CN111728837A - 一种能揉动腹胸和甩蝴蝶袖运动按摩带及其制备方法 - Google Patents
一种能揉动腹胸和甩蝴蝶袖运动按摩带及其制备方法 Download PDFInfo
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Abstract
本发明公开了一种能揉动腹胸和甩蝴蝶袖运动按摩带及其制备方法,该能揉动腹胸和甩蝴蝶袖运动按摩带包括腹胸按摩带、手臂绑带、牵引带;腹胸按摩带可分为囊包、牵引带接口件、按摩带等部件,利用手臂摆动力牵引或机械动力牵引或外用震动器按压腹腰按摩带或胸部按摩带,使囊包内的凸形物往复搓揉腹腰皮下脂肪或胸部,使得腹腰脂肪增温加速新陈代谢,或胸变大、降低***病变的风险;所述的按摩带由抗菌涤纶材料制成,可以减少因运动出汗产生细菌造成皮肤炎症的问题。
Description
技术领域
本发明属于运动保健技术领域,具体涉及一种能揉动腹胸和甩蝴蝶袖运动按摩带及其制备方法。
背景技术
运动按摩带具有恢复肢体功能、健身按摩,舒筋活血,调节神经,消除疲劳,防病治病,强身保健的功效;按摩带主要利用手臂摆动力量、设备制动牵引力量、震动器力量起到按摩的作用;运动时,按摩带可利用按摩带内侧凸起物增加对肉体的夹抓力;当作用力量产生时,增加对肉体区域的推揉震动力量,从而达到恢复肢体功能、健身按摩,舒筋活血,调节神经,消除疲劳,防病治病,强身保健的功效,同时,按摩带的填充物(如红外线电气石、磁铁、震动器、发热器、微电流金属导片等)起到积极的促进血液循环、加速燃脂的作用;另一方面,由于运动出汗,按摩带也容易滋生细菌,按摩带与人体皮肤接触摩擦过程中,也容易使皮肤在毛细孔扩大的状况下接触到滋生细菌,易造成皮肤过敏或炎症等不良反应;所以,研发一种由抗菌涤纶材料制成的运动保健按摩带,显得尤为重要。
发明内容
为了解决上述技术问题,本发明是提供一种能揉动腹胸和甩蝴蝶袖运动按摩带及其制备方法,该运动按摩带由抗菌涤纶材料制成,减少因运动出汗产生细菌造成皮肤炎症的问题。
本发明的目的在于提供一种能揉动腹胸和甩蝴蝶袖运动按摩带。
本发明的另一目在于是提供上述能揉动腹胸和甩蝴蝶袖运动按摩带的制备方法。
本发明上述目的通过以下技术方案实现:
一种能揉动腹胸和甩蝴蝶袖运动按摩带,包括:腹胸按摩带、手臂绑带、牵引带等部件;所述腹胸按摩带可分为囊包、牵引带接口件、按摩带等部件;
所述囊包可设置有凸形物,凸出物高度2mm-20mm宽度0.8cm-10cm,排列为竖条型(上开口袋,可更换内置物)(间距宽3cm-15cm);
作为优选,所述囊包也可设置为满天星颗粒型(分埋入或不埋入红外线电气石;磁铁;)(直径2mm-20mm,间距0.5cm-5cm);竖条与颗粒混搭型;
作为优选,竖条型上开口袋放内置物充填凸出物高度,所述内置物可为:红外线电气石;磁铁;震动器;发热器;微电流金属导片;无作用实物,可更换并选择单一种类搭配或一种以上混搭。(用移动电源);
作为优选,所述满天星颗粒型可分为埋入或不埋入红外线电气石;磁铁;间距0.5cm-5cm;
作为优选,所述囊包可设置为混合型:即凸形物为竖条型及满天星颗粒型混搭型;
所述按摩带可分为腹腰按摩带和胸部按摩带;
所述按摩带可分为圆环型、杯罩型和半截穿戴型按摩带;
所述按摩带内侧贴靠人体皮肤设置有囊包;
所述的手臂绑带与按摩带选用相同材料制得;
作为优选,所述手臂绑带与按摩带在实际使用时通过牵引带连接为整体使用,所述牵引带一端与手臂绑带相连,另一端与腹腰按摩带上设置的牵引带接口件连接;
所述能揉动腹胸和甩蝴蝶袖运动按摩带的动力来源来自于手臂摆动力牵引或机械动力牵引或外用震动器;
使用上述发明结构的有益效果是:利用手臂摆动力牵引或机械动力牵引或外用震动器按压腹腰按摩带,使凸形物直接镶入夹紧拽拉腹腰皮下脂肪时往复搓揉,利用凸形物口袋内置物的能量,使脂肪增温加速新陈代谢,影响表皮下深度可达十个厘米,此外,手臂摆动力牵引或机械动力牵引或外用震动器按压胸部按摩带,胸罩内侧设有的囊包往复搓揉,一方面可使胸变大,另一方面可降低***病变的风险。
所述运动按摩带的按摩带选用抗菌涤纶面料制得,抗菌涤纶面料材料具有如下结构式:
式中m:n=1:5~20。
制备上述运动按摩带的抗菌涤纶面料材料的反应流程及制备方法如下:
1.氮气环境下,将硫代乙酰胺和2-溴代-1-(4-氰基-苯基)-乙酮加入支口烧瓶中,140℃下反应24h。反应完成后,用乙酸乙酯/水萃取,合并的有机相,用水、盐水洗涤,干燥,过滤并浓缩,纯化,得4-(4-氰基-苯基)-2-甲基-噻唑。
2.氮气环境下,在4-(4-氰基-苯基)-2-甲基-噻唑的CCl4溶液中,加入NBS,100℃下反应2h,反应完成后,将反应混合物减压蒸发至干,纯化,得5-溴代-2-溴甲基-4-(4-氰基-苯基)-噻唑。
3.氮气环境下,在支口烧瓶中,加入4-(5-溴代-2-溴甲基-噻唑-4-基)-苄腈和DMF溶液,待4-(5-溴代-2-溴甲基-噻唑-4-基)-苄腈完全溶解后,加入2,6-二氟代-3-羟基-苯甲酰胺和碳酸钾,25℃下反应24h,反应混合物减压蒸发至干,纯化,得3-[5-溴代-4-(4-氰基-苯基)-噻唑-2-基甲氧基]-2,6-二氟代-苯甲酰胺。
4.氮气保护下,将3-[5-溴代-4-(4-氰基-苯基)-噻唑-2-基甲氧基]-2,6-二氟代-苯甲酰胺,5-乙烯基间苯二甲酸,碳酸钠和DMF加入到施莱克管中,将醋酸钯和三苯基膦溶于DMF注入到上述施莱克管,150℃反应12h,反应液冷却至室温,乙酸乙酯和去离子水萃取三次,取有机相,饱和食盐水洗涤,无水硫酸镁干燥,过滤除去硫酸镁,旋蒸浓缩,纯化,得到5-(2-(2-((3-氨基甲酰-2,4-二氟苯氧基)甲基)4-(4-苯腈)噻唑-5-基)乙烯基)间苯二甲酸M1。
5.在圆底烧瓶中加入M1、乙二醇(EG)、N,N'-二环己基碳酰亚胺(DCC)、N,N-对二甲氨基吡啶(DMAP),用等体积干燥二氯甲烷溶解,在室温下反应24h后过滤除去不溶物,50~80℃下蒸发滤液溶剂,以二氯甲烷为洗脱剂,通过硅胶柱色谱分离得到聚酯M2。
所述M1、EG、DCC、DMAP的投料摩尔比为1:3:5:0.2。
M2的结构式如下:
式中,m的取值为1~3。
6.在圆底烧瓶中加入对苯二甲酸二甲酯(DMT)、乙二醇(EG)、催化剂醋酸锰,通入N2,在240~260℃下进行酯交换反应。当冷凝回收的甲醇的体积不低于理论体积的90%时,酯交换反应结束,制得对苯二甲酸乙二醇酯。
所述DMT、EG的投料摩尔比为1:2,醋酸锰的投料量为DMT质量的0.05%。
对苯二甲酸乙二醇酯的结构式如下:
7.按一定的比例将M2和对苯二甲酸乙二醇酯投入圆底烧瓶中,N2保护下,温度升高至240~260℃时,启动真空泵,真空度控制在800~1000Pa内0.5~1h进行预缩聚,将温度升高至250~280℃,真空度低于50Pa,开始终缩聚反应1~2h,用氮气解除真空并出料,得到共聚酯。
所述M2、对苯二甲酸乙二醇酯的投料摩尔比为1:5~20。
8.将共聚酯切片喂入螺杆挤出机,经计量、挤出、冷却、拉伸、热定型和卷绕制得抗菌聚酯纤维,再将抗菌聚酯纤维经高速剪切分散到水相中制备得到抗菌聚酯纤维悬浮液,将制备得到的抗菌聚酯纤维悬浮液均匀涂覆在基布层的表面,干燥后得到厚度为5~8μm的抗菌涤纶面料。
所述挤出温度为260~290℃,冷却的风温为20~30℃,风速为0.4~0.5m/s,送风相对湿度为70~80%,纺丝速度为3000~4000m/min,热定型温度为135~155℃。
本发明具有如下优点和有益效果:
(1)本发明提供一种能揉动腹胸和甩蝴蝶袖运动按摩带及其制备方法,利用手臂摆动力牵引或机械动力牵引或外用震动器按压按摩带,使凸形物直接镶入夹紧拽拉腹腰皮下脂肪时往复搓揉,利用凸形物口袋内置物的能量,使脂肪增温加速新陈代谢,影响表皮下深度可达十个厘米。
(2)将按摩带与手臂或机械制动的绑带进行收紧,使凸形物收缩靠紧腹部器官附近,经动力牵引拉动收紧的贴身按摩带时,挤动的腹肌肉间接影响有:胃、膀胱、摄护腺、卵巢、大肠、小肠、十二指肠、子宫、生殖器官、肾脏、肝、脾、胰等,同时利用口袋内置物的能量增加血液流畅,协助器官间接按摩蠕动,加强能力及活性。
(3)作为环绕在手臂的绑带,当手臂前后摆动时牵引按摩带,负重拉扯的部位正是手臂的蝴蝶袖赘肉,只需要在手臂绑带的夹层放置红外线电气碎石,运动中有助消减蝴蝶袖赘肉。
(4)将本发明的按摩带制作成罩杯型按摩罩,以动力模式牵引按摩罩进行揉动升温,使很少活动的胸部能促进血液循环,营养有效送达细胞,肌肉恢复应有的弹性。
(5)运动按摩带材料由抗菌涤纶材料制成,减少因运动出汗产生细菌造成皮肤炎症的问题。
附图说明
图1为本发明圆环型腹腰按摩带的结构示意图。
图2为本发明贴近型腹部按摩带的结构示意图。
图3为本发明罩杯型胸部按摩带的结构示意图。
图4为本发明半截穿戴型腹胸按摩带内侧视图的结构示意图。
图5为本发明半截穿戴型腹胸按摩带外侧视图的结构示意图。
附图标记:1为圆环型腹腰按摩带,10为腹板,11为囊包,12为透气孔,13为扣环,20为第一腰带,21为第一连接件,22为第一连接扣环,30为第二腰带,31为第二连接件,32为第二连接扣环,4为罩杯型胸部按摩带,41为肩带,42为罩杯,43为粘扣带,44为背带,5为半截穿戴型腹胸按摩带。
具体实施方式
实施例1:图1和图2为本发明提供一种腹腰按摩带,图3圆环型腹腰按摩带的结构示意图,图4为贴近型腹部按摩带的结构示意图,是本发明的一种具体实施方式。
一种圆环型腹腰按摩带1,包含腹板10、第一腰带20、第二腰带30、牵引带及手臂绑带,所述腹板10具有数个囊包11、数个透气孔12及两扣环13,该囊包11设置于该腹板10朝向人体腹部的一面,囊包为埋入红外线电气石、磁铁、震动器、发热器、微电流金属导片的满天星颗粒型,各囊包11的大小,囊包内有凸形物,凸形物的大小高度依照该囊包11上的结构可为相同或不同,排列为竖条型,上开口袋,口袋间距宽10cm,可更换内置物,该囊包11的长边平行于该腹板10上缘,即该囊包11为横向设置,所述透气孔12贯穿于该腹板10上各长形凸块11之间的间隙处,供人体腹部透气用;两扣环13分别设置于该腹板10的两侧,所述牵引带一端与手臂绑带相连,另一端与腹腰按摩带上设置的牵引带接口件连接,手臂绑带与按摩带选用相同材料制得,能揉动圆环型腹腰按摩带的动力来源来自于手臂摆动力牵引或机械动力牵引或外用震动器。
实施例2:图3为本发明提供一种罩杯型胸部按摩带的结构示意图,是本发明的一种具体实施方式。
一种罩杯型胸部按摩带4,它由两肩带41、罩杯42、粘扣带43、背带44组成,被罩42下端有胸部按摩囊包41,该囊包41设置于被罩42朝向人体腹部的一面,囊包里埋入红外线电气石、磁铁、震动器、发热器、微电流金属导片,囊包内有凸形物,凸形物的大小高度依照该胸部按摩囊包41上的结构可为相同或不同,凸形物上开口袋,可更换内置物,能揉动圆环型腹腰按摩带的动力来源来自于手臂摆动力牵引或机械动力牵引或外用震动器。
实施例3:图4和图5为本发明提供一种半截穿戴型腹胸按摩带的结构示意图,图3为半截穿戴型腹胸按摩带内侧视图,图4为半截穿戴型腹胸按摩带外侧视图,是本发明的一种具体实施方式。
一种半截穿戴型腹胸按摩带5,包含罩杯42,半截穿戴型腹胸按摩带5具有数个囊包11、数个透气孔12及两扣环13,该囊包11设置于该半截穿戴型腹胸按摩带5朝向人体腹部的一面,囊包为埋入红外线电气石、磁铁、震动器、发热器、微电流金属导片的满天星颗粒型,各囊包11的大小,囊包内有凸形物,凸形物的大小高度依照该囊包11上的结构可为相同或不同,排列为竖条型,上开口袋,口袋间距宽10cm,可更换内置物,该囊包11的长边平行于半截穿戴型腹胸按摩带5上缘,即该囊包11为横向设置,所述透气孔12贯穿于该半截穿戴型腹胸按摩带5上各长形凸块11之间的间隙处,供人体腹部透气用;两锁扣51分别设置于半截穿戴型腹胸按摩带5的两侧,被罩44下端有胸部按摩囊包41,该囊包41设置于被罩42朝向人体腹部的一面,囊包里埋入红外线电气石、磁铁、震动器、发热器、微电流金属导片,囊包内有凸形物,凸形物的大小高度依照该胸部按摩囊包41上的结构可为相同或不同,凸形物上开口袋,可更换内置物,能揉动圆环型腹腰按摩带的动力来源来自于手臂摆动力牵引或机械动力牵引或外用震动器。
实施例4
抗菌单体的制备。
(1)氮气环境下,将硫代乙酰胺(60mmol)和2-溴代-1-(4-氰基-苯基)-乙酮(5mmol)加入100mL支口烧瓶中,加入30mL N,N-二甲基甲酰胺,140℃下反应24h,TLC监测反应进程,用乙酸乙酯/水萃取三次(3x100mL),合并的有机相并用水、盐水洗涤,Na2SO4干燥,过滤并浓缩,1%EtOAc-己烷作为洗脱剂,将粗产物置于硅胶上纯化,得4-(4-氰基-苯基)-2-甲基-噻唑,产率为72.3%。
(2)氮气环境下,将4-(4-氰基-苯基)-2-甲基-噻唑(5mmol)加入100mL支口烧瓶中,加入20mL CCl4溶解,再加入NBS(8.5mmol),100℃下反应2h,TLC监测反应进程,浓缩粗产物,1%乙酸乙酯/己烷为洗脱剂,将粗产物置于硅胶上纯化,得4-(5-溴代-2-溴甲基-噻唑-4-基)-苄腈,产率为41.3%。
(3)氮气环境下,将4-(5-溴代-2-溴甲基-噻唑-4-基)-苄腈(1.0mmol)加入支口烧瓶中,加入5ml无水DMF溶液溶解,再加入2,6-二氟代-3-羟基-苯甲酰胺(1.0mmol)和碳酸钾(2.0mmol),25℃下反应24h,浓缩粗产物,乙酸乙酯/己烷(30:70)为洗脱剂,将粗产物置于硅胶上纯化,得3-[5-溴代-4-(4-氰基-苯基)-噻唑-2-基甲氧基]-2,6-二氟代-苯甲酰胺,产率74.6%。
(4)氮气保护下,将3-[5-溴代-4-(4-氰基-苯基)-噻唑-2-基甲氧基]-2,6-二氟代-苯甲酰胺(2.0mmol),5-乙烯基间苯二甲酸(2.4mmol),碳酸钠(2.2mmol)和4mL DMF加入到施莱克管中,将醋酸钯(10μmol)和三苯基膦(10μmol)溶于5mL DMF注入到上述施莱克管,90℃反应12h,反应液冷却至室温,乙酸乙酯和去离子水萃取三次,取有机相,饱和食盐水洗涤,无水硫酸镁干燥,过滤除去硫酸镁,旋蒸浓缩,纯化,得到5-(2-(2-((3-氨基甲酰-2,4-二氟苯氧基)甲基)4-(4-苯腈)噻唑-5-基)乙烯基)间苯二甲酸M1,产率92.5%。
实施例5
抗菌涤纶面料的制备。
(1)在50mL圆底烧瓶中加入M1(2.0mmol)、乙二醇(EG)(6.0mmol)、N,N'-二环己基碳酰亚胺(DCC)(10mmol)、4-二甲氨基吡啶(DMAP)(0.4mmol),用25mL干燥二氯甲烷溶解,在室温下反应24h后过滤除去不溶物,50~80℃下蒸发滤液溶剂,以二氯甲烷为洗脱剂,通过硅胶柱色谱分离得到聚酯M2。
(2)对苯二甲酸乙二醇酯的制备。
9.在50mL圆底烧瓶中加入对苯二甲酸二甲酯(DMT)(20mmol)、乙二醇(EG)(40mmol)、催化剂醋酸锰(1.16mmol),通入N2,在240~260℃下进行酯交换反应。当冷凝回收的甲醇的体积不低于理论体积的90%时,酯交换反应结束,制得对苯二甲酸乙二醇酯。
(3)共聚酯的制备。
按M2、对苯二甲酸乙二醇酯的投料摩尔比为1:5~20投入50mL圆底烧瓶中,N2保护下,温度升高至240℃时,启动真空泵,真空度控制在800Pa内1h进行预缩聚,将温度升高至280℃,真空度低于50Pa,开始终缩聚反应2h,用氮气解除真空并出料,得到共聚酯。
(4)抗菌涤纶面料的制备。
将共聚酯切片喂入螺杆挤出机,经计量、挤出、冷却、拉伸、热定型和卷绕制得抗菌聚酯纤维,挤出温度为260℃,冷却的风温为20℃,风速为0.4m/s,送风相对湿度为70%,纺丝速度为3000m/min,热定型温度为135℃,再将抗菌聚酯纤维经高速剪切分散到水相中制备得到抗菌聚酯纤维悬浮液,将制备得到的抗菌聚酯纤维悬浮液均匀涂覆在基布层的表面,干燥后得到厚度为1mm的抗菌涤纶面料。
Claims (6)
1.一种能揉动腹胸和甩蝴蝶袖运动按摩带,包括:腹胸按摩带、手臂绑带、牵引带等部件;其特征在于:所述腹胸按摩带可分为囊包、牵引带接口件、按摩带等部件;
所述囊包可设置有凸形物,凸出物高度2mm-20mm宽度0.8cm-10cm,排列为竖条型(上开口袋,可更换内置物)(间距宽3cm-15cm);
所述囊包也可设置为满天星颗粒型(分埋入或不埋入红外线电气石;磁铁;)(直径2mm-20mm,间距0.5cm-5cm);竖条与颗粒混搭型;
所述竖条型上开口袋放内置物充填凸出物高度,所述内置物可为:红外线电气石;磁铁;震动器;发热器;微电流金属导片;无作用实物,可更换并选择单一种类搭配或一种以上混搭(用移动电源);
所述满天星颗粒型可分为埋入或不埋入红外线电气石;磁铁;间距0.5cm-5cm;
所述囊包可设置为混合型:即凸形物为竖条型及满天星颗粒型混搭型;
所述按摩带可分为腹腰按摩带和胸部按摩带;
所述按摩带可分为圆环型、杯罩型和半截穿戴型按摩带;
所述按摩带内侧贴靠人体皮肤设置有囊包;
所述的手臂绑带与按摩带选用相同材料制得;
所述手臂绑带与腹腰按摩带在实际使用时通过牵引带连接为整体使用,所述牵引带一端与手臂绑带相连,另一端与腹腰按摩带上设置的牵引带接口件连接;
所述能揉动腹胸和甩蝴蝶袖运动按摩带的动力来源来自于手臂摆动力牵引或机械动力牵引或外用震动器;
所述的能揉动腹胸和甩蝴蝶袖运动按摩带的材料,其特征在于,所述能揉动腹胸和甩蝴蝶袖运动按摩带的材料为抗菌涤纶材料,其结构式如式(I)所示:
式中m:n=1:5~20。
2.根据权利要求1所述抗菌涤纶材料的制备方法,其特征在于,包括如下步骤:
(1)氮气环境下,将硫代乙酰胺和2-溴代-1-(4-氰基-苯基)-乙酮加入支口烧瓶中,140℃下反应24h,得4-(4-氰基-苯基)-2-甲基-噻唑。
(2)氮气环境下,在4-(4-氰基-苯基)-2-甲基-噻唑的CCl4溶液中,加入NBS,100℃下反应2h,得5-溴代-2-溴甲基-4-(4-氰基-苯基)-噻唑。
(3)氮气环境下,在支口烧瓶中,加入4-(5-溴代-2-溴甲基-噻唑-4-基)-苄腈和DMF溶液,待4-(5-溴代-2-溴甲基-噻唑-4-基)-苄腈完全溶解后,加入2,6-二氟代-3-羟基-苯甲酰胺和碳酸钾,25℃下反应24h,得3-[5-溴代-4-(4-氰基-苯基)-噻唑-2-基甲氧基]-2,6-二氟代-苯甲酰胺。
(4)氮气保护下,将3-[5-溴代-4-(4-氰基-苯基)-噻唑-2-基甲氧基]-2,6-二氟代-苯甲酰胺,5-乙烯基间苯二甲酸,碳酸钠和DMF加入到施莱克管中,将醋酸钯和三苯基膦溶于DMF注入到上述施莱克管,150℃反应12h,得5-(2-(2-((3-氨基甲酰-2,4-二氟苯氧基)甲基)4-(4-苯腈)噻唑-5-基)乙烯基)间苯二甲酸M1。
(5)在圆底烧瓶中加入M1、乙二醇(EG)、N,N'-二环己基碳酰亚胺(DCC)、N,N-对二甲氨基吡啶(DMAP),用干燥二氯甲烷溶解,在室温下反应24h,得聚酯M2,其结构式(II)如下:
式中,m的取值为1~3。
(6)在圆底烧瓶中加入对苯二甲酸二甲酯(DMT)、乙二醇(EG)、催化剂醋酸锰,通入N2,在240~260℃下进行酯交换反应,当冷凝回收的甲醇的体积不低于理论体积的90%时,酯交换反应结束,得对苯二甲酸乙二醇酯,其结构式(III)如下:
(7)按一定的比例将M2和对苯二甲酸乙二醇酯投入圆底烧瓶中,N2保护下,温度升高至240~260℃时,启动真空泵,真空度控制在800~1000Pa内0.5~1h进行预缩聚,将温度升高至250~280℃,真空度低于50Pa,开始终缩聚反应1~2h,用氮气解除真空并出料,得到共聚酯。
(8)将共聚酯切片喂入螺杆挤出机,经计量、挤出、冷却、拉伸、热定型和卷绕制得抗菌聚酯纤维,再将抗菌聚酯纤维经高速剪切分散到水相中制备得到抗菌聚酯纤维悬浮液,将制备得到的抗菌聚酯纤维悬浮液均匀涂覆在基布层的表面,干燥后得到厚度为5~8μm的抗菌涤纶面料。
3.根据权利要求2所述抗菌涤纶材料的制备方法,其特征在于,所述步骤(5)中,M1、EG、DCC、DMAP的投料摩尔比为1:3:5:0.2。
4.根据权利要求2所述抗菌涤纶材料的制备方法,其特征在于,所述步骤(6)中,所述DMT、EG的投料摩尔比为1:2,醋酸锰的投料量为DMT质量的0.05%。
5.根据权利要求2所述抗菌涤纶材料的制备方法,其特征在于,所述步骤(7)中,所述M2、对苯二甲酸乙二醇酯的投料摩尔比为1:5~20。
6.根据权利要求2所述抗菌涤纶材料的制备方法,其特征在于,所述步骤(8)中,所述螺杆挤出机的挤出温度为260~290℃,冷却的风温为20~30℃,风速为0.4~0.5m/s,送风相对湿度为70~80%,纺丝速度为3000~4000m/min,热定型温度为135~155℃。
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