Two main approaches can be used for determining the age of an ink: indirect dating and direct dating. Indirect dating is based on the chemical analysis of an ink followed by comparison with known samples in a reference collection. The collection should contain information about the inks including the market introduction dates. This approach may allow for an anachronism to be detected. The second concept is based on measuring ink components that change with age. The analysis of solvents in ballpoint inks may be a useful parameter for determining the age of ink on paper. In a previous study, the authors demonstrated that thermal desorption of ink directly from paper, followed by chemical analysis using gas chromatography-mass spectrometry (GC-MS), is a promising procedure for characterizing ink-binder resins and solvents. Preliminary tests showed that monitoring the evaporation of ink solvent from ink on paper is not a suitable method for ink dating. Thermal analysis of ink on paper in two steps revealed that fresh ink releases a relative amount of solvent at a certain low temperature in a defined period of time, which decreases as the ink ages. As a consequence, this relative amount of solvent released at a certain low temperature, and its decrease with time, can be used to estimate ink age. This age-dependent parameter was studied in 85 different inks ranging in age from 1 week to 1.5 years. It was found that some inks showed a significant decrease of this parameter up to an age of several months, and that the aging process can be monitored within this period. For other inks, however, the age-dependent parameter decreases relatively fast, e.g., within a few days, to a constant level, which can be too fast for casework. Based on these results, a general procedure for assessing the age of ballpoint pen inks on paper was developed.

The characterization of ink on paper is of importance for dating and comparing questioned ink entries in forensic document examination. Inks are commonly characterized by their colorant profile that is identified by well-established analytical methods. Numerous ink formulations show identical colorant profiles, though. In order to differentiate inks that are not distinguishable by colorant analysis, a method for the characterization of colorless ink ingredients, namely binders, solvents and additives is necessary. In this paper, we propose a technique for the analysis of colorless compounds in ballpoint inks using direct thermal desorption of the ink on paper followed by chemical analysis of the desorbed volatile compounds by gas chromatography-mass spectrometry. As compared to liquid extraction and subsequent analysis of the extracts, the technique avoids possible contamination risks. Sensitivity is very high due to the enrichment of volatile components by thermal desorption. Even from old samples, the chromatograms obtained by the method enable the determination of binder polymers, solvents and additives. Pure binders as used by ink manufacturers were analyzed for unambiguous assignment of analytical results to specific polymers. To prove the practical applicability, we analyzed 121 ballpoint pens, not all having the same colorant profile, and grouped the pens into resin and solvent categories.

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The latter compound contains a bridging isonitrile ligand of fluxionial behavior as proved by high temperature 'H NMR spectroscopy. The u + B bonded character of the isonitrile bridge was established by X-ray c~st~o~aphy.Much attention has been paid to the addition of small donor molecules to the formally unsaturated [C,H,Mo(CO), I2 [2]. Careful investigations have been carried out recently on the symmetrical addition of allenes [3]. In contrast, relatively little is known about the reaction with heteroallenes, X=C=Y. As a first example we showed that (C~R~)~M~(CO)~ (R = H, CH,) reacts with boiling S=C=S to give complexes of the type CSR,(CO),Mo-Mo(CO),(q'-CS,)C~R~, containing a nonbridging, terminal q2-CS, ligand [4]. Stimulated by this result, we are using other heteroallenes, e.g. isothiocyanates and carbodiimides. In this paper we report on the reaction of [C+Me,(CO),Mo], with CH,N=C=S. Ex~~mentaI sectionAll procedures were carried out under nitrogen with solvents freshly distilled under nitrogen from appropriate drying agents. I was prepared according to a published procedure [5], CH,NCS was obtained from Fluka.