Details
| Original language | English |
|---|---|
| Pages (from-to) | 6957-6966 |
| Number of pages | 10 |
| Journal | Materials Advances |
| Volume | 5 |
| Issue number | 17 |
| Early online date | 6 Aug 2024 |
| Publication status | Published - 2024 |
Abstract
The interest in hydrogels has grown considerably across a number of disciplines, including but not limited to the immobilization of (bio)catalysts in matrices and in the medical sector, for example, in drug delivery systems, contact lenses, biosensors, electrodes, and tissue engineering. Consequently, the characterization of these materials is frequently the subject of cutting-edge research. However, hydrogels are often insoluble, which precludes the use of many analytical methods, such as nuclear magnetic resonance (NMR). Consequently, other established analytical techniques, such as attenuated total reflection (ATR), infrared spectroscopy (IR), Raman spectroscopy, or rheological measurements, are frequently employed. These methods are generally straightforward to use and can be completed rapidly. However, IR spectroscopy, for instance, is inherently limited by the interference of water's vibrational bands. In this study, we present a method for the characterization of hydrogels that can simultaneously observe the gelation and polymerization of hydrogels.
ASJC Scopus subject areas
- Chemistry(all)
- Chemistry (miscellaneous)
- Materials Science(all)
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In: Materials Advances, Vol. 5, No. 17, 2024, p. 6957-6966.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - A novel characterization technique for hydrogels
T2 - in situ rheology-Raman spectroscopy for gelation and polymerization tracking
AU - Lambrecht, Sina
AU - Biermann, Marek
AU - Kara, Selin
AU - Jopp, Stefan
AU - Meyer, Johanna
N1 - Publisher Copyright: © 2024 RSC.
PY - 2024
Y1 - 2024
N2 - The interest in hydrogels has grown considerably across a number of disciplines, including but not limited to the immobilization of (bio)catalysts in matrices and in the medical sector, for example, in drug delivery systems, contact lenses, biosensors, electrodes, and tissue engineering. Consequently, the characterization of these materials is frequently the subject of cutting-edge research. However, hydrogels are often insoluble, which precludes the use of many analytical methods, such as nuclear magnetic resonance (NMR). Consequently, other established analytical techniques, such as attenuated total reflection (ATR), infrared spectroscopy (IR), Raman spectroscopy, or rheological measurements, are frequently employed. These methods are generally straightforward to use and can be completed rapidly. However, IR spectroscopy, for instance, is inherently limited by the interference of water's vibrational bands. In this study, we present a method for the characterization of hydrogels that can simultaneously observe the gelation and polymerization of hydrogels.
AB - The interest in hydrogels has grown considerably across a number of disciplines, including but not limited to the immobilization of (bio)catalysts in matrices and in the medical sector, for example, in drug delivery systems, contact lenses, biosensors, electrodes, and tissue engineering. Consequently, the characterization of these materials is frequently the subject of cutting-edge research. However, hydrogels are often insoluble, which precludes the use of many analytical methods, such as nuclear magnetic resonance (NMR). Consequently, other established analytical techniques, such as attenuated total reflection (ATR), infrared spectroscopy (IR), Raman spectroscopy, or rheological measurements, are frequently employed. These methods are generally straightforward to use and can be completed rapidly. However, IR spectroscopy, for instance, is inherently limited by the interference of water's vibrational bands. In this study, we present a method for the characterization of hydrogels that can simultaneously observe the gelation and polymerization of hydrogels.
UR - http://www.scopus.com/inward/record.url?scp=85200746108&partnerID=8YFLogxK
U2 - 10.1039/d4ma00543k
DO - 10.1039/d4ma00543k
M3 - Article
VL - 5
SP - 6957
EP - 6966
JO - Materials Advances
JF - Materials Advances
IS - 17
ER -