CN106139742A - 一种亚麻复合纤维过滤材料 - Google Patents
一种亚麻复合纤维过滤材料 Download PDFInfo
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- 239000000835 fiber Substances 0.000 title claims abstract description 75
- 239000002131 composite material Substances 0.000 title claims abstract description 42
- 238000001914 filtration Methods 0.000 title claims abstract description 38
- 239000000463 material Substances 0.000 title claims abstract description 36
- 241000208202 Linaceae Species 0.000 title claims abstract description 21
- 235000004431 Linum usitatissimum Nutrition 0.000 title claims abstract description 21
- 229920000728 polyester Polymers 0.000 claims abstract description 17
- 229910052582 BN Inorganic materials 0.000 claims abstract description 16
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000003365 glass fiber Substances 0.000 claims abstract description 16
- 239000013078 crystal Substances 0.000 claims abstract description 14
- 239000002994 raw material Substances 0.000 claims abstract description 7
- 239000002253 acid Substances 0.000 claims abstract description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 33
- 239000007788 liquid Substances 0.000 claims description 20
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 13
- 239000004202 carbamide Substances 0.000 claims description 7
- 235000013877 carbamide Nutrition 0.000 claims description 7
- 238000005530 etching Methods 0.000 claims description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- 230000002378 acidificating effect Effects 0.000 claims description 6
- 239000008367 deionised water Substances 0.000 claims description 6
- 229910021641 deionized water Inorganic materials 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical class [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 239000006228 supernatant Substances 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 230000009514 concussion Effects 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 238000011010 flushing procedure Methods 0.000 claims description 3
- 235000011149 sulphuric acid Nutrition 0.000 claims description 3
- 238000004804 winding Methods 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 230000008014 freezing Effects 0.000 claims description 2
- 238000007710 freezing Methods 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 230000000284 resting effect Effects 0.000 claims description 2
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 2
- 229910001948 sodium oxide Inorganic materials 0.000 claims description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 1
- 229910052796 boron Inorganic materials 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 230000003628 erosive effect Effects 0.000 claims 1
- 238000001179 sorption measurement Methods 0.000 abstract description 4
- 230000035699 permeability Effects 0.000 abstract description 2
- 239000000428 dust Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 210000003928 nasal cavity Anatomy 0.000 description 1
- 230000002685 pulmonary effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
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Abstract
本发明公开了一种过滤材料,尤其是涉及空气过滤材料,其主要原料包括亚麻纤维、六方晶系氮化硼、聚酯纤维和玻璃纤维。本发明的过滤材料具有很强的通透性,且其过滤性能优异。本发明制得的过滤材料的原料易得,因此本发明的过滤材料造价低廉,并且其工作环境要求低、吸附过滤性能强,适用于办公室、卧室等各种场所。本发明的亚麻复合纤维过滤材料具有抗静电、耐高温、耐酸碱、使用安全性好等优点。
Description
技术领域
本发明涉及一种过滤材料,尤其是涉及空气过滤材料。
背景技术
对于空气过滤技术的主要是过滤掉空气中的污染源,而污染源主要是指微尘和细菌二大类。一般通过空气过滤器来过滤掉室内一定空间环境的空气中的污染源;通过口罩、防毒面具来过滤进入鼻腔和肺部的空气中的污染源。目前空气过滤技术主要采用过滤分离方法:通过设置不同性能的过滤器,除去空气中的悬尘埃粒子和微生物,也即通过滤料将尘埃粒子捕集截留下来,以保证送入风量的洁净度要求。它所用的滤料为较细直径的纤维,既能使气流顺利通过,也能有效地捕集尘埃粒子。
现有技术的过滤材料普遍存在吸附微尘和细菌效果不佳,吸附持续时间不长的问题。
发明内容
本发明所要解决的问题是,针对上述现有技术中的缺点,提出创新方案,尤其是一种能够有效解决现有过滤材料吸附微尘和细菌效果不佳,吸附持续时间不长的问题的方案。
为解决上述问题,本发明采用的方案如下:一种亚麻复合纤维过滤材料,其特征在于,其主要原料包括亚麻纤维、六方晶系氮化硼、聚酯纤维和玻璃纤维;
取聚酯纤维加入10%-30%的氢氧化钠溶液中,保持溶液温度在50-80摄氏度,对聚酯纤维进行碱减量处理,然后取出烘干,制成聚酯纤维束;
取六方晶系氮化硼加入去离子水,使用超声波震荡,形成六方晶系氮化硼的均相混合液A;
将亚麻纤维加入混合液A中,并降温至0摄氏度,并向其中加入氢氧化钠、尿素,然后持续搅拌20-30分钟,制得混合液B;
将混合液B在零下15摄氏度的温度下存放1-4小时,然后取出在室温下结冻,并搅拌30-40分钟,制得亚麻纤维和六方晶系氮化硼形成的均相混合液C;
将混合液C喷射如高速搅拌的盐酸溶液中出去多余的氢氧化钠,得到亚麻纤维与六方晶系氮化硼复合纤维,并用去离子水冲洗至冲洗液的pH值达到7,用烘箱将复合纤维烘干,得到干燥的复合纤维;
取石灰水上清层,并向其中加入干燥的复合纤维和活性炭粉,然后放入高速搅拌机中搅拌20-50分钟,形成改性复合纤维;
玻璃纤维放入酸性蚀刻液中浸润2-7分钟,进行表面处理;所述酸性蚀刻液为浓度为15%的KClO3和浓度为40%的H2SO4的混合液,形成改性玻璃纤维;
将改性复合纤维和改性玻璃纤维交叉缠绕设置在聚酯纤维束上,形成亚麻复合纤维过滤材料。
进一步,根据上述设计方案所述亚麻复合纤维过滤材料,所述加入混合液A中的氢氧化钠、尿素和亚麻纤维的重量比例为3:2:3。
进一步,根据上述设计方案所述亚麻复合纤维过滤材料,所述氢氧化钠、尿素和亚麻纤维加入混合液A后搅拌30分钟。
进一步,根据上述设计方案所述亚麻复合纤维过滤材料,所述混合液B在零下15摄氏度的温度下存放时间为4小时。
进一步,根据上述设计方案所述亚麻复合纤维过滤材料,所述混合液B结冻后搅拌时间为40分钟。
根据权利要求1所述亚麻复合纤维过滤材料,其特征在于,所述干燥的复合纤维和活性炭粉加入石灰水上清层后搅拌时间为40分钟。
进一步,根据上述设计方案所述亚麻复合纤维过滤材料,所述玻璃纤维放入酸性蚀刻液中浸润时间为5分钟。
本发明的技术效果如下:本发明公开了一种过滤材料,尤其是涉及空气过滤材料,其主要原料包括亚麻纤维、六方晶系氮化硼、聚酯纤维和玻璃纤维。本发明的过滤材料具有很强的通透性,且其过滤性能优异。本发明制得的过滤材料的原料易得,因此本发明的过滤材料造价低廉,并且其工作环境要求低、吸附过滤性能强,适用于办公室、卧室等各种场所。本发明的亚麻复合纤维过滤材料具有抗静电、耐高温、耐酸碱、使用安全性好等优点。
具体实施方式
下面结合实施例对本发明做进一步详细说明。
实施例:一种亚麻复合纤维过滤材料,其特征在于,其主要原料包括亚麻纤维、六方晶系氮化硼、聚酯纤维和玻璃纤维;
取聚酯纤维加入10%-30%的氢氧化钠溶液中,保持溶液温度在50-80摄氏度,对聚酯纤维进行碱减量处理,然后取出烘干,制成聚酯纤维束;
取六方晶系氮化硼加入去离子水,使用超声波震荡,形成六方晶系氮化硼的均相混合液A;
将亚麻纤维加入混合液A中,并降温至0摄氏度,并向其中加入氢氧化钠、尿素,然后持续搅拌20-30分钟,制得混合液B;
将混合液B在零下15摄氏度的温度下存放1-4小时,然后取出在室温下结冻,并搅拌30-40分钟,制得亚麻纤维和六方晶系氮化硼形成的均相混合液C;
将混合液C喷射如高速搅拌的盐酸溶液中出去多余的氢氧化钠,得到亚麻纤维与六方晶系氮化硼复合纤维,并用去离子水冲洗至冲洗液的pH值达到7,用烘箱将复合纤维烘干,得到干燥的复合纤维;
取石灰水上清层,并向其中加入干燥的复合纤维和活性炭粉,然后放入高速搅拌机中搅拌20-50分钟,形成改性复合纤维;
玻璃纤维放入酸性蚀刻液中浸润2-7分钟,进行表面处理;所述酸性蚀刻液为浓度为15%的KClO3和浓度为40%的H2SO4的混合液,形成改性玻璃纤维;
将改性复合纤维和改性玻璃纤维交叉缠绕设置在聚酯纤维束上,形成亚麻复合纤维过滤材料。
Claims (7)
1.一种亚麻复合纤维过滤材料,其特征在于,其主要原料包括亚麻纤维、六方晶系氮化硼、聚酯纤维和玻璃纤维;
取聚酯纤维加入10%-30%的氢氧化钠溶液中,保持溶液温度在50-80摄氏度,对聚酯纤维进行碱减量处理,然后取出烘干,制成聚酯纤维束;
取六方晶系氮化硼加入去离子水,使用超声波震荡,形成六方晶系氮化硼的均相混合液A;
将亚麻纤维加入混合液A中,并降温至0摄氏度,并向其中加入氢氧化钠、尿素,然后持续搅拌20-30分钟,制得混合液B;
将混合液B在零下15摄氏度的温度下存放1-4小时,然后取出在室温下结冻,并搅拌30-40分钟,制得亚麻纤维和六方晶系氮化硼形成的均相混合液C;
将混合液C喷射如高速搅拌的盐酸溶液中出去多余的氢氧化钠,得到亚麻纤维与六方晶系氮化硼复合纤维,并用去离子水冲洗至冲洗液的pH值达到7,用烘箱将复合纤维烘干,得到干燥的复合纤维;
取石灰水上清层,并向其中加入干燥的复合纤维和活性炭粉,然后放入高速搅拌机中搅拌20-50分钟,形成改性复合纤维;
玻璃纤维放入酸性蚀刻液中浸润2-7分钟,进行表面处理;所述酸性蚀刻液为浓度为15%的KClO3和浓度为40%的H2SO4的混合液,形成改性玻璃纤维;
将改性复合纤维和改性玻璃纤维交叉缠绕设置在聚酯纤维束上,形成亚麻复合纤维过滤材料。
2.根据权利要求1所述亚麻复合纤维过滤材料,其特征在于,所述加入混合液A中的氢氧化钠、尿素和亚麻纤维的重量比例为3:2:3。
3.根据权利要求1所述亚麻复合纤维过滤材料,其特征在于,所述氢氧化钠、尿素和亚麻纤维加入混合液A后搅拌30分钟。
4.根据权利要求1所述亚麻复合纤维过滤材料,其特征在于,所述混合液B在零下15摄氏度的温度下存放时间为4小时。
5.根据权利要求1所述亚麻复合纤维过滤材料,其特征在于,所述混合液B结冻后搅拌时间为40分钟。
6.根据权利要求1所述亚麻复合纤维过滤材料,其特征在于,所述干燥的复合纤维和活性炭粉加入石灰水上清层后搅拌时间为40分钟。
7.根据权利要求1所述亚麻复合纤维过滤材料,其特征在于,所述玻璃纤维放入酸性蚀刻液中浸润时间为5分钟。
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