TY - JOUR
T1 - Evaluation of esterification routes for long chain cellulose esters
AU - Willberg-keyriläinen, Pia
AU - Ropponen, Jarmo
N1 - Project 121828
Funding Information:
The authors thank Eija Silvasti and Mari Leino for their excellent technical assistance in laboratory experiments.
Publisher Copyright:
© 2019 The Authors
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2019/11/1
Y1 - 2019/11/1
N2 - Long chain cellulose esters are internally plasticized bio-based materials, which have good future potential in several applications such as coatings, films and plastics. The long chain cellulose esters with different side chain lengths were synthesized using different esterification methods. When homogeneous esterification was used, the acyl chloride method was the most effective esterification method and cellulose esters prepared using this method have the highest degree of substitution values (DS). In this case, the long chain cellulose esters showed DS values from 0.3 to 1.3 depending on the side chain length of cellulose esters. CDI activation, vinyl transesterification and anhydride routes resulted in somewhat lower DS values. The cellulose was also pretreated with ozone, which decreased cellulose molar mass, and resulted in synthesized cellulose esters having higher DS and better reaction efficiency than untreated cellulose. When heterogeneous esterifications were used, only acyl chloride method seemed to work.
AB - Long chain cellulose esters are internally plasticized bio-based materials, which have good future potential in several applications such as coatings, films and plastics. The long chain cellulose esters with different side chain lengths were synthesized using different esterification methods. When homogeneous esterification was used, the acyl chloride method was the most effective esterification method and cellulose esters prepared using this method have the highest degree of substitution values (DS). In this case, the long chain cellulose esters showed DS values from 0.3 to 1.3 depending on the side chain length of cellulose esters. CDI activation, vinyl transesterification and anhydride routes resulted in somewhat lower DS values. The cellulose was also pretreated with ozone, which decreased cellulose molar mass, and resulted in synthesized cellulose esters having higher DS and better reaction efficiency than untreated cellulose. When heterogeneous esterifications were used, only acyl chloride method seemed to work.
KW - Cellulose
KW - Esterification
KW - Long chain cellulose ester
KW - Materials chemistry
UR - http://www.scopus.com/inward/record.url?scp=85075266083&partnerID=8YFLogxK
U2 - 10.1016/j.heliyon.2019.e02898
DO - 10.1016/j.heliyon.2019.e02898
M3 - Article
SN - 2405-8440
VL - 5
SP - e02898
JO - Heliyon
JF - Heliyon
IS - 11
M1 - e02898
ER -