SEM/EDS法和XRF法在电工胶带检验中的应用

目的探索电工胶带带基的元素检验方法。方法利用扫描电镜/能谱法（SEM/EDS）对电工胶带带基中的主体元素进行定量分析,通过SPSS软件对SEM/EDS定量分析法检测出的主体元素（Cl和Ca）相对含量进行统计分析;利用X射线荧光光谱法（XRF）对电工胶带带基中的微量元素进行定性分析。结果34个品牌红色电工胶带组成的561组样品对通过SEM/EDS定量分析法可以区分539组,区分率达到96.1%;根据XRF法定性分析测出的Mg、Al、Si、S、Ti、Sb、Ba、Pb微量元素的不同组合可将34种电工胶带分成11组,两种方法结合可使不同品牌红色电工胶带的区分率达到98.4%。结论SEM/EDS法和XRF法结合可以实现同种颜色、不同品牌电工胶带的高效区分。     

蓝色电工胶带的扫描电镜／能谱法检验

目的研究不同品牌蓝色电工胶带的检验方法。方法利用扫描电镜／能谱法对蓝色电工胶带进行检验。结果11个厂家生产的15种品牌的蓝色电工胶带组成的105组样品对有104组可以区分,区分率达到99．0％。结论扫描电镜／能谱法能够区分绝大多数蓝色电工胶带,该方法具有操作简便、快速、结果准确的优点,能够用于同色电工胶带的鉴别。     

光谱成像检验同种同色涂抹掩盖字迹研究

目的建立一种无损、灵敏、直观的同种同色涂抹掩盖字迹的显现方法。方法依据涂抹掩盖字迹油墨物质的同色异谱特征,利用可见光滤波型多光谱成像检验系统进行检验。结果黑色圆珠笔、蓝色圆珠笔、黑色签字笔和蓝色签字笔相互涂抹掩盖形成的同种同色涂抹掩盖样本,利用可见光滤波型多光谱成像检验系统进行检验,显效率分别为90.5%、69.1%、49.5%、78.6%,显现效果良好。结论多光谱成像技术可以显现同种同色涂抹掩盖字迹,且具有良好的显现效果。     

运用光谱成像技术区分同色棉纤维

目的研究同色棉纤维的检验方法。方法运用成像光谱法对红、蓝、黑3个颜色组的棉纤维进行区分。结果红色棉纤维的鉴别率为62．2％，蓝色棉纤维的鉴别率为77．8％，黑色棉纤维的鉴别率为69．6％。结论实验结果表明，光谱成像技术可以区分大部分同色棉纤维。拓宽了纤维检验的方法，解决了同色棉纤维的区分问题，该方法能够用于对微量同色棉纤维的快速鉴别。     

透明胶带的厚度检验

目的研究不同品牌透明胶带的区分方法。方法利用测厚仪对35种不同品牌透明胶带的厚度进行检验,并对所得数据进行统计分析。结果 35种品牌透明胶带组成的595组样品对中有458组可以区分,区分率为77.0%。结论厚度检验法能够在一定程度上区分不同品牌的透明胶带,厚度检验结果可与化学成分检验相互佐证,使得鉴定结论更加准确可靠,为法庭科学领域透明胶带物证的区分提供了一种预检验方法。     

基于光谱成像的人血和两种动物血痕迹的函数型数据分析

目的研究现场勘查和实验室检验鉴定中光谱成像技术显现和区分人体血液痕迹与动物血液痕迹的能力。方法使用光谱成像技术分别采集人血、鸡血、蛇血在不同介质表面的光谱影像数据,利用函数型数据分析方法依次分析了四种介质上的血迹数据,主要的分析方法包括:1)基于函数型数据主成分分析定量确定三种血迹光谱主成分贡献率及差异主要集中的波段;2)利用三种血迹的主成分进行聚类分析;3)基于函数型数据Fisher判别分析对样本进行判别。结果利用函数型数据进行血迹种类判别,对四种介质上三种血迹的识别准确率分别达到了96.6%、98.8%、99.0%和94.6%。结论研究表明,利用光谱成像技术和函数型分析方法来区分现场人血与动物血痕迹物证是行之有效的。     

透射光谱成像技术检验黑色签字笔涂抹掩盖字迹研究

目的 对透射光谱成像技术和反射光谱成像技术检验黑色签字笔间涂抹掩盖字迹进行比较研究,探寻一种无损、高效、直观的黑色签字笔涂抹掩盖字迹的显现方法,提高黑色签字笔间涂抹掩盖字迹显现效率。方法根据不同黑色签字笔油墨物质成分不同,不同物质对光的透射率各异的特征,在相同条件下使用反射光谱成像技术与透射光谱成像技术分别对多个黑色签字笔间涂抹掩盖字迹实验样本进行检验。本文将显现效果分为可显现和不可显现两类。分类标准为从未看过原字迹的非文检人员是否可以辨认出被涂抹掩盖字迹。结果 利用透射光谱成像检验系统检验黑色签字笔涂抹掩盖字迹样本,306个样本中,可显现的有231个,不可显现的75个,显效率为75.49%;反射光谱成像技术检验306个样本,其中可显现的有159个,不可显现的有147个,显现效率为51.96%。实验结果表明透射光谱成像检验黑色签字笔涂抹掩盖字迹的显现率高于反射光谱成像检验的检验。结论 除了无法显现原字迹与涂抹掩盖笔迹的油墨物质成分、浓度以及组成配比相同或相近的样本之外,透射光谱成像技术能检验常规的光谱成像技术无法显现的黑色签字笔间涂抹掩盖字迹,其显现效果和效率都优于反射光谱成像技术,是一种高效的显现方法 ,可以应用于刑事物证检验领域。     

光谱成像中光谱基准点选取的研究

目的研究物证检验应用光谱成像标准化规范化的操作技术方法。方法比较相同数据采集条件下选择不同光谱基准点区分物质的效果。结果选择不同基准点对光谱成像检验效果影响很大。结论应用光谱成像方法检验物证时针对不同检验目的选择不同基准点具有很强的规律性。     

显微光谱成像技术在汽车油漆截面检验中的应用

目的对汽车多层油漆的横截面进行分层和比对研究。方法运用显微光谱成像技术对收集的12个省市623个汽车漆片样本进行分层,并对截面结构相同或相似的油漆样本进行了区分。结果 623个油漆样本均可以分层,分析出漆层为两层及以上的油漆样本数占总数的87.26%;截面结构相同或相似的油漆样本能够多层同时区分。结论该方法具有科学及实用价值,检验结果可靠,可见光谱成像技术完全可运用拓展到微量物证的检验中。     

显微共焦拉曼光谱技术区分喷墨打印机打印的彩色图文墨迹

目的建立显微共焦拉曼光谱法区分喷墨打印机打印的彩色图文墨迹的方法。方法利用显微共焦拉曼光谱技术所具有微量、微区、原位分析及非破坏性等特点,对24种常见彩色墨水墨迹分别进行检验。结果品红色墨点墨迹成分归类区分效果最好,其次是黄色墨点,最后是蓝色墨点。结论采用显微共焦拉曼光谱技术对彩色打印墨迹进行不同颜色单点分析可大大提高喷墨打印机厂家型号的识别率,是一种有效的检测手段。     

Hyperspectral imaging of gel pen inks: An emerging tool in document analysis

Hyperspectral imaging (HSI) is a useful technique in the examination of writing inks, including gel pen inks, which combines digital imaging with % reflectance spectroscopy. This facilitates the detection of subtle differences between chemically similar inks. This study analysed a variety of blue, red and black gel inks on white office paper using HSI. The potential of the technique for ink discrimination compared to other analytical methods of examination is highlighted. Discriminating powers of 1.00, 0.90 and 0.40 were achieved using HSI for red, blue and black gel inks respectively. The overall discriminating power of 0.76 for the technique combined with its non-destructive nature and minimal sampling requirements demonstrates promise for this type of application.     

Analysis and discrimination of electrical tapes: part II. Backings

The backings of 90 black electrical tapes were analyzed to evaluate the chemical components of these films, the ability of individual techniques to discriminate samples, and the ability of the techniques combined to distinguish samples. The techniques utilized and their respective discrimination results were stereomicroscopy and physical measurements, to include observation of surface features of the backing, width, and thickness measurements (c. 64%); Fourier transform infrared spectroscopy (FTIR) using a microscope accessory (c. 83%); pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS; c. 81%); and scanning electron microscopy/energy-dispersive spectroscopy (SEM/EDS; c. 87%). Ninety-four percent of the backings were discriminated through this combination of analytical methods. Finally, evaluating these results in conjunction with previously published data on the analysis of the adhesives from the same set of electrical tapes provided an overall discrimination of nearly 96%.     

Forensic utility of carbon isotope ratio variations in PVC tape backings

Forensic interest in adhesive tapes with polyvinyl chloride (PVC) backings (electrical tape) derives from their use in a variety of illicit activities. Due to the range of physical characteristics, chemical compositions, and homogeneity within a single roll of tape, traditional microscopic and chemical analyses can offer a high degree of discrimination between tapes, permitting the assessment of potential associations between evidentiary tape samples. The carbon isotope ratios of tapes could provide additional discrimination among tape samples. To evaluate whether carbon isotope ratios may be able to increase discrimination of electrical tapes, particularly with regards to different rolls of tape of the same product, we assessed the δ(13)C values of backings from 87 rolls of PVC-based black electrical tape (~20 brands, >60 products) Prior to analysis, adhesives were removed to prevent contamination by adhering debris, and plasticizers were extracted because of concern over their potential mobility. This result is consistent with each of these tapes having approximately the same plasticizer δ(13)C value and proportion of carbon in these plasticizers. The δ(13)C values of the 87 PVC tape backings ranged between -23.5 and -41.3 (‰, V-PDB), with negligible carbon isotopic variation within single rolls of tape, yet large variations among tape brands and tape products. Within this tape population, carbon isotope ratios permitted an average exclusion power of 93.7%, using a window of +/-0.3‰; the combination of carbon isotope ratio measurement with additional chemical and physical analyses raises the discrimination power to over 98.9%, with only 41 out of a possible 3741 pairs of tape samples being indistinguishable. There was a linear relationship between the δ(13)C value of tape backings and the change in δ(13)C value with the extraction of plasticizers. Analyses of pre- and post-blast tape sample pairs show that carbon isotope signatures are within 0.3‰ of pre-blast values, indicating that carbon isotope values are largely preserved during an explosion.     

The Discrimination of Colored Acrylic,Cotton, and Wool Textile Fibers Using Micro‐Raman Spectroscopy. Part 1: In situ Detection and Characterization of Dyes

Raman spectroscopy has been applied to characterize fiber dyes and determine the discriminating ability of the method. Black, blue, and red acrylic, cotton, and wool samples were analyzed. Four excitation sources were used to obtain complementary responses in the case of fluorescent samples. Fibers that did not provide informative spectra using a given laser were usually detected using another wavelength. For any colored acrylic, the 633‐nm laser did not provide Raman information. The 514‐nm laser provided the highest discrimination for blue and black cotton, but half of the blue cottons produced noninformative spectra. The 830‐nm laser exhibited the highest discrimination for red cotton. Both visible lasers provided the highest discrimination for black and blue wool, and NIR lasers produced remarkable separation for red and black wool. This study shows that the discriminating ability of Raman spectroscopy depends on the fiber type, color, and the laser wavelength.     

Evaluation of Raman spectroscopy for the analysis of colored fibers: a collaborative study

A collaborative study on Raman spectroscopy was carried out by members of the ENFSI (European Network of Forensic Science Institutes) European Fibres Group (EFG) on three dyed fibers: two red acrylics and one red wool. Raman instruments from six different manufacturers were tested as well as nine different laser wavelengths ranging from blue (lambda = 458 nm) to near infrared-NIR (lambda = 1064 nm). This represents the largest comparison study of Raman analytical parameters carried out on identical fiber samples. For the chosen fiber and dye samples, red lasers (lambda = 633 and 685 nm) gave the poorest spectral quality whereas blue (458 nm), green (514 nm) and near infrared lasers (785, 830 and 1064 nm) provided average results. Blue (488 nm) and green lasers (532 nm) globally gave the best quality spectra. Fluorescence problems were often encountered with some of the excitation wavelengths and therefore a flexible Raman instrument equipped with different lasers can be recommended to measure forensic fiber samples. The instrument should also be equipped with a Raman microscope in order to be able to focus on a single fiber. This study shows that Raman spectroscopy usually enables the identification of the main dye present in a colored fiber; however, minor dye components are much more difficult to detect. SERRS (Surface Enhanced Resonance Raman Scattering) techniques give an improvement of the dye's spectral intensity but no spectral improvement was observed for the two red acrylic and red wool fibers tested.     

Enhancing contrast of fingerprints on plastic tape

Many of the currently available fingerprinting methods have limited ability to visualize fingerprints on plastic tape without expensive equipment or significant handling of the sample. This is especially true for visualizing fingerprints on black electrical tape. This study sought a hands-off method to produce easy visualization of fingerprints on different types of plastic tape, including black electrical tape, without the need for expensive equipment. The methods selected were to sublime disperse dyes into the tape, both with and without the fuming of cyanoacrylate, everywhere except for where the fingerprint was applied. The resulting color contrasts provided enough differentiation to visualize fingerprints on plastic tape under ambient light. Sequential fuming with cyanoacrylate followed by disperse dyes provided the best visualizations on all tapes, and cyanoacrylate followed by disperse yellow 211 clearly visualized fingerprints on black electrical tape.