Practical Application of ±250‐kV DC‐XLPE Cable for Hokkaido–Honshu HVDC Link

The long‐term dc properties of DC‐XLPE insulation materials, which have been developed for dc use, were investigated. It was found that the lifetime of DC‐XLPE under dc voltage application is extended by the addition of nano‐sized filler. The time dependence of the space charge distribution at 50 kV/mm was observed for 7 days. Almost no accumulation of space charge in DC‐XLPE was found. The 250‐kV DC‐XLPE cables and accessories were manufactured and subjected to a type test and PQ test for use in the Hokkaido–Honshu dc link facility owned by the Electric Power Development Co., Ltd. These tests were performed under conditions that included a polarity reversal test for line commutated converter (LCC) systems as recommended in CIGRE TB 219. The test temperature was 90 °C. The type test and PQ test were successfully completed. The DC‐XLPE cable and accessories were installed in summer 2012 for the Hokkaido–Honshu dc link. After the installation of the dc extruded cable system, a dc high‐voltage test at 362.5 kV (=1.45 PU) for 15 min was successfully completed in accordance with CIGRE TB 219. This dc extruded cable system was put into operation in December 2012 as the world's highest‐voltage extruded dc cable in service and the world's first dc extruded cable for a LCC system including polarity reversal operation.     

多乙烯多胺桥联受阻酚类抗氧剂的合成及其清除DPPH·性能

以二乙烯三胺和三乙烯四胺为桥联基，β-(3,5-二叔丁基-4-羟基苯基)丙酰氯为抗氧化功能基团，通过酰胺化缩合反应合成了两类具有不同对位桥联基团的受阻酚类抗氧剂。采用傅里叶红外光谱和核磁共振氢谱证实了合成的多乙烯多胺桥联受阻酚类抗氧剂的化学结构。DPPH法研究了多乙烯多胺桥联受阻酚类抗氧剂清除自由基的性能，并探索了酚羟基个数和对位桥联基结构对受阻酚类抗氧剂清除自由基性能的影响。结果表明，多乙烯多胺桥联受阻酚类抗氧剂具有良好的清除DPPH·能力，且随着抗氧剂分子中酚羟基个数的增加，清除DPPH·的活性增加，分子中含有4个酚羟基的三乙烯四胺受阻酚类抗氧剂的抗氧化效率（AE）达到2.65×10^-2 L/(mol·s)。对位桥联基结构对受阻酚类抗氧剂清除DPPH·能力有较大影响，季戊四醇为桥联基的受阻酚类抗氧剂1010清除DPPH·能力最强，其抗氧化效率（AE）为3.08×10^-2L/(mol·s)；乙二胺为核的1.0代树枝状受阻酚类抗氧剂清除DPPH·能力最弱，其抗氧化效率（AE）为2.60×10^-2 L/(mol·s)。     

Comparative study of wear performance of particulate and fiber-reinforced nano-ZnO/ultra-high molecular weight polyethylene hybrid composites using response surface methodology

The effects of two types of filler reinforcements i.e. particulate (talc particles) and fiber (Glass Fiber (GF)) as secondary reinforcements in ultra-high molecular weight polyethylene (UHMWPE)-based composites on the wear and friction properties were discussed in this paper. These UHMWPE hybrid composites were fabricated by the addition of 10 wt% of talc and glass fiber at a fixed nano-ZnO loading of 10 wt% using a hot compression moulding technique. The wear and friction properties of these hybrid composites were investigated using a pin-on-disc tester with different operating conditions of applied loads, sliding speeds and sliding distances based on response surface Box–Behnken design. Response Surface Methodology (RSM) was applied to model the effects of various variables of applied load, sliding speed and distance on the wear volume loss and average coefficient of friction (COF) of UHMWPE hybrid composites. The mathematical regression models of the wear volume and average COF were derived from the analysis of variance (ANOVA). Optimization of the independent variables to minimize the wear and friction responses of both UHMWPE composites was estimated using RSM. The mathematical models showed that applied load, sliding speed and distance have significant effects on the wear and friction properties of both UHMWPE composites in the tested range of variables. The most significant, in order of the variables that affect the volume loss and friction of UHMWPE composites is load, followed by sliding distance and speed. In addition, the combined effects of load and distance indicate the highest significance on volume loss and average COF for both UHMWPE hybrid composites as compared to other variable interactions. GF/ZnO/UHMWPE exhibited better wear performance compared to talc/ZnO/UHMWPE hybrid composites. The severity of worn surfaces of the GF/ZnO/UHMWPE was less than that of talc/ZnO/UHMWPE. The GF/ZnO/UHMWPE produced transfer films that were more uniform and had better coverage compared to talc/ZnO/UHMWPE.     

In situ fibre‐reinforced composite films of poly(lactic acid)/low‐density polyethylene blends: effects of composition on morphology,transport and mechanical properties

This study aimed to investigate the effects of blend composition on packaging‐related properties of poly(lactic acid) (PLA) and low density polyethylene (LDPE) blown films. Blend films with PLA contents of 5–20 wt% were produced and compared. Scanning electron micrographs of cross‐sectional cryofractured surfaces of the blend films revealed that in situ fibre‐reinforced composites were obtained. Viscosity ratio of the polymer components of ca 1 confirmed that fibre formation was favourable for this blend system. PLA microdomains were dispersed throughout the film in forms of long fibres (length‐to‐diameter ratio > 100) and ribbons. The number of fibres and ribbons increased with an increase of PLA content. Critical content of PLA was found to be 20 wt% for effective improvement of both moduli and gas barrier properties. Incorporation of poly[ethylene‐co‐(methyl acrylate)] compatibilizer showed minimal effect on PLA structure. However, it did improve moduli and O₂ barrier properties when sufficient amount (1.5 pph) was used in 10 wt% PLA/LDPE. In short, flow behaviour, ratio of polymer components and degree of compatibility together played intricate roles in the morphology and hence mechanical and transport properties of PLA/LDPE immiscible blends. © 2017 Society of Chemical Industry     

LDPE装置循环水节约实例研究

文中详细介绍了在高压低密度聚乙烯（LDPE）装置中用热水罐外排污水替代紧急放空塔循环水溢流的做法,探索了节水降耗、清洁生产的经验。     

Injectable polyethylene glycol-laponite composite hydrogels as articular cartilage scaffolds with superior mechanical and rheological properties

In this study, injectable PEG-based hydrogels containing Laponite particles with mechanical and structural properties close to the natural articular cartilage are introduced. The nanocomposites are fabricated by imide ring opening reactions utilizing synthesized copolymers containing PEG blocks and nanoclay through a two-step thermal poly-(amic acid) process. Butane diamine is used as nucleophilic reagent and hydrogels with interconnected pores with sizes in the range of 100–250?µm are prepared. Improved viscoelastic properties compared with the conventional PEG hydrogels are shown. Evaluation of cell viability utilizing human mesenchymal stem cells determines cytocompatibility of the nanocomposite hydrogels.     

Effects of annealing on the hierarchical crystalline structures and mechanical properties of injection‐molded bars of high‐density polyethylene

The effect of annealing on the microstructural evolution and mechanical properties of high‐density polyethylene parts molded via gas‐assisted injection molding was investigated using scanning electron microscopy, differential scanning calorimetry, two‐dimensional wide‐angle X‐ray diffraction and tensile testing. The results indicated that a variety of annealing temperatures could induce considerable variations in the hierarchical structures, crystallinity, lamellar thickness and yield stress of the molded bars. According to these results, the annealing temperatures could be divided into three regions. In the low‐temperature region of annealing at 80 °C, the spatial variation of the superstructure developed along the thickness direction and mechanical properties of the annealed sample were mainly unchanged and similar to those of the original specimen. At 100 and 120 °C, the intermediate temperature region of annealing, the thickness of the crystals, degree of orientation and yield stress of annealed samples were greatly improved. Finally, at 127 °C, the degree of orientation decreased and yield stress slightly improved, an indication of the high‐temperature annealing region being characterized by increasing melting/recrystallization and causing relaxation of oriented molecular chains. A model is proposed to interpret the mechanism of the annealing treatment of the samples at various temperatures. © 2013 Society of Chemical Industry