Abstract: The present disclosure relates to a process for preparing surface-modified carbonaceous particles, wherein said carbonaceous particles are coated with a surface layer of amorphous carbon by dispersing carbonaceous material with an amphiphilic compound, spray drying of the dispersion and subsequent calcination of the dried material. The disclosure also pertains to surface-modified carbonaceous particles coated with amorphous carbon, which can for example be obtained by the process of the invention. The present disclosure further relates to the use of the surface-modified carbonaceous particles in a variety of technical applications, such as its use as an active material for negative electrodes of lithium ion batteries. The present disclosure also relates to a carbon brush or a polymer composite material, and generally compositions comprising said surface-modified carbonaceous particles, optionally together with other carbonaceous or non-carbonaceous materials.

Abstract: Surface-modified carbon hybrid particles may be characterized by a high surface area and a high mesopore content. Surface-modified carbon hybrid particles may be in agglomerated form. Surface-modified carbon hybrid particles may be used, for example, as conductive additives. Dispersions of such compounds in a liquid medium in the presence of a surfactant may be used, for example, as conductive coatings. Polymer compounds filled with the surface-modified carbon hybrid particles may be formed. Surface-modified carbon hybrid particles may be used, for example, as carbon supports.

Abstract: Surface-modified, low surface area synthetic graphite may have a BET surface from 1.0 to 4.0 m2/g and a crystallite size Lc to crystallite size La ratio of greater than 1. Processes for modifying the surface of low surface area synthetic graphite may result in surface-modified, low surface area synthetic graphite have a BET surface from 1.0 to 4.0 m2/g and a crystallite size Lc to crystallite size La ratio of greater than 1. Such synthetic graphite may have many uses, including for example, as a negative electrode material in lithium-ion batteries.

Abstract: The present invention relates to a dental glass containing 50 to 70 wt. % of SiO2, 5 to 18 wt. % of Al2O3, 6.1 to 30 wt. % of MgO, 1 to 15 wt. % of La2O3, 1 to 15 wt. % of WO3, 0.1 to 8 wt. % of ZrO2, and optionally further oxides except for the oxides of Sr, Ba or alkali metals, wherein the stated quantities in total add up to 100 wt. %.

Abstract: The present invention relates to a dental glass containing 50 to 70 wt. % of SiO2, 5 to 18 wt. % of Al2O3, 6.1 to 30 wt. % of MgO, 1 to 15 wt. % of La2O3, 1 to 15 wt. % of WO3, 0.1 to 8 wt. % of ZrO2, and optionally further oxides except for the oxides of Sr, Ba or alkali metals, wherein the stated quantities in total add up to 100 wt. %.