A process is provided to separate a hydrocarbon stream comprising a mixture of light olefins and light paraffins, the process comprising sending the hydrocarbon stream through a pretreatment unit to remove impurities selected from the group consisting of sulfur compounds, arsine, phosphine, methyl acetylene, propadiene, and acetylene to produce a treated hydrocarbon stream; vaporizing the treated hydrocarbon stream to produce a gaseous treated hydrocarbon stream; adding liquid or vapor water to the gaseous treated hydrocarbon stream; then contacting the gaseous treated hydrocarbon stream to a membrane in a membrane system comprising one or more membrane units to produce a permeate stream comprising about 96 to 99.9 wt % light olefins and a retentate stream comprising light paraffins.

A photo sensitive variable hydrophilic membrane includes a membrane substrate, and a photocatalyst layer deposited on the membrane substrate and including an oxide, wherein a hydrophilic property of the photocatalyst layer is increased when a light is irradiated and a method of the same are provided.

Described are SCR catalyst systems comprising a first SCR catalyst composition and a second SCR catalyst composition arranged in the system, the first SCR catalyst composition promoting higher N.sub.2 formation and lower N.sub.2O formation than the second SCR catalyst composition, and the second SCR catalyst composition having a different composition than the first SCR catalyst composition, the second SCR catalyst composition promoting lower N.sub.2 formation and higher N.sub.2O formation than the first SCR catalyst composition. The SCR catalyst systems are useful in methods and systems to catalyze the reduction of nitrogen oxides in the presence of a reductant.

In this disclosure, a process of recycling acid, base and the salt reagents required in the Li recovery process is introduced. A membrane electrolysis cell which incorporates an oxygen depolarized cathode is implemented to generate the required chemicals onsite. The system can utilize a portion of the salar brine or other lithium-containing brine or solid waste to generate hydrochloric or sulfuric acid, sodium hydroxide and carbonate salts. Simultaneous generation of acid and base allows for taking advantage of both chemicals during the conventional Li recovery from brines and mineral rocks. The desalinated water can also be used for the washing steps on the recovery process or returned into the evaporation ponds. The method also can be used for the direct conversion of lithium salts to the high value LiOH product. The method does not produce any solid effluent which makes it easy-to-adopt for use in existing industrial Li recovery plants.

In this disclosure, a process of recycling acid, base and the salt reagents required in the Li recovery process is introduced. A membrane electrolysis cell which incorporates an oxygen depolarized cathode is implemented to generate the required chemicals onsite. The system can utilize a portion of the salar brine or other lithium-containing brine or solid waste to generate hydrochloric or sulfuric acid, sodium hydroxide and carbonate salts. Simultaneous generation of acid and base allows for taking advantage of both chemicals during the conventional Li recovery from brines and mineral rocks. The desalinated water can also be used for the washing steps on the recovery process or returned into the evaporation ponds. The method also can be used for the direct conversion of lithium salts to the high value LiOH product. The method does not produce any solid effluent which makes it easy-to-adopt for use in existing industrial Li recovery plants.

Provided are catalytic assemblies which include a hollow fiber membrane permeable to a gas; a reactive coating permeable to the gas and a contaminant; and a plurality of catalytic nanoparticles embedded in the reactive coating adapted to catalyze a reaction between the gas and the contaminant. Also provided are preparation methods for the catalytic assemblies, and use thereof for treating contaminated water.

In this disclosure, a process of recycling acid, base and the salt reagents required in the Li recovery process is introduced. A membrane electrolysis cell which incorporates an oxygen depolarized cathode is implemented to generate the required chemicals onsite. The system can utilize a portion of the salar brine or other lithium-containing brine or solid waste to generate hydrochloric or sulfuric acid, sodium hydroxide and carbonate salts. Simultaneous generation of acid and base allows for taking advantage of both chemicals during the conventional Li recovery from brines and mineral rocks. The desalinated water can also be used for the washing steps on the recovery process or returned into the evaporation ponds. The method also can be used for the direct conversion of lithium salts to the high value LiOH product. The method does not produce any solid effluent which makes it easy-to-adopt for use in existing industrial Li recovery plants.

A process is provided to separate a hydrocarbon stream comprising a mixture of light olefins and light paraffins, the process comprising sending the hydrocarbon stream through a pretreatment unit to remove impurities selected from the group consisting of sulfur compounds, arsine, phosphine, methyl acetylene, propadiene, and acetylene to produce a treated hydrocarbon stream; vaporizing the treated hydrocarbon stream to produce a gaseous treated hydrocarbon stream; adding liquid or vapor water to the gaseous treated hydrocarbon stream; then contacting the gaseous treated hydrocarbon stream to a membrane in a membrane system comprising one or more membrane units to produce a permeate stream comprising about 96 to 99.9 wt % light olefins and a retentate stream comprising light paraffins.

An ultra-thin anion exchange membrane incorporates functional additives to provide improved water management. Without the functional additives the ultra-thin membrane may have high cross-over and not be effective for many applications. A composite anion exchange membrane includes a porous scaffold support such as a porous polymer. The anion exchange polymer may be coupled to the porous scaffold, such as by being imbibed into the pores of the porous scaffold. The functional additives may contribute to increase water production, water retention, back-diffusion and reduce the gas crossover. A functional additive may include a reactive species, including a catalyst that reacts with oxygen or hydrogen, a plasticizer, a hygroscopic material and/or a radical scavenger.

A porous composite includes a porous base material and a porous collection layer provided on a collection surface of the base material. The collection layer includes particles deposited in pores of the collection surface. In a plan view of the collection surface, the proportion of the area of a covered region that is covered with the collection layer out of the collection surface is less than or equal to 70%, and the proportion of the area of a pore region out of a non-covered region that is not covered with the collection layer is less than or equal to 15%.