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Theoretical exploration into the favourable impact on the actual cold weather decomposition associated with RDX in tetrahydrofuran, acetone, toluene, and also benzene.
Herein, a novel cellulose derivative has been synthesized and investigated as a nature-derived solid polymer electrolyte for lithium batteries. Cellulose is oxidized in a two-step process to dicarboxylic acid cellulose to allow for grafting low molecular weight poly(ethylene glycol) monomethyl ether (550 g mol-1) via Fischer-Speier esterification at the thus obtained carboxyl groups. The chemical structure of the synthesized materials is confirmed by Fourier-transform infrared (FT-IR) and nuclear magnetic resonance (NMR) spectroscopy as well as X-ray diffraction. Incorporating lithium bis(trifluoromethane-sulfonyl)imide (LiTFSI) as conducting salt and N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (Pyr14TFSI) ionic liquid as plasticizer results in the realization of an amorphous and solvent-free solid polymer electrolyte. These electrolyte membranes are characterized by high thermal and electrochemical stability and ionic conductivities of about 1×10-5 S cm-1 at 20 °C and 2.5×10-4 S cm-1 at 80 °C, which enables very stable lithium stripping and plating for more than 800 h.Monosaccharide composition analysis after acid hydrolysis is the first step towards structural characterization of the polysaccharides. To modernize the hydrolytic procedure, we used a polymerase chain reaction (PCR) instrument to accomplish the task, which allows to generate monosaccharide products from up to 96 samples simultaneously within 30 min. Fucoidan, chitosan and propylene glycol alginate sodium sulfate (PSS) were chosen as representatives of complex, basic and acidic polysaccharides to optimize the hydrolytic conditions, respectively, through the orthogonal L9 (34) experiments. The hydrolysis loss ratio for monosaccharide standards were also measured. Using this assay, the hydrolysis plus 1-phenyl-3-methyl-5-pyrazolone (PMP) labeling of the monosaccharide products could be accomplished in 90 min with the RSD values less than 5 % based on HPLC analysis. We further confirmed the reliability of the assay by HPLC coupled MS analysis. In conclusion, PCR instrument-based hydrolysis assay is suitable for monosaccharide composition analysis of complex, acidic and basic polysaccharides.Two bottom-up strategies, disaccharide and oligosaccharide analyses, were applied to elucidate the structure of a fucosylated chondroitin sulfate (FCS). The FCS was hydrolyzed with mild acid. The remained part was digested with CS lyase for disaccharide analysis. The products from each step were analyzed and the results revealed that mild sulfuric acid mainly released sulfated fucose branches, but also affected some residues and sulfo-groups on the backbone. Over 140 oligosaccharide fragments were generated by catalytic oxidation and identified by HPSEC-MS, including sulfated fucose oligosaccharides exclusively from branches, sulfated backbone fragments, and junctional fragments. Based on the results provided by these two methods, the proposed backbone of the FCS is mainly composed of GlcA→GalNAc4S6S and GlcA→GalNAc6S, and the branch is mainly located at GalNAc. The longest branch observed is nonasaccharide, and most of the fucose on the branches are mono and/or di-sulfated. NMR results supported the conclusion.In this work, two new chitosan-Schiff base derivatives (HCS-GSP and LCS-GSP) were synthesized by the condensation reaction of high molecular weight chitosan (HCS) and low molecular weight chitosan (LCS) with (-)-gossypol (GSP), respectively. For this purpose, racemic gossypol was isolated from cotton seeds and it was further enantiomerically purified by diastereomeric resolution technique using l-tryptophan methyl ester hydrochloride. Then, chitosan polymers were derivatized with (-)-gossypol by the condensation reaction. The isolated and synthesized coumpounds were characterized by physical measurements and spectroscopic methods (elemental analysis C,H,N, Uv-vis, FT-IR, 1H&13C NMR and TG/DTG/DTA). The antioxidant activity of high molecular weight chitosan (HCS), low molecular weight chitosan (LCS) and their gossypol derivatives was evaluated as radical scavengers against 1,1-diphenyl-2-picrylhydrazyl radicals (DPPH). The results showed that both of the chitosan-gossypol derivatives (HCS-GSP and LCS-GSP) had a better ability to scavenging DPPH radical (IC50, 12 μg/mL and 16 μg/mL, respectively) than its unmodified chitosan.Chlorite is one of the representative iron-bearing silicates gangue minerals existed in the specularite ores which the traditional depressants are incapable of action in specularite/chlorite separation flotation. https://www.selleckchem.com/peptide/box5.html An attempt was conducted for the separation of specularite/chlorite with chitosan as a novel depressant through microflotation tests, Zeta potential measurements, adsorption tests, FT-IR, and XPS analysis. The microflotation results show that chitosan selectively depresses chlorite while specularite still keeps in high floatability. Zeta potential measurements and adsorption tests indicate that chitosan mainly adsorbed on chlorite surface, hindering the subsequent adsorption of dodecan-1-amine and leading the hydrophobicity distinction. The FT-IR spectra of chlorite validate the adsorption of chitosan on chlorite. The results of XPS illustrate that electrons partially transferred from chitosan to the aluminum, iron, magnesium, silicon, and adjacent oxygen atoms of silicon atoms in chlorite during the adsorption process.The effect of six anions (Cl-, OH-, NO3-, SO42-, C6H10O62- and PO43-) on a starch (St)-enzyme (thermostable α-amylase, TαA)-calcium (Ca) system was investigated in a low-moisture solid state. Two levels of Ca salts (1 and 10 mmol/100 g St) added to potato starch with and without TαA were analyzed by FT-IR, DSC and SEM. The surface morphologies of the St-Ca complexes were different in the presence of various anions, and the residual Ca salts around the St granules might decrease the enzymatic action. For bioextrusion, TαA (0.5‰ and 1.5‰) were introduced for a relatively low Ca content (1 mmol/100 g). Significant differences in enzyme activity were observed, increasing the activity of TαA by SO42- (146.54 %) > C6H10O62- > Cl- > control > NO3- > OH- ≈ PO43- and C6H10O62- (123.20 %) ≈ Cl- ≈ SO42- > control > PO43 > OH- > NO3- for the low and high enzyme levels, respectively.
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