• Journal of the Korean Wood Science and Technology
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• v.10 no.4
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• pp.67-75
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• 1982

모텔리그닌의 펄프화(化) 처리(處理) 및 폐액(廢液)리그닌의 반응생성물(反應生成物)로부터 알칼리 및 설페이트 펄프화중(化中)에 일어나는 반응양식(反應樣式)을 조사(調査)한 것이다. 알칼리의 처리결과(處理結果)는 친핵시약(親核試藥)에 의해 페놀레이트 이온이 생성(生成), 퀴논메타이드 중간체(中間體)를 걸쳐 $C_6-C_3$ 단위(單位)의 ${\alpha}$위(位) aryl은 탈리(脫離)하여, 리그닌은 저분자화(低分子化)가 시작되고, 저분자생성물(低分子生成物)은 축합반응(縮合反應)에 의해 극(極)히 일부(一部)는 고분자화(高分子化)된다. 저분자화(低分子化)된 리그닌은 산화(酸化)에 의해 퀴노이드 착색구조(着色構造)를 형성(形成)한다. 페놀성의 일부(一部) 및 비(非)페놀성리그닌은 oxirane와 thiirane의 중간체(中間體)를 거쳐 $C_6-C_3$ 단위(單位)의 ${\beta}$위(位)의 arylether가 탈리(脫離)된다. 그러나, hydrosulfide 이온은 hydroxide 이용 보다 강(强한)한 친핵종(親核種)이므로 thiirane의 중간체(中間體) 생성(生成)이 용량(容量)하여 개열(開裂)이 더욱 촉진(促進)된다. 저분자(低分子)리그닌의 고분자축합(高分子縮合)은 벤젠핵(核)의 2.6 위(位)보다 5위(位)에 축합(縮合)이 많이 일어 난다.

• Journal of Microbiology
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• v.39 no.4
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• pp.279-285
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• 2001

Vibrio parahaemolyticus is a halophilic bacterium associated with seafood gastroenteritis. An unusual strain of Kanagawa-positive urease producing Vibrio parahaemolyticus O1:K1 was isolated from the environment and identified . A polymerase chain reaction assay revealed that this strain harbored both the tdh and the genes. The urease from this strain was studied. Maximum urease production was induced in LB medium containing 0.2% urea, 0.5% glucose, 2% NaCl and pH 5.5 with 6h of culti-vation at 37$\^{C}$ under aeration. Purification of urease was achieved by the process of whole cell lysate, 65% ammonium sulphate precipitation, DEAE-cellulose ion exchange column chromatography, Sepharose CL-6B gel filtration and oxirane activated Sepharose 6B-urea affinity chromatography with 203 fold purification and 2.2% yield. Analysis of the purified enzyme by SDS-PAGE demonstrated the presence of the subunits with a molecular weight of 85kDa, 59kDa, 41kDa and the molecular weight for the native enzyme by nondenaturing PAGE and gel filtration chromatography was 255kDa. The purified urease was stable at pH 7.5 and the opeimal pH in HEPES buffer was 8.0 The enzyme was stable at 60$\^{C}$ for 2 h with a residual activity of 32% . The addition of 10$\mu$M if NiCl$_2$maintained stability for 30 min. The Km value of the purified enzyme was 35.6 mM in urea substrate. The TD$\_$50/(median toxic dose) of the purified urease was 2.5$\mu\textrm{g}$/ml on human leukemia cells.

• Applied Chemistry for Engineering
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• v.32 no.6
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• pp.607-612
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• 2021

Silicon (Si) is one of the promising active materials to replace the widely used graphite because of its low electrochemical potential and high theoretical capacity. However, Si anodes still face in problems with the huge volume expansion and continuous decomposition of the electrolyte during repeated charge and discharge processes. To address these issues, a cross-linkable waterborne polyurethane (CWPU) based on a bio-oil, castor oil, was prepared and reacted with Tris(2,3-epoxypropyl) isocyanurate (TGIC) linkers, resulting in the formation of a mechanically robust 3D network structure. Si anodes fabricated with the CWPU-TGIC exhibited stable cycling performances and excellent discharge capacities. The results revealed that the CWPU-TGIC binder efficiently accommodates the large volume change for Si anode during charge and discharge cycles. Overall, the eco-friendly binder shows great promise in improving the electrochemical performances of Si anodes.

• Applied Chemistry for Engineering
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• v.31 no.3
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• pp.267-276
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• 2020

Poly(epichlorohydrin) copolyol series (PECH copolyols) were synthesized via cationic ring-opening copolymerization (ROCP) of oxirane-based monomers and effects of reaction temperature, solvent type, and initiator were studied. As a comonomer, two types of alkylene oxides were used, and polymerization conditions were conducted both with diethylene glycol (DEG) as an initiator in methylene chloride (MC) solvent and tripropylene glycol (TPG) in toluene solvent. In order to induce the active monomer (AM) mechanism in the ring-opening copolymerization reaction, the monomer was injected by an incremental monomer addition (IMA) method using a syringe pump, and the polymerization was performed at -5 ℃. PECH copolyol, a synthesized ephichorohydrin (ECH)-based copolyol, was converted to glycidyl azide-based energy-containing copolyol (GAP copolyol) by azadizing the ECH unit through a substitution reaction. It was confirmed that the synthesized azide copolyol had little effects on changes of the solvent and the initiator. Also, the molecular weight increased 500 after the azide reaction, thereby the GAP copolyol was polymerized as designed. As the content of the comonomer increased, both the T_g and viscosity tended to decrease due to the influence of the alkyl chain length. It is possible to fundamentally prevent CH₃N₃ amount produced in the azide reaction process, and it is expected that a large-scale process could be achievable.