1996
DOI: 10.1016/s0008-6215(96)90795-8
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The influence of the conformational state of κ- and τ-carrageenan on the rate of acid hydrolysis

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Cited by 20 publications
(81 citation statements)
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“…On the hypothesis of Hjerde, Smidsrød, & Christensen (1996) and 121 Tanford (1961), and glycoside bonds on KC have a similar susceptibility 122 to scission. 123…”
Section: Theoretical Basis: Degradation Rate 111mentioning
confidence: 99%
“…On the hypothesis of Hjerde, Smidsrød, & Christensen (1996) and 121 Tanford (1961), and glycoside bonds on KC have a similar susceptibility 122 to scission. 123…”
Section: Theoretical Basis: Degradation Rate 111mentioning
confidence: 99%
“…16,17 In previous works we have investigated the depolymerization by acid hydrolysis of -and -carrageenan both in the ordered and disordered conformations. 18 -20 The hydrolysis was monitored both by the decrease in specific viscosity and increase in the number of reducing end groups, 18,19 as well as by monitoring the changes in molecular weight and molecular weight distribution. 20 These results were interpreted in terms of double-stranded structures for the ordered conformations of both -and -carrageenan, partly supported by the observation of a twofold decrease in M w when going from the ordered to the disordered state.…”
Section: 8 -12mentioning
confidence: 99%
“…3,19 High concentrations may favor nonspecific interactions leading to concentration-dependent networks. In most cases, such as for carrageenans, the ordered state is formed from a disordered state by first dissolving the polymer above T m (e.g., in pure water) and then inducing the ordered state by lowering T or increasing the ionic strength.…”
Section: 8 -12mentioning
confidence: 99%
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