

Rotational Rheometer for Polymer Melts
聚合物熔体用旋转流变仪
- SKU RHE-0001
- Rheometers
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Torque range | 0.5 µN·m to 200 mN·m |
|---|---|
| Angular velocity | 10⁻⁷ to 300 rad/s |
| Oscillation frequency | 10⁻⁴ to 100 Hz |
| Temperature range | −40 to 400 °C with oven |
| Temperature accuracy | ±0.2 °C |
| Normal force range | 0.01–50 N |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 3219, ISO 11443, ISO 6721-10
What is the Rotational Rheometer for Polymer Melts?
A rotational rheometer applies controlled shear or oscillation to a polymer melt between parallel plates, cones or cylinders, measuring viscosity and viscoelastic moduli. It is the instrument of choice when molecular structure or additive effects must be linked to elasticity rather than only to viscosity.
What is the Rotational Rheometer for Polymer Melts?
A rotational rheometer applies controlled shear or oscillation to a polymer melt between parallel plates, cones or cylinders, measuring viscosity and viscoelastic moduli. It is the instrument of choice when molecular structure or additive effects must be linked to elasticity rather than only to viscosity.
Overview
The instrument consists of a temperature-controlled oven, a motor that applies torque or rotation, a torque or normal force transducer, and interchangeable geometries of defined diameter and angle. In steady shear mode it yields a flow curve of viscosity against shear rate; in oscillatory mode it yields storage modulus, loss modulus and complex viscosity against frequency, and the crossover point of the two moduli gives an indication of molecular weight distribution. Typical torque resolution is better than 1 µN·m with a range covering several orders of magnitude, enabling both low-viscosity and highly filled melts to be measured. Temperature control from below ambient to about 400 °C is usual for polymer work, and nitrogen purge protects oxidation-sensitive materials.
How does it work?
A rheometer applies a controlled deformation to a polymer sample and measures the resulting force or torque. Rotational instruments use parallel plates, cones or concentric cylinders and can work in steady shear, giving shear viscosity against shear rate, or in oscillation, giving storage and loss moduli against frequency. Capillary instruments force melt through a die of known diameter and length at a controlled piston speed, measuring pressure to calculate apparent shear viscosity at shear rates that reach those of real extrusion. Torque rheometers mix material in a heated chamber and record the torque needed to turn the rotors, which tracks gelation, fusion and degradation in a compounding context. The choice depends on the shear rate range, the sample form and whether elasticity or only viscosity is required.
What are the key features?
- Torque resolution better than 1 µN·m
- Steady shear and oscillatory measurement modes
- Oven from below ambient to 400 °C
- Interchangeable parallel plate, cone and cylinder geometries
- Normal force measurement for elasticity evaluation
- Nitrogen purge for oxidation-sensitive polymers
What are the technical specifications?
A typical rotational rheometer for polymer melts configuration offers torque range of 0.5 µN·m to 200 mN·m, angular velocity of 10⁻⁷ to 300 rad/s, oscillation frequency of 10⁻⁴ to 100 Hz, temperature range of −40 to 400 °C with oven, temperature accuracy of ±0.2 °C and normal force range of 0.01–50 N. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Rotational Rheometer for Polymer Melts is used in molecular weight comparison of polymer grades, effect of additives on melt elasticity, long-chain branching assessment and recycled melt quality evaluation. Across the wider Rheometers class, laboratories also deploy it for molecular weight and molecular weight distribution comparison, processing behaviour prediction for extrusion and moulding and filler and additive effect on melt viscosity.
Which standards and certifications apply?
Relevant standards and methods include ISO 3219, ISO 11443, ISO 6721-10, ASTM D3835, ASTM D4440, ASTM D2538 and IEC 61010-1. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Sample preparation dominates repeatability: dry hygroscopic polymers, compression-mould discs of defined thickness for rotational testing, and ensure filled samples are homogeneous. Set the gap and check it with a zero-gap routine before each series, because a small gap error changes the calculated viscosity. In capillary work, verify piston speed and pressure transducer calibration, and apply the Bagley and Rabinowitsch corrections when true viscosity is required. Purge the oven with nitrogen for high-temperature or oxidation-sensitive polymers. Clean dies and plates thoroughly, since degraded residue changes the surface and the measured torque, and record temperature, geometry and gap with every result.
How do I select the right Rotational Rheometer for Polymer Melts?
Choose a rotational rheometer when you need viscoelastic data, yield stress or low-shear viscosity, or when sample mass available is small. Confirm torque sensitivity against the lowest-viscosity material you must measure, and specify the temperature range including any need below ambient. Ask for a range of plate diameters because a geometry that is too large can exceed the torque limit on stiff melts.
How does it compare with other Rheometers variants?
Match the instrument to the shear rate range that governs your process. Rotational rheometers cover low shear rates and are the only option when viscoelastic data, yield stress or normal force are required, making them suitable for molecular weight comparisons and additive studies. Capillary rheometers reach the high shear rates of extrusion and injection moulding and are more tolerant of filled and highly viscous materials. Torque rheometers are used when the question concerns compounding behaviour, gelation or thermal stability under shear rather than a fundamental viscosity value. Inline instruments are selected for continuous process monitoring and never replace laboratory characterisation, because they see only one fixed measurement point.
Full specifications
| Torque range | 0.5 µN·m to 200 mN·m |
|---|---|
| Angular velocity | 10⁻⁷ to 300 rad/s |
| Oscillation frequency | 10⁻⁴ to 100 Hz |
| Temperature range | −40 to 400 °C with oven |
| Temperature accuracy | ±0.2 °C |
| Normal force range | 0.01–50 N |
| Gap resolution | 1 µm |
| Geometry diameter | 8–50 mm plates, 1–4° cones |
| Purge gas | Nitrogen, 5–20 L/h |
| Power supply | 220 V, 50/60 Hz |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Molecular weight comparison of polymer grades
- Effect of additives on melt elasticity
- Long-chain branching assessment
- Recycled melt quality evaluation
Key features
- Torque resolution better than 1 µN·m
- Steady shear and oscillatory measurement modes
- Oven from below ambient to 400 °C
- Interchangeable parallel plate, cone and cylinder geometries
- Normal force measurement for elasticity evaluation
- Nitrogen purge for oxidation-sensitive polymers
Frequently asked questions about Rotational Rheometer for Polymer Melts
Most polymer work uses 0.01 to 100 rad/s, which spans the terminal and plateau regions of the relaxation spectrum. The low-frequency end is sensitive to molecular weight and branching, while the high-frequency end reflects local chain dynamics. The accessible range depends on instrument inertia and on the thermal stability of the sample.
The polymer is usually compression moulded into a disc of about 1 to 2 mm thickness and slightly larger than the geometry diameter, then trimmed after loading while the melt is hot. Thickness uniformity matters because the gap is set from the disc, and air bubbles or unmelted granules must be avoided.
The frequency at which storage modulus equals loss modulus marks the transition from liquid-like to solid-like response and shifts with molecular weight distribution. A wider distribution or long-chain branching moves the crossover and changes its slope, so the value is useful for comparing grades that have similar shear viscosity.
A rotational rheometer measures viscosity in steady or oscillatory shear at low shear rates, where the material response is dominated by molecular relaxation. A capillary rheometer measures at high shear rates that match extrusion and injection moulding. The two techniques overlap in a mid-range and should agree after corrections, but each covers a shear rate window the other cannot reach.
Viscosity is calculated from measured torque, angular velocity and the gap between the geometries, so an error in gap propagates directly into the result. Compression of the sample and thermal expansion change the effective gap, which is why a zero-gap routine and a constant sample thickness are used before each series.
They can, but filler particles may slip at the plate surface, settle, or bridge the gap, so the measured viscosity can be too low. Practical measures are to use serrated or roughened plates, larger gaps, and lower filler loadings where possible, and to compare results only between samples of the same filler content and particle size.
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