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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.
Antifungal Activities of Anthocyanins from Purple Sweet Potato in the Presence of Food Preservatives
Huiliang Wen,Jingjing Kang,Dandan Li,Wen Wen,Fubin Yang,Haiwei Hu,Chongbo Liu 한국식품과학회 2016 Food Science and Biotechnology Vol.25 No.1
Effects of anthocyanins from purple sweet potato (APSP) against the fungal growth of Geotrichum candidum and Candida albicans were assessed. Response surface methodology was applied for optimization of proportions of sodium benzoate, potassium sorbate, and APSP. Optimum concentrations against G. candidum were 0.300 mg/mL of sodium benzoate, 0.290mg/mL of potassium sorbate, and 13.9mg/mL of APSP. Optimum concentrations against C. albicans were 0.380 mg/mL of sodium benzoate, 0.240 mg/mL of potassium sorbate, and 3.56 mg/mL of APSP. APSP exhibited enhanced antifungal properties in the presence of food preservatives.
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.
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.
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.
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.
Wang, Yingfeng,Guo, Han,Harbuzaru, Alexandra,Uddin, Mohammad Afsar,Arrechea-Marcos, Iratxe,Ling, Shaohua,Yu, Jianwei,Tang, Yumin,Sun, Huiliang,Ló,pez Navarrete, Juan Teodomiro,Ortiz, Rocio Ponce American Chemical Society 2018 JOURNAL OF THE AMERICAN CHEMICAL SOCIETY - Vol.140 No.19
<P>Development of high-performance unipolar n-type organic semiconductors still remains as a great challenge. In this work, all-acceptor bithiophene imide-based ladder-type small molecules BTI<I>n</I> and semiladder-type homopolymers PBTI<I>n</I> (<I>n</I> = 1-5) were synthesized, and their structure-property correlations were studied in depth. It was found that Pd-catalyzed Stille coupling is superior to Ni-mediated Yamamoto coupling to produce polymers with higher molecular weight and improved polymer quality, thus leading to greatly increased electron mobility (μ<SUB>e</SUB>). Due to their all-acceptor backbone, these polymers all exhibit unipolar n-type transport in organic thin-film transistors, accompanied by low off-currents (10<SUP>-10</SUP>-10<SUP>-9</SUP> A), large on/off current ratios (10<SUP>6</SUP>), and small threshold voltages (∼15-25 V). The highest μ<SUB>e</SUB>, up to 3.71 cm<SUP>2</SUP> V<SUP>-1</SUP> s<SUP>-1</SUP>, is attained from PBTI1 with the shortest monomer unit. As the monomer size is extended, the μ<SUB>e</SUB> drops by 2 orders to 0.014 cm<SUP>2</SUP> V<SUP>-1</SUP> s<SUP>-1</SUP> for PBTI5. This monotonic decrease of μ<SUB>e</SUB> was also observed in their homologous BTI<I>n</I> small molecules. This trend of mobility decrease is in good agreement with the evolvement of disordered phases within the film, as revealed by Raman spectroscopy and X-ray diffraction measurements. The extension of the ladder-type building blocks appears to have a large impact on the motion freedom of the building blocks and the polymer chains during film formation, thus negatively affecting film morphology and charge carrier mobility. The result indicates that synthesizing building blocks with more extended ladder-type backbone does not necessarily lead to improved mobilities. This study marks a significant advance in the performance of all-acceptor-type polymers as unipolar electron transporting materials and provides useful guidelines for further development of (semi)ladder-type molecular and polymeric semiconductors for applications in organic electronics.</P> [FIG OMISSION]</BR>
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.