Patent classifications
C09D1/00
IRON ELECTRODE EMPLOYING A POLYVINYL ALCOHOL BINDER
The present invention provides one with an iron electrode employing a binder comprised of polyvinyl alcohol (PVA) binder. In one embodiment, the invention comprises an iron based electrode comprising a single layer of a conductive substrate coated on at least one side with a coating comprising an iron active material and a binder, wherein the binder is PVA. This iron based electrode is useful in alkaline rechargeable batteries, particularly as a negative electrode in a Ni—Fe battery.
METHOD FOR SYNTHESIZING CARBON MATERIALS FROM CARBON AGGLOMERATES CONTAINING CARBINE/CARBYNOID CHAINS
Provided is a method for synthesizing carbon agglomerates containing metastable carbyne/carbynoid chains; a method for synthesizing carbon or carbon compound allotropes from the agglomerates containing metastable carbyne/carbynoid chains; and the uses of the methods. The method for synthesizing carbon agglomerates containing metastable carbyne/carbynoid chains includes the following steps: a) forming carbon vapor precursors, containing carbine/carbynoid chains, by decomposing a carbon gas selected from among CH.sub.4, C.sub.2H.sub.2, C.sub.2H.sub.4, gaseous toluene, and benzene in the form of vapors at a temperature T such that 1 500° C.<T≦3 000° C.; and b) condensing the carbon vapor precursors, obtained in Step a), on the surface of a substrate, the temperature Ts of which is less than the temperature T. The invention is particularly of use in the field of electronics.
METHOD FOR SYNTHESIZING CARBON MATERIALS FROM CARBON AGGLOMERATES CONTAINING CARBINE/CARBYNOID CHAINS
Provided is a method for synthesizing carbon agglomerates containing metastable carbyne/carbynoid chains; a method for synthesizing carbon or carbon compound allotropes from the agglomerates containing metastable carbyne/carbynoid chains; and the uses of the methods. The method for synthesizing carbon agglomerates containing metastable carbyne/carbynoid chains includes the following steps: a) forming carbon vapor precursors, containing carbine/carbynoid chains, by decomposing a carbon gas selected from among CH.sub.4, C.sub.2H.sub.2, C.sub.2H.sub.4, gaseous toluene, and benzene in the form of vapors at a temperature T such that 1 500° C.<T≦3 000° C.; and b) condensing the carbon vapor precursors, obtained in Step a), on the surface of a substrate, the temperature Ts of which is less than the temperature T. The invention is particularly of use in the field of electronics.
PREPARATION METHOD OF SILICA AEROGEL-CONTAINING BLANKET AND SILICA AEROGEL-CONTAINING BLANKET PREPARED BY USING THE SAME
Provided are a preparation method of a silica aerogel-containing blanket which includes mixing a water glass solution, a polar organic solvent, and a silazane-based surface modifier to prepare a sol, preparing a silica gel-base material composite by immersion and gelation of a base material for a blanket in the sol, and drying the silica gel-base material composite, and a silica aerogel-containing blanket prepared by using the preparation method.
A silica aerogel-containing blanket having a high degree of hydrophobicity as well as excellent physical properties, particularly, low tap density, high porosity, and excellent mechanical flexibility may be prepared by the minimal use of a surface modifier without a surface modification step by the above method.
PREPARATION METHOD OF SILICA AEROGEL-CONTAINING BLANKET AND SILICA AEROGEL-CONTAINING BLANKET PREPARED BY USING THE SAME
Provided are a preparation method of a silica aerogel-containing blanket which includes mixing a water glass solution, a polar organic solvent, and a silazane-based surface modifier to prepare a sol, preparing a silica gel-base material composite by immersion and gelation of a base material for a blanket in the sol, and drying the silica gel-base material composite, and a silica aerogel-containing blanket prepared by using the preparation method.
A silica aerogel-containing blanket having a high degree of hydrophobicity as well as excellent physical properties, particularly, low tap density, high porosity, and excellent mechanical flexibility may be prepared by the minimal use of a surface modifier without a surface modification step by the above method.
COMPOSITIONS AND METHODS FOR FORMING STABLE, LIQUID METAL OXIDE/HYDROXIDE FORMULATIONS
Dry mixtures and liquid formulations are provided that comprise metal oxide and/or metal hydroxide nanocrystalline particles. The dry mixtures are advantageously formulated with select surfactants to be readily solubilized and stable in liquid carriers. Additional select components are provided in preferred combinations that are capable of achieving improved biocidal and chemical agent efficacy. Notably, the inventive formulations provided herein allow for easier delivery of the formulations and increased shelf stability.
COMPOSITIONS AND METHODS FOR FORMING STABLE, LIQUID METAL OXIDE/HYDROXIDE FORMULATIONS
Dry mixtures and liquid formulations are provided that comprise metal oxide and/or metal hydroxide nanocrystalline particles. The dry mixtures are advantageously formulated with select surfactants to be readily solubilized and stable in liquid carriers. Additional select components are provided in preferred combinations that are capable of achieving improved biocidal and chemical agent efficacy. Notably, the inventive formulations provided herein allow for easier delivery of the formulations and increased shelf stability.
LARGE SCALE PRODUCTION OF THINNED GRAPHITE, GRAPHENE, AND GRAPHITE-GRAPHENE COMPOSITES
Embodiments described herein relate generally to large scale synthesis of thinned graphite and in particular, few layers of graphene sheets and graphene-graphite composites. In some embodiments, a method for producing thinned crystalline graphite from precursor crystalline graphite using wet ball milling processes is disclosed herein. The method includes transferring crystalline graphite into a ball milling vessel that includes a grinding media. A first and a second solvent are transferred into the ball milling vessel and the ball milling vessel is rotated to cause the shearing of layers of the crystalline graphite to produce thinned crystalline graphite.
LARGE SCALE PRODUCTION OF THINNED GRAPHITE, GRAPHENE, AND GRAPHITE-GRAPHENE COMPOSITES
Embodiments described herein relate generally to large scale synthesis of thinned graphite and in particular, few layers of graphene sheets and graphene-graphite composites. In some embodiments, a method for producing thinned crystalline graphite from precursor crystalline graphite using wet ball milling processes is disclosed herein. The method includes transferring crystalline graphite into a ball milling vessel that includes a grinding media. A first and a second solvent are transferred into the ball milling vessel and the ball milling vessel is rotated to cause the shearing of layers of the crystalline graphite to produce thinned crystalline graphite.
COATING COMPOSITIONS FOR GLASS SUBSTRATES
The present disclosure provides a coated glass substrate, first and second coating compositions, and a process for coating the substrate. The first composition includes a source of tin, a source of fluorine, a source of titanium, and a solvent. The second composition includes a source of tin, a source of fluorine, and a solvent, and can be free of titanium. The first composition is applied to the substrate under elevated temperatures, and a first or sub layer is formed on the substrate via pyrolysis. The second composition is then applied, to form a second or top layer over the sub layer.