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71.
A. Domingue K. Piyakis E. Sacher M. Di Renzo S. D nomm e T. H. Ellis 《The Journal of Adhesion》1993,40(2):151-162
The irreversibly bound interfacial layer deposited by the γ-aminopropysilanetriol adhesion promoter onto a crystalline silicon substrate, which remains even after profuse washing, was found by XPS to have resulted from the fragmentation and rearrangement of the original γ-aminopropylsilanetriol molecule. A mechanism is proposed, involving the homolytic scission of the terminal N-C bond. One of the subsequent reactions is believed to involve hydrogen loss by abstraction and the formation of a terminal vinyl group, which bonds to the substrate. Support for this mechanism is found in IR spectroscopy of this layer. 相似文献
72.
Zinc Coated Steel/Epoxy Adhesive Systems: Investigation of the Interfacial Zone by FTIR Spectroscopy
The present study takes advantage of the ability of Fourier Transform Infrared Spectroscopy (FTIR) for the analysis of ultrathin organic films on metals. FTIR in the reflection mode (IRRAS) is used in order to study the interaction of ultrathin films of dicyandiamide (hardener of most one-pack epoxy resins) with various substrates, model ones such as gold or zinc and industrial ones such as steel and zinc-coated steels.
Pure zinc surfaces and, to a lesser extent, zinc-coated steels are shown to react with dicyandiamide after heating at 180°C, as evidenced by the frequency shift of the absorption band (at about 2200 cm-1) characteristic for nitrile groups. As real systems consist of thick layers of a fully formulated adhesive cured onto a metallic substrate, the direct investigation of such a buried interphase is no longer possible by FTIR and by most of the known spectroscopies. Some mechanically tested specimens are then analysed, after failure, by FTIR microspectrometry. The spectra obtained, corresponding to the fracture initiation zone which is about 100 μm in diameter, advocate for the presence of an ultrathin layer of modified polymer still covering the substrate. 相似文献
Pure zinc surfaces and, to a lesser extent, zinc-coated steels are shown to react with dicyandiamide after heating at 180°C, as evidenced by the frequency shift of the absorption band (at about 2200 cm-1) characteristic for nitrile groups. As real systems consist of thick layers of a fully formulated adhesive cured onto a metallic substrate, the direct investigation of such a buried interphase is no longer possible by FTIR and by most of the known spectroscopies. Some mechanically tested specimens are then analysed, after failure, by FTIR microspectrometry. The spectra obtained, corresponding to the fracture initiation zone which is about 100 μm in diameter, advocate for the presence of an ultrathin layer of modified polymer still covering the substrate. 相似文献
73.
Symon M. Mahungu Steven L. Hansen William E. Artz 《Journal of the American Oil Chemists' Society》1994,71(4):453-455
Static headspace and capillary gas chromatography/infrared spectroscopy-mass spectrometry were used to collect, separate,
identify and quantitate the oxidative and thermal decomposition products in heated triolein. Approximately 4 L of triolein
was heated in a deep-fat fryer at 190°C for 12 h each day for a total of 60 h, until it contained>-20% polymeric material.
The concentration of heptane and octane increased after 12 h heating, then decreased upon further heating, while the concentration
of volatile aldehydes decreased gradually during heating. After 12 h of heating, the concentrations of the major volatiles
changed as follows: heptane (16.36 to 30.17 ppm), octane (24.48 to 40.77 ppm), heptanal (21.68 ppm to 9.11 ppm), octanal (35.53
to 36.64 ppm), nonanal (68.95 to 43.16 ppm), (E)-2-decenal (135.00 to 89.00 ppm) and (E)-2-undecenal (88.50 to 61.00 ppm).
After 60 h of heating, when the oil contained over 20% polymeric material, the concentrations of heptane, octane, heptanal,
octanol, nonanal, (E)-2-decenal and (E)-2-undecenal were 5.16, 4.39, 5.45, 7.02, 18.07, 12.50 and 6.00 ppm, respectively. 相似文献
74.
75.
Crosslinked copolymers of acrylamide (AA) and ethylacrylate and some ion exchangers derived from them containing either primary amine groups, obtained by the Hofmann degradation of the amide groups, or carboxylic groups, obtained by the alkaline hydrolysis of the ester groups, were studied. Divinylbenzene and N,N′‐methylenebisacrylamide were used as crosslinkers. The starting copolymers and the corresponding ion exchangers were characterized by IR spectroscopy, swelling behavior, and thermogravimetric analysis. The ion‐exchanger properties were correlated with the crosslinker nature and the chemical reactions performed on the AA copolymers. The average molecular weight between two crosslinks, determined from the swelling data in water, was compared with that calculated on the basis of the copolymerization stoichiometry only for the carboxylic cation exchangers. In this way, the preservation of the crosslink density after the hydrolysis was revealed. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2701–2707, 2003 相似文献
76.
77.
有机磷化物制备羟基磷灰石工艺条件的探讨 总被引:1,自引:0,他引:1
探索用有机磷化物制备羟基磷灰石的工艺条件:采用硝酸钙、氨水、磷酸三丁酯为原料进行正交对比研究,优化得到了制备较佳羟基磷灰石的工艺条件。优化的工艺条件为:原料中Ca/P(molar ratio)1.67;Ca(NO3)2、4H2O/NH3H2O(g/g)为0.99;烧结温度为850℃:恒温时间为5h,并对合成的样品进行了化学和红外光谱的分析。 相似文献
78.
Yasuhiko H. Mori Takehiro Nosoko Atsushi Mikami Tetsuya Ohyama 《Chemical Engineering Communications》1990,92(1):95-102
The shape of interfaces formed by the contact of two liquid phases, immiscible with each other, and a gaseous phase can be predicted on the condition that the tension to work at each interface is known with a sufficient accuracy. In general, interfacial tension data available are not so accurate, however, as to be useful as they are in predicting the shape of interfaces, particularly when the spreading coefficient of either liquid (liquid 1) on the other (liquid 2) has a negative value of a small magnitude. Presented in this note is a simple method to rectify the interfacial tension data, with the aid of a measurement of the radius of a lens of liquid 1 of a known volume placed on the horizontal surface of liquid 2, and thereby make them usable for predicting interfacial geometries. The method is tested by applying it to benzene/water and n-pentane/water systems. 相似文献
79.
The pyrolysis under nitrogen of salt free and salt treated cellulose was studied by infrared spectroscopy. The results confirm the unzipping mechanism suggested by DTA and TGA studies, and show this mechanism to apply to the untreated and salt treated samples. The results also show the unzipping to stop at the stage of char formation. The onset of this stage was found to occur after the volatilization of only 45–50% of the initial sample of the borax treated cellulose, compared with 65–70% of the KCl treated cellulose and 80–85% of the untreated cellulose. 相似文献
80.
玉米芯木聚糖硫酸酯化条件的研究 总被引:1,自引:0,他引:1
用碱提法从玉米芯中提取木聚糖,采用氯磺酸吡啶法进行硫酸酯化,通过正交试验确定最佳工艺条件为:吡啶与氯磺酸摩尔比1∶1,温度65℃,时间6h;木聚糖硫酸酯wisX-S通过DEAESepharoseFF层析柱分离得到一个相对分子量为1.3×104的组分,硫酸基取代度为2.24。对此木聚糖硫酸酯进行红外光谱分析,结果显示在波数1259、1228和813cm-1处分别有S=O和C-O-S键的特征吸收峰。 相似文献