• Title/Summary/Keyword: $KIO_4$

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Development of Metal Compound Explosives Using KIO4 and TiH2 (KIO4와 TiH2를 이용한 금속복합화약 개발)

  • Ahn, Gilhwan;Kim, Sangbaek;Kim, Junhyung;Ryu, Byungtae
    • Journal of the Korean Society of Propulsion Engineers
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    • v.24 no.1
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    • pp.58-63
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    • 2020
  • THPP is a type of metallic complex explosive used in initiators, consisting of TiH2 and KClO4. In this case KClO4 includes ClO4- which is a harmful substance that may cause thyroid dysfunction or tumors. In this study KIO4 is applied to a new type of environmentally friendly explosive as a substitute to the conventional KClO4. Tests were carried out to see if KIO4 can be made a successful replacement for KClO4.

($H_{2}S$ Adsorption Capacity of $Na_{2}CO_{3}$ and $KIO_{3}$ Impregnated Activated Carbon (($Na_{2}CO_{3}$$KIO_{3}$ 첨착 왕겨활성탄의 $H_{2}S$ 흡착특성)

  • Kim, Jun-Suk;Kim, Myung-Soo
    • Journal of the Korean Applied Science and Technology
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    • v.19 no.3
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    • pp.213-221
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    • 2002
  • Activated carbons with high surface area of 2,600 $m^{2}/g$ and high pore volume of 1.2 cc/g could be prepared by KOH activation of rice hulls at a KOH:char ratio of 4:1 and $850^{\circ}C$. In order to increase the adsorption capacity of hydrogen sulfide, which is one of the major malodorous component in the waste water treatment process, various contents of $Na_{2}CO_{3}$ and $KIO_{3}$ were impregnated to the rice-hull activated carbon. The impregnated activated carbon with 5 wt.% of $Na_{2}CO_{3}$ showed improved $H_{2}S$ adsorption capacity of 75 mg/g which is twice of that for the activated carbon without impregnation and the impregnated activated carbon with 2.4 wt.% of $KIO_{3}$ showed even higher $H_{2}S$ adsorption capacity of 97 mg/g. The improvement of $H_{2}S$ adsorption capacity by the introduction of those chemicals could be due to the $H_{2}S$ oxidation and chemical reaction with impregnated materials in addition to the physical adsorption of activated carbon.

($H_2S$ Adsorption Characteristics of $KIO_3$ Impregnated Activated Carbon (($KIO_3$ 첨착활성탄의 황화수소 흡착 성능평가)

  • Kim, Jun-Suk;Kim, Myung-Chan;Kang, Eun-Jin;Kim, Myung-Soo
    • Journal of the Korean Applied Science and Technology
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    • v.20 no.1
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    • pp.72-79
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    • 2003
  • The impregnated activated carbons were prepared by the incipient wetness method with the contents of $KIO_3$ varied from 1.0${\sim}$10 wt% as the impregnation material. The specific surface area and micropore volume of the rice hulls activated carbon were $2,600{\sim}2,800$ $m^2$/g and 1.1${\sim}$1.4 cc/g, respectively. With increasing the contents of impregnation materials, the surface area and micropore volume decreased by 3${\sim}$21%. However, The amounts of hydrogen sulfide adsorbed increased by 2.1${\sim}$2.8 times depending on the impregnation content. The optimum contents of $KIO_3$ were 2.4 wt%. Although the breakthrough time and adsorption capacity of hydrogen sulfide decreased with increasing temperature in the case of the unimpregnated activated carbons, they increased by 1.2${\sim}$ 3.2 times for the case of the impregnated activated carbons. The optimum aspect ratio(L/D) was 1.0 and the adsorption amount of hydrogen sulfide enhanced with increasing the gas flow rate. The regeneration temperature was determined as 400$^{\circ}C$ from the TGA experiment. The adsorption capacity of hydrogen sulfide with the impregnated activated carbon decreased gradually as the regeneration continued. The hydrogen sulfide adsorption amount of the regenerated activated carbon up to 4 times was still higher than that of the unimpregnated activated carbon.

Spectrophotometric Determination of Reducing Drugs (Ascorbic Acid, Potassium Antimonyl Tartrate, Isonicotinic Acid Hydrazide) with $Bis(2,4-diaminophenyl)phosphonate-KIO_3$ ($Bis(2,4-diaminophenyl)phosphonate-KIO_3$에 의한 환원성의약품(Ascorbic Acid, Potassium Antimonyl Tartrate, Isonicotinic Acid Hydrazide)의 분광광도정량)

  • Suh, Jung-Hyun;Kam, Sang-Kyu
    • YAKHAK HOEJI
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    • v.34 no.1
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    • pp.22-33
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    • 1990
  • Aqueous solution of bis(2,4-diaminophenyl)phosphonate(APP) was very stable, especially below pH 2.0 and the red-color compound formed by the reaction of APP and $IO_3-$ was stable at room temperature. A simple and rapid spectrophotometric method for the determination of ascorbic acid, potassium antimonyl tartrate (PAT), and isonicotinic acid hydrazide (INAH) was established by the reaction of $IO_3-$ and these reducing drugs, and the absorbance measurements were made at 500 nm. In the reaction of $IO_3-$ and each of the reducing drugs, the conditions of pH were suitable below 2.5 for ascorbic acid, below 2.0 for PAT, and below 1.5 for INAH. Beer's law did hold in the range of $17.6{\sim}1549.9\;ug$ for ascorbic acid, $33.4{\sim}2871.8{\mu}g$ for PAT,and $6.9{\sim}548.6\;{\mu}g$ for INAH. Many common ingredients present in pharmaceutical dosage forms did not interfere. The average recoveries for ascorbic acid and INAH in pharmaceutical formulations were 99.8 $-100.3\;{\pm}\;0.2{\sim}0.4%$, $99.8\;{\pm}\;0.3%$, respectively.

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Catalytic Spectrophotometry for the Determination of Manganese at Trace Levels by a Novel Indicator Reaction (새로운 지시약 반응에 의해 극미량 수준의 망간 측정을 위한 촉매 반응의 분광 광도 측정법)

  • Gurkan, Ramazan;Caylak, Osman
    • Journal of the Korean Chemical Society
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    • v.54 no.5
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    • pp.556-566
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    • 2010
  • A new kinetic spectrophotometric method is developed for the measurement of Mn(II) in natural water samples. The method is based on the catalytic effect of Mn(II) with the oxidation of Gallocyanin by $KIO_4$ using nitrilotriacetic acid (NTA) as an activation reagent at 620 nm. The optimum conditions obtained are $4.00{\times}1^{-5}\;M$ Gallocyanin, $KIO_4$, $1.00{\times}10^{-4}\;M$ NTA, 0.1 M HAc/NaAc buffer of pH = 3.50, the reaction time of 5 min and the temperature of $30^{\circ}C$. Under the optimum conditions, the proposed method allows the measurement of Mn(II) in a range of $0.1\;-\;4.0\;ng\;mL^{-1}$ and with a detection limit of down to $0.025\;ng\;mL^{-1}$. The recovery efficiency in measuring the standard Mn(II) solution is in a range of 98.5 - 102%, and the RSD is in a range of 0.76 - 1.25%. The newly developed kinetic method has been successfully applied to the measurement of Mn(II) in both some environmental water samples and certified standard reference river water sample, JAC-0031 with satisfying results. Moreover, few cations and anions interfere with the measurement of Mn(II). Compared with the other catalytic-kinetic methods and instrumental methods, the proposed kinetic method shows fairly good selectivity and sensitivity, low cost, cheapness, low detection limit and rapidity. It can easily and successfully be applied to the real water samples with relatively low salt content and complex matrices such as bottled drinking water, cold and hot spring waters, lake water, river water samples.

Electrochemical Corrosion and Chemical Mechanical Polishing(CMP) Characteristics of Tungsten Film using Mixed Oxidizer (혼합 산화제를 사용한 텅스텐 막의 전기화학적 부식 및 CMP 특성)

  • Na, Eun-Young;Seo, Yong-Jin;Lee, Woo-Sun
    • Journal of the Korean Institute of Electrical and Electronic Material Engineers
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    • v.18 no.4
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    • pp.303-308
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    • 2005
  • In this paper, the effects of oxidants on tungsten chemical mechanical polishing (CMP) process were investigated using three different oxidizers such as Fe(NO₃)₃, KIO₃ and H₂O₂. Moreover, the interaction between the tungsten film and the oxidizer was discussed by potentiodynamic polarization measurement with three different oxidizers, in order to compare the effects of W-CMP and electrochemical characteristics on the tungsten film as a function of oxidizer. As an experimental result, the tungsten removal rate reached a maximum at 5 wt% Fe(NO₃)₃concentration, and when 5 wt% H₂O₂was added in the slurry, the removal rate of W increased. Also, the microstructures of surface layer by atomic force microscopy(AFM) image were greatly influenced by the slurry chemical composition of oxidizers. It was shown that the surface roughness and removal rate of the polished surface were improved in Fe(NO₃)₃than KIO₃. The electrochemical results indicate that the corrosion current density of the 5 wt% H₂O₂ and 5 wt% H₂O/sub 2+/+ 5 wt% Fe(NO₃)₃was higher than the other oxidizers. Therefore, we conclude that the W-CMP characteristics are strongly dependent on the kinds of oxidizers and the amounts of oxidizer additive.

Silver Nanoparticles Enhanced Chemiluminescence of Luminol-KIO4 System for the Determination of Mandelic Acid (Mandelic Acid 정량을 위한 은 나노입자에 의해 증가된 화학발광분석법)

  • Alam, MD R-Mahmnur;Kamruzzaman, Mohammad;Kim, So Yeon;Jo, Hae Jin;Lee, Sang Hak;Kim, Young Ho;Choi, Jong Ha
    • Applied Chemistry
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    • v.15 no.1
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    • pp.21-24
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    • 2011
  • A sensitive silver nanoparticles (Ag NPs) enhanced chemiluminescence (CL) method is reported for the determination of mandelic acid (MA). This method is based on the luminol-KIO4 system catalyzed by Ag NPs to produce CL spectra. Prepared Ag NPs were characterized by UV-visible spectra and TEM image. Under optimal condition, CL spectra of the system were responded linearly with the concentration of MA in the range of 2.5×10-9 to 2.0×10-8 mol L-1 (r=0.9989) with a detection limit of 1.2×10-10 mol L-1. The relative standard deviation of 1.0×10-7 mol L-1 MA was found 1.45 (n=9).

Metal CMP Characteristics by Oxidizer Modification (Oxidizer modify에 의한 Metal CMP 특성)

  • Park, Suno-Woo;Kim, Chul-Bok;Kim, Sang-Yong;Lee, Woo-Sun;Chang, Eui-Goo;Seo, Yong-Jin
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2004.11a
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    • pp.727-730
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    • 2004
  • In this paper, so as to investigate the influence of oxidizer for each metal film using the alumina-based slurry, we have peformed the W/Ti metal-CMP process by adding $H_2O_2$ as a representative oxidizer from 1 wt% to 9 wt%, respectively. As an experimental result, for the case of 5 wt% oxidizer added, the removal rates were improved and polishing selectivity of 1.4 : 1 was obtained. Also, we compared the effects of oxidizer or W-CMP process with three different kind of oxidizers with 5 wt% hydrogen peroxide such as $Fe(NO_3)_3$, $H_2O_2$, and $KIO_3$. Finally, atomic force microscope (AFM) measurements were carried out for the analysis of surface morphology and root mean square (RMS) roughness after CMP Process.

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Synthesis of (S)-5-iodo-2-aminoindan.HCI ((S)-5-요오드 -2-아미노인단.염산염의 합성)

  • 마은숙
    • YAKHAK HOEJI
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    • v.45 no.6
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    • pp.582-587
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    • 2001
  • (S)-5-iodo-2-aminoindan.HCI (7) was synthesized for developing a serotonergic agent. (S)- Phenylalanine was protected with trifuoroacetyl group and compound 2 was prepared by direct iodination in acetic acid and in the presence of I$_2$, KIO$_4$, and sulfuric acid. Compound 3 was cyclized by Friedel-Crafts reaction and reduced with NaBH$_4$ to form 5-iodo-2-(N-trifluoroacetyl)aminoindan-1-ol (4) . This compound was reduced to indan derivative 5 using the triethylsilane and BF$_3$ . Et$_2$O. It was basified with $K_2$CO$_3$ solution and treated with saturated HCl in ethyl ether to isolate compound 7.

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Development of Anticancer Agents from Korean Medicinal Plants (Part 8). - Cytotoxic Activity of Taraxaci Herba Extract against Human Skin Melanoma Cells - (한국산 생약으로부터 항암물질의 개발(제 8보) - 포공령 추출물이 인체 피부흑색종세포에 미치는 세포독성작용 -)

  • Oh, In-Kio;Yoo, Eun-Ah;Han, Du-Seok;Kang, Kil-Ung;Baek, Seung-Hwa
    • Korean Journal of Pharmacognosy
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    • v.29 no.3
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    • pp.198-203
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    • 1998
  • In the present study, we have evaluated cytotoxic effects of Taraxaci herba extract on human skin melanoma cells. The light microscopic study showed morphological changes of the treated cells. Disruptions in cell organelles were determined by calorimetric methods: MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazoliumbromide), NR (Neutral red) and SRB (Sulforhodamine B protein) assay. These results suggest that Taraxaci herba retains a potential antitumor activity.

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