Pyrolysis, water formation

With aldehydes, primary alcohols readily form acetals, RCH(OR )2. Acetone also forms acetals (often called ketals), (CH2)2C(OR)2, in an exothermic reaction, but the equiUbrium concentration is small at ambient temperature. However, the methyl acetal of acetone, 2,2-dimethoxypropane [77-76-9] was once made commercially by reaction with methanol at low temperature for use as a gasoline additive (5). Isopropenyl methyl ether [116-11-OJ, useful as a hydroxyl blocking agent in urethane and epoxy polymer chemistry (6), is obtained in good yield by thermal pyrolysis of 2,2-dimethoxypropane. With other primary, secondary, and tertiary alcohols, the equiUbrium is progressively less favorable to the formation of ketals, in that order. However, acetals of acetone with other primary and secondary alcohols, and of other ketones, can be made from 2,2-dimethoxypropane by transacetalation procedures (7,8). Because they hydroly2e extensively, ketals of primary and especially secondary alcohols are effective water scavengers. 

Flash vacuum pyrolysis of 2-methoxycarbonylpyrrole (11) gives the ketene (12), characterized by IR absorption at 2110 cm. On warming to -100 to -90 °C the dimer (13) is formed (82CC360). Flash vacuum pyrolysis of indole-2-carboxylic acid (14) results in loss of water and the formation of a ketene (15) showing absorption at 2106 cm (82CC360). 

In this study, we extend the range of inorganic materials produced from polymeric precursors to include copper composites. Soluble complexes between poly(2-vinylpyridine) (P2VPy) and cupric chloride were prepared in a mixed solvent of 95% methanol 5% water. Pyrolysis of the isolated complexes results in the formation of carbonaceous composites of copper. The decomposition mechanism of the complexes was studied by optical, infrared, x-ray photoelectron and pyrolysis mass spectroscopy as well as thermogravimetric analysis and magnetic susceptibility measurements. 

Based on these results, the reduction of Au(III) requires the formation of hot cavitation bubbles which cause pyrolysis of water and 1-propanol molecules. In addition, it is suggested that the number of hot cavitation bubbles and/or the bubble temperatures increase with increasing ultrasound intensity in the irradiation system. 

The highly oxygenated bio oil can be de-oxygenated, and thereby upgraded, over acidic zeolite catalysts through the formation of mainly water at low temperatures and C02 and CO at higher temperatures [1-3], Successful catalytic pyrolysis of woody biomass over Beta zeolites has been performed in a fluidized bed reactor in [4]. A drawback in the use of pure zeolitic materials has been the mechanical strength of the pelletized zeolite particles in the fluidized bed. 

Kinetic parameters of fast pyrolysis were derived while assuming a single process for the decomposition of wood, including three parallel first-order decay reactions for the formation of the product classes. This is the so-called Shafizadeh scheme [56]. The three lumped product classes are permanent gas, liquids (biooil, tar), and char a classification that has become standard over the years. The produced vapors are subject to further degradation to gases, water and refractory tars. Charcoal, which is also being formed, catalyzes this reaction and therefore needs to be removed quickly [57]. 

Deoxygenation reactions are catalyzed by acids and the most studied are solid acids such as zeolites and days. Atutxa et al. [61] used a conical spouted bed reactor containing HZSM-5 and Lapas et al. [62] used ZSM-5 and USY zeolites in a circulating fluid bed to study catalytic pyrolysis (400-500 °C). They both observed excessive coke formation on the catalyst, and, compared with non-catalytic pyrolysis, a substantial increase in gaseous products (mainly C02 and CO) and water and a corresponding decrease in the organic liquid and char yield. The obtained liquid product was less corrosive and more stable than pyrolysis oil. 

The CSCIF2O2 adduct is a white solid, stable at 25°C. Vacuum pyrolysis at 80°-100°C yields CsF and FCIO2 (142), demonstrating that the formation reaction is reversible. It fumes in moist air and reacts explosively with water (142). Controlled hydrolysis (54) proceeds according to... 

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