拉曼光谱法在彩绘文物分析中的应用进展

拉曼光谱法是一种较为理想的彩绘文物分析技术,在取样量很少的情况下能获取较多的彩绘文物信息,实现对彩绘文物成分的无损或微损分析。本文通过大量彩绘文物颜料及胎体成分的拉曼光谱分析实例,介绍了该技术在文物分析中的优势,并阐述了拉曼光谱在彩绘胶料分析、产地分析和年代测定等方面应用的可行性和广阔前景。     

拉曼光谱技术在文物有机物鉴定中的应用

拉曼光谱作为一种"指纹光谱"可提供物质分子结构的有用信息,已广泛应用于考古及文物保护领域。拉曼光谱技术在文物有机物鉴定中具有测量简便、无损和微区检测等优势,成为文物鉴定的重要手段。本文系统阐述了拉曼光谱技术在文物有机染料、彩绘胶料、有机物残留物等分析方面的应用,指出了该技术应用于文物有机物鉴定研究的广阔前景,并展望了今后的发展方向。     

高光谱成像技术在彩绘文物分析中的研究综述

彩绘文物是文化遗产研究的重要内容之一。目前,许多的化学、光谱以及数字成像等分析技术应用于彩绘文物研究中,其中,高光谱成像技术集光谱分析与成像技术为一体,具有无损、快速成像以及"图谱合一"的特点。其技术特点使得高光谱成像技术在非接触、无样本的条件下对彩绘文物进行无损研究,既可以获得彩绘文物的整体形貌特征,还可以深入分析彩绘文物的光谱特征,是高光谱成像技术相比于其他彩绘文物研究方法的独特优势。利用高光谱成像技术研究彩绘文物分为数据采集、数据分析以及数据应用三步,其中数据分析与数据应用是研究的主要内容。通过对高光谱成像技术在彩绘文物中的相关研究成果进行总结归纳,其数据处理方法主要包括高光谱数据降维、光谱特征参量化、光谱解混合以及分类方法四个方面,并分别描述了四类处理方法的主要功能、常用方法和已有案例。从具体应用方向上,可归纳为视觉增强、隐含信息挖掘、保护监测和颜料分析四类,具体描述了四类应用方向所涵盖的内容以及所解决的问题。最后对相关研究中存在的挑战和发展前景进行了总结和展望。     

无损光谱技术在彩绘陶质文物分析中的应用进展

彩绘陶质文物拥有丰富的信息内涵,对于研究我国古代历史文化、经济商贸、科学技术发展起到极其重要的作用。但由于彩绘陶质文物的珍贵性和不可破坏性,普通分析技术难以满足其测试要求,近年来无损光谱技术被引入文物分析检测领域并逐渐得到应用。本工作从彩绘颜料分析、陶胎分析以及器物信息提取等三个方面阐述了激光拉曼显微光谱、激光诱导击穿光谱、能量色散X射线荧光光谱等无损光谱技术应用的现状、方法原理、特点及局限性,并对无损光谱技术在彩绘陶质文物分析中的应用进行了展望。     

红外光谱法研究古代彩绘蛋白胶料光老化的二级结构变化

动物胶和蛋清是古代重要彩绘文物蛋白胶结材料,对其光老化蛋白质结构变化的研究与探索彩绘文物病变机理和选择科学保护材料、修复方法密切相关。以维也纳艺术历史博物馆的动物胶(骨胶、兔皮胶、鲟鱼胶)和蛋清为研究对象,利用红外光谱技术,结合酰胺Ⅰ带去卷积和高斯拟合法研究光老化过程中蛋白质二级结构的改变。结果表明,四种胶光老化后仍然具备蛋白质红外光谱的典型吸收特征。但红外吸收峰出现了不同程度的位移,其中蛋清糖苷键明显蓝移。酰胺Ⅰ带去卷积和高斯拟合结果显示,蛋白胶的二级结构占比发生了改变。其中,骨胶α-螺旋结构占比降低22.24%,逐渐解螺旋,无规则卷曲结构占比明显增高(9.76%);兔皮胶和鲟鱼胶α-螺旋结构占比分别降低5.31%,4.15%,前者无规则卷曲增幅最低(6.96%),后者反而减少,推测两者的光老化稳定性高。蛋清α-螺旋占比降低程度最高(44.45%),无规则卷曲占比增幅极大(27.49%),光老化稳定性最差。证实利用红外光谱技术,结合酰胺Ⅰ带去卷积和高斯拟合法研究文物蛋白胶料二级结构变化的方法是可行的,但其转化机理还需后期进一步探讨。     

便携式拉曼光谱用于文物及文物保护材料光老化作用的快速评价

文物保护与考古工作者最为关心的是从文物中无损提取各种有用信息,了解文物老化状况,以便采取合适的保护措施.文章选用桑蚕丝、书画和彩绘文物常用材料印章、胭脂、朱砂、朱膘国画颜料为样品,采用便携式拉曼光谱仪检测样品在紫外光辐照前后光谱变化,进行文物光老化研究.结果表明,在360 nm波长,照度0.68 w·m-2的紫外光下.蚕丝样品47 h发生明显降解现象;便携式拉曼光谱仪采集的光谱能清晰鉴别出印章印泥种类和来源,灵敏检测出印泥和其他国画颜料经163 h紫外辐照后发生氧化分解及颜料分子结构的变化.该工作为文物现场检测、研究实际环境因素对文物影响作用,为研究文物衰变规律提供了一种便捷检测手段.     

光谱分析技术在彩绘文物颜料分析中的应用

对颜料进行准确、无损或微损分析是文物保护领域研究的热点与难点。随着文物保护研究的不断开展及多学科技术的广泛交叉、融汇,各种光谱技术逐渐被应用到彩绘文物颜料的分析之中。从元素分析、结构分析、微区与形貌分析三方面探讨了X荧光光谱分析法、激光拉曼光谱法、光导纤维反射光谱法等常用光谱分析技术在彩绘文物颜料分析中的应用、特点、局限性及应用前景。     

红外光谱结合PCA-LDA对嘉峪关戏台文物建筑彩画胶料种类的判别

为了判别嘉峪关戏台文物建筑彩画的胶料种类,采用皮胶、鱼鳔胶、蛋清、蛋黄、牛奶为参考样品,使用傅里叶红外光谱仪采集了参考样品及三件文物样品胶料的红外吸收光谱,利用主成分分析结合线性判别分析(PCA-LDA)构建胶料种类判别的数学模型,并应用于文物样品.发现参考样品红外光谱在1800～1000 cm-1区间包含了丰富的分子...     

汉阳陵陶俑彩绘颜料的拉曼光谱分析

本文利用拉曼光谱对陕西汉阳陵陶俑彩绘颜料进行了分析 ,成功地测定出彩绘颜料的成分。这一研究工作表明 ,显微拉曼光谱分析技术非常适合于考古学样品的成分分析 ,这一技术有可能成为文物产地研究的有力手段之一。     

龙门石窟彩绘颜料的拉曼光谱、X射线荧光和扫描电镜分析

作为一种无损分析技术,拉曼光谱近几十年来被越来越广泛地应用于文物艺术品分析和考古学领域。色彩是艺术品的灵魂,颜料分析是研究文物艺术品的一个重要课题。本文利用显微拉曼光谱技术,测量了龙门石窟洞窟中彩绘使用的颜料的拉曼光谱,通过对这些光谱的解析,对颜料的化学成分做出了识别。利用X射线荧光光谱进行的元素分析确定金色装饰为高纯度黄金,扫描电镜分析进一步测出了贴金的厚度。这些分析结果对于进一步开展龙门石窟彩绘的保护和修复有着重要的参考价值。     

Assessment of Raman microscopy coupled with principal component analysis to examine egg yolk–pigment interaction based on the protein C?H stretching region (3100–2800 cm−1)

This work seeks to identify the slight changes in the characteristic C H stretching region (3100–2800 cm⁻¹) of a protein‐based binder and fatty acid esters from egg yolk, which may occur in complex paint samples due to the presence of particular pigments. To date, this protein region—where historic pigments do not show characteristic Raman bands—has not been used to identify possible interactions between painting materials, in spite of its potential due to the mentioned feature. This study is based on the investigation of pure egg yolk model samples and tempera model samples prepared by mixing this binder with some historic pigments (cinnabar, raw Sienna, lead white, gypsum, calcite, azurite, lapis lazuli and smalt) as binary samples. All samples were analyzed in this region by Raman microscopy (RM) coupled with principal component analysis (PCA) for three color groups (red, white and blue) separately. The results show relevant spectral changes in the C H stretching region of amino acids and polyunsaturated fatty acids esters of the egg yolk binder, particularly in the azurite, lead white and gypsum‐based tempera samples. Lesser interactions were discerned in the tempera samples made with smalt, as well as shift in the region of polyunsaturated fatty acid esters of the egg yolk binder in the cinnabar and raw Sienna‐based tempera paintings. No interactions were recognized between the egg yolk and the pigments calcite and lapis lazuli. The effectiveness of applying RM combined with PCA for identifying interaction processes between binders and pigments is demonstrated. Copyright © 2011 John Wiley & Sons, Ltd.     

卵黄低密度脂蛋白结构的红外光谱和激光拉曼光谱分析

低密度脂蛋白是把胆固醇运输到肝脏合成胆酸一种重要的脂蛋白。低密度脂蛋白结构的研究对弄清动脉硬化发病机理有着非常重要的意义。用硫酸铵分离法快速分离鸡蛋黄中各种蛋白成分,用Sephadex G-200柱层析分离、纯化获得纯度很高的低密度脂蛋白,对其进行SDS-聚丙烯酰胺凝胶电泳(SDS-PAGE)检测,结果显示低密度脂蛋白主要包含5种脱辅基蛋白。激光拉曼和红外光谱测定,检测出低密度脂蛋白中对称CH2以及不对称CH2的伸缩振动。红外光谱还检测到脂蛋白肽键中C=O伸缩振动、脂链中P=O的伸缩振动和磷脂中胆碱聚集体的N+(CH3)3的不对称振动。两种光谱分析为研究低密度脂蛋白的结构提供了有效信息。     

常温0～1GPa压力下重晶石的拉曼光谱研究

利用碳化硅压腔装置研究了高压下重晶石的S-O对称伸缩振动v987和对称弯曲振动v452及v462的拉曼光谱变化特征.实验结果表明:在常温和0～1GPa压力范围内重晶石稳定,其拉曼谱峰随压力升高向高波数方向移动,二者的关系表达式分别为:v987=0.004 4p+987.42,v452=0.002 3p+452.6,v462=0.001 8p+462.42,而且伸缩振动受压力的影响比弯曲振动大.重晶石的987 cm-1拉曼谱峰强度约为石英464 cm-1拉曼谱峰的六倍,可作为压腔中良好的压力标定物.实验得到压力与重晶石987 cm-1峰偏移量的关系为:p(MPa)=223.16×(△vp)987-90.35(987 cm-1相似文献   

台湾蓝玉髓的振动光谱表征

蓝玉髓是中国台湾所产的名贵宝石之一,素有"台湾蓝宝"的美誉.文章通过红外吸收光谱和激光拉曼光谱,对不同颜色及质地的台湾蓝玉髓的振动光谱特征进行了研究.结果表明,台湾蓝玉髓均显示典型的石英质玉石的振动光谱特征.其红外吸收光谱主要表现为:1 250～1 110 cm-1为最强吸收区,属Si-O非对称伸缩振动,800～600 cm-1间中等强度的吸收窄带,由Si-O-Si对称伸缩振动致,Si-O弯曲振动位于600～300 cm-1内.台湾蓝玉髓样品的激光拉曼光谱散射峰主要分布在499 cm-1,464 cm-1和214～208cm-1处,分别归属为"Moganite"石英中的Si-O对称弯曲振动、Si-O弯曲振动和[SiO4]的旋转振动或平移振动.     

2-(4-异丁基苯基)丙酸的激光拉曼光谱

２┐（４┐异丁基苯基）丙酸的激光拉曼光谱鲍培谛黄天荃刘新民（四川联合大学成都６１００６４）ＲａｍａｎＳｐｅｃｔｒａｏｆ２┐（４┐ｉｓｏｂｕｔｙｌｐｈｅｎｙｌ）ｐｒｏｐｉｏｎｉｃａｃｉｄＢａｏＰｅｉｄｉ，ＨｕａｎｇＴｉａｎｑｕａｎ，ＬｉｕＸｉｎｍｉｎ（...     

DKDP晶体的拉曼散射谱分析

根据空间群理论分析和指认了磷酸二氘钾晶体[K(D_xH_1-x)₂PO₄,简称DKDP]的拉曼活性晶格振动模,测量了其室温拉曼光谱。结果表明DKDP晶体的晶格振动谱主要是由D₂PO-₄阴离子团簇的内振动引起的。与H₂PO-₄阴离子稀溶液的拉曼谱和NaD₂(PO₄)₂晶体的拉曼谱比较,DKDP晶体中D₂PO-₄阴离子的四个特征内振动模可被指认为881 cm-1(ν₁),357 cm-1(ν₂),514/541 cm-1(ν₃),965 cm-1(ν₄)。     

Discrimination of aged mixtures of lipidic paint binders by Raman spectroscopy and chemometrics

This work explores the application of chemometric techniques to Raman spectra to study aged lipidic paint binders. These binders, commonly known as drying oils, were widely used by artists throughout history both individually and in mixtures. We prepared various model samples of the pure binders (linseed, poppy‐seed and walnut oils and egg yolk) and of binary mixtures thereof. These model samples were left to age naturally for six years and further characterized by Raman spectroscopy. A comparative study of the Raman spectral features before and after ageing process was carried out. This showed changes mainly in the bands located at 1267, 1655 and 3011 cm^–1, which correspond to vibrations in cis double bonds. Multivariate analysis was performed by applying principal component analysis and partial least‐squares discriminant analysis on the corresponding Raman spectra to test whether spectral differences allowed samples to be distinguished on the basis of their composition. The CH stretching region was found to be especially useful for discrimination between the different binders. Furthermore, good sensitivity and specificity were found in the discriminant analysis particularly for the identification of binders containing egg yolk. The results of these multivariate analyses demonstrated the potential use of both chemometric approaches in the field of Cultural Heritage for drying oil characterization and identification, and also for gaining a deeper insight into the ageing process. Copyright © 2011 John Wiley & Sons, Ltd.     

Temperature Dependence for the Relative Raman Cross Section of the Ammonia/Water Complex

The Raman spectra of aqueous ammonia solutions have been obtained between -40 and 25 degrees C. The Raman spectrum of neat water was also obtained at 25 degrees C and is characterized by two broad peaks observed at 3200 and 3400 cm(-1). The spectrum due to water is subtracted to determine the NH(3) spectrum at all temperatures. In ammonia-water solutions, the spectrum shows three features at measured displacements of 3250, 3316, and 3400 cm(-1). The feature at 3316 cm(-1) is assigned to the Q branch of the symmetric stretch. The broad, weak features at 3250 and 3400 cm(-1), previously assigned to rotational bands, are assigned to combination bands. The NH(3) combination bands are assigned by comparing with sum frequency generation (SFG) experiments, monitoring changes with temperature, and analyzing the polarization data. The rotational structure of the Q band is also discussed. As the temperature is lowered from 25 to -40 degrees C, an increase in the Raman intensity is observed for all bands. The relative Raman scattering cross section is determined from the numerically integrated area of the NH(3) Q branch at each temperature. Copyright 2001 Academic Press.