• Title/Summary/Keyword: Carbonate Ion

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Evaluating the Durability of Concrete Combined with Ground Granulated Blast Furnace Slag using Electrolysis Alkaline Aqueous as Mixing Water (전기분해 알칼리수를 배합수로 사용한 고로슬래그 미분말 혼입 콘크리트의 내구성)

  • Jeong, Su-Mi;Kim, Ju-Sung;Park, Sun-Gyu
    • Journal of the Korea Institute of Building Construction
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    • v.23 no.4
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    • pp.349-358
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    • 2023
  • This research aimed to enhance the initial strength of concrete that is mixed with ground granulated blast furnace slag, as well as to fortify its resistance to carbonation and chloride ion permeation. To achieve this, alkaline aqueous, produced through the electrolysis of potassium carbonate, was employed as the mixing water in the preparation of concrete. To substantiate the increment in initial strength, compressive strength measurements of the concrete were executed. Additionally, an accelerated carbonation test and a chloride ion permeation resistance test were undertaken. The results confirmed that the initial strength of the concrete, which utilized electrolysis alkaline aqueous as mixing water, exhibited an improvement in comparison to concrete mixed with conventional water. It was also verified that both carbonation resistance and chloride ion permeation resistance showed enhancements.

The Cycling Performance of Graphite Electrode Coated with Tin Oxide for Lithium Ion Battery (리튬이온전지용 주석산화물이 도포된 흑연전극의 싸이클 성능)

  • Kang, Tae-Hyuk;Kim, Hyung-Sun;Cho, Won-Il;Cho, Byung-Won;Ju, Jeh-Beck
    • Journal of the Korean Electrochemical Society
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    • v.5 no.2
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    • pp.52-56
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    • 2002
  • Tin oxide was coated on graphite particle by sol-gel method and an electrode with this material having microcrystalline structure for lithium ion battery was obtained by heat treatment in the range $400-600^{\circ}C$. The content of tin oxide was controlled within the range of $2.25wt\%\~11.1wt\%$. The discharge capacity increased with the content of tin oxide and also initial irreversible capacity increased. The discharge capacity of tin oxide electrode showed more than 350 mAh/g at the initial cycle and 300 mAh/g after the 30th cycle in propylene carbonate(PC) based electrolyte whereas graphite electrode without surface modification showed 140 mAh/g. When the charge and discharge rate was changed from C/5 to C/2, The discharge capacity of tin oxide and graphite electrode showed $92\%\;and\;77\%$ of initial capacity, respectively. It has been considered that such an enhancement of electrode characteristics was caused because lithium $oxide(Li_2O)$ passive film formed from the reaction between tin oxide and lithium ion prevented the exfoliation of graphite electrode and also reduced tin enhanced the electrical conduction between graphite particles to improve the current distribution of electrode.

Improvement of Electrochemical Performance of KVO3 as High Capacity Negative Electrode Material for Lithium-ion Batteries (리튬이온 이차전지용 고용량 KVO3 음극의 전기화학적 성능개선)

  • Kim, Tae Hun;Gim, Gyeong Rae;Park, Hwandong;Kim, Haebeen;Ryu, Ji Heon
    • Journal of the Korean Electrochemical Society
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    • v.22 no.4
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    • pp.148-154
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    • 2019
  • Vanadium oxide based materials have been studied as novel negative electrode materials in lithium-ion batteries (LIBs) because of their high specific capacity. In this study, potassium metavanadate ($KVO_3$) was synthesized and its electrochemical properties are evaluated as a negative electrode materials. The aqueous solution of $NH_4VO_3$ is mixed with a stoichiometric amount of KOH. The solution is boiled to remove $NH_3$ gas and dried to obtain a precipitate. The obtained $KVO_3$ powders are heat-treated at 300 and $500^{\circ}C$ for 8 h in air. As the heat treatment temperature increases, the initial reversible capacity decreases, but the cycle performance and Coulombic efficiency are improved slightly. On the contrary, the electrochemical performances of the $KVO_3$ electrodes are greatly improved when a polyacrylic acid (PAA) as binder was used instead of polyvinylidene fluoride (PVDF) and a fluoroethylene carbonate (FEC) was used as electrolyte additive. The initial reversible capacity of the $KVO_3$ is 1169 mAh/g and the Coulombic efficiency is improved to 76.3% with moderate cycle performance. The $KVO_3$ has the potential as a novel high-capacity negative electrode materials.

Improvement of Cycle Performance of Graphite-Silicon Monoxide Mixture Negative Electrode in Lithium-ion Batteries (흑연과 실리콘 일산화물의 혼합물로 구성된 리튬이온 이차전지용 음극의 사이클 성능개선 연구)

  • Kim, Haebeen;Kim, Tae Hun;Ryu, Ji Heon
    • Journal of the Korean Electrochemical Society
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    • v.22 no.4
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    • pp.155-163
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    • 2019
  • Mixture electrodes of a graphite having a good cycle performance and a silicon monoxide (SiO) having a high capacity are fabricated and their cycle performances are evaluated as negative electrodes for lithium-ion batteries. The electrode prepared by mixing the natural graphite and carbon-coated SiO in a mass ratio of 9:1 shows a reversible capacity of $480mAh\;g^{-1}$, 33% higher than that of graphite. However, the capacity deteriorates continuously upon cycling due to the volume change of silicon monoxide. In this study, the factors that can improve the cycle performance have been discussed through the change in the configurations of the electrode and the electrolyte. The electrode using the carboxymethyl cellulose (CMC) binder shows the best cycle performance compared to the conventional binders. The electrode sing the CMC and styrene-butadiene rubber (SBR) binder not only has almost the similar cycle characteristics with the electrode using the CMC binder but also has the better rate capability. When the fluoroethylene carbonate (FEC) is used as an electrolyte additive, the cycle life is improved. However, the electrolyte with 5 wt% of FEC is appropriate because the rate capability decreases when the content of FEC is increased to 10 wt%. In addition, when the mass loading of the electrode is lowered, the cycle performance is greatly improved. Also, enhanced cycle performance is achieved using the roughened Cu current collector polished by abrasive paper.

Preparation of Cathode Materials for Lithium Rechargeable Batteries using Transition Metals Recycled from Li(Ni1-x-yCoxMny)O2 Secondary Battery Scraps (Li(Ni1-x-yCoxMny)O2계 이차전지 공정 스크랩으로부터 회수한 전이금속을 활용한 리튬이차전지 양극재 제조)

  • Lee, Jae-Won;Kim, Dae Weon;Jang, Seong Tae
    • Journal of Powder Materials
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    • v.21 no.2
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    • pp.131-136
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    • 2014
  • Cathode materials and their precursors are prepared with transition metal solutions recycled from the the waste lithium-ion batteries containing NCM (nickel-cobalt-manganese) cathodes by a $H_2$ and C-reduction process. The recycled transition metal sulfate solutions are used in a co-precipitation process in a CSTR reactor to obtain the transition metal hydroxide. The NCM cathode materials (Ni:Mn:Co=5:3:2) are prepared from the transition metal hydroxide by calcining with lithium carbonate. X-ray diffraction and scanning electron microscopy analyses show that the cathode material has a layered structure and particle size of about 10 ${\mu}m$. The cathode materials also exhibited a capacity of about 160 mAh/g with a retention rate of 93~96% after 100 cycles.

Development of Polymer Film Mass Production by ion Beam Implantation (이온빔을 이용한 고분자 대전방지 처리 양산기술 개발)

  • Kil, Jae-Keun;Lee, Chan-Young;Shon, Chang-Won;Lee, Jae-Hyung
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2004.07b
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    • pp.1138-1141
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    • 2004
  • 고분자 재료에 이온을 주입하면 표면전기저항이 이온주입조건에 따라 $10^{16}\Omega/sq$ 에서 $10^7\Omega/sq$ 까지 변하게 되며, 광학적 특성도 변하게 된다. 이는 산업적으로 대전방지 등에 적용이 가능하며 이러한 신소재 개발을 위하여 산업용 이온빔 표면처리 장치를 제작하고 인출광학을 기초로 이온빔을 제어하여 고분자 재료의 이온주입처리 양산기술을 개발하였다. 본 연구에서는 대면적, 대전류 이온빔 인출을 위한 이온원의 광학적 설계 및 빔라인에서의 솔레노이드 전자석을 이용한 빔프로파일 제어방법을 설명하였다. 사용된 고분자 소재는 PC(PolyCarbonate) 및 PET(PolyEthylene Teraphthalate)이며, 질소이온주입조건은 이온에너지 40-50 keV, 이온주입량 $5\times10^{15}$, $1\times10^{16}$, $7\times10^{16}ions/cm^2$의 조건으로 공정을 수행하였다. 또한 대전방지용 고분자 대량생산을 위한 연속 생산조건과 양산공정조건에 따른 표면전기저항변화를 관찰하였다.

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Ionic Liquid-based Electrolytes for Li Metal/Air Batteries: A Review of Materials and the New 'LABOHR' Flow Cell Concept

  • Bresser, Dominic;Paillard, Elie;Passerini, Stefano
    • Journal of Electrochemical Science and Technology
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    • v.5 no.2
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    • pp.37-44
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    • 2014
  • The $Li-O_2$ battery has been attracting much attention recently, due to its very high theoretical capacity compared with Li-ion chemistries. Nevertheless, several studies within the last few years revealed that Li-ion derived electrolytes based on alkyl carbonate solvents, which have been commonly used in the last 27 years, are irreversibly consumed at the $O_2$ electrode. Accordingly, more stable electrolytes are required capable to operate with both the Li metal anode and the $O_2$ cathode. Thus, due to their favorable properties such as non volatility, chemical inertia, and favorable behavior toward the Li metal electrode, ionic liquid-based electrolytes have gathered increasing attention from the scientific community for its application in $Li-O_2$ batteries. However, the scale-up of Li-$O_2$ technology to real application requires solving the mass transport limitation, especially for supplying oxygen to the cathode. Hence, the 'LABOHR' project proposes the introduction of a flooded cathode configuration and the circulation of the electrolyte, which is then used as an oxygen carrier from an external $O_2$ harvesting device to the cathode for freeing the system from diffusion limitation.

A Study on Calcium Ion Reduction in Power Plant Water using High Voltage Impulse (고전압 임펄스를 활용한 발전용수 칼슘농도 저감에 관한 연구)

  • Kim, TaeHui;Chang, In-Soung;Jung, Jae-Hwan;Hong, Woong ki;Lee, June-Ho
    • The Transactions of The Korean Institute of Electrical Engineers
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    • v.66 no.3
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    • pp.545-550
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    • 2017
  • As an alternate technique for water softening, high voltage impulse (HVI) is introduced and verified if it can control the $CaCO_3$ scale formation in industrial water treatment. After HVI was applied to the artificial hard water containing $100{\pm}5mg/L$ $Ca^{2+}$ for 4 hours, the $Ca^{2+}$ concentration and the electrical conductivity were measured. The concentration of $Ca^{2+}$ was reduced from 94.5 to 86.3 mg/L (8.7% reduction) after 4 hour contact of HVI under 5 kV condition. The $Ca^{2+}$ was decreased from 92 to 77.7 mg/L (15.6% reduction) at 8kV and from 90.1 to 75.4 mg/L (16.3% reduction) at 12 kV condition. Both of the contact time and the applied voltage were important parameters affecting the calcium ion reduction. With these results, it was verified that HVI technique could be potential candidate for control of $CaCO_3$ scale formation.

The properties of hydrophobic concrete prepared by biomimetic mineralization method

  • Huang, Chung-Ho;Fang, Hao-Yu;Zhang, Jue-Zhong
    • Computers and Concrete
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    • v.23 no.5
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    • pp.351-359
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    • 2019
  • In this study, the calcium hydroxide, an inherent product of cement hydration, was treated using biomimetic carbonation method of incorporating stearic acid to generate the hydrophobic calcium carbonate on concrete surface. Carbonation reaction was carried out at various $CO_2$ pressure and temperatures and utilizing the Scanning Electron Microscope (SEM), chloride-ion penetration test apparatus, and compression test machine to investigate the hydrophobicity, durability, and mechanical properties of the synthesized products. Experimental results indicate that the calcium stearate may change the surface property of concrete from hydrophilicity to hydrophobicity. Increasing reaction temperature can change the particles from irregular shapes to needle-rod structures with increased shear stress and thus favorable to hydrophobicity and microhardness. The contact angle against water for the concrete surface was found to increase with increasing $CO_2$ pressure and temperature, and reached to an optimum value at around $90^{\circ}C$. The maximum static water contact angle of 128.7 degree was obtained at the $CO_2$ pressure of 2 atm and temperature of $90^{\circ}C$. It was also found that biomimetic carbonation increased the permeability, acid resistance and chloride-ion permeability of the concrete material. These unique results demonstrate that the needle-rod structures of $CaCO_3$ synthetized on concrete surface could enhance hydrophobicity, durability, and mechanical properties of concrete.

Triallyl Borate as an Effective Separator/Cathode Interphase Modifier for Lithium-ion Batteries

  • Ha Neul Kim;Hye Rim Lee;Taeeun Yim
    • Journal of Electrochemical Science and Technology
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    • v.14 no.3
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    • pp.272-282
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    • 2023
  • Ni-rich layered oxides cathode has recently gained attention as an advanced cathode material due to their applicable energy density. However, as the Ni component in the layered site is increased, the high reactivity of Ni4+ results in parasitic reaction associated with decomposing electrolyte, which leads to a rapid decreasing the lifespan of the cell. The electrolyte additive triallyl borate (TAB) improves interfacial stability, leading to a stable cathode-electrolyte interphase (CEI) layer on the LNCM83 cathode. A multi-functionalized TAB additive can produce a uniformly distributed CEI layer via electrochemical oxidation, which implies an increase in long-term cycling performance. After 100 cycles at elevated temperature, the cell tested by 0.75 TAB retained 88.3% of its retention ratio, whereas the cell performed by TAB-free electrolyte retained 64.1% of its retention. Once the TAB additive formed CEI layers on the LNCM83 cathode, it inhibited the decomposition of carbonate-based solvents species in addition to the dissolution of transition metal components from the cathode. The addition of TAB to LNCM83 cathode material is believed to be a promising way to increase the electrochemical performance.