Patent classifications
C10G2/30
Use of a bifunctional catalyst based on IZM-2 with a specific Si/Al ratio for the isomerization of long paraffinic feedstocks to middle distillates
The present invention describes a process for the isomerization of paraffinic feedstocks operating at a temperature of between 200 C. and 500 C., at a total pressure of between 0.45 MPa and 7 MPa, at a hydrogen partial pressure of between 0.3 and 5.5 MPa, at an hourly space velocity of between 0.1 and 10 kilograms of feedstock introduced per kilogram of catalyst and per hour and using a catalyst comprising at least one metal of group VIII of the periodic table of elements, at least one matrix and at least one zeolite IZM-2, in which the ratio between the number of moles of silicon and the number of moles of aluminium of the zeolite IZM-2 network is between 25 and 55, preferably between 25 and 50, and preferably between 30 and 50.
Thermal and chemical utilization of carbonaceous materials, in particular for emission-free generation of energy
A process for the generation of energy and/or hydrocarbons and other products utilizing carbonaceous materials. In a first process stage (P1) the carbonaceous materials are supplied and are pyrolysed, wherein pyrolysis coke (M21) and pyrolysis gas (M22) are formed. In a second process stage (P2), the pyrolysis coke (M21) from the first process stage (P1) is gasified, wherein synthesis gas (M24) is formed, and slag and other residues (M91, M92, M93, M94) are removed. In a third process stage (P3), the synthesis gas (M24) from the second process stage (P2) is converted into hydrocarbons and/or other solid, liquid, and/or gaseous products (M60), which are discharged. The three process stages (P1, P2, P3) form a closed cycle. Surplus gas (M25) from the third process stage (P3) is passed as recycle gas into the first process stage (P1), and/or the second process stage (P2), and pyrolysis gas (M22) from the first process stage (P1) is passed into the second process stage (P2), and/or the third process stage (P3).
Integrated GTL process
An integrated process for converting light hydrocarbon gases into products. Pre-packaged equipment such as a gas turbine and process compressors may be used to efficiently integrate the process. The gas turbine may provide a portion of the oxygen required in the process as compressed air. An additional oxygen rich stream may be provided by a separate air separation process so that the combined air and oxygen rich streams have an oxygen content of 25% to 50%. The gas turbine may also provide thermal energy to pre-heat the oxygen rich stream and feed gas stream and power to run compressors, air separation, and auxiliaries in the process.
Integrated methods for chemical synthesis
Among other things, the present invention encompasses the applicant's recognition that epoxide carbonylation can be performed industrially utilizing syngas streams containing hydrogen, carbon monoxide and varying amounts carbon dioxide. Contrary to expectation, the epoxide carbonylation reaction proceeds selectively in the presence of these mixed gas streams and incorporates excess CO in the syngas stream into valuable chemical precursors, resulting in hydrogen streams substantially free of CO. This is economically and environmentally preferable to performing WSGR which releases the excess carbon as CO2. The integrated processes herein therefore provide improved carbon efficiency for processes based on coal or biomass gasification or steam methane reforming.
SYNTHESIS GAS CONVERSION PROCESS
The disclosed invention relates to a method for restarting a synthesis gas conversion process which has stopped. The synthesis gas conversion process may be conducted in a conventional reactor or a microchannel reactor. The synthesis gas conversion process may comprise a process for converting synthesis gas to methane, methanol or dimethyl ether. The synthesis gas conversion process may be a Fischer-Tropsch process.
Method for Recycling Carbon Dioxide
The method for recycling carbon dioxide according to the present invention includes: injecting a reaction gas containing carbon dioxide and a carbon raw material into a rotary heating furnace; reacting the reaction gas and the carbon raw material with each other in the rotary heating furnace to generate a hydrocarbon precursor containing carbon monoxide; and converting the hydrocarbon precursor into a hydrocarbon compound, thereby exhibiting excellent conversion rate of carbon dioxide.
Use of a bifunctional catalyst based on zeolite IZM-2 for the hydroisomerization of light paraffinic feedstocks resulting from Fischer-Tropsch synthesis
A process is described for producing middle distillates from a paraffinic feedstock produced by Fischer-Tropsch synthesis and divided into a light fraction (cold condensate) and a heavy fraction (waxes). The process involves fractionation of the waxes to obtain a light fraction, the final boiling point of which is between 350 C. and 400 C., and a heavy fraction which boils above the light fraction. The light fraction is mixed with at least one portion of the cold condensate. The resultant mixture is hydrotreated in the presence of a hydrotreatment catalyst of at least one portion of the resultant effluent is hydroisomerized in the presence of a catalyst comprising at least one noble metal from Group VIII and at least one zeolite IZM-2. At least one portion of the heavy fraction is subjected to hydrocracking and hydroisomerization in the presence of a hydrocracking catalyst. The resultant effluents are fractionated to obtain at least one middle distillates fraction.
PROCESS FOR ENRICHMENT OF THE CO2 CONCENTRATION IN THE CO2-STREAMS FROM THE POST-COMBUSTION AND PRE-COMBUSTION STATIONARY SOURCES OF CO2 EMISSION UPSTREAM OF FURTHER PROCESSING
The present process invention in continuation to the U.S. Ser. No. 14/392,066 appertains to Advanced Combustion in post-combustion carbon capture, wherein the CO.sub.2-containing flue gas, said CO2-Stream, is cleaned from harmful constituents, recirculated, oxygenized and employed for combustion for the fossil fuels, referred to Flue Gas Oxy-Fueling in order to obtain a CO.sub.2-rich gas upstream to CO2-CC with significantly less gas flow rate subject to further processing. This continuation process patent also presents processing to prepare a CO.sub.2-rich CO2-Stream for the pre-combustion carbon capture downstream of gasification and gas cleaning process; or from the secondary CO2-Stream that stems from the cathodic syngas [CO/2H.sub.2] downstream of HPLTE-SG of patent parent, then downstream of the HP/IP-water shift converters in [CO.sub.2/3H.sub.2] composition, whereas the CO.sub.2-rich CO2-Stream from either pre-combustion process is routed to the CO2-CC for CO.sub.2 cooling and condensation section of the U.S. Ser. No. 14/392,066 to obtain liquid carbon dioxide for re-use as new fossil energy resource.
Synthesis gas conversion process
The disclosed invention relates to a method for restarting a synthesis gas conversion process which has stopped. The synthesis gas conversion process may be conducted in a conventional reactor or a microchannel reactor. The synthesis gas conversion process may comprise a process for converting synthesis gas to methane, methanol or dimethyl ether. The synthesis gas conversion process may be a Fischer-Tropsch process.
Process for producing hydrocarbons
The present application relates to a process for producing normally gaseous, normally liquid, and optionally normally solid hydrocarbons from synthesis gas in a three-phase reactor, said reactor comprising a top middle and bottom part wherein the bottom and top part are fluidly connected via one or more reactor tubes, wherein one or more reactor tubes comprise randomly stacked catalyst bodies held stationary in the reactor tube and the reactor is at least partially filled with a liquid medium, said process comprising the steps of: (i) introducing the synthesis gas into the reactor via the bottom part; and (ii) contacting the synthesis gas with a stationary catalyst to catalytically convert the synthesis gas at an elevated temperature to obtain the normally gaseous, normally liquid, and optionally normally solid hydrocarbons from synthesis gas; (iii) withdrawing the normally gaseous, normally liquid, and optionally normally solid hydrocarbons; wherein the catalyst bodies have an open celled foam structure.