973 resultados para Ethyl esters


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This work presents the biofuel production results of the esterification of fatty acids (C12-C18) and high-acid-content waste vegetable oils from different soap stocks (soybean, palm, and coconut) with methanol, ethanol, and butanol by acid catalysis. We used Amberlyst-35 (A35) sulfonic resin as a heterogeneous acid catalyst and p-toluenesulfonic acid as a homogeneous catalyst for comparison. Both the heterogeneous (A35) and homogeneous (p-toluenesulfonic acid) reactions were performed with 5% w/w of catalyst. The final products were analyzed by proton nuclear magnetic resonance (1H NMR). The homogeneous catalyzed esterification of fatty acids with methanol, ethanol, and butanol produced esters with yields higher than 90%. In the reaction with fatty acids and methanol catalyzed by A35, the best results were achieved with lauric acid and methanol, with a yield of 97%. An increase in the hydrocarbon chain decreased the rate of conversion and yield for stearic acid with methanol, which was 90%. Maximum biodiesel production was achieved from coconut and soybean soap stocks and methanol (96%-98%), which showed conversions very close to those obtained from their respective fatty acids. Microwave irradiation reduced the reaction time from 6 to 1 h in the esterification reaction of fatty acids with butanol.

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Specimens of Leonotis nepetiflolia were obtained from cultivated and wild environments to verify their influences in chemical composition. Phytochemical analyses were conducted for the ethyl acetate phase obtained by partitioning the crude ethanol extract from the cultivated leaves of L. nepetifolia. In doing so, flavonoid 3',4',5-trimethoxy-6,7-dihidroxyflavone (cirsiliol), a chemotaxonomic marker of the family Lamiaceae, was isolated. The results reveal that all phases and extracts tested exhibited weak to moderate antimicrobial activity against the strains of bacteria tested. The evaluation of in vitrocytotoxic and antitumor activity showed that the ethyl acetate phases obtained from both wild and cultivated leaves exhibit high potential cytotoxic and antitumor (> 78.0% of inhibition) activity. The major component of these phases was identified by high-performance liquid chromatography-diode array detector and nuclear magnetic resonance analyses using both 1D and 2D methods. The results further indicate that the flavonoid cirsiliol is the agent responsible for the activity observed in these phases.

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We report the single-step derivatization reaction of a biopolymer based onL -lysine with D -biotin analogs:Co -poly(L -lysine)-graft-(ε-N -[X-D-biotinyl]-L -lysine) (PLL-X-Biotin). The valeric acid carboxylate of D -biotin is activated to an NHS ester for direct modification of amine groups in proteins and other macromolecules. NHS esters react by nucleophilic attack of an amine in the carbonyl group, releasing the NHS group, and forming a stable amide linkage. NHS-X-Biotin is the simplest biotinylation reagent commercially available. In contrast withD -biotin, it has a longer spacer arm off the valeric acid side chain allowing better binding potential for avidin or streptavidin probes. Derivatization of poly(L -lysine) (PLL) with NHS-X-Biotin led to a copolymer PLL-X-Biotin. UV-Visible, IR-FT and 1H NMR characteristics derived from synthesis are briefly discussed.

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A fast gas chromatography with a flame ionisation detector (GC-FID) method for the simultaneous analysis of methyl palmitate (C16:0), stearate (C18:0), oleate (C18:1), linoleate (C18:2) and linolenate (C18:3) in biodiesel samples was proposed. The analysis was conducted in a customised ionic-liquid stationary-phase capillary, SLB-IL 111, with a length of 14 m, an internal diameter of 0.10 mm, a film thickness of 0.08 µm and operated isothermally at 160 °C using hydrogen as the carrier gas at a rate of 50 cm s-1 in run time about 3 min. Once methyl myristate (C14:0) is present lower than 0.5% m/m in real samples it was used as an internal standard. The method was successful applied to monitoring basic and acidic catalysis transesterification reactions of vegetable oils such as soybean, canola, corn, sunflower and those used in frying process.

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Herbicides such as trifluralin, simazine, atrazine, metribuzin and metolachlor are used in Brazilian agriculture. The efficiency of a small scale method for determination of these herbicides and two degradation products (deisopropylatrazine and deethylatrazine) in soil samples was evaluated. The compounds were extracted from soil samples (5 g) with 20 ml of ethyl acetate in a mechanical shaker for 50 min. Following the extraction, the supernatant was dried through anhydrous sodium sulphate, concentrated and analysed by high resolution gas chromatography (HRGC) with thermionic specific detection (TSD). Mean recoveries obtained from soil samples fortified at three different levels ranged from 81 to 115% with relative standard deviation (RSD) values varying from 1.2 to 12.7%. The method detection limits ranged from 0.01 to 0.06 mg kg-1. The methodology was applied using soil samples from farms located near the town of Araraquara, in the State of São Paulo, Brazil.

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Polymeric materials have been used in dental applications for decades. Adhesion of polymeric materials to each other and to the tooth substrate is essential to their successful use. The aim of this series of studies was two-folded. First, to improve adhesion of poly(paraphenylene) based rigid rod polymer (RRP) to other dental polymers, and secondly, to evaluate the usability of a new dentin primer system based on RRP fillers. Poly(paraphenylene) based RRP would be a tempting material for dental applications because of its good mechanical properties. To be used in dental applications, reliable adhesion between RRP and other dental polymers is required. In this series of studies, the adhesion of RRP to denture base polymer and the mechanical properties of RRP-denture base polymer-material combination were evaluated. Also adhesion of BisGMA-TEGDMA-resin to RRP was determined. Different surface treatments were tested to improve the adhesion of BisGMA-TEGDMA-resin to RRP. Results were based on three-point bending testing, Vickers surface hardness test and scanning electron microscope analysis (SEM), which showed that no reliable adhesion between RRP and denture base polymer was formed. Addition of RRP filler to denture base polymer increased surface hardness and flexural modulus but flexural strength decreased. Results from the shear bond strength test and SEM revealed that adhesion between resin and RRP was possible to improve by surface treatment with dichloromethane (DCM) based primer and a new kind of adhesive surface can be designed. The current dentin bonding agents have good immediate bond strength, but in long term the bond strength may decrease due to the detrimental effect of water and perhaps by matrix metalloproteinases. This leads to problems in longevity of restorations. Current bonding agents use organic monomers. In this series of studies, RRP filled dentin primer was tested in order to decrease the water sorption of the monomer system of the primers. The properties of new dentin primer system were evaluated in vitro by comparing it to commercial etch and rinse adhesive system. The results from the contact angle measurements and SEM showed that experimental primer with RRP reinforcement provided similar resin infiltration to dentin collagen and formed the resin-dentin interface as the control primer. Microtensile bond strength test and SEM revealed that in short term water storing, RRP increased bond strength and primer with BMEP-monomer (bis[2-(methacryloyloxy)-ethyl]phosphate) and high solvent concentration provided comparable bonding properties to the commercial control primers. In long term water storing, the high solvent-monomer concentration of the experimental primers decreased bond strength. However, in low solvent-monomer concentration groups, the long-term water storing did not decrease the bond strength despite the existence of hydrophilic monomers which were used in the system. These studies demonstrated that new dentin primer system reached the mechanical properties of current traditional etch and rinse adhesive system in short time water storing. Improved properties can be achieved by further modifications of the monomer system. Studies of the adhesion of RRP to other polymers suggest that adhesion between RRP and other dental polymers is possible to obtain by certain surface treatments.

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Previous studies have demonstrated that volatile organic compounds (VOCs), produced by the yeast Saccharomyces cerevisiae, were able to inhibit the development of phytopathogenic fungi. In this context, the nematicidal potential of the synthetic mixture of VOCs, constituted of alcohols and esters, was evaluated for the control of the root-knot nematode Meloidogyne javanica, which causes losses to crops of high economic value. The fumigation of substrate containing second-stage juveniles with VOCs exhibited nematicidal effect higher than 30% for the lowest concentration tested (33.3 µL g-1 substrate), whereas at 66.6 and 133.3 µL g-1 substrate, the nematode mortality was 100%. The present results stimulate other studies on VOCs for nematode management.

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Teve-se o objetivo de avaliar a eficiência de um conjunto de equipamentos de proteção individual no controle das exposições proporcionadas ao tratorista aplicando herbicidas nas culturas de soja e de amendoim com o pulverizador de barra e a segurança dessas condições de trabalho. Os pulverizadores utilizados foram os convencionais empregados nas duas culturas para as aplicações de herbicidas em pré-plantio incorporado (ppi), em pré-emergência (pré) e em pós-emergência inicial (pós), com volumes de 200 L ha-1, e 150 L ha-1 apenas na aplicação em pós, na cultura de soja. As exposições sem EPIs foram de 102,77 mL de calda por dia nas aplicações em ppi, 39,62 em pré e 47,14 em pós-emergência. A eficiência dos EPIs no controle das exposições dérmicas foi de 76,5% em ppi, 50,9% em pré e 75,3% em pós-emergência. Na cultura de soja, foram seguras para o tratorista, sem ou com EPIs, as aplicações de pendimethalin, imazaquin e flumetsulam em ppi; de pendimethalin, acetochlor, clomazone, flumioxazin, imazaquin, metribuzin, sulfentrazone, dimethenamid e flumetsulamem em pré, e de bentazone, glyphosate, imazethapyr, quizalofop-ethyl, chlorimuron ethyl e oxasulfuron em pós. Na cultura de amendoim, sem e com EPIs, foi segura a aplicação de pendimethalin em ppi; em pré, a aplicação de alachlor foi classificada como insegura, sem ou com o uso dos EPIs.

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O objetivo do trabalho foi avaliar se a utilização de adjuvantes nas misturas em tanque de glyphosate + chlorimuron-ethyl e glyphosate + carfentrazone-ethyl influenciam na qualidade da aplicação e eficiência de controle de Ipomoea grandifolia. Treze tratamentos, dispostos em delineamento inteiramente casualizado, foram constituídos pelas misturas em tanque de glyphosate + chlorimuron-ethyl (1.440 + 12,5 g ha-1) e glyphosate + carfentrazone-ethyl (1.440 + 10 g ha-1) isoladas e associados aos adjuvantes Nimbus®, Joint Oil®, Naturl'Oil®, Triunfo 515® e All Fix ®, e uma testemunha sem aplicação. Os adjuvantes utilizados foram eficientes na redução da tensão superficial das caldas; no entanto, não influenciaram nos valores de deposição e na eficiência do controle. Os adjuvantes proporcionaram efeitos distintos na redução da tensão superficial, no pH e na qualidade da aplicação (diâmetro mediano volumétrico, densidade de gotas, potencial de perdas por deriva, área coberta e diâmetro médio das gotas) das misturas em tanque de glyphosate + chlorimuron-ethyl e glyphosate + carfentrazone-ethyl, mas não interferiram na deposição da calda de pulverização sobre os alvos I. grandifolia e lâminas de vidro. Glyphosate + carfentrazone-ethyl apresentou maior velocidade de controle de I. grandifolia em relação ao glyphosate + chlorimuron-ethyl, na ausência ou na presença dos adjuvantes, apesar de o glyphosate + carfentrazone-ethyl associado com Nimbus® e Joint Oil® terem proporcionado às plantas-alvo início de desenvolvimento de novas folhas.

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In this thesis, biocatalysis is defined as the science of using enzymes as catalysts in organic synthesis. Environmental aspects and the continuously expanding repertoire of available enzymes have firmly established biocatalysis as a prominent means of chemo-, regio- and stereoselective synthesis. Yet, no single methodology can solve all the challenges faced by a synthetic chemist. Therefore, the knowledge and the skills to combine different synthetic methods are relevant. Lipases are highly useful enzymes in organic synthesis. In this thesis, an effort is being made to form a coherent picture of when and how can lipases be incorporated into nonenzymatic synthesis. This is attempted both in the literature review and in the discussion of the results presented in the original publications contained in the thesis. In addition to lipases, oxynitrilases were also used in the work. The experimental part of the thesis comprises of the results reported in four peer-reviewed publications and one manuscript. Selected amines, amino acids and sugar-derived cyanohydrins or their acylated derivatives were each prepared in enantio- or diastereomerically enriched form. Where applicable, attempts were made to combine the enzymatic reactions to other synthetic steps either by the application of completely separate sequential reactions with isolated intermediates (kinetic and functional kinetic resolution of amines), simultaneously occurring reactions without intermediate isolation (dynamic kinetic resolution of amino acid esters) or sequential reactions but without isolating the intermediates (hydrocyanation of sugar aldehydes with subsequent diastereoresolution). In all cases, lipase-catalyzed acylation was the key step by which stereoselectivity was achieved. Lipase from Burkholderia cepacia was a highly selective enzyme with each substrate category, but careful selection of the acyl donor and the solvent was important as well.

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Vaahdotusta käytetään yleisesti erottamaan eri mineraaleja malmista. Tässä menetelmässä käytetään erityisiä pinta-aktiivisia aineita, joita kutsutaan kokoojakemikaaleiksi, muuntamaan halutut mineraalit hydrofobisiksi ja erottamaan ne hydrofiilisistä partikkeleista ilmakuplien avulla. Eräs tärkeimmistä kokoojakemikaalien ryhmistä on ksantaatit. Ksantaateilla on havaittu taipumusta hajota useiksi erilaisiksi hajoamistuotteiksi vaahdotusprosessin aikana. Näillä hajoamistuotteilla voi olla monia haitallisia vaikutuksia vaahdotuksen tuloksiin. Näiden tuotteiden tunnistaminen ja määrittäminen on tärkeää vaahdotusprosessin paremman ymmärtämisen kannalta. Työn kirjallisuusosassa vaahdotusprosessi, ksantaatit ja niiden yleisimmät hajoamistuotteet on esitelty, kuten myös käytetty analyysimenetelmä, kapillaarielektroforeesi. Työn kokeellisessa osassa etsittiin sopivaa erotusmenetelmää etyyliksantaatin, etyylitiokarbonaatin, etyyliperksantaatin ja etyyliksantyylitiosulfaatin erottamiseksi kapillaarilelektroforeesilla. Pääasiassa keskityttiin kahteen eri erotusmenetelmään. Ensimmäinen menetelmä kykeni erottamaan kaikki tutkitut tuotteet puhdasvesinäytteissä, ja toinen menetelmä oli sopiva näiden tuotteiden erottamiseen prosessivesinäytteissä. Jälkimmäistä menetelmää kokeiltiin käytännössä rikastamolla, jossa sillä kyettiin erottamaan isobutyyliksantaatti, isobutyylitiokarbonaatti, ja suurella todennäköisyydellä myös isobutyyliperksantaatti.

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Conduziu-se um ensaio em campo na Estação Experimental Agronômica da Universidade Federal do Rio Grande do Sul, em Eldorado do Sul, RS, em 1989/90. O objetivo foi determinar o efeito dos herbicidas clomazone, chlorimuronethyl, imazaquin e imazethaphyr, aplicados em três doses à superfície do solo (PRE) ou incorporados no mesmo (PPI), sobre o rendimento de aquênios de girassol e seus componentes. Os herbicidas de solo para controle de plantas daninhas na cultura da soja com maior potencial de dano ao girassol cultivado em sucessão, conforme indicado pelo rendimento de aquênios, foram os seguintes, em ordem decrescente: imazaquin > clomazone > imazethapyr> chlorimuron-ethyl. O efeito mais pronunciado dos herbicidas foi a redução da população de plantas. Este foi o fator que mais influenciou no rendimento do girassol.

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Brittleness is a well-known material characteristic but brittleness of paper is vaguely covered. The objective of this thesis was to characterize the phenomenon and causes around brittleness of paper and to clarify if it is a measurable property. Brittleness of paper was approached from the perspectives of paper physics and paper mills. Brittleness is a property of dry paper and it causes problems at the finishing stages of paper machine. According to paper physics, brittle materials fail in the elastic regime, while ductile materials can locally accumulate a plastic deformation prior to the fracture and they are often able to withstand higher stresses. Brittleness of paper is vastly affected by the surrounding conditions: paper as a hygroscopic material tries to get to the equilibrium. It is also affected by the quality of the pulp used. Measurement techniques can be divided into two categories: based on the viscoelastic behavior of paper and on the exposure to the mechanical stress of sort. The experimental part of the thesis was based on the trials with brittle and non-brittle mill-made LWC papers. It is divided into three parts: strength testing of the brittle and non-brittle papers, analysis of the conditions that may contribute the brittleness and the experimental methods to evaluate brittle behavior. The strength measurements confirmed the influence of the moisture content, but only tensile energy absorption and the fracture toughness measurements provided modest differences between the brittle and non-brittle papers. Versatile analysis of the possible contributing factors resulted into speculation, while the brittle papers contained higher amount of starch, triglycerides and steryl esters. The experimental research proved that the formation, the sensory impression and the variation of local strains may contain the crucial information of paper brittleness.

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O objetivo deste trabalho foi investigar o grau de tolerância de cultivares de trigo e aveia aos herbicidas diclofop-methyl, fenoxaprop-ethyl e haloxyfop-methyl, visando a utilização seletiva desses produtos para controlar espécies gramíneas infestantes dessas culturas. Foi instalado um experimento de campo e outro de casa-de-vegetação. Os tratamentos testados no experimento de campo foram diclofop-methyl (540 g/ha), fenoxaprop-ethyl (180 g/ha), haloxyfop-methyl (120 g/ha) e uma testemunha sem tratamento herbicida, aplicados sobre as cultivares 'CTC-1', 'UFRGS-7' e 'UPF-16' de aveia branca, e em aveia-preta. No experimento de casa-de-vegetação testaram-se três doses de fenoxaprop-ethyl (0, 90 e 120 g/ha), aplicadas sobre sete cultivares de trigo ('BR-23', 'BR-35', 'BR-38', 'E-16', 'E-40', 'E-49' e 'E-52'), aveia-branca, aveia-preta e azevém. Como resultados do ensaio de campo, constatou-se que todos os herbicidas testados controlaram com eficiência (acima de 90%) as cultivares de aveia-branca. A aveia-preta mostrou alta sensibilidade ao fenoxaprop-ethyl e ao haloxyfop-methyl e alguma tolerância ao diclofop-methyl; já o trigo mostrou-se tolerante ao diclofop-methyl e ao fenoxaprop-ethyl. Em casa-de-vegetação, as cultivares de trigo 'BR-38', 'E-16', 'E-49' e 'E-52' apresentaram níveis aceitáveis de fitotoxicidade para fenoxaprop-ethyl a 90 g/ha, enquanto as demais cultivares ('BR-23', 'BR-35' e 'E-40') apresentaram danos moderados ao herbicida. Já fenoxaprop-ethyl a 120 g/ha causou aumento no nível de fitotoxicidade para as cultivares de trigo, exceto para 'E-16' e 'E-52'. O azevém mostrou-se tolerante ao herbicida fenoxaprop-ethyl. Conclui-se que existe potencial de uso do herbicida fenoxaprop-ethyl em lavouras de trigo para controlar seletivamente aveia-branca e aveia-preta. O herbicida diclofop-methyl apresenta controle elevado de aveia-branca e reduzido de aveia-preta. Haloxyfop-methyl não evidenciou seletividade ao trigo, controlando com eficiência as gramíneas testadas.

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Vaahdotusprosessia käytetään yleisesti erottamaan arvokkaita mineraaleja malmeista. Toimiakseen tehokkaasti prosessi tarvitsee kokoojakemikaaleja, joiden tehtävänä on sitoa halutut mineraalit ilmakupliin. Jotta näiden kemikaalien käyttäytymistä prosessissa voitaisiin ymmärtää paremmin ja prosessin ohjausta tehostaa, pitää kokoojia pystyä analysoimaan prosessivesistä. Työn kirjallisuusosassa on koottu ja vertailtu erilaisia kirjallisuudesta löytyneitä analyysimenetelmiä kokoojakemikaaleille. Kokeellisessaosassa on kehitetty kaksi kapillaarielektroforeesimenetelmää näiden kemikaalien tutkimiseen. Menetelmien toteamisrajat tutkituille kemikaaleille olivat seuraavanlaiset: natrium diiosobutylditiofosfaattille (DTP) 2,7 mg/L puhtaassa vedessä ja 6,7 mg/L prosessivedessä; natrium diisobutyldithiofosfinaatille (DTPI) vastaavasti 4,5 mg/L ja 6,7 mg/L; etyyli ksantaatille 0,025 mg/L ja 0,16 mg/L; ja isobutyyli ksantaatille 0,41 mg/L ja 0,62 mg/L. Näitä menetelmiä voidaan tulevaisuudessa kehittää kokoojien hajoamistuotteiden analysointia varten sekä prosessien on-line mittauksiin.