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JOURNAL OF SOLID STATE CHEMISTRY · 2021 · IF 3.498

Crystallization behavior of boron in low-temperature immobilization of iodine waste

Yaxin Feng,Guilin Wei,Yi Liu,Wenhong Han,Yan Chen,Runjie Sun,Lin Peng,Meihua Ma,Yu Zhang,Zhentao Zhang,Xirui Lu

The immobilization of iodine waste is a challenge in the field of nuclear waste . In this work, iodine waste (silver-coated silica gel with different iodine loadings) was immobilized at low-sintering temperatures (500, 550, and 600 ​°C). XRD represented that the crystallized phases of the sintered matrix consist of AgI and B 2 O 3 . The crystallization behavior of boron can be found as the sintering temperature increased from 500 ​°C to 600 ​°C. FT-IR results proved that in the process of crystallization, part of the microstructure related to B–O stretching transformed from [BO 4 ] to [BO 3 ] units, which benefits low-temperature iodine waste immobilization due to the bonding energy of [BO 3 ] is higher than that of [BO 4 ]. Our work reveals the B-related microstructure transition in low-temperature immobilization iodine waste.

研究领域: 核废物处理 · 材料科学 · 无机化学 · 放射化学 · 环境工程
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF POLYMER SCIENCE · 2015 ·Vol. 33 ·期 7 ·976-987 · IF 1.835

Enhanced ultraviolet resistance of polypropylene random copolymer filled by ZnO-supported mesoporous zeolite

Li Mei,Li Gu,Zhang Zi-shou,Dai Xin,Yang Yue-wen,Mai Kan-cheng

To enhance the ultraviolet resistance of ZnO based polymer materials, ZnO-supported mesoporous zeolite (M-ZnO) was prepared and characterized by atomic absorption spectroscopy and scanning electron microscopy. The ultraviolet resistance, crystallization behavior and melting characteristics of ZnO and M-ZnO filled PPR composites were compared by FTIR spectra and differential scanning calorimetry. The ultraviolet resistance of M-ZnO filled PPR composites is higher than that of ZnO filled PPR composites, indicating higher ultraviolet resistance of M-ZnO than that of ZnO. The crystallization temperatures of mesoporous zeolite filled PPR were higher than those of M-ZnO and decreased with increasing UV-irradiation time. But the crystallization temperatures of M-ZnO filled PPR composites were not influenced by UV-irradiation time. The ZnO supported on the surface of zeolite is effective in enhancing the ultraviolet resistance of ZnO based polymer materials.

研究领域: 高分子材料科学 · 功能复合材料 · 材料老化与稳定性 · 纳米复合材料 · 聚合物改性
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2017 ·Vol. 29 ·期 2 ·982-988 · IF 1.907

Quadruple-shape-memory effect of TPI/LDPE/HDPE composites

Jiayu Xian,Jieting Geng,Yan Wang,Lin Xia

Shape-memory polymers are important smart materials with potential applications in smart textiles, medical devices, and sensors. We prepared trans-1,4-polyisoprene, low-density polyethylene (LDPE), and high-density polyethylene (HDPE) shape-memory composites using a simple mechanical blend method. The mechanical, thermal, and shape-memory properties of the composites were studied. Our results showed that the shape-memory composites could memorize 3 temporary shapes, as revealed by the presence of broad melting transition peaks in the differential scanning calorimetry curves. In the trans-1,4-polyisoprene/LDPE/HDPE composites, the cross-linked network and the crystallization of the LDPE and HDPE portions can serve as fixed domains, and all crystallizations can act as reversible domains. We proposed a schematic diagram to explain the vital role of the cross-linked network and the crystallization in the shape-memory process.

研究领域: 高分子材料科学 · 生物医学工程 · 智能材料 · 功能高分子 · 热响应材料
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2018 · IF 5.091

Crystallization and properties of poly(ethylene terephthalate)/layered double hydroxide nanocomposites

Siyuan Dong,Yingqi Jia,Xiaozhi Xu,Jianeng Luo,Jingbin Han,Xiaoli Sun

Poly(ethylene terephthalate) (PET) generally suffers from low crystallization rate and long molding duration, which as a result limit its application as engineering plastics. To overcome these drawbacks, series of PET/layered double hydroxide (LDH) nanocomposites were prepared by a solution blending process. The effect of metal composition (MgAl and CaAl) and organo-modification (stearic acid intercalated) for LDH fillers on the crystallization behavior of the nanocomposites was investigated. It was revealed that, compared with PET/CaAl-LDH, the PET/MgAl-LDH nanocomposite exhibits a higher crystallization temperature and faster crystallization rate, which is associated with the superior nucleation ability of MgAl-LDH. The nucleation mechanism of PET induced by LDHs was explored by means of Avrami equation and theory of Hoffman-Lauritzen, pointing out that the incorporation of LDHs reduce the free energy of nucleation and the fold surface free energy of PET. In order to improve the compatibility between LDH and PET, stearic acid (SA) intercalated MgAl-LDH was prepared and filled into PET matrix. The resultant PET/MgAl-LDH-SA shows a further enhanced crystallization temperature and accelerated crystallization rate, in comparison with PET/MgAl-LDH nanocomposites. In addition, the thermal stability, gas barrier and mechanical properties of PET/LDH composites were improved upon incorporation of LDH fillers.

研究领域: 高分子科学 · 材料化学 · 纳米复合材料 · 结晶动力学 · 聚合物物理 · 功能材料 · 工程塑料
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