Provided is a resin composition comprising a starch and a polyvinyl alcohol, which is excellent in the breaking strength and breaking elongation at a low temperature, and at the same time, has the good gas barrier property. The resin composition comprises modified starch and polyvinyl alcohol, and where in a cross section photograph by a transmission electron microscope, a cross-sectional area of each of particles of the polyvinyl alcohol dispersed is calculated, and a cross-sectional shape of each of the particles of the polyvinyl alcohol is postulated to be circular based on the cross-sectional area, the particles of the polyvinyl alcohol have a conversion particle diameter of 50 to 300 nm, and the conversion particle diameter has a dispersity of 3.0 or less.

Provided is a powder material for forming a three-dimensional object, the powder material containing granulated particles containing: a resin; and inorganic particles of which primary particles have a volume average particle diameter of 1 micrometer or less, wherein the granulated particles have a volume average particle diameter of 10 micrometers or greater but 70 micrometers or less and a BET specific surface area of 6 m.sup.2/g or greater but 8 m.sup.2/g or less.

In this specification, a method for the manufacture of solid dosage forms is disclosed. The method includes extruding a plasticized matrix through an exit port of an extrusion channel to form one or more plasticized fibers, structuring said fibers to a three dimensional structural network by patterning on a translating or rotating stage, and solidifying the patterned structure.

A method of removing polyvinyl alcohol (PVA)-based scaffold from a 3D printed part formed by a 3D printing process that renders a finished product for immediate use. The method principally involves preparing an acidic-aqueous cleansing solution comprising a mixture of carboxylic acid and water; immersing the 3D printed part conventionally bonded with PVA-based scaffold into the acidic-aqueous cleansing solution for a select amount of time to break down and remove the PVA-based scaffold from the 3D printed part; and adding to the acidic-aqueous cleansing solution a select quantity of polymeric carbohydrate to crosslink and bond with the PVA-based scaffold to effect dissolution thereof into the acidic-aqueous cleansing solution.

The present application is related to a container made of a polymer and containing a single unit dose of a detergent composition. The detergent composition contains at least two complexing agents (A) dissolved in an aqueous medium. The complexing agents (A) are (A1) at least one alkali metal salt of methyl glycine diacetic acid (MGDA), and (A2) at least one alkali metal salt of glutamic acid diacetic acid (GLDA). The complexing agents (A1) and (A2) are partially neutralized with alkali and the weight ratio of (A1) and (A2) ranges from 1:9 to 9:1. The aqueous medium contains at least 25% by weight of water relative to the entire liquid phase.

A grafted polyvinyl alcohol polymer includes a polyvinyl alcohol main chain and a plurality of side chains grafted to the polyvinyl alcohol main chain. One or more of the side chains from the plurality of side chains include one or more units selected from: an aliphatic carboxylic acid, an aliphatic amide, an amino alkyl (meth)acrylate, a hydroxylated alkyl (meth)acrylate, or any combinations thereof. The grafted polyvinyl alcohol polymer can be included in a formulation that also includes water, and the formulation can be used as an adhesive in a creping process.

A method for producing bone grafts using 3-D printing is employed using a 3-D image of a graft location to produce a 3-D model of the graft. This is printed using a 3-D printer and a printing medium that produces a porous, biocompatible, biodegradable material that is conducive to osteoinduction. For example, the printing medium may be PCL, PLLA, PGLA, or another approved biocompatible polymer. In addition such a method may be useful for cosmetic surgeries, reconstructive surgeries, and various techniques required by such procedures. Once the graft is placed, natural bone gradually replaces the graft.

An apparatus, and a system for manufacturing a bioplastic material from a blend solution of gum arabica (GA) and polyvinyl alcohol (PVA) is provided. The apparatus includes a panel having a first end, a second end distal to the first end, and a plurality of walls extending from a periphery of the panel, the panel configured to accommodate the blend solution. The apparatus further includes a plurality of support members coupled to the first end and the second end of the panel and configured to adjust a slope angle of the panel; and one or more vibration generating units coupled to the plurality of support members and configured to vibrate the panel when the blend solution flows from the first end to the second end of the panel. A method of preparing the bioplastic material is also disclosed.

Methods and apparatus are provided for eyeglass lens made using a solution casting process. The method may include providing a first soluble polymer solution. The method may include providing a first dye solution including at least one dye. The method may include adding the first dye solution to the first soluble polymer solution to form a first dyed solution. The method may include casting the first dyed solution to form a first film. The method may include providing a second soluble polymer solution. The method may include providing a second dye solution comprising at least one dye. The method may include adding the second dye solution to the second soluble polymer solution to form a second dyed solution. The method may include casting the second dyed solution onto the first film to form a two-layer film. The method may include laminating or casting the two-layer film to the eyeglass lens.

A method for producing a 3D-printed tissue substitute is disclosed, utilizing a 3D printing device including a tank including a yield stress fluid in which the material is printed, the printing material delivered by the cartridge includes polyvinyl alcohol and gelatin, the method including a step following which, after printing the material in the yield stress fluid, a printed intermediate device is solidified in the yield stress fluid by lowering the temperature of the tank. The intermediate device is removed from the tank, rinsed and dried in order to obtain the tissue substitute.