A radiation-emitting component includes a radiation source; a transparent material disposed in the beam path of the component and including a polymer material and filler particles, wherein the filler particles include an inorganic filler material and a phosphonic acid derivative or phosphoric acid derivative attached to a surface thereof and through which the filler particles are crosslinked with the polymer material.

The present invention relates to the use of a new polymeric aqueous emulsion for surface treating particles of mineral matter.

The present invention is directed to methods of making an electrophoretic dispersion comprising pigment particles dispersed in a solvent or solvent mixture, wherein said pigment particles comprises at least one polymer chain comprising a terminal thiocarbonylthio group, attached to the particle surface. The invention also relates to pigment particles suitable for use in an electrophoretic dispersion and methods for their preparation through a RAFT polymerization technique.

A method for coating pigment particles is provided, the method comprising heating a polymer resin in a carrier fluid to dissolve the polymer resin; suspending in the carrier fluid white pigment particles to be coated; and cooling the carrier fluid at a rate of 2° C./hr or less to effect precipitation of the polymer resin from the carrier fluid such that a coating of the resin is formed on the pigment particles, thereby producing the white liquid electrophotographic ink composition.

A composition comprising a pigment particle that is coated with a cationic material and isopropyl titanium tri-isostearate. The pigment particle can be included in a cleansing composition for deposition on a surface, such as skin.

A paint composition, which comprises a stanchion-encapsulated pigment such as titanium dioxide, can provide enhanced paint quality with reduced cost.

Despite significant progress in the synthesis of nanocomposite materials, integration of several components with various functions remains a big challenge, which significantly limits control over nanocomposite properties. The disclosure provides a multifunctional micro particle based on incorporation of titania nanoparticles combined into a porous polylactic acid (PLA) matrix. PLA is used as a biodegradable and biocompatible polymer and titania nanoparticles represent photocatalytically active nanofillers capable of degradation of organic compounds under solar irradiation. Titania nanoparticles are integrated with PLA by using ‘mixed’ and ‘in situ grown’ approaches. The hybrid systems effectively absorbed and degraded organic impurities from water. The sorption capacity, dye degradability, and PLA disintegration were controlled by varying the concentration of incorporated titania. The hybrid degradable systems can be applied as novel non-toxic photocatalytic materials for such as environmental cleanup of contaminated waters.

Metal oxide-polymer composite particles have a median particle size D50 of 40-75 nm or 100-150 nm and an average RTA of at least 0.06. Alternatively or in addition, metal oxide-polymer composites comprise two or more populations of metal oxide particles differing in size, particle size distribution, or shape. Alternatively or in addition, the use of a multicomponent hydrophobizing system including an alkylsilane to fabricate metal oxide-polymer composite particles increases the tribocharge of the composite particles.

A process for producing a particulate TiO.sub.2 includes supplementing metatitanic acid with an alkali compound in a quantity of 1200 ppm to 2400 ppm of alkali, with a phosphorus compound in a quantity of 0.1 wt.-% to 0.3 wt.-% by weight of P, expressed as phosphorus, and with an aluminum compound in a quantity of 1 ppm to 1000 ppm of Al, expressed as Al, to obtain a mixture. The quantity of the alkali compound, of the phosphorus compound, and of the aluminum compound are with respect to the TiO.sub.2 content. The mixture is calcined at a constant temperature of 940° C. to 1020° C. until a numerical fraction X.sub.50 of TiO.sub.2 has a primary crystallite size of at least 200 nm, to obtain a calcined mixture. The calcined mixture is cooled to obtain a cooled calcined mixture. The cooled calcined mixture is grinded to obtain the particulate TiO.sub.2.

The present invention relates to a method which uses non-core-shell polymer particles to form polymer film on a pre-formed solid substrate surface, said non-core-shell polymer particles comprising two covalently coupled polymer regions of different molecular composition, wherein (a) one of the two polymer regions is a crosslinked RAFT polymer region and the other polymer region is a film forming polymer region, (b) the crosslinked RAFT polymer region comprising particle aggregation prevention means selected from one or more of charged and steric stabilising functionality, and (c) the film forming polymer region comprising 0-3 wt. % of charged polymerised monomer residues relative to the total amount of polymerised monomer residues present in that region.