𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Photocrosslinking Polymerization of Methacrylate Modified Triethoxysilanes Polycondensates and Multifunctional Methacrylates

✍ Scribed by Juraj Pavlinec; Norbert Moszner


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
117 KB
Volume
288
Category
Article
ISSN
1438-7492

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Densely crosslinked polymer networks were prepared by fast, visible light‐induced polymerization at 20–22 °C. The two methacrylate functionalized triethoxysilanes polycondensates (MSiP) either alone, or in a mixture with methacrylate modified oxozirconium clusters, were polymerized separately and as comonomers to multimethacrylate monomers in a weight ratio of 1:0.9. Pure organic networks based on 1,6‐bis(2‐hydroxy‐3‐methacryloyloxyethoxycarbonylamino)‐2,2,4‐trimethylhexane (UDMA) were used for comparison in the same ratio to other comonomers. The networks based on organic bifunctional monomers showed high, around 85% conversion of double bonds. Nevertheless the non‐reacted monomer that migrates to the toluene amounts from 5.6 to 11.65 wt.‐%. Copolymerization of UDMA with tetrafunctional components resulted in networks with higher residual unsaturation up to 27.7%. This result points out the important role that functionality and the spacer structure between the monomer double bonds play in the extent of reaction. Based only on modified inorganic SiOSi nano‐structures the networks are characterized by nearly complete building up of MSiP in the network, extreme crosslinks density, and mostly less than 1 wt.‐% of soluble substances. However, residual unsaturations exceeded 22%. The advantage of copolymerization of MSiP with proper organic comonomers as potential solvent free matrices for dental composites was demonstrated by a network consisting of MSiP II and UDMA. The 13.7% of unreacted double bonds and 99.65 wt.‐% gel content approximated efforts to minimize residual unsaturation and maximize monomer conversion in cured networks.

Monomers used for the synthesis of the densely crosslinked polymer.

magnified imageMonomers used for the synthesis of the densely crosslinked polymer.


📜 SIMILAR VOLUMES


Polymerization of multifunctional methac
✍ Miyazaki, Koji ;Horibe, Takashi 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 652 KB

The cross-linking reaction of 15 dimethacrylates, one trimethacrylate and five diacrylates was studied by means of differential scanning calorimetry (DSC) and high performance liquid chromatography (HPLC) to investigate the relationship between the polymerization characteristics and the chemical str

Modified emulsifier-free emulsion polyme
✍ Xiao-Jun Xu; Fengxi Chen 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 98 KB 👁 1 views

## Abstract A modified emulsifier‐free emulsion polymerization of butyl methacrylate (BMA) with ionic or/and nonionic comonomers was successfully used to prepare nanosized poly(butyl methacrylate) (PBMA) latices with high polymer contents. After seeding particles were generated in an initial emulsi

A new class of transparent polymeric mat
✍ Toru Doi; Noriyuki Ishikawa; Akira Akimoto 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 316 KB 👁 2 views

Transparent polymeric materials with high heat resistance and low water absorption were designed based on the alternating copolymers of N-substituted maleimide (RMI) with isobutene (IB). The N-substituent of the maleimide significantly affected the glass transition temperature (T,) and water absorpt