Recent developments in biodegradable block copolymers

Author(s):  
Sunil U. Tekale ◽  
Yakir Rottenberg ◽  
Rajita D. Ingle ◽  
Abraham J. Domb ◽  
Rajendra P. Pawar
2021 ◽  
Author(s):  
Amit Kumar Pandey ◽  
Shinichi Sakurai

Despite the extensive studies of poly(L-lactic acid)(PLLA), the crystallization of PLLA-based materials is still not completely understood. This chapter presents recent developments of crystallization of PLLA-based blends, block copolymers and nanocomposites. The first section of the chapter discusses the acceleration of PLLA crystallization by the inclusion of biobased (solid and liquid state) additives. It was found that the solid state additives work as a nucleating agent while the liquid-state additive works as a plasticizer. Both type of the additives can significantly enhance the crystallization of PLLA, as indicated by crystallization half-time (t0.5) values. Such composites are of great interest as they are 100% based on renewable resources. The second section talks about the enhanced formation of stereocomplex (SC) crystals in the PLLA/PDLA (50/50) blends by adding 1% SFN. It was found that the loading of SFN enhances the formation of SC crystals and it suppresses the formation of HC (homocrystal). The third section deals with confined crystallization of poly(ethylene glycol) (PEG) in a PLLA/PEG blend. The PLLA/PEG (50/50) blend specimen was heated up to 180.0°C and kept at this temperature for 5 min. Then, a two-step temperature-jump was conducted as 180.0°C → 127.0°C → 45.0°C. For this particular condition, it was found that PEG can crystallize only in the preformed spherulites of PLLA, as no crystallization of PEG was found in the matrix of the mixed PLLA/PEG amorphous phase. The last section describes the confined crystallization of PCL in the diblock and triblock copolymers of PLA-PCL. Furthermore, enantiomeric blends of PLLA-PCL and PDLA-PCL or PLLA-PCL-PLLA and PDLA-PCL-PDLA have been examined for the purpose of the improvement of the poor mechanical property of PLLA to which the SC formation of PLLA with PDLA components are relevant.


1976 ◽  
Vol 49 (2) ◽  
pp. 237-246 ◽  
Author(s):  
E. Helfand

Abstract Most of the polymeric materials one encounters so widely are heterogeneous. For instance, commercial plastics may be blends of immiscible polymers; they may contain antioxidants or other modifiers which are not totally soluble; andfrequently they have added inorganic fillers. Other examples of inhomogeneity in polymer systems are composites, partially crystalline materials, surface layers, ionomers, and block and graft copolymers. In some cases the heterogeneity is the essence of the material's virtue (e.g., its mechanical properties). In other cases heterogeneity is an affliction. But, whether one's goal is to maximize or minimize the effect of nonuniformity, it is well to understand the factors which determine the features of inhomogeneous polymers. This we will attempt to do in a qualitative way by describing, from a simple molecular point of view, the entropy and energy terms which control the systems' physical features. Rather than dealing in generalities, however, let us focus on two particular cases : interfaces between immiscible polymers, and block copolymers. This should provide the reader with some insight into the myriad of recent developments in the field of polymer blends, composites, and microheterogeneities.


2015 ◽  
Vol 6 (13) ◽  
pp. 2369-2381 ◽  
Author(s):  
Elizabeth A. Rainbolt ◽  
Katherine E. Washington ◽  
Michael C. Biewer ◽  
Mihaela C. Stefan

Synthetic modification of caprolactone monomers and polymers provides a route to self-assembling block copolymers for use in drug carrier applications.


2011 ◽  
Vol 64 (9) ◽  
pp. 1183 ◽  
Author(s):  
Hazrat Hussain ◽  
Elkin Amado ◽  
Jörg Kressler

This review deals with the synthesis, physical properties, and applications of amphiphilic block copolymers based on hydrophilic poly(ethylene oxide) (PEO) or hydrophobic poly(propylene oxide) (PPO). Oligomeric PEO and PPO are frequently functionalized by converting their OH end groups into macroinitiators for atom-transfer radical polymerization. They are then used to generate additional blocks as part of complex copolymer architectures. Adding hydrophobic and hydrophilic blocks, respectively, leads to polymers with amphiphilic character in water. They are surface active and form micelles above a critical micellization concentration. Together with recent developments in post-polymerization techniques through quantitative coupling reactions (‘click’ chemistry) a broad variety of tailored functionalities can be introduced to the amphiphilic block copolymers. Examples are outlined including stimuli responsiveness, membrane penetrating ability, formation of multi-compartmentalized micelles, etc.


Author(s):  
Xiaodan Gu ◽  
Ilja Gunkel ◽  
Thomas P. Russell

To meet the increasing demand for patterning smaller feature sizes, a lithography technique is required with the ability to pattern sub-20 nm features. While top-down photolithography is approaching its limit in the continued drive to meet Moore’s law, the use of directed self-assembly (DSA) of block copolymers (BCPs) offers a promising route to meet this challenge in achieving nanometre feature sizes. Recent developments in BCP lithography and in the DSA of BCPs are reviewed. While tremendous advances have been made in this field, there are still hurdles that need to be overcome to realize the full potential of BCPs and their actual use.


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