A cellulose nanocrystal-modified ceramic blank and a preparation method thereof are disclosed. Cellulose nanocrystals are added into a ceramic blank in gelcasting. The cellulose nanocrystal-modified ceramic blank comprises, by weight, 0.1 to 10 parts of cellulose nanocrystals, 0.1 to 30 parts of organic gel and 70 to 99 parts of ceramic powder. The cellulose nanocrystal has length of 100 to 300 nm, a diameter of 10 to 20 nm, a slenderness ratio of 10 to 15 , and an elastic modulus of 100 to 150 GPa. The drying strength of the ceramic blank with the cellulose nanocrystals is obviously improved.

Systems and methods for rapid drying of ceramic greenwares having a high graphite content are disclosed. The methods include employing microwave drying to bring the dryness of the ceramic greenware to a first select dryness and then employing close-coupled hot-air drying to bring the dryness to the final target dryness. The judicious use of close-coupled hot-air drying reduces end defects due to unevenness in the microwave drying process while also substantially speeding up the drying process. Various configurations for and combinations of microwave drying and close-coupled hot-air drying are disclosed.

Methods of forming a polycrystalline table may involve disposing a plurality of particles comprising a superabrasive material, a substrate comprising a hard material, and a catalyst material in a mold. The plurality of particles may be partially sintered in the presence of the catalyst material to form a brown polycrystalline table having a first permeability attached to an end of the substrate. The substrate may be removed from the brown polycrystalline table and catalyst material may be removed from the brown polycrystalline table. The brown polycrystalline table may then be fully sintered to form a polycrystalline table having a reduced, second permeability. Intermediate structures formed during a process of attaching a polycrystalline table to a substrate may include a substantially fully leached brown polycrystalline table. The substantially fully leached brown polycrystalline table may include a plurality of interbonded grains of a superabrasive material.

Powder particles for forming a homogeneous green body having a sufficient strength and a process for producing a green body by using the powder particles. A green body is shaped by using powder particles of composite particles in which thermoplastic resin particles are scattered on surfaces of large particles in an amount within a predetermined volume ratio range with respect to the large particles, and loaded to form resin pools in contact point peripheral areas of adjoining ones of the large particles and form voids in areas other than the contact point peripheral areas when the thermoplastic resin particles are melted. A green body packed with the powder particles each having a small amount of the thermoplastic resin particles attached thereon is placed under a melting condition of the thermoplastic resin particles, the thermoplastic resin is melted and gathers around contact points (or proximal points) of the adjoining powder particles.

Particles each having a sinterable core and a polymeric coating on at least a part of the core, wherein the polymeric coating includes a polymer that can be removed via decomposition by heat, catalytically or by solvent treatment, and wherein the polymeric coating is present in an amount of 0.10 to 3.00% by weight, relative to the total weight of the particles, as well as the use of these particles in an additive manufacturing process such as a powder bed and inkjet head 3D printing process. The particles and the process are able to provide a green part having improved strength and are thus suitable for the production of delicate structures which require a high green strength in order to minimize the risk of structural damage during green part handling.

The present invention provides a method for producing a ceramic green body molded article, comprising: a raw material blending step of kneading 100 parts by mass of a ceramic raw material with 0.1 to 20 parts by mass of a cellulose complex comprising cellulose and a water-soluble polymer to obtain a kneaded product; and a step of molding the kneaded product.

The application discloses a dental zirconia restoration material with uniform transition of strength and color, and a preparation method thereof. The preparation method includes the following steps: (1) pouring colored zirconia powder into a dry pressing mould in accordance with a sequence of the strength from high to low and the color from dark to light for each layer, and performing dry pressing; (2) performing isostatic cool pressing after the dry pressing; (3) performing pre-sintering after the isostatic cool pressing to obtain a greenware; and (4) performing CAD/CAM cutting on the greenware, and finally performing final sintering to obtain the dental zirconia restoration material. In the present application, the strength of a restoration can gradually increase from a cut end to the neck, the wear to adjacent teeth and jaw teeth is reduced, and long-bridge restoration can be realized due to the high strength of the neck.

A method performs evaluation of properties of a clay rod, with which a honeycomb structural body is produced. The method mixes raw materials to produce a clay, and extrudes the clay and compresses the extruded clay to produce a clay rod. The method performs NMR to detect at least one of a T1 relaxation time and a T2 relaxation time in each of a normal part and an abnormality part extracted from the clay rod. Each of the T1 relaxation time and the T2 relaxation time corresponds to a relaxation time of nuclear spins of water protons magnetically excited in each of the normal part and the abnormality part. The method performs the evaluation of uniformity of a mixed state and a compression state of the clay rod based on a difference in T1 relaxation time and T2 relaxation time between the normal part and the abnormality part.

A batch made of refractory mineral materials for lining of assemblies used for nonferrous metal melts, contains over 90% by weight of a mixture of the following constituents:from 3 to 74% by weight of at least one coarse-grain raw olivine material with at least 70% by weight forsterite content and having grain sizes of 50% by weight over 0.1 mmfrom 25 to 49% by weight of at least one ground magnesia with grain sizes of 50% by weight?1 mmfrom 0.9 to 14% by weight of at least one ground silicon carbide (SiC) with grain sizes of 50% by weight?1 mmfrom 0.1 to 10% by weight of at least one fine-particle dry pulverulent silica with particle sizes?500 ?mfrom 0 to 4% by weight of at least one antioxidant known per se for refractory productsfrom 0 to 4% by weight of at least one additional granulated refractory raw material known per se, more particularly having grain sizes of 50% by weight, in particular of 80% by weight, preferably of 100% by weight over 0.1 mmfrom 0 to 2% by weight of at least one additive known per se for the production of refractory products from batchesfrom 0 to 4% by weight of at least one additional substance known per se made of ground refractory materials and/or in the form of what is known as medium-grain-size material and/or of what is known as coarse-grain-size materialfrom 0 to 10% by weight of at least one binder known per se for refractory materials, e.g. in dry form or in ancillary packaging in liquid form.

In a monolithic refractory, in terms of a proportion in 100 mass % of a refractory raw material having a grain size of 8 mm or smaller, an amount of Ca.sub.XSr.sup.1XAl.sub.2O.sub.4 (where, 0X0.5) is 0.5 mass % or more and 10 mass % or less, and a polyvalent metal salt of oxycarboxylic acid is 0.05 mass % or more and 1.0 mass % or less.