A method for separating mixed xylene includes steps that the mixed xylene is subjected to adsorption separation by means of an adsorbent having a metal organic framework material, so that one or more of xylene isomers are separated out. An organic ligand in the metal organic framework material is 2,5-dihydroxy-1,4-benzoquinone. Xylene isomers can be effectively separated using this method.

The present invention relates to the adsorbent for separating organochloride compound from liquid hydrocarbon and a process thereof, wherein said adsorbent is the silica and aluminosilicate composite having infiltrate structure subjected to the modification of the surface property with small metal having high electronegativity.

The present invention relates to the adsorbent for separating organochloride compound from liquid hydrocarbon and a process thereof, wherein said adsorbent is the silica and aluminosilicate composite having infiltrate structure subjected to the modification of the surface property with small metal having high electronegativity.

A portable pressure swing adsorption system and method for fuel gas conditioning. A fuel gas conditioning system includes a pressure swing adsorption (PSA) system fluidly coupled to a compressed rich gas stream, the PSA system including a plurality of adsorbent beds and configured to condition the compressed rich natural gas stream and produce therefrom a high-quality fuel gas and gaseous separated heavier hydrocarbons, a product end of the adsorbent beds fluidly coupled to a fuel gas line, and a feed end of the adsorbent beds configured to be fluidly coupled to the compressed rich natural gas stream or a raw natural gas stream, wherein the produced gaseous separated heavier hydrocarbons are desorbed at at least 50 psia and recirculated into the rich natural gas stream or the raw natural gas stream without post-desorption compression.

A portable pressure swing adsorption system and method for fuel gas conditioning. A fuel gas conditioning system includes a pressure swing adsorption (PSA) system fluidly coupled to a compressed rich gas stream, the PSA system including a plurality of adsorbent beds and configured to condition the compressed rich natural gas stream and produce therefrom a high-quality fuel gas and gaseous separated heavier hydrocarbons, a product end of the adsorbent beds fluidly coupled to a fuel gas line, and a feed end of the adsorbent beds configured to be fluidly coupled to the compressed rich natural gas stream or a raw natural gas stream, wherein the produced gaseous separated heavier hydrocarbons are desorbed at at least 50 psia and recirculated into the rich natural gas stream or the raw natural gas stream without post-desorption compression.

Various illustrative embodiments of a system and process for recovering high-quality biomethane and carbon dioxide product streams from biogas sources and utilizing or sequestering the product streams are provided. The system and process synergistically yield a biomethane product which meets gas pipeline quality specifications and a carbon dioxide product of a quality and form that allows for its transport and sequestration or utilization and reduction in greenhouse gas emissions. The system and process result in improved access to gas pipelines for products, an improvement in the carbon intensity rating of the methane fuel, and improvements in generation of credits related to reductions in emissions of greenhouse gases.

Various illustrative embodiments of a system and process for recovering high-quality biomethane and carbon dioxide product streams from biogas sources and utilizing or sequestering the product streams are provided. The system and process synergistically yield a biomethane product which meets gas pipeline quality specifications and a carbon dioxide product of a quality and form that allows for its transport and sequestration or utilization and reduction in greenhouse gas emissions. The system and process result in improved access to gas pipelines for products, an improvement in the carbon intensity rating of the methane fuel, and improvements in generation of credits related to reductions in emissions of greenhouse gases.

A permanently porous vanadium(II)-containing metal-organic framework (MOF) with vanadium(II) centers and methods for synthesis of such MOF frameworks are provided. Methods for using such compounds to selectively react with N.sup.2 over CH.sub.4 are provided. In the synthetic methods, a vanadium source, such as VY.sub.2(tmeda).sub.2, where Y is a halogen and tmeda is N,N,N′,N′-tetramethylethane-1,2-diamine and a H.sub.2(ligand) are reacted in the presence of acid in a solvent at between 110° C. and 130° C. to form an intermediate product. The intermediate product is collected and washed with a washing agent, such as DMF and acetonitrile, and the vanadium(II) based MOF is activated by heating the washed intermediate product to at least 160° C. under dynamic vacuum.

A permanently porous vanadium(II)-containing metal-organic framework (MOF) with vanadium(II) centers and methods for synthesis of such MOF frameworks are provided. Methods for using such compounds to selectively react with N.sup.2 over CH.sub.4 are provided. In the synthetic methods, a vanadium source, such as VY.sub.2(tmeda).sub.2, where Y is a halogen and tmeda is N,N,N′,N′-tetramethylethane-1,2-diamine and a H.sub.2(ligand) are reacted in the presence of acid in a solvent at between 110° C. and 130° C. to form an intermediate product. The intermediate product is collected and washed with a washing agent, such as DMF and acetonitrile, and the vanadium(II) based MOF is activated by heating the washed intermediate product to at least 160° C. under dynamic vacuum.

A permanently porous vanadium(II)-containing metal-organic framework (MOF) with vanadium(II) centers and methods for synthesis of such MOF frameworks are provided. Methods for using such compounds to selectively react with N.sup.2 over CH.sub.4 are provided. In the synthetic methods, a vanadium source, such as VY.sub.2(tmeda).sub.2, where Y is a halogen and tmeda is N,N,N′,N′-tetramethylethane-1,2-diamine and a H.sub.2(ligand) are reacted in the presence of acid in a solvent at between 110° C. and 130° C. to form an intermediate product. The intermediate product is collected and washed with a washing agent, such as DMF and acetonitrile, and the vanadium(II) based MOF is activated by heating the washed intermediate product to at least 160° C. under dynamic vacuum.