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  • 1970-1974  (11)
  • Physical Chemistry  (11)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 553-565 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of O(3P), prepared from the Hg photosensitization of N2O, with C2HCl3 was studied at 25°C. The products of the reaction in the absence of O2 were CO, CHCl3, and polymer (as well as N2 from the N2O). The quantum yields of CO and CHCl3 were 0.23 ± 0.01 and 0.14 ± 0.05, is respectively independent of reaction conditions. The reaction mechanism is with k14a/k14 = 0.23, where k14a + k14b. Most of the HCl and CCl2 combine to form CHCl3, but some other products must also be formed to account for the difference in the CO and CHCl3 quantum yields. The C2HCl3O* adduct polymerizes without involving additional C2HCl3 molecules, since the quantum yield of C2HCl3 disappearance, —Φ{C2HCl3}, was about 1.0 at high values of [N2O]/[C2HCl3]. The rate coefficient for the reaction of O(3P) with C2HCl3 is 0.10 that for the reaction of O(3P) with C2F4.In the presence of O2 the free radical chain oxidation occurs because of the reaction The main product is CHCl2CCl(O) with smaller amounts of CO and CCl2O, and some CO2. The chain lengths were long and values of — Φ {C2HCl3} up to 90 were observed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 3 (1971), S. 501-508 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ozone was photolyzed at room temperature in the presence of N2O at 2537 Å and 2288 Å to produce O(1D) atoms. These atoms can react with either O3 or N2O via From the quantum yield of N2, the relative rate constants k6a/k6 and k2/k6 could be obtained, where k6 + k6a + k6b. The former rate constant ratio was found to be 0.37 ± 0.03 at 2537 Å and 0.33 ± 0.03 at 2288 Å, in good agreement with an earlier report from our laboratory. The ratio k2/k6 was found to be 2.6 at 2537 Å, but 4.1 at 2288 Å. The difference in the two numbers, if real, may reflect differences in reactivity due to different amounts of excess translational energy in the O(1D) atom at the two wavelengths.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 3 (1971), S. 269-282 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photolysis of pure N2O, N2O and N2, and N2O and C3H6 mixtures at 1470 Å and room temperature has been studied to determine the relative importance of the primary processes. The results are where φ{O(1D)} = 0.515 represents both the O(1D) produced in the primary act and that produced by collisional quenching of O(1S); φ{N2(3Σ)} = 0.084 represents only that portion of N2(3φ) which dissociates N2O on deactivation; and φ{O(1S)} = 0.38 - ±{N(2D)} represents only that portion of O(1S) which enters into chemical reaction with N2O. If the reaction of O(1S) with N2O yields only N2 and O2 as products, which seems likely from potential-energy curve considerations then ±{O(1S)} = 0.135 ± 0.06 and φ{N(2D)} = 0.245 ± 0.06. Young and coworkers [4] have found from spectroscopic observations that the total quantum yield of O(1S) is about 0.5. Thus it can be concluded that collisional removal of O(1S) by N2O yields mainly O(1D) with chemical reaction being less important. Furthermore, most of the O(1D) is produced this way, and the true primary yield of O(1D) is about 0.15. The metastable N(2D) is not deactivated by N2O, but is removed by chemical reaction to produce N2 and NO. The results further indicate that N2(3Σ) dissociates N2O at least 80% of the time during quenching. The relative efficiency of N2O compared to N2 is about 2 for the removal of O(1D). O(1S) is removed about 90 times as efficiently by C3H6 as by N2O.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 3 (1971), S. 319-341 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mercury-photosensitized oxidation of CO was studied at 275°C over a wide range of [O2]/[CO] ratios in the absence and presence of the oxygen atom scavenger 2-trifluoromethylpropene (TMP) and at 25°C at low [O2]/[CO] ratios in the presence of TMP. By following the quantum yield of CO2 production, Φ {CO2}, as a function of the [O2]/[CO] ratio, the reactions of vibrationally excited CO (v υ 9) and electronically excited O2, probably in the c1Σ-u state, were studied. At low [O2]/[CO] ratios the predominant reactions are of vibrationally excited CO (v υ 9). Relative rate constants for chemical reaction versus deactivation of CO (v υ 9) were obtained. At higher [O2]/[CO] ratios, the principal reactions are of electronically excited O2. Relative rate constants for chemical reactions and deactivation of this electronically excited O2 with CO, O2, and TMP were obtained. From the effect of total pressure on Φ {CO2}, it is proposed that an intermediate CO3 is formed in the reaction of electronically excited O2 with CO.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 417-432 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The room-temperature photolysis of N2O (10-100 torr) at 2139 Å to produce O(1D) has been studied in the presence of CH4 (10-891 torr). The reactions of O(1D) with CH4 were found to be \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {(4)} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm CH}_{\rm 4} } & \to & {{\rm HO + CH}_{\rm 3} } & {0.95 \pm 0.05} \\ {(8)} & {} & \to & {{\rm O(}^{\rm 3} P{\rm)} + {\rm CH}_{\rm 4} } & {{\rm 0}{\rm .05} \pm {\rm 0}{\rm .05}} \\ {} & {} & \to & {{\rm CH}_{\rm 2} + {\rm H}_{\rm 2} {\rm O}} & {{\rm 〈 0}{\rm .03}} \\ {} & {} & \to & {{\rm CH}_{\rm 3} {\rm OH}} & {{\rm 〈 0}{\rm .01}} \\ {} & {} & \to & {{\rm CH}_{\rm 2} {\rm O + H}_{\rm 2}} & {{\rm 〈 0}{\rm .002}} \\\end{array}$$\end{document} The method of chemical difference was used to measure the rate constant ratio k4/(k2 + k3), where reactions (2) and (3) are \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {(2)} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm N}_{\rm 2} {\rm O}} & { \to {\rm N}_{\rm 2} + {\rm O}_{\rm 2} } \\ {(3)} & {} & { \to 2{\rm NO}} \\\end{array}$$\end{document} The CH3 radicals produced in reaction (4) react with the O2 and NO produced in reactions (2) and (3). Thus, near the endpoint of the internal titration, φ{C2H6} gives an accurate measure of k4/(k2 + k3). For the translationally energetic O(1D) atoms produced in the photolysis, k4/(k2 + k3) = 2.28 ± 0.20. However, if He is added to remove the excess translational energy, then k4/(k2 + k3) drops to 1.35 ± 0.3.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 529-540 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: NO2 was photolyzed with 2288 Å radiation at 300° and 423°K in the presence of H2O, CO, and in some cases excess He. The photolysis produces O(1D) atoms which react with H2O to give HO radicals \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (3)}} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm H}_{\rm 2} {\rm O} \to 2{\rm HO}} \\\end{array}$$\end{document} or are deactivated by CO to O(3P) atoms \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (5)}} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm CO} \to {\rm O(}^{\rm 3} P{\rm) + CO}} \\\end{array}$$\end{document} The ratio k5/k3 is temperature dependent, being 0.33 at 300°K and 0.60 at 423°K. From these two points, the Arrhenius expression is estimated to be k5/k3 = 2.6 exp(-1200/RT) where R is in cal/mole - °K. The OH radical is either removed by NO2 \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (1)}} & {{\rm OH} + {\rm NO}_{\rm 2} {\rm (+M)} \to {\rm HNO}_{\rm 3} {\rm (+M)}} \\\end{array}$$\end{document} or reacts with CO \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (2)}} & {{\rm OH} + {\rm CO} \to {\rm H} + {\rm CO}_{\rm 2} } \\\end{array}$$\end{document} The ratio k2/kα is 0.019 at 300°K and 0.027 at 423°K, and the ratio k2/k0 is 1.65 × 10-5M at 300°K and 2.84 × 10-5M at 423°K, with H2O as the chaperone gas, where kα = k1 in the high-pressure limit and k0[M] = k1 in the low-pressure limit. When combined with the value of k2 = 4.2 × 108 exp(-1100/RT) M-1sec-1, kα = 6.3 × 109 exp (-340/RT)M-1sec-1 and k0 = 4.0 × 1012M-2sec-1, independent of temperature for H2O as the chaperone gas. He is about 1/8 as efficient as H2O.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 3 (1971), S. 467-482 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The competitive reactions between 2-trifluoromethylpropene (TMP) and OCS for O(3P) atoms were studied between 300° and 523°K, using the mercury-senstitized photolysis of N2O as a source of O(3P). From the known value for the rate constant of the O(3P) + TMP reaction, k3 was found to be 1.6 × 10-11 exp (-4500/RT) cm3/particle-sec, where reaction (3) is \documentclass{article}\pagestyle{empty}\begin{document}$${\rm (3) O(}^{\rm 3} {\rm P)} + {\rm OCS} \to {\rm CO} + {\rm SO}$$\end{document}Mixtures of O3 and OCS were photolyzed at 197°, 228°, 273°, and 299°K with radiation above 4300 Å to produce O(3P) from the photolysis of O3, and thus study the competition between reaction (3) and \documentclass{article}\pagestyle{empty}\begin{document}$${\rm (1)O(}^{\rm 3} {\rm P)} + {\rm O}_{\rm 3} \to 2{\rm O}_{\rm 2}$$\end{document} From the above value of k3, k1 could be computed. When combined with all the previous data, the best espression for k1 is k1 = 1.2 × 10-11 exp (-4300/RT) cm3/particle-sec.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 231-241 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N2O was photolyzed at 2139 Å to produce O(1D) atoms in the presence of H2O and CO. The O(1D) atoms react with H2O to produce HO radicals, as measured by CO2 production from the reaction of OH with CO. The relative importance of the various possible O(1D )-H2O reactions is The relative rate constant for O(1D) removal by H2O compared to that by N2O is 2.1, in good agreement with that found earlier in our laboratory. In the presence Of C3H6, the OH can be removed by reaction with either CO or C3H6: From the CO2 yield, k3/k2 = 75,0 at 100°C and 55.0 at 200°C to within ± 10%. When these values are combined with the value of k2 = 7.0 × 10-13exp (-1100/RT) cm3/sec, k3 = 1.36 × 10-11 exp (-100/RT) cm3/sec. At 25°C, k3 extrapolates to 1.1 × 10-11 cm3/sec.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 497-512 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The method of chemical difference was utilized to accurately determine the relative importance of all the reaction steps in the direct photolysis of N2O at 2139 Å (25° and 250°C) and 1849 Å (25° C), as well as in the Hg6(1P1)-sensitized photolysis of N2O at 1849 Å (25°C). In all cases, the primary process is predominantly, if not exclusively, \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (1)}} & {{\rm N}_{\rm 2} {\rm O} + hv{\rm or H}_{\rm g} 6(^1 P_1) \to {\rm N}_{\rm 2} + {\rm O(}^{\rm 1} D{\rm)}} \\\end{array}$$\end{document} Experiments with trace amounts of C3H6 added showed a slight, but not significant, difference in product ratios (N2 and O2). From these experiments the quantum yield of O(3P) from all possible sources was estimated as 0.02 ± 0.02. Experiments with excess N2 at 1849 Å indicated that O(1S) was not produced in the direct photolysis. The O(1S) yield is probably zero, and certainly 〈0.05. The O(1D) atom can react with N2O via \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} \begin{array}{*{20}c} {{\rm (2)}} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm N}_{\rm 2} {\rm O} \to {\rm N}_{\rm 2} + {\rm O}_2 } \\\end{array} \\ \begin{array}{*{20}c} {{\rm (3)}} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm N}_{\rm 2} {\rm O} \to 2{\rm NO}} \\\end{array} \\ \end{array}$$\end{document} The ratio k2/k3 was found to be 0.69 ± 0.05 in all cases. When combined with other data from our laboratory, the average value is 0.65 ± 0.07. This represents the value for translationally energetic O(1D) atoms. When excess He was added to remove the excess translational energy, k2/k3 rose to 0.83 ± 0.06, which is in reasonable agreement with the value of 1.01 ± 0.06 found in another laboratory. We conclude that for O(1D) atoms with no excess thermal energy, k2/k3 = 0.90 ± 0.10.
    Additional Material: 4 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 575-589 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of NO2 with C2F4 was studied at 30°, 68°, 114°, and 157°C by in situ monitoring the infrared absorption bands of the products. The major primary products of the reaction are O2NCF2CFO and FNO. Smaller amounts of CF2O (and presumably NO) are also produced. There was no evidence for other primary products, though they may have been produced in minor amounts. The rate laws for the production of both O2NCF2CFO and CF2O are first order in both [NO2] and [C2F4]. CF2O production is at least partly heterogeneous as demonstrated by packing the quartz reaction vessel with Pyrex beads and by using a Monel cell. The homogeneous rate constant obtained from the high-temperature results gives a rate constant of 3.4 × 108 exp (minus;17000/RT) M-1sec-1 for CF2O production. Actually these Arrhenius parameters represent lower limits, since the heterogeneous reaction may still be playing a significant role. The production rate of O2NCF2CFO is not much affected by changing the nature of the surface or the surface to volume ratio. However the reaction may be heterogeneous, since the rate constant for its formation of 1.3 × 104 e×p (-7500/RT) M-1sec-1 has an abnormally low pree×ponential factor. E×periments in the presence of NO indicate that the mechanism for O2NCF2CFO formatlon is \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} \begin{array}{*{20}c} {(11)} & {{\rm NO}_{\rm 2} + {\rm C}_{\rm 2} {\rm F}_{\rm 4} \to {\rm O}_{\rm 2} {\rm NCF}_{\rm 2} {\rm CF}_{\rm 2} } \\ \end{array} \\ \begin{array}{*{20}c} {(12)} & {{\rm O}_{\rm 2} + {\rm NCF}_{\rm 2} {\rm CF}_{\rm 2} + {\rm NO}_{\rm 2} \to {\rm O}_{\rm 2} {\rm NCF}_{\rm 2} {\rm CFO} + {\rm FNO}} \\ \end{array} \\ \end{array}$$\end{document} The intermediate can also react with NO: \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {(13)} & {{\rm O}_{\rm 2} {\rm NCF}_{\rm 2} {\rm CF}_{\rm 2} + {\rm NO} \to {\rm O}_{\rm 2} {\rm NCF}_{\rm 2} {\rm CF}_{\rm 2} {\rm NO}} \\ \end{array}$$\end{document} with k13/k12 = 1.3.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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