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What is scorch, why does it happen, how is it prevented?

Causes of scorch (premature vulcanisation) in rubber: mixing temperature, accelerator choice, storage. Mooney scorch measurement and the solution steps with Vulkalent G (CTP) and Vulkalent E.

Updated: 1 November 2026 · Mete Kimya technical team

Definition

Scorch is partial crosslinking of the compound before shaping is finished – in the Banbury, on the calender, in the extruder or while flowing into the mould. Result: non-flowing stock, unfilled moulds, surface defects and scrap. The Mooney scorch test (t5, 120 °C) and rheometer t2 measure processing safety.

Main causes

Too high a dump temperature or too long a mix; adding the accelerator too early; too fast an accelerator or excess thiuram; heat build-up from high filler/low oil; warm storage; ingredients that activate accelerators, such as resins or PPD derivatives.

How does a retarder work?

CTP (Vulkalent G) scavenges the active mercaptobenzothiazole formed as the sulphenamide breaks down and so delays the onset of cure; the effect is linear with dosage and barely changes optimum cure time. Vulkalent E is the nitrosamine-free sulphonamide type and also works in thiazole/thiuram systems.

Step-by-step fix

1) Lower the dump temperature by 5–10 °C and add the accelerator in a second pass. 2) Try 0.2–0.3 phr Vulkalent G; confirm with rheometer t2. 3) If still insufficient, switch to a more delayed accelerator (MBT→MBTS, CBS→DCBS) or cut thiuram. 4) Limit storage temperature and shelf time.

Why is too much retarder bad?

Above 0.5 phr CTP can bloom, with a slight modulus drop and longer cure. The retarder treats the symptom; the root cause is temperature and the accelerator system.

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