Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 31 (1992), S. 2110-2118 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 30 (1991), S. 2396-2404 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 31 (1992), S. 164-171 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 34 (1995), S. 1882-1888 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 39 (1993), S. 1342-1354 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: N2O decomposition and formation during the oxidation of NH3 and HCN were studied in a quartz flow reactor in the presence of CO, NO and other gases. The emphasis is on the influence of CO and NO. In addition, the homogeneous nitrogen chemistry of fluidized bed combustion and the selective noncatalytic reduction of NO (SNR) are discussed. The rate of N2O decomposition in N2 agrees with a first-order rate expression. The presence of CO or H2 increases the decomposition rate regardless of the additional presence of O2For the formation of N2O, HCN oxidation is more efficient than NH3 oxidation. The presence of NO increases the amount of N2O formed during the oxidation of HCN or NH3.CO moves the N2O formation toward lower temperatures. H2O increases the reaction rate where few components are present, whereas H2O has little influence in the presence of large amounts of a combustible component such as CO. There are indications that NO is a necessary intermediate for any significant formation of N2O during the oxidation of NH3 and HCN. NO reduction is obtained when NO is initially present during oxidation of both NH3 and HCN. These results are comparable to the respective SNR results with reductant ammonia and urea.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 43 (1997), S. 3070-3084 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: In coal-fired combustion systems solid calcium species may be present as ash components or limestone added to the combustion chamber. In this study heterogeneous reactions involving HCN over seven different limestones were investigated in a laboratory fixed-bed quartz reactor at 873-1,173 K. Calcined limestone is an effective catalyst for oxidation of HCN. Under conditions with complete conversion of HCN at O2 concentrations above about 5,000 ppmv the selectivity for formation of NO and N2O is 50-70% and below 5%, respectively. Nitric oxide can be reduced by HCN to N2 in the absence of O2 and to N2 and N2O in the presence of O2. At low O2 concentrations or low temperatures, HCN may react with CaO, forming calcium cyanamide, CaCN2. The selectivities for formation of NO and N2O from oxidation of CaCN2 is 20-25% for both species. The catalytic activity of limestone for oxidation of HCN decreases with increasing degree of sulfation. Simultaneously the selectivity for formation of NO decreases while tht for N2O increases. The catalytic activity of sulfated limestone in-creases with decreasing SO2 concentration, indicating a competition between SO2 and HCN for sites on the surface. The results indicate that heterogeneous oxidation of HCN is important in calciners and fluidized-bed combustors with limestone addition or when burning coals with an ash with a high catalytic activity.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 26 (1994), S. 421-436 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have investigated the impact of surface reactions such as NH3 decomposition and radical adsorption on quartz flow reactor data for Thermal DeNOx using a model that accounts for surface chemistry as well as molecular transport. Our calculations support experimental observations that surface effects are not important for experiments carried out in low surface to volume quartz reactors. The reaction mechanism for Thermal DeNOx has been revised in order to reflect recent experimental results. Among the important changes are a smaller chain branching ratio for the NH2 + NO reaction and a shorter NNH lifetime than previously used in modeling. The revised mechanism has been tested against a range of experimental flow reactor data for Thermal DeNOx with reasonable results. The formation of N2O in Thermal DeNOx has been modelled and calculations show good agreement with experimental data. The important reactions in formation and destruction of N2O have been identified. Our calculations indicate that N2O is formed primarily from the reaction between NH and NO, even though the NH2 + NO2 reaction possibly contributes at lower temperatures. At higher temperatures N2O concentrations are limited by thermal dissociation of N2O and by reaction with radicals, primarily OH. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 27 (1995), S. 1207-1220 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The NH3/NO2 system has been investigated experimentally in an isothermal flow reactor in the temperature range 850-1350 K. The experimental data were interpreted in terms of a detailed reaction mechanism. The flow reactor results, supported by a theoretical analysis of the NH2—NO2 complex, suggest that the NH2 + NO2 reaction has two major product channels, both proceeding without activation barriers: Our findings indicate that the N2O + H2O channel is dominant at low temperatures while H2NO + NO dominates at high temperatures. The rate constant for reaction (R21) is estimated to be 3.5 · 1012 cm3/mol-s in the temperature range studied with an uncertainty of a factor of 3. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 28 (1996), S. 773-790 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An experimental and theoretical study on the effect of SO2 on moist CO oxidation with and without NO present has been carried out. The experiments were performed in an isothermal quartz flow reactor at atmospheric pressure in the temperature range 800-1300 K. Inlet concentrations of SO2 ranged from 0 to 1800 ppmv, while the NO ranged between 0, 100, or 1500 ppm.SO2 inhibits CO oxidation under the conditions investigated, shifting the fast oxidation regime 20-40 K towards higher temperatures at 1500 ppm SO2. The inhibition is most pronounced at high O atom levels. The experimental data supported by model analysis suggest that SO2 primarily reacts with O atoms forming SO3, which is subsequently consumed mainly by reaction with O and HO2. Addition of NO significantly diminishes the effect of SO2. Since NO is usually present in combustion flue gases, the impact of SO2 on CO burnout in most practical systems is projected to be small.The H/S/O thermochemistry and reaction subset has been revised based on recent experimental and theoretical results, and a chemical kinetic model has been established. The model provides a reasonable overall description of the effect of SO2 and NO on moist CO oxidation, while the SO3/SO2 ratio is well predicted over the range of conditions investigated. In order to enhance model performance further, rate constants for a number of SO2 and SO3 reactions need to be determined with higher accuracy. © 1996 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...