Determination of Tamarindus Indica Seed Fatty Acid Components Using Ultrasound- Assisted Microwave Extraction Method

In this study aimed to determine the effect of ultrasound and microwave assisted extraction on fatty acids yield. Fatty acid components of Tamarindus Indica (T. Indica) seed were determined using ultrasound assisted microwave extraction method. T. Indica is cultivated in the tropics and in Egypt and India. Its fruits are 12-15 cm long, brown and leguminous. In addition to its positive effects on the digestive system, it is an excellent source of vitamin C and a rich antioxidant. It has also been proven beneficial in keeping blood sugar balanced. Fatty acid components were determined by Gas Chromatography-Mass Spectroscopy (GC-MS) method. In addition, the effects of the solvent on the fatty acid yield were investigated. When the results of the analysis were examined, the highest yield was obtained when ethyl alcohol and methyl alcohol were used as solvents. Another important solvent is acetone. The least product was achieved when hexane was used as solvent. Linoleic acid and arachidic acid were detected in each type of solvent used. Capric acid, ligroseric acid and nervotic acid, which are important fatty acids, are detected only in methyl alcohol extraction. The ultrasound assisted microwave extraction method was found to be much faster than the traditional Soxhlet extraction method.

SYNTHESIS AND PROPERTIES OF ORGANOSILICON EPISULFIDES

A study was made of the interaction of thiourea with saturated and unsaturated organosilicon oxiranes in absolute methyl alcohol in a medium of potassium hydroxide, and methods were developed for the synthesis of unsaturated and unsaturated organosilicon silicides with a yield of 65–75%.The studies carried out revealed that the synthesized organosilicon episulfides are very reactive compounds and can react with nucleophilic and electrophilic reagents, while forming the corresponding silicon derivatives. The IR- spectra of the products were studied. It should be noted that, when comparing the IR- spectra of oxiranes and episulfides, it was revealed that the stretching vibrations of the CH2 group of the episulfide ring are underestimated by 50–70 cm-1 in comparison with the oxirane ring

The use of plant materials for the synthesis of superplasticizer

The paper presents data on the synthesis of phloroglucinol-furfural modifier (1,3,5-trihydroxybenzene-2-furaldehyde oligomer) based on 2-furaldehyde (furfural) and 1,3,5-trihydroxybenzene (phloroglucinol). The synthesis of a modifier with different molar ratios of phloroglucinol/furfural was carried out. It was found that an increase in the molar ratio leads to an increase in the plasticizing ability of the modifier. The optimal concentration of the catalyst was determined to be equal to 50% by weight of phloroglucinol. Two chemical forms of the modifier were obtained: H-form and Na-form. The structure of various forms of the modifier has been studied by scanning electron microscopy. It was found that the oligomers used in the work for the synthesis of the modifier, in addition to 2-furyl methyl alcohol, do not have plasticizing properties. Purified 2-furyl methyl alcohol has weak plasticizing properties. It is shown that to achieve the best plasticizing effect, it is necessary to gradually introduce a condensing agent into the reaction mixture. With gradual introduction, a complete condensation reaction occurs between the monomers, which affects the improvement of the plasticizing properties of the resulting product. The spread of the cement mixture when using 0.3% of the additive based on the mass of cement in terms of dry matter is 19 cm.

Substantiation of parameters for the inertial mixer in a biodiesel production reactor

This paper reports results of the theoretical and experimental studies into the processes of transesterification of oils with methyl alcohol, which determined the material balance and established the molecular weight of the components involved in the process of transesterification as input and output products. The theoretical and experimental studies were carried out to calculate the indicators of the process of transesterification of fat-containing wastes depending on a change in the reaction duration and diameter of the inertial mixer of the reactor to accelerate the process of transesterification of oils with methyl alcohol. The process of transesterification is one of the basic methods for modifying the molecular composition of fat raw materials. With transesterification, the composition of fat fatty acids does not change, their statistical redistribution occurs in a mixture of triacylglycerols, which leads to a change in the physicochemical properties of fat mixtures as a result of changes in molecular composition. Transesterification of high-melting animal and vegetable fats with methyl alcohol improves the conversion of oils for the production of biodiesel from fat-containing waste. The results of the theoretical and experimental studies have helped determine the value of the flow rate of the reaction mixture, as well as the values of the geometric dimensions of the reactor, were determined (the diameter of the mixer, d=100÷500 mm; the length of the reactor is 1.5÷2.0 m). Processing of the reaction mixture made it possible to obtain a high degree of homogeneity in the concentration of components with large diameters of the inertial mixer ‒ 300...500 mm at average rotational speeds. The oil conversion has been improved, as well as productivity, by using equipment to produce biodiesel from fat-containing waste. Optimal pump performance is also ensured with minimal power consumption and reactor operation

Synthesis, Structural and Physicochemical Characterization of a Titanium(IV) Compound with the Hydroxamate Ligand N,2-Dihydroxybenzamide

The siderophore organic ligand N,2-dihydroxybenzamide (H2dihybe) incorporates the hydroxamate group, in addition to the phenoxy group in the ortho-position and reveals a very rich coordination chemistry with potential applications in medicine, materials, and physical sciences. The reaction of H2dihybe with TiCl4 in methyl alcohol and KOH yielded the tetranuclear titanium oxo-cluster (TOC) [TiIV4(μ-O)2(HOCH3)4(μ-Hdihybe)4(Hdihybe)4]Cl4∙10H2O∙12CH3OH (1). The titanium compound was characterized by single-crystal X-ray structure analysis, ESI-MS, 13C, and 1H NMR spectroscopy, solid-state and solution UV–Vis, IR vibrational, and luminescence spectroscopies and molecular orbital calculations. The inorganic core Ti4(μ-O)2 of 1 constitutes a rare structural motif for discrete TiIV4 oxo-clusters. High-resolution ESI-MS studies of 1 in methyl alcohol revealed the presence of isotopic distribution patterns which can be attributed to the tetranuclear clusters containing the inorganic core {Ti4(μ-O)2}. Solid-state IR spectroscopy of 1 showed the presence of an intense band at ~800 cm−1 which is absent in the spectrum of the H2dihybe and was attributed to the high-energy ν(Ti2–μ-O) stretching mode. The ν(C=O) in 1 is red-shifted by ~10 cm−1, while the ν(N-O) is blue-shifted by ~20 cm−1 in comparison to H2dihybe. Density Functional Theory (DFT) calculations reveal that in the experimental and theoretically predicted IR absorbance spectra of the ligand and Ti-complex, the main bands observed in the experimental spectra are also present in the calculated spectra supporting the proposed structural model. 1H and 13C NMR solution (CD3OD) studies of 1 reveal that it retains its integrity in CD3OD. The observed NMR changes upon addition of base to a CD3OD solution of 1, are due to an acid–base equilibrium and not a change in the TiIV coordination environment while the decrease in the complex’s lability is due to the improved electron-donating properties which arise from the ligand deprotonation. Luminescence spectroscopic studies of 1 in solution reveal a dual narrow luminescence at different excitation wavelengths. The TOC 1 exhibits a band-gap of 1.98 eV which renders it a promising candidate for photocatalytic investigations.

Coffee berry borer (Hypothenemus hampei Ferrari) trapping in coffee (Coffea arabica L.) with artisan traps at el Paraíso, Guerrero, Mexico

Objective: To evaluate three proportions of alcohol in traps with one and three windows and two different colors to capture Hypothenemus hampei Ferrari in Coffea arabica L. plants. Design/methodology/approach: The experiment followed a completely randomized design with a complete factorial arrangement and four replications. From March to July 2007, three mixtures of ethyl: methyl alcohol were evaluated in different proportions (1: 0, 0: 1 and 1: 1). In addition, green and transparent traps were used, designed with a single or three windows. The number of captured coffee berry borers, water loss, attractant evaporation and damaged fruits percentage was evaluated. The data were analyzed through an analysis of variance and a test of means differences (Tukey, p ? 0.05). Results: The mixture of ethyl: methyl alcohol 1: 1 was the best, with an average catch of 980 trapped - insects week-1. The single window of transparent color traps was the most efficient to avoid water loss, with an average loss of 1,129.79 mL and 905 mL respectively. Limitations on study/implications: The design and color of the traps did not influence the capture efficiency and the evaporation of the attractant during the evaluated months. Therefore, it should be further evaluated during other important phenological stages for the crop. Findings/conclusions: Transparent color traps with a window and 1: 1 ethyl: methyl alcohol were efficient for capturing H. hampei and lowering their population.

INVESTIGATION OF DIAZINON DEGRADATION IN MODEL SOLUTIONS USING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY

Aim of our war was to investigate the degradation of diazinon in the model mixture in comparison with the experimental preparation. Methyl alcohol was used as a basis for the manufacture of diazinon drops and the model mixture. The concentration of diazinon was determined by reversed-phase high performance liquid chromatography on the third, fourteenth and twenty-first day after preparation of the model mixture and experimental preparation when stored at room temperature. Despite the large number of publications studying the degradation of diazinon under the influence of various factors, there is a need to study this process in mixtures of a specific composition, in particular in new veterinary drugs that have not yet been studied. This article presents the results of determining the content of diazinon in 10% of the drug and the model mixture based on methyl alcohol. The analyzes were performed on a Knauer liquid chromatograph with a spectrophotometric detector equipped with a Luna® Omega Polar C 18 150 × 4.6 mm column filled with a 5 μm particle sorbent from Phenomenex with a universal C 18 pre-column 4 × 3.0 mm ID. Mobile phase: degassed mixture of acetonitrile: water in the ratio 65:35, flow rate was 1.1 ml/min, temperature of the column was ambient. Diazinone was detected at 245 nm. Injection volume was 0.050 ml and the time of one separation – 20 minutes. The appearance of an unknown peak on the 3 min chromatogram of the solution of the production experimental preparation was revealed. On the twenty-first day of storage of the experimental drug, the content of diazinon decreased to 34 % of the stated amount. On the third and twenty-first day of storage of the model mixture, a decrease in the content of diazinon by 16 % and 79%, respectively, and the appearance of an additional peak were observed. The use of methyl alcohol with other components is likely to be a factor in the breakdown of diazinon in the drug. According to the recipe of the drug, methanol is about half the content of ingredients. This composition does not provide stability of the proposed dosage form of the drug. The next step will be to study the effect of other solvents on maintaining the stated concentration of diazinon.