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Adapting XRF Sample Preparation for Green Steel Production

Green steel production promises lower emissions, but it also introduces a more unpredictable analytical environment. Scrap variability, hydrogen reduction chemistry, and evolving slag compositions generate conditions where small material differences can produce large analytical deviations. In many laboratories, this is exposing the limitations of conventional X-ray fluorescence (XRF) sample preparation methods and accelerating the adoption of fusion-based workflows designed to improve repeatability across highly variable sample matrices.

 

How Green Steel Production Alters Sample Chemistry

Traditional ironmaking relies on relatively stable ore streams with predictable mineralogy and chemistry. Green steel production changes those conditions considerably. Hydr

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Hidden Variables: Eliminating Sample-to-Flux Ratio Errors in High-Volume Mineral Labs

High-throughput mineral laboratories operate under relentless pressure to deliver accurate analytical data at speed. Exploration programs, process control systems, and commercial assay operations all depend on reproducible fused bead preparation. Small variations in the sample-to-flux ratio remain a persistent challenge during X-ray fluorescence (XRF) analysis, often destabilizing both bead chemistry and calibration performance. When sample preparation consistency declines, laboratories face rising rework rates, calibration drift, and interruptions that lower overall throughput efficiency.

 

The Technical Importance of the Sample-to-Flux Ratio

The sample-to-flux ratio determines how well a mineral sample dissolves into the borate matrix throughout t

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A Brief Guide to Choosing the Right Flux for High-Sulphide Copper Ores

Few materials test the limits of X-Ray Fluorescence (XRF) fusion as severely as high-sulphide copper ores. Chalcopyrite, bornite, and related concentrates generate complex fusion conditions where oxidation control becomes just as important as temperature itself. Without the correct balance of borate chemistry and oxidizing capacity, sulphides can remain partially unreacted, leading to bead defects, poor homogeneity, and gradual platinum degradation. Selecting the appropriate flux is therefore a critical step in producing stable glass beads and maintaining reliably copper assay performance.

 

Why Standard Fluxes Often Fail With High-Sulphide Copper Ores

Many laboratories begin copper fusion work using standard lithium borate formulations designed for routine o

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