scholarly journals Eosin Y-catalyzed photooxidation of triarylphosphines under visible light irradiation and aerobic conditions

RSC Advances ◽  
2017 ◽  
Vol 7 (22) ◽  
pp. 13240-13243 ◽  
Author(s):  
Yanbin Zhang ◽  
Cong Ye ◽  
Shijie Li ◽  
Aishun Ding ◽  
Guangxin Gu ◽  
...  

A novel method for Eosin Y-catalyzed photooxidation of triarylphosphines under visible light irradiation and aerobic conditions was reported.

2018 ◽  
Vol 42 (17) ◽  
pp. 14083-14086 ◽  
Author(s):  
Yuan Xue ◽  
Yonggang Lei ◽  
Xiangyu Liu ◽  
Yanan Li ◽  
Wanan Deng ◽  
...  

A single-atom Pt cocatalyst anchored onto g-C3N4 nanosheets could efficiently catalyze H2 evolution from an Eosin Y-sensitized system under 520 nm irradiation.


2013 ◽  
Vol 815 ◽  
pp. 567-573
Author(s):  
Xiao Pei Zhang ◽  
Yue Lin Wei ◽  
Shu Hong Chen ◽  
Jing Xu ◽  
Huang Zhao ◽  
...  

A novel and highly efficient photocatalyst, Eosin Y-sensitized Pt-intercalated nanotube Pt/HLa Nb2O7, was found to be very active for hydrogen generation within triethanolamine (TEOA) solution as the electron donor under visible-light irradiation (λ420 nm). The photocatalysts were characterized by X-ray diffraction (XRD), UV-vis diffuse reflectance spectra (DRS), scan electron microscope (SEM) and energy dispersive spectrometer (EDS). The results showed that the significant enhancement of photocatalytic activity was achieved via Pt intercalating and subsequent dye sensitization of Pt/HLaNb2O7. The highest rate for hydrogen evolution was 4.45 mmol·g-1·h-1under irradiation with a wavelength longer than 420 nm, and the probable mechanism of photosensitized hydrogen evolution have also been discussed.


RSC Advances ◽  
2015 ◽  
Vol 5 (3) ◽  
pp. 1852-1858 ◽  
Author(s):  
Mingcai Yin ◽  
Shuang Ma ◽  
Chaojun Wu ◽  
Yaoting Fan

With CoL2 as cocatalyst and eosin Y as sensitizer, the noble-metal-free heterogeneous CoL2/TiO2 system shows much efficient and more stable hydrogen evolution activity than that of the homogeneous system under visible light irradiation.


Nano Energy ◽  
2017 ◽  
Vol 36 ◽  
pp. 331-340 ◽  
Author(s):  
Liuqing Yang ◽  
Jianfeng Huang ◽  
Li Shi ◽  
Liyun Cao ◽  
Wei Zhou ◽  
...  

Catalysts ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 627 ◽  
Author(s):  
Arsou Arimi ◽  
Ralf Dillert ◽  
Gerald Dräger ◽  
Detlef W. Bahnemann

A commercial carbon-modified titanium dioxide, KRONOClean 7000, was applied as a UV(A) and visible-light active photocatalyst to investigate the conversion of the antipsychotic pharmaceutical chlorpromazine in aqueous phase employing two monochromatic light sources emitting at wavelengths of 365 and 455 nm. Photocatalytic and photolytic conversion of chlorpromazine under both anaerobic and aerobic conditions was analyzed using a HPLC-MS technique. Depending on the irradiation wavelength and presence of oxygen, varying conversion rates and intermediates revealing different reaction pathways were observed. Upon visible light irradiation under aerobic conditions, chlorpromazine was only converted in the presence of the photocatalyst. No photocatalytic conversion of this compound under anaerobic conditions upon visible light irradiation was observed. Upon UV(A) irradiation, chlorpromazine was successfully converted into its metabolites in both presence and absence of the photocatalyst. Most importantly, chlorpromazine sulfoxide, a very persistent metabolite of chlorpromazine, was produced throughout the photolytic and photocatalytic conversions of chlorpromazine under aerobic conditions. Chlorpromazine sulfoxide was found to be highly stable under visible light irradiation even in the presence of the photocatalyst. Heterogeneous photocatalysis under UV(A) irradiation resulted in a slow decrease of the sulfoxide concentration, however, the required irradiation time for its complete removal was found to be much longer compared to the removal of chlorpromazine at the same initial concentration.


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