Applications

Edible oils comprise a significant portion of any diet, and they also have important roles in the production of foods, cosmetics, and skincare products. For these reasons, a convenient and accurate method for materials identification of a variety of fats and oils is highly desirable. Historically, authentication of fats and oils was performed through intensive laboratory techniques involving chromatographic methods. Here, Raman spectroscopy combined with Principle Component Analysis (PCA) has been used for materials identification with 16 different edible oils, with excellent results. Raman is an ideal technique for evaluation of fats, as carboncarbon double- and single-bonds give strong Raman signals. PCA analysis in combination with Raman spectroscopy is a powerful tool for qualification and verification of different fats and oils, as there are few visual differences between spectra of edible oils.

Chemical manufacturing such as polyurethane production is characterized by a cost intensive production process combined with a negative ecological impact. These adverse effects can be significantly improved by using vibrational spectroscopy. This analytical technique can assist the operator of the plant to reduce costs and minimize the impact onthe environment as is demonstrated in the present white paper.

Quality control is impacted by multiple challenges, which can have an influence on the functioning of the QC lab. The present White Paper provides approaches, how to simplify the daily quality control using near-infrared spectroscopy combined with a dedicated smart software like Vision Air.

Norms and Standards 21 CFR Part 11 is the FDA rule relating to the use of electronic records and electronic signatures.Recognizing the increasing impact of electronic media on critical data in regulated environments, the FDA met with members of the pharmaceutical industry in the early 1990s. The pharmaceutical industry and the FDA were interested in how they could accommodate paperless record systems and ensure the reliability, trustworthiness, and integrity of electronic records.

The analytical challenges of environmental analysis increase in difficulty from year to year. As well as analysis of particularly toxic types of metals such as chromium(VI), highly diverse and partially persistent organic fluorine compounds (e.g., trifluoroacetic acid) are presently in focus. The analysis of toxic oxohalides such as bromate and perchlorate is also a current subject of investigation.

Analyzer systems monitoring product quality can offer substantial advantages when organized in a client-server network compared to the more traditional local installation. This white paper presents different client-server setups and their benefits. Security aspects that need to be considered are discussed based on the example of the client-server Vis-NIR (visible near-infrared) spectroscopy software Vision Air, widely used for quality control in the chemical, polymer, pharmaceutical, and petrochemical industry.

Data Integrity is currently a hot topic issue that has created much attention and has raised concern within companies working in regulated environments. This White Paper explains some of the key terms used in the context of Data Integrity and outlines how the requirements of Data Integrity can be understood and implemented.

Analytical Instrument Qualification (AIQ) according to the United States Pharmacopeia (USP) ensures that instruments perform as intended and users may have confidence in data quality. As the Pharma industry adopts handheld Raman instruments for incoming materials identification and verification, producers of such systems must provide suitable calibration and validation routines. Upon completion of these tests, end users are assured that all measurements are in accordance with agreed standards at Metrohm Raman, we have sophisticated AIQ routines in place to confirm the quality of your results.

Free white paper describes the effective use of electrochemical techniques to measure corrosion and the effectiveness of inhibitors.

High-Performance Liquid Chromatography (HPLC) and Ion Chromatography (IC) are commonly used in the pharma, food, and environmental sectors to analyze samples for specific components and to verify compliance with norms and standards. However, users of HPLC may run into the limitations of this technique, e.g., when analyzing standard anions or certain pharmaceutical impurities. This white paper outlines how such challenges can be overcome with IC.