Edelweiss Applied Science and Technology ISSN: 2576-8484 Vol. 2, No. 1, 10-17 2018 DOI: 10.33805/2576.8484.107 © 2018 by the authors © 2018 by the authors History: Received: December 01, 2017; Accepted: December 22, 2017; Published: January 01, 2018 * Correspondence: nocaseoche@yahoo.com Forensic Examination of Inks Extracted from Printed Documents Using Fourier Transform Infrared Spectroscopy Paul Ocheje Ameh1*, Musa Suud Ozovehe1 1Department of Chemistry and Forensic Sciences, Nigeria Police Academy, Wudil, Kano, Nigeria; nocaseoche@yahoo.com (P.O.A). Abstract: Yellow, cyan, magenta and black inks were extracted from documents printed using two common brands of printing cartridge in Nigerian market and analyzed to identify / compare the functional groups present using Fourier Transform Infra-red Spectroscopy (FTIR). The FTIR spectra obtained were found to show highly characteristic absorption bands depending on the composition of the printer inks. Also, the results indicated the presence of triarylmethane dyes, epoxy resins, alkyd resin and esters in all the inks as they are peaks assigned to the vibration of aliphatic ester, asymmetrical and symmetrical stretching. The pure ink and its extract from the same band were also found to exhibit similar FTIR spectra while inks extract from different brands exhibits marked difference in absorption bands. This research can provide valuable information if an admitted sample is provided for comparing with the suspect printed document. Keywords: Forensic science, ink analysis, Document examination, FTIR. 1. Introduction Examination of inks on questioned documents has become common, and law enforcement agencies using this technique during their criminal investigations. Questioned documents can include diary entries, or whole diary, reconstructed files and false dated correspondence, prepared to show a particular sequence of events, occurred in the past or more simply a forged signature or an altered cheque [1,2]. Subtle alteration to documents, such as papers involving medical malpractice, tax returns, will scripts and insurance claims, divorce judgments, copyright certificates, agreements related to labour management disputes; employee problem settlements and a variety of contracts etc. can have significance financial implications. These kinds of many cases have been submitted by a number of crime reporters or document investigators. Incidents of forgery have increased tremendously and to alter these documents printers, copiers (inkjet printer) are widely used. The detection of alterations or additions to a document and an assessment of when the document was written have become a prime concern of document examiners and ink chemists [3,4]. Document examiners have invented methods which have been successfully used for examining and identifying printing inks scientifically. These techniques include paper chromatography, paper electrophoresis, luminescence, micro spectrometry, diffuse reflectance Fourier transform infrared, luminescence photography, laser excitation and spectroscopy, thin-layer chromatography, high-performance liquid chromatography, and capillary electrophoresis [1-10]. There is little or no information regarding the application of a sequence of selected standard techniques to the Nigerian population of inks used in printing. Also, no report presenting result of characterization/ comparison of inkjet printer inks collected from the market in Nigeria. There is a need to make effort in filling the gap in current analytical methodology of forensic questioned document examination in the country. Characterization of writing/printing instruments used to produce the document such as ink, paper etc. may be a leading step in the investigation of forgery in Nigeria. The aim of this study therefore is to analyze, compare and contrast ink extracted from printed documents using two brands of printing cartridge in the Nigerian market. This will be achieved by subjecting the extracted inks to Fourier Transform Infrared Spectroscopy (FTIR) analysis. It is hoped that the results from this study will provide valuable information / data if an admitted sample is provided for comparison with the suspect printed document in Nigeria. Also, the proposed method in the study could be used for examination of ink on documents taking extremely small (negligible portion) of the sample from an unimportant area of the document with the permission of the court. 2. Materials and Method 2.1. Materials All reagents used were analytical grade reagents obtained Sigma Aldrich Company U.S.A. Double distilled water was used throughout for the preparation of samples and dilution of the stock standard solutions. The glass wares used in the study were decontaminated by overnight soaking in 5 % HNO3. 2.2. Sample collection The method used in sample collection is that of Sharma et al. [11]. Five colored printouts each containing of cyan, magenta, yellow and black color were printed from inkjet printers of two leading ink printing manufacturers (Silver tosh and Hewlett Packard) in Nigerian Market. White paper of A4 size was used to take all samples. All four printed color i.e. cyan, magenta, yellow, and black from each printout were extracted, analyzed and interpreted. The two leading manufacturers were marked as A and B respectively and their different models were marked as 1, 2, 3and so on. The samples were given marking as A1, A2, A3 ,A4,A5,….A10 for different models of brand ‘A’ and B1, B2,B3,B4…; for different models of brand ‘B’. 2.3. Separation of ink from printed Document The ink from the printed document was separated following the method of Sharma et al. [11]. A colored squared block of constant area was taken from the sample document and cut into small pieces. The pieces of paper were then transferred to 15 ml beaker and titurated with 5 ml of methanol. The sample was then allowed to be extracted at room temperature with intermittent shaking. The methanol extract was then transferred to 10 ml volumetric flasks after filtering through a filter paper. The extract was made up to 4 ml. The same procedure was followed for all samples for cyan, magenta, yellow and black. In order to avoid any interference and to record the response of matrix i.e. paper and the reagent i.e. methanol towards IR, the blank samples of matrix and reagent were also prepared following the same procedure. 11 Edelweiss Applied Science and Technology ISSN: 2576-8484 Vol. 2, No. 1: 10-17, 2018 DOI: 10.33805/2576.8484.107 © 2018 by the authors 2.4. Preparing Pellet for Scanning 2ml of methanolic solution was taken in a china dish and evaporated at room temperature to dryness and heated for about 10minutes in an oven. The residue was scratched from the walls of china dish and mixed intimately with dry KBr. After this process pellets were prepared by using a pellet maker. The same procedure was followed for all samples of Cyan, Magenta, Yellow and Black Color. 2.5. Scanning of Samples The FTIR analyses of the samples were carried using a spectrometer from Agilent technology. The scanning was done through a wave range of 3500 to 400 wave number cm-1 3. Results and Discussions 3.1. FTIR study Figures 1-5 shows the FTIR spectra of pure and extracted inks of Brand A while the spectra obtained for Brand B are presented in Figures 6,7. Peaks obtained from the various spectra as well as assignments to the respective peaks are presented in Tables 1-5. The results presented show the various % transmittances corresponding to the respective wave length of absorption. It should be noticed that most of the absorption bands in the inks spectra are complex peaks, and exhibited band in different areas that are common to many organic compounds typically used in ink formulation. For instance Peaks in the range from 2000 to 1700 cm_1 were observed, which is the characteristic frequency of carbonyl (C=O) stretching vibration indicating that aliphatic acids or their esters are present in the ink colors studied [12]. Table 1. Peaks of FTIR absorption, % transmittance and functional group assignments for pure and extracted magenta ink of Brand A. Pure ink Extracted ink Functional group (Assignment) %Transmittance Peaks(cm-1) %Transmittance Peaks(cm-1) 61.095 655 C‒H “Opp” 85.866 996 N‒H Wag 82.466 1000 ≡CH 81.86 1045 73.079 1048 C‒O Asymmetric stretching 85.674 1082 82.572 1127 C‒O Symmetric stretching 86.898 1141 C‒O‒C Symmetric stretching 85.236 1182 C‒O‒C Symmetric stretching 85.709 1302 C‒N Stretch 86.038 1346 84.958 1346 C‒N Stretch 85.42 1395 C‒N Stretch 86.155 1469 83.545 1473 C‒H Bend 87.33 1495 C‒H Bend 60.252 1659 C=N stretching 96.097 2121 96.228 2125 ‒C≡C‒ stretch 45.102 3268 44.163 3268 N‒H stretch Table 2. Peaks of FTIR absorption, % transmittance and functional group assignments for pure and extracted cyan ink of Brand A. Pure ink Extracted ink Functional group (Assignment) %Transmittance Peaks(cm-1) %Transmittance Peaks(cm-1) 83.85 992 84.061 996 N‒H Wag 75.687 1045 76.584 1045 C‒O Asymmetric Stretching 83.989 1115 84.706 1119 ‒C‒H Wag 82.871 1220 85.183 1220 Aromatic Ether (Ar‒O) vibration 84.918 1465 C‒H Bend 84.924 1473 C‒H Stretch 63.847 1640 61.929 1644 C=C Stretch 96.1 2106 96.081 2121 ‒C≡C‒ Stretch 42.638 3305 43.452 3268 O‒H Stretch (Carboxylic Acid) Table 3. Peaks of FTIR absorption, % transmittance and functional group assignments for pure and extracted black ink of Brand A. Pure Ink Extracted ink Functional group (Assignment) %Transmittance Peaks(cm-1) %Transmittance Peaks (cm-1) 19.426 1026 19.5 1026 C‒O stretch 87.309 1119 87.229 1119 ‒C‒H Wag 83.434 1424 83.368 1424 C‒H (In ring) stretch 82.222 1454 82.169 1454 C‒H Bend 96.735 1663 96.524 1663 C=N stretching 100.373 2005 ‒C≡C‒ stretch 100.295 2125 100.286 2125 ‒C≡C‒ stretch 77.091 2836 76.977 2836 C‒H stretch 76.663 2944 75.654 2944 ‒C‒H stretch Table 4. Peaks of FTIR absorption, % transmittance and functional group assignments for pure and extracted yellow ink of Brand A. Pure ink Extracted ink Functional group (Assignment) %Transmittance Peaks(cm-1) %Transmittance Peaks(cm-1) 77.2 762 C‒H “Opp”(Aromatic) 23.14 1026 18.751 1026 C‒O stretch 86.668 1119 87.487 1119 ‒C‒H Wag 83.228 1413 83.431 1424 C‒C(In ring)stretch 12 Edelweiss Applied Science and Technology ISSN: 2576-8484 Vol. 2, No. 1: 10-17, 2018 DOI: 10.33805/2576.8484.107 © 2018 by the authors Pure ink Extracted ink Functional group (Assignment) %Transmittance Peaks(cm-1) %Transmittance Peaks(cm-1) 82.534 1454 82.211 1454 C‒H bend 92.968 1659 97.472 1711 C=N stretching 99.832 2125 ‒C≡C‒ stretch 78.061 2836 76.956 2836 C‒H stretch 76.21 2948 75.61 2944 ‒C‒H stretch There are indications of the presence of triarylmethane dyes, epoxy resin, alkyd resin, and solvents in the inks as there were peaks assigned to the vibration of aromatic ether (Ar – O), asymmetrical and symmetrical stretch vibration of aliphatic ether (C – O), asymmetrical and symmetrical stretch vibration of the C – O –C bonds. Table 5. Peaks of FTIR absorption, % transmittance and functional group assignments for extracted yellow ink of Brand B. Extracted ink Functional group (Assignment) %Transmittance Peaks(cm-1) 18.191 1026 C‒O stretch 87.838 1119 ‒C‒H Wag 83.92 1421 C‒H (In ring) stretch 82.621 1454 C‒H Bend 100.403 2125 ‒C≡C‒ stretch 77.248 2832 C‒H stretch 76.515 2944 ‒C‒H stretch 68.872 3320 O‒H stretch (Carboxylic acid) Table 6. Peaks of FTIR absorption, % transmittance and functional group assignments for extracted black ink of Brand B. Extracted ink Functional group (Assignment) %Transmittance Peaks(cm-1) 23.463 1026 C‒O Stretch 87.876 1119 ‒C‒H wag 85.066 1413 C‒H (In ring) stretch 83.096 1454 C‒H bend 100. 205 2125 ‒C≡C‒ stretch 77.499 2832 C‒H stretch 77.443 2944 ‒C‒H stretch 69.655 3324 O‒H stretch (Carboxylic) Table 7. Peaks of FTIR absorption, % transmittance and functional group assignments for extracted cyan ink of Brand B. Extracted ink Functional group (Assignment) %Transmittance Peaks(cm-1) 20.197 1026 C‒O stretch 86.38 1119 ‒C‒H wag 83.319 1413 C‒H (In ring) stretch 82.322 1454 C‒H bend 94.587 1674 C=N stretching 99.959 2125 ‒C≡C‒ stretch 77.649 2836 C‒H stretch 76.22 2948 ‒C‒H stretch The FTIR spectra obtained were also found to show highly characteristic absorption bands depending upon the compositions of the printer inks as it could be seen that every printer ink batch exhibits characteristic IR spectra. Table 8. Peaks of FTIR absorption, % transmittance and functional group assignments for extracted magenta ink of Brand B. Extracted ink Functional group (Assignment) %Transmittance Peaks(cm-1) 18.093 1026 C‒O stretch 87. 258 1119 ‒C‒H wag 83.647 1424 C‒H (In ring) stretch 82.335 1454 C‒H Bend 100.31 2113 ‒C≡C‒ stretch 77.172 2832 C‒H stretch 76.102 2944 ‒C‒H stretch 13 Edelweiss Applied Science and Technology ISSN: 2576-8484 Vol. 2, No. 1: 10-17, 2018 DOI: 10.33805/2576.8484.107 © 2018 by the authors Figure 1. FTIR spectra of (A) pure (B) extracted magenta ink of Brand. Different brands of ink cartridge also exhibited different characteristic IR spectra. Also, some common ingredients in different brands gave similar FTIR spectral bands for those components. It was also found that pure ink and its extract from the same brand exhibited similar FTIR spectra. For instance, similar peaks for O‒H Stretch, C‒O asymmetric were stretching for the same brand. However, ink extracts from different cartridges of different brands on the same paper exhibit marked differences. Figure 2. FTIR spectra of (A) pure and (B) extracted cyan of Brand A. Figure 3. FTIR spectra of (A) pure and (B) extracted yellow ink of Brand A. 14 Edelweiss Applied Science and Technology ISSN: 2576-8484 Vol. 2, No. 1: 10-17, 2018 DOI: 10.33805/2576.8484.107 © 2018 by the authors The difference between various samples of ink can be seen by observing at the intensity of main peak, the pattern of each spectrum and the absence or presence of some characteristic bands. Figure 4. FTIR spectra of (A) pure and (B) extracted black ink of Brand A. Figure 5. FTIR spectra of (A) methanol (B) methanol and paper extract. Figure 6. FTIR spectra of extracted (A) black ink of brand B and (B) magenta of Brand B. 15 Edelweiss Applied Science and Technology ISSN: 2576-8484 Vol. 2, No. 1: 10-17, 2018 DOI: 10.33805/2576.8484.107 © 2018 by the authors Figure 7. FTIR spectra of extracted (A) yellow ink of brand B and (B) cyan of Brand B. For instance C‒H “Opp” (Aromatic) peak which was observed at 762 in the yellow ink extracted of brand A was absent in brand B, the ‒C≡C‒ stretch peak at 2125 present in the black ink extract of brand A was absent in brand B, the N‒H Wag at 996 in the extracted cyan ink sample of brand A was absent in brand B Cyan ink sample, the ≡CH peak at 1000 in the magenta ink sample extract of brand A was absent in brand B. According to Beer-Lambert law, absorption is related to concentration (C in mole), path length (d in cm) and molar absorptivity ( in Lmol-1cm-1) according to the following equation [13],     dC A = (1) If the incident radiation entering the sample cell is given by I0 and the amount transmitted is It. The transmittance of the solution is defined as the fraction of the incident radiation that is transmitted and can be written as, 0      tIT I = (2) On the other hand, percentage transmittance is given in equation 3 while equation 4 gives 0 100      1 tIT I =  (3) The amount of light that is absorbed (Ia): 0      a tI I I= − (4) From the logarithm of equation 4, equation 5 is obtained, 0 0             a t t I logI logI logI log I =   = −     (5) The left hand side of equation 5 corresponds to absorbance (Ia). Therefore, the relationship between absorbance and transmittance is given according to equation 6, 1        A log T   =     (6) Since % transmittance is equal to transmittance x 100, equation 5 can also be written as 100 1                2 % A log log T T     = = −        (7) Figure 8. Variation of absorbance with wave number of FTIR absorption by pure and extracted magenta ink of Brand A. Using equation 6, values of absorbance were calculated and plotted with their corresponding wave numbers. These are presented in Figures 8-15. In Figures 8-11, plots showing the variation of absorbance with wave number of FTIR absorption by pure and extracted inks of Brand A are presented. Figures 12-15, show plots of the variation of absorbance with wave number of FTIR absorption by inks extracted from documents printed using the different studied brands (Brand A and B). From the plot, it can be seen that two brands exhibited marked differences in their absorbance. 16 Edelweiss Applied Science and Technology ISSN: 2576-8484 Vol. 2, No. 1: 10-17, 2018 DOI: 10.33805/2576.8484.107 © 2018 by the authors Figure 9. Variation of absorbance with wave number of FTIR absorption by pure and extracted black ink of Brand A. Figure 10. Variation of absorbance with wave number of FTIR absorption by pure and extracted cyan ink of Brand A. Figure 11. Variation of absorbance with wave number of FTIR absorption by pure and extracted yellow ink of Brand A. From the plot, it can be seen that both pure and extracted inks of the same brand exhibited maximum absorption at the same wave number and also show similarity or closeness to similarity in each other wave number. This shows that the extracted ink has some compatibility factors with the pure ink of brand A. Figure 12. Variation of absorbance with wave number of FTIR absorption by yellow ink extracted from printed documents of Brand A and B inks. Figure 13. Variation of absorbance with wave number of FTIR absorption by black ink extracted from printed documents of Brand A and B inks. 17 Edelweiss Applied Science and Technology ISSN: 2576-8484 Vol. 2, No. 1: 10-17, 2018 DOI: 10.33805/2576.8484.107 © 2018 by the authors Figure 14. Variation of absorbance with wave number of FTIR absorption by cyan ink extracted from printed documents of Brand A and B inks. Figure 15. Variation of absorbance with wave number of FTIR absorption by magenta ink extracted from printed documents of Brand A and B inks. 4. Conclusion Based on the obtained results the following conclusion can be drawn. Fourier Transform Infrared Spectroscopy, though strictly not nondestructive could be used for examination of inks on documents taking extremely small (Negligible portion) of the sample from an unimportant area of the document with the permission of the court. Fourier Transform Infrared Spectroscopy is a simple, direct and reproducible method of comparing computer printing inks. Inks when extracted from printed documents will exhibit similar absorption spectra while those from different brands will give marked differences in their absorption bands. References [1] I. Tebbett, "Chromatographic Analysis of Inks for Forensic Science Applications," Forensic Science Review, vol. 3, no. 2, pp. 71-82, 1991. [2] J. Harris, "A preliminary report on the nondestructive examination of ballpoint pen ink on questioned documents by FT-IR spectroscopy," Canadian Society of Forensic Science Journal, vol. 24, no. 1, pp. 5-21, 1991. [3] J. Egan, K. Hagan, and J. Brewer, "Forensic analysis of black ballpoint pen inks using capillary electrophoresis," Forensic Science Communications, vol. 7, no. 3, p. 21, 2005. [4] W. J. Egan et al., "Forensic discrimination of photocopy and printer toners. III. Multivariate statistics applied to scanning electron microscopy and pyrolysis gas chromatography/mass spectrometry," Analytical and Bioanalytical Chemistry, vol. 376, pp. 1286-1297, 2003. https://doi.org/10.1007/s00216-003-2099-3 [5] N. El-Din, M. Sabaa, and H. Hamed, "Influence of three chemical erasures on different types of inks marked on several document papers: An analysis of the chemical reactions occurring on paper between different liquid erasures and writing inks," International Journal of Forensic Document Examiners , vol. 4, no. 2, p. 9, 1998. [6] E. Fabianska and B. M. Trzcinska, "Differentiation of ballpoint and liquid inks-a comparison of methods in use," Problems of Forensic Sciences, vol. 46, pp. 383-400, 2001. https://doi.org/10.1520/jfs15061j [7] S. Fanali and M. Schudel, "Some separations of black and red water-soluble fiber-tip pen inks by capillary zone electrophoresis and thin-layer chromatography," Journal of Forensic Sciences, vol. 36, no. 4, pp. 1192-1197, 1991. https://doi.org/10.1520/jfs13135j [8] I. Geiman, M. Leona, and J. R. Lombardi, "Application of Raman spectroscopy and surface‐enhanced Raman scattering to the analysis of synthetic dyes found in ballpoint pen inks," Journal of Forensic Sciences, vol. 54, no. 4, pp. 947-952, 2009. https://doi.org/10.1111/j.1556-4029.2009.01058.x [9] R. Hofer, "Dating of ballpoint pen inks " Journal of Forensic Science, vol. 49, pp. 1-5, 2004. [10] R. A. Horton and L. K. Nelson, "An evaluation of the use of laser-induced infrared luminescence to differentiate writing inks," Journal of Forensic Sciences, vol. 36, no. 3, pp. 838-843, 1991. https://doi.org/10.1520/jfs13093j [11] R. Sharma, K. Goyal, A. Chattree, T. Baggi, and A. Gupta, "Comparative analysis of inkjet printer inks extracted from printed documents by FT-IR spectrophotometry," IOSR Journal of Applied Chemistry , vol. 5, no. 3, pp. 36-41, 2013. [12] P. Ameh, "A comparative study of the inhibitory effect of gum exudates from khaya senegalensis and albizia ferruginea on the corrosion of mild medium," International Journal of Metals, pp. 1-3, 2015. [13] N. Eddy, P. Ameh, and A. Ibrahim, "Physicochemical characterization and corrosion inhibition potential of ficum benjamina (FB) gum for aluminum in 0.1 M," Walailak Journal of Science and Technology , vol. 12, pp. 1121-1136, 2015. https://doi.org/10.4152/pea.201403183 https://doi.org/10.1007/s00216-003-2099-3 https://doi.org/10.1520/jfs15061j https://doi.org/10.1520/jfs13135j https://doi.org/10.1111/j.1556-4029.2009.01058.x https://doi.org/10.1520/jfs13093j https://doi.org/10.4152/pea.201403183