Stone cutting industry waste-supported zinc oxide nanostructures for ultrasonic assisted decomposition of an anti-inflammatory non-steroidal pharmaceutical compound

被引:51
作者
Soltani, Reza Darvishi Cheshmeh [1 ]
Miraftabi, Zahra [1 ]
Mahmoudi, Mansoureh [1 ]
Jorfi, Sahand [2 ]
Boczkaj, Grzegorz [3 ]
Khataee, Alireza [4 ,5 ,6 ]
机构
[1] Arak Univ Med Sci, Sch Hlth, Dept Environm Hlth Engn, Arak, Iran
[2] Ahvaz Jundishapur Univ Med Sci, Sch Hlth, Dept Environm Hlth Engn, Ahvaz, Iran
[3] Gdansk Univ Technol, Fac Chem, Dept Proc Engn & Chem Technol, G Narutowicza St 11-12, PL-80233 Gdansk G, Poland
[4] Ton Duc Thang Univ, Nanomat Based Water Treatment Res Grp, Ho Chi Minh City, Vietnam
[5] Ton Duc Thang Univ, Fac Appl Sci, Ho Chi Minh City, Vietnam
[6] Univ Tabriz, Fac Chem, Dept Appl Chem, Res Lab Adv Water & Wastewater Treatment Proc, Tabriz 5166616471, Iran
关键词
Advanced oxidation processes; Sonocatalysis; Immobilization; Powdered waste stone; Nanocatalyst; Bio-refractory drug; HIGHLY EFFECTIVE DEGRADATION; ADVANCED OXIDATION PROCESSES; SONOCATALYTIC DEGRADATION; ACTIVATED CARBON; FACILE SYNTHESIS; WATER TREATMENT; ORGANIC-DYES; RHODAMINE-B; TEXTILE DYE; REMOVAL;
D O I
10.1016/j.ultsonch.2019.104669
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Powdered stone waste (PSW) obtained from a stone cutting industrial unit was applied as support for the immobilization of nano-sized ZnO to be utilized as an effective catalyst for the catalytic conversion of acetaminophen (ACE) under ultrasonication. The incorporation of ZnO nanostructures into PSW structure enhanced the specific surface area and pore volume of the as-prepared nanocompound. The change in the value of zero point of charge (pH(zpc)) of the PSW after being covered also demonstrated the good immobilization and distribution of ZnO nanostructures on the surface of PSW. The sonocatalysis of ACE over ZnO/PSW followed pseudo-first order kinetic (reaction rate of 2.27 x 10(-2) 1/min). The highest degradation efficiency of 98.1% was attained when the ZnO/PSW-contained sono-reactor was irradiated by UVC light. The presence of t-butanol led to the lowest degradation efficiency (57.7%), indicating that the sonocatalytic conversion of ACE was hydroxyl radical ((OH)-O-center dot)-dependent. Although the mineralization efficiency of ACE by the process was not excellent, biotoxicity assessment on the effluent revealed decreasing the inhibition percent from 50.8 to 16.7% within reaction time of 240 min.
引用
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页数:14
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