Articles
Dipl. Chem. FH Ch. Schanzer and Prof. Dr H.G. Bührer
Department of Chemistry, Zurich University of Applied Sciences Winterthur (ZHW), CH-8401 Winterthur, Switzerland
S.E.J. Bell,a* E.S.O. Bourguignon,a A. O’Grady,a J. Villaumiea and A.C. Dennisb
aSchool of Chemistry, The Queen’s University of Belfast, Belfast, BT9 5AG, Northern Ireland, UK
bAvalon Instruments Ltd, 10 Malone Road, Belfast BT9 5BN, Northern Ireland, UK
J. Sabine Becker
Central Department of Analytical Chemistry, Research Centre Jülich, D-52425 Jülich, Germany
The study of the mineralogical phases of archaeological ceramics may be very helpful in unravelling the history of an ancient sherd, particularly by means that investigate the process of its production. Micro-Raman spectroscopy offers advantages as a non-destructive, or even better, a non-sampling technique.
Luis Oliveira and Manuel Pais Clemente
CETO – Centro de Ciências e Tecnologias Ópticas, Rua Caldas Xavier, Nº38, 6º E, 4150 Porto, Portugal. E-mail: [email protected]
Marion Menzel and Bernhard Blümich
Institut für Technische Chemie und Makromolekulare Chemie, RWTH Aachen, Worringerweg 1, D-52056 Aachen, Germany
Chemical imaging spectroscopy is an exciting new analytical advance that answers commonly asked questions such as what chemical species are in a sample, how much of each is present, and most importantly, where are they located? Through the fusion of traditional infrared spectroscopy with powerful microscopic and macroscopic imaging capabilities, chemical imaging spectroscopy answers all these questions simultaneously, in a single rapid measurement.
This article discusses the development of new Certified Reference Materials (CRMs) for use in determining the essential accuracy and linearity of the Transmission scale of a conventional UV/vis spectrophotometer.
Ed McCurdy* and Don Potter
Agilent Technologies, Lakeside, Cheadle Royal Business Park, Stockport, Cheshire SK8 3GR, UK. E-mail: [email protected], [email protected]
A stage in the ever-increasing magnetic field strengths in NMR spectroscopy.
A comprehensive and logically ordered list of categories of ordinate error that can occur in conventional Fourier Transform Spectroscopy.
