• Biotechnology and Bioprocess Engineering:BBE
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• 제1권1호
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• pp.26-31
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• 1996

Since biosynthesis of lignin peroxidase from Phanerochaete chrysosporium was known to be sensitive to shear, it is interesting to understand the effects of the shear sensitivity for the overproduction of lignin peroxidase. In stirred-tank fermentor, the shear-sensitivity in lignin peroxidase biosynthesis was quantified by using Kolmogorov length scale. It was found that agitation at 80$\mu$m Kolmogorov length scale is advantageous for the production of lignin peroxidase from P. chrysosporium. To overcome the shear sensitivity in lignin peroxidase biosynthesis caused by the agitation,P. chrysosporium was immobilized on various solid carriers. The nylon-immobilized P. chrysosporium was chosen in the present study as a way to overcome the shear sensitivity at the ranges of above 50$\mu$m Kolmogorov length scale. The adhesion force between immobilized cell and carrier can be predicted by thermodynamic approach and used as a criteria to select an adequate carrier materials for immobilization.

• 임산에너지
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• 제18권1호
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• pp.17-24
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• 1999

액화목재는 목재 및 목질계 자원으로부터 신소재 개발을 위한 새로운 유효이용법의 하나이다. 이 액화목재의 주요 성분변화를 조사하기 위한 실험으로서 액화 전후의 리그닌의 구조적 변화를 알기 위하여 잣나무 KP리그닌과 리그닌설포산을 액화시켜서 유기용매로 분리하고, IR, 1H(13C)-NMR, GC-MS분석기기로 분석하였다. 액화리그닌 중에는 다수의 페놀성 물질들 즉, diguaiacol, acetic acid phenyl ester, phenol, 1-phenyl ethanone 등이 분석되었다.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2002년도 생물공학의 동향 (X)
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• pp.473-476
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• 2002

A lignin degradation bacteria, symbiotic bacteria was isolated from the gut of Sympetrum depressiusculum and tested for its lignin degrading activity using lignin model compounds and related aromatic compounds. The strain was identified as Serratia marcescens HY-5 based on the 165 rDNA, cellular fatty acid composition, biochemical and physiological characteristics. S. marcescens showed 40-50% lignin degrading activity in the media that contained vaillin, guaiacol and dealkaline lignin. S. marcescens showed three ligninase activities [Jaccase, lignin peroxidase(LiP) and Manganase peroxidase(MnP)]. Addition of dealkaline lignin to the basal media increased about 6fold of laccase activity. Vanillic acid or vanillin increase 1.3fold of MnP activity and p-coumaric acid increased 12fold of LiP activity which added to the basal medium.

• 대한화학회지
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• 제20권2호
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• pp.153-157
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• 1976

1기압하에서 한국산 소나무로부터 lignin을 추출할 수 있는 실험실에서의 최적 조건을 구했고, m.p, 증색반응, IR등의 방법으로 순수한 lignin임을 확인했다. 추출한 순수 lignin을 진한 황산으로 탄화한 후 전기로 속에서 650$^{\circ)C$로 공기 부활하여 활성탄을 제조하였다. 이 활성탄의 광전 비색계에 의한 흡착능을 조사한 결과 89%였다.

• Journal of Electrochemical Science and Technology
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• 제15권1호
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• pp.111-131
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• 2024

Lignin-derived porous carbon has been identified as a versatile electrode material for supercapacitors (SCs) in energy storage systems (ESSs) owing to their intrinsic advantages including good electrical conductivity, low cost, high thermal and chemical stability, and high porosity, which stem from high surface, appropriate pore distribution, tailored morphologies, heterostructures, and diverse derivates. In this review, to provide a fundamental understanding of the properties of lignin, we first summarize the origin, historical development, and basic physicochemical properties. Next, we describe essential strategies for the preparation of lignin-derived porous carbon electrode materials and then highlight the latest advances in the utilization of lignin-derived porous carbon materials as advanced electrode materials. Finally, we provide some of our own insights into the major challenges and prospective research directions of lignin-derived porous carbon materials for supercapacitors. We believe that this review will provide general guidance for the design of next-generation electrode materials for supercapacitors.

• 임산에너지
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• 제17권1호
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• pp.56-70
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• 1998

This study was carried out to investigate the structural characteristics of kraft lignin and the wood degrading characteristics, the productivity of ligninolytic enzymes and the enzymatic degradation of kraft lignin by white-rot fungi. To purify kraft lignin, precipitation of kraft pulping black liquors of pitch pine meal was done by titration with lN $H_{2}SO_{4}$ reaching to pH 2, and isolation of the precipitates done by centrifugation. The isolated precipitates from pitch pine were redissloved in lN NaOH, reprecipitated by titration with lN $H_{2}SO_{4}$, washed with deionized water, and kept ofr analysis after freeze drying. Fractionation of the precipitates in solution by successive extraction with $CH_{2}Cl_{2}$ and MeOH, and the fractionates were named SwKL, SwKL I, SwKL II, and SwKL III for pitch pine kraft lignin. The more molecular weights of kraft lignin increased, the less phenolic hydroxyl groups and the more aliphatic hydroxyl groups. Because as the molecular weights increased, the ratio of etherified guaiayl/syringyl(G/S ratio) and the percentage were increased. The spectra obtained by 13C NMR and FTIR assigned by comparing the chemical shifts of various signals with shifts of signals from autherized ones reported. The optimal growth temperature and pH of white-rot fungi in medium were $28^{\circ}C$ and 4.5-5.0, respectively. Especially, in temperature and pH range, and mycelial growth, the best white-rot fungus selected was Phanerochaete chrysosporium for biodegradation. For the degradation pathways, the ligninolytic fungus jcultivated with stationary culture using medium of 1% kraft lignin as a substrate for 3 weeks at $28^{\circ}C$. The weight loss of pitch pine kraft lignin was 15.8%. The degraded products extracted successively methoanol, 90% dioxane and diethyl ether. The ether solubles were analyzed by HPLC. Kraft lignin degradation was initiated in $\beta$-O-4 bonds of lignin by the laccase from Phanerochaete chrysosporium and the degraded compounds were produced from the cleavage of $C\alpha$-$C\beta$ linkages at the side chains by oxidation process. After $C\alpha$-$C\beta$ cleavage, $C\alpha$-Carbon was oxidized and changed into aldehyde and acidic compounds such as syringic acid, syringic aldehyde and vanilline. And the other compound as quinonemethide, coumarin, was analyzed. The structural characteristics of kraft lignin were composed of guaiacyl group substituted functional OHs, methoxyl, and carbonyl at C-3, -4, and -5 and these groups were combinated with $\alpha$ aryl ether, $\beta$ aryl ether and biphenyl. Kraft lignin degradation pathways by Phanerochaete chrysosporium were initially accomplished cleavage of $C\alpha$-$C\beta$ linkages and $C\alpha$ oxidation at the propyl side chains and finally cleavage of aromatic ring and oxidation of OHs.

• Journal of the Korean Wood Science and Technology
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• 제43권3호
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• pp.355-363
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• 2015

본 연구에서는 초임계 에탄올 및 Ru/C 촉매를 이용하여 초본류 바이오매스 유래 아시안 리그닌을 효과적으로 분해하였으며, 분해 생성된 리그닌오일의 물리화학적 특성을 다양한 분석방법을 이용하여 조사하였다. 리그닌오일의 수율은 반응온도가 $250^{\circ}C$에서 $350^{\circ}C$로 상승함에 따라 89.5 wt%에서 32.1 wt%로 감소하는 경향을 보였지만 분자량 및 다분산지수는 $350^{\circ}C$ 조건에서 아시안 리그닌(3698Da, 2.68) 대비 각각 85%, 44% 감소하여 효과적인 탈중합 반응이 진행되었음을 확인할 수 있었다. 리그닌오일의 GC/MS 분석 결과 guaiacol, 4-ethylphenol, 4-methylguaiacol, syringol, and 4-methysyringol 등 단량체 수준의 페놀화합물은 반응온도가 증가할수록 24.1 mg/g of lignin ($250^{\circ}C$)에서 64.8 mg/g of lignin ($350^{\circ}C$)으로 증가하였으며, 반응기 내부에 수소가스와 촉매(Ru/C)를 첨가하였을 때 최대 76.1 mg/g of lignin 수준까지 향상되는 것을 확인할 수 있었다. 한편 리그닌오일의 원소분석 결과 반응온도가 증가함에 따라 탄소함량은 증가한 반면 산소함량은 점차 감소하였으며, 이를 통해 아시안 리그닌 탈중합 공정 중 수첨탈산소반응 및 수소첨가반응이 진행됨을 간접적으로 확인할 수 있었다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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• pp.251.2-251.2
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• 2010

Plant biomass has been proposed to be an alternative source for petroleum-based chemical compounds. Especially, phenolic chemical compounds can be obtained from lignin by chemical depolymerization processes because lignin consists of complex aromatic polymer such as trans-p-coumaryl, coniferyl and sinapyl alcohols, etc. Phenolic chemical compounds from lignin were usually produced in super critical water. However, we applied Near-critical water (NCW) system because NCW is known as a good solvent for lignin depolymerization. Organic matter like lignin can be solved in NCW system and the system has a unique acid-base property without conventional non-eco-friendly chemicals such as sulfuric acid and sodium hydroxide. In this work, we tried to optimize the NCW depolymerization system by adjusting the processing variables such as reaction time, temperature and pressure. Moreover, the amount of additional phenol was optimized by changing the molar ratio between water and phenol. Phenol was used as capping agent to prevent re-polymerization of active fragment such as formaldehyde. Alkali-lignin was used as a starting material and characterized by a Solid State 13C-NMR, FT-IR and EA (Elemental Analysis). GC-MS analysis confirmed that o-cresol, p-cresol, anisole and 4-hydroxyphathalic acid were the main product and they were quantitatively analyzed by HPLC.

• 임산에너지
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• 제20권1호
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• pp.35-41
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• 2001

리그닌 모델화합물 Ⅰ-Ⅳ의 시료를 315℃에서 열분해 시킨 결과, 리그닌 모델호합물 Ⅰ, Ⅱ의 열분해에서는 guaiacol이 0.47mol, DMP가 0.57mol로, DMAP는 0.12와 0.23mol로 각각 생성되었으며, 리그닌 모델화합물 Ⅲ, Ⅳ의 열분해에서는 guaiacol의 생성이 0.26mol, DMP가 0.30mol로 TMAP는 0.09mol 과 0.15mol이 각각 생성되었다. 리그닌 모델화합물 열분해 메커니즘으로서는 우선 탈수되고, 이어서 β-O-4 결합이 개열되어 guaiacol, DMP, DMAP와 TMAP가 생성되는 것을 알 수 있었다.

• Journal of the Korean Wood Science and Technology
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• 제25권1호
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• pp.1-7
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• 1997

Kraft oak lignin and ricestraw lignin from acetosolve pulping were dissolved in 50/50 mixture of tetralin/m-cresol solvent. The dissolved lignin was reacted in the pressurized autoclave which was operating at $350{\sim}500^{\circ}C$ of reaction temperature and 10~20 atms of reaction pressure respectively_Hydrogen pressure of 60~80kg/$cm^2$ was exercising into the pressurized autoclave reactor to create thermochemical hydrogenolysis reaction. It was identified by GLC, GC-MS and HPLC that the alkyl-aryl-${\beta}$-O-4 ether bond of lignin was cleaved and degraded into various smaller molecules of aromatic compound such as phenols and cresols under the reaction conditions around $300^{\circ}C$ and 10 atms of reaction temoerature and pressure. Hydrogenolysis reaction of lignin compound which was done above $500^{\circ}C$ of reaction temperature and 20 atms of reaction pressure showed that the amount of aromatic compound such as phenols and cresols degraded from reactant lignin was decreasing with newly present and increasing water out of product mixtures. It was supposed that new aliphatic compound of high molecular weight hydrocarbon is composed due to higher reaction temperature and pressure of hydrogenolysis reaction such as $500^{\circ}C$ and 20 atms, even though it was almost impossible, to identify what kind of degraded products it was by HPLC.