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Showing papers on "Precipitated silica published in 1974"


Patent
31 Oct 1974
TL;DR: In this article, a new method for producing precipitated silicas having a unique combination of physical and chemical properties is disclosed, which is produced by acidulating a solution of an alkali metal silicate having a specific SiO 2 /Na 2 O mol ratio with an acid until precipitation just begins.
Abstract: A new method for producing precipitated silicas having a unique combination of physical and chemical properties is disclosed. The silicas are produced by acidulating a solution of an alkali metal silicate having a specific SiO 2 /Na 2 O mol ratio with an acid until precipitation just begins. At this point, the reaction mass is aged for a period of time and thereafter the acid addition is continued until the precipitated product is obtained. Products produced in accordance with the invention exhibit lower wet cake moisture and are characterized by their low structure, low oil absorption, high abrasiveness and high pack density, and as such are distinctly different from silicas used as reinforcing fillers in rubber. In a particularly advantageous embodiment, an adduct material, such as aluminum, is added to control the refractive index of the precipitated pigment silica. Products produced in this manner have particular utility for use as abrasion and gelling agents in clear toothpaste compositions.

40 citations


Patent
George Christie1
07 Feb 1974
TL;DR: A heat vulcanizable silicone rubber composition which is resistant to degradation by hydrocarbon oils and having a specific gravity in the cured state of 1.20 to 1.70 comprising an organopolysiloxane polymer and blends of organopoly-siloxanes polymers having a viscosity of anywhere from 1,000,000 to 200, 000,000 centipoise at 25*C, a curing catalyst, a silica filler selected from the class consisting of fumed silica, precipitated silica and mixtures thereof, an inorganic filler which may be any
Abstract: A heat vulcanizable silicone rubber composition which is resistant to degradation by hydrocarbon oils and having a specific gravity in the cured state of 1.20 to 1.70 comprising an organopolysiloxane polymer and blends of organopolysiloxane polymers having a viscosity of anywhere from 1,000,000 to 200,000,000 centipoise at 25*C, a curing catalyst, a silica filler selected from the class consisting of fumed silica, precipitated silica and mixtures thereof, an inorganic filler which may be any of the well known inert organic fillers such as, ground silica, diatomaceous earth and etc., and a small concentration of magnesium oxide and mixtures of various magnesium oxide.

23 citations


Journal ArticleDOI
TL;DR: In this article, an ion exchange mechanism between H aq + in the outer Helmholtz layer and M aq+ in solution is suggested, where the hydrated cation is assumed to be held to a negative surface site by electrostatic forces.

17 citations


Journal ArticleDOI
TL;DR: The ability of styrene-methyl methacrylate copolymers to stabilize silica dispersions has been investigated in this paper, and the results show that the copolymer with styrene contents in excess of ca. 60% does not stabilize in trichloroethylene but does so in carbon tetrachloride.
Abstract: The ability of styrene–methyl methacrylate copolymers to stabilize silica dispersions has been investigated. Random, block, and graft copolymers covering the entire composition range have been employed in carbon tetrachloride, trichloroethylene, and benzene solutions. Equilibrium sediment volumes and dispersion turbidities provide adequate and concordant estimates of stabilization efficiency. Polystyrene is not adsorbed by precipitated silica from trichloroethylene or benzene and does not stabilize dispersions in these liquids; although adsorbed from carbon tetrachloride, there is no stabilization. Poly(methyl methacrylate) is an efficient dispersion stabilizer, and its performance is independent of molecular weight over a wide range. Random copolymers having styrene contents in excess of ca. 60% do not stabilize in trichloroethylene but do so in carbon tetrachloride, although well adsorbed in both cases. With this major exception, and that of a low-styrene graft copolymer in carbon tetrachloride, copolymers of all structures and compositions stabilize well, better than poly(methyl methacrylate) in the solvents examined. A substantial degree of surface coverage is necessary for optimum stabilization. Subsidiary solution adsorption and layer thickness measurements are also reported.

9 citations


Patent
12 Nov 1974
TL;DR: In this article, the authors provided antifoam compositions comprising a dimethylpolysiloxane and a precipitated silica reacted with hexamethyldisilazane, and a process for the preparation and use thereof.
Abstract: There are provided antifoam compositions comprising a dimethylpolysiloxane and a precipitated silica reacted with hexamethyldisilazane and a process for the preparation and use thereof.

8 citations