TY - JOUR
T1 - Laccase/TEMPO oxidation in the production of mechanically strong arabinoxylan and glucomannan aerogels
AU - Parikka, Kirsti
AU - Nikkilä, Ida
AU - Pitkänen, Leena
AU - Ghafar, Abdul
AU - Sontag-Strohm, Tuula
AU - Tenkanen, Maija
PY - 2017/11/1
Y1 - 2017/11/1
N2 - New wheat arabinoxylan and konjac glucomannan hydrogels and aerogels were prepared by hemiacetal crosslinking induced by laccase/TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) ‐catalysed oxidation, which selectively converts the primary hydroxyl groups to aldehydes. The degree of oxidation of the product aldehydes was ca. 10% of the total carbohydrates of the polysaccharides, and the determination of storage and viscous moduli of the oxidised samples showed that they had formed true hydrogels. Two freezing methods for the hydrogels, conventional freezing and ice crystal templating, were investigated for aerogel production, the ice crystal templated products especially were mechanically strong in compression test against the ice crystals' growth direction. The compressive moduli were ca. 1200 kPa for wheat arabinoxylan aerogels and ca. 650 kPa for konjac glucomannan aerogels. A morphological study with a scanning electron microscope revealed the inner structure of the aerogels. Ice crystal templated konjac glucomannan aerogel formed round pores with a diameter of ca. 50–100 μm. The arabinoxylan aerogel consisted of long and narrow pores with a length of a few hundred μm and width of 50–100 μm, which had formed in the direction of the ice crystals' formation. Konjac glucomannan and wheat arabinoxylan are approved food-grade materials, and wheat arabinoxylan is particularly interesting because it can be obtained from cereal processing side streams − thus, these novel products have potential in various applications, including the food, food packaging, and pharmacological fields.
AB - New wheat arabinoxylan and konjac glucomannan hydrogels and aerogels were prepared by hemiacetal crosslinking induced by laccase/TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) ‐catalysed oxidation, which selectively converts the primary hydroxyl groups to aldehydes. The degree of oxidation of the product aldehydes was ca. 10% of the total carbohydrates of the polysaccharides, and the determination of storage and viscous moduli of the oxidised samples showed that they had formed true hydrogels. Two freezing methods for the hydrogels, conventional freezing and ice crystal templating, were investigated for aerogel production, the ice crystal templated products especially were mechanically strong in compression test against the ice crystals' growth direction. The compressive moduli were ca. 1200 kPa for wheat arabinoxylan aerogels and ca. 650 kPa for konjac glucomannan aerogels. A morphological study with a scanning electron microscope revealed the inner structure of the aerogels. Ice crystal templated konjac glucomannan aerogel formed round pores with a diameter of ca. 50–100 μm. The arabinoxylan aerogel consisted of long and narrow pores with a length of a few hundred μm and width of 50–100 μm, which had formed in the direction of the ice crystals' formation. Konjac glucomannan and wheat arabinoxylan are approved food-grade materials, and wheat arabinoxylan is particularly interesting because it can be obtained from cereal processing side streams − thus, these novel products have potential in various applications, including the food, food packaging, and pharmacological fields.
KW - Aerogel
KW - Aldehyde
KW - Guar galactomannan
KW - Hydrogel
KW - Konjac glucomannan
KW - Laccase
KW - Oxidation
KW - TEMPO
KW - Wheat arabinoxylan
UR - http://www.scopus.com/inward/record.url?scp=85027278295&partnerID=8YFLogxK
U2 - 10.1016/j.carbpol.2017.07.074
DO - 10.1016/j.carbpol.2017.07.074
M3 - Article
AN - SCOPUS:85027278295
VL - 175
SP - 377
EP - 386
JO - Carbohydrate Polymers
JF - Carbohydrate Polymers
SN - 0144-8617
ER -