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YIGSR peptide radiopharmaceutical applications |
| OF THE PREFERRED EMBODIMENTS OF THE INVENTION (BEST MODES FOR CARRYING OUT THE INVENTION) Using ... |
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| We claim: 1. A compound of the formula ##STR43## wherein R.sup.1 is hydrogen or a conventional ... |
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System for whole body imaging and count profiling with a scintillation camera |
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Substituted phenyl piperidines |
| We claim: 1. A compound characterized by the formula ##STR63## wherein n is 1 or 2, Y is OH, R.sup.1... |
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Dental prophylaxis containing alkylamine fluorophosphates |
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Process for preparing silica-alumina
| Details |
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Inventors: Shyr, Yen-Shin; Johnson, Marvin M.;
Assignee: Phillips Petroleum Company (Bartlesville, OK)
Primary Examiner: Dees; Carl F.
Assistant Examiner:
Attorney, Agent or Firm: Brandes; K. K.
A process for preparing silica-alumina compositions comprises mixing a first aqueous solution containing an aluminum salt (preferably KAl(SO.sub.4).sub.2) and an ammonium salt (preferably (NH.sub.4).sub.2 SO.sub.4) with a second solution containing an alkali metal silicate (preferably Na.sub.2 SiO.sub.3), wherein the mol ratio of the alkali metal silicate to the aluminum salt is in the range of from about 2:1 to about 20:1, and the concentration of the ammonium salt is chosen so as to afford coprecipitation of silica-alumina hydrogel (preferably at a pH of about 3-6). The thus coprecipitated silica-alumina hydrogel can be separated from the mixture of the two solutions, optionally washed, and calcined so as to prepare acidic silica-alumina suitable as cracking catalyst material. |
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DETAILED DESCRIPTION OF THE INVENTION The term "silica-alumina hydrogel" as used herein is defined as a coagulated colloid of coprecipitated, hydrated silica-alumina containing an embedded aqueous phase. The terms "acidic sites" and "acidity" of silica-alumina compositions as used herein refer to the presence of any sites (on the surface of the silica-alumina composition) which can chemically interact with any Bronsted or Lewis base. The acidity of silica-alumina can be determined by any of the methods described in the literature such as in "Solid Acids and Bases--Their Catalytic Properties" by Kozo Tanabe, 1970, Academic Press, New York, NY, pages 5-23, and "Surface Acidity of Solid Catalysts" by H. A. Benesi et al, Advances in Catalysis, Volume 27, 1978, Academic Press, pages 99-112, both literature citations being herein incorporated by reference. The process for making silica-alumina in accordance with this invention comprises the step of mixing a first aqueous solution, comprising an aluminum salt plus an ammonium salt of an acid having a pKa of less than 2, with a second aqueous solution comprising an alkali metal silicate, wherein the amount of the ammonium salt in said first solution is such that a silica-alumina hydrogel is coprecipitated upon said mixing. Suitable aluminum salts are those that are substantially water-soluble such as Al(NO. sub. 3). sub. 3, Al. sub. 2 (SO. sub. 4). sub. 3, KAl(SO. sub. 4). sub. 2, NH. sub. 4 Al(SO. sub. 4). sub. 2, aluminum acetate and the like. Suitable ammonium salts include NH. sub. 4 Cl, NH. sub. 4 Br, NH. sub. 4 NO. sub. 3, (NH. sub. 4). sub. 2 SO. sub. 4, NH. sub. 4 ClO. sub. 4, ammonium trichloroacetate and the like. Suitable water-soluble alkali metal silicates include Na. sub. 2 SiO. sub. 3, K. sub. 2 SiO. sub. 3, Cs. sub. 2 SiO. sub. 3, Na. sub. 2 Si. sub. 2 O. sub. 5, K. sub. 2 Si. sub. 2 O. sub. 5, Na. sub. 2 Si. sub. 2 O. sub. 7, Na. sub. 4 SiO. sub. 4 and the like. Presently preferred process ingredients are KAl(SO. sub. 4). sub. 2. 16H. sub. 2 O, (NH. sub. 4). sub. 2 SO. sub. 4 and Na. sub. 2 SiO. sub. 3. Preferably, the mixing of the two solutions is carried out with agitation, e
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