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61.
62.
Interactions of anionic dye Eriochrome Blue Black R (EBBR) with various cationic micelles of surfactants n-alkyltrimethylammonium CnTAB (n=12; 14; 16 and 18) have been investigated spectrophotometrically at 25°C in premicellar and postmicellar region. The results have shown that with increasing the alkyl chain length of surfactants, the maximum absorbance of EBBR shifted to a higher wavelength and the binding constants of EBBR to cationic micelles (Kb) increases. This confirms that the surfactant micelle, which has a longer alkyl hydrocarbon chain, enables greater solubilization of dye. Thus, the hydrophobic interaction of the dye with micelles increases in the order: C12TAB相似文献   
63.
Ensemble averaging measurements obscure the link between the electrochemical performance and the specific properties of an individual because of the interplay of inhomogeneity and heterogeneity. Nanocollision electrochemistry has attracted increasing interest because of its extremely high sensitivity, revealing the intrinsic properties of individual entities that are masked in the traditional ensemble measurements. In this perspective review, we summarized the recent developments in nanocollision-based single entity electrochemistry and photoelectrochemistry, the combined nanocollision electrochemistry with the other complementary techniques, as well as accurate data process. In closing, future challenges, opportunities, and destinations related to nanocollison electrochemistry were discussed.  相似文献   
64.
A new series of substituted pryrrolobenzimidazoles have been prepared via regioselective displacement of chlorine atom from dichloropyrrolobenzimidazoles with various amine nucleophiles. The dichloro compounds were obtained from the reaction of ortho phenylene diamine compounds with dichloromaleic anhydride.  相似文献   
65.
In this work, a fast and simple magnetic dispersive solid phase extraction methodology was developed utilizing Ag@magnetite nanoparticles@graphene nanocomposite as an efficient magnetic nanosorbent for preconcentration and determine of five aromatic amines in water samples. The sorbent was characterized by diverse characterization techniques. After the extraction, high‐performance liquid chromatography with UV detection was utilized to analysis the aromatic amines. The effects of different factors on the extraction process were studied thoroughly via design of experiment and desirability function. Detection limits and linear dynamic ranges were obtained in the range of 0.10–0.20 and 0.3–300 μg/L, respectively. The relative standard deviations (n = 5) were in the range of 4.3–6.5%. Eventually, the method was employed for determination of target aromatic amines in various water samples.  相似文献   
66.
Callus, suspension and bioreactor cultures of Verbena officinalis were established, and optimized for biomass growth and production of phenylpropanoid glycosides, phenolic acids, flavonoids and iridoids. All types of cultures were maintained on/in the Murashige and Skoog (MS) media with 1 mg/L BAP and 1 mg/L NAA. The inoculum sizes were optimized in callus and suspension cultures. Moreover, the growth of the culture in two different types of bioreactors—a balloon bioreactor (BB) and a stirred-tank bioreactor (STB) was tested. In methanolic extracts from biomass of all types of in vitro cultures the presence of the same metabolites—verbascoside, isoverbascoside, and six phenolic acids: protocatechuic, chlorogenic, vanillic, caffeic, ferulic and rosmarinic acids was confirmed and quantified by the HPLC-DAD method. In the extracts from lyophilized culture media, no metabolites were found. The main metabolites in biomass extracts were verbascoside and isoverbascoside. Their maximum amounts in g/100 g DW (dry weight) in the tested types of cultures were as follow: 7.25 and 0.61 (callus), 7.06 and 0.48 (suspension), 7.69 and 0.31 (BB), 9.18 and 0.34 (STB). The amounts of phenolic acids were many times lower, max. total content reached of 26.90, 50.72, 19.88, and 36.78 mg/100 g DW, respectively. The highest content of verbascoside and also a high content of isoverbascoside obtained in STB (stirred-tank bioreactor) were 5.3 and 7.8 times higher than in extracts from overground parts of the parent plant. In the extracts from parent plant two iridoids—verbenalin and hastatoside, were also abundant. All investigated biomass extracts and the extracts from parent plant showed the antiproliferative, antioxidant and antibacterial activities. The strongest activities were documented for the cultures maintained in STB. We propose extracts from in vitro cultured biomass of vervain, especially from STB, as a rich source of bioactive metabolites with antiproliferative, antioxidant and antibacterial properties.  相似文献   
67.
The composition of the essential oil of fresh and air-dried Salvia palaestina Benth. (Lamiaceae) growing wild in Jordan has been studied using gas chromatography-mass spectrometry analysis. The essential oils of fresh and air-dried S. palaestina were mainly composed of sesquiterpene hydrocarbons (52.66% and 65.98%, respectively). The major component detected in the oils of fresh and dry S. palaestina was germacrene D (21.18% and 26.02%, respectively). Air drying resulted in a general increase of sesquiterpene hydrocarbons and a great decrease in the percentage of monoterpene hydrocarbons.  相似文献   
68.
Ethanolic and aqueous extracts of the leaves and flowers of Alstonia scholaris were evaluated for their antioxidant activity by investigating their effect on blood glutathione levels in alloxan-induced diabetic rats. The ethanolic extract of the leaves was the most active; therefore, its cytotoxicity against HepG2 cells was also tested. Promising GI?? values of 1.96, 4.34 and 4.65?μg?mL?1 were observed for the extract, its chloroform and ethyl acetate fractions, respectively. The chloroform active subfraction I (GI???=?2.97?μg?mL?1) yielded betulin (1), betulinic acid (2) and ursolic acid (3) upon purification. Compounds 1-3 were identified using spectroscopic techniques and by comparison with reported data. GLC of unsaponifiable and saponifiable fractions of the hexane extract revealed β-sitosterol (7.37%) and n-tetracosane (54.4%) to be the major sterol and hydrocarbon components, respectively. Linoleic acid (48.89%) was the predominant fatty acid.  相似文献   
69.
A novel type of porous metal-organic framework (MOF) was obtained from thiol-modified silica nanoparticles and the copper(II) complex of trimesic acid. It is shown that this nanocomposite is well suitable for the preconcentration of Hg(II) ions. The nanocomposite was characterized by Fourier transfer infrared spectroscopy, X-ray powder diffraction, energy-dispersive X-ray diffraction and scanning electron microscopy. The effects of pH value, sorption time, elution time, the volume and concentration of eluent were investigated. Equilibrium isotherms were studied, and four models were applied to analyze the equilibrium adsorption data. The results revealed that the adsorption process obeyed the Langmuir model. The maximum monolayer capacity and the Langmuir constant are 210 mg g?1 and 0.273 L mg?1, respectively. The new MOF-based nanocomposite is shown to be an efficient and selective sorbent for Hg(II). Under the optimal conditions, the limit of detection is 20 pg mL?1 of Hg(II), and the relative standard deviation is <7.2 % (for n?=?3). The sorbent was successfully applied to the rapid extraction of Hg(II) ions from fish, sediment, and water samples.
Figure
Schematic illustration of Hg(II) sorption onto SH@SiO2/MOF nanocomposite.  相似文献   
70.
Phosphotungstic acid (PWA) was used for accumulation of nickel ions at the carbon paste electrode for preparation of PWA-modified CPE (PWA/CPE). The PWA was evenly mixed with graphite powder and paraffin oil. Then, for preparation of Ni/PWA/CPE, Ni ions were included onto the PWA/CPE surface through immersion method at open circuit condition. The scanning electron microscopy (SEM), energy-dispersive spectroscopy and electrochemical methods were used to verify the prepared electrodes. The SEM images reveal that morphology of the CPE was influenced by PWA addition. Application of the Ni/PWA/CPE for methanol oxidation was explored by various electrochemical techniques. Electrochemical response of methanol oxidation at the surface of Ni/PWA/CPE was 2.5 times higher than that Ni/CPE. The obtained results indicated that the modified electrode exhibited high electrocatalytic activity toward methanol oxidation. Then, catalytic rate constant was found to be 8.25 × 104 cm3 mol ?1 s?1 using chronoamperometry method. Furthermore, the effects of several parameters, such as PWA loading, NiSO4 concentration, accumulation time and methanol concentration toward methanol oxidation at the surface of this modified electrode as well as stability, have been investigated.  相似文献   
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