• 제목/요약/키워드: acidic chemical

검색결과 916건 처리시간 0.034초

Double treated mixed acidic solution texture for crystalline silicon solar cells

  • Kim, S.C.;Kim, S.Y.;Yi, J.S.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2009년도 제38회 동계학술대회 초록집
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    • pp.323-323
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    • 2010
  • Saw damage of crystalline silicon wafer is unavoidable factor. Usually, alkali treatment for removing the damage has been carried out as the saw damage removal (SDR) process for priming the alkali texture. It usually takes lots of time and energy to remove the sawed damages for solar grade crystalline silicon wafers We implemented two different mixed acidic solution treatments to obtain the improved surface structure of silicon wafer without much sacrifice of the silicon wafer thickness. At the first step, the silicon wafer was dipped into the mixed acidic solution of $HF:HNO_3$=1:2 ration for polished surface and at the second step, it was dipped into the diluted mixed acidic solution of $HF:HNO_3:H_2O$=7:3:10 ratio for porous structure. This double treatment to the silicon wafer brought lower reflectance (25% to 6%) and longer carrier lifetime ($0.15\;{\mu}s$ to $0.39\;{\mu}s$) comparing to the bare poly-crystalline silicon wafer. With optimizing the concentration ratio and the dilution ratio, we can not only effectively substitute the time consuming process of SDR to some extent but also skip plasma enhanced chemical vapor deposition (PECVD) process. Moreover, to conduct alkali texture for pyramidal structure on silicon wafer surface, we can use only nitric acid rich solution of the mixed acidic solution treatment instead of implementing SDR.

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표면처리 활성탄소섬유에 의한 U(VI)의 전기흡착 (Electrosorption of U(VI) by Surface-Modified Activated Carbon Fiber)

  • 이유리;정종헌;유승곤;오원진
    • Korean Chemical Engineering Research
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    • 제43권1호
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    • pp.60-65
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    • 2005
  • 연속적 전기흡착 셀에서 활성탄소섬유 부직포 전극을 사용하여 U(VI) 함유 폐액을 처리하였다. 더 낮은 전위에서 U(VI)의 전기흡착 효율을 높이기 위하여 ACFs를 화학약품으로 표면처리하고 그의 세공구조 및 관능기의 변화를 조사하였으며 처리조건이 U(VI)의 흡착에 미치는 영향을 고찰하였다. 표면처리한 모든 ACFs의 비표면적은 감소하였다. 중성염 및 염기성 용액으로 처리한 ACFs의 산성관능기는 감소했지만 산성 용액으로 처리한 ACFs의 산성관능기는 증가하였다. 산성관능기는 U(VI)의 흡착을 차단하여 산성용액 처리 ACFs 전극은 처리하지 않은 ACFs 전극에 비하여 U(VI)의 흡착용량이 감소했다. 중성염과 염기성 용액으로 처리한 ACFs 전극은 흡착용량이 크게 증가하여 -0.3 V의 낮은 전위에서도 처리하지 않은 ACFs 전극의 -0.9 V에 상응하는 결과를 얻었다. 이러한 결과는 ACFs 표면의 산성관능기 감소에 의한 이온의 차단효과(Shielding effect)가 줄어들 뿐만 아니라 음전위 가용에 의한 전기이중층 내에서의 $OH^-$의 증가로 U(VI) 흡착이 효율적으로 진행되었기 때문이다.

몰리브덴 산화물이 도핑된 티타늄 나노튜브전극의 수소 발생 반응 연구 (Study of Hydrogen Evolution Reaction by Molybdenum Oxide Doped TiO2 Nanotubes)

  • 오기석;유현석;이기백;최진섭
    • 한국표면공학회지
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    • 제49권6호
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    • pp.521-529
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    • 2016
  • In this study, titanium nanotubes, prepared by anodization method, showing high surface and strong chemical stability in acidic and basic media, have been employed for the application to the electrodes for water splitting in KOH solution. Due to its high polarization resistance of $TiO_2$ itself, proper catalysts are essentially required to reduce overpotentials for water oxidation and reduction. Most of academic literature showed noble metal catalysts for foreign dopants in $TiO_2$ electrodes. From commercialization point of view, screening of low-cost catalyst is important. Herein, we propose molybdenum oxide as low-cost catalysts among various catalysts tested in the experiments, which exhibits the highest performance for hydrogen evolution reaction in highly alkaline solution. We showed that molybdenum oxide doped electrode can be operated in extreme acidic and basic conditions as well.

활성알루미나를 이용하여 방사성 폐수 중 I-와 IO3-를 제거하는 방법 (Removal of I- and IO3- from Aqueous Solution)

  • 임헌성;이석근
    • 분석과학
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    • 제22권6호
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    • pp.519-523
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    • 2009
  • 본 연구는 수용액 중에 존재하는 방사성 동위원소인 요오드 즉, 요오드이온($I^-$), 요오드산이온(${IO_3}^-$)및 요오드($I_2$)를 효과적으로 제거하는 방법에 관한 것이다. 별도로 물리적 화학적 변화의 과정이 필요하지 않고, 표면 개질된 활성 산화알루미늄과 활성탄을 이용하여 완전하게 제거할 수 있어 방사성 폐수 및 일반 산업폐수에도 유용하게 적용될 수 있다. 요오드이온($I^-$), 요오드산이온(${IO_3}^-$)의 혼합수용액 중의 각 이온들을 은 처리된 염기성 알루미나와 산성 알루미나를 이용한 흡착제거 방법으로 각각 99% 이상 제거하는 효과를 나타내었다.

Poly(benzyl-L-histidine)-b-Poly(ethylene glycol) Micelle Engineered for Tumor Acidic pH-Targeting, in vitro Evaluation

  • Lee, Eun-Seong;Youn, Yu-Seok
    • Bulletin of the Korean Chemical Society
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    • 제29권8호
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    • pp.1539-1544
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    • 2008
  • A polymeric micelle, based on the poly(benzyl-L-histidine)-b-poly(ethylene glycol) (polyBz-His-b-PEG) diblock copolymer, was designed as a tumor-specific targeting carrier. The micelles (particle size: 67-80 nm, critical micelle concentration (CMC); 2-3 $\mu$g/mL) were formed from the diafilteration method at pH 7.4, as a result of self-assembly of the polyBz-His block at the core and PEG block on the shell. Removing benzyl (Bz) group from polyBz-His block provided pH-sensitivity of the micellar core; the micelles were physically destabilized in the pH range of pH 7.4-5.5, depending on the content of the His group free from Bz group. The ionization of His group at a slightly acidic pH promoted the deformation of the interior core. These pHdependent physical changes of the micelles provide the mechanism for pH-triggering anticancer drug (e.g., doxorubicin: DOX) release from the micelle in response to the tumor’s extracellular pH range (pH 7.2-6.5).

Influence of Surface area, Surface Chemical Structure and Solution pH on the Adsorption of Pb(II) Ions on Activated Carbons

  • Goyal, Meenakshi;Amutha, R.
    • Carbon letters
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    • 제7권2호
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    • pp.97-104
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    • 2006
  • The influence of carbon surface area, carbon-oxygen groups associated with the carbon surface and the solution pH on the adsorption of Pb(II) ions from aqueous solutions has been studied using three activated carbons. The adsorption isotherms are Type I of BET classification and the data obeys Langmuir adsorption equation. The BET surface area has little effect on the adsorption while it is strongly influenced by the presence of acidic carbon oxygen surface groups. The amount of these surface groups was enhanced by oxidation of the carbons with different oxidizing agents and reduced by eliminating these groups on degassing at different temperatures. The adsorption of Pb(II) ions increases on each oxidation and decreases on degassing the oxidized carbons. The increase in adsorption on oxidation has been attributed to the formation of acidic carbon-oxygen surface groups and the decrease to the elimination of these acidic surface groups on degassing. The adsorption is also influenced by the pH of the aqueous solution. The adsorption is only small at pH values lower than 3 but is considerably larger at higher pH values. Suitable mechanisms consistent with the adsorption data have been suggested.

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Effect of Hot Water Boiling and Autoclaving on Physicochemical Properties of American Ginseng (Panax quinquefolium L.)

  • Kim, Kyung-Tack;Yoo, Kyung-Mi
    • Journal of Ginseng Research
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    • 제33권1호
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    • pp.40-47
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    • 2009
  • This study evaluates changes in the chemical composition and bioactivities of American ginseng (Panax quinquefolius L.) processed by boiling in water, $75^{\circ}C$ for 10, 20, 30, and 40 min, and autoclaving at high temperatures, $115^{\circ}C$ for 30 and 60 min and $130^{\circ}C$ for 90 and 120 min. Total ginsenoside contents of boiled ginseng remained relatively unchanged, whereas the contents of autoclaved ginseng samples significantly decreased with an increase of both time and temperature. Compared to unheated ginseng (control), the color of both boiled and autoclaved ginseng decreased in lightness and increased in redness. The acidic polysaccharide contents, the total phenolic contents and the antioxidant capacity of boiled and autoclaved ginseng were higher than the untreated ginseng, with the highest values being exhibited by the autoclaved samples. In particular, the antioxidant capacity of unheated ginseng increased about 2.5 times ($285.7{\pm}14.03\;mg$/100g to $777.2{\pm}26.4\;mg$/100g) when ginseng was autoclaved at $130^{\circ}C$ for 120 min as compared to the control. It was concluded that as American ginseng was processed at a high temperature, especially steam-heated in an autoclave, its chemical constituents changed and, in particular, acidic polysaccharides, total phenolics and antioxidant capacity were considerably increased.

CO2 Solubilities in Amide-based Brønsted Acidic Ionic Liquids

  • Palgunadi, Jelliarko;Im, Jin-Kyu;Kang, Je-Eun;Kim, Hoon-Sik;Cheong, Min-Serk
    • Bulletin of the Korean Chemical Society
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    • 제31권1호
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    • pp.146-150
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    • 2010
  • A distinguished class of hydrophobic ionic liquids bearing a Br${\o}$nsted acidic character derived from amide-like compounds were prepared by a neutralization reaction of N,N-diethylformamide, N,N-dibutylformamide, 1-formylpiperidine, and $\varepsilon$-caprolactam with trifluoroacetic acid and physical absorptions of $CO_2$ in these ionic liquids were demonstrated and evaluated. $CO_2$ solubilities in these ionic liquids were influenced by the molecular structure of the cation and were apparently increased with the molar volume. Comparison based on a volume unit reveals that $CO_2$ solubilities in these liquids are relatively higher than those in imidazolium-based ionic liquids. Henry's coefficients calculated from low-pressure solubility tests at 313 to 333 K were used to derive the thermodynamics quantities. Enthalpy and entropy of solvation may share equal contributions in solubility.

Heterologous Expression of a Putative $K^+/H^+$ Antiporter of S. coelicolor A3(2) Enhances $K^+$, Acidic-pH Shock Tolerances, and Geldanamycin Secretion

  • Song, Jae Yang;Seo, Young Bin;Hong, Soon-Kwang;Chang, Yong Keun
    • Journal of Microbiology and Biotechnology
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    • 제23권2호
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    • pp.149-155
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    • 2013
  • Heterologous expression of a putative $K^+/H^+$ antiporter of Streptomyces coelicolor A3(2) (designated as sha4) in E. coli and Streptomyces hygroscopicus JCM4427 showed enhanced tolerance to $K^+$ stress, acidic-pH shock, and/or geldanamycin production under $K^+$ stress. In a series of $K^+$ extrusion experiments with sha4-carrying E. coli deficient in the $K^+/H^+$ antiporter, a restoration of impaired $K^+$ extrusion activity was observed. Based on this, it was concluded that sha4 was a true $K^+/H^+$ antiporter. In different sets of experiments, the sha4-carrying E. coli showed significantly improved tolerances to $K^+$ stresses and acidic-pH shock, whereas sha4-carrying S. hygroscopicus showed an improvement in $K^+$ stress tolerance only. The sha4-carrying S. hygroscopicus showed much higher geldanamycin productivity than the control under $K^+$ stress condition. In another set of experiments with a production medium, the secretion of geldanamycin was also significantly enhanced by the expression of sha4.

Simultaneous Determination of Anions and Cations in Natural Water by Ion-exclusion/Cation-exchange Chromatography with a Weakly Acidic Cation-exchange Resin Column

  • Lee, Kwang-Pill;Choi, Seong-Ho;Park, Yu-Chul;Bae, Zun-Ung;Lee, Mu-Sang;Lee, Sang-Hak;Chang, Hye-Yong;Kwon, Se-Mok;Kazuhiko Tanaka
    • Bulletin of the Korean Chemical Society
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    • 제24권9호
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    • pp.1324-1328
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    • 2003
  • The simultaneous determination of anions ($SO_4 ^{2-},\;Cl^-,\;and\;NO_3^-$) and cations ($Na^+,\;NH^{4+},\;K^+,\;Mg^{2+},\;and\;Ca^{2+}$) in natural water obtained by Nakdong River waters system in Korea were performed by ion-exclusion/cationexchange chromatography with conductimetric detection. The stationary phase was a polymethacrylate-based weakly acidic cation-exchange resin column in the $H^+$-form and a weak-acid eluent. When using only a 1.4 mM sulfosalicylic acid/6 mM 18-crown-6 ether as an eluent, good resolution of both anions and cations, minimum time required for the separation, and satisfactory detection sensitivity were obtained in a reasonable time. The method was successfully applied to the simultaneous determination of anions and cations in natural waters.