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991.
Satoru Iwamori Takehiro Miyashita Shin Fukuda Shouhei Nozaki Nobuhiro Fukuda Kazufuyu Sudoh 《The Journal of Adhesion》1997,63(4):309-321
Peel strength between a copper (Cu) thin film and a polyimide (pyromellitic dianhydride-oxydianiline, or PMDA-ODA) substrate is reduced by heat treatment at 150°C in air. In this work, we investigated the peel strength, the morphology of the interface between Cu films and polyimide substrates using optical microscopy and electron microscopy, and chemical change of the interface using Auger electron spectroscopy (AES) and micro X-ray photoelectron spectroscopy (XPS). The analysis showed that CuO “lumps” were present on the peeled surface of PMDA-ODA after heat treatment at 150°C in air. The peeled surfaces of other polyimide substrates were also analyzed: biphenyl dianhydride-para phenylene diamine (BPDA-PDA) and biphenyl dianhydride-oxydianiline (BPDA-ODA). CuO lumps were present on the peeled surface of BPDA-ODA after the heat treatment, but not that of BPDA-PDA. Compared with the adhesion strength for the Cu thin film, the adhesion strength was high for the Cu/PMDA-ODA and Cu/BPDA-ODA laminates, but the adhesion strength was very low for the Cu/BPDA-PDA laminate. This low strength is the reason that CuO lumps were not detected on the peeled surface of the BPDA-PDA substrate. These CuO lumps were related to the adhesion degradation of the Cu/polyimide laminates after the heat treatment. 相似文献
992.
Understanding the molecular-level processes underlying interfacial phenomena is important in the area of adhesion. We briefly introduce IR-visible sum-frequency generation spectroscopy (SFG) using a total-internal-reflection geometry for the study of polymer-air, polymer-solid, and polymer-polymer interfaces. The following examples, predominantly of work done in our lab, illustrating differences in molecular structure and dynamic properties at interfaces are presented: the air- and solid-interface structure of an amorphous polystyrene (PS) and a semicrystalline polymer with side-chain crystallinity, poly(octadecyl acrylate) (PA-18); structure of a polymer-polymer interface between thin films of a semicrystalline polymer with side-chain crystallinity, poly(vinyl-N-octadecylcarbamate- co-vinyl acetate), and an amorphous PS; thermal order-to-disorder transitions of the air and solid interface of PA-18, and the interface of this polymer with PS; and dynamic surface-relaxation studies of a rubbed PS film. 相似文献
993.
Sang Hern Kim Won Keun Son Yong Joo Kim Eu‐Gene Kang Dong‐Won Kim Chang Woo Park Whan‐Gi Kim Hyung‐Joong Kim 《应用聚合物科学杂志》2003,88(3):595-601
A polystyrene (PS)/poly(butyl acrylate) (PBA) composite emulsion was produced by seeded emulsion polymerization of butyl acrylate (BA) with PS seed particles which were prepared by emulsifier‐free polymerization of styrene with potassium persulfate (KPS) under a nitrogen atmosphere at 70°C for 24 h with stirring at 60 rpm and swelled with the BA monomer in an ethanol/water medium. The structure of the PS/PBA composite particles was confirmed by the presence of the characteristic absorption band attributed to PS and PBA from FTIR spectra. The particles for pure PS and PS/PBA with a low content of the BA monomer were almost spherical and regular. As the BA monomer content was increased, the particle size of the PS/PBA composite particles became larger, and more golf ball‐like particles were produced. The surface morphology of the PS/PBA composite particles was investigated by AFM and SEM. The Tg's attributed to PS and PBA in the PS/PBA composite particles were found at 110 and ?49°C, respectively. The thermal degradation of the pure PS and PS/PBA composite particles occurred in one and two steps, respectively. With an increasing amount of PBA, the initial thermal decomposition temperature increased. On the contrary the residual weight at 450°C decreased with an increasing amount of PBA. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 595–601, 2003 相似文献
994.
The micellar properties of aqueous binary mixed solutions for two systems consisting of sodium cholate (NaC)-octaoxyethylene
glycol mono n-decyl ether (C10E8) and sodium glycocholate (NaGC)-C10E8 have been studied on the basis of surface tensions, polarity of the micelle interior and the mean aggregation number. Application
of two theoretical treatments, based on regular solution and excess thermodynamic quantities for critical micellar concentration
(CMC) data from surface tension curves of two mixed systems showed that the mole fraction of each bile salt in the mixed micelles
near the CMC is lower than that of the corresponding prepared mole fraction in the mixed solution. The polarity of the interior
suggested that the hydrophobicity of intramicelles increased with the increase of the mole fraction of bile salt in the mixed
solution and that the mixed micelles become dramatically more hydrophobic at a mole fraction of 0.68 for NaGC−C10E8 system and 0.75 for NaC−C10E8 system, respectively. This implies that the micelles become richer in the bile salt molecules and the tendency appears strongly
for NaGC−C10E8 system due to the strong cohesion between the conjugated glycines in the NaGC molecules. The decrease of aggregation number
with the increase of the mole fraction of bile salts shows that the micelles approach those of the single system of each bile
salt. This supports the previously mentioned facts. 相似文献
995.
Two surface modification methods—plasma surface treatment and chemical agent treatment—were used to investigate their effects on the surface properties of ultrahigh‐molecular‐weight polyethylene (UHMWPE) fibers. In the analyses, performed using electron spectroscopy for chemical analysis, changes in weight, and scanning electron microscope observations, demonstrated that the two fiber‐surface‐modified composites formed between UHMWPE fiber and epoxy matrix exhibited improved interfacial adhesion and slight improvements in tensile strengths, but notable decreases in elongation, relative to those properties of the composites reinforced with the untreated UHMWPE fibers. In addition, three kinds of epoxy resins—neat DGEBA, polyurethane‐crosslinked DGEBA, and BHHBP‐DGEBA—were used as resin matrices to examine the tensile and elongation properties of their UHMWPE fiber‐reinforced composites. From stress/strain measurements and scanning electron microscope observations, the resin matrix improved the tensile strength apparently, but did not affect the elongation. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 655–665, 2007 相似文献
996.
对用化学方法制备的天然胶乳浸渍制品表面起皱进行了研究。分析了天然胶乳浸渍制品表面起皱的原理,确定了起皱剂的选择.同时对影响起皱的因素(增稠剂、预干燥规律)进行了研究。 相似文献
997.
998.
The importance of some relative surface characteristics which determines the strength of adhesive joints: specific surface of substrate , relative contact area β and specific contact area β in the adhesion interaction process were emphasised. Existing and potential methods of experimental evaluation of these characteristics were shortly analysed. The durability of the adhesive joints in water media significantly increases with growth of specific surface * of chemically treated substrate evaluated from the SEM micrographs. Specific surface calculated from the experimental data of hexane adsorption measurements for iron particles (particulate model of steel substrate) is more then ten times greater than respective * values. The relative contact area β of the Al2O3 particles (in wide range of ) with PE melt was in a roundabout way evaluated by experimental determination of the affect of on kinetic of peel strength formation of adhesive joints: Al2O3 filled PE-steel. The speculation was based on the ability of Al2O3 to adsorb low-molecular products of contact oxidation of PE which takes place in the process of formation of adhesive joints and determines their strength. The ability of sorption in its turn is proportional to efficient value of β. The availability of the Al2O3 surface was evaluated. 相似文献
999.
Functional polyurethane surfactants (di‐block and tri‐block) were synthesized by addition polymerization of 2,4‐toluenediisocyanate with poly(propylene oxide) and monoallyl‐end‐capped poly(ethylene oxide). The chemical structure of the polyurethane surfactants was confirmed by Fourier transform infrared and 1H NMR spectroscopy. These polymeric surfactants were found to have excellent surface activity. The lowest surface tension of polyurethane surfactant aqueous solutions could be reduced to 37.6 mN m?1. All the polyurethane surfactants synthesized had low critical micelle concentrations and could reduce the surface tension even at very low concentration levels (10?6–10?5 mol L?1). The solubilization of toluene in micelles of the synthesized polyurethane surfactants was studied using UV‐visible spectroscopy, and the results showed that they all exhibited good solubilization capacity. Possible solubilization positions of toluene in the micelles are conjectured. Copyright © 2006 Society of Chemical Industry 相似文献
1000.
Using one of the generic models (CO oxidation on Pt with surface-oxide formation) predicting kinetic oscillations in heterogeneous catalytic reactions, we show that the efficiency of two-variable periodic perturbations with respect to converting natural period-1 oscillations to period-l oscillations at the forcing frequency is remarkably sensitive to the kind of perturbations used. Counter-phase perturbations are much more effective compared to in-phase perturbations. The physics underlying these findings is suggestive of their applicability to many other models and/or real systems exhibiting kinetic oscillations. 相似文献