CN105007952A - 用于形成多孔吸收性结构的组合物 - Google Patents
用于形成多孔吸收性结构的组合物 Download PDFInfo
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- CN105007952A CN105007952A CN201480011375.6A CN201480011375A CN105007952A CN 105007952 A CN105007952 A CN 105007952A CN 201480011375 A CN201480011375 A CN 201480011375A CN 105007952 A CN105007952 A CN 105007952A
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Abstract
本发明公开了多孔吸收性结构,其包括吸收性颗粒和具有低于约百万分之1000的残留的单烯键不饱和单体的超吸收性聚合物材料,所述超吸收性聚合物材料基本上包被吸收性颗粒并将颗粒连接成多孔网络以形成多孔吸收性结构。
Description
发明领域
本发明一般地涉及多孔吸收性材料领域,更具体地涉及可以喷涂到多种表面上的多孔吸收性微粒结构。
发明背景
良好的卫生是全球性的需要,并且使用一次性吸收性制品时常是满足该需要的更容易且更卫生的途径。术语“吸收性制品”通常是指可以吸收并容纳流体的装置。例如,个人护理吸收性制品是指贴着或接近皮肤放置以吸收并容纳从身体排出的各种流体的装置。术语“一次性的”在本文中用来描述这样的吸收性制品,在单次使用后不打算对其进行洗涤或另外储存或作为吸收性制品重新使用。这样的一次性吸收性制品的实例包括但不限于,个人护理吸收性制品、健康/医疗吸收性制品和家用/工业吸收性制品。
由于一些吸收性制品需要复杂且昂贵的制造,吸收性制品的可用性在一些领域中会受到限制。必要的材料可能不是当地可得的。传统的一次性吸收性制品可以包括顶片、底片和设置在两者之间的吸收芯。
还已知供选择的形成一次性服装的方法。例如,本领域已知通过浸渍和喷涂形成的服装。Giloh的第6,987,210号美国专利公开了一次性保护性内衣,其可以通过将模型浸渍在弹性的液体可渗透的材料中形成。吸收垫可以连接到浸渍形成的服装的胯部区域。服装可以使用粘合剂喷涂,以使棉或其他纤维可以连接到服装内部。在另一个实例中,Torres的第8,124,549号美国专利公开了用于通过将组合物喷涂到支撑表面上而形成织物的组合物。组合物包括纤维、粘合剂和稀释剂。组合物可以直接喷涂到人体上以形成衬衫或连衣裙。在一些实施方案中,组合物可以喷涂在放置在人体上的网架上,以使产生的服装具有特定的形状。然而,Torres公开的组合物没有足够的吸收性以发挥作为最常见的可得的吸收性制品的替代品或替换物的作用。
在世界各地都仍然需要具有吸收性且容易制造的制品,所述制品具有完整性、覆盖范围和吸收能力以满足消费者的需要。
发明概述
本发明涉及多孔吸收性结构以及形成多孔吸收性结构的方法。在一个实施方案中,形成多孔吸收性结构的方法可以包括提供粘度小于约10,000cp的超吸收性聚合物材料的步骤。
吸收性颗粒,包括但不限于有机吸收性颗粒,可以加入到超吸收性聚合物材料中以形成混合物。混合物的超吸收性聚合物材料与吸收性颗粒的重量比可以为大于3:1,并且在一些实施方案中,大于约3.5:1且小于约6:1。本发明的某些实施方案可以包括平均长宽比小于约5,优选地小于约3的吸收性颗粒。所述吸收性颗粒可以具有大于约20微米且小于约100微米的平均长度。
将超吸收性聚合物材料和吸收性颗粒的混合物喷涂到模型上,并干燥混合物以产生基本上符合模型形状的多孔吸收性结构。在一些实施方案中,模型可以是人体的至少一部分。然而,模型还可以是非织造材料、织造材料、纸、膜或其组合。形成多孔吸收性结构的方法还可以包括从模型上移除所述多孔吸收性结构的步骤。
在选择的实施方案中,超吸收性聚合物材料具有低于约百万分之1000的残留的单烯键不饱和单体,其可以是丙烯酸。
在某些实施方案中的多孔吸收性结构可以由以下方法形成:提供粘度小于约10,000cp的超吸收性聚合物材料,并且将吸收性颗粒加入到超吸收性聚合物材料中以形成混合物,其中混合物中的超吸收性聚合物材料与吸收性颗粒的重量比为大于3:1且小于约6:1。将所述混合物施加到模型上并干燥以产生基本上符合模型形状的多孔吸收性结构。
多孔吸收性结构可以包括吸收性颗粒和超吸收性聚合物材料,所述超吸收性聚合物材料基本上包被吸收性颗粒并将吸收性颗粒连接成如附图所示的多孔吸收性网络。多孔吸收性结构中的超吸收性聚合物材料与吸收性颗粒的重量比可以为大于1:1,并且可以为大于1.1:1,并且在一些实施方案中可以为小于1.5:1。这样的多孔吸收性结构可以具有至少约10%的峰值拉伸,在某些实施方案中具有至少约25%的峰值拉伸。多孔吸收性结构还可以具有至少约150g/cm的峰值能,并且在一些实施方案中具有至少约250g/cm的峰值能量。
当多孔吸收性结构连接到材料如非织造材料时,本发明还适合用作吸收性揩巾。超吸收性聚合物材料和吸收性颗粒的混合物可以通过喷涂、倾倒或其他施加方法直接施加到非织造材料,以提高非织造材料的吸收性。
吸收性制品可以使用适合固定到人体的外罩形成,所述外罩具有内侧。包括吸收性颗粒和超吸收性聚合物材料的多孔吸收性结构可以施加到外罩的内侧。供选择地,超吸收性聚合物材料和吸收性颗粒的混合物可以喷涂到外罩的内侧上,多孔吸收性结构在外罩上直接形成,所述外罩可以充当多孔吸收性结构的模型。
多孔吸收性结构中的超吸收性聚合物材料可以基本上包被吸收性颗粒并将颗粒连接成多孔网络。在选择的实施方案中,多孔吸收性结构中的超吸收性聚合物材料与吸收性颗粒的重量比为大于0.8:1且小于1.4:1。
以下将参照附图中说明的具体实施方案更详细地描述本发明。
附图简要说明
图1是本发明的多孔吸收性结构的一个实施方案的剖视图;
图2是本发明的多孔吸收性结构的一个实施方案的放大的剖视图;
图3是本发明的多孔吸收性结构的一个实施方案的近视图;
图4是本发明的多孔吸收性结构的上表面视图;和
图5是本发明的多孔吸收性结构的上表面的放大视图。
详述
现在将详细参照本发明的实施方案,在附图中说明其一个或多个实施例。每个实施例通过解释本发明的方式提供,并不意味着限制本发明。例如,作为一个实施方案的部分说明或描述的特征可以与另一个实施方案一起使用,以产生又一个实施方案。本发明旨在包括本文所述的实施方案的修改和变化。
本发明涉及多孔吸收性结构和用于形成多孔吸收性结构的方法。本发明的多孔吸收性结构的一个实施方案显示在图1-5中。根据本发明的多孔吸收性结构包括吸收性颗粒,其基本上被超吸收性聚合物材料或组合物包被。所述超吸收性聚合物材料还将吸收性颗粒连接成多孔吸收性网络。在这样的实施方案中,多孔吸收性结构中的超吸收性聚合物材料与吸收性颗粒的重量比可以为大于1:1且小于约1.5:1。在一个优选的实施方案中,多孔吸收性结构中的超吸收性聚合物材料与吸收性颗粒的重量比为1.1:1。如本文所使用,术语“超吸收性”是指水可溶胀的、水不溶性的有机或无机材料,其在最有利的条件下在含有0.9wt%氯化钠的水溶液中能够吸收其重量的至少约10倍或其重量的至少约15倍。超吸收性材料可以是天然的、合成和修饰的天然聚合物和材料。此外,超吸收性材料可以是无机材料,如硅胶,或有机化合物,如交联的聚合物。超吸收性聚合物材料基本上覆盖颗粒并将其结合在一起。本发明的选择的实施方案包括超吸收性聚合物材料和吸收性颗粒的混合物,其可以使用通常可得的低成本手动喷雾瓶施加。
在图1-5中显示的具体实施方案是由超吸收性聚合物材料中的微粒化的纤维素颗粒形成的。混合物可以直接喷涂在溅出物或人体的一部分上,并且在干燥时变成多孔吸收性组合物。如果希望,一旦多孔吸收性组合物吸收了溅出物或渗出物,其可以被移除并替换。例如,混合物可以直接施加到伤口。当混合物干燥成多孔吸收性结构时,其吸收伤口中的渗出物。多孔吸收性结构保持其完整性并且可以从伤口中移除,而不破坏周围的组织。本发明的多孔吸收性结构具有足够的完整性以保持其形状,并保持与其所喷涂到其上的模型的连接。
供选择地,混合物可以喷涂到低成本的通常可得的基材上,所述基材可以具有或不具有吸收特性。组合可以用作吸收性服装或制品,如揩巾。在多孔吸收性材料已经吸收渗出物后,多孔吸收性材料可以容易地从基材上移除,并在施加另外的混合物后重新使用基材。
用于形成这样的多孔吸收性结构的方法包括提供超吸收性聚合物材料,其在选择的实施方案中具有允许通过通常可得的低成本常规手动喷雾器或喷雾瓶递送超吸收性聚合物材料的粘度。在一些实施方案中,超吸收性聚合物材料的粘度为低于约10,000cP且高于约500cP。在其他实施方案中,超吸收性聚合物材料的粘度优选地为低于2,000cP,且更优选地低于1000cP。在一些实施方案中,超吸收性聚合物材料的粘度为高于500cP,在其他实施方案中高于650cP。根据第7,312,286号美国专利中概述的测试程序,超吸收性聚合物材料的粘度在16小时时测量。如其中所解释,超吸收性聚合物材料的粘度使用可得自Brookfield Engineering,Middleboro,Mass.,U.S.A.的Brookfield DVII+可程序化粘度计测量。在25-盎司的塑料杯中取约200-250ml的超吸收性聚合物材料。粘度计通常首先使用希望的转子归零。对于超吸收性聚合物材料,使用3号转子。在20RPM和22.±.1℃的温度下测量粘度。
适用于本发明的超吸收性聚合物材料在Soerens等人的第6,849,685号、Lang等人的第7,312,286号和Lang等人的第7,335,713号美国专利中被描述为超吸收性粘合剂聚合物溶液,将这些参考文献各自的全部内容引入本文作为参考。其中描述的超吸收性粘合剂聚合物溶液能够在施加后水分诱导交联。虽然大多数超吸收性聚合物需要加入内部交联剂来加固聚合物,但由于有机单体充当内部交联剂,因此用于本发明的超吸收性聚合物材料不需要加入交联剂。内部交联剂允许通过将水溶性前体聚合物包被在基材上,然后去除水以活化潜在的交联剂来形成超吸收性聚合物材料。
Soerens等人在第6,737,491号美国专利中描述了可以在本发明中用作超吸收性聚合物材料的吸收性粘合剂组合物。Soerens等人公开的吸收性粘合剂组合物是单烯键不饱和聚合物和含有烷氧基硅烷官能团的丙烯酸酯或甲基丙烯酸酯,其特别适合用于制造吸收性制品。Soerens等人还描述的是制备吸收性粘合剂组合物的方法,其包括以下步骤:制备单体溶液,将单体溶液加入到引发剂系统,以及活化报导为基于醇的水溶性粘合剂组合物的引发剂系统中的聚合引发剂。如本文所使用的“单体(或多种单体)”包括单体,低聚物,聚合物,单体、低聚物和/或聚合物的混合物,以及能够与单烯键不饱和羧酸、磺酸或磷酸或其盐共聚的任意其他反应性化学物质。含有三烷氧基硅烷官能团的烯键不饱和单体适用于本发明并且是希望的。希望的烯键不饱和单体包括丙烯酸酯和甲基丙烯酸酯,如含有烷氧基硅烷官能团的丙烯酸酯和甲基丙烯酸酯。
在上述参考文献中公开的超吸收性粘合剂聚合物组合物是以下的反应产物:至少15质量%的单烯键不饱和羧酸、磺酸或磷酸或其盐;含有烷氧基硅烷官能团的丙烯酸酯或甲基丙烯酸酯,所述烷氧基硅烷官能团在暴露于水时形成硅醇官能团,所述硅醇官能团缩合以形成交联聚合物;含有酯单体的可共聚的亲水性二醇;和/或增塑剂。
单烯键不饱和单体可优选地为丙烯酸。其他适合的单体包括含有羧基的单体:例如,单烯键不饱和单羧酸或多羧酸,如(甲基)丙烯酸(是指丙烯酸或甲基丙烯酸;下文中使用类似的表示)、马来酸、富马酸、巴豆酸、山梨酸、衣康酸和肉桂酸;含羧酸酐基团的单体:例如,单烯键不饱和多羧酸酐(如马来酸酐);含羧酸盐的单体:例如,单烯键不饱和单羧酸或多羧酸(如(甲基)丙烯酸钠、(甲基)丙烯酸三甲胺、(甲基)丙烯酸三乙醇胺)的水溶性盐(碱金属盐、铵盐、胺盐等)、马来酸钠、马来酸甲胺;含磺酸基的单体:例如脂族或芳族乙烯基磺酸(如乙烯基磺酸、烯丙基磺酸、乙烯基甲苯磺酸、苯乙烯磺酸)、(甲基)丙烯酸磺酸[如(甲基)丙烯酸磺丙酯、2-羟基-3-(甲基)丙烯酰氧基丙磺酸];含磺酸盐基团的单体:例如,如上所述的含磺酸基单体的碱金属盐、铵盐、胺盐;和/或含酰胺基的单体:乙烯基甲酰胺、(甲基)丙烯酰胺、N-烷基(甲基)丙烯酰胺(如N-甲基丙烯酰胺、N-己基丙烯酰胺)、N,N-二烷基(甲基)丙烯酰胺(如N,N-二甲基丙烯酰胺、N,N-二正丙基丙烯酰胺)、N-羟烷基(甲基)丙烯酰胺[如N-羟甲基(甲基)丙烯酰胺、N-羟乙基(甲基)丙烯酰胺]、N,N-二羟烷基(甲基)丙烯酰胺[如N,N-二羟乙基(甲基)丙烯酰胺]、乙烯基内酰胺(如N-乙烯基吡咯烷酮)。
适合地,单烯键不饱和羧酸、磺酸或磷酸或其盐的量相对于超吸收性粘合剂聚合物组合物的重量可以为约15重量%至约99.9重量%。希望将酸基团中和至至少约25mol%的程度,也就是说,酸基团优选地作为钠、钾或铵盐存在。中和的程度优选地为至少约50mol%。
制备水溶性聚合物的问题之一是保留在聚合物中的残留的单烯键不饱和单体含量的量。对于在个人卫生中的应用,要求超吸收性聚合物组合物的残留的单烯键不饱和单体含量的量为小于约1000ppm,更优选地小于500ppm,甚至更优选地小于100ppm。第7,312,286号美国专利公开了至少一种方法,借助其可以制造吸收性粘合剂组合物以使残留的单烯键不饱和单体含量为至少小于百万分之1000。残留的单烯键不饱和单体的分析根据第7,312,286号美国专利公开的残留的单烯键不饱和单体测试进行测定。更具体地,残留的单烯键不饱和单体分析使用由聚合物溶液或超吸收性组合物获得的固体膜进行。根据用于该测试描述的实例,单烯键不饱和单体为丙烯酸。带有SPD-IOAvp Shimadzu UV检测器的高效液相色谱(HPLC)(可得自营业地点在Columbia,Md.,U.S.A的Shimadzu Scientific Instruments)用于测定残留的丙烯酸单体含量。为了测定残留的丙烯酸单体,使用3.5cm Lx0.5cmW磁力搅拌棒在500rpm的速度下在100ml 0.9%NaCl溶液中搅拌约0.5克的固化膜16h。过滤混合物并随后使滤液通过Nucleosil C8 100A反相柱(可得自具有位于Ontario,Calif.,U.S.A.的办公室的企业Column EngineeringIncorporated)以分离丙烯酸单体。丙烯酸单体在特定时间洗脱,检测限为约10ppm。随后使用由色谱图计算的得到的洗脱液的峰面积来计算膜中残留的丙烯酸单体的量。最初,通过绘制纯丙烯酸洗脱液针对其已知量(ppm)的响应面积来生成校正曲线。获得了相关系数大于0.996的线性曲线。
将吸收性颗粒加入超吸收性聚合物材料中以形成混合物,所述混合物基本上尚未交联,但当交联发生时将产生多孔吸收性结构。如本文所使用,术语“吸收性颗粒”一般地是指可以吸收并容纳流体的颗粒。
吸收性颗粒可以是有机或无机的。适合的有机吸收性颗粒包括但不限于纤维素、大米、小麦粉、埃塞俄比亚画眉草、蚕豆、杏仁坚果粉、洋麻和玉米淀粉。适合的无机颗粒包括但不限于亚利桑那砂、浮石、硅藻土和白垩。
在选择用于本发明的吸收性颗粒时,必须小心以避免使超吸收性聚合物材料的交联升高至足够高的水平,使产生的材料太易碎而不能适当地保持作为吸收性材料的完整性和功能。
优选地选择吸收性颗粒的尺寸以允许颗粒将足够的吸收性加入到多孔吸收性材料,而不干扰混合物的递送方法。例如,某些纤维可能阻塞典型的手动喷雾器。优选的是平均长宽比小于约5的颗粒。甚至更优选的是平均长宽比小于约3的吸收性颗粒。在许多优选的实施方案中,吸收性颗粒具有大于约20微米且小于约80微米的平均长度。
吸收性颗粒可以加入到超吸收性聚合物材料(可得自EvonickStockhausen,LLC的聚丙烯酸钠的水溶液,名为“SR1717”或“吸收性粘合剂A”,其根据第7,312,286号美国专利制造),以使超吸收性聚合物材料与吸收性颗粒的重量比为大于约3:1,以及在一些实施方案中为大于或等于3.5:1。在选择的实施方案中,混合物中的超吸收性聚合物材料与吸收性颗粒的重量比为小于约6:1。在某些实施方案中,将吸收性颗粒加入到超吸收性聚合物材料中以形成这样的混合物,其中混合物中的超吸收性聚合物材料与吸收性颗粒的重量比为大于3:1且小于约6:1。在这些范围内的比例能够实现具有适合的完整性和吸收性的多孔吸收性结构的形成。
在混合吸收性颗粒直到其分散在超吸收性聚合物材料中且已达到希望的重量比之后,其他添加剂可以加入混合物中。例如,丙三醇可以加入超吸收性聚合物材料和吸收性颗粒的混合物中,以提高多孔吸收性材料的柔性和伸长率。可以利用其他添加剂来提高多孔吸收性材料的柔性和完整性,以及其他特性。例如,一些实施方案可以包括按重量计约百分之十五(15%)的量的分子量为8000的聚(乙二醇)(PEG)。
混合物可以倾倒或喷涂到希望的模型上。在一些情况下,混合物可以直接施加到其中需要吸收特性的区域。例如,混合物可以直接喷涂到伤口或其中需要吸收性的人体的另一区域上。在这样的实例中,模型将是人体。在本发明中有用的其他模型包括纸、膜、织造材料、非织造材料及其组合。例如,混合物可以施加到非织造材料以提高其吸收性,从而使复合材料可以用作用于任意数量的表面的揩巾,所述表面包括但不限于皮肤。“非织造”或“非织造纤网”是指材料和纤网或具有单一纤维或纤丝的结构的材料,所述单个纤维或纤丝是互层的,但不是像在编织织物中以可辨认的方式互层。非织造织物或纤网已经由许多方法形成,例如熔喷法、纺粘法、气流法和粘合梳理纤网法。在某些实施方案中,刚性模型可以用于成型多孔吸收性结构,之后该多孔吸收性结构可以从模型上移除并单独使用或作为吸收性制品的部分使用。
当使用第7,312,286号美国专利中描述的离心保留能力测试测量时,超吸收性聚合物材料或单独的组合物的吸收能力应为至少每克超吸收性聚合物材料一(1)克流体,在一些实施方案中,每克超吸收性聚合物材料至少三(3)克流体。
在选择的实施方案中,当使用第7,312,286号美国专利中描述的离心保留能力测试测量时,本发明的多孔吸收性结构的保留能力优选地为大于10g/g,更优选地为大于12g/g。
形成了许多样品并且这些样品的测试值报告在表1和2中。用于每种样品的超吸收性聚合物材料获得自Evonik Stockhausen,LLC(Greensboro,NorthCarolina,U.S.A.),其名为“SR1717”或“吸收性粘合剂A”,其根据第7,312,286号美国专利制造。吸收性粘合剂A是聚丙烯酸钠的水溶液。将两(2)克的表中列举的每种物质加入到七(7)克的该超吸收性聚合物材料中并搅拌三分钟。对于藻酸盐样品,将两(2)克的藻酸盐加入到七(7)克的吸收性粘合剂A。对于表1中列举的第一样品,不将颗粒或其他物质加入到超吸收性聚合物材料。将每种混合物倾倒到通常可得的圆形玻璃蒸发皿中,并放在一边干燥至少20分钟。产生的多孔吸收性结构符合玻璃皿的形状。
为了测量多孔吸收性结构的强度和韧度,对一系列样品进行拉伸测试。MTS Insight Electromechanical 1kN Extended Length单元用于使用100N的头(型号820-1XLTEL/0060.MTS Systems Corp.,Eden Prairie,MN)进行测试。样品为约6cm的圆形或正方形。还使用数显卡尺测量每种样品的厚度。报告在表1和2中的测试值包括峰值负载、峰值拉伸和峰值能量。峰值拉伸是材料的延展性的量度并且在拉伸测试中测定。其为断裂后测量的样品长度的增加(即,断裂后样品的长度减去原始样品长度)除以原始样品长度。更高的伸长率表明更高的延展性。峰值能量是直到最大负载的点处由样品吸收的能量。对于表1和2中报告的样品,最大负载对应于断裂(样品在断裂前可以吸收的能量)或大于100N的量。如表中所报告的,峰值负载是在测试过程中样品达到的最高值。
在表1中列举的超吸收性聚合物材料样品显示合理平衡的特性,但是缺乏实现本发明必要的适合的颗粒浓度。包括藻酸盐粉末的样品比希望的显示更低的峰值负载,并缺乏提高材料吸收性所必需的颗粒。
杏仁坚果壳粉形成具有比其他吸收性颗粒更低的完整性的多孔吸收性结构,但仍然是满意的。表1中许多多孔吸收性结构的样品是使用面粉(小麦粉(得自The J.M.Smucker Co,Orrville Ohio,U.S.A.的BestAll-Purpose Flour)、大米粉、埃塞俄比亚画眉草粉和鹰嘴豆和蚕豆粉(均可得自Bob’s Red Mill,Milwaukee,Oregon,U.S.A.))和玉米淀粉(可得自Pinnacle Foods Corp.,Cherry Hill,New Jersey U.S.A)形成的。所有使用这些颗粒制成的多孔吸收性结构均显示良好的完整性。使用洋麻颗粒形成的多孔吸收性结构显示特别良好的负载性质,但是峰值拉伸值低于期望的。然而,当形成多孔吸收性结构时,丙三醇可以加入到颗粒和超吸收性聚合物材料以增强多孔吸收性结构的拉伸和柔性。微粒化的纤维素用于形成多孔吸收性结构,其也报告在表1中,具有良好的完整性。
表1
图1-5是使用微粒化的纤维素形成的多孔吸收性结构的视图。图1是使用微粒化的纤维素形成的多孔吸收性结构的横截面的扫描电子显微镜图像。图2和3是部分横截面视图的放大。从图2和3中可看出,吸收性颗粒基本上包被有超吸收性聚合物材料,所述超吸收性聚合物材料还起到将吸收性颗粒结合到一起的作用。多孔吸收性结构的孔隙率通过蒸发水来产生,所述蒸发水还允许超吸收性聚合物材料有效地交联。
认为当多孔吸收性结构与流体接触时,超吸收性聚合物材料首先吸收流体。虽然在一些实施方案中,吸收性颗粒可以基本上或完全被超吸收性聚合物材料覆盖,但由于其被设置成从超吸收性聚合物材料中吸收流体,因此吸收性颗粒仍有助于多孔吸收性结构的吸收能力。
使用表2中列举的颗粒形成的样品是以与表1中列举的样品相同的方式形成的。使用亚利桑那砂(可得自CR Minerals Co.,Golden,Colorado,U.S.A.)和浮石(可得自Charles B.Crystal Co.,New York,New York,U.S.A.)形成的多孔吸收性结构显示良好的完整性和强度。这些多孔吸收性结构的表面与细粒度砂纸类似。膨润土颗粒(可得自Acros Organics,Fair Lawn New Jersey,U.S.A)形成具有非常高的峰值负载值的材料。硅藻土(可得自AldrichChemical Company,Milwaukee Wisconsin,U.S.A.)和二氧化硅样品(Sigma-Aldrich Chemical Co.Milwaukee Wisconsin,U.S.A.)形成的结构由于其缺乏完整性而不能被测试。其一个可能的原因是这些颗粒在该实例中提供了过多的交联能力。
表2
基于上述样品,本发明的优选的实施方案可以具有至少约150g/cm的峰值能量,以及可以优选地具有至少约500g/cm的峰值能量。
多孔吸收性结构可以用于多种吸收性产品中,如绷带、训练裤、尿布、尿布裤、揩巾、女性卫生产品、泳衣、失禁产品、吸收性毛巾、其他个人护理或健康护理服装,包括医疗服装等。这样的吸收性产品可以包括适于固定到人体的外罩。在外罩的内表面上可以形成多孔吸收性结构或在形成后可以施加多孔吸收性结构。
本领域技术人员应理解,可以对本文所述的分配器的特征作出各种修改和变化,特别是对分配器的机械和控制电路方面,而不脱离本发明的范围和精神。本发明旨在包括所有这样的变化。
Claims (28)
1.一种形成多孔吸收性结构的方法,其包括以下步骤:
提供粘度小于约10,000cp的超吸收性聚合物材料;
将吸收性颗粒加入到超吸收性聚合物材料中以形成混合物,使得超吸收性聚合物材料与吸收性颗粒的重量比大于3:1;
将超吸收性聚合物材料和吸收性颗粒的混合物喷涂到模型上;和
干燥混合物以产生基本上符合模型形状的多孔吸收性结构。
2.根据权利要求1的方法,其中所述超吸收性聚合物材料具有低于约百万分之1000的残留的单烯键不饱和单体。
3.根据权利要求1的方法,其中所述模型是人体的至少一部分。
4.根据权利要求1的方法,其中所述模型选自:非织造材料、织造材料、纸、膜或其组合。
5.根据权利要求1的方法,其进一步包括从模型上移除所述多孔吸收性结构的步骤。
6.根据权利要求1的方法,其中所述单烯键不饱和单体为丙烯酸。
7.根据权利要求1的方法,其中所述吸收性颗粒为有机颗粒。
8.根据权利要求1的方法,其中所述吸收性颗粒的平均长宽比为小于约5。
9.根据权利要求1的方法,其中所述干燥混合物的步骤进一步包括干燥混合物以诱导超吸收性聚合物材料中的交联以及产生基本上符合模型形状的多孔吸收性结构。
10.根据权利要求1的方法,其中所述吸收性颗粒的平均长度为大于20微米。
11.根据权利要求1的方法,其中所述混合物中的超吸收性聚合物材料与吸收性颗粒的重量比为小于约6:1。
12.根据权利要求11的方法,其中所述混合物中的超吸收性聚合物材料与吸收性颗粒的重量比为大于3.5:1。
13.根据权利要求1的方法,其中所述将吸收性颗粒加入到超吸收性聚合物材料中的步骤进一步包括其中超吸收性聚合物材料基本上包被吸收性颗粒。
14.一种多孔吸收性结构,其由包括以下步骤的方法形成:
提供粘度小于约10,000cp的超吸收性聚合物材料;
将吸收性颗粒加入到超吸收性聚合物材料中以形成混合物,其中混合物中的超吸收性聚合物材料与吸收性颗粒的重量比为大于3:1且小于约6:1;
将超吸收性聚合物材料和吸收性颗粒的混合物施加到模型上;和
干燥混合物以产生基本上符合模型形状的多孔吸收性结构。
15.根据权利要求14的多孔吸收性结构,其中所述超吸收性聚合物材料具有低于约百万分之1000的残留的单烯键不饱和单体。
16.根据权利要求14的多孔吸收性结构,其中所述模型是人体的至少一部分。
17.根据权利要求14的多孔吸收性结构,其中所述模型选自:非织造材料、织造材料、纸、膜或其组合。
18.根据权利要求14的多孔吸收性结构,其进一步包括从模型上移除所述多孔吸收性结构的步骤。
19.一种多孔吸收性结构,其包括:
吸收性颗粒;
超吸收性聚合物材料,其基本上包被所述吸收性颗粒并将所述吸收性颗粒连接成多孔吸收性网络;和
其中多孔吸收性结构中的超吸收性聚合物材料与吸收性颗粒的重量比为大于1:1且小于1.5:1。
20.根据权利要求19的多孔吸收性结构,其中所述超吸收性聚合物材料具有低于约百万分之1000的残留的单烯键不饱和单体。
21.根据权利要求19的多孔吸收性结构,其中所述超吸收性聚合物材料与吸收性颗粒的重量比为1.1:1。
22.根据权利要求19的多孔吸收性结构,其中所述多孔吸收性结构的峰值拉伸为至少约10%。
23.根据权利要求19的多孔吸收性结构,其中所述多孔吸收性结构的峰值能量为至少约150g/cm。
24.根据权利要求19的多孔吸收性结构,其进一步包括非织造材料。
25.根据权利要求24的多孔吸收性结构,其中所述非织造材料和多孔吸收性结构形成揩巾。
26.一种吸收性制品,其包括:
外罩,其适于固定到人体,所述外罩具有内侧;
多孔吸收性结构,其包括:
吸收性颗粒,和
超吸收性聚合物材料,其基本上包被吸收性颗粒并将所述颗粒连接成多孔网络以形成放置在外罩的内侧上的吸收芯,其中所述多孔吸收性结构中的所述超吸收性聚合物材料与吸收性颗粒的重量比为大于0.8:1且小于1.4:1。
27.根据权利要求26的吸收性制品,其中所述超吸收性聚合物材料具有低于约百万分之1000的残留的单烯键不饱和单体。
28.根据权利要求26的吸收性制品,其中所述多孔吸收性结构的峰值拉伸为至少约10%。
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- 2014-03-05 BR BR112015020387-6A patent/BR112015020387B1/pt active IP Right Grant
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- 2014-03-05 EP EP14763761.5A patent/EP2968642B1/en active Active
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KR20150121231A (ko) | 2015-10-28 |
MX358573B (es) | 2018-08-20 |
MX347437B (es) | 2017-04-25 |
WO2014141010A1 (en) | 2014-09-18 |
JP6165274B2 (ja) | 2017-07-19 |
IL240711A0 (en) | 2015-10-29 |
US20140276513A1 (en) | 2014-09-18 |
JP2016516564A (ja) | 2016-06-09 |
CL2015002470A1 (es) | 2016-02-05 |
EP2968642A4 (en) | 2016-11-16 |
EP2968642A1 (en) | 2016-01-20 |
MX2015011309A (es) | 2015-12-03 |
BR112015020387A2 (pt) | 2017-07-18 |
AU2014229396B2 (en) | 2015-12-17 |
BR112015020387B1 (pt) | 2020-05-12 |
AU2014229396A1 (en) | 2015-10-29 |
US9078947B2 (en) | 2015-07-14 |
KR101634536B1 (ko) | 2016-06-29 |
RU2599493C1 (ru) | 2016-10-10 |
EP2968642B1 (en) | 2018-10-10 |
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