Sulfuric acid formulations

Catalysts. Commercial sulfuric acid catalysts typically consist of vanadium and potassium salts supported on sUica, usually diatomaceous earth (see Diatomite). Catalyst peUets are available in various formulations, shapes, and sizes depending on the manufacturer and the particular converter pass in which they are to be used. A detailed discussion of oxidation catalysts for sulfuric acid production is available (107). 

Copper-plating bath compositions of various types have been used. A typical bath formulation consists of 200 g copper sulfate crystals, 30 mL cone, sulfuric acid, 2 mL phenylsulfonic acid, and 1000 mL distUled water. A pure copper anode may be used a copper anode containing a trace of phosphoms reduces sludge accumulation in the plating bath. 

ABS plastic, a polymer consisting of polybutadiene spheroids is dispersed in a continuous phase of poly(styrene—acrylonitrile). The chromic acid attacks the polybutadiene at a much higher rate than the continuous phase. This gives an excellent microroughened surface with superior metal-to-plastic bond strength. A typical recommended formulation consists of 20 vol % sulfuric acid, 420 g/L chromic acid, and 0.1—1.0% of a fluorocarbon wetting agent. The plastic is treated with this formulation for 6—10 min at 60—65°C. 

Pla.tinum, Platinum plating has found appHcation in the production of platinised titanium, niobium, or tantalum anodes which are used as insoluble anodes in many other plating solutions (see Metalanodes). Plating solutions were often based on platinum "P" salt, which is diamminedinitroplatiniim (IT). A dinitroplatinite sulfate—sulfuric acid bath has been used to plate direcdy onto titanium (129). This bath contains 5 g/L of the platinum salt, pH adjusted to 2.0 with sulfuric acid. The bath is operated at 40°C at 10—100 A/m. Other baths based on chloroplatinic acid have been used in both acid and alkaline formulations the acid bath uses 20 g/L of the platinum salt and 300 g/L hydrochloric acid at 65° C and 10—200 A/m. The alkaline bath uses 10 g/L of the platinum salt, 60 g/L of ammonium phosphate and ammonium hydroxide to give a pH of 2.5—9.0. The alkaline bath can be plated directly onto nickel-base alloys acid baths require a gold strike on most metals. 

Cyclization of hydrazonyl chloride 797 with aniline gave triazolotriazine 798 (R2 = PhNH) (80JHC209). Cyclization of 797 was also effected by the action of sodium acetate to give 798 (R2 = Cl) (83JHC285). Cyclization of 799 by the action of sulfuric acid gave a triazolotriazine formulated as 800 or 801 (83JHC285). 

The dilute sulfuric acid obtained as a coupled product in stoichiometric ratios is used in the fertilizer industry. Formerly it was neutralized to sodium sulfate, but this practice is now of minor interest since fillers have been withdrawn from most detergent formulations. 

Preparation of Emulsions. The entire aqueous phase was stirred until all solids were dissolved. Sufficient water was withheld from the formulation so small volumes of experimental and control components could be added to emulsion subsamples. Sulfuric acid (1 N) was added to the aqueous phase to decrease the pH to 5.7. The two phases in separate containers were blanketed with nitrogen, sealed, and heated to 75 in an 80 water bath (about 30 minutes). The hot oil phase was stirred slowly and blanketed with nitrogen, then the hot aqueous phase was quickly added while stirring. The emulsion was blanketed with nitrogen and slowly stirred (about 2 hours) in the stoppered container until ambient temperature ( 25 ) was reached. Subsamples of the master batch were removed for the addition of experimental components and stored in 1-oz containers. The containers had been washed with hot tap water, deionized water, and methanol, then dried at 120 . 

Massaccesi reported the development of a two-phase titration method for the analysis of miconazole and other imidazole derivatives in pure form and in pharmaceutical formulation [14], To the sample (10 mg) are added 10 mL of water, 10 mL of 1 M-sulfuric acid, 25 mL of dichloromethane and 1 mL of 0.05% indophenol blue (C.I. No. 49700) in dichloromethane solution and the solution is titrated with 10 mM sodium dodecyl sulfate until the color of the organic phase changes from blue to pale yellow. Results obtained for the drug in pure form, tablets, suppositories, cream and lotion agreed with the expected values and the coefficient of variation (n = 6) were 0.3-0.35%. Imidazole and the other constituents of the pharmaceutical preparations did not interfere. 

Sastry et al. [50] estimated primaquine in its tablet formulation. Powdered tablets equivalent to 100 mg of primaquine phosphate were dissolved in water, filtered, and filtrate was diluted to 100 mL with water. Portions of the solution were shaken with 3 mL of 5 mM brucine-0.16 M sulfuric acid, 1.5 mL of 5 mM sodium periodate and 2 mL of 1.2 M sulfuric acid and diluted to 9 mL with water. The solution was set aside for 20 min in a boiling water bath, cooled, and diluted to 10 mL with water. The absorbance was measured at 510 nm versus a reagent blank. Beer s law was obeyed from 20 to 140 pg/mL of primaquine phosphate. The coefficient of variation was 1.56% (n = 8). Recovery was 99.2%. 

In contrast to the above, other reactions have been found to require base assistance by water in the rate-determining step, i.e. the water activity does appear in the rate law. The mechanism formulated for the condensation of acetaldehyde in sulfuric acid is given in equation (63), following on from the enolization of Scheme 7, subsequent dehydration to crotonaldehyde occurring as shown in Scheme 8. The ky k2, k3 and k 3 steps shown were all studied.246... 

Equation (6.13) is an expression assuming that all sulfuric acid formed will react with the cement. For practical reasons, the following expression can be formulated ... 

The mutagenic aminophenazines 71 are present as impurities of carbendazim (72) fungicides and its formulations. They were determined by HPLC-UVD (diode array), using 0.02% sulfuric acid in MeOH, and measuring at 270 and 453 nm186. 

Gas Chromatography Analysis of Water for Pesticides. All analyses for pesticides in water were done by gas chromatography. Solvents used for extraction were checked by gas chromatography for purity and interferences and all glassware used in the extraction was cleaned in a chromic acid/sulfuric acid mixture. Standards consisted of mixtures of various pesticides (actual commercial formulations) suspended or dissolved in water. These aqueous standards were extracted in the same manner as unknown solutions. The standard concentrations encompassed the concentration of unknowns to be determined. A standard curve normally consisted of a set of four pesticide concentrations. Blanks were run and an internal standard (eicosane) was used. The internal standard concentration was kept constant for all analyses. The conditions for GC analysis were guided by the pesticides expected in the water. For the more complex mixtures, such as those employed in the synthetic waste and those encountered in the field, a 6 ft., 3 percent SE-30 on GAS CHROM Q column sufficed. A typical chromatogram of a complex pesticide mixture is shown in Figure 2. ( )... 

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