镁合金超疏水表面制备的研究进展

利用超疏水表面可望减少材料与液体介质的直接接触来提高材料的耐蚀性能,在制备自清洁表面等方面得到了广泛研究。超疏水表面一般通过构造一定表面粗糙度和用低表面自由能物质修饰表面而成。在简要概括固体表面润湿性理论的基础上,针对镁合金的特点,综述了当前镁合金上超疏水表面制备的最新进展,并讨论了提高其性能的可能途径和未来的发展方向。     

Magnetic particles stabilized by chemically adsorbed monolayers for use in functional fluids

Chemically adsorbed monolayers were applied to magnetic particle surfaces for preparing functional fluids. Fluorocarbon silanes were used to form the monolayers, as the methoxysilyl groups of fluorocarbon silanes can form a strong chemical bond with the surface of a magnetic particle without degrading its properties. Fluorocarbon oils were used as the carrier liquid because of their high affinity with the fluorocarbon group of the monolayers, enabling the particles to disperse easily in it. Also, fluorocarbon oils can sustain high temperature and low pressure. The functional fluids prepared using these materials showed magnetorheological characteristics and can be used under high-vacuum and/or high-temperature conditions like those encountered in space.     

WH-1038氟碳面层涂料的性能研究

氟碳涂料是指使用了含氟树脂为基料的新型涂料,其树脂结构中的F—C键是键长最短、键能最大的化学键。氟碳涂料表面张力很低,因此具有非常出色的耐污染和自洁功能。通过对WH-1038氟碳涂料进行的工艺模拟性能试验,得出了涂料的喷涂工艺流程,并指出了使用中存在的问题。     

Surface characterization and platelet adhesion studies of aliphatic polyurethanes grafted by fluorocarbon oligomers: effect of fluorocarbon chain length and carboxylic acid group

The surfaces of aliphatic polyurethane films, which were synthesized by 1,6 hexamethylene diisocyanate, poly(tetramethylene glycol) and 1,4 butanediol, were modified by grafting different chain length of fluorocarbon oligomers. The fluorocarbon oligomers on polyurethane surfaces were terminated with trifluorocarbon or carboxylic acid functionality. The alkyl groups were also grafted onto polyurethane surfaces for comparison. The surface characterization and platelet-contacting property were studied using electron spectroscopy for chemical analysis (ESCA), static contact angle analysis and in vitro platelet adhesion experiments. The effects of fluorocarbon oligomers and their terminal functionalities are discussed. The ESCA results demonstrate the fluorocarbon enrichment at the outmost layer in fluorocarbon oligomer grafted polyurethanes. The fluorocarbon content at the surface increases with increasing the chain length of fluorocarbon oligomers. The fluorocarbon oligomer grafted polyurethanes exhibit highly hydrophobic surfaces, while alkyl groups grafted polyurethanes show relatively hydrophobic surfaces compared with the untreated polyurethane. The in vitro platelet adhesion experiments indicated that the fluorocarbon oligomer and carboxylic acid functionality significantly reduced the number and the degree of activation of the adherent platelets.     

基于低表面能树脂的海洋防污涂料的研究进展

从基团转移聚合、阳离子聚合、阴离子聚合、活性官能团之间的反应和自由基聚合5个方面简单综述了低表面能树脂的聚合机理;详细介绍了以有机硅树脂、氟碳树脂、氟硅树脂以及不含氟硅元素树脂为基体的防污涂料;分析讨论了低表面能海洋防污涂料的控制因素;并展望了低表面能防污技术的发展方向。     

氟碳涂料中主组分对涂层性能的影响

为促进低表面能氟碳涂料的研究应用,使用能谱仪（EDS）、扫描电镜（SEM）、接触角测量仪和划格试验法对FEVE（氟烯烃一乙烯基醚或酯的共聚物）氟碳涂料涂膜表面进行表征和测试,考察了氟碳涂料中的偶联剂、填料及颜料含量对涂层性能的影响。结果表明：涂层表层比底层的氟含量要高,且存在纳米级的“突起”;偶联剂含量大于3．O％时涂...     

Analysis of coatings which inhibit epoxy bleeding in electronic packaging

The bleeding of epoxy resin around surfaces, undergoing bonding in electronic packaging assembly, has for long caused sporadic yield-loss. This loss is more severe in advanced and dense packages. Previously it has been supposed that the loss results from surface contaminants which are reduced by vacuum bakeout. In fact, that procedure generates coatings of hydrocarbons as we show by surface analysis. The coatings very strongly affect the wettabilities and measured surface energies of substrates. In particular, the comparatively low surface energy of hydrocarbon films on gold surfaces shows how the surfaces can be engineered, with coatings of “appropriate cleanliness”, to systematically inhibit epoxy bleeding. This revised version was published online in July 2006 with corrections to the Cover Date.     

Multifunctional superhydrophobic coatings fabricated from basalt scales on a fluorocarbon coating base

Superhydrophobic coatings are increasingly being evaluated as anticorrosion interventions in exceed-ingly hydrated environments.However,concerns about their long-term durability and amenability to large-area applications in marine environments are still hindering commercial-scale deployment.This study is focused on development of easy-to-apply superhydrophobic coatings,with multifunctional capa-bilities,in order to extend the integrity and durability of the coatings in harsh marine environments.Here,a set of facile methods involving selective chemical etching using concentrated NaOH,as well as fluori-nation with perfluoropolyether methyl ester were adopted to fabricate a superhydrophobic surface on basalt scales,having the required rough hierarchical micro-nanotextured and low surface energy.The superhydrophobic basalt scales were subsequently aligned atop a fluorocarbon resin,pre-deposited on a metal substrate,to yield a multifunctional superhydrophobic coating(3 μL water droplet;contact angle=165.1°,rolling angle=0.7°),easily amenable to large surface area application and having excellent wear resistance,UV-aging resistance,salt spray resistance,corrosion resistance and antibacterial capabilities.     

Surface modification of polymers by ion-assisted reaction

This paper deals with a new surface modification technique of polymers, the so-called ion-assisted reaction (IAR) to improve the surface properties of polymers and provides outstanding experimental results regarding wettability and adhesion of various polymers. In the IAR, polymer surfaces were subjected to low energy ion irradiation at different dosage in reactive gas environment. Dramatic improvements in wettability and surface energy are observed for the IAR-treated polymer surfaces and can be explained by the addition of functional groups, responsible for the increase of polar component in surface energy. The formation of functional groups results from the interaction among ion, reactive gas and polymer chain involved in IAR treatment, depending on the reactive ion species, the flow rate of the reactive gas and the irradiating ion fluence. The improvement in adhesion between the IAR-treated polymers and coating materials was explained in terms of the increased surface energy as well as surface roughness in the polymers modified by the IAR and possible adhesion enhancement mechanism is to be discussed.     

Designing novel hybrid materials by one-pot co-condensation: from hydrophobic mesoporous silica nanoparticles to superamphiphobic cotton textiles

This work reports the synthesis and characterization of mesoporous silica nanoparticles (MSNs) functionalized with tridecafluorooctyltriethoxysilane (F13) and their in situ incorporation onto cotton textiles. The hybrid MSNs and the functional textiles were prepared by a one-pot co-condensation methodology between tetraethylorthosilicate (TEOS) and F13, with hexadecyltrimethylammonium chloride (CTAC) as the template and triethanolamine as the base. The influence of the F13 to TEOS molar ratio (1:10, 1:5 and 1:3) on the nanoparticle morphology, porosity, degree of functionalization, and hydro/oleophobic properties is discussed. The hybrid nanosilicas presented high colloidal stability and were spherical and monodispersed with average particle size of ～45 nm. They also showed high surface areas, large pore volumes, and a wormhole-type mesoporous structure. The increase in the organosilane proportion during the co-condensation process led to a more radially branched wormhole-like mesoporosity, a decrease in the surface area, pore volume, and amount of surface silanol groups, and an enrichment of the surface with fluorocarbon moieties. These changes imparted hydrophobic and oleophobic properties to the materials, especially to that containing the highest F13 loading. Cotton textiles were coated with the F13-MSNs through an efficient and less time-consuming route. The combination between surface roughness and mesoporosity imparted by the MSNs, and the low surface energy provided by the organosilane resulted in superhydrophobic functional textiles. Moreover, the textile with the highest loading of fluorocarbon groups was superamphiphobic.     

Plasmapolymerschichten als Basis für maßgeschneiderte funktionale Oberflächen

Plasmapolymer coatings for tailor‐made functional surfaces The tailoring of surface properties via polymer coatings is currently a strongly pursued topic in various fields ranging from microsystem technology to bioanalytics. A precise tuning of surface properties, however, is only possible if chemically well‐defined processes are used that usually require reactive surface moieties to which molecules can be coupled. In this contribution we summarize studies that aimed at the modification of inert surfaces. For this purpose reactive groups at the surfaces are generated by plasma polymerisation of allyl amine which results in layers that contain amino groups. Initiator molecules for free radical polymerization processes are then coupled to these amino groups resulting in surfaces from which polymers can then be grown via surface‐initiated polymerization. Using these processes, polymer monolayers with very different properties can be generated by simply using different monomers.     

Chemical nature of superhydrophobic aluminum alloy surfaces produced via a one-step process using fluoroalkyl-silane in a base medium

Various surface characterization techniques were used to study the modified surface chemistry of superhydrophobic aluminum alloy surfaces prepared by immersing the substrates in an aqueous solution containing sodium hydroxide and fluoroalkyl-silane (FAS-17) molecules. The creation of a rough micronanostructure on the treated surfaces was revealed by scanning electron microscopy (SEM). X-ray photoelectron spectroscopy (XPS) and infrared reflection absorption spectroscopy (IRRAS) confirmed the presence of low surface energy functional groups of fluorinated carbon on the superhydrophobic surfaces. IRRAS also revealed the presence of a large number of OH groups on the hydrophilic surfaces. A possible bonding mechanism of the FAS-17 molecules with the aluminum alloy surfaces has been suggested based on the IRRAS and XPS studies. The resulting surfaces demonstrated water contact angles as high as ~166° and contact angle hystereses as low as ~4.5°. A correlation between the contact angle, rms roughnesses, and the chemical nature of the surface has been elucidated.     

A nanoscale fluorocarbon coating on PET surfaces improves the adhesion and growth of cultured coronary endothelial cells

Plasma deposition was applied to deposit smooth and nanostructured fluorocarbon coatings on polyethylene terephthalate substrates, with the aim to obtain surfaces with identical chemical composition but different roughness to improve the endothelialization process on PET surfaces. We found that increased roughness was associated with enhanced endothelial cell response, as shown by the ability of cells to grow and adhere to nanostructures. We also observed specific interaction of filopodia protruding from the cell membrane with individual nanostructures, leading to increased cell attachment, spreading and cell viability. Among the modified surfaces, one termed PET-tfl90 emerged as the one capable of best sustaining the formation of a confluent monolayer of endothelial cells. In conclusion, PET modified by nanostructured fluorocarbon film represents an improved graft material, over conventional PET, for endothelial cell adhesion and growth.     

低表面能防污涂料的最新研究进展

低表面能防污涂料(有机硅系列和氟化物系列)因具有独特的性能而在许多领域得到广泛应用.介绍了低表面能防污涂料防污的作用机理、特点,综述了低表面能防污涂料的应用和最新进展,并阐述了低表面能防污涂料有待解决的问题和今后的发展方向.     

Proliferation of osteoblasts and fibroblasts on model surfaces of varying roughness and surface chemistry

Physical and chemical properties of the surfaces of implants are of considerable interest for dental and orthopedic applications. We used self-assembled monolayers (SAMs) terminated by various functional chemical groups to study the effect of surface chemistry on cell behavior. Cell morphology and proliferation on silicon wafers of various roughnesses and topographies created by chemical etching in caustic solution and by corundum sandblasting were analyzed as well. Water contact angle data indicated that oxidized wafer surfaces displayed high hydrophilicity, modification with poly(ethylene glycol) (PEG) created a hydrophilic surface, and an amino group (NH₂) led to a moderately wettable surface. A hydrophobic surface was formed by hydrocarbon chains terminated by CH₃, but this hydrophobicity was even further increased by a fluorocarbon (CF₃) group. Cell proliferation on these surfaces was different depending primarily on the chemistry of the terminating groups rather than on wettability. Cell proliferation on CH₃ was as high as on NH₂ and hydrophilic oxidized surfaces, but significantly lower on CF₃. Precoating of silicon wafers with cell culture serum had no significant influence on cell proliferation. Scanning electron microscopy indicated a very weak initial cell-surface contact on CF₃. The cell number of osteoblasts was significantly lower on sandblasted surfaces compared with other rough surfaces but no differences were detected with 3T3 mouse fibroblasts. The different surface roughnesses and topographies were recognized by MG-63 osteoblasts. The cells spread well on smooth surfaces but appeared smaller on a rough and unique pyramid-shaped surface and on a rough sandblasted surface.     

Superhydrophobic Coatings on Cellulose‐Based Materials: Fabrication,Properties, and Applications

Wettability of a solid surface by a liquid plays an important role in several phenomena and applications, for example in adhesion, printing, and self‐cleaning. In particular, wetting of rough surfaces has attracted great scientific interest in recent decades. Superhydrophobic surfaces, which possess extraordinary water repelling properties due to their low surface energy and specific nanometer‐ and micrometer‐scale roughness, are of particular interest due to the great variety of potential applications ranging from self‐cleaning surfaces to microfluidic devices. In recent years, the potential of superhydrophobic cellulose‐based materials in the function of smart devices and functional clothing has been recognized, and in the past few years cellulose‐based materials have established themselves among the most frequently used substrates for superhydrophobic coatings. In this Review, over 40 different approaches to fabricate superhydrophobic coatings on cellulose‐based materials are discussed in detail. In addition to the anti‐wetting properties of the coatings, particular attention is paid to coating durability and other incorporated functionalities such as gas permeability, transparency, UV‐shielding, photoactivity, and self‐healing properties. Potential applications for the superhydrophobic cellulose‐based materials range from water‐ and stain‐repellent, self‐cleaning and breathable clothing to cheap and disposable lab‐on‐a‐chip devices made from renewable sources with reduced material consumption.     

金属表面超疏水性的研究进展

超疏水金属表面在表面自清洁、抗腐蚀、流动减阻及微流体无损输送等方面有着潜在的应用价值.综述了金属表面巯水性在理论及实现方法上的新进展,介绍了目前国内外提高金属表面疏水性的途径,重点归纳了金属超疏水表面的制备方法及相关应用,展望了今后的研究方向.     

Modifizierung unpolarer Polymeroberflächen

Modification of non‐polar polymer surfaces In numerous technological relevant processes the adhesion in compound systems is of central importance. It concerns for example surface coatings and the manufacturing of composites. Particular problems result at the compounding of polyolefins, silicones and fluoropolymers due to their very low surface energy. The modification of such polymer surfaces with the aim of functionalisation and with it of increasing the surface energy results in an improvement of adhesion properties of the materials. A well‐established procedure, particularly in the automotive industry, is the flame treatment of the surfaces. However, a defined chemical modification of the surface depends on many parameters and thus is very difficult to standardize. A defined change of the surface can be better achieved through a targeted plasma treatment, in which in our case the surface is stabilized by a subsequent wet chemical process step.     

Plasma im Beutel

Plasma in a bag — Internal coating of bags using atmospheric pressure plasmas for cell culturing. “Plasma in a bag” stands for a new low‐cost technique for coating the inside of closed plastic bags by means of atmospheric pressure plasma. The technique allows the deposition of homogeneous, long‐term stable functional layers on the inner surfaces of cell culture bags. The area density of functional amino groups was determined by chemical derivatization in combination with ATR‐FTIR spectroscopy. A prototype of an equipment was built for the automated and reproducible deposition of coatings under standard laboratory conditions maintaining the sterility of the bag. High yields of adherent grown human mesenchymal stem cells can be achieved even after long periods of storage of the bag before use. With suitable variation of the film‐forming agent different functionalities can be obtained on the surface. Future goals are the deposition of migration barriers as well as the coating of bottles with hydrophobic surfaces.     

Tuning Molecular Self‐Assembly on Bulk Insulator Surfaces by Anchoring of the Organic Building Blocks

Molecular self‐assembly constitutes a versatile strategy for creating functional structures on surfaces. Tuning the subtle balance between intermolecular and molecule‐surface interactions allows structure formation to be tailored at the single‐molecule level. While metal surfaces usually exhibit interaction strengths in an energy range that favors molecular self‐assembly, dielectric surfaces having low surface energies often lack sufficient interactions with adsorbed molecules. As a consequence, application‐relevant, bulk insulating materials pose significant challenges when considering them as supporting substrates for molecular self‐assembly. Here, the current status of molecular self‐assembly on surfaces of wide‐bandgap dielectric crystals, investigated under ultrahigh vacuum conditions at room temperature, is reviewed. To address the major issues currently limiting the applicability of molecular self‐assembly principles in the case of dielectric surfaces, a systematic discussion of general strategies is provided for anchoring organic molecules to bulk insulating materials.