scholarly journals Efficient Reduction of CO2 to Formate Using in Situ Prepared Nano-Sized Bi Electrocatalyst

Author(s):  
Jingjing Bei ◽  
ChemSusChem ◽  
2017 ◽  
Vol 10 (15) ◽  
pp. 3044-3048 ◽  
Author(s):  
Qingyuan Bi ◽  
Xin Wang ◽  
Feng Gu ◽  
Xianlong Du ◽  
Hongliang Bao ◽  
...  

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1486
Author(s):  
Ganesh Shimoga ◽  
Eun-Jae Shin ◽  
Sang-Youn Kim

Two xerogels made of 4-pyridyl cholesterol (PC) and silver-nanocomposites (SNCs) thereof have been studied for their efficient reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) in the presence of aqueous sodium borohydride. Since in-situ silver doping will be effective in ethanol and acetone solvents with a PC gelator, two silver-loaded PC xerogels were prepared and successive SNCs were achieved by using an environmentally benign trisodium citrate dehydrate reducing agent. The formed PC xerogels and their SNCs were comprehensively investigated using different physico-chemical techniques, such as field emission scanning electron microscopy (FE-SEM), Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), powdered X-ray diffraction (XRD) and UV-Visible spectroscopy (UV-Vis). The FE-SEM results confirm that the shape of xerogel-covered silver nanoparticles (SNPs) are roughly spherical, with an average size in the range of 30–80 nm. Thermal degradation studies were analyzed via the sensitive graphical Broido’s method using a TGA technique. Both SNC-PC (SNC-PC-X1 and SNC-PC-X2) xerogels showed remarkable catalytic performances, with recyclable conversion efficiency of around 82% after the fourth consecutive run. The apparent rate constant (kapp) of SNC-PC-X1 and SNC-PC-X2 were found to be 6.120 × 10-3 sec-1 and 3.758 × 10-3 sec-1, respectively, at an ambient temperature.


Author(s):  
Peter G. Loutzenhiser ◽  
M. Elena Ga´lvez ◽  
Illias Hischier ◽  
Anastasia Stamatiou ◽  
Aldo Steinfeld

Using concentrated solar energy as the source of high-temperature process heat, a two-step CO2 splitting thermochemical cycle based on Zn/ZnO redox reactions is applied to produce renewable carbon-neutral fuels. The solar thermochemical cycle consists of: 1) the solar endothermic dissociation of ZnO to Zn and O2; 2) the non-solar exothermic reduction of CO2 with Zn to CO and ZnO; the latter is the recycled to the 1st solar step. The net reaction is CO2 = CO + 1/2 O2, with products formed in different steps, thereby eliminating the need for their separation. A Second-Law thermodynamic analysis indicates a maximum solar-to-chemical energy conversion efficiency of 39% for a solar concentration ratio of 5000 suns. The technical feasibility of the first step of the cycle has been demonstrated in a high-flux solar furnace with a 10 kW solar reactor prototype. The second step of the cycle is experimentally investigated in a hot-wall quartz aerosol flow reactor, designed for in-situ quenching of Zn(g), formation of Zn nanoparticles, and oxidation with CO2. The effect of varying the molar flow ratios of the reactants was investigated. Chemical conversions were determined by gas chromatography and X-ray diffraction. Chemical conversions of Zn to ZnO of up to 88% were obtained for a residence time of ∼ 3.05 s. For all of the experiments, the reactions primarily occurred outside the aerosol jet flow on the surfaces of the reaction zone.


Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 581 ◽  
Author(s):  
Sonam Goyal ◽  
Maizatul Shaharun ◽  
Chong Kait ◽  
Bawadi Abdullah ◽  
Mariam Ameen

The efficient reduction of CO2 into valuable products such as methanol, over metal-organic frameworks (MOFs) based catalyst, has received much attention. The photocatalytic reduction is considered the most economical method due to the utilization of solar energy. In this study, Copper (II)/Zeolitic Imidazolate Framework-8 (Cu/ZIF-8) catalysts were synthesized via a hydrothermal method for photocatalytic reduction of CO2 to methanol. The synthesized catalysts were characterized by X-ray Photoelectron Spectroscopy (XPS), Field Emission Scanning Electron Microscopy (FESEM) coupled with Energy Dispersive X-ray (EDX), Ultraviolet-visible (UV-vis) spectroscopy, and X-Ray Diffraction (XRD). The host ZIF-8, treated with 2 mmol copper prepared in 2M ammonium hydroxide solution showed the highest photocatalytic activity. The crystal structures of ZIF-8 and 2Cu/ZIF-8N2 catalysts were observed as cubic and orthorhombic, respectively and the XPS analysis confirmed the deposition of Cu (II) ions over ZIF-8 surface among all the prepared catalysts. The orthorhombic structure, nano-sized crystals, morphology and Cu loading of the 2Cu/ZIF-8N2 catalyst were the core factors to influence the photocatalytic activity. The yield of Methanol was found to be 35.82 µmol/L·g after 6 h of irradiations on 2Cu/ZIF-8N2 catalyst in the wavelength range between 530–580 nm. The copper-based ZIF-8 catalyst has proven as an alternative approach for the economical photocatalytic reduction of CO2 to CH3OH.


ChemCatChem ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 1295-1302 ◽  
Author(s):  
Qingyuan Bi ◽  
Xieyi Huang ◽  
Guoheng Yin ◽  
Tianyuan Chen ◽  
Xianlong Du ◽  
...  

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