Application of Lanthanum in High Strength and High Conductivity Copper Alloys

China is quite poor in argent resource. Roughly 80% of this industrial argent is imported every year. In order to improve the situation, we took advantage of rare earth (RE) mineral resource and successfully developed the non-argent Lanthanum-tellurium-copper alloy as a substitute for industry argent-copper. In our research, we were able to successfully apply rare earth lanthanum to copper alloy. The defects as porosity, inclusion, etc. originating from nonvacuum melting processing were controlled. Fine grain was obtained. Meanwhile, the comprehensive properties of the copper alloy, such as strength, conductivity and thermal conductivity were improved. The research results in increasing conductivity and thermal conductivity by 5% and 15%, respectively, while the tensile strength is increased by 6% higher than Ag-Cu alloy. The anti-electric corrosion property is good, and there is no argent-cadmium steam population originating from the electric arc effect. The addition of lanthanum further reduces the content of oxygen and hydrogen. The optimum quantity of the addition of RE lanthanum in the copper alloy is 0.010% - 0.020% .

Electrical properties of dry polycrystalline olivine mixed with various chromite contents: Implications for the high conductivity anomalies in subduction zones

Chromite,a crucial high-conductivity mineral phase of peridotite in ophiolite suites,has a significant effect on the electrical structure of subduction zones.The electrical conductivities of sintered polycrystalline olivine containing various volume percents of chromite(0,4,7,10,13,16,18,21,23,100 vol.%)were measured using a complex impedance spectroscopic technique in the frequency range of 10^(−1)-10^(6) Hz under the conditions of 1.0-3.0 GPa and 873-1223 K.The relationship between the conductivities of the chromite-bearing olivine aggregates and temperatures conformed to the Arrhenius equation.The positive effect of pressure on the conductivities of the olivine-chromite systems was much weaker than that of temperature.The chromite content had an important effect on the conductivities of the olivine-chromite systems,and the bulk conductivities increased with increasing volume fraction of chromite to a certain extent.The inclusion of 16 vol.%chromites dramatically enhanced the bulk conductivity,implying that the percolation threshold of interconnectivity of chromite in the olivine-chromite systems is-16 vol.%.The fitted activation enthalpies for pure polycrystalline olivine,polycrystalline olivine with isolated chromite,polycrystalline olivine with interconnected chromites,and pure polycrystalline chromite were 1.25,0.78-0.87,0.48-0.54,and 0.47 eV,respectively.Based on the chemical compositions and activation enthalpies,small polaron conduction was proposed to be the dominant conduction mechanism for polycrystalline olivine with various chromite contents.Furthermore,the conductivities of polycrystalline olivine with interconnected chromite(10-1.5-100.5 S/m)provides a reasonable explanation for the high conductivity anomalies in subduction-related tectonic environments.

On the Origin of Crustal High Conductivity Zone in theWestern Tibet Plateau

The subduction of the Indian continental lithosphere under the Asian continent caused the uplift of the Tibet Plateau,resulting in the formation of a thickened continental crust twice of the normal value and the crustal shortening of at least 1500 km.Therefore,many models have been proposed to explain the shortening and material transportation mechanism of the Tibetan Plateau.

High Conductivity Water Treatment Using Water Surface Discharge with Nonmetallic Electrodes

Although electrohydraulic discharge is effective for wastewater treatment,its application is restricted by water conductivity and limited to the treatment of low conductivity water. For high conductivity water treatment,water-surface discharge is the preferred choice.However. the metallic electrodes are easily corroded because of the high temperature and strong oxidative environment caused by gas phase discharge and the electrochemical reaction in water.As a result. the efficiency of the water treatment might be affected and the service life of the reactor might be shortened.In order to avoid the corrosion problem,nonmetallic electrode water-surface discharge is introduced into high conductivity water treatment in the present study.Carbon-felt and water were used as the high voltage electrode and ground electrode,respectively.A comparison of the electrical and chemical characteristics showed that nonmetallic electrode discharge maintained the discharge characteristics and enhanced the energy efficiency,and furthermore,the corrosion of metal electrodes was avoided.

Ni-P-SBR composite-electroless-plating enables Si anode with high conductivity and elasticity for high performance Li-ion batteries application

Silica-based anode is widely employed for high energy density Li-ion batteries owing to their high theoretical specific capacity(4200 m A h g-1).However,it is always accompanied by a huge volume expansion(300%)and shrinks during the lithiation/delithiation process,further leading to low cycle stability.Efforts to mitigate the adverse effects caused by volume expansion such as robust binder matrix,Coreshell structure,etc.,inevitably affect the electronic conductivity within the electrode.Herein,a high conductivity and elasticity Si anode(Ni-P-SBR(styrene-butadiene rubber)@Si)was designed and fabricated via the Ni-P-SBR composite-electroless-plating process.In this design,the Si particles are surrounded by SBR polymer and Ni particles,where the SBR can adapt to the volume change and Ni particles can provide the electrode with high electronic conductivity.Therefore,the Ni-P-SBR@Si delivers a high initial capacity of 3470 m A h g-1and presents capacity retention of 49.4%within 200 cycles at 600 m A g-1.Additionally,a high capacity of 1153 m A h g-1can be achieved at 2000 m A g-1and can be cycled stably under bending conditions.This strategy provides feasible ideas to solve the key issues that limit the practical application of Si anodes.

High strength and high conductivity Cu alloys: A review

High strength and high conductivity(HSHC) Cu alloys are widely used in many fields,such as high-speed electric railway contact wires and integrated circuit lead frames. Pure Cu is well known to have excellent electrical conductivity but rather low strength. The main concern of HSHC Cu alloys is how to strengthen the alloy efficiently. However,when the Cu alloys are strengthened by a certain method,their electrical conductivity will inevitably decrease to a certain extent. This review introduces the strengthening methods of HSHC Cu alloys. Then the research progress of some typical HSHC Cu alloys such as Cu-Cr-Zr,Cu-Ni-Si,Cu-Ag,Cu-Mg is reviewed according to different alloy systems. Finally,the development trend of HSHC Cu alloys is forecasted. It is pointed out that precipitation and micro-alloying are effective ways to improve the performance of HSHC Cu alloys. At the same time,the production of HSHC Cu alloys also needs to comply with the large-scale,low-cost development trend of industrialization in the future.

High conductivity polymer electrolyte with comb-like structure via a solvent-free UV-cured method for large-area ambient all-solid-sate lithium batteries

A novel solid polymer electrolyte with comb-like structure is prepared via a solvent-free UV-cured method.The relationship between conductivity and molecular weight is investigated and revealed.The optimal electrolyte presents a considerably high conductivity of 1.44·10^(-4)S·cm^(-1)at 30℃.Meanwhile,it shows excellent compatibility with metallic lithium and wide electrochemical window(>5 V).To investigate the safety and cycling performance,the coin cell and soft package battery are assembled respectively.The LiFePO_(4)/Li coin cells exhibit initial discharge specific capacities of 163.2,147.7,137.3 and 108.7 mA·h·g^(-1)at 0.1,0.2,0.5 and 1C under 60℃,respectively.Notably,when the coin cells work at 30℃,the initial discharge specific capacities at 0.05,0.1,0.2 and 0.5C are 140.5,133.5,107.7 and 55.6 mA·h·g^(-1).Significantly,a 3.5 cm×7 cm solid-state soft pack battery is fabricated and cycling at 30℃.The first discharge capacity reaches to 137.5 mA·h·g^(-1)and the capacity retention is as high as 84.4%after 100 cycles at 0.2C and remain 95.5%after 100 cycles at 0.5C,respectively.These results shows a promising solid polymer electrolyte for solid-state batteries with good cycling and safety performance.

Polymer dispersed ionic liquid electrolytes with high ionic conductivity for ultrastable solid-state lithium batteries

Solid polymer electrolytes(SPEs)have emerged as one of the most promising candidates for building solid-state lithium batteries due to their excellent flexibility,scalability,and interfacial compatibility with electrodes.However,the low ionic conductivity and poor cyclic stability of SPEs do not meet the requirements for practical applications of lithium batteries.Here,a novel polymer dispersed ionic liquid-based solid polymer electrolyte(PDIL-SPE)is fabricated using the in situ polymerization-induced phase separation(PIPS)method.The as-prepared PDIL-SPE possesses both outstanding ionic conductivity(0.74 mS cm^(-1) at 25℃)and a wide electrochemical window(up to 4.86 V),and the formed unique three-dimensional(3D)co-continuous structure of polymer matrix and ionic liquid in PDIL-SPE can promote the transport of lithium ions.Also,the 3D co-continuous structure of PDIL-SPE effectively accommodates the severe volume expansion for prolonged lithium plating and stripping processes over 1000 h at 0.5 mA cm^(-2) under 25℃.Moreover,the LiFePO_(4)//Li coin cell can work stably over 150 cycles at a 1 C rate under room temperature with a capacity retention of 90.6%from 111.1 to 100.7 mAh g^(-1).The PDIL-SPE composite is a promising material system for enabling the ultrastable operation of solid-state lithium-metal batteries.

Analysis of Glutamic Acid in Cerebrospinal Fluid by Capillary Electrophoresis with High Frequency Conductivity Detection

A rapid method to determine glutamic acid (Glu) in cerebrospinal fluid (CSF) by capillaryelectrophoresis with high frequency conductivity detection (contactless conductivity detection) wasdescribed. The CSF sample was pretreated with silver cation resin to remove high concentration ofCl- ions in CSF. The separation was achieved in the buffer solution of 10 mmol/L Tris and 8mmol/L boric acid at the separation voltage of 20.0 kV. Glu showed linear response in the range of5.0×10-6 to 6.0×10-3 mol/L, the limit of detection was 1.0×10-6 mol/L. The method was used foranalysis Glu in CSF satisfactorily with a recovery of 97.8-98.8%.

New Activated Carbon with High Thermal Conductivity and Its Microwave Regeneration Performance

Using a walnut shellas a carbon source and ZnCl_2 as an activating agent,we resolved the temperature gradient problems of activated carbon in the microwave desorption process.An appropriate amount of silicon carbide was added to prepare the composite activated carbon with high thermalconductivity while developing VOC adsorption-microwave regeneration technology.The experimentalresults show that the coefficient of thermalconductivity of SiC-AC is three times as much as those of AC and SY-6.When microwave power was 480 W in its microwave desorption,the temperature of the bed thermaldesorption was 10 ℃ to 30 ℃ below that of normalactivated carbon prepared in our laboratory.The toluene desorption activation energy was 16.05 k J·mol^（-1）,which was 15% less than the desorption activation energy of commercialactivated carbon.This study testified that the process could maintain its high adsorption and regeneration desorption performances.

Highly Active Interfacial Sites in SFT-SnO_(2) Heterojunction Electrolyte for Enhanced Fuel Cell Performance via Engineered Energy Bands:Envisioned Theoretically and Experimentally

Extending the ionic conductivity is the pre-requisite of electrolytes in fuel cell technology for high-electrochemical performance.In this regard,the introduction of semiconductor-oxide materials and the approach of heterostructure formation by modulating energy bands to enhance ionic conduction acting as an electrolyte in fuel cell-device.Semiconductor(n-type;SnO_(2))plays a key role by introducing into p-type SrFe_(0.2)Ti_(0.8)O_(3-δ)(SFT)semiconductor perovskite materials to construct p-n heterojunction for high ionic conductivity.Therefore,two different composites of SFT and SnO_(2)are constructed by gluing p-and n-type SFT-SnO_(2),where the optimal composition of SFT-SnO_(2)(6∶4)heterostructure electrolyte-based fuel cell achieved excellent ionic conductivity 0.24 S cm^(-1)with power-output of 1004 mW cm^(-2)and high OCV 1.12 V at a low operational temperature of 500℃.The high power-output and significant ionic conductivity with durable operation of 54 h are accredited to SFT-SnO_(2)heterojunction formation including interfacial conduction assisted by a built-in electric field in fuel cell device.Moreover,the fuel conversion efficiency and considerable Faradaic efficiency reveal the compatibility of SFT-SnO_(2)heterostructure electrolyte and ruled-out short-circuiting issue.Further,the first principle calculation provides sufficient information on structure optimization and energy-band structure modulation of SFT-SnO_(2).This strategy will provide new insight into semiconductor-based fuel cell technology to design novel electrolytes.

Performance of High Thermal Conductivity Dense Silica Bricks and Their High Thermal Conductivity Mechanism

High thermal conductivity dense silica bricks have the higher thermal conductivity than ordinary silica bricks,which is conducive to the realization of energy saving and emission reduction in the iron and steel industry.The performance of ordinary silica bricks and high thermal conductivity dense silica bricks was compared,and the high thermal conductivity mechanism was analyzed.The results show that(1)compared with ordinary silica bricks,high thermal conductivity dense silica bricks have the characteristics of higher thermal conductivity,lower apparent porosity,higher tridymite content,higher compressive strength,and higher thermal expansion;(2)by increasing the tridymite content and reducing the porosity,the close packing of honeycombα-tridymite improves the density and continuity of the SiO_(2)frame structure of the silica bricks,and the larger area perpendicular to the heat transfer direction improves the thermal conductivity of the bricks;(3)the densification of the silica bricks also increases the thermal expansion of the bricks,but they still meet the standard requirements.

Highly Thermally Conductive and Structurally Ultra‑Stable Graphitic Films with Seamless Heterointerfaces for Extreme Thermal Management

Highly thermally conductive graphitic film(GF)materials have become a competitive solution for the thermal management of high-power electronic devices.However,their catastrophic structural failure under extreme alternating thermal/cold shock poses a significant challenge to reliability and safety.Here,we present the first investigation into the structural failure mechanism of GF during cyclic liquid nitrogen shocks(LNS),which reveals a bubbling process characterized by“permeation-diffusion-deformation”phenomenon.To overcome this long-standing structural weakness,a novel metal-nanoarmor strategy is proposed to construct a Cu-modified graphitic film(GF@Cu)with seamless heterointerface.This well-designed interface ensures superior structural stability for GF@Cu after hundreds of LNS cycles from 77 to 300 K.Moreover,GF@Cu maintains high thermal conductivity up to 1088 W m^(−1)K^(−1)with degradation of less than 5%even after 150 LNS cycles,superior to that of pure GF(50%degradation).Our work not only offers an opportunity to improve the robustness of graphitic films by the rational structural design but also facilitates the applications of thermally conductive carbon-based materials for future extreme thermal management in complex aerospace electronics.

Defect chemistry engineering of Ga-doped garnet electrolyte with high stability for solid-state lithium metal batteries

Ga-doped Li_(7)La_(3)Zr_(2)O_(12)(Ga-LLZO)has long been considered as a promising garnet-type electrolyte candidate for all-solid-state lithium metal batteries(ASSLBs)due to its high room temperature ionic conductivity.However,the typical synthesis of Ga-LLZO is usually accompanied by the formation of undesired LiGaO_(2) impurity phase that causes severe instability of the electrolyte in contact with molten Li metal during half/full cell assembly.In this study,we show that by simply engineering the defect chemistry of Ga-LLZO,namely,the lithium deficiency level,LiGaO_(2) impurity phase is effectively inhibited in the final synthetic product.Consequently,defect chemistry engineered Ga-LLZO exhibits excellent electrochemical stability against lithium metal,while its high room temperature ionic conductivity(~1.9×10^(-3)S·cm^(-1))is well reserved.The assembled Li/Ga-LLZO/Li symmetric cell has a superior critical current density of 0.9 mA·cm^(-2),and cycles stably for 500 hours at a current density of 0.3 mA·cm^(-2).This research facilitates the potential commercial applications of high performance Ga-LLZO solid electrolytes in ASSLBs.

A cerium-doped NASICON chemically coupled poly(vinylidene fluoride-hexafluoropropylene)-based polymer electrolyte for high-rate and high-voltage quasi-solid-state lithium metal batteries

The isolated inorganic particles within composite polymer electrolytes(CPEs) are not correlated to the Li^(+)transfer network,resulting in the polymer dominating the low ionic conductivity of CPEs.Therefore,we developed novel quasi-solid-state CPEs of a Ce-doped Na super ion conductors(NASICON)Na_(1.3+x)Al_(0.3)Ce_(x)Ti_(1.7-x)(PO_(4))_(3)(NCATP) chemically coupled poly(vinylidene fluoride-hexafluoropropylene)(PVDF-HFP)/Li-bis(trifluoromethanes-ulfonyl)imide(LiTFSI) matrix.A strong interaction between Ce^(3+)from NCATP and TFSI-anion from the polymer matrix contributes to the fast Li+transportation at the interface.The PVDF-HFP/NCATP CPEs exhibit an ionic conductivity of 2.16 × 0^(-3) S cm^(-1) and a Li^(+) transference number of 0.88.A symmetric Li/Li cell with NCATP-integrated CPEs at 0.1 mA cm^(-2) presents outstanding cycling stability over 2000 h at 25℃.The quasi-solid-state Li metal batteries of Li/CPEs/LiFePO_(4) at 2 C after 400 cycles and Li/CPEs/LiCoO_(2) at 0.2 C after 120 cycles deliver capacities of 100 and 152 mAh g^(-1) at 25℃,respectively.

Highly conductive S-doped FeSe_(2-x)S_(x)microsphere with high tap density for practical sodium storage

Metal selenides have been explored as promising sodium storage materials owing to their high theoretical capacity.However,sluggish Naþdiffusion and low electronic conductivity of selenides still hinder their practical applications.Herein,FeSe_(2-x)S_(x)microspheres have been prepared via a self-doping solvothermal method using NH4Fe(SO4)2 as both the Fe and S source,followed by gas phase selenization.The density functional theory calculation results reveal that S doping not only improves the Na adsorption,but also lower the diffusion energy barrier of Na atoms at the S doping sites,at the same time enhance the electronic conductivity of FeSe_(2-x)S_(x).The carbon-free nature of the FeSe_(2-x)S_(x)microspheres results in a low specific surface area and a high tap density,leading to an initial columbic efficiency of 85.6%.Compared with pure FeSe_(2),such FeSe_(2-x)S_(x)delivers a high reversible capacity of 373.6 mAh⋅g^(-1)at a high current density of 5 A⋅g^(-1)after 2000 cycles and an enhanced rate performance of 305.8 mAh⋅g^(-1)at even 50 A⋅g1.Finally,the FeSe_(2-x)S_(x)//NVP pouch cells have been assembled,achieving high energy and volumetric energy densities of 118 Wh⋅kg1 and 272 mWh⋅cm3,respectively,confirming the potential of applications for the FeSe_(2-x)S_(x)microspheres.

Facile synthesis of high electrical conductive CoP via solid-state synthetic routes for supercapacitors

Co-P precursor was prepared by a mechanical alloying method and then is controlled to synthesis of CoP phase through an annealing method. The optimal conditions of ball milling and annealing temperature are investigated. The CoP exhibits higher electrical conductivity than graphite and cobalt oxide, showing excellent pseudocapacitive properties due its high electrical conductivity which can result in a fast electron transfer in high rate charge-discharge possess. The as-obtained CoP electrode achieves a high specific capacitance of 447.5 Fig at 1 Aug, and displays an excellent rate capability as well as good cycling stability. Besides, the asymmetric supercapacitor (ASC) based on the CoP as the positive electrode and activated carbon (AC) as the negative electrode was assembled and displayed a high rate capability (60% of the capacitance is retained when the current density increased from 1 Aug to 12 Aug), excellent cycling stability (96.7% of the initial capacitance is retained after 5000 cycles), and a superior specific energy of 19 Wh/kg at a power density of 350.8 W/kg. The results, suggest that the CoP electrode materials have a great potential for developing high-performance electrochemical energy storage devices. (C) 2016 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.

Highly Ordered Thermoplastic Polyurethane/Aramid Nanofiber Conductive Foams Modulated by Kevlar Polyanion for Piezoresistive Sensing and Electromagnetic Interference Shielding

Highly ordered and uniformly porous structure of conductive foams is a vital issue for various functional purposes such as piezoresistive sensing and electromagnetic interference(EMI) shielding. With the aids of Kevlar polyanionic chains, thermoplastic polyurethane(TPU) foams reinforced by aramid nanofibers(ANF) with adjustable pore-size distribution were successfully obtained via a nonsolvent-induced phase separation. In this regard, the most outstanding result is the in situ formation of ANF in TPU foams after protonation of Kevlar polyanion during the NIPS process. Furthermore, in situ growth of copper nanoparticles(Cu NPs) on TPU/ANF foams was performed according to the electroless deposition by using the tiny amount of pre-blended Ti_(3)C_(2)T_(x) MXene as reducing agents. Particularly, the existence of Cu NPs layers significantly promoted the storage modulus in 2,932% increments, and the well-designed TPU/ANF/Ti_(3)C_(2)T_(x) MXene(PAM-Cu) composite foams showed distinguished compressive cycle stability. Taking virtues of the highly ordered and elastic porous architectures, the PAM-Cu foams were utilized as piezoresistive sensor exhibiting board compressive interval of 0–344.5 kPa(50% strain) with good sensitivity at 0.46 kPa^(-1). Meanwhile,the PAM-Cu foams displayed remarkable EMI shielding effectiveness at 79.09 dB in X band. This work provides an ideal strategy to fabricate highly ordered TPU foams with outstanding elastic recovery and excellent EMI shielding performance, which can be used as a promising candidate in integration of satisfactory piezoresistive sensor and EMI shielding applications for human–machine interfaces.

Highly Thermally Conductive Polymer/Graphene Composites with Rapid Room‑Temperature Self‑Healing Capacity

Composites that can rapidly self-healing their structure and function at room temperature have broad application prospects.However,in view of the complexity of composite structure and composition,its self-heal is facing challenges.In this article,supramolecular effect is proposed to repair the multistage structure,mechanical and thermal properties of composite materials.A stiff and tough supramolecular frameworks of 2-[[(butylamino)carbonyl]oxy]ethyl ester(PBA)–polydimethylsiloxane(PDMS)were established using a chain extender with double amide bonds in a side chain to extend prepolymers through copolymerization.Then,by introducing the copolymer into a folded graphene film(FGf),a highly thermally conductive composite of PBA–PDMS/FGf with self-healing capacity was fabricated.The ratio of crosslinking and hydrogen bonding was optimized to ensure that PBA–PDMS could completely self-heal at room temperature in 10 min.Additionally,PBA–PDMS/FGf exhibits a high tensile strength of 2.23±0.15 MPa at break and high thermal conductivity of 13±0.2 W m^(−1)K^(−1);of which the self-healing efficiencies were 100%and 98.65%at room temperature for tensile strength and thermal conductivity,respectively.The excellent self-healing performance comes from the efficient supramolecular interaction between polymer molecules,as well as polymer molecule and graphene.This kind of thermal conductive self-healing composite has important application prospects in the heat dissipation field of next generation electronic devices in the future.

On the high conductive layer near the Moho and the transitional zone between the crust and mantle in Tianshui region

On the basis of MTS and DSS data in and near Tianshui region,the deep structure contour of the region was expounded.The regional distribution of the high conductive layer near the Moho in the region becomes one of the most obvious characters of the conductivity structure in the crust and mantle,and it is corresponding to the low S wave velocity zone near the Moho and is guessed as the transitional zone between the crust and mantle in the region.In this paper,the behaviour of medium and the thermodynamic circumstance of the conductive low shear velocity layer near the Moho were demonstrated emphatically,and the cause of formation of the layer was roughly explained under specified conditions of geographical environment and deep structure characters in this region.