The present disclosure relates to materials, and specifically to materials such as sheet, molded or extruded polymer materials containing flake, formed, powdered, granulated or splintered borosilicate glass for heat rejection or mitigation and enhanced durability and strength. The invention provides a synthetic substrate that includes: 1 to 70 wt % borosilicate glass having an average size of 0.1 to 50 um; and 30 to 99 wt % polymer material, wherein the synthetic substrate has either a denier ranging between 0.1 to 20.0 or a thickness ranging between 0.1 to 20 MIL, which provides thermal management properties including reduction in solar absorptance and net power absorbed by surfaces. The greater the intensity of the solar radiation the more reactive the borosilicate becomes, reflecting and dissipating an increased level of energy.

A method of producing a glass briquette in which reclaimed glass fines are mixed with a binder material to create a mixture. The mixture is subsequently compressed in a chamber to form a briquette having the shape of the interior of the chamber. The reclaimed glass includes glass fines of a size of smaller than 10 mm. The method is performed without melting the glass fines such that the resulting briquette contains the discrete glass fines held in the binder and may be used as a furnace ingredient for later glass product production. The glass briquette may contain other batch ingredients required in the production of glass.

A glass pharmaceutical package having a glass composition of 68.00 mol % to 81.00 mol % SiO.sub.2, from 4.00 mol % to 11.00 mol % Al.sub.2O.sub.3, from 0.10 mol % to 16.00 mol % Li.sub.2O, from 0.10 mol % to 12.00 mol % Na.sub.2O, from 0.00 mol % to 5.00 mol % K.sub.2O, from 0.10 mol % to 8.00 mol % MgO, from 0.10 mol % to 5.00 mol % CaO, from 0.00 mol % to 0.20 mol % fining agent. The glass pharmaceutical package is delamination resistant, and has class 1 or class 2 chemical durability in acid, base, and water. The glass pharmaceutical package may have a surface compressive stress of at least 350 MPa.

The present disclosure relates to a method for forming a glass structure having a metallized surface portion. The method may comprise forming a structure using a flowable first material, adapted to form a glass, which includes a metal component. The structure is then treated to remove substantially all solvents and organic components contained in the first flowable material. Finally, the structure is exposed to a bath of a metal salt during which nucleation occurs and a metallized surface coating is formed on at least a portion of an outer surface of the structure.

A pseudo-reference electrode comprising a pseudo-reference glass material backed by a silver conductor comprising silver metal, wherein the pseudo-reference glass material is a chalcogenide glass comprising a silver chalcogenide Ag2Ch, wherein Ch denotes a chalcogen, or a halide glass comprising a silver halide and at least one glass-forming oxide of a metal or a metalloid, a mixture of two or more of these glasses, or a composite of at least one of these glasses. This pseudo-reference electrode can be used in ion-selective electrode (ISE) sensors and ion-selective field effect transistors (ISFETs).

Disclosed are a transition metal chalcogenide thin-layer material, a preparation method and an application thereof. The preparation method comprises: uniformly spreading a transition metal source between two substrates to prepare a sandwich structure; performing a heat treatment on the sandwich structure to fuse and bond the two substrates together, and performing a chemical vapor deposition reaction on a chalcogen element source and the fused and bonded sandwich structure under the protection of a protective gas, wherein the transition metal source is heated to dissolve and diffuse at a reaction temperature, separated out from surfaces of the substrates, and reacts with the chalcogen element source. The prepared thin-layer material is uniformly distributed in a centimeter-level substrate.

A method of manufacturing a resorbable, macroporous bioactive glass scaffold comprising approximately 15-45% CaO, 30-70% SiO.sub.2, 0-25% Na.sub.2O, 0-17% P.sub.2O.sub.5, 0-10% MgO and 0-5% CaF.sub.2 by mass percent, produced by mixing with pore forming agents and specified heat treatments.

A method of fabricating a ceramic component includes hot pressing a composite component with a glass powder / filler cover mixture to form a consolidated glass-based coating on the composite component.

Ceramic colours containing effect pigments and a liquid glass forming component for decoration of metallic, ceramic and glassy articles and a process for the preparation of a ceramic glaze.

Methods of synthesizing particles and the resulting particles are disclosed. The methods include synthesizing the particles in the presence of one or more additives. The resulting particles are smaller and easier to disperse in solution. Also described are methods of processing particles and the resulting particles. In particular embodiments, the particles are suited for incorporation into films.