• Anhydrosugars
    Analysis at Celignis


Anhydrosugars are defined as sugars in which one or more molecule of water has been eliminated. The 1,6-anhydrosugars involve the loss of one water molecule and tend to be the most common type. They are formed from the elimination of water from a pair of hydroxyl groups on the same molecule which results in the formation of a new heterocyclic ring of a different size through an intramolecular glycosidic linkage. This linkage is usually between the anomeric hydroxyl and the hydroxyl of C-6 in the pyranose form with both the interacting groups at C-1 and C-5 being axial (1,6-anhydroaldohexoses). However, the intramolecular rings can also form in other positions (for example there can be 2,3-anhydrosugars and 1,2-anhydrosugars).

The intramolecular linkages in anhydrosugars can be readily opened by the actions of acids, resulting in hydrolysis to the corresponding aldoses (e.g. from levoglucosan to glucose).

Anhydrosugars are often found in the bio-oil produced in pyrolysis processes and come from the pyrolysis of cellulose and hemicellulose. Click here to read more about bio-oil and the analysis methods we use to characterise it.

Analysis of Anhydrosugars at Celignis

Using our ion chromatography system we are able to directly analyse a number of anhydrosugars. These are detailed below:


Levoglucosan

Levoglucosan (also known as 1,6-Anhydro-beta-glucopyranose) is the 1,6-anhydrosugar form of glucose and is formed during the pyrolysis of glucose-containing carbohydrates such as cellulose. Some pyrolysis technologies specifically target the production of levoglucosan in high yields. In recent years there has been significant research on developing uses and conversion pathways for levoglucosan. For example, sorbitol has been synthesised from this anhydrosugar whilst microorganisms capable of directly fermenting levoglucosan (without requiring hydrolysis to glucose) have been tested.

Cellobiosan

Cellobiosan (also known as 1,6-Anhydro-beta-cellobiose) is an anhydrosugar formed from the elimination of one water molecule from cellobiose. This water is lost from one of the glucose sugars in the disaccharide and a 1,6 glycosidic linkage is formed within that sugar.

After levoglucosan, cellobiosan is the most abundantly produced product from the pyrolysis of cellulose. As a result of this there has been much work on finding ways in which it can be valorised or further converted to other products. For instance, cellobiosan can be hydrolysed to glucose using acids or, like levoglucosan, it can be directly fermented using some micro-organisms.

Mannosan

Mannosan (also known as 1,6-Anhydro-beta-mannopyranose) is an anhydrosugar formed from the elimination of one water molecule from mannose. It can be present in pyrolysis bio-oil in cases where the starting biomass feedstock had mannose residues within its hemicelluloses.

Galactosan

Galactosan (also known as 1,6-Anhydro-beta-galactopyranose) is an anhydrosugar formed from the elimination of one water molecule from galactose. It can be present in pyrolysis bio-oil in cases where the starting biomass feedstock had galactose residues within its hemicelluloses.

Our Analysis Packages for Anhydrosugars

We currently have three analysis packages for detailing the amount of anhydrosugars in a solution. These are detailed below. Packages P61 and P62 will quantify the amount of four different anhydrosugars (levoglucosan, cellobiosan, mannosan, and galactosan) in the water extract of pyrolysis bio-oils or other aqueous solutions. Package P63 analyses the bio-oil directly for a range of different semi-volatile oxygenated components, but only one anhydrosugar (levoglucosan). Please click on the links below for further information.

Furthermore, if there are other anyhydrosugars that you would like us to determine then please get in touch.



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