4.7 Article

Influence of Pressure on Boron Cross-Linked Polymer Gels

Journal

MACROMOLECULES
Volume 41, Issue 21, Pages 8181-8186

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma801187q

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Funding

  1. Office of Basic Energy Sciences
  2. Division of Chemical Sciences
  3. U.S. Department of Energy [W-31-109-ENG-38]

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Using steady-shear rheometry in combination with high-pressure B-11 nuclear magnetic resonance spectroscopy (B-11 NMR), we have found that gels formed from water-soluble polymers containing vicinal hydroxyl groups cross-linked with various boron-containing compounds undergo significant structural changes that result in a pronounced loss of viscosity when placed under pressure. Importantly, gels from other cross-linking agents tested, including Ti(IV) and Zr(IV), did not show this loss in viscosity. The experimental study probed pressure-induced changes to both galactomannan and polyvinyl alcohol (PVA) gets cross-linked with either aryl boronic acids or alkali metal boron-containing salts using pressure conditions that ranged from atmospheric to 680 bar and temperatures that ranged from 20 to 65 degrees C. Significantly, the pressure-induced losses in viscosity and, to a somewhat lesser extent, the concomitant pressure-induced B-11 NMR spectral changes were found to be reversed upon lowering the pressure.

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