Architectural structures including an inorganic material carrier including cement and particles or fibers of a glass including a plurality of Cu.sup.1+ ions. In aspects, the glass may have a glass phase and a cuprite phase. In aspects, the glasses may include a plurality of Cu.sup.1+ ions, a degradable phase including B.sub.2O.sub.3, P.sub.2O.sub.5 and K.sub.2O and a durable phase including SiO.sub.2. In other aspects, the glass can have a plurality of Cu.sup.1+ ions disposed on the surface of the glass and in the glass network and/or the glass matrix. The glasses and articles disclosed herein can exhibit a 2 log reduction or greater in a concentration of at least one of Staphylococcus aureus, Enterobacter aerogenes, Pseudomonas aeruginosa bacteria, Methicillin Resistant Staphylococcus aureus, and E. coli, under the EPA Test Method for Efficacy of Copper Alloy as a Sanitizer testing condition and under Modified JIS Z 2801 for Bacteria testing conditions.

The invention relates to glass articles suitable for use as electronic device housing/cover glass which comprise a glass ceramic material. Particularly, a cover glass comprising an ion-exchanged glass ceramic exhibiting the following attributes (1) optical transparency, as defined by greater than 90% transmission at 400-750 nm; (2) a fracture toughness of greater than 0.6 MPa.Math.m.sup.1/2; (3) a 4-point bend strength of greater than 350 MPa; (4) a Vickers hardness of at least 450 kgf/mm.sup.2 and a Vickers median/radial crack initiation threshold of at least 5 kgf; (5) a Young's Modulus ranging between about 50 to 100 GPa; (6) a thermal conductivity of less than 2.0 W/m° C., and (7) and at least one of the following attributes: (i) a compressive surface layer having a depth of layer (DOL) greater and a compressive stress greater than 400 MPa, or, (ii) a central tension of more than 20 MPa.

A method is provided for calculating gaseous diffusion and oxidation evolution of a ceramic matrix composite (CMC) structure, which includes determining temperature and load distribution in a structural member; determining matrix crack distribution in the structure; establishing an equivalent diffusion coefficient model of a fiber bundle scale to predict a gas flow channel in a fiber bundle: averaging a total amount of gaseous diffusion in the channel to establish the equivalent diffusion coefficient model of the fiber bundle composite scale related to the matrix crack distribution; establishing a representative volume element (RVE) model; establishing an equivalent diffusion coefficient model of a RVE scale; calculating the distribution of the gas concentration and oxidation products in the structure; calculating a growth thickness of an oxide at cracks and pores in each element; and updating sealing conditions of the gas channel, and calculating a new equivalent diffusion coefficient field and the distribution of the oxidation products again.

A preparation method includes the following steps: Step (1): pressing and then drying body powder to form a green brick; Step (2): applying a ground coat on the surface of the green brick; Step (3): inkjet-printing a pattern on the surface of the green brick having the ground coat, and applying an isolation glaze; Step (4): applying a fully polished glaze on the surface of the green brick having the isolation glaze; and Step (5): drying, firing, and polishing the green brick having the fully polished glaze to obtain a hard wear-resistant polished glazed ceramic tile. The phase composition of the fired fully polished glaze is as follows: 10 to 20 percent by weight of corundum, 20 to 30 percent by weight of hyalophane, 0.5 to 1.0 percent by weight of hematite, and 50 to 68 percent by weight of amorphous phase.

A glass-ceramic that includes a first crystal phase including (Mg.sub.xZn.sub.1-x)Al.sub.2O.sub.4, where x is ≤1, and a second crystal phase including tetragonal ZrO.sub.2. The glass-ceramic may be substantially free of arsenic, tin, antimony, and cesium, each of the arsenic, tin, antimony, and cesium present at less than 0.01% (by mole of oxide). Further, the glass-ceramic may include a transmittance of at least about 80% to light having a wavelength of 380 nm to 760 nm.

A connected substrate of the present invention includes a plurality of element substrate regions partitioned by dividing grooves, wherein the connected substrate is a glass ceramic sintered body having precipitated therein an anorthite crystal.

Disclosed in the present invention is a multi-crystal nucleus transparent glass-ceramic and a preparation method therefor, said preparation method comprising the following steps: during glass production, adding a plurality of types of nucleation agents, and after processing, acquiring a mother glass having certain outer dimensions; and placing the mother glass obtained in S2 under a temperature of T1 and heating for 1 h-6 h to perform annealing treatment, after the annealing treatment is complete, placing under a temperature of T2 and heating 1 h-6 h to perform nucleation treatment, and after nucleation treatment is complete, placing under a temperature of T3 and heating 0-3 h to perform crystallization treatment. T1<T2. The present invention produces a glass-ceramic containing multiple types of crystal nuclei and having crystal phases of lithium disilicate and petalite. The multiple crystal nuclei reduces the nucleation and crystallization energies required for devitrification, thus being able to reduce thermal treatment temperature and time, and adjust the ratio of crystals. The glass-ceramic prepared by means of the present preparation method features an increased damage resistance, good fracture toughness, and a broad application range.

The present invention provides a silicate glass that can reduce a color change in base material zirconia even when simultaneously fired with an unsintered zirconia. The present invention also provides a dental product using same. The present invention relates to a silicate glass comprising: 65.0 to 90.0 mol % SiO.sub.2, 4.0 to 15.0 mol % Al.sub.2O.sub.3, 1.0 to 10.0 mol % K.sub.2O, 0.1 to 7.0 mol % Na.sub.2O, and 0.01 to 15.0 mol % CaO, the silicate glass being essentially free of B.sub.2O.sub.3, and satisfying the relation {(number of moles of Al.sub.2O.sub.3)/(total number of moles of RO+R.sub.2O)}≥0.70, wherein R in the metal oxide represented by RO represents a metallic element in group 2 or 12 of the periodic table, and R in the metal oxide represented by R.sub.2O represents a metallic element in group 1 of the periodic table. The present invention also relates to a composite comprising the silicate glass and a base material formed of a ceramic; a sintered body as a fired product of the composite; and a dental product comprising the sintered body.

A composition includes 30 mol % to 60 mol % SiO.sub.2; 15 mol % to 40 mol % Al.sub.2O.sub.3; 5 mol % to 25 mol % Y.sub.2O.sub.3; 5 mol % to 15 mol % TiO.sub.2; and 0.1 mol % to 15 mol % RO, such that RO is a sum of MgO, CaO, SrO, and BaO.

A glass ceramic includes feldspar crystal phases, non-crystalline glass phases, Al.sub.2O.sub.3 phases, and SiO.sub.2 phases. At least one pair of the Al.sub.2O.sub.3 phases is bonded via at least one of the feldspar crystal phases.