Sorbent materials comprising a nanofiber composite including a polymeric material defining a continuous phase and at least one metal organic framework (MOF) material defining a discontinuous phase are provided. The at least one MOF material is dispersed throughout the continuous phase of the polymeric material. Fibrous mats comprising the sorbent materials are also provided. Water harvesting devices utilizing the sorbent materials are also provided.

An adsorbent system including a body having or defining a channel therein, wherein the body is configured to be coupled to a humidity-controlled environment such that a first end of the channel is in selective fluid communication with the ambient environment and such that a second end of the channel is in fluid communication with said humidity-controlled environment. The system further includes an adsorbent material in the channel, wherein the channel and adsorbent material are configured such that inlet fluid flowing from the first end to the second end through the channel is flowable over the adsorbent material, and such that outlet fluid flowing from the second end to the first end is flowable over a majority of the adsorbent material that is flowable over by the inlet fluid. The system also includes a valve system positioned at or adjacent to or in fluid communication with the first end of the channel.

The present invention relates to a method for modifying the crystalline inorganic framework of an adsorbent with coatings to provide rate selectivity for one gas over others is described. The method described herein narrows the effective pore size of crystalline porous solids with pores less than about 5 Å for rate selective separations. This method of the invention comprises treating the hydrated or partially hydrated zeolite with a silicone derived binding agent followed by subsequent heat treatment. The additive content and treatment are adjusted to match effective pore size to specific separations. The superior adsorbent has the added convenience of bead forming simultaneously with pore modification as well as having the treatment result in the yielding of high crush strength products.

A media design for modular use in an air cleaning or HVAC systems to removes gas phase contaminants. The design allows for a control of gas contaminant removal using variable media length, path length, and contact time to ensure a contained MTZ length and low pressure drop. In one embodiment, the design includes a filter module at an angle to an airflow and an air filter mounted within the filter frame. The filter module may include channels therethrough that are oriented at the optimum angle in relation to the airflow to provide the required dwell time and pressure drop for a given application.

An carbon molecular sieve for adsorbing water molecules in an alcohol solution to separate an alcohol from the water molecules, wherein the total volume of pores with an inlet diameter of 0.33 nm or more as determined by a molecular probe method is not less than 3 times the total volume of pores with an inlet diameter of 0.46 nm or more. This carbon molecular sieve is an alcohol concentration material that is capable of efficiently concentrating alcohol without performing a distillation step and that is easily reusable.

A nucleophilic substitution reaction to crosslink cyclodextrin (CD) polymer with rigid aromatic groups, providing a high surface area, mesoporous CD-containing polymers (P-CDPs). The P-CDPs can be used for removing organic contaminants from water. By encapsulating pollutants to form well-defined host-guest complexes with complementary selectivities to activated carbon (AC) sorbents. The P-CDPs can rapidly sequester pharmaceuticals, pesticides, and other organic micropollutants, achieving equilibrium binding capacity in seconds with adsorption rate constants 15-200 times greater than ACs and nonporous CD sorbents. The CD polymer can be regenerated several times, through a room temperature washing procedure, with no loss in performance.

Embodiments of the present disclosure provide a metal-organic framework composition including a metal-organic framework having an ana topology, the metal-organic framework including one or more metals connected to one or more organic linkers. Embodiments of the present disclosure further provide a method of separating chemical species including contacting a metal-organic framework having an ana topology with a flow of paraffins and separating the paraffins.

A method for preparing a nanoporous silica sol-gel matrix containing at least one amine reactant selected from hydroxylamine, methylhydroxylamine, tertbutylhydroxylamine, methoxyamine, tetraethylenepentamine, dicarboxylic acid dihydrazides, particularly adipic acid dihydrazide, and the salts thereof, said method including the following steps: a) synthesising a gel from tetramethoxysilane or from a mixture of tetramethoxysilane and another organosilicon precursor selected from among phenyltrimethoxysilane, phenyltriethoxysilane, a fluoroalkyltrimethoxysilane, a fluoroalkyltriethoxysilane, a chloroalkylmethoxysilane, a chloroalkylethoxysilane, an alkyltrimethoxysilane, an alkyltriethoxysilane, an aminopropyltriethoxysilane and the mixtures thereof, the synthesis being performed in an aqueous medium at a temperature ranging from 10 to 70° C. in the presence of at least one amine reactant selected from among hydroxylamine, methylhydroxylamine, tertbutylhydroxylamine, methoxyamine, dicarboxylic acid dihydrazides, particularly adipic acid dihydrazide, and the salts thereof; b) drying the gel obtained during step a) so as to obtain a sol-gel matrix containing at least one amine reactant.

A system and method for sulfur recovery, including hydrogenating Claus tail gas, quenching the hydrogenated gas, adsorbing water and hydrogen sulfide from the quenched gas, and regenerating adsorbent with carbon dioxide and/or nitrogen and heating the adsorbent in a regeneration temperature ramp to desorb primarily hydrogen sulfide in a first part of the temperature ramp.

Described are storage and dispensing systems, and related methods, for storing and selectively dispensing high purity reagent gas from a storage vessel in which the reagent gas is held in sorptive relationship to pyrolyzed carbon adsorption particles.