Soft Matter
·
2019
·Vol. 15
·期 27
·5529-5536
·
IF 3.399
Han Jia,Xu Leng,Peng Lian,Yugui Han,Qiuxia Wang,Shaoyan Wang,Tunan Sun,Yipu Liang,Pan Huang,Kaihe Lv
Additional HCl can facilely control the dynamic noncovalent interaction between anionic surfactant sodium dodecyl benzene sulfonate (SDBS) and additional organic matter, 4,4′-oxydianiline (ODA), at the water/oil interface. At low HCl concentration (ODA/HCl molar ratio (r) = 1 : 1.5, [ODA] = 250 mg L−1), the ODA+ ions effectively enhanced the SDBS ability to reduce the water/oil interfacial tension (IFT) by about two orders of magnitude, while the (SDBS)2/ODA2+ gemini-like surfactants could be constructed at a relatively high HCl concentration (r = 1 : 4, [ODA] = 250 mg L−1), which could largely reduce the IFT to 1.19 × 10−3 mN m−1. Molecular simulation was employed to explore the interfacial activity of ODAn+ (ODA+/ODA2+) ions and the SDBS/ODAn+ interaction. The control experiments used another three surfactants to verify the proposed model. The pH-switchable gradual protonation of amino groups in ODA molecules determined the SDBS/ODA interfacial assembly, which was responsible for the reversal of IFT variations and the related emulsion behaviors.
研究领域:
化学
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界面科学
·
胶体与表面化学
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DOI
PubMed
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2023
·
IF 5.2
Xiaofang Li,Zechen Yan,Kangxing Wei,Xu Zhu,Lei Zhu,Tianci Huo,Yan Li,Qingzhong Xue
In order to investigate the flow behavior and oil displacement of ultralow interfacial tension (IFT) surfactant flooding, the experimentally validated computational fluid dynamics simulation model is constructed by coupling the Navier-Stokes equations and the Cahn-Hilliard equation. The mixed surfactant solution is prepared using the ionic liquid surfactant and the nonionic surfactant , and the fluid parameters are measured experimentally. Due to the reduced oil-water IFT, the low pressure drop in porous medium and the decreased oil viscosity, ultralow IFT surfactant contributes to increasing the mobility ability of the fluid front in pores, and its optimal injection velocity is 0.01 m/s. In addition, the sweep area of surfactant flooding in oil-wet porous medium is significantly larger than that of brine flooding because of wettability alteration. Finally, for different porosity models, the residual oil content and the pressure drop of surfactant flooding show a 66.7% and 71.4% decrease than those of brine flooding, respectively, proving its better displacement performance.
研究领域:
石油工程
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化学工程
·
计算流体力学
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DOI
高影响因子
JOURNAL OF SURFACTANTS AND DETERGENTS
·
2018
·Vol. 22
·期 1
·47-60
·
IF 1.454
Limin Yan,Ji Ma,Zhenggang Cui,Jianzhong Jiang,Binglei Song,Xiaomei Pei
A new series of sulfobetaine surfactants with double-chain single-head structure were derived from 1,3-dialkyl glyceryl ethers and their performances in reducing Daqing crude oil/connate water interfacial tension (IFT) in the absence of alkali were studied. With a large hydrophilic head group and double hydrophobic chains, these surfactants are efficient at reducing crude oil/connate water IFT. Those with didecyl and dioctyl are good hydrophobic surfactants that can reduce Daqing crude oil/connate water to ultra-low IFT by mixing with a small molar fraction of various conventional single-chain hydrophilic surfactants, such as α-olefin sulfonates, dodecyl polyoxyethylene (10) ether, and cetyl dimethyl hydroxypropyl sulfobetaine. The asymmetric double-chain sulfobetaine derived from 1-decyl-3-hexyl glyceryl ether can reduce Daqing crude oil/connate water IFT to ultra-low solely over a wide concentration range (0.03–10 mM or 0.0017–0.58 wt.%), which allows for use of an individual surfactant instead of mixed surfactants to avoid chromatographic separation in the reservoir. In addition, formulations rich in sulfobetaine surfactants show low adsorption on sandstone, keeping the negatively charged solid surface water-wet, and forming crude oil-in-water emulsions. These new sulfobetaine surfactants are, therefore, good candidates for surfactant-polymer flooding free of alkali. Graphical
研究领域:
石油化学
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界面科学
·
采油工程
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产品关联
DOI
高影响因子
FLUID PHASE EQUILIBRIA
·
2017
·
IF 2.473
Qiaoyan Shang,Shuqian Xia,GuanWei Cui,Bo Tang,Peisheng Ma
Interfacial tension (IFT) is crucial for characterizing the phase and interphase behavior in the enhanced oil recovery (EOR) process. CO 2 and N 2 are commonly used as injection gases in the EOR process. In this work, an experimental apparatus using the pendent drop method was adopted to measure IFTs for the EOR process with different injection gases, temperatures (40.0–120.0 °C) and pressures (0.22–17.32 MPa). The relative Gibbs adsorption isotherm ( Γ ij ) of a species i on species j were calculated by the experimental IFTs. Theoretically, new correlations were proposed to predict paraffin IFTs for pure CO 2 and mixture gas (CO 2 + N 2 ) injection. A total of 561 and 268 experimental IFTs were used to derive the correlations for pure CO 2 and mixture gas injection, respectively. The square of correlation coefficient ( R 2 ), root mean square error ( RMSE ) and average absolute relative deviations ( AARD ) for pure CO 2 were 0.9884, 0.58 and 5.45%, respectively. For the mixture gas injection, the R 2 , RMSE and AARD of the correlation were 0.9851, 0.57 and 4.47%, respectively.
研究领域:
石油工程
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化学工程
·
热力学
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DOI
高影响因子
JOURNAL OF PETROLEUM SCIENCE AND ENGINEERING
·
2021
·
IF 4.346
Qi Wu,Yan Xu
Stimulus-responsive surfactant is becoming a hot research topic with high controllability and excellent emulsifying properties. In this work, an amidine naphthenate surfactant was synthesized for the first time by the reaction between alkyl amidine and naphthenic acid. Surface activity and emulsion performance of this novel surfactant in oil/water emulsion were investigated. Compared with the previously synthesized amidine bicarbonate surfactants, amidine naphthenate surfactants exhibited a superior emulsification performance above 60 °C due to their lower critical micelle concentration (CMC) and interfacial tension (IFT). The presence of two long alkyl groups is recognized as the main reason for its superior properties than amidine bicarbonate having only one long alkyl group. Increased hydrophobic interactions between the long alkyl chains and electrostatic interactions between the ionic head groups lead to the easier formation of micelles. Notably, the amidine naphthenate has a characteristic of CO 2 -responsive property. The amidine naphthenate emulsion can be demulsified by CO 2 bubbling which destroys the chemical structure of amidine naphthenate, accompanied by the formation of amidine cations and naphthenic acids. Then, the emulsion was completely demulsified due to the demulsification effect of naphthenic acid. Therefore, the synthesized amidine naphthenate surfactant possesses not only high interface activity but also CO 2 responsive property, which endows it an extensive application prospect for enhanced oil recovery (EOR) operations in the oil industry.
研究领域:
化学
·
材料科学
·
石油工程
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产品关联
DOI
高影响因子
JOURNAL OF SURFACTANTS AND DETERGENTS
·
2021
·Vol. 24
·期 5
·749-760
·
IF 1.902
Hongyan Cai,Wenli Luo,Yancheng Zheng,Yi Zhang,Lu Lai,Shanfa Tang
Surface tension of a series of poly(ethylene glycol)-octyl sulfosuccinates at different temperatures was measured, and the interfacial properties were investigated in the absence and presence of inorganic salts. Surface tension results indicate that critical micelle concentration (CMC) values of five surfactants (C8-PEG200, C8-PEG400, C8-PEG600, C8-PEG800, and C8-PEG1000) decrease as the molecular weight of polyethylene glycol (PEG) segments and the experimental temperature increases. The surface activity of the C8-PEG series changes with temperature, and the surface tension at the CMC ( γ CMC ) of the C8-PEG series decreases initially and then increases as the PEG molecular weight increases. This behavior may be attributed to the dehydration of the surfactant molecules, resulting in the change of hydrophile–lipophile balance for the different EO numbers in the surfactant molecules, which form a different surface energy film at the air–water interface. Negative ΔG m indicates that the micellization process of these surfactants is spontaneous and an entropically driven process. For the water/alkane interface, these surfactants have low interfacial activity. The interfacial tension (IFT) between these surfactants and alkanes increases first and then decreases with the increase in the molecular weight of PEG segments. After the addition of salt, the interfacial activity of the investigated surfactants increases significantly. The IFT between C8-PEG800 and 10–12 alkanes and between C8-PEG1000 and 12–16 alkanes reaches a low IFT magnitude of 10 −2 mN m −1 in the presence of 0.5% CaCl 2 or the mixed inorganic salts 0.5% NaCl+0.5% CaCl 2 .
研究领域:
物理化学
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胶体科学
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表面活性剂化学
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产品关联
DOI
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2022
·Vol. 30
·期 8
·20006-20019
·
IF 5.19
Lin Qinghua,Hong Mei
Fractional wettability is common in the dense non-aqueous phase liquids (DNAPL) contaminated sites. However, it is still unclear how fractional wettability affects surfactant-enhanced DNAPL immiscible mobilization in saturated porous media. The macro-contact angle of the fractional wettability media was measured. The results of column experiments showed that the entrapped tetrachloroethene (PCE) saturations after sodium dodecyl benzene sulfonate (SDBS) flooding were lower in the media where NAPL-wet sand was present compared with those in water-wet media. In the media which contained 25% octadecyltrichlorosilane (OTS)-treated sand, the entrapped PCE saturations decreased to the minimum, and the decrease was much larger in fine sand media. The SDBS-enhanced PCE recoveries were jointly affected by fractional wettability, particle size, and interfacial tension (IFT). When NAPL-wet sand was present and SDBS concentration was just 0.125 g⋅L −1 , the SDBS-enhanced PCE recoveries increased significantly. As the SDBS concentration continues to increase to 0.5 g⋅L −1 , they only increased slightly. In the fine sand media, the SDBS-enhanced PCE recoveries were higher, and they increased more obviously with the increase of NAPL-wet sand fractions. The influence weight of fractional wettability on SDBS-enhanced PCE recoveries was the largest (47.09%) under the experimental conditions. These findings indicate that it is important to consider fractional wettability characteristics when establishing a DNAPL immiscible mobilization strategy, because it is not sufficient to consider only IFT reduction, especially in media with finer pore structures.
研究领域:
环境科学
·
化学工程
·
水文地质学
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产品关联
DOI
PubMed
高影响因子
ACS ES&T Engineering
·
2022
·
IF 0
Ruobin Dai,Jiansuxuan Chen,Hongyi Han,Huimin Zhou,Zhiwei Wang
Polymeric membranes, which are typically synthesized from fossil-based polymers, will reach their end of life (EOL) and then be replaced, due to the inevitable accumulation of membrane fouling even though the periodic cleaning is applied. The conventional disposal methods of the EOL membranes are landfilling and incineration, which will lead to additional carbon emission and fossil resource depletion. Herein, we proposed a surfactant-regulated interfacial polymerization strategy, by adding sodium dodecylbenzene sulfonate (SDBS) in the piperazine (PIP) aqueous solution, for the one-step upcycling of the EOL polymeric microfiltration membrane to obtain a thin-film composite polyamide (PA) nanofiltration (NF) membrane. Revealed by the quartz crystal microbalance with dissipation analysis and molecular dynamics simulation, the presence of SDBS reduced interfacial tension (IFT) and regulated interfacial wettability, thereby facilitating adequate and uniform uptake of PIP monomers. The resulting upcycled NF membrane with 4 critical micelle concentration (CMC) of SDBS addition exhibited a favorable pure water permeance (20.1 ± 0.6 L m–2 h–1 bar–1) and a satisfactory Na2SO4 rejection of 98.6 ± 0.4% owing to the formation of a continuous PA layer with high cross-linking degree (89.3 ± 0.5%). The Na2SO4 permeability of the 4 CMC upcycled NF membrane was more than 1 magnitude lower than that of the upcycled NF membrane without SDBS addition. This study provides a facile, rapid, and cost-effective method for the one-step upcycling of EOL polymeric membranes, which thus improves the sustainability of membrane technology.
研究领域:
材料科学
·
环境工程
·
膜技术
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产品关联
DOI