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1. |
Editorial |
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Ozone: Science & Engineering,
Volume 20,
Issue 5,
1998,
Page 340-340
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PDF (42KB)
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ISSN:0191-9512
DOI:10.1080/01919519809480352
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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2. |
Ozonation of p-Hydroxybenzoic Acid Solution |
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Ozone: Science & Engineering,
Volume 20,
Issue 5,
1998,
Page 343-360
Ya-Wen Ko,
Pen-Chi Chiang,
E. E. Chang,
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PDF (771KB)
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摘要:
The objective of this study was to examine the reaction between ozone and p-hydroxybenzoic acid, in view of kinetic regime and by-product formation. It was found that the highest specific reduction efficiency of p-hydroxybenzoic acid, THMFP and HAAFP occurred within the kinetic regime of slow reaction, other than the very slow reaction regime. Besides, the efficient way to decrease the glyoxal formation, the ozonation by-product, is to control the reaction duration before the ozonation time of peak glyoxal, which fell within the slow reaction kinetic regime as well.
ISSN:0191-9512
DOI:10.1080/01919519809480347
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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3. |
An Empirical Analysis of Ozone Decay Kinetics in Natural Waters |
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Ozone: Science & Engineering,
Volume 20,
Issue 5,
1998,
Page 361-379
Nicholas J. Oke,
Daniel W. Smith,
Hongde Zhou,
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PDF (766KB)
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摘要:
Ozone decay kinetics in various natural waters and their impact on modeling dissolved ozone concentration profiles in a bubble column contactor were studied. The results demonstrated that the commonly-used first-order kinetics with a constant rate constant were unable to describe the ozone decay behavior, particularly in cases where the initial ozone demand was significant. An explanation is that the water's reactivity toward ozone changes substantially as the ozonation depletes those readily reactive compounds. As a result, an exponentially decreasing function was proposed to provide better estimates of the ozone decay curves.
ISSN:0191-9512
DOI:10.1080/01919519809480348
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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4. |
Ozonation of Amino Acids: Ozone Demand and Aldehyde Formation |
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Ozone: Science & Engineering,
Volume 20,
Issue 5,
1998,
Page 381-402
L. Hureki,
J.P. Croué,
B. Legube,
M. Doré,
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PDF (707KB)
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摘要:
This study is related to the ozonation of free and combined amino acids, which present a high reactivity with ozone. Amino acids reactivities studied in the presence or absence of tert-butyl alcohol as radical scavenger were found to be related to their structures. Amino acid side chains seem to be the main sites that are responsible for the high ozone reactivity in polypeptide structures. Ozonation of amino acids led to the formation of aldehydes such as formaldehyde, acetaldehyde, glyoxal and glyoxal derivatives. The direct ozone reaction has been shown to favor aldehyde production.
ISSN:0191-9512
DOI:10.1080/01919519809480349
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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5. |
Comparison Of Ozonation Kinetic Data From Film and Danckwerts Theories |
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Ozone: Science & Engineering,
Volume 20,
Issue 5,
1998,
Page 403-420
F.J. Beltrán,
L.A. Fernández,
P. Álvarez,
E. Rodriguez,
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PDF (642KB)
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摘要:
Danckwerts and film theories have been compared through the aqueous ozonation kinetic study of three organics: crotonic, cinnamic and 0hydroxycinnamic acids. At the conditions investigated, these compounds areremoved from water exclusively by direct reactions with ozone and the kinetic regime of ozone absorption corresponds to a fast second order irreversiblereaction. In this regime, Danckwerts theory provides wider possibilities than film theory for the determination of the rate constant and individual liquid side masstransfer coefficients. The ozonation reactor was operated as an agitated cell to determine the rate constant and as an agitated tank to obtain the mass transfercoefficient. Rate constants were found to increase with increasing pH. AtpH 7 the ozone reactivity of these compounds was in the following increasing order:Cinnamic acid <⃒ crotonic acid <⃒ o‐hydroxycinnamic acid. AtpH 3 differences in reactivity were not significant.
ISSN:0191-9512
DOI:10.1080/10874506.01919512.1998
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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6. |
VUV Intensity Measurement of a 172 nm Xe Excimer Lamp by means of Oxygen Actinometry |
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Ozone: Science & Engineering,
Volume 20,
Issue 5,
1998,
Page 421-432
Zs László,
I. Ilisz,
G. Peintler,
A. Dombi,
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PDF (1412KB)
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摘要:
The light power of a xenon excimer VUV source was determined by means of oxygen actinometiy. It was found that the method is notapplicable for direct measurement of the light power mainly because of the side-reactions of ozone with oxygen atoms. Model calculations led to a simple equation between the quantum yield and the concentrations of ozone and oxygen. The correlation between the overall quantum yield and the ozone and oxygen concentration at room temperature is Φ = 2 - 1.l0[O3]/(O2]1.94, and at atmospheric oxygen pressure Φ = 2 - 520 [O3].
ISSN:0191-9512
DOI:10.1080/01919519809480350
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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