Author Keywords: Infrared spectrometry; Fourier transform; Wall and canvas painting analysis; Restoration/conservation of works of art 相似文献
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91.
研究乙酰丙酮-meso-四-(对-氯代)苯基卟啉及其Nd、Sm、Eu、Gd、Tb、Dy、Ho、Er、Lu配合物在3600~220cm-1范围内的傅立叶变换红外光声光谱,对其主要谱带进行经验归属.实验结果表明,四-(对-氯代)苯基卟啉与稀土乙酰丙酮配合物中的金属离子配位,削弱乙酰丙酮环上的M-O键伸缩振动,使该谱带向低波数方向移动.金属敏感带出现在~1558、~1474、~1427、~1219、~798、~733、~250cm-1. 相似文献
92.
Joannie Chin Amanda Forster Lipiin Sung Kirk Rice 《Polymer Degradation and Stability》2007,92(7):1234-1246
In recent years, poly(p-phenylene-2,6-benzobisoxazole) (PBO) fibers have become prominent in high strength applications such as body armor, ropes and cables, and recreational equipment. The objectives of this study were to expose woven PBO body armor panels to elevated temperature and moisture, and to analyze the chemical, morphological and mechanical changes in PBO yarns extracted from the panels. A 30% decrease in yarn tensile strength, which was correlated to changes in the infrared peak absorbance of key functional groups in the PBO structure, was observed during the 26 week elevated temperature/elevated moisture aging period. Substantial changes in chemical structure were observed via infrared spectroscopy, as well as changes in polymer morphology using microscopy and neutron scattering. When the panels were removed to an ultra-dry environment for storage for 47 weeks, no further decreases in tensile strength degradation were observed. In a follow-on study, fibers were sealed in argon-filled glass tubes and exposed to elevated temperature; less than a 4% decrease in tensile strength was observed after 30 weeks, demonstrating that moisture is a key factor in the degradation of these fibers. 相似文献
93.
Ruifeng Liu Paula R. Moody Alex S. Vanburen Jeffrey A. Clark Joel A. Krauser Dennis R. Tate 《Vibrational Spectroscopy》1996,10(2):325-329
Results of ab initio and density functional theory calculations on the structure and vibrational frequencies of hypophosphite anion indicate earlier experimental assignments of the fundamental vibrational modes are correct while the recent reassignments of several modes proposed by Bickley et al. are inconsistent with the calculated results. 相似文献
94.
在280~320K的温度范围内考察了30%十六烷基三甲基溴化铵水溶液的红外光谱随温度的变化。结果表明该体系的凝聚胶-液晶相转变温度为300K。在300K以下的凝聚胶相,分子的极性头部基团处于高度“固定”的状态,分子的碳氢链以有序的相互平行方式排列,极性头与碳氢链之间有一定的倾斜角。在300K以上的液晶相,极性头内部CH_3-(N~+)基团以及整个极性头与碳氢链之间发生了旋转,碳氢链变为以六方亚晶胞填充形式存在,旦扭曲式构象异构体数量显著增多,极性头与碳氢链之间已不存在倾斜角,分子的亲水极性头和疏水碳氢链部分都处于“融化”状态。 相似文献
95.
M. T. Dom nech Carb F. Bosch Reig J. V. Gimeno Adelantado V. Periz Martí nez 《Analytica chimica acta》1996,330(2-3):207-215
This paper is a study of the analytical capacity of Fourier transform infrared spectroscopy (FT-IR) for any type of samples from works of art. The analytical information obtained with this technique on organic and inorganic compounds is extremely useful in the preliminary studies necessary for diagnosis and to decide on the conservation process. This paper reports the analysis and study with FT-IR on samples extracted from the microlayers in several works of art from different periods (16th to 18th century) comprising wall paintings and canvas. The most outstanding of these being the frescoes by A. Palomino from two ceilings in the Santos Juanes church. The analytical procedures for the different components of the works studied such as
1. (a) varnish applied to wood panels and canvas paintings,
2. (b) binding media and pigments used by the artists,
3. (c) inerts, mortars, stuccos and grounds have been optimized. The FT-IR technique offers a quick analysis of microsamples (less than 0.5 mg) and is able to characterise the different molecular groups which provide information on the nature of the different materials of organic and inorganic origin used by the artist and thus permits the diagnosis of pathologies requiring conservation treatment.
96.
Using infrared reflection absorption spectroscopy (IRRAS), quartz crystal microbalance (QMB) measurements, and X-ray photoelectron spectroscopy (XPS) in combination with chemical derivatization techniques the VUV photolysis of polyethylene (PE), polypropylene (PP), and polystyrene (PS) was investigated. A mass balance obtained from the quantification of the data was used to suggest reaction path ways. Although PE and PP behave similar, the mass loss is about 8 times higher in the case of PP. These differences originate from the higher disproportionation to recombination ratio for the branched polymer. Both polymers form double bonds and at extended treatment times they tend to crosslink. PS is rather stable due to the possibility of the energy dissipation by fluorescence. 相似文献
97.
The composition of solvent mixtures employed in the paint industry was determined by Fourier transform infrared spectrometry. A procedure based on the use of the ratio between the absorbance of characteristic bands of each component permits the ratio between two solvents in a binary mixture to be determined, independently of the thickness of the sample film. Typical mixtures of xylol with butan-1-ol and with butyl acetate (xylol=mixture of o-, m- and p-xylenes) were used as model systems to develop the proposed procedure and the accuracy was determined using synthetic formulations. Another possible application of the procedure is the characterization of azeotropic mixtures. 相似文献
98.
Z. Guennoun A. Coupeaud I. Couturier-Tamburelli N. Pitri S. Coussan J.-P. Aycard 《Chemical physics》2004,300(1-3):143-151
The structures and energies of the 1:1 acetylene/cyanoacetylene, acetylene/dicyanoacetylene and cyanoacetylene/dicyanoacetylene complexes in solid argon matrices have been investigated using FT-IR spectroscopy and ab initio calculations, at the B3LYP/6-31G** level of theory. For the three complexes, predicted frequency shifts for the L shaped structures, characterized by a hydrogen bond between the nitrogen of the cyano group and the acetylenic proton, were found to be in good agreement with those experimental. Only in the case of acetylene/cyanoacetylene complex, we obtained a second minimum with a T shaped structure characterized by an interaction between the proton of cyanoacetylene and the Π system of acetylene. It appears clearly that HC3N acts as an electrophile or as a nucleophile in these complexes. 相似文献
99.
The infrared spectra of 4-Cl 2-Me, 4-Cl 3-Me and 6-Cl 3-Me phenols have been recorded. The vibrational spectrum has been analysed
assuming that the molecules belong toC
s
point group and a tentative assignment of the observed frequencies to various modes of vibration has been proposed. The near
ultraviolet absorption spectrum of these compounds has also been recorded. Assuming the transition to be electronically allowed
the strongest band on the longer wavelength side has been assigned as the (0, 0) band in each case. The spectrum has been
analysed in terms of several excited state frequencies which have been correlated with the ground state frequencies observed
in the infrared spectrum. 相似文献
100.
Peter Grosse 《Vibrational Spectroscopy》1990,1(2)
In condensed matter, optical properties can be described by a dielectric function (DF), and the structures observed in spectra are then related to the poles and zeros of the DF. As an example, model functions are calculated by a fit to measured spectroscopic data for polystyrene and silica. The first material shows weak, narrow bands and the latter strong, broad bands and a negative real part of the DF.Based on these model DFs, spectra are simulated which are expected to be obtained by “conventional” methods such as transmittance or reflectance measurements, or by “unconventional” methods such as reflectance at oblique incidence, diffuse reflectance, photoacoustic spectroscopy and attenuated total reflectance. A variety of simulated, typical spectra are plotted as a small “atlas”. Conditions are discussed that allow a straightforward procedure for interpreting the spectra quantitatively, i.e., the evaluation of the resonance frequency and the concentration of the oscillators under consideration.It is shown that for systems characterized by weak, narrow oscillator lines, mostly an intuitive interpretation is possible, looking only at the position and strength of “lines” in the spectra. Materials showing strong polar vibrations, however, require more sophisticated procedures for interpreting the spectra. 相似文献