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      Selective Hydrogenolysis of Glycerol to 1,2-Propanediol Over Bimetallic Cu-Ni Catalysts Supported on γ-Al2O3

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          Abstract

          <p>A series of Cu or Ni monometallic and Cu-Ni bimetallic catalysts supported on γ-Al<sub>2</sub>O<sub>3</sub> were synthesized by incipient wetness impregnation method. X-ray diffraction results exhibited the formation of bimetallic Cu-Ni phase in the reduced Cu-Ni(1:1)/γ-Al<sub>2</sub>O<sub>3</sub> catalyst. Among the catalyst examined for hydrogenolysis of glycerol, bimetallic catalysts exhibited higher catalytic activity than monometallic catalysts due to synergetic effect of Cu-Ni bimetal. Cu-Ni(1:1)/γ-Al<sub>2</sub>O<sub>3</sub> catalyst displayed a maximum glycerol conversion of 71.6% with 92.8% selectivity to 1,2-propanediol at 210 °C and 4.5 MPa hydrogen pressure. The superior performance of Cu-Ni(1:1)/γ-Al<sub>2</sub>O<sub>3</sub> catalyst was attributed to the formation of bimetallic Cu-Ni phase, high active metal surface area, small Cu-Ni particle size, and high acidic strength of the catalyst. Stability and reusability of Cu-Ni(1:1)/γ-Al<sub>2</sub>O<sub>3</sub> catalyst was performed and detailed characterization results of fresh and used catalysts suggested that bimetallic Cu-Ni phase remained stable after reuses.</p>

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          Efficient and limiting reactions in aqueous light-induced hydrogen evolution systems using molecular catalysts and quantum dots.

          Hydrogen produced from water and solar energy holds much promise for decreasing the fossil fuel dependence. It has recently been proven that the use of quantum dots as light harvesters in combination with catalysts is a valuable strategy to obtain photogenerated hydrogen. However, the light to hydrogen conversion efficiency of these systems is reported to be lower than 40%. The low conversion efficiency is mainly due to losses occurring at the different interfacial charge-transfer reactions taking place in the multicomponent system during illumination. In this work we have analyzed all the involved reactions in the hydrogen evolution catalysis of a model system composed of CdTe quantum dots, a molecular cobalt catalyst and vitamin C as sacrificial electron donor. The results demonstrate that the electron transfer from the quantum dots to the catalyst occurs fast enough and efficiently (nanosecond time scale), while the back electron transfer and catalysis are much slower (millisecond and microsecond time scales). Further improvements of the photodriven proton reduction should focus on the catalytic rate enhancement, which should be at least in the hundreds of nanoseconds time scale.
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            The Last Globally Stable Extended Alkane

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              An Iron Electrocatalyst for Selective Reduction of CO2 to Formate in Water: Including Thermochemical Insights

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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                jbchs
                Journal of the Brazilian Chemical Society
                J. Braz. Chem. Soc.
                Sociedade Brasileira de Química (São Paulo )
                1678-4790
                August 2015
                : 26
                : 8
                : 1551-1564
                Affiliations
                [1 ] Indian Institute Of Technology Roorkee India
                [2 ] State University of New York United States
                Article
                S0103-50532015000801551
                10.5935/0103-5053.20150123
                692d142d-952b-4109-b457-2d25f9fe5242

                http://creativecommons.org/licenses/by/4.0/

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                SciELO Brazil

                Self URI (journal page): http://www.scielo.br/scielo.php?script=sci_serial&pid=0103-5053&lng=en
                Categories
                CHEMISTRY, MULTIDISCIPLINARY

                General chemistry
                glycerol hydrogenolysis,Cu-Ni bimetallic catalysts,1,2-propanediol,catalyst stability

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