The present disclosure provides cassettes for use in automated cell engineering systems that include cell concentration filters for reducing fluid volume of a cell sample during or following automated processing. The disclosure also provides methods of concentrating a cell population, as well as automated cell engineering systems that can utilize the cassettes and carry out the methods.

The present disclosure provides cassettes for use in automated cell engineering systems that include cell concentration filters for reducing fluid volume of a cell sample during or following automated processing. The disclosure also provides methods of concentrating a cell population, as well as automated cell engineering systems that can utilize the cassettes and carry out the methods.

A gas separation membrane, a method for making the gas separation membrane, and a method for using the gas separation membrane are provided. An exemplary gas separation membrane includes a polyether-block-polyamide (PEBA) matrix and a cross-linked network including functionalized polyhedral oligomeric silsesquioxane (POSS) nanoparticles dispersed through the PEBA matrix.

M(SiF.sub.6)(pyz).sub.3 (M=Cu, Zn, Co, or Ni) has a pore size between a size of H.sub.2 and a size of CO.sub.2, and thus exhibits prominent screening performance for H.sub.2/CO.sub.2. A strong interaction between Cu(SiF.sub.6)(bpy).sub.2 and a CO.sub.2 molecule can hinder the transport of the CO.sub.2 molecule. The above two MOFs both can achieve the H.sub.2/CO.sub.2 separation. By preparing a dense MSiF.sub.6/polymer layer, MSiF.sub.6 is uniformly dispersed in the polymer and is fixed, and subsequently, MSiF.sub.6 is converted into M(SiF.sub.6)(pyz).sub.3 or Cu(SiF.sub.6)(bpy).sub.2 by interacting with an organic ligand. Through vapor-induced in-situ conversion, MOF particles can be well dispersed without interface defects between the MOF particles and the polymer. Even at a doping amount of 80%, the mechanical flexibility and stability of the MMM can still be retained.

The extraction of benzene from benzene/cyclohexane mixture described herein is a process that removes benzene from a benzene/cyclohexane mixture with high selectivity, resulting in an enriched cyclohexane content in the retentate. The process involves adding an aqueous solution of poloxamer 188 to the benzene/cyclohexane mixture and waiting for the mixture to partition into an organic layer above an aqueous layer. Benzene, being more polar than cyclohexane, is selectively drawn into the aqueous layer. Benzene is then removed from the aqueous layer by pervaporation through a composite PDMS (polydimethylsiloxane)/polystyrene membrane. Cyclohexane is recovered from the retentate by drawing off the organic layer of the retentate by any known method. About 97% of benzene has been removed from a 50-50 wt % mixture by pervaporation in the static mode, and about 99% by pervaporation in the continuous mode.

An energy efficient process for NGL recovery and production of compressed natural gas (CNG) in which natural gas is fed to a first gas separation membrane-based separation stage where it is separated into a permeate and a retentate. The high C.sub.3+ concentration first stage permeate is chilled and separated to provide liquid phase NGL and a gaseous phase. The first stage retentate is separated at a second gas membrane-based separation stage to produce a retentate meeting pipeline specifications for CNG (including hydrocarbon dewpoint) and a permeate that is recycled to the first stage. The gaseous phase, constituting a low BTU fuel, may be used in on-site power generation equipment and/or in internal combustion engines. The second stage permeate (and optionally the third stage retentate) is (are) recycled back to the first stage to enhance the production of NGL and CNG. The gaseous phase may instead be fed to a third stage to produce a third permeate and a third residue, in which case the third permeate is recycled to the first stage and the third retentate is a low BTU fuel which may be used in on-site power generation equipment and/or in internal combustion engines.

The present invention relates to a separation membrane including a thermoplastic polymer selected from a cellulose ester and a polyamide, in which, when regions obtained by dividing a cross-sectional surface perpendicular to a longitudinal direction of the separation membrane into 5 at an equal interval are defined as regions 1 to 5, all the regions 1 to 5 have a number average pore diameter changing rate α.sub.i of −0.25 to 0.25, and at least one of the regions 1 to 5 is a region P that satisfies conditions (a) and (b): (a) a value of area average pore diameter D.sub.s/number average pore diameter D.sub.n is 2.50 to 6.00; and (b) a number average W of fine pores that are located at a distance smaller than L.sub.a from a center of respective coarse pores is 10 to 30.

The present invention relates to a separation membrane including a thermoplastic polymer selected from a cellulose ester and a polyamide, in which, when regions obtained by dividing a cross-sectional surface perpendicular to a longitudinal direction of the separation membrane into 5 at an equal interval are defined as regions 1 to 5, all the regions 1 to 5 have a number average pore diameter changing rate α.sub.i of −0.25 to 0.25, and at least one of the regions 1 to 5 is a region P that satisfies conditions (a) and (b): (a) a value of area average pore diameter D.sub.s/number average pore diameter D.sub.n is 2.50 to 6.00; and (b) a number average W of fine pores that are located at a distance smaller than L.sub.a from a center of respective coarse pores is 10 to 30.

A thin film composite gas separation membrane comprising a polyether block amide copolymer coating layer and a nanoporous asymmetric support membrane with nanopores on the skin layer surface of the support membrane and gelatin polymers inside the nanopores on the skin layer surface of the support membrane. A method for making the thin film composite gas separation membrane is provided as well as the use of the membrane for a variety of separations such as separations of hydrogen sulfide and carbon dioxide from natural gas, carbon dioxide removal from flue gas, fuel gas conditioning, hydrogen/methane, polar molecules, and ammonia mixtures with methane, nitrogen or hydrogen and other light gases separations, but also for natural gas liquids recovery and hydrogen sulfide and carbon dioxide removal from natural gas in a single step.

A thin film composite gas separation membrane comprising a polyether block amide copolymer coating layer and a nanoporous asymmetric support membrane with nanopores on the skin layer surface of the support membrane and gelatin polymers inside the nanopores on the skin layer surface of the support membrane. A method for making the thin film composite gas separation membrane is provided as well as the use of the membrane for a variety of separations such as separations of hydrogen sulfide and carbon dioxide from natural gas, carbon dioxide removal from flue gas, fuel gas conditioning, hydrogen/methane, polar molecules, and ammonia mixtures with methane, nitrogen or hydrogen and other light gases separations, but also for natural gas liquids recovery and hydrogen sulfide and carbon dioxide removal from natural gas in a single step.