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Copper at Scale: Reducing Calibration in High-Throughput Exploration Labs

Large copper drilling campaigns generate analytical workloads that only high-throughput laboratories can sustain. To process the thousands of prepared geological samples per day, laboratories rely heavily on X-ray fluorescence (XRF) systems, which provide the speed required for rapid resource delineation. Under continuous operation, XRF calibration stability is becoming increasingly difficult to maintain. As X-ray tubes age, excitation intensity gradually declines; X-ray detector response shifts with thermal cycling, and electronic components slowly modify signal amplification. Individually, each source of variation remains minor. Over extended analytical runs, however, their cumulative impact emerges when calibration drifts, progressively biasing copper measurements and introducing unc

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Pressed Pellets vs. Fusion Beads: Which Method Wins for Lower-Grade Deposit Optimization?

The transition to renewable energy, electric vehicles, and advanced electronics has intensified global reliance on lithium, copper, and rare earth elements (REEs). At the same time, declining head grades, complex mineralogy, variable gangue chemistry, and tighter capital discipline are compressing operating margins and increasing processing costs per tonne in new mine developments and expansion projects. Many new feasibility-stage and newly commissioned mining operations advancing lower-grade lithium, copper, and rare earth deposits now proceed at head grades of these target elements close to economic cut-off, where minor fluctuations in reported elemental concentrations can shift resource classification or recovery forecasts. High-quality elemental data generated by X-ray fluorescence

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Why XRF is Critical for Lithium Miners (Even if it Doesn’t Measure the Li)

Lithium mining has shifted from discovery to optimization. As operators process lower-grade, more complex deposits, operating margins and processing efficiency depend on precise chemical control across the flowsheet. At first glance, X-ray fluorescence (XRF) may appear ill-suited because it cannot directly measure lithium in fused samples. Yet recovery is rarely limited by lithium concentration alone. It is governed by the surrounding element matrix, including iron, magnesium, aluminium, silicon, sulfur, and trace elements that influence roasting, leaching, and impurity control. XRF measures the chemistry that ultimately controls reaction stability, impurity behavior, and yield. Even without directly measuring lithium, it provides the elemental visibility required to protect recovery an

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