• 펄프종이기술
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• 제32권2호
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• pp.58-67
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• 2000

This study was carried out to acquire basic data necessary for the use of non-wood pulp. Various chemical pulping methods for rice straw to achieve higher yield, lower Kappa No. were investigated and then the physical properties of various pulps were tested. The results of this study were as follows: When various chemical pulps (Soda, Soda-AQ, Soda-$H_2O_2$, Soda-$Na_2S_2$, AS, AS-AQ, AS-$Na_2S_2O_3$, AS-$Na_2S_2O_4$, Kraft) were produced with rice-straw, the pulps with the highest yield and lowest Kappa No. were obtained with Soda-$Na_2S_2$and AS-$Na_2S_2O_4$pulps. For the breaking length, Soda and Soda-additive pulps(7.5~9.2km) were better than AS and AS-additive pulps(6.2~8.1km). Similarly, for the burst index, Soda and Soda-additive pulps(6.0~7.0 kPa.$m^2$/g) were better than AS and AS-additive pulps(4.5~6.3 kPa.m$^2$/g). But the tear index was showed 21.8-30.9 mN.$m^2$/g with a little different between pulping methods.

• 한국펄프종이공학회:학술대회논문집
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• 한국펄프종이공학회 2006년도 PAN PACIFIC CONFERENCE vol.1
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• pp.167-172
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• 2006

High-yield Pinus radiate kraft pulps with various Kappa number were produced from flow-through laboratory pulping. The samples were prepared and scanned using a rapid scan photoacoustic Fourier transform infrared (PAS-FTIR) spectrometer. A partial-least-squares (PLS) model was established based on the spectral data collected at different mirror velocities. The model was used to predict the Kappa number of the pulps and its robustness was statistically evaluated. The outcomes indicate that the PLS model can be used to predict the Kappa number of Pinus radiata kraft pulps with a high degree of accuracy provided that the moving mirror velocity is ${\leq}\;0.5cm/s$.

• 펄프종이기술
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• 제32권3호
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• pp.57-64
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• 2000

This study was carried out to acquire basic data necessary for the use of non-wood pulp. It investigated various chemical pulping methods using bamboo to achieve higher yield lower kappa no. and then the physical properties of various pulps were tested. The results of this study were as follows. When various chemical pulps(Soda, Soda-AQ, Soda-AQ-H2O2, Soda-urea, AS, AS-AQ, Kraft) were produced with bamboo. the pulps with the higher yield and lower kappa no. were AS-AQ and Kraft. In the case of the breaking length Soda pulps(5.77∼6.46 km) showed the greatest and Soda-urea pulps(3.81∼4.522km) showed the lower value. Similarly for the burst index Soda pulps (3.28∼3.50 kPa$.$m2/g) were the best and Soda-urea pulps(2.29∼2.39 kPa$.$m2/g) were worst. On the other hand the tearing indexes of AS-AQ pulps(73.6∼89.7mN$.$m2/g) showed the tendency which was higher then those of other pulps.

• 한국펄프종이공학회:학술대회논문집
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• 한국펄프종이공학회 2011년도 춘계학술발표회 논문집
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• pp.151-156
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• 2011

• Journal of the Korean Wood Science and Technology
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• 제15권1호
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• pp.1-11
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• 1987

소나무 크라프트 펄프제조과정중 회수된 폐액으로 Black liquor-phenol formaldehyde. Methylolated kraft lignin-phenol formaldehyde 및 Lignin cake-phenol rein 세 종류의 접착제가 제조되었다. Black liquor-phenol formaldehyde resin 제조시 Phenol의 약 60%를 크라프트 폐액으로 대치할 수 있다. 본 접착제의 최적압착조건은 $160^{\circ}C$에서 7분간이였다.(상태접착력 : 15.77kg/$cm^2$ 내수접착력 : 8.54kg/$cm^2$). Methylolated kraft lignin-pheno] formaldehyde resin 제조시 Phenol의 약 80~90%를 Methylolated kraft lignin으로 대용할 수 있었다. 본 접착제 제조시 pH를 2.6 용매로서 Methanol, 접착제 1g 당 $0.2m\ell$ Formaldehyde를 첨가하는 것이 접착력이 가장 높았다(상대접착력 : 18.54kg/$cm^2$, 내수 접착력 : 10.08kg/$cm^2$. Lignin cake-phenol ressin에서 Phenol양과 Kraft lignin양이 1 : 1일 경우에 접착력이 높았다. 본 접착제의 최적 압착조건은 $150^{\circ}C$에서 4분간이었다.(상태 접착력 : 18.46kg/$cm^2$, 내수접착력 : 12.3kg/$cm^2$).

• Journal of Forest and Environmental Science
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• 제9권1호
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• pp.67-80
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• 1993

무공해 대체 펄프화법 개발의 일환으로 비교척 최근에 많은 연구가 이루어지고 있는 아세트산-물 용매 증해법을 이용하여 현사시나무와 소나무률 펄프화 하였다. 펄프 특성의 변화에서 현사시나무는 거의 모든 아세트산 충해초건에서 우수한 펄프화 경향을 보였지만 소나무는 저온에서 충해가 거의 일어나지 않았다. 현사시나무의 최적 중해조건은 중해농도 95%, 중해온도 $185^{\circ}C$, 증해시간 0.5hr이었다. 구성당 성분의 거동은 현사시나무와 소나무에서 glucose만이 소량 감소하는 반면 그외의 당성분들은 다량 용출되었다. 폐액중의 용출 아세트산 리그닌에 대한 기초척인 성질을 살펴본 결과 현사시나무의 아세트산 리그닌의 원소조성은 C가 63.88%, H가 5.45%, O가 30.67%이며 $C_9$의 formular는 $C_9H_{9.15}O_{3.24}$였고 소나무의 아세트산 리그닌의 조성온 C가 61.85%, H가 6.14%, O가 32.01% 이며 $C_9$의 formular는 $C_9H_{9.15}O_{3.50}$이었으며 두 수종의 아세트산 리그닌 중합 명균분자량은 현사시나무가 731이며 소나무는 725였다.

• 펄프종이기술
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• 제36권5호
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• pp.69-77
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• 2004

Degradations of pine, yellow poplar and sweet gum by two fungi, Pycnoporus cinnabarinus and Trichophyton rubrum LSK-27 were investigated. P. cinabarinus degraded pine block samples much faster than T rub rum LSK-27, whereas P. cinnabarinus and T rubrum LSK-27 degraded yellow poplar and sweet gum at almost the same rate. In an effort to get a better understanding of how fungi degrade lignin in wood, contents of various functional groups were analyzed. After three-months of degradation of pine flour by these fungi, the following changes were observed: an increase in condensed phenolic OH group and carboxylic acid group content, a decrease in the guaiacyl phenolic OH content, and little change of aliphatic OH group content. Further studies in the degradation of pine flour by P. cinnabarinus indicated that the increase in condensed phenolic OH group content and the decrease in guaiacyl phenolic OH group content occurred in the first month of the degradation. The changes of functional group contents in the degradation of unbleached softwood kraft pulp by P. cinnabarinus had the same trends as those in the degradation of pine flour. That is, structural alteration of lignin due to the kraft pulping process had little effect on how P. cinnabarinus degraded lignin.

• 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.

• 청정기술
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• 제27권2호
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• pp.190-197
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• 2021

펄프 및 제지산업에서 목재의 셀룰로오스 성분 활용 후 남는 부산물인 크라프트 리그닌(kraft lignin)은 촉매적 저분자화 공정을 통해 바이오연료나 고부가가치 페놀 단량체로 전환될 수 있다. 본 연구에서는 크라프트 리그닌의 효율적인 저분자화를 위한 촉매로 수소화 금속 및 산-염기점을 동시에 지니는 Ru-Mg-Al-oxide 복합 촉매를 제조하고, 리그닌 분해 성능을 평가하고자 하였다. 촉매 내 다양한 활성점들(산점, 염기점, 수소화 금속)이 리그닌 분해 반응에 미치는 영향을 파악하기 위해 MgO, Mg-Al-oxide, Ru-Mg-Al-oxide의 세 가지 촉매를 제조하여 초임계 에탄올 용매 상에서 리그닌 분해 반응을 수행하였고, 리그닌 분해 성능은 바이오오일(bio-oil) 수율 및 분자량, 그리고 페놀계 단량체 수율을 통해 평가하였다. 그 결과, Ru-Mg-Al-oxide 촉매가 다양한 활성점들의 시너지 효과로 인해 가장 높은 수율의 바이오오일 및 페놀 단량체들을 생산한다는 것을 확인하였다. Ru-Mg-Al-oxide 촉매 상에서 분해 효율을 최적화하기 위해 다양한 반응 조건(온도, 시간, 촉매양)에 따른 분해 효율을 평가하였고, 최종적으로 반응온도 350 ℃, 리그닌 대비 촉매 비율 10%, 4 h 반응을 통해 72%의 높은 바이오오일 수율과 무촉매 대비 3.5배 이상 증가한 페놀 단량체를 생산할 수 있었다.

• Journal of Forest and Environmental Science
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• 제13권1호
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• pp.143-152
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• 1997

백색부후균인 Fomes pini (Thore) Lloyd에 의해 처리된 chip을 anthraquinone(AQ)을 첨가하여 화학 펄프화를 실시하여 얻은 결과를 미처리재의 것과 비교하였다. 균처리함에 의해 카파값 20에서의 H factor는 소다와 크라프트 증해에서 각각 17%와 15%가 감소되었다. 이러한 결과는 목재를 백색부후균으로 처리함으로 인해 탈리그닌이 용이해졌음을 나타내는 것이다. 비페놀성 ${\beta}$-O-4 화합물인 veratrylglycerol-${\beta}$-guaiacyl ether(I)와 페놀성 ${\beta}$-O-4 화합물인 syringylglycerol-${\beta}$-syringyl ether(III)에 백색부후균을 작용시키면 반응생성물로서 각각 ${\alpha}$-guaiacoxy-${\beta}$-hydroxypropioveratrone(II)과 ${\alpha}$-syringyloxy-${\beta}$-hydroxypropiosyringone(IV)이 생성됨이 밝혀졌다. 따라서 목재에 균처리를 함으로서 카르보닐기가 리그닌의 측쇄 ${\alpha}$ 위에 도입되어 그로 인해 탈리그닌이 용이하게 된 것으로 여겨진다.