The present disclosure is directed to stationary phase materials for performing size exclusion chromatography. Embodiments of the present disclosure feature hydroxy-terminated polyethylene glycol surface modified silica particle stationary phase materials, which are optionally also methoxy-terminated polyethylene glycol surface modified.

The present disclosure is directed to stationary phase materials (e.g., porous inorganic-organic hybrid particles) for performing size exclusion chromatography. Embodiments of the present disclosure feature hydroxy-terminated polyethylene glycol surface modified stationary phase materials.

The present disclosure is directed to methods for performing size exclusion chromatography. Embodiments of the present disclosure feature methods for improving separations of proteinaceous analytes in size exclusion chromatography, for example, by using low concentrations of amino acids or derivatives thereof in the mobile phase.

The invention includes methods for removing higher acetylenes from a gaseous stream that includes a hydrogen fraction and a non-hydrogen fraction, wherein the gaseous stream includes less than about 4% in total of diacetylene and vinylacetylene, where the method includes the following steps: (i) an adsorption that passes the gaseous stream at a preselected superficial linear gas velocity across an adsorption bed supported within an enclosure, the adsorption bed containing a crystalline porous ceramic adsorbent to adsorb the higher acetylenes onto the adsorbent, thereby producing a saturated adsorption bed and a purified gaseous stream including less than about 25 ppm of diacetylene that regenerates the saturated adsorbent bed by passing a regeneration gas across the saturated adsorption bed to desorb the higher acetylenes retained thereupon, thereby producing a regenerated adsorbent bed and a contaminated gas stream bearing the higher acetylenes; and (iii) a purging step that removes the contaminated gas stream from the enclosure. The invention also includes systems for removing diacetylene and vinylacetylene from a hydrogen-dominant acetylene-hydrogen gaseous stream.

A honeycomb structure comprising a pillar-shaped honeycomb structure body having a porous partition wall disposed so as to surround a plurality of cells, wherein let that A denotes an absolute value of open frontal area (%) in a plane of the honeycomb structure body orthogonal to the extending direction of the cells and P denotes an absolute value of porosity (%) of the partition wall, the honeycomb structure has a value represented by the following expression (1) that is 0.05 to 0.12, let that D denotes an average pore diameter (m) of the partition wall and G denotes a geometric surface area (mm.sup.2/mm.sup.3) of the partition wall, the honeycomb structure has a value represented by the following expression (2) that is 8 to 50 (μm×mm.sup.2/mm.sup.3), and the honeycomb structure has a hydraulic diameter of the cells that is 1.1 mm or more,
(1−A/100)×(1−P/100),  Expression (1)
D×G.  Expression (2)

An oil absorbent is manufactured by including performing heat treatment on a non-woven fabric for low-temperature carbonization, and has the effect of adsorbing and evaporating oil having various carbon numbers ranging from a low boiling point to a high boiling point to remove the oil, has photothermal conversion efficiency, high evaporation efficiency of oil by sunlight, and a high adsorption amount and high adsorption rate, thereby making the adsorption-evaporation cycle fast and efficiently performing the adsorption-evaporation, and has an environmentally friendly effect that does not cause any environmental problems even if the oil absorbent is put into a river, a sea, or the like and then lost.

A method of trapping and removing contaminants from a source of contamination using a microparticle media includes the steps of: providing the microparticle media, wherein the microparticle media includes a plurality of microparticles, and wherein each of the microparticles includes a substrate having pores; prehydrating the pores of the microparticles by mixing the microparticle media with at least one of a water or water of a electrolysis supernatant solution to form a prehydrated microparticle media having a portion of the water or water of the electrolysis supernatant solution absorbed or adsorbed in the pores of the microparticles; introducing the prehydrated microparticle media to the contaminants, wherein the prehydrated microparticle media trap or bind to the contaminants; and separating the prehydrated microparticle media and the contaminants trapped or bound to the prehydrated microparticle media from the source of contamination.

In one aspect, the present invention provides a chromatographic stationary phase material for various different modes of chromatography represented by Formula 1: [X](W).sub.a(Q).sub.b(T).sub.c (Formula 1). X can be a high purity chromatographic core composition having a surface comprising a silica core material, metal oxide core material, an inorganic-organic hybrid material or a group of block copolymers thereof. W can be absent and/or can include hydrogen and/or can include a hydroxyl on the surface of X. Q can be a functional group that minimizes retention variation over time (drift) under chromatographic conditions utilizing low water concentrations. T can include one or more hydrophilic, polar, ionizable, and/or charged functional groups that chromatographically interact with the analyte. Additionally, b and c can be positive numbers, with the ratio 0.05≤(b/c)≤100, and a≥0.

The present invention relates to calcium hydroxide particles having a total pore volume greater than 0.18 cm.sup.3/g, said total pore volume being calculated with the BJH method for a range of pores having a diameter of between 20 and 1000 Å, said particles being characterized in that the BJH partial pore volume for the range of pores having a diameter of between 20 and 100 Å corresponds to more than 20% of said BJH total pore volume.

This disclosure pertains to performance enhancing conditioning and storage solvents containing low levels of buffer and salt for reproducible and improved size exclusion chromatography (SEC). In some embodiments, the present disclosure pertains to storage solvents for protein-based size exclusion chromatography that comprise water, a water-miscible organic solvent, a phosphate salt, and a neutral salt. In some embodiments, the present disclosure pertains to columns for protein-based size exclusion chromatography that comprise porous particles and such a storage solvent