4 research outputs found

    Determination of Boron, Phosphorus, and Molybdenum Content in Biosludge Samples by Microwave Plasma Atomic Emission Spectrometry (MP-AES)

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    A novel analytical method for accurate determination of boron (B), phosphorous (P), and molybdenum (Mo) content in biosludge samples based on a relatively recent analytical technique, microwave plasma atomic emission spectrometry (MP-AES), is developed in the present work. Microwave assisted acid digestion method is utilized to extract B, P, and Mo from biosludge. To demonstrate the reliability and accuracy of the present MP-AES method, its results are compared with those obtained using two well-established techniques, i.e., flame atomic absorption spectrometry (FAAS) and inductively coupled plasma optical emission spectrometry (ICP-OES). Matrix variation in the MP-AES technique is found to result in minimal changes. Precision and accuracy of the developed method are demonstrated using replicate analyses of certified sewage sludge reference material, EnviroMAT (BE-1). The limit of quantification and detection of B, P, and Mo in the extracts are determined; the linear regression coefficient was greater than 0.998 for all the three techniques. Analytical wavelengths are selected according to the sensitivity and interference effects. The results obtained in this work demonstrate the potential of MP-AES technique for the determination of B, P, and Mo content in biosludge, which achieved lower detection limits, higher accuracy, and better reproducibility as compared to other techniques

    Labor Market Digest, March 1990

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    1410-1417We have synthesized two new potassium metal coordination polymers {[K(CH3COCH3)3][Cu(btdt)2]}n (1) and {[K(CH3CN)2][Cu(btdt)2]}n (2) of diverse dimensionality based on a copper coordination complex [CuIII(btdt)2]1− ({btdt}2– = 2,1,3-benzenethiadiazole-5,6-dithiolate). Recrystallization of the dark brown solid, obtained from the reaction mixture of H2btdt, KOH and CuCl2·2H2O in MeOH, from the coordinating solvents acetone and acetonitrile results in the formation of 3-D and 2-D extended networks in compounds (1) and (2) respectively. The crystal structures of (1) and (2) have been discussed in comparison with those of recently reported sodium coordination polymers {[Na(CH3OH)4][Au(btdt)2]}n (3), [Na(DMF)2][Au(btdt)2]}n (4) and {[Na(CH3CN)2][Au(btdt)2]}n (5). Compounds (1) and (2) have additionally been characterized by routine spectroscopy including elemental analyses

    Simultaneous determination of telmisartan and amlodipine in human plasma by LCâMS/MS and its application in a human pharmacokinetic study

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    A rapid and sensitive liquid chromatographyâtandem mass spectrometric (LCâMS/MS) assay method has been developed and fully validated for the simultaneous quantification of telmisartan and amlodipine in human plasma. Carbamazepine was used as an internal standard. Analytes and the internal standard were extracted from human plasma by solid-phase extraction technique using Waters Oasis® HLB 1 cm3 (30 mg) extraction cartridge. The reconstituted samples were chromatographed on a Hypurity advance C18 column (50 mmÃ4.6 mm, 5 μm) using a mixture of acetonitrileâ5 mM ammonium acetate buffer (pH-4.0) (50:50, v/v) as the mobile phase at a flow rate of 0.8 mL/min. The calibration curve obtained was linear (râ¥0.99) over the concentration range of 2.01â400.06 ng/mL for telmisartan and 0.05â10.01 ng/mL for amlodipine. Method validation was performed as per FDA guidelines and the results met the acceptance criteria. A run time of 2.5 min for each sample made it possible to analyze more than 400 human plasma samples per day. The proposed method was found to be applicable to clinical studies. Keywords: Telmisartan, Amlodipine, Human plasma, Solid-phase extraction, LCâMS/MS, Pharmacokinetic

    Determination of Boron, Phosphorus, and Molybdenum Content in Biosludge Samples by Microwave Plasma Atomic Emission Spectrometry (MP-AES)

    No full text
    A novel analytical method for accurate determination of boron (B), phosphorous (P), and molybdenum (Mo) content in biosludge samples based on a relatively recent analytical technique, microwave plasma atomic emission spectrometry (MP-AES), is developed in the present work. Microwave assisted acid digestion method is utilized to extract B, P, and Mo from biosludge. To demonstrate the reliability and accuracy of the present MP-AES method, its results are compared with those obtained using two well-established techniques, i.e., flame atomic absorption spectrometry (FAAS) and inductively coupled plasma optical emission spectrometry (ICP-OES). Matrix variation in the MP-AES technique is found to result in minimal changes. Precision and accuracy of the developed method are demonstrated using replicate analyses of certified sewage sludge reference material, EnviroMAT (BE-1). The limit of quantification and detection of B, P, and Mo in the extracts are determined; the linear regression coefficient was greater than 0.998 for all the three techniques. Analytical wavelengths are selected according to the sensitivity and interference effects. The results obtained in this work demonstrate the potential of MP-AES technique for the determination of B, P, and Mo content in biosludge, which achieved lower detection limits, higher accuracy, and better reproducibility as compared to other techniques
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