Patent classifications
B01D2258/02
APPARATUS AND METHOD FOR CONVERTING TOXIC GAS OF STERILIZATION PROCESSES TO BENIGN SUBSTANCES
An apparatus for converting a toxic gas to benign substances comprises a housing characterized with multi-stages including a first stage, a second stage, a third stage and a fourth stage coupled to one another in sequence, wherein the first stage comprises a catalytic system configured to convert the toxic gas into its derivatives; the second stage comprises a carbonaceous fibrous material adapted to capture the remaining toxic gas and the derivatives; the third stage comprises at least one oxidizer to oxidize the remaining toxic gas to benign substances including CO.sub.2 and water; and the fourth stage comprises a scrubber configured to remove all of volatile organic compounds or water molecules generated as part of the first and third stages.
Processes and systems for producing light olefins and aromatics from a mixed plastics stream
Methods and systems for producing aromatics and light olefins from a mixed plastics stream are described. The method may include feeding a plastic feedstock to a dechlorination operation to melt the plastic feedstock to release HCl and generate a liquid plastic stream; feeding the liquid plastic stream to a pyrolysis reactor, the pyrolysis reactor to generate hydrocarbon vapors; feeding the hydrocarbon vapors to an acid gas removal reactor with a solid inorganic alkali salt disposed within the reaction vessel to remove residual HCl and sulfur-containing compounds from the hydrocarbon vapors to generate a plastic derived oil; and feeding the plastic derived oil to a steam enhanced catalytic cracking reactor to generate a product stream comprising light olefins having a carbon number of C.sub.2-C.sub.4 and aromatics. The associated system for processing mixed plastics into aromatics and light olefins is also described.
EVAPORATIVE FUEL VAPOR EMISSION CONTROL SYSTEMS
An evaporative emission control canister system comprises an initial adsorbent volume having an effective incremental adsorption capacity at 25° C. of greater than 35 grams n-butane/L between vapor concentration of 5 vol % and 50 vol % n-butane, and at least one subsequent adsorbent volume having an effective incremental adsorption capacity at 25° C. of less than 35 grams n-butane/L between vapor concentration of 5 vol % and 50 vol % n-butane, an effective butane working capacity (BWC) of less than 3 g/dL, and a g-total BWC of between 2 grams and 6 grams. The evaporative emission control canister system has a two-day diurnal breathing loss (DBL) emissions of no more than 20 mg at no more than 210 liters of purge applied after the 40 g/hr butane loading step.
METHOD FOR THE DRY FILTRATION OF A GAS FLOW CARRYING FOREIGN OBJECTS, AND FILTER DEVICE FOR CLEANING RAW GAS CARRYING FOREIGN OBJECTS
A method and a filter device for the dry filtration of a gas flow carrying foreign objects in a filter device for purifying waste gas produced in additive manufacturing technologies, conducting a raw gas flow containing foreign objects into a raw gas space of a filter unit having at least one filter surface separating a raw gas side from a clean gas side, feeding oxidant to a reaction region located on the raw gas side of the filter surface downstream of the filter surface, such that foreign objects contained in material cleaned off from the filter surface and/or in the raw gas flow react with the oxidant in the reaction region to form foreign objects containing oxides.
Methods for optimizing gas utilization
The invention provides for the optimal utilization of gas by a fermentation process, whereby the various components within the gas stream are separated to increase the efficiency of the microorganisms. The invention is capable of tailoring the composition of the gas being used by the fermentation process so as to enhance the production of various products. The invention is capable of applying such controlled separation and utilization of gas to produce different products in two parallel fermentation processes. The invention is also capable of applying such controlled separation and utilization of gas to produce one product in a first fermentation process, which may be converted to a different product in a second fermentation process. The invention is additionally capable of mitigating culture inhibition.
Polluted CO.SUB.2 .capturing with lime produced from phosphogypsum calcination using sulfur as non-CO.SUB.2 .fuel
A new integrated method to capture polluted CO.sub.2 using CaO produced from phosphogypsum calcination using sulfur as non-CO.sub.2 fuel where (1) both pollutants of phosphogypsum and CO.sub.2 are transformed into environmentally neutral or useful products such as limestone or clinker and sulfuric acid; (2) low-CO.sub.2 CaO produced from calcination of phosphogypsum with sulfur as fuel can be used to produce low-CO.sub.2 clinker that replaces the use of high-CO.sub.2 limestone as raw material; (3) the use of sulfur as fuel to calcine phosphogypsum allows the production of low-cost sulfuric acid.
A NOBLE GAS RECOVERY SYSTEM
A system comprising a pumping system configured to pump respective exhaust gases from each of a plurality of chemical etching process chambers and to combine the exhaust gases to provide a combined exhaust gas, and a noble gas recovery system configured to process the combined exhaust gas to remove one or more noble gases therefrom.
Systems and methods for managing hydrocarbon emissions
A system for reducing the release of hydrocarbons emitted from a hydrocarbon source into the atmosphere includes a hydrocarbon supply conduit configured to receive the emitted hydrocarbons. In addition, the system includes an air supply conduit coupled to an air source. Further, the system includes a combustion device coupled to an outlet end of the hydrocarbon supply conduit and an outlet end of the air supply conduit. The combustion device is configured to receive the hydrocarbons from the hydrocarbon supply conduit and the air from the air supply conduit, and combust the hydrocarbons. Still further, the system includes a catalytic converter spaced apart from the combustion device and a transfer conduit extending from an outlet of the combustion device to an inlet of a catalytic converter. The catalytic converter is configured to receive the combustion products and any un-combusted hydrocarbons from the transfer conduit, and oxidize the un-combusted hydrocarbons.
MOLECULAR SIEVE COMPLEX, COMPOSITE MATERIAL AND APPLICATION THEREOF
A molecular sieve complex contains an oxide of aluminum, an oxide of an alkaline earth metal and a rare earth-modified molecular sieve. The rare earth-modified molecular sieve is a molecular sieve doped by a rare earth element. The percentage of the pore volume occupied by pores of 3 nm or less to the total pore volume in the molecular sieve complex is greater than or equal to 63.5%. The content of the rare earth element and the contents of the oxide of aluminum, the oxide of the alkaline earth metal and the molecular sieve satisfy a certain relationship. The composite material contains a molecular sieve complex and an auxiliary agent loaded on the molecular sieve complex, and the composite material may be applied to flue gas adsorption and desulfurization.
Supported catalyst for organic substance decomposition and organic substance decomposing apparatus
A supported catalyst for decomposing an organic substance that includes a carrier and catalyst particles supported on the carrier. The catalyst particles contain a perovskite-type composite oxide represented by A.sub.xB.sub.yM.sub.zO.sub.w, where A contains at least one of Ba and Sr, B contains Zr, M is at least one of Mn, Co, Ni, and Fe, y+z=1, x>1, z<0.4, and w is a positive value that satisfies electrical neutrality. An organic substance decomposition rate after the supported catalyst is subjected to a heat treatment at 950° C. for 48 hours is greater than 0.97 when the organic substance decomposition rate before the heat treatment is regarded as 1, and an amount of the catalyst particles peeled off when the supported catalyst is ultrasonicated in water at 28 kHz and 220 W for 15 minutes is less than 1 wt % of the catalyst particles before untrasonication.