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Hydrogen peroxide reactor

A fixed-bed reactor for this hydrolysis that uses feed-forward control has been described (11) the reaction, which is first order ia both reactants, has also been studied kiaeticaHy (12—14). Hydrogen peroxide interacts with acetyl chloride to yield both peroxyacetic acid [79-21-0] and acetyl peroxide... [Pg.81]

Most of the controlled corrosion studies on beryllium have been carried out in the USA in simulated reactor coolants. The latter have usually been water, aerated and de-aerated, containing small amounts of hydrogen peroxide and at temperatures up to 300-350°C. Many variables have been examined, covering surface condition, chemical composition, temperature, pH, galvanic effects and mechanical stress . [Pg.834]

In a falling film evaporator (4) a water-paraffin mixture is distilled off and completely pumped back to the reactor. The resulting product is separated into a 60% sulfuric acid fraction and paraffin-containing alkanesulfonic acid (5), which is bleached by hydrogen peroxide (6). In a stirred vessel (7) the alkanesulfonic acid is neutralized by 50% sodium hydroxide solution until the pH is exactly 7. The composition of the neutralized product is also given in Table 2. [Pg.148]

The utihty stream gets started at operating temperature and flow rate. In the following experiments, the utihty stream is heated so as to initiate the reaction. The main and secondary process tines are fed with water at room temperature and with the same flow rate as one of the experiments. Once steady state is reached, operating parameters are recorded. Process tines are then fed with the reactants, hydrogen peroxide and sodium thiosulfate. At steady state, operating parameters are recorded, and a sample of a known mass of reactor products is introduced in the Dewar vessel. Temperature in the Dewar vessel is recorded until equilibrium is reached, that is, until the reaction ends. This calorimetric method is aimed at calculating the conversion rate at the product outlet and thus the conversion rate in the reactor. The latter is also determined by thermal balances between process inlet and outlet of the reactor. Finally, the reactor is rinsed with water. This procedure is repeated for each experiment... [Pg.278]

To test the validity of this hypothesis, a 30% solution of hydrogen peroxide, a good source of hydroxyl radicals, was injected into the reactor during photockalytic methane... [Pg.412]

Such improvements in conversion were reported for the oxidation of ethanol by hydrogen peroxide to acetic acid. This is a well-studied reaction, carried out in a continuous stirred-tank reactor (CSTR). Near-complete conversion (> 99%) at near-complete selectivity (> 99%) was found in a micro-reaction system [150]. Processing in a CSTR resulted in 30-95% conversion at > 99% selectivity. [Pg.67]

In this context, the esterification of 4-(l-pyrenyl)butyric acid with an alcohol to the corresponding ester was investigated [171]. Without the presence of sulfuric acid no reaction to the ester was foimd in the micro reactor. On activating the surface by a sulfuric acid/hydrogen peroxide mixture, however, a yield of 9% was achieved after 40 min at 50 °C. On making the surface hydrophobic by exposure to octadecyltrichlorosilane, no product formation was observed. Using silica gel in a laboratory-scale batch experiment resulted in conversion, but substantially lower than in the case of the micro reactor. The yield was no higher than 15% (40 min ... [Pg.75]

Acetone was accidentally introduced into a reactor containing a sulphuric acid/nitric acid/hydrogen peroxide mixture. This led to an explosion due to acetone oxidation by the peroxymonosulphuric acid formed by the oxidising mixture. [Pg.309]

Chand et al. [88] degraded phenol under sonication at different frequencies with H2O2 and O3 in presence of zero valent iron and copper. The effectiveness of 300 kHz sonochemical reactor was found to be the maximum for the generation of OH radicals among 20, 300 and 520 kHz. The complete removal of phenol was achieved when sonicated with 300 kHz frequency with zero valent iron compared to zero valent copper. In their mechanism it was supposed that at first iron metal was corroded in the presence of hydrogen peroxide, under acidic conditions, oxidizing Fe° to Fe2+, which on further reaction with H202 produce OH radicals and Fe3+. The Fe° then reduces the Fe3+ back to Fe2+ and the chain was maintained as... [Pg.292]

Chand R, Ince NH, Gogate PR, Bremner DH (2009) Phenol degradation using 20, 300 and 520 kHz ultrasonic reactors with hydrogen peroxide, ozone and zero valent metals. Sep Purif Technol 67 103-109... [Pg.311]

Keairns and Manning AIChE J., 15 (660), 1969] have used the reaction between sodium thiosulfate and hydrogen peroxide in a well-stirred flow reactor to check a computer simulation of adiabatic CSTR operation. Data on their experimental conditions and the reaction parameters are listed below. The reaction may be considered second-order in sodium thiosulfate. [Pg.386]


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See also in sourсe #XX -- [ Pg.189 ]




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