CN114875573B - 一种屋顶防滑用sm无纺布的制备方法 - Google Patents

一种屋顶防滑用sm无纺布的制备方法 Download PDF

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CN114875573B
CN114875573B CN202210503842.3A CN202210503842A CN114875573B CN 114875573 B CN114875573 B CN 114875573B CN 202210503842 A CN202210503842 A CN 202210503842A CN 114875573 B CN114875573 B CN 114875573B
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melt
woven fabric
temperature
preparation
spun
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CN114875573A (zh
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黄文胜
刘雨佳
张卫东
邱锦晶
孙伟峰
黄志国
袁珊珊
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Dongying Junfu Purification Technology Co ltd
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Dongying Junfu Purification Technology Co ltd
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Priority to PCT/CN2023/088578 priority patent/WO2023216810A1/zh
Priority to US18/570,620 priority patent/US20240263371A1/en
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    • DTEXTILES; PAPER
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    • D04H1/4282Addition polymers
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Abstract

本发明公开了一种屋顶防滑用SM无纺布的制备方法,属于屋顶材料技术领域,包括制备纺粘无纺布原料,制备纺粘无纺布,制备熔喷无纺布原料,制备初级SM无纺布,后处理;所述制备纺粘无纺布原料,将低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV‑531,聚乙烯醇,增强剂,粘性剂,纳米二氧化钛混合均匀后得到纺粘无纺布原料;本发明能够避免SM无纺布在结合时不能完全粘合在一起,容易分层的问题,还能够解决高速生产过程中容易出现断布的问题,同时还能够提高SM无纺布的耐磨性,强度和硬挺度,并且制备的SM无纺布生产成本低,易回收,环保性能好。

Description

一种屋顶防滑用SM无纺布的制备方法
技术领域
本发明涉及屋顶材料技术领域,具体涉及一种屋顶防滑用SM无纺布的制备方法。
背景技术
SM无纺布属于复合无纺布,是纺粘无纺布和熔喷无纺布的复合产品,具有强力高、过滤性能好、透气性能好、不含粘合剂、无毒等优点,目前主要用于医疗卫生劳动防护产品如屋顶、手术服、手术帽、防护服、洗手衣、手袋等。
相对于单独使用纺粘无纺布,SM无纺布在屋顶材料中主要作为防滑材料使用时的优点有:表面凹凸不平,防滑效果好,并且添加抗老化母粒,具备抗UV功能,避免长时间阳光照射导致的布面粉化。但是现有的SM无纺布有两种工艺,一种是SM热轧法,该方法加工的材料,其强度高,但是由于过轧机将材料完全融为一体,导致产品的布面光滑,只能靠单纯纺粘轧机轧点起到防滑作用,防滑效果甚微。另一种工艺是将熔喷层喷覆在纺粘层上面,不经过轧机热轧,但由于熔喷铺网过程中迅速结晶,导致熔喷层和纺粘层在结合时不能完全粘合在一起,容易分层,造成后加工过程中,由于两种无纺布材料强力等性能不同,拉伸张力也不一致,高速生产过程中容易出现断布的情况,此外,由于熔喷无纺布的耐磨性差,强度不度,硬挺度不够,导致了SM无纺布的耐磨性,强度和硬挺度较差。
为了解决上述问题,目前最常用的方法为使用热压粘合将两种无纺布粘合到一起,但是该方法会影响制备的SM无纺布的防滑效果,而且不能从根本上解决两种无纺布材料强力等性能不同,拉伸张力也不一致,高速生产过程中容易出现断布的问题,也不能解决SM无纺布的耐磨性,强度和硬挺度较差的问题。
发明内容
针对现有技术存在的不足,本发明提供了一种屋顶防滑用SM无纺布的制备方法,能够避免SM无纺布在结合时不能完全粘合在一起,容易分层的问题,还能够解决两种无纺布材料强力等性能不同,拉伸张力也不一致,高速生产过程中容易出现断布的问题,同时还能够提高SM无纺布的耐磨性,强度和硬挺度,并且制备的SM无纺布生产成本低,易回收,环保性能好。
为解决以上技术问题,本发明采取的技术方案如下:
一种屋顶防滑用SM无纺布的制备方法,包括制备纺粘无纺布原料,制备纺粘无纺布,制备熔喷无纺布原料,制备初级SM无纺布,后处理。
所述制备纺粘无纺布原料,将低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛混合均匀后得到纺粘无纺布原料;
所述低熔融指数聚丙烯的熔融指数为25-35g/10min;
所述高熔融指数聚丙烯的熔融指数为800-900g/10min;
其中,低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛的重量比为120-130:7-9:3-5:0.5-0.7:2-4:1-2:6-8:7-9:3-4:2-4。
所述增强剂的制备方法为:将六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠置于球磨机中进行球磨,控制球磨时的球料比为20-25:1,球磨转速为200-300rpm,球磨时的温度为60-65℃,球磨时间为20-30min,球磨结束后得到初级增强剂,将初级增强剂进行真空加热处理,控制真空加热处理的真空度为100-120Pa,温度为70-80℃,真空加热处理结束得到增强剂;
其中,六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠的重量比为20-22:8-10:3-5:7-10。
所述粘性剂的制备方法为:将聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺加入去离子水中,在60-65℃下以200-240rpm的搅拌速度搅拌40-50min后进行喷雾干燥,控制喷雾干燥的进风温度为140-160℃,出风温度为60-70℃,真空喷雾干燥结束得到粘性剂;
所述阳离子聚丙烯酰胺的分子量为500-600万,离子度为15-20%;
其中,聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺,去离子水的重量比为30-35:3-4:5-7:1-3:50-55。
所述制备纺粘无纺布,将纺粘无纺布原料加入混料装置中,经熔融挤压、熔体过滤、模头喷丝、铺网、热轧、上液、烘干、卷绕收卷、分切,得到纺粘无纺布;
所述模头喷丝步骤中的风箱压力为2800-3000Pa,风机转速比为80-82%,上下冷风的温度为22-25℃;
所述热轧步骤中的花辊温度为155-160℃,光辊温度为140-145℃,网带速度为630-650m/min,热轧压力为80-90daN/cm。
所述制备熔喷无纺布原料,将聚丙烯,聚丁烯对苯二甲酸酯,聚乙烯,纳米二氧化硅,椰油酸单异丙醇酰胺,改性增容剂,增粘剂混合均匀后得到熔喷无纺布原料;
所述改性增容剂的制备方法为:将高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯加入搅拌机中,控制搅拌机的转速为250-280rpm,搅拌机的温度为2-5℃,在2-5℃下低温处理20-25min后,加入过氧化二异丙苯,正十二烷基硫醇,然后以1-1.2℃/min的升温速度升温至40-45℃,在40-45℃下搅拌15-20min,加入甲基丙烯酸羟乙酯,过硫酸钠,然后以0.8-1℃/min的升温速度升温至50-55℃,在50-55℃下搅拌20-25min,自然恢复至室温,得到改性增容剂;
高熔融指数聚丙烯的熔融指数为800-900g/10min;
其中,高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯,过氧化二异丙苯,正十二烷基硫醇,甲基丙烯酸羟乙酯,过硫酸钠的重量比为100-110:5-6:2-3:0.5-0.8:0.6-0.7:3-4:0.2-0.4。
所述增粘剂的制备方法为:将黄原胶,阳离子瓜尔胶,海藻多糖混合均匀后置于密闭容器中,将密闭容器抽真空至真空度为100-200Pa后通入氧气,控制密闭容器内氧气的气体压力为70-90kPa,然后将密闭容器的温度控制到60-65℃,在60-65℃下处理40-45min后得到增粘剂;
其中,黄原胶,阳离子瓜尔胶,海藻多糖的重量比为25-30:15-20:4-6。
所述制备初级SM无纺布,将熔喷无纺布原料进行加热熔融,熔体过滤,熔体分配后由模头上的喷丝孔挤出,使用热风牵伸得到熔喷纤维,将熔喷纤维喷覆于纺粘无纺布上进行成网,得到初级SM无纺布;
所述加热熔融中螺杆区的温度分别为200-205℃,210-215℃,230-235℃;
所述熔体过滤中的过滤器温度为230-235℃;
所述熔体分配中的计量泵温度为230-235℃,转速为25-30rpm;
所述热风牵伸中的风温为200-210℃,转速为700-710rpm;
所述成网的速度为25-27rpm;
所述喷丝孔的孔径为0.45-0.55mm;
所述熔喷纤维的纤维直径为10-12μm。
所述后处理,在40-45℃下对初级SM无纺布表面喷淋活性液,控制活性液的使用量为50-60g/m2,喷淋结束后在40-45℃下烘干,得到SM无纺布;
所述活性液的组成,按重量份计,包括:100-110份去离子水,7-9份麦芽糊精,5-6份三聚磷酸钠,2-3份十二烷基硫酸钠,0.2-0.5份聚二烯丙基二甲基氯化铵。
与现有技术相比,本发明的有益效果为:
(1)本发明的屋顶防滑用SM无纺布的制备方法,能够避免SM无纺布在结合时不能完全粘合在一起,容易分层的问题,将本发明制备的屋顶防滑用SM无纺布置于温度为38℃,湿度85%下静置10天,20天,30天,60天,90天后,按照ASTM D5035定伸长10%测试,不会发生分层现象;
(2)本发明的屋顶防滑用SM无纺布的制备方法,能够解决两种无纺布材料强力等性能不同,拉伸张力也不一致,高速生产过程中容易出现断布的问题;
(3)本发明的屋顶防滑用SM无纺布的制备方法,能够提高SM无纺布的耐磨性,强度和硬挺度,本发明制备的SM无纺布的横向强度为39-43N,纵向强力为52-55N,摩擦系数为1.2-1.5;
(4)本发明制备的屋顶防滑用SM无纺布,克重为45-49g/m2,孔隙率为56-61%,纤维细度为11-13μm,透气量为2900-3100mm/s,厚度为0.37-0.42mm;
(5)本发明制备的屋顶防滑用SM无纺布,生产成本低,易回收,环保性能好。
具体实施方式
为了对本发明的技术特征、目的和效果有更加清楚的理解,现说明本发明的具体实施方式。
实施例1
一种屋顶防滑用SM无纺布的制备方法,具体为:
1.制备纺粘无纺布原料:将低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛混合均匀后得到纺粘无纺布原料;
所述低熔融指数聚丙烯的熔融指数为25g/10min;
所述高熔融指数聚丙烯的熔融指数为800g/10min;
其中,低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛的重量比为120:7:3:0.5:2:1:6:7:3:2。
所述增强剂的制备方法为:将六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠置于球磨机中进行球磨,控制球磨时的球料比为20:1,球磨转速为200rpm,球磨时的温度为60℃,球磨时间为20min,球磨结束后得到初级增强剂,将初级增强剂进行真空加热处理,控制真空加热处理的真空度为100Pa,温度为70℃,真空加热处理结束得到增强剂;
其中,六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠的重量比为20:8:3:7。
所述粘性剂的制备方法为:将聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺加入去离子水中,在60℃下以200rpm的搅拌速度搅拌40min后进行喷雾干燥,控制喷雾干燥的进风温度为140℃,出风温度为60℃,真空喷雾干燥结束得到粘性剂;
所述阳离子聚丙烯酰胺的分子量为500万,离子度为15%;
其中,聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺,去离子水的重量比为30:3:5:1:50。
2.制备纺粘无纺布:将纺粘无纺布原料加入混料装置中,经熔融挤压、熔体过滤、模头喷丝、铺网、热轧、上液、烘干、卷绕收卷、分切,得到纺粘无纺布;
所述模头喷丝步骤中的风箱压力为2800Pa,风机转速比为80%,上下冷风的温度为22℃;
所述热轧步骤中的花辊温度为155℃,光辊温度为140℃,网带速度为630m/min,热轧压力为80daN/cm。
3.制备熔喷无纺布原料:将聚丙烯,聚丁烯对苯二甲酸酯,聚乙烯,纳米二氧化硅,椰油酸单异丙醇酰胺,改性增容剂,增粘剂混合均匀后得到熔喷无纺布原料;
所述改性增容剂的制备方法为:将高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯加入搅拌机中,控制搅拌机的转速为250rpm,搅拌机的温度为2℃,在2℃下低温处理20min后,加入过氧化二异丙苯,正十二烷基硫醇,然后以1℃/min的升温速度升温至40℃,在40℃下搅拌15min,加入甲基丙烯酸羟乙酯,过硫酸钠,然后以0.8℃/min的升温速度升温至50℃,在50℃下搅拌20min,自然恢复至室温,得到改性增容剂;
高熔融指数聚丙烯的熔融指数为800g/10min;
其中,高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯,过氧化二异丙苯,正十二烷基硫醇,甲基丙烯酸羟乙酯,过硫酸钠的重量比为100:5:2:0.5:0.6:3:0.2。
所述增粘剂的制备方法为:将黄原胶,阳离子瓜尔胶,海藻多糖混合均匀后置于密闭容器中,将密闭容器抽真空至真空度为100Pa后通入氧气,控制密闭容器内氧气的气体压力为70kPa,然后将密闭容器的温度控制到60℃,在60℃下处理40min后得到增粘剂;
其中,黄原胶,阳离子瓜尔胶,海藻多糖的重量比为25:15:4。
4.制备初级SM无纺布:将熔喷无纺布原料进行加热熔融,熔体过滤,熔体分配后由模头上的喷丝孔挤出,使用热风牵伸得到熔喷纤维,将熔喷纤维喷覆于第2步制备的纺粘无纺布上进行成网,得到初级SM无纺布;
所述加热熔融中螺杆区的温度分别为200℃,210℃,230℃;
所述熔体过滤中的过滤器温度为230℃;
所述熔体分配中的计量泵温度为230℃,转速为25rpm;
所述热风牵伸中的风温为200℃,转速为700rpm;
所述成网的速度为25rpm;
所述喷丝孔的孔径为0.45mm;
所述熔喷纤维的纤维直径为10μm。
5.后处理:在40℃下对初级SM无纺布表面喷淋活性液,控制活性液的使用量为50g/m2,喷淋结束后在40℃下烘干,得到SM无纺布;
所述活性液的组成,按重量份计,包括:100份去离子水,7份麦芽糊精,5份三聚磷酸钠,2份十二烷基硫酸钠,0.2份聚二烯丙基二甲基氯化铵。
本实施例在制备过程中未出现断布情况。
实施例2
一种屋顶防滑用SM无纺布的制备方法,具体为:
1.制备纺粘无纺布原料:将低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛混合均匀后得到纺粘无纺布原料;
所述低熔融指数聚丙烯的熔融指数为30g/10min;
所述高熔融指数聚丙烯的熔融指数为850g/10min;
其中,低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛的重量比为125:8:4:0.6:3:1.5:7:8:3.5:3。
所述增强剂的制备方法为:将六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠置于球磨机中进行球磨,控制球磨时的球料比为22:1,球磨转速为250rpm,球磨时的温度为62℃,球磨时间为25min,球磨结束后得到初级增强剂,将初级增强剂进行真空加热处理,控制真空加热处理的真空度为110Pa,温度为75℃,真空加热处理结束得到增强剂;
其中,六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠的重量比为21:9:4:8。
所述粘性剂的制备方法为:将聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺加入去离子水中,在62℃下以220rpm的搅拌速度搅拌45min后进行喷雾干燥,控制喷雾干燥的进风温度为150℃,出风温度为65℃,真空喷雾干燥结束得到粘性剂;
所述阳离子聚丙烯酰胺的分子量为550万,离子度为17%;
其中,聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺,去离子水的重量比为32:3.5:6:2:52。
2.制备纺粘无纺布:将纺粘无纺布原料加入混料装置中,经熔融挤压、熔体过滤、模头喷丝、铺网、热轧、上液、烘干、卷绕收卷、分切,得到纺粘无纺布;
所述模头喷丝步骤中的风箱压力为2900Pa,风机转速比为81%,上下冷风的温度为23℃;
所述热轧步骤中的花辊温度为157℃,光辊温度为142℃,网带速度为640m/min,热轧压力为85daN/cm。
3.制备熔喷无纺布原料:将聚丙烯,聚丁烯对苯二甲酸酯,聚乙烯,纳米二氧化硅,椰油酸单异丙醇酰胺,改性增容剂,增粘剂混合均匀后得到熔喷无纺布原料;
所述改性增容剂的制备方法为:将高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯加入搅拌机中,控制搅拌机的转速为260rpm,搅拌机的温度为3℃,在3℃下低温处理22min后,加入过氧化二异丙苯,正十二烷基硫醇,然后以1.1℃/min的升温速度升温至42℃,在42℃下搅拌17min,加入甲基丙烯酸羟乙酯,过硫酸钠,然后以0.9℃/min的升温速度升温至52℃,在52℃下搅拌22min,自然恢复至室温,得到改性增容剂;
高熔融指数聚丙烯的熔融指数为850g/10min;
其中,高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯,过氧化二异丙苯,正十二烷基硫醇,甲基丙烯酸羟乙酯,过硫酸钠的重量比为105:5.5:2.5:0.7:0.6:3.5:0.3。
所述增粘剂的制备方法为:将黄原胶,阳离子瓜尔胶,海藻多糖混合均匀后置于密闭容器中,将密闭容器抽真空至真空度为150Pa后通入氧气,控制密闭容器内氧气的气体压力为80kPa,然后将密闭容器的温度控制到62℃,在62℃下处理42min后得到增粘剂;
其中,黄原胶,阳离子瓜尔胶,海藻多糖的重量比为27:17:5。
4.制备初级SM无纺布:将熔喷无纺布原料进行加热熔融,熔体过滤,熔体分配后由模头上的喷丝孔挤出,使用热风牵伸得到熔喷纤维,将熔喷纤维喷覆于第2步制备的纺粘无纺布上进行成网,得到初级SM无纺布;
所述加热熔融中螺杆区的温度分别为202℃,212℃,232℃;
所述熔体过滤中的过滤器温度为232℃;
所述熔体分配中的计量泵温度为232℃,转速为27rpm;
所述热风牵伸中的风温为205℃,转速为705rpm;
所述成网的速度为26rpm;
所述喷丝孔的孔径为0.5mm;
所述熔喷纤维的纤维直径为11μm。
5.后处理:在40-45℃下对初级SM无纺布表面喷淋活性液,控制活性液的使用量为55g/m2,喷淋结束后在42℃下烘干,得到SM无纺布;
所述活性液的组成,按重量份计,包括:105份去离子水,8份麦芽糊精,5.5份三聚磷酸钠,2.5份十二烷基硫酸钠,0.3份聚二烯丙基二甲基氯化铵。
本实施例在制备过程中未出现断布情况。
实施例3
一种屋顶防滑用SM无纺布的制备方法,具体为:
1.制备纺粘无纺布原料:将低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛混合均匀后得到纺粘无纺布原料;
所述低熔融指数聚丙烯的熔融指数为35g/10min;
所述高熔融指数聚丙烯的熔融指数为900g/10min;
其中,低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛的重量比为130:9:3:0.7:4:2:8:9:4:4。
所述增强剂的制备方法为:将六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠置于球磨机中进行球磨,控制球磨时的球料比为25:1,球磨转速为300rpm,球磨时的温度为65℃,球磨时间为30min,球磨结束后得到初级增强剂,将初级增强剂进行真空加热处理,控制真空加热处理的真空度为120Pa,温度为80℃,真空加热处理结束得到增强剂;
其中,六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠的重量比为22:10:5:10。
所述粘性剂的制备方法为:将聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺加入去离子水中,在65℃下以240rpm的搅拌速度搅拌50min后进行喷雾干燥,控制喷雾干燥的进风温度为160℃,出风温度为70℃,真空喷雾干燥结束得到粘性剂;
所述阳离子聚丙烯酰胺的分子量为600万,离子度为20%;
其中,聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺,去离子水的重量比为35:4:7:3:55。
2.制备纺粘无纺布:将纺粘无纺布原料加入混料装置中,经熔融挤压、熔体过滤、模头喷丝、铺网、热轧、上液、烘干、卷绕收卷、分切,得到纺粘无纺布;
所述模头喷丝步骤中的风箱压力为3000Pa,风机转速比为82%,上下冷风的温度为25℃;
所述热轧处理步骤中的花辊温度为160℃,光辊温度为145℃,网带速度为650m/min,热轧压力为90daN/cm。
3.制备熔喷无纺布原料:将聚丙烯,聚丁烯对苯二甲酸酯,聚乙烯,纳米二氧化硅,椰油酸单异丙醇酰胺,改性增容剂,增粘剂混合均匀后得到熔喷无纺布原料;
所述改性增容剂的制备方法为:将高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯加入搅拌机中,控制搅拌机的转速为280rpm,搅拌机的温度为5℃,在5℃下低温处理25min后,加入过氧化二异丙苯,正十二烷基硫醇,然后以1.2℃/min的升温速度升温至45℃,在45℃下搅拌20min,加入甲基丙烯酸羟乙酯,过硫酸钠,然后以1℃/min的升温速度升温至55℃,在55℃下搅拌25min,自然恢复至室温,得到改性增容剂;
高熔融指数聚丙烯的熔融指数为900g/10min;
其中,高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯,过氧化二异丙苯,正十二烷基硫醇,甲基丙烯酸羟乙酯,过硫酸钠的重量比为110:6:3:0.8:0.7:4:0.4。
所述增粘剂的制备方法为:将黄原胶,阳离子瓜尔胶,海藻多糖混合均匀后置于密闭容器中,将密闭容器抽真空至真空度为200Pa后通入氧气,控制密闭容器内氧气的气体压力为90kPa,然后将密闭容器的温度控制到65℃,在65℃下处理45min后得到增粘剂;
其中,黄原胶,阳离子瓜尔胶,海藻多糖的重量比为30:20:6。
4.制备初级SM无纺布:将熔喷无纺布原料进行加热熔融,熔体过滤,熔体分配后由模头上的喷丝孔挤出,使用热风牵伸得到熔喷纤维,将熔喷纤维喷覆于第2步制备的纺粘无纺布上进行成网,得到初级SM无纺布;
所述加热熔融中螺杆区的温度分别为205℃,215℃,235℃;
所述熔体过滤中的过滤器温度为235℃;
所述熔体分配中的计量泵温度为235℃,转速为30rpm;
所述热风牵伸中的风温为210℃,转速为710rpm;
所述成网的速度为27rpm;
所述喷丝孔的孔径为0.55mm;
所述熔喷纤维的纤维直径为12μm。
5.后处理:在45℃下对初级SM无纺布表面喷淋活性液,控制活性液的使用量为60g/m2,喷淋结束后在45℃下烘干,得到SM无纺布;
所述活性液的组成,按重量份计,包括:110份去离子水,9份麦芽糊精,6份三聚磷酸钠,3份十二烷基硫酸钠,0.5份聚二烯丙基二甲基氯化铵。
本实施例在制备过程中未出现断布情况。
对比例1
采用实施例1所述的屋顶防滑用SM无纺布的制备方法,其不同之处在于:在第1步制备纺粘无纺布原料步骤中使用六方氮化硼粉末代替增强剂。
本对比例在第4步制备初级SM无纺布过程中出现了断布情况。
对比例2
采用实施例1所述的屋顶防滑用SM无纺布的制备方法,其不同之处在于:在第1步制备纺粘无纺布原料步骤中使用聚乙烯醇2488代替粘性剂。
本对比例在制备过程中未出现断布情况。
对比例3
采用实施例1所述的屋顶防滑用SM无纺布的制备方法,其不同之处在于:在第3步制备熔喷无纺布原料步骤中省略改性增容剂的加入。
本对比例在第4步制备初级SM无纺布过程中出现了断布情况。
对比例4
采用实施例1所述的屋顶防滑用SM无纺布的制备方法,其不同之处在于:省略第5步后处理。
本对比例在制备过程中未出现断布情况。
将实施例1-3和对比例1-4制备的屋顶防滑用SM无纺布置于温度为38℃,湿度85%下静置10天,20天,30天,60天,90天后统计分层情况,统计结果如下:
Figure SMS_1
对实施例1-3和对比例1-4制备的屋顶防滑用SM无纺布的克重,孔隙率,纤维细度,透气量,横向强力,纵向强力,厚度,摩擦系数进行测试,测试结果如下:
Figure SMS_2
除非另有说明,本发明中所采用的百分数均为质量百分数。
最后应说明的是:以上所述仅为本发明的优选实施例而已,并不用于限制本发明,尽管参照前述实施例对本发明进行了详细的说明,对于本领域的技术人员来说,其依然可以对前述各实施例所记载的技术方案进行修改,或者对其中部分技术特征进行等同替换。凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。

Claims (6)

1.一种屋顶防滑用SM无纺布的制备方法,其特征在于,包括制备纺粘无纺布原料,制备纺粘无纺布,制备熔喷无纺布原料,制备初级SM无纺布,后处理;
所述制备纺粘无纺布原料,将低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛混合均匀后得到纺粘无纺布原料;
所述制备纺粘无纺布原料步骤中低熔融指数聚丙烯,高熔融指数聚丙烯,海藻酸钠,抗氧剂1010,硬脂酸锌,紫外线吸收剂UV-531,聚乙二醇6000,增强剂,粘性剂,纳米二氧化钛的重量比为120-130:7-9:3-5:0.5-0.7:2-4:1-2:6-8:7-9:3-4:2-4;
所述增强剂的制备方法为:将六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠置于球磨机中进行球磨,控制球磨时的球料比为20-25:1,球磨转速为200-300rpm,球磨时的温度为60-65℃,球磨时间为20-30min,球磨结束后得到初级增强剂,将初级增强剂进行真空加热处理,控制真空加热处理的真空度为100-120Pa,温度为70-80℃,真空加热处理结束得到增强剂;
其中,六方氮化硼粉末,轻质碳酸钙,十六烷基三甲基溴化铵,六偏磷酸钠的重量比为20-22:8-10:3-5:7-10;
所述制备熔喷无纺布原料,将聚丙烯,聚丁烯对苯二甲酸酯,聚乙烯,纳米二氧化硅,椰油酸单异丙醇酰胺,改性增容剂,增粘剂混合均匀后得到熔喷无纺布原料;
所述改性增容剂的制备方法为:将高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯加入搅拌机中,控制搅拌机的转速为250-280rpm,搅拌机的温度为2-5℃,在2-5℃下低温处理20-25min后,加入过氧化二异丙苯,正十二烷基硫醇,然后以1-1.2℃/min的升温速度升温至40-45℃,在40-45℃下搅拌15-20min,加入甲基丙烯酸羟乙酯,过硫酸钠,然后以0.8-1℃/min的升温速度升温至50-55℃,在50-55℃下搅拌20-25min,自然恢复至室温,得到改性增容剂;
所述改性增容剂的制备中,高熔融指数聚丙烯,马来酸酐,甲基丙烯酸甲酯,过氧化二异丙苯,正十二烷基硫醇,甲基丙烯酸羟乙酯,过硫酸钠的重量比为100-110:5-6:2-3:0.5-0.8:0.6-0.7:3-4:0.2-0.4;
所述后处理,在40-45℃下对初级SM无纺布表面喷淋活性液,控制活性液的使用量为50-60g/m2,喷淋结束后在40-45℃下烘干,得到SM无纺布;
所述活性液的组成,按重量份计,包括:100-110份去离子水,7-9份麦芽糊精,5-6份三聚磷酸钠,2-3份十二烷基硫酸钠,0.2-0.5份聚二烯丙基二甲基氯化铵。
2.根据权利要求1所述的屋顶防滑用SM无纺布的制备方法,其特征在于,所述低熔融指数聚丙烯的熔融指数为25-35g/10min;所述高熔融指数聚丙烯的熔融指数为800-900g/10min。
3.根据权利要求1所述的屋顶防滑用SM无纺布的制备方法,其特征在于,所述粘性剂的制备方法为:将聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺加入去离子水中,在60-65℃下以200-240rpm的搅拌速度搅拌40-50min后进行喷雾干燥,控制喷雾干燥的进风温度为140-160℃,出风温度为60-70℃,喷雾干燥结束得到粘性剂;
所述阳离子聚丙烯酰胺的分子量为500-600万,离子度为15-20%;
其中,聚乙烯醇2488,环糊精,羟乙基纤维素,阳离子聚丙烯酰胺,去离子水的重量比为30-35:3-4:5-7:1-3:50-55。
4.根据权利要求1所述的屋顶防滑用SM无纺布的制备方法,其特征在于,所述制备纺粘无纺布,将纺粘无纺布原料加入混料装置中,经熔融挤压、熔体过滤、模头喷丝、铺网、热轧、上液、烘干、卷绕收卷、分切,得到纺粘无纺布;
所述模头喷丝步骤中的风箱压力为2800-3000Pa,风机转速比为80-82%,上下冷风的温度为22-25℃;
所述热轧步骤中的花辊温度为155-160℃,光辊温度为140-145℃,网带速度为630-650m/min,热轧压力为80-90daN/cm。
5.根据权利要求1所述的屋顶防滑用SM无纺布的制备方法,其特征在于,所述增粘剂的制备方法为:将黄原胶,阳离子瓜尔胶,海藻多糖混合均匀后置于密闭容器中,将密闭容器抽真空至真空度为100-200Pa后通入氧气,控制密闭容器内氧气的气体压力为70-90kPa,然后将密闭容器的温度控制到60-65℃,在60-65℃下处理40-45min后得到增粘剂;
其中,黄原胶,阳离子瓜尔胶,海藻多糖的重量比为25-30:15-20:4-6。
6.根据权利要求1所述的屋顶防滑用SM无纺布的制备方法,其特征在于,所述制备初级SM无纺布,将熔喷无纺布原料进行加热熔融,熔体过滤,熔体分配后由模头上的喷丝孔挤出,使用热风牵伸得到熔喷纤维,将熔喷纤维喷覆于纺粘无纺布上进行成网,得到初级SM无纺布;
所述加热熔融中螺杆区的温度分别为200-205℃,210-215℃,230-235℃;
所述熔体过滤中的过滤器温度为230-235℃;
所述熔体分配中的计量泵温度为230-235℃,转速为25-30rpm;
所述热风牵伸中的风温为200-210℃,转速为700-710rpm;
所述成网的速度为25-27rpm;
所述喷丝孔的孔径为0.45-0.55mm;
所述熔喷纤维的纤维直径为10-12μm。
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Denomination of invention: Preparation method of SM non-woven fabric for roof anti slip

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