This investigation adopts a new perspective on wettability alteration as a function of temperature. Colloidal (i.e., DLVO) theory and calculations are used to interpret results from laboratory-scale displacements. Water imbibition tests were conducted with 9 reservoir cores from a diatomaceous reservoir. Permeability and porosity of cores varied from 0.2 to 0.7 md and 46% to 65%, respectively. The experiments included spontaneous counter-current water imbibition followed by forced co-current water imbibition to residual oil saturation. The fluids were 34 degrees API crude oil and synthetic formation brine. All tests were isothermal and temperatures ranged from 45 to 230 degrees C at pressures sufficient to maintain liquid water. The experimental results show that an increase in temperature results in: (1) a substantial increase in imbibition rate and extent of oil recovery, (2) a slight reduction in residual oil saturation, and (3) a significant shift in the Amott wettability index from intermediate and weakly water wet to strongly water wet. DLVO calculations illustrate detachment of fines from pore surfaces at high temperature. Fines detachment is a mechanism for altering wettability. Release of fines coated with oil exposes clean water-wet pore surfaces. Further calculations indicate the water-oil contact angle decreases as temperature increases indicating a systematic increase in water wettability consistent with experimental measurements of the Amott index. (c) 2006 Elsevier B.V. All rights reserved.
机构:
Department of Petroleum Engineering, Faculty of Chemical Engineering, Tarbiat Modares UniversityDepartment of Chemical Engineering Sanandaj Branch, Islamic Azad University
Mostafa Hosseini
Ebrahim Tangestani
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Faculty of Chemical Engineering, Tarbiat Modares UniversityDepartment of Chemical Engineering Sanandaj Branch, Islamic Azad University
Ebrahim Tangestani
Seyyed Ebrahim Mousavi
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Faculty of Chemical Engineering, Tarbiat Modares UniversityDepartment of Chemical Engineering Sanandaj Branch, Islamic Azad University
Seyyed Ebrahim Mousavi
Mohammad Niazi
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Faculty of Chemical Engineering, Tarbiat Modares UniversityDepartment of Chemical Engineering Sanandaj Branch, Islamic Azad University
机构:
China Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R ChinaChina Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China
Xu, Derong
Bai, Baojun
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China Univ Petr Beijing Karamay, Sch Petr Engn, Karamay 834000, Peoples R China
Missouri Univ Sci & Technol, Dept Geosci & Geol & Petr Engn, Rolla, MO 65409 USAChina Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China
Bai, Baojun
Wu, Hairong
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China Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R ChinaChina Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China
Wu, Hairong
Hou, Jirui
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China Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R ChinaChina Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China
Hou, Jirui
Meng, Ziyu
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China Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R ChinaChina Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China
Meng, Ziyu
Sun, Renxian
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China Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R ChinaChina Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China
Sun, Renxian
Li, Zhe
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China Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R ChinaChina Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China
Li, Zhe
Lu, Yao
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China Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R ChinaChina Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China
Lu, Yao
Kang, Wanli
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China Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China
China Univ Petr East China, Sch Petr Engn, Qingdao 266000, Peoples R ChinaChina Univ Petr, Inst Enhanced Oil Recovery Res, Beijing 102249, Peoples R China