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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 718479Erstellt: 24. Oktober 2026

Sulfuric Acid → Zirconium hydroxide (Zr(OH)4), (T-4)-

https://huagongshe.com/de/reaction/718479

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktSodium aluminateHCID 14766—
EduktSodium HydroxideHCID 14798—
EduktSodium orthosilicateHCID 26051—
EduktChloro hypochlorite;zirconiumHCID 71304769—
KatalysatorTitanium oxide (Ti3O)HCID 162651—
LösungsmittelWaterHCID 962—
ProduktZirconium hydroxide (Zr(OH)4), (T-4)-HCID 84465—
ProduktAluminum HydroxideHCID 10176082—
ProduktSilicon(4+) tetrahydroxideHCID 23617461—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Fine titanium oxide particle (Sakai Chemical Industry Co., Ltd., STR-100N) was added to water, to prepare 150 g/L aqueous slurry of TiO2. This slurry (5.0 L) was heated to 90° C. under stirring. While maintaining this temperature, a 150 g/L aqueous solution of sodium silicate, which corresponded to 6% by mass (in terms of SiO2) of TiO2, was added to the slurry. Then, 30% sulfuric acid was added thereto over 180 minutes such that the pH of the slurry should be 9. The resultant slurry was aged for 60 minutes. Next, under stirring, the temperature of the slurry was regulated so as to be 45° C. While the pH of the slurry was maintained to 8.5, a 100 g/L aqueous solution of zirconium oxychloride, which corresponded to 3.0% by mass (in terms of ZrO2) of TiO2, and 30% aqueous sodium hydroxide were added to the slurry as a single portion over 90 minutes. The resultant slurry was aged for 30 minutes. Then, under stirring, while the pH of the slurry was maintained to 8.5, a 250 g/L aqueous solution of sodium aluminate, which corresponded to 4.5% by mass (in terms of Al2O3) of TiO2, and 30% sulfuric acid were added to the slurry as a single portion over 120 minutes. The resultant slurry was aged for 30 minutes. Thus, on the surface of TiO2, coating layers of silicon hydroxide, zirconium hydroxide, and aluminum hydroxide were formed in the order as set forth.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09193871B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-95f5547fb1f149799f092f4895268fd6
Quellennotizuspto-grants-2015_11