Poly(amidoamine)-type dendrimers (PAMAM) were synthesized by divergent routes, and generations (G0.5, G1.0, G1.5, G2.0 and G2.5) along with hydroxylated half-generation polymers (G0.5-OH, G1.5-OH and G2.5-OH) were characterized by Fourier-transform infrared spectroscopy, thermogravimetric analysis and differential scanning calorimetry. Carbon dioxide (CO2) capture tests were performed using thermogravimetric analysis. Among the absorption temperatures tested, 60 °C was the most promising: 0.77, 1.08, and 1.14 mol CO2 L 1 for G0.5-OH, G1.5-OH and G2.5-OH, respectively, of CO2 and partial pressure of 45 kPa. This showed that dendrimers with larger molecular structures have more hydroxyl groups and consequently capture more CO2. However, at low partial pressures (< 2 kPa), CO2 solubility in PAMAM increased with temperature reduction, confirmed by Henry’s solubility constant (398.4 mol m3 kPa 1, in G2.5-OH at 40 °C). According to the thermodynamic properties of CO2 solubilization, the process was spontaneous (∆Gsol < 0) and exothermic (∆Hsol < 0). Polyamidoaminetype Poly amidoamine type (PAMAM routes G0.5, G05 G G0 5 (G0.5 G10 G1 0 G1.0 G15 G1.5 G20 G2 G2. G2.5 G25 halfgeneration half generation G0.5OH, G05OH GOH G0.5 OH, OH (G0.5-OH G1.5OH G15OH G2.5OH G25OH Fouriertransform Fourier transform spectroscopy calorimetry CO (CO2 tested 6 C promising 077 77 0.77 108 08 1.08 114 14 1.1 G0.5-OH G2.5OH, respectively 4 However ( kPa, , kPa) reduction Henrys Henry s 398.4 3984 398 (398. m °C. . °C) solubilization ∆Gsol Gsol ∆Hsol Hsol 0. (G0. G1. 5OH G0.5OH G0. (CO 07 7 0.7 10 1.0 11 1. 398. 39 (398 (G0 3 (39 (G (3

One of the main phenomena causing problems in the oil industry is the precipitation of waxes, which can crystallize and form deposits, clogging lines and reducing flows. Many studies have been conducted seeking to overcome this problem, mainly through application of chemical to increase flow. Some studies have shown that the asphaltenes present in crude oil can also be involved in the process of wax deposition. In this study, model systems were investigated to determine the influence of a natural additive, a chemical additive and their combined use on the fluidity of the samples. The natural additive, consisting of a refinery asphalt residue (ASPR), was studied in relation to the influence of its aggregation states on the fluidity of the wax model systems. All samples were evaluated through the pour point test, according to the ASTM D-97 standard. The results indicated that both the ASPR and the commercial poly(ethylene-co-vinyl acetate) can improve the fluidity. Synergistic effect, using both together, was verified by the significant reduction of pour point for model systems with wax content as high as 13% m v-1. That action was closely related to the concentration of ASPR and its aggregation state, as indicated by tests with different wax concentrations. waxes deposits flows problem flow deposition study ASPR, , (ASPR) test D97 D 97 D-9 standard polyethylenecovinyl poly ethylene co vinyl acetate effect together 13 v1. v1 v 1. 1 v-1 state concentrations (ASPR D9 9 D- v-

Cardanol acts to stabilize asphaltene particles in crude oil, but its derivative polycardanol, synthesized with BF3.O(C2H5)2 as initiator, exhibits divergent behavior, acting as both asphaltenes stabilizer and flocculant. This behavior could be related to structural differences in polycardanol samples. Therefore, in this work, we study the influence of some polymerization conditions (monomer purity, initiator concentration, and reaction time) on the structures and molar masses of the reaction products, and the reaction conversion. The materials were characterized by size exclusion chromatography and hydrogen and carbon nuclear magnetic resonance. When reacting with distilled cardanol, the conversion, the molar mass, and the homogeneity of structures increased as increasing initiator concentration in the range tested (1-3% m/m). For both monomers (different purity degrees), when using a lower initiator concentration (1% m/m), the product contained a larger amount of unreacted monomer and different structures were obtained due to the occurrence of rearrangements. The presence of triolefinic molecules in the monomer provoked crosslinked structures for higher initiator concentration (2-3% m/m). This study elucidated the differences among the reaction products of polycardanol. oil BF3.OC2H52 BF3OC2H52 BFOCH BF3.O C2H5 2 BF3 O BF C H BF3.O(C2H5) flocculant samples Therefore work time conversion resonance cardanol mass 13% 13 1 3% 3 (1-3 m/m. mm m/m . m m/m) degrees, degrees , degrees) 1% (1 m/m, rearrangements 23% 23 (2-3 OC2H52 OC BF3.OC2H5 BF3OC2H5 BF3O BFO CH C2H BF3.O(C2H5 (1- ( (2- OCH OC2H5 BF3.OC2H BF3OC2H BF3.O(C2H (2 OC2H

Resumen Este estudio describe la síntesis de resinas poliméricas a base de estireno (STY), metacrilato de glicidilo (GMA) y divinilbenceno (DVB), modificadas químicamente mediante reacciones de sulfonación durante diferentes intervalos de tiempo, para conocer la influencia de la estructura de los materiales en su capacidad de adsorción y evaluar su potencial de aplicación en la remoción de amonio de aguas residuales a niveles que cumplan con la norma técnica NT202, R-10 (INEA, 1986). Los resultados mostraron que, además de la duración de la reacción de sulfonación, factores como el área superficial y el diámetro de los poros también contribuyeron significativamente al proceso de absorción de amonio. La eficácia de las formulaciones fue en orden decreciente DVB(7:3)(2)S, DVB(7:3)(24)S, STY-DVB(7:3)(2)S y GMA-DVB(7:3)(2)S. De estos, DVB(7:3)(2)S tenía la mayor área superficial pero tenía una baja capacidad de intercambio iónico. La resina con mayor capacidad de intercambio fue STY-DVB(7:3)(2)S, pero tuvo una eficiencia aproximadamente un 20% menor que la resina anterior, mostrando un resultado muy cercano al de GMA-DVB (7:3)(2)S.

Abstract This study describes the synthesis of polymeric resins based on styrene (STY), glycidyl methacrylate (GMA) and divinylbenzene (DVB), modified chemically through sulfonation reactions during different time intervals, to learn the influence of the materials’ structure on their adsorption capacity and evaluate their potential for application in the removal of ammonium from wastewater to levels compliant with the technical standard NT202, R-10 (INEA, 1986). The results showed that besides the duration of the sulfonation reaction, factors such as surface area and pore diameter also contributed significantly to the ammonium absorption process. The efficiency of the formulations was in decreasing order DVB(7:3)(2)S, DVB(7:3)(24)S, STY-DVB(7:3)(2)S and GMA-DVB(7:3)(2)S. Of these, DVB(7:3)(2)S had the greatest surface area but had low ion exchange capacity. The resin with the greatest exchange capacity was STY-DVB(7:3)(2)S, but it had efficiency about 20% lower than the former resin, showing a result very near that of GMA-DVB(7:3)(2)S.

The conditions of petroleum extraction may allow asphaltenes to precipitate, causing deposition that clogs wells, pipes and equipment, consequently reducing productivity. In this work, the solubility parameters and precipitation onset of polar fractions of heavy crudes from Brazilian fields were estimated using a simplified system of n-heptane/toluene mixtures. Asphaltenes were extracted by two different methods with regard to pressure and temperature. The samples were physically and chemically characterized, and both density (1053-1159 kg m-3) and molecular weight (1176-5316 g mol-1) were estimated based on the density of diluted asphaltenes in toluene solutions. The solubility of those fractions was studied as well as their solubility parameter (ca. 19-23 MPa0.5) based on regular solution theory, Flory-Hüggins theory and empirical correlation. The influence of asphaltene concentration (between 0.5 and 5.0 g L-1) on the solubility parameter and precipitation onset was studied, and a strong linear correlation between them was not found.

One of the methods used by the oil industry to increase production is to inject water, containing polymer, into the reservoir. The viscosity of the aqueous solution is primarily responsible for the efficiency of this method, and is achieved using polymers with high molar mass. However, polymer degradation can occur during pumping and fluid displacement in the porous medium, reducing the efficiency of the polymer flooding method. Therefore, it is important to monitor the molar mass of the polymer in the produced water. Size-exclusion chromatography (SEC) is a powerful method for determining average molar mass of polymers, but the impurities present in the produced water, such as salts and residual oil, can significantly affect the analysis. There is no method described in the literature for pretreating produced water before injecting it into the chromatograph. Therefore, the purpose of this work was to develop a reliable method for this pretreatment, without affecting the molar mass of the polymer. The results showed that an efficient method, which does not cause polymer degradation, must contain four steps: (i) heating, (ii) regular filtration, (iii) elution in poly(divinylbenzene) resin, and (iv) dialysis.

Predicting the compatibility of crude oils from different streams can be done by applying models that use the solubility parameter of the oils. The approximate solubility parameter value of a given crude oil can be calculated by observing the asphaltene precipitation onset caused by titration with n-heptane. For oils whose precipitation onset is not well defined, a small quantity of another petroleum with easily detected onset can be added. It would be ideal to always use the same petroleum for this addition, but this is obviously not possible. The purpose of this study was to replace this petroleum by a synthetic molecule. Therefore, molecules were selected and synthesized to obtain structures containing aromatic ring, aliphatic chain and heteroatom. The molecules were characterized by infrared spectrometry, gas chromatography-mass spectrometry, elemental analysis and gel permeation chromatography. Nitrated cardanol, polycardanol obtained by addition polymerization (PCA) and nitrated PCA presented the desired behavior. However, the concentration of the molecule in toluene needs to be adjusted in function of the characteristics of the petroleum. For a particular crude oil, when model molecule present solubility in a wider solubility parameter range, lower concentration will require to identify the precipitation onset of that oil.

Crude oils containing large quantities of waxes, and in situations where sudden temperature drops occur, a crystalline network can be formed, generating flow difficulties in production, transfer and offloading lines. Despite the scientific and economic importance of this phenomenon, correlations between the behavior of petroleum in relation to its pour point are scarce in the literature. In this work, nine crude oil samples were characterized regarding density, water content, wax fraction (one- and two-dimensional chromatography), pour point, yield stress and wax appearance temperature. The results showed that the storage conditions and oil characteristics had a strong influence on the pour point. Yield stress was influenced by initial temperature of the sample, cooling rate and shear rate during cooling. Finally, the content of aromatic compounds in oil with low concentration of n-alkanes can contribute to increase the pour point.

In this study, microparticles of poly(lactic acid) (PLA) were produced to encapsulate cardanol, varying molar mass of the polymer matrix, concentration of the emulsifier (PVA) and concentration of the chemical additive (cardanol). The droplet size distribution, polydispersity index, morphology, the interaction between cardanol and PLA, cardanol encapsulation efficiency and release profile of this chemical additive were assessed. The morphological characterization showed that the microparticles containing cardanol were presented as microcapsules up to a maximum cardanol concentration limit that could be incorporated. The addition of cardanol during the production of the microparticles led to an increase in the average diameter of the microparticles obtained, both those with low and high molar mass (MPLA3 and MPLA100, respectively), with the increase depending on the quantity of cardanol incorporated. DSC results showed a shift in melting point and a change in Tg and Tm with the incorporation of cardanol, suggesting an interaction between cardanol and PLA matrix. Higher encapsulation efficiency and slower release of cardanol were achieved when using microparticles with higher molar mass (MPLA100). The microparticles of MPLA100/1PVA/50C provided the slowest additive release among the formulations tested. Therefore, the processes for encapsulation and controlled release of cardanol in the PLA matrix were efficient.

Clays such as smectite have high technical and economic viability due to their large adsorption capacity. These properties can be improved by treatment with acids or other modifications. This paper describes experiments to prepare and characterize organoclays and to evaluate their ability to remove oil from contaminated water in comparison with clay in its natural state. We used natural smectite clay from the municipality of Presidente Dutra, Maranhão State, modified with the quaternary ammonium salt cetyltrimethylammonium bromide. Characterization was performed by X-ray diffraction, Fourier transform infrared spectroscopy, X-ray fluorescence, thermogravimetry and determination of surface area by the Brunauer-Emmett-Teller (BET) method. The results showed appropriate conditions of the organophilization process, indicating the intercalation of quaternary ammonium cations between the clay layers. The adsorption tests showed that the natural clay reduced the amount of oil contained in the aqueous medium by 76.16%, while the corresponding removal rates of all organoclays tested were above 92%, which makes them potentially applicable to remove oil from wastewaters.

Asphaltenes are blamed for various problems in the petroleum industry, especially formation of solid deposits and stabilization of water-in-oil emulsions. Many studies have been conducted to characterize chemical structures of asphaltenes and assess their phase behavior in crude oil or in model-systems of asphaltenes extracted from oil or asphaltic residues from refineries. However, due to the diversity and complexity of these structures, there is still much to be investigated. In this study, asphaltene (sub)fractions were extracted from an asphaltic residue (AR02), characterized by NMR, elemental analysis, X-ray fluorescence and MS-TOF, and compared to asphaltene subfractions obtained from another asphaltic residue (AR01) described in a previous article. The (sub)fractions obtained from the two residues were used to prepare model-systems containing 1 wt% of asphaltenes in toluene and their phase behavior was evaluated by measuring asphaltene precipitation onset using optical microscopy. The results obtained indicated minor differences between the asphaltene fractions obtained from the asphaltic residues of distinct origins, with respect to aromaticity, elemental composition (CHN), presence and content of heteroelements and average molar mass. Regarding stability, minor differences in molecule polarity appear to promote major differences in the phase behavior of each of the asphaltene fractions isolated.

O parâmetro de solubilidade (δ) de uma molécula é extremamente importante, visto que novas moléculas são frequentemente desenvolvidas para serem aplicadas em sistemas líquidos. Neste trabalho, nós buscamos técnicas alternativas simples e confiáveis para determinar δ de moléculas de baixa e alta massa molar. Pireno, fenantreno e naftaleno tiveram seus δ determinados por microcalorimetria (µDSC), ultravioleta (UV) e calorimetria (DSC). Resultados de UV foram similares àqueles obtidos por DSC e àqueles citados na literatura. Amostras de poliestireno e poliestireno sulfonado tiveram seus δ determinados por UV, µDSC e viscosidade intrínseca ([η]). Os resultados de [η] foram similares àqueles obtidos por UV. Procedimento de UV foi relativamente simples, de fácil operação e confiável para determinação de δ de moléculas de ampla faixa de massa molar, podendo ser utilizado no desenvolvimento de novas moléculas. O procedimento utilizando μDSC ainda requer alguns ajustes a fim de torná-lo mais preciso do que [η].

The solubility parameter (δ) of a molecule is extremely important, since that new molecules are frequently developed to be applied in liquid systems. In this work, we looked for simple and reliable alternative techniques to determine δ of low and high molecular weight molecules. Pyrene, phenanthrene and naphthalene had their δ determined by microcalorimetry (µDSC), ultraviolet (UV) and calorimetry (DSC). UV results were similar to those obtained by DSC and to those cited in the literature. Polystyrene and sulfonated polystyrene samples had their δ determined by UV, µDSC and intrinsic viscosity ([η]). The [η] results were similar to those obtained by UV. UV procedure was relatively simple, easy operation and reliable for determining δ of molecules in a wide range of molar mass, can be used when developing new molecules. The µDSC procedure still requires some adjustments to become more accurate than [η] procedure.

In the current scenario, there is growing interest in the products of degradation of rubber (natural and synthetic) for specific applications in different industry sectors, whose benefits in replacing conventionally used products are mainly related to sustainability. Since the degradation products of rubber can be used in different areas, several research groups may have the interest aroused by these products, but are not familiar with the aspects related to the chemical behavior of rubber. This review aims to bring together the key information in the published literature on the degradation of natural rubber, emphasizing metatheses reactions, oxidative damage and splitting of the double bond, in order to serve as a reference source for researchers from different fields interested in obtaining such kind of products. The structures and properties as well as additional chemical transformations resulting in oligomers of isoprene, functionalised oligomers and polymers based on both are also described.

O petróleo é produzido na forma de emulsão água em óleo e os asfaltenos são considerados os principais responsáveis pela estabilização dessas emulsões. O objetivo deste trabalho foi avaliar a influência de diferentes frações asfaltênicas sobre a estabilidade de emulsões modelo de petróleo (salmoura em asfaltenos/tolueno) e sobre a eficiência de desemulsificantes. A estabilidade das emulsões foi acompanhada pelo ensaio de garrafa, com e sem a adição de desemulsificante. Os resultados mostram que a amostra de asfaltenos com larga distribuição de polaridade promove maior estabilidade da emulsão do que a amostra com distribuição mais estreita e polaridade intermediária. Além disso, a eficiência do desemulsificante na separação das emulsões está diretamente relacionada à estabilidade original da emulsão. Resultados de tensão interfacial evidenciaram a eficiência de deslocamento dos asfaltenos pelos tensoativos desemulsificantes, o que ocorreu com maior eficiência para as emulsões contendo frações de asfaltenos com distribuição estreita e polaridade intermediária.

Crude oil is produced as water-in-oil emulsion, and asphaltenes have been considered the main responsible by their stabilization. The aim of this work was to evaluate the influence of the asphaltenes subfractions on the stability of petroleum model emulsions and on the efficiency of demulsifiers. Model water-in-oil emulsions were prepared: aqueous phase of brine and oil phase of asphaltenes in toluene. Different asphaltenes fractions were used. The emulsions' stability was assessed by the bottle test, with and without adding demulsifier. The results show that a sample of asphaltenes with broad polarity distribution promotes greater emulsion stability than a sample with narrow distribution and intermediate polarity. Besides this, the efficiency of demulsifiers in separating the emulsions is directly related to the original stability of the emulsion. Measurements of the interfacial tension revealed the efficiency of displacement of the asphaltenes by the demulsifiers, which occurred more efficiently for the emulsions containing asphaltenes fractions with narrow distribution and intermediate polarity.

Foi realizado um estudo para investigar a interação entre asfaltenos (em soluções de tolueno) e resinas (em soluções de n-heptano). Para entender melhor o tipo de interação entre essas frações, quantificou-se o consumo de resina quando asfaltenos (dissolvidos em tolueno) foram precipitados com uma solução de n-heptano contendo resina. Os resultados indicaram que a precipitação de asfaltenos ocorre juntamente com a redução na concentração de resina. Os perfis das isotermas de ligação indicaram que a saturação ocorreu em um caso, em quanto que o efeito cooperativo com posterior platô inicial foi observado para duas outras amostras. Estes resultados confirmaram a hipótese de que resinas podem adsorver em asfaltenos, mas não podem evitar floculação e precipitação de asfaltenos. Além disso, resultados de microcalorimetria sugeriram que a resina e asfalteno interagem por forças fracas de van der Waals. Estes resultados estão em contraste com a escola de pensamento predominante desde a década de 1940 que advoga que as resinas podem peptizar e estabilizar asfaltenos.

A study was carried out to investigate the interaction between asphaltenes (in toluene solutions) and resins (in n-heptane solutions). To better understand the type of interaction between these fractions, it was quantified the resin uptake when asphaltenes (dissolved in toluene) were precipitated by a resin-containing n-heptane solution. These results indicated the asphaltene precipitation occurs together with a reduction in the resin concentration. The binding isotherm profiles indicated that saturation occurred in one case, while collective association following an initial plateau was observed for the other two samples. These results confirmed the hypothesis that resins can adsorb on asphaltenes but cannot prevent asphaltenes from flocculating and precipitating. Furthermore, microcalorimetric results suggested that the resin and asphaltene interact by weak van der Waals forces. These results are in stark contrast with the school of thought prevalent since the 1940s that resins can peptize and stabilize asphaltenes.