Mukerjee

A. K. Singhal, L. W. Keeton, A. K. Majundar, and T. Mukerjee,M Improved Mathematical Formulation for the Computations of Flow Distributions in Manifolds for Compact Heat Exchangers, paper presented at The ASME Winter Annual Meeting, Anaheim, Calif., 1986, p. 105. 

P. Mukerjee and M. J. Mysels, Critical Micelle Concentration ofMqueous Suf actant Systems, NSROS-NBS 36, U.S. Dept, of Commerce, Washiagton, D.C., 1971. 

When the range of chemieal types is restricted, regular behavior is often observed. For example, one might choose to study a series of hydroxylic solvents, thus holding approximately constant the H-bonding capabilities within the series. This is a motivation, also, for solvent studies in a series of binary mixed solvents, often an organic-aqueous mixture whose composition may be varied from pure water to pure organic. Mukerjee et al. defined a quantity H for hydroxylic and mixed hydroxyiic-water solvents by Eq. (8-17). 

Other solvatochromic probes have been proposed. Mukerjee et al. used nitrox-ides for this purpose, finding that their transition energies correlate linearly with Z and t (30). Brooker et al. prepared a polar merocyanine that shows a blue shift... 

J J. R. Johnson, S. Mukerjee, G. D. Adzic, J. J. Reilly, J. McBreen, In situ XAS studies on AB2 type metal hydride alloys for battery ap-... 

The a- and [3-isomers of endosulfan undergo photolysis in laboratory tests after irradiation in polar solvents and upon exposure to sunlight on plant leaves. The a-isomer also undergoes isomerization to the P-isomer, which is relatively more stable (Dureja and Mukerjee 1982). A photolytic half-life of about 7 days was reported for endosulfan by EPA (1982c). The primary photolysis product is endosulfan diol, which is subsequently photodegraded to endosulfan a-hydroxyether. Endosulfan sulfate is stable to direct photolysis at light wavelengths of >300 nm however, the compound reacts with hydroxy radicals, with an estimated atmospheric half-life of 1.23 hours (HSDB 1999). 

DurejaP, Mukerjee SK. 1982. Photoinduced reactions Part IV. Studies on the photochemical fate of 6,7,8,9,10,10-hexachloro-l,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzo(e)dioxathiepin-3-oxide (endosulfan), an important insecticide. Indian J Chem 21B 411-413. 

Mukerjee SK. 1985. The environmental photodegradation of pesticides. Indian J Agric Chem 18 1-9. 

Guild AF, Gancs L, Allen RJ, Mukerjee S (2007) Carbon-supported low-loading rhodium sulfide electrocatalysts for oxygen depolarized cathode applications. Appl Catal A 326 227-235... 

Hatta T, G Mukerjee-Dhar, J Damborsky, H Kiyohara, K Kimbara (2003) Characterization of a novel thermostable Mn(II)-dependent 2,3-dihydroxybiphenyl 1,2-dioxygenase from a polychlorinated biphenyl- and naphthalene-degrading Bacillus sp. JF8. J Biol Chem 278 21483-21492. 

Shimura M, G Mukerjee-Dhar, K Kimbara, H Nagato, H Kiyohara, T Hatta (1999) Isolation and characterization of a thermophilic Bacillus sp. JE8 capable of degrading polychlorinated biphenyls and naphthalene. FEMS Microbiol Lett 178 87-93. 

Similar size effects have been observed in some other electrochemical systems, but by far not in all of them. At platinized platinum, the rate of hydrogen ionization and evolution is approximately an order of magnitude lower than at smooth platinum. Yet in the literature, examples can be found where such a size effect is absent or where it is in the opposite direction. In cathodic oxygen reduction at platinum and at silver, there is little difference in the reaction rates between smooth and disperse electrodes. In methanol oxidation at nickel electrodes in alkaline solution, the reaction rate increases markedly with increasing degree of dispersion of the nickel powders. Such size effects have been reported in many papers and were the subject of reviews (Kinoshita, 1982 Mukerjee, 1990). 

The key parameters of the electronic structure of these surfaces are summarized in Table 9.3. The calculated rf-band vacancy of Pt shows no appreciable increase. Instead, there is a shght charge transfer from Co to Pt, which may be attributable to the difference in electronegativity of Pt and Co, in apparent contradiction with the substantial increase in Pt band vacancy previously reported [Mukerjee et al., 1995]. What does change systematically across these surfaces is the J-band center (s ) of Pt, which, as Fig. 9.12 demonstrates, systematically affects the reactivity of the surfaces. This correlation is consistent with the previous successes [Greeley et al., 2002 Mavrikakis et al., 1998] of the band model in describing the reactivity of various bimetallic surfaces and the effect of strain. Compressive strain lowers s, which, in turn, leads to weaker adsorbate-surface interaction, whereas expansive strain has the opposite effect. 

Mukerjee, P. Mysels, K. J. Critical Micelle Concentrations of Aoueous Surfactant Systems. U. S. Department of Commerce, NSRDS-NBS 36,1971. 

---