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61.
A simple and sensitive field detection and spectrophotometric method for determination of copper described herewith is based on the formation of a red coloured species of copper(II) with 1-[pyridyl-(2)-azo]-naphthol-(2) (PAN), TX-100 and N,N'-diphenylbenzamidine (DPBA) at pH range 7.8-9.4. The red coloured Cu(II)-PAN-(TX-100)-DPBA complex in chloroform shows maximum absorbance at 520 nm with molar absorptivity value of 1.14x10(5) l mol(-1) cm(-1). The detection limit of the method is 2 ng ml(-1) organic phase. The system obeys Beer's law up to 0.6 mug Cu(II) ml(-1) in organic solution. Most of the common metal ions generally found associated with copper do not interfere. The repeatability of the method was checked by finding relative standard deviation (RSD) (n=10) value for solutions each containing 0.2 mug ml(-1) of Cu(II) and the RSD value of the method was found to be 1.5%. The validity of the method has been satisfactorily examined for the determination of copper in soil and airborne dust particulate samples. 相似文献
62.
Roland Prewo Jost H. Bieri Subhendu Narayan Ganguly Max Viscontini 《Helvetica chimica acta》1982,65(3):1094-1099
The Configuration at C(6) of Natural 5,6,7,8-Tetrahydro-L-biopterin and of its Pentaacetate The structure of (6.R)-pentaacetyl-5,6,7,8-tetrahydro-L-biopterin, one of two diastereoisomers obtained by catalytic hydrogenation and subsequent acetylation of L-biopterin, has been determined by X-ray diffraction analysis. The space group is P212121, a=8,053(l), b=14,955(3), c= 21,502 (4) Å. The asymmetric unit contains one molecule of the biopterin derivative and one of ethyl acetate. The R-configuration can be assigned to C(6) by reference to the known configurations of the other asymmetric C-atoms. As hydrolysis of this diastereoisomer yields the natural 5, 6,7,8-tetrahydro-L-biopterin, the latter also possesses the (6 R)-configuration. 相似文献
63.
Praharaj S Ghosh SK Nath S Kundu S Panigrahi S Basu S Pal T 《The journal of physical chemistry. B》2005,109(27):13166-13174
Gold nanoparticles of variable sizes have been synthesized in toluene employing two-phase (water-toluene) extraction of AuCl4- followed by its reduction with sodium borohydride in the presence of a series of cationic surfactants of a homologous series having the general formula C(n)TAC. The solubility features of the gold particles in the organic solvent have been accounted qualitatively by calculating the van der Waals interaction potential between the particles. The effect of thermal energy and medium dielectric constant on the stability of metal particles has been studied by measuring the surface plasmon resonance. The stabilization of surfactant-mediated gold particles as hydrosol or organosol has been elucidated by considering the double-layer interaction as a function of the dielectric constant of the solvent medium. The influence of the counterion of the phase transfer reagent and stabilizing ligand on the photochemical stability of the gold colloids has been investigated. The fluorescence probe 1-methylaminopyrene (MAP) was considered for the surface functionalization of the gold particles, and it has been found that there is an enhancement of molecular fluorescence from the gold-probe assembly. 相似文献
64.
Submerged culture fermentation studies were carried out in batch mode for optimizing the environmental parameters and carbon
source requirement by Pseudomonas elodea for the production of gellan gum. The maximum production of gellan gum was obtained with 16-h-old culture and 8% inoculum
at 30°C and pH 7.0 after 52 h of incubation (6.0 g/L). Of the various carbon sources tested, 2% sucrose, glucose, and soluble
starch yielded considerably high amounts of gellan. Studies on the concentration of various carbohydrates on gellan gum production
indicated that the optimum concentration of glucose and starch was 3%, whereas for sucrose it was 4%. The addition of glucose
in the medium above 3% had a detrimental effect on gellan yield. The investigation of intermediate two-step addition of glucose
under identical conditions of fermentation showed an enhanced production of gellan (8.12 g/L) as compared with the control
(6.0 g/L). To optimize the recovery of gellan from fermented broth, different solvents were tested for precipitation of gellan
gum. Among the various solvents tested, tetrahydrofuran gave better recovery of gellan (82%) as compared with the conventional
solvent isopropanol (49%). 相似文献
65.
A simple, novel diastereoselective synthesis of both (E)- and (Z)-allylsilanes via organoboranes is developed. (E)-1-Alkenylboronate esters easily prepared from the corresponding terminal alkynes via hydroboration with dibromoborane-methyl sulfide complex followed by treatment with 1,3-propane diol readily react with trimethylsilylmethyllithium at −78 °C in methanol followed by reaction with iodine in methanol to produce the corresponding (Z)-allylsilanes in high yields (72-80%) and in high stereochemical purities (98% as evidenced by CMR spectral data). Similarly, the (Z)-1-alkenylboronate esters react with trimethylsilylmethyllithium at −78 °C in methanol followed by treatment with iodine in methanol to produce the corresponding (E)-allylsilanes in moderate yields (57-65%) in high stereochemical purities (>98% as revealed by CMR spectral data). 相似文献
66.
Novel anionic dinuclear mixed-ligand peroxo complexes of the type [(UO2)2(O2)3L(H2O)2]3− (L = Histidinate, aspartate, salicylate, Imidazolate and glutamate) have been synthesized from the interaction of uranyl ion (UO22+) with peroxide (O22−) in the presence of the respective coligand (L) at pH 9–10. The sparingly soluble complexes were characterized by elemental analyses, FT-IR, laser Raman (LR) and UV-vis spectroscopy and solution electrical conductance measurements. Based on these studies, a double bridged dinuclear structure involving one peroxo and the mixed ligand L (via-COO−) has been tentatively proposed. Infra-red coupled with LR spectra evidenced structurally different metal bound peroxides (ν2 and σ:σ). An aqueous solution of the salicylate and aspartate complexes have been shown to convert triphenylphosphine (PPh3), cyclohexene, styrene and SO2 to the corresponding OPPh3, 1,2 cyclohexanediol, phenylethyleneglycol and SO42−, respectively. 相似文献
67.
The viscosity deviation (Δη), the excess molar volume (V
E) and the ultrasonic speed (u) have been investigated from viscosity (η) and density (ρ ) measurements of binary liquid mixtures of 1,2-dimethyoxyethane with methanol, ethanol, propan-1-ol, butan-1-ol,
pentan-1-ol, hexan-1-ol or octan-1-ol over the entire range of composition at 298.15 K. The excess volumes are negative over
the entire range of composition for all of the mixtures with the exception of hexan-1-ol and octan-1-ol. The excess isentropic
compressibilities (K
S
E) and viscosity deviations are negative for all of the mixtures. The magnitudes of the negative values of V
E decrease with the number of carbon atoms of the alkan-1-ol. The trend of increasing K
S
E values with the chain length of the alkanol is similar to that observed in the case of V
E. Graphs of V
E, Δ η, K
S
E, Δ u, L
f
E and Z
E against composition are presented as a basis for a qualitative discussion of the results. 相似文献
68.
M. Patri Varsha R. Hande Swati Phadnis B. Somaiah Suhasini Roychoudhury P. C. Deb 《先进技术聚合物》2004,15(5):270-274
A Novel solid polymer electrolyte (SPE) membrane containing both ? COOH and ? SO3H group has been prepared by simultaneous method of radiation grafting of acrylic acid onto FEP followed by sulfonation. The presence of weakly acidic acrylic acid controls the swelling in water while ? SO3H group provides conductivity due to its strongly ionic characteristic. FEP‐g‐acrylic acid and its sulfonated derivatives were characterized by their properties. While the mechanical properties decreased, other properties such as ion exchange capacity (IEC), water uptake and ionic conductivity increased with increase in graft content. These properties further changed on sulfonation. Acrylic acid being weakly acidic in nature, conductivity values of the grafted membrane were quite low. However, introduction of strong ? SO3H group resulted in conductivity closer to Nafion 117. Few sulfonated membranes have been tested with respect to H2/O2 fuel cell performance. Short‐term fuel cell test for 100 hr gave a stable performance. These membranes are less expensive compared to Nafion. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
69.
Hussain SA Deb S Biswas S Bhattacharjee D 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,61(11-12):2448-2454
This communication reports the surface pressure (pi) versus area per molecule (A) isotherm characteristics of the mixed films of 9-phenyl anthracene (PA) in stearic acid (SA) and polymethyl methacrylate (PMMA) matrices, at the air-water interface. The mixed Langmuir films at the air-water interface have been observed to be easily transferred onto solid substrates to form uniform Langmuir-Blodgett films. By changing various parameters, namely molefraction, surface pressure of lifting and number of layers, the mixed Langmuir-Blodgett (LB) films of various types have been fabricated successfully and their spectroscopic characteristics have been reported. From the isotherm characteristics and the area per molecule versus molefraction plot, it is evident that the PA molecules are successfully incorporated into mixed Langmuir-Blodgett films. UV-vis absorption spectroscopic study of the mixed LB films at various molefractions of PA in two different matrices reveal that formation of I-type aggregate in PMMA matrix whereas both I- and H-type aggregates are playing their dominant role in SA matrix. Moreover, fluorescence spectroscopic study reveals reabsorption effect. Molecular movement persists in the freshly prepared LB films, as is evident from the time dependent changes in both UV-vis absorption and fluorescence spectra of the mixed LB films in both matrices. From our observation it is evident that about 200 h is required to get the LB films in a stable condition. Dimers and higher order n-mers are formed at a higher surface pressure of 30 mNm(-1). 相似文献
70.
Ditzler WR Hill D Hoftiezer J Johnson KF Lopiano D Shima T Shimizu H Spinka H Stanek R Underwood D Wagner RG Yokosawa A Burleson GR Faucett JA Fontenla CA Garnett RW Luchini C Rawool-Sullivan MW Bhatia TS Glass G Hiebert JC Kenefick RA Nath S Northcliffe LC Damjanovich R Jarmer JJ Vaninetti J Jeppesen RH Tripard GE 《Physical review D: Particles and fields》1992,46(7):2792-2830