Analytical Instrument Documents

Gas Analysis Solutions with JEOL Mass Spectrometers

We investigated the structural analysis of the polyethylene-terephthalate (PET) polymer exposed to the on-plate alkaline degradation method by using the JMS-S3000 "SpiralTOFTM-plus" with TOF-TOF option. The SpiralTOFTM-plus uses an ultra-high resolution TOF for MS1 which allows monoisotopic precursor selection and a reflectron TOF for MS2 to analyze the product ion spectra produced from high energy collisional induced dissociation (HE-CID).

In this work, we introduce the msFineAnalysis software and use it to automatically combine data acquired by GC/EI and GC/soft ionization for the qualitative analysis of compounds produced by the pyrolysis of a vinyl acetate resin.

In this report, we have applied this combined method to analyze a polyethylene terephthalate (PET) that was degraded by ultraviolet (UV) irradiation.

In this report, we have expanded MALDI-MSI to analyzing a PET film that was exposed to UV radiation. Additionally, a SEM was used to look at the morphological differences in the PET film before and after UV irradiation.

NOAH (NMR by Ordered Acquisition using 1H-detection)[1] is a group of nested NMR experiments combining several conventional two-dimensional (2D) NMR pulse sequences, such as COSY, HSQC and HMBC, into one supersequence. Therefore, two or more 2D NMR data can be obtained from a single NOAH experiment. By using a single relaxation delay, the NOAH method significantly reduces the total data collection time and increases the throughput of an NMR instrument in structure elucidation of small organic molecules.

13C NMR spectra provide wide range chemical shift, and it suggests that can easily distinguish each signals. But carbon resolution of 2D spectra such as HSQC and HMBC is worse than 1D 13C spectra due to small data points. In order to analyze a compound with close 13C chemical shifts, a high resolution 2D spectrum is required frequently. In this document, some improvements to distinguish each signals on 13C axis of 2D hetero nuclear experiments are presented.

The NMR signal of a spin reflects its local magnetic environment. If a spin due to chemical exchange samples two magnetically different states then its NMR signal would reflect both states. Its appearance on a NMR spectrum would be determined by the dynamics of the exchange event. In the case of chemical exchange that is slow on the NMR time scale, it is possible to observe two distinct signals for the same spin, one signal for each state under exchange. Presence of chemical exchange is often demonstrated with the exchange experiment (2D NOESY experiment). A exchange peak (cross peak) of the same sign can be observed between the two autopeaks (diagonal peaks) that represent the two states under exchange. Because the same results can be interpreted in a different way based on NOE, further evidence is desirable.

In this study, we used the JMS-S3000 to test several matrices for PSD effects and to measure high resolution mass spectra of intact insulin, ubiquitin and cytochrome C.

In this report, we investigate a MSI visualization method for synthetic polymers that uses Mn, Mw and D as indices for visualization.