• 제목/요약/키워드: alkali metal salt

검색결과 33건 처리시간 0.019초

중성염이 Poly(ethylene terephthalate) 직물의 알칼리 가수분해에 미치는 영향(II) (Effects of Neutral Salts on Alkaline Hydrolysis of Poly(ethylene terephthalate) (II) - Anionic Effect -)

  • 도성국;조환
    • 한국염색가공학회지
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    • 제6권2호
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    • pp.10-16
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    • 1994
  • Neutral salts have negative or positive effects on the rates of many chemical reactions and also on the rates of acidic and alkaline hydrolysis of carboxylic esters. The direction of neutral salt effects on the hydrolysis of ester depends on the charge of esters. Neutral salts accelerate alkaline hydrolysis of esters with negative charge, but decelerate alkaline hydrolysis of esters with positive charge, and have little effect on the alkaline hydrolysis of neutral esters. It is expected that the rate of the alkaline hydrolysis of Poly(ethylene terephthalte) (PET), polymeric solid carboxylic polyester with carboxyl end group at the polymer end, is also influenced positively by neutral salts. In the present work, to clarify the mechanism of the neutral salt effect on the alkaline hydrolysis of PET, many salts with different anions like NaF, NACl, NaBr, NaI 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 decrease in the nucleophilicity of anions of neutral salts, i.e., in the order of $F^-$ <$Cl^-$<$Br^-$<$I^-$. It was thought that the reaction rate was increased in the order of $F^-$ <$Cl^-$<$Br^-$<$I^-$. because the completion of anions with $OH^-$ for carbonyl carbon became weaker with the decrease in the nucleophilicity and with the increase in the size of anions.

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크라온에테르를 이용한 탈륨(I) 이온 선택성 전극 (Tallium(I) Ion-Selective Electrodes Based on Crown Ethers)

  • 김성민;정성욱;김진은;김재상
    • 대한화학회지
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    • 제37권8호
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    • pp.773-778
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    • 1993
  • Tl$^+$이온 센서로서 크라운 에테르 B15C5와 DB18C6를 중성운반체로 한 PVC 액체막 이온 선택성 전극을 제작하였다. 막용매로는 DOA, NPPE 및 NPOE를 사용하였으며 친유성 염, KTClPB의 농도를 변화시킨 여러가지 조성의 막을 시험하였다. B15C5와 DB18C6 막 전극의 감응전위는 농도범위, 10$^{-1}$∼10$^{-5}$M에서 직선으로 나타났으며 최대 기울기는 전극에 따라서 40∼55 mV/decade였다. 선택계수는 분리용액법으로 결정하였으며 알카리금속 이온, 알칼리토금속 이온 및 일부 전이금속 이온에 대하여 좋은 선택성을 나타냈다. 제작된 액체막 전극은 Ph > 3 에서 안정한 감응전위를 보였다.

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알칼리금속을 함침시킨 아미노산 염 수용액의 이산화탄소 흡수특성 연구 (CO2 Absorption by Alkali-modified Amino Acid Salts)

  • 임윤희;조영민;박준석
    • 공업화학
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    • 제22권5호
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    • pp.526-531
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    • 2011
  • 본 연구는 이산화탄소 흡수성능을 향상시키기 위하여 아미노산에 알칼리금속을 함침시키는 것이다. 사용된 아미노산은 글리신이었으며, 알칼리성분 추가에 따라 pH가 11까지 증가하였다. 시험제조한 아미노산 염은 회분식과 연속식 흡수공정에서 이산화탄소의 포집능을 평가하였다. 치환된 금속종류에 따른 이산화탄소 흡수량은 Sodium Glycinate (Na-Gly) ${\geq}$ Lithium Glycinate (Li-Gly) > Potassium Glycinate (K-Gly) 순으로 나타났다. 흡수반응온도에 따른 $CO_2$ 흡수량 시험결과, $20^{\circ}C$에서는 알칼리금속을 함침시킨 아미노산 염이 1차 아민보다 약간 낮은 흡수능을 보였으나, 연속식 흡수반응기에서는 10% $CO_2$ 흐름에 대하여 반응기 내부온도가 상승하면서($40^{\circ}C$, $60^{\circ}C$) 아미노산 염의 흡수량 증가폭이 아민에 비하여 상대적으로 크게 나타났다.

용융염법을 이용한 저차원 구조의 금속 칼코겐 화합물의 합성 및 구조 특성연구 (Synthesis and Characterization of Low-Dimensional Chalcogenide Compound via a Molten Salt Method)

  • 최덕수;윤혜식;오화숙;김돈;윤호섭;박윤봉
    • 대한화학회지
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    • 제48권5호
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    • pp.504-509
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    • 2004
  • 구리 금속 분말과 혼합 알칼리금속 다셀레늄화물 용융염 ($KNaSe_x$) 과의 반응을 통하여 판상형태의 결정을 갖는 $KCu_4Se_3$ 화합물을 얻었다. $KCu_4Se_3$화합물의 구조는 X-선 단결정 회절법에의해 결정되었으며 사반면상을 갖는다. (P4/mmm, a=4.013(1)${\AA}$, c=9.712(1)${\AA}$, z=1, R=6.7%). 그 구조는 안티 PbO 구조를 갖는 $Cu_2Se_2$ 층이 겹쳐짐으로서 만들어지는 $[Cu_4Se_3]_n^{n-}$의 이중층으로 구성되어있다. $KCu_4Se_3$의 단결정에 대한 온도 변화에 따른 저항 측정을 통하여 전도체의 특성을 확인하였으며 300 K에서 $1.8{\times}10^{-4}{\Omega}{\cdot}cm$과 20 K에서 $1.0{\times}10^{-6}{\Omega}{\cdot}cm$의 저항 값을 갖는다.

첨가제가 담배 연기성분에 미치는 영향 (The Effect of Some Additives on the Components of Cigarette Smoke)

  • 나도영;제병권;이창국;조시형;이동욱
    • 한국연초학회지
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    • 제27권1호
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    • pp.40-50
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    • 2005
  • The influence of tobacco additives on the composition of the combustion products in mainstream smoke is discussed. The effect of additives on the chemical composition of smoke have been further evaluated in order to discover additives that would alter the chemical composition of smoke. Tobacco was uniformly treated at a 1-5$\%$ level with 8 classes of additives. Group M treated with alkali metal salt and group S, F, O give lower tar, nicotine and CO values than the control. Group AN treated with natural antioxidant gives higher tar and CO values than the control. The increases are most probably due to the high transfer rate of the ingredients to smoke. M3 and P1 reduced above the $50\%$ of TSNA from the smoke. M4 and P1 reduced above the $50\%$ of HCN from the smoke. These results suggest that tobacco additives alter pyrolysis or combustion product distribution and provide fundamental data to lead the development of a RRP(reduced risk product).

The Potentiometric Performance of Mercury (II) Ion-Selective Electrode Based on Tetracycline Antibiotics

  • Baek, Jong-Gyu;Rhee Paeng, In-Sook
    • 전기화학회지
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    • 제11권1호
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    • pp.59-63
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    • 2008
  • Poly (vinylchloride) (PVC) membrane electrodes based on neutral carrier, tetracycline was prepared as an active sensor for Hg(II) ion, and tested in different contents of the potassium tetrakis (4-chlorophenyl) borate (KTpClPB) as lipophilic salt. Bis (2-ethylhexyl) sebacate (DOS), bis(l-butylpentyl) adipate (BBPA), 2-nitrophenyl octyl ether (NPOE) and dibutyl phthalate (DBP) were used as diverse plasticizing solvent mediators. This electrode shows excellent potentiometric response characteristics and display good linearity with log $[Hg^{+2}]$ versus EMF response, over a range of concentrations between $10^{-7}$ and $10^{-3}M$. With 30.8mV/decade Nernstian slope, the detection limit was $6.9{\times}10^{-9}M$ and the response time was less than 20s. The proposed electrode yields very good selectivity for mercury (II) ion over many cations such as alkali, alkaline earth, transition and heavy metal ions. And it shows a very stable potential values in a wide pH range. This reliable electrode prepared was kept at least a month without considerable alteration in their response to Hg (II) ion.

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

  • 도성국;조환
    • 한국염색가공학회지
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    • 제6권1호
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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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Preliminary design and assessment of a heat pipe residual heat removal system for the reactor driven subcritical facility

  • Zhang, Wenwen;Sun, Kaichao;Wang, Chenglong;Zhang, Dalin;Tian, Wenxi;Qiu, Suizheng;Su, G.H.
    • Nuclear Engineering and Technology
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    • 제53권12호
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    • pp.3879-3891
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    • 2021
  • A heat pipe residual heat removal system is proposed to be incorporated into the reactor driven subcritical (RDS) facility, which has been proposed by MIT Nuclear Reactor Laboratory for testing and demonstrating the Fluoride-salt-cooled High-temperature Reactor (FHR). It aims to reduce the risk of the system operation after the shutdown of the facility. One of the main components of the system is an air-cooled heat pipe heat exchanger. The alkali-metal high-temperature heat pipe was designed to meet the operation temperature and residual heat removal requirement of the facility. The heat pipe model developed in the previous work was adopted to simulate the designed heat pipe and assess the heat transport capability. 3D numerical simulation of the subcritical facility active zone was performed by the commercial CFD software STAR CCM + to investigate the operation characteristics of this proposed system. The thermal resistance network of the heat pipe was built and incorporated into the CFD model. The nominal condition, partial loss of air flow accident and partial heat pipe failure accident were simulated and analyzed. The results show that the residual heat removal system can provide sufficient cooling of the subcritical facility with a remarkable safety margin. The heat pipe can work under the recommended operation temperature range and the heat flux is below all thermal limits. The facility peak temperature is also lower than the safety limits.

다양한 촉매들을 통한 모델 바이오매스-초임계수 촉매 가스화에서 수소 생산 성능에 대한 연구 (The Study on of Hydrogen Production Performance by Model Biomass-supercritical Water Gasification with Various Catalysts)

  • 허동현;황종하;이루세;손정민
    • 한국수소및신에너지학회논문집
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    • 제26권1호
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    • pp.8-14
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    • 2015
  • In this study, the model biomass was used for hydrogen production by supercritical water gasification (SCWG). Model biomasses were glycerol, glycine, lignin and cellulose. The feed concentration was set to 1 wt%. Experiments were conducted in a reactor at $440^{\circ}C$ and above 26.3 MPa for 30 min. The effects of catalysts such as alkali metal salt ($K_2CO_3$ and $Na_2CO_3$) and transition metal salts ($Ni(NO_3)_2$, $Fe(NO_3)_3$ and $Mn(NO_3)_2$) on the gasification were systematically investigated. No tar or coke was observed in all experiments. The results showed that the gasification efficiency increased with various catalysts. For the cellulose and glycerol, all catalysts were effective for the promoted $H_2$ production compared with no catalyst. The significant decrease of $H_2$ production compared with no catalyst was observed with $Na_2CO_3$ and $Fe(NO_3)_3$ for glycine and lignin. respectively. The highest H2 production, 1.24 mmol was obtained for glycerol-SCWG with $Mn(NO_3)_2$. Conclusively, the addition of $Mn(NO_3)_2$ enhanced all model biomass gasification efficiency and increased the hydrogen production promoting the supercritical water reaction.

정삼투 공정의 유도용질로서의 식물 화학물질 기반의 탄닌산 유도체 (Phytochemical-based Tannic Acid Derivatives as Draw Solutes for Forward Osmosis Process)

  • 김태형;주창하;강효
    • 멤브레인
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    • 제28권3호
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    • pp.157-168
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    • 2018
  • 우리는 정삼투 공정의 유도용질로서 잠재적인 활용 가능성을 확인하기 위해 식물화학물질인 tannic acid (TA)에 알칼리 염 처리한 alkali tannate 염 중 하나인 potassium tannate (TA-K)를 평가하였다. TA-K의 정삼투 특성과 회수 특성은 체계적으로 조사되었다. 정삼투 공정을 active layer facing feed solution (AL-FS) 방식으로 적용했을 때, TA-K 유도용액의 투수량은 TA 유도용액의 투수량 보다 훨씬 많은 반면, TA 유도용액의 투수량이 거의 확인되지 않았다. 100 mM 저농도에서의 TA-K 유도용액의 삼투압(1,135 mOsmol/kg)은 NaCl 수용액의 삼투압(173 mOsmol/kg)의 약 6.5배로 확인되었다. 100 mM 농도의 TA-K의 투수량과 specific salt flux (6.14 LMH, 1.26 g/L)는 동일한 농도의 NaCl 유도용액의 투수량과 specific salt flux (2.46 LMH, 2.63 g/L)의 약 2.5배 및 0.5배로 각각 확인되었다. TA-K를 재사용하기 위해, 금속 이온 침전법을 이용하여 TA-K유도용질을 침전시킨 후, membrane filtration을 이용하여 유도용질을 회수하였다. 이 연구는 식물화학물질을 정삼투 공정의 유도용질로서의 적용 가능성을 보여준다.