The reaction kinetics and gelation behavior in atom transfer radical polymerization (ATRP), reversible addition-fragmentation chain transfer (RAFT), and conventional free radical copolymerizations (FRP) of oligo(ethylene glycol) methyl ether methacrylate (OEGMEMA) and oligo(ethylene glycol) dimethac
Photocalorimetric monitoring of the polymerization of an oligo(ethylene glycol) dimethacrylate in oligo(ethylene glycol) dimethyl ethers
✍ Scribed by Barbara Sandner; Norbert Kotzian; Jens Tübke; Siegfried Wartewig; Otfried Lange
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 592 KB
- Volume
- 198
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The course of the 2,4,6‐trimethylbenzoyldiphenylphosphine oxide initiated free‐radical photopolymerization of an oligo(ethylene glycol) dimethacrylate ((EG)~23~DMA) in two oligo(ethylene glycol) dimethyl ethers ((EG)~3~DME and (EG)~11~DME) in the presence of LiCF~3~SO~3~ has been studied by means of differential scanning calorimetry (DSC), FT‐Raman spectroscopy and sol‐gel analysis. In order to obtain the kinetical data of the fast photopolymerization, the photo‐DSC curves were corrected numerically. Both, the initial and the maximum polymerization rates were found to depend on the concentration of the monomer and the photo‐initiator with the order 2,5 and 0,2, respectively. Upon addition of LiCF~3~SO~3~, the polymerization rate is increased. Grafting reactions from (EG)~11~DME were observed resulting in its partially linking to the poly(methacrylate) network.
📜 SIMILAR VOLUMES
## Abstract **Summary:** New injectable, in situ curable liquid formulations consisting of biodegradable aliphatic polyester, i.e., poly(3‐allyloxy‐1,2‐propylene)succinate (PSAGE), methyl methacrylate (MMA), and hydrophilic oligo(ethylene glycol) dimethacrylates (OEGDMA) were investigated. The effe
## Abstract A side chain polyrotaxane bearing photoresponsive and nonresponsive recognition sites, i.e., azobenzene (Azo) and heptamethylene (C7) moieties, respectively, linked with a long linker is synthesized. The photoregulated switching of the position of the rotor, i.e., α‐cyclodextrin (α‐CD),