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1.
Thermal degradation studies of alkyl-imidazolium salts and their application in nanocomposites 总被引:1,自引:0,他引:1
Walid H Awad Jeffrey W Gilman Marc Nyden Thomas E Sutto Paul C Trulove Douglas M Fox 《Thermochimica Acta》2004,409(1):3-11
Increasing the thermal stability of organically-modified layered silicates is one of the key points in the successful technical application of polymer-layered silicate nanocomposites on the industrial scale. To circumvent the detrimental effect of the lower thermal stability of alkyl ammonium-treated montmorillonite, a series of alkyl-imidazolium molten salts were prepared and characterized by elemental analysis, thermogravimetry (TGA) and thermal desorption mass spectroscopy (TDMS). The effect of counter ion, alkyl chain length and structural isomerism on the thermal stability of the imidazolium salts was investigated. Alkyl-imidazolium-treated montmorillonite clays were prepared by ion exchange of the imidazolium salts with Na-montmorillonite. These organically-modified clays were characterized by X-ray diffraction (XRD), TDMS and thermogravimetry coupled with Fourier transform infrared spectroscopy (TGA-FTIR), and compared to the conventional quaternary alkyl ammonium montmorillonite. Results indicate that the counter ion has an effect on the thermal stability of the imidazolium salts, and that imidazolium salts with PF6−, N(SO2CF3)2− and BF4− anions are thermally more stable than the halide salts. A relationship was observed between the chain length of the alkyl group and the thermo-oxidative stability; as the chain length increased from propyl, butyl, decyl, hexadecyl, octadecyl to eicosyl, the stability decreased. The results also show that the imidazolium-treated montmorillonite has greater thermal stability compared to the imidazolium halide. Analysis of the decomposition products by FTIR provides an insight about the decomposition products which are water, carbon dioxide and hydrocarbons. 相似文献
2.
Chouhaid Nasr Prashant V. Kamat Surat Hotchandani 《Journal of Electroanalytical Chemistry》1997,420(1-2)
A photoelectrochemical cell with a coupled SnO2|CdSe nanocrystalline semiconductor electrode has been prepared by sequential deposition of SnO2 and CdSe films onto an optically transparent electrode (OTE), and its photoelectrochemical behavior has been studied. The results show that the coupling of CdSe with SnO2 leads to an improvement in the performance of OTE|SnO2|CdSe over OTE|CdSe cells in terms of increased incident photon-to-current conversion efficiency, increased stability and smaller reversal of current. The favorable positioning of the energy bands of SnO2 and CdSe is responsible for the above observations. Various photoelectrochemical parameters of the OTE|SnO2|CdSe cell obtained for an incident light power of 0.31 mW cm−2 at 470nm, are as follows: Isc ≈ 25–30 μA cm−2, Voc ≈ 0.5–0.6 V, ƒƒ = 0.47 and a power conversion efficiency of about 2.25%. 相似文献
3.
M. Nasr H. H. Zoorob A. Zayed M. T. El-Wassimi 《Monatshefte für Chemie / Chemical Monthly》1979,110(4):913-918
Condensation of 4-bromomethylquinoline derivatives1 a-1 c with glycine and thioglycolic acid gave the corresponding quinolylmethylglycine and quinolylmethylthioacetic acid derivatives2 a-2 c and2 d-2 f, respectively. Cyclization of2 a-2 f was affected either by polyphosphoric acid or concentrated sulphuric acid to give3 a-3 f. Chlorination of2 a-2 f and3 a-3 f were also accomplished.
Die Reaktivität von 4-Brommethylchinolin-Derivaten gegenüber Glycin und Thioglycolsäure. Ein neues Ringsystem
Zusammenfassung Die Reaktion von 4-Brommethylchinolin-Derivaten1 a-c mit Glycin und Thioglycolsäure gab die entsprechenden Kondensationsprodukte2 a-c und2d-f.2 a-f konnten mit Polyphosphorsäure bzw. mit konzentrierter Schwefelsäure zu Benzo[c]-2,6-naphthyridinen3 a-f zyklisiert werden.2 a-f und3 a-f waren einer Chlorierung (POCl3) zugängig.相似文献
4.
LetF(b, M) (b ≠ 0 complex,M>1/2) denote the class of functionsf(z) =z + Σ n=2 ∞ a n z n analytic in U={z:|z|<1} which satisfy for fixedM, f(z)/z ≠ 0 inU and \(\left| {\frac{{b - 1 + \left[ {zf'{{\left( z \right)} \mathord{\left/ {\vphantom {{\left( z \right)} {f\left( z \right)}}} \right. \kern-0em} {f\left( z \right)}}} \right]}}{b} - M} \right|< M, z \in U\) . In this note we obtain various representations for functions inF(b, M). We maximize |a3=μa 2 2 | over the classF(b, M). Also sharp coefficient bounds are established for functions inF(b, M). We also obtain the sharp radius of starlikeness of the classF(b, M). 相似文献
5.
Cssio Luiz Coutinho Almeida-da-Silva Nallusamy Sivakumar Homer Asadi Anna Chang-Chien M. Walid Qoronfleh David M. Ojcius Musthafa Mohamed Essa 《Molecules (Basel, Switzerland)》2022,27(13)
Boswellia trees, found throughout the Middle East and parts of Africa and Asia, are the source of frankincense oil. Since antiquity, frankincense has been traded as a precious commodity, but it has also been used for the treatment of chronic disease, inflammation, oral health, and microbial infection. More recently, the bioactive components of Boswellia trees have been identified and characterized for their effects on cancer, microbial infection (especially infection by oral pathogens), and inflammation. Most studies have focused on cell lines, but more recent research has also investigated effects in animal models of disease. As natural products are considered to be safer than synthetic drugs, there is growing interest in further developing the use of substances such as frankincense oil for therapeutic treatment. 相似文献
6.
7.
The effect of swelling in kerosene on the electrical conductance of 60, 80, and 100 part per hundred parts of rubber by weight of Fast Extrusion Furnace (FEF) carbon black-loaded styrene-butadiene rubber (SBR, 1502) was studied. It was found that there is a characteristic time of swelling after which a sudden decrease in conductivity appears. An ideal and simple model is suggested to calculate the carbon-carbon interspacing distance, D, in the carbon/rubber matrix. The dependence of D on the swelling time is also discussed. 相似文献
8.
Synthesis,spectroscopic characterization,thermal behaviour,in vitro antimicrobial and anticancer activities of novel ruthenium tricarbonyl complexes containing monodentate V‐shaped Schiff bases
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The interaction of Ru3(CO)12 with a novel family of monodentate V‐shaped Schiff base ligands (L1–4; L1: (E)‐1‐(4‐((4‐bromobenzylidene)amino)phenyl)ethanone, L2: (E)‐1‐(3‐(4‐(dimethylamino)benzylideneamino)phenyl)ethanone, L3: (E)‐1‐(4‐(4‐(dimethylamino)benzylideneamino)phenyl)ethanone, L4: (E)‐1‐(3‐(3,4‐dimethoxybenzylideneamino)phenyl)ethanone) in air under atmospheric pressure afforded the novel complexes [Ru(CO)3(L1–4)2]. The parent ligands and their complexes were characterized using elemental analyses and spectroscopic techniques. In addition, the structure of the representative ligand L1 was determined using single‐crystal X‐ray analysis. The stereochemistry and theoretical optimization of the three‐dimensional geometry of the ligands and their complexes were justified. In vitro antimicrobial screening against bacterial stains Escherichia coli and Staphylococcus aureus and fungus Candida albicans was conducted. Cytotoxicity of the compounds as anti‐tumour agents was evaluated against liver carcinoma (HepG2), breast carcinoma (MCF7) and colon carcinoma (HCT‐116) cell lines relative to cisplatin and doxorubicin. The complexes showed variable in vitro cytotoxic activities against the three studied cell lines, with IC50 values less than those of cis‐platin, and thus appear to be building blocks for promising anti‐tumour agents. 相似文献
9.
J. Oueslati A. Rayes C. Ben Nasr F. Lefebvre 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):693-705
The synthesis and structures of two new compounds with the general formula N(C2H4NH3)3(H2TO4)(HTO4)·2H2O (T = P, As) are reported. They crystallize with triclinic unit cells and are isotropic. We determined the structure of phosphate salt. The following unit cell parameters were found: a = 9.886(4), b = 9.308(2), c = 10.140(3) Å, α = 109.38(2), β = 108.83(3), γ = 74.40(3)°, V = 819.2(5) Å3, and ρcal. = 1.537 g · cm?3. The crystal structure was solved with a final R = 0.042 for 3748 with I > 3σ I). The space group is P-1 and Z = 2. The atomic arrangement can be described as a three-dimensional network of hydrogen bonds made up from HnPO4 3?n (n = 1, 2) anions and H 2 O molecules between which are trapped the tris(2-ammoniumethyl)amine cations. Solid-state 13C and 31P MAS-NMR spectroscopies are in agreement with X-ray structure. Ab initio calculations allow the attribution of the phosphorus signals to the independent crystallographic sites. 相似文献
10.
Galal H. Elgemeie Wafaa A. Zaghary Tamer M. Nasr Kamelia M. Amin 《Journal of carbohydrate chemistry》2013,32(6):345-356
Reported is the first method to prepare a new class of thienopyrazole thioglycosides via a one‐pot reaction of the sodium thienopyrazolthiolate salts with 2,3,4,6‐tetra‐O‐acetyl‐α‐D‐gluco‐and galactopyranosyl bromides. The sodium thienopyrazolthiolate salts are prepared using pyrazoldithioic acids and their corresponding mono ‐ and dithiolate salts. 相似文献