首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >High-Flux Nanofiltration Membranes Prepared by Adsorption of Multilayer Polyelectrolyte Membranes on Polymeric Supports
【24h】

High-Flux Nanofiltration Membranes Prepared by Adsorption of Multilayer Polyelectrolyte Membranes on Polymeric Supports

机译:通过在聚合物载体上吸附多层聚电解质膜制备的高通量纳滤膜

获取原文
获取原文并翻译 | 示例
           

摘要

Layer-by-layer deposition of anionic and cationic polyelectrolytes readily converts polymeric ultrafiltration membranes into materials capable of nanofiltration.ATR-FTIR spectra confirm that layer-by-layer deposition occurs on the ultrafiltration substrates,and adsorption of as few as 2.5 bilayers of poly(styrenesulfonate) (PSS)/protonated poly(allylamine) (PAH) or 3.5 bilayers of PSS/poly(diallyldimethylammonium chloride) (PDADMAC) reduces the molecular weight cutoff of polyethersulfone ultrafiltration supports from 50 kDa to <500 Da.Deposition of multilayer polyelectrolyte films on 300 and 500 kDa membranes also decreases molecular weight cutoffs,but solute rejections are significantly lower when using these supports,suggesting that the polyelectrolyte films do not completely cover large (0.2-0.4 mum in diameter) pores.On the 50 kDa substrates,PSS/PDADMAC films containing 3.5 bilayers exhibit a 95% rejection of SO_4~(2-)and a chloride/ sulfate selectivity of 27,whereas 4.5-bilayer PSS/PAH coatings show a glucose/raffinose selectivity of 100.Pure water flux for [PSS/PAH]_3PSS-coated membranes at 4.8 bar is 1.6 m~3/(m~2day),which is more than 2-fold higher than that through a commercial 500 Da membrane.
机译:阴离子和阳离子聚电解质的逐层沉积易于将聚合的超滤膜转化为具有纳滤能力的材料。ATR-FTIR光谱证实,在超滤基质上发生了逐层沉积,并吸附了多达2.5个双层的聚(苯乙烯磺酸盐)(PSS)/质子化聚(烯丙胺)(PAH)或3.5双层PSS /聚(二烯丙基二甲基氯化铵)(PDADMAC)将聚醚砜超滤载体的截留分子量从50 kDa降低至<500 Da。在300 kDa和500 kDa膜上的膜也可降低分子量的截留值,但使用这些载体时溶质截留率明显降低,这表明聚电解质膜不能完全覆盖大(直径为0.2-0.4微米)的孔。在50 kDa的基底上,包含3.5个双层的PSS / PDADMAC膜表现出95%的SO_4〜(2-)截留率和27个氯化物/硫酸盐选择性,而4.5双层PS S / PAH涂层对葡萄糖/果糖的选择性为100。[PSS / PAH] _3PSS涂层膜在4.8 bar下的纯水通量为1.6 m〜3 /(m〜2day),是其的2倍以上。通过商业化的500 Da膜

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号