The invention relates to a method of testing silanization, which permits inline control of the in situ silanization of light-colored fillers, especially precipitated silicas. This enables continuous in situ silanization in the production of rubber mixtures comprising silanized light-colored fillers, and representative control of the rubber mixture under production conditions. The process is additionally nondestructive and has a high tolerance for carbon black as an additional constituent of the rubber mixture.

A particulate metal oxide has a metal oxide core and a coating layer containing an inorganic material and (i) a quaternary silane coupling agent, and/or (ii) a silane coupling agent and a hydrophobizing agent. Preferred materials are titanium dioxide core particles, an amino organosilane coupling agent and a fatty acid hydrophobizing agent. The particulate metal oxide is suitable for use in forming a dispersion, and the particles and dispersion can be used in an end-use sunscreen composition which is transparent, exhibits effective UV absorption properties, reduced photoactivity, and/or improved skin feel.

In order to provide a filler composition for fabricating a high-performance filler achieving good productivity while preventing worsening of a working environment and production of a VOC and to provide a filler and a method for producing the filler, a filler composition of the present invention contains wet silica, a polyoxyethylene unsaturated fatty acid ester, and a sulfur-containing silane coupling agent.

According to the present disclosure, a hydrophobic polymeric composite comprising a hydrophobic polymer matrix with hydrophobically modified particles dispersed therein is provided. The hydrophobically modified particles may be derived from hydrophilic particles modified with organic moieties. The hydrophobically modified particles may also take in the form of core-shell fibers with hydrophilic particles encapsulated inside the core of said fibers or in the form of monolithic fibers embedded with hydrophilic particles. The method for making hydrophobic polymeric composite comprising each of the various hydrophobically modified particles is also provided. The hydrophobic polymer matrix can be chosen from poly(alpha-hydroxyesters), of carbonates, polyurethanes or polyalkanoates. For example, hydrophilic particles, such as barium sulphate, zirconium oxide, tantalum oxide or bismuth oxide, are dispersed in the hydrophobic biodegradable polymers, such as poly-(L-lactide) (PLLA).

According to the present disclosure, a hydrophobic polymeric composite comprising a hydrophobic polymer matrix with hydrophobically modified particles dispersed therein is provided. The hydrophobically modified particles may be derived from hydrophilic particles modified with organic moieties. The hydrophobically modified particles may also take in the form of core-shell fibers with hydrophilic particles encapsulated inside the core of said fibers or in the form of monolithic fibers embedded with hydrophilic particles. The method for making hydrophobic polymeric composite comprising each of the various hydrophobically modified particles is also provided. The hydrophobic polymer matrix can be chosen from poly(alpha-hydroxyesters), of carbonates, polyurethanes or polyalkanoates. For example, hydrophilic particles, such as barium sulphate, zirconium oxide, tantalum oxide or bismuth oxide, are dispersed in the hydrophobic biodegradable polymers, such as poly-(L-lactide) (PLLA).

An embodiment of the present application discloses a display panel, a manufacturing method thereof, and a display device thereof. The display panel includes a light emission functional layer and a color filter layer, the color filter layer includes a light shielding units, a light shielding material in the light shielding units includes a light shielding composition. The light shielding composition includes a plurality of carbon black particles and at least one function group located on surfaces of the carbon black particles. The function group is an acidic functional group or a free radical capture group, the acidic functional group is one of a carboxyl group, a hydroxy group, and a carbonyl group. The free radical capture group is a ketone group.

There are disclosed aqueous pigment dispersions containing dispersant-improving-agents, and methods of preparing and using the same.

A coated powder comprises (a) particles, and (b) a coating on the surface of the particles including (1) silica moieties, (2) organo oxysilane moieties selected from the group consisting of mono-organo oxysilane moieties, bi-organo oxysilane moieties and tri-organo oxysilane moieties, and (3) poly(dialkyl)siloxane moieties. The amount by weight in SiO.sub.2 equivalents of the organo oxysilane moieties and the silica moieties is at least 0.0625% of the total coated powder weight per m.sup.2/g of the specific surface area of the particle to be coated.

A coated powder comprises (a) particles, and (b) a coating on the surface of the particles including (1) silica moieties, (2) organo oxysilane moieties selected from the group consisting of mono-organo oxysilane moieties, bi-organo oxysilane moieties and tri-organo oxysilane moieties, and (3) poly(dialkyl)siloxane moieties. The amount by weight in SiO.sub.2 equivalents of the organo oxysilane moieties and the silica moieties is at least 0.0625% of the total coated powder weight per m.sup.2/g of the specific surface area of the particle to be coated.

A coating film-forming composition includes a hydrolysis-condensation product of a hydrolyzable silane and fine inorganic particles subjected to a special dispersion treatment, that can be formed into a highly heat-resistant, highly transparent coating film capable of exhibiting a high refractive index and having a large thickness and excellent storage stability as a coating composition; and a process for producing the coating film-forming composition.