Photocatalytic Decomposition of Gas-Phase Chlorobenzene with Transition Metal–Doped KLaTi2O6 Under Visible Light Irradiation

2014 ◽  
Vol 31 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Dandan Pang ◽  
Minhua Dong ◽  
Xiaodong Ma ◽  
Feng Ouyang
Keyword(s):  
Transition Metal ◽  
Visible Light ◽  
Gas Phase ◽  
Visible Light Irradiation ◽  
Light Irradiation ◽  
Photocatalytic Decomposition ◽  
Metal Doped

An investigation of transition metal doped TiO2 photocatalysts for the enhanced photocatalytic decoloration of methylene blue dye under visible light irradiation

2021 ◽  
Vol 9 (4) ◽  
pp. 105254
Author(s):  
Periyakaruppan Karuppasamy ◽  
Nagoorkani Ramzan Nilofar Nisha ◽  
Arivalagan Pugazhendhi ◽  
Sabariswaran Kandasamy ◽  
Sakthivel Pitchaimuthu
Keyword(s):  
Methylene Blue ◽  
Transition Metal ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Light Irradiation ◽  
Blue Dye ◽  
Methylene Blue Dye ◽  
Tio2 Photocatalysts ◽  
Doped Tio2 ◽  
Metal Doped

scholarly journals Fabrication of AgCl/Ag3PO4/graphitic carbon nitride heterojunctions for enhanced visible light photocatalytic decomposition of methylene blue, methylparaben and E. coli

RSC Advances ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 6383-6394 ◽  
Author(s):  
Haishuai Li ◽  
Linlin Cai ◽  
Xin Wang ◽  
Huixian Shi
Keyword(s):  
Methylene Blue ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Irradiation ◽  
Carbon Nitride ◽  
Light Irradiation ◽  
Graphitic Carbon Nitride ◽  
Photocatalytic Decomposition ◽  
E Coli ◽  
Visible Light Photocatalytic

A noval ternary nanocomposite AgCl/Ag3PO4/g-C3N4 was successfully synthesized for photocatalytic degradation of methylene blue, methylparaben and inactivation of E. coli under visible light irradiation, showing excellent photocatalytic degradation performance and stability.

scholarly journals TiO2 Photocatalyzed C–H Bond Transformation for C–C Coupling Reactions

Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 355 ◽  
Author(s):  
Yi Wang ◽  
Anan Liu ◽  
Dongge Ma ◽  
Shuhong Li ◽  
Chichong Lu ◽  
...  
Keyword(s):  
Transition Metal ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Transition Metal Catalysis ◽  
Light Irradiation ◽  
Coupling Reactions ◽  
Metal Catalysis ◽  
Bond Functionalization ◽  
Tio2 Photocatalysis ◽  
Mild Conditions

Fulfilling the direct inert C–H bond functionalization of raw materials that are earth-abundant and commercially available for the synthesis of diverse targeted organic compounds is very desirable and its implementation would mean a great reduction of the synthetic steps required for substrate prefunctionalization such as halogenation, borylation, and metalation. Successful C–H bond functionalization mainly resorts to homogeneous transition-metal catalysis, albeit sometimes suffering from poor catalyst reusability, nontrivial separation, and severe biotoxicity. TiO2 photocatalysis displays multifaceted advantages, such as strong oxidizing ability, high chemical stability and photostability, excellent reusability, and low biotoxicity. The chemical reactions started and delivered by TiO2 photocatalysts are well known to be widely used in photocatalytic water-splitting, organic pollutant degradation, and dye-sensitized solar cells. Recently, TiO2 photocatalysis has been demonstrated to possess the unanticipated ability to trigger the transformation of inert C–H bonds for C–C, C–N, C–O, and C–X bond formation under ultraviolet light, sunlight, and even visible-light irradiation at room temperature. A few important organic products, traditionally synthesized in harsh reaction conditions and with specially functionalized group substrates, are continuously reported to be realized by TiO2 photocatalysis with simple starting materials under very mild conditions. This prominent advantage—the capability of utilizing cheap and readily available compounds for highly selective synthesis without prefunctionalized reactants such as organic halides, boronates, silanes, etc.—is attributed to the overwhelmingly powerful photo-induced hole reactivity of TiO2 photocatalysis, which does not require an elevated reaction temperature as in conventional transition-metal catalysis. Such a reaction mechanism, under typically mild conditions, is apparently different from traditional transition-metal catalysis and beyond our insights into the driving forces that transform the C–H bond for C–C bond coupling reactions. This review gives a summary of the recent progress of TiO2 photocatalytic C–H bond activation for C–C coupling reactions and discusses some model examples, especially under visible-light irradiation.

Photocatalytic Decomposition of Methylene Blue with Lanthanum Doping TiO2 under Visible Light Irradiation

2013 ◽  
Vol 734-737 ◽  
pp. 2163-2167
Author(s):  
Guang Xiu Cao ◽  
Zhong Hou Zhang ◽  
Bin Zhai
Keyword(s):  
Methylene Blue ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
Light Irradiation ◽  
Photocatalytic Decomposition ◽  
Lanthanum Doping ◽  
X Ray ◽  
Degradation Rates ◽  
Vis Spectroscopy

Lanthanum doped TiO2 powders were prepared by hydrolysis of titanium tetra-n-butyl oxide and La (NO3)3 in solution. The resulting powders were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-Vis absorption spectroscopy. The photocatalytic activities of doped samples were evaluated by the decomposition of methylene blue under visible light irradiation. The XRD results showed that the doping of lanthanum could not only efficiently inhibit the grain growth but also suppress the phase transition of anatase to rutile. UV-Vis spectroscopy of lanthanum doping TiO2 indicated that the absorption onset red-shifted to the visible light region. XPS results revealed that La2O3 had formed which could enhance the surface area. The degradation rates of methylene blue verified that the visible light photocatalytic activity of TiO2 has been enhanced by the doping of lanthanum.

Photocatalyst- and transition-metal-free α-allylation of N-aryl tetrahydroisoquinolines mediated by visible light

2020 ◽  
Vol 22 (3) ◽  
pp. 646-650 ◽  
Author(s):  
Zhuohua Li ◽  
Pengju Ma ◽  
Yongzhu Tan ◽  
Yufei Liu ◽  
Min Gao ◽  
...  
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Light Irradiation ◽  
Metal Free

A convenient and efficient α-allylation of N-aryl tetrahydroisoquinolines has been achieved. This transformation can be realized under only visible light irradiation without the aid of transition metals or photocatalysts.

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