A no bake process is provided for preparing a foundry shape. A major amount of an appropriate foundry aggregate, especially a sand that has been mechanically-reclaimed, is mixed with an amount of halloysite tubes. A binder system, especially a water-based binder, such as an aqueous alkaline phenolic resole resin, is added to the mixed aggregate and halloysite, and a liquid co-reactant for curing the binder is also added. By intimately mixing the components, a foundry molding compound is formed and it can be placed into a mold or patter to cure into a foundry shape. When removed from the mold or pattern, the foundry shape can be used to cast molten metal.

A no bake process is provided for preparing a foundry shape. A major amount of an appropriate foundry aggregate, especially a sand that has been mechanically-reclaimed, is mixed with an amount of halloysite tubes. A binder system, especially a water-based binder, such as an aqueous alkaline phenolic resole resin, is added to the mixed aggregate and halloysite, and a liquid co-reactant for curing the binder is also added. By intimately mixing the components, a foundry molding compound is formed and it can be placed into a mold or patter to cure into a foundry shape. When removed from the mold or pattern, the foundry shape can be used to cast molten metal.

A high-strength geopolymer hollow microsphere, a preparation method thereof and a phase change energy storage microsphere are provided, including: dissolving sodium hydroxide, sodium silicate and spheroidizing aid in water to form a solution A, and adding active powder to the solution A, stirring and uniformly mixing to form a slurry B, adding the slurry B to an oil phase, stirring and dispersing into balls, filtering to obtain geopolymer microspheres I, washing the geopolymer microspheres I, and then carrying out a high-temperature calcination to obtain the high-strength geopolymer hollow microspheres II; using the high-strength geopolymer hollow microsphere as a carrier, absorbing a phase change material into the carrier, and mixing a microsphere carrying the phase change material with an epoxy resin, adding a powder dispersant and stirring to disperse the microsphere, after the epoxy resin is solidified, screening the superfluous powder dispersant to obtain the phase energy storage microsphere.

Aggregates useful in building materials such as concrete are described. The aggregates may include fly ash and an inorganic polymer binder, which may be present as an outer layer on a core of fly ash. Methods of preparing the aggregates and concrete mixtures comprising the aggregates are also described. For example, the aggregates may be prepared by contacting fly ash agglomerates with an alkaline solution. The concrete mixtures may comprise the aggregates and a hydraulic cement.

Aggregates useful in building materials such as concrete are described. The aggregates may include fly ash and an inorganic polymer binder, which may be present as an outer layer on a core of fly ash. Methods of preparing the aggregates and concrete mixtures comprising the aggregates are also described. For example, the aggregates may be prepared by contacting fly ash agglomerates with an alkaline solution. The concrete mixtures may comprise the aggregates and a hydraulic cement.

The present invention provides a preparation method for a high-performance water infiltration resisting material. Components of the water infiltration resisting material are mixed by the following weight ratio: wherein the content of ammonia silicate is 2.0-7.0 wt %, the content of sodium ethylsiliconate is 1.2-20.5 wt %, the content of polyacrylate-diatomite is 6.0-13.0 wt %, the content of sandy soil is 15.0-40.0 wt %, the content of coarse sand is 4.0-12.0 wt %, the content of calcia is 6.0-17.0 wt %, the content of cement is 30.0-50.0 wt %, and the content of additive is 0.02-0.09 wt %. The present invention can be used in dams, baths, pools, basements, building roofs and other fields of water infiltration resisting, and has the characteristics of high resistance to water infiltration, long effective water resistance time, being non-toxic and harmless, and convenient use.

A high-strength geopolymer hollow microsphere, a preparation method thereof and a phase change energy storage microsphere are provided, including: dissolving sodium hydroxide, sodium silicate and spheroidizing aid in water to form a solution A, and adding active powder to the solution A, stirring and uniformly mixing to form a slurry B, adding the slurry B to an oil phase, stirring and dispersing into balls, filtering to obtain geopolymer microspheres I, washing the geopolymer microspheres I, and then carrying out a high-temperature calcination to obtain the high-strength geopolymer hollow microspheres II; using the high-strength geopolymer hollow microsphere as a carrier, absorbing a phase change material into the carrier, and mixing a microsphere carrying the phase change material with an epoxy resin, adding a powder dispersant and stirring to disperse the microsphere, after the epoxy resin is solidified, screening the superfluous powder dispersant to obtain the phase energy storage microsphere.

A composition of matter for use as an electrode in batteries, fuel cells and other applications, that may or may not be primarily composed of graphite, Portland Cement, pozzolans and water. Organic polymers, additives, reinforcements, fillers, catalysts, current collectors, and other materials may be included in vast ranges and proportions. Large graphite electrodes and other useful products are fabricated integrating concrete with chemical and electrical sciences. Batteries, fuel cells, thermal energy systems, conductive paints, fireproof coatings, metal casting forms, crucibles, fire bricks, graphite electrodes for electroplating, electric arc furnaces, and other applications may make use of the composition. For example, an air battery cathode composed of 50 grams white portland cement, 7 grams metakaolin pozzolan, and 700 grams of properly mixed graphite particle sizes. Dry components mixed with a water based liquid component start the cementing reactions. Mixing, forming and curing play important roles in the final composition properties.

A method of controlling the setting time of a geopolymer by coating aluminosilicate particles with nanoparticles to slow the geopolymerization reaction. The coating effectiveness of the nanoparticles may be enhanced by pretreating the aluminosilicate particles with a layer-by-layer assembly of polyelectrolytes. A geopolymer is formed by mixing about 39% to about 66% by weight aluminosilicate source, about 0% to about 40% by weight sand, about 19% to about 33% by weight of alkali activator solution, and about 1% to about 4% nanoparticles.

A method of controlling the setting time of a geopolymer by coating aluminosilicate particles with nanoparticles to slow the geopolymerization reaction. The coating effectiveness of the nanoparticles may be enhanced by pretreating the aluminosilicate particles with a layer-by-layer assembly of polyelectrolytes. A geopolymer is formed by mixing about 39% to about 66% by weight aluminosilicate source, about 0% to about 40% by weight sand, about 19% to about 33% by weight of alkali activator solution, and about 1% to about 4% nanoparticles.