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Aluminum Cleaning Acid

A number of chemical or electrochemical treatments may be applied after the forming of aluminum or aluminum alloy products. Solvent, acid and alkaline solutions, and detergents can be used to clean soils such as oil and grease from the aluminum surface. Acid and alkaline solutions can be used to etch the product or brighten its surface. Acid solutions are also used for deoxidizing and desmutting. [Pg.201]

Fluorotitanic acid is used as a metal surface cleaning agent, as a catalyst, and as an aluminum finishing solvent (see Metal surface treatments). Fluorotitanates are used in abrasive grinding wheels and for incorporating titanium into aluminum aHoys (see Abrasives Aluminumand aluminum alloys). [Pg.255]

Hexafluorozirconic acid is used ia metal finishing and cleaning of metal surfaces, whereas the fluorozirconates are used in the manufacture of abrasive grinding wheels, in aluminum metallurgy, ceramics industry, glass manufacturing, in electrolytic cells, in the preparation of fluxes, and as a fire retardant (see Abrasives Metal surface treati nts). [Pg.263]

Although abrasive polishing is the most common metal polishing operation, other forms of polishing and chemical brightening are used ia iadustrial operations. Aluminum tmck trailers often are cleaned and brightened by treatments with strong acids or alkaHes, which chemically remove oxides. Chemical methods can also remove tarnish from other metals (55,56). [Pg.211]

Hydrated amorphous silica dissolves more rapidly than does the anhydrous amorphous silica. The solubility in neutral dilute aqueous salt solutions is only slighdy less than in pure water. The presence of dissolved salts increases the rate of dissolution in neutral solution. Trace amounts of impurities, especially aluminum or iron (24,25), cause a decrease in solubility. Acid cleaning of impure silica to remove metal ions increases its solubility. The dissolution of amorphous silica is significantly accelerated by hydroxyl ion at high pH values and by hydrofluoric acid at low pH values (1). Dissolution follows first-order kinetic behavior and is dependent on the equilibria shown in equations 2 and 3. Below a pH value of 9, the solubility of amorphous silica is independent of pH. Above pH 9, the solubility of amorphous silica increases because of increased ionization of monosilicic acid. [Pg.488]

Clean metallic aluminum is extremely reactive. Even exposure to air at ordinary temperatures is sufficient to promote immediate oxidation. This reactivity is self-inhibiting, however, which determines the general corrosion behavior of aluminum and its alloys due to the formation of a thin, inert, adherent oxide film. In view of the great importance of the surface film, it can be thickened by anodizing in a bath of 15% sulfuric acid (H2SO4) solution or by cladding with a thin layer of an aluminum alloy containing 1 % zinc. [Pg.90]

The new continuous casting processes, in contrast to ingot cast products, provide tin mill products which are exceptionally clean and formable. The deoxidizing processes required for continuous casting involve either aluminum or silicon killing, which adds aluminum or silicon to the steel. Experience with type D steels indicates that the added aluminum will not cause a corrosion problem. Laubscher and Weyandt (18) have shown that the silicon found in silicon killed, continuous cast, heavily coated ETP will not adversely affect the corrosion performance of plain cans packed with mildly acid food products in which tin usually protects steel. The data on enameled cans is not definitive. Additional published data are required to determine whether or not silicon actually reduces the performance of enameled cans made from enameled, heavily coated, silicon killed, continuous cast ETP. [Pg.11]

C) for cast iron and up to 140 °F for marstenitic SS (60 °C). Not suitable for galvanizing, aluminum, or enamels. Formic acid solvents containing the appropriate corrosion inhibitors and iron stabilizers can be very successful in cleaning larger units, such as once-through boilers. [Pg.638]

Sulfamic acid (HOS02NH2). Clean at only 120 °F (49 °C) for cast iron and up to 140 °F for marstenitic SS (60 °C). It is not suitable for galvanizing or aluminum over 150 °F, but it is suitable for copper, brass, and SS. Sulfamic acid tends to be used only in small systems because of its relatively high cost. It is a ciystalline solid and so is easily transported. Additionally, in the diy form it is relatively safe and has a negligible effect on skin. Typically, it is used at 10% strength, and when 5% sodium chloride is added, it is reasonably successful at dissolving ferric oxide. [Pg.641]

Hydrocarbons and carbonized or coke deposits can be removed by chromic acid. The chromic acid oxidizes the binders holding the deposits together. Use a 10 to 20% solution for 12 to 24 hours at 190 to 200 °F. Chromic acid cannot be effectively inhibited and is not suitable for cleaning copper, brass, aluminum, zinc, or cast iron because these are all rapidly attacked. [Pg.651]

P 17] In order to have a catalyst with a sufficiently high specific surface area, pretreatment of the micro channels made of aluminum was necessary [17], Following a cleaning procedure, an oxide layer with a regular system of nanopores was generated by anodic oxidation (1.5% oxalic acid 25 °C 50 V DC 2 h exposure using an aluminum plate cathode followed by calcination). [Pg.624]

Alkylation of dianions occurs at the more basic carbon. This technique permits alkylation of 1,3-dicarbonyl compounds to be carried out cleanly at the less acidic position. Since, as discussed earlier, alkylation of the monoanion occurs at the carbon between the two carbonyl groups, the site of monoalkylation can be controlled by choice of the amount and nature of the base. A few examples of the formation and alkylation of dianions are collected in Scheme 1.7. In each case, alkylation occurs at the less stabilized anionic carbon. In Entry 3, the a-formyl substituent, which is removed after the alkylation, serves to direct the alkylation to the methyl-substituted carbon. Entry 6 is a step in the synthesis of artemisinin, an antimalarial component of a Chinese herbal medicine. The sulfoxide serves as an anion-stabilizing group and the dianion is alkylated at the less acidic a-position. Note that this reaction is also stereoselective for the trans isomer. The phenylsulfinyl group is removed reductively by aluminum. (See Section 5.6.2 for a discussion of this reaction.)... [Pg.36]


See other pages where Aluminum Cleaning Acid is mentioned: [Pg.105]    [Pg.105]    [Pg.13]    [Pg.693]    [Pg.927]    [Pg.1442]    [Pg.1442]    [Pg.165]    [Pg.528]    [Pg.334]    [Pg.131]    [Pg.138]    [Pg.226]    [Pg.462]    [Pg.337]    [Pg.170]    [Pg.433]    [Pg.458]    [Pg.232]    [Pg.148]    [Pg.149]    [Pg.212]    [Pg.1599]    [Pg.60]    [Pg.953]    [Pg.1016]    [Pg.349]    [Pg.637]    [Pg.641]    [Pg.397]    [Pg.312]    [Pg.316]    [Pg.17]    [Pg.68]    [Pg.565]    [Pg.581]    [Pg.55]   


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Aluminum cleaning

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