## Abstract Spectra of 10 monomers and polymers of methacrylate esters and of methyl chloroacrylate have been studied between 6000β450 cm^β1^. A number of known regularities are confirmed. The CH~2~ and CH~3~ deformation vibrations in the 1500β1350 cm^β1^ region of the polymer unit can be distingu
Characterization of methacrylic polymers by calorimetry and infrared analyses
β Scribed by Claudia R. E. Mansur; Elisabeth E. C. Monteiro
- Book ID
- 101253130
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 266 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
Methyl methacrylate-methacrylic acid (MMA-MAA) copolymers, prepared by the action of concentrated nitric acid (65% HNO 3 ) on methyl methacrylate in absence of other reagents, were characterized using calorimetry (DSC) and infrared (FTIR) analyses. DSC curves of ester/acid copolymers suggested the anhydride formation at Γ 200ΠC, which was corroborated by thermogravimetry (TG). This structure was assigned by FTIR spectra. The results obtained by DSC data are in good agreement with the hydrolysis degree of the MMA-MAA copolymers obtained from chemical titration. The molecular weight of the copolymers were estimated by viscometry. α§ 1998
π SIMILAR VOLUMES
## Abstract Xβray photoelectron spectroscopy (XPS) and static secondary ion mass spectrometry (SIMS) were used to identify and quantify different isomeric butyl methacrylate polymers. The samples examined were normalβ, isoβ and __tert__β butyl methacrylate (__n__β, __i__β and __t__βBuMA) homopolyme
## Abstract The synthesis of new methacrylic monomers H~2~Cο£ΏC(CH~3~)ο£ΏCOOCH~2~ο£ΏG where G is a pyridine, a pyrazole or a bipyrazole group has been achieved. Their homopolymerization was studied and gave fairly low molecular mass polymers. Their copolymerization with styrene gave copolymers tending to
Soluble polymers have been produced from technical-grade 2-hydroxyethyl methacrylate (HEMA) and hydroxypropyl methacrylate (HPHA) using a combination of vacuum distillation and solvent extractions to purify the monomers prior to solution polymerization. These extractions, particularly of HEMA with h