The present application discloses an eco-friendly long-lasting heat-sensitive paper, including a substrate layer, a base color layer, a heat-sensitive covering layer, and a protective layer that are arranged sequentially from bottom to top, where the heat-sensitive covering layer is prepared as follows: coating a heat-sensitive covering layer raw material on the base color layer, and oven-drying a resulting product, where the heat-sensitive covering layer raw material is an emulsion obtained by mixing an acrylic hollow microsphere with a host resin. In the present application, an acrylic hollow microsphere that can change from an opaque state to a transparent state after rupturing under heat is used as a heat-sensitive covering layer to cover a base color layer to obtain the heat-sensitive paper with heat-sensitive color development characteristics.

Described is a treated inorganic particle having an organic treatment layer, which can provide crystallization benefits to polymer resins. The treated inorganic particle has a mean particle size of about 0.1-10 m, and the organic treatment layer is an alkali metal salt or alkaline earth metal salt of an acid; where the acid is an aromatic acid or organic diacid. The treated inorganic particles increase crystallization temperature, increase crystal formation rate, and/or decrease cooling time needed for the solidification of the polymer compared with pigmented resins using other inorganic particles.

The invention relates to nanoparticles of a composite material comprising a light absorbing agent dispersed in a matrix of a mineral oxide, to a method for the preparation of such nanoparticles, to the use of said method to modify the hue of nanoparticles of composite material comprising a light absorbing agent, and to an ophthalmic lens comprising such nanoparticles.

A nanoparticulate organic hybrid material comprising inorganic nanoparticles covalently grafted with at least one anion of an organic sodium or lithium salt is provided. In addition, a process for preparing the nanoparticulate organic hybrid material and its use in the preparation of electrolytes suitable for lithium and sodium secondary batteries are provided.

Methods for of synthesizing a polymer functionalized nanoparticle are provided. The method can comprise: attaching an anchoring compound to a nanoparticle; attaching a RAFT agent to the anchoring compound; and polymerizing a plurality of butadiene-derived monomers on the anchoring compound to form a polymeric chain covalently bonded to the nanoparticle via the anchoring compound. Polymer functionalized nanoparticles are also provided that include a nanoparticle defining a surface; a butadiene-derived polymeric chain covalently bonded to the surface of the nanoparticle. Nanocomposites are also provided that include a plurality of such polymer functionalized nanoparticles dispersed within a polymeric matrix.

The present invention includes a process for producing treated filler that includes (a) treating a slurry that includes untreated filler, where the untreated filler has not been previously dried, with a treating composition that includes a treating agent, thereby forming a treated filler slurry, and (b) drying the treated filler slurry to produce treated filler. The treating agent can include a polymer having (i) at least one first group that interacts with the untreated filler and (ii) at least one second group that interacts with a rubber matrix into which the treated filler is incorporated. The present invention also is directed to treated filler prepared by the process, as well as rubber compounding compositions and tires including the treated filler.

The present invention includes a process for producing treated filler that includes (a) treating a slurry that includes untreated filler, where the untreated filler has not been previously dried, with a treating composition that includes a treating agent, thereby forming a treated filler slurry, and (b) drying the treated filler slurry to produce treated filler. The treating agent can include a polymer having (i) at least one first group that interacts with the untreated filler and (ii) at least one second group that interacts with a rubber matrix into which the treated filler is incorporated. The present invention also is directed to treated filler prepared by the process, as well as rubber compounding compositions and tires including the treated filler.

A set of spherical inorganic particles having the particular property of being spontaneously individualized, both in dry state in the form of a powder and when they are dispersed in a matrix. The method for producing the particles, and the materials produced by including the particles in the matrices are also described.

The present invention includes a process for producing treated filler that includes (a) treating a slurry that includes untreated filler where the untreated filler has not been previously dried, with a treating composition that includes a treating agent, thereby forming a treated filler slurry, and (b) drying the treated filler slurry to produce treated filler. The treating agent can include a polymer having (i) at least one first group that interacts with the untreated filler and (ii) at least one second group that interacts with a rubber matrix into which the treated filler is incorporated. The present invention also is directed to treated filler prepared by the process, as well as rubber compounding compositions and tires including the treated filler.

The invention relates to a hydrophobic silica powder which is unprecedentedly insensitive to environmental humidity with which electrophotographic toner can possess stable electro static charge that leads to stable quality of printed image.

The hydrophobic silica powder has the following physicochemical properties;

average primary particle size (D) is 30-2000 nm,

B*D<430 nm, whilst B stands for weight % of adsorbed water vapor on silica (100 weight %) when the partial pressure of water to the equilibrium vapor pressure of water at 25 C. is 80% and D stands for average primary particle size (nm) of the silica powder,

B/C<2.7, whilst C stands for weight % of adsorbed water vapor on silica (100 weight %) when the partial pressure of water to the equilibrium vapor pressure of water at 25 C. is 20%, and

carbon content >0.30 wt.-%.