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- W2085054764 abstract "The cyclization reaction (formation of 3,6-anhydro-α-d-galactose and 3,6-anhydro-α-d-galactose 2-sulfate units from α-d-galactose 6-sulfate and 2,6-disulfate residues, respectively) of carrageenans follows a pseudo-first-order kinetics. This reaction can be carried out, at reasonable rates, in sodium hydroxide solutions less concentrated than those usually employed or by using a milder base such as sodium carbonate. Rate constants were also determined at a fixed sodium hydi oxide concentration but using different ionic strengths. No specific salt effects were observed at a given sodium hydroxide concentration and ionic strength." @default.
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- W2085054764 date "1997-03-01" @default.
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- W2085054764 title "Alkaline modification of carrageenans. Part III. Use of mild alkaline media and high ionic strengths" @default.
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- W2085054764 doi "https://doi.org/10.1016/s0144-8617(96)00130-0" @default.
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