CN108927014A - 一种口罩中pva复合空气过滤膜的制备方法 - Google Patents

一种口罩中pva复合空气过滤膜的制备方法 Download PDF

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CN108927014A
CN108927014A CN201810832035.XA CN201810832035A CN108927014A CN 108927014 A CN108927014 A CN 108927014A CN 201810832035 A CN201810832035 A CN 201810832035A CN 108927014 A CN108927014 A CN 108927014A
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film
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李德喜
陈宗明
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Suzhou City Tianao Special Embroidery Co Ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D71/00Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/06Organic material
    • B01D71/44Polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, not provided for in a single one of groups B01D71/26-B01D71/42
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D46/00Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
    • B01D46/54Particle separators, e.g. dust precipitators, using ultra-fine filter sheets or diaphragms
    • B01D46/543Particle separators, e.g. dust precipitators, using ultra-fine filter sheets or diaphragms using membranes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D67/00Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
    • B01D67/0079Manufacture of membranes comprising organic and inorganic components
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D69/00Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
    • B01D69/12Composite membranes; Ultra-thin membranes
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/44Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/50Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polyalcohols, polyacetals or polyketals
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/184Carboxylic acids; Anhydrides, halides or salts thereof
    • D06M13/207Substituted carboxylic acids, e.g. by hydroxy or keto groups; Anhydrides, halides or salts thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/16Synthetic fibres, other than mineral fibres
    • D06M2101/18Synthetic fibres consisting of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/24Polymers or copolymers of alkenylalcohols or esters thereof; Polymers or copolymers of alkenylethers, acetals or ketones
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/10Repellency against liquids
    • D06M2200/12Hydrophobic properties

Abstract

本发明提供了一种口罩中PVA复合空气过滤膜的制备方法,包括以下步骤:S1.将纳米粉煤灰溶解于盐酸溶液中,采用湿法研磨后,过滤,洗净盐酸,烘干后备用;S2.将纳米高岭土和步骤S1中制备的粉煤灰混合改性,得到改性纳米颗粒;S3.将PVA溶解于去离子水中配置成PVA纺丝液;S4.将改性纳米颗粒加入纺丝液中,得到含有改性纳米颗粒的PVA纺丝液;S5.分别用步骤S3和S4.制备的PVA纺丝液分别进行纺丝,得到纯PVA膜和改性PVA膜;S6.将步骤S5制备的两种PVA膜进行防水整理;S7.然后将改性PVA膜和纯PVA膜复合后,热处理得到复合空气过滤膜。本发明制备的过滤膜的过滤效果非常优异。

Description

一种口罩中PVA复合空气过滤膜的制备方法
技术领域
本发明涉及纺织材料领域,具体涉及一种口罩中PVA复合空气过滤膜的制备方法。
背景技术
市场上的口罩一般分为两大类,一类以活性炭或者棉布为主要材料制造而成,相比其它材料,这两种材料对空气中颗粒物的拦截吸附能力较好。然而,粒径小于纤维孔隙的微粒,如PM2.5,总能穿过过滤层,进入到人体肺部,威胁心肺功能,对健康造成不利影响。另外一类口罩应用高科技材料作为滤芯,虽然能够有效地过滤空气中的PM2.5,但却给人的呼吸过程带来很大阻力,缺乏一定的舒适度。基于此,我们考虑探究一种新型材料作为口罩滤芯。静电纺丝是一种特殊的纤维制造工艺,可以制备出纤维直径在微纳米量级的聚合物细丝。
发明内容
要解决的技术问题:本发明的目的是提供一种PVA复合空气过滤膜,得到的过滤膜具有很强的吸附和拦截能力,为制造新型口罩提供了一个较好的选择。
技术方案:一种口罩中PVA复合空气过滤膜的制备方法,包括以下步骤:
S1. 将纳米粉煤灰按照1:3-6的质量比溶解于浓度为5-15wt%的盐酸溶液中,采用湿法研磨后,过滤,洗净盐酸,烘干后备用;
S2. 将纳米高岭土和步骤S1中制备的粉煤灰按质量比1:0.3-1.5混合均匀,加入水,用模具压成型,干燥后在860-930℃焙烧130-150min,冷却后用研钵研磨后过25000目筛,得到改性纳米颗粒;
S3. 将PVA溶解于去离子水中配置成浓度为10-20wt%的PVA纺丝液;
S4. 将改性纳米颗粒加入纺丝液中,纳米颗粒的浓度为0.5-3.5wt%,在水浴为40-50℃下超声分撒均匀,得到含有改性纳米颗粒的PVA纺丝液;
S5. 分别用步骤S3和S4.制备的PVA纺丝液分别进行纺丝,得到纯PVA膜和改性PVA膜;
S6. 将步骤S5制备的两种PVA膜进行防水整理;
S7. 然后将改性PVA膜和纯PVA膜复合后,热处理得到复合空气过滤膜。
进一步的,所述步骤S3中PVA的平均分子质量为20000-30000 g/mol,水解度88%。
进一步的,所述步骤S5中采用螺旋式纺丝机,纺丝参数设置为纺丝距离为20cm,电压为80kV,纺丝头旋转速率为10rpm。
进一步的,所述步骤S6中防水整理为将PVA膜浸泡于浓度为23.5-28wt%的柠檬酸乙醇溶液中在温度为50-60℃下浸泡30-60min。
进一步的,所述步骤S7中热处理的温度为170-180℃,热处理时间为120-160min
进一步的,所述步骤S7中复合方法为改性PVA膜和纯PVA膜三层复合,中间层为改性PVA膜。
有益效果:本发明的PVA复合空气过滤膜具有以下优点:首先本发明的空气过滤膜具有很强的过滤和吸附作用,其次加入粉煤灰和高岭土,由于粉煤灰和高岭土的多孔结构,对空气中的固体颗粒具有很强的吸附作用,最后通过静电纺丝,得到的薄膜自身带有静电,具有多孔结构,其纤维直径在2至3微米之间,并通过多层复合,使得本发明的过滤的膜的过滤效果更加好。
具体实施方式
实施例1
一种口罩中PVA复合空气过滤膜的制备方法,包括以下步骤:
S1. 将纳米粉煤灰按照1:3的质量比溶解于浓度为15wt%的盐酸溶液中,采用湿法研磨后,过滤,洗净盐酸,烘干后备用;
S2. 将纳米高岭土和步骤S1中制备的粉煤灰按质量比1:0.3混合均匀,加入水,用模具压成型,干燥后在860℃焙烧150min,冷却后用研钵研磨后过25000目筛,得到改性纳米颗粒;
S3. 将分子质量为20000g/mol,水解度88%的PVA溶解于去离子水中配置成浓度为20wt%的PVA纺丝液;
S4. 将改性纳米颗粒加入纺丝液中,纳米颗粒的浓度为0.5wt%,在水浴为50℃下超声分撒均匀,得到含有改性纳米颗粒的PVA纺丝液;
S5. 分别用步骤S3和S4.制备的PVA纺丝液分别进行纺丝,采用螺旋式纺丝机,纺丝参数设置为纺丝距离为20cm,电压为80kV,纺丝头旋转速率为10rpm,得到纯PVA膜和改性PVA膜;
S6. 将步骤S5制备的两种PVA膜分别浸泡于浓度为28wt%的柠檬酸乙醇溶液中在温度为50℃下浸泡60min,进行防水整理;
S7. 然后将改性PVA膜和纯PVA膜复合后,热处理温度为170℃,热处理时间为120min,将改性PVA膜和纯PVA膜三层复合,中间层为改性PVA膜,得到复合空气过滤膜。
实施例2
一种口罩中PVA复合空气过滤膜的制备方法,包括以下步骤:
S1. 将纳米粉煤灰按照1:6的质量比溶解于浓度为5wt%的盐酸溶液中,采用湿法研磨后,过滤,洗净盐酸,烘干后备用;
S2. 将纳米高岭土和步骤S1中制备的粉煤灰按质量比1:1.5混合均匀,加入水,用模具压成型,干燥后在930℃焙烧150min,冷却后用研钵研磨后过25000目筛,得到改性纳米颗粒;
S3. 将分子质量为30000g/mol,水解度88%的PVA溶解于去离子水中配置成浓度为10wt%的PVA纺丝液;
S4. 将改性纳米颗粒加入纺丝液中,纳米颗粒的浓度为3.5wt%,在水浴为50℃下超声分撒均匀,得到含有改性纳米颗粒的PVA纺丝液;
S5. 分别用步骤S3和S4.制备的PVA纺丝液分别进行纺丝,采用螺旋式纺丝机,纺丝参数设置为纺丝距离为20cm,电压为80kV,纺丝头旋转速率为10rpm,得到纯PVA膜和改性PVA膜;
S6. 将步骤S5制备的两种PVA膜分别浸泡于浓度为28wt%的柠檬酸乙醇溶液中在温度为60℃下浸泡30min,进行防水整理;
S7. 然后将改性PVA膜和纯PVA膜复合后,热处理温度为180℃,热处理时间为160min,将改性PVA膜和纯PVA膜三层复合,中间层为改性PVA膜,得到复合空气过滤膜。
实施例3
一种口罩中PVA复合空气过滤膜的制备方法,包括以下步骤:
S1. 将纳米粉煤灰按照1:3的质量比溶解于浓度为12wt%的盐酸溶液中,采用湿法研磨后,过滤,洗净盐酸,烘干后备用;
S2. 将纳米高岭土和步骤S1中制备的粉煤灰按质量比1:0.5混合均匀,加入水,用模具压成型,干燥后在880℃焙烧150min,冷却后用研钵研磨后过25000目筛,得到改性纳米颗粒;
S3. 将分子质量为24000 g/mol,水解度88%的PVA溶解于去离子水中配置成浓度为12wt%的PVA纺丝液;
S4. 将改性纳米颗粒加入纺丝液中,纳米颗粒的浓度为3wt%,在水浴为50℃下超声分撒均匀,得到含有改性纳米颗粒的PVA纺丝液;
S5. 分别用步骤S3和S4.制备的PVA纺丝液分别进行纺丝,采用螺旋式纺丝机,纺丝参数设置为纺丝距离为20cm,电压为80kV,纺丝头旋转速率为10rpm,得到纯PVA膜和改性PVA膜;
S6. 将步骤S5制备的两种PVA膜分别浸泡于浓度为25-27wt%的柠檬酸乙醇溶液中在温度为50℃下浸泡30min,进行防水整理;
S7. 然后将改性PVA膜和纯PVA膜复合后,热处理温度为170℃,热处理时间为150min,将改性PVA膜和纯PVA膜三层复合,中间层为改性PVA膜,得到复合空气过滤膜。
实施例4
一种口罩中PVA复合空气过滤膜的制备方法,包括以下步骤:
S1. 将纳米粉煤灰按照1:6的质量比溶解于浓度为8wt%的盐酸溶液中,采用湿法研磨后,过滤,洗净盐酸,烘干后备用;
S2. 将纳米高岭土和步骤S1中制备的粉煤灰按质量比1:1.2混合均匀,加入水,用模具压成型,干燥后在910℃焙烧130min,冷却后用研钵研磨后过25000目筛,得到改性纳米颗粒;
S3. 将分子质量为28000 g/mol,水解度88%的PVA溶解于去离子水中配置成浓度为18wt%的PVA纺丝液;
S4. 将改性纳米颗粒加入纺丝液中,纳米颗粒的浓度为1.5wt%,在水浴为40℃下超声分撒均匀,得到含有改性纳米颗粒的PVA纺丝液;
S5. 分别用步骤S3和S4.制备的PVA纺丝液分别进行纺丝,采用螺旋式纺丝机,纺丝参数设置为纺丝距离为20cm,电压为80kV,纺丝头旋转速率为10rpm,得到纯PVA膜和改性PVA膜;
S6. 将步骤S5制备的两种PVA膜分别浸泡于浓度为25-27wt%的柠檬酸乙醇溶液中在温度为60℃下浸泡60min,进行防水整理;
S7. 然后将改性PVA膜和纯PVA膜复合后,热处理温度为180℃,热处理时间为130min,将改性PVA膜和纯PVA膜三层复合,中间层为改性PVA膜,得到复合空气过滤膜。
实施例5
一种口罩中PVA复合空气过滤膜的制备方法,包括以下步骤:
S1. 将纳米粉煤灰按照1:3-6的质量比溶解于浓度为19wt%的盐酸溶液中,采用湿法研磨后,过滤,洗净盐酸,烘干后备用;
S2. 将纳米高岭土和步骤S1中制备的粉煤灰按质量比1:1混合均匀,加入水,用模具压成型,干燥后在900℃焙烧150min,冷却后用研钵研磨后过25000目筛,得到改性纳米颗粒;
S3. 将分子质量为26000 g/mol,水解度88%的PVA溶解于去离子水中配置成浓度为15wt%的PVA纺丝液;
S4. 将改性纳米颗粒加入纺丝液中,纳米颗粒的浓度为2wt%,在水浴为45℃下超声分撒均匀,得到含有改性纳米颗粒的PVA纺丝液;
S5. 分别用步骤S3和S4.制备的PVA纺丝液分别进行纺丝,采用螺旋式纺丝机,纺丝参数设置为纺丝距离为20cm,电压为80kV,纺丝头旋转速率为10rpm,得到纯PVA膜和改性PVA膜;
S6. 将步骤S5制备的两种PVA膜分别浸泡于浓度为27wt%的柠檬酸乙醇溶液中在温度为55℃下浸泡40min,进行防水整理;
S7. 然后将改性PVA膜和纯PVA膜复合后,热处理温度为175℃,热处理时间为140min,将改性PVA膜和纯PVA膜三层复合,中间层为改性PVA膜,得到复合空气过滤膜。
对比例1
对比例1中纳米粉煤灰和高岭土未处理,直接添加到PVA纺丝液中。
对比例2
对比例2中直接制备改性PVA膜,不复合直接过滤。
采用Certi Test 8130型全自动过滤测试仪,在室温条件下,测量气体过滤效率和过滤阻力(毫米水柱高度压力的压降)。采用氯化钠(NaCl)气溶胶作为过滤介质,用BS224S型Sartorius电子天平称取20 g NaCl固体,加入到1000 mL去离子水中,在室温条件下,用玻璃棒搅拌至固体完全溶解,得到均匀的浓度为5wt%的测试用NaCl溶液,通过测试仪器转化为NaCl气溶胶。气溶胶颗粒质量中值直径为260 nm,数量中值直径为75 nm。将PVA纳米纤维膜连同基布一起进行测试,有效面积100 cm2,根据GB 19083-2010 《医用防护口罩技术要求》,气溶胶流量85 ± 0.2 L/min,每种试样测3次,取平均值。

Claims (6)

1.一种口罩中PVA复合空气过滤膜的制备方法,其特征在于,包括以下步骤:
S1. 将纳米粉煤灰按照1:3-6的质量比溶解于浓度为5-15wt%的盐酸溶液中,采用湿法研磨后,过滤,洗净盐酸,烘干后备用;
S2. 将纳米高岭土和步骤S1中制备的粉煤灰按质量比1:0.3-1.5混合均匀,加入水,用模具压成型,干燥后在860-930℃焙烧130-150min,冷却后用研钵研磨后过25000目筛,得到改性纳米颗粒;
S3. 将PVA溶解于去离子水中配置成浓度为10-20wt%的PVA纺丝液;
S4. 将改性纳米颗粒加入纺丝液中,纳米颗粒的浓度为0.5-3.5wt%,在水浴为40-50℃下超声分撒均匀,得到含有改性纳米颗粒的PVA纺丝液;
S5. 分别用步骤S3和S4.制备的PVA纺丝液分别进行纺丝,得到纯PVA膜和改性PVA膜;
S6. 将步骤S5制备的两种PVA膜进行防水整理;
S7. 然后将改性PVA膜和纯PVA膜复合后,热处理得到复合空气过滤膜。
2.根据权利要求1所述的口罩中PVA复合空气过滤膜的制备方法,其特征在于:所述步骤S3中PVA的平均分子质量为20000-30000 g/mol,水解度88%。
3.根据权利要求1所述的口罩中PVA复合空气过滤膜的制备方法,其特征在于:所述步骤S5中采用螺旋式纺丝机,纺丝参数设置为纺丝距离为20cm,电压为80kV,纺丝头旋转速率为10rpm。
4.根据权利要求1所述的口罩中PVA复合空气过滤膜的制备方法,其特征在于:所述步骤S6中防水整理为将PVA膜浸泡于浓度为23.5-28wt%的柠檬酸乙醇溶液中在温度为50-60℃下浸泡30-60min。
5.根据权利要求1所述的口罩中PVA复合空气过滤膜的制备方法,其特征在于:所述步骤S7中热处理的温度为170-180℃,热处理时间为120-160min。
6.根据权利要求1所述的口罩中PVA复合空气过滤膜的制备方法,其特征在于:所述步骤S7中复合方法为改性PVA膜和纯PVA膜三层复合,中间层为改性PVA膜。
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