Jianfeng Zhang

Blending poly(lactic acid) (PLA) with wheat starch compatibized by maleic anhydride (MA) was performed with a lab-scale co-extruder. An initiator, 2,5-bis(tert-butylperoxy)-2,5 dimethylhexane (L101), was used to improve compatability among PLA, starch and MA. Interfacial adhesion between PLA and starch was significantly improved. Mechanical properties increased markedly compared to the virgin composites of PLA/starch. The PLA/starch composites at a constant ratio of 55/45 compatibilized by 1% MA and initiated by 10% L101 (MA basis) resulted in the highest tensile strength and elongation.

Abstract To avoid the complex core surface functionalization or pretreatment that is necessary in order to coat latex and silica colloids with a uniform, complete metal shell, the solvent‐assisted route has been explored to prepare a complete metal (Ag or Au) shell with controlled thickness on polystyrene (PS) colloids and the electroless plating approach, based on electrostatic attraction, has been explored to prepare a complete silver shell with controlled thickness on silica colloids. Without any additional surface treatment, the as‐prepared complex core–shell colloids can be crystallized directly into long‐range‐ordered structures with photonic bandgaps, as reported here for the first time. These ordered structures may find potential applications as substrates or physical systems for the enhancement of Raman scattering studies, besides applications as photonic crystals. The optical plasmon resonance of the composite core–shell colloids changes with metal shell thickness, the wavelength varying over hundreds of nanometers. Our coating routes are facile and versatile, and can be extended to coat PS and silica colloids with any other metal whose ion or complex can be reduced in solution.

The core−shell structure nanofibers of poly(ethylene oxide)/chitosan have been electrospun from the homogeneous solution of chitosan (CS, as shell) and poly(ethylene oxide) (PEO, as core). The preparation process of core−shell structure was quite simple and efficient without any complex electrospinning setup or post-treatment. The core−shell structure and major component of each layer had been characterized by TEM and further supported by SEM, XRD, DSC, and EDS studies. The blending ratio of PEO and CS, molecular weight of chitosan, and temperature of electrospinning were thought to be the key influence factors on the formation of core−shell structure. Because of the chitosan outer layer and shell thickness being controllable, the core−shell structure nanofiber would show a potential application for the biomedical fields involving wound care and tissue engineering.

Abstract Poly(lactic acid) (PLA)/starch blends were prepared blending with dioctyl maleate (DOM). DOM acted as a compatibilizer at low concentrations (below 5%), and markedly improved tensile strength of the blend. However, DOM functioned as a plasticizer at concentrations over 5%, significantly enhancing elongation. Compatibilization and plasticization took place simultaneously according to the analysis of, for example, mechanical properties and thermal behavior. With DOM as a polymeric plasticizer, thermal loss in the blends was not significant. Water absorption of PLA/starch blends increased with DOM concentration. DOM leaching in an aqueous environment was inhibited. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1697–1704, 2004

A variety of methods have been developed for polydimethylsiloxane (PDMS) elastomer surface functionalization, particularly for the improvement of hydrophilicity. However, in addition to difficulties in avoiding undesired physical changes to the modified surface, including surface cracking, "hydrophobic recovery" frequently leads hydrophilically modified surfaces to completely return over time to their hydrophobic nature, with accompanying loss of accessible functional groups. Thiol-ene chemistry provides a mild and robust technology for synthetic elaboration. We demonstrate the introduction of thiol groups onto the PDMS surface via base-catalyzed equilibration of MTS ((MeO)3Si(CH2)3SH). Thiols in the product elastomer were shown to be located primarily at the air interface using EDX, XPS, and fluorescence labeling initially, and after extended periods of time: total thiol concentrations at the surface and in the bulk were established by complementary chemical titrations with DTDP (4,4'-dithiodipyridine) and iodine titrations in different solvents. The surface density of thiols was readily controlled by reaction conditions: the rate of hydrophobic recovery, which led to incomplete loss of accessible functional groups, was determined. Thiol-ene click chemistry was then used to introduce a variety of hydrophilic moieties onto the surface including a silicone surfactant and maleic anhydride, respectively. In the latter case, molecular functionalization with both small (fluorescent labels) and polymeric nucleophiles (poly(ethylene glycol), chitosan) could be subsequently induced by simple ring-opening nucleophilic attack leading to permanently functional surfaces.