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Calcite Wettability in the Presence of Dissolved Mg2+ and SO42-

机译:Mg2 +和SO42-存在下的方解石润湿性

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摘要

The wettability of mineral surfaces controls a range of phenomena in. natural and industrial processes. In reservoirs, rock wettability determines the effectiveness of oil production; thus, modification of mineral surface properties can lead to enhanced oil recovery. Recent work reports that potential determining ions in seawater, Mg2+, Ca2+, and SO42-, are responsible for altering the wettability of calcite surfaces. In favorable conditions, e.g., elevated temperature, calcium at the calcite surface can be replaced by magnesium, making organic molecules bind more weakly and water molecules bind more strongly,, rendering the surface more hydrophilic. We used atomic force microscopy in chemical force mapping mode to probe the adhesion forces between a hydrophobic CH3-terminated AFM tip and a freshly cleaved calcite {10.4} surface to investigate wettability change in the presence of Mg2+ and SO42- at 75 and 80 degrees C. We made submicrometer scale maps of adhesion force and contact angle and demonstrated that the adhesion force between the hydrophobic tip and calcite decreases when both. Mg and SO4 are present. Surface analysis with X-ray photoelectron spectroscopy showed Mg associated with calcite even after rinsing with CaCO3-saturated deionized water, suggesting sorption on or in calcite. When the calcite saturated solution of MgSO4 was replaced by calcite-saturated NaCl at the same ionic strength, adhesion force increased again, indicating that the effect is reversible and suggesting Mg replacement by Ca. Experiments with solutions of Na2SO4 and MgCl2 suggest that Mg2+ uptake is favored when SO42- is also present.
机译:矿物表面的润湿性控制着自然和工业过程中的一系列现象。在储层中,岩石的润湿性决定了采油的有效性。因此,改变矿物表面性质可以提高采油率。最近的工作报告指出,海水,Mg2 +,Ca2 +和SO42-中潜在的决定性离子与改变方解石表面的润湿性有关。在有利的条件下,例如高温,方解石表面的钙可以被镁替代,从而使有机分子更弱地结合而水分子更强地结合,从而使表面更具亲水性。我们使用原子力显微镜以化学力作图模式研究了疏水CH3端接的AFM尖端与刚裂解的方解石{10.4}表面之间的粘附力,以研究在75和80摄氏度下Mg2 +和SO42-存在下的润湿性变化我们绘制了粘附力和接触角的亚微米比例图,并证明了疏水性尖端和方解石之间的粘附力均会降低。存在Mg和SO4。用X射线光电子能谱进行的表面分析表明,即使在用CaCO3饱和的去离子水冲洗后,镁也与方解石有关,这表明方解石上或内部有吸附。当以相同的离子强度用方解石饱和的NaCl代替MgSO4的方解石饱和溶液时,粘附力再次增加,这表明该作用是可逆的,表明Mg被Ca替代。用Na2SO4和MgCl2溶液进行的实验表明,当还存在SO42-时,Mg2 +的吸收会受到促进。

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  • 来源
    《Energy & fuels》 |2017年第1期|1005-1014|共10页
  • 作者单位

    Univ Copenhagen, Dept Chem, NanoSci Ctr, DK-2100 Copenhagen, Denmark;

    Univ Copenhagen, Dept Chem, NanoSci Ctr, DK-2100 Copenhagen, Denmark;

    Univ Copenhagen, Dept Chem, NanoSci Ctr, DK-2100 Copenhagen, Denmark;

    Univ Copenhagen, Dept Chem, NanoSci Ctr, DK-2100 Copenhagen, Denmark;

    Univ Copenhagen, Dept Chem, NanoSci Ctr, DK-2100 Copenhagen, Denmark;

    Univ Copenhagen, Dept Chem, NanoSci Ctr, DK-2100 Copenhagen, Denmark;

    Univ Copenhagen, Dept Chem, NanoSci Ctr, DK-2100 Copenhagen, Denmark;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 00:39:30

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