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11.
A holographic image subtraction technique is proposed. The vector nature of light is utilized in introducing a phase difference of π between the two reconstructed object waves. The experimental results are also presented. 相似文献
12.
A. Saxena D. Fabris G. Prete D. V. Shetty G. Viesti B. K. Nayak D. C. Biswas R. K. Choudhury S. S. Kapoor M. Lunardon S. Moretto G. Nebbia S. Pesente V. Rizzi A. M. Samant M. Barbui E. Fioretto M. Cinausero A. Brondi G. La Rana R. Moro E. Vardaci N. Gelli F. Lucarelli 《Nuclear Physics A》2004,730(3-4):299-315
Pre-scission and post-scission multiplicities of neutrons and alpha particles have been simultaneously measured for the fission-like reactions of 340 MeV 28Si on 232Th. Dynamical model calculations using HICOL code predict that about 90% of the observed events are of quasi-fission type while the remaining 10% are from compound nucleus fission decay. Moving source fits were carried out to the observed neutron and alpha particle spectra, measured at different angles with respect to the fragment directions. The pre-scission and post-scission neutron multiplicities are deduced to be 8.7±2.0 and 9.4±2.0, respectively. The corresponding multiplicity values for alpha particles are found to be 0.22±0.08 and 0.1±0.03. From the measured post-scission neutron multiplicity, it is inferred that about 65±20 MeV of the initial excitation energy remains at scission. This may be compared to the value of 85±30 MeV estimated from PACE2 statistical model calculations, adjusted to reproduce the measured pre-scission neutron multiplicity. From a comparison of the Statistical Model predictions with the measured pre-scission neutron multiplicity, the fission delay is estimated to be of 5+7−3×10−20 s which overlaps with the average duration of fission-like process from the contact to the scission point (2×10−20 s) as determined from HICOL-based dynamical calculations. For the delay time deduced as above, the pre-scission alpha particle multiplicity calculated by the PACE2 code is about a factor two larger than the experimental one, demonstrating the difficulties in modelling the alpha particle emission from highly elongated shapes that characterize the fissioning system from the contact point to scission. 相似文献
13.
Dipak Ghosh Madhumita Lahiri Argha Deb Susobhan Das Krishnadas Purkait Biswanath Biswas Jayanta Roy Choudhury Rini Chatterjee Abdul Kayum Jafry 《Zeitschrift fur Physik C Particles and Fields》1996,71(1):243-249
The scaled factorial moments and the multifractal moments have been investigated in differentη-intervals to study the dynamical fluctuation of pions produced in 200 AGeV32S-Ag/Br interaction. In order to investigate the detail characteristics of intermittency behaviour, theF-moments are extracted up to the eighth order of moments in differentM-intervals. The analysis indicates a non-thermal phase transition and different regime of particle production during the hadronisation process. 相似文献
14.
15.
D. Choudhury R. C. Borah R. L. Goswamee H. P. Sharmah P. G. Rao 《Journal of Thermal Analysis and Calorimetry》2007,89(3):965-970
Pyrolysis of petroleum refinery sludge has received global acclamation as a clean conversion technique for providing solution
of sludge disposal as well as efficient resource utilization. This communication reports the kinetics study of pyrolysis of
petroleum refinery sludge. Experiments were carried out by means of thermogravimetric analysis at different heating rates
of 5, 10 and 20°C min−1. The pyrolytic reaction is significant in the temperature range of 200–350°C and analysis and evaluation of kinetic parameters
is done in the 100–500°C region of non-isothermal TG curves obtained in nitrogen atmosphere.
The activation energy is calculated by iso-conversional method, then other kinetic parameters are determined by considering
single reaction and two reaction global kinetic model. Two-reaction model is found to fit satisfactorily the experimental
results. 相似文献
16.
A. G. Pramanik P. K. Choudhury 《Journal of polymer science. Part A, Polymer chemistry》1970,8(7):1713-1724
Sodium amylopectin xanthate was prepared by xanthation of potato amylopectin in alkaline medium. The pure product was characterized by I2 solution and ultraviolet spectra of the xanthate groups. The polyelectrolyte behavior of Na amylopectin xanthate in aqueous and salt solutions was investigated by viscometry and light scattering. Its polyelectrolyte behavior in aqueous solution as studied viscometrically was completely different from that of Na amylose xanthate, which is characteristic of linear polyelectrolyte molecules. This difference in behavior could be partly due to the branched structure of amylopectin molecule. A dissymmetry study of Na amylopectin xanthate in aqueous and salt solutions, however, showed that Na amylopectin xanthate molecule underwent expansion in water by about 1.3 times its linear dimension in 0.5M NaCl (unperturbed value). Light-scattering measurements confirmed that the Na amylopectin xanthate molecule had a polydisperse random-coil chain configuration in 0.25M NaCl. Its molecular weight, end-to-end length, and other parameters in salt and alkali solutions were also determined, and the data were then compared with those of Na amylose xanthate in the same media. The solution behavior of Na amylopectin xanthate in 1M NaOH was further investigated and linear expansion factor α, excluded volume factor A2M W/[η], and Flory's hydrodynamic constant φ were evaluated. 相似文献
17.
Methods have been developed to allow applications of membrane introduction mass spectrometry (MIMS) to monitor solution phase components of fermentation broths using electron ionization. The solutions are transported by flow injection analysis (FIA) through a direct insertion membrane probe, fitted with a silicone membrane in the sheet configuration. Analytes of interest pass through the membrane and are ionized by electron implant ionization. The compounds monitored are ammonia, acetic acid, and ethanol, with ammonia being detected as the monochloramine derivative which is generated at pH 10 upon addition of hypochlorite. Quantitation is achieved using external standard solutions. The dynamic range for the quantification of ammonia is 2-8000 ppm, and for ethanol and acetic acid 10-1000 ppm. This method provides rapid detection of analytes of interest, on-line monitoring capabilities, and the advantage of electron ionization. The introduction of samples into the mass spectrometer is achieved readily and automatically, the response time is a few seconds, and there are no memory effects. 相似文献
18.
A. G. Pramanik P. K. Choudhury 《Journal of polymer science. Part A, Polymer chemistry》1968,6(5):1121-1134
Sodium amylose xanthate has been studied in dilute solution. Potato starch was fractionated for this purpose into amylose and amylopectin fractions. Amylose was xanthated in solution under alkaline conditions and the Na amylose xanthate was then characterized by reaction with I2 solution and ultraviolet spectra of the xanthate groups determined. Stability of the xanthate in alkaline condition under both oxygen and nitrogen atmospheres was also investigated. From light scattering measurements of dilute salt solutions of Na amylose xanthate, the weight-average molecular weight M w as well as the molecular dimensions were determined. In 0.11M NaCl, which conforms to the θ solvent, Na amylose xanthate molecules appear to have a random-coil configuration. Two other configurational parameters, such as the effective bond length b, and the steric factor σ, i.e., (R02)1/2/(Rf2 )1/2, where (R02)1/2 is the Root-mean-square end-to-end distance in the unperturbed state and (Rf2 )1/2 is the unperturbed value calculated on the assumption of free rotation about each intermonomer C? O bond of the amylose chain were also calculated and found to be 6.24 and 1.020, respectively. It is thus concluded that the amylose chain in Na amylose xanthate behaves as a typical flexible coil in dilute salt solution. 相似文献
19.
Gurucharan Mukherjee Sailendra Nath Poddar Kingshuk Choudhury Kamalendu Dey 《Transition Metal Chemistry》1988,13(1):58-63
Summary Iron(III) complexes of a quadridentate N2S2 donor ligand, 1,2-di(o-aminophenylthio)ethane (DAPTE) and its Schiff Base with salicylaldehyde, a hexadentate N2S2O2 donor ligand,viz. 1,2-di(o-salicylaldiminophenylthio)ethane (H2DSALPTE) have been synthesised and characterised.The Schiff base ligand (1 mol) gave a dark green tri-iron(III) [Fe3(DSALPTE)(HDSALPTE)Cl3]Cl2 complex when reacted with anhydrous iron(III) chloride (1 mol). The Mössbauer data of this complex suggest the presence of three iron sites, one of which is octahedral and the other two tetrahedral. On the other hand, Fe(ClO4)3 reacted smoothly with H2DSALPTE in ethanol to give a mononuclear pseudo-octahedral complex in which the ligand functions in a dibasic hexadentate fashion. Mössbauer data suggest the presence of a low-spin-high-spin equilibrium in the solid state. The manganese(III) and cobalt(III) complexes of the Schiff base, H2DSALPTE, are also studied for the sake of comparison with the corresponding iron(III) complex. The N2S2 ligand, however, formed a low-spin pseudo-octahedral iron(III) complex. The complexes have been characterised by elemental analysis, molar conductance values, cryomagnetic data and i.r., electronic and Mössbauer spectral data. 相似文献
20.