纳米颗粒吸附岩心表面的强疏水特征

通过将疏水的纳米颗粒吸附在岩心微通道壁面,可以形成具有类荷叶表面的双重微结构表面,从而在注水开发的过程中在岩心微通道壁面产生水流滑移,达到降低注水压力、增加注水量的目的.研究纳米颗粒吸附岩心切片表面的强疏水特征对纳米颗粒吸附法减阻技术具有重要的意义.本文简要叙述了荷叶、蚊子腿以及水黾腿的超疏水特征;介绍了制备具有亚微米、纳米双重微结构的强疏水表面的纳米颗粒吸附法;给出了规则排列时纳米颗粒吸附岩心切片表面的强疏水特征的物理机制,根据真实的纳米颗粒吸附岩心切片,给出了接触角的范围,计算结果与实验数据一致.岩心流动实验结果表明,经纳米颗粒分散液处理后,岩心的平均水相渗透率提高94%.     

表面活性剂对气-液界面纳米颗粒吸附规律的影响

通过测定及分析纳米颗粒和表面活性剂-纳米颗粒复配体系在自由吸附过程与动态收缩过程中表面张力的变化,总结了纳米颗粒在气-液界面的吸附排布规律以及表面活性剂对其吸附规律的影响.实验结果表明,自由吸附过程中,随矿化度增加、阳离子活性剂浓度增加,平衡表面张力降低,这与颗粒吸附密度增加及颗粒润湿性改变有关.浓度低于临界胶束浓度(CMC)时,阳离子活性剂体系与混合体系的表面张力差异证明了阳离子活性剂可以通过静电作用吸附于纳米颗粒表面,进而部分溶解于水相;而阴离子活性剂与纳米颗粒相互作用力较弱,对表面张力影响较小.纳米颗粒体系在液滴收缩过程中,表面张力从自由吸附平衡态进一步降低大约9 m N/m,说明自由吸附过程中纳米颗粒不能达到紧密排布;同时表面张力呈现为缓慢降低、快速降低和达到平衡三部分,表面压缩模量可达70 m N/m,满足了液膜Gibbs稳定准则,这将有助于提高泡沫或者乳液稳定性.纳米颗粒-表面活性剂体系在液滴收缩过程中表面张力降低值随活性剂浓度增加而减小;表面压缩模量由高到低依次为:纳米颗粒>阳离子活性剂-纳米颗粒>阴离子-纳米颗粒>表面活性剂.     

表面活性剂辅助二氧化硅纳米颗粒在非水基液中的分散研究（英文）

研究了粒径10~100nm的二氧化硅纳米颗粒在非水基液中的表面活性剂辅助分散。结合颗粒表面特定官能团结构,针对性选择了合适的表面活性剂,氢键桥梁作用和长链分子空间位阻作用抑制了颗粒团聚行为。当表面活性剂体积分数6%的时候,动态光散射测试结果表明颗粒中位尺度30.2nm,与透射电镜测试结果吻合,展现了良好的分散性。     

表面活性剂辅助二氧化硅纳米颗粒在非水基液中的分散研究

研究了粒径10~100 nm的二氧化硅纳米颗粒在非水基液中的表面活性剂辅助分散。结合颗粒表面特定官能团结构,针对性选择了合适的表面活性剂,氢键桥梁作用和长链分子空间位阻作用抑制了颗粒团聚行为。当表面活性剂体积分数6%的时候,动态光散射测试结果表明颗粒中位尺度30.2 nm,与透射电镜测试结果吻合,展现了良好的分散性。     

水基ZnO纳米流体电导和热导性能研究

利用水热法生成了形状规则、粒径均匀的球形ZnO纳米颗粒, 并超声分散于水中, 制备得到稳定的水基ZnO纳米流体. 实验测量水基ZnO纳米流体在体积分数和温度变化时的电导率, 并测试室温下水基ZnO纳米流体在不同体积分数下的热导率. 实验结果表明, ZnO纳米颗粒的添加较大地提高了基液(纯水)的热导率和电导率, 水基ZnO纳米流体的电导率随纳米颗粒体积分数增加呈非线性增加关系, 而电导率随温度变化呈现出拟线性关系; 纳米流体的热导率与纳米颗粒体积分数增加呈近似线性增加关系. 本文在经典Maxwell热导模型和布朗动力学理论的基础上, 同时考虑了吸附层、团聚体和布朗运动等因素对热导率的影响, 提出了热导率修正模型.将修正模型预测值与实验值对比, 结果表明修正模型可以较为准确地计算出纳米流体的热导率. 关键词： 水热法 电导率 热导率 热导模型     

纳米粒子构建表面的超疏水性能实验研究

采用疏水纳米粉体压片法和岩心吸附法构建了具有微纳米结构的表面,测试了这些表面的接触角,拍摄了水滴在吸附纳米粒子的岩石表面的滚动过程照片,采用扫描电子显微镜(scanning electron microscope,SEM)检测了表面的微结构.实验结果表明：无机纳米粒子经弱疏水性材料修饰后,其表面润湿性由强亲水变为强疏水;疏水纳米粒子吸附表面的接触角均大于120°,滚动角约7°,显示出超疏水特性;SEM照片显示,这些超疏水表面是具有不规则微纳米结构的气固复合面,符合Cassie-Baxter的复合表面模型. 关键词： 超疏水 纳米粒子 微纳米结构表面 接触角     

超疏水纳米结构表面池沸腾特性

本文通过采用物理气相沉积法于TiO2纳米管阵列表面修饰一层聚四氟乙烯(PTFE)纳米颗粒,得到超疏水表面,并研究此超疏水纳米结构表面的池沸腾特性.研究表明,超疏水纳米结构表面沸腾特性类似于膜沸腾,沸腾工质难以浸润该表面,其沸腾传热系数及临界热流密度均较低.分析表明,固液处于Cassie-Baxter接触状态,纳米结构表...     

纳米Fe3O4磁性液体稳定性的研究

从理论上解析了磁性颗粒之间的相互作用对纳米磁性液体稳定性的影响 ,指出磁粒半径和浓度 ,表面活性剂的包覆是影响磁液稳定性的重要因素 .采用湿化学共沉淀法制备了纳米Fe3O4 磁性液体 ,经过TEM等手段的表征 ,证明平均粒径为 10nm ,稳定性良好 .实验研究了加料方式、搅拌速度、分散作用、表面活性剂包覆时机、包覆时间和加入量以及pH值诸多工艺因素对磁液稳定性的影响 ,并分析了这些因素的影响机制     

憎水性金属纳米粒子及其LB膜的制备与光谱表征

用油酸钠和十四烷基硫醇作为稳定剂,制备了高度单分散的疏水性银和金纳米溶胶。考察了单粒子层的π－Ａ曲线并建造了纳米粒子的ＬＢ膜。通过紫外可见光谱讨论了纳米粒子的分散状态,由红外光谱结果讨论了纳米粒子表面有机吸附层的状态。     

α-烯烃减阻聚合物隔离包覆中吸附过程的分子动力学模拟

采用分子动力学模拟方法,在α-烯烃聚合物颗粒聚氨酯类隔离体包覆机理的基础上,对α-烯烃减阻聚合物隔离包覆过程所涉及的吸附过程进行了研究. 结果表明,不同表面活性剂与同一多元羟基化合物、不同多元羟基化合物与同一表面活性剂相互之间的作用类似,呈现出吸附分布程度不同、与颗粒表面接近程度不一的现象,通过模拟给出了接近程度的顺序;包覆过程中进行的加成聚合反应其控制步骤为吸附传质过程,多元羟基化合物的分布离颗粒表面越近,越利于其与异氰酸酯在表面进行反应,模拟结果给出了表面活性剂和多元羟基化合物的选择配伍关系.     

疏水表面滑移流动及减阻特性的格子Boltzmann方法模拟

采用格子Boltzmann方法研究了固体壁面对流体的作用强度与其润湿性的关系,在此基础上进一步模拟了疏水表面微通道内的流体流动,获得了润湿性对疏水表面滑移流动及减阻特性的影响规律,证实了疏水表面表观滑移的存在性并揭示了其产生机理.结果表明,疏水性作用在疏水表面的近壁区诱导了一个低密度层,而表观滑移则发生在低密度层上.表观滑移是疏水表面具有减阻作用的直接原因,减阻效果随滑移长度的增大而增大.对于特定的流体系统,滑移长度是疏水表面的固有属性,仅是壁面润湿性的单一函数,而与流动本身的性质无关.     

The role of poly(methacrylic acid) conformation on dispersion behavior of nano TiO2 powder

To exploit the advantages of nanoparticles for various applications, controlling the dispersion and agglomeration is of paramount importance. Agglomeration and dispersion behavior of titanium dioxide (TiO₂) nanoparticles was investigated using electrokinetic and surface chemical properties. Nanoparticles are generally stabilized by the adsorption of a dispersant (polyelectrolyte) layer around the particle surface and in this connection ammonium salt of polymethacrylic acid (Darvan C) was used as dispersant to stabilize the suspension. The dosages of polyelectrolyte were optimized to get best dispersion stability by techniques namely particle charge detector (13.75 mg/g) and adsorption (14.57 mg/g). The surface charge of TiO₂ particles changed significantly in presence of dispersant Darvan C and isoelectric point (iep) shifted significantly towards lower pH from 5.99 to 3.37. The shift in iep has been quantified in terms of free energy of interaction between the surface sites of TiO₂ and the adsorbing dispersant Darvan C. Free energies of adsorption were calculated by electrokinetic data (−9.8 RT unit) and adsorption isotherms (−10.56 RT unit), which corroborated well. The adsorption isotherms are of typical Langmuir type and employed for calculation of free energy. The results indicated that adsorption occurs mainly through electrostatic interactions between the dispersant molecule and the TiO₂ surface apart from hydrophobic interactions.     

适配体纳米金比色分析技术研究进展

核酸适配体作为一种生物识别分子,其本质是一段单链DNA或RNA,折叠形成特定的二级、三级构象后与靶标分子以高亲和力高特异性结合。纳米金具有强烈的粒子间距光学效应,其在分散状态下呈红色,发生凝聚后变为蓝色。适配体可以通过共价偶联或静电吸附与纳米金结合,通过结合靶标来控制纳米金的颜色变化,从而提供了一种简单、快速、灵敏、可以肉眼观察的快速分析技术。综述了适配体纳米金比色分析技术的研究进展,通过对不同方法比较和讨论,提出了未来的研究方向。     

Melting evolution and diffusion behavior of vanadium nanoparticles

Molecular dynamics calculations have been performed to study the melting evolution, atomic diffusion and vibrational behavior of bcc metal vanadium nanoparticles with the number of atoms ranging from 537 to 28475 (diameters around 2–9 nm). The interactions between atoms are described using an analytic embedded-atom method. The obtained results reveal that the melting temperatures of nanoparticles are inversely proportional to the reciprocal of the nanoparticle size, and are in good agreement with the predictions of the thermodynamic liquid-drop model. The melting process can be described as occurring in two stages, firstly the stepwise premelting of the surface layer with a thickness of 2–3 times the perfect lattice constant, and then the abrupt overall melting of the whole cluster. The heats of fusion of nanoparticles are also inversely proportional to the reciprocal of the nanoparticle size. The diffusion is mainly localized to the surface layer at low temperatures and increases with the reduction of nanoparticle size, with the temperature being held constant. The radial mean square vibration amplitude (RMSVA) is developed to study the anharmonic effect on surface shells.     

Adsorption of surface functionalized silica nanoparticles onto mineral surfaces and decane/water interface

The adsorption of silica nanoparticles onto representative mineral surfaces and at the decane/water interface was studied. The effects of particle size (the mean diameters from 5 to 75?nm), concentration and surface type on the adsorption were studied in detail. Silica nanoparticles with four different surfaces [unmodified, surface modified with anionic (sulfonate), cationic (quaternary ammonium (quat)) or nonionic (polyethylene glycol (PEG)) surfactant] were used. The zeta potential of these silica nanoparticles ranges from ?79.8 to 15.3?mV. The shape of silica particles examined by a Hitachi-S5500 scanning transmission electron microscope (STEM) is quite spherical. The adsorption of all the nanoparticles (unmodified or surface modified) on quartz and calcite surfaces was found to be insignificant. We used interfacial tension (IFT) measurements to investigate the adsorption of silica nanoparticles at the decane/water interface. Unmodified nanoparticles or surface modified ones with sulfonate or quat do not significantly affect the IFT of the decane/water interface. It also does not appear that the particle size or concentration influences the IFT. However, the presence of PEG as a surface modifying material significantly reduces the IFT. The PEG surface modifier alone in an aqueous solution, without the nanoparticles, yields the same IFT reduction for an equivalent PEG concentration as that used for modifying the surface of nanoparticles. Contact angle measurements of a decane droplet on quartz or calcite plate immersed in water (or aqueous nanoparticle dispersion) showed a slight change in the contact angle in the presence of the studied nanoparticles. The results of contact angle measurements are in good agreement with experiments of adsorption of nanoparticles on mineral surfaces or decane/water interface. This study brings new insights into the understanding and modeling of the adsorption of surface-modified silica nanoparticles onto mineral surfaces and water/decane interface.     

Magnetic properties of NiO nano particles: Contributions of the antiferromagnetic and ferromagnetic subsystems in different magnetic field ranges up to 250 kOe

The magnetic properties of antiferromagnetic NiO nanoparticles prepared by thermal decomposition of nickel hydroxocarbonate are investigated. According to the data of magnetization measurements in fields of up to 250 kOe, the magnetic moment linearly grows in strong fields, which is caused by the contribution of the antiferromagnetically ordered nanoparticle core, and the antiferromagnetic susceptibility corresponds to that of bulk polycrystalline NiO. This allowed the antiferromagnetic and ferromagnetic contributions to the total magnetic response of a sample to be quantitatively determined. The latter occurs due to the incomplete spin compensation in an antiferromagnetic nanoparticle caused by defects on its surface. It is demonstrated that to correctly determine the superparamagnetic blocking temperature, it is necessary to take into account the antiferromagnetic susceptibility of the particle core.     

疏水表面减阻的格子Boltzmann方法数值模拟

采用格子Boltzmann方法的多松弛模型和Shan-Chen多相流模型对雷诺数为100的疏水表面方柱绕流进行了数值模拟, 分析了疏水表面接触角和来流含气率对方柱绕流流场的影响. 研究结果表明: 疏水表面接触角一定时, 来流含气率在一定范围内, 疏水表面具有减阻的能力, 超出这一范围时会出现阻力系数、升力系数升高的现象, 同时在方柱近壁面处伴随涡的形成产生了气团脱落; 当来流含气率处于适当水平时, 接触角越大, 绕流物体近壁面处含气率越稳定, 减阻效果越明显. 分析发现疏水表面减阻的关键在于保证近壁面处气层的稳定性, 此时接触角越大, 减阻效果越明显. 本文从含气率角度出发分析疏水表面的减阻现象, 为进一步探索疏水表面减阻机理提出了新的思路.     

Environmental response nanosilica for reducing the pressure of water injection in ultra-low permeability reservoirs

The super-hydrophobic silica nanoparticles are applied to alter the wettability of rock surface from water-wet to oil-wet. The aim of this is to reduce injection pressure so as to enhance water injection efficiency in low permeability reservoirs. Therefore, a new type of environmentally responsive nanosilica (denote as ERS) is modified with organic compound containing hydrophobic groups and “pinning” groups by covalent bond and then covered with a layer of hydrophilic organic compound by chemical adsorption to achieve excellent water dispersibility. Resultant ERS is homogeneously dispersed in water with a size of about 4–8 nm like a micro-emulsion system and can be easily injected into the macro or nano channels of ultra-low permeability reservoirs. The hydrophobic nanosilica core can be released from the aqueous delivery system owing to its strong dependence on the environmental variation from normal condition to injection wells (such as pH and salinity). Then the exposed silica nanoparticles form a thin layer on the surface of narrow pore throat, leading to the wettability from water-wet to oil-wet. More importantly, the two rock cores with different permeability were surface treated with ERS dispersion with a concentration of 2 g/L, exhibit great reduce of water injection pressure by 57.4 and 39.6%, respectively, which shows great potential for exploitation of crude oil from ultra-low permeability reservoirs during water flooding.

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Experimental investigation on underwater drag reduction using partial cavitation

For underwater drag reduction, one promising idea is to form a continuous gas or discrete bubbly layer at the submerged surface. Owing to the lower viscosity of gas than of water, this could considerably reduce underwater drag by achieving slippage at the liquid–gas interface. This paper presents an experimental investigation on underwater drag reduction using partial cavitation. Dense hydrophobic micro-grooved structures sustain gas in the valleys, which can be considered as defects that weaken the strength of the water body. Therefore, partial cavities are easily formed at lower flow speeds, and the dense cavities connect to form a lubricating gas layer at the solid–liquid interface. The results indicate that the proposed method achieves drag reduction without any additional energy or gas-providing devices, which should stimulate the development of underwater vehicles.     

疏水表面减阻环带实验研究

针对疏水功能材料在流动减阻方面的应用, 选取典型不同粗糙度、不同疏水性的功能涂层表面, 通过新型环带实验研究了其阻力特性, 并获得了相应的扭矩和减阻率曲线. 实验采用测量圆盘带动环带旋转时的扭矩的方法间接计算环带表面所受的摩阻, 突破了传统微管道实验在尺度上的限制, 避免了水洞实验中影响因素过多的弊端, 对疏水材料的宏观应用有着重要意义. 实验证实了在宏观尺度下疏水涂层在低雷诺数时的减阻作用; 但在高雷诺数时, 减阻作用减弱, 甚至部分涂层有增阻作用, 而压差阻力的迅速增大是造成增阻的主要原因. 通过对比分析认为: 低雷诺数时, 疏水特性对于减阻效果影响更大; 而高雷诺数时, 粗糙度起更大作用, 甚至可能起到增阻的反效果. 关键词： 疏水表面 环带实验 粗糙度 减阻