Provided herein are metal organic frameworks comprising metal nodes and N-donor organic ligands which have high selectivity and stability in the present of gases and vapors including H.sub.2S, H.sub.2O, and CO.sub.2. Methods include capturing one or more of H.sub.2S, H.sub.2O, and CO.sub.2 from fluid compositions, such as natural gas.

The present invention relates to a process for upgrading a petroleum product comprising mixing the petroleum product with an upgrading solution to provide a two-phase mixture consisting of an extract phase and a raffinate phase, wherein the upgrading solution comprises a pyrolysis oil and optionally a polar organic solvent. In other aspects, the invention provides an upgrading solution comprising a pyrolysis oil and optionally a polar organic solvent and uses thereof. Furthermore, an upgraded petroleum product and raffinate phase is provided.

There is described a process for producing biodiesel and related products from mixtures. There is also described a process for producing precursors and feedstock materials for producing biodiesel and related products. The processes use esterification and trans-esterification, separation and purification. Other process steps such as acidification and distillation can also be used.

The invention relates to a process (100) for producing liquefied natural gas using a feedstock mixture that contains at least methane, one or more components boiling at a temperature lower than methane and one or more hydrocarbons boiling at a temperature higher than methane, wherein the hydrocarbon(s) boiling at a temperature higher than methane comprise one or more hydrocarbons freezing at a higher temperature, with a freezing point higher than 50 C. According to the invention the feedstock mixture is fed into a pressure swing adsorption process (10), in which a first fraction containing methane and a second fraction containing methane are formed, the first fraction containing methane contains, in addition to the methane, at least the predominant portion of the components of the feedstock mixture that boil more readily than methane and is low in or free from the hydrocarbons boiling less readily than methane, and the second fraction containing methane contains, in addition to the methane, at least the predominant portion of the hydrocarbons from the feedstock that boil less readily than methane and is low in or free from the components that boil more readily than methane, and the first fraction containing methane, or a portion thereof, is supplied for liquefaction (20). The invention also relates to a corresponding plant.

Systems and methods for separating hydrocarbons on an internal combustion powered vehicle via one or more metal organic frameworks are disclosed. Systems and methods can further include utilizing separated hydrocarbons and exhaust to generate hydrogen gas for use as fuel.

The present invention generally relates to a process for responding to feed flow variations by changing the process cycle and thereby increasing the productivity and capacity of the system significantly over constant process systems. This increases the flexibility a PSA system for customers that do not require a constant or uniform product flow rate and/or for processes and applications that experience feed streams that vary in flow, temperature, and/or composition.

Primary, secondary (1,2) alkylethylenediamine- and alkylpropylenediamine-appended variants of metal-organic framework are provided for CO.sub.2 capture applications. Increasing the size of the alkyl group on the secondary amine enhances the stability to diamine volatilization from the metal sites. Two-step adsorption/desorption profiles are overcome by minimizing steric interactions between adjacent ammonium carbamate chains. For instance, the isoreticularly expanded framework Mg.sub.2(dotpdc) (dotpdc.sup.4=4,4-dioxido-[1,1:4,1-terphenyl]-3,3-dicarboxylate), yields diamine-appended adsorbents displaying a single CO.sub.2 adsorption step. Further, use of the isomeric framework Mg-IRMOF-74-II or Mg.sub.2(pc-dobpdc) (pc-dobpdc.sup.4=3,3-dioxidobiphenyl-4,4-dicarboxylate, pc=para-carboxylate) also leads to a single CO.sub.2 adsorption step with bulky diamines. By relieving steric interactions between adjacent ammonium carbamate chains, these frameworks enable step-shaped CO.sub.2 adsorption, decreased water co-adsorption, and increased stability to diamine loss. Variants of Mg.sub.2(dotpdc) and Mg.sub.2(pc-dobpdc) functionalized with large diamines such as N-(n-heptyl)ethylenediamine have utility as adsorbents for carbon capture applications.

This invention uses a fixed-bed adsorber, interchangeably called a capacitor herein, to process the product stream coming out of a regenerable adsorption system such as a temperature swing adsorption system (TSA) or pressure swing adsorption system (PSA). The fluid stream coming out of this fixed-bed capacitor will have a more uniform composition than the one entering the adsorption system or the capacitor. The fixed-bed adsorber operates in a once-through non-cyclic manner, similar to a conventional fixed bed reactor or adsorber.

A method for recovering sulfur within a gas processing system is described herein. The method includes contacting a natural gas stream including an acid gas with a solvent stream within a co-current contacting system to produce a sweetened natural gas stream and a rich solvent stream including an absorbed acid gas. The method also includes removing the absorbed acid gas from the rich solvent stream within a regenerator to produce a concentrated acid gas stream and a lean solvent stream. The method further includes recovering elemental sulfur from hydrogen sulfide (H.sub.2S) within the concentrated acid gas stream via a sulfur recovery unit.

The present disclosure is directed to a method for making a MER framework type zeolite, a MER framework type zeolite having a stick-like morphology, and processes for the selective separation of carbon dioxide (CO.sub.2) from multi-component feedstreams containing CO.sub.2 using the zeolite.