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Water thermal effects

Measuring the gross heating value (mass) is done in the laboratory using the ASTM D 240 procedure by combustion of the fuel sample under an oxygen atmosphere, in a bomb calorimeter surrounded by water. The thermal effects are calculated from the rise in temperature of the surrounding medium and the thermal characteristics of the apparatus. [Pg.180]

Thermal effects on aquatic organisms have been given critical scientific review. Annual reviews of the thermal effects Hterature have been pubUshed beginning in 1968 (12). Water temperature criteria for protection of aquatic life were prepared by the NAS in 1972, and these criteria have formed the basis of the EPA recommendations for estabUshing water temperature standards for specific water bodies (13,14). [Pg.474]

Bead Polymerization Bulk reaction proceeds in independent droplets of 10 to 1,000 [Lm diameter suspended in water or other medium and insulated from each other by some colloid. A typical suspending agent is polyvinyl alcohol dissolved in water. The polymerization can be done to high conversion. Temperature control is easy because of the moderating thermal effect of the water and its low viscosity. The suspensions sometimes are unstable and agitation may be critical. Only batch reaciors appear to be in industrial use polyvinyl acetate in methanol, copolymers of acrylates and methacrylates, polyacrylonitrile in aqueous ZnCh solution, and others. Bead polymerization of styrene takes 8 to 12 h. [Pg.2102]

The major reasons for the beluu ior of vertical temperature in water bodies are the low thermal condnctii ity and the absorption of heat in the first few meters. As tlie surface waters begin to heat, transfer to low er layers is reduced and a stability condition develops. The prediction of thermal behavior in lakes and reser oirs is an important power plant siting consideration and also is a major factor in preienting e.xcessive thermal effects on sensitive ecosystems. Furthermore, the extent of thermal stratification influences the vertical dissolved ox)gen (DO) profiles where reduced DO often results from minimal exchiuige with aerated water. ... [Pg.362]

For other environments, such as in sea-water or in chemical plants, exposure conditions that most nearly duplicate those of the related service and are at the same time reproducible, are used. Impingement by water or water carrying entrained solids, thermal effects and physical abuse are among the factors to be considered. [Pg.1081]

Parent polyfthicnylene vinylene) has also been synthesized by an aldol precursor route [122]. In this method, 5-methyl-2-thiophenecarbaldehyde 76 is treated with a base and the monomer polymerizes yielding a precursor 77 which is soluble in water. Thermal treatment in an acidic solution at 80 nC yields the fully conjugated material. Alternatively, the solid polymer may be healed to 280 C to effect elimination of water. Fully conjugated material exhibits low conductivity (10 8 S cm"1) in its pristine stale. [Pg.343]

This difference originates from the different heat capacities of the reaction mixtures. The large difference between the process heats could not be attributed to dilution of the aromatic compound in the nitric acid/water mixture. The difference increased by adding a larger amount of nitric acid.The heat of the solvent process, that was run in such a way that the heat flux was kept constant, only increased slightly due to the aromatic dilution by the acid added to the reaction mixture. In contrast, extra acid addition resulted in a significant rise of the thermal effect of the water process (to 209 kJ/kg), indicating that formation of a di-nitro compound proceeds. [Pg.374]

A DSC instrument was used to assess the possible consequences of a potential thermal runaway using post-nitration mixtures for evaluations (see Fig. 5.4-65). For the solvent process two minor peaks between 150 and 220 °C appeared, which correspond to thermal effects of -15 kJ/kg and -9 kJ/kg. In contrast, a large thermal effect (-730 kJ/kg) was observed for the reaction mixture from the water process, located between 90 and 160 °C. Based on these data the risk of a thermal runaway for both processes was assessed. [Pg.374]

The reduction of NO also produced water, which however did not desorb immediately, showing a delay of about 50 s due to adsorption onto the catalyst and most likely onto Ba sites to form Ba(OH)2. The stepwise addition of hydrogen to the reactor was accompanied by a small increase of the catalyst temperature (3-5°C), due to the occurrence of the exothermic reduction, so that the run was actually performed in the absence of significant thermal effects. The following main reactions were thus likely involved in the reduction of stored NO by H2 ... [Pg.192]

Sharma et al. [153] have devised a gentle accelerated corrosion test using a kinetic rate equation to establish appropriate acceleration factors due to relative humidity and thermal effects. Using an estimate for the thermal activation energy of 0.6 eV and determining the amount of adsorbed water by a BET analysis on Au, Cu and Ni, they obtain an acceleration factor of 154 at 65°C/80% RH with respect to 25 °C/35-40% RH. [Pg.278]

In reservoirs with discharge of hypolimnetic water, the effects on the water temperature have been widely studied. If there is stratification, water temperature downstream from the dam is higher in winter, colder in summer, the daily and annual thermal amplitude is reduced and the maximum annual temperature is delayed [5-7]. Recently, it has been observed that hypolimnetic discharges can reduce the variability of the temperature of the water in reduced time scales, in the range of days to weeks [8]. The low temperatures in summer can modify the composition of the fluvial community, but they can also bring the river to a previous stage of the river continuum [9, 10]. [Pg.79]

Thermogravimetry can be used to measure the amount of water [232] or other molecule adsorbed on a zeolite. DSC can be uhlized to study the thermal effects during adsorption and desorphon of water [233] because the peak area under the heat flow time curve is related to the sorption heat. [Pg.156]

Cook (1958), Ionization in Shock Waves (pp 153-58) Thermal Effects of Shock Waves in Solids (213-16) Stability of a Shock Wave in an Inert Solid (216) Chapter 13. Shock Waves in Gaseous and Condensed Media, which includes Mechanism of Formation and Propagation of Shock Waves in Air and Water (322-24) Formation of Pressure Wave (324-26) Propagation of Pressure Wave in... [Pg.539]

Thermal Expansion. Most manufacturers literature (87,119,136—138) quotes a linear expansion coefficient within the 0—300°C range of 5.4 x 10"7 to 5.6 x 10 7 /°C. The effect of thermal history on low temperature expansion of Homosil (Heraeus Schott Quarzschmelze GmbH) and Osram s vitreous silicas is shown in Figure 4. The 1000, 1300, and 1720°C curves are for samples that were held at these temperatures until equilibrium density was achieved and then quenched in water. The effect of temperature on linear expansion of vitreous silica is compared with that of typical soda—lime and borosilicate glasses in Figure 5. The low thermal expansion of vitreous silica is the main reason that it has a high thermal shock resistance compared to other glasses. [Pg.505]

When in contact with some skin or an eye, the very concentrated corrosives, dissolve the water of tissues. Before they really lead to a chemical bum, or simultaneously, these very concentrated corrosives can cause a bum by dehydration and/or by thermal effect. [Pg.39]


See other pages where Water thermal effects is mentioned: [Pg.123]    [Pg.123]    [Pg.119]    [Pg.47]    [Pg.505]    [Pg.340]    [Pg.473]    [Pg.474]    [Pg.390]    [Pg.509]    [Pg.2055]    [Pg.274]    [Pg.176]    [Pg.214]    [Pg.372]    [Pg.241]    [Pg.65]    [Pg.145]    [Pg.239]    [Pg.162]    [Pg.165]    [Pg.237]    [Pg.85]    [Pg.221]    [Pg.225]    [Pg.394]    [Pg.235]    [Pg.1120]    [Pg.1121]    [Pg.480]    [Pg.203]    [Pg.473]    [Pg.474]    [Pg.501]    [Pg.73]   
See also in sourсe #XX -- [ Pg.224 ]




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