CN109610173B - 纺织品耐久性抗皱、吸湿速干、抗起毛起球整理液及整理方法 - Google Patents
纺织品耐久性抗皱、吸湿速干、抗起毛起球整理液及整理方法 Download PDFInfo
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Abstract
纺织品耐久性抗皱、吸湿速干、抗起毛起球整理液及整理方法,其特征是整理液包含醚化改性二羟甲基二羟基乙烯脲树脂60‑80g/L、催化剂10‑15g/L、有机硅乳液10‑30g/L、阳离子封端型聚氨酯树脂20‑40g/L。使织物经一次整理即能够得到良好的抗皱、吸湿速干、抗起毛起球的功能效果,且整理后织物手感柔软,强力损伤小,耐洗性良好。
Description
技术领域
本发明涉及的是纺织品后整理加工技术领域,具体涉及一种纺织品用耐久性抗皱、吸湿速干、抗起毛起球后整理液及其整理工艺。经该整理液加工的织物产品可以同时具备抗皱、吸湿速干、抗起毛起球的功能特点,且对织物强力损伤小,有优异的耐水洗牢度,适用于各种织物。
背景技术
随着人们生活水平的提高,人们对服饰的要求也在不断提高,不仅要求穿着舒适,而且对保持外观平整,容易打理,以及具有一定的穿着强力,耐水洗等方面也尤为看重。例如一些衬衫类、运动装类的服装产品,人们要求面料手感柔软、弹性好、抗皱性佳,吸湿速干、透湿透气性好,服用过程中保持服装外观平整,不易起毛起球,耐水洗牢度好。针对这些性能要求,通常需要对织物采用不同的助剂进行后整理来实现。在选择后整理助剂及工艺时,既要达到各个功能整理的理想效果,又要保证整理助剂相互之间良好的复配性能,同时还要保证整理工艺的协同和简便,达到最优的整理效果。
纤维分子链间易发生相对滑移是产生褶皱的重要原因。许多棉、麻、粘胶等纤维的纯纺及混纺都容易产生褶皱。抗皱的原理主要是通过固定纤维中分子链的相对位置,从而防止和减少分子链间滑移的产生。上世纪70年代后,二羟甲基二羟基乙烯脲树脂抗皱整理的技术趋于成熟,应用较为广泛。但此类化合物在整理加工、后期储存和穿着过程中都会有甲醛的释放,且普遍存在强力下降,整理后织物泛黄的现象。
吸湿速干也称为“吸湿排汗”,这一词包含两层含义:①快速吸收,且排放出人体的汗液,不易产生闷热和发粘的现象;②通过吸湿性和放湿性,对穿着空间和外部环境的湿度变化进行响应,即具有调节湿度使人们服用时感到舒适的性能。吸湿速干织物是指织物同时具有吸水性和快干性,无论天然还是合成纤维都很难兼具这两种性能,可以通过后整理技术使织物获得快速吸湿、散湿的高舒适性能。目前市场上常见的吸湿速干整理剂多为聚酯聚醚嵌段共聚物,这类整理剂在制备过程中能耗较大,且通常只应用在涤纶或其混纺类织物上,在其他类型织物上的作用效果及耐洗性均比较一般。
织物起毛起球是一个渐变的过程,当织物受到的外界摩擦力大于纤维强力,或纤维间的摩擦力或者抱合力时,纤维末梢被拉出形成圈环和绒毛;绒毛露出一定长度后,在一定距离间因揉搓摩擦,反复伸长和回缩而纠结成球,此谓起毛起球;在后整理工艺中,通常采用树脂整理法来改善织物的抗起毛起球性能。利用树脂在纤维表面交联网状成膜的功能,使纤维表面包裹一层耐磨的树脂膜,此树脂膜使纤维的滑移减弱;同时,树脂均匀地交联凝聚在纱线的表层,使纤维端粘附于纱线上,摩擦时不易起球,从而有效地提高织物抗起球性。但是经此法整理得到的织物往往手感偏硬,亲水性能较差。
CN108330695A专利公开了“一种织物防皱处理方法”,选用多元羧酸改性有机硅与聚氨酯改性有机硅,复合多种渗透剂对织物进行抗皱整理,避免了甲醛的释放。但是其未对除***平纹织物以外的织物种类进行测评,且由于此发明整理剂所含大量的多元羧酸,其整理过程中经烘干时发生降解后会对织物的强力带来大幅度且永久性的损伤,整理后断裂强力普遍下降40%以上。
CN108517689A专利公开了“一种提高棉织物强力及手感的抗皱整理方法”,采用将经免烫整理后的织物依次进行液氨整、重免烫整理、和重液氨整理,所选用免烫整理的助剂为N-羟甲基树脂或多元羧酸或聚氨酯反应型交联剂中的一种。经此方法整理后的棉织物抗皱性能良好(折痕回复角>276°),织物撕破强力较常规工艺有所提高(撕破强力保留率>80%)。但是其不足之处在于该方法工艺较为复杂,工序较多,且涉及到使用液氨于-60~-40℃条件进行整理,能耗较大,成本相对较高;并未对除纯棉织物以外的织物进行测评,且未提及断裂强力的保留程度。
CN106758202A专利公开了“一种衬衫的防缩吸湿快干型免烫整理液及其整理方法”,分别合成了以丙烯酸丁酯、丙烯酸、丙烯酸2-甲氧基乙酯为主要单体的阳离子型有机硅改性丙烯酸酯聚合物,以及以壳聚糖和马来酸酐为原料合成的多元羧酸类聚合物,将此两种聚合物作为整理剂,按照特殊工艺对纯棉织物进行整理,使整理后的纯棉织物具有良好的抗皱及免烫效果,快干效果,且有穿着舒适且无甲醛释放等优点。其存在缺点为,一是起抗皱作用的组分实质为多元羧酸类聚合物,整理后会对织物强力带来较大程度的降低;二是其整理后织物的亲水性能一般,滴水扩散时间明显高于5s,不能够称为吸湿速干织物;三是其制备过程中使用的DMF溶剂属于非环保类溶剂,且与水互溶,难以除去,污水易产生环境污染。
CN102409537A专利公开了“一种防缩防皱、吸湿快干型衬衫领衬的后整理工艺”,选取聚乙烯硅氧烷的改性物作为吸湿快干整理剂,可单独使用,也可与一定量浓度的树脂、催化剂配制成工作液对织物进行浸轧,赋予织物柔软手感、吸湿快干的效果,适用于棉、涤及其混纺织物。但其整理后织物不具备耐久性,同时并未对织物除吸湿速干以外的其他功能性进行研究。
CN107904955A专利公开了“一种复合抗皱抗起毛处理剂及其制备方法”,采用含氢硅油乳液与酸酐在引发剂作用下发生自由基聚合,再加入有机硅及乳化剂进行乳化复配得到复合抗皱起毛处理剂。经此助剂整理后的织物提高了抗皱性及抗起毛起球性能。例如棉织物整理后,折痕回复角较整理前可提高119°;断裂强力保留率>95%;抗起毛起球等级从2级提高至5级。但未对除纤维素纤维织物(棉、竹、麻)以外的织物进行探讨,且不具有吸湿速干性能。
CN107057030A专利公开了“阳离子聚氨酯其制备方法、织物预处理液及其应用”,可以使整理后的织物有效的改善前道加工工序造成的纤维结构损伤,提升强力,改善抗起毛起球性能。实施例进行应用测评时未提及所整理织物的具体种类、规格,整理后织物的抗起毛起球性能可从2.5-3级提高至3-4级,断裂延伸率可提高1-5%。但未讨论整理后织物各功能的耐洗性,且整理后织物未对抗皱性及吸湿速干性进行探讨。
CN104532589A专利公开了“纺织品耐久性透气、抗菌、补强、吸湿速干整理剂及制备方法”,采用聚氨基甲酸酯粘合剂、封端异氰酸酯、吸湿速干整理剂、抗菌整理剂混合制得,适用于涤纶和纯棉面料,使整理后的产品同时具备透气、抗菌、补强、吸湿速干的功能特点,且有优异的耐水洗牢度。经此整理剂整理后的纯棉及涤纶织物,断裂强力有1-8%不等的提高,且经过50次水洗后仍可有所提高。其补强性与耐水洗性由氨基甲酸酯粘合剂与封端异氰酸酯共同作用实现。其缺点在于所发明整理剂中,聚氨基甲酸酯粘合剂与封端异氰酸酯用量较大,同属阴离子性,无法与呈阳离子性的二羟甲基二羟基乙烯脲树脂类抗皱整理剂进行配伍,进行同浴整理;且封端异氰酸酯属于交联剂,硬段占比较多,烘干交联后成膜较硬,影响织物手感;未对涤纶及纯棉以外的织物进行探讨,未对整理后织物的抗皱性及抗起毛起球性进行探讨。
综上,想要使织物同时得到理想的抗皱性能、吸湿速干性能及抗起毛起球性能,往往需要进行2、3次的整理。而且用现有的抗皱整理剂单独整理时,织物的强力普遍下降较大;用现有的吸湿速干整理剂单独整理时,与织物的结合牢度即耐洗性能相对较差;用现有的抗起毛起球剂单独整理剂时,织物的亲水性普遍能较差,整理后织物无法具有良好吸湿速干效果,且手感较硬。若把上述多种助剂同时进行整理时,又需要考虑各个助剂相互之间的配伍性、加工可持续性、在各类织物上的适用性,以及整理后各个助剂的功能效果是否相互影响,是否能够发挥协同作用。
目前尚未有一种可以适用各种织物的后整理工作液,使织物经过一次整理后即可具有优异的抗皱性能、吸湿速干性能及抗起起球性能,并且使整理后织物手感柔软、强力损伤较小、耐水洗牢度高。
发明内容
本发明目的是提供一种纺织品后整理液及其整理工艺,使织物经一次整理即能够得到良好的抗皱、吸湿速干、抗起毛起球的功能效果,且整理后织物手感柔软,强力损伤小,耐洗性良好。
本发明纺织品耐久性抗皱、吸湿速干、抗起毛起球整理液:
包含醚化改性二羟甲基二羟基乙烯脲树脂60-80g/L、催化剂10-15g/L、有机硅乳液10-30g/L、阳离子封端型聚氨酯树脂20-40g/L。
所述醚化改性二羟甲基二羟基乙烯脲树脂,可选辽宁恒星精细化工有限公司的FS-528C产品、亨斯曼化学的KNITTEX-7636产品、广东德美精细化工股份有限公司的DM-3510产品,其中的一种;
所述催化剂,为氯化镁、氯化锌、氯化铝中的一种,优选氯化镁;
所述有机硅乳液,为辽宁恒星精细化工有限公司的FS-909产品;
所述阳离子封端型聚氨酯树脂,为辽宁恒星精细化工有限公司的FS-530A产品。
本发明纺织品耐久性抗皱、吸湿速干、抗起毛起球整理方法:
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂、催化剂、有机硅乳液、阳离子封端型聚氨酯树脂、水,混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂60-80g/L、催化剂10-15g/L、有机硅乳液10-30g/L、阳离子封端型聚氨酯树脂20-40g/L的水溶液,得整理液;
(2)浸轧处理
将织物用上述步骤(1)到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
所述醚化改性二羟甲基二羟基乙烯脲树脂,可选辽宁恒星精细化工有限公司的FS-528C产品、亨斯曼化学的KNITTEX-7636产品、广东德美精细化工股份有限公司的DM-3510产品,其中的一种;
所述催化剂,为氯化镁、氯化锌、氯化铝中的一种,优选氯化镁;
所述有机硅乳液,为辽宁恒星精细化工有限公司的FS-909产品;
所述阳离子封端型聚氨酯树脂,为辽宁恒星精细化工有限公司的FS-530A产品。
本发明提供的是一种纺织品功能性后整理液及其整理工艺,整理液所选用的各个组分均为阳离子或非离子水溶性物质,相互之间的配伍性良好,整理液的稳定性及加工持续性优异,长时间使用亦不会出现如破乳、漂油、粘辊、沉淀等不良反应,可以使织物通过一次浸轧整理即得到良好的抗皱、吸湿速干及抗起毛起球性能,改善了为达到以上功能性能通常需进行多次整理的弊端,节省了加工成本。整理后的织物手感柔软,强力损伤小,具有良好的耐洗性。
抗皱性能方面,醚化改性二羟甲基二羟基乙烯脲树脂是在二羟甲基二羟基乙烯脲树脂的环上和侧基上醚化接枝改性而得来。二羟甲基二羟基乙烯脲树脂含有多个羟基,可以与纤维上的羟基、氨基等活性基团进行反应,同时羟甲基基团间也进行脱水缩合,再脱出甲醛,新生成的甲醛为织物所吸收,再进一步与纤维素羟基反应,如此反应过程中有若干缩合型长分子链的交联形成,达到耐久防皱的效果。而本发明所选用的醚化改性二羟甲基二羟基乙烯脲树脂通过醚化接枝改性,极大的减少了烘干后甲醛的释放量,改性后树脂的游离甲醛量低于0.4%,整理后织物的释放甲醛量小于50ppm,可符合OEKO-Texstandard100的II类标准。在抗皱性能和强力保留方面较普通二羟甲基二羟基乙烯脲树脂也有所提高。同时在抗皱性能、强力保留及价格方面,无醛型的产品均无法与之相比,是目前做织物抗皱整理的最佳选择。
吸湿速干性能方面,所选用的有机硅乳液(FS-909)是环氧基团与端羟基聚醚基团共同改性的有机硅三元共聚物。环氧基团可以在高温时可与端羟基发生自交联在纤维表面形成亲水薄膜,也可以渗透进纤维中与纤维大分子发生交联反应,从而获得牢固的吸附;侧链上大量的聚醚基团作为亲水基团聚集在织物表面及渗透入纤维内部,不仅提高了织物的亲水速度和吸水率,同时也提高了水分在织物中的传导及扩散性能,使织物所吸收的水分能够快速的蒸发排入大气,达到吸湿速干的效果;聚合物主链为有机硅柔性链段,可赋予织物柔软的手感,有利于提升织物的撕破强力;
抗起毛起球方面,本发明所选用的阳离子型封端聚氨酯(FS-530A),在合成时采用特殊的三官能度大分子量聚醚多元醇,制备的聚氨酯树脂具有多支链结构,整理后在织物表面及纤维内部沉积,经烘干会形成大分子网状结构,网状大分子成膜作用强,柔软且富有弹性,在达到抗起毛起球效果的同时,可以改善织物的手感,且有一定的抗皱效果;同时,由于大分子聚醚链段的存在,使得成膜具有较好的亲水性,与有机硅乳液(FS-909)中的侧链聚醚基团共同提高了织物的亲水及水分传导能力,达到吸湿速干的效果。
本发明所选用的阳离子型封端聚氨酯(FS-530A),其合成预聚体时采取封端处理,将异氰酸酯基团进行封闭,经高温焙烘后释放出活性的异氰酸酯基团,可与织物中含活泼氢的基团进行反应,增强与织物的交联成膜性能,进一步提升织物的断裂强力,增强织物的耐洗性;同时,释放的活性异氰酸酯基团也可以与醚化改性二羟甲基二羟基乙烯脲树脂及有机硅乳液(FS-909)中的羟基发生反应,化学键合成网状结构,增加交联牢度,增强织物的耐洗性。
此外,活性的异氰酸酯基团与纤维大分子中的氨基和羟基反应,在纤维大分子上形成柔性网状交联结构,部分沉积在纤维无定形区,依靠摩擦阻力和氢键限制了纤维分子链或基本结构单元的相对滑移,两种作用赋予了整理后织物的抗皱性和弹性。断裂强力和断裂伸长率的保留,原因是聚氨酯分子链较长,具有优异的弹性,结构中含有较大比例的软段,软链段中含有C-O单键和C-C单键,这些单键内旋转频率高,在常温下会有各种构象,具有柔顺性,与纤维可形成柔***联,交联后纤维的活动性得到了加强,在收到外力的作用时,分子链段可以通过滑移来补偿和平衡各个分子链上的应力分布,分散了应力,减小了纤维的受力不均,故拉伸及断裂强力有所提高。
本发明纺织品后整理工作液,通过助剂的选择与配伍,使织物进行整理后可以得到良好的抗皱性能、吸湿速干性能、抗起毛起球性能,并通过化学键合提升织物的强力保留,耐水洗牢度优异,适用于各类织物。
具体实施方式
实施例1
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂(KNITTEX-7636)、氯化镁、有机硅乳液(FS-909)、阳离子封端型聚氨酯树脂(FS-530A)、水,混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂(KNITTEX-7636) 80g/L,氯化镁15g/L,有机硅乳液(FS-909) 10g/L,阳离子封端型聚氨酯树脂(FS-530A) 20g/L的水溶液,得整理液;
(2) 浸轧整理
将纯棉基布(规格:60×60/90×88 斜纹)用上述步骤(1)得到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
实施例2
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂(DM-3510)、氯化镁、有机硅乳液(FS-909)、阳离子封端型聚氨酯树脂(FS-530A)、水,混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂(DM-3510) 80g/L,氯化镁15g/L,有机硅乳液(FS-909) 10g/L,阳离子封端型聚氨酯树脂(FS-530A) 20g/L的水溶液,得整理液;
(2) 浸轧整理
将纯棉基布(规格:60×60/90×88 斜纹)用上述步骤(1)得到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
实施例3
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂(FS-528C)、氯化镁、有机硅乳液(FS-909)、阳离子封端型聚氨酯树脂(FS-530A)、水,混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂(FS-528C) 80g/L,氯化镁15g/L,有机硅乳液(FS-909) 10g/L,阳离子封端型聚氨酯树脂(FS-530A) 20g/L的水溶液,得整理液;
(2) 浸轧整理
将纯棉基布(规格:60×60/90×88 斜纹)用上述步骤(1)得到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
实施例4
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂(KNITTEX-7636)、氯化铝、有机硅乳液(FS-909)、阳离子封端型聚氨酯树脂(FS-530A)、水,混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂(KNITTEX-7636) 60g/L,氯化镁10g/L,有机硅乳液(FS-909) 30g/L,阳离子封端型聚氨酯树脂(FS-530A) 40g/L的水溶液,得整理液;
(2) 浸轧整理
将涤棉基布(规格:45T/C×45T/C 涤纶/棉65/35 平纹)用上述步骤(1)得到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
实施例5
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂(DM-3510)、氯化铝、有机硅乳液(FS-909)、阳离子封端型聚氨酯树脂(FS-530A)、水,混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂(DM-3510) 60g/L,氯化镁10g/L,有机硅乳液(FS-909) 30g/L,阳离子封端型聚氨酯树脂(FS-530A) 40g/L的水溶液,得整理液;
(2) 浸轧整理
将涤棉基布(规格:45T/C×45T/C 涤纶/棉65/35 平纹)用上述步骤(1)得到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
实施例6
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂(FS-528C)、氯化铝、有机硅乳液(FS-909)、阳离子封端型聚氨酯树脂(FS-530A)、水,混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂(FS-528C) 60g/L,氯化镁10g/L,有机硅乳液(FS-909) 30g/L,阳离子封端型聚氨酯树脂(FS-530A) 40g/L的水溶液,得整理液;
(2) 浸轧整理
将涤棉基布(规格:45T/C×45T/C 涤纶/棉65/35 平纹)用上述步骤(1)得到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
实施例7
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂(KNITTEX-7636)、氯化锌、有机硅乳液(FS-909)、阳离子封端型聚氨酯树脂(FS-530A)、水,混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂(KNITTEX-7636) 70g/L,氯化镁15g/L,有机硅乳液(FS-909) 20g/L,阳离子封端型聚氨酯树脂(FS-530A) 30g/L的水溶液,得整理液;
(2) 浸轧整理
将锦棉基布(规格:36S/2锦纶/棉60/40 平纹)用上述步骤(1)得到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
实施例8
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂(DM-3510)、氯化锌、有机硅乳液(FS-909)、阳离子封端型聚氨酯树脂(FS-530A)、水混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂(DM-3510) 70g/L,氯化镁15g/L,有机硅乳液(FS-909) 20g/L,阳离子封端型聚氨酯树脂(FS-530A) 30g/L的水溶液,得整理液;
(2) 浸轧整理
将锦棉基布(规格:36S/2锦纶/棉60/40 平纹)用上述步骤(1)得到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
实施例9
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂(FS-528C)、氯化锌、有机硅乳液(FS-909)、阳离子封端型聚氨酯树脂(FS-530A)、水,水混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂(FS-528C) 70g/L,氯化镁15g/L,有机硅乳液(FS-909) 20g/L,阳离子封端型聚氨酯树脂(FS-530A) 30g/L的水溶液,得整理液;
(2) 浸轧整理
将锦棉基布(规格:36S/2锦纶/棉60/40 平纹)用上述步骤(1)得到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟。
性能测试评价
检测结果表明,经本发明后整理液整理后的纯棉织物折痕回复角可提高72-91°,水洗后可提高60-82°;水洗前后的吸湿速干性均符合国标机织类产品标准;抗起毛起球性能可从3.5级提高至4.5级,洗后无变化;整理后织物的断裂强力保留率>87%,洗后>84%,撕破强力与基布持平。
检测结果表明,经本发明后整理液整理后的纯棉织物折痕回复角可提高77-87°,水洗后可提高65-78°;水洗前后的吸湿速干性均符合国标机织类产品标准;抗起毛起球性能可从3级提高至4.5级,洗后无变化;整理后织物的断裂强力保留率>92%,洗后>90%;撕破强力提升18%以上。
检测结果表明,经本发明后整理液整理后的纯棉织物折痕回复角可提高84-96°,水洗后可提高72-88°;水洗前后的吸湿速干性均符合国标机织类产品标准;抗起毛起球性能可从3.5级提高至4.5级,洗后无变化;整理后织物的断裂强力保留率>92%,洗后>90%;撕破强力提升3%以上。
综上所述,经本发明后整理液整理后的纯棉、涤棉、锦棉织物,均获得了良好的抗皱性能、吸湿速干性能及抗起毛起球性能,强力损伤小,且具有良好的耐洗性能。
应用测试评价方法如下:
水洗测试评定标准:GB/T 8629-2001《纺织品 试验用家庭洗涤和干燥程序》(5A程序,20次,烘干);
抗皱性能测试评定标准:GB/T 3819-1997《纺织品 织物折痕回复性的测定 回复角法》;
吸湿速干性能测试评定标准:GB/T 21655.1-2008《纺织品 吸湿速干性的评定 第1部分:单项组合试验法》。
抗起毛起球性能测试评定标准:GB/T 4802.2-2008《纺织品 抗起毛起球性能的测定 第2部分:改型马丁代尔法》;
断裂强力、伸长率测试标准:GB/T 3923.1-2013《纺织品 织物拉伸性能 第1部分:断裂强力和断裂伸长率的测定(条样法)》;
撕破强力测试标准:GB/T 3917.2-2009《纺织品 织物撕破性能 第2部分:裤型试样(单缝)撕破强力的测定》。
Claims (2)
1.纺织品耐久性抗皱、吸湿速干、抗起毛起球整理液,其特征是:
包含醚化改性二羟甲基二羟基乙烯脲树脂60-80g/L、催化剂10-15g/L、有机硅乳液10-30g/L、阳离子封端型聚氨酯树脂20-40g/L;
所述催化剂,为氯化镁、氯化锌、氯化铝中的一种;
所述有机硅乳液,为辽宁恒星精细化工有限公司的FS-909产品;
所述阳离子封端型聚氨酯树脂,为辽宁恒星精细化工有限公司的FS-530A产品。
2.纺织品耐久性抗皱、吸湿速干、抗起毛起球整理方法,其特征是:
(1)整理液制备
将醚化改性二羟甲基二羟基乙烯脲树脂、催化剂、有机硅乳液、阳离子封端型聚氨酯树脂、水,混合均匀,配成醚化改性二羟甲基二羟基乙烯脲树脂60-80g/L、催化剂10-15g/L、有机硅乳液10-30g/L、阳离子封端型聚氨酯树脂20-40g/L的水溶液,得整理液;
(2)浸轧处理
将织物用上述步骤(1)到的整理液进行浸轧整理;两浸两轧,轧余率为60-80%,100-120℃烘干1-2分钟, 150-170℃焙烘1-2分钟;
所述催化剂,为氯化镁、氯化锌、氯化铝中的一种;
所述有机硅乳液,为辽宁恒星精细化工有限公司的FS-909产品;
所述阳离子封端型聚氨酯树脂,为辽宁恒星精细化工有限公司的FS-530A产品。
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