高校化学工程学报
高校化學工程學報
고교화학공정학보
JOURNAL OF CHEMICAL ENGINEERING OF CHINESE UNIVERSITIES
2010年
2期
274-279
,共6页
陈岩%赵宜江%周守勇%褚效中%邢卫红
陳巖%趙宜江%週守勇%褚效中%邢衛紅
진암%조의강%주수용%저효중%형위홍
凹凸棒粘土%丙烯酰胺%复合吸附材料%制备%表征
凹凸棒粘土%丙烯酰胺%複閤吸附材料%製備%錶徵
요철봉점토%병희선알%복합흡부재료%제비%표정
attapulgite%acrylamide%adsorbent composite%preparation%characterization
采用溶液聚合法在硅烷化凹凸棒粘土(OATP)表面接枝丙烯酰胺(AM),制备聚丙烯酰胺/凹凸棒粘土(PAM/ATP)复合吸附材料.通过考察PAM/ATP复合吸附材料对汞离子吸附性能的影响,对其制备条件进行了优化.采用热重/差示扫描量热(TG/DSC)和傅里叶变换红外光谱(FT-IR)对PAM/ATP进行了表征.结果表明,当AM质量分数(相对OATP质量,下同)为30%,聚合反应时间为6 h,引发剂质量分数为3.0%,反应温度为80℃时,制备的PMA/ATP对汞离子的最大吸附容量可达到135.5 mg·g~(-1).TG/DSC分析表明,PAM/ATP的DSC曲线在345℃出现一有机物分解吸热峰,且PAM/ATP的热失重率(18.0%) 明显高于ATP(5.0%) 和OATP(7.0%);FT-IR分析表明,PAM/ATP在1604 cm~(-1) (-NH_2或-NH的弯曲振动) 和3190 cm~(-1)(-NH_2或-NH伸缩振动)及1671 cm~(-1)(-C=O伸缩振动) 有新的吸收峰出现,表明PAM成功接枝于OATP表面.与ATP、OATP相比,PAM/ATP对Hg~(2+)离子的吸附容量增大了6倍以上.
採用溶液聚閤法在硅烷化凹凸棒粘土(OATP)錶麵接枝丙烯酰胺(AM),製備聚丙烯酰胺/凹凸棒粘土(PAM/ATP)複閤吸附材料.通過攷察PAM/ATP複閤吸附材料對汞離子吸附性能的影響,對其製備條件進行瞭優化.採用熱重/差示掃描量熱(TG/DSC)和傅裏葉變換紅外光譜(FT-IR)對PAM/ATP進行瞭錶徵.結果錶明,噹AM質量分數(相對OATP質量,下同)為30%,聚閤反應時間為6 h,引髮劑質量分數為3.0%,反應溫度為80℃時,製備的PMA/ATP對汞離子的最大吸附容量可達到135.5 mg·g~(-1).TG/DSC分析錶明,PAM/ATP的DSC麯線在345℃齣現一有機物分解吸熱峰,且PAM/ATP的熱失重率(18.0%) 明顯高于ATP(5.0%) 和OATP(7.0%);FT-IR分析錶明,PAM/ATP在1604 cm~(-1) (-NH_2或-NH的彎麯振動) 和3190 cm~(-1)(-NH_2或-NH伸縮振動)及1671 cm~(-1)(-C=O伸縮振動) 有新的吸收峰齣現,錶明PAM成功接枝于OATP錶麵.與ATP、OATP相比,PAM/ATP對Hg~(2+)離子的吸附容量增大瞭6倍以上.
채용용액취합법재규완화요철봉점토(OATP)표면접지병희선알(AM),제비취병희선알/요철봉점토(PAM/ATP)복합흡부재료.통과고찰PAM/ATP복합흡부재료대홍리자흡부성능적영향,대기제비조건진행료우화.채용열중/차시소묘량열(TG/DSC)화부리협변환홍외광보(FT-IR)대PAM/ATP진행료표정.결과표명,당AM질량분수(상대OATP질량,하동)위30%,취합반응시간위6 h,인발제질량분수위3.0%,반응온도위80℃시,제비적PMA/ATP대홍리자적최대흡부용량가체도135.5 mg·g~(-1).TG/DSC분석표명,PAM/ATP적DSC곡선재345℃출현일유궤물분해흡열봉,차PAM/ATP적열실중솔(18.0%) 명현고우ATP(5.0%) 화OATP(7.0%);FT-IR분석표명,PAM/ATP재1604 cm~(-1) (-NH_2혹-NH적만곡진동) 화3190 cm~(-1)(-NH_2혹-NH신축진동)급1671 cm~(-1)(-C=O신축진동) 유신적흡수봉출현,표명PAM성공접지우OATP표면.여ATP、OATP상비,PAM/ATP대Hg~(2+)리자적흡부용량증대료6배이상.
Using solution polymerization, polyacrylamide/attapulgite (PAM/ATP) adsorbent was synthesized by grafting acrylamide (AM) onto the silane coupling reagent modified ATP (OATP). The preparing conditions of the PAM/ATP were investigated, and the analyses by TG/DSC and FT-IR were conducted to characterize the synthesized PAM/ATP. The results show that the prepared PAM/ATP gives a maximum Hg~(2+) adsorption capacity of 135.5 mg·g~(-1) under following conditions: AM mass concentration of 30.0% (relative to OATP mass, the same hereinafter), reaction time of 6 h, initiator dosage of 3.0% (weight) and reaction temperature of 80℃. TG/DSC analyses reveal that the DSC curve of the PAM/ATP exhibits an endothermic peak of organic decomposition at 345℃, and in the temperature range of 280℃ to 600℃, the weight loss of the PAM/ATP (18.0%) is much more than those of the ATP (5.0%) and the OATP (7.0%). The FT-IR spectra show that the new absorption bands at 1604 cm~(-1) (-NH_2 or -NH bending vibration), 3190 cm~(-1) (-NH_2 or -NH stretching vibration) and 1671 cm~(-1) (-C=O stretching vibration) appear on the spectrum of PAM/ATP; It indicates that the PAM is successfully grafted onto the surface of OATP. It was found that the Hg~(2+) adsorption capacity of the PAM/ATP prepared under the above conditions is more than 6 folds compared with those of the ATP and OATP.