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Huiliang Zhang,Yan Zhao 한국화학공학회 2016 Korean Journal of Chemical Engineering Vol.33 No.3
Poly(lactic acid) (PLA)/poly(ethylene octene) grafted with glycidyl methacrylate (POE-g-GMA denoted as GPOE) blends were prepared via simple melt compounding method at GPOE loadings from 5 to 20wt%. GPOE can significantly affect the physical properties of PLA. Compared to neat PLA, the elongation at break and impact strength of the blends were significantly improved. Scanning electron micrograph analysis revealed large numbers of cavities in the fracture surface of the blends, and the size of the cavities increased along with the increase of GPOE content in the PLA/GPOE blends. Furthermore, the overall crystallization rates were faster in the PLA/GPOE blends than that in neat PLA. However, the crystallization mechanism and crystal structure of these blends remained unchanged despite the presence of GPOE. The addition of GPOE decreased the degree of crystallinity of PLA. The toughened PLA could be of great use and importance for wider practical applications.
Ye Zhang,Yan Zhao,Hongwei Pan,Xianzhong Lang,Huili Yang,Huiliang Zhang,Huixuan Zhang,Lisong Dong 한국고분자학회 2016 폴리머 Vol.40 No.3
Polylactide (PLA) was plasticized with poly(diethylene glycol adipate) (PDEGA). The plasticized PLA was further blended with core-shell structured particles of glycidyl methacrylate-functionalized methyl methacrylate-butyl acrylate copolymer (GACR) using a twin-screw extruder, and the extruded samples were blown using the blown thin film technique. Both PDEGA and GACR significantly influenced the physical properties of the films. Compared to neat PLA, the elongation at break and tear strength of the films were significantly improved. The shear yielding induced by cavitation of GACR particles was the major tearing mechanism. GACR could act as a tear resistance modifier for PLA blown films. The spherulite size of the PLA/PDEGA/GACR films decreased with the addition of GACR. The biodegradability of the PLA/PDEGA/GACR films decreased slightly. These findings contributed new knowledge to the additive area and gave important implications for designing and manufacturing polymer packaging materials.
Ye Zhang,Shiling Jia,Pan Hongwei,Lijuan Wang,Junjia Bian,Yang Guan,Bohao Li,Huiliang Zhang,Huili Yang,Lisong Dong 한국화학공학회 2021 Korean Journal of Chemical Engineering Vol.38 No.8
A series of poly(lactic acid) (PLA), poly(butylene adipate-co-terephthalate) (PBAT) and glycidyl methacrylate- grafted poly(ethylene octene) (GPOE) blends and films with different GPOE content were prepared by melt blending and blowing film technique. The effect of GPOE on the rheological behavior, melt strength, crystallization behavior, crystallization morphology, miscibility, mechanical property, phase morphology, thermal stability and water vapor permeability were studied. The addition of GPOE improved melt rheological properties. Results of DSC showed that addition of GPOE encouraged the mobility of PLA molecular chains and enhanced crystalline ability. POM observations revealed that the addition of GPOE made the density of spherulite nucleation increase and the size of crystalline particles decrease. From DMA and SEM analysis, it was demonstrated that PLA/PBAT blend was an immiscible system and GPOE in the blend could improve compatibility between PLA and PBAT. Results of mechanical test showed that the PLA/PBAT/GPOE blends and films obtained had excellent mechanical properties. The elongation at break of 50/30/ 20 w/w/w PLA/PBAT/GPOE blend (477%) was higher by about 2.2 times than that of 70/30/0 w/w/w PLA/PBAT/ GPOE blend (220%). The tensile strength of all the PLA/PBAT/GPOE blends exceeded 31 MPa. The tensile strength reached 32.9MPa (MD) and 22.5MPa (TD), the elongation at break exceeded 210% and tear strength exceeded 140 kN/m for 50/30/20 w/w/w PLA/PBAT/GPOE film. With increasing GPOE content, thermal stability and water vapor barrier property also improved.
Feng, Kui,Zhang, Xianhe,Wu, Ziang,Shi, Yongqiang,Su, Mengyao,Yang, Kun,Wang, Yang,Sun, Huiliang,Min, Jie,Zhang, Yujie,Cheng, Xing,Woo, Han Young,Guo, Xugang American Chemical Society 2019 ACS APPLIED MATERIALS & INTERFACES Vol.11 No.39
<P>Imide functionalization is one of the most effective approaches to develop electron-deficient building blocks for constructing n-type organic semiconductors. Driven by the attractive properties of imide-functionalized dithienylbenzodiimide (TBDI) and the promising device performance of TBDI-based polymers, a novel acceptor with increased electron affinity, fluorinated dithienylbenzodiimide (TFBDI), was designed with the hydrogen replaced by fluorine on the benzene core, and the synthetic challenges associated with this highly electron-deficient fluorinated imide building block are successfully overcome. TFBDI showed suppressed frontier molecular orbital energy levels as compared with TBDI. Copolymerizing this new electron-withdrawing TBDI with various donor co-units afforded a series of n-type polymer semiconductors TFBDI-T, TFBDI-Se, and TFBDI-BSe. All these TFBDI-based polymers exhibited a lower-lying lowest unoccupied molecular orbital (LUMO) energy level than the polymer analogue without fluorine. When applied in organic thin-film transistors, three polymers showed unipolar electron transport with large on-current/off-current ratios (<I>I</I><SUB>on</SUB>/<I>I</I><SUB>off</SUB>) of 10<SUP>5</SUP>-10<SUP>7</SUP>. Among them, the selenophene-based polymer TFBDI-Se with the deepest-positioned LUMO and optimal chain stacking exhibited the highest electron mobility of 0.30 cm<SUP>2</SUP> V<SUP>-1</SUP> s<SUP>-1</SUP>. This result demonstrates that the new TFBDI is a highly attractive electron-deficient unit for enabling n-type polymer semiconductors, and the fluorination of imide-functionalized arenes offers an effective approach to develop more electron-deficient building blocks in organic electronics.</P> [FIG OMISSION]</BR>
Yanping Hao,Huili Yang,Huiliang Zhang,Zhishen Mo 한국섬유공학회 2018 Fibers and polymers Vol.19 No.1
Blends of poly(butylene terephthalate) (PBT)/thermoplastic polyurethane (TPU) were prepared by melt compounding. The miscibility, crystallization behaviors and toughening mechanism of the PBT/TPU blends were studied. Dynamic mechanical analysis results demonstrated that PBT was immiscible with TPU. Differential scanning calorimetry and wide angle X-ray diffraction results showed that the crystallinity of PBT decreased with increasing TPU content. Furthermore, blending with TPU did not modify the crystal structure of PBT. The small angle X-ray scattering resultsindicated that the crystal layer thickness decreased and the amorphous layer thickness increased with increasing TPU content, indicating that TPU mainly resided in the interlamellar region of PBT spherulites in the blends. An obvious improvement in toughness of PBT was achieved with addition of TPU. Neat PBT had elongation at break and impact strength of about 15 %and 2.9 kJ/m2, respectively. However, the elongation at break and impact strength of the 70/30 PBT/TPU blend reached 410 % and 62.9 kJ/m2, respectively. The morphology of the PBT/TPU blends after tensile and impact tests was investigated, and the corresponding toughening mechanism is discussed. It was found that the PBT showed obvious shear yielding in theblend during the tensile and impact tests, which induced dissipation of energy and, therefore, led to the improvement in toughness of the PBT/TPU blends.
Yanping Hao,Yi Li,Zhigang Liu,Xiangyu Yan,Yi Tong,Huiliang Zhang 한국섬유공학회 2019 Fibers and polymers Vol.20 No.9
In this study, polyaryl polymethylene isocyanate (PAPI) was used as a chain extender for poly(lactic acid) (PLA)to produce a high molecular weight material with better rheological, thermal and mechanical properties. The reactionbetween PLA chains and PAPI was proved by FTIR during reactive blending. The results showed that the molecular weightand molecular weight distribution were increased with the addition of PAPI content due to the chain extension. Chainextension was also responsible for the increased modulus and complex viscosity. The glass transition temperature (Tg) andthermal stability increased by incorporating with PAPI. The results of mechanical properties showed that a considerablyhigher tensile strength and Young’s modulus of the reactive blends compared with neat PLA.
Yan Zhao,Hongyu Liang,Dandan Wu,Junjia Bian,Yanping Hao,Guibao Zhang,Sanrong Liu,Huiliang Zhang,Lisong Dong 한국고분자학회 2015 폴리머 Vol.39 No.2
Poly(1,2-propylene glycol adipate) (PPA) was used as an environmentally friendly plasticizer in flexible poly(vinyl chloride) (PVC). Thermal, mechanical, and rheological properties of the PVC/PPA blends were characterized by differential scanning calorimetry, dynamic mechanical analysis, tensile test, scanning electron microscopy and small amplitude oscillatory shear rheometry. The results showed that PPA lowered the glass transition temperature of PVC. The introduction of PPA could decrease tensile strength and Young’s modulus of the PVC/PPA blends; however, elongationat-break was dramatically increased due to the plastic deformation. The plasticization effect of PPA was also manifested by the decrease of dynamic storage modulus and viscosity in the melt state of the blends. The results indicated that PPA had a good plasticizing effect on PVC.
Hongwei Pan,Yanping Hao,Yan Zhao,Xianzhong Lang,Ye Zhang,Zhe Wang,Huiliang Zhang,Lisong Dong 한국화학공학회 2017 Korean Journal of Chemical Engineering Vol.34 No.5
Poly(butylene adipate-co-terephthalate) (PBAT) was blended with poly(propylene carbonate) (PPC) by a twin screw extruder and then the blends were made onto films via the blown film technique. PPC dispersed uniformly in the PBAT matrix, and the glass transition temperature (Tg) of PBAT were decreased with the increasing content of PPC. Wide angle X-ray diffraction confirmed that the crystallite dimension of PBAT was decreased after blending PBAT with the amorphous PPC. The results of mechanical tests indicated that the PBAT/PPC films showed high tensile strength and tear strength. In addition, the PBAT/PPC films showed high carbon dioxide permeability and moderate oxygen and nitrogen permeability. After embedding in soil, the weight loss and mechanical properties analysis demonstrated that the films were remarkably biodegraded. These findings contributed to application of the biodegradable materials, such as design and manufacture polymer packaging.