Interfacial tension during mass transfer of decanoic acid from hexane to an aqueous solution containing NaOH

1989 ◽  
Vol 36 (1) ◽  
pp. 13-27 ◽  
Author(s):  
M. Vermeulen ◽  
P. Joos
SPE Journal ◽  
2020 ◽  
Vol 25 (03) ◽  
pp. 1042-1056 ◽  
Author(s):  
Weiqi Fu ◽  
Zhiyuan Wang ◽  
Litao Chen ◽  
Baojiang Sun

Summary In the development of deepwater crude oil, gas, and gas hydrates, hydrate formation during drilling operations becomes a crucial problem for flow assurance and wellbore pressure management. To study the characteristics of methane hydrate formation in the drilling fluid, the experiments of the methane hydrate formation in water with carboxmethylcellulose (CMC) additive are performed in a horizontal flow loop under flow velocity from 1.32 to 1.60 m/s and CMC concentration from 0.2 to 0.5 wt%. The flow pattern is observed as bubbly flow in experiments. The experiments indicate that the increase of CMC concentration impedes the hydrate formation while the increase of liquid velocity enhances formation rates. In the stirred reactor, the hydrate formation rate generally decreases as the subcooling condition decreases. However, in this work, with the subcooling condition continuously decreasing, hydrate formation rate follows a “U” shaped trend—initially decreasing, then leveling out and finally increasing. It is because the hydrate formation rate in this work is influenced by multiple factors, such as hydrate shell formation, fracturing, sloughing, and bubble breaking up, which has more complicated mass transfer procedure than that in the stirred reactor. A semiempirical model that is based on the mass transfer mechanism is developed for current experimental conditions, and can be used to predict the formation rates of gas hydrates in the non-Newtonian fluid by replacing corresponding correlations. The rheological experiments are performed to obtain the rheological model of the CMC aqueous solution for the proposed model. The overall hydrate formation coefficient in the proposed model is correlated with experimental data. The hydrate formation model is verified and the predicted quantity of gas hydrates has a discrepancy less than 10%.


2012 ◽  
Vol 550-553 ◽  
pp. 2738-2744 ◽  
Author(s):  
Han Min Xiao ◽  
Ling Hui Sun ◽  
Hui Hui Kou

Experiments on chromatography separation are taken for ASP flooding. Mass transfer equation is estabilished and mutiple adsorption factor is obtained. Mutiple adsorption factor is used to analyze the experiment results. The Mass transfer property of alkali, surfactant and polymer during single fooding and ASP flooding and the effect on interfacial tension of oil/solution are discussed. The results show the diffrence of hesteris degree of alkali, surfactant and polymer deduce the chromatography separation, lowing the active of ASP flooding. Accoding to interfacial tension, the efficent length of ASP slug is discussed.


1999 ◽  
Vol 33 (2) ◽  
pp. 372-372
Author(s):  
Linda K. Weavers ◽  
Michael R. Hoffmann

2008 ◽  
Vol 273-276 ◽  
pp. 776-781 ◽  
Author(s):  
Patricia F. Lito ◽  
Carlos Manuel Silva

Two models comprising external and intraparticle mass transfer resistances developed to describe ion exchange in microporous materials are compared. Maxwell-Stefan and Nernst-Planck equations account for both concentration and electric potential gradients. However, under certain conditions, Maxwell-Stefan approach can be more advantageous particularly due to taking into account ion-ion and ion-solid interactions separately. The models were tested and compared with data available in the literature, namely batch experiments on cadmium (II) removal from aqueous solution using ETS-4 microporous titanosilicate. Calculated results reveal both models provide good and similar representations as well as fine predictive capability. Therefore, under the conditions investigated, both models can be successfully applied to describe intraparticle ionic transport.


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