Desorption by ultrasound: Phenol on activated carbon and polymeric resin

被引:124
作者
Rege, SU
Yang, RT [1 ]
Cain, CA
机构
[1] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
关键词
D O I
10.1002/aic.690440706
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
An experimental feasibility study of using ultrasound to accomplish the difficult desorption of phenol from activated carbon and polymeric resin adsorbents is discussed. The desorption rates of activated carbon were found to significantly increase by ultrasound at 40 kHz and 1.44 MHz. Attrition of the activated carbon due to cavitation could be prevented by operating at a higher frequency and with an intensity below the threshold of the pulverization of carbon. According to the structural stability study of Amberlite XAD-4 and Dowex Optipore L-493 resins to withstand the abrasive cavitational effects of ultrasound at 40 Wiz, the Dowex Optipore resin was stable under experimental conditions and phenol desorption rates were enhanced significantly with sonication. The ultrasonic desorption rates were favored by decreased temperature, aerated liquid medium, and increased ultrasound intensity. The desorption rates obtained without ultrasound appeared to be limited by pore diffusion whereas those obtained in the presence of ultrasound were limited by surface reaction. The rate enhancement was due to an increase in diffusive transport within the pores caused by acoustic vortex microstreaming. The activation energy for desorption decreased with an increase in ultrasonic power density, thus making the ultrasound weaken the adsorption bond.
引用
收藏
页码:1519 / 1528
页数:10
相关论文
共 37 条
[1]  
ARKHANGELSKII ME, 1973, PHYSICAL PRINCIPLES, V2, P294
[2]   SOLVENT REGENERATION OF ACTIVATED CARBON [J].
COONEY, DO ;
NAGERL, A ;
HINES, AL .
WATER RESEARCH, 1983, 17 (04) :403-410
[3]  
Crank John, 1979, MATH DIFFUSION, V3rd, P91
[4]  
ENSMINGER D, 1988, ULTRASONICS FUNDAMEN, P405
[5]   Effect of frequency on sonochemical reactions .2. Temperature and intensity effects [J].
Entezari, MH ;
Kruus, P .
ULTRASONICS SONOCHEMISTRY, 1996, 3 (01) :19-24
[6]   ADSORPTION OF PHENOL AND BENZOIC-ACID FROM DILUTE AQUEOUS-SOLUTION ONTO A MACRORETICULAR RESIN [J].
FARRIER, DS ;
HINES, AL ;
WANG, SW .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1979, 69 (02) :233-237
[7]   INTRAPARTICLE DIFFUSION OF PHENOLS WITHIN BIDISPERSED MACRORETICULAR RESIN PARTICLES [J].
FURUYA, E ;
TAKEUCHI, Y .
JOURNAL OF CHEMICAL ENGINEERING OF JAPAN, 1989, 22 (06) :670-676
[8]   ADSORPTION EQUILIBRIA OF PHENOL ON ANION-EXCHANGE RESINS IN AQUEOUS-SOLUTION [J].
GOTO, S ;
GOTO, M ;
UCHIYAMA, S .
JOURNAL OF CHEMICAL ENGINEERING OF JAPAN, 1984, 17 (02) :204-205
[9]   MECHANISM OF IRREVERSIBLE ADSORPTION OF PHENOLIC-COMPOUNDS BY ACTIVATED CARBONS [J].
GRANT, TM ;
KING, CJ .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1990, 29 (02) :264-271
[10]   Application of ultrasonic irradiation for the degradation of chemical contaminants in water [J].
Hoffmann, MR ;
Hua, I ;
Hochemer, R .
ULTRASONICS SONOCHEMISTRY, 1996, 3 (03) :S163-S172