End groups in acrylic copolymers. 1. Identification of end groups by carbon-13 NMR

1988 ◽  
Vol 21 (6) ◽  
pp. 1598-1603 ◽  
Author(s):  
K. R. Carduner ◽  
R. O. Carter ◽  
M. Zinbo ◽  
J. L. Gerlock ◽  
D. R. Bauer
Author(s):  
Maria Cristina KANTUN-UICAB ◽  
Isis RODRÍGUEZ-SÁNCHEZ ◽  
Francisco Javier RODRÍGUEZ-GONZÁLEZ ◽  
Juan Gregorio HORTELANO-CAPETILLO

In this work, the reactive compatibilization of Polylactic Acid/Thermoplastic Starch (PLA/TPS, 80/20% w/w) blends using acrylic copolymers of methyl methacrylate-glycidyl methacrylate (MMA-GMA) was examined. The compatibilization was studied using torque rheometry, thermal analysis (DSC), Scanning Electron Microscopy (SEM) and mechanical properties. During melt mixing, the torque of PLA/TPS blends decreased, this was related to the breakup of starch chains. The addition of MMA-GMA copolymer increased the torque during the mixing period. This torque increasing is evidence of a viscosity increase and it was related to the reactions between the epoxy group present in the acrylic copolymer, the end-groups of the PLA and TPS hydroxyl groups. The morphologies of the compatibilized blends showed a decrease in the particle size of the TPS domains and an increase in elongation of 30%. The reactive compatibilization is an interesting technique to expand the property range of PLA materials, which can potentially substitute oil-based materials.


1988 ◽  
Vol 21 (6) ◽  
pp. 1604-1607 ◽  
Author(s):  
J. L. Gerlock ◽  
D. F. Mielewski ◽  
D. R. Bauer ◽  
K. R. Carduner

1992 ◽  
Vol 35 (3) ◽  
pp. 219-228 ◽  
Author(s):  
K.R. Carduner ◽  
D.R. Bauer ◽  
J.L. Gerlock ◽  
D.F. Mielewski

2004 ◽  
Vol 19 (2) ◽  
pp. 146-154
Author(s):  
Jim Parkås ◽  
Magnus Paulsson ◽  
Shiming Li ◽  
Knut Lundquist ◽  
Ulla Westermark
Keyword(s):  

2020 ◽  
Vol 17 (2) ◽  
pp. 85-89
Author(s):  
Francisco J. Hidalgo ◽  
Nathan A.P. Lorentz ◽  
TinTin B. Luu ◽  
Jonathan D. Tran ◽  
Praveen D. Wickremasinghe ◽  
...  

: Maltodextrins have an increasing number of biomedical and industrial applications due to their attractive physicochemical properties such as biodegradability and biocompatibility. Herein, we describe the development of a synthetic pathway and characterization of thiol-responsive maltodextrin conjugates with dithiomaleimide linkages. 19F NMR studies were also conducted to demonstrate the exchange dynamics of the dithiomaleimide-functionalized sugar end groups.


1976 ◽  
Vol 31 (8) ◽  
pp. 1017-1018 ◽  
Author(s):  
H. Oehling ◽  
F. Baer

Abstract Polymethine oxonols show temperature dependent 1H-NMR-spectra because of restricted rotation of the end groups. The dependence of the value of the corresponding free enthalpy of activation AGt on the length of the poly-methine chain can be explained by the change of the π-electron contribution to ⊿G≠.


1953 ◽  
Vol 203 (2) ◽  
pp. 575-582 ◽  
Author(s):  
Sidney F. Velick ◽  
Sidney Udenfriend
Keyword(s):  

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