Patent classifications
C08L3/02
Container and preparation method thereof
A container and a preparation method thereof are provided. A material forming the container includes at least two types of oxidized nanocelluloses interlaced with each other, the at least two types of oxidized nanocelluloses being configured to have different degrees of expansion after absorbing moisture in a same environment. In a dry condition, the at least two types of oxidized nanocelluloses do not expand, so the structure of the container is relatively dense and the air permeability is poor, which can sufficiently maintain moisture of an article stored in the container. In case the article itself or other reasons cause high humidity, different oxidized nanocelluloses of the container expand after absorbing moisture, so that gaps between different oxidized nanocelluloses becomes larger, and the air permeability of the container becomes better, which can discharge excessive moisture, enabling the container to self-adjust the air permeability based on humidity.
Formaldehyde free binder compositions with urea-aldehyde reaction products
Binder compositions are described that contain (1) a reducing sugar and (2) a reaction product of a urea compound and an aldehyde-containing compound. A specific example of the binder compositions include dextrose and an imidazolidine compound such as 4,5-dihydroxyimidazolidin-2-one. The binder compositions may be applied to collections of fibers and cured to form a fiber-containing composite, such as fiberglass insulation.
Home Compostable Label
The present disclosure relates to a home compostable label and its facestock, and a method for manufacturing such label and facestock. The facestock comprises a core layer comprising a top surface, a bottom surface, and a core compostable material; and a first skin layer comprising a first compostable material, said first skin layer being positioned proximate to at least a portion of the top surface of the core layer.
Home Compostable Label
The present disclosure relates to a home compostable label and its facestock, and a method for manufacturing such label and facestock. The facestock comprises a core layer comprising a top surface, a bottom surface, and a core compostable material; and a first skin layer comprising a first compostable material, said first skin layer being positioned proximate to at least a portion of the top surface of the core layer.
Thermally conductive three-dimensional (3-D) graphene polymer composite materials, methods of making, and uses thereof
A thermally conductive three-dimensional (3-D) graphene-polymer composite material, methods of making, and uses thereof are described. The thermally conductive three-dimensional (3-D) graphene-polymer composite material contains: (a) a porous 3-D graphene structure comprising a network of graphene layers that are attached to one another through a carbonized organic polymer bridging agent; and (b) a polymer material impregnated within the porous 3-D graphene structure, wherein the thermally conductive 3-D graphene-polymer composite material has a thermal conductivity of 10 W/m.Math.K to 16 W/m.Math.K.
Thermally conductive three-dimensional (3-D) graphene polymer composite materials, methods of making, and uses thereof
A thermally conductive three-dimensional (3-D) graphene-polymer composite material, methods of making, and uses thereof are described. The thermally conductive three-dimensional (3-D) graphene-polymer composite material contains: (a) a porous 3-D graphene structure comprising a network of graphene layers that are attached to one another through a carbonized organic polymer bridging agent; and (b) a polymer material impregnated within the porous 3-D graphene structure, wherein the thermally conductive 3-D graphene-polymer composite material has a thermal conductivity of 10 W/m.Math.K to 16 W/m.Math.K.
Thermally conductive three-dimensional (3-D) graphene polymer composite materials, methods of making, and uses thereof
A thermally conductive three-dimensional (3-D) graphene-polymer composite material, methods of making, and uses thereof are described. The thermally conductive three-dimensional (3-D) graphene-polymer composite material contains: (a) a porous 3-D graphene structure comprising a network of graphene layers that are attached to one another through a carbonized organic polymer bridging agent; and (b) a polymer material impregnated within the porous 3-D graphene structure, wherein the thermally conductive 3-D graphene-polymer composite material has a thermal conductivity of 10 W/m.Math.K to 16 W/m.Math.K.
Process for sugar modulation
The present invention relates to a method for producing a food product comprising hydrolysed starch, as well as to products obtainable by the method. The method has the advantage of reducing the amount of sugar (i.e. maltose) produced by hydrolysis as compared to conventional methods of starch hydrolysis and present the additional advantage of providing good processability for the food product.
Process for sugar modulation
The present invention relates to a method for producing a food product comprising hydrolysed starch, as well as to products obtainable by the method. The method has the advantage of reducing the amount of sugar (i.e. maltose) produced by hydrolysis as compared to conventional methods of starch hydrolysis and present the additional advantage of providing good processability for the food product.
Water-soluble film, production method thereof, and chemical agent package
A water-soluble film is provided, which is less susceptible to curling even after long-term storage. The water-soluble film includes a polyvinyl alcohol resin (A) , and has a first surface, which has a crystal Unity index Xa, and a second surface, which is opposite to the first surface and has a crystallinity index Xb, where: Xa≥Xb; Xa−Xb is from 0.015 to 0.10; and the crystallinity indexes Xa and Xb are measured through an infrared spectroscopic analysis by an attenuated total reflection method and represented by: ABS.sub.1141/ABS.sub.1093, wherein ABS.sub.1141 and ABS.sub.1093 are absorbances at wavenumbers of 1141 cm.sup.−1 and 1093 cm.sup.−1, respectively.