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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.
Pilot plant operation has shown that ethanol pulping produces pulp superior to sulphite pulp at a lower cost. Lignin and hemicellulose are recovered in high yields. In 1987 the APR process was renamed the Alcell process. The process uses aqueous ethanol solutions (40–60% v/v) to delignifying wood at temperatures from 180 to 210 °C and 2–3. ...
The concentration of alkylsulfates in effluent from waste water treatment plants (WWTP) has been measured at 10 micrograms per litre (5.8 × 10 −9 oz/cu in) and lower. Alkyl sulfates biodegrade easily, even starting likely before reaching the WWTP. Once at the treatment plant, they are rapidly removed by biodegradation. Invertebrates were ...
The more popular methods for production of ethanol and cellulosic ethanol use enzymes that must be isolated first to be added to the biomass and thus convert the starch or cellulose into simple sugars, followed then by yeast fermentation into ethanol. This process does not need the addition of such enzymes as these microorganisms make their own.
the reaction steps presented here are just a part of the reaction sequence, see reference for more details. Photocatalytic oxidation with TiO 2: [15] TiO 2 + UV → e − + h + (irradiation of the photocatalytic surface leads to an excited electron (e −) and electron gap (h +)) Ti(IV) + H 2 O ⇌ Ti(IV)-H 2 O (water adsorbs onto the catalyst ...
The most pervasive is the application of non-toxic cosolvents with water to produce formulations that can dissolve hydrophobic molecules while maintaining cohesion with biological systems. Common cosolvents for this purpose are ethanol, propylene glycol, glycerine, glycofural, and polyethylene glycols. [7]
The conversion of ethanol to ethylene is a fundamental example: [3] [4] CH 3 CH 2 OH → H 2 C=CH 2 + H 2 O. The reaction is accelerated by acid catalysts such as sulfuric acid and certain zeolites. These reactions often proceed via carbocation intermediates as shown for the dehydration of cyclohexanol. [5] Some alcohols are prone to dehydration.
Ethanol-water mixtures have less volume than the sum of their individual components at the given fractions. Mixing equal volumes of ethanol and water results in only 1.92 volumes of mixture. [77] [82] Mixing ethanol and water is exothermic, with up to 777 J/mol [83] being released at 298 K. Hydrogen bonding in solid ethanol at −186 °C