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C breaking

A small sample in a sealed glass capillary exploded violently at 181°C, breaking the surrounding oil bath. [Pg.706]

Equation (c) breaks down when A(co) co which is the case for instance... [Pg.511]

It was shown by E. Marsden and Thomas Barratt and independently by Hahn and Meitner that thorium C breaks down into thorium C and thorium C" (20, 34, 76). The last member of this series, thorium D, or thorio-lead, ends what Soddy has called the stately procession of element evolution (57). Thus thorium disintegrates in cascade to form the successive products mesothorium 1, mesothorium 2, radiothorium, thorium X, thoron, and thorium A, B, C, C, C", and D. [Pg.827]

Equation (c) breaks down when A(co) => which is the case for instance with the Gaussian distribution. Then values of time over a range can be tried until the results of integration of Equation (b) assume a constant value. This technique is applied In problems P5.07.04, P5.07.14 and P5.07.15. [Pg.500]

If the reaction occurs in a single step, the electron distribution about the three nuclei must change in the course of the collision such that a new bond, A-B, develops at the same time the old bond, B-C, breaks. Between the reactant and product stages, the nuclei pass through a configuration in which all three atoms are weakly linked together. We can picture the progress of the reaction as... [Pg.499]

Place a mixture of 7.0 g (0.018 mol) of tetraphenylcyclopentadienone (Expt 7.7) 1.9 g (0.019 mol) of maleic anhydride (Expt 5.218) and 5 ml of bromo-benzene in a 100-ml round-bottomed flask fitted with a reflux condenser. Reflux gently in a fume cupboard (carbon monoxide is evolved) for 1.5 hours during this period the dark brown colour of the cyclic ketone disappears. Cool to room temperature, add about 15 ml of light petroleum, b.p. 60-80 °C, break up the solid and filter. Wash with light petroleum and dry. The yield of crude product, m.p. 237-240 °C, is 7.5 g (90%). Dissolve the solid in hot benzene (120 ml), filter and add light petroleum, b.p. 60-80 °C (120 ml), to the hot filtrate and cool. Collect the solid which separates, wash with light petroleum and dry. The yield of pure tetraphenyldihydrophthalic anhydride, m.p. 235-240 °C, is 6.2 g (75%). The m.p. depends on the rate of heating. [Pg.1121]

Bocard, C. Gatellier, C. Breaking of Fresh and Weathered Emulsions by Chemicals in Proceedings of the Oil Spill Conference, API Publication 4452, American Petroleum Institute Washington, DC, 1981, pp. 601—607. [Pg.418]

Note that c breaks up the material into two sentences. [Pg.130]

Development Manufacture B-C Break Even after Launch... [Pg.249]

Perfluoro polyethers (Fomblin) (Krytox ) (3 x IO 8) If exposed to too much heat, decomposes to a gas rather than breaking down. Is resistant to oxidation and chemically resistant with few exceptions. No polymers are formed under energetic particle bombardment. Can be regenerated for reuse. Provides somewhat lower pumping speeds than other oils. High initial cost. Above 300 - 350°C, breaks down into aggressive and toxic compounds. To effectively remove it, chlorofluorocarbons must be used. [Pg.380]

Molecular weights of 30,000-60,000 could be obtained. The polymers showed outstanding thermal stability (TGA 550°C. break, air or nitrogen), are all soluble in common organic solvents (up to 15 wt. % ), form clear films, are colorless, and amorphous. The thermal decomposition of these polymers has been shown to take place by the loss of pendant phenyl groups as phenyl radicals. Thus, the thermal treatment of a film under nitrogen produces a crosslinked film which is still amorphous but insoluble no appreciable main chain degradation takes place. [Pg.651]

Indeed, one can point out two cases in which (4) with the usual quantum expression for C breaks down badly. The first one is given in Fig. 4. The zero-point energy corresponding to the vibration along OX will appear in (4), not, however, in reality, since the potential barrier is very thin. [Pg.178]

C Break When Value Is true Break When Value Changes... [Pg.277]

It reacts with hydrochloric or hydriodic acids, giving acetic acid, naphthalene, and a mercuric halide four atoms of iodine react giving acetic acid, mercuric iodide, and iodonaphthalene sodium amalgam on the alcoholic solution yields mercury, acetic acid, and naphthalene alcoholic hydrogen sulphide or ammonium sulphide at 100° C. break the compound down into acetic acid, mercuric sulphide, and naphthalene. [Pg.97]

There are other problems in the wet oxidation method. For one, the precision of the method is far from good. Customarily, three replicates are taken from each water sample. After acidification, bubbling, and the addition of persulfate (not necessarily in diat order), the sample ampoules are sealed with a torch. They are then held until it is convenient to heat them, usually for 1 hr at 140 °C, break the ampoule, and measure the carbon dioxide evolved. Since there is often a considerable delay between sampling and analysis, sometimes as much as a month, there is no opportunity to retrieve mistakes or accidents. Our own experience has been that wild values, perhaps caused by contamination, occur in about 20% of the samples. The use of either subjective judgment or some empirical rule-of-thumb not far removed from subjective judgment, for the elimination of these wild values is widespread. [Pg.154]

Formula (VBA) f Project jW/1, W tAType — - — -, J/tfatchhxpression 1 C BtBdkVthen/pluelsIrue C Break. Mien rfatue Change., "... [Pg.277]

Figure 3.104 Effect of UV irradiation in a QUV Weather-o-meter on the tensile properties of PVF, PVDF and ETFE (a) tensile modulus b) tensile strength (c) break elongationJ i... Figure 3.104 Effect of UV irradiation in a QUV Weather-o-meter on the tensile properties of PVF, PVDF and ETFE (a) tensile modulus b) tensile strength (c) break elongationJ i...
Fig. 3. Reaction coordinate diagram showing how a reaction will proceed through a preassociation complex (R.C.) when the associated intermediate and catalyst (I.C.) breaks down to reactants faster than it dissociates to separated I and C. Additional stabilisation of I.C. may occur through hydrogen-bonding. Fig. 3. Reaction coordinate diagram showing how a reaction will proceed through a preassociation complex (R.C.) when the associated intermediate and catalyst (I.C.) breaks down to reactants faster than it dissociates to separated I and C. Additional stabilisation of I.C. may occur through hydrogen-bonding.
Procedure After 90 minutes of stirring, cool the mixture to 80 °C Break vacuum and add 20% citric acid solution to inactivate the catalyst, while mechanically stirring for 15 minutes Post bleach with 0.5% bleaching earth under vacuum for 30 minutes at90°C ... [Pg.430]

C. breaks down into carbon and water vapor when heated... [Pg.98]


See other pages where C breaking is mentioned: [Pg.114]    [Pg.518]    [Pg.518]    [Pg.54]    [Pg.59]    [Pg.28]    [Pg.58]    [Pg.243]    [Pg.413]    [Pg.138]    [Pg.66]    [Pg.249]    [Pg.34]    [Pg.4417]    [Pg.67]    [Pg.84]    [Pg.27]    [Pg.85]    [Pg.284]    [Pg.434]    [Pg.71]    [Pg.239]    [Pg.128]    [Pg.134]    [Pg.71]    [Pg.4416]    [Pg.409]   
See also in sourсe #XX -- [ Pg.492 ]




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Breaking H—C Bonds Dehydrogenation

C-H bond breaking

C-N bond breaking

C-S bond breaking

ETFE examples of tensile stress (TS) elongation at break (EB) retentions () versus temperature (C)

PVF examples of tensile stress (TS) elongation at break (EB) retentions () versus temperature (C)

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