Relevant bibliographies by topics / Transfer reaction

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Transfer reaction'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Transfer reaction"

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Rasaiah, Jayendran C., and Jianjun Zhu. "Reaction coordinates for electron transfer reactions." Journal of Chemical Physics 129, no. 21 (December 7, 2008): 214503. http://dx.doi.org/10.1063/1.3026365.

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KIMURA, Yoshifumi, Koji OSAWA, and Issei KOBAYASHI. "Electron Transfer Reaction and Proton Transfer Reaction in Supercritical Water." Review of High Pressure Science and Technology 23, no. 4 (2013): 300–308. http://dx.doi.org/10.4131/jshpreview.23.300.

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Ashok, Konda, Prashant V. Kamat, and Manapurathu V. George. "Electron transfer reactions. Reaction of dibenzobarrelenes with potassium." Research on Chemical Intermediates 13, no. 3 (September 1990): 203–20. http://dx.doi.org/10.1163/156856790x00094.

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Ashok, Konda, Pallikkaparambil M. Scaria, Prashant V. Kamat, and Manapurathu V. George. "Electron transfer reactions. Reaction of nitrones with potassium." Canadian Journal of Chemistry 65, no. 9 (September 1, 1987): 2039–49. http://dx.doi.org/10.1139/v87-339.

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Treatment of nitrones (1a–d, 26a,b, 34, 49) with potassium in tetrahydrofuran (THF) gives rise to radical anion (2a–d, 27a,b, 35, 50) and dianion intermediates (3a–d, 28a,b, 36) through electron transfer reactions. These intermediates undergo further transformations to give a variety of products. Thus, the aldehydonitrones (1a–d) give the corresponding aldehydes (10a–c), carboxylic acids (25a–c), and azobenzenes (19a,d), whereas the ketonitrones (26a,b) give deoxygenation products (31a,b). The nitrone 34 gave a mixture of products consisting of benzoic acid (25a), dibenzyl (48), the dimeric product 38, and tetraphenylpyrazine (46), whereas 49 did not give any isolable product. Cyclic voltammetric studies have been employed to measure the reduction potentials for both one-electron and two-electron transfer processes, leading to the radical anions and dianions respectively. These intermediates have been characterized through their electronic spectra and they were quenched by oxygen. Pulse radiolysis of the nitrones 1a–d, 26a,b, 34, and 49 also gave the corresponding radical anions 2a–d, 27a,b, 35, and 50, characterized by their spectra.
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Niki, Katsumi, and Takamasa Sagara. "Electron transfer reaction of electron transfer proteins." Kobunshi 39, no. 11 (1990): 830–33. http://dx.doi.org/10.1295/kobunshi.39.830.

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Douhal, Abderrazzak, Françoise Lahmani, and Ahmed H. Zewail. "Proton-transfer reaction dynamics." Chemical Physics 207, no. 2-3 (July 1996): 477–98. http://dx.doi.org/10.1016/0301-0104(96)00067-5.

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Tripathi, R., S. Sodaye, K. Ramachandran, S. K. Sharma, and P. K. Pujari. "Incomplete mass transfer processes in 28Si +93Nb reaction." International Journal of Modern Physics E 27, no. 02 (February 2018): 1850010. http://dx.doi.org/10.1142/s0218301318500106.

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Cross sections of reaction products were measured in [Formula: see text]Si[Formula: see text]Nb reaction using recoil catcher technique involving by off-line gamma-ray spectrometry at beam energies of 105 and 155[Formula: see text]MeV. At [Formula: see text][Formula: see text]MeV, the contribution from different incomplete mass transfer processes is investigated. Results of the present studies show the contribution from deep inelastic collision (DIC), massive transfer or incomplete fusion (ICF) and quasi-elastic transfer (QET). The contribution from massive transfer reactions was confirmed from the fractional yield of the reaction products in the forward catcher foil. The present results are different from those from the reactions with comparatively higher entrance channel mass asymmetry with lighter projectiles, for which dominant transfer processes are ICF and QET which involve mass transfer predominantly from projectile to target. The [Formula: see text] values of the products close to the target mass were observed to be in a wide range, starting from [Formula: see text] of the target ([Formula: see text]Nb) and extending slightly below the [Formula: see text] of the composite system, consistent with the contribution from DIC and QET reactions. At [Formula: see text][Formula: see text]MeV, a small contribution from QET was observed in addition to complete fusion.
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Muneer, Mohammed, Prashant V. Kamat, and Manapurathu V. George. "Electron transfer reactions. Reaction of nitrogen heterocycles with potassium." Canadian Journal of Chemistry 68, no. 6 (June 1, 1990): 969–75. http://dx.doi.org/10.1139/v90-152.

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The results of our studies on potassium-induced transformations of some selected nitrogen heterocycles are presented. The substrates under investigation include 2,3-diphenylindole (1a), 2,3-diphenyl-1-methylindole (1b), 1,2,3-triphenylindole (1c), 2,3,4,5-tetraphenylpyrrole (5a), 1,2,3,5-tetraphenylpyrrole (5b), 1-benzyl-2,3,5-triphenylpyrrole (5c), 2,4,5-triphenyloxazole (15a), 4,5-diphenyl-2-methyloxazole (15b), 2,4-diphenyl-5-methyloxazole (15c), and 2,4,5-triphenylimidazole (19). Treatment of 1a with potassium in THF gave 9H-dibenzo[a,c]carbazole (3a), whereas 1c gave a mixture of 9-phenyl-9H-dibenzo-[a,c]carbazole (3c) and 2,3-diphenylindole (1a). Under identical conditions, 1b gave only the cleavage product 1a. In contrast, when the reactions of 1a,c were carried out with potassium in THF saturated with oxygen, and with potassium superoxide in benzene containing 18-crown-6, a mixture of 2-benzamidobenzophenone (4a), the carbazoles 3a,c, and 1a was formed. Although no product was isolated on treatment of 5a with potassium in THF, the reaction of 5a with potassium in THF saturated with oxygen gave a mixture of tetraphenylpyrazine (7a), the benzoylaminostilbene 8a, the lactam 12a, benzamide (11a), and benzoic acid (14). Similar results were obtained in the reaction of 5a with potassium superoxide. The reaction of N-substituted pyrroles such as 5b,c with potassium gave the NH pyrrole 9b in each case, whereas the reaction of 5b,c with potassium in THF, saturated with oxygen, gave a mixture of 9b, the butanone 10b, the 1,4-dione 13b, the lactam 12b, the amides 11a–c, and benzoic acid (14). Attempted reactions of 5b,c with potassium superoxide did not give any isolable product; most of the starting material could be recovered unchanged in each case. A mixture of N-(1,2-diphenylethyl)benzamide (18a) and benzoic acid (14) was formed in the reaction of the oxazole 15a with potassium, whereas 15b,c, under analogous conditions, gave the N-vinylamides 17b,c and benzoic acid (14). In contrast, treatment of the imidazole 19 with potassium in THF did not give any product; however, when the reaction of 19 was carried out with potassium in THF saturated with oxygen, and with potassium superoxide, dibenzamide (21) was isolated, in each case.Radical ions have been invoked as intermediates in the transformation of the different substrates to the observed products. Cyclic voltammetric studies have been carried out to measure the reduction potentials of these radical anion intermediates. These radical anions have also been generated by pulse radiolysis in methanol, and their absorption spectra recorded. Keywords: nitrogen heterocycles, radical ions, potassium-induced transformations, pulse radiolysis, cyclic voltammetry.
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Yamaguchi, Yasuchika, Noriaki Tatsuta, Kenji Hayakawa, and Ken Kanematsu. "Chirality transfer from the furan ring transfer reaction." Journal of the Chemical Society, Chemical Communications, no. 8 (1989): 470. http://dx.doi.org/10.1039/c39890000470.

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Arseneau, D. J., D. G. Fleming, M. Senba, I. D. Reid, and D. M. Garner. "The ion–molecule reactivity of the positive muon molecular ions HeMu+ and NeMu+." Canadian Journal of Chemistry 66, no. 8 (August 1, 1988): 2018–24. http://dx.doi.org/10.1139/v88-325.

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Thermal (300 K) ion–molecule reaction rates are measured, using the µSR (muon spin rotation) technique, for the muonated rare gas molecular ions HeMu+ and NeMu+ reacting with NO, O2, N2O, NH3, CF4, C2H4, TMS, and CH3NO2. In almost every case (excepting O2), both charge transfer (ke) and muon transfer (kµ) contribute to the reaction rate. Reaction is believed to occur from ro-vibrational excited states, [HeMu+]* and [NeMu+]*, due to the poor efficiency of He and Ne moderators for collisional deactivation. The total experimental rate constants, kexp = kµ + ke, are generally in excellent agreement with total capture rates predicted by the simple ADO theory, regardless of the degree of internal excitation. Comparisons with literature values for corresponding protonated ion reaction rates with O2 and C2H4 reveal little or no isotope effect, although it is noted that these reactions are dominated by proton transfer, in contrast to the µSR results.
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Dissertations / Theses on the topic "Transfer reaction"

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Gillespie, Stephen. "Indirect studies of astrophysical reaction rates through transfer reactions." Thesis, University of York, 2017. http://etheses.whiterose.ac.uk/16376/.

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The work in this thesis describes two experiments which use transfer reactions to perform spectroscopic studies of nuclei in order to improve reaction rates in astrophysical environments. The first experiment is an indirect study of the 34S(p,γ)35Cl reaction rate at energies relevant to classical novae temperatures. By reducing uncertainties in this reaction it may be possible to use 32S/34S isotopic ratio as a diagnostic tool to determine pre-solar grain paternity. A study of the 34S(3He,d)35Cl transfer reaction was performed to identify energy levels in the astrophysically relevant energy region and assign spin and parity to these new states. A new reaction rate has been calculated from this spectroscopic information and is the first experimental measurement of the 34S(p,γ)35Cl reaction rate. Using this new rate it was concluded that it is now possible to determine the paternity of pre-solar grains using the 32S/34S isotopic ratio. The second experiment measured two proton transfer reactions, (3He,d) and (α,t), with the aim of making spin assignments of states above the neutron threshold in 27Al. Combined with information from complementary experiments this information would be used to calculate new 26Al(n,p/α) reaction rates. Direct comparison of the two transfer reactions should allow for low and high spin states to be identified, however due to lower than expected cross sections useful information could not be extracted from the (α,t) reaction. The experimental resolution was insufficient to resolve individual states with the (3He,d) reaction, however due to the selectivity of the reaction it appears that many of the previously known states show low spin behaviour and are likely not relevant to the reaction rate at astrophysical temperatures. In addition, the non-observation of 23 states known to exist in 27Al may indicate they are high spin and further measurements of these states should be performed in order to calculate new 26Al(n,p/α) reaction rates.
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Duff, Jack Lawrence. "Single electron transfer in nucleophilic reactions of substituted norbornanes." Thesis, Georgia Institute of Technology, 1989. http://hdl.handle.net/1853/27444.

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Maza, William Antonio. "Reaction Enthalpy and Volume Profiles for Excited State Reactions Involving Electron Transfer and Proton-Coupled Electron Transfer." Scholar Commons, 2013. http://scholarcommons.usf.edu/etd/4539.

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Electron transfer, ET, and proton-coupled electron transfer, PCET, reactions are central to biological reactions involving catalysis, energy conversion and energy storage. The movement of electrons and protons in either a sequential or concerted manner are coupled in a series of elementary reaction steps in respiration and photosynthesis to harvest and convert energy consumed in foodstuffs or by absorption of light into high energy chemi-cal bonds in the form of ATP. These electron transfer processes may be modulated by conformational dynamics within the protein matrix or at the protein-protein interface, the energetics of which are still not well understood. Photoacoustic calorimetry is an estab-lished method of obtaining time-resolved reaction enthalpy and volume changes on the nanosecond to microsecond timescale. Photoacoustic calorimetry is used here to probe 1) the energetics and volume changes for ET between the self-assembled anionic uroporphy-rin:cytochrome c complex and the role of the observed volume changes in modulating ET within the complex, 2) the enthalpy and volume change for the excited state PCET reac-tion of a tyramine functionalized ruthenium(II) bis-(2,2'-bipyridine)(4-carboxy-4'-methyl-2,2'-bipyrine) meant to be a model for the tyrosine PCET chemistry carried out by cyto-chrome c oxidase and photosystem II, 3) the enthalpy and volume changes related to car-bon monoxide and tryptophan migration in heme tryptophan catabolic enzyme indoleam-ine 2,3-dioxygenase.
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Serbetcioglu, Serpil. "Mass transfer and catalytic reaction in a three-phase monolith reactor." Thesis, University of Bath, 1993. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.332665.

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Lekakou, Constantina. "Simulation of flow, reaction and heat transfer in reaction injection moulding." Thesis, Imperial College London, 1987. http://hdl.handle.net/10044/1/47048.

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Hasegawa, Jun-ya. "Theoretical Study on the Excited States and Electron Transfer Reactions in Photosynthetic Reaction Center." Kyoto University, 1998. http://hdl.handle.net/2433/77871.

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Tran, Thu-Trang. "Electron and multielectron reaction characterizations in molecular photosystems by laser flash photolysis, towards energy production by artificial photosynthesis." Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLS320.

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La demande énergétique de l’humanité augmente rapidement et ne montre aucun signe de ralentissement. Parallèlement à cette problématique, l'utilisation abusive de combustibles fossiles est l'une des principales causes d'augmentation de la concentration de CO₂ dans l'atmosphère. Ces problèmes doivent être résolus en termes de limitation des émissions de CO₂ et de recherche de sources d'énergie renouvelables pour remplacer les combustibles fossiles. De nos jours, l’énergie solaire est l’une des sources d’énergie renouvelables les plus efficaces. La conversion de l'énergie de la lumière solaire en électricité dans le photovoltaïque ou en énergie chimique par le biais de processus photocatalytiques implique invariablement un transfert d'énergie photo-induit et un transfert d'électrons. Dans ce contexte, l'objectif de la thèse est d'étudier les processus photo-induits dans les photosystèmes moléculaires utilisant la photolyse par flash laser. Le premier thème de cette thèse porte sur l’étude du transfert monoélectronique dans des systèmes de dyades donneur-accepteur en vue d’optimiser l’efficacité de la séparation des charges et de son application dans la cellule solaire organique photovoltaïque. Le deuxième thème de cette thèse porte sur l’étude de deux systèmes modèles de photosynthèse artificielle étudiés pour la possibilité d’une accumulation de charge par étapes. Ensuite, différents systèmes photocatalytiques, développés pour la photoréduction du CO₂, ont été étudiés. La compréhension des processus photo-induits devraient permettre l’amélioration de l'efficacité de la réduction du CO₂ dans les systèmes photocatalytiques pratiques
The energy demand of humanity is increasing rapidly, and shows no signs of slowing. Alongside this issue, abuse using fossil fuels is one of the main reasons which leads to an increase in atmospheric CO₂ concentration. These problems have to be solved in terms of both limiting CO₂ emission and finding renewable energy sources to replace fossil fuels. Nowadays, solar energy appears as one of the most effective renewable energy sources. Conversion of solar light energy to electricity in photovoltaics or to chemical energy through photocatalytic processes invariably involves photoinduced energy transfer and electron transfer. In this context, the aim of the thesis focuses on studying photoinduced processes in molecular photosystems using laser flash photolysis. The first theme of this thesis focus on studying single electron transfer in Donor-Acceptor Dyad systems towards optimization efficiency of charge separation and application in the photovoltaic organic solar cell. In the second theme of this thesis, two model systems of artificial photosynthesis were investigated to assess the possibility of stepwise charge accumulation on model molecules. A fairly good global yield of approximately 9% for the two charge accumulation on MV²⁺ molecule was achieved. Then, different photocatalytic systems, which have developed for CO₂ reduction, were studied. Understanding of the photoinduced processes is an important step toward improving the efficiency of reduction of CO₂ in practical photocatalytic systems
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Clower, Caroline Elizabeth. "Proton-transfer dynamics of novel photoexcited hydroxyarenes." Diss., Georgia Institute of Technology, 2001. http://hdl.handle.net/1853/27858.

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Lee, Lester Y. C. "Transmembrane electron transfer in artificial bilayers /." Full text open access at:, 1985. http://content.ohsu.edu/u?/etd,86.

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Cooper, Ian Blake. "Photosynthetic water oxidation and proton-coupled electron transfer." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/26707.

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Thesis (Ph. D.)--Chemistry and Biochemistry, Georgia Institute of Technology, 2009.
Committee Chair: Bridgette Barry; Committee Member: El-Sayed, Mostafa; Committee Member: Fahrni, Christoph; Committee Member: Kröger, Nils; Committee Member: McCarty, Nael. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Books on the topic "Transfer reaction"

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Ellis, Andrew M., and Christopher A. Mayhew. Proton Transfer Reaction Mass Spectrometry. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118682883.

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International, Geological Congress (29th 1992 Kyoto Japan). Metamorphic reaction: Kinetics and mass transfer. Utrecht: VSP, 1994.

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Heterogeneous photochemical electron transfer. Boca Raton, Fla: CRC Press, 1989.

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W, Rees Charles, ed. Electron transfer reactions in organic chemistry. Berlin: Springer-Verlag, 1987.

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Ling, Juliette Roseanne. Enhancement of the interfacial transfer of iodine by chemical reaction. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1999.

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Dʹi︠a︡konov, Vladimir A. Dzhemilev reaction in organic and organometallic synthesis. New York: Nova Science Publishers, 2010.

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1941-, Ulstrup Jens, ed. Electron transfer in chemistry and biology: An introduction to the theory. Chichester: Wiley, 1999.

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Dʹi︠a︡konov, Vladimir A. Dzhemilev reaction in organic and organometallic synthesis. Hauppauge, N.Y: Nova Science Publishers, 2009.

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Sengupta, Tapan Kumar. Instabilities of flows: With and without heat transfer and chemical reaction. Wien: Springer Verlag, 2010.

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Sengupta, Tapan K., and Thierry Poinsot, eds. Instabilities of Flows: With and Without Heat Transfer and Chemical Reaction. Vienna: Springer Vienna, 2010. http://dx.doi.org/10.1007/978-3-7091-0127-8.

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Book chapters on the topic "Transfer reaction"

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Ghana, Priyabrata. "Plumbylidyne Transfer Reaction." In Synthesis, Characterization and Reactivity of Ylidyne and μ-Ylido Complexes Supported by Scorpionato Ligands, 165–78. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-02625-7_9.

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Nagnibeda, Ekaterina, and Elena Kustova. "Reaction Rate Coefficients." In Heat and Mass Transfer, 171–90. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01390-4_7.

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Tembe, Bhalachandra L. "Activated Thermal Electron Transfer in Polar Liquids." In Reaction Dynamics, 135–55. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-662-09683-3_6.

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Huppert, D., and E. Pines. "Intermolecular Proton Transfer." In Advances in Chemical Reaction Dynamics, 171–78. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4734-4_11.

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Ašperger, Smiljko. "Electron-Transfer Reactions." In Chemical Kinetics and Inorganic Reaction Mechanisms, 177–201. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-9276-5_6.

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Viehland, Larry A. "Momentum-Transfer Theory." In Gaseous Ion Mobility, Diffusion, and Reaction, 95–115. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-04494-7_3.

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Starks, Charles M., Charles L. Liotta, and Marc E. Halpern. "Phase-Transfer Catalysis Reaction with Strong Bases." In Phase-Transfer Catalysis, 383–451. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0687-0_8.

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Khomenko, Iuliia, and Brian Farneti. "Proton-Transfer-Reaction–Mass Spectrometry." In Food Aroma Evolution, 217–40. 1st edition. | Boca Raton : CRC Press, 2019. | Series: Food analysis & properties, 2475-7551: CRC Press, 2019. http://dx.doi.org/10.1201/9780429441837-11.

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Gregory, R. P. F. "Electron Transfer within Reaction-Centre Complexes." In Photosynthesis, 61–82. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0391-3_4.

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Hynes, James T. "Charge Transfer Reaction Dynamics in Solutions." In Perspectives in Quantum Chemistry, 83–95. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0949-6_5.

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Conference papers on the topic "Transfer reaction"

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Rasaiah, Jayendran C., and Jianjun Zhu. "Solvent dynamics and electron transfer reactions." In Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45397.

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Elsaesser, Thomas. "Femtosecond intramolecular proton transfer in hydrogen bonded systems." In Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45384.

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Fonseca, Teresa, and Branka M. Ladanyi. "Computer simulation studies of electron transfer in methanol." In Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45393.

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Martin, Monique M., and Pascal Plaza. "Solvent controlled ultrafast intramolecular charge transfer and internal rotation." In Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45396.

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Karlström, G., and P. Å Malmqvist. "Theoretical aspects on electron transfer in the Fe2+–Fe3+ system." In Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45416.

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Chandler, David, John N. Gehlen, and Massimo Marchi. "On the mechanism of the primary charge transfer in photosynthesis." In Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45411.

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Rai, Yasuhiro, Kazuya Tatsumi, and Kazuyoshi Nakabe. "Experimental Study on a Compact Methanol-Fueled Reformer With Heat Regeneration Using Ceramic Honeycomb." In 2010 14th International Heat Transfer Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/ihtc14-22742.

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On the way to a new era of our society which will be based on hydrogen energy, it is needed to develop on-site hydrogen production systems to cover current insufficient infrastructures of hydrogen supply network systems. For this, a highly efficient compact reformer can be one of the most suitable solutions for on-site production of hydrogen which is supplied to distributed electric power-generation systems. But, the local and overall energy balance in the reformer should be precisely controlled since the reforming reaction processes of hydrocarbon fuels are very sensitive to reaction temperature in the reformer. For smaller reformers, in particular, the amount of heat loss through the outer surfaces is large enough to dominate the reactions. An appropriate way for thermal energy management, therefore, is necessary to accomplish highly efficient reformers. For these backgrounds, a compact tubular-typed fuel reformer was fabricated in this study, and was applied to produce hydrogen from methanol, focusing on the partial oxidation reaction (POR). The reformer was composed of a stainless steel pipe as the reactor exterior and ceramic honeycomb blocks inserted in two locations of the reactor. The honeycomb blocks are expected to assist the reforming reactions and transfer the thermal energy of the exhaust gas to the reaction region, acting as a heat regenerator. The upstream-side honeycomb block was aimed to perform an effective heat exchange from the reactor wall to the reactant gas. By inserting the block, the reforming reaction became stable at right after the block. The maximum hydrogen production was achieved in the condition of equivalence ratio, around 3.5. The other honeycomb block was inserted in the downstream of the reaction zone to convert the thermal energy of exhaust gas to radiation energy which can be transferred to the upstream reaction region. Comparing to the case without the downstream-side block, the temperature of the reaction region became higher. Gas temperatures in the downstream region, on the other hand, became lower. Methanol conversion ratio and hydrogen production ratio enhanced due to the higher temperature at the reaction region. These results indicate that the thermal energy possessed by the exhaust gas was regenerated in the reaction region by the downstream-side honeycomb block and contributes to enhance the efficiency of the fuel reformer.
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Limbach, H. H., G. Scherer, L. Meschede, F. Aguilar-Parrilla, B. Wehrle, J. Braun, Ch Hoelger, et al. "NMR studies of elementary steps of hydrogen transfer in condensed phases." In Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45383.

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JONES, K. L., J. M. ALLMOND, D. W. BARDAYAN, A. BEY, J. BEENE, J. A. CIZEWSKI, A. GALINDO-URIBARRI, et al. "TRANSFER REACTION EXPERIMENTS WITH FISSION FRAGMENTS." In Proceedings of the Fifth International Conference on ICFN5. WORLD SCIENTIFIC, 2013. http://dx.doi.org/10.1142/9789814525435_others30.

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Catford, W. N. "Transfer Reaction Studies with Exotic Nuclei." In TOURS SYMPOSIUM ON NUCLEAR PHYSICS V; Tours 2003. AIP, 2004. http://dx.doi.org/10.1063/1.1737110.

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Reports on the topic "Transfer reaction"

1

Dutton, P. (Electron transfer mechanisms in reaction centers). Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/5624150.

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Dutta, P. K. Photoinduced electron transfer reaction in zeolite cages. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6433626.

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Georgiadou, Anastasia. Nuclear reaction studies: Transfer and Neutron-induced reactions on medium-range nuclei. Office of Scientific and Technical Information (OSTI), March 2020. http://dx.doi.org/10.2172/1602737.

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Ibrahim, Hassan. The ^2H(e,e'p)n Reaction at High Four-Momentum Transfer. Office of Scientific and Technical Information (OSTI), December 2006. http://dx.doi.org/10.2172/917020.

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Tominaga, Keisuke, Gilbert C. Walker, Tai J. Kang, Paul F. Barbara, and Teresa Fonseca. Reaction Rates in the Phenomenological Adiabatic Excited State Electron Transfer Theory. Fort Belvoir, VA: Defense Technical Information Center, May 1991. http://dx.doi.org/10.21236/ada235583.

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Valentini, J. J. Single-collision studies of hot atom energy transfer and chemical reaction. Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/5872757.

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Valentini, J. J. Single-collision studies of hot atom energy transfer and chemical reaction. Final report. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/10124118.

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Thompson, Neil. Analysis of the 12C (e,e'pd) Reaction at High Energy Transfer. Office of Scientific and Technical Information (OSTI), March 2011. http://dx.doi.org/10.2172/1411414.

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Valentini, J. J. Single-collision studies of energy transfer and chemical reaction. Progress report, April 1992--March 1993. Office of Scientific and Technical Information (OSTI), July 1993. http://dx.doi.org/10.2172/10166359.

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Huang, Hai, Benjamin W. Spencer, and Guowei Cai. GRIZZLY Model of Multi-Reactive Species Diffusion, Moisture/Heat Transfer and Alkali-Silica Reaction for Simulating Concrete Aging and Degradation. Office of Scientific and Technical Information (OSTI), September 2015. http://dx.doi.org/10.2172/1244622.

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