scholarly journals Crystallization, Structures, and Properties of Different Polyolefins with Similar Grafting Degree of Maleic Anhydride

Polymers ◽  
2020 ◽  
Vol 12 (3) ◽  
pp. 675
Author(s):  
Ying Wang ◽  
Ying Shi ◽  
Wenjun Shao ◽  
Yi Ren ◽  
Wanyu Dong ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Maleic Anhydride ◽  
Lamellar Structure ◽  
Crystal Size ◽  
Mechanical And Thermal Properties ◽  
Elongation At Break ◽  
Long Period ◽  
Crystallization Ability ◽  
Structures And Properties ◽  
Grafting Degree

Maleic anhydride (MAH) grafting to different polyolefins with similar grafting degree can have different effects on crystallization, crystal structure, and mechanical and thermal properties. The grafting leads to a smaller crystal size, less ordered lamellar structure, and a shorter long period for HDPE, LLDPE, and PP. The grafting makes PP lamellar packing less ordered the most and almost no effect to LLDPE. The grafting does not have that much impact on the crystallization ability of the HDPE, LLDPE, and HDPE/PP blend, but appreciably reduces the crystalline ability of PP-g-MAH, due to a dramatical drop in its molecular weight during the grafting process. As a result, the grafting makes PP a very brittle material with a lowered average melting point than the corresponding neat PP, but the grafting has almost no effect on elongation at break for LLDPE and some effect on HDPE (decreased by one-third). However, the PP degradation due to MAH grafting can be avoided in the presence of PE component, i.e., making the grafting of PP and PE at the same time with HDPE/PP blend. The grafted HDPE/PP blend shows a significantly improved compatibility, which leads to overall appreciably better mechanical properties than the neat HDPE/PP blend.

scholarly journals Sericin cocoon bio-compatibilizer for reactive blending of thermoplastic cassava starch

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Thanongsak Chaiyaso ◽  
Pornchai Rachtanapun ◽  
Nanthicha Thajai ◽  
Krittameth Kiattipornpithak ◽  
Pensak Jantrawut ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Maleic Anhydride ◽  
Crystal Size ◽  
Thermoplastic Starch ◽  
Cassava Starch ◽  
Chain Extension ◽  
Amino Groups ◽  
Reactive Blending ◽  
Elongation At Break ◽  
Small Crystal Size

AbstractCassava starch was blended with glycerol to prepare thermoplastic starch (TPS). Thermoplastic starch was premixed with sericin (TPSS) by solution mixing and then melt-blended with polyethylene grafted maleic anhydride (PEMAH). The effect of sericin on the mechanical properties, morphology, thermal properties, rheology, and reaction mechanism was investigated. The tensile strength and elongation at break of the TPSS10/PEMAH blend were improved to 12.2 MPa and 100.4%, respectively. The TPS/PEMAH morphology presented polyethylene grafted maleic anhydride particles (2 μm) dispersed in the thermoplastic starch matrix, which decreased in size to approximately 200 nm when 5% sericin was used. The melting temperature of polyethylene grafted maleic anhydride (121 °C) decreased to 111 °C because of the small crystal size of the polyethylene grafted maleic anhydride phase. The viscosity of TPS/PEMAH increased with increasing sericin content because of the chain extension. Fourier-transform infrared spectroscopy confirmed the reaction between the amino groups of sericin and the maleic anhydride groups of polyethylene grafted maleic anhydride. This reaction reduced the interfacial tension between thermoplastic starch and polyethylene grafted maleic anhydride, which improved the compatibility, mechanical properties, and morphology of the blend.

scholarly journals Sericin cocoon bio-compatibilizer for reactive blending of thermoplastic cassava starch

2021 ◽  
Author(s):  
Thanongsak Chaiyaso ◽  
Pornchai Rachtanapun ◽  
Nanthicha Thajai ◽  
Krittameth kiattipronpithak ◽  
Pensak Jantrawut ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Maleic Anhydride ◽  
Crystal Size ◽  
Thermoplastic Starch ◽  
Cassava Starch ◽  
Chain Extension ◽  
Amino Groups ◽  
Reactive Blending ◽  
Elongation At Break ◽  
Small Crystal Size

Abstract Cassava starch was blended with glycerol to prepare thermoplastic starch (TPS). TPS was premixed with sericin (TPSS) by solution mixing and then melt-blended with polyethylene grafted maleic anhydride (PEMAH). The effect of sericin on the mechanical properties, morphology, thermal properties, rheology, and reaction mechanism was investigated. The tensile strength and elongation at break of the TPSS10/PEMAH blend were improved to 12.2 MPa and 100.4%, respectively. The TPS/PEMAH morphology presented PEMAH particles (2 µm) dispersed in the TPS matrix, which decreased in size to approximately 200 nm when 5% sericin was used. The melting temperature of PEMAH (121°C) decreased to 111°C because of the small crystal size of the PEMAH phase. The viscosity of TPS/PEMAH increased with increasing sericin content because of the chain extension. Fourier-transform infrared spectroscopy (FTIR) confirmed the reaction between the amino groups of sericin and the maleic anhydride groups of PEMAH. This reaction reduced the interfacial tension between TPS and PEMAH, which improved the compatibility, mechanical properties, and morphology of the blend.

Pengaruh Pendopingan Karbon Terhadap Struktur Kristal dan Morfologi TIO2

2019 ◽  
Vol 2 (2) ◽  
Author(s):  
Frastica Deswardani ◽  
Helga Dwi Fahyuan ◽  
Rimawanto Gultom ◽  
Eif Sparzinanda
Keyword(s):  
Thin Film ◽  
Crystal Structure ◽  
Grain Size ◽  
Tio2 Thin Film ◽  
Crystal Size ◽  
Diffraction Peak ◽  
Carbon Doping ◽  
Tio2 Anatase ◽  
Spray Method ◽  
Carbon Analysis

Telah dilakukan penelitian mengenai pengaruh konsentrasi doping karbon pada lapisan tipis TiO2 yang ditumbuhkan dengan metode spray terhadap struktur kristal dan morfologi TiO2. Hasil karakterisasi SEM menunjukkan bahwa penambahan doping karbon dapat meningkatkan ukuran butir. Lapisan TiO2 doping karbon 8% diperoleh ukuran butir terbesar adalah 1.35 μm, sedangkan ukuran tekecilnya adalah 0.45 μm. Sementara itu, untuk lapisan tipis TiO2 didoping karbon 15% memiliki ukuran butir terbesar yaitu 1.76 μm dan terkecil 0.9 μm. Hasil XRD menunjukkan seluruh puncak difraksi lapisan tipis TiO2 dengan doping karbon 8% dan 15% merupakan TiO2 anatase. Ukuran kristal lapisan TiO2 didoping karbon 8% diperoleh sebesar 638,08 Å dan untuk pendopingan 15% karbon ukuran kristal lapisan tipis TiO2 adalah 638,09 Å, hal ini menunjukkan ukuran kristal kedua sampel tidak mengalami perubahan yang signifikan.   TiO2 thin film with carbon doping has been successfully grown by spray method. The research on the effect of carbon doping on crystal structure and morfology of TiO2 has been prepared by varying carbon concentration (8% and 15% carbon). Analysis of SEM showed that the addition of carbon may increase the grain size. Thin film of TiO2 doped carbon 8% has the largest grain size 1.35 μm, while the smallest grain size is 0.45 μm. Meanwhile, for thin film TiO2 doped carbon 15% has the largest grain size 1.76 μm and smallest 0.9 μm. The XRD results showed the entire diffraction peak of thin film TiO2 doped carbon 8% and 15% were TiO2 anatase. The crystal size of thin film TiO2 doped carbon 8% was obtained at 638.08 Å and for thin film TiO2 doped carbon 15% the crystalline size of TiO2 thin film was 638.09 Å, this shows that the crystal size of both samples did not change significantly.    

Melting and Crystallization of Poly(oxyethylene) Mixtures

1995 ◽  
Vol 60 (11) ◽  
pp. 1855-1868 ◽  
Author(s):  
Ivo Lapeš ◽  
Josef Baldrian ◽  
Ján Biroš ◽  
Julius Pouchlý ◽  
Hanes Mio
Keyword(s):  
Melting Point ◽  
Lamellar Structure ◽  
Composition Dependence ◽  
Eutectic Phase ◽  
Eutectic Melting ◽  
Pure Polymer ◽  
X Ray ◽  
Long Period ◽  
Solid Liquid ◽  
Melting And Crystallization

Solid-liquid eutectic phase diagrams of mixtures of poly(oxyethylene) (M.w. 2 000) with hydroxy and methoxy endgroups, crystallizing in extended-chain macroconformation only, with glutaric acid, benzoic acid or 1,2-diphenylethane are given. The composition dependence of the melting temperature can be fitted by the Flory-Huggins equation. Interaction parameters X and interaction energy densities B evaluated from the diluent branch of the phase diagram are consistent with those obtained from the polymer branch provided the calorimetric value of enthalpy of polymer fusion is used in the latter computation. Measurements of small- and wide-angle X-ray scatterings showed a stacked lamellar structure of POE. Below the eutectic melting point, the long period of the polymer is almost independent of the diluent concentration. On raising temperature gradually from this melting point to the melting point of pure polymer, the increasing long period indicates the penetration of the diluent between the lamellae. As follows from SAXS measurements, the crystallinity of poly(oxyethylene) in the mixtures remains unchanged compared to that of the pure polymer.

scholarly journals Study on the Electrical, Structural, Chemical and Optical Properties of PVD Ta(N) Films Deposited with Different N2 Flow Rates

Coatings ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 937
Author(s):  
Yingying Hu ◽  
Md Rasadujjaman ◽  
Yanrong Wang ◽  
Jing Zhang ◽  
Jiang Yan ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Optical Properties ◽  
Photoelectron Spectroscopy ◽  
Crystal Size ◽  
Silicon Substrates ◽  
X Ray Diffraction ◽  
Dc Magnetron Sputtering ◽  
Flow Rates ◽  
X Ray ◽  
N2 Flow Rate

By reactive DC magnetron sputtering from a pure Ta target onto silicon substrates, Ta(N) films were prepared with different N2 flow rates of 0, 12, 17, 25, 38, and 58 sccm. The effects of N2 flow rate on the electrical properties, crystal structure, elemental composition, and optical properties of Ta(N) were studied. These properties were characterized by the four-probe method, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and spectroscopic ellipsometry (SE). Results show that the deposition rate decreases with an increase of N2 flows. Furthermore, as resistivity increases, the crystal size decreases, the crystal structure transitions from β-Ta to TaN(111), and finally becomes the N-rich phase Ta3N5(130, 040). Studying the optical properties, it is found that there are differences in the refractive index (n) and extinction coefficient (k) of Ta(N) with different thicknesses and different N2 flow rates, depending on the crystal size and crystal phase structure.

scholarly journals Structure and Properties of Polyoxymethylene/Silver/Maleic Anhydride-Grafted Polyolefin Elastomer Ternary Nanocomposites

Polymers ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 1954
Author(s):  
Yang Liu ◽  
Xun Zhang ◽  
Quanxin Gao ◽  
Hongliang Huang ◽  
Yongli Liu ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Thermal Stability ◽  
Maleic Anhydride ◽  
Ag Nanoparticles ◽  
Decomposition Temperature ◽  
Melt Mixing ◽  
Elongation At Break ◽  
Maximum Value ◽  
Polyolefin Elastomer ◽  
Local Defects

In the present study, silver (Ag) nanoparticles and maleic anhydride-grafted polyolefin elastomer (MAH-g-POE) were used as enhancement additives to improve the performance of the polyoxymethylene (POM) homopolymer. Specifically, the POM/Ag/MAH-g-POE ternary nanocomposites with varying Ag nanoparticles and MAH-g-POE contents were prepared by a melt mixing method. The effects of the additives on the microstructure, thermal stability, crystallization behavior, mechanical properties, and dynamic mechanical thermal properties of the ternary nanocomposites were studied. It was found that the MAH-g-POE played a role in the bridging of the Ag nanoparticles and POM matrix and improved the interfacial adhesion between the Ag nanoparticles and POM matrix, owing to the good compatibility between Ag/MAH-g-POE and the POM matrix. Moreover, it was found that the combined addition of Ag nanoparticles and MAH-g-POE significantly enhanced the thermal stability, crystallization properties, and mechanical properties of the POM/Ag/MAH-g-POE ternary nanocomposites. When the Ag/MAH-g-POE content was 1 wt.%, the tensile strength reached the maximum value of 54.78 MPa. In addition, when the Ag/MAH-g-POE content increased to 15wt.%, the elongation at break reached the maximum value of 64.02%. However, when the Ag/MAH-g-POE content further increased to 20 wt.%, the elongation at break decreased again, which could be attributed to the aggregation of excessive Ag nanoparticles forming local defects in the POM/Ag/MAH-g-POE ternary nanocomposites. Furthermore, when the Ag/MAH-g-POE content was 20 wt.%, the maximum decomposition temperature of POM/Ag/MAH-g-POE ternary nanocomposites was 398.22 °C, which was 71.39 °C higher than that of pure POM. However, compared with POM, the storage modulus of POM/Ag/MAH-g-POE ternary nanocomposites decreased with the Ag/MAH-g-POE content, because the MAH-g-POE elastomer could reduce the rigidity of POM.

Influence of Mineralogical Origin of Limestone Powder on the Performance of Complex Binder Material

2011 ◽  
Vol 477 ◽  
pp. 136-141
Author(s):  
Qin Wang ◽  
Jia Long Chen ◽  
Chang Cheng Zhang ◽  
Wei Niu
Keyword(s):  
Crystal Structure ◽  
Clay Mineral ◽  
Lamellar Structure ◽  
Perfect Crystal ◽  
Limestone Powder ◽  
Elemental Component ◽  
Binder Material ◽  
Complex Binder ◽  
Main Components ◽  
Perfect Crystal Structure

The effect of mineralogical origin, elemental component, crystal structure of three types of limestone powder on the fluidity of cement-limestone paste and mortar was investigated. The results show that the limestone powder originated from the mine of limestone and river pebble have better water-reducing effect, which is closely correlated with the main components of Calcite and Dolomite. These two mineral have relatively regular, orderly and perfect crystal structure with few defects and unfilled pores which are liable to adsorb more water and water-reducing agents. On the contrary, the limestone powder derived from the mine of sandstone has nearly no water-reducing effect which is ascribed to the large amount of clay mineral which exhibit lamellar structure leading to the large quantity of consumption of water.

The crystal structure of maleic anhydride

1962 ◽  
Vol 15 (1) ◽  
pp. 35-41 ◽  
Author(s):  
R. E. Marsh ◽  
E. Ubell ◽  
H. E. Wilcox
Keyword(s):  
Crystal Structure ◽  
Maleic Anhydride

Self-Extinguishing and Non-Drip Flame Retardant Polyamide 6 Nanocomposite: Mechanical, Thermal, and Combustion Behavior

2018 ◽  
Vol 1 (1) ◽  
pp. 1-13 ◽  
Author(s):  
Hao Wu ◽  
Rogelio Ortiz ◽  
Renan De Azevedo Correa ◽  
Mourad Krifa ◽  
Joseph H. Koo
Keyword(s):  
Maleic Anhydride ◽  
Flame Retardant ◽  
Polymer Matrix ◽  
Flame Retardants ◽  
Polyamide 6 ◽  
Twin Screw Extrusion ◽  
Elongation At Break ◽  
Combustion Behavior ◽  
Screw Extrusion ◽  
Twin Screw

AbstractIncorporation of flame-retardant (FR) additives and nanoclay fillers into thermoplastic polymers effectively suppresses materials flammability and melt dripping behavior. However, it largely affects other properties, such as toughness and ductility. In order to recover the lost toughness and ductility of flame retardant polyamide 6, various loadings of maleic anhydride modified SEBS elastomer were added and processed by twin screw extrusion. TEM images showed exfoliated nanoclay platelets and reveals that the clay platelets well dispersed in the polymer matrix. By balancing the ratio of flame retardants, nanoclay and elastomers, formulation with elongation at break as high as 76% was achieved. Combining conventional intumescent FR and nanoclay, UL-94 V-0 rating and the LOI value as high as 32.2 were achieved. In conclusion, effective self-extinguishing and non-drip polyamide 6 nanocomposite formulations with significant improvement in toughness and ductility were achieved.

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