CN101107301A - 用于清洁表面的混合物和方法 - Google Patents
用于清洁表面的混合物和方法 Download PDFInfo
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- CN101107301A CN101107301A CNA2006800029944A CN200680002994A CN101107301A CN 101107301 A CN101107301 A CN 101107301A CN A2006800029944 A CNA2006800029944 A CN A2006800029944A CN 200680002994 A CN200680002994 A CN 200680002994A CN 101107301 A CN101107301 A CN 101107301A
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- ester
- aminoplastics
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Classifications
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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
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/32—Amides; Substituted amides
- C11D3/323—Amides; Substituted amides urea or derivatives thereof
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- 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
- C11D3/16—Organic compounds
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- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
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- C11D2111/14—Hard surfaces
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- C11D2111/10—Objects to be cleaned
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- C11D2111/20—Industrial or commercial equipment, e.g. reactors, tubes or engines
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- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
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- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
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Abstract
本发明公开了包含如下物质的混合物:(a)平均直径为50μm至5mm(重均)的开孔氨基塑料泡沫块,(b)水,(c)至少一种表面活性剂,和(d)任选油相或脂相。
Description
本发明涉及包含如下物质的混合物:
(a)平均直径为50μm至5mm(重均)的开孔氨基塑料泡沫块,
(b)水,
(c)至少一种表面活性剂,和
(d)合适的话油或脂相,
以及涉及一种生产本发明混合物的方法。
此外,本发明还涉及一种使用包含如下物质的混合物清洁表面的方法:
(a)平均直径为50μm至5mm(重均)的开孔氨基塑料泡沫块,
(b)水,
(c)至少一种表面活性剂,和
(d)合适的话油或脂相。
此外,本发明还涉及本发明混合物作为清洁剂的用途。
表面清洁和适合于此的清洁剂具有显著的经济重要性。就此而言,不仅考虑工业清洁,而且考虑生产适合工业领域和个人领域的清洁剂。
此处特别重要的是一方面清洗身体,尤其是清洗身体的非常脏的部位。因此,例如难以在操作中从手上完全除去润滑油残留物而不伤害皮肤。特别重要的是牙齿表面,其应能够完全清洁沉积物(齿斑)。还重要的是物体表面,其也简称为表面。在许多情况下表面应确保令人愉悦的外观,然而例如被顽固污渍弄脏的表面并不令人愉悦。污渍痕迹或薄膜也应完全除去。
在另一方面,具有很大重要性的是清洁脂、油的有光泽的表面,尤其是树脂化残留物而不使所述表面受损如变模糊。在许多情况下例如使用硅胶或具有摩擦作用的清洁材料如海绵来摩擦材料,这些材料有助于除去顽固残留物。残留物越顽固,使用更强摩擦的清洁剂如海绵,或在清洁剂中使用更强的摩擦剂,因此对待清洁表面造成损坏的风险也越大。具体而言,在清洁牙齿时,必须确保齿根不受损,而这在使用强摩擦剂时可能发生。
因此本发明的目的是提供适合清洗身体和清洁表面,尤其是光泽表面并避免现有技术缺点的混合物。本发明的另一目的是提供一种避免现有技术缺点的清洁表面的方法。
因此,找到了开头所定义的混合物,其包含:
(a)平均直径为50μm至5mm(重均)的开孔氨基塑料泡沫块,
(b)水,
(c)至少一种表面活性剂,和
(d)合适的话油或脂相。
就此而言,本发明混合物的组分(a)-(d)如下所定义。
本发明混合物包含开孔氨基塑料泡沫块(a)。这些块的平均直径(重均)为50μm至5mm,优选75μm至3mm,特别优选100μm至2mm。
存在于本发明混合物中的开孔氨基塑料泡沫块(a)可具有宽或窄的直径分布。在形成直径(质均)与直径(数均)的商时,因此商例如可为1.1-10,优选1.2-3。
存在于本发明混合物中的开孔氨基塑料泡沫块(a)可具有规则或不规则形状。规则形状的实例为立方体、长方体、球形或椭圆形。不规则形状的实例为颗粒、碎片和碎屑。
在本发明的一个实施方案中,开孔氨基塑料泡沫块(a)为基于合成有机泡沫如脲-甲醛树脂的那些,尤其是基于氨基塑料-甲醛树脂,非常特别优选蜜胺-甲醛树脂的氨基塑料泡沫,其中基于蜜胺-甲醛树脂的氨基塑料也称为蜜胺泡沫。
在本发明的一个实施方案中,开孔氨基塑料泡沫块(a)为其中至少50%,优选60-100%,特别优选65-99.9%的所有薄片是开孔的氨基塑料泡沫,其根据DIN ISO 4590测定。
在本发明的一个实施方案中,开孔氨基塑料泡沫块(a)由硬质氨基塑料泡沫制成,即对本发明而言,根据DIN 53577测定,在压缩40%时压缩强度为1kPa或更大的氨基塑料泡沫。
在本发明的一个实施方案中,开孔氨基塑料泡沫块(a)由密度为5-500kg/m3,优选6-300kg/m3,特别优选7-300kg/m3的氨基塑料泡沫制成。
存在于本发明混合物中的开孔氨基塑料泡沫块(a)通过分析截面的显微照片测定的平均孔径(数均)为1μm至1mm,优选50-500μm。
在本发明的一个实施方案中,存在于本发明混合物中的开孔氨基塑料泡沫块(a)由每m2具有至多20个,优选至多15个,特别优选至多10个孔且孔直径至多为20mm的氨基塑料泡沫制备。其它孔通常具有较小的直径。
在本发明的一个实施方案中,存在于本发明混合物中的开孔氨基塑料泡沫块(a)的根据DIN 66131测定的BET表面积为0.1-50m2/g,优选0.5-20m2/g。
在本发明的一个实施方案中,存在于本发明混合物中的开孔氨基塑料泡沫块(a)由根据DIN 52215在2000Hz的频率和50mm的所述泡沫(a)的层厚度下测量的吸声系数大于50%的氨基塑料泡沫制备。
在本发明的特定实施方案中,存在于本发明混合物中的开孔氨基塑料泡沫块(a)由根据DIN 52212在2000Hz的频率和40mm的所述泡沫(a)的层厚度下测量的吸声系数大于0.5的氨基塑料泡沫制成。
存在于本发明混合物中的开孔氨基塑料泡沫块(a)可由氨基塑料泡沫例如通过粉碎而得到。合适的粉碎方法尤其为机械粉碎方法如浇铸、冲压、切割、切屑、刨片、锯、研磨、盘磨、剪。
特别适合机械粉碎氨基塑料泡沫的装置为磨机、锯、切碎机、磨碎机、破碎机和研磨机。
在本发明的一个实施方案中,开孔氨基塑料泡沫块(a)由密度为5-500kg/m3且平均孔径为1μm至1mm的氨基塑料泡沫通过机械粉碎而制备。
特别适合作为进行本发明方法的原料的蜜胺泡沫本身是已知的。它们例如通过使:
i)除甲醛外还可以缩合形式包含其它羰基化合物如醛类的蜜胺-甲醛预缩合物在如下物质存在下发泡而制备:
ii)一种或多种推进剂,
iii)以及合适的话一种或多种乳化剂,
iv)一种或多种硬化剂。
蜜胺-甲醛预缩合物i)可以是未改性的,尽管它们也可以被改性,例如至多20mol%蜜胺可由其它本身已知的热固性塑料形成体如烷基取代的蜜胺、脲、氨基甲酸酯、羧酰胺、双氰胺、胍、硫酰胺、磺酰胺、脂族胺、苯酚和苯酚衍生物替代。作为除甲醛以外的其它羰基化合物,改性的蜜胺-甲醛预缩合物例如可以缩合形式包含乙醛、三羟甲基乙醛、丙烯醛、糠醛、乙二醛、邻苯二甲醛和对苯二甲醛。
合适的推进剂ii)例如为水,惰性气体,尤其是二氧化碳以及所谓的物理推进剂。物理推进剂为对进料组分呈惰性且优选在室温下为液体但在形成氨基塑料的条件下汽化的化合物。优选这些化合物的沸点低于110℃,尤其低于80℃。物理推进剂还包括引入进料组分i)和ii)中的或溶于它们中的惰性气体如二氧化碳、氮气或稀有气体。
在室温下为液体的合适化合物选自具有至少4个碳原子的链烷烃和/或环烷烃,二烷基醚、酯类、酮类、缩醛类、具有1-8个碳原子的氟代链烷烃,以及在烷基链中具有1-3个碳原子的四烷基硅烷,尤其是四甲基硅烷。
可提及的实例为丙烷、正丙烷、异丁烷、环丁烷、正戊烷、异戊烷、环戊烷、环己烷、二甲醚、甲基乙基醚、甲基叔丁基醚、甲酸甲酯、丙酮,以及可在对流层中分解并因此对臭氧层无害的氟代链烷烃如三氟甲烷、二氟甲烷、1,1,1,3,3-五氟丁烷、1,1,1,3,3-五氟丙烷、1,1,1,2-四氟乙烷、1,1,1-三氟-2,2,2-三氯乙烷、1,1,2-三氟-1,2,2-三氯乙烷、二氟乙烷和七氟丙烷。所述物理推进剂可单独使用或以它们之间任何相互的组合使用。
使用全氟代链烷烃产生细孔由EP-A 0 351 614已知。
可使用的乳化剂iii)为常规非离子、阴离子、阳离子或内铵盐表面活性剂,尤其是C12-C30烷基磺酸化物,优选C12-C18烷基磺酸化物以及聚乙氧基化C10-C20烷基醇,尤其是具有式R1-O(CH2-CH2-O)x-H的聚乙氧基化烷基醇,其中R1选自C10-C20烷基且x例如可为5-100的整数。
合适的硬化剂iv)尤其为酸性化合物如无机布朗斯台德酸如硫酸或磷酸,有机布朗斯台德酸如乙酸或甲酸,路易斯酸以及所谓的潜酸。
合适的蜜胺泡沫的实例及其制备方法由EP-A 0 017 672给出。
氨基塑料泡沫当然可以包含常用于泡沫化学的添加剂和聚集体,例如抗氧化剂、阻燃剂、填料、着色剂如颜料或染料以及生物杀伤剂如:
氨基塑料泡沫块(a)可具有规则形式如球体或椭圆体,或者尤其是不规则形式。
本发明混合物进一步包含可去离子或含盐的水(b)。
本发明混合物还包含至少一种表面活性剂(c)。表面活性剂(c)选自离子、两性离子,优选非离子表面活性剂。离子表面活性剂可为阳离子或阴离子表面活性剂。
在本发明的一个实施方案中,表面活性剂(c)选自无毒的表面活性剂。
就阴离子表面活性剂而言,盐的含义优选理解为镁盐、铵盐和碱金属盐,尤其是钾和钠盐。优选的铵盐例如为三乙醇铵盐和未取代氨的盐。
阴离子表面活性剂的实例为酰基氨基酸及其盐,例如:
-酰基谷氨酸盐,尤其是酰基谷氨酸钠,其中酰基例如可为乙酰基、丁酰基、肉豆蔻酰基、月桂酰基或椰油酰基,
-肌氨酸盐如肉豆蔻酰基肌氨酸、月桂酰基肌氨酸三乙醇铵盐、月桂酰基肌氨酸钠和椰油酰基肌氨酸钠。
阴离子表面活性剂的其它实例为磺酸及其盐例如:
-酰基羟乙磺酸盐,其中酰基例如可为乙酰基、丁酰基、肉豆蔻酰基、月桂酰基或椰油酰基,所述盐例如为椰油酰基羟乙磺酸钠或椰油酰基羟乙磺酸铵,
-磺基琥珀酸化物,例如琥珀酸二辛酯磺酸钠、月桂基聚氧乙烯醚磺基琥珀酸二钠、磺基琥珀酸月桂酯二钠、十一碳烯酰基单乙醇胺磺基琥珀酸酯二钠盐、月桂基聚氧乙烯(5)柠檬酸酯磺基琥珀酸二钠及其衍生物,以及硫酸半酯如:
-烷基醚硫酸盐如钠盐、铵盐、镁盐、单异丙醇铵,月桂基聚氧乙烯醚硫酸三异丙醇铵,十四烷基聚氧乙烯醚硫酸钠和C12-13烷基聚氧乙烯醚硫酸钠,
-烷基硫酸盐如月桂基硫酸的钠盐、铵盐和三乙醇铵盐。
其它有利的阴离子表面活性剂为:
-牛磺酸盐如月桂酰基牛磺酸钠和甲基椰油酰基牛磺酸钠,
-醚羧酸如月桂基聚氧乙烯(13)醚羧酸钠和聚氧乙烯(6)椰油酰胺羧酸钠、聚氧乙烯(7)橄榄油羧酸钠,
-磷酸酯和盐如油基聚氧乙烯(10)醚磷酸二乙醇胺和二[月桂基聚氧乙烯(10)醚]磷酸酯,
-取代的烷基磺酸盐如椰油酸单甘油酯硫酸钠、C12-C14-α-烯烃磺酸钠、月桂基乙酸酯磺酸钠和聚氧乙烯(3)椰油酰胺硫酸镁,
-酰基谷氨酸盐如棕榈酰基天冬氨酸二(三乙醇胺)和辛酸/癸酸谷氨酸钠,
-酰基肽如棕榈酰基水解牛奶蛋白、椰油酰基水解大豆蛋白钠盐和椰油酰基水解胶原钠/钾盐(由椰油酰基肽分解的胶原),
在本发明范围内,此处TEA为三乙醇铵盐,DEA为二乙醇铵盐。此外,在本发明范围内,PEG在每种情况下为聚乙二醇,其后的数目在每种情况下为平均每分子的氧化乙烯单元的数目。
其它有利的阴离子表面活性剂为羧酸及其衍生物如盐或酯:
-尤其是月桂酸、硬脂酸铝、C1-C10醇镁和十一烯酸锌,羧酸酯如硬脂酰乳酰乳酸钙、月桂基聚氧乙烯(6)醚柠檬酸酯和聚氧乙烯(4)月桂酰胺酯钠盐,
-烷基酰基磺酸盐如式R2-Ar-SO3M1,其中R2优选为未支化的C10-C13烷基,Ar例如为亚苯基或亚萘基,尤其是对亚苯基或1,5-亚萘基,M1为单价阳离子,尤其是钠阳离子。
对本发明而言,优选阳离子表面活性剂为季铵盐表面活性剂。季铵盐表面活性剂包含至少一个与4个相同或不同的有机非离子基团如C1-C30烷基或C6-C14芳基键接的N原子。
对本发明而言,有利的阳离子表面活性剂还有:
-C10-C30烷基胺,
-C1-C30烷基咪唑,
-单-或多-,尤其是单-至十乙氧基化的C10-C30烷基胺如椰油脂肪胺,
-以及尤其是其盐,尤其是卤化物如氯化物和溴化物。
有利的两性离子表面活性剂的实例为:
-C1-C20-酰基-/二-C1-C30烷基乙二胺如N-(C1-C20-酰胺乙基)-N-(羟乙基)乙酸钠、N-(C1-C20-酰胺乙基)-N-(羟乙基)二丙酸钠、N-(C1-C30-酰胺乙基)-N-(羟乙基)二乙酸钠,优选N-(C10-C25-烷基酰胺乙基)-N-(羟乙基)二乙酸钠,N-(C1-C20-酰胺乙基)-N-(羟乙基)羟丙基磺酸钠、N-(C1-C20-酰胺乙基)-N-(羟乙基)二乙酸钠、N-(C1-C20-酰胺乙基)-N-(羟乙基)丙酸钠和N-(椰油脂肪酰胺基乙基)-N-(羟乙基)氨基乙酸钠盐,
-N-C1-C30烷基氨基酸,优选N-C10-C25烷基氨基酸,例如氨基丙基-C1-C30烷基谷氨酰胺,优选氨基丙基-C10-C25烷基谷氨酰胺,N-C1-C30烷基氨基丙酸,优选N-C10-C25烷基氨基丙酸,C1-C30烷基亚胺二丙酸钠,优选C10-C25烷基亚胺二丙酸钠和N-(月桂酰胺基乙基)-N-(羟基乙基)-N-羧甲基氨基乙酸钠,
-C1-C20烷基甜菜碱、C1-C20烷基酰胺基丙基甜菜碱和C1-C20烷基酰胺基丙基羟基磺基甜菜碱。
有利的非离子表面活性剂的实例为:
-链烷醇酰胺如单-或二-ω-C2-C4-链烷醇-C1-C30-羧酰胺如椰油酰胺MEA/DEA/MIPA,
-通过C2-C30羧酸与甘油、脱水山梨糖醇或其它醇或与氧化乙烯的酯化而形成的酯,
-例如单-或聚乙氧基化C2-C30醇,尤其是3-80重乙氧基化的C2-C30链烷醇,乙氧基化羊毛脂,乙氧基化聚硅氧烷,丙氧基化POE醚,烷基聚糖苷如月桂基葡糖苷、正癸基葡糖苷和椰油葡糖苷,HLB值为至少20的糖苷(如BelsilSPG 128V(Wacker))。
其它有利的非离子表面活性剂为C12-C30链烷醇和C12-C30胺氧化物如椰油酰胺基丙胺N-氧化物。
在本发明的一个实施方案中,存在于本发明混合物中的表面活性剂(c)或存在于本发明混合物中的至少一种表面活性剂(c)的HLB值超过25,优选HLB值超过35。此处HLB值的含义应理解为根据W.C.Griffin的HLB值,即含义理解为氧化乙烯(EO)、氧化丙烯(PO)、甘油或脱水山梨糖醇在特定的表面活性剂分子中的质量分数的20倍。
其它合适的表面活性剂(c)为多重,尤其是3-50重乙氧基化的失水山梨糖醇的单-、二-或三脂肪酸酯,所谓的乙氧基化山梨糖醇酯例如:
-聚氧乙烯(20)失水山梨醇醚单月桂酸酯(Tween 20,CAS No.9005-64-5)
-聚氧乙烯(4)失水山梨醇醚单月桂酸酯(Tween 21,CAS No.9005-64-5)
-聚氧乙烯(4)失水山梨醇醚单硬脂酸酯(Tween 61,CAS No.9005-67-8)
-聚氧乙烯(20)失水山梨醇醚三硬脂酸酯(Tween 65,CAS No.9005-71-4)
-聚氧乙烯(20)失水山梨醇醚单油酸酯(Tween 80,CAS No.9005-65-6)
-聚氧乙烯(5)失水山梨醇醚单油酸酯(Tween 81,CAS No.9005-65-5)
-聚氧乙烯(20)失水山梨醇醚三油酸酯(Tween 85,CAS No.9005-70-3)。特别合适的表面活性剂(c)为:
-聚氧乙烯(20)失水山梨醇醚单棕榈酸酯(Tween 40,CAS No.9005-66-7)
-聚氧乙烯(20)失水山梨醇醚单硬脂酸酯(Tween 60,CAS No.9005-67-8)。
在本发明混合物中可存在一种或多种不同的表面活性剂(c),其中例如烷氧基化脂肪醇的混合物通常在合成中生产,其中在本发明范围内,例如将仅在烷氧基化程度方面略微不同的各分子看作表面活性剂(c)。
本发明混合物还可包含油或脂相(d)。油或脂相(d)例如可由一种或多种天然或合成油、脂肪或蜡形成。
在本发明的一个实施方案中,油或脂相(d)由一种或优选多种下列成分组成。
油和/或脂相(d)的成分例如可选自卵磷脂和甘油三脂肪酸酯,如链长度为8-24个,尤其是12-18个碳原子的饱和和/或不饱和,支化和/或未支化链烷羧酸的甘油三酯。甘油三脂肪酸酯例如可有利地选自合成、半合成和天然油如橄榄油、向日葵油、大豆油、花生油、菜籽油、杏仁油、棕榈油、椰子油、蓖麻油、小麦胚芽油、葡萄籽油、蓟油、月见草油和澳洲坚果油。
油和/或脂相(d)的其它成分可选自链长度为3-30个碳原子的饱和和/或不饱和,支化和/或未支化链烷羧酸和链长度为3-30个碳原子的饱和和/或不饱和,支化和/或未支化醇的酯,以及选自芳族羧酸和链长度为3-30个碳原子的饱和和/或不饱和,支化和/或未支化醇的酯。优选实例为肉豆蔻酸异丙酯、棕榈酸异丙酯、硬脂酸异丙酯、油酸异丙酯、硬脂酸正丁酯、月桂酸正己酯、油酸正癸酯、硬脂酸异辛酯、硬脂酸异壬酯、异壬酸异壬酯、棕榈酸2-乙基己酯、月桂酸2-乙基己酯、硬脂酸2-己基癸酯、棕榈酸2-辛基十二烷基酯、油酸油醇酯、芥子酸油醇酯、油酸二十二碳烯酯、芥子酸二十二碳烯酯、碳酸二辛酯(Cetiol CC)和椰油单、双、三甘油酯(如Myritol 331),丁二醇二辛酸酯/二癸酸酯和己二酸二丁酯,以及这些酯的合成、半合成和天然混合物如霍霍巴油。
油或脂相(d)的其它成分可选自支化和未支化烃和烃蜡,硅油,二-C5-C20烷基醚,饱和或不饱和、支化或未支化C12-C30醇,其也可起表面活性剂作用。
上述成分的任何混合物也可用作本发明混合物中的油或脂相(d)。
有利的是使用蜡如棕榈酸鲸蜡酯作为油相的单独脂组分。
油或脂相(d)的优选成分选自异硬脂酸2-乙基己酯、辛基十二烷醇、异壬酸异十三烷基酯、异二十烷、椰油酸2-乙基己酯、苯甲酸C12-C15烷基酯、甘油三(辛酸/癸酸)酯、二辛酰基醚。
油或脂相(d)成分的优选混合物的实例选自苯甲酸C12-C15烷基酯和异硬脂酸2-乙基己酯的混合物,苯甲酸C12-C15烷基酯和异壬酸异十三烷基酯的混合物,苯甲酸C12-C15烷基酯、异硬脂酸2-乙基己酯和/或异壬酸异十三烷基酯的混合物。
根据本发明,作为极性为5-50mN/m的油,特别优选使用甘油三脂肪酸酯,尤其是大豆油和/或杏仁油。
在烃类中,例如可以使用石蜡油、角鲨烷、角鲨烯,尤其是合适的话使用水合的聚异丁烯作为油或脂相(d)。
在本发明的一个实施方案中,油或脂相(d)可选自吉尔伯特醇。吉尔伯特醇本身已知且例如可通过例如在Na和/或Cu存在下加热2当量通式R2-CH2-CH2-OH的醇产生式R2-CH2-CH2-CHR2-CH2-OH的醇而得到。此处R2为C2-C20烷基,支化或优选未支化,尤其是未支化C3-C14烷基,例如在每种情况下为未支化丙基、丁基、戊基、己基、庚基、辛基、壬基、癸基、十一烷基、十二烷基、十三烷基或十四烷基。特别适合作为油或脂相(d)的吉尔伯特醇为2-正丁基辛醇(R2=正-C4H9)和2-正己基癸醇(R2=正-C6H13)以及上述吉尔伯特醇的混合物。
在本发明的一个实施方案中,油或脂相(d)可选自聚烯烃,尤其是聚α-烯烃。在聚烯烃中,优选聚正癸烯。
在本发明的一个实施方案中,油或脂相(d)可由环状或线性硅油组成或优选包含环状或线性硅油。
硅油通常为在室温下为液体,优选由如下通式定义的聚硅氧烷:
R3、R4、R5和R6各自可相同或不同且选自C1-C10烷基,尤其是甲基或苯基。变量n为1-200的整数。在环状聚硅氧烷化合物中,R5和R6一起为(SiR3R4)基团。
有利的是选择聚三甲基苯基硅氧烷作为硅油。其它硅油例如聚二甲基硅氧烷、六甲基环三硅氧烷、聚二甲基苯基硅氧烷、环状聚二甲基硅氧烷(如十甲基环五硅氧烷)、六甲基环三硅氧烷、聚二甲基硅氧烷、聚(甲基苯基硅氧烷)、聚二甲基鲸蜡基硅氧烷、聚二甲基山萮氧基硅氧烷也可用作油或脂相(d)。还有利的是聚二甲基硅氧烷和异壬酸异十三烷基酯的混合物,以及环状聚二甲基硅氧烷和异硬脂酸2-乙基己酯的混合物。
在本发明的一个实施方案中,可选用的硅油为将其有机侧链衍生化如聚乙氧基化和/或聚丙氧基化的那些聚硅氧烷化合物。这些化合物例如包括聚硅氧烷聚烷基-聚醚共聚物如含聚氧乙烯或聚氧丙烯侧链的聚二甲基鲸蜡基硅氧烷。有利的是将环状聚二甲基硅氧烷(八甲基环四硅氧烷)用作特定的硅油。
在本发明的一个实施方案中,油或脂相(d)选自植物蜡、动物蜡、地蜡和石油化学蜡。例如小烛树蜡、巴西棕榈蜡、日本蜡、西班牙草蜡、软木蜡、guaruma wax、米胚芽油蜡、甘蔗蜡、浆果蜡、小冠巴西棕蜡、褐煤蜡、霍霍巴蜡、牛油树脂、蜂蜡、紫胶蜡、鲸蜡、羊毛脂(羊毛蜡)、羽脂(uropygial grease)、纯地蜡、地蜡、石蜡和微晶蜡是有利的。
在本发明的一个实施方案中,油或脂相(d)可选自化学改性蜡和合成蜡,例如SyncrowaxHRC(三山萮酸甘油酯)和SyncrowaxAW 1C(C18-C36脂肪酸)、褐煤酯蜡、沙索蜡(sasol waxe)、氢化霍霍巴蜡、合成或改性的蜂蜡(如含有聚氧乙烯或聚氧丙烯侧链的聚二甲基硅氧烷蜂蜡和/或C30-C50烷基蜂蜡)、蓖麻酸十六烷酯、聚亚烷基蜡,尤其是聚乙烯蜡,聚乙二醇蜡,化学改性脂如氢化植物油如氢化蓖麻油和/或氢化椰油脂肪酸甘油酯),氢化甘油三酸酯如氢化大豆甘油酯、三(羟基硬脂酸)甘油酯,脂肪酸,脂肪酸酯和乙二醇酯如硬脂酸C20-C40烷基酯、C20-C40烷基羟基硬脂酰基硬脂酸酯和/或乙二醇褐煤酸酯。某些与所述脂和/或蜡组分具有类似物理性能的有机硅化合物如十八烷氧基三甲基硅烷也是有利的。
在本发明的一个实施方案中,油或脂相(d)可选自磷脂。磷脂为酰化甘油的磷酸酯。在磷脂酰胆碱中特别重要的例如是卵磷脂,其可由如下通用结构描述:
其中R7和R8可相同或不同且选自未支化的脂族的或具有15或17个碳原子且具有至多4个反式双键的烯属烃基。
本发明混合物也可包含一种或多种香料或芳香物质(e)。
合适的香料可以为纯物质或释放香味的天然或合成的挥发性化合物的混合物。天然香料为来自花(百合、熏衣草、玫瑰、茉莉、苦橙花、依兰),茎和叶(老鹳草、广藿香、苦橙叶),果实(茴香、芫荽、芡蒿子、刺柏),果皮(香柠檬、柠檬、橙),根(肉豆蔻、当归、芹菜、小豆蔻、闭鞘姜、鸢尾、石菖蒲),木(松木、檀香木、愈创木、雪松木、蔷薇木),香草和草(龙蒿、香茅草、鼠尾草、百里香),针和枝(云杉、冷杉、松树、矮松),树脂和香脂(古蓬香脂、榄香脂、安息香、没药、乳香、愈伤草树脂)的萃取物。动物原料也是合适的,例如麝猫香和海狸香。典型的合成香料化合物为酯类、醚类、醛类、酮类、醇类和烃类的产物。酯类香料例如为乙酸苄酯、异丁酸酚氧基乙酯、乙酸4-叔丁基环己酯、乙酸芳樟酯、乙酸二甲基苄基原酯、乙酸苯乙酯、苯甲酸芳樟酯、甲酸苄酯、甲基苯基氨基乙酸乙酯、环己基丙酸烯丙基酯、丙酸苏合香酯和水杨酸苄酯。醚类香料例如包括苯基·乙基醚,醛类香料例如包括具有8-18个碳原子的线性链烷醛、柠檬醛、香茅醛、香茅基含氧乙醛、仙客来醛、羟基香茅醛、铃兰醛和波洁红醛(bourgeonal),酮类香料例如包括芷香酮、cc-异甲基紫罗兰酮和甲基柏木酮,醇类香料包括茴香脑、香茅醇、丁子香酚、异丁子香酚、香叶醇、芳樟醇、苄醇、苯乙醇和松油醇,以及烃类香料主要包括萜类和香脂。然而,优选使用一起产生令人愉悦香味的不同香料的混合物。主要用作芳香组分的低挥发性精油也适合用作香料,例如鼠尾草油、春黄菊油、丁子香油、蜜蜂花油、薄荷油、肉桂叶油、莱姆花油(linden blossom oil)、刺柏油、岩兰油、乳香油、古蓬油、labolanum油和杂薰衣草油。优选单独或混合使用如下物质:香柠檬油、二氢月桂烯醇、铃兰醛、新铃兰醛(lyral)、香茅醇、苯乙醇、α-己基肉桂醛、α-戊基肉桂醛、香叶醇、苄基丙酮、仙客来醛、芳樟醇、boisambreneForte、龙涎呋喃(ambroxan)、吲哚、二氢茉莉酮酸甲酯(hedione)、sandelice、柠檬油、橘子油、橙油、戊基甘醇酸烯丙酯、cyclovertal、杂熏衣草油、鼠尾草油、β-突厥酮、波旁香叶油、水杨酸环己酯、合成橡苔(evernyl)、γ-甲基紫罗兰酮(iraldein gamma)、苯乙酸、乙酸香叶酯、乙酸苄酯、氧化玫瑰、Romillat、Irotyl和Floramat。
本发明混合物也可包含一种或多种添加剂(f)。添加剂(f)可选自调理剂、抗氧化剂、乙氧基化的甘油单-或二脂肪酸酯、增稠剂、发泡剂、润湿剂和保湿剂、生物杀伤剂、有机溶剂如乙醇或异丙醇、发光物质和/或其它效果物质(如颜色条纹)。发光物质和/或其它效果物质(如颜色条纹)具有显著的感觉重要性。
调理剂的实例列于International Cosmetic lngredient Dictionary andHandbook(第4卷,编辑:R.C.Pepe,J.A.Wenninger,G.N.McEwen,The Cosmetic,Toiletry,and Fragrance Association,第9版,2002)第4部分,如下关键词下:发用调理剂、保湿剂、皮肤调理剂、皮肤调理剂-润肤剂、皮肤调理剂-保湿剂、皮肤调理剂-混杂、皮肤调理剂-吸留剂和皮肤保护剂。调理剂的其它实例为在EP-A 0 934 956(第11-13页)中在“水溶性调理剂”和“油溶性调理剂”下列出的化合物。其它有利的调理剂例如为根据INCI称为聚季铵盐的化合物(尤其是聚季铵盐-1至聚季铵盐-56)。非常特别优选的调理剂为N,N-二甲基-N-2-丙烯基-2-丙烯氯化铵(聚季铵盐-7)。
有利的调理剂的其它实例为纤维素衍生物和季铵化的瓜耳胶衍生物,尤其是瓜耳羟丙基氯化铵(如Jaguar Excel、Jaguar C 162(Rhodia)、CAS65497-29-2、CAS 39421-75-5)。
根据本发明还可有利地使用非离子聚N-乙烯基吡咯烷酮/聚乙酸乙烯酯共聚物(如LuviskolVA 64(BASF)),阴离子丙烯酸盐共聚物(如LuviflexSoft(BASF)),和/或两性酰胺/丙烯酸盐/甲基丙烯酸盐共聚物(如Amphomer(National Starch))。有利的调理剂的其它实例为季铵化的聚硅氧烷。
乙氧基化的甘油单-或二脂肪酸酯的实例为聚氧乙烯(10)橄榄油甘油酯、聚氧乙烯(11)鳄梨油甘油酯、聚氧乙烯(11)可可脂甘油酯、聚氧乙烯(13)向日葵油甘油酯、聚氧乙烯(15)甘油醚异硬脂酸酯、聚氧乙烯(9)椰油脂肪酸甘油酯、聚氧乙烯(54)氢化蓖麻油、聚氧乙烯(7)氢化蓖麻油、聚氧乙烯(60)氢化蓖麻油、霍霍巴油乙氧基化物(聚氧乙烯(26)霍霍巴脂肪酸、聚氧乙烯(26)霍霍巴醇)、甘油聚氧氧乙烯(5)椰油酸酯、聚氧乙烯(9)椰油脂肪酸甘油酯、聚氧乙烯(7)甘油醚椰油酸酯、聚氧乙烯(45)棕榈仁油甘油酯、聚氧乙烯(35)蓖麻油、橄榄油聚氧乙烯(7)酯、聚氧乙烯(6)辛酸/癸酸甘油酯、聚氧乙烯(10)橄榄油甘油酯、聚氧乙烯(13)向日葵油甘油酯、聚氧乙烯(7)氢化蓖麻油、氢化棕榈仁油甘油酯、聚氧乙烯(6)酯、聚氧乙烯(20)玉米油甘油酯、聚氧乙烯(18)甘油醚油酸酯椰油酸酯、聚氧乙烯(40)氢化蓖麻油、聚氧乙烯(40)蓖麻油、聚氧乙烯(60)氢化蓖麻油、聚氧乙烯(60)玉米油甘油酯、聚氧乙烯(54)氢化蓖麻油、聚氧乙烯(45)棕榈仁油甘油酯、聚氧乙烯(80)甘油醚椰油酸酯、聚氧乙烯(60)杏仁油甘油酯、聚氧乙烯(60)月见草甘油酯、聚氧乙烯(200)氢化甘油醚棕榈酸酯、聚氧乙烯(90)甘油醚异硬脂酸酯。
优选乙氧基化的甘油单-或二脂肪酸酯为聚氧乙烯(7)甘油醚椰油酸酯、聚氧乙烯(9)椰油甘油酯、聚氧乙烯(40)氢化蓖麻油、聚氧乙烯(200)氢化甘油醚棕榈酸酯。
为了不同目的将乙氧基化的甘油单-或二脂肪酸酯用于本发明混合物中。每分子具有3-12个氧化乙烯单元的乙氧基化的甘油单-或二脂肪酸酯用作加脂剂(refatting agent)以改进皮肤干燥后的感觉,每分子具有30-50个氧化乙烯单元的乙氧基化的甘油单-或二脂肪酸酯用作非极性物质如香料的助溶剂。每分子具有超过50个氧化乙烯单元的乙氧基化的甘油单-或二脂肪酸酯用作增稠剂。
合适的抗氧化剂的实例为常规的或适合化妆品和/或皮肤病学应用的所有抗氧化剂。
抗氧化剂优选选自下列物质:氨基酸(如甘氨酸、组氨酸、酪氨酸、色氨酸),咪唑(如咪唑丙烯酸),肽如D,L-肌肽、D-肌肽、L-肌肽及其衍生物(如鹅肌肽),类胡萝卜素,胡萝卜素(如α-胡萝卜素、β-胡萝卜素、γ-番茄红素),绿原酸及其衍生物,类视色素如视黄醇、视黄醛和/或视黄酸及其相应的酯,硫辛酸及其衍生物(如二氢硫辛酸),金硫葡萄糖,丙硫氧嘧啶和其它硫醇(如硫氧还蛋白、谷胱甘肽、半胱氨酸、胱氨酸、胱胺及其糖基、N-乙酰基、甲基、乙基、丙基、戊基、丁基和月桂基、棕榈酰基、油基、γ-亚油基、胆甾烯基和甘油基酯)及其盐,硫代二丙酸二月桂酯,硫代二丙酸二硬脂醇酯,硫代二丙酸及其衍生物(酯、醚、肽、类脂、核苷酸、核苷和盐),以及非常低剂量(如pmol-μmol/kg本发明混合物)的磺酰亚胺化合物(如丁硫堇磺酰亚胺、高半胱氨酸磺酰亚胺、丁硫堇砜、戊硫堇磺酰亚胺、己硫堇磺酰亚胺、庚硫堇磺酰亚胺),以及(金属)螯合剂(如α-羟基脂肪酸、棕榈酸、植酸、乳铁蛋白),α-羟基酸(如柠檬酸、乳酸、马来酸),腐殖酸,胆汁酸,胆汁萃取物,胆红素,脱氢胆红素,EDTA,EGTA,不饱和脂肪酸(如γ-亚麻酸、亚油酸、油酸),叶酸,泛醌和泛醌醇,维生素C及衍生物(如棕榈酸抗坏血酸酯、抗坏血酸磷酸镁,乙酸抗坏血酸酯),生育酚及衍生物(如维生素E乙酸酯),维生素A及衍生物(维生素A棕榈酸酯),以及安息香树脂的苯甲酸松柏酯,芸香亭酸及其衍生物,α-糖基芸香苷,阿魏酸,亚糠基葡糖醇,肌肽,丁基羟基甲苯,丁基羟基苯甲醚,去甲二氢愈创木酸,去甲二氢愈创木脂酸,三羟基苯丁酮,尿酸及其衍生物,甘露糖及其衍生物,锌及其衍生物(如ZnO,ZnSO4),硒及其衍生物(如硒代蛋氨酸),均二苯代乙烯及其衍生物(如均二苯代乙烯氧化物,尤其是反式均二苯代乙烯氧化物)和合适衍生物(盐、酯、醚、糖、核苷酸、核苷、肽和类脂)。
适合本发明混合物的增稠剂为交联的聚丙烯酸及其衍生物,角叉菜胶,黄原胶,多糖如黄原胶、瓜耳胶、琼脂、藻酸盐和甲基纤维素,纤维素衍生物如羧甲基纤维素、羟基羧甲基纤维素、羟乙基丙基纤维素、羟丁基甲基纤维素、羟丙基甲基纤维素,以及较高分子量的聚乙二醇单-和二脂肪酸酯,脂肪醇,甘油单酯和脂肪酸,聚乙烯醇和聚乙烯基吡咯烷酮。
合适的增稠剂例如还有亲水性热解硅胶、聚丙烯酰胺、聚乙烯醇和聚乙烯基吡咯烷酮,脂肪酸与多元醇如季戊四醇或三羟甲基丙烷的酯,具有窄同系物分布的脂肪醇乙氧基化物或C1-C20烷基低聚葡糖苷,以及电解质如氯化钠和氯化铵。
适合本发明混合物的生物杀伤剂为对革兰氏阳性细菌有特定作用的试剂,例如玉洁纯(2,4,4’-三氯-2’-羟基二苯醚)、洗必泰(1,1’-六亚甲基双[5-(4-氯苯基)双胍]和TTC(3,4,4’-三氯均二苯脲)。高度合适的生物杀伤剂还有异噻唑酮如5-氯-2-甲基-3(2H)异噻唑酮和2-甲基-3(2H)异噻唑酮。季铵盐化合物原则上也是适合的,但优选用于消毒皂和洗剂中。许多香料也具有生物杀伤性能。还有大量精油或其特征成分,例如丁香油(丁子香酚)、薄荷油(薄荷醇)或百里香油(百里酚),表现出显著的抗微生物效果。其它合适的生物杀伤剂为例如适合龋齿预防的氟化合物如NaF和胺氟化物。
发泡剂的实例例如可为上述表面活性剂(c),尤其是十二烷基硫酸钠。
许多上述表面活性剂(c)也可用作润湿剂,润湿剂的特别优选的实例为具有式R9-C6H4-SO3M1的烷基苯磺酸盐,其中M1如上所定义且R9为C8-C12烷基。优选烷基苯磺酸盐为所谓的LAS(线性烷基苯磺酸盐),其使用线性C8-C12链烷制备。
保湿剂的实例为山梨糖醇,分子量Mn例如为200-1000g/mol的聚乙二醇。
本发明混合物也可包含着色剂如染料或颜料,发光物质和/或其它效果物质(如颜色条纹)。
在本发明的一个实施方案中,本发明混合物包含:
0.1-10重量%,优选1-5重量%氨基塑料泡沫块(a),
总共1-99.8重量%,优选10-85重量%表面活性剂(c),
0-20重量%,优选1-15重量%油或脂相(d),
0-10重量%,优选0.1-5重量%香料或芳香物质(e),
总共0-5重量%,优选1-4重量%添加剂(f),
其中重量%中的数据基于整个本发明混合物,余量优选为水(b)。
在一个实施方案中,本发明混合物可以以总共0.001-3重量%,特别优选0.05-2重量%,尤其是0.1-1重量%的量包含一种或多种抗氧化剂。如果维生素E和/或其衍生物为抗氧化剂,则优选含量为0.001-1重量%。如果维生素A或维生素A衍生物或胡萝卜素为本发明混合物中的抗氧化剂,则优选含量为0.001-1重量%。
在本发明的一个实施方案中,本发明混合物可包含0.1-0.3重量%生物杀伤剂。
在本发明的一个实施方案中,本发明混合物的pH为2-12,优选3-10,特别优选5-9。此处,如果这些混合物意欲用于清洗身体,则优选pH为2-12,优选4-9,特别优选5-8。
在本发明的一个实施方案中,本发明混合物在23℃下的动态粘度为100-100 000mPa·s。动态粘度例如使用Brookfield粘度计测量。
本发明混合物当然可以包含一种或多种本身已知的摩擦剂如硅胶、硅酸盐、浮石、大理石、聚乙烯、杏仁壳、超吸收剂。然而,优选本发明混合物不包含摩擦剂。
本发明混合物尤其适用于清洗身体和各种类型的表面。在本发明混合物用于清洗身体的情况下,例如清洗严重粘有油的手时,首先观察到所述身体部位变得易于清洁并且甚至无需施加很大的力。其次,皮肤受到保护,没有观察到或仅观察到程度显著降低的在使用强摩擦剂时经常观察到的皮肤开裂。
本发明混合物例如可用作清洁剂、盆浴或淋浴凝胶、去皮剂、牙膏、洗手膏或用于制备清洁剂、盆浴或淋浴凝胶、去皮剂、牙膏、洗手膏。清洁剂的实例为通用型清洁剂、喷雾清洁剂、清洁剂用浓缩物、窗和玻璃清洁剂、挡风玻璃清洁剂、汽车用香波、烘箱清洁剂、液体合成皂、地板清洁剂如肥皂清洁剂和地板消毒清洁剂、人造革清洁剂、塑料清洁剂、冲刷组合物如液体冲刷组合物和冲刷粉末,地毯清洁剂如用于地毯的泡沫清洁剂和喷雾萃取清洁剂,例如用于织物的洗涤膏。
本发明混合物例如可具有略微粘稠或高度粘稠液体,糊,清洁乳,凝胶或皂如洗手皂的外观。
因此本发明进一步提供了本发明混合物作为清洁剂的用途。本发明进一步提供了一种使用本发明混合物清洁表面的方法。
就此而言,表面如上所定义。
在本发明特别优选的变型方案中,表面为由有光泽材料如瓷釉,玻璃,金属如不锈钢,塑料,尤其是有光泽塑料,陶瓷如瓷砖或瓷器制成的表面。
为进行本发明方法,起点为污染表面,其可被均匀或不均匀地污染至较高或较低的程度。
待除去的污物例如为:
脂,油,蜡如聚乙烯蜡、石蜡,石蜡油,酯油,天然油和脂,润滑脂,轴承润滑脂,Stauffer脂,褐煤蜡,
阴离子表面活性剂的金属盐如石灰皂,
生物膜如霉菌或假单胞菌的生物膜,
聚合物如喷漆枪、聚氨酯泡沫、聚硅氧烷,
金属氧化物如氧化铜、氧化铅或氧化镍或者例如由腐蚀产生的锈,或锈颗粒或航空器锈,尤其是可为中性、酸性或碱性的铁氧化物、金属氢氧化物和金属碳酸盐,尤其是氢氧化铁、氢氧化铜、氢氧化镍、氢氧化铝、氢氧化镁、MgCO3、碱式MgCO3、CaCO3、碱式碳酸铜,其中金属氧化物、金属碳酸盐和金属氢氧化物可例如由工具或材料的结构表面的基础金属通过腐蚀形成,或者可以是二次沉积的,
润滑剂残留物如部分碳化或者部分或完全树脂化的润滑剂以及破坏的乳液。可提及的实例为:例如在链锯上的树脂化的天然酯油,或在纺丝聚酯丝纤维中使用的热板上的碳化油,以及例如来自自动化领域和汽车或自行车的润滑油,
如水泥或石膏的沉积物和结块,
通常的室内污物如与来自厨房区域的脂、油脂混合的房屋灰尘,还呈树脂化形式如焙烧脂或油炸的油。
待除去的污物的其它实例例如为圆珠笔或毡尖笔书写痕迹。
污物例如可以以点、环、溅泼点或膜的形式均匀或不均匀地分布在待清洁表面上。
本发明方法的时间例如可选择为从数秒如5秒至24小时,优选1分钟至3小时,特别优选至多1小时。
为进行本发明的清洁方法,程序例如可包括将本发明混合物以纯的形式或以稀释形式,尤其是以用水稀释形式施加至待清洁表面。
为进行本发明的清洁方法,可使用的辅助工具为一种或多种布、刷或海绵。
本发明进一步提供了一种生产本发明混合物的方法,其也称为本发明的生产方法。本发明生产方法例如可通过将如下组分以任何顺序一起混合如搅拌而进行:
(a)平均直径为50μm至5mm(重均)的开孔氨基塑料泡沫块,
(b)水,
(c)至少一种表面活性剂,和
(d)合适的话油或脂相。
如果希望生产糊状的本发明混合物,则优选使用高速搅拌器,特别优选在减压下如在20-100毫巴下进行混合。
在实际进行本发明生产方法之后,可配制如挤出或加工本发明混合物而得到皂状条。
本发明通过如下操作实施例说明。
I.1制备氨基塑料泡沫
在开口容器中,将喷雾干燥的蜜胺/甲醛预缩合物(摩尔比1∶3,分子量约500g/mol)加入具有3重量%甲酸和1.5%在烷基中具有12-18个碳原子的烷基磺酸钠盐的混合物乳化剂(购自Bayer AG的K 30)的水溶液中,其中百分数基于蜜胺/甲醛预缩合物。蜜胺/甲醛预缩合物的浓度基于蜜胺/甲醛预缩合物和水的整个混合物为74重量%。将如此得到的混合物剧烈搅拌,然后加入20重量%正戊烷。将混合物进一步搅拌(约3分钟)直至形成看上去均相的分散体。将该分散体刮涂至作为载体的特氟隆化的玻璃布上并在干燥烘箱中发泡和固化,其中烘箱中盛行150℃的空气温度。在此过程中,在这些条件下在泡沫内建立的块温度为正戊烷的沸点温度,即37.0℃。在7-8分钟之后,达到泡沫的最大高度。将泡沫在150℃的干燥烘箱中再放置10分钟;然后在180℃下加热处理30分钟。这得到氨基塑料泡沫。
对氨基塑料泡沫测得如下性能:
根据DIN ISO 4590,99.6%开孔,
根据DIN 53577测定的压缩强度(40%)为1.3kPa,
根据EN ISO 845测定的密度为7.6kg/m3,
通过分析截面的显微照片测得的平均孔径为210μm,
根据DIN 66131测定的BET表面积为6.4m2/g,
根据DIN 52215测定的吸声系数为93%,
根据DIN 52212测定的吸声系数超过0.9。
I.2通过研磨制备氨基塑料泡沫块(a.1)
使用高速切削刀操作的实验室分析磨机(型号A10)研磨根据I.1的氨基塑料泡沫立方体,然后通过网孔宽度为250μm的振摇筛筛分。这得到平均直径为至多250μm的开孔氨基塑料泡沫块(a.1)。除去筛分残留物。
I.3制备本发明混合物
I.3.1制备室内清洁剂,通用程序
将如下组分一起混合:
3g 正-C12H25-SO4Na(c.1)
0.5g 硬脂酸钠(c.2)
2g 油烯基鲸蜡醇与17当量氧化乙烯的乙氧基化产物(c.3)
2g 正-C18H37-OH与7当量氧化乙烯的乙氧基化产物(c.4)
0.5g 乙醇
0.2g香料(e.1)-(e.5)的混合物,其包含相同重量份的α-戊基肉桂醛、α-己基肉桂醛、4-正丁基苯基甲基丙醛
0.1g苄醇、芳樟醇
1g烷基苄基二甲基氯化铵(生物杀伤剂,(f.1))
并用水(b)补足100g。
这得到不含摩擦剂的清洁剂V-R.5,将其置于150ml的烧杯中。然后使用玻璃棒按表1加入开孔氨基塑料泡沫块(a.1)并用玻璃棒搅拌。这得到根据表1的本发明混合物R.1-R.4,其也称为本发明清洁剂R.1-R.4。在每种情况下,测试了沉淀性能和清洁效果。
I.3.2制备沐浴凝胶
沐浴凝胶通过混合所谓的表面活性剂相和所谓的水相而制备。
为制备表面活性剂相,将如下组分一起混合:
3000g 28重量%的正-C12H25-(OCH2CH2)3-OSO3 -Na+水溶液
600g N-(椰油酰胺基乙基)-N-(羟基乙基)氨基乙酸钠
770g 13重量%季铵盐-44[SHBN006]水溶液
300g 月桂基聚氧乙烯醚硫酸钠
50g 香油(香味:苹果-梨)
2000g 蒸馏水
这得到表面活性剂相。
为制备水相,将如下组分一起混合:
100g D-泛醇(D-(+)-2,4-二羟基-N-(3-羟丙基)-3,3-二甲基丁酰胺
10g 5-氯-2-甲基-3(2H)异噻唑酮和2-甲基-3(2H)异噻唑酮的3∶1混合物(重量份)
30g 柠檬酸
100g 氯化钠
0.15g黄色-橙色85 E 110
2440g蒸馏水
这得到水相。
为制备不含摩擦剂的沐浴凝胶,将如下组分一起混合:73.7g表面活性剂相(参见上文)和26.7g水相。这得到沐浴凝胶V-DG.5。
为制备本发明沐浴凝胶,首先引入100g不含摩擦剂的沐浴凝胶V-DG.1。然后使用玻璃棒按表2加入开孔氨基塑料泡沫块(a.1)并用玻璃棒搅拌。这得到根据表2的本发明混合物DG.1-DG.4,其也称为本发明沐浴凝胶DG.1-DG.4。在每种情况下,测试了沉淀性能和清洁效果。
II.清洁表面
II.1使用根据实施例I.3.1的室内清洁剂清洁表面
为测试清洁效果,使用覆盖石灰痕的不锈钢。在每种情况下,将两滴根据I.3.1的纯清洁剂施加至湿布上并擦去石灰。然后视觉评价清洁效果。
表1:本发明清洁剂和对比清洁剂的组成和清洁效果
清洁剂 | 添加剂(a.1)[g] | 沉淀性能 | 清洁效果的评价 |
R.1 | 1 | 立刻沉淀 | 良好,无划痕 |
R.2 | 2 | 立刻沉淀 | 良好,无划痕 |
R.3 | 5 | 立刻沉淀 | 良好,无划痕 |
R.4 | 10 | 立刻沉淀 | 良好,无划痕 |
V-R.5 | - | - | 令人满意,无划痕 |
V-R.6 | - | 立刻沉淀 | 良好,但留下划痕 |
V-R.5没有加摩擦剂的根据实施例I.3.1的不含摩擦剂的清洁剂。
V-R.6与V-R.5对应并且还在其中加入2g浮石粉作为摩擦剂。
II.2清洁被润滑油(自行车链)污染的手
双手均被润滑油(自行车链)污染。用水将手润湿。在手中放上数滴根据表2的一种本发明沐浴凝胶和一种对比沐浴凝胶并擦手。用热水简单地漂洗手并用手巾干燥并视觉评价清洁效果。
表2:本发明沐浴凝胶和对比沐浴凝胶的组成和清洁效果
沐浴凝胶 | 添加剂(a.1)[g] | 沉淀性能 | 清洁效果的评价 |
DG.1 | 1 | 立刻沉淀 | 良好,皮肤没有变红 |
DG.2 | 2 | 立刻沉淀 | 良好,皮肤没有变红 |
DG.3 | 5 | 立刻沉淀 | 良好,皮肤没有变红 |
DG.4 | 10 | 立刻沉淀 | 良好,皮肤没有变红 |
V-DG.5 | - | - | 中等,皮肤没有变红 |
V-R.6 | - | 立刻沉淀 | 良好,但皮肤变红 |
V-DG.5没有加摩擦剂的根据实施例I.3.2的不含摩擦剂的清洁剂。
V-DG.6与V-DG.5对应并且还在其中加入2g聚乙烯作为摩擦剂。
Claims (10)
1.一种包含如下物质的混合物:
(a)平均直径为50μm至5mm(重均)的开孔氨基塑料泡沫块,
(b)水,
(c)至少一种表面活性剂,和
(d)合适的话油或脂相。
2.根据权利要求1的混合物,其中表面活性剂(c)选自无毒的表面活性剂。
3.根据权利要求1或2的混合物,其中所述混合物在23℃下的动态粘度为100-100000mPa·s。
4.根据权利要求1-3中任一项的混合物,其中开孔氨基塑料泡沫块(a)由密度为5-500kg/m3且平均孔径为1μm至1mm的氨基塑料泡沫通过机械粉碎而制备。
5.根据权利要求1-4中任一项的混合物,其额外包含至少一种香料或芳香物质(e)。
6.一种使用至少一种根据权利要求1-5中任一项的混合物作为清洁剂来清洁表面的方法。
7.根据权利要求6的方法,其中所述表面为由有光泽材料制成的表面。
8.根据权利要求1-5中任一项的混合物作为清洁剂或沐浴凝胶的用途。
9.一种生产根据权利要求1-5中任一项的混合物的方法,其中将如下组分一起混合:
(a)平均直径为50μm至5mm(重均)的开孔氨基塑料泡沫块,
(b)水,
(c)至少一种表面活性剂,和
(d)合适的话油或脂相。
10.根据权利要求9的方法,其以多段进行。
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DE102005023801.7 | 2005-05-19 | ||
DE102005023801A DE102005023801A1 (de) | 2005-05-19 | 2005-05-19 | Verfahren zur Reinigung von Oberflächen |
DE200510029745 DE102005029745A1 (de) | 2005-06-24 | 2005-06-24 | Verfahren zur Reinigung von Oberflächen |
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