Patents by Inventor Mark Feaviour

Mark Feaviour has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20190299159
    Abstract: An oxidation catalyst is described for treating an exhaust gas produced by a diesel engine comprising a catalytic region and a substrate, wherein the catalytic region comprises a catalytic material comprising: bismuth (Bi), antimony (Sb) or an oxide thereof; a platinum group metal (PGM) selected from the group consisting of (i) platinum (Pt), (ii) palladium (Pd) and (iii) platinum (Pt) and palladium (Pd); and a support material, which is a refractory oxide; wherein the platinum group metal (PGM) is supported on the support material; and wherein the bismuth (Bi), antimony (Sb) or an oxide thereof is supported on the support material and/or the refractory oxide comprises the bismuth, antimony or an oxide thereof.
    Type: Application
    Filed: June 20, 2019
    Publication date: October 3, 2019
    Inventors: Andrew Francis Chiffey, Oliver Cooper, Christopher Daly, Mark Feaviour, Steven Merrick, Francois Moreau, Matthew O'Brien, David Thompsett
  • Patent number: 10357743
    Abstract: An oxidation catalyst is described for treating an exhaust gas produced by a diesel engine comprising a catalytic region and a substrate, wherein the catalytic region comprises a catalytic material comprising: bismuth (Bi), antimony (Sb) or an oxide thereof; a platinum group metal (PGM) selected from the group consisting of (i) platinum (Pt), (ii) palladium (Pd) and (iii) platinum (Pt) and palladium (Pd); and a support material, which is a refractory oxide; wherein the platinum group metal (PGM) is supported on the support material; and wherein the bismuth (Bi), antimony (Sb) or an oxide thereof is supported on the support material and/or the refractory oxide comprises the bismuth, antimony or an oxide thereof.
    Type: Grant
    Filed: October 14, 2016
    Date of Patent: July 23, 2019
    Assignee: Johnson Matthey Public Limited Company
    Inventors: Andrew Francis Chiffey, Oliver Cooper, Christopher Daly, Mark Feaviour, Steven Merrick, Francois Moreau, Matthew O'Brien, David Thompsett
  • Publication number: 20170106337
    Abstract: An oxidation catalyst is described for treating an exhaust gas produced by a diesel engine comprising a catalytic region and a substrate, wherein the catalytic region comprises a catalytic material comprising: bismuth (Bi), antimony (Sb) or an oxide thereof; a platinum group metal (PGM) selected from the group consisting of (i) platinum (Pt), (ii) palladium (Pd) and (iii) platinum (Pt) and palladium (Pd); and a support material, which is a refractory oxide: wherein the platinum group metal (PGM) is supported on the support material; and wherein the bismuth (Bi), antimony (Sb) or an oxide thereof is supported on the support material and/or the refractory oxide comprises the bismuth, antimony or an oxide thereof.
    Type: Application
    Filed: October 14, 2016
    Publication date: April 20, 2017
    Inventors: Andrew Francis CHIFFEY, Oliver COOPER, Christopher DALY, Mark FEAVIOUR, Steven MERRICK, Francois MOREAU, Matthew O'BRIEN, David THOMPSETT
  • Publication number: 20070254805
    Abstract: A reforming catalyst comprising precious metal particles dispersed on a support material, wherein the support material comprises ceria, and characterised in that the support material further comprises magnesium aluminate is disclosed. Catalysed components and fuel processing systems comprising the catalyst, and reforming processes using the catalyst are also disclosed.
    Type: Application
    Filed: December 7, 2004
    Publication date: November 1, 2007
    Inventors: Mark Feaviour, Jillian Bailie
  • Publication number: 20060272213
    Abstract: A method of operating a methanation reactor to reduce carbon monoxide concentration in a reformate stream in a fuel cell reformer. The reactor includes a flowpath with a noble metal catalyst supported by a ceramic support such that the reactor preferentially converts carbon monoxide via methanation over that of carbon dioxide. The reduced level of carbon monoxide present in the reformate stream after passing through the methanation reactor reduces the likelihood of poisoning of the catalyst used on the fuel cell anode.
    Type: Application
    Filed: August 11, 2006
    Publication date: December 7, 2006
    Inventors: Mark Feaviour, Julia Rowe
  • Publication number: 20050207958
    Abstract: A method of reducing an amount of carbon monoxide in process fuel gas in a water gas shift converter with no methane formation. The method includes placing a high activity water gas shift catalyst system into a water gas shift converter; and passing the process fuel gas through the water gas shift converter in effective contact with the high activity water gas shift catalyst system and converting a portion of the carbon monoxide in the process fuel gas into carbon dioxide and hydrogen by a water gas shift reaction with no methane formation at a temperature in a range of about 200° C. to about 425° C.
    Type: Application
    Filed: March 18, 2004
    Publication date: September 22, 2005
    Inventors: Anca Faur-Ghenciu, Sailesh Mullapudi, Mark Feaviour, Nathan Trusty, Jessica Reinkingh
  • Publication number: 20050172555
    Abstract: Methods and apparatus for producing hydrogen are provided. The methods and apparatus utilize reforming catalysts in order to produce hydrogen gas. The reforming catalysts may be platinum group metals on a support material, and they may be located in a reforming reaction zone of a primary reactor. The support material may an oxidic support having a ceria zirconia promoter. The support material may be an oxidic support and a neodymium stabilizer. The support material may also be an oxidic support material and at least one Group IA, Group IIA, manganese, or iron metal promoter. The primary reactor may have a first and second reforming reaction zones. Upstream reforming catalysts located in the first reforming reaction zone may be selected to perform optimally under the conditions in the first reforming reaction zone. Downstream reforming catalysts located in the second reforming reaction zone may be selected to perform optimally under the conditions in the second reforming reaction zone.
    Type: Application
    Filed: March 3, 2005
    Publication date: August 11, 2005
    Inventors: Michael Petch, Jonathan Frost, Suzanne Ellis, Jessica Reinkingh, Mark Feaviour, Jillian Bailie, David Wails, Paul Millington
  • Publication number: 20050005520
    Abstract: A method of reducing the amount of carbon monoxide in process fuel gas in a water gas shift converter. The method includes placing a high activity water gas shift catalyst system into a water gas shift converter, and passing the process fuel gas through the water gas shift converter in effective contact with the high activity water gas shift catalyst system and converting a portion of the carbon monoxide in the process fuel gas into carbon dioxide and hydrogen by a water gas shift reaction. The high water gas shift catalyst system includes a noble metal, a support comprising a mixed metal oxide of cerium oxide and at least one of zirconium oxide or lanthanum oxide. A promoter of yttrium, an alkali metal, or alkaline earth metal can be included. A support dopant can also be included.
    Type: Application
    Filed: July 10, 2003
    Publication date: January 13, 2005
    Inventors: Anca Faur-Ghenciu, Nathan Trusty, Mark Feaviour, Jessica Reinkingh, Phillip Shady, Paul Andersen