Structural-mechanical properties of organosilicate composites with introduced curing agents

A systematic investigation on the rheological properties of five organosilicate suspensions of the “polyorganosiloxane-muscovite-talc-rutile-aminopropyltriethoxysilane-toluene” composition is undertaken. It is established that the sedimentation processes affect the energy characteristics of the surface of the organosilicate coatings prepared by curing the initial suspensions. The chemical processes occurring during long-term storage of the composites with introduced curing agents have an effect on the redistribution of the contributions from the polar and dispersion components to the total surface energy of the coating.     

Application of nanotechnologies to organosilicate materials

The use of fullerenes C₆₀ + C₇₀ and polyhedral multilayered nanoparticles (astralenes) in organosilicate coatings of the “polyorganosiloxane-silicate-inorganic pigment” composition leads to an increase in the physicomechanical and protective properties of the coating, as well as to a change in the energy characteristics of the coating surface. The decrease observed in the polar component of the surface energy of the coatings is especially pronounced upon introduction of astralenes.     

The current state of the art in materials science of organosilicate composites

Physicochemical regularities of processes occurring in the “polyorganosiloxane-silicate-metal oxide” system are investigated over a wide range of temperatures. The results of investigations are used to design organosilicate materials, such as heat-resistant functional coatings, high-temperature adhesives, and vacuum-tight sealants, which find wide application in various fields of engineering. Modern materials science of organosilicate composites is a dynamic knowledge system.     

Investigation of the functional role of sepiolite in organosilicate composites

The functional role of sepiolite in organosilicate composites is investigated. It is demonstrated that the addition of the organomodified sepiolite to organosilicate composites during their fabrication in amounts of 1 wt % increases the thixotropy and pseudoplasticity of “polydimethylphenylsiloxane-silicate-inorganic pigment” suspensions and prevents sedimentation of pigments and fillers, as well as the formation of dense sediments in the course of storage. Upon introduction of this stabilizing additive, the physicomechanical and protective properties of organosilicate coatings remain good. Original Russian Text ? S.V. Chuppina, 2008, published in Fizika i Khimiya Stekla.     

低氟含量低表面能自清洁氟碳涂料的研究

以氟单体和丙烯酸酯类单体通过聚合物的分子结构设计，合成了一类总氟含量不超过12％的低氟含量的含氟丙烯酸树脂，所制备的氟碳涂料的涂层的表面能低，具有自清洁功能。分析了该涂层中极性与非极性官能团的分子取向机理，测定了纯水水珠在不同含氟单体均聚物和共聚物清漆漆膜上以及在含氟丙烯酸树脂涂层上的接触角，探明了含氟丙烯酸树脂涂层的总氟含量与表面能的关系、含氟官能团在涂层中的分布，探讨了低氟含量的含氟丙烯酸树脂涂料的涂层自清洁机理。     

Comparison of drag characteristics of self-polishing co-polymers and silicone foul release coatings: A study of wettability and surface roughness

An experimental study has been carried out to evaluate the drag characteristics of different self-polishing co-polymers (SPC) (tin based and tin-free) and a silicone foul release (FR) coating. Drag measurements have been performed on a smooth aluminum cylinder connected to a rotor device. Various coatings on cylinders were examined and differential length technique was also used to avoid the end effects during rotation. Surface energy of the coated samples was determined using static contact angle measurement. Characteristic roughness measurements of the coated surfaces were evaluated with atomic force microscopy (AFM) technique.Drag measurements showed that the frictional resistance of the FR coated cylinders was lower than that of SPC coated samples.Contact angle results showed that the critical surface tension and its polar component for silicone FR coating are less than SPC coatings. This prevents firm adhesion of fouling organisms on underwater hulls.AFM studies revealed a lower surface roughness for silicone FR coating as compared to SPC coatings. Also, its surface texture is considerably different from SPC coatings.It can be concluded that the drag characteristics of a surface are affected by its free energy and roughness parameters.     

Comparison of drag characteristics of self-polishing co-polymers and silicone foul release coatings: A study of wettability and surface roughness

An experimental study has been carried out to evaluate the drag characteristics of different self-polishing co-polymers (SPC) (tin based and tin-free) and a silicone foul release (FR) coating. Drag measurements have been performed on a smooth aluminum cylinder connected to a rotor device. Various coatings on cylinders were examined and differential length technique was also used to avoid the end effects during rotation. Surface energy of the coated samples was determined using static contact angle measurement. Characteristic roughness measurements of the coated surfaces were evaluated with atomic force microscopy (AFM) technique.

Drag measurements showed that the frictional resistance of the FR coated cylinders was lower than that of SPC coated samples.

Contact angle results showed that the critical surface tension and its polar component for silicone FR coating are less than SPC coatings. This prevents firm adhesion of fouling organisms on underwater hulls.

AFM studies revealed a lower surface roughness for silicone FR coating as compared to SPC coatings. Also, its surface texture is considerably different from SPC coatings.

It can be concluded that the drag characteristics of a surface are affected by its free energy and roughness parameters.     

Chemical oxidation of high-density polyethylene: Surface energy,functionality, and adhesion to liquid epoxy

The application of polyolefins has increased significantly over the past few decades. However, their chemical inertness and low surface energy limits their application in many industries where high adhesion to polar materials is required, such as for composites and protective coatings. Herein, six different acids are used to create polar functional groups on High-Density Polyethylene's (HDPE) surface and to increase its adhesion to liquid epoxy (LE). Contact angle measurements, Fourier Transform Infrared Spectroscopy (FTIR), X-ray Photoelectron Spectroscopy (XPS), and pull-off strength measurements are used to analyze the surface energy and functionality of HDPE and to measure its adhesion to LE. The results show that each acid increases both the polar and disperse surface energies of HDPE to a different extent, but that this is not necessarily a function of acid strength. Chlorosulfonic acid and chromic acid increase the oxygen to carbon ratio by a factor of 8 and increase HDPE's adhesion to LE by more than 400%. Furthermore, a comparison between predicted work of adhesion values from the OWRK model and experimental results shows that the latter are significantly higher than what is predicted, especially with increasing surface polarity.     

Surface-Energy Determinations of Tin Oxide-Coated Soda–Lime–Silica Glass

The dispersive and polar surface-energy components, as well as the total surface energy, of tin oxide coatings on soda–lime–silica glass were determined by the Owens–Wendt method. The total surface energy of tin oxide is greater than soda–lime–silica glass and, more importantly, exhibits significantly more-dispersive and less-polar character. These results indicate that tin oxide is significantly more covalent than soda–lime–silica glass. It is postulated that the more-covalent tin oxide coatings increase the bond strength of organic coatings to soda–lime–silica glass. These effects improve the friction-damage resistance of glass surfaces coated with metal oxides and organics, compared with glass surfaces coated with organics only.     

The role of surface modification in digital printing on polymer‐coated packaging boards

Digital printing is increasingly being used for package printing. One of the major techniques of digital printing is dry‐toner electrophotography. This paper evaluates the printability of three different extrusion coatings used for packaging boards: low‐density polyethylene (PE‐LD), ethylene methyl acrylate (E/MA) and polyethylene terephthalate (PET). Extrusion coatings in general have an impervious, chemically inert, nonporous surface with low surface energies that cause them to be non‐receptive to bonding with toners. The most common methods used in improving the adhesion properties of polymer coatings are different surface treatments. These increase the surface energy and also provide the polar molecular groups necessary for good bonds between the toner and polymer molecules. The polymer coatings have been modified with electrical corona discharge treatment. The effects of corona on polymer surfaces and the correlation between surface modification and print quality have been evaluated. Results show that sufficiently high surface energy and surface‐charge uniformity are necessary for even print quality and toner adhesion. E/MA and PET have the required surface‐energy level without the corona treatment, but PE‐LD needs surface modification in order to succeed in the electrophotographic process. E/MA also has exceptional surface‐charge properties compared with PET and PE‐LD. Polym. Eng. Sci. 44:2052–2060, 2004. © 2004 Society of Plastics Engineers.     

The influence of ageing of epoxy coatings on adhesion of polyurethane topcoats and protective properties of coating systems

The dependence of adhesion and protective properties of coating systems on surface properties of epoxy intermediate coatings, aged and non-aged before an application of polyurethane topcoats, were examined. The intermediate coatings were aged 500 h in UV chamber. The surface free energy and polar groups were estimated after ageing. After applying polyurethane topcoats on aged and non-aged epoxy coatings, resistance to salt spray and thermal shocks were tested as well as internal stresses were measured before and after corrosion tests.The results showed that adhesion in coating systems with polyurethane topcoats applied on aged epoxy coatings depends strongly on the degradation degree of epoxy intermediate coatings and the value of generated internal stresses. Coatings with good adhesion retention in corrosion environments have good protective properties even when temporary blistering has occurred.     

Low surface energy self-polishing polymer grafted MWNTs for antibacterial coating and controlled-release property of Cu2O

Marine biofouling had been a headache when engaging in marine activities. The most effective and convenient method for dealing with this problem was to apply antifouling coatings. But now a single anti-fouling system was hard to satisfy the requirement of anti-fouling simultaneously. Therefore, it was particularly important to develop novel multi-system anti-fouling technology. In the work, a novel polymer coatings with polydimethylsiloxane (PDMS) segments in the main chain and hydrolysable side chain was designed and synthesized which showed low surface energy and self-polishing performance, and then we creatively covalently immobilized the polyurethane on the surface of multi-carbon nanotubes (MWNTs) to form multisystem antifouling coating. The results showed that the polymer coating would produce hydrolysable regions in the hydrophobic PDMS segment to endure the polymer coating hydrophobic and hydrolysis properties when contacted with water. In addition, the self-polishing rate and the surface energy could be regulated by varying its copolymerization, and the addition of MWNTs could kill the microorganisms and endowed the polymer coating itself enhanced antibacterial effect. Furthermore, considering the high specific surface area and physicochemical characteristics of MWNTs, it could be combined with antifoulant Cu₂O through a polar or non-polar combination as a carrier to control the release rate of Cu₂O in coatings.     

On the Predominant Electron-Donicity of Polar Solid Surfaces

The reasons for the predominant electron-donicity of almost all solid polar surfaces and its implications are discussed in this paper. By contact angle or interfacial tension measurements, the electron-accepting as well as the electron-donating properties of polar liquids can be ascertained, through the interplay between their energies of adhesion and cohesion. For the solid-liquid interface, direct interfacial tension measurements are not possible, but indirectly, solid/liquid interfacial tensions of polar systems can be obtained by contact angle measurement. However, as the energy of cohesion of a solid does not influence the contact angle formed by a liquid drop placed upon its surface, one can only measure the solid surface'ks residual polar property, manifested by the energy of adhesion between solid and liquid. This residual polar property is of necessity the dominant component; in most cases this turns out to be its electron donicity. When, by means of contact angle measurements with polar liquids, both electron-accepting and electron-donating potentials are found on a polar solid, it is most likely still partly covered with a polar liquid: usually water. The amount of residual water of hydration of a polar solid follows from its polar (Lewis acid-base) surface tension component (γ^AB). The degree of orientation of the residual water of hydration on a polar solid can be expressed by the ratio of the electron-donating to electron-accepting potentials (γ^⊖/γ^⊕), measured on the hydrated surface.     

Effect of DC glow discharge treatment on the surface energy and surface resistivity of thin film of polypropylene

A change in the surface energy and surface resistivity of a thin film of polypropylene (PP) of thickness 100 μm was investigated, using direct current (DC) glow discharge. The thin film of the PP was treated for various discharge powers and treatment time and the modification in the surface energy and the surface resistivity was observed. To investigate the modification in the surface energy after DC glow discharge treatment, contact angle of two test liquids formamide and de‐ionized water over the surface of PP film was measured. By measuring the contact angle the change in surface energy and its two polar and dispersive components have been measured. It was observed that at a given power level of DC glow discharge surface energy and its polar component increases with increase of the treatment time, attains a maximum value, and then becomes almost constant. Correspondingly, with increase in surface energy, a decrease in surface resistivity was observed. Also, a change in surface morphology was observed by atomic force microscopy and by FT‐IR spectra generation of polar groups at the surface of PP film. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 767–772, 2007     

Surface energy of untreated and surface-modified cellulose fibers

Average advancing and receding contact angles made against cotton and glass fibers by a set of probe liquids are determined using the Wilhelmy technique. The dispersive and polar components of the surface energy are calculated from the measured contact angles using both the geometric and the harmonic mean methods. It is found that these components are similar for untreated cellulose and glass fibers, and that they both have a high polar component, corresponding to a hydrophilic surface. Changes in surface energy caused by treatment of the cellulose fiber surfaces with melamine, polyethyleneimine (PEI), and a silane coupling agent are reported. It is found in particular that polyethyleneimine treatment of cellulose significantly reduces the polar component of its surface energy. While treatment of glass fibers with a silane coupling agent reduces the polar component and increases the dispersive component of the surface energy it shows little effect on the surface energy of cellulose.     

Surface modification of PTFE by 60Co γ-ray irradiation

Surface carboxyl groups were formed during the ⁶⁰Co γ-ray irradiation of poly(tetrafluoroethylene) (PTFE) in air. Fourier transform infrared spectroscopy enables the detection of surface carboxyl groups. The contact angles were used to calculate the dispersive and polar components of the surface free energy according to a two-liquid method. The γ-ray irradiation of PTFE mainly caused degradation of the polymer. The concentration of carboxyl groups, the wettability, the friction, and the dispersive and polar components of the surface energy and the crystallinity on PTFE surface were increased, while the particle size of PTFE decreased with increasing irradiation dose. A highly modified PTFE was used to reduce the aqueous liquid repellent properties of PTFE. A 20 kGy dose for modified PTFE surface was suitable in air additivity in antifriction, anticorrosion, antifouling, lubrication, and noise reduction coatings. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 435–441, 1998     

^60Co辐照对PTFE表面结构和表面能的影响

为了改善氟聚合物加工性和二次加工性,研究了PTFE聚合物的加工技术。以不同剂量辐照PTFE,PTFE粉末辐照后表面晶相没有发生变化。模压辐照的PTFE,其密实性较好,表面光滑。同时,辐照PTFE后表面有大量的极性亲水基团出现,使表面极性分量增加;而色散分量变化较小。辐照产生的表面极性基团减小了由于不同模压产生的表面所引起的接触角变化。     

On the Predominant Electron-Donicity of Polar Solid Surfaces

The reasons for the predominant electron-donicity of almost all solid polar surfaces and its implications are discussed in this paper. By contact angle or interfacial tension measurements, the electron-accepting as well as the electron-donating properties of polar liquids can be ascertained, through the interplay between their energies of adhesion and cohesion. For the solid-liquid interface, direct interfacial tension measurements are not possible, but indirectly, solid/liquid interfacial tensions of polar systems can be obtained by contact angle measurement. However, as the energy of cohesion of a solid does not influence the contact angle formed by a liquid drop placed upon its surface, one can only measure the solid surface'ks residual polar property, manifested by the energy of adhesion between solid and liquid. This residual polar property is of necessity the dominant component; in most cases this turns out to be its electron donicity. When, by means of contact angle measurements with polar liquids, both electron-accepting and electron-donating potentials are found on a polar solid, it is most likely still partly covered with a polar liquid: usually water. The amount of residual water of hydration of a polar solid follows from its polar (Lewis acid-base) surface tension component (γ^AB). The degree of orientation of the residual water of hydration on a polar solid can be expressed by the ratio of the electron-donating to electron-accepting potentials (γ^?/γ^⊕), measured on the hydrated surface.     

Physicochemical and Adhesion Characteristics of High-Density Polyethylene when Treated in a Low-Pressure Plasma under Different Electrodes

The present investigation studys the effects of different electrodes such as copper, nickel, and stainless steel under low-pressure plasma on physicochemical and adhesion characteristics of high-density polyethylene (HDPE). To estimate the extent of surface modification, the surface energies of the polymer surfaces exposed to low-pressure plasmas have been determined by measuring contact angles using two standard test liquids of known surface energies. It is observed that the surface energy and its polar component increase with increasing exposure time, attain a maximum, and then decrease. The increase in surface energy and its polar component is relatively more important when the polymer is exposed under a stainless-steel electrode followed by a nickel and then a copper electrode. The dispersion component of surface energy remains almost unaffected. The surfaces have also been studied by optical microscopy and electron spectroscopy for chemical analysis (ESCA). It is observed that when the HDPE is exposed under these electrodes, single crystals of shish kebab structure form, and the extent of formation of crystals is higher under a stainless-steel electrode followed by nickel and then copper electrodes. Exposure of the polymer under low-pressure plasma has essentially incorporated oxygen functionalities on the polymer surface as detected by ESCA. Furthermore the ESCA studies strongly emphasize that higher incorporation of oxygen functionalities are obtained when the polymer is exposed to low-pressure plasma under a stainless-steel electrode followed by nickel and then copper electrodes. These oxygen functionalities have been transformed into various polar functional groups, which have been attributed to increases in the polar component of surface energy as well as the total surface energy of the polymer. Therefore, the maximum increase in surface energy results in stronger adhesion of the polymer when the polymer is exposed under a stainless-steel electrode rather than nickel and copper electrodes.     

阳极氧化二氧化钛纳米管涂层地热水腐蚀和沉积特性

拟采用金属二次阳极氧化等表面工程技术抑制地热水的腐蚀和结垢现象。在纯钛和钛合金(Ti-6Al-4V)板基底上采用二次阳极氧化法制备了二氧化钛微纳米管阵列涂层,探讨了制备工艺参数对涂层结构的影响,并进一步采用浸渍法对涂层进行了超疏水化处理。通过场发射环境扫描电镜表征了涂层的微观结构形貌。应用视频光学接触角测量仪检测了涂层表面的静态接触角,估算了表面自由能。对涂层的粗糙度也进行了测量。采用静态浸渍法评估了涂层的防垢性能。采用电化学线性极化曲线法研究了涂层在地热水中的耐腐蚀效果。结果表明,在钛及钛合金基底上,采用二次阳极氧化和浸渍工艺,可以制得具有规整二氧化钛微纳米管阵列结构和较低表面能的功能涂层;该涂层与基底相比,在地热水中的耐腐蚀性能得以提高;在碳酸钙饱和溶液中的污垢沉积速率降低约15%。同时,涂层与基底有较好的结合性能,疏水涂层经历多次胶带剥离和砂纸磨损实验后,依然保持着较高的疏水性。