• 제목/요약/키워드: Acid and Alkali

검색결과 584건 처리시간 0.021초

산-염기 처리한 게 껍질에 의한 수풍의 납 이온 제거 (Removal of Pb2+ ion from aqueous solution Using crab shell treated by acid and alkali)

  • 김동석
    • 한국환경과학회지
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    • 제12권4호
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    • pp.469-476
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    • 2003
  • In order to examine the pre-treatment effect of crab shell en Pb$^{2+}$ removal by crab shell in aqueous solution, acid and alkali pre-treated crab shell were used. Electron microscopy techniques such as TEM (transmission electron microscopy) and SEM (scanning electron microscopy), and EDX (energy dispersive X-ray) and FTIR (Fourier transform infrared) spectrometry techniques were used to investigate the process of Pb$^{2+}$ removal by acid and alkali pre-treated crab shell. The Pb$^{2+}$ removal by acid pre-treated crab shell was much lower than that by untreated crab shell because of the decrease of CaCO$_3$ from the crab shell. However, the Pb$^{2+}$removal by alkali pre-treated crab shell increased compared to that by untreated crab shell. The results were confirmed by TEM, SEM, EDX and FTIR.nd FTIR.

유지의 알칼리 이성질화에 의한 Conjugated Linoleic Acid 농축물의 제조 (Preparation of Conjugated Linoleic Acid Concentrate from Vegetable Oils by Alkali Isomerization)

  • 김지호;신효선
    • 한국식품과학회지
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    • 제31권6호
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    • pp.1453-1457
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    • 1999
  • 항산화 및 항암 작용이 있는 것으로 알려진 conjugated linoleic acid(CLA)를 식물성 유지로부터 알칼리 이성질화에 의해 고 농도의 CLA 농축물을 얻기 위한 최적 조건을 연구하였다. 지방산 조성이 상이한 식물성 유지를 알칼리 이성질화 하였을 때 CLA 생성량은 유지중 linoleic acid 함량이 많은 것이 가장 높았다. 홍화유를 알칼리 이성질화할 때 KOH 농도는 $8{\sim}11%$, 가열온도는 $180{\sim]185^{\circ}C$에서 cis-9, trans-11 CLA와 총 CLA 생성량이 가장 높았고, 가열시간은 CLA 생성량에 큰 영향을 미치지는 않았으나 $20{\sim}40$분이 가장 적당하였다. 홍화유를 silicic acid column chromatograph)에 의해 중성, 당 및 인지방질의 lipid class를 분획하여 알칼리 이성질화를 시켰을 때 중성지방질의 획분에 CLA가 가장 많이 함유되었다. 알칼리 이성질화시킨 홍화유를 요소처리와 HPLC 분획에 의해 95.4%의 CLA 농축물을 얻을 수 있었다.

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이온성 크라운에테르 포스포닉산에 의한 알칼리 금속 양이온과 알칼리 토금속 양이온의 용매추출 (Solvent Extractions of Alkali Metal Cations and Alkaline Earth Cations by Ionizable Crown Ether Phosphonic Acids)

  • 정연진
    • 한국응용과학기술학회지
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    • 제22권1호
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    • pp.50-55
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    • 2005
  • A comparison of alkali metal cation and alkaline earth cation solvent extraction was made for three additional monoionizable crown ethers and one diionizable crown ether. sym-(n-Octyldibenzo)-16-crown-5-oxyacetic acid $\underline{1}$ exhibited high efficiency and selecvity in solvent extraction of alkali metal cations with respect to that observed with alkaline earth cations. Sizes of $Na^+$ and $Ca^{2+}$ appropriately match with the cavity size of monoethyl sym-bis[4(5)-tert-butylbenzo]-16-crown-5-oxymethylphosphonic acid $\underline{3}$. As the result, $Na^+$ and $Ca^{2+}$ are the best extracted. sym-(n-Octyldibenzo)-16-crown-5-oxymethyldiphosphonic acid $\underline{4}$was found to be somewhat selective for $Na^+$ over $Li^+$ and other alkaline earth metal cations. In the complexation of alklaine earth cations by crown ether diphosphonic acid $\underline{4}$, $Ca^{2+}$ and $Sr^{2+}$ are the appropriate sizes, but lager $Ba^{2+}$ may be due to favorable formation of a sandwich type complex between the crown ether cavity and the dianion of the deprotonated crown ether phoaphonic acid moiety.

알칼리 활성화 슬래그 시멘트 모르타르의 내황산성 (Resistance of Alkali Activated Slag Cement Mortar to Sulfuric Acid Attack)

  • 민경산;이승헌
    • 한국세라믹학회지
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    • 제44권11호
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    • pp.633-638
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    • 2007
  • The setting time of alkali activated slag cement tends to be much faster than ordinary Portland cement, and its compressive strength had been higher from the 1 day but became lower than that of the cement on the 28 days. According to the results of the surface observation, weight loss, compressed strength, and erosion depth tests on the sulphuric acid solution. It has been drawn that alkali activated slag cement has a higher sulphate resistance than ordinary Portland cement, and in particular, the alkali activated slag cement added 5 wt% alumina cement has little deterioration on the sulphuric acid solution. The reason why the alkali activated slag cement has higher sulphate resistance than other hardened cement pastes is that it has no $Ca(OH)_2$ reactive to sulphate ion, and there is little $CaSO_4{\cdot}2H_2O$ production causing volume expansion, unlike other pastes. And it is supposed that $Al(OH)_3$ hydrates with high sulphate resistance, which is produced by adding the alumina cement increases the sulfate resistance.

산 및 알칼리 공정으로 조제한 수리미 가열 겔의 물성 특성 (Rheological Properties of Heat-Induced Gels of Surimi from Acid and Alkali Process)

  • 최영준;박주동;김진수;조영제
    • 한국수산과학회지
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    • 제35권4호
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    • pp.309-314
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    • 2002
  • 알칼리 pH에서 어육 단백질을 녹인 후 등전점 처리를 통하여 단백질을 회수하고, 중성으로 pH를 조절하여 조제한 알칼리 수리미 가열 겔의 파괴강도와 변형값은 수세 과정을 통해 조제한 기존의 수리미 가열 겔에 비하여 손색이 없는 것으로 나타났으나, 백색도 값은 수리미에 남아있는 혈색소와 육 색소로 인하여 낮게 나타났다. 산처리 수리미의 저장 modulus 값은 수분 함량이 감소함에 따라 감소하였으나, 알칼리 수리미의 경우는 증가하였다. 수리미의 최종 pH는 저장 modulus 값에 영향을 미치고 형태는 산처리와 알칼리 처리 수리미 간에 다소 차이를 보였다. Potassium bromide는 S-S 결합의 형성을 통해 가열 겔의 저장 modulus를 증가시키는 것으로 나타났다. 알칼리 처리 수리미는 파괴강도, 변형값 및 백색도에 미루어 어묵 grade의 연제품 제조를 위한 원료로는 손색이 없는 것으로 판단하였다.

한천의 산 당화에 의한 Furan화합물의 생성 및 제거 (Formation of Furans during the Acid Hydrolysis of Agar and Their Removal by Treatments of Lime, Steam-stripping and Hydrophobic Resins)

  • 김나현;이재원;서영범;윤민호
    • 농업과학연구
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    • 제36권2호
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    • pp.225-232
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    • 2009
  • The ratio of saccharification and formation of furans during the acid hydrolysis of agar with oxalic acid and sulfuric acid were examined base on the contents of the agar and acids. The ratio of saccharification in oxalic acid appeared to be 51~59% somewhat higher than 49~61% of sulfuric acid. Formation of the furans during the acid hydrolysis increased proportional to the contents of agar and acid. The relative formation ratio was high 10~47% for furfural (FUR) and 15~29% for hydroxy-methyl furfural (HMF) in 0.5~1.25% sulfuric acid rather than those of oxalic acid. When comparing the removal efficiency of the furans using an alkali treatment, steam stripping and hydrophobic resins, FUR was eliminated 60% by the alkali treatment, 62~90% by steam stripping and 71~75% by Amberlite XAD4 and 7HP, while HMF was removed to low levels of 10.5%, 4~17% and 13~25%, respectively. The loss of reducing sugar was also observed in process of the removal of furans, and the loss rate was the level of 2~4% in alkali treatment, 11~16% in steam stripping and 7~9% in Amberlite resins.

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크라운에테르 카르복시산과 크라운에테르 포스포닉산을 포함한 알칼리 금속과 알칼리 토금속 양이온 혼합물의 경쟁적 용매추출 (Competitive Solvent Extraction of the Mixture of Alkali Metal and Alkaline Earth Metal Cation containing Crown Ether Carboxylic Acid and Crown Ether Phosphonic Acid)

  • 정용진
    • 한국응용과학기술학회지
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    • 제22권3호
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    • pp.219-227
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    • 2005
  • Competitive solvent extraction of the mixure of alkali metal and alkaline earth cation from water into organic solvent containing the crown ether carboxylic acid and anlogous crown ether phosphonic acid was investigated as follows. The lipophilic group is found to strongly influence to the selective extraction in the mixed systems from only alkali metal cation for sym-(n-decyldibenzo)-16-crown-5-oxyacetic acid $\underline{1}$ to mostly alkaline earth metal cation for sym-bis[4(5)-tert-butylbenzo]-16-crown-5-oxyacetic acid $\underline{3}$. Monoethyl sym-(n-decyldibenzo)-16-crown-5-oxymethylphosphonic acid $\underline{2}$. and monoethyl-sym- bis]4(5)-tert-butylbenzo]-16-crown-5-oxymethylphosphonic acid $\underline{4}$ showed good selectivity for $Na^+$ over $Mg^{2+}$, the second extracted ion. Structural variation in the crown ether phosphonic acid somewhat was influenced to the extraction selectivity in the mixed systems. when variation of the ionized group is influenced in the mixed systems, the selectivity of $Na^+$ as the second extracted ion was much better crown ether carboxylic acid $\underline{1}$ than crown ether phosphonic acid $\underline{2}$, while the efficiency of $Na^+$ extraction was better $\underline{2}$ (83% total loading) than $\underline{1}$ (32%).

알칼리와 CTAB 처리에 의한 양모섬유의 개질(I) -화학적 성질의 변화- (Modification of Wool Treated with Alkali and Alkali/CTAB (I) -Changes of chemical properties-)

  • 김영리;유효선
    • 한국의류학회지
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    • 제20권5호
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    • pp.728-737
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    • 1996
  • The purpose of this study is to investigate the change of the chemical properties of wool treated with six kinds of alkali (NaOH, Naac03, NH40H, NH2CH3CH30H, TMAH and BTMAH) with or without CTAB. Content of bound fatty acid liberated from wool surface, elemental composition and allw6rden time were measured to compare the surface modification of untreated and alkali treated wool. Also, the chemical degradation of the fiber was investigated by measuring cystine contents and urea-hydrogensulfite solubility. The result were as follows: 1. By the alkali treatment of wool, the covalently bound fatty acid of the epicuticle was removed and the allworden time was shortened, and in the case of wool treated with TMAH, BTMAH, the allw6rden sacs were formed unevenly and rarely. Also, cystine contents and urea-hydrogensulfite solubility were decreased by alkali treatment on wool. 2. The modification of epicuticle and the chemical degradation of wool were occurred due to alkaline hydrolysis in the order of TMAH, BTMAH > NaOH, Na3c03> NH2CH3CHaOH, NH40H. 3. As a treating time increased, the modification of epicuticle and chemical degradation of wool were accelerated. By the addition of CTAB to the alkali solution, the modification of epicuticle was increase, and the cystine contents and urea-hydrogensulfite solubility were reduced than that of wool teated with alkli without CTAB due to reduction of negative charge on the wool surface by the adhesion of CTAB.

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Surface Treatment Technology for Metal Corrosion Layer Focusing on Copper Alloy

  • Yang, Eun-Hee;Han, Won-Sik;Choi, Kwang-Sun;Lee, Young-Hoon;Ham, Chul-Hee;Hong, Tae-Kee
    • 한국응용과학기술학회지
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    • 제31권2호
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    • pp.176-182
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    • 2014
  • Using alkali treatment solution, neutrality treatment solution and acid treatment solution, the surface corrosion layer of copper plates and bronze plates that have been artificially corroded using HCl, $H_2SO_4$ and $HNO_3$ solutions were removed. In the case of alkali treatment solution, only air oxidation in the form of black tenorite and white cuproous chloride remained without being removed. In the case of using a neutrality treatment solution, a anhydrous type layer of reddish brown cupric chloride remained without being removed, together with this black and white corrosion substance. In the case of using an acid treatment solution, this red corrosion substance also remained, but all of the oxide was removed on the surface of the specimen that was treated by alternatively using alkali treatment solution and acid treatment solution. In the case of this treatment solution with the order of alkali-acid, oxidation no longer proceeded only through the distilled water cleaning process after treatment, thereby showing that oxidation from the cleaning solution no longer proceeded.

알칼리 촉매와 고정화 효소를 이용한 폐식용유로 부터 바이오 디젤 생산 1. 지방산 조성 (Biodiesel Production from Waste Cooking Oil Using Alkali Catalyst and Immobilized Enzyme 1. Fatty Acid Composition)

  • 신춘환
    • 한국환경과학회지
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    • 제19권10호
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    • pp.1247-1256
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    • 2010
  • Since biodiesel as bioenergy is defined as ester compounds formed by esterification of animal/vegetable oils, in this study three vegetable cooking oils (market, waste and refined waste ones) were esterified by reactions of alkali catalyst and immobilized enzyme. The fatty acid composition of the formed ester compounds was analyzed to investigate the feasibility of biodiesel production. By lipolysis (i.e, hydrolysis of Triglyceride (TG)), all three vegetable oils used in this study were found to produce Diglyceride (DG), Monoglyceride (MD) and Fatty acid ethylester (FAEE). However, the amount of produced FAEE (which can be used as an energy source) was in the increasing order of market cooking oil, waste one and refined waste one. With NaOH catalyst, FAEE was produced about 24.92, 17.63 and 11.31 % for the respective oils while adding Lipozyme TL produced FAEE about 43.54, 38.16 and 24.47 %, respectively. This indicates that enzyme catalyst is more effective than alkali one for transesterification. In addition, it was found that the composition of fatty acids produced by hydrolysis of TG was unchanged with alkali and immobilized enzyme reactions. Thus it can be expected that stable conditions remain in the course of mixing with gasoline whose composition is similar to that of the fatty acids.