R.S. Seright, B. Henrici – 1990

Abstract

This paper examines xanthan stability to define the polymer’s temperature limitations as a mobility-control agent. Experiments probed the relative importance of hydrolysis, oxidation, and helix-coil transitions in xanthan degradation. In the absence of dissolved oxygen, free-radical oxidation/reduction reactions are not the dominant degradation mechanism. Depending on pH, acid-catalyzed hydrolysis and base-catalyzed fragmentation reactions may play important roles. Using Arrhenius calculations, under ideal conditions — no dissolved oxygen, pH 7–8, and moderate-to-high salinities — xanthan is estimated to maintain at least half its original viscosity for 5 years if temperature does not exceed 75–80°C. Above this temperature, new polymers are needed for chemical floods requiring mobility control.

Key Takeaways

  • In the absence of dissolved oxygen, oxidative free-radical reactions are not the dominant mechanism of xanthan degradation — confirming that eliminating oxygen is the highest-priority stability measure for field applications.
  • Acid-catalyzed hydrolysis and base-catalyzed fragmentation are important xanthan degradation mechanisms at elevated temperatures, making pH control (pH 7–8 optimal) a critical operational parameter in addition to oxygen exclusion.
  • Arrhenius analysis estimates xanthan can maintain at least half its original viscosity for 5 years at temperatures up to 75–80°C under ideal conditions (no dissolved oxygen, pH 7–8, moderate-to-high salinity).
  • Above 75–80°C, xanthan does not have sufficient thermal stability for long-residence-time polymer flood applications — new polymer chemistries are required for chemical floods targeting higher-temperature reservoirs.
  • Helix-coil transitions in xanthan are a recognized structural change but not a dominant viscosity-loss mechanism under typical polymer flood conditions — the primary concern remains chemical degradation through hydrolysis and oxidation.

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