• 제목/요약/키워드: Lithium chloride

검색결과 120건 처리시간 0.022초

Dioxane을 용매로 한 PVC-LMO 비드의 제조와 Li+ 흡착특성 (Preparation of PVC-LMO Bead with Dioxane Solvent and Adsorptive Properties of Lithium Ions)

  • 감상규;유해나;이민규
    • 한국환경과학회지
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    • 제23권7호
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    • pp.1289-1297
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    • 2014
  • In this study, PVC-LMO beads were prepared by immobilizing lithium manganese oxide (LMO) with poly vinyl chloride (PVC) diluted in dioxane solvent. XRD and SEM analysis confirmed that LMO was immobilized well in PVC-LMO beads. The diameter of PVC-LMO beads prepared by dioxane solvent was about 2 mm. The adsorption experiments of lithium ions by PVC-LMO beads were conducted batchwise. The optimum pH was pH 10. The adsorption characteristics of lithium ions by PVC-LMO beads was well described by the pseudo-second-order kinetic model. The maximum adsorption capacity obtained from Langmuir model was 24.25 mg/g. The thermodynamic parameters such as ${\Delta}H^{\circ}$, ${\Delta}S^{\circ}$ and ${\Delta}G^{\circ}$ were evaluated. The calculated ${\Delta}G^{\circ}$ was between -6.16 and -4.14 kJ/mol (below zero), indicating the spontaneous nature of $Li^+$ adsorption on PVC-LMO beads. Also, the results showed that PVC-LMO beads prepared in this study could be used for the removal of lithium ions from seawater containing coexisting ions such as $Na^+$, $K^+$, $Mg^{2+}$ and $Ca^{2+}$.

가소화된 Poly(vinyl chloride)-g-Poly(oxyethylene methacrylate) 가지형 고분자 전해질막 제조 및 분석 (Preparation and Characterization of Plasticized Poly(vinyl chloride)-g-Poly(oxyethylene methacrylate) Graft Copolymer Electrolyte Membranes)

  • 서진아;고종관;고주환;김종학
    • 멤브레인
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    • 제21권3호
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    • pp.222-228
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    • 2011
  • Poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) 가지형 공중합체를 원자전달라디칼 중합을 통해 합성하여 전기변색소자의 전해질에 적용하였다. 가소화된 고분자 전해질은 가소제로서 propylene carbonate (PC)/ethylene carbonate (EC) 혼합물을 도입하여 제조하였으며, Lithium tetrafluoroborate ($LiBF_4$), lithium perchlorate ($LiClO_4$), lithium iodide (LiI) and lithium bistrifluoromethanesulfonimide (LiTFSI)를 사용하여 염의 종류에 따른 영향을 조사하였다. 광각 x-선 산란(WAXS)과 시차주사 열량법(DSC) 측정 결과 고분자 전해질의 구조와 유리전이온도($T_g$)가 변하였고, 이는 POEM 내의 에테르의 산소와 리튬염 사이의 상호작용으로 인해 변했다는 것을 FT-IR 분광법을 통하여 확인하였다. 투과전자현미경(TEM) 측정 결과 PVC-g-POEM 가지형 공중합체의 미세상분리 구조가 PC/EC와 리튬염의 도입에도 변하지 않는 것을 관찰하였다. 가소화된 고분자 전해질은 poly(3-hexylthiophene) (P3HT) 전도성 고분자를 이용한 전기변색소자에 적용되었다.

다이메틸설폭시화물 용매를 사용한 PVC-LMO 비드의 제조와 리튬 이온 흡착 특성 (Preparation of PVC-LMO Beads Using Dimethyl Sulfoxide Solvent and Adsorption Characteristics of Lithium Ions)

  • 유해나;이동환;이민규
    • 청정기술
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    • 제20권2호
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    • pp.154-159
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    • 2014
  • 본 연구에서는 노말 메틸 피로리돈(N-methyl-2-pyrrolidone, NMP)을 대신하여 다이메틸설폭시화물(dimethyl sulfoxide, DMSO)을 용매로 사용하여 폴리염화비닐 (poly vinyl chloride, PVC)로 리튬망간산화물(lithium manganese oxide, LMO)를 고정화하여 PVC-LMO 비드를 제조하였다. XRD 분석을 통해 PVC-LMO 비드내에 LMO가 잘 고정화 된 것을 확인 하였다. 합성한 PVC-LMO 비드의 크기는 약 4 mm였다. PVC-LMO 비드에 의한 리튬이온 흡착 실험은 회분식으로 수행하였다. 랭뮤어 모델식으로 부터 구한 최대 흡착량은 21.31 mg/g였다. PVC-LMO 비드에 의한 리튬이온 흡착특성은 유사 2차 속도모델식으로 잘 설명되었으며, 내부확산 단계가 흡착속도 결정단계인 것으로 사료되었다.

보란-염화리튬에 의한 유기화합물의 환원반응 (Effect of Lithium Chloride on the Borane Reduction of Organic Compound)

  • 윤능민;차진순
    • 대한화학회지
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    • 제22권1호
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    • pp.37-44
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    • 1978
  • $BH_3$-THF 용액에 염화리튬을 가한 새로운 환원계의 환원특성에 대한 연구가 대표적인 작용기를 가진 유기화합물을 가지고 표준조건($0^{\circ}$, THF)에서 이루어졌다. 조사 연구된 화합물중 벤조페논, 4가지 에스테르 및 시클로헥센은 $BH_3$ 환원과 별 차이를 보이지 않았으나, 2-헵탄온, 아세토페논, 염화벤조일, 프탈산무수물, 그리고 3가지 에폭시화물은 소량의 염화리튬에 의해 빠른 속도로 환원이 완결 되었다. 특히 에폭시화시클로헥센의 환원에 있어서는 소량의 염화리튬 존재하에서는 정량적으로 시클로헥산올을 생성하였으나 염화리튬의 양이 증가하면 2-클로로시클로헥산올이 시클로헥산올과 함께 생성됨을 알았다. 또한, 에폭시화시클로헥센과의 반응에 있어서 질산리튬은 염화리튬과는 달리 별로 효과가 없었다. 따라서 보란-염화리튬용액에 클로로수소화붕소리튬의 생성가능성을 논의하였다.

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Electrochemical Properties of Acetylene Black/Multi-walled Carbon Nanotube Cathodes for Lithium Thionyl Chloride Batteries at High Discharge Currents

  • Song, Hee-Youb;Jung, Moon-Hyung;Jeong, Soon-Ki
    • Journal of Electrochemical Science and Technology
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    • 제11권4호
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    • pp.430-436
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    • 2020
  • Lithium thionyl chloride (Li/SOCl2) batteries exhibit the highest energy densities seen in commercially available primary batteries because of their high operating voltages and discharge capacities. They are widely used in various extreme environments; however, they show signs of degradation at high discharge currents. The discharge performance of Li/SOCl2 is considered to be greatly dependent on the carbon materials used in the cathode. Therefore, suitable carbon materials must be chosen to improve discharge performances. In this work, we investigated the discharge properties of Li/SOCl2 batteries in which the cathodes contained various ratios of acetylene black (AB) and multi-walled carbon nanotubes (MWCNTs) at high discharge currents. It was confirmed that the MWCNTs were effectively dispersed in the mixed AB/MWCNT cathodes. Moreover, the discharge capacity and operating voltage improved at high discharge currents in these mixed cathodes when compared with pure AB cathodes. It was found that the mesopores present in the cathodes have a strong impact on the discharge capacity, while the macropores present on the cathode surface influence the discharge properties at high discharge rates in Li/SOCl2 batteries. These results indicate that the ratio of mesopores and macropores in the cathode is key to improving the discharge performance of Li/SOCl2 batteries, as is the dispersion of the MWCNTs.

Cycling Behavior of Binder-Free Graphite-Lithium Intercalation Anode In AICI3-EMIC-LiCI-SOCI2 Room-Temperature Molten Salt

  • Koura, Nobuyuki;Minami, Takuto;Etoh, Keiko;Idemoto, Yasushi;Matsumoto, Futoshi
    • 전기화학회지
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    • 제5권4호
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    • pp.178-182
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    • 2002
  • The electrochemical behavior of binder-free carbon anode, comprising of only artificial and natural graphite (AG and NG) particles, for intercalation and deintercalation of lithium ion $(Li^+)$ in aluminum chloride (AICI_3)-I-ethyl­3-methylimidazolium chloride (EMIC)-lithium chloride (LiCl)-thionyl chloride $(SOCI_2)$ room-temperature molten salt (RTMS) was studied. Binder-free carbon electrodes were fabricated using electrophoretic deposition (EPD) method. The binder-free carbon anodes provided a relatively flat charge and discharge potentials $(0\;to\;0.2V\;vs.\;Li/Li^+)$ and current capabilities $(250-340mAh{\cdot}g^{-1})$ for the intercalation and deintercalation of $Li^+$. Stability of the binder-free carbon anodes for intercalation and deintercalation of 50 cycles was confirmed.

리튬 및 발프로에이트 병용 처치가 PC12 세포에서 ERK1/2 인산화와 ELK1 및 C-FOS 전사활성에 미치는 영향 (Effects of Combined Treatments of Lithium and Valproate on the Phosphorylation of ERK1/2 and Transcriptional Activity of ELK1 and C-FOS in PC12 Cells)

  • 차승근;김세현;하규섭;신순영;강웅구
    • 생물정신의학
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    • 제20권4호
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    • pp.159-165
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    • 2013
  • Objectives Mechanisms of clinical synergistic effects, induced by co-treatments of lithium and valproate, are unclear. Extracellular signal-regulated kinase (ERK) has been suggested to play important roles in mechanisms of the action of mood stabilizers. In this study, effects of co-treatments of lithium and valproate on the ERK1/2 signal pathway and its down-stream transcription factors, ELK1 and C-FOS, were investigated in vitro. Methods PC12 cells, human pheochromocytoma cells, were treated with lithium chloride (30 mM), valproate (1 mM) or lithium chloride + valproate. The phosphorylation of ERK1/2 was analyzed with immunoblot analysis. Transcriptional activities of ELK1 and C-FOS were analyzed with reporter gene assay. Results Single treatment of lithium and valproate increased the phosphorylation of ERK and transcriptional activities of ELK1 and C-FOS, respectively. Combined treatments of lithium and valproate induced more robust increase in the phosphorylation of ERK1/2 and transcriptional activities of ELK1 and C-FOS, compared to those in response to single treatment of lithium or valproate. Conclusions Co-treatments of lithium and valproate induced synergistic increase in the phosphorylation of ERK1/2 and transcriptional activities of its down-stream transcription factors, ELK1 and C-FOS, compared to effects of single treatment. The findings might suggest potentiating effects of lithium and valproate augmentation treatment strategy.

Neuroprotection of Lithium is Associated with Inhibition of Bax Expression and Caspase 8 Activation

  • Kwon, Gee-Youn;Kim, Soo-Kyung
    • The Korean Journal of Physiology and Pharmacology
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    • 제5권5호
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    • pp.389-396
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    • 2001
  • Neuroprotective properties of lithium were investigated by using in vivo NMDA excitotoxicity model. The appearance of TUNEL positive cells was prominent within 24 h of NMDA (70 mg/kg, i.p.) injection in the regions of the cortex, hippocampal formation, and thalamus of mouse cerebrum. NMDA treatment resulted in the extensive enhancement of Bax immunoreactivity in the cortical and hippocampal regions. NMDA also increased the immunoreactivity of caspase 8 in the similar regions of the mouse cerebrum. However, the increased immunoreactivity of Bax and caspase 8 were dramatically attenuated by chronic lithium pretreatment (lithium chloride, 300 mg/kg/d, i.p. for $7{\sim}10$ days). At the same time, lithium ion blocked the appearance of TUNEL positive cells, and the morphological assessment indicated an effective neuroprotection by lithium against NMDA excitotoxicity. Although the exact action mechanism of lithium is not straightforward at this time, we propose that the inhibition of Bax and caspase cascade is involved in the neuroprotective action of lithium.

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SEPARATION OF STRONTIUM AND CESIUM FROM TERNARY AND QUATERNARY LITHIUM CHLORIDE-POTASSIUM CHLORIDE SALTS VIA MELT CRYSTALLIZATION

  • WILLIAMS, AMMON N.;PACK, MICHAEL;PHONGIKAROON, SUPATHORN
    • Nuclear Engineering and Technology
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    • 제47권7호
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    • pp.867-874
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    • 2015
  • Separation of cesium chloride (CsCl) and strontium chloride ($SrCl_2$) from the lithium chloride-potassium chloride (LiCl-KCl) salt was studied using a melt crystallization process similar to the reverse vertical Bridgeman growth technique. A ternary $SrCl_2-LiCl-KCl$ salt was explored at similar growth rates (1.8-5 mm/h) and compared with CsCl ternary results to identify similarities. Quaternary experiments were also conducted and compared with the ternary cases to identify trends and possible limitations to the separations process. In the ternary case, as much as 68% of the total salt could be recycled per batch process. In the quaternary experiments, separation of Cs and Sr was nearly identical at the slower rates; however, as the growth rate increased, $SrCl_2$ separated more easily than CsCl. The quaternary results show less separation and rate dependence than in both ternary cases. As an estimated result, only 51% of the total salt could be recycled per batch. Furthermore, two models have been explored to further understand the growth process and separation. A comparison of the experimental and modeling results reveals that the nonmixed model fits reasonably well with the ternary and quaternary data sets. A dimensional analysis was performed and a correlation was identified to semipredict the segregation coefficient.

Experimental study of correlation between aqueous lithium chloride-air temperature difference and mass transfer performance

  • Fatkhur, Rokhmaw;Agung, Bakhtiar;Choi, Kwang-Hwan
    • 한국태양에너지학회:학술대회논문집
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    • 한국태양에너지학회 2011년도 춘계학술발표대회 논문집
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    • pp.195-198
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    • 2011
  • Liquid desiccant material, such as lithium chloride (LiCl) or halide slits are usually used on air conditioning application for controlling the humidity of high Outdoor Air (OA). Solar energy is usually used to heat the liquid in regeneration process of those desiccant. The mass transfer it self is driven by the temperature different between the liquid desiccant and the input air. This experiment study is analyzing the characteristic of the aqueous LiCl-air temperature different in variance specific gravity, especially in range of temperature different using the solar energy as the heat generator. The experiment has done by variating the concentration of the LiCl with specific gravity 1.210 and 1.150. For the comparison the pure water is also used. The result show that the mass transfer rate is increased in every variation as the increases of the temperature different, and the weeker aqueous solution of the LiCl the highest mass transfer coefficient.

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