[Distribution of Micro-plastics in the Soil Covered by Different Vegetation in Yellow River Delta Wetland].

Micro-plastics (MPs) pollution has been a hotspot in soil environment. To explore the correlation of the vegetation cover and the distribution of MPs in Yellow River Delta wetland, the characters of MPs in the soil sampled at 16 sites where reed (Phragmites communis, a low-salt dominant species) and Suaeda salsa (a high-salt dominant species) covered were investigated. The abundance of MPs here ranged to 80-4640 n·kg-1, and the particle size ranged to 13 µm-5 mm. The main components of MPs with large size were polyethylene (PE), polyethylene terephthalate (PET) and polystyrene (PS), and the content of PET ranged to 0.22-1.16 µg·kg-1. The barrier effect of reed on MPs was higher than that of Suaeda salsa. The average abundance of MPs and PET contents at the sites where reed covered were 1423 n·kg-1 and 0.62 µg·kg-1, and they mainly consisted of small particles with a size less than 50 µm. The average abundance of MPs and PET contents at the site Suaeda salsa covered were 584 n·kg-1 and 0.33 µg·kg-1, and they mainly consisted of fragments and fibers with a size ranged to 100-1000 µm. The abundance of MPs in the soil was significantly correlated with the growth statues of the vegetations (P=0.001). Therefore, the distribution of MPs in the soil in the same area covered by different vegetation might be spatial different.

Supernucleation, crystalline structure and thermal stability of bacterially synthesized poly(3-hydroxybutyrate) polyester tailored by thymine as a biocompatible nucleating agent.

Naturally occurring thymine (TM) was incorporated into bacterial poly(3-hydroxybutyrate) (PHB) polyester to fabricate a novel and green biocomposite. Both 0.5% and 1% TM exhibit supernucleation effect on PHB, and crystallization kinetics suggests TM significantly increased Tc and Xc, and substantially shortened t1/2 of PHB. Epitaxial nucleation caused by a perfect crystal lattice matching between PHB and TM, was proposed to elucidate nucleation mechanism of PHB. Hydrogen bond interaction exists between CO, C-O-C groups of PHB and -CH3 (or -CH)/-NH- group of TM. TM interacted with CO group of PHB crystalline phase rather than that of amorphous one. In addition, two new IR crystalline bands assigned to C-O-C group of PHB appeared in the presence of TM, which arises from shift of two amorphous ones, respectively. TM enhanced onset thermal degradation temperature of PHB, mainly attributed to increased degree of crystallinity of PHB and flame retardance effect of TM.

Effects of crystallization temperature of poly(vinylidene fluoride) on crystal modification and phase transition of poly(butylene adipate) in their blends: a novel approach for polymorphic control.

Effects of the isothermal crystallization temperatures of poly(vinylidene fluoride), T(IC,PVDF), on polymorphic crystalline structure, phase transition, fractional crystallization, and enzymatic degradation of poly(butylene adipate) (PBA) in crystalline/crystalline blends have been investigated. The crystal modifications of PBA can be regulated by T(IC,PVDF). Lower T(IC,PVDF) (e.g., 80 °C) facilitates the formation of PBA α crystals in both the isothermal and nonisothermal melt crystallizations and also favors the ß-to-α phase transition of PBA upon annealing at elevated temperatures. This might be attributable to the decreased equilibrium melting temperature of PBA when T(IC,PVDF) is decreased. Higher T(IC,PVDF) is favorable for the fractional crystallization of PBA, which tends to segregate in the interlamellar regions of the PVDF matrix under these conditions. PBA shows faster enzymatic degradation in the blends with a lower T(IC,PVDF) than those with a higher T(IC,PVDF), attributable to the preferential formation of α crystals at a lower T(IC,PVDF). This study provides a new method to control the crystal modification and physical properties of polymorphic polymers in their blend systems.