Patent classifications
F25J2205/70
LIQUEFIED HYDROGEN PRODUCTION DEVICE
Liquid hydrogen is produced while reducing emission of carbon dioxide to the atmosphere. Provided is a liquid hydrogen production device including: a carbon dioxide cycle plant (2), which includes a turbine (23) using a carbon dioxide fluid as a driving fluid, and is configured to drive the turbine (23) to generate motive power with use of a carbon dioxide cycle in which the carbon dioxide fluid discharged from the turbine (23) is increased in pressure and heated and is then re-supplied to the turbine (23); and a liquefaction plant (4) configured to cool gaseous hydrogen by heat exchange with a refrigerant, to obtain liquid hydrogen. The motive power generated by driving of the turbine (23) is used as motive power to be consumed in the liquefaction plant (4).
Natural gas liquid fractionation plant waste heat conversion to simultaneous power and potable water using Kalina cycle and modified multi-effect-distillation system
Certain aspects of natural gas liquid fractionation plant waste heat conversion to simultaneous power and potable water using Kalina Cycle and modified multi-effect-distillation system can be implemented as a system. The system includes a waste heat recovery heat exchanger network coupled to multiple heat sources of a Natural Gas Liquid (NGL) fractionation plant. The heat exchanger network is configured to transfer at least a portion of heat generated at the multiple heat sources to a first buffer fluid and a second buffer fluid flowed through the first heat exchanger network. The system includes a first sub-system configured to generate power. The first sub-system is thermally coupled to the waste heat recovery heat exchanger. The system includes a second sub-system configured to generate potable water from brackish water. The second sub-system is thermally coupled to the waste heat recovery heat exchanger.
Apparatus and system for swing adsorption processes
Provided are apparatus and systems for performing a swing adsorption process. This swing adsorption process may involve performing a startup mode process prior to beginning a normal operation mode process to remove contaminants from a gaseous feed stream. The startup mode process may be utilized for swing adsorption processes, such as TSA and/or PSA, which are utilized to remove one or more contaminants from a gaseous feed stream.
SYNTHESIS GAS PRODUCTION PROCESS FOR THE IMPLEMENTATION OF A NATURAL GAS LIQUEFACTION
Natural gas liquefaction process in combination with a synthesis gas production process, where the steam derived from the synthesis gas production process is used as a heating source for the implementation of the pre-treatment step for eliminating the impurities liable to freeze during the natural gas liquefaction process.
Cryogenic adsorption process for xenon recovery
An adsorption process for xenon recovery from a cryogenic liquid or gas stream is described wherein a bed of adsorbent is contacted with the aforementioned xenon containing liquid or gas stream and adsorbs the xenon selectively from this fluid stream. The adsorption bed is operated to at least near full breakthrough with xenon to enable a deep rejection of other stream components, prior to regeneration using the temperature swing method. Operating the adsorption bed to near full breakthrough with xenon, prior to regeneration, enables production of a high purity product from the adsorption bed and further enables oxygen to be used safely as a purge gas, even in cases where hydrocarbons are co-present in the feed stream.
System and method for recovery of non-condensable gases such as neon, helium, xenon, and krypton from an air separation unit
A system and method for recovery of rare gases such as neon, helium, xenon, and krypton in an air separation unit is provided. The rare gas recovery system comprises a non-condensable stripping column linked in a heat transfer relationship with a xenon-krypton column via an auxiliary condenser-reboiler. The non-condensable stripping column produces a rare gas containing overhead that is directed to the auxiliary condenser-reboiler where most of the neon is captured in a non-condensable vent stream that is further processed to produce a crude neon vapor stream that contains greater than about 50% mole fraction of neon with the overall neon recovery exceeding 95%. The xenon-krypton column further receives two streams of liquid oxygen from the lower pressure column and the rare gas containing overhead from the non-condensable stripping column and produces a crude xenon and krypton liquid stream and an oxygen-rich overhead.
SYSTEM AND METHOD FOR RECOVERY OF NON-CONDENSABLE GASES SUCH AS NEON, HELIUM, XENON, AND KRYPTON FROM AN AIR SEPARATION UNIT
A system and method for recovery of rare gases such as neon, helium, xenon, and krypton in an air separation unit is provided. The rare gas recovery system comprises a non-condensable stripping column linked in a heat transfer relationship with a xenon-krypton column via an auxiliary condenser-reboiler. The non-condensable stripping column produces a rare gas containing overhead that is directed to the auxiliary condenser-reboiler where most of the neon is captured in a non-condensable vent stream that is further processed to produce a crude neon vapor stream that contains greater than about 50% mole fraction of neon with the overall neon recovery exceeding 95%. The xenon-krypton column further receives two streams of liquid oxygen from the lower pressure column and the rare gas containing overhead from the non-condensable stripping column and produces a crude xenon and krypton liquid stream and an oxygen-rich overhead.
NATURAL GAS LIQUID FRACTIONATION PLANT WASTE HEAT CONVERSION TO SIMULTANEOUS POWER AND POTABLE WATER USING KALINA CYCLE AND MODIFIED MULTI-EFFECT-DISTILLATION SYSTEM
Certain aspects of natural gas liquid fractionation plant waste heat conversion to simultaneous power and potable water using Kalina Cycle and modified multi-effect-distillation system can be implemented as a system. The system includes a waste heat recovery heat exchanger network coupled to multiple heat sources of a Natural Gas Liquid (NGL) fractionation plant. The heat exchanger network is configured to transfer at least a portion of heat generated at the multiple heat sources to a first buffer fluid and a second buffer fluid flowed through the first heat exchanger network. The system includes a first sub-system configured to generate power. The first sub-system is thermally coupled to the waste heat recovery heat exchanger. The system includes a second sub-system configured to generate potable water from brackish water. The second sub-system is thermally coupled to the waste heat recovery heat exchanger.
NATURAL GAS LIQUID FRACTIONATION PLANT WASTE HEAT CONVERSION TO SIMULTANEOUS POWER AND POTABLE WATER USING ORGANIC RANKINE CYCLE AND MODIFIED MULTI-EFFECT-DISTILLATION SYSTEMS
Certain aspects of natural gas liquid fractionation plant waste heat conversion to simultaneous power and potable water using organic Rankine cycle and modified multi-effect distillation systems can be implemented as a system that includes two heating fluid circuits thermally coupled to two sets of heat sources of a NGL fractionation plant. The system includes a power generation system that comprises an organic Rankine cycle (ORC), which includes (i) a working fluid that is thermally coupled to the first heating fluid circuit to heat the working fluid, and (ii) a first expander configured to generate electrical power from the heated working fluid. The system includes a MED system thermally coupled to the second heating fluid circuit and configured to produce potable water using at least a portion of heat from the second heating fluid circuit. A control system actuates control valves to selectively thermally couple the heating fluid circuit to a portion of the heat sources of the NGL fractionation plant.
METHOD FOR PRODUCING BIOMETHANE BY PURIFYING BIOGAS FROM NON-HAZARDOUS WASTE STORAGE FACILITIES AND FACILITY FOR IMPLEMENTING THE METHOD
A method for producing biomethane by purifying biogas from non-hazardous waste storage facilities involves compressing the initial gas flow, introducing the gas flow to be purified into at least one adsorber loaded with adsorbents capable of reversibly adsorbing the VOCs, and subjecting the VOC-depleted gas flow to at least one membrane separation step in order to partially separate the CO.sub.2 and O.sub.2 from the gas flow. The method also involves introducing the retentate from the membrane separation step into at least one adsorber loaded with adsorbents capable of reversibly adsorbing the major portion of the remaining CO.sub.2, subjecting the CO.sub.2-depleted gas flow exiting the adsorber loaded with adsorbents capable of reversibly adsorbing the major portion of the remaining CO.sub.2 to a cryogenic separation step in a distillation column in order to separate the O.sub.2 and N.sub.2 from the gas flow, and recovering the CH.sub.4-rich flow from the cryogenic separation step.