Refrigeration systems with a purge for removing non-condensables from the refrigerant and an acid filter for remove acid from the refrigerant are provided. The acid filter can be operatively connected to the purge. Optionally, the purge can include a separating device for separating non-condensable gases from condensable refrigerant gases and an acid filter is provided to remove acid from the condensable refrigerant gases.

Process for preparing a catalyst or a trapping mass comprising the following steps: bringing a porous oxide support into contact with a metal salt comprising at least one metal belonging to groups VIB, VIIB, VIIIB, IB or IIB, of which the melting point of said metal salt is between 20° C. and 150° C., for a period of between 5 minutes and 5 hours in order to form a solid mixture, the weight ratio of said metal salt to said porous oxide support being between 0.1 and 1; heating the solid mixture with stirring at a temperature between the melting point of said metal salt and 200° C. and for 5 minutes to 12 hours; calcining the solid obtained in the preceding step at a temperature above 200° C. and below or equal to 1100° C. under an inert atmosphere or under an oxygen-containing atmosphere.

Apparatus and methods are disclosed. The apparatus comprises: an abatement chamber of an abatement apparatus which treats an effluent stream from a semiconductor processing tool to provide a combusted effluent stream having effluent particles; and a first atomiser located downstream of the abatement chamber, the first atomiser being configured to produce droplets having a droplet size based on a particle size of the effluent particles to be removed from the combusted effluent stream. In this way, the atomizer may produce droplets which combine with or adhere to the effluent particles which assists in the removal of the effluent particles from the combusted effluent stream.

A long-effect self-cleaning negative-pressure ejector at least comprises a suction chamber, a jet pipe and a flushing member. A side wall of the suction chamber has at least one suction port for communicating with a first fluid pipeline. An exit port of the jet pipe is disposed in the suction chamber and ejects a second fluid so that a negative pressure is generated in the suction chamber, a first fluid in the first fluid pipeline obliquely enters the suction chamber, and a first included angle is between a direction in which the first fluid being sucked into the suction chamber and an ejection direction of the second fluid. The flushing member optionally provides a third fluid to flush the suction chamber and/or the first fluid pipeline. At least one air jet nozzle is disposed on the first fluid pipeline to inject gas into the first fluid pipeline.

A wet scrubber at least comprises a treatment tank, a jet pipe, a gas-liquid separation component, and a spray component. The treatment tank is used to contain a cleaning solution. The jet pipe is disposed in the treatment tank, by injecting the cleaning solution to suck in an exhaust gas, and mixing the cleaning solution with the exhaust gas, and directly injecting into the cleaning solution contained in the treatment tank, thereby forming a plurality of microbubbles in the cleaning solution to dissolve the exhaust gas and capture solid particles in the exhaust gas. The gas-liquid separation component is used to filter and block water mist raised in the cleaning solution. The spray component is used to prevent the solid particles from clogging the gas-liquid separation component.

The present description relates to a process for producing magnesium metal from dihydrate magnesium chloride comprising the steps of dehydrating MgCI.sub.2.2H.sub.2O with anhydrous hydrochloric acid (HCI) to obtain anhydrous magnesium chloride in an inert environment, releasing the mixture of hydrous HCI and protection gas; and electrolyzing the anhydrous magnesium chloride in an electrolytic cell fed with hydrogen gas under free oxygen atmosphere content, wherein magnesium metal and anhydrous hydrogen chloride are produced, wherein a part of the hydrous HCI is passed through a scrubbing unit to obtain a hydrochloric acid solution, the other part of the hydrochloric chloride gas is dehydrated by contact with a desiccant agent in a drying unit to produce anhydrous HCI, and wherein the anhydrous HCI produced by at least one of the electrolytic cell and the drying unit is reused to dehydrate the of MgCI.sub.2.2H.sub.2O.

Membranes, methods of making the membranes, and methods of using the membranes are described herein. The membrane can include a support layer, and a selective polymer layer disposed on the support layer. The selective polymer layer can include a selective polymer matrix (e.g., hydrophilic polymer, a cross-linking agent, an amino compound, a CO.sub.2-philic ether, or a combination thereof), and optionally graphene oxide dispersed within the selective polymer matrix. The membranes can be used to separate carbon dioxide from hydrogen. Also provided are methods of purifying syngas using the membranes described herein.

Provided herein are gas permeable membranes comprising an amine-containing selective layer on top of a gas permeable polymer support as well as methods of making and using thereof. The membranes are useful for the separation of CO.sub.2 from N.sub.2-containing gases.

Membranes, methods of making the membranes, and methods of using the membranes are described herein. The membranes can comprise a gas permeable support and a continuous phase comprising a selective inorganic material disposed within the gas permeable support. In some embodiments, the membranes can exhibit a CO.sub.2:N.sub.2 selectivity of at least 10 at 24° C. The membranes can be bendable, such that when the membranes are wrapped around a 1.5-inch diameter cylinder and returned to a planar conformation, the CO.sub.2:N.sub.2 selectivity of the membranes is at least 25% of the CO.sub.2:N.sub.2 selectivity of the membranes prior to having been wrapped around the cylinder.

A hydrated lime product exhibiting superior reactivity towards HCl and SO.sub.2 in air pollution control applications. Also disclosed is a method of providing highly reactive hydrated lime and the resultant lime hydrate where an initial lime feed comprising calcium and impurities is first ground to a particle-size distribution with relatively course particles. Smaller particles are then removed from this ground lime and the smaller particles are hydrated and flash dried to form a hydrated lime, which is then milled to a significantly smaller particle size than that of the relatively course particles. The resultant lime hydrate product has available CaOH of greater than 92%, a citric acid reactivity of less than 20 seconds, a BET surface area greater than 18, a D90 less than 10 μm, a D50 less than 4 μm, a D90/D50 less than 3, and a large pore volume of greater than 0.2 BJH.