Patent classifications
B01J12/00
PROCESS, REACTOR AND SYSTEM FOR FABRICATION OF FREE-STANDING TWO-DIMENSIONAL NANOSTRUCTURES USING PLASMA TECHNOLOGY
The present invention relates to a process, reactor and system to produce self-standing two-dimensional nanostructures, using a microwave-excited plasma environment. The process is based on injecting, into a reactor, a mixture of gases and precursors in stream regime. The stream is subjected to a surface wave electric field, excited by the use of microwave power which is introduced into a field applicator, generating high energy density plasmas, that break the precursors into its atomic and/or molecular constituents. The system comprises a plasma reactor with a surface wave launching zone, a transient zone with a progressively increasing cross-sectional area, and a nucleation zone. The plasma reactor together with an infrared radiation source provides a controlled adjustment of the spatial gradients, of the temperature and the gas stream velocity.
Process and a system for hydrocarbon steam cracking
A process for steam cracking hydrocarbon feedstock in a steam cracking furnace, the process comprising superheating hydrocarbon feedstock using flue gas from a radiant section of the steam cracking furnace in hydrocarbon feedstock superheating means or the hydrocarbon feedstock superheater, superheating steam from the steam generator using the flue gas from the radiant section of the steam cracking furnace in second heat exchanging means or a second heat exchanger, steam cracking the super-heated hydrocarbon feedstock from the hydrocarbon feedstock superheating means or the hydrocarbon feedstock superheater into cracked gas in a fired tubular reactor, vaporizing the hydrocarbon feedstock, using hydrocarbon feedstock vaporizing means, wherein the hydrocarbon feedstock vaporizing means or the hydrocarbon feedstock vaporizer are heated with a heat transfer medium having a temperature less than or equal to 350° C. and feeding the vaporized hydrocarbon feedstock to the steam cracking furnace.
Apparatus for converting a feed gas into a product gas
Apparatus for converting feed gas (28) into a product gas (29), comprising at least one reactor (1) with a reaction chamber (15) bounded by the inner wall of an outer tube (4) closed at a first outer end and an inner tube (14) received coaxially in this outer tube (4) and provided at both its outer ends with openings, which reactor (1) is provided with an inlet chamber (11) and with an outlet chamber (10), wherein a first wall (31) of the outlet chamber (10) encloses the outer tube (4) and extends therefrom, and a second wall (12) of the outlet chamber (10) lying opposite the first wall (31) encloses the outer tube (4) and extends therefrom, and the inlet chamber (11) is bounded by the second wall (12) of the outlet chamber (10) and a third wall (47) which lies opposite this second wall (12), encloses the outer tube (4) and extends therefrom.
COMBUSTION CHAMBER HOT FACE REFRACTORY LINING
A refractory lining in a combustion chamber operating in a reducing atmosphere. The lining includes at least one or more Zirconia (Zr)-based refractory lining members comprising one or more Zr-based parts. The Zr-based parts comprise at least 90 wt. %, preferably at least 95 wt. %, of monoclinic ZrO.sub.2 and/or partially stabilized ZrO.sub.2 and/or fully stabilized ZrO.sub.2, wherein the total content of tetragonal and cubic ZrO.sub.2 amounts to at least 20 wt. %, preferably more than 35 wt. %, as well as Zr based refractory lining members and methods for manufacturing the Zr based refractory lining members.
SYNTHESIS METHOD FOR HIGHLY SELECTIVE 2-METHYLALLYL CHLORIDE AND SYNTHESIS REACTOR THEREOF
The present invention relates to a synthesis method and synthesis reactor of high-selectivity 2-methylallyl chloride by taking isobutylene and chlorine gas as raw materials and performing a gas-phase chlorination reaction in a microchannel reactor with a cooling surface. The isobutylene and the chlorine gas are reacted in a T-shaped microchannel reactor, and the mixing speed is extremely fast. Meanwhile, the huge heat exchange area per unit volume can ensure that the reaction proceeds stably at a substantially constant temperature and has good controllability. Therefore, side reactions caused by excessive local temperature can be effectively suppressed, the reaction selectivity is high, and no coking phenomenon occurs.
CRACKER MODULAR PROCESSING FACILITY
The various processes of an ethane cracker plant may be segmented into separate process blocks, which may be interconnected using fluid conduits and/or electrical connections. These process blocks may be directly connected, for example without an external piperack or other external piping interconnecting process blocks. Each process block may be formed of one or more modules The process blocks can include an ethane cracking furnace, a steam generation process, a water stripper, a water quench, a compression, a caustic scrubber, a drier, a deethanizer, an acetylene conversion, a demethanizer, a refrigerator, or a splitter.
PROCESS FOR CONVERTING ALKANES TO OLEFINS
A process and apparatus for converting an alkane to an olefin. In one embodiment, the process involves oxidative coupling of an alkane, e.g., methane, with an oxidant, such as air, to produce an olefin having twice the number of carbon atoms as the alkane, e.g., ethylene. In another embodiment, the process involves oxidative dehydrogenation of an alkane, e.g., ethane, with an oxidant to form an olefin having the same number of carbon atoms as the alkane, e.g., ethylene. The process involves passing a flow of the oxidant from a first flow passage through a porous medium; diffusing a flow of the alkane from a second flow passage into the porous medium; and contacting the reactant alkane and the oxidant in the presence of a catalyst within the porous medium to produce the olefin.
HEAT INTEGRATED REFORMER WITH CATALYTIC COMBUSTION FOR HYDROGEN PRODUCTION
An apparatus for the production of hydrogen from a fuel source includes a combustor configured to receive a combustor fuel and convert the combustor fuel into a combustor heat; a reformer disposed annularly about the combustor, a removable structured catalyst support disposed within the gap and coated with a catalyst to induce combustor fuel combustion reactions that convert the combustor fuel to the combustor heat, and a combustor fuel injection aperture configured for mixing combustion fuel into the combustion catalyst. The combustor fuel injection aperture being disposed along a length of the combustion zone. The reformer and the combustor define a gap therebetween and the reformer is configured to receive the combustor heat.
COMBUSTION CHAMBER HOT FACE REFRACTORY LINING
A method for producing a refractory lining in a combustion chamber operating in a reducing atmosphere. The lining includes at least one or more Zirconia (Zr)-based refractory lining members comprising one or more Zr-based parts. The Zr-based parts comprise at least 90 wt. %, preferably at least 95 wt. %, of monoclinic ZrO.sub.2 and/or partially stabilized ZrO.sub.2 and/or fully stabilized ZrO.sub.2, wherein the total content of tetragonal and cubic ZrO.sub.2 amounts to at least 20 wt. %, preferably more than 35 wt. %, as well as Zr based refractory lining members and methods for manufacturing the Zr based refractory lining members.
METHOD FOR OPERATING A REACTOR FACILITY
A method for operating a reactor facility for equilibrium-limited reactions, includes: converting starting materials to a product in a reaction chamber under a pressure p1, wherein an absorbent is loaded with the product and absorbs starting materials; discharging the loaded absorbent from the reaction chamber; lowering the pressure of the absorbent to a pressure p2 which is lower than pressure p1 and the product and starting materials are discharged in the gaseous state from the liquid absorbent; separating the gaseous products by condensation from the gaseous starting materials at the same time as a pressure p3 higher than pressure p1 is applied to the liquid absorbent, under pressure p3 into a liquid jet gas compressor in which the gaseous starting materials separated from the products are aspirated and dissolved in the liquid absorbent; and then introduced under pressure p4, which is lower than pressure p3, into the reaction chamber.