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排序方式: 共有74条查询结果,搜索用时 15 毫秒
1.
Xiaohong Gu Tinh Nguyen Mounira Oudina David Martin Bouchra Kidah Joan Jasmin Aziz Rezig Lipiin Sung Eric Byrd Jonathan W. Martin Derek L. Ho Y. C. Jean 《Journal of Coatings Technology and Research》2005,2(7):547-556
Atomic force microscopy (AFM) has been used to study the morphology and microstructure of an amine-cured epoxy before and
after outdoor exposure. Measurements were made from samples prepared in an essentially CO2-free, H2O-free glove box and from samples prepared in ambient conditions. For those prepared in a CO2-free glove box, AFM imaging was conducted on (1) an unexposed air/coating surface, (2) an unexposed coating bulk, (3) an
unexposed coating/substrate interface, and (4) a field exposed air/coating surface. For samples prepared in ambient conditions,
only the unexposed air/coating surface was investigated. The same regions of the exposed samples were scanned periodically
by the AFM to monitor changes in the surface morphology of the coating as UV exposure progressed. Small angle neutron scattering
and Fourier transform infrared spectroscopy (FTIR) studies were performed to verify the microstructure and to follow chemical
changes during outdoor exposure, respectively. The results have shown that amine blushing, which occurs only under ambient
conditions, had a significant effect on the surface morphology and microstructure of the epoxy. The surface morphology of
the samples prepared under CO2-free, dry conditions was generally smooth and homogeneous. However, the interface and the bulk samples clearly revealed a
two-phase structure consisting of bright nodular domains and dark interstitial regions, indicating an inhomogeneous microstructure.
Such heterogeneous structure of the bulk was in good agreement with results obtained by small angle neutron scattering of
unexposed samples and by AFM phase imaging of the degraded sample surface. The relationship between submicrometer physical
changes and molecular chemical degradation is discussed.
Presented at the 82nd Annual Meeting of the Federation of Societies for Coatings Technology, October 27–29, 2004, in Chicago,
IL. 相似文献
2.
Li-Piin Sung Joan Jasmin Xiaohong Gu Tinh Nguyen Jonathan W. Martin 《Journal of Coatings Technology and Research》2004,1(4):267-276
Laser scanning confocal microscopy (LSCM) has been used to characterize the changes in film thickness and local surface morphology
of polymer coatings during the UV degradation process. With the noninvasive feature of LSCM, one can obtain thickness information
directly and nondestructively at various exposure times without destroying the specimens or deriving the thickness values
from IR measurement by assuming uniform film ablation. Two acrylic polymer coatings were chosen for the study, and the physical
and chemical changes of the two systems at various exposure times were measured and analyzed. Those measurable physical changes
caused by UV exposure include film ablation, formation of pits and other surface defects, and increases in surface roughness.
It was found in both coatings that changes in measured film thickness by LSCM were not correlated linearly to the predicted
thickness loss using the changes in the CH band obtained by the Fourier Transform Infrared (FTIR) spectroscopy measurements
in the later degradation stages. This result suggested it was not a uniform film ablation process during the UV degradation.
At later stages, where surface deformation became severe, surface roughness and profile information using LSCM were also proven
to be useful for analyzing the surface degradation process
Presented at the 81st Annual Meeting of the Federation of Societies for Coatings Technology, November 13–14, 2004 in Philadelphia,
PA. 相似文献
3.
Aziz Rezig Tinh Nguyen David Martin Lipiin Sung Xiaohong Gu Joan Jasmin Jonathan W. Martin 《Journal of Coatings Technology and Research》2006,3(3):173-184
The relationship between chemical degradation and thickness loss of an unpigmented, non UV-stabilized, crosslinked amine-cured
epoxy coating exposed to three UV conditions was investigated. Spin-coated samples having a thickness of approximately 7 μm
on an Si substrate were prepared from a stochiometric mixture of a bisphenol A epoxy resin and a tetra-functional amine curing
agent. Samples were exposed outdoors and to two accelerated laboratory UV environments. Chemical degradation and thickness
loss were measured by transmission Fourier transform infrared spectroscopy (FTIRS) and laser scanning confocal microscopy
(LSCM), respectively. In addition, surface roughness and morphological changes were measured by atomic forcemicrosocopy (AFM)
and LSCM. Substantial chemical degradation, thickness loss, and morpholocal changes occurred in the exposed films, and the
rate of chemical degradation was greater than that due to the thickness loss. This additional chemical loss was attributed
to an inhomogeneous degradation process in which nanoscale localized depressions initiate at certain sites on the surface,
which then enlarge and deepen with exposure time. The results of this study provide a better understanding of the degradation
mechanism and should lead to the development of scientific-based models for predicting the service life of crosslinked amine-cured
epoxy coatings.
Presented at the 82nd Annual Meeting of the Federation of Societies for Coatings Technology, October 27–29, 2004, in Chicago,
IL 相似文献
4.
Tinh Nguyen W. Eric Byrd David Alshed Joannie Chin Cyril Clerici Jon Martin 《The Journal of Adhesion》2007,83(6):587-610
Water at the polymer/substrate interface is often the major cause of adhesion loss in coatings, adhesives, and fiber-reinforced polymer composites. This study critically assesses the relationship between the interfacial water layer and the adhesion loss in epoxy/siliceous substrate systems. Both untreated and silane-treated Si substrates and untreated and silane-treated E-glass fibers were used. Thickness of the interfacial water layer was measured on epoxy/Si systems by Fourier transform infrared-multiple total internal reflection (FTIR-MTIR) spectroscopy. Adhesion loss of epoxy/Si systems and epoxy/E-glass fiber composites was measured by peel adhesion and short-beam shear tests, respectively. Little water accumulation at the epoxy/Si substrate interface was observed for silane-treated Si substrates, but about 10 monolayers of water accumulated at the interface between the epoxy and the untreated Si substrate following 100 h of exposure at 24 °C. More than 70% of the initial epoxy/untreated Si system peel strength was lost within 75 h of exposure, compared with 20% loss after 600 h for the silane-treated Si samples. Shear strength loss in composites made with untreated E-glass fiber was nearly twice that of composites fabricated with silane-treated fiber after 6 months of immersion in 60 °C water. Further, the silane-treated composites remained transparent, but the untreated fiber composites became opaque after water exposure. Evidence from FTIR-MTIR spectroscopy, adhesion loss, and visual observation strongly indicated that a water layer at the polymer/substrate interface is mostly responsible for the adhesion loss of epoxy/untreated siliceous substrate systems and epoxy/untreated glass fiber composites and that FTIR-MTIR is a viable technique to reliably and conveniently assess the adhesion loss attributable to water sorption at the interface. 相似文献
5.
Engineering with Computers - This paper is devoted to numerical investigations on mechanical behavior of cracked composite functionally graded (FG) plates. We thus develop an efficient adaptive... 相似文献
6.
Efficiency improvement of InGaP/GaAs/Ge solar cells by hydrothermal-deposited ZnO nanotube structure
Chen-Chen Chung Binh Tinh Tran Kung-Liang Lin Yen-Teng Ho Hung-Wei Yu Nguyen-Hong Quan Edward Yi Chang 《Nanoscale research letters》2014,9(1):338
In this paper, a zinc oxide (ZnO) nanotube, fabricated by the hydrothermal growth method on triple-junction (T-J) solar cell devices to enhance efficiency, is investigated. Compared to those of bare T-J solar cells (without antireflection (AR) coating) and solar cells with Si3N4 AR coatings, the experimental results show that the T-J solar cells, which use a ZnO nanotube as an AR coating, have the lowest reflectance in the short wavelength spectrum. The ZnO nanotube has the lowest light reflection among all experimental samples, especially in the range of 350 to 500 nm from ultraviolet (UV) to visible light. It was found that a ZnO nanotube can enhance the conversion efficiency by 4.9%, compared with a conventional T-J solar cell. The Si3N4 AR coatings also enhance the conversion efficiency by 3.2%.The results show that a cell with ZnO nanotube coating could greatly improve solar cell performances. 相似文献
7.
Deborah?S.?JacobsEmail author Sin-Ru?Huang Yu-Lun?Cheng Savelas?A.?Rabb Justin?M.?Gorham Peter?J.?Krommenhoek Lee?L.?Yu Tinh?Nguyen Lipiin?Sung 《Journal of Coatings Technology and Research》2016,13(5):735-751
Many coating properties such as mechanical, electrical, and ultraviolet (UV) resistance are greatly enhanced by the addition of nanoparticles, which can potentially increase the use of nanocoatings for many outdoor applications. However, because polymers used in all coatings are susceptible to degradation by weathering, nanoparticles in a coating may be brought to the surface and released into the environment during the life cycle of a nanocoating. Therefore, the goal of this study is to investigate the process and mechanism of surface degradation and potential particle release from a commercial nanosilica/polyurethane coating under accelerated UV exposure. Recent research at the National Institute of Standards and Technology (NIST) has shown that the matrix in an epoxy nanocomposite undergoes photodegradation during exposure to UV radiation, resulting in surface accumulation of nanoparticles and subsequent release from the composite. In this study, specimens of a commercial polyurethane (PU) coating, to which a 5 mass% surface-treated silica nanoparticle solution was added, were exposed to well-controlled, accelerated UV environments. The nanocoating surface morphological changes and surface accumulation of nanoparticles as a function of UV exposure were measured, along with chemical change and mass loss using a variety of techniques. Particles from the surface of the coating were collected using a simulated rain process developed at NIST, and the collected runoff specimens were measured using inductively coupled plasma optical emission spectroscopy to determine the amount of silicon released from the nanocoatings. The results demonstrated that the added silica nanoparticle solution decreased the photodegradation rate (i.e., stabilization) of the commercial PU nanocoating. Although the degradation was slower than the previous nanosilica epoxy model system, the degradation of the PU matrix resulted in accumulation of silica nanoparticles on the nanocoating surface and release to the environment by simulated rain. These experimental data are valuable for developing models to predict the long-term release of nanosilica from commercial PU nanocoatings used outdoors and, therefore, are essential for assessing the health and environmental risks during the service life of exterior PU nanocoatings. 相似文献
8.
Difficulty in imposing essential boundary conditions in the standard element-free Galerkin method (EFG) is due to the lack of Kronecker’s delta function property of shape functions generated by moving least square approximation (MLS). In this paper, we further apply a meshfree model based on the moving Kriging interpolation method (MK) to free vibration analysis of first-order shear deformable plates. The deflection and two rotation field variables of plate are approximated by the MK method, which is employed to construct the shape functions having the delta function property. With this approach, the drawback in enforcement of the boundary conditions caused by the MLS is now avoided. The present formulation is based on the first-order shear deformation plate theory (FSDT) associated with an effective elimination of the shear-locking phenomenon completely, and hence the approach is applicable to both moderately thick and thin plates. Numerical examples considering various aspect ratios and different boundaries are examined and solutions on natural frequencies obtained by the present method are then compared with existing reference solutions, and very good agreements are observed. 相似文献
9.
Mark R. VanLandingham Tinh Nguyen W. Eric Byrd Jonathan W. Martin 《Journal of Coatings Technology》2001,73(923):43-50
The atomic force microscope (AFM) was used to monitor changes in surface features of an acrylic melamine coating that was
exposed to a variety of conditions. Exposure to ultraviolet (UV) radiation and high relative humidity caused general roughening
of the surface and the formation of pits. Further, the damage of the coating surface was much more substantial for exposure
to high relative humidity compared to exposure to dry environments. This difference in degradation rates correlated with measurements
of chemical degradation determined using infrared spectra that were acquired along with the AFM images.
Building Materials Division, 100 Bureau Dr., Stop 8621, Gaithersburg, MD 20899-8621. 相似文献
10.
Tinh Nguyen 《The Journal of Adhesion》2013,89(3-4):283-294
The study of surface modification to prepare an optimum surface for bonding is of practical importance for the production of glued materials. Lignocellulosic materials contain many chemical groupings such as phenolic and alcoholic hydroxyls, carbonyl groups, etc., capable of being readily activated by physical or chemical methods. These active sites can then react under heat and pressure, either with active sites from another surface, or through a crosslinking agent to form a glued product. This paper reports the role of lignin in the reactions between lignocellulosic materials and hydrogen peroxide studied by a differential scanning calorimetry method. The results showed that lignin is much more reactive toward hydrogen peroxide than is cellulose, and that the lignin-hydrogen peroxide reaction yields the highest enthalpy. Correlation between lignin and enthalpy, and enthalpy and bonding will also be discussed. 相似文献