Forensic Paint Analysis and Comparison Guidelines by SWGMAT Paint Subgroup, Part 2 (FSC, July 1999)
8.2. A reasonable scheme for forensic paint examinations is outlined in Figure 1. A variety of potentially useful techniques for the discrimination of paint binders, pigments, and additives are listed. The major steps in Figure 1 correspond to the discussions presented in this section (e.g., 8.8. Solvent/Microchemical Tests). For any given comparison, not all the techniques listed in Figures 1A, 1B, and 1C are necessarily required. Sample size, condition, and layer structure complexity should be considered when determining which techniques to use. The forensic coatings examiner should always use the more specific and least destructive tests prior to those that require more sample preparation or consumption. A review of the general technique descriptions, listed in 8.8. Solvent/Microchemical Tests and the subsections that follow, provides guidance for the selection of appropriate methods.
8.3. Figure 1 does not imply that other examinations should be excluded or that the order of the procedures in the chart is irrevocable. Samples that are neither constrained by amount nor condition should be subjected to analyses that will determine the color and texture of the paint as well as the number, order, colors, and textures of the layers in a multilayered sample. In most cases, instrumental techniques should be employed to analyze and compare both the pigment and binder portions of the sample. A combination of techniques, which provides discrimination between as many types of paints and coatings as possible, should be used. These techniques should also be selected to provide either or both classification or component identification information to be used in significance assessments. For samples that are limited in layer structure complexity, techniques for the comparison of both the binder and pigment portion of the coating must be used. The choice of techniques may change depending upon sample characteristics. For instance, pyrolysis gas chromatography (PGC) may be used for identifying and comparing the binder portion of samples that exhibit a low binder concentration. Likewise, scanning electron microscopy-energy dispersive X-ray analysis (SEM-EDS), X-ray fluorescence (XRF), and X-ray diffraction (XRD) may be used for identifying and comparing the pigment portion of samples that exhibit a low pigment concentration.
8.4. The flowchart in Figure 2 is a guide to the determination of the possible origins of a motor vehicle paint in an investigative case. It is usually possible to differentiate motor vehicle repaint from the original equipment manufacturer (OEM) paint by microscopical examination. If no OEM paint is present, then only the vehicle color can be reported. For OEM paint, the color of the topcoat layers and of the undercoat layers will each be useful in identifying manufacturer, model, and year. Often the two systems provide complementary information. In most cases a range of possible makes, models, and years will be generated by the search. Further specific information can often be developed through chemical analysis of the individual layers. Any of the techniques shown in Figure 1 can be used, depending on the databases available. Reference collections and databases may fall into one of the following categories: books of color chips produced by automotive refinish paint manufacturers for use by body shops and automotive repair facilities, manufacturer topcoat and undercoat colors, chemical standards, street samples collected from damaged motor vehicles, OEM information on paint formulations, and collections of infrared spectra or pyrograms of known paints. Examples of databases include the Royal Canadian Mounted Police/Scientific Working Group on Materials Analysis (RCMP/SWGMAT) database, the National Automotive Paint File maintained by the Federal Bureau of Investigation, the Collaborative Testing Services reference collection of automotive paints, and the Georgia Bureau of Investigation Paint Library of infrared spectra.
8.5. Sample Description
8.5.2. The initial evaluation should begin with a critical review of the chain of custody, package sealing, and identification markings of the sample or samples and any potential cross-contamination between samples. If the items are found to be suitable for further evaluation, a detailed accounting and description of the paint fragments and any commingled material should be documented. This involves describing the general condition, weathering characteristics, size, shape, exterior colors, and major layers present in each sample. This description can be accomplished by examining each item using a stereo microscope.
8.5.3. Written descriptions, sketches, photography, or other imaging methods must be used to document each sample's characteristics. The goal is to produce documentation that will be meaningful to a reviewer in the absence of the recording examiner. The resulting notes must be sufficient to document the conclusions reached in the examiner's report. Although documentation is discussed at this point in the guidelines, it is an essential part of all steps in an analysis.
8.6. Physical Match
8.6.2. Physical matches must be documented with descriptive notes. Photography, photo transparency overlays, or other appropriate imaging techniques may be a useful adjunct. When imaging methods are used to document a physical match, the examiner must ensure that the method employed is dimensionally accurate and has associated measuring scales. Images must be well-preserved and retained as part of the documentation.
8.7. Sample Preparation
and Layer Analysis
8.7.2. Paint layer structure can be observed by using a scalpel blade to make an oblique cut through a sample. The larger surface area created by this angled cut may enhance layer visualization and assist in the detection of layer inhomogeneities. The preparation of thin-sections and the separation of paint layers can be accomplished with a scalpel blade. Preliminary solvent tests can be conducted on the manually prepared sections and layer fractions.
8.7.3. Subtle differences in color, pigment appearance, surface details, inclusions, metallic and pearlescent flake size and distribution, and layer defects may require microscopical comparisons of the edge, oblique cut, and surface views of known and questioned paint samples. These comparisons must be carried out with both samples positioned side by side and in the same field of view.
8.7.4. Cross sections (embedded or thin-section preparations) may provide additional information as to the layer sequence, layer thickness, color, pigment distribution, pigment size, and composition of the individual layers that may not be possible to obtain with gross examination. Embedded preparations can be prepared by polishing, microtomy, or both. Thin-sections can be prepared using a variety of microtomy techniques. Examination and analysis of the cross sections can be conducted using a variety of analytical techniques that may include light microscopy, UV-visible microspectrophotometry, infrared microspectrophotometry, and electron microscopy. Laing et al. (8), Allen (9), and Stoecklein and Tuente (10) offer a concise discussion of thin-section paint analysis.
8.8. Solvent/Microchemical Tests
8.8.2. Solvent/microchemical tests are destructive and should be applied first to known samples in order to evaluate their efficacy to a specific case, and they should be used only in situations in which an adequate questioned sample is available.
8.8.3. Solvent/microchemical examinations should be applied to both questioned and known materials concurrently. The effects of various tests are recorded immediately and then at reasonable intervals for the duration of each test. It is desirable to apply such tests not only to intact paint films but also to peels of each individual layer to avoid interaction with neighboring layers and to observe the dissolution process more critically.
8.8.4. Reactions such as softening, swelling, curling or wrinkling, layer dissolution, pigment filler effervescence, flocculation, and color changes are some of the features that may be noted. The results of these tests are inherently difficult to quantify. Therefore, they are primarily used for preliminary classification and comparison.
8.9. Polarized Light Microscopy (PLM)
8.9.2. Suitable samples for examination by PLM include but are not limited to thin peels, thin-sections, pyrolysis and low-temperature ashing residues, sublimation condensates, and dispersed particles in a solvent oil or other mounting medium.
8.9.3. The use of PLM for the identification of paint components requires advanced training and experience. Preparation and identification of paint components by PLM are discussed by McCrone (11) and Kilbourn and Marx (12).
8.10. Vibrational Spectroscopy
8.10.2. If a multiple-layer coating system is to be subjected to an infrared examination, optimal results can be obtained if each layer is isolated and analyzed separately. Methods that use solvents to assist in the sample preparation should be used with caution because they might alter the sample or result in the production of residual solvent spectral absorptions.
8.10.3. An infrared microscope accessory permits the analysis of a small sample or a small area of a sample. Samples of individual layers may be prepared manually using scalpels, blades, needles, forceps, or other similar tools. Peels or sections can be placed on a salt plate or appropriate mount for analysis. The infrared microscope accessory may also be used to sequentially sample individual layers of a multiple-layer coating system that has been cross-sectioned either manually or by microtome. Generally, it is desirable to press such a sample after sectioning to produce a wider width for each layer and to produce a more uniform thickness. The aperture for an individual layer should be chosen so that its edges are as far from the adjacent layers as practicable. This minimizes the amount of stray light produced by diffraction that may be detected. All spectra of individual layers should be examined to determine if absorptions of adjacent layers are contributing to the spectrum.
8.10.4. Certain types of coatings, including automotive undercoats and many types of architectural coatings (particularly those with low luster finishes), usually contain significant amounts of inorganic pigments. These pigments tend to have most of their significant infrared absorptions in the lower frequency spectral regions, and several have all of their absorptions in the region below 700 cm-1. An FTIR spectrometer equipped with cesium iodide (CsI) optics and a deuterated triglycine sulfate (DTGS) detector can collect spectral data to 220 cm-1. The DTGS detector is less sensitive than the mercury cadmium telluride (MCT) detector used with IR microscopes, and the DTGS detector also requires a longer time to acquire each spectrum. CsI optics also have the disadvantage of lower energy throughput compared to potassium bromide (KBr) optics. Thus, a far-IR instrument requires longer analysis times.
8.10.5. Transfers of coatings resulting in smears on various substrates may be sampled in situ using an appropriate attenuated total reflectance (ATR) accessory or an ATR objective for an infrared microscope. As a control, the substrate itself (not a metal) should also be analyzed to verify that its absorptions are not contributing to the spectrum of the smear. Any contributions from the substrate should be considered. If the substrate is a metal or highly reflecting, it may be possible to obtain a reflection-absorption spectrum of the smear using the reflectance mode of an infrared microscope accessory. This produces a double-pass transmittance spectrum of the material, and a background spectrum of the substrate itself (or uncoated mirror) should be used as a reference.
8.10.6. General information about the forensic analysis of coatings using infrared spectroscopy is discussed by O'Neill (13), Suzuki (14), and Ryland (15). Forensic infrared microsampling of coatings using a beam condenser is described by Tweed et al. (16), Rodgers et al. (17), and Schiering (18). Analyses using infrared microspectroscopy are described by Wilkinson et al. (19), Allen (20), Bartick et al. (21), and Ryland (15). The identification of specific binders, pigments, and additives using infrared spectroscopy is described by Rodgers et al. (17, 22, 23), Norman et al. (24), Ryland (15), and Suzuki et al. (25-27). Infrared spectral data for a number of binders, pigments, additives, and solvents are presented in a compilation produced by the Federation of Societies for Coatings Technology (28).
8.10.7. Raman spectroscopy can also be used to obtain information about binders, pigments, and additives used in coatings. Because this technique is based on light scattering rather than absorption, Raman spectra provide information that is complementary to that produced by infrared spectroscopy. Some paint components, for example, may give rise to both infrared absorption bands and Raman bands, but the relative absorption or scattering intensities of these bands will differ significantly between the two techniques. Other paint components may have vibrational modes that produce no infrared absorption bands but may produce Raman bands. In addition, Raman spectroscopy can be useful for the analysis of inorganic pigments and additives because it, like far-infrared spectroscopy, can provide information about low-frequency vibrational transitions.
8.10.8. In most cases, Raman instrumentation using near-infrared lasers will be needed to avoid strong fluorescence produced by various paint components. Because near-infrared excitation produces considerably weaker Raman scattering than visible excitation, dispersive instruments equipped with diode array detection systems or Fourier transform Raman spectrometers are recommended. Some applications of Raman spectroscopy for the analyses of coatings are discussed by Kuptsov (29) and Claybourn et al. (30).
8.11. Pyrolysis Gas Chromatography
8.11.2. Pyrograms, the chromatograms of the pyrolytic products, are influenced by numerous sample characteristics and instrumental parameters. These may include sample size, shape and condition, ramping rates, final pyrolytic temperature, type of capillary column or columns, gas-flow rates, temperature programs, and detector type or types. The resulting patterns of peaks in the known and questioned sample pyrograms are used for comparison purposes. If pyrolysis and chromatographic conditions are kept constant over time, then PGC can be used as an aid in the characterization of binder types by comparison with pyrograms of paints or resins from a reference collection.
8.11.3. The applicability of this technique depends on the paint type, layer complexity, and the amount of sample consumption that can be tolerated. PGC analysis may be conducted with as little as 5-10 micrograms of sample. Run times are typically 20-40 minutes in duration. PGC is best applied to individual paint layers for purposes of both binder classification and comparison. With multilayered paint samples, layer thickness variations, sample orientation in the pyrolysis accessory, and incomplete pyrolysis make reproducible pyrograms more difficult to obtain.
8.11.4. The user must ensure that reproducibility is maintained and that there is no sample carryover between runs. The necessity and frequency of replicate and blank runs must be established for each system and sample type.
8.11.5. The identification of pyrolysis products may be accomplished by pyrolysis gas chromatography-mass spectrometry (PGC-MS). Besides the detection of binder components, the reconstructed total ion chromatogram may contain information about additives, organic pigments, and impurities. McMinn et al. (41) and Challinor (42) provide discussions of mass spectrometric detection for PGC.
8.11.6. Information about the binder composition of some samples can be increased if the paints have been derivatized during pyrolysis. The use of derivatizing reagents such as tetramethyl-ammonium-hydroxide (TMAH) is discussed by Challinor (43-45).
8.12.2. Microspectrophotometry may be required to provide objective color data for paint comparison because of the typically small size of samples. The technique can be applied to the outer surfaces of paint films by diffuse reflectance (DR) measurements with visible spectrum illumination.
8.12.3. Diffuse reflectance measurements of paint surfaces are affected profoundly by surface conditions such as weathering, abrasion, contamination, and texture. This fact can provide useful discriminating information when an examiner is faced with distinguishing different surfaces that were originally painted with the same paint formulation. Careful reference sampling is essential to the success of color comparisons of such surfaces.
8.12.4. Diffuse reflectance techniques can also be used on the edges of thin paint layers much as it is on outer paint surfaces. Before analysis, questioned and known samples can be mounted side by side on edge and polished to a smooth surface using a polish of 3-micron grit size or less. Microtomed samples without surface defects may be used without polishing. The requirement for consistent surface finish characteristics for all samples is achieved easily if the known and questioned samples are mounted and prepared in a single mount.
8.12.5. When required for the discrimination of similarly colored paint layers, the surface finish of a polished sample must approach the size of the smallest pigment particles present.
8.12.6. Comparison of paint layers by transmission microspectroscopy of thin cross sections offers a more definite form of color analysis for these samples, compared to reflectance techniques. Transmission microspectroscopy demands the most care in preparation. Consistent sample thickness and choice of measurement size and location are essential for meaningful comparisons. Although thin cross sections can be manually prepared, improved reproducibility can be achieved using a microtome. Even when using a microtome, the slice thickness, blade angle, cutting speed, lubrication, and mounting block stiffness or resilience must be selected and controlled carefully. A discussion of these parameters is presented by Derrick (47).
8.13. Scanning Electron Microscopy
8.13.2. X-rays are produced as a result of high-energy electrons creating inner-shell ionizations in sample atoms, with subsequent emission of X-rays unique to those atoms. The minimum detection limit under many conditions is 0.1 percent. Elements with atomic numbers greater than or equal to 11 are customarily detectable. Detection of elements with atomic numbers greater than or equal to 4 is possible using a detector with an organic film window or a windowless detector. Analysis can be performed in a rastered beam mode for bulk-layer analysis or static beam (spot) mode for individual particle analysis. Goldstein et al. (48) present a general treatment of all aspects of SEM and X-ray microanalysis.
8.13.3. Comparison of the composition of layers is generally performed by a nonquantitative method, such as direct spectral comparison or peak ratioing. Because accurate quantitative EDS requires sample homogeneity to a level of several microns, quantitative methods are not generally used for paint analysis. In order to produce a representative spectrum of a paint layer, the summing of spectra from multiple areas or the use of a beam raster area larger than 30 square microns is often required. The homogeneity of modern household paints and their examination by SEM-EDS is discussed by Gardiner (49).
8.13.4. The analysis of individual pigment particles in paint layers by static beam (spot) analysis can be useful. However, variations in the absorption and fluorescence factors caused by particle size and shape and fluorescence contributions from adjacent particles preclude the application of small, single-particle, X-ray correction routines.
8.13.5. The depth from which X-rays are produced (the analytical volume) is dependent upon beam energy, composition and density of the sample, and energy of the X-rays. Generally, the primary X-ray spatial resolution obtained in the analysis of paint systems is less than 10 mm. Secondary X-ray fluorescence further enlarges the analytical volume beyond the scanned image area visible in the SEM image. Optimal results are obtained from samples prepared in cross section, either by microtomy or polishing. The low bulk density and low average atomic number of organic polymer-based paint layers make them susceptible to electron and X-ray penetration that can yield analytical X-ray contributions from adjacent layers. Care must be taken to ensure that the EDS data generated are representative only of the paint layer of interest or that any adjacent layer contributions are reproducible.
8.13.6. Additional sample preparation methods such as thin peels or stair stepping may be used. Stair-step sample preparation and analysis allows larger areas to be analyzed and possibly avoids inhomogeneity concerns but faces the potential for penetration into the underlying layer and difficulties in obtaining flat analytical surfaces and reproducible layer thicknesses. If samples are prepared as single-layer peels, the concerns of penetrating or sampling adjacent layers or both are avoided. Elements in low concentrations may not be as readily detected in these thin peels without longer count times.
8.13.7. Mapping of elements across the cross section of a multilayer paint can be useful for explaining or demonstrating elemental distributions and elemental associations. However, elemental maps are generally not quantitative and may lack the sensitivity to demonstrate minor sample differences.
8.13.8. Because a wavelength
dispersive spectrometer (WDS) generally has better spectral resolution,
lower detection limits, and superior light element detection
capability than EDS, its use can supplement EDS to more completely
characterize the elemental composition of paints. For example,
WDS may resolve overlapping Ti K and Ba L lines, which is not
possible by EDS. Because WDS has critical X-ray focusing requirements,
the sample analyzed must generally be flat, and the analysis
area must generally be smaller than that allowed for EDS. Goldstein
et al. (48) present a complete discussion of wavelength and energy
8.14. X-Ray Fluorescence Spectrometry
8.14.2. Because of the significant penetration depth of the primary X-rays, XRF analysis will generally yield elemental data from several, if not all, layers of a typical multilayer paint fragment simultaneously. Because variations in layer thickness may cause variations in the X-ray ratios of elements present, this technique can be used only comparatively or qualitatively. Fischer and Hellmiss (50) present a general discussion of the forensic applications of X-ray fluorescence. Howden et al. (51) discuss XRF analysis as applied to single-layer household paints.
8.15. X-Ray Diffraction (XRD)
8.15.2. XRD instruments usually employ a copper target X-ray tube to generate the X-ray beam and a diffractometer to measure both the diffraction angles and peak intensities characteristic of the crystal structure. Beam/sample geometry is critical in producing the correct diffraction pattern.
8.15.3. Commercially available databases of diffraction patterns of crystalline materials can be used to facilitate qualitative analysis. Because the diffraction pattern of a mixture may be difficult to interpret, the identification of each component may require information provided by other analytical techniques such as elemental analysis.
8.15.4. Most paints need no sample preparation. Surface contaminants (e.g., sand particles), however, should be removed. Individual layer analysis is preferred over multilayer or bulk analysis in order to associate components to their respective layers.
You are invited to submit constructive feedback on the Document Comments Form.
FORENSIC SCIENCE COMMUNICATIONS JULY 1999 VOLUME 1 NUMBER 2