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排序方式: 共有258条查询结果,搜索用时 15 毫秒
1.
Vandana Singh Ashutosh TiwariDevendra Narayan Tripathi Tulika Malviya 《Tetrahedron letters》2003,44(39):7295-7297
O-Methylation is of outstanding importance in structural polysaccharide chemistry. A novel method for the methylation of polysaccharides using microwave (MW) irradiation is described. Seed gum from Cyamopsis tetragonolobus (Guar) was fully methylated with dimethyl sulphate and sodium hydroxide using 100% microwave power for 4 min in 68% yield. The completely methylated seed gum thus obtained was hydrolyzed by 70% formic acid followed by 0.5N H2SO4 under full microwave power for 1.16 and 1.66 min, respectively. The partially methylated monosaccharides were separated and identified. 相似文献
2.
Cerium(IV) mediated grafting of polyacrylonitrile on to guar gum was studied. Grafting parameters were studied gravimetrically, as a function of temperature, initiator concentration and Guar to acrylonitrile ratio. Higher temperatures resulted in higher monomer conversion and homopolymer formation. Both monomer conversion and extent of grafting increased with increase in cerium ion concentration in the range studied (0.91–9.12 mmol/l). Similar results were obtained with increase in monomer to guar gum ratio from 1 to 5. Grafting with this initiator was found to be generally good with high grafting efficiencies and low homopolymer formation for most experiments. The copolymers obtained were subjected to alkaline hydrolysis to convert nitrile groups in to carboxylic acid groups and the water absorbency of the resulting anionic guar gum was studied. Materials with water absorption up to 300 g/g could be obtained from this study. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
3.
4.
I Sebastián-Francisco 《Analytica chimica acta》2004,508(2):135-140
A quantitative assay for guar gum in carob gum, based on the extraction of proteins in acetonitrile-water (7:3), separation by capillary electrophoresis and multiple linear regression (MLR) using the areas of nine selected peaks as predictors, was improved by performing the extraction in the presence of gamanase. In the absence of the enzyme, peak migration times and areas depended on the guar content, which complicated peak identification and evaluation. Manual correction of the migration times by comparison with standard electropherograms obtained with pure carob and carob-guar mixtures was required; however, when the proteins were extracted under sonication at 60 °C for 30 min in the presence of gamanase, the migration times and peak areas did not vary with the composition of the carob-guar mixtures, and its reproducibility improved largely. These effects were attributed to the reduction of the viscosity of the extracts and the removal of the galactomannose interactions with the proteins and the capillary walls. Peak identification and evaluation were easily and directly performed on these electropherograms without further processing. An MLR model constructed with 36 carob-guar mixtures containing up to 20% guar, and by measuring the areas of 12 selected peaks and using eight of them as predictors, yielded a detection limit of 2.8% guar (α=β=0.05 criterion). A model of similar quality was obtained by partial least-squares (PLS) regression. 相似文献
5.
Most of the common classes of organic compounds chromatograph normally on Superoxes. There is no tailing or adverse effect from excessively different activity different activity coefficients. Superoxes are therefore universal phases for gas chromatography. This is also expressed by a wide useful temperature range from ~50° to ~300°. High MW Superox-4 has a MAOT about 20° higher than the lower MW Superox-0.1. Several applications illustrating the versatility of Superox phases in (GC)2 are presented. 相似文献
6.
Durcilene A. da Silva 《European Polymer Journal》2007,43(6):2620-2629
The synthesis of cashew gum-g-polyacrylamide was carried out at 60 °C by a radical polymerisation using potassium persulphate as the redox initiator under N2 atmosphere. A series of graft copolymers, varying in acrylamide concentration and keeping the concentration of the initiator and polysaccharide constant, was prepared. These graft copolymers were characterised by elemental analysis, infrared and 13C NMR spectroscopy, rheological studies, differential scanning calorimetry and thermogravimetric analysis. Comparisons amongst grafting parameters of the reaction of various natural polysaccharides with polyacrylamide (PAM) were carried out. High percentages of acrylamide conversion (%C) and grafting efficiency (%E) were obtained for cashew gum (CG), even with a low acrylamide/gum ratio. All copolymers had intrinsic viscosity and thus the hydrodynamic volume much higher than the CG value and closer to the PAM. The CG-g-PAM solution had an absolute viscosity at 2.5% concentration (wt./vol.) up to 33 and 3.3 times the CG and PAM values, respectively. Grafting of PAM chains onto the polysaccharide enhances its thermal stability. 相似文献
7.
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
8.
Glutaraldehyde-crosslinked O-carboxymethyl chitosan (O-CMC)–gum Arabic (GA) coacervates were characterized against coacervation acidity. As the coacervation pH increased from 3.0 to 6.0, the crosslinking degree of the coacervates and its sensitivity to glutaraldehyde concentration variation declined gradually, but the elasticity increased markedly. Crosslinking improved the structure compactness and thermal stability of the coacervates and high coacervation pH favored the increase of the two parameters, but a reverse trend was observed regarding swelling ratio in the simulated gastric fluid. It was concluded that glutaraldehyde-crosslinked O-CMC–GA coacervates with required properties could be tailored by selecting an appropriate complexation acidity. 相似文献
9.
The photoinitiating ability of some sulfur ylides was studied. Diphenylsulfonium bis (methoxycarbony1)methylide (DPSY) could photoinitiate methyl methacrylate and styrene. A free radical mechanism was confirmed by a kinetic study, the inhibiting effect of benzoquinone, and the copolymer composition. From an analysis of the photodecomposition products it is suggested that the phenyl radical generated from the bond fission between the sulfur atom and the phenyl group participates in the initiation of this free radical polymerization. Methylphenylsulfonium bis (methoxycarbonyl) methylide, as well as DPSY, served as a photoinitiator, but dimethylsulfonium bis (methoxycarbony1)methylide did not. The differences are explained based on UV spectra. 相似文献
10.
4-Amino-, chloro-, and bromo-substituted salicylic acid-formaldehyde polymers and their metal chelates were screened for their antifungal activity. Various copolymers prepared from 4-chloro-(bromo)salicylic acid, formaldehyde, and other comonomers were also screened for their antifungal activity. All these polymers, copolymers, and polychelates were found active against several fungi Their fungicidal activities are compared with those of the corresponding monomers and monomeric chelates. 相似文献