• Title/Summary/Keyword: carbon neutral

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Plasma Characterization of Facing Target Sputter System for Carbon Nitride Film Deposition

  • Lee, Ji-Gong;Lee, Sung-Pil
    • Transactions on Electrical and Electronic Materials
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    • v.5 no.3
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    • pp.98-103
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    • 2004
  • The plasma properties in the facing target sputtering system during carbon nitride film deposition have been investigated. The ionized nitrogen species of the deposited films increased with increasing discharge current and were independent of the nitrogen pressure. The nitrogen content in the films did not vary significantly with the variation of nitrogen gas. The electron temperature was high close to that in the inter-cathode region, reduced as the electrons moved away from the most intense region of magnetic confinement and increased again outside this region. Calculations based on the film composition showed that the ion to carbon atom ratio at the substrate was about 50 and that the ratio between the ionized and neutral nitrogen molecules was about 0.25.

Energy Loss of Hydrogen Atom due to Charge Exchange in Neutral Particle Energy Analyzer (중성입자 에너지 분석장치에서 전하교환용 탄소박막에 의한 수소원자의 에너지 손실특성)

  • Kim, Kye-Ryung;Kim, Wan;Lee, Yong-Hyun;Kang, Hee-Dong
    • Journal of Sensor Science and Technology
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    • v.7 no.3
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    • pp.179-187
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    • 1998
  • A neutral particle energy analyzer, which has the carbon stripping foil and the $90^{\circ}$ cylindrical electrostatic deflection plate, was designed and constructed for measuring of ion temperature in plasma. The energy calibration and energy resolution were studied in detail for a hydrogen ion at the $0.5{\sim}3.0\;keV$ energy using a duoplasmatron ion source. An energy of hydrogen ion to the deflection plate voltage at the peak ion count rate could be fitted by the expression $E_{o}(keV)$=3.83V(kV). The measured energy resolution, which was about 2 % at the energy of 3.0 keV and 9 % at the energy of 0.5keV, was better for the increased hydrogen ion energy. For the charge exchanged hydrogen atom due to the carbon stripping foil, the energy calibration, energy loss and resolution were measured to the $0.5{\sim}2.0{\mu}g/cm^{2}$ thickness of the carbon stripping foil. An energy of the charge exchanged hydrogen atom as a function of the deflection plate voltage and carbon foil thickness could be fitted by the expression $E_{o}(keV)=(0.53d+4.4){\cdot}V(kV)$. The energy loss was $0.23{\sim}0.89\;keV $ to the $0.5{\sim}2.0{\mu}g/cm^{2}$ carbon foil thickness and the $0.5{\sim}3.0\;keV$ energy of the incident neutral hydrogen atom, it could be fitted by the expression ${\Delta}E=(0.12d+0.27){\cdot}{E_{o}}^{1/2}(keV)$. The measured energy resolution for the neutral hydrogen atom, which was between 7 % and 35 % in this experiment region, was increased for the increasing neutral hydrogen atom energy and the decreasing carbon stripping foil thickness.

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Kinetic Studies on the Nucleophilic Addition of Thioglycolic Acid to S-Phenyl-S-vinyl-N-p-tosylsulfilimine Derivatives (S-Phenyl-S-vinyl-N-p-tosylsulfilimine 유도체에 대한 Thioglycolic Acid의 친핵성 첨가반응에 관한 반응속도론적 연구)

  • Kim, Tae Rin;Han, Man So;Pyun, Sang Yong
    • Journal of the Korean Chemical Society
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    • v.40 no.10
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    • pp.663-669
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    • 1996
  • The rate constants for the nucleophilic addition reactions of thioglycolic acid to vinylsulfilimine(VSI) derivatives(p-OCH3, H, p-Cl and p-Br) were determined by an ultraviolet spectrophotometric method, and rate equations which can be applied over a wide pH range were obtained. On the basis of rate equation, general base catalysis and substituent effect, a plausible addition reaction mechanism was proposed: Below pH 3.0, the reaction was proceeded via the addition of neutral molecule to carbon-carbon double bond after protonation at the nitrogen atom of the sulfilimine, and in the pH range of 3.0 to 9.0, the neutral molecule and its anion attacked to carbon-carbon double bond competitively. Above pH 9.0, sulfide anion added to the double bond (Michael type addition).

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Detergency of Woven Fabrics in Relation to the Detergents and Washing Temperature (세제의 종류 및 세척온도에 따른 각종 섬유직물의 세척성)

  • Cho Sung Kyo
    • Journal of the Korean Society of Clothing and Textiles
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    • v.3 no.1
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    • pp.49-56
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    • 1979
  • To investigate detergency of various woven fabrics in relation to the detergents and washing temperature. cotton, polyester/cotton (p/c), nylon, acetate, and polyester were soiled in aqueous artificial ($carbon-CCl_4$) soil. Each fabric was washed with soap, alkaline and neutral synthetic detergents at $30^{\circ}C$, $40^{\circ}C$ and $60^{\circ}C$ respectively. The results obtained may be summerized as follows; 1. In soap, ascension of temperature had the most important effect upon washing efficiency and the higher the temperature was, the higher the washing efficiency was showed in all fabrics. And in case of alkaline synthetic detergent, nylon and p/c fabrics were much more difficult to clean at higher temperature and also acetate and polyester had the best efficiency at $40^{\circ}C$. Detergency of neutral detergent was good but the effect of temperature in neutral detergent was less than in soap. 2. Washing efficiency of cotton was less than that of others. 3. The higher the temperature was, the higher the washing efficiency of cotton in all detergents, and the best was in soap. In p/c, detergency of neutral detergent was good but effect of ascension of temperature was lower than in soap. In nylon, washing efficiencies of alkaline synthetic detergent and neutral detergent were excellent at 30°C but detergency of soap at $60^{\circ}C$ was best. In case of acetate, detergency of all detergents was about the same at $30^{\circ}C$ but that of soap at $60^{\circ}C$ was best. In polyester at $30^{\circ}C$, efficiency of neutral detergent was excellent but that of soap was more excellent at higher temperature and the best detergency of alkaline synthetic detergent showed at $40^{\circ}C$. In general. the higher the temperature is, the higher the washing efficiency of soap is. But when synthetic fibers of nylon and polyester are washed with synthetic detergents, washing at lower temperature is advisable.

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Accelerating Effect of Neutral Salts on Alkaline Hydrolysis of Poly(ethylene terephthalate) (I) - Cationic Effect - (중성염의 폴리에틸렌 텔레프탈레이트의 알칼리 가수분해 촉진효과에 관한 연구(I) - 양이온의 영향 -)

  • Do, Sung-Guk;Cho, Hwan
    • Textile Coloration and Finishing
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    • v.6 no.1
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    • pp.33-43
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    • 1994
  • In the present work, to clarify the mechanism of the neutral salt effect on the alkaline hydrolysis of PET, many salts with different cations like LiCl, NaCl, KCl, CsCl were added to the aqueous alkaline solutions. Then PET was hydrolyzed with aqueous solutions of many salts in alkali metal hydroxides under various conditions. Some conclusions obtained from the experimental results were summarized as follows. The reaction rate of the alkaline hydrolysis of PET was increased by the addition of neutral salts and In k was increased nearly linearly with the square root of ionic strength of reaction medium. This fact suggested that the ionic strength effect by Debye-Huckel and Bronsted theory was exerted on the reaction. The specific salt effect was also observed. The reaction rate was increased with the increase in the electrophilicity of cations of neutral salts, i. e., in the order of $Cs^+$/ < $K^+$/ $a^+$/ $i^$^+$. It was considered that the reaction rate was increased in the order of C $s^+$. < $K^+$. $a^+$. $i^+$. because the lowering effect of the cations on the negative charge of PET surface was increased with the electrophilicity of cations. It was thought that $E_{a}$ was increased because the cations of neutral salts decreased the negative charge of PET surface. It, however, was inferred from the increase in ${\Delta}$S* and the decrease in the ${\Delta}$G* that the cations of neutral salts associated with PET increased the collision frequency between carbonyl carbon and OH- ion and then accelerated the reaction rate.te.

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Biochar for soil carbon sequestration (토양탄소격리를 위한 바이오차)

  • Woo, Seung Han
    • Clean Technology
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    • v.19 no.3
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    • pp.201-211
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    • 2013
  • Biochar is charred materials generated during pyrolysis processes in the absence of oxygen using biomass, resulting in high carbon contents. In recent years, biochar has attracted more increasingly due to its potential role in carbon sequestration, renewable energy, waste management, soil amendment for agricultural use, and environmental remediation. Since biochar has a long-term stability in soil for thousands of years, biochar can be carbon negative compared to carbon-neutral biomass energy that decomposes eventually. Moreover, when biochar is applied to soil, crop production can be largely improved due to its high pH and its superior ability to retain water and nutrients. This paper review the research trends of biochar including the principles of carbon sequestration by biochar, its physico-chemical properties, and its applications on agricultural and environmental area.

Cinnamic Acid Derivatives III, The Kinetics and Mechanism of the Nucleophilic Addition of Thioglycolic Acid to Benzalacetophenone Derivatives (신남산 유도체III, Benzalacetophenone 유도체에 대한 Thioglycolic acid의 친핵성 첨가반응 메카니즘과 그 반응속도론적 연구)

  • Lee, Ki-Chang;Hwang, Yong-Hyun;Park, Eun-Kyung;Ryu, Jung-Wook;Lee, Kwang-Il
    • Journal of the Korean Applied Science and Technology
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    • v.7 no.2
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    • pp.33-40
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    • 1990
  • The Kinetics of the addition of benzalacetophenone derivatives was investigated by ultraviolet spectrophotometery in 5% dioxane $H_2O$ at $50^{\circ}C$. A rate equation was obtained in wide range of pH. The substituent effects on benzalacetophenone derivatives were studied, and addition were facilitated by electron attracting groups. The final product was benzalacetophenone-${\beta}$-thioglycolic acid synthesized by the addition of thioglycolic acid to benzalacetophenone. On the base of the rate equation, substituent effect, general base effect and final product, the plausible addition mechanism was proposed: Below pH 9.0, only neutral thioglycolic acid molecule was added to the carbon-carbon double bond, and in the range of pH $9.0{\sim}11.0$, neutral thioglycolic acid molecule and thioglycolic acid anion competitively attacted the double bond. By contrast, above pH 11.0, the reaction was dependent upon only the addition of thioglycolic acid anion.

Studies on the Enzyme Activities of Rhizopus distributed in South Korea(1) - On the amylase, protease and cellulase activities- (한국산 Rhizopus의 효소활성에 관한 연구 (第 1 報) - Amylase, protease 및 cellulase 활성에 관하여-)

  • 이영녹;윤경하;이평우;배광승;박용근;정성균;서항원
    • Korean Journal of Microbiology
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    • v.14 no.2
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    • pp.49-49
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    • 1976
  • Enzyme activities, such as glucoamylase dextrinogenic amylase, cellulase, acid protase and neutral protease, of Rhizopus isolated from various substrates collected throughout South Korea are measured, and their enzyme activities are surveyed from taxonomical, ecological and physiological viewpoint. Effect of carbon sources and phytohormones on the amylalse production of Rhizopus are also measured. Among the 735 strains of Phizopus isolated, strain number 587 exhibiting most prominent dextrinogenic amylase and netral protease activity is selected as the best strain, and the strain number 673, 108, 329, 165 and 728 are seleted for their predominant cellulase, acid protease, glucoamylase, dextrinogenic amylase and neutral protease activities, respectively. R.acidus and R.nigricans which exhibited relatively higher callulalse activity, showed lower activities for both amylase. R.tritici exhibited higher protease activity. The relations between activities and various substrates of wild strains are not outstnading difference, although the strains isolated from inland region exhibited more or less higher amylase and cellulase activities, than those of coast region, generally. Lactose and dextrin are most effective carbon sources for glucoamylase and dextrinogenic amylase production of the Rhizopus niveus, respectively. Although all phytohormones tested are effective for production of amylase by the Rhizopus strains, except nicotinamide for glucoamylase production, biotin and ascorbate are most effective for dextrinogenic amylase and glucoamylase production, respectively.

Studies on the Enzyme Activities of Rhizopus distributed in South Korea(1) - On the amylase, protease and cellulase activities- (한국산 Rhizopus의 효소활성에 관한 연구 (第 1 報) - Amylase, protease 및 cellulase 활성에 관하여-)

  • 이영녹;윤경하;이평우;배광승;박용근;정성균;서항원
    • Korean Journal of Microbiology
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    • v.14 no.2
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    • pp.47-56
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    • 1976
  • Enzyme activities, such as glucoamylase dextrinogenic amylase, cellulase, acid protase and neutral protease, of Rhizopus isolated from various substrates collected throughout South Korea are measured, and their enzyme activities are surveyed from taxonomical, ecological and physiological viewpoint. Effect of carbon sources and phytohormones on the amylalse production of Rhizopus are also measured. Among the 735 strains of Phizopus isolated, strain number 587 exhibiting most prominent dextrinogenic amylase and netral protease activity is selected as the best strain, and the strain number 673, 108, 329, 165 and 728 are seleted for their predominant cellulase, acid protease, glucoamylase, dextrinogenic amylase and neutral protease activities, respectively. R.acidus and R.nigricans which exhibited relatively higher callulalse activity, showed lower activities for both amylase. R.tritici exhibited higher protease activity. The relations between activities and various substrates of wild strains are not outstnading difference, although the strains isolated from inland region exhibited more or less higher amylase and cellulase activities, than those of coast region, generally. Lactose and dextrin are most effective carbon sources for glucoamylase and dextrinogenic amylase production of the Rhizopus niveus, respectively. Although all phytohormones tested are effective for production of amylase by the Rhizopus strains, except nicotinamide for glucoamylase production, biotin and ascorbate are most effective for dextrinogenic amylase and glucoamylase production, respectively.

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Kinetic Studies on the Nucleophilic Addition of Cysteine to 3,4-Methylenedioxyphenylmethylene Malononitrile (3,4-Methylenedioxyphenylmethylene Malononitrile에 대한 Cysteine의 친핵성 첨가반응에 관한 반응속도론적 연구)

  • Tae-Rin Kim;Dong-Suk Rho;Young-Haeng Lee
    • Journal of the Korean Chemical Society
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    • v.26 no.6
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    • pp.407-413
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    • 1982
  • The rate constants of the nucleophilic addition of cysteine to 3,4-methylenedioxyphenylmethylene malononitrile were determined by UV Spectrophotometry and a rate equation which can be applied over wide pH range was obtained. On the basis of rate equation, it may be concluded that the rate constants were dependent upon only the concentration of hydroxide ion above pH 9.0, however, below pH 6.0, the reaction were initiated by the addition of neutral cysteine molecule to carbon-carbon double bond and at pH 7.0~9.0, the addition of a neutral cysteine molecule and it's anion occurred competitively.

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