Effect of permeability and fractures on oil mobilization of unconventional resources during CO2 EOR using nuclear magnetic resonance.

CO2 EOR (enhanced oil recovery) will be one of main technologies of enhanced unconventional resources recovery. Understanding effect of permeability and fractures on the oil mobilization of unconventional resources, i.e. tight oil, is crucial during CO2 EOR process. Exposure experiments based on nuclear magnetic resonance (NMR) were used to study the interaction between CO2 and tight oil reservoirs in Chang 8 layer of Ordos Basin at 40 °C and 12 MPa. Effect of permeability and fractures on oil mobilization of exposure experiments were investigated for the different exposure time. The oil was mobilized from matrix to the surface of matrix and the oil recovery increased as the exposure time increased. The final oil recovery increased as the core permeability increased in these exposure experiments. Exposure area increased to 1.75 times by fractures resulting in that oil was mobilized faster in the initial stage of exposure experiment and the final oil recovery increased to 1.19 times from 28.8 to 34.2%. This study shows the quantitative results of effect of permeability and fractures on oil mobilization of unconventional resources during CO2 EOR, which will support CO2 EOR design in Chang 8 layer of Ordos Basin.

Wormlike micelles formed by sodium erucate in the presence of a tetraalkylammonium hydrotrope.

Anionic wormlike micelles, particularly those formed by long-chain carboxylate surfactants, are relatively less documented though their cationic or zwitterionic counterparts are frequently reported. In this study, the wormlike micelles of sodium erucate (NaOEr), a C22-tailed anionic surfactant with a monounsaturated tail, in the presence of a tetraalkylammonium hydrotrope were investigated for the first time. The different effects of two hydrotropes, benzyl trimethyl ammonium bromide (BTAB) and tetramethyl ammonium bromide (TMAB), on the phase behavior and rheological behaviors were compared, and the influences of surfactant concentration and temperature on the rheological properties of NaOEr solutions were also examined. Both organic salts can lower the Krafft temperature of NaOEr solutions and thus improve its water solubility, but BTAB can make T(K) drop more sharply. At a fixed NaOEr concentration, less BTAB is demanded to induce the formation of viscoelastic solution and to obtain the maximum viscosity of NaOEr solution; at a constant salt concentration, with increasing NaOEr content, the NaOEr-BTAB system shows a larger zero-shear viscosity (η(0)), relaxation time, and plateau modulus but lower overlapping concentration than those of the NaOEr-TMAB system. The occurrence of maximum η(0) with increasing salt content for the NaOEr-BTAB system results from the formation of vesicles and L(3) phases, which were verified by cryo-TEM observations. η(0) shows an exponential decrease with increasing temperature; nevertheless it still remains above 10(3) mPa·s even at 90 °C.

Macromolecular knot in good and poor solvents: a Monte Carlo simulation.

The probability and dimension of the simple macromolecular knots over a wide range of temperatures corresponding from good to poor solvents are investigated by Monte Carlo simulation. Macromolecular knots are modeled as rings of self-avoiding walks on a simple cubic lattice with the nearest neighbor attractions. We found that there is a minimum probability for the unknotted ring at a certain temperature. The size dependence of trivial, trefoil, and figure-eight knots on chain lengths and temperatures is presented. The simulation results for the size dependence on the knot's complication in different solvents are in good qualitative agreement with prediction of the scaling model proposed by Grosberg et al. The critical exponent for long chain is independent of the knot types based on the simulation results, although the mean square radius of gyration is influenced significantly by the knot types for a shorter length macromolecular ring. We calculated the ratio of the topological invariant p of trefoil knot and figure-eight knot and found that the ratio is approaching to 1.3 with the increasing of the chain length.

Effect of divalent cationic ions on the adsorption behavior of zwitterionic surfactant at silica/solution interface.

The adsorption behavior of zwitterionic surfactant dodecyl sulfobetaine (DBS) on a silica/solution interface with Ca(2+), Mg(2+) existing in aqueous solution is explored by atomistic molecular simulations. The interaction energy contribution of van der Waals and electrostatic potentials in the surfactants/water/silica system are respectively calculated, from which the electrical interaction can be found to play a decisive role in the adsorption tendency of DBS on the silica surface with or without inorganic ions, despite different mechanisms. The distinct decrease of energy has been found to be derived from electrical interaction when DBS adsorb on the silica surface covered by Ca(2+) or Mg(2+). Therefore, it can be predicted that the cationic ions combined on the negatively charged silica surface in a mineral water medium might decrease the adsorption trend of DBS on the silica surface, which has been experimentally proven by TOC measurement. Structural information of the close interface layer and the distribution of water molecules are analyzed after the complete molecular dynamics simulation using a ternary model. Ca(2+) and Mg(2+) combined on the silica surface can reduce the adsorption amount of DBS by preventing the direct interaction between DBS and surface, and bringing about the orientation reversal of DBS molecules to break the order of adsorption interface layer. Furthermore, changes in the status of the water spreading on the silica surface caused by the complexation of cations are also an important reason in the adsorption reduction.

A study of dilational rheological properties of polymers at interfaces.

Viscoelastic properties of two polymers, partially hydrolyzed polyacrylamide and partially hydrolyzed modified polyacrylamide, widely used in chemical flooding in the petroleum industry, were investigated at three interfaces, water-air, water-dodecane, and water-crude oil, by means of a dilational method provided by I.T. Concept, France, at 85 degrees C. Polymer solutions were prepared in brine with 10,000 mg/l sodium chloride and 2000 mg/l calcium chloride. It has been shown that the viscoelastic modulus increases with the increment of polymer concentration in the range of 0-1500 mg/l at the water-air interface. Each polymer shows different viscoelatic behavior at different interfaces. Generally speaking, values of the viscoelastic modulus (E), the real part (E'), and the imaginary part (E") at the crude oil-water interface for each polymer are lower than at the air-water or water-dodecane interface. The two polymers display different interfacial properties at the same interface. Polymer No. 2 gives more viscous interfaces than polymer No. 1. All the information obtained from this paper will be helpful in understanding the interfacial rheology of ultra-high-molecular-weight polymer solutions.