CAJ | 학술논문

以丁胺和正十二醇为混合模板剂,采用共沉淀法制备了介孔纳米CuAl2O4.用X射线粉末衍射(XRD)、傅里叶变换红外(FTIR)光谱、N2吸附-脱附对产物的结构进行了表征.采用连续在线原位衰减全反射傅里叶变换红外(ATR-FTIR)光谱技术研究了水溶液中丁基和辛基黄药在介孔CuAl2O4表面的吸附.随着吸附时间的延长,1200和1040 cm-1两处黄药特征峰的高度逐渐增加,根据1200 cm-1处C-O-C伸缩振动峰的变化来评价黄药在CuAl2O4表面的吸附动力学过程.结果表明,介孔纳米CuAl2O4对黄药有很强的吸附能力,在100 min的时间内, CuAl2O4样品对丁基和辛基黄药的吸附量分别达到了236和300 mg·g-1,且属于化学吸附.对实验数据进行理论模拟,发现吸附过程更接近于拟二级吸附动力学方程.
이정알화정십이순위혼합모판제,채용공침정법제비료개공납미CuAl2O4.용X사선분말연사(XRD)、부리협변환홍외(FTIR)광보、N2흡부-탈부대산물적결구진행료표정.채용련속재선원위쇠감전반사부리협변환홍외(ATR-FTIR)광보기술연구료수용액중정기화신기황약재개공CuAl2O4표면적흡부.수착흡부시간적연장,1200화1040 cm-1량처황약특정봉적고도축점증가,근거1200 cm-1처C-O-C신축진동봉적변화래평개황약재CuAl2O4표면적흡부동역학과정.결과표명,개공납미CuAl2O4대황약유흔강적흡부능력,재100 min적시간내, CuAl2O4양품대정기화신기황약적흡부량분별체도료236화300 mg·g-1,차속우화학흡부.대실험수거진행이론모의,발현흡부과정경접근우의이급흡부동역학방정.
In this study, mesoporous nano CuAl2O4 was synthesized through a coprecipitation method using simple mixed templates consisting of butylamine and dodecanol. The sample was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and nitrogen adsorption-desorption techniques. The absorption of butyl and octyl xanthate from aqueous solution onto the synthesized mesoporous CuAl2O4 solid surfaces was studied by a continuous, online, in situ attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) technique. The CuAl2O4 membrane used in the adsorption experiments was prepared on a germanium internal reflection element using the chemical bath deposition method. During the adsorption process, the characteristic peak height of xanthate at 1200 and 1040 cm-1 emerged and gradual y increased. By monitoring changes in the peak height at 1200 cm-1, which was assigned to the stretching vibration caused by C-O-C of the adsorbed xanthate molecules, the adsorption kinetics were studied. The adsorption results show that mesoporous CuAl2O4 has a high chemisorption capacity for xanthate, which reaches 236 and 300 mg·g-1 for butyl and octyl xanthate, respectively, within 100 min. The adsorption kinetics can be described by a pseudo-second-order reaction model.