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US4312845A Expired / Lapsed US ⏱️ 0.0 years remaining

Method of producing amorphous silica of controlled oil absorption

Assignee: JM Huber Corp
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Filing: 1980-09-15
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Granted: 1982-01-26
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Expires: 2000-09-15
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Abstract

Abstract A new silica is formed by hydrothermally reacting an aqueous dispersion of silica and sodium hydroxide, under certain conditions, to form a partly polymerized silicate; spray drying the mixture to form spheres of polysilicate; reacting the polysilicate with sulfuric acid to form a synthetic amorphous silica; and filtering, washing and drying the synthetic silica. This silica is useful as an adsorbent in polyol purification. When milled and air classified to the proper particle size, it is useful as a polishing agent in dentrifrices and as a flatting pigment in paints.

Inventors

  • 👤 Satish K. Wason

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 09:39
CPC Classifications
C; C07; C07C; C07C29/00; C07C29/74; C07C29/76; A; A61; A61K; A61K8/00; A61K8/18; A61K8/19; A61K8/25; A61Q; A61Q11/00; B; B01; B01J; B01J20/00; B01J20/02; B01J20/10; B01J20/103; C01; C01B; C01B33/00; C01B33/113; C01B33/12; C01B33/18; C01B33/187; C09; C09D; C09D7/00; C09D7/40; C09D7/42; A61K2800/00; A61K2800/40; A61K2800/41; A61K2800/412; C01P; C01P2002/00; C01P2002/02; C01P2002/50; C01P2002/52; C01P2004/00; C01P2004/30; C01P2004/32; C01P2004/51; C01P2004/60; C01P2004/61; C01P2006/00; C01P2006/10; C01P2006/12; C01P2006/19; C07B; C07B2200/00; C07B2200/07

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 380 words
A method of producing a synthetic amorphous silica useful as a polishing agent in a dentifrice comprising a solid phase comprising from 10 to 50% by weight of the dentifrice, of said synthetic amorphous silica and a liquid phase comprising water and a polyhydric alcohol humectant selected from the group consisting of sorbitol, glycerin and mixtures thereof; wherein fluoride is present in the dentifrice composition and the dentifrice has an RDA of less than 500 when the silica has 100% of the particles below 44 microns, an oil absorption greater than 60 cc/100 g and a BET surface area between 40 and 420 sq. m/g; as a flatting pigment in a paint coating composition wherein said flatting pigment has a 60 degree gloss of less than 8 when the silica has 100% of the particles below 10 microns and having an average particle size of from 2 to 5 microns, an oil absorption greater than 60 cc/100 g and a BET surface area between 40 and 420 sq. m/g; and as an adsorbent for polyol purification when the silica has at least 70% of the silica larger than 44 microns, an oil absorption of from 60 to 140 cc/100 g and a BET surface area greater than 60 sq. m/g when the synthetic silica contains up to 5% by weight of a metal cation adduct selected from the group consisting of aluminum, magnesium, zinc and calcium, said method comprising the steps of: (a) subjecting an aqueous dispersion including finely divided silica and a sodium hydroxide to hydrothermal treatment at a temperature in the range of from about 138 to 210 degrees Celsius and for a period of time of from about 2.5 to 4.5 hours and sufficient to react the silica and said sodium hydroxide to form a reaction mixture of partly polymerized sodium silicate, said aqueous dispersion having a silica to sodium oxide weight ratio of at least 1.8:1; (b) spray-drying said reaction mixture at a temperature of at least 204 degrees Celsius to form minute hollow spheres of sodium polysilicate having a bulk density of from 0.128 to 0.416 g/cc; (c) reacting the polysilicate with a 5 to 15% sulfuric acid solution to form a synthetic amorphous silica; and (d) filtering, washing and drying the synthetic amorphous silica.
Claim 2
Independent Claim 380 words
A method of producing a synthetic amorphous silica useful as a polishing agent in a dentifrice comprising a solid phase comprising from 10 to 50% by weight of the dentifrice, of said synthetic amorphous silica and a liquid phase comprising water and a polyhydric alcohol humectant selected from the group consisting of sorbitol, glycerin and mixtures thereof; wherein fluoride is present in the dentifrice composition and the dentifrice has an RDA of less than 500 when the silica has 100% of the particles below 44 microns, an oil absorption greater than 60 cc/100 g and a BET surface area between 40 and 420 sq. m/g; as a flatting pigment in a paint coating composition wherein said flatting pigment has a 60 degree gloss of less than 8 when the silica has 100% of the particles below 10 microns and having an average particle size of from 2 to 5 microns, an oil absorption greater than 60 cc/100 g and a BET surface area between 40 and 420 sq. m/g; and as an adsorbent for polyol purification when the silica has at least 70% of the silica larger than 44 microns, an oil absorption of from 60 to 140 cc/100 g and a BET surface area greater than 60 sq. m/g when the synthetic silica contains up to 5% by weight of a metal cation adduct selected from the group consisting of aluminum, magnesium, zinc and calcium, said method comprising the steps of: (a) subjecting an aqueous dispersion including finely divided silica and a sodium hydroxide to hydrothermal treatment at a temperature in the range of from about 138 to 210 degrees Celsius and for a period of time of from about 2.5 to 4.5 hours and sufficient to react the silica and said sodium hydroxide to form a reaction mixture of partly polymerized sodium silicate, said aqueous dispersion having a silica to sodium oxide weight ratio of at least 1.8:1; (b) spray-drying said reaction mixture at a temperature of at least 204 degrees Celsius to form minute hollow spheres of sodium polysilicate having a bulk density of from 0.128 to 0.416 g/cc; (c) reacting the polysilicate with a 5 to 15% sulfuric acid solution to form a synthetic amorphous silica; and (d) filtering, washing and drying the synthetic amorphous silica.

References Cited (Backward Citations)

US3838192A Cited
US3928541A Cited
DE2502111A1 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-01-25 1985-07-27 1986-01-26 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-01-25 1989-07-27 1990-01-26 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-01-25 1993-07-27 1994-01-26 $7700.00 Window Closed / Lapsed

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