的个体#) |
高碱性 | 碱性调理剂I(对照样品) | 70g/100ml/64g | 低-150F | 无 | -0.04 | 2 |
高碱性 | 调理剂A | 70g/100ml/64g | 低-150F | 有 | -0.94 | 20 |
高碱性 | 碱性调理剂I(对照样品) | 70g/100ml/64g | 高-245F | 无 | 0.94 | 6 |
高碱性 | 调理剂A | 70g/100ml/64g | 高-245F | 有 | 0.29 | 16 |
以下表9概括了依据低碱性清洁剂规程使用有和没有氨基官能化硅酮的酯季铵(碱性调理剂II)织物调理剂(组合物D)并在高温下干燥的洗涤毛巾的数据。
表9
清洁剂 | 调理剂 | 干燥器温度(华氏度) | 硅酮 | Δb值 | 柔软性保留 |
低碱性 | 碱性组合物II(对照样品) | 高-200F | 无 | 0.22 | 5.1 |
低碱性 | 组合物D | 高-200F | 有 | -0.24 | 5.9 |
低碱性 | 碱性组合物II(对照样品) | 高-240F | 无 | 0.76 | 5.2 |
低碱性 | 组合物D | 高-240F | 有 | 0.41 | 5.6 |
以下表10概括了依据低碱性清洁剂规程使用有和没有氨基官能化硅酮(组合物B)和有和没有硅酮橡胶(组合物C)的酰氨基胺季铵(碱性调理剂I)织物调理剂并在高温下干燥的洗涤毛巾的数据。
表10
清洁剂 | 调理剂 | 干燥器温度(华氏度) | 硅酮 | Δb值 | 柔软性保留 |
低碱性 | 碱性调理剂I(对照样品) | 高-200F | 无 | -0.09 | -- |
低碱性 | 组合物B | 高-200F | 有 | -1.09 | -- |
低碱性 | 碱性调理剂I(对照样品) | 高-200F | 无 | -0.09 | -- |
低碱性 | 组合物C | 高-200F | 有 | -1.00 | -- |
以下表11概括了依据中等pH值清洁剂规程使用有和没有氨基官能化硅酮(组合物A)的酰氨基胺季铵(碱性调理剂I)并在高温下干燥的洗涤毛巾的数据。
表11
清洁剂 | 调理剂 | 干燥器温度(华氏度) | 硅酮 | 洗涤/干燥循环的# | 视觉白度(选择样品为最白的个体#) | 柔软性保留 | Δb值 |
中等-pH | 调理剂I | 200F | 无 | 10 | -- | -- | 3.55 |
中等-PH | 组合物A | 200F | 有 | 10 | -- | -- | 0.21 |
中等-pH | 调理剂I | 200F | 无 | 15 | 0 | 4.38 | 4.12 |
中等-PH | 组合物A | 200F | 有 | 15 | 22 | 4.37 | 1.12 |
概括在表7-11中的上述数据表明当在高或中等碱性洗涤条件中使用本发明组合物时和/或当干燥器温度是200华氏度或更高时出现样品减少的泛黄。上述数据还表明使用本发明调理剂的样品中柔软性不降低。
Claims (31)
1.织物的调理方法,包括:
(a)让织物与含氨基官能化硅酮和季铵的液态组合物接触,和
(b)干燥所述织物以致织物温度是200华氏度或更高。
2.根据权利要求1的织物的调理方法,其中所述织物调理组合物还包含以下物质中的至少一种:抗静电剂、抗皱剂、染料转印抑制/颜色保护剂、除气/气味捕获剂、污物阻挡/污物释放剂、紫外光防护剂、香料、消毒剂、杀菌剂、防水剂、驱虫剂、抗起球剂、酸化剂、除霉剂、酶、抗过敏剂、淀粉、漂白剂、光学增白剂和它们的混合物。
3.根据权利要求1的织物的调理方法,其中所述组合物的季铵组分包含酰氨基胺季铵、酯季铵、二甲基二牛脂基胺、咪唑啉季胺和它们的混合物中的至少一种。
4.根据权利要求1的织物的调理方法,其中所述织物温度大于220华氏度。
5.根据权利要求1的织物的调理方法,其中当经历至少15个循环时,棉毛圈布毛巾的Δb*比对照样品的Δb*更大(更负),其中一个循环由洗涤步骤继之根据权利要求1的调理步骤和干燥步骤组成。
6.根据权利要求1的方法,其中所述织物的柔软性不降低。
7.根据权利要求1的织物的调理方法,包括在让所述织物与所述织物调理组合物接触之前在pH值大于9的洗剂中洗涤所述织物的步骤。
8.织物的调理方法,包括:
(a)用pH值大于9的洗剂洗涤织物,
(b)让该经洗涤的织物与含氨基官能化硅酮和季铵的组合物接触,和
(c)干燥所述织物以致织物温度是200华氏度或更高。
9.根据权利要求8的织物的调理方法,其中所述织物调理组合物还包含以下物质中的至少一种:抗静电剂、抗皱剂、染料转印抑制/颜色保护剂、除气/气味捕获剂、污物阻挡/污物释放剂、紫外光防护剂、香料、消毒剂、杀菌剂、防水剂、驱虫剂、抗起球剂、酸化剂、除霉剂、酶、抗过敏剂、淀粉、漂白剂、光学增白剂和它们的混合物。
10.根据权利要求8的织物的调理方法,其中所述组合物的季铵组分包含酰氨基胺季铵、酯季铵、二甲基二牛脂基胺、咪唑啉季胺和它们的混合物中的至少一种。
11.根据权利要求8的织物的调理方法,其中所述织物温度大于220华氏度。
12.根据权利要求8的织物的调理方法,其中当经历至少15个根据权利要求8的调理步骤时,棉毛圈布毛巾的Δb*比对照样品的Δb*更大(更负)。
13.根据权利要求8的方法,其中该经处理的织物的柔软性不降低。
14.处理织物的方法,该方法包括:(a)允许织物接触液态织物调理组合物,其中所述组合物包含:(i)酰氨基胺季铵化合物或酯季铵化合物或它们的混合物;和(ii)氨基官能化硅酮化合物,和(b)将所述经调理的织物放入在干燥运转过程中的工业干燥器的内部,其中所述织物温度是200华氏度或更高,并且在15个循环之后所述织物的Δb*比对照样品的Δb*更大(更负),其中一个循环包括洗涤步骤、处理步骤和干燥步骤。
15.根据权利要求14的方法,其中所述织物调理组合物还包含以下物质中的至少一种:抗静电剂、抗皱剂、染料转印抑制/颜色保护剂、除气/气味捕获剂、污物阻挡/污物释放剂、紫外光防护剂、香料、消毒剂、酶、杀菌剂、防水剂、驱虫剂、抗起球剂、酸化剂、除霉剂、抗过敏剂、淀粉、漂白剂、光学增白剂和它们的混合物。
16.根据权利要求14的方法,其中该经处理的织物的柔软性不降低。
17.织物的调理方法,包括:
(a)在高碱性清洁剂中洗涤织物;
(b)让织物与含氨基官能化硅酮和季铵的液态组合物接触,和
(b)干燥所述织物。
18.根据权利要求17的织物的调理方法,其中所述织物调理组合物还包含以下物质中的至少一种:抗静电剂、抗皱剂、染料转印抑制/颜色保护剂、除气/气味捕获剂、污物阻挡/污物释放剂、紫外光防护剂、香料、消毒剂、杀菌剂、防水剂、驱虫剂、抗起球剂、酸化剂、除霉剂、酶、抗过敏剂、淀粉、漂白剂、光学增白剂和它们的混合物。
19.根据权利要求17的织物的调理方法,其中所述组合物的季铵组分包含酰氨基胺季铵、酯季铵、二甲基二牛脂基胺、咪唑啉季胺和它们的混合物中的至少一种。
20.根据权利要求17的织物的调理方法,其中所述织物温度低于180华氏度。
21.根据权利要求17的织物的调理方法,其中当经历至少15个循环时,棉毛圈布毛巾的Δb*比对照样品的Δb*更大(更负),其中一个循环由根据权利要求17的洗涤步骤继之调理步骤和干燥步骤组成。
22.根据权利要求17的方法,其中所述织物的柔软性不降低。
23.根据权利要求17的织物的调理方法,包括在让所述织物与所述织物调理组合物接触之前在pH值大于9的洗剂中洗涤所述织物的步骤。
24.织物的调理方法,包括:
(a)用pH值大于10的洗剂洗涤织物,
(b)让该经洗涤的织物与含氨基官能化硅酮和季铵的组合物接触,和
(c)干燥所述织物。
25.根据权利要求24的织物的调理方法,其中所述织物调理组合物还包含以下物质中的至少一种:抗静电剂、抗皱剂、染料转印抑制/颜色保护剂、除气/气味捕获剂、污物阻挡/污物释放剂、紫外光防护剂、香料、消毒剂、杀菌剂、防水剂、驱虫剂、抗起球剂、酸化剂、除霉剂、酶、抗过敏剂、淀粉、漂白剂、光学增白剂和它们的混合物。
26.根据权利要求24的织物的调理方法,其中所述组合物的季铵组分包含酰氨基胺季铵、酯季铵、二甲基二牛脂基胺、咪唑啉季胺和它们的混合物中的至少一种。
27.根据权利要求24的织物的调理方法,其中当经历至少15个根据权利要求24的调理步骤时,棉毛圈布毛巾的Δb*比对照样品的Δb*更大(更负)。
28.根据权利要求24的方法,其中该经处理的织物的柔软性不降低。
29.处理织物的方法,该方法包括:(a)在具有10或更高的pH值的碱性清洁剂中洗涤织物,(b)使织物接触液态织物调理组合物,其中所述组合物包含:(i)酰氨基胺季铵化合物或酯季铵化合物或它们的混合物;和(ii)氨基官能化硅酮化合物,和(c)将所述经调理的织物放入在干燥运转过程中的干燥器的内部,其中所述织物温度低于200华氏度,并且在15个循环之后所述织物的Δb*比对照样品的Δb*更大(更负),其中一个循环包括洗涤步骤和处理步骤。
30.根据权利要求30的方法,其中所述织物调理组合物还包含以下物质中的至少一种:抗静电剂、抗皱剂、染料转印抑制/颜色保护剂、除气/气味捕获剂、污物阻挡/污物释放剂、紫外光防护剂、香料、消毒剂、酶、杀菌剂、防水剂、驱虫剂、抗起球剂、酸化剂、除霉剂、抗过敏剂、淀粉、漂白剂、光学增白剂和它们的混合物。
31.根据权利要求29的方法,其中该经处理的织物的柔软性不降低。
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
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CN104781381A (zh) * | 2012-11-20 | 2015-07-15 | 荷兰联合利华有限公司 | 洗衣用组合物 |
CN104781381B (zh) * | 2012-11-20 | 2018-02-23 | 荷兰联合利华有限公司 | 洗衣用组合物 |
US11542458B2 (en) | 2015-12-28 | 2023-01-03 | Colgate-Palmolive Company | Fabric conditioners |
CN109415657A (zh) * | 2016-05-06 | 2019-03-01 | 雷克特本克斯尔万尼施公司 | 组合物 |
CN109415657B (zh) * | 2016-05-06 | 2021-12-17 | 雷克特本克斯尔万尼施公司 | 组合物 |
CN111971377A (zh) * | 2018-03-02 | 2020-11-20 | 荷兰联合利华有限公司 | 洗衣方法 |
US11814607B2 (en) | 2018-03-02 | 2023-11-14 | Conopco, Inc. | Laundry additive composition comprising a soil release polymer/silicone mixture |
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WO2008152602A1 (en) | 2008-12-18 |
US9150819B2 (en) | 2015-10-06 |
US20080307586A1 (en) | 2008-12-18 |
JP2010530036A (ja) | 2010-09-02 |
US20150376548A1 (en) | 2015-12-31 |
EP3312336A1 (en) | 2018-04-25 |
EP2158352A4 (en) | 2012-05-02 |
AU2008263396A1 (en) | 2008-12-18 |
BRPI0813148A2 (pt) | 2014-12-23 |
EP2158352B1 (en) | 2017-12-20 |
ES2663408T3 (es) | 2018-04-12 |
EP3312336B1 (en) | 2021-06-09 |
CA2686129A1 (en) | 2008-12-18 |
BRPI0813148B1 (pt) | 2018-09-18 |
AU2008263396B2 (en) | 2012-09-27 |
US8038729B2 (en) | 2011-10-18 |
MX2009012912A (es) | 2010-01-14 |
EP2158352A1 (en) | 2010-03-03 |
US20170096622A1 (en) | 2017-04-06 |
CN101680158B (zh) | 2013-12-25 |
US20110239379A1 (en) | 2011-10-06 |
EP3901357A1 (en) | 2021-10-27 |
CA2686129C (en) | 2015-03-31 |
US10233407B2 (en) | 2019-03-19 |
US20120030882A1 (en) | 2012-02-09 |
ES2886584T3 (es) | 2021-12-20 |
JP5226782B2 (ja) | 2013-07-03 |
US20190055494A1 (en) | 2019-02-21 |
US10113139B2 (en) | 2018-10-30 |
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