Efeito da adição de farinha de linhaça à dieta sobre a concentração de colesterol e ácidos graxos em camarões / The effect of feed added of linseed on cholesterol and fatty acids in shrimp

Avaliou-se a expressão de ácidos graxos, macronutrientes e colesterol de camarões-da-malásia alimentados com dieta adicionada de sementes de linhaça. Quinhentos camarões foram distribuídos em dois grupos e alimentados durante 90 dias com dietas contendo: 1) lipídeo proveniente de linhaça e 2) óleo de soja (controle). A concentração de proteína foi maior (Р<0,05) para o grupo-linhaça, 15,8±0,09%, em relação ao grupo-controle, 15,2±0,04%. O peso corporal também se apresentou maior no grupo-linhaça, 1,38±0,93g, em relação ao grupo-controle, 0,93±0,48g. O grupo-linhaça apresentou teor de colesterol de 120,8±23,9mg/100g e o grupo-controle, 130,2±13,9mg/100g, porém sem diferença estatística significativa. Em relação ao perfil lipídico, a suplementação da dieta com linhaça influenciou a incorporação do ácido oleico (C18:1, ω-9) e melhorou a relação ω-6/ω-3 na carne do camarão (Р<0,05). Concluiu-se que a adição de linhaça à ração promoveu importantes modificações na qualidade nutricional dos tecidos do camarão.

The aim of the present study was to analyze the chemical composition of shrimp fed with a diet added of linseed flour. Five hundred post larvae shrimp were divided into two groups: a linseed group fed with a diet based on casein complemented with linseed and a control group, fed a diet without linseed flour. The cholesterol content for the linseed group was 120.8±23.9 mg/100g while for the control group it was 130.2±13.9 mg/100g. However, the protein content of 15.8±0.09 % and the body weight of 1.38±0.93g for the linseed group were higher than for the control group. It was concluded that the addition of linseed to the diet seems to increase the protein, weight and oleic acid (C18:1, ω-9) in the shrimp tissue. The ratio of polyunsaturated fatty acids/saturated fatty acids and ω-6/ω-3 for the linseed group was more suitable than for the control group.

Fractions composition study of the pyrolysis oil obtained from sewage sludge treatment plant.

In this work the parameters of Low Temperature Conversion--LTC were applied in a centrifuged sludge from a sewage treatment plant located in Rio de Janeiro, Brazil. Before the conversion, the sludge was dried and analyzed by TGA to observe its behavior with increasing temperature. The chemical composition of the crude pyrolysis oil was analyzed by FTIR, 1H NMR and GC-MS. The results showed that the oil is a mixture of hydrocarbons, oxygenated and nitrogenated compounds. Using a catalytic treatment it was possible to fractionate the oil where the predominant constituents were hydrocarbons showing that the cracking was effective. An important result was the difference between the calorific value of dry sludge (10 MJ kg(-1)), the pyrolysis oil (36 MJ kg(-1)) and one of the fractions separated by catalytic cracking (40 MJ kg(-1)) when compared with commercial diesel (45 MJ kg(-1)).

Low temperature conversion (LTC)--an alternative method to treat sludge generated in an industrial wastewater treatment station--batch and continuous process comparison.

In this work low temperature conversion (LTC) process was applied in a dried sludge from a petrochemical industry wastewater treatment station located in Rio de Janeiro, Brazil. The process was performed in two modes: continuous and batch-scale. This process produced a pyrolysis oil (continuous 14%; batch-scale 40% yield); pyrolytic char (continuous 46%; batch-scale 56% yield); gas and water. Pyrolysis oil fraction was analyzed by gas chromatographic mass spectrometry (GCMS) and the main components identified were toluene, ethylbenzene, styrene, isopropyl benzene, alpha-methylstyrene, butanenitrile and 1,3- biphenyl propane. Metals content, sulfur content and calorific value have been determined for the pyrolysis oil fraction. The results showed that the pyrolysis oil obtained could be used for industrial purposes and/or as energetic matrix.

Low temperature conversion of sludge and shavings from leather industry.

Abstract Brazil has one of the largest herds of cattle in the world, with more than 170 million heads. Over 400 farms have exported more than 2,875 ton (in 1997) of leather to Europe. The wet blue tanning process uses chemicals such as chromium compounds and produces liquid wastes that must be treated by physicochemical and biological systems. About 15,000 ton per month of dewatering sludge with 24% solids content is disposed of into landfills. During the process, pre-tanned skins (wet blue leather) are shaved to the desired thickness and the shavings, like sludge, are among the wastes that must have special attention. The organic content and chromium concentration are high. About 12% of the leather production from cattle hides are shavings, and its chromium concentration ranges from 3.5 to 5.5% of dry matter. The Environmentally friendly leather project, a co-operation between Brazilian and German tanneries, universities and technical schools, is looking for process optimisation, waste minimisation and adequate treatment for solid and liquid wastes from the leather industry. This work presents results of Low Temperature Conversion of chrome-containing sludge and shavings in a laboratory batch reactor, offering a solution for these hazardous wastes, recovering the energy content and transforming metals in insoluble sulphides.

Inibiçäo seletiva das atividades das enzimas transcriptase reversa do vírus HIV-1 e DNA polimerases humanas por derivados dipirazolo-piridina / Selective inhibition of reverse transcriptase enzyme activity of HIV-1 virus and human polymerases DNA by dipirazolo-pyridines derivatives

Novos ribonucleosídeos derivados dos sistemas dipirazolo-piridina foram preparados e avaliados quanto à atividade polimerásica das enzimas transcriptase reversa (RT) do vírus HIV-1 e das DNA polimerases humanas alfa e epsilon. Os derivados 1b e 1d inibiram a atividade da transcriptase reversa em concentraçöes de micromolares. Entretanto, as mesmas substâncias näo foram capazes de inibir a atividade polimerase das enzimas DNA-polimerase humana alfa e epsilon.