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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2020 · IF 7.489

Tension gradient-driven oil/water interface rapid particle self-assembly and its application in microdroplet motion control

Xuan Li,Dong Feng,Lei Chen,Ding Weng,Chaolang Chen,Jiadao Wang

Hypothesis A binary mixture was used during injection with one water-miscible component and the other water-immiscible, which can help particles to migrate toward and then self-assemble at the interface. Experiments The ethanol-tetrachloromethane binary mixture was used to verify the self-assembly method, with the diameter of droplets being about 1 mm. As the ethanol diffused into the colloidal solution, the colloidal particles efficiently moved towards and self-assembled on the oil/water interface, while a colloidal particle film with high-coverage was able to rapidly form on the droplet surface even in an ultra-low concentration colloidal solution. The effects of ethanol concentration and particle concentration on self-assembly were investigated. Findings The driving force for self-assembly originated from the tension gradient generated by ethanol's concentration gradient at the particle/liquid interfaces, where the concentrations of ethanol and the colloidal solution had significant effects on self-assembly. The simulation and calculations results aligned well with experiments, providing the theoretical basis for this self-assembly method. Further, as-prepared magnetic particle-coated droplets transformed into a non-wetting soft solid, which had long lifetimes and could be precisely moved, coalesced, and transferred in various two-dimensional and three-dimensional liquid environments. Thus, wider applications are facilitated, such as droplet transfer, microreactor and other potential fields.

研究领域: 材料科学 · 化学工程 · 界面科学
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ADVANCED FUNCTIONAL MATERIALS · 2022 ·Vol. 32 ·期 45 ·2205462 · IF 19.924

Ultrafast Fabrication of Large-Area Colloidal Crystal Micropatterns via Self-Assembly and Transfer Printing

Xuan Li,Lei Chen,Yuan Ma,Ding Weng,Zhaoxin Li,Lele Song,Xuanhe Zhang,Guoxu Yu,Jiadao Wang

Colloidal crystals have brought the promise of revolution to modern engineering, yet commonly used fabrication technologies are still limited by the small preparation area, time-consuming process, and dependence on sophisticated equipment. Here, a surface tension gradient-driven self-assembly strategy is proposed for the ultrafast fabrication of large-area colloidal crystals. The hydrogel loaded with sodium dodecyl sulfate is devised to construct a stable and continuous liquid-air interfacial tension gradient, and the resulting Marangoni effect can drive the micro-nano particles to instantaneously form (within several seconds) highly ordered colloidal crystals. Benefiting from the long range of surface tension gradients, the fabrication area of colloidal crystal films is demonstrated to exceed an astonishing 1000 cm 2 without compromising their quality, showing great potential in scale-up manufacture. Moreover, particles of a wide variety of sizes, materials, and functionalities can form close-packed self-assembly monolayers and be transferred to various substrates without damage, exhibiting great versatility. Inspired by ink microprinting, an ultrafast nanoparticle transfer printing method is further proposed to convert the close-packed nanoparticle monolayers into large-area conformal micropatterns with single-nanoparticle resolution. The great potential of nanoparticle micropatterns is demonstrated in flexible micro-electronics/skin electronics. This user-friendly, efficient self-assembly, and micropatterning strategy provide promising opportunities for academic and real industrial applications.

研究领域: 材料科学 · 纳米技术 · 制造工程
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Journal of Physical Chemistry C · 2018 · IF 4.484

Electrocoalescence of Two Drops with Different Surfactant Concentrations Suspended in Oil

Xiaoming Luo,Haoran Yin,Haipeng Yan,Xin Huang,Donghai Yang,Limin He

In this study, the electrocoalescence characteristic of two drops with different surfactant concentrations suspended in oil is revealed. Different from the symmetrical coalescence of identical drops, the asymmetrical liquid bridge is induced by the capillary force, which involves the interfacial tension gradient between the drops. In addition, a mushroom-like jet is formed during asymmetrical coalescence, causing mixing of drops. A characteristic time considering the interfacial tension gradient is proposed to describe the asymmetrical liquid bridge evolution. The mushroom-like jet is found to be driven by the pressure difference between drops, which has a positive correlation with the interfacial tension gradient. Moreover, it is found that the electrocoalescence time is shortened as the interfacial tension increases. This study indicates that increasing the interfacial tension gradient will enhance the jet flow rate and reduce the coalescence time, which is of significance to improve the mixing efficiency of the drops.

研究领域: 物理学 · 化学工程 · 流体力学
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Petroleum Science · 2022 · IF 4.757

The enhancement of performance and imbibition effect of slickwater-based fracturing fluid by using MoS2 nanosheets

Hang Xu,Yuan Li,Guo-Lin Yu,Sa-Sa Yang,Bo-Jun Li,Fu-Jian Zhou,Er-Dong Yao,Hao Bai,Zhi-Yu Liu

Slickwater-based fracturing fluid has recently garnered significant attention as the major fluid for volumetric fracturing; however, lots of challenges and limitations such as low viscosity, poor salt tolerance, and possible formation damage hinder the application of the conventional simple slickwater-based fracturing fluid. In addition, nanomaterials have proven to be potential solutions or improvements to a number of challenges associated with the slickwater. In this paper, molybdenum disulfide (MoS 2 ) nanosheets were chemically synthesized by hydrothermal method and applied to improve the performance of conventional slickwater-based fracturing fluid. Firstly, the microstructure characteristics and crystal type of the MoS 2 nanosheets were analyzed by SEM, EDS, TEM, XPS, and Raman spectroscopy techniques. Then, a series of evaluation experiments were carried out to compare the performance of MoS 2 nanosheet-modified slickwater with the conventional slickwater, including rheology, drag reduction, and sand suspension. Finally, the enhanced imbibition capacity and potential mechanism of the nanosheet-modified slickwater were systematically investigated. The results showed that the self-synthesized MoS 2 nanosheets displayed a distinct ultrathin flake-like morphology and a lateral size in the range of tens of nanometers. In the nano-composites, each MoS 2 nanosheet plays the role of cross-linking point, so as to make the spatial structure of the entire system more compact. Moreover, nanosheet-modified slickwater demonstrates more excellent properties in rheology, drag reduction, and sand suspension. The nanosheet-modified slickwater has a higher apparent viscosity after shearing 120 min under 90 °C and 170 s −1 . The maximum drag reduction rate achieved 76.3% at 20 °C, and the sand settling time of proppants with different mesh in the nano-composites was prolonged. Spontaneous imbibition experiments showed that the gel-breaking fluid of nanosheet-modified slickwater exhibited excellent capability of oil-detaching, and increase the oil recovery to ∼35.43%. By observing and analyzing the interfacial behavior of MoS 2 nanosheets under stimulated reservoir conditions, it was found that the presence of an interfacial tension gradient and the formation of a climbing film may play an essential role in the spontaneous imbibition mechanism. This work innovatively uses two-dimensional MoS 2 nanosheets to modify regular slickwater and confirms the feasibility of flake-like nanomaterials to improve the performance of slickwater. The study also reveals the underlying mechanism of enhanced imbibition efficiency of the nano-composites.

研究领域: 材料科学 · 石油工程 · 纳米技术
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LANGMUIR · 2020 · IF 3.557

Hydrodynamic Process in the Langmuir-Blodgett Film Method

Wenjie Ji,Wenjing Zhao,Weibin Li,Yuren Wang,Jin Wang,Ding Lan

Preparing organic coatings in a very controlled manner through the spreading of organic molecules on the water surface is one of the emphases for research in Langmuir-Blodgett (LB) technology. For preparing a homogeneous film and improving the quality of the film, it is our concern to have a deeper understanding of the dynamic process involved in spreading. Here, we present an overview of the hydrodynamic process under the influence of assisting the spreading solvent, which mainly focuses on the mechanical mechanisms of related phenomena. A typical spreading experiment of two-component mixed droplets on water substrate for the purpose of preparing LB films was carried out in this research. We perform the spreading of a liquid of silicone oil and oleic acid mixture on the horizontal surface of another immiscible deep water substrate, where the volatile silicone oil is the assisting spreading solvent with low viscosity. We find that it needs to exceed a certain critical value (60% in our experiment) to achieve a uniform and centrosymmetric spreading process, which is a key factor for getting a homogeneous film. We observe that the evolution of a large droplet into liquid film and then into small droplets under the action of surface tension gradient in experiments. Gravity-viscous and surface tension-viscous dominate successively in the whole spreading process, with its spreading radius r(t) ∝ t1/4 and r(t) ∝ t3/4, respectively. However, we also obtain singular values of scaling exponents −0.033 and −0.180, which is attributed to nonuniform distribution of the Laplace pressure caused by different curvatures near the capillary wave.

CAS / MDL: 112-80-1
研究领域: 物理学 · 材料科学
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LANGMUIR · 2025 · IF 3.9

Self-Swimming Droplets Driven by the Synergistic Effects of the Fast Interfacial Polymerization and Hydrolysis Reactions

Xiaodong Lian,Jingwen Luo,Yizhou Ding,Bin Yuan,Yapei Wang

Self-swimming droplets, as an intriguing phenomenon in the microscopic realm, have traditionally been achieved by harnessing the interfacial properties of small-molecule emulsifiers. Herein, we successfully prepared self-swimming droplets by employing polymers. Leveraging the synergistic effects of fast interfacial polymerization and hydrolysis reactions, a polymer layer is rapidly formed at the oil–water interface, followed by the generation of weakly amphiphilic substances that establish an interfacial tension gradient. Thus, strong Marangoni circulation flows were induced to propel the droplets to move spontaneously. The interfacial behavior of the self-swimming droplets was investigated, revealing regular oscillations and the spontaneous formation of microdroplets on the larger droplet surface. Comparative experiments confirmed the synergistic effects of the two types of reactions in forming self-swimming droplets, as the absence of either reaction hindered autonomous movement. The movement time reaches 758 s, and the maximum speed of droplet movement reaches 5.08 mm/s. This work not only enriches the variety of self-swimming droplets but also provides theoretical guidance for designing and preparing innovative self-swimming systems.

CAS / MDL: 123-96-6
研究领域: 化学 · 材料科学 · 物理学
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PHYSICS OF FLUIDS · 2021 ·Vol. 33 ·期 2 · IF 3.521

Marangoni-driven instability patterns of an N-hexadecane drop triggered by assistant solvent

Zhao Wenjing,Ma Hongzhi,Ji Wenjie,Li Weibin,Wang Jin,Yuan Quanzi,Wang Yuren,Lan Ding

Flows of thin fluid layers spreading, which have a distinguished history, have been studied since the days of Reynolds, who was among the early researchers to examine flows. Different from surfactant-driven spreading, which is currently the most common subject of study, we observe the spreading process of n -hexadecane driven by volatile silicone oil at the surface of the aqueous substrates and explore the influence of Marangoni flow caused by surface tension gradient on liquid-driven spreading. We find that on different substrates, the initial state of n -hexadecane is different, and there are two instability patterns during the spreading, subsequently, which are analyzed theoretically. While the n -hexadecane drop stationed on the liquid surface is small, it is driven to form a rim and then breaks up into beads, which shows the Rayleigh–Plateau instability patterns. When we put the n -hexadecane drop on the surface of the saturated sodium chloride solution, which spreads out more, it is driven to form a circular belt first and fingering instability subsequently occurs at the inner edge of the circular belt.

研究领域: 流体力学 · 物理化学
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Theranostics · 2023 · IF 12.4

Stiff matrix induced srGAP2 tension gradients control migration direction in triple-negative breast cancer

Chen Li,Zihui Zheng,Xiang Wu,Qiu Xie,Ping Liu,Yunfeng Hu,Mei Chen,Liming Liu,Wangxing Zhao,Linlin Chen,Jun Guo,Ying Song

Rationale: Cells migrating through interstitial matrix enables stiffening of the tumor micro-environment. To overcome the stiff resistance of extracellular matrix, aggressive cells require the extracellular mechanosensory activation and intracellular tension response. Mechanotransduction linker srGAP2 can synergistically control the mechanical-biochemical process of malignant cell migration. Methods: To mimic the tumor micro-environment containing abundant collagen fibers and moving durotaxis of triple-negative breast cancer cells, the stiff-directed matrix was established. The newly designed srGAP2 tension probe was used to real-time supervise srGAP2 tension in living cells. The phosphorylation sites responsible for srGAP2 tension were identified by phosphorylated mutagenesis. Transwell assays and Xenograft mouse model were performed to evaluate TNBC cells invasiveness in vitro and in vivo . Fluorescence staining and membrane protein isolation were used to detect protein localization. Results: The present study shows srGAP2 serves as a linker to transmit the mechanical signals among cytoskeleton and membrane. SrGAP2 exhibits tension gradients among different parts in the stiff-directionally migrating triple-negative breast cancer cells. Cells showing the polarized tension that increased in the leading edge move faster, particularly guided by the stiff interstitial matrix. The srGAP2 tension-directed cell migration results from the upstream events of PKCα-mediated phosphorylation at Ser 206 in the F-bar domain of srGAP2. In addition, Syndecan-4 (SDC4), a transmembrane mechanoreceptor protein, drives PKCα regional recruit on the area of membrane trending deformation, which requires the distinct extent of extracellular mechanics. Conclusion: SDC4-PKCα polarized distribution leads to the intracellular tension gradient of srGAP2, presenting the extra- and intracellular physiochemical integration and essential for persistent cell migration in stiff matrix and caner progression. Targeting the srGAP2-related physicochemical signaling could be developed into the therapeutic strategies of inhibiting breast cancer cell invasion and durotaxis.

CAS / MDL: 674289-55-5
研究领域: 癌症生物学 · 细胞生物学 · 机械生物学 · 分子生物学
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Tension gradient-driven rapid self-assembly method of large-area colloidal crystal film and its application in multifunctional structural color displays

Xuan Li,Lei Chen,Ding Weng,Chaolang Chen,Zhaoxin Li,Jiadao Wang

Liquid-air interface self-assembly (such as the classic L-B method) is the most popular way to form high-quality colloidal crystal monolayers, yet still limited by sophisticated equipment, time-consuming processes and small preparation area. Here, a tension gradient-driven nanoparticle self-assembly method is proposed to realize the high-efficiency and low-cost fabrication of large-area (25 × 18 cm 2 ) colloidal crystal film. The periodic nanoparticle structures composed of various particles with different materials and diameters can be easily obtained in a short time and transferred to various substrates under this self-assembly method. And the preparation area is one to two orders of magnitude higher than the conventional self-assembly method. The simulation results align well with experiments, indicating that the Marangoni effect induced by tension gradient is the main driving force for self-assembly. The influence of various self-assembly parameters is investigated. Inspired by amber, a periodic particle/PDMS/nano-silica particles composite film is further designed to form a large-area durable structural color display. The structural color of the composite film is surprisingly different from that of the periodic particle which was mainly due to the unique semi-coated structure. The composite film has outstanding superhydrophobic and self-cleaning performance with a broad impact on durable structural color displays/sensors, anti-counterfeiting and other aspects.

CAS / MDL: 151-21-3
研究领域: 材料科学 · 纳米技术 · 光学 · 表面科学
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Nature Communications · 2022 ·Vol. 13 ·期 1 ·1-11 · IF 17.694

Generation of Fermat’s spiral patterns by solutal Marangoni-driven coiling in an aqueous two-phase system

Xiao Yang,Ribe Neil M.,Zhang Yage,Pan Yi,Cao Yang,Shum Ho Cheung

The solutal Marangoni effect is attracting increasing interest because of its fundamental role in many isothermal directional transport processes in fluids, including the Marangoni-driven spreading on liquid surfaces or Marangoni convection within a liquid. Here we report a type of continuous Marangoni transport process resulting from Marangoni-driven spreading and Marangoni convection in an aqueous two-phase system. The interaction between a salt (CaCl 2 ) and an anionic surfactant (sodium dodecylbenzenesulfonate) generates surface tension gradients, which drive the transport process. This Marangoni transport consists of the upward transfer of a filament from a droplet located at the bottom of a bulk solution, coiling of the filament near the surface, and formation of Fermat’s spiral patterns on the surface. The bottom-up coiling of the filament, driven by Marangoni convection, may inspire automatic fiber fabrication.

CAS / MDL: 10043-52-4
研究领域: 流体动力学 · 材料科学 · 表面化学
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Journal of Coatings Technology and Research · 2025 · IF 2.8

Method for preparing a self-stratifying epoxy/acrylic resin coating with micron-sized FeSiCr

Zhang Linbo,Hong Mu-Nai Jin,Yang Ruoyu,Jiang Xianyu,Zhou Yusheng,Zhang Tongqing,Yuan Le

This study develops and explores a self-stratifying coating system that incorporates both epoxy and acrylic resins. It examines the impact of film thickness and substrate type on self-stratification behavior, confirms predictions from the surface energy model, and identifies the surface tension gradient as the primary driving mechanism for stratification. Additionally, this research investigates the influence of FeSiCr powder on the stratification behavior of the coating. Results demonstrate that the self-stratifying coating, composed of a blend of epoxy and acrylic resins with FeSiCr powder, exhibits superior corrosion resistance compared to coatings formulated solely from a mixture of epoxy resin and FeSiCr powder. SEM-EDS analysis reveals that the enhanced corrosion resistance can be attributed to the accumulation of epoxy resin and FeSiCr at the bottom of the coating, while the acrylic resin forms an effective protective layer on the surface. Furthermore, the study examines the effects of FeSiCr powder content, solvent addition, and volatilization rate on the stratified structure and appearance of the coating. The findings indicate that at relatively low FeSiCr powder content, the layered structure of the coating remains largely intact, with the powder predominantly residing within the epoxy resin layer. However, increasing the powder content compromises the self-stratification structure, leading to a rougher coating surface. It is also observed that augmenting the quantity of the xylene/butyl acetate mixture reduces pit formation on the surface, while the use of MIBK solvent results in incomplete stratification and exacerbates surface roughness.

研究领域: 材料科学 · 涂层技术 · 腐蚀工程 · 高分子科学 · 表面化学
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