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Blog entry by Finlay Christian

When analyzing particulate materials, understanding particle size distribution is essential for predicting performance in applications ranging from pharmaceuticals to industrial powders and environmental science. Particle size can be assessed either by particle count or by volumetric contribution, and each provides distinct insights that can lead to very different conclusions. Advanced imaging systems are now critical for uncovering hidden complexities in particle populations, offering visual and quantitative data that traditional sizing techniques often miss.

Measuring particle size by number means counting individual particles and determining how many fall into each size class. When the quantity of particles is more relevant than their bulk, number-based sizing is preferred,—for example, in aerosol science where inhalation exposure depends on particle count, or in nanomaterials where biological interactions are often governed by surface area and concentration of individual entities. Digital imaging tools allow precise counting of particles at the micro- and nanoscale, providing a clear picture of how many particles exist at each size. Small particles, though sparse, are prominently revealed through number-based analysis, leading to more accurate risk and efficacy assessments.

In contrast, measuring by volume assigns weight to each particle based on its three-dimensional size, effectively amplifying the contribution of larger particles. A few oversized particles can skew the entire volume profile. This is often the preferred method in industries where flow properties, settling rates, or mixing behavior are critical—such as in concrete production or paint formulation. Bulk property predictors such as sedimentation and flow modeling rely on volume-weighted data. However, they can obscure the presence of small particles that contribute little to volume but may significantly influence other properties.

Imaging bridges the gap between these two methods by allowing direct visualization of particle morphology and size. In contrast to models based on averaged physical interactions, imaging reveals irregular shapes, agglomerations, and surface features that profoundly affect how particles behave. A seemingly uniform particle in bulk data may be a fractal-like agglomerate, leading to misinterpretation of its true nature. Imaging shows whether a volume-dominated peak is due to a few large, dense particles or a cluster of smaller ones bound together.

Moreover, imaging enables the calculation of both number and volume distributions from the same dataset. From pixel-level measurements, algorithms compute individual particle volumes and tally counts, and then generate corresponding number and volume distributions side by side. The contrast between number and volume profiles uncovers hidden heterogeneity. For instance, A bulk volume profile may appear homogeneous, 動的画像解析 while particle counts reveal a bimodal population. This indicates potential instability or contamination.

The practical implications of this distinction are significant. In drug delivery, a volume-based analysis might indicate that most particles are within the ideal size range for lung deposition, but imaging could reveal that the majority of particles by count are far too small to be effective, potentially leading to wasted dosage or unintended systemic absorption. In environmental monitoring, a volume-based measurement of airborne dust might suggest low risk, but imaging could expose high concentrations of ultrafine particles capable of penetrating deep into the respiratory system.

Ultimately, imaging transforms particle size analysis from a statistical exercise into a visual science. It compels a shift from mathematical estimations to direct physical observation. Number counts expose particle density and exposure potential; volume measures reflect bulk behavior and macroscopic influence. Only by integrating all three dimensions—count, volume, and morphology—can true particle behavior be understood. Depending solely on volume or number leads to blind spots; imaging-integrated analysis eliminates ambiguity.