THERMAL SCIENCE

International Scientific Journal

ACTIVE COMPONENTS IN LEAVES OF RHUS CHINENSIS MILL.

ABSTRACT
Rhus chinensis Mill is a high-quality eco-economic resource for potential sustainable development. To analyze the chemical constituents of extracts from the leaves of Rhus chinensis Mill for resource values, the following analytical methods were performed: Fourier transform infrared (FT-IR) spectrum, gas chromatography-mass spectrometry (GC-MS), thermogravimetry, and pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS). The results showed that the leaves of Rhus chinensis Mill were rich in volatile substances that could be exploited and used
KEYWORDS
PAPER SUBMITTED: 2019-05-29
PAPER REVISED: 2019-09-06
PAPER ACCEPTED: 2019-08-11
PUBLISHED ONLINE: 2020-02-08
DOI REFERENCE: https://doi.org/10.2298/TSCI190529045S
CITATION EXPORT: view in browser or download as text file
THERMAL SCIENCE YEAR 2020, VOLUME 24, ISSUE Issue 3, PAGES [1729 - 1735]
REFERENCES
  1. Tan, D. P., et al., Chemical Constituents of Rhus chinensis. Chem Nat. Compounds 51.3 (2015), pp. 542-543.
  2. Gu, Q., et al., A New Benzofuranone and Anti-HIV Constituents from the Stems of Rhus chinensis, Planta Medica 73.3 (2007), pp. 279-282.
  3. Zhu, B., et al., Chemical Variation in Leaf Essential Oils of Rhus chinensis from Eight Locations in Southern and Eastern China, Chem. Nat. Compounds 43.6 (2007), pp. 741-743.
  4. Shim, Y. J., et al., Inhibitory effect of aqueous extract from the gall of Rhus chinensis on alpha-glucosidase activity and postprandial blood glucose, J. Ethnopharmacol. 85.2-3 (2003), pp. 283-287.
  5. Li, C., et al., Preparation and Characterization of a Novel Environmentally Friendly Phenol-Formaldehyde Adhesive Modified with Tannin and Urea, Intl J. Adhesion. Adhesives 66 (2016), pp. 26-32.
  6. Liu, Z. L., et al., A Novel ANFIS-PSO Network for Forecasting Oil Flocculated Asphaltene Weight Percentage at Wide Range of Operation Conditions, Petroleum Sci Tech.
  7. Wang, L., et al., Properties of Antibacterial Bioboard from Bamboo Macromolecule by Hot Press, Saudi J Biol Sci 25.3 (2018), pp. 465-468.
  8. Zolfi Bavariani, M., et al., Influence of Pyrolysis Temperatures on FTIR Analysis, Nutrient Bioavailability, and Agricultural Use of Poultry Manure Biochars, Commun. Soil Scie. Plant Anal. (2019), pp. 1-10.
  9. Streit, J., et al., Above- and below Ground Biomass in a Mixed Cropping System with Eight Novel Winter Faba Bean Genotypes and Winter Wheat Using FTIR Spectroscopy for Root Species Discrimination, Plant Soil (2019).
  10. Chen, J., et al., Molecules and Functions of Rosewood: Diospyros Celebica, Arab J Chem, (2017).
  11. ] Ge, S. B., et al., Biological Analysis on Extractives of Bayberry Fresh Flesh by GC-MS, Saudi J Biol Sci (2017).
  12. Intararuchikul, T., et al., Effects of Centella asiatica Extract on Antioxidant Status and Liver Metabolome of Rotenone-Treated Rats Using GC-MS, Biomed Chromatog 17.2 (2019).
  13. Owen, L., et al., Characterisation and Screening of Antimicrobial Essential Oil Components against Clinically Important Antibiotic-Resistant Bacteria Using Thin Layer Chromatography-Direct Bioautography Hyphenated with GC-MS, LC-MS and NMR, Phytochem Anal (2018).
  14. Luedemann, A., et al., TagFinder for the Quantitative Analysis of Gas Chromatography-Mass Spectrometry (GC-MS)-Based Metabolite Profiling Experiments, Bioinformatics 24.5 (2008), pp. 732-737.
  15. Jiang, S. C., et al., Molecules and Functions of Rosewood: Dalbergia Stevenson. Arab J Chem, (2017).
  16. Dong, J., et al., Study on the Source of Polycyclic Aromatic Hydrocarbons (PAHs) during Coal Pyrolysis by PY-GC-MS, J Hazardous Mat. 243. (2012), pp. 80-85.
  17. Slopiecka, K., et al., Thermogravimetric Analysis and Kinetic Study of Poplar Wood Pyrolysis, Appl Energy 97. (2012).
  18. Jeguirim, M., et al., Pyrolysis Characteristics and Kinetics of Arundo donax Using Thermogravimetric Analysis, Bioresource Technol 100.17 (2009), pp. 4026-4031.
  19. Zuo S. L., et al., FT-IR Analysis of Carbonized Bamboo Catalyzed by Phosphoric Acid, Chem Industry Forest Prod 25.04 (2005), pp. 21-25.
  20. Tomoo, O., et al., Plasma Palmitoleic Acid Content and Obesity in Children, Am J Clini Nut 82.4 (2005), pp. 747.
  21. Lee, J. J., et al., Palmitoleic Acid Is Elevated in Fatty Liver Disease and Reflects Hepatic Lipogenesis, Am J Clinl Nut 101.1 (2015), pp. 34-43.
  22. Atasever-Arslan, B., et al, Screening of New Antileukemic Agents from Essential Oils of Algae Extracts and Computational Modelling of Their Interactions with Intracellular Signalling Nodes, Eur J Pharmaceutl Sci 83 (2015) pp. 120-131.
  23. McCracken, S. T., et al., Synthesis and Antimalarial and Antituberculosis Activities of a Series of Natural and Unnatural 4-methoxy-6-styryl-pyran-2-ones, Dihydro Analogues and Photo-Dimers, Bioorg Med Chem 20.4 (2012), pp. 1482-1493.
  24. Aparna, V., et al., Anti-Inflammatory Property of n-hexadecanoic Acid: Structural Evidence and Kinetic Assessment, Chem BiolDrug Design 80.3 (2012).
  25. Marshall, J. A., et al., Stereoselective Synthesis of Cycloalkene-Fused Butyrolactones via Cyclopropylcarbinol Solvolysis, Org Chem 40.14 (1975), pp. 2070-2073.
  26. Vajravelu, K., et al., Effects of second-order slip and drag reduction in boundary layer flows. Applied Mathematics & Nonlinear Sciences, 3.1 (2018), pp. 291-302.
  27. Plata, S.A., Sáez, S.B. After notes on chebyshev's iterative method. Applied Mathematics & Nonlinear Sciences, 2.3 (2017), pp. 1-12.
  28. Faure, V., The uremic solute p-cresol decreases leukocyte transendothelial migration in vitro, International Immunology 18.10 (2006), pp. 1453-1459.
  29. Wenxia, W., et al., Dealkylation of 6-tert-Butyl-3-Methyl-Phenol to m-Cresol, Petrochemical Technology 41.1 (2012), pp. 62-65.
  30. Geetha, S., et al., Polyaniline reinforced conducting E-glass fabric using 4-chloro-3-methyl phenol as secondary dopant for the control of electromagnetic radiations, Composites Science and Technology 65.6 (2005), pp. 973-980.
  31. Yoshimura, Y., Reaction of 3-methyl phenol with methyl α-eleostearate, Journal of Applied Polymer Science 28.12 (1983), pp. 3859-3872.
  32. Fischer, D., et al., Studies on the Synthesis of Schisandraceae Natural Products: Exploring a Cyclopropylcarbinol Ring Expansion Strategy, European Journal of Organic Chemistry 2007.25 (2007), pp. 4.
  33. Okuma, K., et al., One-pot synthesis of enantiomerically pure (methylenecyclopropyl)carbinol: a key intermediate to the synthesis of the causative agent of Jamaican vomiting sickness, Cheminform 25.11 (2010).
  34. Meyer, C., et al., Stereoselective Synthesis of Polypropionate Units and Heterocyclic Compounds by Cyclopropylcarbinol Ring-Opening with Mercury(II) Salts, Cheminform 35.3 (2004), pp. 766.
  35. Zhang, G. J.,et al., Thermogravimetry, Differential Thermal Analysis, and Mass Spectrometry Study of the Silicon Nitride-Boron Carbide-Carbon Reaction System for the Synthesis of Silicon Carbide-Boron Nitride Composites, Journal of the American Ceramic Society 85.9 (2002), pp. 2256-2260.
  36. Franco, F., et al., Bhigh-temperature x-ray diffraction, differential thermal analysis and thermogravimetry of the kaolinite-dimethylsulfoxide intercalation complex, Clays & Clay Minerals 50.50 (2002), pp. 47-55.
  37. Saraji-Bozorgzad M., Investigation of polymers by a novel analytical approach for evolved gas analysis in thermogravimetry: Gas chromatography comprehensively coupled to single photon ionization mass spectrometry, Journal of Thermal Analysis & Calorimetry volume 105 (2011), pp. 859-866(8).
  38. Parra, D. F., et al., Thermal behavior of the epoxy and polyester powder coatings using thermogravimetry/differential thermal analysis coupled gas chromatography/mass spectrometry (TG/DTA-GC/MS) technique: Identification of the degradation products, Thermochimica Acta 386.2 (2002), pp. 143-151.
  39. Xu, G. C., et al., Thermal kinetic TG-analysis of the mixed-ligand copper(II) and nickel(II) complexes of N-(1-phenyl-3-methyl-4-benzylidene-5-pyrazolone) p-nitrobezoylhydrazide and pyridine, Thermochimica Acta 429.1 (2005), pp. 31-42.
  40. Surzhikov, A., et al., Investigation of structural states and oxidation processes in Li 0.5 Fe 2.5 O 4−δ, using TG analysis, Journal of Thermal Analysis & Calorimetry 108.3 (2012), pp. 1207-1212.

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