Home Physical Sciences Arc erosion behavior of TiB2/Cu composites with single-scale and dual-scale TiB2 particles
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Arc erosion behavior of TiB2/Cu composites with single-scale and dual-scale TiB2 particles

  • Shaolin Li , Xiuhua Guo EMAIL logo , Shengli Zhang , Jiang Feng , Kexing Song and Shuhua Liang
Published/Copyright: December 31, 2019
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Abstract

Arc erosion behaviors of TiB2/Cu composites with single-scale and dual-scale TiB2 particles fabricated by powder metallurgy were studied. It was revealed that the dual-scale TiB2/Cu composites had fewer structure defects compared with the single-scale TiB2/Cu composites, and TiB2 particles with different size were uniformly distributed in the copper matrix. When the ratio of 2 μm over 50 μm TiB2 particles is 1:2, the density of TiB2/Cu composite is 98.5% and shows best mechanical and thermal properties. The arc duration and energy of TiB2/Cu composites increase with the increase of electric current in contact material testing. Compared with the single-scale TiB2/Cu composites, the arc erosion of dual-scale TiB2/Cu composite with 2 μm+50 μm (1:2) TiB2 was slighter. The anode bulge area and cathode erosion pit of dual-scale TiB2/Cu composite was smaller. The dual-scale TiB2 particles optimize the microstructure and thermal stability of the composite, which is conducive to alleviating arc erosion. The synergistic effect of different sized TiB2 particles in the matrix improved the arc erosion resistance of TiB2/Cu composite during arcing.

1 Introduction

Copper matrix composites, which show wide application prospect in the field of transportation, power and so on due to their excellent conductivity, mechanical properties and thermal stability, have been attracting much attention [1, 2, 3, 4]. With the rapid development of transportation, power, communication and other industries, the requirement of material performance is increasing constantly. For example, the level of transmission voltage is continuously improved. Higher transmission voltage would lead to higher temperature and more severe arc erosion of high voltage switch components. The properties of high voltage switch components material directly affect their service life and stability. Thus, developing copper matrix composites with good properties and arc erosion resistance is the key to solve the above problems [5, 6, 7].

Fibers, nanotube and ceramic particles are commonly used reinforcements in composites [8, 9, 10]. TiB2 are widely concerned as a stable ceramic material with high performance due to their low resistivity, high hardness, melting point and elastic modulus. It was shown that the microstructure and mechanical properties of metal matrix composites were improved by adding TiB2 particles [11]. Zhang discussed the dual role of TiB2 particles in the Micro-arc oxidation process of the in-situ TiB2/A201 composites [12]. Zhu studied the ablation resistance behaviors of the TiC-TiB2/xCu ceramic-matrix composites [13]. Our team also carried out some studies on the arc erosion behavior of copper matrix composite [14, 15, 16]. After arc erosion, the quality loss of composites are reduced and the surface erosion pits are shallow by adding TiB2 particles. With the increasing demand of high performance, how to further improve the arc erosion resistance of copper matrix composites is one of the concerns at present.

Some scholars added dual-scale reinforced particles into Fe-based, Al-based, Mg-based and ceramic-based composites. It was shown that the dual-scale reinforced particles greatly improved the hardness, strength, thermal conductivity and thermal stability of the composites due to the different strengthening effects and occupancy of multiple sized particles [17, 18, 19]. Lee presented a transparent electrode based on a dual-scale silver nanowire (AgNW) percolation network embedded in a flexible substrate to demonstrate a significant enhancement in the effective electrical area by filling the large percolative voids present in a long/thick AgNW network with short/thin Ag-NWs [20]. Zou reported a simple strategy for electrosynthesis of silicon carbide nanowires (SiC NWs)-derived carbon with dual-scale nanostructures for high performance supercapacitors [21]. The above research results provide a new idea for the design and development of high performance copper matrix composites. By multiple sized particle, the synergies between different particle sizes can be exerted. The comprehensive properties of copper matrix composites are expected to be further improved accordingly. At present, the fabrication of multiple sized particle reinforced copper matrix composites and their application are rarely reported.

In this paper, TiB2/Cu composite with 5% volume fraction of single-scale and dual-scale TiB2 particles were fabricated by powder metallurgy. Microstructure and comprehensive properties of TiB2/Cu composites with single-scale and dual-scale reinforcements were discussed. The arc erosion behaviors of TiB2/Cu composites were analyzed. The mechanism of arc erosion resistance of dual-scale TiB2/Cu composites was proposed.

2 Material and methods

TiB2 particles (5% vol.) were mixed with electrolytic copper powder. The average particle size of electrolytic copper powder was 75 μm and the purity was more than 99%. The average particle size of TiB2 was 2 μm and 50 μm, respectively. The ratio of 2 μm over 50 μm TiB2 particles were 1:0, 1:1, 1:2, 2:1 and 0:1. The fabrication process was as follows: TiB2 particles were mixed with pure copper powder by ball milling. The milling time was 16 h and ratio of grinding media over material was 5:1. After ball milling, the mixed powder were subjected to a cold isostatic process with the pressure of 280 MPa for 20 min. The size of the compacted samples were Φ = 50×60 mm. ZT-200-22Y sintering furnace was used for vacuum sintering. The sintering temperature was 950C and the holding time was 90 min. After sintering, the sintered samples were further densified by hot extrusion. The extrusion temperature was 900C and the extrusion ratio was 5:1.

Microstructure of the composites were observed with Axio Vert. A1 optical microscope. Hardness of the composite were tested by 320HBS-3000 digital display brinell durometer. The electrical conductivity of the composite were measured by Sigma 2008B1 digital conductivity meter. Thermal conductivity and thermal diffusion coefficient of samples at 25C, 50C, 100C, 150C, 200C, 250C and 280C were measured by LFA447 laser thermal conductivity instrument.

The extruded composite was processed into Φ = 3.8 mm × 10 mm cylindrical sample for arc erosion test by JF04C contact material testing system. Experimental parameters of arc erosion test are as follows: test voltage is 24V, currents are 5 A, 10 A, 15 A and 25 A, on-off frequency is 60 times per minute, contacts closed force is 0.4~0.6 N, number of test is 5000. Arc duration, arc energy and mass change of the samples were recorded. The arc erosion morphologies of the samples were observed by JSM-5610LV scanning electron microscope.

3 Result and discussion

3.1 Structure and properties of the TiB2/Cu composites

Properties of single-scale and dual-scale TiB2/Cu composites are shown in Table 1. Relative densities, hardness and electric conductivity of the dual-scale TiB2/Cu composites are higher than the single-scale ones. When the ratio of 2 μm over 50 μm TiB2 particles is 1:2, the density of the TiB2/Cu composite is 98.5% and shows best properties. Its conductivity and hardness increase by 4.8% and 12.2% respectively,

Table 1

Properties of single-scale and dual-scale TiB2/Cu composites

Particle size of TiB2 / μmRelative density / %Hardness / HBWElectrialconductivity / %IACS
296.961.581.4
5097.363.082.5
2+50(1:1)98.066.884.7
2+50(1:2)98.569.285.3
2+50(2:1)97.66584.3

compared with the composite reinforced by 2 μm single-scale TiB2 particles.

Relative density is an important factor affecting the properties of composite materials. According to Horsfield compact stacking theory, in the dual-scale TiB2/Cu composites, large TiB2 particles served as frame and small TiB2 particles filled the gaps between large particles. The density of the dual-scale TiB2/Cu composites increased accordingly. The different ratio of particle size led to different distribution and occupancy of reinforced particle. In the present work, the better ratio of 2 μm over 50 μm TiB2 particles is 1:2.

Microstructure of single-scale and dual-scale TiB2/Cu composites are shown in Figure 1. In 2 μm single-scale TiB2/Cu composites, the small TiB2 particles are aggregated at grain boundaries (Figure 1(a)). When the composite is loaded, the aggregation of reinforcement at grain boundaries are crack sources and degrade the properties of composite [22]. In 50 μm single-scale TiB2/Cu composite, the interface between TiB2 particles and matrix is poor, and gaps can be found around particles (Figure 1(b)). The gaps may serve as crack sources under loading and jeopardize the properties of composite directly. In dual-scale TiB2/Cu composite, neither aggregation nor gaps are observed since the ratio between large and small TiB2 particles is moderate (Figure 1(c)). In ball milling process, the gaps after copper powder accumulation were filled with large TiB2 particles and small TiB2 particle successively. The density and propertied of the composite increased consequently. As seen in Figure 1(c), large and small TiB2 particles are evenly distributed in matrix. The large particles are surrounded by small particles without aggregation and gap.

Figure 1 Microstructure of single-scale and dual-scale TiB2/Cu composites (a) 2 μm single-scale TiB2/Cu compositel (b) 50 μm single-scale TiB2/Cu compositel (c) 2μm+50μm(1:2) dual-scale TiB2/Cu composite
Figure 1

Microstructure of single-scale and dual-scale TiB2/Cu composites (a) 2 μm single-scale TiB2/Cu compositel (b) 50 μm single-scale TiB2/Cu compositel (c) 2μm+50μm(1:2) dual-scale TiB2/Cu composite

Thermal conductivity and thermal diffusion coefficient of single-scale and dual-scale TiB2/Cu composites are shown in Figure 2. Compared with the single-scale TiB2/Cu composites (both 2 μm and 50 μm), the thermal conductivity and thermal diffusion coefficient of dual-scale TiB2/Cu composite with 2 μm+50 μm (1:2) TiB2 are significantly improved. Dense microstructure without pore, as well as the uniform distribution of particles, contributed to the improvement of thermal properties.

Figure 2 (a) Thermal conductivity; (b) thermal diffusion coefficient; of single-scale and dual-scale TiB2/Cu composites
Figure 2

(a) Thermal conductivity; (b) thermal diffusion coefficient; of single-scale and dual-scale TiB2/Cu composites

3.2 Arc erosion behavior of the TiB2/Cu composites

Arc duration/arc energy versus operation times of single-scale and dual-scale TiB2/Cu composites at 24 V and 25 A are shown in Figure 3. Arc duration and arc energy increased as the number of operation times increased for both single-scale and dual-scale TiB2/Cu composites. The arc duration and energy increase of 50 μm single-scale TiB2/Cu composites were fast. When added 2 μm TiB2 particles into the composite, the increase of arc duration and arc energy were significantly slowed. The high temperature produced by the arc caused the melting of composite surface. Small particles in copper matrix increased the viscosity of molten liquid, which suppressed the splashing of melted metal.

Figure 3 (a) Arc duration; (b) arc energy; versus operation times of single-scale and dual-scale TiB2/Cu composites at 24 V and 25 A
Figure 3

(a) Arc duration; (b) arc energy; versus operation times of single-scale and dual-scale TiB2/Cu composites at 24 V and 25 A

Mass changes of single-scale and dual-scale TiB2/Cu composites after arc erosion test are shown in Figure 4. The mass of cathode decreased and the mass of anode increased after arc erosion. The mass transfer of single-scale TiB2/Cu composites were significant, especially 50 μm single-scale TiB2/Cu composite. The dual-scale TiB2/Cu composite with 2 μm+50 μm (1:2) TiB2 shows lower mass transfer and loss. Dense microstructure and uniform particles distribution of the dual-scale TiB2/Cu composite resulted in favorable mechanical and thermal property, which suppressed the mass loss under are erosion.

Figure 4 Mass changes of single-scale and dual-scale TiB2/Cu composites after arc erosion test
Figure 4

Mass changes of single-scale and dual-scale TiB2/Cu composites after arc erosion test

Arc erosion morphology of single-scale and dual-scale TiB2/Cu composites after 5000 times arc erosion test are shown in Figure 5. The arc erosion morphologies of anode and cathode are quite different. The surface of anode was convex after arc erosion. Arc erosion pits formed at the surface of cathode, with globular particles of molten droplets scattered around the pits. According to the mass transfer measurement, a portion of the cathode material was transferred to the anode under the arc, and another portion caused material loss in the form of splashes.

Figure 5 Arc erosion morphology of single-scale and dual-scale TiB2/Cu composites after 5000 times arc erosion test (the erosion area of 50 μm single-scale TiB2/Cu composite covers almost the entire field of view) (a) 2 μm, anode; (b) 50 μm, anode; (c) 2 μm+50 μm (1:2), anode (bulges on the anodes) (d) 2 μm, cathode; (e) 50 μm, cathode; (f) 2 μm+50 μm (1:2), cathode (erosion pits in the cathodes)
Figure 5

Arc erosion morphology of single-scale and dual-scale TiB2/Cu composites after 5000 times arc erosion test (the erosion area of 50 μm single-scale TiB2/Cu composite covers almost the entire field of view) (a) 2 μm, anode; (b) 50 μm, anode; (c) 2 μm+50 μm (1:2), anode (bulges on the anodes) (d) 2 μm, cathode; (e) 50 μm, cathode; (f) 2 μm+50 μm (1:2), cathode (erosion pits in the cathodes)

The arc erosion of 50 μm single-scale TiB2/Cu composite was severe, and the erosion area covers almost the entire field of view. The erosion area of 2 μm single-scale TiB2/Cu composite was relatively small. Cremens [23] studied the relationship among particle spacing, particle size and particle content,

(1)λ=23d(1v1)

(λ: particle spacing, d: particle size, v: particle volume fraction). With the same content of TiB2 particles, the larger the particle size is, the fewer the particles are in the copper matrix, and the distance between the particles is relatively larger. The large particle spacing resulted in copper enrichment.

Melting occurred in the copper enrichment firstly and then formed molten pools under arc. Then the copper liquid in the molten pool was splashed when the contact closed. A portion of the spray droplet formed a bulge in the anode. When the contact closed again, the anode bulge would first produce an arc. With the increase of contact times, the area of molten pool and spray increased, which resulted in a large arc erosion area.

Compared with single-scale TiB2/Cu composites, the arc erosion of dual-scale TiB2/Cu composite with 2 μm+50 μm (1:2) TiB2 was slighter, characterized by smaller anode bulge area and cathode erosion pit. The density of dual-scale TiB2/Cu composite with 2 μm+50 μm (1:2) TiB2 was higher than the single-scale ones. The structure of single-scale TiB2/Cu composites were relatively loose. Under the action of arc, the loose composite surface melted and absorbed a large amount of external gas. When the temperature dropped, the gases absorbed by the surface formed bubbles in the loose structure. In next arc erosion, these bubbles burst and splashed, and then formed a wide range of arc erosion morphology in anode and cathode.

Arc erosion microstructure of single-scale and dual-scale TiB2/Cu composites at 25A are shown in Figure 6. Melting and gasification of contact materials were the main phase transition processes in arc erosion. With the increase of arc heat flow and temperature, molten metal flowed into contact surfaces. The arc force produced a splash of liquid, causing a large amount of material loss. As shown in Figure 6, the heat generated by the arc caused the copper to melt and splash, then adhere to the surface of the sample after cooling and solidifying. The cathode melt was attached to the anode, resulting in a convex appearance of the anode. The surface of 2 μm single-scale TiB2/Cu composite cathode melt was rough, as shown in Figure 6. This was because there were many small TiB2 particles in the composite. When the high temperature of the arc melted the composite, these small TiB2 particles increased the viscosity of the molten copper solution. After the molten droplets cooled, smaller spherical particles were formed.

Figure 6 Arc erosion microstructure of single-scale and dual-scale TiB2/Cu composites at 25A (large molten droplets in Figure 6(a) and 6(d); large erosion area in Figure 6(e); flat erosion surface and small droplets in Figure 6(c) and 6(f)) (a) 2 μm, anode; (b) 50 μm, anode; (c) 2 μm+50 μm (1:2), anode (d) 2 μm, cathode; (e) 50 μm, cathode; (f) 2 μm+50 μm (1:2), cathode
Figure 6

Arc erosion microstructure of single-scale and dual-scale TiB2/Cu composites at 25A (large molten droplets in Figure 6(a) and 6(d); large erosion area in Figure 6(e); flat erosion surface and small droplets in Figure 6(c) and 6(f)) (a) 2 μm, anode; (b) 50 μm, anode; (c) 2 μm+50 μm (1:2), anode (d) 2 μm, cathode; (e) 50 μm, cathode; (f) 2 μm+50 μm (1:2), cathode

In addition, liquid diffusion occurred on the cathode surface of the composites and metal pools were located near molten droplets, as shown in Figure 6(d), 6(e) and 6(f). In the process of contact between two poles, the melting temperature of the contact material was close to or higher than that of the copper matrix due to the arc. As the bipolar contacts continued to open, the molten bridge broke and arced. The high temperature of the arc melted the contact surface into a pool. Due to the low melting and boiling temperature of the copper matrix, when the two ends of the contact closed, the copper matrix would first melt and splash, resulting in material loss and transfer. As the temperature dropped, the material solidified to form a bulge at the anode and a ball and pool structure at the cathode.

In 50 μm single-scale TiB2/Cu composite, large TiB2 particles resulted in fewer particles and larger particle spacing in the matrix. When the copper matrix was melted by the high temperature of arc, the molten pool area was larger, and the spherical molten material of cathode was large and the surface was smooth. The arc erosion of dual-scale TiB2/Cu composite with 2 μm+50 μm (1:2) TiB2 was relatively slight. Compared with the single-scale TiB2/Cu composites, the dual-scale TiB2/Cu composites combined the supporting effect of large particles with the increasing viscosity effect of small particles. At the same time, the mixing effect of multiple sized particles overcame the large spacing caused by large particles, resulting in finer molten particles and shallow etch pit.

3.3 Mechanism of arc erosion resistance of dual-scale TiB2/Cu composites

The arc erosion morphology of the TiB2/Cu composites is closely related to plasma impact, thermal convection, Lorentz force and surface tension [24]. In the arc initiation phase, cations are rapidly bombarded the cathode pool due to the accelerating effect of electric field on cations. This rapid and massive plasma shock can cause flow in the central area of the cathode pool. In addition, Lorentz forces generated by electric current drive the solution to flow outward to both sides of the side wall of the molten pool. The cathode pool splashes during the collision of anode and cathode. However, thermal convection causes molten metal to flow inward from the sides of the pool. And the surface tension of the molten metal will restrict the flow of the solution. Therefore, plasma impact and Lorentz force are the main factors causing the spatter, while thermal convection and surface tension are the main factors preventing the spatter. Compared with the cathode eroded by arc, the anode molten pool has the same four kinds of forces, but the anode is mainly bombarded by free electrons with lower mass. And its influence on the anode is much less than that on the cathode, so that the sputtering rarely happens. This is the main reason why the anode of TiB2/Cu composite produces bulges while the cathode produces erosion pits and spray droplets under arc.

As seen in Figure 7, there are some defects in the contact surface of anode and cathode, such as cracks, pores, etc. The contact was on and off over and over again under the high temperature of arc erosion, which had a strong thermal impact on the surface of the material. Under the action of thermal stress, cracks formed by arc erosion materials usually expanded in multiple directions. When the cracks in these directions grew to cross each other, the physical properties of the contact surface of anode and cathode of the material would decline, and the arc erosion would be more serious. In this case, one of the potential causes of crack initiation and propagation was thermal tensile stress. The thermal conductivity and thermal expansion coefficient of ceramic particles and copper matrix were different in the composites. As the material was heated or cooled, a thermal gradient was thus generated between the components. Therefore, under the high temperature of arc erosion, cracks would inevitably appear in ceramic particle reinforced copper matrix composites. The maximum temperature gradient of material without forming cracks (T), namely thermal shock parameter of materials (R), is [25]

Figure 7 (a) Pores; (b) cracks; on the surface of TiB2/Cu composites after arc erosion
Figure 7

(a) Pores; (b) cracks; on the surface of TiB2/Cu composites after arc erosion

(2)R=ΔT=kσC/Eα

(k: thermal conductivity, σ: material strength, E: Young modulus, α: coefficient of thermal expansion, C: constraint coefficient). According to equation (2), the generation of cracks in TiB2/Cu composite during arc erosion was related to its thermal conductivity. The composites with good thermal conductivity had better thermal shock resistance. The thermal conductivity of the dual-scale TiB2/Cu composite with 2 μm+50 μm(1:2) TiB2 was higher than the single-scale ones. Therefore, the dual-scale TiB2/Cu composite with 2 μm+50 μm(1:2) TiB2 had better thermal shock resistance. In dual-scale TiB2/Cu composite, the larger particles played a supporting role, while the smaller ones strengthened the matrix and increased the viscosity of the molten pool during arc erosion. Therefore, the effect of dual-scale TiB2 particles effectively improved the arc erosion resistance of the composite. The schematic of arc erosion behavior of dual-scale TiB2/Cu composite is shown in Figure 8.

Figure 8 Schematic of arc erosion behavior of dual-scale TiB2/ Cu composite
Figure 8

Schematic of arc erosion behavior of dual-scale TiB2/ Cu composite

Moreover, in the dual-scale TiB2/Cu composite with 2 μm+50 μm (1:2) TiB2, large TiB2 particles appeared as particle fracture under loading, while small grain size particles deflected cracks. The large TiB2 particle can inhibit crack initiation, while the small TiB2particle size can resist crack propagation. Therefore, in the arc erosion under the same conditions, it was more difficult for the dual-scale TiB2/Cu composite with 2 μm+50 μm (1:2) TiB2 to form cracks, which improved its arc erosion resistance.

4 Conclusion

  1. For TiB2/Cu composite with 5% volume fraction of single-scale and dual-scale TiB2 particles, the dual-scale TiB2/Cu composites have few structure defects, and TiB2 particles with different size are uniformly distributed in the copper matrix. When the ratio of 2 μm over 50 μm TiB2 particles is 1:2, the density of TiB2/Cu composite is 98.5% and shows best mechanical and thermal properties.

  2. In the process of arc erosion, the arc duration and energy of TiB2/Cu composites increase with the increase of current. Compared with single-scale TiB2/Cu composites, the arc erosion of the dual-scale TiB2/Cu composite with 2 μm+50 μm(1:2) TiB2 was slighter, characterized by smaller anode bulge area and cathode erosion pit.

  3. On the one hand, dual-scale TiB2 particles optimize the microstructure and thermal stability of the composite, which is conducive to alleviating arc erosion. On the other hand, the synergistic effect of different sized TiB2 particles in the matrix improves the arc erosion resistance of TiB2/Cu composite during arcing.

Acknowledgement

This work was supported by the National Natural Science Foundation of China (Grant Nos. U1502274 and 51605146); The China Postdoctoral Science Foundation (Grant No. 2018M632769); Henan Plan Project for College Youth Backbone Teacher (Grant No. 2018GGJS045).

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Received: 2019-10-18
Accepted: 2019-11-05
Published Online: 2019-12-31

© 2019 S. Li et al., published by De Gruyter

This work is licensed under the Creative Commons Attribution 4.0 Public License.

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  10. Effect of PVA fiber on durability of cementitious composite containing nano-SiO2
  11. Cr effects on the electrical contact properties of the Al2O3-Cu/15W composites
  12. Experimental evaluation of self-expandable metallic tracheobronchial stents
  13. Experimental study on the existence of nano-scale pores and the evolution of organic matter in organic-rich shale
  14. Mechanical characterizations of braided composite stents made of helical polyethylene terephthalate strips and NiTi wires
  15. Mechanical properties of boron nitride sheet with randomly distributed vacancy defects
  16. Fabrication, mechanical properties and failure mechanism of random and aligned nanofiber membrane with different parameters
  17. Micro- structure and rheological properties of graphene oxide rubber asphalt
  18. First-principles calculations of mechanical and thermodynamic properties of tungsten-based alloy
  19. Adsorption performance of hydrophobic/hydrophilic silica aerogel for low concentration organic pollutant in aqueous solution
  20. Preparation of spherical aminopropyl-functionalized MCM-41 and its application in removal of Pb(II) ion from aqueous solution
  21. Electrical conductivity anisotropy of copper matrix composites reinforced with SiC whiskers
  22. Miniature on-fiber extrinsic Fabry-Perot interferometric vibration sensors based on micro-cantilever beam
  23. Electric-field assisted growth and mechanical bactericidal performance of ZnO nanoarrays with gradient morphologies
  24. Flexural behavior and mechanical model of aluminum alloy mortise-and-tenon T-joints for electric vehicle
  25. Synthesis of nano zirconium oxide and its application in dentistry
  26. Surface modification of nano-sized carbon black for reinforcement of rubber
  27. Temperature-dependent negative Poisson’s ratio of monolayer graphene: Prediction from molecular dynamics simulations
  28. Finite element nonlinear transient modelling of carbon nanotubes reinforced fiber/polymer composite spherical shells with a cutout
  29. Preparation of low-permittivity K2O–B2O3–SiO2–Al2O3 composites without the addition of glass
  30. Large amplitude vibration of doubly curved FG-GRC laminated panels in thermal environments
  31. Enhanced flexural properties of aramid fiber/epoxy composites by graphene oxide
  32. Correlation between electrochemical performance degradation and catalyst structural parameters on polymer electrolyte membrane fuel cell
  33. Materials characterization of advanced fillers for composites engineering applications
  34. Humic acid assisted stabilization of dispersed single-walled carbon nanotubes in cementitious composites
  35. Test on axial compression performance of nano-silica concrete-filled angle steel reinforced GFRP tubular column
  36. Multi-scale modeling of the lamellar unit of arterial media
  37. The multiscale enhancement of mechanical properties of 3D MWK composites via poly(oxypropylene) diamines and GO nanoparticles
  38. Mechanical properties of circular nano-silica concrete filled stainless steel tube stub columns after being exposed to freezing and thawing
  39. Arc erosion behavior of TiB2/Cu composites with single-scale and dual-scale TiB2 particles
  40. Yb3+-containing chitosan hydrogels induce B-16 melanoma cell anoikis via a Fak-dependent pathway
  41. Template-free synthesis of Se-nanorods-rGO nanocomposite for application in supercapacitors
  42. Effect of graphene oxide on chloride penetration resistance of recycled concrete
  43. Bending resistance of PVA fiber reinforced cementitious composites containing nano-SiO2
  44. Review Articles
  45. Recent development of Supercapacitor Electrode Based on Carbon Materials
  46. Mechanical contribution of vascular smooth muscle cells in the tunica media of artery
  47. Applications of polymer-based nanoparticles in vaccine field
  48. Toxicity of metallic nanoparticles in the central nervous system
  49. Parameter control and concentration analysis of graphene colloids prepared by electric spark discharge method
  50. A critique on multi-jet electrospinning: State of the art and future outlook
  51. Electrospun cellulose acetate nanofibers and Au@AgNPs for antimicrobial activity - A mini review
  52. Recent progress in supercapacitors based on the advanced carbon electrodes
  53. Recent progress in shape memory polymer composites: methods, properties, applications and prospects
  54. In situ capabilities of Small Angle X-ray Scattering
  55. Review of nano-phase effects in high strength and conductivity copper alloys
  56. Progress and challenges in p-type oxide-based thin film transistors
  57. Advanced materials for flexible solar cell applications
  58. Phenylboronic acid-decorated polymeric nanomaterials for advanced bio-application
  59. The effect of nano-SiO2 on concrete properties: a review
  60. A brief review for fluorinated carbon: synthesis, properties and applications
  61. A review on the mechanical properties for thin film and block structure characterised by using nanoscratch test
  62. Cotton fibres functionalized with plasmonic nanoparticles to promote the destruction of harmful molecules: an overview
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