Bulk production of porous TiO2 nanowires by unique solvo-plasma oxidation approach for combating biotic and abiotic water contaminants

Author(s):  
Gul Afreen ◽  
Jose Antonio Lara-Ramos ◽  
Niraj Ashutosh Vidwans ◽  
Veerendra Atla ◽  
Vivekanand Kumar ◽  
...  
2013 ◽  
Vol 181 ◽  
pp. 146-153 ◽  
Author(s):  
Zhen Jin ◽  
Fan-Li Meng ◽  
Yong Jia ◽  
Tao Luo ◽  
Jin-Yun Liu ◽  
...  

2014 ◽  
Vol 145 ◽  
pp. 231-236 ◽  
Author(s):  
Byungho Lee ◽  
Jae Ik Kim ◽  
Sangheon Lee ◽  
Taehyun Hwang ◽  
Seunghoon Nam ◽  
...  

2017 ◽  
Vol 10 (4) ◽  
pp. 395-401 ◽  
Author(s):  
Yonglun Tang ◽  
Haibo Ren ◽  
Jiarui Huang

2017 ◽  
Vol 17 (6) ◽  
pp. 1740-1747
Author(s):  
Abolfazl Zakersalehi ◽  
Hyeok Choi

Abstract Non-selectivity of TiO2-based photocatalysis is a known drawback of this technology for full scale water treatment applications. It results in significant decline in decomposition of toxic target contaminants when other non-toxic organic compounds such as natural organic matter (NOM) compete in the reaction. Previously, size exclusion of large NOM onto the mesoporous structure of TiO2 photocatalyst was proven to improve the selective decomposition of small size target chemicals. In this study, manipulation of reaction pH as a crucial parameter in governing the adsorption and decomposition of organic chemicals was combined with the size exclusion of NOM. The effects of size-based adsorption/exclusion and pH-dependent electrostatic attraction/repulsion were investigated by using humic acid as model NOM and ibuprofen and methylene blue as model target contaminants. Adsorption and decomposition of the targets were dependent on their hydrodynamic size and ionization state. Mesoporous TiO2 suppressed physical access of large NOM onto its surface while reaction pH influenced the surface charge of TiO2 and the speciation of the chemicals and thus controlled their adsorption and decomposition. The results imply that selecting a proper pH can significantly improve selective decomposition of a target onto porous TiO2 in the presence of NOM.


2016 ◽  
Vol 387 ◽  
pp. 469-476 ◽  
Author(s):  
Yun-Chang Yao ◽  
Xin-Rong Dai ◽  
Xiao-Ye Hu ◽  
Su-Zhen Huang ◽  
Zhen Jin

1983 ◽  
Vol 17 (9) ◽  
pp. 394-394 ◽  
Author(s):  
JGMM Smeenk

TAPPI Journal ◽  
2012 ◽  
Vol 11 (8) ◽  
pp. 51-58
Author(s):  
ANTTI HAAPALA ◽  
MIKA KÖRKKÖ ◽  
ELISA KOIVURANTA ◽  
JOUKO NIINIMÄKI

Analysis methods developed specifically to determine the presence of ink and other optically active components in paper machine white waters or other process effluents are not available. It is generally more interest¬ing to quantify the effect of circulation water contaminants on end products. This study compares optical techniques to quantify the dirt in process water by two methods for test media preparation and measurement: direct process water filtration on a membrane foil and low-grammage sheet formation. The results show that ink content values obtained from various analyses cannot be directly compared because of fundamental issues involving test media preparation and the varied methodologies used to formulate the results, which may be based on different sets of assumptions. The use of brightness, luminosity, and reflectance and the role of scattering measurements as a part of ink content analysis are discussed, along with fine materials retention and measurement media selection. The study concludes with practical tips for case-dependent measurement methodology selection.


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