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Epoxy Resin Exhibits Long-Term Durability and Chemical Stability as a Well Sealant 环氧树脂作为井密封剂具有长期耐久性和化学稳定性
Pub Date : 2021-11-29 DOI: 10.2118/204374-ms
F. Sabins, A. Apblett, R. Shafer, L. Watters
The necessity to verify epoxy resin sealant's reliability for well applications is amplified as its use increases. Limited data exists to confirm resin's long-term durability or chemical stability under exposure to well fluids at temperature and pressure. This paper presents laboratory results illustrating durability and stability of epoxy resin exposed to a range of well fluids over a span of temperatures. Additionally, results of accelerated thermal degradation testing further quantify long-term thermal and chemical stability. Epoxy resins formulated for a range of remedial and abandonment applications were cured in fresh water, CaCl2 brine, and hydrocarbon at 170°F up to one year. Additional samples cured in fresh water and water containing CO2 and H2S at elevated temperatures (220°F to 320°F) for up to six weeks to produce accelerated degradation reactions allowed the assessment of resin degradation verses temperature. Thermal Gravimetric Analysis (TGA) evaluated chemical and mechanical degradation verses time at temperatures ranging from 200°C to 400°C. Arrhenius calculations were performed to forecast long term stability of resins across their intended temperature ranges. Resulting data were analyzed to develop an inclusive assessment of resin stability and durability in well environments. Results indicate properly formulated epoxy resin is a mechanically, chemically, and thermally durable sealant for well applications.
随着环氧树脂密封胶使用量的增加,验证其可靠性的必要性也越来越大。目前的数据有限,无法证实树脂在温度和压力下的长期耐久性或化学稳定性。本文介绍了实验室结果,说明了环氧树脂在一定温度范围内暴露于一系列井液中的耐久性和稳定性。此外,加速热降解测试的结果进一步量化了长期热稳定性和化学稳定性。为一系列补救和废弃应用而配制的环氧树脂在170°F的淡水、CaCl2盐水和碳氢化合物中固化长达一年。额外的样品在淡水和含有CO2和H2S的水中在高温下(220°F至320°F)固化长达6周,以产生加速降解反应,从而评估树脂降解随温度的变化。热重分析(TGA)在200°C至400°C的温度范围内评估了化学和机械降解随时间的变化。进行阿伦尼乌斯计算来预测树脂在其预期温度范围内的长期稳定性。分析所得数据,对树脂在井环境中的稳定性和耐久性进行全面评估。结果表明,配方合理的环氧树脂是一种机械、化学和热耐用的井用密封胶。
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引用次数: 0
Mechanical Properties of API Class C Cement Contaminated with Oil-Based Mud OBM at Elevated Temperatures and Early Curing Time 油基泥浆OBM污染的API C类水泥在高温和早期养护条件下的力学性能
Pub Date : 2021-11-29 DOI: 10.2118/204302-ms
Nachiket Arbad, F. Rincón, C. Teodoriu, M. Amani
The catastrophic events faced by the Oil and Gas industry in the past depict the importance of maintaining the integrity of the well. The cement acts as a crucial barrier throughout the life cycle of the well. The contamination of the cement occurs due to inefficiency in cementing practices and operations. Experimental investigations have been done on the reduction in mechanical properties of different API class cement considering contamination with water-based mud and oil-based mud. This study focuses on analyzing the changes in mechanical properties of API Class C cement on varying the following parameters: OBM contamination (0%, 0.6%, 1.1%, 2.2%, 4.3%) Curing time (4 hrs, 6 hrs, 8 hrs, 1 day, 3 days, 7 days) Temperature (25˚C, 75 ˚C) API recommendations were followed for preparing the cement slurries. The destructive, as well as non-destructive tests were carried out on the cement samples at ambient room temperature to measure the uniaxial compressive strength (UCS) for OBM contaminated class C cement slurries. The general trend observed is that the UCS increases with an increase in curing time and temperature. UCS decreases with an increase in OBM contamination. Logarithmic trends were obtained for UCS vs curing time for different contaminations at a given temperature. Exceptions were observed at lower curing times where contaminated samples showed better results than the neat cement slurries. These observations play a critical role in understanding contaminated cement behavior. This widespread work was carried out only on API Class C cement to provide reliable data for future references. The correlations presented in this paper will help operators estimate the deterioration in mechanical properties of Class C cement in the presence of low OBM contamination. Email: nachiket.arbad@ou.edu & cteodoriu@ou.edu
过去油气行业所面临的灾难性事件说明了保持油井完整性的重要性。水泥在井的整个生命周期中都是至关重要的屏障。水泥污染的发生是由于固井方法和操作效率低下。对不同原料药级水泥在考虑水基泥浆和油基泥浆污染的情况下力学性能的降低进行了实验研究。本研究重点分析了API C类水泥在以下参数变化时力学性能的变化:OBM污染(0%,0.6%,1.1%,2.2%,4.3%)养护时间(4小时,6小时,8小时,1天,3天,7天)温度(25˚C, 75˚C) API推荐的水泥浆制备方法。在室温条件下对水泥样品进行了破坏性和非破坏性试验,以测量OBM污染的C类水泥浆的单轴抗压强度(UCS)。观察到的总体趋势是,随固化时间和温度的增加,UCS增加。UCS随着OBM污染的增加而降低。在给定温度下,获得了不同污染的UCS与固化时间的对数趋势。在较短的养护时间内观察到例外情况,其中污染样品比干净的水泥浆表现出更好的结果。这些观察结果对理解受污染水泥的行为起着关键作用。这项广泛的工作仅在API C级水泥上进行,为将来参考提供可靠的数据。本文给出的相关性将有助于作业者估计低OBM污染情况下C级水泥力学性能的恶化情况。电子邮件:nachiket.arbad@ou.edu & cteodoriu@ou.edu
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引用次数: 2
Evaluation of Lignosulfonate Based Retarders for Thickening Time as a Function of Dosage and Temperature 木质素磺酸盐基缓凝剂增稠时间随用量和温度的变化规律
Pub Date : 2021-11-29 DOI: 10.2118/204327-ms
Justin Montgomery, T. McNally, Jay Hunger, S. Subramanian
The retardation of class H Portland cement using lignosulfonates was investigated in the temperature range between 54°C and 153°C. Lignosulfonates with varying extent of modification was used in the study, and the optimum retarder dosage and temperature range to achieve desired thickening time was identified for different lignosulfonate types (non-modified, modified and highly modified). In general, a linear thickening response was observed at low retarder dosage, while a near exponential increase in thickening time response was observed at higher dosages. Defining the retarder dosage temperature relationship is essential for proper cement slurry design for securing desired placement of cement slurry. A significant finding is that the thickening time responses trend from near linear at low dosages, transitioning to near exponential at higher dosages. The observed results varied depending on the extent of modification performed on the lignosulfonate retarder. Pure lignosulfonate retarders produce optimal dosage response from 54°C to 97°C. Modified retarders work best in the range of 97°C to 118°C. While highly modified retarders perform best in the range of 118°C to 153°C. Defining the retarder dosage temperature relationship is essential for proper cement slurry design for securing desired placement of cement slurry.
在54 ~ 153℃的温度范围内,研究了木质素磺酸盐对H类硅酸盐水泥的缓凝作用。研究中使用了不同改性程度的木质素磺酸盐,并对不同类型的木质素磺酸盐(未改性、改性和高度改性)确定了达到理想增稠时间的最佳缓凝剂用量和温度范围。一般来说,在低缓凝剂剂量下观察到线性增稠响应,而在高剂量下观察到近指数增长的增稠时间响应。确定缓凝剂掺量与温度的关系对于设计合适的水泥浆以确保水泥浆的理想位置至关重要。一个重要的发现是,增稠时间的响应趋势,从近线性在低剂量,过渡到近指数在高剂量。观察到的结果取决于对木质素磺酸盐缓凝剂进行改性的程度。纯木质素磺酸盐缓凝剂在54°C至97°C范围内产生最佳剂量反应。改性缓速剂在97°C至118°C范围内工作最佳。而高度改性缓凝剂在118 ~ 153℃范围内表现最佳。确定缓凝剂掺量与温度的关系对于设计合适的水泥浆以确保水泥浆的理想位置至关重要。
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引用次数: 0
Dry Cationic Friction Reducers: New Alternative for High TDS Slickwater 干式阳离子减摩剂:高TDS滑溜水的新选择
Pub Date : 2021-11-29 DOI: 10.2118/204286-ms
Linping Ke, Josselyne Chano, Melissa C. Weston, Hong Sun, Dong Shen
Currently, well stimulation in North America has evolved almost entirely to slickwater fracturing with friction reducers (FRs). Some parts of North America are notorious for their poor water quality, so wells are commonly treated using high total dissolved solids (TDS)-containing flow-back or produced water. Cationic FRs are usually applied in these systems due to their tolerance to multivalent cations in such waters. Additionally, dry friction reducers have gained momentum for better economics and logistics. In this paper, a dry cationic FR is systematically studied with respect to its "on the fly" hydration capability, friction reduction, mechanical stability, compatibility with other anionic chemical additives, and thermal stability in different levels of TDS brines. The cationic FR solution was subjected to varying shearing rates to understand its hydration capability, friction reduction, and mechanical stability. Its compatibility with anionic additives, such as a scale inhibitor, was also tested in a laboratory friction loop. Thermal stability of the cationic FR solution was studied at 150°F using a viscometer and Multi-Angle Laser Light Scattering (MALLS) method to obtain molecular weight information. The charge characteristics of the cationic FR, indicative of self-degradation properties, with exposure to heat, were also studied. Potential formation damage of the FR solution was evaluated with core flow tests in the absence of oxidizing breakers. Friction reduction and hydration tests show that the FR performs well in high TDS waters, even at low temperature, reaching its peak performance rapidly. The cationic FR possesses high mechanical stability even after being exposed to high pumping rates in the friction loop. It is well known that cationic FRs are not compatible with polyanionic scale inhibitors; in this study, a compatible scale inhibitor, SI-1, is identified. Additionally, there has historically been hesitation to use such cationic materials due to concerns of formation compatibility with negatively charged source rocks or flocculation in water treatment plants. Thermal testing with cationic FRs reveals that the material degrades to anionic without the aid of any other additive, which is confirmed by the fact that addition of polycationic additive, C1, caused coacervation in the heat-treated sample. As a result, concerns over effects of rock wettability or incompatibility with water treatment additives can be alleviated. No anionic FRs undergo similar change of the ionic charge. Thermal testing with cationic FR solutions also shows a significant viscosity drop, surprisingly without pronounced molecular weight loss (via MALLS). However, core flow testing of cationic FR fluids shows good regained permeability, even without breakers, further confirming self-cleaning capability. The degradation mechanism of these FRs will be shown. The self-cleaning capability of the dry cationic FR, even at relatively low bottomhole temperature
目前,北美地区的增产措施几乎完全发展为使用减摩剂(FRs)的滑水压裂。北美部分地区因水质差而臭名昭著,因此通常使用含高总溶解固体(TDS)的返排液或采出水进行处理。阳离子FRs通常应用于这些系统,因为它们对这些水中的多价阳离子具有耐受性。此外,干摩擦减速器已经获得了更好的经济和物流动力。本文系统地研究了一种干法阳离子FR在不同浓度TDS盐水中的“动态”水化性能、减阻性能、机械稳定性、与其他阴离子化学添加剂的相容性以及热稳定性。研究人员对阳离子FR溶液进行了不同剪切速率的实验,以了解其水化能力、摩擦减量和机械稳定性。它与阴离子添加剂(如阻垢剂)的相容性也在实验室摩擦环中进行了测试。利用粘度计和多角度激光散射(mall)方法研究了阳离子FR溶液在150°F下的热稳定性。还研究了阳离子FR的电荷特性,表明其在高温下的自降解性能。在没有氧化破冰剂的情况下,通过岩心流动试验评估了FR溶液对地层的潜在损害。减摩试验和水化试验表明,FR在高TDS水体中表现良好,即使在低温条件下也能迅速达到峰值性能。即使在摩擦环中暴露于高泵送速率后,阳离子FR也具有很高的机械稳定性。众所周知,阳离子fr与聚阴离子阻垢剂不相容;在本研究中,确定了一种相容性阻垢剂SI-1。此外,由于担心与带负电荷的烃源岩的地层相容性或水处理厂中的絮凝,人们一直在犹豫是否使用这种阳离子材料。用阳离子FRs热测试表明,材料在没有任何其他添加剂的情况下降解为阴离子,这一事实被多阳离子添加剂C1在热处理样品中引起凝聚的事实所证实。因此,可以减轻对岩石润湿性影响或与水处理添加剂不相容的担忧。阴离子FRs没有发生类似的离子电荷变化。用阳离子FR溶液进行热测试也显示出明显的粘度下降,令人惊讶的是没有明显的分子量损失(通过mall)。然而,阳离子FR流体的岩心流动测试显示,即使没有破冰剂,其恢复渗透率也很好,进一步证实了其自清洁能力。本文将介绍这些fr的降解机理。干阳离子FR的自清洁能力,即使在相对较低的井底温度(BHT)下,再加上其高耐盐性,使其成为多种应用的优秀减阻剂,特别是在低质量的水中。
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引用次数: 1
Critical Examination of Variables Effecting Friction Loop Results for Friction Reducer Selection 影响摩擦回路结果的变量对减速器选择的关键检验
Pub Date : 2021-11-29 DOI: 10.2118/204280-ms
C. Aften, Yaser Asgari, Lee Bailey, Gene Middleton, F. Muhammed, Parasmani Pageni, Keith Sullivan
Friction reducer evaluations for field application selection are conducted in laboratory benchtop recirculating flow loops or once-through systems. Industry standard procedures and benchtop flow loop (loop) system specifications for friction reduction assessment are nonexistent, though standardization efforts are recently documented. Research and papers correlating friction reducer performance to brine and additives have been published, however other key variables can significantly affect performance and therefore must be addressed to maximize product recommendation accuracy. This paper illustrates how variances affect results. Benchtop recirculating loops used for testing friction reduction products for a specific field's application vary significantly in system components, configurations, and test analyses. Crucial loop system variance examples include differing pipe diameters, pump configurations, flow meter types and placement, differential pressure section and full run lengths, reservoir designs, mixing conditions, and end performance calculations. Oil and gas producers and service companies are trending towards outsourcing friction reducers to independent testing laboratories for loop assessment results prior to recommending friction reducers for end use field applications. These recommendations may have inherent selection bias depending upon the loop system's components and configuration. Friction reduction calculations during loop testing do not consistently consider changes in viscosity and temperature, thereby altering absolute results when evaluating performance. To apply the simplified assumptions in standard pressure, drop methodology, equivalency in flow rate, density, viscosity, and temperature within the run must be maintained. Performance of the friction reducer in a specific brine and additive test run should primarily be dependent upon dosage and method of injecting friction reducer into the loop, however other variables can contribute to performance results. We presume equivalency in pipe roughness and proper loop cleansing. The effects of these variables on friction reduction response applying wide-ranging factors of flowrate, density, viscosity, and temperature are evaluated using designed experiments with responses plotted and illustrated in Cartesian and contour graphs. The result of these designed experiments identified that certain variables are more influential on friction reducers’ measured performances in standard loop experiments and require observation and documentation during performance testing. The final study in this work generated vastly different performance curves when all of the aspects of loop design, entry and differential run lengths, flow rate, injection method, friction reducer types and loadings, and brine types, densities, viscosities, and temperatures were held constant. The goal of benchtop loop testing is scaling for actual field applications. Scaling discrepancies persist however due to diffe
现场应用选择的减速器评估是在实验室台式再循环回路或直通系统中进行的。工业标准程序和工作台流回路(循环)系统规范的摩擦减少评估是不存在的,尽管标准化的努力最近记录。已经发表了将摩擦减速器性能与卤水和添加剂相关联的研究和论文,但是其他关键变量会显著影响性能,因此必须加以解决,以最大限度地提高产品推荐的准确性。本文说明了方差是如何影响结果的。用于测试特定领域应用的减阻产品的台式循环回路在系统组件,配置和测试分析方面差异很大。关键的循环系统差异示例包括不同的管径、泵配置、流量计类型和位置、压差段和全下钻长度、油藏设计、混合条件和末端性能计算。油气生产商和服务公司倾向于将减速器外包给独立的测试实验室,以获得循环评估结果,然后再推荐减速器用于最终的现场应用。根据回路系统的组件和配置,这些建议可能存在固有的选择偏差。环路测试中的摩擦减少计算没有始终考虑粘度和温度的变化,因此在评估性能时改变了绝对结果。为了在标准压降方法中应用简化的假设,必须保持下入过程中流量、密度、粘度和温度的等效性。在特定的卤水和添加剂测试中,摩擦减速器的性能主要取决于向循环注入摩擦减速器的剂量和方法,但其他变量也会影响性能结果。我们假定管道粗糙度和适当的回路清洗是相等的。应用流量、密度、粘度和温度等广泛因素对这些变量对摩擦减少响应的影响进行了评估,使用设计的实验对响应进行了绘制,并在笛卡尔和等高线图中进行了说明。这些设计实验的结果表明,在标准环试验中,某些变量对摩擦减速器的测量性能影响更大,需要在性能测试中进行观察和记录。在环路设计、入口和差速下入长度、流量、注入方式、减摩剂类型和载荷、盐水类型、密度、粘度和温度保持不变的情况下,最后的研究得出了截然不同的性能曲线。台式回路测试的目标是针对实际的现场应用进行扩展。然而,由于管道直径、流体回路设计、泵类型和速率的不同,再加上盐水成分、支撑剂和化学添加剂对减阻剂产品的影响,结垢差异仍然存在。了解不同的台式循环,或可能相同的台式循环,将产生不同的结果是有趣的,但令人不安的。
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引用次数: 0
Water-Based Nanofluid-Alternating-CO2 Injection for Enhancing Heavy Oil Recovery: Underlying Mechanisms that Influence its Efficiency 水基纳米流体交替注入二氧化碳提高稠油采收率:影响其效率的潜在机制
Pub Date : 2021-11-29 DOI: 10.2118/204331-ms
Changxiao Cao, Zhaojie Song, Shan Su, Zihan Tang, Zehui Xie, Xuya Chang
The efficiency of CO2 water-alternating-gas (WAG) flooding is highly limited in low-permeability heavy oil reservoirs due to the viscosifying action of W/O emulsification and high mobility contrast between oil and CO2. Here we propose a new enhanced oil recovery (EOR) process which involves water-based nanofluid-alternating-CO2 (NWAG) injection, and investigate the synergistic effect of nanofluid and CO2 for enhancing heavy oil recovery. Firstly, the oil-nanofluid and oil-water emulsions were prepared, and the bulk rheology and interfacial properties of emulsion fluid were tested. Then, core flooding tests were conducted to examine the NWAG flooding efficiency and its underlying mechanisms. The results showed that the bulk viscosity and viscoelasticity of oil-nanofluid emulsion reported much lower than those of oil-water emulsion, and nanofluid presented a positive contribution to the phase inversion from W/O to O/W emulsification. Compared with oil-water emulsion, the interfacial storage modulus of oil-nanofluid emulsion was obviously increased, which confirmed that more of crude oil heavy components with surface activity (e.g., resin and asphaltene) were adsorbed on interfacial film with the addition of silica nanoparticles (NPs). However, the interfacial viscosity of oil-nanofluid emulsion was much lower than that of oil-water emulsion, showing the irregularity of interfacial adsorption. This implied that the self-assembly structure of crude oil heavy component of the oil-water interface was destroyed due to the surface activity of silica NPs. During the core flooding experiments, NWAG injection could reduce the displacement pressure by 57.14% and increase oil recovery by 23.31% compared to WAG injection. By comparing produced-oil components after WAG and NWAG injection, we found that more of crude oil light components were extracted by CO2 during NWAG flooding, showing that the interaction between CO2 and crude oil was improved after oil-nanofluid emulsification. These findings clearly indicated two main EOR mechanisms of NWAG injection. One was the phase inversion during the nanofluid flooding process. The addition of silica NPs promoted phase-inversion emulsification and thus improved the displacement efficiency. The other was the enhanced interaction between CO2 and crude oil after oil-nanofluid emulsification. Because of the enhanced adsorption of crude oil heavy component on the oil-water interface, the proportion of light hydrocarbon increased in the bulk phase, and so the interaction between CO2 and oil phase was improved. This work could provide a new insight into the high-efficiency exploitation of low-permeability heavy oil reservoirs.
在低渗透稠油油藏中,由于水/油乳化的增粘作用和油与二氧化碳的高流动性对比,CO2水-气交替驱(WAG)的效率受到很大限制。本文提出了一种新型的水基纳米流体-交替注入二氧化碳(NWAG)提高采收率的方法,并研究了纳米流体和二氧化碳对稠油采收率的协同效应。首先,制备了油纳米流体和油水乳液,测试了乳化液的整体流变性能和界面性能。然后,进行岩心驱油试验,以检验NWAG驱油效率及其潜在机制。结果表明:油-纳米流体乳化液的体粘度和粘弹性明显低于油水乳化液,纳米流体对W/O乳化向O/W乳化的相转化有积极的贡献;与油水乳状液相比,油纳米流体乳状液的界面储存模量明显增加,这证实了二氧化硅纳米颗粒(NPs)的加入使更多具有表面活性的原油重质组分(如树脂和沥青质)被吸附在界面膜上。然而,油纳米流体乳状液的界面粘度远低于油水乳状液,显示出界面吸附的不规律性。这说明二氧化硅纳米粒子的表面活性破坏了油水界面原油重组分的自组装结构。岩心驱替实验中,注入NWAG可使驱替压力比注入WAG降低57.14%,采收率提高23.31%。通过对比注入WAG和NWAG后的产出油组分,我们发现NWAG驱油过程中,更多的原油轻质油组分被CO2萃取,说明油纳米流体乳化后,CO2与原油的相互作用得到改善。这些发现清楚地表明了NWAG注入的两种主要提高采收率机制。一是纳米流体驱油过程中的相反转。二氧化硅NPs的加入促进了相反转乳化,从而提高了驱替效率。二是油纳米流体乳化后CO2与原油的相互作用增强。由于原油重质组分在油水界面上的吸附增强,使得体积相中轻烃的比例增加,从而改善了CO2与油相的相互作用。该研究为低渗透稠油油藏高效开发提供了新的思路。
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引用次数: 0
Facile Fabrication of Nanoemulsions through the Efficient Catanionic Surfactants for Spontaneous Imbibition in Tight Oil Reservoirs: Experimental and Numerical Simulation 利用高效阳离子表面活性剂制备致密油自吸纳米乳液:实验与数值模拟
Pub Date : 2021-11-29 DOI: 10.2118/204336-ms
B. Wei, Runxue Mao, Haoran Tang, Lele Wang, Dianlin Wang, Yiwen Wang, Junyu You, Jun Lu
Spontaneous imbibition (SI) is an essential method for accelerating mass exchange between fracture and matrix in tight oil reservoirs. However, conventional systems such as brine and surfactant solution have limited imbibition effects, so there is still abundant remaining oil in the matrix. Nanoemulsion holds the most promising potential in improving tight oil recovery owing to the favorable surface activity and nanoscale droplets, but it still lacks economic and facile methods to fabricate nanoemulsions. Therefore, in this paper, we prepared a kind of O/W nanoemulsion of catanionic surfactants with a low dosage of surfactant and energy consumption, which was then used to assess spontaneous imbibition performance in Changqing outcrop cores by experimental and numerical simulation. We have fully considered the possible imbibition mechanisms of nanoemulsion including wettability alteration, IFT reduction, solubilization and emulsification, etc., and successfully applied to the nanoemulsion imbibition model. The model and experimental data were found to be in good agreement. The results showed that the imbibition rate and oil recovery factor of the nanoemulsion in the first 100 hours are lower than that of brine. In the late stage, we observed a longer equilibrium time and a faster and higher oil imbibition process in nanoemulsion with ultralow IFT. Finally, we confirmed that solubilization and emulsification is one of the domiant mechanisms for nanoemulsion imbibition by comparing with the modelling without considering solubilization and emulsification.
自发渗吸是致密油储层加速裂缝与基质间物质交换的重要手段。然而,卤水和表面活性剂等常规体系的吸胀效果有限,因此基质中仍然存在大量的剩余油。纳米乳液由于具有良好的表面活性和纳米级的液滴,在提高致密油采收率方面具有很大的潜力,但目前还缺乏经济、简便的制备方法。为此,本文制备了一种低表面活性剂用量、低能耗的阳离子表面活性剂O/W纳米乳液,并通过实验和数值模拟对长庆露头岩心的自吸性能进行了评价。我们充分考虑了纳米乳液可能的吸胀机制,包括润湿性改变、IFT还原、增溶和乳化等,并成功应用于纳米乳液的吸胀模型。模型与实验数据吻合较好。结果表明,纳米乳在前100小时的吸胀速率和采收率低于盐水;在后期,我们观察到超低IFT纳米乳的平衡时间更长,吸油速度更快,吸油速率更高。最后,通过与不考虑增溶和乳化的模型对比,证实了增溶和乳化是纳米乳吸胀的主要机理之一。
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引用次数: 1
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