The present disclosure is directed to mixed mode chromatography media comprising a ligand directly attached to a solid support. In some aspects, the ligand has a chemical formula of ##STR00001##
The mixed mode chromatography media is useful for binding and purifying proteins from a solution.

The present invention is a solid lubricant treatment medium, usually but not always in bead form, suitable to be brought into contact with lubricants to remediate and to condition them. A key feature of the medium, typically a polymeric resin, is the presence of relatively very large pores, which are able to capture and remove fine lubricant contaminants and breakdown products (such as small phosphate ester varnish, soot, coke, dissolved metal or other small semi-soluble or insoluble particles). Resins and adsorbents of the prior art have proven unable to remove fine contaminants like phosphate ester varnish that have a deleterious impact on industrial equipment performance and reliability. The mean pore size diameter of the medium is between about 8,000 and 100,000 and, more preferably, in the range of about 20,000 to about 80,000 .

The present invention is a solid cooling fluid treatment medium, usually but not always in bead form, suitable to be brought into contact with coolants to remediate and to condition them. A key feature of the medium, typically a polymeric resin, is the presence of relatively very large pores, which are able to capture and remove ultrafine coolant contaminants and breakdown products (such as colloids, soot, coke, organics, scale or other small semi-soluble or insoluble particles). Resins and adsorbents of the prior art have proven unable to remove ultrafine contaminants like these that have a deleterious impact on industrial equipment performance and reliability. The mean pore size diameter of the medium is between about 1,500 and 100,000 and, more preferably, in the range of about 1,500 to about 80,000 .

An adsorption structure unit prevents water leakage from an adsorption structure and improves the durability of the adsorption structure and the durability of the adsorption structure unit. An adsorption structure has a filter portion having a plurality of flow paths divided by a plurality of partition walls and a plugged portion shutting a feed water inflow or outflow end of the plurality of flow paths, a water-impermeable outer tube accommodating the filter portion, and a seal material blocking a gap between the filter portion and the outer tube in at least one end portion of the filter portion. An adsorption structure unit has the adsorption structure, a housing supplying feed water from one end of the adsorption structure, and discharging the feed water from the other end, and a ring member disposed between end portions on both sides of the outer tube and an inner surface of the housing.

Disclosed is a separation material comprising hydrophobic polymer particles and a coating layer covering at least a portion of a surface of the hydrophobic polymer particles, wherein the coating layer comprises a hydrophilic polymer having hydroxy groups, and the hydrophilic polymer has a group represented by NHR-L or an epoxy group, wherein R represents a hydrocarbon group and L represents a carboxy group or an amino group.

A composite filter aid may include diatomaceous earth, natural glass, and a precipitated silica binder, wherein the filter aid has a permeability ranging from 3 to 20 darcys. A composite filter aid may include diatomaceous earth, perlite, and a precipitated silica binder, wherein the filter aid has an alpha density less than 15 lbs/ft.sup.3. A method for making a composite material may include blending diatomaceous earth and perlite, adding alkali silicate to the blended diatomaceous earth and perlite, and precipitating the alkali silicate as a binder to make the composite material. A method for filtering a beverage may include using a composite filter aid and/or composite material.

A hydrated lime product exhibiting superior reactivity towards HCl and SO.sub.2 in air pollution control applications. Also disclosed is a method of providing highly reactive hydrated lime and the resultant lime hydrate where an initial lime feed comprising calcium and impurities is first ground to a particle-size distribution with relatively course particles. Smaller particles are then removed from this ground lime and the smaller particles are hydrated and flash dried to form a hydrated lime, which is then milled to a significantly smaller particle size than that of the relatively course particles. The resultant lime hydrate product has available CaOH of greater than 92%, a citric acid reactivity of less than 20 seconds, a BET surface area greater than 18, a D90 less than 10 m, a D50 less than 4 m, a D90/D50 less than 3, and a large pore volume of greater than 0.2 BJH.

The present disclosure provides an extraction coating for an SPME sampling instrument, where the extraction coating includes a sorptive material immobilized in a fluorocarbon polymer that is compatible with thermal-assisted desorption techniques, solvent-assisted desorption techniques, or both. The disclosure also provides SPME sampling instruments, methods of making an SPME sampling instrument, and methods of extracting an analyte from a sample matrix using the SPME coating.

An agent for removing a halogen gas, such as chlorine, in a waste gas by means of reduction; a method for producing this agent; a method for removing a halogen gas by use of this agent; and a system for removing a halogen gas. The agent for removing the halogen gas contains at least pseudo-boehmite, that serves as a host material, and a sulfur-containing reducing agent, that serves as a guest material. 1-8% by weight of the reducing agent, in terms of elemental sulfur, based on the total amount of the pseudo-boehmite and sulfur-containing reducing agent is present in the agent. At least one inorganic compound selected from among oxides, carbonates salts and hydrocarbon salts of alkaline earth metal elements, transition metal elements and zinc group elements is additionally contained in the agent as a third component.

The invention concerns high-performance adsorbents based on activated carbon of high meso- and macroporosity which are present in the form of discrete grains of activated carbon, wherein: at least 55% of the total pore volume of the high-performance adsorbents are formed by pores (i.e. meso- and macropores) having pore diameters of more than 20 , the high-performance adsorbents have a measure of central tendency pore diameter of more than 25 , and the high-performance adsorbents have a BET surface area of at least 1250 m.sup.2/g. These high-performance adsorbents are obtainable by a novel process comprising specific two-stage activation, and have, in addition to the aforementioned properties, an excellent abrasion and bursting resistance, so that they are useful for a multiplicity of different applications.