The present specification provides a dental glass ionomer cement (GIC) composition comprising a zwitterionic material and a glass ionomer cement, and a method of preparing the same.

The present disclosure discloses an oil shale semicoke adsorption inhibitor and use thereof in concrete preparation. The adsorption inhibitor is prepared by the following steps: sequentially adding 50-52.5 weight parts of an anti-corrosion rheological agent, 5-20 weight parts of methanol, 0.5-2 weight parts of sulfonated melamine, 2-5 weight parts of EDTA, 20-30 weight parts of an organosilicon compound, and 5-10 weight parts of stearate into a mixing container, and performing stirring well. The anti-corrosion rheological agent is a microbead. The adsorption inhibitor solves problems of strong water absorption, high adsorption of a water reducing agent, etc. of oil shale semicoke, reduces the use amount of the water reducing agent in concrete production, and can also reduce power consumption during grinding, thereby realizing high-value resource utilization of the oil shale semicoke.

The present disclosure discloses an oil shale semicoke adsorption inhibitor and use thereof in concrete preparation. The adsorption inhibitor is prepared by the following steps: sequentially adding 50-52.5 weight parts of an anti-corrosion rheological agent, 5-20 weight parts of methanol, 0.5-2 weight parts of sulfonated melamine, 2-5 weight parts of EDTA, 20-30 weight parts of an organosilicon compound, and 5-10 weight parts of stearate into a mixing container, and performing stirring well. The anti-corrosion rheological agent is a microbead. The adsorption inhibitor solves problems of strong water absorption, high adsorption of a water reducing agent, etc. of oil shale semicoke, reduces the use amount of the water reducing agent in concrete production, and can also reduce power consumption during grinding, thereby realizing high-value resource utilization of the oil shale semicoke.

A plurality of granules comprising ceramic particles bound together with an inorganic binder, the inorganic binder comprising reaction product of at least alkali silicate and hardener, wherein the ceramic particles are present as at least 50 percent by weight of each granule, based on the total weight of the respective granule, wherein each granule has a total porosity in a range from greater than 0 to 50 percent by volume, based on the total volume of the respective granule, and wherein the granule has a minimum Total Solar Reflectance of at least 0.7. The granules are useful, for example, as roofing granules.

A plurality of granules comprising ceramic particles bound together with an inorganic binder, the inorganic binder comprising reaction product of at least alkali silicate and hardener, wherein the ceramic particles are present as at least 50 percent by weight of each granule, based on the total weight of the respective granule, wherein each granule has a total porosity in a range from greater than 0 to 50 percent by volume, based on the total volume of the respective granule, and wherein the granule has a minimum Total Solar Reflectance of at least 0.7. The granules are useful, for example, as roofing granules.

Geopolymer cement slurries, cured geopolymer cements, and methods of making cured geopolymer cement and methods of using geopolymer cement slurries are provided. The geopolymer cement slurry comprises Saudi Arabian volcanic ash, an aqueous solution, Na.sub.2SiO.sub.3, NaOH, and a resin. The Saudi Arabian volcanic ash comprises SO.sub.3, CaO, SiO.sub.2, Al.sub.2O.sub.3, Fe.sub.2O.sub.3, MgO, and K.sub.2O.

Geopolymer cement slurries, cured geopolymer cements, and methods of making cured geopolymer cement and methods of using geopolymer cement slurries are provided. The geopolymer cement slurry comprises Saudi Arabian volcanic ash, an aqueous solution, Na.sub.2SiO.sub.3, NaOH, and a resin. The Saudi Arabian volcanic ash comprises SO.sub.3, CaO, SiO.sub.2, Al.sub.2O.sub.3, Fe.sub.2O.sub.3, MgO, and K.sub.2O.

The present invention provides a dry mix composition of a low-viscosity cellulose ether (50 to 750 mPa.Math.s at 1 wt. % solids, at 20 C, and a 514 s-1 shear rate, using a strain-controlled rotational rheometer (for example, ARES-G2™, TA Instruments), a graded aggregate, and a hydraulic cement, or a granular wet cement composition of the cement, graded aggregate and an admixture therefor including the cellulose ether. The wet granular hydraulic cement composition behaves like asphalt compositions and has zero or near zero slump, a high lubricity and from 5 wt. % to less than 13 wt. % of water, or, preferably from greater than 5 to 10.5 wt. %, based on the total weight of the granular wet cement composition. The low-viscosity cellulose ether enables lubricity without impairing compaction and without causing air entrainment.

The present invention provides a dry mix composition of a low-viscosity cellulose ether (50 to 750 mPa.Math.s at 1 wt. % solids, at 20 C, and a 514 s-1 shear rate, using a strain-controlled rotational rheometer (for example, ARES-G2™, TA Instruments), a graded aggregate, and a hydraulic cement, or a granular wet cement composition of the cement, graded aggregate and an admixture therefor including the cellulose ether. The wet granular hydraulic cement composition behaves like asphalt compositions and has zero or near zero slump, a high lubricity and from 5 wt. % to less than 13 wt. % of water, or, preferably from greater than 5 to 10.5 wt. %, based on the total weight of the granular wet cement composition. The low-viscosity cellulose ether enables lubricity without impairing compaction and without causing air entrainment.

Thermoset ceramic compositions and a method of preparation of such compositions. The compositions are advanced organic/inorganic hybrid composite polymer ceramic alloys. The material combines strength, hardness and high temperature performance of technical ceramics with the strength, ductility, thermal shock resistance, density, and easy processing of the polymer. Consisting of a branched backbone of silicon, and alumina, with highly coordinated Si—O—Si or Al—O—Al bonds, the material undergoes sintering at 7 to 300 centigrade for 2 to 94 hours from water at a pH between 0 to 14, humidity of 0 to 100%, with or without vaporous solvents.