Submitted by Ana Hilda Fonseca (anahilda@ufba.br) on 2016-02-26T13:54:44Z No. of bitstreams: 1 Tese Final_Anaildes.pdf: 2041985 bytes, checksum: 94248283056f958235943f529a088431 (MD5) / Approved for entry into archive by Ana Hilda Fonseca (anahilda@ufba.br) on 2016-05-04T19:43:15Z (GMT) No. of bitstreams: 1 Tese Final_Anaildes.pdf: 2041985 bytes, checksum: 94248283056f958235943f529a088431 (MD5) / Made available in DSpace on 2016-05-04T19:43:15Z (GMT). No. of bitstreams: 1 Tese Final_Anaildes.pdf: 2041985 bytes, checksum: 94248283056f958235943f529a088431 (MD5) / CNPq / O biodiesel, combustível alternativo ao diesel, é composto de mono-ésteres de alquila de ácidos graxos preparados a partir de óleos vegetais ou gordura animal. É um biocombustível renovável, que pode contribuir na diminuição das emissões de alguns poluentes. Entretanto, deve-se considerar que o biodiesel produzido a partir de óleos vegetais pode ser mais propenso à oxidação do que um diesel de petróleo típico. Neste sentido, foi realizado um estudo detalhado sobre a estabilidade oxidativa do biodiesel de soja e de seus produtos de oxidação. O propósito da primeira etapa desta tese foi verificar através de um planejamento de misturas, à proporção que se obtém a melhor resposta (período de indução), através de misturas ternárias de amostras de biodiesel de soja, sebo e mamona. O melhor período de indução foi obtido com a seguinte proporção: 82,5% (v/v) de soja, 7,5% (v/v) de sebo e 10,0% (v/v) de mamona. Na segunda parte do trabalho, foram propostos procedimentos para avaliar alguns fatores que influenciam o período de indução do biodiesel de soja. A utilização de reatores ultrassônicos induziu a oxidação da amostra de biodiesel. Uma alternativa viável para um maior controle da oxidação foi adição de um fluxo de gás nitrogênio durante a produção do biodiesel. Verificou-se que as amostras de biodiesel armazenadas em recipientes de diferentes materiais, aumentaram o teor de água ao longo de nove meses de armazenamento, enquanto o período de indução diminuiu neste tempo. Observou-se que o recipiente mais adequado para armazenar o biodiesel foi o vidro âmbar. No terceiro trabalho, foi proposta a quantificação e avaliação de espécies inorgânicas (Na+, K+, NH4 +, Cl-, NO3 -, C2O4 2- e PO4 3-) e espécies orgânicas (formiato, acetato, propionato, lactato e succinato) utilizando a cromatografia iônica em amostras de óleo e biodiesel de soja submetida à degradação acelerada utilizando o Rancimat. Verificou-se que as espécies que mais contribuíram para o aumento da condutividade do sistema foram formiato e acetato. Na quarta etapa do trabalho, um método foi proposto para capturar os compostos carbonílicos formados durante a degradação do óleo e biodiesel de soja para quantificá-los posteriormente por CLAE-DAD. Os aldeídos identificados como produtos da oxidação do óleo e biodiesel de soja foram: formaldeído, acetaldeído, acroleína, propanal, crotonaldeído, metacroleína, butanal, pentanal, hexanal, heptanal e octanal. Sendo que, o acetaldeído, propanal e hexanal apresentaram maiores taxas de formação para todos os tempos de coleta. Esse trabalho contribuiu para o entendimento sobre a estabilidade oxidativa do biodiesel de soja, além da identificação e quantificação dos seus produtos de oxidação. / Biodiesel, an alternative fuel to diesel, is composed of mono-alkyl esters of fatty acids prepared from vegetable oils or animal fat. It is a renewable bio-fuel, which can contribute to the reduction of emissions of certain pollutants. However, biodiesel made from vegetable oils may be more unstable than a typical diesel oil. In this work, a detailed study on the oxidative stability of soybean biodiesel and its oxidation products was performed. The purpose of the first stage of this thesis was to verify through a design mixtures, the proportion that gets the best response (induction period), using ternary mixtures of samples of soybean biodiesel, tallow and castor. The best induction period was obtained with the following proportions: 82.5% (v / v) soy, 7.5% (v / v) of tallow and 10.0% (v / v) castor oil. In the second part of the work, procedures to assess some factors that influence the induction period of soybean biodiesel have been proposed. The use of ultrasonic reactors induced oxidation of the sample of biodiesel. A viable alternative for greater control of oxidation was adding a flow of nitrogen gas during the production of biodiesel. It was found that samples of biodiesel stored in containers of different materials, the increased water content over nine months of storage, while the induction period decreased at this time. It was observed that the most suitable for storing the biodiesel was amber glass container. In the third study, quantification and evaluation of inorganic species (Na+, K+, NH4 +, Cl-, NO3 -, and C2O4 2- PO4 3-) and organic species (formate, acetate, propionate, lactate, and succinate) was proposed using ion chromatography in samples of oil and soybean biodiesel subjected to accelerated degradation using the Rancimat. It was found that the species that contributed most to the increase in conductivity of the system were formate and acetate. In the fourth stage of the work, a method was proposed to capture the carbonyl compounds formed during the degradation of oil and soybean biodiesel to quantify them later by HPLC-DAD. The aldehydes identified as the oxidation of soybean oil and biodiesel products were formaldehyde, acetaldehyde, acrolein, propanal, crotonaldehyde, methacrolein, butanal, pentanal, hexanal, heptanal and octanal. Since, acetaldehyde, propanal and hexanal showed higher rates of training for all collection times. This work contributed to the understanding of the oxidative stability of soybean biodiesel, besides the identification and quantification of their oxidation products.

Orientadores: Miriam Dupas Hubinger, Vanessa Martins da Silva / Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos / Made available in DSpace on 2018-08-22T08:01:27Z (GMT). No. of bitstreams: 1 Carvalho_AnaGabrieladaSilva_M.pdf: 18654651 bytes, checksum: b9cbc1f805b1d0974af4067819e06088 (MD5) Previous issue date: 2013 / Resumo: O óleo de café verde merece destaque na área cosmética por sua capacidade de bloquear a radiação solar UVB (290-320 nm) e por suas propriedades emolientes. Nesse contexto, para melhor aproveitar as propriedades desse óleo e aumentar a sua estabilidade oxidativa, pretendeu-se com este trabalho produzir micropartículas de óleo de café verde, pelo processo físico de spray drying. Como agentes encapsulantes foram utilizados lecitina, um fosfolipídeo de caráter aniônico quando em pH 3,0, quitosana, um polissacarídeo de caráter catiônico também em pH 3,0 e solúvel somente em sistemas ácidos diluídos, além de sólidos de xarope de milho ou amidos modificados derivados do milho, HiCap 100 e Snow-Flake. O preparo das emulsões foi feito através da técnica de estabilização por atração eletrostática de cargas opostas entre a lecitina e a quitosana. Com o propósito de se obter emulsões com dupla camada estáveis à separação de fase, foi utilizado um rotor-estator e um homogeneizador a alta pressão. As emulsões foram analisadas quanto à estabilidade, distribuição de tamanho e diâmetro médio das gotas, microscopia ótica, potencial zeta e comportamento reológico. As emulsões preparadas com Snow-Flake e xarope de milho/Snow-Flake (50/50) apresentaram comportamento pseudoplástico, além de apresentarem os maiores diâmetros de gota variando de 3,70 a 5,19 µm. Contudo, as emulsões com xarope de milho, HiCap 100 e xarope de milho/HiCap 100 (50/50) apresentaram comportamento de fluidos Newtonianos e diâmetros menores de gota, entre 1,15 e 1,51 µm. Para o processo de secagem foi utilizado um secador laboratorial do tipo mini spray dryer, com temperatura do ar de secagem de 170 °C. As micropartículas obtidas foram caracterizadas em relação ao conteúdo de umidade, atividade de água, distribuição de tamanho e diâmetro médio de partículas e microestrutura. Além disso, foram também determinados: a eficiência de encapsulação, o fator de proteção solar in vitro das micropartículas e estabilidade oxidativa pelo método Rancimat. As micropartículas apresentaram diâmetro entre 14,51 e 29,19 µm e excelentes valores de eficiência de encapsulação, superiores a 84%. As partículas produzidas com os amidos modificados apresentaram formato esférico sem rachaduras ou poros, já as micropartículas produzidas com somente xarope de milho apresentaram alguns poros e rachaduras, que causaram a menor estabilidade oxidativa dessas micropartículas. As micropartículas produzidas com HiCap 100 e xarope de milho/HiCap 100 (50/50) estabilizadas por lecitina-quitosana apresentaram maior estabilidade oxidativa. O fator de proteção das partículas variou entre 1,37 e 2,45, sendo de 2,12 para o óleo de café verde puro / Abstract: The green coffee oil stands out for its ability to block the UVB radiation (290-320 nm) and its emollient property. In this context, to improve the properties of this oil and increase its stability, the aim of this work was to produce microparticles of green coffee oil by spray drying. Encapsulating agents used were lecithin, a phospholipid with anionic character at pH 3.0, chitosan, a polysaccharide with cationic character also in pH 3.0 and soluble only in diluted acid solutions and corn syrup solids or corn modified starches as HiCap 100 and Snow-Flake. Emulsions preparation involved the technique of stabilization by electrostatic attraction between lecithin and chitosan. A rotor-stator homogenizer and a high pressure homogenizer were used in order to obtain stable emulsions by electrostatic layer-by-layer deposition. The emulsions were analyzed in relation to stability, size distribution and droplet diameter, optical microscopy, zeta potential and rheological behavior. The emulsions prepared with Snow-Flake and corn syrup/Snow-Flake (50/50) showed pseudoplastic behavior, besides having the biggest droplet diameters ranging from 3.70 to 5.19 µm. However emulsions prepared with corn syrup, HiCap 100 and corn syrup/HiCap 100 (50/50) showed Newtonian behavior and smaller droplet diameters ranging from 1.15 to 1.51 µm. For the drying process, a laboratory spray dryer and air temperature of 170 °C were used. Microparticles were characterized with respect to moisture content, water activity, particle size distribution and microstructure. Furthermore, encapsulation efficiency, sun protection factor in vitro and oxidative stability by the Rancimat method were determined. The microparticles had a diameter ranging from 14.51 and 29.19 µm and high values of encapsulation efficiency, above 84%. The particles produced with modified starches showed spherical shape without cracks or pores and those produced with only corn syrup showed some holes and cracks, that caused lower oxidative stability of these microparticles. The microparticles produced with HiCap 100 and corn syrup/HiCap 100 (50/50) stabilized by lecithin-chitosan showed the highest oxidative stability. The sun protection factor of particles ranged from 1.37 and 2.45 and 2.12 for the pure green coffee oil / Mestrado / Engenharia de Alimentos / Mestra em Engenharia de Alimentos

Made available in DSpace on 2014-12-17T15:41:47Z (GMT). No. of bitstreams: 1 AnneGDS_DISSERT.pdf: 3113468 bytes, checksum: a8146612a95169da2fa541dd638d6763 (MD5) Previous issue date: 2010-02-26 / The search for new sources of environmentally friendly energy is growing every day. Among these alternative energies, biodiesel is a biofuel that has had prominence in world production. In Brazil, law 11.097, determine that all diesel sold in the country must be made by mixing diesel/biodiesel. The latter called BX, , where X represents the percent volume of biodiesel in the diesel oil, as specified by the ANP. In order to guarantee the quality of biodiesel and its mixtures, the main properties which should be controlled are the thermal and oxidative stability. These properties depend mainly of the chemical composition on the raw materials used to prepare the biodiesel. This dissertation aims to study the overall thermal and oxidative stability of biodiesel derived from cotton seed oil, sunflower oil, palm oil and beef tallow, as well as analyze the properties of the blends made from mineral oil and biodiesel in proportion B10. The main physical-chemical properties of oils and animal fat, their respective B100 and blends were determined. The samples were characterized by infrared and gas chromatography (GC). The study of thermal and oxidative stability were performed by thermogravimetry (TG), pressure differential scanning calorimeter (PDSC) and Rancimat. The obtained biodiesel samples are within the specifications established by ANP Resolution number 7/2008. In addition, all the blends and mineral diesel analyzed presented in conformed withthe ANP Regularion specifications number 15/2006. The obtained results from TG curves data indicated that the cotton biodiesel is the more stable combustible. In the kinetic study, we obtained the following order of apparent activation energy for the samples: biodiesel from palm oil > sunflower biodiesel > tallow biodiesel > cotton biodiesel. In terms of the oxidative stability, the two methods studied showed that biodiesel from palm oil is more stable then the tallow. Within the B100 samples studied only the latter were tound to be within the standard required by ANP resolution N? 7. Testing was carried out according to the EN14112. This higher stability its chemical composition / A busca por novas fontes de energia, que sejam ecologicamente corretas, cresce a cada dia. Dentre essas energias alternativas, o biodiesel ? um dos biocombust?veis que vem tendo destaque na produ??o mundial. No Brasil, a Lei n? 11.097, determina que todo diesel vendido no pa?s, deve ser constitu?do pela mistura de ?leo diesel/biodiesel, denominado BX, onde X representa o percentual em volume de biodiesel no ?leo diesel, conforme especifica??o da Ag?ncia Nacional do Petr?leo (ANP). Entre as principais propriedades que devem ser controladas para garantir a qualidade do biodiesel est?o as estabilidades t?rmica e oxidativa, as quais dependem, basicamente, da composi??o da mat?ria prima utilizada. Este trabalho tem como objetivo estudar a estabilidade t?rmica e oxidativa de biodieseis provenientes dos ?leos de algod?o, girassol, dend? e do sebo bovino, assim como analisar as propriedades das blendas feitas do ?leo mineral com biodiesel, na propor??o B10. Foram determinadas as principais propriedades f?sico-qu?micas dos ?leos vegetais e gordura animal, das respectivas amostras de B100 e suas misturas, al?m de caracteriza??es atrav?s de infravermelho e cromatografia a g?s. O estudo das estabilidades t?rmica e oxidativa foram realizados atrav?s de Termogravimetria (TG), Calorimetria Explorat?ria Diferencial sob Press?o (PDSC) e Rancimat. As amostras de biodiesel obtidas est?o dentro das especifica??es estabelecidas pela Resolu??o da ANP No7/2008. As misturas analisadas e o diesel mineral apresentaram todos os resultados em conformidade com as especifica??es da Portaria da ANP N?15/2006. Os resultados obtidos via TG apontam o biodiesel de algod?o como o mais est?vel. No estudo cin?tico, obteve-se a seguinte ordem de energia de ativa??o aparente: biodiesel de dend? > biodiesel de girassol > biodiesel de sebo > biodiesel de algod?o. Em rela??o ? estabilidade oxidativa os resultados obtidos via PDSC e Rancimat indicaram que o biodiesel de dend? foi o mais est?vel, e em seguida o de sebo. Dentre os B100 estudados, o de dend? e sebo bovino, se encontraram dentro dos padr?es exigidos na Resolu??o ANP N?7 (tempo de indu??o 6h), os ensaios foram realizados de acordo com a norma Europ?ia EN14112, a temperatura de 110?C. A maior estabilidade do biodiesel de dend? pode ser atribu?do ? sua composi??o qu?mica

Made available in DSpace on 2016-08-19T12:56:36Z (GMT). No. of bitstreams: 1 MIRELA GHISI.pdf: 1324849 bytes, checksum: 5d9ca5c5a49c366f3bf4959e2e942a14 (MD5) Previous issue date: 2011-05-16 / Conselho Nacional de Desenvolvimento Científico e Tecnológico / The metals content in biodiesel is directly related with the raw material used and also with the utilized biodiesel production method. In this work, an evaluation of the main metals present in biodiesel samples from different sources was done. The qualitative analysis of the metal content was assessed using the Inductively Coupled Plasma Mass Spectrometry technique after sample digestion in microwave oven. The main metals identified in the analyzed biodiesel samples were Al, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Sr and Zn. Metals like Ag, As, Ba, Cd, Co, Tl and V have not significant presence in the samples. Among these, Cu and Fe were selected due to their relevance and importance in oxidative process of biodiesel, to the development of an analytical methodology to be used in the determination by Electrothermal Atomic Absorption Spectrometry, and also evaluate the effect of these metals over the oxidative stability of the soy biodiesel. The samples were prepared with tetramethylammonium hydroxide (TMAH), and the pyrolysis and atomization temperatures were optimized pyrolysis and atomization curves. The high pyrolysis temperature adopted, 1000 oC, certainly minimized potential interferences, but calibration had to be carried out with aqueous standard solutions in the presence of the TMAH. The detection limits in the sample (3s, n=10), were quite low 15 ng g-1 and 24 ng g-1 for Cu and Fe, respectively. Seven biodiesel samples, produced from different raw materials, including vegetable seed, waste frying oil and animal fat were analyzed. Accuracy was validated by applying the recovery test (recoveries from 105% to 120%) and through comparison with the obtained results by High Resolution Continuum Source Electrothermal Atomic Absorption Spectrometry. The precision, expressed by the relative standard deviation, was better than 3% for Cu and than 7% for Fe. Copper could be quantified in two and Fe in three of the seven samples. The biodiesel sample from fodder turnip was especially rich in the analytes in comparison to the other samples. The influence of metals Cu and Fe on soy biodiesel oxidative stability was evaluated by Rancimat method through induction period, according with the Standard EN 14112. The metals Cu2+ and Fe3+ were added to the biodiesel samples in the form of theirs salts, and different storage times of the samples were evaluated. Due to the catalytic behaviour of these metals, the oxidative stability of the samples was affected, even under low metal concentrations. Compared to Cu2+, the effect over the biodiesel stability was higher when Fe3+ was added. / A presença de metais no biodiesel está diretamente relacionada com a matéria-prima utilizada e também com o processo utilizado para a obtenção do biodiesel. Neste trabalho realizou-se uma avaliação dos principais metais presentes em amostras de biodiesel provenientes de diferentes fontes. A análise semi-quantitativa nas amostras de biodiesel foi realizada utilizando a técnica de Espectrometria de Massa com Plasma Indutivamente Acoplado após a digestão das amostras em micro-ondas. Os principais metais identificados nas amostras de biodiesel analisadas são Al, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Sr e Zn. Metais como Ag, As, Ba, Cd, Co, Tl e V não estão presentes em concentrações significativas nessas amostras. Em função de sua relevância e importância em processos oxidativos do biodiesel, selecionou-se Cu e Fe para o desenvolvimento de uma metodologia analítica para a determinação destes por Espectrometria de Absorção Atômica com Atomização Eletrotérmica e também a avaliação do efeito destes metais sobre a estabilidade oxidativa do biodiesel de soja. As amostras foram preparadas com hidróxido de tetrametilamônio (TMAH), e as temperaturas de pirólise e atomização foram otimizadas através de curvas de pirólise e atomização. A alta temperatura de pirólise adotada, 1000 oC, certamente ajudou a minimizar possíveis interferências; porém, a calibração teve de ser realizada com padrões aquosos na presença de TMAH. Os limites de detecção (3s, n = 10), na amostra, foram baixos, 15 ng g-1 e 24 ng g-1 para Cu e Fe, respectivamente. Sete amostras de biodiesel, produzidas de diferentes matérias-primas, incluindo óleos vegetais, óleo de fritura e gordura animal foram analisadas. A exatidão foi avaliada através do teste de recuperação (recuperações de 105% a 120%) e através da comparação com os resultados obtidos por Espectrometria de Absorção Atômica de Alta Resolução com Fonte Contínua e Atomização Eletrotérmica. A precisão, expressa pelo desvio padrão relativo foi melhor que 3% para Cu e que 7% para Fe. Cobre pôde ser quantificado em duas e Fe em três das sete amostras. A amostra de biodiesel proveniente do nabo forrageiro era especialmente rica nos analitos comparada às outras amostras. A influência dos metais Cu e Fe sobre a estabilidade oxidativa do biodiesel de soja foi avaliada pelo método Rancimat através do período de indução, de acordo com a Norma EN 14112. Os metais Cu2+ e Fe3+ foram adicionados nas amostras de biodiesel na forma de seus sais, e foram avaliados diferentes tempos de armazenamento das amostras. Devido ao efeito catalítico destes metais, a estabilidade oxidativa das amostras analisadas foi reduzida mesmo na presença de baixas concentrações dos metais. O efeito do Fe3+ sobre a estabilidade do biodiesel foi significativamente maior quando comparado ao Cu2+.

The major objectives of this study were to investigate the antioxidant properties of flaxseed lignans secoisolariciresinol (SECO 2) and secoisolariciresinol diglycoside (SDG 1) and their major oxidative compounds using 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH 47) in an in vitro model of lipid peroxidation. This investigation was facilitated by the structural elucidation of the major oxidative compounds and the ability of flaxseed lignans to delay the onset of oxidation in two model systems. <p>This study showed that SECO 2 oxidation occurs at the aromatic (4-OH) and aliphatic (9-OH) hydroxyl groups. Conversely for SDG 1, only compounds derived from the oxidation of aromatic hydroxyl groups were obtained because the 9-OH position is glucosylated. <p>SECO 2 oxidation with AAPH 47 showed that the intermediate 2a is most likely involved in the generation of early-forming (48 and 52) and 2c for the formation of late-forming (49, 50 and 51) oxidation compounds. Compound 48 is formed from dimerization of 2a that is converted to 52 and then to 51. Compound 50 was formed by the addition of a carbon-centre free radical of AAPH (AP radical) to 2c. Compounds 50 and 51 trap carbon-centered AP radicals supporting SECO 2 as a chain-breaking antioxidant and AAPH 47 as a proper model for study of SECO 2 oxidation in vitro. <p>SDG 1 oxidation with AAPH 47 indicated that intermediates 1b and 1c are most likely involved for the formation of early forming compounds (55 and 58) and 1a leads to the late forming compounds (56 and 57). Compound 55 is a result of dimerization. Compound 56 may be directly formed via intermediate radical 1a by adding AP free radicals. Compound 56 was a stable non-radical compound that could trap AP free radicals, thereby supporting SDG 1 as a chain-breaking antioxidant. Hydrogen abstraction from 4-hydroxyl yielded the radical 1a and hydroxyl radical addition to 1a yielded 57. Compound 58 formed from the addition of OH or H2O to 1c. <p>This study demonstrated that AAPH 47 produces carbon-centred AP radicals upon thermal decomposition and mimics the formation of lipid peroxyl radicals. Interaction of carbon-centred AP radicals with SECO 2 and SDG 1 provides a good model to study the antioxidant reactions of SECO 2 in vitro. p*The relative antioxidant capacity of the flaxseed lignans versus BHT 17, in two model systems, was determined. The stoichiometric ratio for SECO 2 and SDG 1 were 1.5 and 1.1-1.2, respectively, compared to BHT 17 (2.0). The induction time by Rancimat analyzer measured inhibition of autoxidation mediated by flaxseed lignans SECO, SDG and SDG polymer in comparison with BHT 17. The induction time data demonstrated that SECO 2 protected canola oil better than either SDG 1 or SDG polymer 3. <p>These results are important for better understanding about the chemistry behind flaxseed lignan antioxidant activities. This study provided useful evidence that flaxseed lignans can be used as natural antioxidants.

The major objectives of this study were to investigate the antioxidant properties of flaxseed lignans secoisolariciresinol (SECO 2) and secoisolariciresinol diglycoside (SDG 1) and their major oxidative compounds using 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH 47) in an in vitro model of lipid peroxidation. This investigation was facilitated by the structural elucidation of the major oxidative compounds and the ability of flaxseed lignans to delay the onset of oxidation in two model systems. <p>This study showed that SECO 2 oxidation occurs at the aromatic (4-OH) and aliphatic (9-OH) hydroxyl groups. Conversely for SDG 1, only compounds derived from the oxidation of aromatic hydroxyl groups were obtained because the 9-OH position is glucosylated. <p>SECO 2 oxidation with AAPH 47 showed that the intermediate 2a is most likely involved in the generation of early-forming (48 and 52) and 2c for the formation of late-forming (49, 50 and 51) oxidation compounds. Compound 48 is formed from dimerization of 2a that is converted to 52 and then to 51. Compound 50 was formed by the addition of a carbon-centre free radical of AAPH (AP radical) to 2c. Compounds 50 and 51 trap carbon-centered AP radicals supporting SECO 2 as a chain-breaking antioxidant and AAPH 47 as a proper model for study of SECO 2 oxidation in vitro. <p>SDG 1 oxidation with AAPH 47 indicated that intermediates 1b and 1c are most likely involved for the formation of early forming compounds (55 and 58) and 1a leads to the late forming compounds (56 and 57). Compound 55 is a result of dimerization. Compound 56 may be directly formed via intermediate radical 1a by adding AP free radicals. Compound 56 was a stable non-radical compound that could trap AP free radicals, thereby supporting SDG 1 as a chain-breaking antioxidant. Hydrogen abstraction from 4-hydroxyl yielded the radical 1a and hydroxyl radical addition to 1a yielded 57. Compound 58 formed from the addition of OH or H2O to 1c. <p>This study demonstrated that AAPH 47 produces carbon-centred AP radicals upon thermal decomposition and mimics the formation of lipid peroxyl radicals. Interaction of carbon-centred AP radicals with SECO 2 and SDG 1 provides a good model to study the antioxidant reactions of SECO 2 in vitro. p*The relative antioxidant capacity of the flaxseed lignans versus BHT 17, in two model systems, was determined. The stoichiometric ratio for SECO 2 and SDG 1 were 1.5 and 1.1-1.2, respectively, compared to BHT 17 (2.0). The induction time by Rancimat analyzer measured inhibition of autoxidation mediated by flaxseed lignans SECO, SDG and SDG polymer in comparison with BHT 17. The induction time data demonstrated that SECO 2 protected canola oil better than either SDG 1 or SDG polymer 3. <p>These results are important for better understanding about the chemistry behind flaxseed lignan antioxidant activities. This study provided useful evidence that flaxseed lignans can be used as natural antioxidants.

<p>Podizanje novih zasada i povećanje kapaciteta prerade<br />grožđa povećava količinu otpada sa kojim se suočava<br />industrija proizvodnje vina i rakije. Najbolji i najodgovorniji<br />način upravljanja otpadom je njegovo dalje iskori&scaron;ćenje<br />kao nusproizvoda. U ovoj disertaciji sagledavana je mogućnost iskori&scaron;ćenja<br />nusproizvoda iz različitih faza proizvodnje u vinarijama i<br />destilerijama za dobijanje semenki grožđa koje su<br />kori&scaron;ćene za proizvodnju hladno presovanog ulja. Hipoteza<br />se zasniva na činjenici da semenke grožđa raznih sorti iz<br />različitih faza proizvodnje vina (bela, roze ili crvena vina),<br />odnosno, rakije mogu imati sasvim različit hemijski sastav i<br />kvalitet koji svakako može da se reflektuje na kvalitet,<br />bioaktivne komponente i održivost hladno presovanog ulja.<br />Ovakav proizvod, obzirom da je dobijen hladnim<br />presovanjem, može biti veoma atraktivan za potro&scaron;ače,<br />zbog svojih specifičnih senzorskih i nutritivnih<br />karakteristika.<br />Za potrebe izrade disertacije prikupljeni su nusproizvodi<br />i pripremljeni su uzorci iz vinarija i destilerija fru&scaron;kogorskog<br />vinogorja. Dobijene su semenke i proizvedeno hladno<br />presovano ulje od semenki crnog grožđa sorte Merlot,<br />belog grožđa sorte Italijanski rizling i belog grožđa sorte<br />Sila, kao autohtone sorte vinove loze. Hladno presovana<br />ulja su proizvedena od semenki grožđa koje nisu pro&scaron;le<br />nikakav tretman, odnosno dobijene su nakon presovanja,<br />prilikom proizvodnje belih (Italijanski rizling i Sila) i roze<br />(Merlot) vina, zatim od semenki koje su pro&scaron;le proces<br />fermentacije prilikom proizvodnje crvenih vina (Merlot) i od<br />semenki koje su pro&scaron;le proces fermentacije i destilacije<br />prilikom proizvodnje rakije (Merlot, Italijanski rizling i Sila).<br />Pored navedenih semenki i ulja, pripremljen je i prosečan<br />proizvodni uzorak koji predstavlja uzorak dobijen od svih<br />prikupljenih semenki. Kao uporedni uzorci kori&scaron;ćeno je<br />nerafinisano i rafinisano ulje od semenki grožđa nabavljeno<br />na trži&scaron;tu. Za realizaciju postavljenog cilja, rad na izvođenju ove<br />disertacije obuhvatio je različite faze. U prvoj fazi<br />prikupljene su semenke grožđa i ispitivane su njihove<br />tehničko-tehnolo&scaron;ke karakteristika i kvalitet. Zatim su od<br />navedenih semenki proizvedena hladno presovana ulja.<br />U sledećim fazama, ovako dobijena uja, zajedno sa<br />uzorkom nerafinisanog i rafinisanog ulja od semenki<br />grožđa sa trži&scaron;ta ispitivana su sa aspekta senzorskog i<br />nutritivnog kvaliteta i praćene su razlike u održivosti ulja.<br />Izvr&scaron;ena je senzorska analiza, određivane su frakcije<br />pigmenata, karotenoidi i hlorofili, merena je transparencija,<br />a parametri boje ulja određivani su i instrumentalno.<br />Nutritivni kvalitet ulja sagledavan je na osnovu sadržaja i<br />sastava bioaktivnih komponenti, pre svega tokoferola i<br />tokotrienola, fenola i sterola. Budući da ova jedinjenja<br />ispoljavaju značajne antioksidativne aktivnosti izvr&scaron;eno je i<br />ispitivanje antiradikalske aktivnosti uzoraka. Odživost ulja<br />od semenki grožđa sagledana je na osnovu početnog<br />kvaliteta i oksidativnog stanja, kao i rezultata ubrzanih<br />testova, kao &scaron;to je Rancimat test, Schaal-oven test i<br />fluorescentni test.<br />Na osnovu dobijenih rezultata, može se konstatovati da<br />su svi dobijeni uzorci semenki imali dobru skladi&scaron;nu vlagu,<br />koja, obzirom na mali sadržaj ulja u semenkama, može da<br />osigura čuvanje semenki u dužem periodu. Sadržaj ulja u<br />semenkama, pored uticaja sorte vinove loze, zavisi i od<br />uticaja procesa kome su podvrgnute semenke pre<br />presovanja (fermentacija, destilacija).<br />Senzorska analiza ulja od semenki grožđa pokazala je<br />značajne razlike u karakteristikama koje su posledica ne<br />samo načina dobijanja ulja (hladno presovano ili rafinisano), sorte vinove loze, već i postupka dobijanja,<br />porekla i kvaliteta semenki grožđa. Uslovi kojima su<br />semenke grožđa izložene u toku alkoholne fermentacije i<br />posebno destilacije utiču na formiranje specifične arome<br />hladno presovanog ulja. I pored toga &scaron;to se pojavljuje<br />izuzetno &scaron;irok spektar različitih aroma, mirisa i ukusa u ulju<br />i &scaron;to postoje značajne razlike u aromi ulja u zavisnosti od<br />sorte grožđa, moguće je prepoznati da li je hladno<br />presovano ulje dobijeno od semenki grožđa bez<br />fermentacije, posle fermentacije ili posle destilacije.<br />Takođe, sa aspekta boje ulja može se kazati da rafinisano<br />ulje od semenki grožđa ima svetlo žutu boju sa<br />zelenkastom nijansom, dok su hladno presovana ulja<br />intenzivnijih boja i kreću se od žuto-zelenkaste, preko<br />zelenkasto žute i svetlo zelenkaste do tamno zelene. Veći<br />udeo zelene boje imaju hladno presovana ulja od semenki<br />grožđa dobijenih posle destilacije.<br />U radu je pokazano da sadržaj pigmenata (karotenoida i<br />hlorofila) u velikoj meri zavisi od porekla semenki.<br />Postupak fermentacije doprinosi povećanju sadržaja<br />pigmenata, dok postupak destilacije, zbog visokih<br />temperatura ima negativan efekat.<br />Transparencija uzoraka hladno presovanih ulja od<br />semenki grožđa proizvedenih za potrebe disertacije kretala<br />se od 32,8% do 53,8%.<br />Sadržaj nezasićenih masnih kiselina u svim uzorcima<br />ulja od semenki grožđa veći je od 90%, pri čemu<br />dominantnu masnu kiselinu čini linolna, omega-6, masna<br />kiselina.<br />Sadržaj tokotrienola je veći od sadržaja tokoferola u uljima od semenki grožđa, a dominantni tokoferol je alfatokoferol.<br />Njegov sadržaj je veći u uzorcima ulja dobijenim<br />iz semenki nakon fermentacije i destilacije.<br />Sadržaj fenolnih jedinjenja, u zavisnosti od sorte, u<br />proseku je ne&scaron;to vi&scaron;i u hladno presovanim uljima dobijenim<br />od crvene sorte grožđa, ali uočava se i značajan porast<br />(akumulacija) fenola u hladno presovanim uljima dobijenim<br />iz semenki grožđa nakon procesa fermentacije i destilacije.<br />Najveći pojedinačni sadržaju u ulju od semenki grožđa ima<br />ursolna kiselina, a pored nje značajniji sadržaj, mada<br />mnogo manji, pokazuju rezveratrol, kemferol i vanilinska<br />kiselina.<br />Najzastupljeniji steroli ulja semenki grožđa su &beta;-<br />sitosterol sa udelom od 62,59-69,74%, stigmasterol sa<br />udelom od 12,13-15,00% i kampesterol sa udelom od 6,59-<br />11,94% u ukupnim sterolima. Na sadržaj fitosterola u<br />uljima od semenki grožđa nemaju uticaja procesi<br />fermentacije i destilacije kojima su podvrgnute semenke<br />pre preosvanja.<br />U radu je dokazan negativan uticaj procesa fermentacije<br />i destilacije kojima su povrgnute semenke grožđa na<br />antiradikalski potencijal dobijenih ulja. Antiradikalski<br />potencijal ulja od semenki grožđa zavisi i od sorte vinove<br />loze, kao i od načina dobijanja ulja (hladno presovano ili<br />rafinisano).<br />Procesi fermentacije i destilacije utiču i na osnovni<br />hemijski kvalitet dobijenih hladno presovanih ulja na način<br />da dovode do povećanja kiselinskog i peroksidnog broja.<br />Hladno presovana ulja od semenki grožđa pokazuju<br />dobru oksidativnu stabilnost. Rancimat test je pokazao razlike u indukcionom periodu hladno presovanih ulja od<br />semenki grožđa kao posledicu razlike u sorti, kao i u<br />načinu dobijanja semenki. Proces fermentacije utiče na<br />povećanje, a proces destilacije na smanjenje indukcionog<br />perioda.<br />Na osnovu svih dobijenih rezultata istraživanja može se<br />konstatovati da su hladno presovana ulja od semenki<br />grožđa pokazala različit nutritivni kvalitet i oksidativnu<br />stabilnost, zbog specifičnih razlika koje su posledica razlika<br />u sorti i poreklu semenki, tj. zbog specifičnog efekta<br />fermentacije i destilacije na semenke od kojih je ulje<br />proizvedeno, čime je i potvrđena hipoteza.</p> / <p>Raising new plantations and increasing the grape<br />processing capacity increases the amount of waste faced<br />by the wine and brandy industry. The best and most<br />responsible way of waste management is its further<br />exploitation as by-products.<br />In this dissertation, the possibility of using by-products from different stages of production in wineries and distilleries for<br />obtaining grape seeds, which were used for the production<br />of cold pressed oil, was examined. The hypothesis is<br />based on the fact that grape seeds of various varieties<br />from different stages of wine production (white, rose or red<br />wine), that is, brandy can have a completely different<br />chemical composition and quality that can certainly be<br />reflected on the quality, bioactive components and stability<br />of cold pressed oil.<br />Such a product, as it is obtained by cold pressing, can<br />be very attractive to consumers, due to its specific sensory<br />and nutritional characteristics.<br />For the needs of the dissertation, the by-products were<br />collected and samples were prepared from the wineries<br />and distilleries of the Fru&scaron;ka Gora vineyard. Seeds were<br />obtained and cold pressed oil produced from Merlot grape<br />seed, as representatives of red grape varieties, Italian<br />Riesling, as representatives of white grape varieties and<br />Sila, as new white grape varieties. Cold pressed oils were<br />produced from grape seeds that did not undergo any<br />treatment, that is, they were obtained after pressing, during<br />the production of white (Italian Riesling and Sila) and rose<br />(Merlot) wines, then from the seeds that were fermented<br />during the production of red wines (Merlot ) and seeds that<br />have undergone fermentation and distillation process<br />during the production of brandy (Merlot, Italian Riesling and<br />Sila). In addition to the mentioned seeds and oils, an<br />average production sample was prepared, which is a<br />sample obtained from all collected seeds. Unrefined and<br />refined grape seed oil purchased on the market was used<br />as comparative samples. For realization of the set goal, the work on the<br />performance of this dissertation encompassed different<br />phases. In the first phase, grape seed were collected and<br />their technical and technological characteristics and quality<br />were examined. Then cold-pressed oils were produced<br />from these seeds.<br />In the following phases, the resulting ear, together with a<br />sample of unrefined and refined grape seed oil from the<br />market, were examined from the aspect of sensory and<br />nutritional quality and differences in oil stability were<br />observed. Sensory analysis was performed, pigmentate<br />fractions, carotenoids and chlorophylls were determined,<br />transparency was measured, and oil color parameters<br />were also determined instrumentally. The nutritive oil<br />quality was examined based on the content and<br />composition of bioactive components, primarily tocopherols<br />and tocotrienols, phenols and sterols. Since these<br />compounds exhibit significant antioxidant activities, the<br />antiradical activity of the samples was also tested. The<br />stability of grape seed oils was examined based on the<br />initial quality and the oxidative state, as well as the results<br />of accelerated tests, such as Rancimat test, Schaal-oven<br />and fluorescence test.<br />On the basis of the obtained results, it can be concluded<br />that all the obtained seed samples had good storage<br />moisture, which, given the small content of oil in the seeds,<br />can ensure the storage of seeds for a longer period. The<br />content of oil in the seed, in addition to the influence of the<br />grape variety, depends on the influence of the process to<br />which the seeds are subjected to pressing (fermentation,<br />distillation). Sensory analysis grape seed oils showed significant<br />differences in characteristics that are due not only to the<br />method of obtaining oil (cold pressed or refined), grape<br />varieties, but also the method of obtaining, the origin and<br />quality of grape seed. The conditions for grape seeds<br />exposed during fermentation and especially distillation<br />affect the formation of a specific cold pressed oil. Although<br />an extremely wide range of different flavors, odors and<br />flavors in oil appear, and there are significant differences in<br />the aroma of the oil, depending on the grape variety, it is<br />possible to recognize whether the cold-pressed oil is<br />derived from the grape seed without fermentation, after<br />fermentation or after distillation. Also, from the aspect of oil<br />color it can be said that refined grape seed oil has a light<br />yellow color with a greenish shade, while cold pressed<br />grape seed oils have more intense colors range from<br />yellowish-greenish, over greenish yellow and light greenish<br />to dark green. A higher proportion of green color has cold<br />pressed grape seed oils obtained after distillation.<br />The thesis has shown that the content of pigments<br />(carotenoids and chlorophyll) depends to a great extent on<br />the origin of the seed. The fermentation process<br />contributes to increasing the content of pigments, while the<br />distillation process has a negative effect due to high<br />temperatures.<br />Transparency of cold pressed grape seed oils produced<br />for the dissertation ranged from 32.8% to 53.8%.<br />The content of unsaturated fatty acids in all samples of<br />grape seed oil is greater than 90%, with the dominant fatty<br />acid being linoleic, omega-6, fatty acid. The content of tocotrienols is higher than the content of<br />tocopherols in grape seed oils, and the dominant<br />tocopherol is alpha-tocopherol. Its content is higher in oil<br />samples obtained from the seed after fermentation and<br />distillation.<br />The content of phenol compounds, depending on the<br />variety, is somewhat higher in cold pressed oils obtained<br />from red grape varieties, but there is also a significant<br />increase in accumulation of phenol in cold pressed oils<br />obtained from the grape seed after the fermentation and<br />distillation process. The largest individual oil content of<br />grape seeds has ursolic acid, and besides it, significant<br />content, although much smaller, shows rezveratrol,<br />kemferol and vanillinic acid.<br />The most prevalent sterols of grape seed oils are &beta;-<br />sitosterol with a share of 62.59-69.74%, stigmasterol with a<br />share of 12.13-15.00% and campesterol with a share of<br />6.59-11.94% in total sterols. Fermentation and distilation<br />processes, to which the seeds have been exposed, have<br />no effect on the content of phytosterols in grape seed oils.<br />The paper has shown the negative influence of the<br />fermentation and distillation process, to which the seeds<br />have been exposed, onto the antiradical potential of the<br />obtained oils. The antiradical potential of grape seed oils<br />depends on grape varietes, as well as on the way oil is<br />obtained (cold pressed or refined).<br />Processes of fermentation and distillation also affect the<br />basic chemical quality of obtained cold pressed oils in such<br />a way as to increase the acid and peroxide values.<br />Cold pressed grape seed oils show good oxidative stability. The Rancimat test showed differences in the<br />induction period of cold pressed grape seed oils as a result<br />of the variation in the variety, as well as in the method of<br />obtaining the seed. The fermentation process affects the<br />increase, and the process of distillation decreases the<br />induction period.<br />Based on all the obtained results, it can be concluded<br />that cold pressed grape seed oils showed different<br />nutritional quality and oxidative stability due to specific<br />differences resulting from differences in variety and seed<br />origin, i.e. due to the specific effect of fermentation and<br />distillation processes on the seeds from which the oil was<br />produced, thus confirming the hypothesis.</p>