• Journal of the Korean Wood Science and Technology
• /
• 제41권2호
• /
• pp.87-99
• /
• 2013

Waste paper stands for the major biodegradable organic fraction of most of municipal solid waste. The potential of waste paper for glucose production was investigated in this current work. The pretreatment was accomplished by first subjecting waste paper to disintegration time (30 s), followed by ink removal of disintegrated waste paper using an deinking agent. Concentrated acid hydrolysis of waste paper with sulfuric acid was optimized to maximize glucose conversion. The concentrated acid hydrolysis conditions for waste paper (disintegrated time: 30 s, deinking agent loading : 15 ml) were optimized by using central composite design and response surface methodology. The optimization process employed a central composite design, where the investigated variables were acid concentration (60~80%), loading sulfuric acid (1~5 ml) and reaction time (1~5 h). All the tested variables were identified to have significant effects (p < 0.05) on glucose conversion. The optimum concentrated acid hydrolysis conditions were acid concentration of 70.8%, loading sulfuric acid of 3.2 ml and a reaction time of 3.6 h. This research of concentrated acid hydrolysis was a promising method to improve glucose conversion for waste paper.

• 상하수도학회지
• /
• 제7권1호
• /
• pp.20-28
• /
• 1993

The Wastewater from the weight reduction process of polyester is more difficult to be treated biologically than the general wastewater from dyeing and finishing processes in textile industries. Above wastewater shows high pH, high organic strength and wide variation of organic loading. These characteristics are due to TPA and EG resulting from alkaline weight-reduction process and make trouble in the operation of activated sludge process. Therefore, the objective of this study is to develop the pretreatment method for the successful operation of treatment process. For the successful pretreatment process, the wastewater from weight-reduction process should be segregated from other wastewater stream and then acidified with concentrated sulfuric acid to precipitate out TPA from DST solution. At the optimum pH of 2. 2, the initial $COD_{cr}$ 60,000mg/l is reduced to 11,500mg/l and the removal efficiency of $COD_{cr}$ is 81.1%. The required amount of sulfuric acid for pretreatment is not greater than the amount for the the existing neutralization process. Moreover, the supernatant of pretreatment process can be reused in acidification of wastewater.

• 청정기술
• /
• 제17권2호
• /
• pp.156-165
• /
• 2011

본 연구에서는 바이오에탄올 생산을 위한 목질계 바이오매스의 전처리, 당화, 당/산 분리, 발효, 정제에 이르는 전 공정을 조합하고, 상용공정모사기(PRO/II)를 사용하여 공정모사를 수행하였다. 주요 공정으로 강산에 의한 전처리 및 당화, SMB(simulated moving bed)를 사용한 당/산 분리, 그리고 증류 및 투과증발법(Pervaporation)을 이용한 에탄올 탈수 공정을 사용하였다. 열회수 공정을 이용하여 전 공정의 에너지 소비가 최소화 되도록 하고 강산당화공정에 의한 바이오에탄올 생산공정의 물질수지 및 열 수지를 확인하였다. 공정모사 결과, 1 kg의 에탄올을 생산하는데 필요한 바이오매스는 4.07 kg, 소요된 열량은 3,572 kcal로 계산되었다. 기존 묽은 산 당화공정(SRI 자료)에 비해 26%의 수율 증가와 30% 정도의 에너지 절감이 가능할 것으로 예상되었다. 이러한 수율을 얻기 위해서는 강산당화공정에 의한 전처리 및 당화공정에서 셀룰로오스 및 헤미셀룰로오스의 전환율이 90% 정도에 이르러야한다. 또한 5탄당 발효공정이 개발되어야 한다. 효율적 에너지 절감을 위해서는 SMB 공정에서 분리된 황산수용액의 농도가 20% 이상 되어야하며, SMB 공정에 의한 당/산분리 공정이 실용화되어야 강산당화공정에 의한 목절계 바이오에탄올 생산공정이 상용화될 것이다.

• 한국환경농학회지
• /
• 제16권4호
• /
• pp.311-319
• /
• 1997

광산폐수, 산업폐수등으로 부터 Cd, Pb, Zn 및 Cu등의 중금속에 강한 내성을 지니고 있을 뿐만 아니라 균체내 중금속 축적능력이 우수한 중금속 내성 미생물 균주 Pseudomonas putida(Cd), Pseudomonas aeruginosa(Pb), Pseudomonas chlororaphis(Zn) 및 Pseudomonas stutzeri(Cu)를 각각 분리하여, 여러가지 물리화학적인 방법으로 세포를 전처리하여 세포구성성분을 인위적으로 조절한 후 세포내 중금속이온의 흡수 거동 및 조단백질 함량과 중금속 축적관계를 조사한 결과는 다음과 같다. 세포를 알카리로 전처리하였을 경우 세포내 중금속 축적은 매우 감소되었으며, 메탄올과 클로포름으로 전처리하였을 경우에는 중금속 축적에 큰 영향을 미치지 않았으나, 메탄올과 클로로포름으로 전처리한 후 다시 알카리로 재차 처리하였을 경우에는 중금속 축적이 매우 감소되었다. 전처리된 세포내 중금속 축적은 용출되지 않고 남아있는 조단백질 함량이 감소됨에 따라 더 얼마나 크게 감소되었으므로 세포 구성물질중 단백질이 중금속 축적에 중요한 역할을 하는 물질인 것으로 판단되었다.

• 대한치과보철학회지
• /
• 제25권1호
• /
• pp.95-118
• /
• 1987

This study was undertaken to observe the elemental transition of Interface depending on different pretreatment methods, the number of filings, the kinds of porcelain powders and the various alloys in ceramo-metal restoration. The materials used in this study were Pors-on $4^{(R)}$ and Ceramco porcelain powder to compare the differences depending on the pretreatement methods and the number of firings. Ceramco porcelain powder and Vita porcelain powder were used to compare the differences of elemental transition depending on the porcelain powders. The $Parasil^{(R)},\;PGV^{(R)}$ and Pors-on $4^{(R)}$ as Pd-Ag alloy were used to compare the difference of elemental transition depending on the various alloys. The pretreatment methods were : no treatment, treatment under vacuum and air, treatment with 50 % hydrofluoric acid and double heat tretament. The number of firings were 3, 5 and 7 repeated firings All specimens were observed by SEM and concentration of elements were analyzed quantitatively with EPMA The results of this study were obtained as follows : 1. In the groups of air-treatment, concentration of Sn were the highest and widest. A high concentration of In were in the groups of vacuum and air treatment. 2. There were no significant differences in concentration of Sn between the group of vacuum, 5 minutes hydrofluoric acid and double heat treatment. (p>0.05) 3. As the period of time of hydrofluoric acid treatment increased, not only were the trace elements reduced but the main components such as Pd and Ag were also reduced. 4. Concentration of Sn and In increased and diffused with repeated firings but 5 repeated and 7 repeated firings groups had no significant differences. (p>0.05) 5. Sn were more concentrated in the group of Ceramco porcelaion powder than Vita porcelain powder. 6. The higher concentration of trace elements in the alloy, the more increasing concentration of Sn and In in the interface.

• 한국산업보건학회지
• /
• 제9권1호
• /
• pp.23-40
• /
• 1999

The analysis of thiodiglycolic acid in urine has been used as an index of biological exposure to vinyl chloride. Unfortunately thiodiglycolic acid has a strong hydrophilic character, because it has two carboxylic groups, so that it can only be extracted with organic solvent with a great difficulty. Underivatized thiodiglycolic acid tends to tail because of non-specific interaction with the inert support. Therefore, esterification is the obvious first choice for derivatization of thiodiglycolic acid, particularly for gas chromatography. In this study, the focus of interest is to compare two method of esterifications (methylation and silylation). Methylation is to make the methyl ester of thiodiglycolic acid by reaction with diazomethane. Silylation is to make the trimethylsilyl ester of thiodiglycolic acid by reaction with N-trimethylsily-ldiethylamine. The results and conclusions are as the following: 1. The detection limit (sensitivity) of methylated thiodiglycolic acid was $5.00{\mu}g/m{\ell}$ and silylated thiodiglycolic acid was $3.07{\mu}g/m{\ell}$ by gas chromatography with flame ionization detector. 2. The optimal liquid-liquid extraction of thiodiglycolic acid was as following: To each of the tubes, $15m{\ell}$ of urine, concentrated sulfuric acid (pH 1 - 2) and 5 gsodium sulfate were added. The samples was extracted three times with $5m{\ell}$ ethylacetate each time. 3. The methylated thiodiglycolic acid was more stable than silylated thiodiglycolic acid in extractional solvent which contained humidity. 4. The precision (pooled coefficient of variation for 4 days) of the analysis was 0.07324 in methylated thiodiglycolic acid with external standard calibration, and 0.07033 in methylated thiodiglycolic acid with internal standard calibration. 5. The precision (pooled coefficient of variation for 4 days) of the analysis was 0.10914 in silylated thiodiglycolic acid with external standard calibration, and 0.13602 in silylated thiodiglycolic acid with internal standard calibration. From the above results, the analysis of methylated thiodiglycolic acid was more sensitive (limit of detection) than silylated thiodiglycolic acid by gas chromatography. However, the methylated thiodiglycolic acid was stable in the humidity and was separated sharply on chromatogram. Also, analysis of methylated thiodiglycolic acid was more precise (pooled coefficient of variation for 4 days) than silylated thiodiglycolic acid. In conclusion, it is established that the analysis of methylated thiodiglycolic acid is appropriate for biological monitoring of exposure to vinyl chloride.

• 한국펄프종이공학회:학술대회논문집
• /
• 한국펄프종이공학회 2011년도 추계학술발표회 논문집
• /
• pp.167-177
• /
• 2011

Renewable energy resources and technologies have the potential to provide long-lasting solutions of the global energy-requirements faced by the economic and environmental sectors of a nation. Therefore, waste money bills were used as renewable energy source for the production of bio-ethanol. In this study, different concentrated NaOH 0.5%. 1.0%, 2.0%, 3.0% and 0.0% (as a control) were used for 10, 20 and 30 mins at $121^{\circ}C$/15 psi in an autoclave. Saccharification and fermentation (aerobic and anaerobic) were carried out through commercial enzyme Celluclast 1.5 L, Novozymes 188 and Saccharomyces cerevisiae KCCM 11304 respectively. The results of pretreatment showed that the NaOH pre-treated substrate enhanced enzyme action and released more amount of glucose. The amount of glucose was found with the increasing concentration of NaOH and time $44996.95{\pm}6.30$, $46763.10{\pm}3.56$, $53421.32{\pm}4.72$, $63431.25{\pm}6.95$ and $56850.98{\pm}6.75\;ng/{\mu}l$ for 30 min respectively. As for bioethanol, the conversion rate of NaOH resulted $1010.08{\pm}4.71$, $1050.25{\pm}4.37$, $1109.49{\pm}4.39$, $1139.25{\pm}3.26$ and $1020.77{\pm}3.89$ ppm for aerobic; $16730.54{\pm}6.67$, $17076.45{\pm}6.25$, $17516.17{\pm}4.49$, $19782.68{\pm}6.19$ and $17973.39{\pm}7.50$ ppm for anaerobic and $18935.02{\pm}4.59$, $19895.45{\pm}5.39$, $21912.95{\pm}4.83$, $24895.21{\pm}6.72$ and $18961.21{\pm}4.90$ ppm for anaerobic condition with benzoic acid for respective condition. Thus, the results of the present work clearly revealed that with the increasing of alkali concentration might be more effective for bio-ethanol production from waste money bill, which is economic and environmental friendly.

• 한방재활의학과학회지
• /
• 제32권4호
• /
• pp.9-18
• /
• 2022

Objectives This study was conducted to confirm the anti-inflammatory effect of Naetakbaekryeom-san (NTB), and whether it could be another treatment for inflammatory diseases. Methods The NTB water extract was extracted with hot water at 100℃ for 2 hours, concentrated at 80℃ under reduced pressure, and used. After 2 hours of pretreatment with NTB and positive control Bay11-7082, nitric oxide (NO), inducible NO synthase (iNOS), interleukin (IL)-6, IL-1𝛽, tumor necrosis factor alpha (TNF-𝛼) were measured in RAW264.7 cells activated with lipopolysaccharides (LPS) 500 ng/mL. After 2 hours of pretreatment with NTB, the anti-inflammatory effect of NTB was evaluated by measuring nuclear factor kappa-light-chain-enhancer of activated B cells (NF-𝜅B) in RAW264.7 cells and 293T cells activated with phorbol 12-myristate 13-acetic acid (PMA) 30 ng/mL. Results In RAW264.7 cells activated with LPS, NTB at concentrations of 0.1, 0.3, and 1.0 mg/mL showed no cytotoxicity, significantly inhibited NO production and inhibition of iNOS expression. TNF-𝛼 cytokine levels was not regulated, but NTB at each concentration inhibited the production of IL-1𝛽 and IL-6, and the effect was higher than that of the positive control Bay11-7082 (20 𝜇M). In PMA-activated RAW264.7 cells and 293T cells, each concentration of NBT decreased the NF-𝜅B transcriptional activity, with the greatest decrease at 1 mg/mL. Conclusions These results demonstrated the anti-inflammatory effect of NTB water extracts, but further studies such as comparison of anti-inflammatory effects and antioxidant effects by NTB component, comparison of effects according to extraction solvents, and clinical studies are needed.

• Journal of the Korean Wood Science and Technology
• /
• 제43권6호
• /
• pp.826-837
• /
• 2015

본 연구에서는 목질계 바이오매스로부터 옥살산 전처리 액상 가수분해산물을 이용하여 바이오에탄올을 생산하였다. 생산된 바이오에탄올은 투과증발에 의해 분리, 농축하였으며 투과증발 잔류물에 대한 항산화 활성을 측정하였다. 옥살산 전처리 후 액상 가수분해산물에는 자일로스($37.28g/{\ell}$)가 대부분을 차지하고 있었으며 발효저해물질인 초산, 푸르푸랄 및 페놀성 화합물을 포함하고 있었다. 전기투석에 의해 초산을 제거하였으며 전기투석 후 가수분해산물로 발효를 수행한 결과 $12.21g/{\ell}$의 에탄올을 생산하였다. 에탄올 농축 후 투과증발 잔류물의 에틸아세테이트 분획에서는 86.81 mg/100 g(추출물)의 페놀성 화합물을 함유하고 있었으며 DPPH, ABTS 라디칼 소거활성 및 환원력에 대한 $IC_{50}$ 값은 각각 $0.87mg/m{\ell}$, $0.85mg/m{\ell}$, $0.59mg/m{\ell}$로 나타났다. GC-MS로 구성성분을 확인한 결과 당 분해산물과 페놀 유도체들이 검출되었다.

• Applied Biological Chemistry
• /
• 제10권
• /
• pp.1-13
• /
• 1968

phytin은 phytic acid의 금속염(金屬鹽)(주(主)로 Ca 와 Mg)임으로 그중(中)의 P,Ca 및 Mg를 정량(定量)하면 순도(純度)를 알 수 있고, 또 분자식(分子式)을 추정(推定)할 수 있다. 저자(著者)는 phytin 중(中)의 P,Ca 및 Mg를 정량분석(定量分析)하는 새로운 방법(방법)으로 서 phytin을 건식(乾式) 분해(分解)하고 ion 교환수지(交換樹脂)로 처리한 다음 Chelate 법(法)으로 정량(定量)하는 방법(方法)을 확정(確定)켰으며 그 결과(結果)를 요약(要約)하면 다음과 같다. 1) phytin 분석(分析)의 전처리과정(前處理課程)으로서는 phytin을 conc. $HNO_3$로 적시면서 $550{\sim}660^{\circ}C$에서 회화(灰化)하는 건식분해법(乾式分解法)을 썼다. 이 방법(方法)은 습식분해법(濕式分解法)보다 분석결과(分析結果)가 정확(正確)하다. 2) phytin을 건식분해(乾式分解)한 시료(試料)를 가지고 종래법(從來法)과 새로운 분석법(分析法) (본법(本法))에 의하여 P,Ca 및 Mg를 정량(定量)하였으며, 본법(本法)은 다음고 같다. phytin 회분(灰分 HCl 용액(溶液)을 양(陽) ion 교환수지(交換樹脂)로 처리하여 양(陽) ion 구분(區分)과 음(陰) ion 분리(分離)하고 양(陽) ion 구분(區分)의 일부(一部)를 pH 7.0로 한다음 완충액(緩衝液)($NH_3-NH_4Cl$으로 pH 10으로 하고 BT 지시약(指示藥)을 써서 표준(標準) EDTA 용액(溶液적정(滴定)하여 Ca와 Mg의 합계치(合計値)를 얻었다. 또 양(陽) ion 구분(區分)의 일부(一部)를 pH 7.0로 하고 표준(標準) EDTA 용액(溶液)을 소량(少量)넣고 8N-KOH로 pH $12{\sim}13$으로 하고 N-N 희석분말(稀釋粉末)을 지시약(指示藥) 으로써 표준(標準) EDTA 용액(溶液)으로 적정(滴定)하여 Ca 치(値)를 얻었다. Ca와 Mg의 합계결정치(合計決定値)와 Ca 적정치(滴定値) 차(差)로 Mg 치(値)를 얻었다. 음(陰) ion 구분(區分)으로부터 상법(常法)에 의하여 $MgNH_4PO_4$의 침전(沈澱)을 만들어서 HCl에 녹키고 일정량(一定量)의 표준(標準) EDTA 용액(溶液)을 넣어 pH 7.0로 한다음 완충액(緩衝液)으로 pH 10으로 하고 BT 지시약(指示藥)을 써서 표준(標準) Mg $SO_4$용액(溶液)으로 적정(滴定)하여 P 치(値)를 얻었다. 본법(本法)으로 Na-phytate를 분석(分析)한 결과(結果) Na-phytate의 분자식(分子式)을 $C_6H_6O_{24}P_6Mg_4CaNa_2{\cdot}5H_2O$라고 하였을 때의 이론치(理論値)에 비(比)하여 P가 98.9% Cark 97.1%, Mg가 99.1%이고 통계처리(統計處理)한 결과분석치(結果分析値)와 이론치(理論値)는 잘 일치(一致)된다. 그러나 종래법(從來法)에 의(依)한 분석치(分析値)는 이론치(理論値)에 비(比)하여 P가 92.40%, Cark 86.80%, Mg가 93.80%로서 이론치(理論値)와 일치(一致)하지 않는다. 3) Na-phytate를 전분(澱粉)과 일정(一定)한 비(比)로 혼합(混合)하고 본법(本法)으로 P,Ca 및 Mc를 정량(定量)한 결과(結果) 이들의 회수율(回收率)은 거의 100%이었다. 4) 본분석법(本分析法)의 정확성(正確性)을 재확인(再確認)하기 위하여 phytic acid 수용액(水溶液)에 $CaCl_2$수용액(水溶液)을 phytic acid 1M:$CaCl_25M:McCl_220M$의 비(比)로 반응(反應)서키어서 Ca 1 원자(原子), Mg 4원자함유(原子含有)된 Na-phytate를 합성(合成)하였으며 이것의 P,Ca 및 Mg 분석치(分析値)와 의(依한) 조제(調製) Naphytate의 분석치(分析値)와 일치(一致)되었다. 이상(以上)과 같이 phytin 시료(試料)를 건식분해(乾式分解)하고 ion 교환수지(交換樹脂)로 처리(處理)한 다음 Chelate 법(法)으로 P,Ca 및 Mg를 정량(定量)하는 본법(本法)은 정확(正確)하고 신속(迅速)한 phytin의 새 분석방법(分析方法)이라고 사료(思料)되는 바이다.