CN109112823A - 一种涤纶羊毛混纺面料 - Google Patents
一种涤纶羊毛混纺面料 Download PDFInfo
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- 239000004744 fabric Substances 0.000 title claims abstract description 52
- 229920004933 Terylene® Polymers 0.000 title claims abstract description 25
- 239000005020 polyethylene terephthalate Substances 0.000 title claims abstract description 25
- 210000002268 wool Anatomy 0.000 title claims abstract description 22
- 239000000835 fiber Substances 0.000 claims abstract description 23
- 229920000728 polyester Polymers 0.000 claims abstract description 17
- 239000003795 chemical substances by application Substances 0.000 claims description 30
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 22
- 238000001694 spray drying Methods 0.000 claims description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
- 239000002002 slurry Substances 0.000 claims description 16
- 239000002994 raw material Substances 0.000 claims description 15
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 14
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 claims description 14
- 239000012153 distilled water Substances 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 14
- 230000008569 process Effects 0.000 claims description 14
- 238000010298 pulverizing process Methods 0.000 claims description 14
- 229910021389 graphene Inorganic materials 0.000 claims description 13
- 239000011159 matrix material Substances 0.000 claims description 13
- 239000002243 precursor Substances 0.000 claims description 13
- 239000011032 tourmaline Substances 0.000 claims description 12
- 229940070527 tourmaline Drugs 0.000 claims description 12
- 229910052613 tourmaline Inorganic materials 0.000 claims description 12
- 239000002041 carbon nanotube Substances 0.000 claims description 10
- 229910021393 carbon nanotube Inorganic materials 0.000 claims description 10
- 235000019441 ethanol Nutrition 0.000 claims description 9
- 239000000243 solution Substances 0.000 claims description 9
- 238000005406 washing Methods 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 7
- 230000000996 additive effect Effects 0.000 claims description 7
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 7
- 239000000920 calcium hydroxide Substances 0.000 claims description 7
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 7
- 239000001569 carbon dioxide Substances 0.000 claims description 7
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 7
- VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 claims description 7
- 238000000227 grinding Methods 0.000 claims description 7
- 239000011261 inert gas Substances 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 7
- 238000002604 ultrasonography Methods 0.000 claims description 7
- 229910052845 zircon Inorganic materials 0.000 claims description 7
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 5
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical group CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 claims description 4
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 claims description 4
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- 238000012545 processing Methods 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 3
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- 238000007598 dipping method Methods 0.000 claims description 3
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- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 239000004408 titanium dioxide Substances 0.000 claims description 3
- 239000011259 mixed solution Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims 1
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- 238000010792 warming Methods 0.000 claims 1
- 150000002500 ions Chemical class 0.000 abstract description 5
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- 102000004169 proteins and genes Human genes 0.000 abstract description 2
- 108090000623 proteins and genes Proteins 0.000 abstract description 2
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- 238000012360 testing method Methods 0.000 description 6
- 230000000844 anti-bacterial effect Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000000463 material Substances 0.000 description 4
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- 244000146553 Ceiba pentandra Species 0.000 description 1
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- 206010009866 Cold sweat Diseases 0.000 description 1
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- 241000233866 Fungi Species 0.000 description 1
- 240000000249 Morus alba Species 0.000 description 1
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- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 230000000721 bacterilogical effect Effects 0.000 description 1
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- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000037336 dry skin Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
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- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
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- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/73—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with carbon or compounds thereof
- D06M11/74—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with carbon or compounds thereof with carbon or graphite; with carbides; with graphitic acids or their salts
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- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
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- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/40—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the structure of the yarns or threads
- D03D15/47—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the structure of the yarns or threads multicomponent, e.g. blended yarns or threads
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- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
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Abstract
本发明涉及混纺面料技术领域,具体地,涉及一种涤纶羊毛混纺面料,包括羊毛纤维32~46份、涤纶纤维20~40份,如此,本申请中,在制备涤纶纤维具有负电离子,从而制备形成的用品能够调节人体周边空气,吸附异味,且负离子能使空气中微米级肉眼看不见的漂尘,通过正负离子吸引、碰撞形成分子团下沉落地,从而使本申请的混纺面料具有自洁功能,降低了外接的灰尘附着在面料上的概率,进一步的,本申请混纺面料上的负离子能使细菌蛋白质两级性颠倒,而使细菌生存能力下降或致死,从而达到健康卫生的效果。
Description
技术领域:
本发明涉及混纺面料技术领域,具体地,涉及一种涤纶羊毛混纺面料。
背景技术:
随着人们生活水平的不断提高,人们对穿着舒适性的要求越来越高,服装面料的科技含量也在逐步提升。服装面料发展的趋势,是把高科技与时代经济、文化发展紧密结合,舒适、休闲、时尚、绿色、环保和健康的功能性面料成为发展潮流。
人们选择织物不仅追求漂亮的外观,还希望得到最周到的保护。尤其是在炎热的夏季和进行运动的时候,人们希望一可以尽情玩耍而无汗流挟背和闷热湿冷的后顾之忧,因此对面料的吸湿排汗性能提出了更高的要求。在夏季由于人们经常出汗,所以与湿度有关的感觉如不吸水性、黏贴感等对于夏季服装的整体舒适性起着很重要的作用。汗水产生与传送的问题是评估湿热舒适性的重要因素,当汗水出现在皮肤与衣服之间,穿着者便觉得很不舒适,像是湿、热、冷的触感,贴在身上不仅妨碍活动,而且容易使人生病。汗水只有快速移除,保持皮肤干燥,人体才会感觉舒适,这就要求织物面料具有良好的吸湿快干性能,抗菌面料具有良好的安全性,它可以高效完全去除织物上的细菌、真菌和霉菌,保持织物清洁,并能防止细菌再生和繁殖。菌再生和繁殖。
现有技术中,为了使得服装面料具有上述各种功能,一般是通过将混纺好的面料经过整理液改性处理,从而使得具备抗菌、快干等性能,但由于整理液和混纺棉料之间的结合性差,服装的抗菌、快干等特点并不能长久维持。
发明内容:
本发明克服现有技术的缺陷,提供一种涤纶羊毛混纺面料。
本发明所要解决的技术问题采用以下的技术方案来实现:一种涤纶羊毛混纺面料,按重量份计,包括羊毛纤维32~46份、涤纶纤维20~40份;
上述原料采用以下步骤制备:
(1)将羊毛纤维和涤纶纤维混纺面料采用本行业通用方法进行混纺,制得混纺纱,再将该混纺纱采用本行业通用方法织造成羊毛和涤纶的混纺面料;
(2)将步骤(1)中得到的混纺面料垂直悬挂,并采用压力为20~22bar,流量为400~600slpm的的热风机进行正面吹拂处理,至混纺面料蓬松为准;
(3)将经过吹拂处理后的混纺面料浸渍在含有改性剂的水溶液中,所述改性剂和水的体积比为1:40,浸渍时间为20~60min;
(4)将浸渍后的混纺面料晾干,然后采用烘培机在110~115℃下处理5~8min,然后通过0.5MPa,120℃的饱和蒸汽下浸蒸50min,冷却至室温后采用高红外线辐射干燥。
优选的,所述涤纶纤维经由以下步骤制备:
(1)分散制浆:将配置好的原料、酸和表面活性剂在搅拌下加入到水、乙醇的混合溶液中,制得电气石浆液,其中混合液中是体积比水:醇=1:2,质量比为原料:混合液=1:12,质量比原料:酸:表面活性剂=1:1~3:4;
(2)入釜:将配置好的电气石浆液进行温控水热反应,水热温度为150℃,时间为24h;
(3)洗涤:将反应好的电气石浆液过滤,并先后分别用去离子水和乙醇洗涤三遍;
(4)干燥:将洗涤抽滤完所得滤饼置于烘箱内80~150℃烘干,最后得到粉末B;
(5)将步骤(4)中的粉末B和涤纶按照比例1:(20~40)的质量比共混,挤出、切片,制得涤纶切片,将涤纶切片加热熔融,挤压,喷丝成型,得到所述涤纶纤维。
优选的,所述步骤(1)中的原料包括电气石60~70份,二氧化钛6~12份。
优选的,所述改性剂经由以下步骤制备:
(1)将锆石投入到蒸馏水中,并通过球磨机粉碎处理至粒径为2~12um后,在常温下混合搅拌4~6分钟,得到混合液A;
(2)将质量比2:1石墨烯和碳纳米管投入到蒸馏水中,并通过超声初步粉碎处理后,在常温下混合搅拌4~6分钟,然后在惰性气体保护的环境下以2~4℃/min的速度升温至40~60℃,再保温4~6h,然后自然冷却至室温,得到混合液B;
(3)将混合液A和混合液B以体积比(1~2):1的比例的混合搅拌,得到锆-碳前驱体,并将锆-碳前驱体通过闭式循环喷雾干燥机进行干燥,闭式循环喷雾干燥机的进口温度和出口温度分别为800~960℃和70~60℃,闭式循环喷雾干燥机的雾化器的转速为24000~26000r/min,形成初步改性剂;
(4)将质量为初步改性剂质量5%的5-磺酸钠间苯二甲酸二甲酯加入到氢氧化钙浆料中并在压力为20~22bar,流量为400~600slpm的条件下通入15%的二氧化碳,在室温条件下反映至溶液呈中性,干燥,研磨制得所述添加剂。
优选的,所述步骤(1)中的表面活性剂为十二烷基苯磺酸。
与现有技术相比,本发明的有益效果是:
1、本申请中,在制备涤纶纤维具有负电离子,从而制备形成的用品能够调节人体周边空气,吸附异味,且负离子能使空气中微米级肉眼看不见的漂尘,通过正负离子吸引、碰撞形成分子团下沉落地,从而使本申请的混纺面料具有自洁功能,降低了外接的灰尘附着在面料上的概率,进一步的,本申请混纺面料上的负离子能使细菌蛋白质两级性颠倒,而使细菌生存能力下降或致死,从而达到健康卫生的效果;
2、本申请提供的改性剂是以石墨烯和碳纳米管为主体,首先通过石墨烯和碳纳米管的改性处理,该过程中形成的为石墨烯和碳纳米管之间的包覆结构,碳纳米管裂解形成无定型碳包覆在石墨烯表面,形成一种碳包覆结构,同时锆吸附至石墨烯表面,并于石墨烯表面的碳成键,从而使混纺面料具有凉滑舒适的感觉,且改性剂结构的比表面积大,经过改性处理后,其表面能够形成较多的有机链,能够和涤纶纤维相似相溶,从而使得改性剂长期稳定附着在面料上,在不影响涤纶纤维的强度的前提下,持久稳定保持面料的抗菌、凉滑特性。
具体实施方式:
为了使本发明实现的技术手段、创作特征、达成目的与功效易于明白了解,下面结合具体实施例,进一步阐述本发明。
实施例1:
一种涤纶羊毛混纺面料,羊毛纤维:涤纶纤维的混纺质量比为39:30.
上述原料采用以下步骤制备:
(1)将羊毛纤维和涤纶纤维混纺面料采用本行业通用方法进行混纺,制得混纺纱,再将该混纺纱采用本行业通用方法织造成羊毛和涤纶的混纺面料;
(2)将步骤(1)中得到的混纺面料垂直悬挂,并采用压力为20~22bar,流量为400~600slpm的的热风机进行正面吹拂处理,至混纺面料蓬松为准;
(3)将经过吹拂处理后的混纺面料浸渍在含有改性剂的水溶液中,所述改性剂和水的体积比为1:40,浸渍时间为20~60min;
(4)将浸渍后的混纺面料晾干,然后采用烘培机在110~115℃下处理5~8min,然后通过0.5MPa,120℃的饱和蒸汽下浸蒸50min,冷却至室温后采用高红外线辐射干燥。
涤纶纤维经由以下步骤制备:
(1)分散制浆:将配置好的原料、酸和十二烷基苯磺酸在搅拌下加入到水、乙醇的混合溶液中,制得电气石浆液,其中混合液中是体积比水:醇=1:2,质量比为原料:混合液=1:12,质量比原料:酸:十二烷基苯磺酸=1:1~3:4;
(2)入釜:将配置好的电气石浆液进行温控水热反应,水热温度为150℃,时间为24h;
(3)洗涤:将反应好的电气石浆液过滤,并先后分别用去离子水和乙醇洗涤三遍;
(4)干燥:将洗涤抽滤完所得滤饼置于烘箱内80~150℃烘干,最后得到粉末B;
(5)将步骤(4)中的粉末B和涤纶按照比例1:(20~40)的质量比共混,挤出、切片,制得涤纶切片,将涤纶切片加热熔融,挤压,喷丝成型,得到所述涤纶纤维。
所述步骤(1)中的原料包括电气石650g,二氧化钛90g。
所述改性剂经由以下步骤制备:
(1)将锆石投入到蒸馏水中,并通过球磨机粉碎处理至粒径为2~12um后,在常温下混合搅拌4~6分钟,得到混合液A;
(2)将质量比2:1石墨烯和碳纳米管投入到蒸馏水中,并通过超声初步粉碎处理后,在常温下混合搅拌4~6分钟,然后在惰性气体保护的环境下以2~4℃/min的速度升温至40~60℃,再保温4~6h,然后自然冷却至室温,得到混合液B;
(3)将混合液A和混合液B以体积比1:1的比例的混合搅拌,得到锆-碳前驱体,并将锆-碳前驱体通过闭式循环喷雾干燥机进行干燥,闭式循环喷雾干燥机的进口温度和出口温度分别为800~960℃和70~60℃,闭式循环喷雾干燥机的雾化器的转速为24000~26000r/min,形成初步改性剂;
(4)将质量为初步改性剂质量5%的5-磺酸钠间苯二甲酸二甲酯加入到氢氧化钙浆料中并在压力为20~22bar,流量为400~600slpm的条件下通入15%的二氧化碳,在室温条件下反映至溶液呈中性,干燥,研磨制得所述添加剂。
实施例2:
本实施例内容和实施例1内容基本相同,相同之处不再重述,不同之处在于:所述改性剂经由以下步骤制备:
(1)将锆石投入到蒸馏水中,并通过球磨机粉碎处理至粒径为2~12um后,在常温下混合搅拌4~6分钟,得到混合液A;
(2)将质量比2:1石墨烯和碳纳米管投入到蒸馏水中,并通过超声初步粉碎处理后,在常温下混合搅拌4~6分钟,然后在惰性气体保护的环境下以2~4℃/min的速度升温至40~60℃,再保温4~6h,然后自然冷却至室温,得到混合液B;
(3)将混合液A和混合液B以体积比1.5:1的比例的混合搅拌,得到锆-碳前驱体,并将锆-碳前驱体通过闭式循环喷雾干燥机进行干燥,闭式循环喷雾干燥机的进口温度和出口温度分别为800~960℃和70~60℃,闭式循环喷雾干燥机的雾化器的转速为24000~26000r/min,形成初步改性剂;
(4)将质量为初步改性剂质量5%的5-磺酸钠间苯二甲酸二甲酯加入到氢氧化钙浆料中并在压力为20~22bar,流量为400~600slpm的条件下通入15%的二氧化碳,在室温条件下反映至溶液呈中性,干燥,研磨制得所述添加剂。
实施例3:
本实施例内容和实施例1结构基本相同,相同之处不再重述,不同之处在于:所述改性剂经由以下步骤制备:
(1)将锆石投入到蒸馏水中,并通过球磨机粉碎处理至粒径为2~12um后,在常温下混合搅拌4~6分钟,得到混合液A;
(2)将质量比2:1石墨烯和碳纳米管投入到蒸馏水中,并通过超声初步粉碎处理后,在常温下混合搅拌4~6分钟,然后在惰性气体保护的环境下以2~4℃/min的速度升温至40~60℃,再保温4~6h,然后自然冷却至室温,得到混合液B;
(3)将混合液A和混合液B以体积比2:1的比例的混合搅拌,得到锆-碳前驱体,并将锆-碳前驱体通过闭式循环喷雾干燥机进行干燥,闭式循环喷雾干燥机的进口温度和出口温度分别为800~960℃和70~60℃,闭式循环喷雾干燥机的雾化器的转速为24000~26000r/min,形成初步改性剂;
(4)将质量为初步改性剂质量5%的5-磺酸钠间苯二甲酸二甲酯加入到氢氧化钙浆料中并在压力为20~22bar,流量为400~600slpm的条件下通入15%的二氧化碳,在室温条件下反映至溶液呈中性,干燥,研磨制得所述添加剂。
对比例1
本对比例内容和实施例1内容基本相同,相同之处不再重述,不同之处在于:所述改性剂经由以下步骤制备:
(1)将锆石投入到蒸馏水中,并通过球磨机粉碎处理至粒径为2~12um后,在常温下混合搅拌4~6分钟,得到混合液A;
(2)将质量比2:1石墨烯和碳纳米管投入到蒸馏水中,并通过超声初步粉碎处理后,在常温下混合搅拌4~6分钟,然后在惰性气体保护的环境下以2~4℃/min的速度升温至40~60℃,再保温4~6h,然后自然冷却至室温,得到混合液B;
(3)将混合液A和混合液B以体积比0.5:1的比例的混合搅拌,得到锆-碳前驱体,并将锆-碳前驱体通过闭式循环喷雾干燥机进行干燥,闭式循环喷雾干燥机的进口温度和出口温度分别为800~960℃和70~60℃,闭式循环喷雾干燥机的雾化器的转速为24000~26000r/min,形成初步改性剂;
(4)将质量为初步改性剂质量5%的5-磺酸钠间苯二甲酸二甲酯加入到氢氧化钙浆料中并在压力为20~22bar,流量为400~600slpm的条件下通入15%的二氧化碳,在室温条件下反映至溶液呈中性,干燥,研磨制得所述添加剂。
对比例2
本对比例内容和实施例1内容基本相同,相同之处不再重述,不同之处在于:所述改性剂经由以下步骤制备:
(1)将锆石投入到蒸馏水中,并通过球磨机粉碎处理至粒径为2~12um后,在常温下混合搅拌4~6分钟,得到混合液A;
(2)将质量比2:1石墨烯和碳纳米管投入到蒸馏水中,并通过超声初步粉碎处理后,在常温下混合搅拌4~6分钟,然后在惰性气体保护的环境下以2~4℃/min的速度升温至40~60℃,再保温4~6h,然后自然冷却至室温,得到混合液B;
(3)将混合液A和混合液B以体积比3:1的比例的混合搅拌,得到锆-碳前驱体,并将锆-碳前驱体通过闭式循环喷雾干燥机进行干燥,闭式循环喷雾干燥机的进口温度和出口温度分别为800~960℃和70~60℃,闭式循环喷雾干燥机的雾化器的转速为24000~26000r/min,形成初步改性剂;
(4)将质量为初步改性剂质量5%的5-磺酸钠间苯二甲酸二甲酯加入到氢氧化钙浆料中并在压力为20~22bar,流量为400~600slpm的条件下通入15%的二氧化碳,在室温条件下反映至溶液呈中性,干燥,研磨制得所述添加剂。
参照例
选用市场上常见的混纺面料进行测试,具体选用浙江国诚纺织有限公司生产的桑蚕丝亚麻混纺面料。
性能测试:
依据《SFJJ-QWX25-2006负离子浓度检验细则》对实施例1~3,对比例1~2所制得的蚕丝、木棉和涤纶混纺面料测试。
采用国家标准GB/T20944.3-2008《纺织品抗菌性能的评价第3部分:振荡法》进行抗菌性定量测试,采用耐洗色牢度试验机洗涤方法,测试水洗30次后的织物,测试结果见表1。
采用国家标准GB18401进行性能测试,测试径向和维向撕破强力,其测试结果见表1:
表1
以上显示和描述了本发明的基本原理和主要特征和本发明的优点。本行业的技术人员应该了解,本发明不受上述实施例的限制,上述实施例和说明书中描述的只是说明本发明的原理,在不脱离本发明精神和范围的前提下,本发明还会有各种变化和改进,这些变化和改进都落入要求保护的本发明范围内。本发明要求保护范围由所附的权利要求书及其等效物界定。
Claims (5)
1.一种涤纶羊毛混纺面料,其特征在于,按重量份计,包括羊毛纤维32~46份、涤纶纤维20~40份;
上述原料采用以下步骤制备:
(1)将羊毛纤维和涤纶纤维混纺面料采用本行业通用方法进行混纺,制得混纺纱,再将该混纺纱采用本行业通用方法织造成羊毛和涤纶的混纺面料;
(2)将步骤(1)中得到的混纺面料垂直悬挂,并采用压力为20~22bar,流量为400~600slpm的的热风机进行正面吹拂处理,至混纺面料蓬松为准;
(3)将经过吹拂处理后的混纺面料浸渍在含有改性剂的水溶液中,所述改性剂和水的体积比为1:40,浸渍时间为20~60min;
(4)将浸渍后的混纺面料晾干,然后采用烘培机在110~115℃下处理5~8min,然后通过0.5MPa,120℃的饱和蒸汽下浸蒸50min,冷却至室温后采用高红外线辐射干燥。
2.根据权利要求1所述的涤纶羊毛混纺面料,其特征在于,所述涤纶纤维经由以下步骤制备:
(1)分散制浆:将配置好的原料、酸和表面活性剂在搅拌下加入到水、乙醇的混合溶液中,制得电气石浆液,其中混合液中是体积比水:醇=1:2,质量比为原料:混合液=1:12,质量比原料:酸:表面活性剂=1:1~3:4;
(2)入釜:将配置好的电气石浆液进行温控水热反应,水热温度为150℃,时间为24h;
(3)洗涤:将反应好的电气石浆液过滤,并先后分别用去离子水和乙醇洗涤三遍;
(4)干燥:将洗涤抽滤完所得滤饼置于烘箱内80~150℃烘干,最后得到粉末B;
(5)将步骤(4)中的粉末B和涤纶按照比例1:(20~40)的质量比共混,挤出、切片,制得涤纶切片,将涤纶切片加热熔融,挤压,喷丝成型,得到所述涤纶纤维。
3.根据权利要求2所述的涤纶羊毛混纺面料,其特征在于,所述步骤(1)中的原料包括电气石60~70份,二氧化钛6~12份。
4.根据权利要求1所述的涤纶羊毛混纺面料,其特征在于,所述改性剂经由以下步骤制备:
(1)将锆石投入到蒸馏水中,并通过球磨机粉碎处理至粒径为2~12um后,在常温下混合搅拌4~6分钟,得到混合液A;
(2)将质量比2:1石墨烯和碳纳米管投入到蒸馏水中,并通过超声初步粉碎处理后,在常温下混合搅拌4~6分钟,然后在惰性气体保护的环境下以2~4℃/min的速度升温至40~60℃,再保温4~6h,然后自然冷却至室温,得到混合液B;
(3)将混合液A和混合液B以体积比(1~2):1的比例的混合搅拌,得到锆-碳前驱体,并将锆-碳前驱体通过闭式循环喷雾干燥机进行干燥,闭式循环喷雾干燥机的进口温度和出口温度分别为800~960℃和70~60℃,闭式循环喷雾干燥机的雾化器的转速为24000~26000r/min,形成初步改性剂;
(4)将质量为初步改性剂质量5%的5-磺酸钠间苯二甲酸二甲酯加入到氢氧化钙浆料中并在压力为20~22bar,流量为400~600slpm的条件下通入15%的二氧化碳,在室温条件下反映至溶液呈中性,干燥,研磨制得所述添加剂。
5.根据权利要求2所述的涤纶羊毛混纺面料,其特征在于,所述步骤(1)中的表面活性剂为十二烷基苯磺酸。
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