• 환경위생공학
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• 제13권3호
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• pp.141-147
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• 1998

Under high temperature and high pressure, cyanogen disinter gration distruction mechanism brought followings results through continuous plug flow reactor system. 1. The temperature was a important reacting factor in cyanogen disintegration. Over $612.8^{\cird}K$ high disintegration rate or 99.99% was shown even under $2000{\;}mg/{\ell}$ cyanogen density. 2. The conditions of cyanogen disintegration was gained through experimenting the supercrietical condition of water in basic. To gain 99.99% disintegration rate under $1000{\;}mg/{\ell}$ early cyanogen density, the pressure showed 52.8 seconds at $523^{\cird}K$ and 84.2 atm and gained $0.56{\;}mg/{\ell}$ operating density. 3. Here is the reaction velocity formula of cyanogen disintegration by hydrolysis: This formula indicates the high possibility of cyanogen disintegration within a short time. And it also implys the potential possibility on treating NBDICOD and the technology in developing the environment cleaning progress as small size automatic controlling equipment.

• Biomolecules & Therapeutics
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• 제15권1호
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• pp.65-72
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• 2007

Flax seed(Linseed, Linum usitatissimum L.) and its oil, a richest source of alpha-linolenic acid(ALA)(${\omega}-3$), contain saturated fatty acids, neurotoxic cyanogen glycosides and immuno-suppressive cyclic-nonapeptides. Present paper describes the development of two chemical processes, Process-A and -B, to remove saturated fatty acids and to destroy cyclic nonapeptides and cyanogen glycosides from flax seed oil. Process-A consists of three major steps, i.e., extraction of fatty acid mixture by alkaline saponification, removal of saturated fatty acid by urea-complexation, and triglyceride reconstruction of unsaturated fatty acid via fatty acyl-chloride activation using oxalyl chloride. Process-B consists of preparation of fatty acid ethyl ester by transesterification, elimination of saturated fatty acid ester by urea-complexation, and reconstruction of triglyceride by interesterification with glycerol-triacetate (triacetin). The destruction of lipophilic cyclic nonapeptide during saponification or transesterification processes could be demonstrated indirectly by the disappearance of antibacterial activity of bacitracin, an analogous cyclic-decapeptide. The cyanogen glycosides were found only in the dregs after hexane extraction, but not in the flax seed oil. The reconstructed triglyceride of flax seed oil, obtained by these two different pathways after elimination of saturated fatty acid and toxic components, showed agreeable properties as edible oil in terms of taste, acid value, iodine and peroxide value, glycerine content, and antioxidant activity.

• Journal of Microbiology and Biotechnology
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• 제14권2호
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• pp.297-301
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• 2004

The dTDP-D-glucose 4,6-dehydratase from Salmonella enterica was immobilized using covalent binding to cyanogen bromide activated sepharose. The immobilized enzyme was used to produce dTDP-4-keto-6-deoxy-D-glucose, a key sugar intermediate that can be used economically to produce diverse classes of unusual sugars appended in various antibiotics. The enzyme was immobilized on the sepharose after activation with cyanogen bromide. The maximum immobilization (80.03％) was achieved after 14 h of coupling. The covalently immobilized enzyme was stable, and an average of 78.4 ％ conversion was achieved until 120 h of immobilization when it was repeatedly used. Similar conversion was noticed for the first batch using the enzyme entrapped-hydrogel but activity was gradually decreased in the following batches. The production of dTDP-4-keto-6-deoxy-D-glucose by using an immobilized enzyme has high potential for commercial application.

• Bulletin of the Korean Chemical Society
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• 제32권9호
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• pp.3382-3388
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• 2011

Reaction of barbituric acid (BA), 1,3-dimethyl barbituric acid (DMBA) and 2-thiobarbituric acid (TBA) with cyanogen bromide and aldehydes in the presence of L-(+)-tartaric acid afforded a new route for the synthesis of stable heterocyclic 5-aryl-1H,1'H-spiro[furo[2,3-d]pyrimidine-6,5'-pyrimidine]2,2',4,4',6'(3H,3'H,5H)-pentaones which is a dimeric form of barbiturate (uracil and thiouracil derivative). In the reaction of 1,3-diethyl thiobarbituric acid (DETBA) the Knoevenagel condensation and then Michael adducts were obtained under the same condition. Structure elucidation is carried out by $^1H$ NMR, $^{13}C$ NMR, FT-IR and Mass analyses. Mechanism of the formation is discussed.

• 한국군사과학기술학회지
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• 제18권6호
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• pp.829-834
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• 2015

A simple and sensitive hydrogel-based detecting gel has been presented for the qualitative determination of cyanogen chloride(CK) using Konig reaction. To optimize Konig reaction conditions, the effects of pyridine and barbituric acid concentration were investigated. Under the optimized conditions, CK gas concentration was directly related with absorbance change at 567 nm. Based on aqueous solution test results, we finally prepared CK detecting hydrogel by absorbing pyridine and barbituric acid solution. Color change of the prepared CK detecting hydrogel was clearly observed when the detecting gel was exposed to 10 ppm CK gas.

• Current Research on Agriculture and Life Sciences
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• 제3권
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• pp.166-173
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• 1985

��신을 DEAE-cellulose, CM-cellulose, Sepharose-4B와 porous glass beads을 사용(使用)하여 고정화(固定化)시켰던 바 그 결과(結果)를 요약(要約)하면 다음과 같다. 1. CM cellulose와 DEAE-cellulose의 ��신 흡착량(吸着量)은 건조된 bead 1 gr에 대하여 각각 10 mg와 15 mg이었고 glutaralde을 사용(使用)함으로서 20 mg와 27 mg로 흡착량(吸着量)이 증가(增加)하였고 효소(酵素)의 활력(活力)은 용해성효소(溶解性酵素)에 비해 각각 22%, 24%로 나타났다. 2. Sepharose-4B을 cyanogen bromide을 사용(使用)하여 활성화(活性化)시킨후 glutaraldehyde을 사용(使用)하여 공유결합을 유도하였던 바 건조된 bead 1 gr에 ��신 19 mg가 통합(統合)되었고 효소(酵素)의 활력(活力)은 23%로 나타났다. 3. Porous glass beads의 표면(表面)을 succineamido - propyl glass beads의 형태(形態)로 유도체를 만든후 ��신을 고정화(固定化)시켰을 때 bead 1 gr가 ��신 40 mg을 통합(統合)할 수 있었고 효소(酵素)의 활력(活力)은 용해성효소(溶解性酵素)에 비해 45%로 나타났다.

• Carbon letters
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• 제8권4호
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• pp.280-284
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• 2007

Samples of active carbon of $1150\;m^2/g$ surface area were impregnated with ammoniacal salts of copper, chromium and silver, with and without triethylenediamine. The samples of impregnated carbon were aged at $50^{\circ}C$, with and without 90% RH (relative humidity), for a little more than one year and chemically evaluated periodically. Initially copper (II) and chromium (VI) reduced very fast in the samples in humid atmosphere to the extent of 30% and 60% respectively in four months. These values were found to be unaffected by the presence of triethylenediamine (TEDA) indicating that the chemical did not retard the reduction process of chromium (VI) and copper (II). However, in the absence of humidity the reduction of the impregnants was significantly less (10-12%, w/w) in four months. It was quite evident; therefore, that the moisture was mainly responsible for the reduction of chromium (VI) and copper (II) species in impregnated carbons. The prolonged ageing of the samples with and without triethylenediamme after four months with and without humid atmosphere showed that the extent of reduction of chromium (VI) was very low, i.e. 5-10% and of copper (II) was 2-25%. Silver is not reduced due to carbon, as it remained unchanged in concentration on storage. The impregnated carbon samples (100 g) without triethylenediamine, which were aged at room temperature for 5 years in absence of humidity and unaged when evaluated against cyanogen chloride (CNCl) at a concentration of 4 mg/L and airflow rate of 30 lpm showed a high degree of protection (80- 110 minutes).

• Corrosion Science and Technology
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• 제6권6호
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• pp.304-307
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• 2007

As to the reflection electrode of LCD (liquid crystal displays), silver-copper-gold alloy (hereafter, it is called as ACA (Ag98%, Cu1%, Au1%)) is an effective material of which weathering resistance can be improved more compared with pure silver. However, there is a problem that gold remains on the substrate as residues when ACA is etched in cerium ammonium nitrate solution or phosphoric acid. Gold can not be etched in these etchants as readily as the other two alloying elements. Gold residue has actually been removed physically by brushing etc. This procedure causes damage to the display elements. Another etchant of iodine/potassium iodide generally known as one of the gold etchants can not give precise etch pattern because of remarkable difference in etching rates among silver, copper and gold. The purpose of this research is to obtain a practical etchant for ACA alloy. The results are as follows. The cyanogen complex salt of gold generates when cyanide is used as the etchant, in which gold dissolves considerably. Oxygen reduction is important as the cathodic reaction in the dissolution of gold. A new etchant of sodium cyanide / potassium ferricyanide whose cathodic reduction is stronger than oxygen, can give precise etch patterns in ACA alloy swiftly at room temperature.

• 대한화학회지
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• 제55권6호
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• pp.940-951
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• 2011

Reaction of 1-methylpyrimidine-(1H,3H,5H)-2,4,6-trione (1-MBA 1) as an unsymmetrical barbituric acid with cyanogen bromide and various aldehydes in the presence of triethylamine and/or pyridine afforded diastereomeric mixtures of new class of heterocyclic stable 5-aryl-1,1'-dimethyl- and 5-aryl-3,1'-dimethyl-1H,1'H-spiro[furo[2,3-d]pyrimidine-6,5'-pyrimidine]2,2',4,4',6'(3H,3'H,5H)-pentaones which are dimeric forms of 1-methyl barbiturate at the range of $0^{\circ}C$ to room temperature. In the reaction of some aldehydes with 1-MBA and BrCN were afforded a mixture of diastereomers. Another two aldehydes such as 4-cyano- and 2-hydroxybenzaldehydes gave exclusively two diastereomers in which binded to the salt of triethylammonium hydrobromide by intermolecular H-bond in ratio of 1:1. 4-Hydroxybenzaldehyde and 2-pyridinecarbaldehyde gave exclusively one diastereomer under the same condition. Aldehydes possessing strong electron-donor were produced exclusively two geometric isomers of Knoevenagel adduct (E- and Z-isomers). The structures of compounds were deduced by $^1H$ NMR, $^{13}C$ NMR and FT-IR spectroscopy. Mechanism of the formation is discussed.

• 보존과학회지
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• 제25권3호
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• pp.283-291
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• 2009

현재까지 문화재 훈증제로서 사용되어왔던 브롬화메틸(Methyl Bromide, 이하 M.B)은 온실 가스로 지구 오존층 파괴의 원인물질로 판명되어, 1987년 몬트리올 의정서에 의해 선진국에서는 2005년부터 사용이 금지되었다. 또한, 2007년 발리 협약에 의해 우리나라도 점진적으로 사용 규제가 예상되므로, 본 실험에서는 Methyl Bromide를 대체할 Ethylene Oxide + HFC 134a, Methyl Iodide, Cyanogen, Argon 훈증법이 금속(은, 구리, 철), 목재(미송), 안료(황, 장단, 양청, 백분, 먹), 섬유(삼베, 모시, 황마, 도침 비단, 비도침 비단 / 쪽, 황벽, 홍화 염색), 지류(닥지 4종, 중성지 1종) 시편 재질에 미치는 안정성 평가를 실시하였다. 훈증 실험 결과, Ethylene Oxide + HFC 134a가 훈증 전, 후 실험 시편의 중량, 색도 변화 등에 가장 영향이 없었다. 표면변화는 지류와 금속시편에서 부분적으로 변색이 발생하였다. 색도변화는 대부분의 시편에서 0.5에서 1.5내외의 근소한 색차를 나타내었다. Methyl Iodide는 훈증 전, 후 중량변화가 거의 없는 것으로 나타났다. 색도변화는 대부분의 실험시편에서 1.0 이상의 색차를 나타내었다. 특히, 염색된 대부분의 섬유시편에서 비교적 큰 색도변화가 나타났다. 표면변화는 양청안료시편에서 육안으로 관찰 가능한 변색이 관찰되었다. Cyanogen은 훈증 전, 후 실험 시편의 중량변화에 큰 영향이 없는 것으로 나타났다. 색도변화는 전반적으로 실험시편에서 1.5이상 정도의 색차를 보였다. 특히, 섬유시편의 변색에 큰 영향을 주는 것으로 나타났다. Argon으로 훈증한 실험시편은 중량변화가 3~6% 내외로 감소한 것으로 나타났다. 표면변화는 지류시편에서 부분적으로 변색이 발생한 것을 관찰할 수 있었다. 색도변화는 2주 훈증 조건에서 홍화와 황벽으로 염색한 황마시편이 6.3, 6.0의 현저한 색차를 나타냈다.