The average relaxation time relaxation times corresponding to seg-q 0 , mental motion and group rotations of a series of binary mixtures of q 1 q 2 , poly(ethylene glycols) (PEG 200 ] PEG 300, PEG 400 ] PEG 600, PEG 1500 ] PEG 4000, PEG 6000 ] PEG 9000, PEG 200 ] PEG 1500, PEG 300 ] PEG 4000, PEG 40
Solvent effects on microwave dielectric relaxation in poly(ethylene glycols)
β Scribed by Sengwa, R. J.
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 207 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0959-8103
No coin nor oath required. For personal study only.
β¦ Synopsis
This paper reports the results of a systematic study of microwave dielectric relaxation times of poly(ethylene glycols), average molecular weight 200Γ9000, in dilute solutions of benzene at 9Γ83 GHz. These results are compared with the values of relaxation times obtained earlier in carbon tetrachloride solutions. This shows that the average relaxation times and the relaxation time q 0 corresponding to segmental reorientation are inΓuenced by the solvent q 1 environment. The variation in chain Γexibility in these polymers with the increase in degree of polymerization and formation of intra-and inter-molecular hydrogen bonding in benzene and carbon tetrachloride solutions is discussed with the help of relaxation data. The relaxation time corresponding to group q 2 rotations has been determined. It is found that the value is independent of q 2 solvent environment and degree of polymerization, and may be attributed to the rotation of chain wOH end-groups around the CwO bonds in dynamic equilibrium, with the formation of a Γve-membered ring due to intra-molecular hydrogen bonding at the end of the chain.
1998 SCI. ( . Int. 45 43Γ46 (1998)
Polym
π SIMILAR VOLUMES
The effect of the matrix on poly(ethylene glycol) (PEG) cationization was investigated using an equimolar mixture of CsCl and LiCl as cationizing agents. It was observed that for both carboxylic acid and noncarboxylic acid matrices used, PEG cationization by a given alkali metal ion depends on the m
The e β ect of anionic (sodium butylbenzene sulfonate, sodium butylmonoglycol sulfate), cationic (tetrabutyl ammonium bromide), nonionic(Tween 20) and amphoteric (proline) surface active additives on the partitioning of proteins and enzymes, such as BSA, lysozyme, glucose oxidase and b-lactoglobulin,
## Abstract Covalent modification of purified __Trigonopsis variabilis__ Dβamino acid oxidase using maleimideβactivated poly(ethylene glycol) 5000 yielded a stable bioconjugate in which three surfaceβexposed cysteine side chains were selectively derivatized. Compared with the native enzyme, the PEG