scholarly journals Extraction and Characterization of Sugarcane Peel Wax

ISRN Agronomy ◽  
2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Mangesh B. Inarkar ◽  
S. S. Lele
Keyword(s):  
Fatty Acids ◽  
Molecular Weight ◽  
Gas Chromatography ◽  
Fourier Transform ◽  
Dry Weight ◽  
Weight Basis ◽  
Ft Ir ◽  
Gas Chromatography Mass Spectroscopy ◽  
Layer Chromatography

Sugarcane peel is an agrowaste product and contains considerable amount of wax. This has a good technoeconomic potential. In view of this, the present study aims at extraction and characterization of wax from sugarcane peel. The yield of crude wax was 0.95% on dry weight basis. During Fourier transform-infrared spectroscopy (FT-IR) prominent peaks obtained at 2921.73 and 2851.64 (–CH), 1463.44 (–CH2), 1376.96 (–CH3), 1108.4 and 1170.16 (–C–O) 3395.60 (–OH), 1710.25 (–CHO), and 1736.63 (–COOH) indicate presence of alkanes, ketones, alcohols, aldehydes, and carboxylic acids, respectively. Alcohol and hydrocarbon fractions were also found by thin layer chromatography (TLC). Melting point of crude wax was observed to be 62.1°C. Molecular weight of wax was estimated to be 1706 Dalton. Composition of crude wax found using gas chromatography-mass spectroscopy (GC-MS) was alkanes (28.83%), ester (66.26%), fatty acids (4.58%), aldehyde (0.11%), and alcohol (0.22%).

ASSESSMENT OF PHYTOCONSTITUENTS OF MEDICINAL IMPORTANCE FROM MILLETTIA PEGUENSIS ALI (SYN. MILLETTIA OVALIFOLIA KURZ)

INDIAN DRUGS ◽  
2020 ◽  
Vol 57 (05) ◽  
pp. 43-50
Author(s):  
Arshpreet Kaur ◽  
◽  
M. C. Sidhu
Keyword(s):  
Gas Chromatography ◽  
Fourier Transform ◽  
Mass Spectroscopy ◽  
Biologically Active ◽  
Leaf Extracts ◽  
Single Compound ◽  
Ft Ir ◽  
Ethanol Extracts ◽  
Gas Chromatography Mass Spectroscopy ◽  
Layer Chromatography

The present study was aimed to investigate the biologically active compounds present in the seed and leaf extracts of Millettia peguensis. Screening was done through preliminary qualitative analysis of phytochemicals and Gas Chromatography-Mass Spectroscopy (GC-MS) method. The study revealed the presence of alkaloids, carbohydrates, flavonoids, glycosides, gum and mucilage, phenolics, quinones, steroids and terpenoids in both aqueous and ethanol extracts of leaves and seeds. The GC-MS analysis of ethanol extracts of seeds and leaves have yielded 29 and 23 phytoconstituents, respectively. These observations were further validated by Fourier transform infrared spectroscopy (FT-IR) of the leaves and seeds powder. FT-IR has provided detailed information of the various functional groups associated with the compounds present in the samples. A single compound was isolated through Column Chromatography and Thin Layer Chromatography whose characterization was done through mass spectroscopy and IR spectroscopy.

scholarly journals Phytochemical characterization of the ethanolic extract of Kaempferia galanga rhizome for anti-oxidant activities by HPTLC and GCMS

2022 ◽  
Vol 8 (1) ◽  
Author(s):  
Flavius Phrangsngi Nonglang ◽  
Abhijeet Khale ◽  
Surya Bhan
Keyword(s):  
Gas Chromatography ◽  
High Performance ◽  
Freeze Drying ◽  
Ethanolic Extract ◽  
Dry Weight ◽  
Kaempferia Galanga ◽  
Anti Oxidant ◽  
Gas Chromatography Mass Spectroscopy ◽  
Layer Chromatography

Abstract Background The rhizome of Kaempferia galanga (K. galanga) was collected from Meghalaya, India, and its ethanolic extract was obtained by freeze-drying or lyophilization process, which was then assessed for its in vitro anti-oxidant activity and phytochemical characterization using high-performance thin-layer chromatography (HPTLC) and gas chromatography-mass spectroscopy (GCMS). Results In vitro anti-oxidant activity analysis shows an inhibitory concentration (IC50) value of 1.824 mg/mL and 0.307 mg/mL for, α, α-diphenyl-ρ-picrylhydrazyl (DPPH) and 2, 2′-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS) assays, respectively. Total polyphenol content (TPC) of 23.55 ± 0.5 mg gallic acid equivalent (GAE)/g dry weight of extract and total flavonoid content (TFC) of 100 ± 1.414 mg rutin equivalents (RE)/g dry weight of extract were found. High-performance thin-layer chromatography (HPTLC) analysis shows the best separation of bands at different retention factor (Rf) values, when employing the solvent system 2-butanol/1-propanol/water in the ratio of 3:1:1 (v/v/v). Gas chromatography-mass spectroscopy (GCMS) analysis confirms the presence and identification of various phytocompounds, with ethyl p-methoxycinnamate identified as the major active compound. Conclusion Freeze-dried ethanolic extract of K. galanga (rhizome) possesses anti-oxidant activity. Ethyl p-methoxycinnamate is present as the major bioactive component (about 94.87% of the total area composition), and since it has very important and diverse medicinal properties, a freeze-drying process (lyophilization) can be utilized for its isolation and extraction.

scholarly journals Characterization of Neocarya Macrophylla Seed Oil using Gas Chromatography-Mass Spectrometry (GC-MS) and Fourier Transform Infra-Red (FT-IR) Techniques

2019 ◽  
pp. 1-7
Author(s):  
Aliyu Ahmad Warra ◽  
Lawal Gusau Hassan ◽  
Leye Jonathan Babatola ◽  
Adedara Adejoju Omodolapo ◽  
Richard Undigweundeye Ukpanukpong ◽  
...  
Keyword(s):  
Fatty Acids ◽  
Gas Chromatography ◽  
Fourier Transform ◽  
Seed Oil ◽  
Saturated Fatty Acids ◽  
Soxhlet Extraction ◽  
Industrial Applications ◽  
Pharmaceutical Products ◽  
Gas Chromatography Mass Spectrometry ◽  
Ft Ir

Aim: Modern researches described incorporating gingerbread plum (Neocarya macrophylla) kernel oils into food, cosmetics and pharmaceutical products by exploiting its physicochemical properties. Study Design: Experimental and instrumental study was done to determine the general and the saturated fatty acids present in the seed oil and its suitability for industrial applications. This study examined the fatty acids by qualitative determination from hexane extracts of Neocarya macrophylla seed using GC-MS. Materials and Methods: Indigenous Neocarya macrophylla   seeds obtained from Gingerbread plum tree were collected in the Month of August from Birnin Kebbi, Kebbi State, Nigeria. soxhlet extraction method was used for the oil extraction. The GC-MS analysis was by coupling system of Shimadzu QP2010 series gas chromatography with Shimadzu QP2010 plus mass spectroscopy detector (GCMS).  For the FT-IR analysis, software of OMNIC operating system (Version 7.0 Thermo Nicolet) was connected to Fourier Transform Infrared Spectrometer Nicolet 8400S equipped with a detector of deuterated triglycine sulphate (DTGS). Conclusion: These results showed the potential of this oil in cosmetic industry.

scholarly journals Fourier Transform Infra-Red (FT-IR) Characterization of Plant Oils from Selected Cultivars Grown in Nigeria

2019 ◽  
pp. 1-10
Author(s):  
A. A. Warra ◽  
L. J. Babatola ◽  
L. G. Hassan ◽  
M. N. V. Prasad ◽  
A. A. Odutuga ◽  
...  
Keyword(s):  
Fatty Acids ◽  
Fourier Transform ◽  
Energy Demand ◽  
Alternative Energy ◽  
Degree Of Saturation ◽  
Plant Oils ◽  
Background Spectrum ◽  
Infra Red ◽  
Ft Ir

Background and Objectives: The developments of fourier transform infrared (FT-IR) spectroscopic instrumentation, and application, over the years has made it a powerful analytical tool in the study of oils and fats. This work has explored fourier transform Infra-Red for characterization of plant oils from selected cultivars grown in Nigeria. The selection of these plants oils that flourishes in Nigeria aside their used primarily for nutritional applications, is dependent on the fatty acid (FA) composition of triacylglycerol (TAG which make them potential for bioenergy and biofiuel production considering the explosion of energy demand through alternative energy sources. They are also needed for the preparations of chemical feedstocks, biopolymer and composites, skin care products. Oils from these plants can provide renewable sources of high-value fatty acids for both the chemical and health-related industries. We report here several areas where these plant oils can have a significant impact on the emerging bioeconomy. Materials and Methods: The samples were each placed in contact with KBr disc and FT-IR spectra were collected in frequency 4500-400 cm-1 by coadding 32 scans and at resolution of 4 cm-1. All spectra were rationed against a background spectrum. In each scan, a new reference background spectrum was detected. Results: The spectra of oils of the present investigation revealed the following bands 1522, 1449.55, 1364.68, 1444.73, 1364.68, 1445.09, 1369.50, 1447.62, 1362.75, 1449.55, 1371.43, 1447.62, 1366.54, 1447.62, 1450.5, 1360.82, 1370.47, 1446.66, 1246.06, 1364.47, 1448.59 for Adansonia digitata, Ricinus communis, Sesamum indicum, Jatropha curcas, Allium cepa, Cucumis melo, Lannea microcarpa, Lagenaria vulgaris and Sesamun indicum seed oil respectively. 1450 cm-1- 1444 is related to bending vibration of CH2, and CH3; (cis =C–H bending) and at 1360 - 1370 cm-1 is concerned with the bending vibrations CH2 groups which showed total unsaturation. The results obtained shows that all the oils are unsaturated because there is no band around 3005- 3009 which is the band that normally determine the index of degree of unsaturation. Conclusion: The FT- IR spectroscopy proved to be an important technique for identification, analysis, determination of degree of saturation of fatty acids in oils suitable for industrial applications.

scholarly journals THE MOLECULAR WEIGHT OF RHODOPSIN AND THE NATURE OF THE RHODOPSIN-DIGITONIN COMPLEX

1954 ◽  
Vol 37 (3) ◽  
pp. 381-399 ◽  
Author(s):  
Ruth Hubbard
Keyword(s):  
Molecular Weight ◽  
Single Molecule ◽  
Extinction Coefficient ◽  
Dry Weight ◽  
Weight Basis ◽  
Sedimentation Behavior ◽  
A Value ◽  
Wet Weight ◽  
Single Boundary ◽  
Stoichiometric Complex

The sedimentation behavior of aqueous solutions of digitonin and of cattle rhodopsin in digitonin has been examined in the ultracentrifuge. In confirmation of earlier work, digitonin was found to sediment as a micelle (D-1) with an s20 of about 6.35 Svedberg units, and containing at least 60 molecules. The rhodopsin solutions sediment as a stoichiometric complex of rhodopsin with digitonin (RD-1) with an s20 of about 9.77 Svedberg units. The s20 of the RD-1 micelle is constant between pH 6.3 and 9.6, and in the presence of excess digitonin. RD-1 travels as a single boundary also in the electrophoresis apparatus at pH 8.5, and on filter paper at pH 8.0. The molecular weight of the RD-1 micelle lies between 260,000 and 290,000. Of this, only about 40,000 gm. are due to rhodopsin; the rest is digitonin (180 to 200 moles). Comparison of the relative concentrations of RD-1 and retinene in solutions of rhodopsin-digitonin shows that RD-1 contains only one retinene equivalent. It can therefore contain only one molecule of rhodopsin with a molecular weight of about 40,000. Cattle rhodopsin therefore contains only one chromophore consisting of a single molecule of retinene. It is likely that frog rhodopsin has a similar molecular weight and also contains only one chromophore per molecule. The molar extinction coefficient of rhodopsin is therefore identical with the extinction coefficient per mole of retinene (40,600 cm.2 per mole) and the E(1 per cent, 1 cm., 500 mµ) has a value of about 10. Rhodopsin constitutes about 14 per cent of the dry weight, and 3.7 per cent of the wet weight of cattle outer limbs. This corresponds to about 4.2 x 106 molecules of rhodopsin per outer limb. The rhodopsin content of frog outer limbs is considerably higher: about 35 per cent of the dry weight, and 10 per cent of the wet weight, corresponding to about 2.1 x 109 molecules per outer limb. Thus the frog outer limb contains about five hundred times as much rhodopsin as the cattle outer limb. But the relative volumes of these structures are such that the ratio of concentrations is only about 2.5 to 1 on a weight basis. Rhodopsin accounts for at least one-fifth of the total protein of the cattle outer limb; for the frog, this value must be higher. The extinction (K500) along its axis is about 0.037 cm.2 for the cattle outer limb, and about 0.50 cm.2 for the frog outer limb.

Tetrachlorodibenzo-p-Dioxin Isomer Differentiation by Capillary Gas Chromatography Fourier Transform-Infrared Spectroscopy

1987 ◽  
Vol 41 (5) ◽  
pp. 809-820 ◽  
Author(s):  
James Grainger ◽  
Leslie T. Gelbaum
Keyword(s):  
Gas Chromatography ◽  
Fourier Transform ◽  
Vapor Phase ◽  
Valence Bond ◽  
Fourier Transform Infrared ◽  
Molecular Geometry ◽  
Ether Linkage ◽  
Relative Electron ◽  
Ft Ir ◽  
Infrared Frequencies

Reference infrared vapor-phase spectra of the 22 tetrachlorodibenzo-dioxin (TCDD) isomers were recorded at low microgram concentrations. These reference spectra of synthetic mixture components separated chromatographically or by spectral subtraction exhibit distinct infrared spectra for each isomer. The infrared frequencies are delineated in correlation tables and are interpreted in terms of substitution patterns which determine the strength of the ether linkage. Absorbance values in the 1330–1280 cm−1 (C-O-C asymmetric stretch) region correlate with specific substitution patterns and molecular geometry. Relative electron-withdrawing capacities for chlorinated aromatic rings in TCDD isomers were estimated on the basis of relative capacities determined for model compounds. Qualitative correlations were established between electron-withdrawing capacities and the effects of resonance and field interactions on the ether linkage absorption frequencies of individual TCDD isomers. Gas chromatography Fourier transform infrared (GC/FT-IR) isomer assignments are generally consistent with those obtained by proton Fourier transform nuclear magnetic resonance (1H FT/NMR) and flame ionization gas chromatography (GC/FID). A chromatographically independent method of assigning TCDD isomer structures on the basis of ether linkage asymmetric stretching frequencies was established by utilization of valence-bond approximations. GC/FT-IR assignments for several TCDD isomers differ from isomer assignments in previously published results. A user-generated, vapor-phase reference library, containing individual TCDD spectra and spectra of isomer pairs that are incompletely resolved on chromatographic columns, correctly identified each isomer in variety of mixtures by means of a software algorithm.

Sign in / Sign up

Export Citation Format

Share Document