China University of Petroleum

About: China University of Petroleum is a education organization based out in Beijing, China. It is known for research contribution in the topics: Catalysis & Oil shale. The organization has 39802 authors who have published 39151 publications receiving 483760 citations. The organization is also known as: Zhōngguó Shíyóu Dàxué & China University of Petroleum (Beijing).

Confinement Correction to Mercury Intrusion Capillary Pressure of Shale Nanopores

Abstract: We optimized potential parameters in a molecular dynamics model to reproduce the experimental contact angle of a macroscopic mercury droplet on graphite. With the tuned potential, we studied the effects of pore size, geometry, and temperature on the wetting of mercury droplets confined in organic-rich shale nanopores. The contact angle of mercury in a circular pore increases exponentially as pore size decreases. In conjunction with the curvature-dependent surface tension of liquid droplets predicted from a theoretical model, we proposed a technique to correct the common interpretation procedure of mercury intrusion capillary pressure (MICP) measurement for nanoporous material such as shale. Considering the variation of contact angle and surface tension with pore size improves the agreement between MICP and adsorption-derived pore size distribution, especially for pores having a radius smaller than 5 nm. The relative error produced in ignoring these effects could be as high as 44%--samples that contain smaller pores deviate more. We also explored the impacts of pore size and temperature on the surface tension and contact angle of water/vapor and oil/gas systems, by which the capillary pressure of water/oil/gas in shale can be obtained from MICP. This information is fundamental to understanding multiphase flow behavior in shale systems.

A multi-aromatic hydrocarbon unit induced hydrophobic metal–organic framework for efficient C2/C1 hydrocarbon and oil/water separation

Abstract: Oil spills have led to more and more energy waste and economic losses all over the world. Developing highly hydrophobic materials for efficient oil/water separation has become key in solving this global issue. Here we report a highly hydrophobic porous metal–organic framework, named UPC-21, constructed from a pentiptycene-based organic ligand, for efficient oil/water separation. Large and pure crystals of UPC-21 could be obtained with high yield through a developed “diauxic growth” strategy. Due to the existence of multi-aromatic hydrocarbon units in the central pentiptycene core of the ligand, UPC-21 exhibits high hydrophobicity with a water contact angle of 145 ± 1° and superoleophilicity with an oil contact angle of 0°. Strikingly, oil/water separation measurements reveal that UPC-21 can efficiently separate toluene/water, hexane/water, gasoline/water, naphtha/water, and crude oil/water with a separation efficiency being above 99.0% except for crude oil/water due to its high viscosity and complex composition. Our work presented here may open a new avenue for the application of porous MOF materials.

Hydrate Film Growth on the Surface of a Gas Bubble Suspended in Water

Abstract: The lateral film growth rate of CH4, C2H4, CO2, CH4 + C2H4, and CH4 + C3H8 hydrates in pure water were measured at four fixed temperatures of 273.4, 275.4, 277.4, and 279.4 K by means of suspending a single gas bubble in water. The results showed that the lateral growth rates of mixed-gas CH4 + C2H4 hydrate films were slower than that of pure gas (CH4 or C2H4) for the same driving force and that of mixed-gas CH4 + C3H8 hydrate film growth was the slowest. The dependence of the thickness of hydrate film on the driving force was investigated, and it was demonstrated that the thickness of hydrate film was inversely proportional to the driving force. It was found that the convective heat transfer control model reported in the literature could be used to formulate the lateral film growth rate v(f) with the driving force DeltaT perfectly for all systems after introduction of the assumption that the thickness of hydrate films is inversely proportional to the driving force DeltaT; i.e., v(f) = psiDeltaT(5/2) is correct and independent of the composition of gas and the type of hydrate. The thicknesses of different gas hydrate films were estimated, and it is demonstrated that the thicknesses of mixed-gas hydrate films were thicker than those of pure gases, which was qualitatively consistent with the experimental result.