Abstract: Disclosed is a micro-macro channel reactor comprising: a top end plate and a bottom end plate assembled on the outskirts of the micro-macro channel reactor; a heat exchanging plate by which a heat exchanging material passes through passages thereof so that heat is transferred between the heat exchanging material and such a fluid as a reactant, a product, or a mixture thereof that passes through a catalyst plate; a catalyst plate stacked and assembled together with the heat exchanging plate and including a catalyst section containing a reaction catalyst necessary to perform a catalytic reaction of the reactant while the reactant is passing through the catalyst section; and a support plate stacked and assembled together with the catalyst plate and configured to provide passages that allows the reactant to pass through the catalyst section of the catalyst plate.

Abstract: Disclosed are methods for producing dimethyl ether using a dimethyl ether (DME)-floating, production, storage and offloading (FPSO) system that can be used in offshore oil fields or stranded gas fields. More particularly, the disclosure relates to producing dimethyl ether from gas extracted from stranded gas fields or from associated gas extracted from oil fields at an FMSO facility, which includes a reforming reactor and a dimethyl ether reactor equipped offshore.

Abstract: Disclosed are a dimethyl ether (DME)-floating, production, storage and offloading (FPSO) system that can be used in offshore oil fields or stranded gas fields and a method for producing dimethyl ether using the same. More particularly, the disclosure relates to a DME-FPSO system capable of producing dimethyl ether from gas extracted from stranded gas fields or from associated gas extracted from oil fields, which includes a reforming reactor and a dimethyl ether reactor equipped offshore, and a method for producing the same.

Abstract: Disclosed is a micro-macro channel reactor comprising: a top end plate and a bottom end plate assembled on the outskirts of the micro-macro channel reactor; a heat exchanging plate by which a heat exchanging material passes through passages thereof so that heat is transferred between the heat exchanging material and such a fluid as a reactant, a product, or a mixture thereof that passes through a catalyst plate; a catalyst plate stacked and assembled together with the heat exchanging plate and including a catalyst section containing a reaction catalyst necessary to perform a catalytic reaction of the reactant while the reactant is passing through the catalyst section; and a support plate stacked and assembled together with the catalyst plate and configured to provide passages that allows the reactant to pass through the catalyst section of the catalyst plate.

Abstract: Disclosed are a gas to liquids (GTL)-floating production, storage and offloading (FPSO) system that can be used in offshore oil fields or stranded gas fields and a method for producing synthetic fuel using the same. More particularly, the disclosure relates to a GTL-FPSO system capable of producing liquid synthetic fuel from gas extracted from stranded gas fields or associated gas extracted from oil fields, including a reforming reactor and a liquid hydrocarbon producer, and a method for producing the same.

Abstract: The present invention relates to synthetic peptides having selectively protected amines of untargeted sites and to methods for production thereof and for specifically conjugating PEG to targeted sites of the synthetic peptides using the same. The present invention provides a much higher yield of PEG conjugated peptides in which PEG is specifically combined to amines at targeted sites.

Abstract: The present invention relates to a structured catalyst for reforming of gasoline and a method of preparing the same, more particularly to a structured catalyst for reforming of gasoline for fuel-cell powered vehicles prepared by wash-coating the transition metal based reforming catalyst on the surface of the ceramic honeycomb support wash-coated with sub-micron sized alumina or its precursor to sufficiently increase the effective surface area and the performance of the catalyst and a method of preparing the same.

Abstract: The present invention relates to a structured catalyst for reforming of gasoline and a method of preparing the same, more particularly to a structured catalyst for reforming of gasoline for fuel-cell powered vehicles prepared by wash-coating the transition metal based reforming catalyst on the surface of the ceramic honeycomb support wash-coated with sub-micron sized alumina or its precursor to sufficiently increase the effective surface area and the performance of the catalyst and a method of preparing the same.

Abstract: The present invention relates to a solid oxide fuel cell for internal reforming of hydrocarbons and carbon dioxide, in particular, to a solid oxide fuel cell in which one side of solid oxide electrolyte (YSZ) is attached to an air electrode (La0.8Sr0.2MnO3) and its other side is attached to a catalyst electrode of Ni-YSZ type or perovskite type metal oxide. The electrochemical conversion system using the solid oxide fuel cell permits the occurrence of internal reforming of hydrocarbons and carbon dioxide concomitantly with the coproduction of a syngas and electricity, and overcomes the shortcomings associated with the catalytic deactivation due to carbon deposition and the high-energy consumption.

Abstract: The present invention relates to a structured catalyst for reforming of gasoline and a method of preparing the same, more particularly to a structured catalyst for reforming of gasoline for fuel-cell powered vehicles prepared by wash-coating the transition metal based reforming catalyst on the surface of the ceramic honeycomb support wash-coated with sub-micron sized alumina or its precursor to sufficiently increase the effective surface area and the performance of the catalyst and a method of preparing the same.

Abstract: The present invention relates to a Ni-based catalyst for preparing syngas and a tri-reforming reaction of methane using the catalyst, particularly to a Ni-based catalyst, where an active ingredient (a nickel) is impregnated in a zirconia support and the zirconia is doped with a yttrium and a metal selected among a lanthanum and an alkaline earth metal to distort the crystal lattice of the zirconia, to facilitate the transfer of oxygen ion and to increase the storage and supply of oxygen, thus inhibiting the carbon deposition on the active nickel metal and maintaining the activity of the catalyst. Particularly, if the catalyst herein is used for the tri-reforming reaction of methane where a mixture of carbon dioxide, oxygen and steam is used as an oxidant, the molar ratio of hydrogen and carbon monoxide (H2/CO) in the syngas may be selectively controlled.

Abstract: Disclosed are a pyrrolidinium type sulphonated zwitterion, a method of preparing the same, a lithium salt prepared by using the same, a method of preparing the salt, an electrolytic composition containing the salt and a lithium secondary battery including the electrolytic composition. Since the pyrrolidinium type sulphonated zwitterions prepared according to the invention are thermally and electrochemically stable, the lithium salt prepared by using the same exhibits a lower hygroscopicity than the conventional lithium salts and strong thermal and electrochemical stabilities. When the lithium salt of the invention is dissolved in an organic solvent independently or together with the ionic liquid, excellent conductivity and electrochemical stability are exhibited. Accordingly, the lithium salt of the invention is very suitable for the electrolyte of the lithium secondary battery.

Abstract: The present invention relates to a solid oxide fuel cell for internal reforming of hydrocarbons and carbon dioxide, in particular, to a solid oxide fuel cell in which one side of solid oxide electrolyte (YSZ) is attached to an air electrode (La0.8Sr0.2MnO3) and its other side is attached to a catalyst electrode of Ni-YSZ type or perovskite type metal oxide. The electrochemical conversion system using the solid oxide fuel cell permits the occurrence of internal reforming of hydrocarbons and carbon dioxide concomitantly with the coproduction of a syngas and electricity, and overcomes the shortcomings associated with the catalytic deactivation due to carbon deposition and the high-energy consumption.

Abstract: The present invention relates to a structured catalyst for reforming of gasoline and a method of preparing the same, more particularly to a structured catalyst for reforming of gasoline for fuel-cell powered vehicles prepared by wash-coating the transition metal based reforming catalyst on the surface of the ceramic honeycomb support wash-coated with sub-micron sized alumina or its precursor to sufficiently increase the effective surface area and the performance of the catalyst and a method of preparing the same.

Abstract: Nitrogen trifluoride is produced with a high yield by the method comprising forming a fast stream of micro droplets of a fused ammonium fluoride salt by rapidly ejecting the fused ammonium fluoride salt into a reactor through a nozzle while circulating the fused ammonium fluoride salt in the reactor from a lower portion to an upper portion; and contacting micro droplets of the fused ammonium fluoride salt with fluorine gas sucked in the reactor through a suction pipe for fluorine by a negative pressure formed around the nozzle due to an ejection of the fused ammonium fluoride salt, whereby excessive generation and regional accumulation of the heat of reaction are prevented, reducing the reaction temperature by 10˜30° C. compared with those of the existing methods, and a side reaction occurs only to a slight extent according to the lowered reaction temperature.

Abstract: The present invention relates to a process for simultaneously preparing tetrafluoroethylene and hexafluoropropylene by the pyrolysis of difluorochloromethane mixed in the molar ratio of super-heated steam/pre-heated difluorochloromethane ([H2O]/[R22]) of 5-10 under the conditions such as a temperature of 730° C. to 760° C. and a residence time of 0.01 to 0.2 seconds, where the unreacted R22 and produced HFP are recycled and controlled to have an appropriate molar ratio of HFP/R22 of 0.01 to 0.1 in order to obtain a high yield of HFP. Thus, the pyrolysis process of the present invention is efficient for preparing TFE and HFP, which are essential monomers in fluorinated resin industry.

Abstract: A refrigerant composition that can be a substitute for chlorodifluoromethane (HCFC-22) comprises: (a) a first constituent of difluoromethane, (b) a second constituent of 1,1,1-trifluoroethane, (c) a third constituent of 1,1-difluoroethane, and (d) a fourth constituent selected from the group consisting of 1,1,1,2,3,3,3-heptafluoropropane, isobutane, 1,1,1,2,3,3-hexafluropropane and butane.

Abstract: The present invention relates to a process for simultaneously preparing tetrafluoroethylene and hexafluoropropylene by the pyrolysis of difluorochloromethane mixed in the molar ratio of super-heated steam/pre-heated difluorochloromethane ([H2O]/[R22]) of 5-10 under the conditions such as a temperature of 730° C. to 760° C. and a residence time of 0.01 to 0.2 seconds, where the unreacted R22 and produced HFP are recycled and controlled to have an appropriate molar ratio of HFP/R22 of 0.01 to 0.1 in order to obtain a high yield of HFP. Thus, the pyrolysis process of the present invention is efficient for preparing TFE and HFP, which are essential monomers in fluorinated resin industry.

Abstract: A refrigerant composition that can be a substitute for chlorodifluoromethane (HCFC-22) comprises: (a) a first constituent of difluoromethane, (b) a second constituent of 1,1,1-trifluoroethane, (c) a third constituent of 1,1-difluoroethane, and (d) a fourth constituent selected from the group consisting of 1,1,1,2,3,3,3-heptafluoropropane, isobutane, 1,1,1,2,3,3-hexafluropropane and butane.

Abstract: Nitrogen trifluoride is produced with a high yield by the method comprising forming a fast stream of micro droplets of a fused ammonium fluoride salt by rapidly ejecting the fused ammonium fluoride salt into a reactor through a nozzle while circulating the fused ammonium fluoride salt in the reactor from a lower portion to an upper portion; and contacting micro droplets of the fused ammonium fluoride salt with fluorine gas sucked in the reactor through a suction pipe for fluorine by a negative pressure formed around the nozzle due to an ejection of the fused ammonium fluoride salt, whereby excessive generation and regional accumulation of the heat of reaction are prevented, reducing the reaction temperature by 10˜30° C. compared with those of the existing methods, and a side reaction occurs only to a slight extent according to the lowered reaction temperature.