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Although nearly 100% sulfuric acid solutions can be made, the subsequent loss of SO 3 at the boiling point brings the concentration to 98.3% acid. The 98.3% grade, which is more stable in storage, is the usual form of what is described as "concentrated sulfuric acid".
The lead chamber process for sulfuric acid production was abandoned, partly because it could not produce sulfur trioxide or concentrated sulfuric acid directly due to corrosion of the lead, and absorption of NO 2 gas. Until this process was made obsolete by the contact process, oleum had to be obtained through indirect methods.
2-Propenoic acid, polymer with 2 p-propenamide, sodium salt / copolymer of acrylamide and sodium acrylate: Friction reducer 71050-62-9: 2-Propenoic acid, polymer with sodium phosphinate (1:1) No record 66019-18-9: 2-propenoic acid, telomer with sodium hydrogen sulfite: No record 107-19-7: 2-Propyn-1-ol / propargyl alcohol: No record 51229-78-8
Sulfuric(IV) acid (United Kingdom spelling: sulphuric(IV) acid), also known as sulfurous (UK: sulphurous) acid and thionic acid, [citation needed] is the chemical compound with the formula H 2 SO 3. Raman spectra of solutions of sulfur dioxide in water show only signals due to the SO 2 molecule and the bisulfite ion, HSO − 3 . [ 2 ]
The most important chemical sodium sulfate production is during hydrochloric acid production, either from sodium chloride (salt) and sulfuric acid, in the Mannheim process, or from sulfur dioxide in the Hargreaves process. [21] The resulting sodium sulfate from these processes is known as salt cake. Mannheim: 2 NaCl + H 2 SO 4 → 2 HCl + Na 2 SO 4
The wet sulfuric acid process (WSA process) is a gas desulfurization process. After Danish company Haldor Topsoe introduced this technology in 1987, it has been recognized as a process for recovering sulfur from various process gases in the form of commercial quality sulfuric acid (H 2 SO 4) with the simultaneous production of high-pressure steam.
A salt containing reactive cations undergo hydrolysis by which they react with water molecules, causing deprotonation of the conjugate acids. For example, the acid salt ammonium chloride is the main species formed upon the half neutralization of ammonia in aqueous solution of hydrogen chloride: [2] NH 3 + HCl(aq) → [NH 4] + Cl − (aq)
If produced from oleochemical feedstock or the Ziegler process, the hydrocarbon chain of the alcohol will be linear. If derived using the oxo process, a low level of branching will appear usually with a methyl or ethyl group at the C-2 position, containing even and odd amounts of alkyl chains. [3] These alcohols react with chlorosulfuric acid: