Search

Made available in DSpace on 2019-10-06T16:18:59Z (GMT). No. of bitstreams: 0 Previous issue date: 2019-07-01 Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Natural deep eutectic solvents (NADES) based on xylitol, citric acid, and malic acid were synthesized and were then characterized using infrared spectroscopy, thermogravimetry (TG), differential scanning calorimetry (DSC), also density and viscosity were measurements. The deep eutectic solvents were used as solvent in ultrasound-assisted extraction (DES-UAE) of plant samples prior to elemental analysis. Inductively coupled plasma-mass spectrometry (ICP-MS) and inductively coupled plasma-optical emission spectrometry (ICP OES) were employed for the determination of As, Ca, Cd, Cu, Fe, K, Mg, Mn, Na, P, and Zn in the extracts. The infrared analyses of the NADES revealed bands characteristic of the initial reagents, with the presence of hydrogen bonds, which confirmed the formation of a NADES. The thermal analyses showed decomposition temperatures of around 170 °C and endothermic events related to degradation of the NADES. The viscosity and density parameters were found to be related to the presence of hydrogen bonds. The extraction recoveries ranged from 80% to 120%, with some analytes presenting poor recoveries. There were no significant differences between the NADES, in terms of the concentrations of the analytes found in the extracts. However, there were differences between the analyte concentrations obtained using the NADES extraction method and the concentrations obtained using microwave-assisted acid digestion (MW-AD), possibly due to the different types of interactions between the solvents and the analytes. Plant tissues are complex matrices containing substantial amounts of silica, so some elements may be tightly bound and consequently difficult to release. The results indicated that UAE using NADES is a promising technique for the elemental extraction of plant samples. São Paulo State University (UNESP) National Institute for Alternative Technologies of Detection Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT-DATREM) Department of Chemistry and Environmental Science Group for Applied Instrumental Analysis Department of Chemistry Federal University of São Carlos Department of Chemistry and Environmental Sciences (DQCA) São Paulo State University (UNESP) Institute of Biosciences Humanities and Exact Sciences (IBILCE) Federal University of Parana Department of Chemistry São Paulo State University (UNESP) National Institute for Alternative Technologies of Detection Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT-DATREM) Department of Chemistry and Environmental Science Department of Chemistry and Environmental Sciences (DQCA) São Paulo State University (UNESP) Institute of Biosciences Humanities and Exact Sciences (IBILCE) FAPESP: #2013/23886-4 FAPESP: #2017/13230-5 FAPESP: #2017/18531-3

Innovative extraction configurations for the biorefining of a biomass waste (citrus peel) were developed in this work. Non-conventional energies, such as microwaves (MW) and ultrasounds (US), were directly irradiated to the fresh orange peel using a versatile MW coaxial dipole antenna. This particular MW configuration enabled us to build two new extraction systems: (1) a coaxial solventless MW-assisted extraction (SMWAE) approach and, (2) a simultaneous ultrasound coaxial MW-assisted hydrodistillation (US-MWHD) method. The yield and chemical composition of the essential oils (EOs) of the orange peel obtained by the two innovative approaches were analyzed as a function of the extraction time and compared with those from coaxial microwave hydrodistillation (MWHD) and conventional hydrodistillation (CH). The EOs were chemically characterized by GC and GC-MS analysis. The residue mash was then used to extract pectin by a MW-assisted procedure. The structure and thermal stability of the pectin were investigated by FTIR and TG. The biorefining of EOs and pectin from a citrus waste maximises the benefits of our proposed green methodologies, which involve safe operability, faster processing and easy scalability. Furthermore, the energy consumed per unit mass of products in each step of the orange peel biorefining clearly showed that the most promising approach is SMWAE (since it is around 27 times lower than the CH approach). MWHD and US-MWHD also showed more than 60% energy savings compared to CH.

A green analytical procedure exploiting cloud point extraction for determination of copper and iron in plant materials is presented. After sample digestion with a diluted oxidant mixture (HNO3 + H2O2) in a closed vessel microwave oven, metal ions were simultaneously extracted as hydrophobic complexes formed with 1,2-tiazolylazo-2-naphthol (TAN) using Triton X-114 as extracting agent. Copper and iron were determined by flame atomic absorption spectrometry (FAAS) and iron also by UV-Vis spectrophotometry. For FAAS, the detection limits (99.7% confidence level) were estimated as 1 and 10 μg L-1 for copper and iron, respectively. Linear responses for both analytes were observed in the 25-200 μg L-1 range. The enrichment factors were estimated as 30 for both analytes and the extraction was quantitative, as evaluated by measurements in the supernatant solution remaining after extraction. For iron determination by UV-Vis spectrophotometry, the detection limit was estimated as 1 μg L-1, with linear response within 6 and 60 μg L-1. The accuracy of the procedure was evaluated by determination of the metals in certified reference materials and the results agreed with the certified values at the 95% confidence level. In the whole procedure, the reagent consumption was 1 mL HNO3, 1.1 mL H2O2, 50 mg Triton X-114 and 150 μg TAN per determination. Um procedimento analítico limpo baseado em extração em ponto nuvem é descrito para a determinação de cobre e ferro em materiais vegetais. Após a digestão da amostra em frascos fechados em forno de microondas, empregando mistura oxidante diluída (HNO3 + H2O2), os íons metálicos foram simultaneamente extraídos como complexos hidrofóbicos formados com 1,2-tiazolilazo-2-naftol (TAN) usando Triton X-114 como agente extrator. Íons cobre e ferro foram determinados por espectrometria de absorção atômica com chama (FAAS) e ferro também por espectrofotometria de absorção molecular UV-Vis. Nas medidas por FAAS, os limites de detecção (99,7% de confiança) foram estimados em 1 e 10 μg L-1 para cobre e ferro, respectivamente. Respostas lineares para ambos os analitos foram observadas no intervalo de 25-200 μg L-1. O fator de enriquecimento foi estimado em 30, com extração quantitativa dos complexos avaliada por medidas na solução sobrenadante remanescente após extração. Para a determinação de ferro por espectrofotometria UV-Vis, o limite de detecção (99,7% de confiança) foi estimado em 1 μg L-1, com resposta linear entre 6 e 60 μg L-1. A exatidão do procedimento foi avaliada pela determinação dos metais em materiais de referência certificados e os resultados foram concordantes com os valores certificados no nível de confiança de 95%. O consumo de reagentes foi de 1 mL HNO3, 1,1 mL H2O2, 50 mg Triton X-114 e 150 μg TAN por determinação.

The spatial distribution pattern of silicon in the leaves of three species of Saccharum has been demonstrated by means of laser induced breakdown spectroscopy (LIBS). The in-situ point detection capability of LIBS was used to determine different elements in leaf samples. The concentrations of silicon and other elements in different parts of the leaves were estimated by measuring the intensities of their corresponding atomic lines. Silicon, deposited in the form of phytoliths, was also isolated by using the dry ash technique. LIBS observations showed that in all three Saccharum species, the concentration of silicon was highest in the midrib followed by that found in margin and vein areas. The concentration of silicon in S. officinarum is higher in comparison to S. spontaneum and S. bengalense. Furthermore, the concentration of silicon at the upper surface of the leaf was larger than at the lower surface. The LIBS spectra of Saccharum species also show the presence of spectral lines of Na, Mg, Ca, Fe, and K.

A post-column fluorigenic reaction with benzamidine coupled to liquid chromatographic separation was used for the determination of reducing carbohydrates in three complex biological samples. This method allows the simultaneous determination of the different reducing sugars, which represents an improvement over batch enzymatic tests where in most instances only single monosaccharides can be determined. This selective liquid chromatographic method has a broad linear range. The method was validated by simultaneous analyses with a specific enzymatic test for glucose. Results are presented for the determination of glucose in human serum and mustard plants and glucose and fructose in white wines.

In this study the investigation of the aroma compounds of dried fruits of Evodia rutaecarpa (Juss.) Benth. and E. rutaecarpa (Juss.) Benth. var. officinalis (Dode) Huang (i.e. E. officinalis Dode) (Rutaceae family) was carried out to identify the odorous target components responsible for the characteristic aroma of these valuable natural products. To avoid the traditional and more time-consuming hydrodistillation, the analyses were carried out by means of headspace solid-phase microextraction (HS-SPME) coupled to gas chromatography-mass spectrometry (GC-MS). The SPME headspace volatiles were collected using a divinylbenzene-carboxen-polydimethylsiloxane (DVB-CAR-PDMS) fiber. The extraction conditions were optimized using a response surface experimental design to analyze the effect of three factors: extraction temperature, equilibrium time and extraction time. The best response was obtained when the extraction temperature was around 80 degrees C, equilibrium time near 25 min and extraction time close to 18 min. Analyses were performed by GC-MS with a 5% diphenyl-95% dimethyl polysiloxane (30 m x 0.25 mm I.D., film thickness 0.25 microm) capillary column using He as the carrier gas and a programmed temperature run. The main components of the HS-SPME samples of E. rutaecarpa (concentration >3.0%) were limonene (33.79%), beta-elemene (10.78%), linalool (8.15%), myrcene (5.83%), valencene (4.73%), beta-caryophyllene (4.62%), linalyl acetate (4.13%) and alpha-terpineol (3.99%). As for E. officinalis, the major compounds were myrcene (32.79%), limonene (18.36%), beta-caryophyllene (9.92%), trans-beta-ocimene (6.04%), linalool (5.88%), beta-elemene (7.85%) and valencene (4.62%).

Glycyrrhizin is one of the main bioactive components in liquorice (Glycyrrhiza uralensis Fisch) which has recently been found to be highly active in inhibiting replication of the severe acute respiratory syndrome (SARS)-associated virus. The separation and purification of glycyrrhizin from a methanol-water (70:30 (v/v)) extract of liquorice roots was achieved using high-speed counter-current chromatography. The separation was performed at a preparative scale in a one-step separation with a two-phase solvent system composed of ethyl acetate-methanol-water (5:2:5 (v/v)). The lower phase was used as the mobile phase in the head-to-tail elution mode. The present method yielded 42.2 mg glycyrrhizin at 96.8% purity from 130 mg of the crude exact with 95.2% recovery as determined by HPLC analysis.

Microwave closed-system wet digestion procedures for plant samples were examined. Each procedure was tested with samples of tobacco and cabbage, and included digestion by the use of different acids composition, almost complete evaporation of the digest, and then dissolution of the residue in 1% nitric acid. Three microwave digestion programs that varied power, duration, and temperature were used. Closed-vessel reactions followed open-vessel reaction-delay time. Using flame atomic absorption spectrometry on the digests, four or five elements were determined to evaluate effectiveness, precision and accuracy of analytes extraction into solution. After a preliminary study of tobacco digests, the four most effective procedures were chosen, and detailed investigations were carried out on both tobacco and cabbage reference materials. Although all four of the final procedures were accurate, the most precise procedure, with the lowest errors of determination, was using reverse ‘aqua regia’ for tobacco and ‘aqua re...

The application of immunoaffinity chromatography for the purification of Taxus plant and cell extracts prior to the HPLC analysis is described. Polyclonal antibodies raised against 10-deacetylbaccatin III (10-DAB III), paclitaxel's main precursor in plant, were characterised by enzymed-linked immunosorbent assay. Immunoglobulins from selected antisera were immobilised on CNBr-activated Sepharose 4B. The immunoaffinity column was used for the purification of plant and plant cell culture extracts prior to their analysis by HPLC. Immunoaffinity chromatography enabled the selective concentration of taxoids and enhanced sample clean-up. (C) 2002 Elsevier Science B.V. All rights reserved.

Rapid analytical methods for the determination of endosulfan isomers and endosulfan-sulfate in air and plant samples were developed. The insecticides were trapped from air using a column containing Florisil and extracted with a low volume of ethyl acetate, assisted by sonication. Pesticide residues were determined by gas chromatography with electron-capture detection using a nonpolar capillary column. Residue identities were confirmed by gas chromatography coupled with mass spectrometry. Recoveries of these compounds from air samples were always higher than 78% with an RSD lower than 11% and the detection limits obtained were at least 0.3 ng/l air. Leaf samples were homogenised with ethyl acetate and extracts cleaned-up on an aluminium oxide column. Pesticides were eluted with a hexane-ethyl acetate (8020, v/v) mixture. Recoveries obtained from plant samples were higher than 78% with an RSD lower than 14% and detection limits in leaves were 0.02 μg/g for each pesticide. These methods were applied to study the volatilisation of endosulfan from tomato leaves under laboratory conditions. A volatilisation rate near 1% of the initial amount of endosulfan per hour was obtained during the first 24 h at room temperature. © 2002 Elsevier Science B.V. All rights reserved.

The major phenolic diterpenes responsible for the antioxidant properties of rosemary extracts, namely carnosol and carnosic acid, were separated by capillary zone electrophoresis (CZE) using a 56 cm long uncoated fused-silica capillary and a 50 mM disodium tetraborate buffer of pH 10.1. The effect of the buffer type, pH and concentration, and the capillary length on the separation, was studied. Carnosol and carnosic acid were identified in the electrophoregrams of rosemary extracts through their migration times and UV spectra obtained by CZE analysis of pure compounds isolated from a rosemary extract by HPLC fractionation. The CZE method had good reproducibility (relative standard deviation less than 5%) and was applied to compare the contents of carnosol and carnosic acid in solid and oil-dispersed commercial extracts of rosemary and in rosemary leaves. The separation of carnosol and carnosic acid was accomplished in less than 11 min. © 2002 Elsevier Science B.V. All rights reserved.

It has been demonstrated that laser induced breakdown spectrometry (LIBS) can be used as an alternative method for the determination of macro (P, K, Ca, Mg) and micronutrients (B, Fe, Cu, Mn, Zn) in pellets of plant materials. However, information is required regarding the sample preparation for plant analysis by LIBS. In this work, methods involving cryogenic grinding and planetary ball milling were evaluated for leaves comminution before pellets preparation. The particle sizes were associated to chemical sample properties such as fiber and cellulose contents, as well as to pellets porosity and density. The pellets were ablated at 30 different sites by applying 25 laser pulses per site (Nd:YAG@1064 nm, 5 ns, 10 Hz, 25J cm(-2)). The plasma emission collected by lenses was directed through an optical fiber towards a high resolution echelle spectrometer equipped with an ICCD. Delay time and integration time gate were fixed at 2.0 and 4.5 μs, respectively. Experiments carried out with pellets of sugarcane, orange tree and soy leaves showed a significant effect of the plant species for choosing the most appropriate grinding conditions. By using ball milling with agate materials, 20 min grinding for orange tree and soy, and 60 min for sugarcane leaves led to particle size distributions generally lower than 75 μm. Cryogenic grinding yielded similar particle size distributions after 10 min for orange tree, 20 min for soy and 30 min for sugarcane leaves. There was up to 50% emission signal enhancement on LIBS measurements for most elements by improving particle size distribution and consequently the pellet porosity.

The volatile components of fresh leaves and roots from Anthriscus sylvestris (L.) Hoffm., obtained through hydrodistillation, were analysed by GC and GC-MS. This was compared to dichloromethane extracts of both fresh and dried leaf and root material. The monoterpene fraction (69-70%) dominated, while beta-phellandrene (39-45%) was the main component in both the leaf and the root oil. Other components in the leaf oil were beta-myrcene (17%), sabinene (6.2%), Z-beta-ocimene (5.4%) and benzene acetaldehyde (4.1%). In the roots we found Z-beta-ocimene (16.9%) and alpha-pinene (4.6%) as other major components. These principle constituents of both essential oils were also present in the dichloromethane extracts of the fresh and dried leaves and the roots, although in much smaller percentages. Comparing hydrodistillation of fresh plant material with a dichloromethane extract, the latter yielded a considerably lower amount of constituents. In addition, air drying and freeze drying resulted in a significant loss of volatile constituents as compared to fresh material (dichloromethane extract). (C) 2002 Elsevier Science B.V. All rights reserved.