Tom Bowman

All Publications

• Professor Irvin Glassman COMBUSTION SCIENCE AND TECHNOLOGY Bowman, C. T., Dryer, F. L. 2021; 193 (4): 539–40

  View details for DOI 10.1080/00102202.2020.1841180

  View details for Web of Science ID 000614806000001

• Impact of vitiation on flow reactor studies of jet fuel combustion chemistry COMBUSTION AND FLAME Wang, K., Xu, R., Bowman, C. T., Wang, H. 2021; 224: 66–72

  View details for DOI 10.1016/j.combustflame.2020.10.044

  View details for Web of Science ID 000609127800009

• Professor Irvin Glassman (1923-2019) IN MEMORIAM COMBUSTION AND FLAME Bowman, C. T., Dryer, F. L. 2021; 223: A1

  View details for DOI 10.1016/j.combustflame.2020.10.027

  View details for Web of Science ID 000599642700001

• A physics-based approach to modeling real-fuel combustion chemistry - V. NOx formation from a typical Jet A COMBUSTION AND FLAME Saggese, C., Wan, K., Xu, R., Tao, Y., Bowman, C. T., Park, J., Lu, T., Wang, H. 2020; 212: 270–78

  View details for DOI 10.1016/j.combustflame.2019.10.038

  View details for Web of Science ID 000515192500023

• Kinetic analysis of distinct product generation in oxidative pyrolysis of four octane isomers PROCEEDINGS OF THE COMBUSTION INSTITUTE Wang, K., Bowman, C. T., Wang, H. 2019; 37 (1): 531–38

  View details for DOI 10.1016/j.proci.2018.06.219

  View details for Web of Science ID 000456612200051

• A Physics-based approach to modeling real-fuel combustion chemistry - III. Reaction kinetic model of JP10 COMBUSTION AND FLAME Tao, Y., Xu, R., Wang, K., Shao, J., Johnson, S. E., Movaghar, A., Han, X., Park, J., Lu, T., Brezinsky, K., Egolfopoulos, F. N., Davidson, D. F., Hanson, R. K., Bowman, C. T., Wang, H. 2018; 198: 466–76

  View details for DOI 10.1016/j.combustflame.2018.08.022

  View details for Web of Science ID 000452581400039

• A physics based approach to modeling real-fuel combustion chemistry - IV. HyChem modeling of combustion kinetics of a bio-derived jet fuel and its blends with a conventional Jet A COMBUSTION AND FLAME Wang, K., Xu, R., Parise, T., Shao, J., Movaghar, A., Lee, D., Park, J., Gao, Y., Lu, T., Egolfopoulos, F. N., Davidson, D. F., Hanson, R. K., Bowman, C. T., Wang, H. 2018; 198: 477–89

  View details for DOI 10.1016/j.combustflame.2018.07.012

  View details for Web of Science ID 000452581400040

• A physics-based approach to modeling real-fuel combustion chemistry - II. Reaction kinetic models of jet and rocket fuels COMBUSTION AND FLAME Xu, R., Wang, K., Banerjee, S., Shao, J., Parise, T., Zhu, Y., Wang, S., Movaghar, A., Lee, D., Zhao, R., Han, X., Gao, Y., Lu, T., Brezinsky, K., Egolfopoulos, F. N., Davidson, D. F., Hanson, R. K., Bowman, C. T., Wang, H. 2018; 193: 520–37

  View details for DOI 10.1016/j.combustflame.2018.03.021

  View details for Web of Science ID 000436899700042

• A physics-based approach to modeling real-fuel combustion chemistry - I. Evidence from experiments, and thermodynamic, chemical kinetic and statistical considerations COMBUSTION AND FLAME Wang, H., Xu, R., Wang, K., Bowman, C. T., Hanson, R. K., Davidson, D. F., Brezinsky, K., Egolfopoulos, F. N. 2018; 193: 502–19

  View details for DOI 10.1016/j.combustflame.2018.03.019

  View details for Web of Science ID 000436899700041

• An experimental and kinetic modeling study of n-dodecane pyrolysis and oxidation COMBUSTION AND FLAME Banerjee, S., Tangko, R., Sheen, D. A., Wang, H., Bowman, C. T. 2016; 163: 12-30

  View details for DOI 10.1016/j.combustflame.2015.08.005

  View details for Web of Science ID 000367278600002

• Shock Tube Measurements of the Rate Constant for the Reaction Ethanol + OH. journal of physical chemistry. A Stranic, I., Pang, G. A., Hanson, R. K., Golden, D. M., Bowman, C. T. 2014; 118 (5): 822-828

  Abstract

  The overall rate constant for the reaction ethanol + OH → products was determined experimentally from 900 to 1270 K behind reflected shock waves. Ethan(18)ol was utilized for these measurements in order to avoid the recycling of OH radicals following H-atom abstraction at the β-site of ethanol. Similar experiments were also performed with unlabeled ethan(16)ol in order to infer the rate constant that excludes reactivity at the β-site. The two data sets were used to directly infer the branching ratio for the reaction at the β-site. Experimental data in the current study and in previous low-temperature studies for the overall rate constant are best fit by the expression koverall = 5.07 × 10(5) T[K](2.31) exp(608/T[K]) cm(3) mol(-1) s(-1), valid from 300 to 1300 K. Measurements indicate that the branching ratio of the β-site is between 20 and 25% at the conditions studied. Pseudo-first-order reaction conditions were generated using tert-butylhydroperoxide (TBHP) as a fast source of (16)OH with ethanol in excess. (16)OH mole fraction time-histories were measured using narrow-line width laser absorption near 307 nm. Measurements were performed at the linecenter of the R22(5.5) transition in the A-X(0,0) band of (16)OH that does not overlap with any absorption features of (18)OH, thus producing a measurement of the (16)OH mole fraction that is insensitive to the presence of (18)OH.

  View details for DOI 10.1021/jp410853f

  View details for PubMedID 24405356

• Shock Tube Measurements of the Rate Constant for the Reaction Ethanol plus OH JOURNAL OF PHYSICAL CHEMISTRY A Stranic, I., Pang, G. A., Hanson, R. K., Golden, D. M., Bowmant, C. T. 2014; 118 (5): 822-828

  Abstract

  The overall rate constant for the reaction ethanol + OH → products was determined experimentally from 900 to 1270 K behind reflected shock waves. Ethan(18)ol was utilized for these measurements in order to avoid the recycling of OH radicals following H-atom abstraction at the β-site of ethanol. Similar experiments were also performed with unlabeled ethan(16)ol in order to infer the rate constant that excludes reactivity at the β-site. The two data sets were used to directly infer the branching ratio for the reaction at the β-site. Experimental data in the current study and in previous low-temperature studies for the overall rate constant are best fit by the expression koverall = 5.07 × 10(5) T[K](2.31) exp(608/T[K]) cm(3) mol(-1) s(-1), valid from 300 to 1300 K. Measurements indicate that the branching ratio of the β-site is between 20 and 25% at the conditions studied. Pseudo-first-order reaction conditions were generated using tert-butylhydroperoxide (TBHP) as a fast source of (16)OH with ethanol in excess. (16)OH mole fraction time-histories were measured using narrow-line width laser absorption near 307 nm. Measurements were performed at the linecenter of the R22(5.5) transition in the A-X(0,0) band of (16)OH that does not overlap with any absorption features of (18)OH, thus producing a measurement of the (16)OH mole fraction that is insensitive to the presence of (18)OH.

  View details for DOI 10.1021/jp410853f

  View details for Web of Science ID 000331153400004

• Shock Tube Measurements of the tert-Butanol + OH Reaction Rate and the tert-C4H8OH Radical ß-Scission Branching Ratio Using Isotopic Labeling. journal of physical chemistry. A Stranic, I., Pang, G. A., Hanson, R. K., Golden, D. M., Bowman, C. T. 2013; 117 (23): 4777-4784

  Abstract

  The overall rate constant for the reaction tert-butanol + OH → products was determined experimentally behind reflected shock waves by using (18)O-substituted tert-butanol (tert-butan(18)ol) and tert-butyl hydroperoxide (TBHP) as a fast source of (16)OH. The data were acquired from 900 to 1200 K near 1.1 atm and are best fit by the Arrhenius expression 1.24 × 10(-10) exp(-2501/T [K]) cm(3) molecule(-1) s(-1). The products of the title reaction include the tert-C4H8OH radical that is known to have two major β-scission decomposition channels, one of which produces OH radicals. Experiments with the isotopically labeled tert-butan(18)ol also lead to an experimental determination of the branching ratio for the β-scission pathways of the tert-C4H8OH radical by comparing the measured pseudo-first-order decay rate of (16)OH in the presence of excess tert-butan(16)ol with the respective decay rate of (16)OH in the presence of excess tert-butan(18)ol. The two decay rates of (16)OH as a result of reactions with the two forms of tert-butanol differ by approximately a factor of 5 due to the absence of (16)OH-producing pathways in experiments with tert-butan(18)ol. This indicates that 80% of the (16)OH molecules that react with tert-butan(16)ol will reproduce another (16)OH molecule through β-scission of the resulting tert-C4H8(16)OH radical. (16)OH mole fraction time histories were measured using narrow-line-width laser absorption near 307 nm. Measurements were performed at the line center of the R22(5.5) transition in the A-X(0,0) band of (16)OH, a transition that does not overlap with any absorption features of (18)OH, hence yielding a measurement of (16)OH mole fraction that is insensitive to any production of (18)OH.

  View details for DOI 10.1021/jp402176e

  View details for PubMedID 23683356

• CFD simulation of a confined axisymmetric laminar methane-air diffusion flame 8th Mediterranean Combustion Symposium Fletcher, D. F., Bowman, C. T., Haynes, B. S. 2013
• Experimental Determination of the High-Temperature Rate Constant for the Reaction of OH with sec-Butanol JOURNAL OF PHYSICAL CHEMISTRY A Pang, G. A., Hanson, R. K., Golden, D. M., Bowman, C. T. 2012; 116 (39): 9607-9613

  Abstract

  The overall rate constant for the reaction of OH with sec-butanol [CH(3)CH(OH)CH(2)CH(3)] was determined from measurements of the near-first-order OH decay in shock-heated mixtures of tert-butylhydroperoxide (as a fast source of OH) with sec-butanol in excess. Three kinetic mechanisms from the literature describing sec-butanol combustion were used to examine the sensitivity of the rate constant determination to secondary kinetics. The overall rate constant determined can be described by the Arrhenius expression 6.97 × 10(-11) exp(-1550/T[K]) cm(3) molecule(-1) s(-1), valid over the temperature range of 888-1178 K. Uncertainty bounds of ±30% were found to adequately account for the uncertainty in secondary kinetics. To our knowledge, the current data represent the first efforts toward an experimentally determined rate constant for the overall reaction of OH with sec-butanol at combustion-relevant temperatures. A rate constant predicted using a structure-activity relationship from the literature was compared to the current data and previous rate constant measurements for the title reaction at atmospheric-relevant temperatures. The structure-activity relationship was found to be unable to correctly predict the measured rate constant at all temperatures where experimental data exist. We found that the three-parameter fit of 4.95 × 10(-20)T(2.66) exp(+1123/T[K]) cm(3) molecule(-1) s(-1) better describes the overall rate constant for the reaction of OH with sec-butanol from 263 to 1178 K.

  View details for DOI 10.1021/jp306977e

  View details for Web of Science ID 000309375300002

  View details for PubMedID 22946741

• High-Temperature Rate Constant Determination for the Reaction of OH with iso-Butanol JOURNAL OF PHYSICAL CHEMISTRY A Pang, G. A., Hanson, R. K., Golden, D. M., Bowman, C. T. 2012; 116 (19): 4720-4725

  Abstract

  This work presents the first direct experimental study of the rate constant for the reaction of OH with iso-butanol (2-methyl-1-propanol) at temperatures from 907 to 1147 K at near-atmospheric pressures. OH time-histories were measured behind reflected shock waves using a narrow-linewidth laser absorption method during reactions of dilute mixtures of tert-butylhydroperoxide (as a fast source of OH) with iso-butanol in excess. The title reaction's overall rate constant (OH + iso-butanol →(k(overall)) all products) minus the rate constant for the β-radical-producing channel (OH + iso-butanol →(k(β)) 1-hydroxy-2-methyl-prop-2-yl radical + H(2)O) was determined from the pseudo-first-order rate of OH decay. A two-parameter Arrhenius fit of the experimentally determined rate constant in the current temperature range yields the expression (k(overall) - k(β)) = 1.84 × 10(-10) exp(-2350/T[K]) cm(3) molecule(-1) s(-1). A recommendation for the overall rate constant, including k(β), is made, and comparisons of the results to rate constant recommendations from the literature are discussed.

  View details for DOI 10.1021/jp302719j

  View details for Web of Science ID 000304073200005

  View details for PubMedID 22515280

• Rate Constant Measurements for the Overall Reaction of OH+1-Butanol -> Products from 900 to 1200 K JOURNAL OF PHYSICAL CHEMISTRY A Pang, G. A., Hanson, R. K., Golden, D. M., Bowman, C. T. 2012; 116 (10): 2475-2483

  Abstract

  The rate constant for the overall reaction OH + 1-butanol → products was determined in the temperature range 900 to 1200 K from measurements of OH concentration time histories in reflected shock wave experiments of tert-butyl hydroperoxide (TBHP) as a fast source of OH radicals with 1-butanol in excess. Narrow-linewidth laser absorption was employed for the quantitative OH concentration measurement. A detailed kinetic mechanism was constructed that includes updated rate constants for 1-butanol and TBHP kinetics that influence the near-first-order OH concentration decay under the present experimental conditions, and this mechanism was used to facilitate the rate constant determination. The current work improves upon previous experimental studies of the title rate constant by utilizing a rigorously generated kinetic model to describe secondary reactions. Additionally, the current work extends the temperature range of experimental data in the literature for the title reaction under combustion-relevant conditions, presenting the first measurements from 900 to 1000 K. Over the entire temperature range studied, the overall rate constant can be expressed in Arrhenius form as 3.24 × 10(-10) exp(-2505/T [K]) cm(3) molecule(-1) s(-1). The influence of secondary reactions on the overall OH decay rate is discussed, and a detailed uncertainty analysis is performed yielding an overall uncertainty in the measured rate constant of ±20% at 1197 K and ±23% at 925 K. The results are compared with previous experimental and theoretical studies on the rate constant for the title reaction and reasonable agreement is found when the earlier experimental data were reinterpreted.

  View details for DOI 10.1021/jp211885p

  View details for Web of Science ID 000301509400010

  View details for PubMedID 22352920

• High-Temperature Measurements of the Rate Constants for Reactions of OH with a Series of Large Normal Alkanes: n-Pentane, n-Heptane, and n-Nonane ZEITSCHRIFT FUR PHYSIKALISCHE CHEMIE-INTERNATIONAL JOURNAL OF RESEARCH IN PHYSICAL CHEMISTRY & CHEMICAL PHYSICS Pang, G. A., Hanson, R. K., Golden, D. M., Bowman, C. T. 2011; 225 (11-12): 1157-1178

  View details for DOI 10.1524/zpch.2011.0156

  View details for Web of Science ID 000299393700002

• Vitiated ethane oxidation in a high-pressure flow reactor COMBUSTION AND FLAME Walters, K. M., Bowman, C. T. 2009; 156 (10): 1886-1897

  View details for DOI 10.1016/j.combustflame.2009.05.012

  View details for Web of Science ID 000274583500004

• High-temperature shock tube study of the reactions CH3+OH -> products and CH3OH+Ar -> products INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Vasudevan, V., Cook, R. D., Hanson, R. K., Bowman, C. T., Golden, D. M. 2008; 40 (8): 488-495

  View details for DOI 10.1002/kin.20334

  View details for Web of Science ID 000257769400004

• Shock tube study of the reaction of CH with N-2: Overall rate and branching ratio JOURNAL OF PHYSICAL CHEMISTRY A Vasudevan, V., Hanson, R. K., Bowman, C. T., Golden, D. M., Davidson, D. F. 2007; 111 (46): 11818-11830

  Abstract

  We have studied the reaction between CH and N2, (1) CH + N2 --> products, in shock tube experiments using CH and NCN laser absorption. CH was monitored by continuous-wave, narrow-line-width laser absorption at 431.1 nm. The overall rate coefficient of the CH + N2 reaction was measured between 1943 and 3543 K, in the 0.9-1.4 atm pressure range, using a CH perturbation approach. CH profiles recorded upon shock-heating dilute mixtures of ethane in argon and acetic anhydride in argon were perturbed by the addition of nitrogen. The perturbation in the CH concentration was principally due to the reaction between CH and N2. Rate coefficients for the overall reaction were inferred by kinetically modeling the perturbed CH profiles. A least-squares, two-parameter fit of the current overall rate coefficient measurements was k1 = 6.03 x 1012 exp(-11150/T [K]) (cm3 mol-1 s-1). The uncertainty in k1 was estimated to be approximately +/-25% and approximately +/-35% at approximately 3350 and approximately 2100 K, respectively. At high temperatures, there are two possible product channels for the reaction between CH and N2, (1a) CH + N2 --> HCN + N and (1b) CH + N2 --> H + NCN. The large difference in the rates of the reverse reactions enabled inference of the branching ratio of reaction 1, k1b/(k1b + k1a), in the 2228-2905 K temperature range by CH laser absorption in experiments in a nitrogen bath. The current CH measurements are consistent with a branching ratio of 1 and establish NCN and H as the primary products of the CH + N2 reaction. A detailed and systematic uncertainty analysis, taking into account experimental and mechanism-induced contributions, yields a conservative lower bound of 0.70 for the branching ratio. NCN was also detected by continuous-wave, narrow-line-width laser absorption at 329.13 nm. The measured NCN time histories were used to infer the rate coefficient of the reaction between H and NCN, H + NCN --> HCN + N, and to estimate an absorption coefficient for the NCN radical.

  View details for DOI 10.1021/jp075638c

  View details for Web of Science ID 000250967800012

  View details for PubMedID 17958405

• Effects of pressure on performance of mesoscale burner arrays for gas-turbine applications JOURNAL OF PROPULSION AND POWER Bardos, A., Walters, K. M., Boutross, M. G., Lee, S., Edwards, C. F., Bowman, C. T. 2007; 23 (4): 884-886

  View details for DOI 10.2514/1.26255

  View details for Web of Science ID 000248073000032

• High-temperature shock tube measurements of methyl radical decomposition JOURNAL OF PHYSICAL CHEMISTRY A Vasudevan, V., Hanson, R. K., Golden, D. M., Bowman, C. T., Davidson, D. F. 2007; 111 (19): 4062-4072

  Abstract

  We have studied the two-channel thermal decomposition of methyl radicals in argon, involving the reactions CH3 + Ar --> CH + H2 + Ar (1a) and CH3 + Ar --> CH2 + H + Ar (1b), in shock tube experiments over the 2253-3527 K temperature range, at pressures between 0.7 and 4.2 atm. CH was monitored by continuous-wave, narrow-line-width laser absorption at 431.1311 nm. The collision-broadening coefficient for CH in argon, 2gamma(CH-Ar), was measured via repeated single-frequency experiments in the ethane pyrolysis system behind reflected shock waves. The measured 2gamma(CH-Ar) value and updated spectroscopic and molecular parameters were used to calculate the CH absorption coefficient at 431.1311 nm (23194.80 cm(-1)), which was then used to convert raw traces of fractional transmission to quantitative CH concentration time histories in the methyl decomposition experiments. The rate coefficient of reaction 1a was measured by monitoring CH radicals generated upon shock-heating highly dilute mixtures of ethane, C2H6, or methyl iodide, CH3I, in an argon bath. A detailed chemical kinetic mechanism was used to model the measured CH time histories. Within experimental uncertainty and scatter, no pressure dependence could be discerned in the rate coefficient of reaction 1a in the 0.7-4.2 atm pressure range. A least-squares, two-parameter fit of the current measurements, applicable between 2706 and 3527 K, gives k(1a) (cm(3) mol(-1) s(-1)) = 3.09 x 1015 exp[-40700/T (K)]. The rate coefficient of reaction 1b was determined by shock-heating dilute mixtures of C2H6 or CH3I and excess O2 in argon. During the course of reaction, OH radicals were monitored using the well-characterized R(1)(5) line of the OH A-X (0,0) band at 306.6871 nm (32606.52 cm(-1)). H atoms generated via reaction 1b rapidly react with O2, which is present in excess, forming OH. The OH traces are primarily sensitive to reaction 1b, reaction 9 (H + O2 --> OH + O) and reaction 10 (CH3 + O2 --> products), where the rate coefficients of reactions 9 and 10 are relatively well-established. No pressure dependence could be discerned for reaction 1b between 1.1 and 3.9 atm. A two-parameter, least-squares fit of the current data, valid over the 2253-2975 K temperature range, yields the rate expression k(1b) (cm(3) mol(-1) s(-1)) = 2.24 x 10(15) exp[-41600/T (K)]. Theoretical calculations carried out using a master equation/RRKM analysis fit the measurements reasonably well.

  View details for DOI 10.1021/jp0677187

  View details for Web of Science ID 000246341200040

  View details for PubMedID 17388279

• High-temperature measurements of the rates of the reactions CH2O+Ar -> Products and CH2O+O-2 -> Products PROCEEDINGS OF THE COMBUSTION INSTITUTE Vasudevan, V., Davidson, D. F., Hanson, R. K., Bowman, C. T., Golden, D. M. 2007; 31: 175-183

  View details for DOI 10.1016/j.proci.2006.07.017

  View details for Web of Science ID 000252858000011

• Mesoscale burner Arrays for gas-turbine reheat applications JOURNAL OF PROPULSION AND POWER Lee, S., Svrcek, M., Edwards, C. F., Bowman, C. T. 2006; 22 (2): 417-424

  View details for Web of Science ID 000236087000015

• Experimental study of confined, swirling, nonpremixed gas flame for validation of simulations JOURNAL OF PROPULSION AND POWER Tribbett, E. J., Sipperley, C. M., Huh, J. Y., Edwards, C. F., Bowman, C. T. 2006; 22 (1): 158-168

  View details for Web of Science ID 000234910900019

• The reaction of CH3+O-2: experimental determination of the rate coefficients for the product channels at high temperatures 30th International Symposium on Combustion Herbon, J. T., Hanson, R. K., Bowman, C. T., GOLDEN, D. M. ELSEVIER SCIENCE INC. 2005: 955–963

  View details for DOI 10.1016/j.proci.2004.08.094

  View details for Web of Science ID 000229944200102

• Evaluated kinetic data for combustion modeling: Supplement II JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA Baulch, D. L., Bowman, C. T., Cobos, C. J., Cox, R. A., Just, T., Kerr, J. A., Pilling, M. J., Stocker, D., Troe, J., Tsang, W., Walker, R. W., Warnatz, J. 2005; 34 (3): 757-1397

  View details for DOI 10.1063/1.1748524

  View details for Web of Science ID 000231310600001

• A shock tube study of the reaction NH2+CH4 -> NH3+CH3 and comparison with transition state theory INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Song, S. H., Golden, D. M., Hanson, R. K., Bowman, C. T., Senosiain, J. P., Musgrave, C. B., Friedrichs, G. 2003; 35 (7): 304-309

  View details for DOI 10.1002/kin.10131

  View details for Web of Science ID 000183601300004

• A shock tube study of the product branching ratio of the NH2+NO reaction at high temperatures JOURNAL OF PHYSICAL CHEMISTRY A Song, S. H., Hanson, R. K., Bowman, C. T., GOLDEN, D. M. 2002; 106 (40): 9233-9235

  View details for DOI 10.1021/jp020943d

  View details for Web of Science ID 000178506700012

• A shock tube study of benzylamine decomposition: Overall rate coefficient and heat of formation of the benzyl radical JOURNAL OF PHYSICAL CHEMISTRY A Song, S., GOLDEN, D. M., Hanson, R. K., Bowman, C. T. 2002; 106 (25): 6094-6098

  View details for DOI 10.1021/jp0200851

  View details for Web of Science ID 000176356400017

• A shock tube study of the enthalpy of formation of OH 29th International Combustion Symposium Herbon, J. T., Hanson, R. K., GOLDEN, D. M., Bowman, C. T. ELSEVIER SCIENCE INC. 2002: 1201–1208

  View details for Web of Science ID 000182866100145

• A shock tube study of the NH2+NO2 reaction 29th International Combustion Symposium Song, S., GOLDEN, D. M., Hanson, R. K., Bowman, C. T. ELSEVIER SCIENCE INC. 2002: 2163–2170

  View details for Web of Science ID 000182866500090

• Shock tube determination of the overall rate of NH2+NO -> products in the Thermal De-NOx temperature window INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Song, S., Hanson, R. K., Bowman, C. T., GOLDEN, D. M. 2001; 33 (11): 715-721

  View details for Web of Science ID 000171483200009

• Flow reactor study of the effect of pressure on the thermal De-NOx process COMBUSTION AND FLAME Schmidt, C. C., Bowman, C. T. 2001; 127 (1-2): 1958-1970

  View details for Web of Science ID 000172022900007

• Experimental study and modeling of the reaction H+O-2+M -> HO2+M (M = Ar, N-2, H2O) at elevated pressures and temperatures between 1050 and 1250 K International Discussion Meeting of the Deutsche-Bunsen-Gesellschaft-fur-Physikalische-Chemie Bates, R. W., GOLDEN, D. M., Hanson, R. K., Bowman, C. T. ROYAL SOC CHEMISTRY. 2001: 2337–42

  View details for Web of Science ID 000169504900021

• Gas-phase reaction mechanisms for nitrogen oxide formation and removal in combustion Conference of the NATO-Advanced-Study-Institute on Pollutants from Combustion Formation and Impact on Atmospheric Chemistry Bowman, C. T. KLUWER ACADEMIC PUBL. 2000: 123–144

  View details for Web of Science ID 000166342300007

• Shock tube determination of the overall rate of NH2+NO -> products at high temperatures 28th International Symposium on Combustion Song, S., Hanson, R. K., Bowman, C. T., GOLDEN, D. M. ELSEVIER SCIENCE INC. 2000: 2403–2409

  View details for Web of Science ID 000169870400112

• A shock tube study of the product branching ratio for the reaction NH2+NO using frequency-modulation detection of NH2 JOURNAL OF PHYSICAL CHEMISTRY A Votsmeier, M., Song, S., Hanson, R. K., Bowman, C. T. 1999; 103 (11): 1566-1571

  View details for Web of Science ID 000079458500017

• CH-radical concentration measurements in fuel-rich CH4/O-2/Ar and CH4/O-2/NO/Ar mixtures behind shock waves COMBUSTION AND FLAME Woiki, D., Votsmeier, M., Davidson, D. F., Hanson, R. K., Bowman, C. T. 1998; 113 (4): 624-626

  View details for Web of Science ID 000073079800016

• An experimental investigation of the effects of compressibility on a turbulent reacting mixing layer JOURNAL OF FLUID MECHANICS Miller, M. F., Bowman, C. T., Mungal, M. G. 1998; 356: 25-64

  View details for Web of Science ID 000072308800002

• Measurement of the rate coefficient of the reaction CH+O-2->products in the temperature range 2200 to 2600 K INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Rohrig, M., Petersen, E. L., Davidson, D. F., Hanson, R. K., Bowman, C. T. 1997; 29 (10): 781-789

  View details for Web of Science ID A1997XX53200007

• Argon broadening of the R(48), R(50) and R(52) lines of CO2 in the (00 degrees 1)<-(00 degrees 0) band JOURNAL OF QUANTITATIVE SPECTROSCOPY & RADIATIVE TRANSFER Wooldridge, M. S., Hanson, R. K., Bowman, C. T. 1997; 57 (3): 425-434

  View details for Web of Science ID A1997WL78700012

• Argon Broadening of the R (48), R (50) and R (52) Lines of CO2 in the (00°1) ¬ (00°0) Band Journal of Quantitative Spectroscopy and Radiative Transfer Wooldridge, M. S., Hanson, R. K., Bowman, C. T. 1997; 57 (3): 425-434

  View details for DOI 10.1016/S0022-4073(96)00074-X

• Mechanisms and Modeling of Gas-Phase Aftertreatment Methods for NO Removal from Combustion Products Physical and Chemical Aspects of Combustion Bowman, C., T. edited by Dryer, F., L., Sawyer, R., F. Gordon and Breach. 1997: 29–68
• A shock tube study of CO+OH->CO2+H and HNCO+OH->products via simultaneous laser adsorption measurements of OH and CO2 INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Wooldridge, M. S., Hanson, R. K., Bowman, C. T. 1996; 28 (5): 361-372

  View details for Web of Science ID A1996UF30600005

• On-line adaptive optimal combustor control IEEE TRANSACTIONS ON CONTROL SYSTEMS TECHNOLOGY PADMANABHAN, K. T., Bowman, C. T., Powell, J. D. 1996; 4 (3): 217-229

  View details for Web of Science ID A1996UG99100002

• A shock tube study of reactions of CN with HCN, OH, and H-2 using CN and OH laser absorption INTERNATIONAL JOURNAL OF CHEMICAL KINETICS WOOLDRIDGE, S. T., Hanson, R. K., Bowman, C. T. 1996; 28 (4): 245-258

  View details for Web of Science ID A1996UB30500002

• High-pressure methane oxidation behind reflected shock waves 26th International Symposium on Combustion Petersen, E. L., Rohrig, M., Davidson, D. F., Hanson, R. K., Bowman, C. T. COMBUSTION INSTITUTE. 1996: 799–806

  View details for Web of Science ID 000083308500095

• Real-time adaptive feedback control of combustion instability 26th International Symposium on Combustion Kemal, A., Bowman, C. T. COMBUSTION INSTITUTE. 1996: 2803–2809

  View details for Web of Science ID 000083308500331

• Measurement of the rate coefficient of H+O-2+M -> HO2+M for M = Ar and N-2 at high pressures 26th International Symposium on Combustion Davidson, D. F., Petersen, E. L., Rohrig, M., Hanson, R. K., Bowman, C. T. COMBUSTION INSTITUTE. 1996: 481–488

  View details for Web of Science ID 000083308500056

• A SHOCK-TUBE STUDY OF METHYL-METHYL REACTIONS BETWEEN 1200 AND 2400 K INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Davidson, D. F., DIROSA, M. D., Chang, E. J., Hanson, R. K., Bowman, C. T. 1995; 27 (12): 1179-1196

  View details for Web of Science ID A1995TG72500004

• SIMULTANEOUS LASER-ABSORPTION MEASUREMENTS OF CN AND OH IN A SHOCK-TUBE STUDY OF HCN+OH-]PRODUCTS INTERNATIONAL JOURNAL OF CHEMICAL KINETICS WOOLDRIDGE, S. T., Hanson, R. K., Bowman, C. T. 1995; 27 (11): 1075-1087

  View details for Web of Science ID A1995TB25000004

• MEASUREMENTS OF ARGON COLLISION BROADENING IN THE CN B-2-SIGMA(+)[-X(2)SIGMA(+)(0,0) SPECTRUM JOURNAL OF QUANTITATIVE SPECTROSCOPY & RADIATIVE TRANSFER WOOLDRIDGE, S. T., Hanson, R. K., Bowman, C. T. 1995; 53 (5): 481-492

  View details for Web of Science ID A1995RD79100002

• AN ADAPTIVE OPTIMAL COMBUSTION CONTROL STRATEGY 25th International Symposium on Combustion PADMANABHAN, K. T., Bowman, C. T., Powell, J. D. ELSEVIER SCIENCE PUBL CO INC. 1995: 101–10

  View details for Web of Science ID A1995QG33100012

• On-line Combustor Performance Optimization Sensing, actuation, and control in aeropropulsion Padmanabhan, K. T., Bowman, C. T., Powell, J. D. 1995: 138–49

  View details for DOI 10.1117/12.210507

• Active adaptive control of combustion 4th IEEE Conference on Control Applications Kemal, A., Bowman, C. T. I E E E. 1995: 667–672

  View details for Web of Science ID A1995BE48V00118

• On-line combustor performance optimization Conference on Sensing, Actuation, and Control in Aeropropulsion PADMANABHAN, K. T., Bowman, C. T., Powell, J. D. SPIE - INT SOC OPTICAL ENGINEERING. 1995: 138–149

  View details for Web of Science ID A1995BD37D00012

• Revised Values for the Rate Coefficients of Ethane and Methane Decomposition International Journal of Chemical Kinetics Davidson, D. F., Hanson, R. K., Bowman, C. T. 1995; 27 (3): 305-308

  View details for DOI 10.1002/kin.550270308

• A Shock Tube Study of Nitric Acid Decomposition Shock Waves @ Marseille II (Springer-Verlag) Wooldridge, M. S., Hanson, R. K., Bowman, C. T. 1995: 83-88

  View details for DOI 10.1007/978-3-642-78832-1_14

• CO2* chemiluminescence in premixed flames COMBUSTION SCIENCE AND TECHNOLOGY Samaniego, J. M., Egolfopoulos, F. N., Bowman, C. T. 1995; 109 (1-6): 183-203

  View details for Web of Science ID 000169110500010

• A SHOCK-TUBE STUDY OF THE OH+OH-]H2O+O REACTION INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Wooldridge, M. S., Hanson, R. K., Bowman, C. T. 1994; 26 (4): 389-401

  View details for Web of Science ID A1994NC58300001

• Reexamination of Shock-Tube Measurements of the Rate Coefficient of H + O2 -> OH + O Journal of Physical Chemistry Yu, C. L., Frenklach, M., Masten, D. A., Hanson, R. K., Bowman, C. T. 1994; 98 (17): 4770-4771

  View details for DOI 10.1021/j100068a048

• An Experimental Investigation of Supersonic Reacting Mixing Layers 32nd Aerospace Sciences Meeting and Exhibit Miller, M. F., Island, T. C., Seitzman, J. M., Bowman, C. T., Mungal, M. G., Hanson, R. K. 1994

  View details for DOI 10.2514/6.1994-823

• A STUDY OF ETHANE DECOMPOSITION IN A SHOCK-TUBE USING LASER-ABSORPTION OF CH3 INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Davidson, D. F., DIROSA, M. D., Hanson, R. K., Bowman, C. T. 1993; 25 (11): 969-982

  View details for Web of Science ID A1993MC21900008

• DEVELOPMENT OF A CW LASER-ABSORPTION DIAGNOSTIC FOR MEASUREMENT OF CN IN SHOCK-TUBE EXPERIMENTS JOURNAL OF QUANTITATIVE SPECTROSCOPY & RADIATIVE TRANSFER WOOLDRIDGE, S. T., Hanson, R. K., Bowman, C. T. 1993; 50 (1): 19-34

  View details for Web of Science ID A1993LJ39100003

• Compressibility effects in a reacting mixing layer 29th Joint Propulsion Conference and Exhibit Miller, M. F., Island, T. C., Seitzman, J. M., Bowman, C. T., Mungal, M. G., Hanson, R. K. 1993

  View details for DOI 10.2514/6.1993-1771

• An Experimental Study of the Structure of a Compressible, Reacting Mixing Layer 31st Aerospace Sciences Meeting Miller, M. F., Island, T. C., Yip, B., Bowman, C. T., Mungal, M. G., Hanson, R. K. 1993

  View details for DOI 10.2514/6.1993-354

• A SHOCK-TUBE STUDY OF REACTIONS OF ATOMIC OXYGEN WITH ISOCYANIC ACID INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Mertens, J. D., Chang, A. Y., Hanson, R. K., Bowman, C. T. 1992; 24 (3): 279-295

  View details for Web of Science ID A1992HE02400005

• Control of Combustion-Generated Nitrogen Oxide Emissions: Technology Driven by Regulation Twenty-Fourth Symposium (International) on Combustion Bowman, C. T. 1992: 859–78

  View details for DOI 10.1016/S0082-0784(06)80104-9

• A SHOCK-TUBE STUDY OF H + HNCO -] NH2 + CO INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Mertens, J. D., KOHSEHOINGHAUS, K., Hanson, R. K., Bowman, C. T. 1991; 23 (8): 655-668

  View details for Web of Science ID A1991FX28900001

• A SHOCK-TUBE STUDY OF REACTIONS OF C ATOMS AND CH WITH NO INCLUDING PRODUCT CHANNEL MEASUREMENTS JOURNAL OF PHYSICAL CHEMISTRY Dean, A. J., Hanson, R. K., Bowman, C. T. 1991; 95 (8): 3180-3189

  View details for Web of Science ID A1991FH09800042

• KINETIC MODELING OF THE REDUCTION OF NITRIC-OXIDE IN COMBUSTION PRODUCTS BY ISOCYANIC ACID INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Miller, J. A., Bowman, C. T. 1991; 23 (4): 289-313

  View details for Web of Science ID A1991FF93700002

• A SHOCK-TUBE STUDY OF THE REACTIONS OF NH WITH NO, O2, AND O INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Mertens, J. D., Chang, A. Y., Hanson, R. K., Bowman, C. T. 1991; 23 (2): 173-196

  View details for Web of Science ID A1991EV72600007

• Chemistry of Gaseous Pollutant Formation and Destruction Fossil Fuel Combustion: A Source Book Bowman, C., T. edited by Bartok, W., Sarofim, A., F. John Wiley. 1991: 215–260
• COMBUSTOR PERFORMANCE ENHANCEMENT THROUGH DIRECT SHEAR-LAYER EXCITATION COMBUSTION AND FLAME McManus, K. R., Vandsburger, U., Bowman, C. T. 1990; 82 (1): 75-92

  View details for Web of Science ID A1990DZ99200006

• SHOCK-TUBE STUDY OF THE REACTION H + O2-]OH + O USING OH LASER-ABSORPTION JOURNAL OF PHYSICAL CHEMISTRY Masten, D. A., Hanson, R. K., Bowman, C. T. 1990; 94 (18): 7119-7128

  View details for Web of Science ID A1990DX31800033

• Effects of Controlling Vortex Dynamics on the Performance of a Dump Combustor Twenty-Third Symposium (International) on Combustion McManus, K. R., Bowman, C. T. 1990

  View details for DOI 10.1016/S0082-0784(06)80369-3

• REACTION-KINETICS OF NH IN THE SHOCK-TUBE PYROLYSIS OF HNCO INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Mertens, J. D., Chang, A. Y., Hanson, R. K., Bowman, C. T. 1989; 21 (11): 1049-1067

  View details for Web of Science ID A1989AV39800006

• MECHANISM AND MODELING OF NITROGEN CHEMISTRY IN COMBUSTION PROGRESS IN ENERGY AND COMBUSTION SCIENCE Miller, J. A., Bowman, C. T. 1989; 15 (4): 287-338

  View details for Web of Science ID A1989CJ39700002

• Effect of fuel spray vaporization on the stability characteristics of a dump combustor 25th Joint Propulsion Conference Vandsburger, U., McManus, K. R., Bowman, C. T. 1989

  View details for DOI 10.2514/6.1989-2436

• An Investigation of the Structure of a Laminar Non-Premixed Flame in an Unsteady Vortical Flow Twenty-Second Symposium (International) on Combustion Lewis, G. S., Cantwell, B. J., Bowman, C. T. 1988: 515–22

  View details for DOI 10.1016/S0082-0784(89)80058-X

• THE STRUCTURE OF A CHEMICALLY REACTING PLANE MIXING LAYER JOURNAL OF FLUID MECHANICS Masutani, S. M., Bowman, C. T. 1986; 172: 93-?

  View details for Web of Science ID A1986F280600006

• CHEMICAL-KINETICS MODELS FOR COMPLEX REACTING FLOWS BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS Bowman, C. T. 1986; 90 (11): 934-940

  View details for Web of Science ID A1986F382200002

• Soot Production in Axisymmetric Laminar Diffusion Flames at Pressure from One to Ten Atmospheres Twenty-First Symposium (International) on Combustion Flower, W. L., Bowman, C. T. 1986: 1115–24

  View details for DOI 10.1016/S0082-0784(88)80342-4

• Shock Tube Study of the Reaction between Hydrogen Cyanide and Atomic Oxygen Twentieth Symposium (International) on Combustion Hanson, R. K., Bowman, C. T. 1985: 647–54

  View details for DOI 10.1016/S0082-0784(85)80554-3

• Measurements of the Structure of Sooting Laminar Diffusion Flames at Elevated Pressure Twentieth Symposium (International) on Combustion Flower, W. L., Bowman, C. T. 1985: 1035–44

  View details for DOI 10.1016/S0082-0784(85)80593-2

• Combustion of Monodisperse Droplet Clouds in a Reactive Environment Twentieth Symposium (International) on Combustion Koshland, C. P., Bowman, C. T. 1985: 1799–1807

  View details for DOI 10.1016/S0082-0784(85)80677-9

• SHOCK-TUBE STUDY OF THE THERMAL-DECOMPOSITION OF CYANOGEN JOURNAL OF CHEMICAL PHYSICS Szekely, A., Hanson, R. K., Bowman, C. T. 1984; 80 (10): 4982-4985

  View details for Web of Science ID A1984SS95800048

• HIGH-TEMPERATURE DETERMINATION OF THE RATE COEFFICIENT FOR THE REACTION H2O+CN-]HCN+OH INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Szekely, A., Hanson, R. K., Bowman, C. T. 1984; 16 (12): 1609-1621

  View details for Web of Science ID A1984AAA2500013

• HIGH-TEMPERATURE DETERMINATION OF THE RATE COEFFICIENT FOR THE REACTION H2+CN-]H+HCN INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Szekely, A., Hanson, R. K., Bowman, C. T. 1983; 15 (9): 915-923

  View details for Web of Science ID A1983RH56700006

• Shock Tube Determination of the Rate Coefficient for the Reaction CN+HCN → C2N2+H INTERNATIONAL JOURNAL OF CHEMICAL KINETICS Hanson, R. K., Bowman, C. T. 1983; 15 (11): 1237-1241

  View details for DOI 10.1002/kin.550151110

• A Three-Zone Model for Coal Particle Swelling Combustion Science and Technology Melia, P. F., Bowman, C. T. 1983; 31: 195-201

  View details for DOI 10.1080/00102208308923640

• Shock Tube Study of the Thermal Decomposition of Hydrogen Cyanide Shock Tubes and Waves Hanson, R. K., Bowman, C. T. 1981
• SHOCK-TUBE MEASUREMENTS OF RATE COEFFICIENTS OF ELEMENTARY GAS REACTIONS JOURNAL OF PHYSICAL CHEMISTRY Bowman, C. T., Hanson, R. K. 1979; 83 (6): 757-763

  View details for Web of Science ID A1979GN84300023

• Effects of Inlet Air Swirl and Fuel Volatility on the Structure of Confined Spray Flames Seventeenth Symposium (International) on Combustion Owen, F. K., Spadaccini, L. J., Kennedy, J. B., Bowman, C. T. 1979: 467–73

  View details for DOI 10.1016/S0082-0784(79)80047-8

• Alternative Hydrocarbon Fuels: Combustion and Chemical Kinetics AIAA Progress in Astronautics and Aeronautics edited by Bowman, C. T. AIAA, New York. 1978; 62

  View details for DOI 10.2514/4.865367

• Pollutant Formation and Energy Release in Confined Turbulent Diffusion Flames Sixteenth Symposium (International) on Combustion Spadaccini, L. J., Owen, F. K., Bowman, C. T. 1977: 105–17

  View details for DOI 10.1016/S0082-0784(77)80317-2

• Probe Measurements in Flames Experimental Diagnostics in Gas Phase Combustion Systems Bowman, C. T. edited by Bowman, C. T., Price, E. W., Skifstad, J. G., Zinn, B. T., Hartley, D. L. AIAA. 1977: 3–24

  View details for DOI 10.2514/5.9781600865275.0003.0024

• Pollutant formation and energy release in liquid-fuel turbulent diffusion flames 15th Aerospace Sciences Meeting Spadaccini, L. J., McVey, J. B., Kennedy, J. B., Owen, F. K., Bowman, C. T. 1977

  View details for DOI 10.2514/6.1977-53

• Kinetics of Thermal Decomposition of Hydrogen Sulfide behind Shock Waves Sixteenth Symposium (International) on Combustion Bowman, C. T., Dodge, L. G. 1977: 971–82

  View details for DOI 10.1016/S0082-0784(77)80389-5

• Kinetics of Pollutant Formation and Destruction in Combustion Progress in Energy and Combustion Science Bowman, C. T. 1975; 1 (1): 33-45

  View details for DOI 10.1016/0360-1285(75)90005-2

• A Shock Tube Investigation of the High-Temperature Oxidation of Methanol Combustion and Flame Bowman, C. T. 1975; 25: 343-354

  View details for DOI 10.1016/0010-2180(75)90106-6

• Non-Equilibrium Radical Concentrations in Shock-Initiated Methane Oxidation Fifteenth Symposium (International) on Combustion Bowman, C. T. 1975: 869–82

  View details for DOI 10.1016/S0082-0784(75)80354-7

• Comment on “molecular beam sampling of H2CO and NO in one-atmosphere methaneair flames” Combustion and Flame Seery, D. J., Bowman, C. T. 1975; 25: 397-398

  View details for DOI 10.1016/0010-2180(75)90113-3

• Kinetics of Nitric Oxide Formation in Combustion Processes Fourteenth Symposium (International) on Combustion Bowman, C. T. 1973: 729–38

  View details for DOI 10.1016/S0082-0784(73)80068-2

• Investigation of Nitric Oxide Formation Kinetics in Combustion Processes: The Hydrogen-Oxygen-Nitrogen Reaction Combustion Science and Technology Bowman, C. T. 1971; 3 (1): 37-45

  View details for DOI 10.1080/00102207108952269

• An Experimental and Analytical Study of Methane Oxidation behind Shock Waves Combustion and Flame Seery, D. J., Bowman, C. T. 1970; 14 (1): 37-47

  View details for DOI 10.1016/S0010-2180(70)80008-6

• An Experimental and Analytical Investigation of the High-Temperature Oxidation Mechanisms of Hydrocarbon Fuels Combustion Science and Technology Bowman, C. T. 1970; 2: 161-172

  View details for DOI 10.1080/00102207008952244

• Vibrational Relaxation of HCl behind Shock Waves J. Chem. Phys. Bowman, C. T., Seery, D. J. 1969; 50: 1904-1905

  View details for DOI 10.1063/1.1671298

• Dissociation of HCl behind Shock Waves J. Chem. Phys. Seery, D. J., Bowman, C. T. 1968; 48: 4314-4317

  View details for DOI 10.1063/1.1669776

• Chemiluminescence in the High-Temperature Oxidation of Methane Combustion and Flame Bowman, C. T., Seery, D. J. 1968; 12: 611-614

  View details for DOI 10.1016/0010-2180(68)90080-1

• Combustion Instability in Gas Rockets AIAA J. Bowman, C. T., Glassman, I., Crocco, L. 1965; 3: 1981-1982

  View details for DOI 10.2514/3.55206

• A Shock Tube Study of the Reactions of NCO with O and NO using NCO Laser Absorption Twenty-Fourth Symposium (International) on Combustion Mertens, J. D., Dean, A. J., Hanson, R. K., Bowman, C. T. 1992: 701–710

  View details for DOI 10.1016/S0082-0784(06)80086-X

• A Shock Tube Study of the Reaction of CN and NCO with NO2 Twenty-Fifth Symposium (International) on Combustion Wooldridge, S. T., Mertens, J. D., Hanson, R. K., Bowman, C. T. 1994: 983–991

  View details for DOI 10.1016/S0082-0784(06)80735-6

• A Shock Tube Study of Methane Decomposition Using Laser Absorption by CH3 Twenty-Fourth Symposium (International) on Combustion Davidson, D. F., DiRosa, M. D., Chang, A. Y., Hanson, R. K., Bowman, C. T. 1992: 589–596

  View details for DOI 10.1016/S0082-0784(06)80072-X

• High Temperature Shock Tube Study of Reactions of CH and C-Atoms with N2 Twenty-Third Symposium (International) on Combustion Dean, A. J., Hanson, R. K., Bowman, C. T. 1990: 259–265

  View details for DOI 10.1016/S0082-0784(06)80268-7

• A Shock Tube Study of the CO+OH → CO2+H Reaction Twenty-Fifth Symposium (International) on Combustion Wooldridge, M. S., Hanson, R. K., Bowman, C. T. 1994: 741–748

  View details for DOI 10.1016/S0082-0784(06)80706-X