• Title/Summary/Keyword: 리그닌 함량

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Characteristics of Lignin Removal in Cellulosic Ethanol Production Process (셀룰로오스 에탄올 생산공정에서 리그닌의 제거특성)

  • Lee, You-Na;Lee, Seung-Bum;Lee, Jae-Dong
    • Applied Chemistry for Engineering
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    • v.22 no.1
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    • pp.77-80
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    • 2011
  • In this study, we measured changes in the lignin content of acidified lignocellulosic biomass such as rice straw, saw dust, chestnut shell and peanut hull and analyzed the conversion property to cellulosic ethanol. It turns out that the lignin content increases in chestnut shell, rice straw, saw dust, peanut hull order and the conversion property to cellulosic ethanol is superior in the reverse order. Thus, the removal of lignin by acidification is necessary. In addition, as the concentration of sulfuric acid increases, the lignin content decreases and the yield of cellulosic ethanol increased. The optimum concentration of sulfuric acid is 20 wt%.

Seasonal Expression of OMT Gene in Relation to Lignin biosynthesis in two Poplar Species (종의 포플라수종에서 리그닌생합성에 관계된 OMT유전자의 발현)

  • Park, Young-Goo;Park, Hee Sung;Choi, Jang Won;Sul, Ill Whan;Chung, Il Kyung;Shin, Dong Ill
    • Journal of Life Science
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    • v.8 no.4
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    • pp.443-448
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    • 1998
  • We analyzed lignin content and wxpression of OMT gene during growth season in two hybrid poplar species. OMT gene expression was observed mainy in the developing secondary xylem where major quantity of lignin occurs. Lignin content in the xylem tissue increased as plant resumed growth in the spring and reached the highest in the late August. Change in lignin content was concurrent with that of OMT gene expression, indicating OMT is a key enzyme in lignin biosynthesis.

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Chemical characterization of the fast-growing industrial hemp (Cannabis sativa) woody core and bast fiber (산업용 대마의 목부와 인피섬유의 화학 조성 분석)

  • Shin, Soo-Jeong;Koo, Bon-Wook;Lee, Jae-Won;Choi, In-Gyu
    • 한국신재생에너지학회:학술대회논문집
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    • 2006.06a
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    • pp.482-484
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    • 2006
  • 대마에 대한 분석 결과, 인피 섬유의 경우 리그닌 함량은 7.6%로 다른 목질계 바이오매스나 일년생 초본류와 비교하여 매우 낮은 리그닌 함량을 나타냈으며 탄수화물 함량은 65.4%로 목질계 바이오매스와 유사하고, 초본류보다는 오히려 높았다. 목부는 리그닌 및 탄수화물 함량이 활엽수와 유사한 경향을 나타내었는데 특히 높은 자일란의 함량이 확인되었다. 또한 회분 함량이 인피섬유와 목부에서 각각 5.0%와 2.3%로 낮은 값을 나타내어 당화 및 발효 공정에 적용될 때 회분에 의한 공정 장애(스케일링 등)의 가능성을 낮추어 줄 것으로 사료되었다. 최종적으로 이러한 화학적 분석을 통해 대체에너지 생산을 위한 자원으로서 대마의 가능성을 확인할 수 있었다.

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Structural Analysis of Milled Wood Lignins Isolated From Aspen Wood (Populus tremuloides L.) Biotreated by Ceriporiopsis subvermispora (Ceriporiopsis subvermispora 처리에 의한 아스펜 목재 리그닌의 구조 변화)

  • Choi, Joon-Weon;Moon, Sung-Hee;Ahn, Sye-Hee;Choi, Don-Ha;Paik, Ki-Hyun
    • Journal of the Korean Wood Science and Technology
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    • v.33 no.6 s.134
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    • pp.79-86
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    • 2005
  • Aspen wood (Populus tremuloides, L.) was biotreated with Ceriporiopsis subvermispora for 1, 2, 4, and 6 weeks to observe the physical/chemical modification of wood components. Milled wood lignins (MWLs) isolated from each decayed wood were analyzed by gel permeation chromatography (GPC) and nitrobenzene oxidation (NBO). As fungal treatment was progressed, lignin contents continuously decreased up to 20% after 6-week treatment. The lignin polymer could be fragmented to low-molecular phenolics, which make an enhancement of alkali solubility. Holocellulose contents were not affected severely during the period of fungal treatment, only reduction of 5~6% compared to the control. Xylose contents were decreased gradually from 23.4% to 18% after 6 weeks, whereas alpha-cellulose remained almost unchanged. Gel permeation chromatography (GPC) indicates that molecular weight of lignin undergoes a slight decrement for 4 weeks of fungal treatment. Nitrobenzene oxidation revealed that total yield of NBO products of lignins were lowered ca 20% after fungal treatment. Sum of syringaldehyde and syringic acid are remarkably decreased. However, increment of sum of vanillin and vanillic acid was surprisingly observed. These results work as indirect evidence that a specific lignolytic reaction, maybe selective demethoxylaytion of S-lignin, can occur during fungal treatment of aspen wood by C. subvermispora.

Biomodification of Ethanol Organolsolv Lignin by Abortiporus biennis and Its Structural Change by Addition of Reducing Agent (Abortiporus biennis에 의한 유기용매 리그닌의 생물학적 변환과 환원제 첨가에 따른 구조 변화)

  • Hong, Chang-Young;Park, Se-Yeong;Kim, Seon-Hong;Lee, Su-Yeon;Ryu, Sun-Hwa;Choi, In-Gyu
    • Journal of the Korean Wood Science and Technology
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    • v.44 no.1
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    • pp.124-134
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    • 2016
  • The main goal of this study was to investigate biomodification mechanism of lignin by white rot fungus, Abortiporus biennis, and to depolymerize ethanol organosolv lignin for industrial application. In nitrogen-limited culture, A. biennis polymerized mainly lignin showing a rapid increase of molecular weight and structural changes depending on incubation days. At the initial incubation days, cleavage of ether bonds increased phenolic OH content, while the results were contrary in of the later part of the culture. Based on these results, ascorbic acid as a reducing agent was used to induce depolymerization of lignin during cultivation with white rot fungus. As a result, the degree of increase of average molecular weight of lignin was significantly declined when compared with those of the ascorbic acid free-experiment, although the molecular weight of fungus treated sample slightly increased than that of control. Furthermore, lignin derived oligomers in culture medium were depolymerized with the addition of ascorbic acid, showing that the average molecular weight was 381 Da, and phenolic OH content was 38.63%. These depolymerized lignin oligomers were considered to be applicable for industrial utilization of lignin. In conclusion, A. biennis led to the polymerization of lignin during biomodification period. The addition of ascorbic acid had a positive effect on the depolymerization and increase of phenolic OH content of lignin oligomers in medium.

Lignocellulose Biodegradation and Interaction between Cellulose and Lignin under Sulfate Reducing Conditions (황산염 환원 조건에서 리그노셀룰로오스의 분해 및 리그닌과 셀룰로오스의 상호작용)

  • Ko, Jae-Jung;Kim, Seog-Ku;Shimizu, Yoshihisa
    • Journal of the Korea Organic Resources Recycling Association
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    • v.15 no.4
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    • pp.131-137
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    • 2007
  • In this study, the biodegradation test on lignocellulose under sulfate reducing conditions was carried out. In particular, the interaction between cellulose and lignin was investigated with various g-cellulose/g-lignin (C/L) ratios: 42.15, 4.59, 2.51, 1.14 and 0.7. It was shown that the rate of cellulose degradation decreased in proportion to the lignin content. Assuming first order degradation kinetics, the consequences of competitive inhibition were graphically shown for different C/L ratios. The relation between cellulose reduction rate and C/L ratio was expressed by logarithm function with a determination coefficient of 0.97. Lignocellulose reduction rate was also described as a logarithm function of C/L ratio showing a inhibition effect by lignin. In the mean time, the rate of lignin decomposition was higher at C/L ratio of 2.51 and 1.14 compared with C/L ratios of 4.59 and 0.7, indicating that excessive extra carbon source is not appropriate for lignin biodegradation.

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Changes of Mass Loss and Nitrogen Content during Root Decomposition in the Chihuahuan Desert (치화화사막에서 뿌리의 분해과정에 따른 질소함량의 변화)

  • ;W.G.Whitford
    • The Korean Journal of Ecology
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    • v.17 no.3
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    • pp.311-318
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    • 1994
  • We examined spatial and temporal patterns of root decomposition for three and half years, from October 1986 to April 1990, in semi-arid Chihuahuan Desert. Decomposition of roots occurred in a two-phased pattern: an early period of rapid mass loss followed by a period of slower loss. The rate of root decomposition had a high negative correlation with the initial lignin concentration in roots (r=-0.84, p<0.05). Annual mass loss rate of Baileya multiradiata, a herbaceous annual, was the highest with the value of 0.60, while that of Panicum obtusum. a perennial grass which was restricted to playa, was the lowest with 0.13. The mass loss rate of roots in the playa was the lowest among the vegetation zones along the transect. After 42 months elapsed, fluffgrass roots in playa lost 40% of the initial mass, while in other sites it lost on average 55% of the initial mass. In all roots except for desert marigold, there was an initial release of nitrogen early in decomposition followed by net nitrogen immobilization. Nitrogen concentration of the desert marigold roots showed linear increase from the beginning. Lignin concentration of perennial grass roots were higher than those of herbaceous annual and woody perennial root.

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The Effects of Cultivars and DAPs(Days After Planting) of Kenaf Plants on Lignin Contents and Dyeability of Their Fibers (품종과 재배기간이 다른 케나프 섬유의 리그닌 함량과 염색성)

  • Rhie, Jeon-Sook;Yoo, Hye-Ja;Ladisch, Christine M.
    • Journal of the Korean Society of Clothing and Textiles
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    • v.31 no.12
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    • pp.1682-1688
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    • 2007
  • The effects of cultivar and DAPs on the lignin content and dyeability of the kenaf fibers were investigated. Four kenaf fiber samples were prepared from two cultivars, Tainung 2 and Everglades 41, and their 60 and 120 DAPs(days after planting) for the experiments. The lignin contents of the kenaf fibers of Tainung 2(T2) and Everglades 41(E41) were $11.29{\sim}12.78%$. Both T2 and E41 kenaf fibers had comparable amount of lignin, and klason lignin of the fibers was $2.5{\sim}3$ times as much as much as acid-soluble lignin. In both T2 and E41, 120 DAPs kenaf have 1% more lignin than 60 DAPs kenaf. The moisture regains of the four kenaf fiber samples were almost the same as $10.25{\pm}0.05%$. The absorbances of residual solution after dyeing for $1{\sim}180$ minutes with Red 81 at maximum wavelength 520 nm and Green 26 at 600 nm were measured. Comparing to Green 26, the dyeing rate of Red 81 was rapid and equilibrium state was reached in 12 minutes. The CIE $L^*,\;a^*, \;b^*,\;{\Delta}E$ and K/S values of the kenaf fibers dyed with Red 81 and Green 26 were measured as well. The dye exhaustion ratio of 60 DAPs kenaf was higher than that of 120 DAP.

Effect of active alkali concentration on the delignification of Larch UKP (활성(活性) 알칼리 농도(濃度)가 일본잎갈나무 UKP의 탈(脫)리그닌에 미치는 영향(影響))

  • Won, Jong-Myoung;Jo, Byoung-Muk
    • Journal of the Korean Wood Science and Technology
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    • v.4 no.1
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    • pp.21-27
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    • 1976
  • This study was carried out in order to obtain the effect of active alkali concentration. Sulfidity 25%, maximum temperature 170$^{\circ}C$, cooking time 3hrs., liquor to wood ratio 5 : 1 in the kraft cooking conditions were maintained. Active alkali concentration were varied at intervals of 3% between 12% and 24%. The rates of de lignification increased with an increase in active alkali concentration and beatability, brightness, and strength of pulp also improved. The total pulp yield trand to decrease with an increase of active alkali concentration. The maximum screened pulp yield were obtained between 18% and 21% A.A.. Therefore, the optimum active alkali concentration was 18~21%.

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Characterization of Pyrolytic Lignin in Biooil Produced with Yellow Poplar (Liriodendron tulipifera) (백합나무 바이오오일에서 회수한 열분해리그닌(Pyrolytic Lignin)의 화학적 특성)

  • Kim, Kwang-Ho;Moon, Sun-Joo;Kim, Tai-Seung;Lee, Soo-Min;Yeo, Hwan-Myeong;Choi, In-Gyu;Choi, Joon-Weon
    • Journal of the Korean Wood Science and Technology
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    • v.39 no.1
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    • pp.86-94
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    • 2011
  • Pyrolytic lignin was obtained from biooil produced with yellow poplar wood. Fast pyrolysis was performed under various temperature ranges and residence times using fluidized bed type reactor. Several analytical methods were adopted to characterize the structure of pyrolytic lignin as well as the effect of pyrolysis temperature and residence time on the modification of the lignin. The yield of pyrolytic lignin increased as increasing pyrolysis temperature and decreasing residence time of pyrolysis products. The molecular weight of pyrolytic lignin determined by gel permeation chromatography (GPC) was approximately 1,200 mol/g, which was approximately a tenth of milled wood lignin (MWL) purified from the same woody biomass. Based on analytical data, demethoxylation and side chain cleavage reaction were dominantly occurred during fast pyrolysis.