Study on Deterioration Characteristics of a Composite Crossarm Mandrel in a 10 kV Distribution Network Based on Multi-Factor Aging.

This paper presents a study that conducted 5000 h of multi-factor aging tests on 10 kV composite crossarms, considering the natural environment in coastal areas and actual power line operations. Various aging conditions, such as voltage, rain, temperature, humidity, salt fog, ultraviolet light, and mechanical stress, were applied during the tests. The research initially analyzed the influence of multi-factor aging on the bending and tensile properties of the full-size composite crossarm. Subsequently, a detailed investigation was carried out to assess the impact of aging on the mechanical properties, electrical insulation properties, and microscopic characteristics of the composite crossarm core bar. Results indicated that the tensile strength and bending strength of the full-size composite crossarm mandrel experienced minimal changes after aging, remaining well within operational requirements. However, the silicone rubber outer sheath's hydrophobicity decreased, leading to the appearance of cracks and holes on the surface, which provided pathways for moisture and salt infiltration into the mandrel. As a consequence, the bending strength and shear strength of the mandrel material were reduced by 16.5% and 37.7%, respectively. Moreover, the electrical performance test demonstrated a slight change in the mandrel's leakage current, while the electrical breakdown strength decreased by 22.8%. Microscopic analysis using SEM, three-dimensional CT, and TGA revealed that a small amount of resin matrix decomposed and microcracks appeared on the surface. Additionally, the fiber-matrix interface experienced debonding and cracking, leading to an increased moisture absorption rate of the mandrel material.

Study on Blending Modification of Bisphenol A Epoxy.

Epoxy-resin-based composites in the field of current electrical materials often work in high temperature, high humidity or salt spray conditions. In order to improve the operation reliability of the composite insulator cross arm in a high temperature, high humidity and high salt spray environment, and analyze the aging mechanism and performance characteristics of resin, in this paper, wet heat aging and salt spray aging experiments were carried out on the blended resin system composed of bisphenol A type epoxy resin (E-51), aliphatic epoxy modified bisphenol A epoxy resin (2021P/E-51) and dimeric acid modified bisphenol A epoxy resin (EPD-172/E-51). Among them, 10 wt% and 20 wt% of 2021P blend resin and 10 wt% of EPD blend resin have superior thermo-mechanical properties. Under humid and hot conditions, the dielectric loss of 10 wt% EPD blend system before and after aging is 39.9% and 49.5% lower than that of pure E51 resin system, respectively. Under the condition of salt spray, the dielectric loss of 20 wt% and 10 wt% EPD blends decreased by 73.1% and 74.6% after aging. The leakage current of 10 wt% 2021P blend resin and 10 wt% EPD blend resin decreased by 7% and 3.8% before aging, respectively. After aging, they decreased by 3.7% and 2.2%, respectively. The bending strength of 2021P blend resin before and after aging reached 29.3 MPa and 26.6 MPa, respectively. The above three blending resin systems exhibit good electrical properties and good mechanical properties, their ageing resistance performance is strong and they are suitable as the matrix resin of compound cross arm mandrel material.

Effect of Sizing Agent on the Mechanical, Thermal, and Electrical Performance of Basalt Fiber/Epoxy Composites.

Basalt fiber and its resin composites have gradually supplanted traditional steel and glass fiber composites due to their superior strength, heat resistance, and corrosion resistance. However, basalt fiber still has significant flaws that restrict the functionality and use of its composites, such as less active functional groups and poor resin adherence. This study examines the effects of sizing agent on the characteristics of basalt fiber/epoxy resin composites. Epoxy resin emulsion and acrylate emulsion are employed as the primary auxiliary film-forming agents in this study. Polyurethane emulsion with various content levels is also used. The findings indicate that a 1% wt. of polyurethane emulsion concentration produces the greatest results, increasing the composite's flexural strength, flexural modulus, tensile strength, and interlaminar shear strength by 122%, 34.0%, 102%, and 10.2%, respectively. At the same time, the storage modulus and Tg of the material will decrease. In addition, the breakdown strength can be raised by 112%, and insulation parameters such as leakage current and dielectric loss factor can be decreased by 26.4% and 15.6%, respectively. The effect of sizing agent B is the best.

Properties of Basalt Fiber Core Rods and Their Application in Composite Cross Arms of a Power Distribution Network.

As basalt fiber has better mechanical properties and stability than glass fiber, cross arms made of continuous basalt-fiber-reinforced epoxy matrix composites are capable of meeting the mechanical requirements in the event of typhoons and broken lines in coastal areas, mountainous areas and other special areas. In this paper, continuous basalt-fiber-reinforced epoxy matrix composites were used to fabricate the core rods and composite cross arms. The results verified that basalt fiber composite cross arms can meet the strict requirements of transmission lines in terms of quality and reliability. In addition to high electrical insulation performance, the flexural modulus and the flexural strength of basalt fiber core rods are 1.8 and 1.06 times those of glass fiber core rods, respectively. Basalt fiber core rods were found to be much better load-bearing components compared to glass fiber core rods. However, the leakage current and the result of scanning electron microscopy (SEM) analysis reveal that the interface bonding strength between basalt fibers and the matrix resin is weak. A 3D reconstruction of micro-CT indicates that the volume of pores inside basalt fiber core rods accounts for 0.0048% of the total volume, which is greater than the 0.0042% of glass fiber rods. Therefore, improving the interface bond between basalt fibers and the resin can further improve the properties of basalt fiber core rods.

A Lithium Ion Highway by Surface Coordination Polymerization: In Situ Growth of Metal-Organic Framework Thin Layers on Metal Oxides for Exceptional Rate and Cycling Performance.

A thin layer of a highly porous metal-organic framework material, ZIF-8, is fabricated uniformly on the surface of nanostructured transition metal oxides (ZnO nanoflakes and MnO2 nanorods) to boost the transfer of lithium ions. The novel design and uniform microstructure of the MOF-coated TMOs (ZIF-8@TMOs) exhibit dramatically enhanced rate and cycling performance comparing to their pristine counterparts. The capacities of ZIF-8@ZnO (nanoflakes) and ZIF-8@MnO2 (nanorods) are 28 % and 31 % higher that of the pristine ones at the same current density. The nanorods of ZIF-8@MnO2 show a capacity of 1067 mAh g-1 after 500 cycles at 1 Ag-1 and without any fading. To further improve the conductivity and capacity, the ZIF-8-coated materials are pyrolyzed at 700 °C in an N2 atmosphere (ZIF-8@TMO-700 N). After pyrolysis, a much higher capacity improvement is achieved: ZIF-8@ZnO-700 N and ZIF-8@MnO2 -700 N have 54 % and 69 % capacity increases compared with the pristine TMOs, and at 1 Ag-1 , the capacity of ZIF-8@MnO2 -700 N is 1060 mAh g-1 after cycling for 300 cycles.

Metal-Organic Frameworks (MOFs) as Sandwich Coating Cushion for Silicon Anode in Lithium Ion Batteries.

A novel metal-organic framework (MOF) sandwich coating method (denoted as MOF-SC) is developed for hybrid Li ion battery electrode preparation, in which the MOF films are casted on the surface of a silicon layer and sandwiched between the active silicon and the separator. The obtained electrodes show improved cycling performance. The areal capacity of the cheap and readily available microsized Si treated with MOF-SC can reach 1700 µAh cm(-2) at 265 µA cm(-2) and maintain at 850 µAh cm(-2) after 50 cycles. Beyond the above, the commercial nanosized Si treated by MOF-SC also shows greatly enhanced areal capacity and outstanding cycle stability, 600 µAh cm(-2) for 100 cycles without any apparent fading. By virtue of the novel structure prepared by the MOFs, this new MOF-SC structure serves as an efficient protection cushion for the drastic volume change of silicon during charge/discharge cycles. Furthermore, this MOF layer, with large pore volume and high surface area, can adsorb electrolyte and allow faster diffusion of Li(+) as evidenced by decreased impedance and improved rate performance.

MOF derived composites for cathode protection: coatings of LiCoO2 from UiO-66 and MIL-53 as ultra-stable cathodes.

A mechanochemical synthetic method of preparing LiCoO2 coated by MOF-derived metal oxide composites is introduced. Mono-dispersed ZrO2 and Al2O3 are applied as protection layers. These composites show 148 mA h g(-1) at a current density of 2325 mA g(-1) and excellent thermal stability (55 °C).

In situ growth of MOFs on the surface of si nanoparticles for highly efficient lithium storage: Si@MOF nanocomposites as anode materials for lithium-ion batteries.

A simple yet powerful one-pot strategy is developed to prepare metal-organic framework-coated silicon nanoparticles via in situ mechanochemical synthesis. After simple pyrolysis, the thus-obtained composite shows exceptional electrochemical properties with a lithium storage capacity up to 1050 mA h g(-1), excellent cycle stability (>99% capacity retention after 500 cycles) and outstanding rate performance. These characteristics, combined with their high stability and ease of fabrication, make such Si@MOF nanocomposites ideal alternative candidates as high-energy anode materials in lithium-ion batteries.

[Synthesis and fluorescence properties of complexes of terbium with red fluorescence].

Two terbium complexes were synthesized, with dibenzoylmethane (HDBM) as the first ligand and 1,10-phenanthroline (phen), dipyrido[3,2-a:2',3'-c] quinoxaline as the second ligand. The studies of elemental analysis, rare earth complexometric titration, molar conduction, IR spectra, UV spectra, fluorescence excitation and emission spectra indicate that the complexes have the compositions of Tb (DBM)3 phen and Tb (DBM)3dpq. The results show that the rare earth ion (Tb3+) was bonded with the carbonyl oxygen atom of DBM and nitrogen atoms of phen and dpq. For the terbium complexes prepared by precipitation, the peak positions of the transitions were similar with the ones of the common complexes. The peaks at 490, 545, 586 and 621 nm were assigned to the D4 --> 7F6, 5D4 --> 7F6, D4 --> 7F6, 5D4 --> 7F6 transitions. For the fluorescence intensities of their 5D4 --> 7F6, 5D4 --> 7F5 and 5D4 --> 7F4 transitions were lower than that of the 5D4 --> 7F3 transition, the terbium complexes did not exhibit the characteristic fluorescence (green), but strong red fluorescence. The reason why terbium complexes exhibit the red fluorescence was investigated in the paper by studying the triplet state of ligands, the energy level transitions of complexes and the aggregation state of particles.

Fluorescent property of the Gd3+-doped terbium complexes and crystal structure of [Tb(TPTZ)(H2O)6]Cl3.3H2O.

The complex of Tb(TPTZ)Cl(3).3H(2)O was synthesized by adding the ethyl alcohol solution of TbCl(3) (1 mmol) to the solution of 2,4,6-tris-(2-pyridyl)-s-triazine(TPTZ, 1 mmol) with constant stirring. The solution which had been filtered was kept at the room temperature for 4 weeks, and then a kind of transparent crystal was formed. Besides, nine kinds of solid complexes in the different molar proportion of terbium to gadolinium had been synthesized by adopting the similar method mentioned above. It was inferred from the elemental analysis and rare earth complexometry that the composition of these complexes is (Tb(x)Gd(y))(TPTZ)Cl(3).3H(2)O (x : y = 0.9 : 0.1, 0.8 : 0.2, 0.7 : 0.3, 0.6 : 0.4, 0.5 : 0.5, 0.4 : 0.6, 0.3 : 0.7, 0.2 : 0.8, 0.1 : 0.9). The absorption spectra and photoluminescence of the complexes were determined in dimethylsulfoxide (DMF), which showed that the excitation of the complexes is mostly ligand based. The triplet state energy level of TPTZ was measured, indicating that the lowest excitation state energy level of Tb(III) and the triplet state energy level of TPTZ match well each other. The fluorescent data indicated that the fluorescent emission intensity of Tb(3+) ions would be enhanced in the complexes after terbium was doped with Gd(3+) ion. When x : y was 0.5 : 0.5, the fluorescent emission intensity was the largest. The result obtained by testing the X-ray diffraction of the monocrystal revealed that the molecular formula of the mono-crystal complex is [Tb(TPTZ)(H(2)O)(6)]Cl(3).3H(2)O. The number of metal ion coordinates is nine, and the tridentate TPTZ and six water molecules are bonded with terbium respectively. Besides, it also revealed that the monocrystal belongs to the monoclinic system, and space group Cc with the following unit cell parameters is a = 1.4785 (3) nm, b = 1.0547 (2) nm, c = 1.7385 (4) nm, beta = 94.42 (3) degrees, V = 2.7028 (9) nm(3) and Z = 4.