scholarly journals Photodegradation of rhodamine B and methyl orange by Ag3PO4 catalyst under visible light irradiation

2014 ◽  
Vol 35 (8) ◽  
pp. 1410-1417 ◽  
Author(s):  
Ming Ge
Keyword(s):  
Methyl Orange ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Rhodamine B ◽  
Light Irradiation

scholarly journals A hierarchical Ca/TiO2/NH2-MIL-125 nanocomposite photocatalyst for solar visible light induced photodegradation of organic dye pollutants in water

RSC Advances ◽  
2020 ◽  
Vol 10 (50) ◽  
pp. 29808-29820 ◽  
Author(s):  
Najmeh Ahmadpour ◽  
Mohammad Hossein Sayadi ◽  
Shahin Homaeigohar
Keyword(s):  
Methyl Orange ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Rhodamine B ◽  
Organic Dye ◽  
Light Irradiation ◽  
Dye Pollutants ◽  
First Time

In this study, for the first time, the Ca/TiO2/NH2-MIL-125 nanocomposite photocatalyst was synthesized for the purpose of photodegradation of Methyl Orange (MO) and Rhodamine B (RhB) dyes under visible light irradiation.

scholarly journals A series of five-coordinated copper coordination polymers for efficient degradation of organic dyes under visible light irradiation

RSC Advances ◽  
2017 ◽  
Vol 7 (38) ◽  
pp. 23432-23443 ◽  
Author(s):  
Lu-Lu Shi ◽  
Tian-Rui Zheng ◽  
Min Li ◽  
Lin-Lu Qian ◽  
Bao-Long Li ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Methyl Orange ◽  
Visible Light ◽  
Coordination Polymers ◽  
Visible Light Irradiation ◽  
Rhodamine B ◽  
Organic Dyes ◽  
Light Irradiation ◽  
Highly Efficient ◽  
Copper Coordination

Five-coordinated copper(ii) coordination polymers 1–5 are highly efficient and universal photocatalysts for the degradation of the organic dyes methylene blue (MB), rhodamine B (RhB) and methyl orange (MO) under visible light irradiation.

SiO2@Ag/AgCl: a low-cost and highly efficient plasmonic photocatalyst for degrading rhodamine B under visible light irradiation

RSC Advances ◽  
2014 ◽  
Vol 4 (110) ◽  
pp. 64747-64755 ◽  
Author(s):  
Xuefeng Xu ◽  
Man Wang ◽  
Yanyan Pei ◽  
Changchun Ai ◽  
Liangjie Yuan
Keyword(s):  
Aqueous Solution ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Rhodamine B ◽  
Photocatalytic Performance ◽  
Low Cost ◽  
Light Irradiation ◽  
Nano Structure ◽  
Plasmonic Photocatalyst ◽  
Highly Efficient

The micro/nano-structure composite SiO2@Ag/AgCl was employed as a low cost photocatalyst for the degradation of RhB in aqueous solution under visible light irradiation, which exhibited excellent photocatalytic performance and stability.

Dechlorination of DDT catalyzed by visible-light-driven system composed of vitamin B12 derivative and Rhodamine B

2013 ◽  
Vol 17 (01n02) ◽  
pp. 135-141 ◽  
Author(s):  
Keishiro Tahara ◽  
Kumiko Mikuriya ◽  
Takahiro Masuko ◽  
Jun-ichi Kikuchi ◽  
Yoshio Hisaeda
Keyword(s):  
Visible Light ◽  
Visible Light Irradiation ◽  
Rhodamine B ◽  
Cobalt Complex ◽  
Light Irradiation ◽  
Vitamin B ◽  
Free Process ◽  
Driven System ◽  
Derivative System ◽  
Visible Light Driven

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.

scholarly journals Photocatalytic Degradation of Methylene Blue and Methyl Orange by Y-PTC Metal-Organic Framework

2021 ◽  
Vol 7 (2) ◽  
pp. 129-141
Author(s):  
Adawiah Adawiah ◽  
Muhammad Derry Luthfi Yudhi ◽  
Agustino Zulys
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Metal Organic Framework ◽  
Light Irradiation ◽  
Bandgap Energy ◽  
Metal Organic ◽  
Organic Framework

The yttrium based metal-organic framework (MOF) Y-PTC was synthesized by the solvothermal method using perylene as the linker and yttrium as metal ion. This study aims to assess the photocatalytic activity of yttrium-perylenetetracarboxylate (Y-PTC) metal-organic framework (MOF) toward methylene blue and methyl orange under visible light irradiation. The results of the FTIR analysis showed that Y-PTC MOF had a different structure and composition from its precursor (Na4PTC). The Y-PTC MOF has a bandgap energy value of 2.20 eV with a surface area of 47.7487 m2/g. The SEM-EDS analysis showed an elemental composition of yttrium, carbon, and oxygen, were 6.9%, 72.1% and 20.7%, respectively. Furthermore, Y-PTC MOF was able to adsorb dyes at the optimum by 78.10% and 35.57% toward methylene blue (MB) and methyl orange (MO) at the dispersion period of 60 mins. Y-PTC MOF exhibited photocatalytic activity towards the degradation of methylene blue and methyl orange under visible light irradiation. The addition of H2O2 inhibited Y-PTC photocatalytic activity towards MO degradation from 50.89% to 26.38%. In contrast to MO, the addition of H2O2 had a positive effect on MB, which increased the degradation from 87.56% to 91.65%. Therefore, Y-PTC MOF possessed the potential of a photocatalyst material in dyes degradation under visible light irradiation.

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