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31.
Walvekar Rashmi Zairin Danial Aminin Khalid Mohammad Mubarak Nabisab Mujawar TCSM Gupta 《Journal of Thermal Analysis and Calorimetry》2022,147(13):7193-7201
Journal of Thermal Analysis and Calorimetry - This study aims to investigate the thermal conductivity, viscosity and thermal degradation of naphthenic-based mineral oil, palm oil methyl ester... 相似文献
32.
K. P. Madhusudanan Shubhra Mittal Susheel Durani R. S. Kapil 《Journal of mass spectrometry : JMS》1985,20(5):323-326
Stereospecific adduct ion formation has been observed in the chemical ionization mass spectra (positive and negative) of certain E- and Z-1,2,3-triaryl-2-propen-1-ones. The Z isomers are found to give higher relative abundances of adduct ions than the E isomers. This has been interpreted in terms of the differences in the proton affinities of the isomers originating from their different degrees of enone resonance. Halide ion (CI? and Br?) attachment spectra of these compounds also show stereochemical differences in the relative abundances of [M]?˙ and [M+halide]? ions, though the effect is not as pronounced as in the case of the positive ion spectra. 相似文献
33.
Chelating resins based on biopolymers, specifically cellulose, offers a green analytical method for determination of metal ions at trace levels present in various samples. It offers a fast, accurate and simple method for separation and pre-concentration of metal ions at low concentrations, prior to their determination by instrumental method. Cellulose based chelating resin (CELL-GLY) has been synthesised by immobilising glycine on it. CELL-GLY was used for the determination of trace amounts of Cu2+ and Ni2+ from aqueous solutions before their determination by FAAS. The preparation of CELL-GLY involves simple steps, based on natural and easily available biopolymer cellulose, which makes its use as chelating resin is a green method. The Cu2+ and Ni2+ can be quantitatively recovered from the CELL-GLY in the pH range 4.8–6.9 and 6.9-7.8 respectively with a recovery of more than 95% for each of these metal ions. Recovery of these metal ions using CELL-GLY was quantitative up to 35 °C. The detection limits for copper and nickel by FAAS were 1.20 ppb and 1.40 ppb, respectively. The method was successfully employed for the determination of trace amounts of Cu2+ and Ni2+ in various samples. 相似文献
34.
Ageratum conyzoides L. and Its Secondary Metabolites in the Management of Different Fungal Pathogens
Rubal Chahal Arun Nanda Esra Küpeli Akkol Eduardo Sobarzo-Snchez Ashwani Arya Deepak Kaushik Rohit Dutt Rashmi Bhardwaj Md. Habibur Rahman Vineet Mittal 《Molecules (Basel, Switzerland)》2021,26(10)
Ageratum conyzoides L. (Family—Asteraceae) is an annual aromatic invasive herb, mainly distributed over the tropical and subtropical regions of the world. It owns a reputed history of indigenous remedial uses, including as a wound dressing, an antimicrobial, and mouthwash as well as in treatment of dysentery, diarrhea, skin diseases, etc. In this review, the core idea is to present the antifungal potential of the selected medicinal plant and its secondary metabolites against different fungal pathogens. Additionally, toxicological studies (safety profile) conducted on the amazing plant A. conyzoides L. are discussed for the possible clinical development of this medicinal herb. Articles available from 2000 to 2020 were reviewed in detail to exhibit recent appraisals of the antifungal properties of A. conyzoides. Efforts were aimed at delivering evidences for the medicinal application of A. conyzoides by using globally recognized scientific search engines and databases so that an efficient approach for filling the lacunae in the research and development of antifungal drugs can be adopted. After analyzing the literature, it can be reported that the selected medicinal plant effectively suppressed the growth of numerous fungal species, such as Aspergillus, Alternaria, Candida, Fusarium, Phytophthora, and Pythium, owing to the presence of various secondary metabolites, particularly chromenes, terpenoids, flavonoids and coumarins. The possible mechanism of action of different secondary metabolites of the plant against fungal pathogens is also discussed briefly. However, it was found that only a few studies have been performed to demonstrate the plant’s dosage and safety profile in humans. Considered all together, A. conyzoides extract and its constituents may act as a promising biosource for the development of effective antifungal formulations for clinical use. However, in order to establish safety and efficacy, additional scientific research is required to explore chronic toxicological effects of ageratum, to determine the probability of interactions when used with different herbs, and to identify safe dosage. The particulars presented here not only bridge this gap but also furnish future research strategies for the investigators in microbiology, ethno-pharmacology, and drug discovery. 相似文献
35.
Feven Mattews Michael Mohammad Khalid Gunasunderi Raju Chantara Thevy Ratnam Rashmi Walvekar Nabisab Mujawar Mubarak 《Molecules (Basel, Switzerland)》2021,26(19)
We studied the reinforcing effects of treated and untreated nanohydroxyapatite (NHA) on poly-lactic acid (PLA). The NHA surface was treated with three different types of chemicals; 3-aminopropyl triethoxysilane (APTES), sodium n-dodecyl sulfate (SDS) and polyethylenimine (PEI). The nanocomposite samples were prepared using melt mixing techniques by blending 5 wt% untreated NHA and 5 wt% surface-treated NHA (mNHA). Based on the FESEM images, the interfacial adhesion between the mNHA filler and PLA matrix was improved upon surface treatment in the order of mNHA (APTES) > mNHA (SDS) > mNHA (PEI). As a result, the PLA-5wt%mNHA (APTES) nanocomposite showed increased viscoelastic properties such as storage modulus, damping parameter, and creep permanent deformation compared to pure PLA. Similarly, PLA-5wt%mNHA (APTES) thermal properties improved, attaining higher Tc and Tm than pure PLA, reflecting the enhanced nucleating effect of the mNHA (APTES) filler. 相似文献
36.
NMR is a fast method for obtaining a holistic snapshot of the metabolome and also offers quantitative information without separating the compounds present in a complex mixture. Identification of the metabolites present in a plant extract sample is a crucial step for all plant metabolomics studies. In the present work, we used various two dimensional (2D) NMR methods such as J-resolved NMR, total correlation spectroscopy (TOCSY), and heteronuclear single quantum coherence sensitivity enhanced NMR spectroscopy for the identification of 36 common metabolites present in Coriandrum sativum L. seed extract. The identified metabolites belong to the following classes: organic acids, amino acids, and carbohydrates. 1H NMR spectra of such complex mixtures in general display tremendous signal overlap due to the presence of a large number of metabolites with closely resonating multiplet signals. This signal overlapping leads to ambiguity in an assignment, and hence, identification of metabolites becomes tedious or impossible in many cases. Therefore, the utility of pure-shift proton spectrum along the indirect (F1) dimension of the F1-PSYCHE-TOCSY spectrum is demonstrated for overcoming ambiguity in assignment of metabolites in crowded spectral regions from Coriandrum sativum L. seed extract sample. Because pure-shift NMR methods yield ultrahigh resolution spectrum (i.e., a singlet peak per chemical site) along one or more dimensions, such spectra provide better identification of metabolites compared with regular 2D TOCSY where signal overlap and peak distortions lead to ambiguity in the assignment. Nine metabolites were unambiguously assigned by pure-shift F1-PSYCHE-TOCSY spectrum, which was unresolved in regular TOCSY spectrum. 相似文献
37.
Kamath Srinivas S. Narayana B. D’Souza Renita Shiny Nayak S. Rashmi Mohan M. P. Dileep B. N. Baburajan A. Ravi P. M. Karunakara N. 《Journal of Radioanalytical and Nuclear Chemistry》2019,322(2):389-397
Tritium concentration was monitored in different water sources collected around Kaiga Nuclear Power plant, India. The concentration was in the ranges?<?1.9–27.4 Bq L?1 (GM?=?4.0 Bq L?1) for groundwater,?<?1.9–42.1 Bq L?1 (GM?=?3.5 Bq L?1) for surface water and in 12.4–42.0 Bq L?1 (GM?=?24.07 Bq L?1) for reservoir water. The concentration values observed in this study are similar to those reported for other PHWR stations of the world. The radiation dose to the public due to ingestion of Tritium through groundwater was computed to be 0.08 μSvy?1.
相似文献38.
Singh N Rashmi Ahuja T Singh S Pasricha R Haranath D 《Journal of colloid and interface science》2012,369(1):40-45
A novel synthesis of the production of luminescent zinc oxide (ZnO), either in its intrinsic, metal, non-metal-doped or composite forms with high yield has been developed by parallel iterative techniques, within a combinatorial library prepared by the reduction of nitroarenes. The reduction of nitroarenes by aluminium/zinc dusts in alkaline medium (pH 10±2) forms azoxy compounds, whereas in acidic medium (pH 4.9±0.2) forms phenyl hydroxylamine and zinc/aluminium dust gets oxidised into respective hydroxide. Here, we demonstrate the reduction of nitroarenes at neutral pH (7.0±0.2), which forms intrinsic as well as doped ZnO at 50±5°C using zinc dust alone or mixtures of salts of several transition and non-transition metals in presence of 1:10 ratio of solvent and water. Interestingly, it is observed that the photoluminescence emission could be tuned in a wide range from 390 to 615 nm useful for many display related devices. 相似文献
39.
The dinuclear complex [Re2Cl2(CO)6S
e] has been prepared and characterized in the solid state by X-ray crystallography. Proton NMR spectroscopy has shown the structure to be stereochemically rigid in solution. 相似文献
40.
K. P. Madhusudanan Rashmi Srivastava D. K. Kulshreshtha D. Fraisse 《Journal of mass spectrometry : JMS》1987,22(6):368-372
Substitution of amino for hydroxyl groups in certain sesquiterpene alcohols has been studied by chemical ionization mass spectrometry using ammonia and ammouia-d3 as the reagent gases, and by mass-analysed ion kinetic energy spectrometry and collision-induced decomposition mass-analysed ion kinetic energy measurements. Depending upon the source conditions and the nature of the substrates, both SNi and SN1 mechanisms have been found to operate. No evidence is obtained for an SN2 mechanism in these compounds. In centdarol and isocentdarol, addition of NH3 to the double bond, followed by elimination of H2O, also contributes to the substitution process. Attack of [NH4]+ on the epoxide function, followed by loss of H2O, appears to lead to the substitution ions in epoxycentdarol, epoxyisocentdarol and epoxyhimachalol. 相似文献