Abstract
The rubber from commercially obtained high-ammonia latex (commercial HA-latex) increased in gel content significantly after long preservation of the latex with 1.0% w/v tetramethylthiuram disulfide (TMTD) and zinc oxide (ZnO). Deproteinization of the HA-latex did not decrease the gel content. The gel fraction of deproteinized commercial HA-latex (DPHA-latex) was not solubilized by toluene containing 1.0% ethanol, showing that the gel fraction is composed of chemically crosslinked rubber. The addition of (NH4) 2HPO4, which is usually added to fresh latex (FL-latex) to remove excess amounts of Mg2+ ions by centrifugation, decreased the gel formation in FL-latex preserved with 0.6 % v/v NH4OH due to the removal of Mg2+ ions. The excess amounts of (NH4) 2HPO4 accelerated the gel formation in preserved FL-latex and commercial HA-latex. The addition of 0.1% w/v TMTD/ZnO to preserved FL-latex treated with 5% w/v (NH4)2HPO4 caused an increase of gel content during storage. The gel formation in the commercial HA-latex during long time storage was presumed to be caused by excess amounts of Mg2+ ions, TMTD/ZnO and (NH4)2HPO 4. Here, TMTD/ZnO accelerated the gel formation at the initial stage of storage, while (NH4)2HPO4 affected in long storage.
| Original language | English |
|---|---|
| Pages (from-to) | 1177-1184 |
| Number of pages | 8 |
| Journal | Rubber Chemistry and Technology |
| Volume | 76 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 2003 |
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