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Optical rotation of dilute aqueous xanthan solutions at elevated hydrostatic pressure
Author(s) -
Stokke B. T.,
Knudsen K. D.,
Smidsrød O.,
Elgsaeter A.
Publication year - 1991
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.1991.070420734
Subject(s) - hydrostatic pressure , aqueous solution , ionic strength , ionic bonding , chemistry , xanthan gum , ambient pressure , analytical chemistry (journal) , polymer , thermodynamics , materials science , ion , chromatography , rheology , composite material , organic chemistry , physics
The optical rotation of dilute aqueous xanthan solutions of ultrasonically depolymerized xanthan have been measured in the pressure range from 0.1 to 50 MPa. This was achieved using a high‐pressure cell in a spectropolarimeter of original design. The conformational melting temperature T m of xanthan was found to decrease with increasing pressure. The pressure coefficients of the melting temperature at constant ionic strengths, I , was found to be (Δ T m /Δ p ) I = −(9.5 ± 4.0) 10 −8 K Pa −1 and (Δ T m /Δ p ) I = −(20 ± 10) 10 −8 K Pa −1 for solution ionic strengths of 10 m M NaCl and 25m M NaCl, respectively. The largest shift in T m of xanthan for an increase in hydrostatic pressure from 0.1 to 50 MPa is less than −10 K. The observed decrease in conformational transition temperature can have significant implications when xanthan is used in polymer or micellar flooding processes in high‐salinity, high‐temperature oil reservoirs where the reservoir temperature is close to the structural transition temperature at ambient pressure.