scholarly journals Enhanced Transformation of Atrazine by High Efficient Visible Light-Driven N, S-Codoped TiO2Nanowires Photocatalysts

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Yanlin Zhang ◽  
Honghai Wu ◽  
Peihong Liu

Advanced oxidation process using titanium dioxide as a photocatalyst under solar irradiation is one of the most attractive technologies to eliminate atrazine, an endocrine disrupting and carcinogen contaminant. The N, S-codoped TiO2nanowires at the calcination of 600°C obtained by a facile hydrothermal method revealed the best photocatalytic performance for the degradation of atrazine under visible light irradiation compared to N, S-codoped TiO2nanoparticles and S-doped TiO2nanowires. TOC removal experiment also exhibited the similar result and achieved 63% of atrazine mineralization within 6 h. The degradation of atrazine was driven mainly by•OH and holes during the photocatalytic process. Reactive species quantities such•OH andO2•-generated by N, S-codoped TiO2nanowires under visible light irradiation were much more than those of S-doped TiO2nanowires and N, S-codoped TiO2nanoparticles. These results were mainly attributed to the synergistic effect of N and S doping in narrowing the band gap, remarkable increase in electron-hole separation, extending the anatase-to-rutile transformation temperature above 600°C, and preferentially exposing high reactive{001}crystal facets of anatase.

2015 ◽  
Vol 3 (36) ◽  
pp. 18622-18635 ◽  
Author(s):  
Susanginee Nayak ◽  
Lagnamayee Mohapatra ◽  
Kulamani Parida

Dispersion of exfoliated CN over the surface of exfoliated LDH composite materials, and its photocatalytic water splitting under visible-light irradiation.


RSC Advances ◽  
2014 ◽  
Vol 4 (88) ◽  
pp. 47615-47624 ◽  
Author(s):  
Ping Li ◽  
Chunbo Liu ◽  
Guoling Wu ◽  
Yang Heng ◽  
Shuang Lin ◽  
...  

In this paper, Fe-doped SrTiO3 (FSTO) photocatalysts were successfully prepared via a facile solvothermal method, and their photocatalytic activities for degrading tetracycline (TC) under visible light irradiation were examined.


2015 ◽  
Vol 2015 ◽  
pp. 1-12 ◽  
Author(s):  
Xiangchao Meng ◽  
Zisheng Zhang

In photocatalysis, the recombination of electron-hole pairs is generally regarded as one of its most serious drawbacks. The synthesis of various composites with heterojunction structures has increasingly shed light on preventing this recombination. In this work, a BiOBr-Bi2WO6photocatalytic heterojunction semiconductor was synthesized by the facile hydrothermal method and applied in the photocatalytic degradation process. It was determined that both reaction time and temperature significantly affected the crystal structure and morphologies of the photocatalysts. BiOBr (50 at%)-Bi2WO6composites were prepared under optimum synthesis conditions (120°C for 6 h) and by theoretically analyzing the DRS results, it was determined that they possessed the suitable band gap (2.61 eV) to be stimulated by visible-light irradiation. The photocatalytic activities of the as-prepared photocatalysts were evaluated by the degradation ofRhodamine B (RhB)under visible-light irradiation. The experimental conditions, including initial concentration, pH, and catalyst dosage, were explored and the photocatalysts in this system were proven stable enough to be reused for several runs. Moreover, the interpreted mechanism of the heterojunction enhancement effect proved that the synthesis of a heterojunction structure provided an effective method to decrease the recombination rate of the electron-hole pairs, thereby improving the photocatalytic activity.


Author(s):  
Zhao Zhang ◽  
Haohua Chen ◽  
Niklas Keller ◽  
Qin Xiong ◽  
Lei Liu ◽  
...  

A visible-light-driven oxidative 6π heterocycilization for the synthesis of structurally diverse π-conjugated polycyclic 1-aminoisoquinolines has been developed. The reaction proceeds under visible-light or sunshine, obviates photocatalyst and transition-metals, and features...


2015 ◽  
Vol 42 (3) ◽  
pp. 1651-1662 ◽  
Author(s):  
Phattranit Dumrongrojthanath ◽  
Anukorn Phuruangrat ◽  
Patcharanan Junploy ◽  
Somchai Thongtem ◽  
Titipun Thongtem

2013 ◽  
Vol 17 (01n02) ◽  
pp. 135-141 ◽  
Author(s):  
Keishiro Tahara ◽  
Kumiko Mikuriya ◽  
Takahiro Masuko ◽  
Jun-ichi Kikuchi ◽  
Yoshio Hisaeda

The visible-light-driven dechlorination of 1,1-bis(4-chlorophenyl)-2,2,2-trichloroethane (DDT) was carried out in the presence of a hydrophobic vitamin B12 , heptamethyl cobyrinate perchlorate and Rhodamine B . DDT was successfully dechlorinated to form 1,1-bis(4-chlorophenyl)-2,2-dichloroethane (DDD) as the mono-dechlorinated product upon visible light irradiation with a tungsten lamp (λ > 440 nm). Upon prolonged visible light irradiation to DDT, DDMU (1-chloro-2,2-bis(4-chlorophenyl)ethylene), DDMS (1-chloro-2,2-bis(4-chlorophenyl)ethane) and DCS (trans-4,4′-dichlorostilbene) were obtained as the di- and tri-dechlorinated products. The use of the photostable organic sensitizer enabled prolonged photocatalysis via a noble-metal-free process. The vitamin B12 derivative was replaced by an imine/oxime-type cobalt complex although the cobalt complex system showed a lower catalytic activity than the B12 derivative system. The dechlorination mechanism in the B12 -Rhodamin B system was investigated by various methods such as UV-vis absorption and fluorescence quenching.


2018 ◽  
Vol 9 (35) ◽  
pp. 4468-4475 ◽  
Author(s):  
Chang Cheng ◽  
Xunchang Wang ◽  
Yaoyao Lin ◽  
Luying He ◽  
Jia-Xing Jiang ◽  
...  

The linear non-fluorinated polymer L-PyBT exhibited an impressive hydrogen evolution rate up to 83.7 μmol h−1 under visible light irradiation.


2019 ◽  
Vol 9 (5) ◽  
pp. 1178-1188 ◽  
Author(s):  
Taiping Xie ◽  
Yaoyu Zhang ◽  
Weiyuan Yao ◽  
Yue Liu ◽  
Haiqiang Wang ◽  
...  

The strong protonated hydroxyl groups around Bi vacancies could efficiently promote the separation of photoexcited electron–hole pairs.


Sign in / Sign up

Export Citation Format

Share Document