Flex-fuel hydrogen generator for IC engines and gas turbines
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
C01B-003/38
F02C-003/20
출원번호
US-0900479
(2013-05-22)
등록번호
US-9440851
(2016-09-13)
발명자
/ 주소
Hwang, Herng Shinn
출원인 / 주소
Hwang, Herng Shinn
대리인 / 주소
Hwang, Herng Shinn
인용정보
피인용 횟수 :
1인용 특허 :
25
초록▼
An on-board Flex-Fuel H2 Generator provides devices and the methods of operating these devices to produce H2 and CO from hydrocarbons and bio-fuels. One or more parallel autothermal reformers are used to convert the fuels into H2 over the Pt group metal catalysts without external heat and power. The
An on-board Flex-Fuel H2 Generator provides devices and the methods of operating these devices to produce H2 and CO from hydrocarbons and bio-fuels. One or more parallel autothermal reformers are used to convert the fuels into H2 over the Pt group metal catalysts without external heat and power. The produced reformate is then cooled and the dry gas is compressed and stored in vessels at a pressure between 1 to 100 atmospheres. For this system, the pressure of the storage vessels and the flow control curves are used directly to control the amount of the reformers' reformate output. To improve thermal efficiency of a mobile vehicle or a distributed power generator, a portion of the reformate from the storage vessels is used to mix with the primary fuels and air as part of a lean burn fuel mixture for the engine/gas turbine. Also, this on-board Flex-Fuel H2 Generator can provide H2 to regenerate the NOx and diesel particulate traps for diesel engines, and/or it can provide H2 for a mobile or a portable fuel cell power generator.
대표청구항▼
1. A method of operating an on-board Flex-Fuel H2 Generator comprising: a). providing one or more parallel autothermal (ATR) reformers for producing H2 and CO from hydrocarbons and/or bio-fuels over supported and/or unsupported Pt group catalysts;b). providing one automatic control system comprising
1. A method of operating an on-board Flex-Fuel H2 Generator comprising: a). providing one or more parallel autothermal (ATR) reformers for producing H2 and CO from hydrocarbons and/or bio-fuels over supported and/or unsupported Pt group catalysts;b). providing one automatic control system comprising a control computer and microprocessors, flow meters/controllers, valves, pumps, sensors and thermocouples;c). providing to the one or more reformers a stream of reactants of an inlet fuel mixture comprising at least one oxidant, at least one fuel and at least one water/steam, wherein the reactants are selected from a reactant supply group consisting of a liquid fuel loop, a gas fuel loop, a water supply loop, an air supply loop, a water electrolyzer loop, an exhaust gas recycle (EGR) loop, a water recycle loop and a reformate recycle loop;d). reacting said stream of the inlet fuel mixture over said catalysts inside the one or more ATR reformers to produce a reformate containing H2 and CO from said reactants;e). providing one or more vessels/manifolds for storing condensed water from the one or more reformers and also storing said reformate produced from the one or more ATR reformers at a pressure between 1 to 100 atmospheres, which is used by a downstream IC engine or gas turbine;f). providing one or more flow control curves defined by pressure in the one or more storage vessels as a function of reformer output capacity for regulating each reactants flow rate, the reformate composition, the one or more reformer's start-up/shutdown and the total reformer's flow output, wherein:f.1). a single point on a given control curve supplies: i. a group of pre-calibrated and pre-stored set points for all flow meters/controllers, which is down loaded from the control computer and/or the microprocessors for the purpose of controlling each reactant's flow rate;ii. a specified reformer's inlet fuel mixture which is at a given O2/C, H2O/C and CO2/C ratios according to said set points;iii. a specified reformate dry gas composition which is produced by the one or more reformers from said inlet fuel mixture and is stored in the one or more storage vessels, andiv. a specified amount of the reformate output which is produced by the one or more reformers at a given flow rate according to the location on the given control curve;f.2). multiple points on the same control curve are capable of producing a series of different flow outputs with the same reformate composition;f.3). multiple different pre-calibrated control curves are used to provide different reformer inlet fuel mixtures, and are used by the same reformer to produce H2 and CO reformate from various fuels and/or bio-fuels. 2. The method of claim 1, wherein each ATR reformer installed in said on-board Flex-Fuel H2 Generator performs the following steps: (a). receiving a stream of the inlet fuel mixture comprising water, one or more fuels and an O2 containing gas in a given range of O2/C, H2O/C and CO2/C ratios into a first CPO/SR reaction zone;(b). reacting said inlet fuel mixture over the Pt group metal catalysts with a residence time <300 milliseconds (calculated at STP) in the first CPO/SR reaction zone to provide a fuel and reformate mixture;(c). reacting further the fuel and reformate mixture from step (b) over the Pt group metal catalysts with a residence time <5 seconds in a second SR reaction zone;(d). producing rapidly in steps (b) and (c) a reformate comprising steam, H2, CO, CO2, N2, O2 and unconverted fuels at a given temperatures between 150-1 and a given pressure between 1 to 100 atmosphere, and(e). feeding the produced reformate from step (d) into a third reaction zone with a residence time <100 seconds and converting portion of a feed water and CO into hydrogen with or without Pt group metal catalysts at a temperatures between 50-500° C. 3. The method of claim 2, wherein the stream of said inlet fuel mixture reacts over the Pt group catalysts to start or re-start the one or more ATR reformers without external heat and electricity, and two or more start-up reactants are selected from the group consisting of fuels, air, the engine or gas turbine's recycle exhaust gas, H2/O2 gases from an electrolyzer, and the reformate in the one or more storage vessels. 4. The method of claim 1, wherein the pressure of the reformate in the storage vessels/manifolds is kept between 30 to 100 atmosphere, and said vessel pressure is used to start up/shut down the reformer or to increase/decrease the total amount of the one or more ATR's flow output according to the one or more control curves. 5. The method of claim 1, wherein said reformate pressure of the storage vessel is used to regulate each reactant's flow rate according to the predefined control curve, and is therefore used to increase or decrease the total amount of the reformate output, which is produced by the one or more ATR reformers with a specified dry reformate composition according to said O2/C, H2O/C and CO2/C ratios of said inlet fuel mixture. 6. The method of claim 1, wherein a portion of the high pressure reformate from the storage vessels, which is at a specified gas composition, is used to assist in lean combustion inside the IC engine or gas turbine, and the ratio of H, (217)/fuel flow (201A) is kept between 0.05 to 0.95, so that a combined final engine or gas turbine's inlet fuel mixture of H2, primary fuel, primary air and secondary air is kept at a lambda ratio between 1.01 to 1.80. 7. The method of claim 1, wherein the high pressure reformate in the one or more storage vessels is used to generate the oxidation reaction heat over the catalysts to start or to re-start quickly the one or more ATR reformers. 8. The method of claim 1, wherein said high pressure reformate in the one or more storage vessels is used as a reducing gas to reduce the supported Pt group metal catalysts, or to regenerate catalysts in catalytic converters, NOx traps and diesel particulate filters. 9. The method of claim 1, wherein said high pressure reformate in the one or more storage vessels is used to provide H2 to a mobile electric vehicle/device which is equipped with a solid oxide or proton exchange membrane fuel cell stack. 10. The method of claim 1, wherein said high pressure reformate in the one or more storage vessels is used to provide reformate to the IC engine or gas turbine, a fuel cell device and/or a catalytic combustor to supply both heat and power as an on-board Auxiliary Power Unit. 11. The method of claim 1, wherein said supported Pt group metal catalysts inside the one or more ATR reformers comprise one or more supported Pt group metal washcoat powder catalysts, and each catalyzed washcoat contains between 0.01 to 10.0 wt % of total Pt group metals supported on oxide powders. 12. The method of claim 11, wherein said supported Pt group metal powder catalyst comprises one or more of Pt, Pd, Rh, Ir, Os, and/or Ru metals which are first impregnated on one or more washcoat powders selected from the group consisting of Al2O3, Ce oxide, Zr oxides, Ce—Zr oxide composite, oxide promoters/thermal stabilizers and mixtures thereof. 13. The method of claim 12, wherein the oxide promoters/stabilizers are one or more oxides of lanthanum, cerium, praseodymium, Rhenium, Zinc, Tin, calcium, potassium, zirconium, yttrium, barium, strontium, magnesium and mixtures thereof. 14. The method of claim 12, wherein the catalyzed washcoat powder is further coated on the surface of a high temperature inert carrier such as a ceramic monolith, metallic monolith, pellet, wire mesh, screen, foam, plate, static mixer and silicon carbide, and the total Pt group metal content is between 0.10 to 2000 g/ft3. 15. The method of claim 2, wherein the catalyst temperature is constantly kept below 1000° C. by controlling the H2O/C ratio of the inlet fuel mixture between 0.05 and 10.0, the O2/C ratio between 0.15 to 0.8, and the CO2/C ratio between 0.0 and 0.5. 16. The method of claim 1, wherein the at least one fuel is any chemical selected from one or more of the following compounds: C1-C16 hydrocarbons, methane, natural gas, methanehydrate, LPG, C1-C8 alcohols, vegetable oils, bio-ethanol, bio-diesel, bio-methane, industrial waste or vent gas containing volatile organic compounds, and any bio-fuels derived from biomass or from agriculture/industrial/animal wastes. 17. The method of claim 1, wherein recycled reformate from the one or more storage vessels and/or the H2/O2 gases from a water electrolyzer are used to start or to re-start the one or more ATR reformers with the system's own heat and power. 18. The method of claim 1, wherein the flow rate of O2/H2 produced by an electrolyzer is controlled by the one or more control curves, and the O2 generated by the electrolyzer is used directly as the one or more ATR reformer's only oxygen source for the purpose of increasing the % H2 in the ATR reformate. 19. The method of claim 1, wherein a flow rate of O2 generated by an electrolyzer is controlled by the one or more control curves, and H2 produced by the electrolyzer is used to regenerate a NOx trap and/or diesel particulate filter. 20. The method of claim 2, wherein a portion of the engine or gas turbine's exhaust gas is recycled to the one or more ATR reformers to provide steam, O2, CO2 and heat. 21. The method of claim 1, wherein one or more fuels selected from the group consisting of natural gas, CNG, LPG, gasoline, methanol or bio-ethanol are used by the one or more reformers to produce H2 and CO reformate according to the one or more control curves, so that said reformate is used to regenerate a diesel engine's NOx traps and/or a diesel particulate filter. 22. The method of claim 1, wherein electricity is generated and used to dissociate distilled water in an electrolyzer to provide both H2 and O2 to start and/or to re-start the one or more reformers. 23. The method of claim 1, wherein a molar ratio of an injected H2 flow (#217) to a primary fuel flow (#201A) is controlled between 0.05 to 0.95. 24. The method of claim 23, wherein a molar ratio of a secondary air flow (#208) to the injected H2 flow (#217) is controlled at a given value, and a position of a throttle valve and/or an air mass flow sensor will determine the amount of the H2, a primary and the secondary air injection, so that a final fuel mixture is kept at a lambda ratio between 1.01 to 1.80. 25. The method of claim 1, wherein, in order to maintain said pressure between 1 to 100 atmosphere, said automatic control system would start up/increase the one or more reformer's flow output when said pressure is low or shutdown/decrease the output when said pressure is high. 26. The method of claim 2, wherein the catalysts comprise a large diameter metallic monolith catalyst with a removable small diameter center core and a large annular outside core as an integral catalyst unit. 27. The method of claim 1, wherein the engine or gas turbine is used by itself as a driving device for automobile, lawn mower, fork lift truck, diesel truck, bus, or motorcycle. 28. The method of claim 1, wherein the engine or gas turbine is used as a stand-alone distributed powerstation to power an electric car, truck, motorcycle, forklift truck, electric utility vehicle, battery charger or backup power generator.
연구과제 타임라인
LOADING...
LOADING...
LOADING...
LOADING...
LOADING...
이 특허에 인용된 특허 (25)
Hwang, Herng Shinn, Catalytic EGR oxidizer for IC engines and gas turbines.
Munshi, Sandeep; McTaggart-Cowan, Gordon P.; Rogak, Steven N.; Bushe, William Kendal, Method and apparatus of fuelling an internal combustion engine with hydrogen and methane.
Boegner Walter (Remseck DEX) Kraemer Michael (Notzingen DEX) Krutzsch Bernd (Denkendorf DEX) Wenninger Guenter (Stuttgart DEX) Wirbeleit Friedrich (Esslingen DEX) Weisweiler Werner (Remchingen DEX), Process and apparatus for selective catalyzed no-reduction in oxygen-containing exhaust gases.
Smith Jack A. ; Podnar Daniel J. ; Cole James J. ; Kubesh John T. ; Bartley Gordon J., Stoichiometric synthesis, exhaust, and natural-gas combustion engine.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.