2021
DOI: 10.1016/j.carbpol.2021.118079
|View full text |Cite
|
Sign up to set email alerts
|

Structure-property relationships on recrystallized β-cyclodextrin solvates: A focus on X-ray diffractometry, FTIR and thermal analyses

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
16
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
3
3
1

Relationship

0
7

Authors

Journals

citations
Cited by 27 publications
(16 citation statements)
references
References 50 publications
0
16
0
Order By: Relevance
“…During the molecular encapsulation process, the fatty acid moieties of the triglycerides contained by chicken lipids progressively replace a part of the water molecules from the β-CD hydrate. Consequently, the water content of a β-CD/hydrophobic compound complex is lower [ 41 , 42 , 44 , 46 , 47 , 53 ]. According to this study, the recovering yield was higher for the β-CD/processed chicken lipid complexes in comparison with that in the raw samples (79.57 (±5.33) and 66.68 (±9.18)%, respectively).…”
Section: Resultsmentioning
confidence: 99%
See 3 more Smart Citations
“…During the molecular encapsulation process, the fatty acid moieties of the triglycerides contained by chicken lipids progressively replace a part of the water molecules from the β-CD hydrate. Consequently, the water content of a β-CD/hydrophobic compound complex is lower [ 41 , 42 , 44 , 46 , 47 , 53 ]. According to this study, the recovering yield was higher for the β-CD/processed chicken lipid complexes in comparison with that in the raw samples (79.57 (±5.33) and 66.68 (±9.18)%, respectively).…”
Section: Resultsmentioning
confidence: 99%
“…On the contrary, the β-CD/processed lipid complexes had significantly higher values for the temperature corresponding to the maximum water dissociation rate (107.8–117.2 °C). This behavior was probably due to the dissociation of the strongly retained water and solvent (from the complexation process) molecules from the β-CD/lipid complexes [ 42 ]. Another difference appeared for the mass loss during the temperature range of 110–275 °C.…”
Section: Resultsmentioning
confidence: 99%
See 2 more Smart Citations
“…The absorption peak present at 1449 cm − 1 is a symmetric stretching peak formed by the dissociation of the hydroxyl group of AM into COO − during the polymerization process 33 . The IR spectral curve of β-CD shows that the absorption peak at 3388 cm − 1 is the O-H stretching vibration peak, and the absorption peak at 1368 cm − 1 is the bending vibration peak of O-H 34 . From the FTIR spectral pro le of P(AA-AM)/β-CD, it can be seen that there are a large number of absorption peaks identical to those of P(AA-AM), but a stronger absorption peak appears at 1374 cm − 1 , which corresponds to the bending vibration peak generated by O-H in β-CD.…”
Section: Fourier Infrared Spectroscopy (Ftir)mentioning
confidence: 99%