CN105440517A - Pvdf超滤膜 - Google Patents

Pvdf超滤膜 Download PDF

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CN105440517A
CN105440517A CN201510936312.8A CN201510936312A CN105440517A CN 105440517 A CN105440517 A CN 105440517A CN 201510936312 A CN201510936312 A CN 201510936312A CN 105440517 A CN105440517 A CN 105440517A
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polyvinylidene difluoride
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徐建林
邹建良
宗建青
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CHANGSHU LIYUAN MEMBRANE TECHNOLOGY Co Ltd
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Abstract

本发明公开了一种PVDF超滤膜,以聚偏氟乙烯为膜的原料,聚偏氟乙烯制备步骤如下:1)反应釜中投入1~2重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。本发明PVDF超滤膜具有耐腐蚀、耐热、耐寒、耐氧化、耐候性能。

Description

PVDF超滤膜
技术领域
本发明涉及PVDF超滤膜。
背景技术
现有超滤膜、分离膜、中空纤维膜的耐腐蚀、耐热、耐寒、耐氧化、耐候性能都有待提高。
发明内容
本发明的目的在于提供一种PVDF超滤膜,以聚偏氟乙烯为膜的原料,制备的膜具有优异的耐腐蚀、耐热、耐寒、耐氧化、耐候性能。
为实现上述目的,本发明的技术方案是设计一种PVDF超滤膜,以聚偏氟乙烯为膜的原料,所述聚偏氟乙烯通过如下步骤制备:
1)反应釜中投入1~2重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;
2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;
3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。
优选的,PVDF超滤膜,以聚偏氟乙烯为膜的原料,所述聚偏氟乙烯通过如下步骤制备:
1)反应釜中投入1重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;
2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;
3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。
优选的,PVDF超滤膜,以聚偏氟乙烯为膜的原料,所述聚偏氟乙烯通过如下步骤制备:
1)反应釜中投入2重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;
2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;
3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。
本发明的优点和有益效果在于:提供一种PVDF超滤膜,以聚偏氟乙烯为膜的原料,制备的膜具有优异的耐腐蚀、耐热、耐寒、耐氧化、耐候性能。
具体实施方式
下面结合实施例,对本发明的具体实施方式作进一步描述。以下实施例仅用于更加清楚地说明本发明的技术方案,而不能以此来限制本发明的保护范围。
本发明具体实施的技术方案是:
实施例1
一种PVDF超滤膜,以聚偏氟乙烯为膜的原料,所述聚偏氟乙烯通过如下步骤制备:
1)反应釜中投入1~2重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;
2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;
3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。
实施例2
PVDF超滤膜,以聚偏氟乙烯为膜的原料,所述聚偏氟乙烯通过如下步骤制备:
1)反应釜中投入1重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;
2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;
3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。
实施例3
PVDF超滤膜,以聚偏氟乙烯为膜的原料,所述聚偏氟乙烯通过如下步骤制备:
1)反应釜中投入2重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;
2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;
3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。
以上所述仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明技术原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。

Claims (3)

1.PVDF超滤膜,其特征在于,以聚偏氟乙烯为膜的原料,所述聚偏氟乙烯通过如下步骤制备:
1)反应釜中投入1~2重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;
2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;
3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。
2.根据权利要求1所述的PVDF超滤膜,其特征在于,以聚偏氟乙烯为膜的原料,所述聚偏氟乙烯通过如下步骤制备:
1)反应釜中投入1重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;
2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;
3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。
3.根据权利要求1所述的PVDF超滤膜,其特征在于,以聚偏氟乙烯为膜的原料,所述聚偏氟乙烯通过如下步骤制备:
1)反应釜中投入2重量份泡花碱、1.6重量份双氧水、1.9重量份无机碱溶液,混合均匀,再投入0.9重量份蓖麻油酸丁酯硫酸钠、15.2重量份六氟乙烷溶剂、0.4重量份磺酰氯溶液,在-5.5℃搅拌反应36分钟;
2)再投入4.7重量份聚甘油单硬脂酸酯、7.3重量份聚丙烯酸溶液、78重量份偏氟乙烯单体、3.8重量份2,2,3-三甲基戊烷,在31℃搅拌反应,压力下降至0.26MPa以下时终止反应;
3)过滤、洗涤、干燥,即得粉末状聚偏氟乙烯。
CN201510936312.8A 2015-12-16 2015-12-16 Pvdf超滤膜 Pending CN105440517A (zh)

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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104448075A (zh) * 2014-12-06 2015-03-25 常熟丽源膜科技有限公司 用于制备热稳定性聚偏氟乙烯的方法

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104448075A (zh) * 2014-12-06 2015-03-25 常熟丽源膜科技有限公司 用于制备热稳定性聚偏氟乙烯的方法

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Application publication date: 20160330