中国有色金属学报(英文版)
中國有色金屬學報(英文版)
중국유색금속학보(영문판)
TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA
2014年
4期
1196-1201
,共6页
络合-超滤%马来酸-丙烯酸共聚物%PVB中空纤维膜%锰%废水处理
絡閤-超濾%馬來痠-丙烯痠共聚物%PVB中空纖維膜%錳%廢水處理
락합-초려%마래산-병희산공취물%PVB중공섬유막%맹%폐수처리
complexation-ultrafitration%copolymer of maleic acid and acrylic acid%poly (vinyl butyral) hollow fiber membrane%manganese%wastewater treatment
用马来酸-丙烯酸共聚物(PMA-100)作络合剂,采用PVB中空纤维膜,研究络合-超滤处理含锰废水。测定了高聚物的羧基含量以及Mn(II)与PMA-100的络合反应速率,研究聚合物与重金属质量比(P/M)、pH、外加盐浓度等因素对锰离子截留率(R)和膜通量(J)的影响。结果表明:高聚物中羧基含量为9.5 mmol/g,对Mn(II)质量浓度为10 mg/L的模拟废水,在pH=6.0时,Mn(II)与PMA-100的络合在5 min内基本可完成,络合率达99.6%。在一定P/M下,pH在2.5~7.0范围内,截留率和膜通量均随着pH的增加而增大;在一定pH下,截留率随着P/M的增加而增加,但膜通量基本不变。外加盐的存在使截留率下降,在同样离子强度下,CaCl2的影响远大于NaCl的。
用馬來痠-丙烯痠共聚物(PMA-100)作絡閤劑,採用PVB中空纖維膜,研究絡閤-超濾處理含錳廢水。測定瞭高聚物的羧基含量以及Mn(II)與PMA-100的絡閤反應速率,研究聚閤物與重金屬質量比(P/M)、pH、外加鹽濃度等因素對錳離子截留率(R)和膜通量(J)的影響。結果錶明:高聚物中羧基含量為9.5 mmol/g,對Mn(II)質量濃度為10 mg/L的模擬廢水,在pH=6.0時,Mn(II)與PMA-100的絡閤在5 min內基本可完成,絡閤率達99.6%。在一定P/M下,pH在2.5~7.0範圍內,截留率和膜通量均隨著pH的增加而增大;在一定pH下,截留率隨著P/M的增加而增加,但膜通量基本不變。外加鹽的存在使截留率下降,在同樣離子彊度下,CaCl2的影響遠大于NaCl的。
용마래산-병희산공취물(PMA-100)작락합제,채용PVB중공섬유막,연구락합-초려처리함맹폐수。측정료고취물적최기함량이급Mn(II)여PMA-100적락합반응속솔,연구취합물여중금속질량비(P/M)、pH、외가염농도등인소대맹리자절류솔(R)화막통량(J)적영향。결과표명:고취물중최기함량위9.5 mmol/g,대Mn(II)질량농도위10 mg/L적모의폐수,재pH=6.0시,Mn(II)여PMA-100적락합재5 min내기본가완성,락합솔체99.6%。재일정P/M하,pH재2.5~7.0범위내,절류솔화막통량균수착pH적증가이증대;재일정pH하,절류솔수착P/M적증가이증가,단막통량기본불변。외가염적존재사절류솔하강,재동양리자강도하,CaCl2적영향원대우NaCl적。
Copolymer of maleic acid and acrylic acid (PMA-100), combining with polyvinyl butyral (PVB) ultrafiltration membrane was used for the removal of Mn(II) from waste water by complexation-ultrafiltration. The carboxylic group content of PMA-100 and the rate of complexation reaction were measured. Effects of the mass ratio of PMA-100 to Mn(II) (n), pH, background electrolyte, etc on the rejection rate (R) and permeate flux (J) were investigated. The results show that carboxylic group content of PMA-100 is 9.5 mmol/g. The complexation of Mn(II) with PMA-100 is rapid and completed within 5 min at pH 6.0. Both R and J increase with pH increasing in the range of 2.5-7.0, and R increases with the increase of n at pH 6.0 while J is little affected. The background electrolyte leads to the decrease of R, and CaCl2 has much greater effect on R than NaCl at the same ionic strength.