Overview
ISO 7884-4:1987 - "Glass - Viscosity and viscometric fixed points - Part 4: Determination of viscosity by beam bending" specifies a laboratory method for measuring the dynamic viscosity of glasses using a rod‑shaped test specimen (a beam) supported at its ends. The standard describes the theoretical basis, required apparatus and measurement procedures: a controlled load is applied at midspan and the viscous deflection rate (midpoint sag vs time) is recorded. From the measured sag, span, cross‑sectional moment of inertia and load the dynamic viscosity is calculated. The method covers a broad viscosity range (~10^9 to 10^15 dPa·s) and includes guidance on temperature control, calibration and sample thermal history.
Key topics and technical requirements
- Test principle: Measure midpoint deflection rate under a known load and convert to dynamic viscosity using beam bending relations and geometric properties of the specimen.
- Specimens: Rod‑shaped beams with rectangular (thickness h, width b) or circular (diameter d) cross sections; must be homogeneous, bubble‑free and properly annealed.
- Apparatus:
- Electrically heated viscometer furnace with temperature uniformity (≤ ±1 °C) and programmable temperature‑time control (heating rates up to ~6 °C/min).
- Thermocouples: Type S (Pt‑10%Rh/Pt) or Type K (NiCr/Ni) per IEC 584‑1, low thermal inertia and properly calibrated.
- Supports and loading assembly (yoke, bending edge, loading rod), support stand materials (vitreous silica or alumina), and loading pieces with accurately known masses.
- Displacement measurement: LVDTs or comparable transducers to record midpoint deflection and total deflection with high resolution.
- Measurement controls:
- Small‑deflection and small‑deflection‑rate assumptions apply (relative midpoint deflection z should remain < 0.05).
- Support ratio and span constraints determine validity of simplified equations; calibration with a reference glass is required when support ratio limits are exceeded.
- Care to avoid devitrification; consider thermal history effects for viscosities > 10^12 dPa·s (structure equilibration may be slow).
- Calibration and traceability: Verify instrument using a reference glass of known viscosity; check span, parallelism and thermal distribution routinely.