Water activity data of several binary water + polymer systems were determined experimentally using both vapor-pressure osmometry (VPO) and improved isopiestic methods. The polymers were poly(ethylene glycol) dimethyl ether 250, poly(ethylene glycol) dimethyl ether 500, poly(ethylene glycol) dimethyl ether 2000, poly(ethylene glycol) monomethyl ether 350, poly(ethylene glycol) 200, poly(ethylene glycol) 6000, and poly(propylene glycol) 400. The obtained water activities data were used to calculate the vapor pressure of solutions as a function of concentration. Water activity of all investigated solutions increased with increasing temperature and polymer molar mass. A comparison is given between the vapor−liquid equilibrium data inferred from VPO and isopiestic methods, for different aqueous polymer solutions at 298.15 K, and there is a good agreement between the results of the investigated methods. Furthermore, the segment-based local composition models, nonrandom two-liquid (NRTL), Wilson, and universal quasichemical (UNIQUAC), were used to correlate the experimental activity data.

The action of particular electrolytes in altering the solution properties of ionic liquids is well documented, although the origin of this effect is not clearly defined. In order to clarify this point, the aim of this work is to obtain further evidence about the salting-out effect produced by the addition of different salts to aqueous solutions of water miscible ionic liquids by evaluating the effect of a large series of salts on the vapor-liquid equilibria, liquid-liquid phase diagram, volumetric, compressibility, and conductometric properties of ionic liquids 1-alkyl-3-methylimidazolium halide ([C(n)mim][X]). In the first part of this work, the experimental measurements of water activity at 298.15 and 308.15 K for aqueous binary and ternary solutions containing 1-alkyl-3-methylimidazolium bromide ([Rmim][Br], R = butyl (C(4)), heptyl (C(7)), and octyl (C(8))), sodium dihydrogen citrate (NaH(2)Cit), disodium hydrogen citrate (Na(2)HCit), and trisodium citrate (Na(3)Cit) are taken using both vapor pressure osmometry (VPO) and improved isopiestic methods. The effect of temperature, charge on the anion of sodium citrate salts, and alkyl chain length of ionic liquids on the vapor-liquid equilibria properties of the investigated systems are studied. The constant water activity lines of all the ternary systems show large negative deviation from the linear isopiestic relation (Zdanovskii-Stokes-Robinson rule) derived using the semi-ideal hydration model, and the vapor pressure depression for a ternary solution is much larger than the sum of those for the corresponding binary solutions with the same molality of the ternary solution. The results have been interpreted in terms of the solute-water and solute-solute interactions. In the second part of this work, the effects of the addition of (NH(4))(3)Cit, K(3)Cit, Na(3)Cit, (NH(4))(2)HPO(4), and (NH(4))(3)PO(4) on the liquid-liquid phase diagram, apparent molar volume, isentropic compressibility, and conductivity of aqueous solutions containing the model ionic liquid 1-butyl-3-methylimidazolium iodide, [C(4)mim][I], are investigated at different temperatures. It was found that there is a relation between the relative concentration of various salts to form two-phase systems with [C(4)mim][I] and apparent molar volume or isentropic compressibility of transfer of [C(4)mim][I] from water to aqueous solutions of the investigated salts.

Removing the precipitated asphaltenes from the facilities of oil industry is of vital importance. In this study, the possibility of the precipitated asphaltene biodegradation from a crude oil sample using indigenous bacterial species isolated from different oil-contaminated samples of a Middle East oilfield has been investigated. On the basis of the achieved designed experiments results using response surface methodology, identified bacteria were cultured in the flasks on pure and consortium. Three levels of temperatures, salinity, pH, and initial asphaltene concentration were considered as growth medium parameters, and the flasks were incubated for 60 days. The CHNS and FT-IR analysis have been performed to evaluate the asphaltene elemental and structural alteration after the biodegradation process. The validity of some kinetic models to predict the behavior of the microbial systems was studied. The maximum asphaltene biodegradation was 41.95% and carbon, hydrogen, and nitrogen content of treated samples decreased significantly during the bacterial activity.

VaporÀliquid equilibria (VLE) measurements have been performed for several binary polymer þ solvent systems at 318.15 K using a vapor pressure osmometry (VPO) method in the semidiluted polymer concentration range. The polymers were poly(ethylene oxide) dimethyl ether 250, poly(ethylene oxide) dimethyl ether 500, poly(ethylene oxide) dimethyl ether 2000, poly(ethylene oxide) 400, and poly(propylene oxide) 400, and the investigated solvents were water, methanol, ethanol, acetonitrile, and 2-propanol. The variations of the activity of solvents with the polymer molar mass and type of polymer and solvent were investigated, and the results have been interpreted in terms of the solvent/polymer interactions. In the second part of this work, the segment-based local composition models, nonrandom two-liquid (NRTL) and Wilson, as well as the FloryÀHuggins model were used to correlate the experimental activity data.

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One of the serious problems in the oil industry is precipitation and deposition of asphaltenes in the different oil production stages including formation, wellbore, production tubing, flow lines, and separation units. This phenomenon causes a dramatic increase in the cost of oil production, processing, and transferring. Thus, it seems to be very necessary to use the removing methods for precipitated asphaltenes in different crude oil production and transferring stages. In this study, the ability of microorganisms for biodegradation of precipitated asphaltenes was investigated. For this purpose, four bacterial consortiums were isolated from oil-contaminated soil, crude oil, reservoir water, and oil sludge samples of an oil field located in the southwest of Iran. Based on the results of the designed experiments, by using response surface methodology (RSM) and central composite design, the bacterial consortiums were cultured in the flasks. Three levels of temperatures, salinity, pH, and initial asphaltene concentration as the substrate were considered as the parameters of culture medium and incubated growth mediums for 60 days. The maximum asphaltene biodegradation was 46.41% caused by the crude oil consortium including Staphylococcus saprophyticus sp. and Bacillus cereus sp. at 45 °C, salinity 160 g·L–1, pH 6.5, and 25 g·L–1 initial asphaltene concentration. Also, it was observed that the negative or positive impacts of culture media conditions such as temperature and salinity on asphaltene degradation depended on the type of the available bacterial consortium. The carbon–hydrogen–nitrogen–sulfur analysis showed that carbon, hydrogen, nitrogen, and in some cases, the sulfur in biodegraded samples are less than in control samples. Moreover, Fourier transform infrared analysis indicated that the alkyne groups were less resistant to biodegradation and were eliminated thoroughly after 2 months of incubation. In addition, alkane components were partially removed in treated asphaltene fraction. The parameters of culture medium were optimized by RSM, and besides, their effects on the performance of bacteria in the asphaltene biodegradation process were discussed. The validity of some available kinetic models to describe the behavior of the studied bacteria consortium was investigated, and it was observed that Tessier, Moser, and Contois models accurately predict the values of asphaltenes and biomass concentration at 30, 45, and 60 °C, respectively.

The presence of carbon dioxide in natural gases can lower the quality of natural gas and can cause CO 2 freezing problems. Therefore, using reliable techniques for the reduction and elimination of carbon dioxide from natural gases is necessary. The aqueous diethanol amine (DEA) solution’s ability to simultaneously absorb H 2 S and CO 2 from sour natural gases makes it possible to use this solution in the natural gas sweetening process. The goal of this work was to determine the maximum amount of the removed CO 2 by an aqueous DEA solution in one of the gas sweetening plants of the National Iranian South Oilfields Company (NISOC). For this purpose, based on the obtained designed experiment results using the L9 orthogonal array Taguchi method, the experiments were conducted and three levels of amine concentrations (25, 28, and 30 wt %), temperatures (40, 50, and 60 °C), and circulation rates of lean amine (220, 240, and 260 m 3 h –1 ) were considered as the key operational parameters on CO 2 removal. To evaluate the ability of the HYSYS simulation software and the Kent–Eisenberg thermodynamic model to predict CO 2 absorption by an aqueous DEA solution in the gas sweetening process, the field data were compared with the results of the simulation. It was observed that the maximum removal of CO 2 is achieved at a lean amine concentration of 30 wt %, a temperature of 40 °C, and a circulation rate of 260 m 3 h –1 . Also, the experimental results indicate that the effects of the selected process variables on CO 2 absorption are not linear and the most effective parameter on carbon dioxide removal is the concentration of amine in an aqueous solution and the temperature of the lean amine has the least effect. Besides, the obtained simulation results are in the range of the unit design basis but have some deviations from field data. The findings of this study can help in better understanding of the selection of the effective variables in the natural gas sweetening process and obtaining their appropriate values to achieve the highest efficiency.