In the early days of dioxin analysis, applied methods were laboratory- and time-consuming. Only GC–HRMS, which is complicated, was used. Nowadays, GC–MS/MS is suitable for control proposes. Using GC–MS/MS means that solvent consumption for sample preparation can be reduced by a factor of 10 and the purity of the obtained fraction can be enhanced, indicating that GC–MS/MS is appropriate for dioxin analysis.
In the early days of dioxin analysis, applied methods were laboratory- and time-consuming. Only GC–HRMS, which is complicated, was used. Nowadays, GC–MS/MS is suitable for control proposes. Using GC–MS/MS means that solvent consumption for sample preparation can be reduced by a factor of 10 and the purity of the obtained fraction can be enhanced, indicating that GC–MS/MS is appropriate for dioxin analysis.
In the early days of dioxin analysis, applied methods were laboratory- and time-consuming. Only GC–HRMS, which is complicated, was used. Nowadays, GC–MS/MS is suitable for control proposes. Using GC–MS/MS means that solvent consumption for sample preparation can be reduced by a factor of 10 and the purity of the obtained fraction can be enhanced, indicating that GC–MS/MS is appropriate for dioxin analysis.
Webinar Date/Time: Airing 1: Wednesday, March 20, 2024 at 11AM EDT / 3PM GMT / 4PM CET Airing 2: Wednesday, March 20, 2024 at 2PM EDT / 1PM CDT / 11AM PST
In plant metabolomics, molecular fingerprints and additional molecular descriptors can be identified using recent developments in polarity-extended separations with serial coupling of reversed-phase LC and HILIC combined with ESI-TOF-MS.
In plant metabolomics, molecular fingerprints and additional molecular descriptors can be identified using recent developments in polarity-extended separations with serial coupling of reversed-phase LC and HILIC combined with ESI-TOF-MS.
In plant metabolomics, molecular fingerprints and additional molecular descriptors can be identified using recent developments in polarity-extended separations with serial coupling of reversed-phase LC and HILIC combined with ESI-TOF-MS.
A new high-throughput LC–MS/MS method meets the challenge of eliminating matrix effects for monitoring, with high specificity, polar organic pesticides such as glyphosate in food and water, while meeting targeted limits of detection.
A new high-throughput LC–MS/MS method meets the challenge of eliminating matrix effects for monitoring, with high specificity, polar organic pesticides such as glyphosate in food and water, while meeting targeted limits of detection.
Forensic scientists often encounter highly complex analytical problems related to crime scenes that would benefit from the capabilities of GC×GC–MS. However, this technique has not been fully explored to help benefit forensic laboratories.
A new method to analyze low concentrations of the drug diclofenac in wastewater.
A new method to analyze low concentrations of the drug diclofenac in wastewater.
A new method to analyze low concentrations of the drug diclofenac in wastewater.
A new method to analyze low concentrations of the drug diclofenac in wastewater.
A new method to analyze low concentrations of the drug diclofenac in wastewater.
Webinar Date/Time: Wed, May 15, 2024 2:00 PM EDT
In this article, we examine how tandem and tandem hybrid mass spectrometry has opened up new frontiers already. We go further and examine how lesser-known experiments are breaking new ground, with alternative fragmentation techniques, as well as the addition of extra levels of orthogonality by parallel separations techniques.
Material identification is a common need in many industries, most notably for pharmaceutical manufacturing where the United States Pharmacopeial Convention (USP) defines many identification tests.
Chiral chromatography has become the preferred tool for enantiomer separations in the early stages of pharmaceutical development for the purpose of accurately identifying single pure enantiomers with pharmacologic, toxicological, and clinical information, as stipulated by the FDA.1
The analysis of contaminants found in environmental waters and originating from personal care products using metalorganic frameworks (MOFs) combined with liquid chromatography (LC) is described. This work expands the use of MOFs from gas chromatography to LC and also meets the requirements of green analytical chemistry.
The analysis of contaminants found in environmental waters and originating from personal care products using metalorganic frameworks (MOFs) combined with liquid chromatography (LC) is described. This work expands the use of MOFs from gas chromatography to LC and also meets the requirements of green analytical chemistry.
Examples from food science illustrate the usefulness of chemometrics techniques like pattern recognition, regression, and classification.
In this instalment of “Column Watch”, a simple method for profiling free naphthenic acids in produced water by GC–MS is proposed.
It is important to develop analytical methods to detect crude MCHM components in environmental water samples. This article describes two microextractive methods based on solid-phase microextraction (SPME) in fibre format and thin film microextraction (TFME) that were developed and validated for 4-MCHM and other constituents of crude MCHM.
It is important to develop analytical methods to detect crude MCHM components in environmental water samples. This article describes two microextractive methods based on solid-phase microextraction (SPME) in fibre format and thin film microextraction (TFME) that were developed and validated for 4-MCHM and other constituents of crude MCHM.
This article reviews how nanomaterials are being used in a variety of sample preparation techniques, such as dispersive solid-phase extraction (dSPE), solid-phase microextraction (SPME), stir-bar sorptive extraction (SBSE), and matrix solid-phase dispersion (MSPD).
This article reviews how nanomaterials are being used in a variety of sample preparation techniques, such as dispersive solid-phase extraction (dSPE), solid-phase microextraction (SPME), stir-bar sorptive extraction (SBSE), and matrix solid-phase dispersion (MSPD).
It is important to develop analytical methods to detect crude MCHM components in environmental water samples. This article describes two microextractive methods based on solid-phase microextraction (SPME) in fibre format and thin film microextraction (TFME) that were developed and validated for 4-MCHM and other constituents of crude MCHM.
This article reviews how nanomaterials are being used in a variety of sample preparation techniques, such as dispersive solid-phase extraction (dSPE), solid-phase microextraction (SPME), stir-bar sorptive extraction (SBSE), and matrix solid-phase dispersion (MSPD).