کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
642251 | 1457030 | 2012 | 9 صفحه PDF | دانلود رایگان |

In this work, separation of poly- and disaccharides is achieved by means of novel biphasic systems based on ionic liquids as alternative to the volatile organic compounds used in large amounts for precipitation of the polysaccharides produced from disaccharides in microbial culture broths. Xanthan and maltose are employed to represent a charged (anionic) polysaccharide and a neutral disaccharide. For the separation, two kinds of systems are applied, a specially designed biphasic system of water/1-hexyl-3-methylimidazolium tetrafluoroborate ([C6mim][BF4]), and an aqueous biphasic system of 3-methyl-1-octylimidazolium chloride/K2HPO4. In the system of [C6mim][BF4] the effects of the alcohol (isopropyl), added as modifier, and of the temperature on the system volume partitioning and separation are investigated. Recycling and reuse of the [C6mim][BF4] are shown. In both ionic liquid-based systems, complete isolation with simultaneous concentration of the polysaccharide in the upper phase of the system is obtained, and 80% of the initial disaccharide is retained in the lower phase. The mechanism of the polysaccharide transfer is revealed in terms of the possible interactions of the xanthan polyanion with the imidazolium cations assisted by the polymer dehydration caused under the addition of isopropyl alcohol or kosmotropic K2HPO4. Drawbacks of the ionic liquid-based biphasic systems are also discussed.
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► A novel biphasic system of water, [C6mim][BF4], and isopropyl alcohol was designed.
► The biphasic system was used for poly-/disaccharide (xanthan/maltose) separation.
► The polysaccharide (xanthan) was isolated and concentrated in one extraction step.
► Poly-/disaccharide (xanthan/maltose) separation factors of five were obtained.
► The ionic liquid ([C6mim][BF4]) recycling and reuse were shown to be fast and easy.
Journal: Separation and Purification Technology - Volume 89, 22 March 2012, Pages 57–65