The objective of this investigation was to observe and evaluate the effects of surfactants on the biodegradation of toluene in the subsurface. Soil microcosms containing gasoline were used to simulate conditions of an aquifer contaminated with hydrocarbons. The surfactants were the nonionics, Surfonic N-40 and N-95. Three volumes of gasoline, 0.005, 0.05, and 0.1 mL, were injected into separate microcosms in order to observe changes in toluene concentration in both adsorbed component conditions and free-phase, interstitial gasoline conditions. The data presented are the results from the microcosms containing 0.005 mL gasoline. -Dissolved toluene was only partially biodegraded in the microcosms containing free-phase hydrocarbons. The lack of complete biodegradation was believed to be due to substrate toxicity. / Master of Science

This article studies the impact of some environmental conditions and the nutrition of culturing medium on the growth of bacteria and theirs capacity of toluene removal. The 5 bacterial strains isolated from leaf samples of three different common houseplants in Vietnam are Gram-negative, rod-shaped bacteria. The cells are single or arranged in chains. The cell size is relatively small and ranged from 0.7 to 2.5μm. These bacteria prefer the incubating temperature from 28°C to 32°C and a neutral pH 6.5 to 7.5. They are able to assimilate different nitrogen and carbon sources. In the liquid SH1 medium containing 200ppm toluene five selected strains have shown the ability to degrade toluene at a rate of 12.8 to 75.2% in comparison with the control at 30°C at a speed of 200rpm for over 120 hours. These 5 studied strains are potentially useful in bioremediation strategies to remove airborne toluene. / 5 chủng vi khuẩn có khả năng phân giải toluene được phân lập từ lá một số cây cảnh phổ biến ở Việt Nam là vi khuẩn G (-), dạng trực khuẩn và kích thước tế bào từ 0,7 – 2,5μm. Một số điều kiện môi trường nuôi cấy thích hợp cho 5 chủng vi khuẩn nghiên cứ gồm nhiệt độ 28°C-32°C, pH 6,5- 7,5, có khả năng đồng hoá nhiều nguồn nitơ và ba nguồn carbon khác nhau. Trong điều kiện môi trường dịch SH1 chứa 200ppm toluene, 5 chủng vi khuẩn này cho thấy khả năng phân giải toluene từ 12,8 – 75,2%. Đây là các chủng vi khuẩn có tiềm năng ứng dụng để loại bỏ toluene từ không khí ô nhiễm.

The Onsager heat of transport for p-tert-butyltoluene was measured, as part of a series of preliminary experiments towards the determination of the importance of temperature gradients on the air-sea flux of carbon dioxide. The results presented in this thesis imply that the temperature gradient is a major contributor to the magnitude of the air-sea flux. The heat of transport has been measured for the p-tert-butyltoluene system by measuring stationary-state pressure changes for known temperature differences on the vapour side of the interface. At the pressure ranges used the number of mean free paths was always outside the Knudsen zone, but the values of Q* were approximately 100 % of the latent heat of vaporisation. Departures from linearity of plots of P against ΔT are attributed to temperature jumps at the surface of the dry upper plate. Both the results taken for p-tert-butyltoluene and the earlier results for water from this laboratory fit to a Type III BET isotherm, where the c parameter is not constant. They also reveal the importance of the temperature gradient in determining the value of the thermal accommodation coefficient, and provide a new method of measuring thermal accommodation coefficients for a variety of surfaces and vapours

Inhalants are a loosely defined diverse group of volatile substances which people abuse. Despite widespread misuse of inhalants, there are limited preclinical methods available to study the reinforcement-like properties of inhalants. One procedure which has demonstrated substantial promise as a tool to investigate inhalant pharmacology is the intracranial self-stimulation (ICSS) procedure. ICSS utilizes pulses of electrical stimulation to the mesolimbic reward pathway to serve as a temporally defined and controlled operant reinforcer with a highly adjustable efficacy. The first aim of the project was to characterize the effects of commonly abused inhalants: including toluene, trichloroethane, nitrous oxide, isoflurane and R134a in ICSS. The second aim was to attenuate inhalant-facilitated ICSS by utilization of compounds which would attenuate the pharmacological actions of toluene on GABAA receptors. The low efficacy benzodiazepine negative modulator Ro15-4513 significantly attenuated the ability of toluene to facilitate ICSS without itself significantly altering baseline ICSS responding. Pretreatment with Ro15-4513 also attenuated methamphetamine ICSS even though there is no evidence of methamphetamine interacting with GABAA receptors. Given these unexpected results, I employed a microdialysis procedure to examine the effect of Ro15-4513 on methamphetamine stimulated dopamine release in the nucleus accumbens. Pretreatment with Ro15-4513 significantly attenuated methamphetamine stimulated dopamine release while having a negligible effect on dopamine release when administered alone. These results suggest that a modest level of benzodiazepine-site negative modulation can reduce the reinforcement enhancing effects of abused drugs regardless of their primary mechanism of action through allosteric modulation of GABAergic neurons within the mesolimbic pathway. Further, these results may have implications for expanding the examination of GABAA negative modulator medications beyond those trials currently being conducted with alcohol. Finally, the effects of chronic intermittent toluene exposure on ICSS and nesting behaviors were examined. Subjects were systemically exposed to air, chronic intermittent toluene (CIT), or escalating chronic intermittent (ECIT) toluene for 15 min at 3300 PPM toluene vapor per exposure. The results show that ECIT resulted in decreased overall responding in ICSS relative to air control and showed a tolerance-like effect to facilitatory effects of 3300 ppm toluene during ICSS compared to CIT group. These results indicate that escalating use of toluene produces reductions in its reward-like effects and may contribute to escalation to other drugs of abuse.

Hidrocarbonetos aromáticos conhecidos como BTEX (benzeno, tolueno, etilbenzeno e xilenos) estão entre os maiores problemas de poluição ambiental. Estes compostos são reconhecidos por sua recalcitrância em ambientes anóxicos, e a remoção destes hidrocarbonetos, de sítios anaeróbios contaminados é dependente da atividade de uma população de microrganismos adaptados capazes de promover a biodegradação destes compostos, nestas condições. Neste sentido, o presente trabalho buscou purificar, caracterizar e utilizar cultura desnitrificante, como inóculo para desenvolvimento de biofilme, em reator anaeróbio de leito fixo preenchido com espumas de poliuretano, além de avaliar o potencial deste biofilme em promover a biodegradação dos compostos de BTEX. Células da cultura apresentaram coloração Gram negativa, com morfologia de cocos (diplococos e cocobacilos). A cultura foi capaz de crescer, sob condições desnitrificantes, utilizando diferentes substratos. A cultura não apresentou capacidade de crescer sob condições sulfetogênicas. Velocidades de crescimento ('mü') de 0,046/h e 0,050/h e tempos de geração (Tg) de 15,1 horas e 13,9 horas foram obtidos para as células crescidas em benzeno e etilbenzeno, respectivamente. A cultura purificada foi utilizada para formar biofilme em RAHLF. Em todas as condições de alimentação as quais os reatores foram submetidos houve remoção da matéria orgânica, nitrato e dos hidrocarbonetos. A menor eficiência de remoção de hidrocarbonetos foi de 89,4%, obtida durante a alimentação dos reatores com benzeno. A matéria orgânica (DQO) foi removida com eficiência média de 87,1%. A eficiência média de remoção de nitrato foi de 94%. O sequenciamento das amostras revelou que o biofilme do RAHLF1 foi formado, principalmente, por espécies de Paracoccus, Pseudomonas e Bacteroides, enquanto que no RAHLF2, alimentado com etilbenzeno, observou-se espécies dos gêneros: Paracoccus, Pseudomonas, Xanthomonas e Variovorax / The monoaromatic hydrocarbons known as BTEX (benzene, toluene, ethylbenzene, and xylene) are among the greatest environmental pollution problems. These compounds are known by their recalcitrance in anoxic environments, and the removal of these toxics from anaerobic contaminated sites depends on the presence of an adapted microbial population capable of to promote the biodegradation of these compounds under such condition. Thus, in the current study a denitrifying culture was purified, characterized and used as inoculum to form a biofilm in a horizontal-flow anaerobic immobilized biomass reactor filled with polyurethane foam, and to assess the potential of this biofilm to promote BTEX compounds biodegradation. Culture cells were Gram negative, with coccus (diplococcus and cocobacilli) morphology. The culture was able to grow, under denitrifying conditions, using different substrates. No growth was seen in sulfate-reducing conditions. Growth velocity('mü') of 0.046/h and 0.050/h, and generation time of 15.1 and 13.9 hours were obtained for cultures isolated in the presence of benzene and ethylbenzene, respectively. The purified culture was used to form a biofilm inside RAHLF. At all feeding conditions the reactors were submitted the organic matter, nitrate and hydrocarbons were removed. The smallest hydrocarbons removal efficiency was 89.4%, obtained during benzene feeding. The organic matter (COD) was removed with mean efficiency of 87.1%. The mean efficiency of nitrate removal was 94.0%. Sequencing of samples showed that the RAHLF1 biofilm was composed specially for Paracoccus, Pseudomonas and Bacteroides species. Biofilm of RAHLF2 reactor, obtained from ethylbenzene feeding, was composed by Paracoccus, Pseudomonas, Xanthomonas and Variovorax species

O verapamil (VER) é um composto quiral comercializado como mistura racêmica dos enantiômeros (+)-(R)-VER e (-)-(S)-VER. O VER é biotransformado em norverapamil (NOR) e em outros metabólitos por vias dependentes do CYP. O tolueno e o n-hexano são solventes orgânicos que podem alterar o metabolismo de medicamentos dependente do CYP. Assim, o estudo investiga a estereosseletividade na farmacocinética do verapamil administrado a ratos na dose de 10 mg kg-1, sob forma racêmica, e do seu metabólito, norverapamil, bem como a influência do n-hexano e do tolueno na disposição cinética dos enantiômeros (+)-(R) e (-)-(S)-VER e (R)- e (S)-norverapamil em animais tratados com os solventes por inalação em câmara de exposição do tipo nose only nas concentrações de 88, 176 e 352 mg/m3 para o n-hexano e 94, 188 e 376 mg/m3 para o tolueno. Os enantiômeros do VER e do NOR foram separados na coluna de fase quiral Chiralpak® AD e analisados por LC-MS/MS (m/z = 441,3->165,5 para os enantiômeros do norverapamil e m/z 455,3->165,5 para os enantiômeros do verapamil). A análise farmacocinética foi realizada com base no modelo monocompartimental. A farmacocinética do verapamil é estereosseletiva em ratos do grupo controle não tratado com os solventes com acúmulo plasmático do eutômero (-)-(S)-VER (AUC0-? = 250,8 vs 120,4 ng mL-1 h; P<=0,05, teste de Wilcoxon). O metabólito (S)-NOR também foi acumulado no plasma dos animais do grupo controle com razão S/R relativa ao parâmetro AUC0-? de 1,5. Os parâmetros farmacocinéticos AUC0-?, Cl/F, Vd/F e t1/2 relativos aos enantiômeros (-)-S e (+)-(R)-VER e aos enantiômeros (S) e (R)-NOR não foram alterados pela exposição em câmara de exposição do tipo nose only ao n-hexano nas concentrações de 88, 176 e 352 mg/m3 e ao tolueno nas concentrações de 94, 188 e 376 mg/m3; teste de Kruskall-Wallis; P<=0,05. No entanto, a exposição ao n-hexano nas concentrações de 176 mg/m3 e 352 mg/m3 e ao tolueno nas concentrações de 94 mg/m3, 188 mg/m3 e 376 mg/m3 resultou em perda da enantiosseletividade observada para o grupo controle. / Verapamil (VER) is a chiral compound which is commercialized as a racemic mixture of the (+)-(R)-VER and (-)-(S)-VER enantiomers. VER is biotransformed into norverapamil (NOR) and other metabolites through CYP-dependent pathways. Toluene and n-hexane are organic solvents that can alter the metabolism of CYP-dependent drugs. The present study investigated the stereoselectivity in the pharmacokinetics of racemic VER administered to rats at a dose of 10 mg kg-1 and of its metabolite NOR. In addition, the influence of n-hexane and toluene on the kinetic disposition of the (+)-(R) and (-)-(S)-VER and (R)- and (S)-NOR enantiomers was analyzed in animals exposed by nose-only inhalation to n-hexane at concentrations of 88, 176 and 352 mg/m3 and to toluene at concentrations of 94, 188 and 376 mg/m3. The VER and NOR enantiomers were separated on a Chiralpak® AD chiral phase column and analyzed by LC-MS/MS (m/z = 441.3->165.5 for the NOR enantiomers and m/z 455.3->165.5 for the VER enantiomers). Pharmacokinetic analysis was performed using a monocompartmental model. The pharmacokinetics of VER was stereoselective in control rats not treated with the solvents, with plasma accumulation of the (-)-(S)-VER eutomer (AUC0-? = 250.8 vs 120.4 ng mL-1 h; P<=0.05, Wilcoxon test). The (S)-NOR metabolite was also found to accumulate in plasma of control animals, with an S/R AUC0-? ratio of 1.5. The pharmacokinetic parameters AUC0-?, Cl/F, Vd/F and t1/2 obtained for the (-)-S-VER, (+)-(R)-VER, (S)-NOR and (R)-NOR enantiomers were not altered by nose-only exposure to n-hexane at concentrations of 88, 176 and 352 mg/m3 or to toluene at concentrations of 94, 188 and 376 mg/m3 (P<=0.05), Kruskal-Wallis test). However, exposure to 176 and 352 mg/m3 n-hexane and to 94, 188 and 376 mg/m3 toluene resulted in the loss of enantioselectivity observed for the control group.

A princípio, foram realizados ensaios de enriquecimento em reatores em batelada, sob agitação, para avaliar a melhor condição nutricional, meio Beller ou meio Zinder, para crescimento microbiano e remoção de sulfato. Posteriormente, esta melhor condição nutricional foi usada para crescimento microbiano e remoção de etanol, tolueno e benzeno em ensaios contínuos em dois reatores anaeróbios horizontais de leito fixo (RAHLF), sob condições de redução de sulfato. Os sistemas foram inoculados com lodo de reator anaeróbio de fluxo ascendente e manta de lodo tratando águas residuárias provenientes de abatedouro de aves. Os RAHLF consistiram de biomassa imobilizada em espumas de poliuretano submetidas a concentrações de 91 e 550 mg/l de sulfato ferroso e sulfato de sódio, respectivamente, para promoção de ambiente sulfetogênico. Tolueno e benzeno foram adicionados, separadamente nos reatores, em concentrações iniciais de 2,0 mg/l, seguidas de aumentos que variaram até as concentrações finais de 9 e 10 mg/l, para tolueno e benzeno, respectivamente. O etanol foi adicionado em ambos reatores a concentração inicial de 170 mg/l, seguido de aumento de até 960 mg/l. Os reatores foram operados a 30 (± 2) ºC com tempo de detenção hidráulica de 12 h. A eficiência na remoção da matéria orgânica nos dois reatores foi próxima a 90% com taxa máxima de degradação de tolueno de 0,06 mg tolueno/mg ssv.d, e 0,07 mg benzeno/mg ssv.d, para benzeno. A redução de sulfato foi de 99,9% em todas as condições nutricionais nos dois reatores. A caracterização microscópica do biofilme revelou diversas morfologias e o perfil de DGGE mostrou variação nas populações de BRS e de representantes do Domínio Bacteria em geral, o que foi associado com as crescentes concentrações de tolueno e benzeno nos meios de alimentação. Finalmente, o presente trabalho demonstrou que unidades compactas de RAHLF, sob condições sulfetogênicas, oferecem alternativa para a biorremediação in situ de compostos aromáticos. / Previously, enrichment assays in batch reactors were used to evaluation of best nutritional condition, Beller or Zinder medium, to microorganism growth and sulfate removal. Further, the chosen nutritional condition was used in two horizontal-flow anaerobic immobilized biomass (HAIB) reactors under sulphate-reducing condition, which were exposed to different amounts of ethanol, toluene and benzene. The systems were inoculated with sludge taken from up-flow anaerobic sludge blanket (UASB) reactors treating refuses from a poultry slaughterhouse. The HAIB reactors comprised of an immobilized biomass on polyurethane foam and ferrous and sodium sulphate solutions were used (91 and 550 mg/L, respectively), to promote a sulphate-reducing environment. Toluene and benzene were added at an initial concentration of 2.0 mg/L followed by an increased range of different amendments. Ethanol was added at an initial concentration of 170 mg/L followed by an increased range of 960 mg/L. The reactors were operated at 30 (± 2) °C with hydraulic detention time of 12 h. Organic matter removal efficiency of 90%, in both systems, with a maximum toluene degradation rate of 0.06 mg toluene/mg vss.d and with a maximum benzene degradation rate of 0.07 mg benzene/mg vss.d. Sulfate reduction was dose to 99.9% for all-nutritional amendments in both systems. Biofilm microscopic characterization revealed a diversity of microbial morphologies and DGGE-profiling showed a variation of bacterial and sulphate reducing bacteria (SRB) populations, which were, significantly, associated with toluene and benzene amendments. Thus, this work demonstrates that compact units of HAIB reactors, under sulphate reducing conditions, are a potential alternative for in situ aromatic compounds bioremediation.

Electroactive textile fibers are key components in smart and interactive textile applications. In previous research on textile base conductive fibers, viscose fibers were coated with poly (3,4-ethylenedioxythiophne) (PEDOT) using oxidative chemical vapor deposition (oCVD) technique[1]. Ferric chloride was used as oxidant and reaction conditions were optimized at which better electrical as well as mechanical properties of conductive viscose fibers could be achieved. In this thesis work, effect of new parameters such as pretreatment of viscose fibers with solvents, drying of oxidant treated viscose fibers at different time and temperature and comparison of two different oxidants have been tried. One new and important oxidant, ferric (III) p-toluene sulfonate or ferric (III) tosylate, used to prepare PEDOT coated viscose fibers and then compared with PEDOT coated viscose fibers prepared using oxidant ferric (III) chloride. Viscose fibers have been treated with two well know solvents, acetone and ethyl acetate before soaking in oxidant solution. Oxidant enriched fibers dried at different temperature for variable time prior to polymerization step. Knitted structures of conductive viscose fibers have been prepared. Hand washing of PEDOT coated viscose fibers with tap water and machine washing of knitted structures according to the international standard ISO EN-6330 have been performed and washing effects were investigated. Effects of all of the above mentioned variables on electromechanical properties of PEDOT coated viscose fibers were studied by using tensile testing, TGA analysis, FTIR spectra and conductivity measurements. Stretch sensing properties of knitted structures; before and after washing, were determined on cyclic tester. The purpose of this study is to enhance the properties of PEDOT-coated viscose fibers by controlling different parameters and to evaluate their usage as stretch sensors as well as to check the washability of PEDOT coated viscose fibers and knitted structures. Better electromechanical properties were achieved on new parameters and PEDOT coated viscose fibers were successfully utilized as stretch sensors. PEDOT coated viscose fibers could have potential to apply in areas such as, military textiles, medical textiles and sensors. / Program: Master programme in Textile Technology

The main purpose of this thesis was to compare GAC adsorption method, VOCs incinerationmethod and Non-treatment alternative by using LCA to find which method or alternative isenvironmentally preferable. The LCA framework proposed by ISO 14040 (1997) has beenconsidered in this research. The comparison was made by considering a flue gas contaminatedby toluene (with three different concentration 100, 1000, 2000 mg/m3). The plant locationwhere the polluted flue gas is emitted has been assumed to be located in Borås, Sweden. Theflow rate of emitted flue gas was 10000m3/hr. The present thesis report contains two mainparts.The results of LCA showed that when the toluene concentration is low (&lt; 100 mg/m3), GACadsorption method, Non-treatment alternative and VOCs incineration method are respectivelypreferable from environmental point of view. On the other side, when the tolueneconcentration of inlet stream is high (&gt;1000 mg/m3), the order of GAC adsorption method,incineration and Non-treatment alternative is more desirable. Furthermore, the resultsillustrated that as toluene plays the role of fuel as a hydrocarbon, VOCs incineration methodis much more suitable when toluene concentration is high due to lower demand on additionalfuel. In the other words, high toluene concentration of influent leads to less environmentalimpact when VOCs incineration method is exploited. Conversely, the environmental impactof GAC adsorption method is increased when the inlet concentration of toluene is escalated.In overall, the weighted result showed that GAC adsorption method is the most preferablemethod while Non-treatment alternative is the worst.

Made available in DSpace on 2014-12-17T15:42:20Z (GMT). No. of bitstreams: 1 JonasAB_DISSERT.pdf: 1695862 bytes, checksum: 814d00e46b0fb400b2ca97afa17cf2f1 (MD5) Previous issue date: 2014-03-31 / Petr?leo Brasileiro SA - PETROBRAS / This work is directed to the treatment of organic compounds present in produced water from oil using electrochemical technology. The water produced is a residue of the petroleum industry are difficult to treat , since this corresponds to 98 % effluent from the effluent generated in the exploration of oil and contains various compounds such as volatile hydrocarbons (benzene, toluene, ethylbenzene and xylene), polycyclic aromatic hydrocarbons (PAHs), phenols, carboxylic acids and inorganic compounds. There are several types of treatment methodologies that residue being studied, among which are the biological processes, advanced oxidation processes (AOPs), such as electrochemical treatments electrooxidation, electrocoagulation, electrocoagulation and eletroredution. The electrochemical method is a method of little environmental impact because instead of chemical reagents uses electron through reactions of oxide-reducing transforms toxic substances into substances with less environmental impact. Thus, this paper aims to study the electrochemical behavior and elimination of the BTX (benzene, toluene and xylene) using electrode of Ti/Pt. For the experiment an electrochemical batch system consists of a continuous source, anode Ti/Pt was used, applying three densities of current (1 mA/cm2, 2,5 mA/cm2 and 5 mA/cm2). The synthetic wastewater was prepared by a solution of benzene, toluene and xylene with a concentration of 5 ppm, to evaluate the electrochemical behavior by cyclic voltammetry and polarization curves, even before assessing the removal of these compounds in solution by electrochemical oxidation. The behavior of each of the compounds was evaluated by the use of electrochemical techniques indicate that each of the compounds when evaluated by cyclic voltammetry showed partial oxidation behavior via adsorption to the surface of the Ti/Pt electrode. The adsorption of each of the present compounds depends on the solution concentration but there is the strong adsorption of xylene. However, the removal was confirmed by UV-Vis, and analysis of total organic carbon (TOC), which showed a percentage of partial oxidation (19,8 % - 99,1 % TOC removed), confirming the electrochemical behavior already observed in voltammetry and cyclic polarization curves / O presente trabalho ? dirigido ao tratamento de compostos org?nicos presentes na ?gua produzida de petr?leo usando a tecnologia eletroqu?mica. A ?gua produzida ? um res?duo da ind?stria do petr?leo de dif?cil tratamento, j? que este efluente corresponde a 98 % do efluente gerado na explora??o do petr?leo e cont?m v?rios compostos, tais como hidrocarbonetos vol?teis (benzeno, tolueno, etilbenzeno e xileno), hidrocarbonetos polic?clicos arom?ticos (HPAs), fen?is, ?cidos carbox?licos e compostos inorg?nicos. Existem v?rios tipos de metodologias de tratamento desse res?duo sendo estudadas, dentre elas est?o os processos biol?gicos, os processos de oxida??o avan?ados (POAS), tratamentos eletroqu?micos como eletroxida??o, eletrocoagula??o, eletroflota??o e eletroredu??o. O tratamento eletroqu?mico ? um m?todo ambientalmente correto, pois em vez de reagentes qu?micos utiliza o el?tron que atrav?s de rea??es de oxido redu??o transforma as subst?ncias t?xicas em subst?ncias de menor impacto ambiental. Assim, este trabalho se prop?e a estudar o comportamento eletroqu?mico e a degrada??o dos BTX (benzeno, tolueno e xileno) usando o eletrodo de Ti/Pt. Para os experimentos foi utilizado um sistema eletroqu?mico em batelada composto por uma fonte de corrente cont?nua, ?nodo de Ti&#8725;Pt, aplicando tr?s densidades de corrente (1,0 mA/cm2, 2,5 mA/cm2 e 5,0 mA/cm2). O efluente sint?tico foi preparado mediante uma solu??o de benzeno, tolueno e xileno com concentra??o de 5 ppm, com objetivo de avaliar o comportamento eletroqu?mico atrav?s de voltametria c?clica e curvas de polariza??o, antes mesmo de avaliar a remo??o desses compostos em solu??o atrav?s de oxida??o eletroqu?mica. O comportamento de cada um dos compostos foi avaliado mediante o uso de t?cnicas eletroqu?micas indicando que cada um dos compostos quando avaliado por voltametria c?clica, mostrou um comportamento de oxida??o parcial via adsor??o na superf?cie do eletrodo de Ti/Pt. A adsor??o de cada um dos compostos depende da concentra??o presente em solu??o, mas destaca-se a forte adsor??o do xileno. Entretanto, a remo??o foi comprovada atrav?s de espectrofotometria UV-Vis, e analises de carbono org?nico total (COT), os quais mostraram um percentual de oxida??o parcial (de 19,8 a 99,1% de COT removido), confirmando o comportamento eletroqu?mico j? observado na voltametria c?clica e curvas de polariza??o