Methods of catalytic hydrogenation for ethylene glycol formation
US-2015375209-A1 · Dec 31, 2015 · US
US2016271589A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016271589-A1 |
| Application number | US-201315029577-A |
| Country | US |
| Kind code | A1 |
| Filing date | Oct 17, 2013 |
| Priority date | Oct 17, 2013 |
| Publication date | Sep 22, 2016 |
| Grant date | — |
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In an embodiment, a photocatalyst for the generation of diatomic hydrogen from a hydrogen containing precursor under the influence of actinic radiation comprises: a semiconductor support of SrTiO 3 and TiO 2 , wherein a molar ratio of SrTiO 3 and TiO 2 in the semiconductor support is at least 0.01; and a gold and palladium alloy on said semiconductor support. Included herein are embodiments of a photocatalyst system, methods of making diatomic hydrogen, and methods of making the photocatalyst.
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We claim: 1 . A photocatalyst for the generation of diatomic hydrogen from a hydrogen containing precursor under the influence of actinic radiation comprising: a semiconductor support of SrTiO 3 and TiO 2 , wherein a molar ratio of SrTiO 3 and TiO 2 in the semiconductor support is at least 0.01; and a gold and palladium alloy on said semiconductor support. 2 . The photocatalyst according to claim 1 , wherein the alloy is present on the semiconductor support as particles having an average major axis length of 1-100 nm. 3 . (canceled) 4 . The photocatalyst according to claim 1 , wherein the alloy comprises greater than or equal to 90 wt %, of palladium and gold, based on the weight of the alloy. 5 . The photocatalyst according to claim 1 , wherein greater than or equal to 90 wt %, of the gold and palladium in the alloy are present in their non-oxidized state. 6 . The photocatalyst according to claim 1 , wherein the alloy further comprises at least one of silver and copper. 7 . The photocatalyst according to claim 1 , wherein the molar ratio of SrTiO 3 and TiO 2 is selected such that the semiconductor support has one or more, bandgaps between 2.8 eV and 3.3 eV. 8 . (canceled) 9 . The photocatalyst according to claim 1 , wherein the photocatalyst has a BET surface area of 30 to 60 m 2 per gram catalyst using the nitrogen absorption technique. 10 . (canceled) 11 . The photocatalyst according to claim 1 , wherein at least part of the alloy is covered with a layer of the semiconductor support. 12 . The photocatalyst according to claim 1 , wherein at least part of the alloy is covered with a layer of the semiconductor support, and wherein the layer has a thickness of 1 to 5 nm. 13 . The photocatalyst according to claim 1 , wherein the semiconductor support is a mixture comprising SrTiO 3 and TiO 2 that is physically inseparable. 14 . A method for preparing a photocatalyst according to claim 1 comprising providing a semiconductor support and depositing gold and palladium so that a gold and palladium alloy is formed on the semiconductor support. 15 . A method for generating diatomic hydrogen from a hydrogen containing precursor, comprising contacting a photocatalyst according to claim 1 with the hydrogen containing precursor while exposing the photocatalyst to actinic radiation. 16 . The method according to claim 15 , wherein the actinic radiation has a photonic energy of at least 2.5 eV and a radiant flux density of at least 0.1 mW/cm 2 . 17 . (canceled) 18 . The method of claim 15 , wherein the hydrogen containing precursor is a mixture of water and alcohol wherein the amount of alcohol is from 0.1 to 10% by volume, a mixture of water and diol wherein the amount of diol is from 0.1 to 10% by volume, or a mixture of water, alcohol, and diol wherein the combined amount of alcohol and diol is from 0.1 to 10% by volume based on the volume of the mixture. 19 . (canceled) 20 . The method of claim 15 , wherein the hydrogen containing precursor is a mixture of water and glycerol wherein the amount of glycerol is from 0.1 to 10% by volume, or a mixture of water, glycerol, and diol wherein the combined amount of glycerol and diol is from 0.1 to 10% by volume based on the volume of the mixture. 21 . The method according to claim 18 , wherein the mixture is an aqueous solution. 22 . (canceled) 23 . (canceled) 24 . A method for preparing a photocatalyst according to claim 1 , comprising: i) combining a titanium precursor, and a strontium salt solution; ii) raising the pH to a value such that precipitation occurs; iii) washing the precipitate from step ii) with water; iv) calcining the precipitate at a temperature in the range of 500 to 800° C. so as to form the support; and v) depositing the gold and palladium onto the support. 25 . The method of claim 24 , wherein step i) further comprises lowering the pH of the mixture obtained by combining said titanium precursor and strontium salt solution to a value of at most 4. 26 . The method according to claim 24 , further comprising heating the support at a temperature of 300° C. to 800° C. in an inert or reducing atmosphere for a period from 1 to 24 hours so as to cover the alloy at least in part with a layer of semiconductor support having a thickness of 1 to 5 nm. 27 . (canceled) 28 . (canceled) 29 . The method according to claim 24 , wherein the titanium precursor comprises a titanium halogenide.
Hydrogen production from non-carbon containing sources, e.g. by water electrolysis · CPC title
Compounds characterised by their crystallite size · CPC title
Scanning electron microscopy; Transmission electron microscopy · CPC title
Nanoparticles · CPC title
Indexing scheme associated with group B01J35/00, related to the analysis techniques used to determine the catalysts form or properties · CPC title
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