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131.
A direct and reagent free procedure has been developed to monitor the fermentation process of pine apple nectar using Attenuated Total Reflectance Fourier-transform mid-infrared spectrometry (FT-IR) and multivariate analysis. A classical 42 design for standards was employed for calibration using the information in the spectral range from 907 to 1531 cm−1 of the first order derivative spectra after mean centering of infrared data. The root mean square error of calibration (RMSEC) of 0.040, 0.021, 0.063 and 0.074% w/w were obtained for glucose, fructose, saccharose and ethanol, respectively, and a mean relative validation error of 2.9, 2.1, 2.6 and 3.6% was achieved for glucose, fructose, saccharose and ethanol. Results obtained by the proposed procedure for the alcohol content at different fermentation levels were statistically comparable with those obtained by a reference spectrometric method. So, FT-IR spectrometry provides a fast alternative to long and tedious classical procedures to ethanol determination and sugar enzymatic analysis. 相似文献
132.
133.
L.L. Carvalho 《European Polymer Journal》2006,42(10):2589-2595
Samples of a methacrylic side-chain azopolymer were synthesized by a radical copolymerization of methyl-methacrylate with the methacrylic derivative of the commercial dye Disperse Red-13 (DR13). Copolymers with different molecular weight were obtained by varying the reaction time and the concentration of initiator. Samples with molecular weight averages (Mw) from 3 to 8 × 104 g/mol and 1.4-1.7 polydispersity were obtained. The glass transition temperature of the samples increased linearly from the lower to the highest molecular weight. Optical quality cast films were prepared for all samples and photoinduced birefringence was successfully carried out in all samples as well as surface relief gratings could be inscribed in the cast films. 相似文献
134.
135.
María Beatriz de la Calle Guntiñas Michiel Ceulemans Claudia Witte Ryszard Łobiński Freddy C. Adams 《Mikrochimica acta》1995,120(1-4):73-82
A method is presented for the selective determination of the volatile selenium species dimethylselenide and dimethyldiselenide, using a commercially available purge-and-trap injection system coupled to capillary gas chromatography-microwave induced plasma-atomic emission spectrometry. The efficiency of the purging step was evaluated and the parameters affecting the purge and trap processes were optimized. The method was applied to the determination of volatile selenium compounds in lake water. Relative detection limits of 2ng/l for dimethylselenide and dimethyldiselenide, corresponding to an absolute detection limit of 10 pg, were achieved. 相似文献
136.
137.
Summary The application of GLC, HPLC and TLC to the analysis of pharmaceutical creams is discussed with special attention to sample clean-up. The results of the determination of hydrocortisone acetate, salicylic acid, benzoic acid, diethyl stilbestrol, chloramphenicol, diphenhydramine HCl, tretinoin and some cream base components by reversed phase HPLC are given.Presented at the 14th International Symposium on Chromatography London, September, 1982 相似文献
138.
D. S. Gouveia R. Rosenhaim M. A. M. A. de Maurera S. J. G. Lima C. A. Paskocimas E. Longo A. G. Souza I. M. G. Santos 《Journal of Thermal Analysis and Calorimetry》2004,75(2):453-460
With the aim of obtaining materials with applications in pigments, CoxZn7-xSb2O12 spinels were synthesized using the Pechini method. This method consists in the formation of a polymeric net, where the metallic
cations are homogeneously distributed. In this work, two types of alcohol (ethyl glycol and ethylene glycol) were used for
the synthesis of a zinc antimoniate spinel, CoxZn7-xSb2O12 (x=0-7). The materials were characterized by termogravimetry (TG) and differential thermal analysis (DTA). TG results indicated
a decrease in total mass loss when cobalt was added to the solution substituting zinc, for samples prepared using the two
different alcohols. Decomposition temperatures, obtained by TG and DTA, presented a decreasing behavior as cobalt was added
to the material. In relation to the alcohols, all results indicated a better polymerization of the resin when ethylene glycol
was used, being the most indicated one for cation immobilization. X-ray diffraction did not show differences between the two
alcohols - both presented the spinel phase (Co, Zn)2.33Sb0.67O4. Samples with higher quantity of cobalt also presented ilmenite phase (Co, Zn)Sb2O6.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
139.
F. F. C. Bazito S. I. Córdoba de Torresi R. M. Torresi 《Journal of Solid State Electrochemistry》2007,11(11):1471-1479
Poly(phenylene sulfide phenyleneamine), PPSA, is a copolymer of poly(aniline) and poly(phenylene sulfide), soluble in conventional
organic solvents as tetrahydrofuran, dimethyl sulfoxide, dimethylformamide, and cyclohexanone. In this research, its electrochemical
behavior has been studied in acetonitrile in the presence of different electrolytes, where the loss of electroactivity was
observed after few cycles. In this paper, the charge compensation dynamics of PPSA is analyzed through electrochemical quartz
crystal microbalance experiments and electroacoustic impedance measurements. Raman spectroscopy data have shown that once
the oxidation of the sulfur atom occurs, a loss of electroactivity is observed, being not possible to recover the pristine
state of the polymer. Fourier transform infrared (FTIR) and X-ray diffraction (XRD) data obtained for the fully oxidized polymer
are consistent with the formation of a networked polymer due to the electrophilic attack of the positive sulfur atom on the
activated aromatic rings. Electrochemical quartz crystal microbalance results clearly show that the degree of irreversibility
fully depends on the chemical nature of the anions with a negligible participation of the cations of the electrolytic solution.
This work is in memoriam of Prof. Dr. Francisco C. Nart, dearest friend and colleague, whose scientific skills and enthusiasm
will always be remembered. 相似文献
140.
Treatment of methyl 3,5-dideoxy-β---pentofuranoside with the Ph3P-CCl4 reagent gave none of the expected 2-chloro derivative but a mixture of l→2 linked oligosaccharides, , with some higher homologues, terminated by αa 2-chloro-2,3,5-trideoxy-α---pentofuranosyl unit at the non reducing end. 相似文献