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41.
The analytical potential of water as an eluent in thin layer chromatographic separation of various anions on plain adsorbent layers (silica gel "G" alumina, and cellulose) as well as on beds containing different combinations of silica gel, alumina, or cellulose has been investigated. In addition to some important separation of anions, microgram separation of IO−4 from milligram quantities of IO−3, Bro−3, MoO2−4, and Fe (CN)3−6 has been realized. The effect on pH of the sample in the separation of IO−4 from accompanying ions has also been studied. The limits of detection and dilution limits of anions on alumina thin layers have been determined. NO−2 in artificial seawater has been detected. The effect of CaCl2, MgCl2, and NaHCO3 on some ternary separations of analytical importance has been examined. 相似文献
42.
Vernon R. Morris Fida Mohammad Lynnette Valdry William M. Jackson 《Chemical physics letters》1994,220(6):448-454
Time-resolved IR emission spectroscopy (TRIES) has been used to study infrared emission in the 3400–3100 cm−1 region from HCN molecules produced when CN radicals abstract a hydrogen atom from ethane, propane, and chloroform. From these observations the nascent vibrational distributions of the HCN produced were derived. The nascent vibrational population distributions of the product HCN in all of the reactions are non-statistical and inverted in both the pure CH stretch (00p) and CH stretch—bend (0np) series. 相似文献
43.
Mohammad M. Mojtahedi Hassan Abbasi M. Saeed Abaee 《Journal of molecular catalysis. A, Chemical》2006,250(1-2):6-8
Various types of alcohols and phenols were rapidly protected by hexamethyldisilazane in good to excellent yields at room temperature in the presence of catalytic amount of magnesium bromide ethyl etherate under solvent-free conditions. Good to excellent chemoselectivity was demonstrated for competitive protection of primary hydroxyls in the presence of secondary and tertiary alcohols. Highly selective protection of phenols in the presence of aromatic amines was also demonstrated successfully. 相似文献
44.
Mohammad Mazloum Ardakani Pouran Pourhakak Masoud Salavati-Niasari 《Analytical sciences》2006,22(6):865-870
A coated-wire ion-selective electrode (CWISE), based on a Schiff base as a neutral carrier, was successfully developed for the detection of Pb(II) in aqueous solution. CWISE exhibited a linear response with a Nernstian slope of 29.4 +/- 0.5 mV/decade within the concentration range of 1.0 x 10(-5) - 1.0 x 10(-1) M lead ion. CWISE has shown detection limits of 5.0 x 10(-6) M. The electrode exhibited good selectivity over a number of alkali, alkaline earth, transition and heavy metal ions. This sensor yielded a steady potential within 10 to 20 s at a linear dynamic range. The electrode was suitable for use in aqueous solutions in a pH range of 2.0 to 5.0. Applications of this electrode for the determination of lead in real samples and as indicator electrode for potentiometric titration of Pb2+ ion using K2CrO4 are reported. 相似文献
45.
Trituration and capillary solid-state spot-tests for 25 anions with a number of organic and inorganic reagents have been examined. A comparative study of the corresponding reactions in solution has also been made. Incorporation of a glass-wool plug in the capillary improves the selectivity. Schemes are presented for possible use of the technique. 相似文献
46.
Titration calorimetry was used to construct the solid-liquid equilibrium line in ternary systems containing the solute and an aqueous mixed solvent by measuring the heat of dissolution of the solid solute during successive additions of the liquid solvent. The plot of cumulated heats versus the mole ratio, nsolvent/nsolute, yields two (almost) linear increases of different slopes. These two lines represent successively the enthalpy of dissolution then the enthalpy of dilution of the medium; their intersection gives the solubility and the enthalpy of dissolution of the solute. Phase diagrams have been established over the whole concentration range for o-anisaldehyde, 1,3,5-trimethoxybenzene and vanillin, in water + methanol, +ethanol, or +n-propanol at 303, 313 and 318 K. 相似文献
47.
Mohammad H. Alizadeh Toktam Kermani Reza Tayebee 《Monatshefte für Chemie / Chemical Monthly》2007,138(2):165-170
Summary. Esterifications of acetic acid with some linear, secondary, tertiary, and benzylic alcohols mediated by catalytic amounts
of Keggin, Wells–Dawson, and Preyssler type heteropolyacids were carried out under reflux at mild reaction conditions with good to excellent yields. Among the examined
catalysts, H3PW12O40 and H14NaP5W30O110 revealed better results than other heteropolyacids. This work was performed with the aim of simplifying the esterification
process by omitting any solvents and mineral acid catalysts. Easy work-up, low cost, and acidic waste reduction, which are
all important features from the environmental and economical points of view, are distinct aspects of this protocol. Heteropolyacid
catalysts could be separated after a simple work-up and reused for several times. 相似文献
48.
Summary. A highly efficient, selective, fast, and cheap protocol is developed for oxidation of aromatic amines and alcohols utilizing
34% hydrogen peroxide in water catalyzed by some W- and Mo-based heteropolyoxometalates. Findings showed that dodecatungstophosphoric
acid, H3PW12O40, was the most efficient catalyst in the examined oxidation reactions. This methodology may prove to be a valuable alternative
for eco-friendly green oxidation. Inherent simplicity, easy work up, and using regenerable catalysts were other key aspects
of this oxidation protocol. 相似文献
49.
Headspace solvent microextraction (HSME) into a single drop is developed for the determination of six trihalomethanes, CH2Cl2, CHCl3, C4H9Cl, CCl4, C2HCl3, and C2Cl4, in aqueous solution. A drop of benzyl alcohol containing bromoform, as an internal standard, is used for extraction. The analytes are extracted by suspending a 3-microL drop directly from the needle of a microsyringe. The needle passes through the septum of a vessel, and the needle tip appears above the surface of the solution. After the prescribed extraction time, the drop is drawn back into the syringe. The syringe is then removed, and its content is injected directly into a gas chromatography column for analysis. The main parameters affecting the HSME process, such as stirring speed, microdrop volume, sample solution temperature, microsyringe needle temperature, sample volume, solution pH, extracting solvent, and ionic strength of the solution, are studied. Also, the linear range and precision of the method are examined. 相似文献
50.
Khodabakhsh NIKNAM Mohammad Ali ZOLFIGOL Zahra HOSSIENINEJAD Nader DANESHVAR 《催化学报》2007,28(7):591-595
以金属硫酸氢盐M(HSO4)n(Ca(HSO4)2,Zn(HSO4)2和过硫酸氢钾制剂oxone○R)为催化剂催化醛、1,3-二羰基化合物和尿素进行缩合反应,在90℃及无溶剂的条件下高收率、一锅法合成了3,4-二氢嘧啶-2(1H)-酮. 相似文献