Interactions between apolar,basic and acidic model oils and a calcite surface

Abstract

In this study, the atomic force microscopy colloidal probe technique was employed to investigate the interaction between apolar, basic and acidic model oil probes and a calcite surface in solutions containing different concentrations of NaCl, CaCl₂ and Na₂SO₄. In the presence of SO₄^2?, hydration and structural forces were observed between apolar model oil probes and a calcite surface on approach. Relatively low adhesion forces were observed between the basic model oil probes and the calcite surface, while higher adhesion forces were observed between the acidic model oil probes and the calcite surface. Furthermore, the adhesion forces between the basic model oil probes and the calcite surface significantly increased in the presence of SO₄^2?, while the adhesion force between the acidic model oil probes and the calcite surface decreased in the presence of Ca²⁺ or SO₄^2?. The differences in the adhesion forces are related to electrostatic attraction and ion bridging forces between the model oil probes and the calcite surface.     

Improved solution of displacements due to a compacting reservoir over a rigid basement

Geertsma’s analytical method is often used to compute strain and stress changes around a compacting geological reservoir. The present work extends Geertsma’s solution by adding a rigid layer beneath the compacting reservoir. Analytical formulae are presented for all the components of displacement of a point in the subsurface. Our derivation includes the correction of an error found in the paper written by Sharma in 1956.     

Extended UNIQUAC model for thermodynamic modeling of CO2 absorption in aqueous alkanolamine solutions

The extended UNIQUAC model [K. Thomsen, P. Rasmussen, Chem. Eng. Sci. 54 (1999) 1787–1802] was applied to the thermodynamic representation of carbon dioxide absorption in aqueous monoethanolamine (MEA), methyldiethanolamine (MDEA) and varied strength mixtures of the two alkanolamines (MEA–MDEA). For these systems, altogether 13 interaction model parameters are adjusted. Out of these parameters, 11 are temperature dependent.     

Spectral Evidence for a 2:1 Complex Between Titanium Tetrachloride and Ethyl Benzoate

Abstract

Infrared spectra of codeposited ethyl benzoate with excess titanium tetrachloride at 80 K revealed a novel 2:1 complex, where the inorganic entity is proposed to be a dimeric, triple bridged titanium tetrachloride unit. The ester is complexed to one of the octahedral titanium units through the carbonyl group. Compared to the 2:2 complex there are ν_c=o' ν _α-C-Oand ν_Ti-O shifts of -40/-47, +4/+24 and +16/17 cm^?1, depending on which of the ¹⁸O-carbonyl or d⁵-ethyl isotopic congeners is considered.     

A Dynamic Two-Phase Pore-Scale Model of Imbibition

We present a dynamic pore-scale network model of imbibition, capable of calculating residual oil saturation for any given capillary number, viscosity ratio, contact angle, and aspect ratio. Our goal is not to predict the outcome of core floods, but rather to perform a sensitivity analysis of the above-mentioned parameters, except from the viscosity ratio. We find that contact angle, aspect ratio, and capillary number all have a significant influence on the competition between piston-like advance, leading to high recovery, and snap-off, causing oil entrapment. Due to significant CPU-time requirements we did not incorporate long-range correlations among pore and throat sizes in our network, but were limited to small-range correlations. Consequently, the gradual suppression of snap-off occurs within one order of magnitude of the capillary number. At capillary numbers around 10⁸ - 10⁷ snap-off has been entirely inhibited, in agreement with results obtained by Blunt (1997) who used a quasi-static model. For higher aspect ratios, the effect of rate and contact angle is more pronounced.     

Experimental investigation of liquid chromatography columns by means of computed tomography

The efficiency of packed chromatographic columns was investigated experimentally by means of computed tomography (CT) techniques. The measurements were carried out by monitoring tracer fronts in situ inside the chromatographic columns. The experimental results were fitted using the equilibrium dispersive model (EDM) and varying the so called apparent axial dispersion coefficient. The additivity of the first and second central moments was exploited to estimate column efficiency in different regions of the column. The results showed that the columns under investigation offered a higher column efficiency in the centre compared to the wall region. Furthermore the void fraction in the vicinity of the walls was lower than that in the column core. For this reason the bands were conveyed faster in the central region of the column where the permeability was higher. This result is in good agreement with earlier findings.     

Ergodic Theory and Maximal Abelian Subalgebras of the Hyperfinite Factor

Let T be a free ergodic measure-preserving action of an abelian group G on (X,μ). The crossed product algebra R_T=L^∞(X,μ)? G has two distinguished masas, the image C_T of L^∞(X,μ) and the algebra S_T generated by the image of G. We conjecture that conjugacy of the singular masas S_T⁽¹⁾ and S_T⁽²⁾ for weakly mixing actions T⁽¹⁾ and T⁽²⁾ of different groups implies that the groups are isomorphic and the actions are conjugate with respect to this isomorphism. Our main result supporting this conjecture is that the conclusion is true under the additional assumption that the isomorphism γ : R_T⁽¹⁾→R_T⁽²⁾ such that γ(S_T⁽¹⁾)=S_T⁽²⁾ has the property that the Cartan subalgebras γ(C_T⁽¹⁾) and C_T⁽²⁾ of R_T⁽²⁾ are inner conjugate. We discuss a stronger conjecture about the structure of the automorphism group Aut(R_T,S_T), and a weaker one about entropy as a conjugacy invariant. We study also the Pukanszky and some related invariants of S_T, and show that they have a simple interpretation in terms of the spectral theory of the action T. It follows that essentially all values of the Pukanszky invariant are realized by the masas S_T, and there exist non-conjugate singular masas with the same Pukanszky invariant.     

Direct measurement of gas solubility and diffusivity in poly(vinylidene fluoride) with a high-pressure microbalance

We present solubility and diffusion data for the gases methane and carbon dioxide in the polymer poly(vinylidene fluoride). The polymer was cut from extruded piping intended for use in offshore oil and gas applications. Measurements were carried out using a purpose-built high-pressure microbalance. These properties were determined in the temperature range 80-120 °C and in the pressure range 50-150 bar for methane and 20-40 bar for carbon dioxide. In general, good agreement was obtained for similar measurements reported in the literature. Solubility follows a Henry’s law (linear) dependence with pressure. Diffusion coefficients for each of the gases in the polymer were also measured using the balance. Activation energies for diffusion and heats of solution for the two gases in the polymer were also determined.     

一类联图的距离谱半径以及盖理论（英文）

令X=(n₁,n₂,…,n_t),Y=(m₁,m₂,…,m_t)是两个t维递减序列.如果对所有的j,1≤j≤t,都有∑_i=1~j、n_i≥∑_i=1~j m_i以及∑_i=1~t n_i=∑_i=1~t m_i,则称X可盖Y,记作X■Y.如果X≠Y,则记作X■Y.本文考虑联图G(n₁,n₂,…,n_t;a)=(K_n1∪_n2∪…∪K_nt)∨K_a的谱半径,这里n₁+n₂+…+n_t+a=n,(n₁,n