• 제목/요약/키워드: hydrogen yield

검색결과 476건 처리시간 0.03초

비이온성 계면활성제의 운점이 OMG 배합비가 증가된 폐 신문지 탈묵효율에 미치는 영향 (Effects of Cloud Point of Non-ionic Surfactant on Deinking Efficiency of ONP at High Blending Ratio of OMG)

  • 이태주;서진호;류정용
    • 펄프종이기술
    • /
    • 제47권6호
    • /
    • pp.164-169
    • /
    • 2015
  • Nowadays blending ratio of OMG (old magazine) in recovered paper used for manufacturing newspaper have been increased. When large amount of OMG is consumed in newsprint mill, brightness can be improved by inorganic pigments of coating layer. On the other hand decrease in yield of deinking process will be encountered because the pigments can be removed as reject of froth flotation process. Therefore selection of the optimal deinking agent is an important. Non-ionic surfactant have been used widely in newsprint mill. Non-ionic surfactant has amphoteric characteristics. Hydrophilic group is ethylene and propylene oxide that can induce hydrogen bonding with water molecules. In this regard, cloud point is an important parameter in order to control efficiency of deinking process because hydration of the hydrophobic group can be varied according to temperature of a system. In this study, deinking properties of ONP at high blending ratio of OMG was analyzed according to cloud points of non-ionic surfactants. $L^*$, $a^*$, $b^*$, brightness and effective residual ink concentration did not affected by the change of cloud points. Especially, flotation reject decreased significantly according to increase in cloud point of the non-ionic surfactant. Consequently, when a nonionic surfactant having a cloud point higher than the temperature of the system is used, properties of the deinked pulp can be maintained and yield of deinking process can be improved.

이트라코나졸 항진균제의 효과적인 합성법 개발 (Development of the Efficient Synthetic Route for Itraconazole Antifungal Agent)

  • 백두종
    • 공업화학
    • /
    • 제17권6호
    • /
    • pp.633-637
    • /
    • 2006
  • 본 연구에서는 triazole계 항진균제인 이트라코나졸의 대량합성을 위한 효과적인 합성법을 제시하였다. Janssen Pharmaceutica에 의해 발표된 기존의 의약화학적 합성경로는 2,4-dichloroacetophenone을 출발물질로 하는 직렬(linear) 합성의 14 단계로서 전체수율이 1.4%에 불과하였고 대량합성에 부적합한 위험물질로서 methanesulfonyl chloride ($CH_{3}SO_{2}Cl$)와 수소기체 및 sodium hydride (NaH)를 사용하고 있다. 또한 고가의 1-acetyl-4-(4-hydroxyphenyl)piperazine 및 팔라듐을 사용함으로써 생산 단가가 높은 문제점이 있었다. 이를 개선하기 위해서 병렬(convergent) 합성 전략을 수립하였는데, 이트라코나졸의 대략 반에 해당하는 중간체 II와 III을 각각 합성한 다음 두 부분을 결합시키는 12단계의 합성공정을 개발하였고 전체 수율은 12.0%로서 합성효율이 크게 개선되었다. 이 과정에서 공정을 간략화하고 위험물질 및 고가의 반응물의 사용을 배제함으로써 생산 원가를 크게 절감시킬 수 있었다.

Catalytic Gasification of Mandarin Waste Residue using Ni/CeO2-ZrO2

  • Kim, Seong-Soo;Kim, Jeong Wook;Park, Sung Hoon;Jung, Sang-Chul;Jeon, Jong-Ki;Ryu, Changkook;Park, Young-Kwon
    • Bulletin of the Korean Chemical Society
    • /
    • 제34권11호
    • /
    • pp.3387-3390
    • /
    • 2013
  • Catalytic gasification of mandarin waste residue was carried out using direct and indirect catalyst-contact methods for the first time. In the indirect method, non-catalytic reaction in a reactor was followed by catalytic upgrading of vapor product in another reactor. Two different catalysts, $Ni/{\gamma}-Al_2O_3$ and $Ni/CeO_2-ZrO_2$, were employed. $CeO_2-ZrO_2$ support was prepared using hydrothermal synthesis in supercritical water. The catalysts were characterized by $H_2$-temperature programmed reduction and Brunauer-Emmett-Teller analyses. Under the condition of equivalent ratio (ER) = 0, the indirect catalyst-contact method led to a higher gas yield than the direct method. Under ER = 0.2, the yield of biogas obtained over $Ni/CeO_2-ZrO_2$ was higher than that obtained over $Ni/{\gamma}-Al_2O_3$. Also, the coke formation of $Ni/CeO_2-ZrO_2$ was lower than that of $Ni/{\gamma}-Al_2O_3$. Such results were attributed to the higher reducibility and better lattice oxygen mobility of $Ni/CeO_2-ZrO_2$, which were advantageous for partial oxidation reaction.

Efficient Enantioselective Synthesis of (R)-[3,5-Bis(trifluoromethyl)phenyl] Ethanol by Leifsonia xyli CCTCC M 2010241 Using Isopropanol as Co- Substrate

  • Ouyang, Qi;Wang, Pu;Huang, Jin;Cai, Jinbo;He, Junyao
    • Journal of Microbiology and Biotechnology
    • /
    • 제23권3호
    • /
    • pp.343-350
    • /
    • 2013
  • (R)-[3,5-Bis(trifluoromethyl)phenyl] ethanol is a key chiral intermediate for the synthesis of aprepitant. In this paper, an efficient synthetic process for (R)-[3,5- bis(trifluoromethyl)phenyl] ethanol was developed via the asymmetric reduction of 3,5-bis(trifluoromethyl) acetophenone, catalyzed by Leifsonia xyli CCTCC M 2010241 cells using isopropanol as the co-substrate for cofactor recycling. Firstly, the substrate and product solubility and cell membrane permeability of biocatalysts were evaluated with different co-substrate additions into the reaction system, in which isopropanol manifested as the best hydrogen donor of coupled NADH regeneration during the bioreduction of 3,5-bis(trifluoromethyl) acetophenone. Subsequently, the optimization of parameters for the bioreduction were undertaken to improve the effectiveness of the process. The determined efficient reaction system contained 200mM of 3,5-bis(trifluoromethyl) acetophenone, 20% (v/v) of isopropanol, and 300 g/l of wet cells. The bioreduction was executed at $30^{\circ}C$ and 200 rpm for 30 h, and 91.8% of product yield with 99.9% of enantiometric excess (e.e.) was obtained. The established bioreduction reaction system could tolerate higher substrate concentrations of 3,5- bis(trifluoromethyl) acetophenone, and afforded a satisfactory yield and excellent product e.e. for the desired (R)-chiral alcohol, thus providing an alternative to the chemical synthesis of (R)-[3,5-bis(trifluoromethyl)phenyl] ethanol.

Potential use of ultrasound in antioxidant extraction from Ecklonia cava

  • Lee, Seung-Hong;Kang, Min-Cheol;Moon, Sang-Ho;Jeon, Byong-Tae;Jeon, You-Jin
    • ALGAE
    • /
    • 제28권4호
    • /
    • pp.371-378
    • /
    • 2013
  • Water and methanolic extracts of Ecklonia cava, a marine brown alga, were prepared by ultrasonic extraction (UE) and conventional extraction (CE) methods. The radical-scavenging activity and the inhibitory effects against hydrogen peroxide ($H_2O_2$)-induced DNA damage of the extracts were investigated. All extracts prepared by CE exhibited higher total polyphenolic content than that in the extracts prepared by UE. Extraction yield and total phenolic content increased as the UE time increased. The radical-scavenging activities increased as the UE time increased. All extracts prepared by CE exhibited higher 1,1-diphenyl-2-pricrylhydrazyl (DPPH) and hydroxyl radical-scavenging activities than did those prepared by UE. Extracts prepared by UE showed stronger scavenging activities on alkyl radical and $H_2O_2$ than those prepared by CE did. Methanolic extract with UE 12 h (100MEU-12h) and methanolic extract with CE 24 h (100MEC-24h) were selected and evaluated by comet assay for their inhibitory effect against $H_2O_2$-induced DNA damage. 100MEU-12h showed slightly greater protective effect against $H_2O_2$-induced DNA damage than 100MEC-24h. Thus, UE can be effectively used as a seaweed extraction technique, and there is potential for scale-up of the extraction process.

원자로 내부구조물 균열개시 민감도에 미치는 영향인자 고찰 (Review of Factors Affecting IASCC Initiation of Stainless Steel in PWRs)

  • 황성식;최민재;김성우;김동진
    • Corrosion Science and Technology
    • /
    • 제20권4호
    • /
    • pp.210-229
    • /
    • 2021
  • To safely operate domestic nuclear power plants approaching the end of their design life, the material degradation management strategy of the components is important. Among studies conducted to improve the soundness of nuclear reactor components, research methods for understanding the degradation of reactor internals and preparing management strategies were surveyed. Since the IGSCC (Intergranular Stress Corrosion Cracking) initiation and propagation process is associated with metal dissolution at the crack tip, crack initiation sensitivity was decreased in the hydrogenated water with decreased crack sensitivity but occurrence of small surface cracks increased. A stress of 50 to 55% of the yield strength of the irradiated materials was required to cause IASCC (Irradiation Assisted Stress Corrosion Cracking) failure at the end of the reactor operating life. In the threshold-stress analysis, IASCC cracks were not expected to occur until the end of life at a stress of less than 62% of the investigated yield strength, and the IASCC critical dose was determined to be 4 dpa (Displacement Per Atom). The stainless steel surface oxide was composed of an internal Cr-rich spinel oxide and an external Fe and Ni-rich oxide, regardless of the dose and applied strain level.

벼와 옥수수 부산물로 제조한 바이오차의 NH4+ 흡착 특성 평가 (Adsorption Characteristics of NH4+ by Biochar Derived from Rice and Maize Residue)

  • 강윤구;이재한;천진혁;오택근
    • 한국환경농학회지
    • /
    • 제40권3호
    • /
    • pp.161-168
    • /
    • 2021
  • BACKGROUND: Biochar has ability to reduce N loss, increase crop yield, and sequestrate carbon in the soil However, there is still limited study concerning the interactive effects of various biochars on NH3 loss and plant growth. This study, therefore, was conducted to investigate the NH4+ adsorption characteristics of biochar derived from rice and maize residues. METHODS AND RESULTS: By-products were pyrolyzed under oxygen-limited conditions at 300-700℃ for 1 hour and used for experiment of NH4+ adsorption in aqueous solution. The adsorption characteristics of biochar were studied using Langmuir isotherm. Biochar yield and hydrogen content decreased with increasing pyrolysis temperatures, whereas pH, EC, and total carbon content increased. The biochar pyrolyzed at lower temperatures was more efficient at NH4+ adsorption than those produced at higher temperatures. In addition, the RL values, indicating equilibrium coefficient were between 0 and 1, confirming that the result was suitable for Langmuir isotherm. CONCLUSION: The maize stalk biochar pyrolyzed at 300℃ was the most efficient to adsorb NH4+ from the aqueous solution. Furthermore, the adsorption results of this experiment were lower than those of other prior studies, which were ascribed to different experimental conditions such as ingredients, and pyrolysis conditions.

The Mechanism of the Photocyclization of N-(2-Haloarylmethyl)Pyridinium and N-(arylmethyl)-2-Halopyridinium Salts

  • Yong-Tae Park;Chang-Han Joo;Chung-Do Choi;Kum-Soo Park
    • Bulletin of the Korean Chemical Society
    • /
    • 제12권2호
    • /
    • pp.163-169
    • /
    • 1991
  • The photochemical and photophysical properties of N-(2-haloarylmethyl)pyridinium, N-(arylmethyl)-2-halopyridinium, N-(2-haloarylmethyl)-2-halopyridinium salts and N-(2-halobenzyl)-isoquinolinium salt are studied. The pyridinium salts photocyclize to afford isoindolium salts, while the isoquinolium salts do not. In the photocyclization of N-(2-chlorobenzyl)-2-chloropyridinium salts, pyrido[2,1-a]-4-chloroisoindolium salt is formed by the cleavage of chlorine of pyridinium ring. This indicates that the excited moiety is not the phenyl ring, but the pyridinium ring. The triplet states of the pyridinium salts are believed to be largely involved in the photocyclization, since oxygen retards most of the reaction. Some assistance of a ${\pi}$-complex between the excited chlorine moiety of the salt and phenyl plane of the same molecule is required to explain the reactivity of the salts. N-(Benzyl)-2-chloropyridinium salt is two times more reactive than N-(2-chlorobenzyl)pyridinium salt. N-(Benzyl)-2-chloropyridinium salt can form ${\pi}-complex$ effectively because of the electron-rich phenyl group. The ${\pi}$-complex affords an intermediate, phenyl radical by cleaving the chlorine atom. The photocyclized product, isoindolium salt is obtained by losing the hydrogen atom from the phenyl radical. The reactive pyridinium salts 1a, 2a and 3a have a low fluorescence quantum yield (${\Phi}F$ < 0.01) and a higher triplet energy (ET > 68 kcal/mole) than the unreactive quinolinium salt. The unreactivity of isoquinolinium salt can be understood in relation to its high fluorescence quantum yield and its low triplet energy $(E_T = 61 kcal/mole).$.

황화물(黃化物) 및 불화물(弗化物)이 수도생육(水稻生育)과 수량(收量)에 미치는 영향(影響);I. 오염지역(汚染地域)에서의 생육장해(生育障害) 및 수량감소(收量減少) (Influence of Sulfur and Fluorine Compounds on the Growth and Yield of Rice Plants;I. Growth Retardation and Yield Reduction under Various Stressed Conditions in the Field)

  • 박완철;신응배;김광호
    • 한국환경농학회지
    • /
    • 제6권2호
    • /
    • pp.53-65
    • /
    • 1987
  • 본(本) 연구(硏究)는 1981년(年)부터 1984년(年)까지 4개년(個年)에 걸쳐 울산공업단지주변(蔚山工業團地周邊) 21 개지점(個地點)에서 수행(遂行)되었다. 대기중(大氣中) 황화물(黃化物) 및 불화물(弗化物)이 수도(水稻)의 생육(生育) 및 수량(收量)에 미치는 영향(影響)을 구명(究明)하기 위해 수도(水稻)의 수량구성요소(收量構成要素), 수량(收量), 대기중(大氣中)의 류황산화물(硫黃酸化物), 엽내류황(葉內硫黃) 및 불소함량(弗素含量), 엽피해율(葉被害率)을 조사(調査)하여 검토(檢討)한 결과(結果)는 다음과 같다. 1. 수도(水稻)의 수량(收量)에 대(對)한 수량구성요소(收量構成要素)의 기여율(寄與率)은 주당수수(株當穗數)의 기여율(寄與率)이 매년(每年) 제일 높았으며, 타(他) 수량구성요소(收量構成要素)들의 기여율(寄與率)은 주당수수(株當穗數)보다 현저히 낮았고, 이들의 기여정도(寄與程度)는 조사년도(調査年度)에 따라 차이(差異)가 있었다. 2. 수량(收量)과 주당수수(株當穗數) 및 등열율(登熱率)에 대(對)해서는 매년(每年) 엽내불소함량(葉內弗素含量)에 의한 영향도(影響度)는 엽내류황(葉內硫黃)에 의한 것보다 크고, 수당입수(穗當粒數)에 대(對)한 엽내류황(葉內硫黃)과 불소(弗素)에 의한 영향도(影響度)는 조사년도(調査年度)에 따라 일정(一定)한 경향(傾向)이 없었으며, 이들 오염지표(汚染指標)와 천립중간(千粒重間)에는 상관(相關)의 유의성(有意性)이 인정(認定)되지 않았다. 그리고 수량(收量) 및 수량구성요소(收量構成要素)에 대(對)한 월별(月別) 오염물(汚染物)이 영향(影響)은 조사연도(調査年度)에 따라 차이(差異)가 있었으며, 매년(每年) 주당수수(株當穗數)의 감소(減少)에 가장 큰 영향(影響)을 미친 월별(月別) 오염물(汚染物)이 최종수량(最終收量)의 감소(減少)에도 가장 영향(影響)이 컸다. 3. 수도(水稻)의 수량추정(收量推定)에 적용(適用)할 오염지표(汚染指標)를 선정(選定)할 때 월별(月別) 엽내류황(葉內硫黃) 및 불소함량(弗素含量)과 엽피해율(葉被害率)을 함께 적용(適用)하는 것이 PSS 값이 제일 낮았다. 그리고 PSS에 의해 선정(選定)된 오염지표(汚染指標)를 이용(利用)하여 만든 회귀식(回歸式)에 의한 예측수량(豫測收量)과 실측수량간(實測收量間)에는 높은 상관관계(相關關係)가 인정(認定)되었다.

  • PDF

과산화수소 엽면 처리에 의한 수수에서 한발 스트레스 완화 효과 (Mitigation Effects of Foliar-Applied Hydrogen Peroxide on Drought Stress in Sorghum bicolor)

  • 심두보;이승하;정종일;김민철;정정성;이영훈;전승호;송기은;심상인
    • 한국작물학회지
    • /
    • 제65권2호
    • /
    • pp.113-123
    • /
    • 2020
  • 본 논문은 과산화수소 엽면 처리를 통해 수수에서 한발 스트레스 완화 효과가 있는지 알아보기 위하여 과산화수소 처리에 따른 생육 및 생리적 특성 변화와 단백질 변화를 분석하였다. 1. 포장 실험에서 한발 스트레스는 수수 생장을 감소시켰으나, 과산화수소 처리구에서는 과산화수소 무처리구보다 생육이 우수하였다. 또한 한발 조건에서 과산화수소 처리는 무처리에 비해 수량 관련 형질들의저하를 막는 효과를 보였다. 2. 엽 녹색도(SPAD) 및 엽록소 형광(Fv/Fm), 광합성 형질 조사에서 과산화수소 처리가 과산화수소 무처리보다 높았고, 포장 실험에서 엽내 과산화수소 함량은 적습+H2O2 처리가 적습+H2O 처리보다 과산화수소 함량이 227.8 µmol·g-1 높았고, 한발 조건에서 엽내 과산화수소 함량은 한발+H2O2 처리가 한발+H2O 처리보다 16.7 µmol·g-1으로 낮았다. 3. 한발 조건에서 과산화수소 처리는 여러 단백질의 발현을 변화시켰으며, 특히 광합성 관련 단백질인 ATP synthase deltal chain, cytochrome b6-f complex iron-sulfur subunit, ATP synthase subunit gamma, putative uncharacterized protein Sb02g002690, Sb07g027500와 Superoxide 라디칼을 제거해주는 superoxide dismutase가 증가한 것을 확인하였다. 그리고 단백질 보호와 복원에 관련된 heat shock protein의 발현 증가도 확인되었다. 종합적으로 과산화수소 엽면 처리가 한발 하에서 광합성 관련 단백질의 발현을 증가와 기공 개도를 높여 광합성 능력을 향상시켰다. 특히 엽내에 축적될 수 있는 활성산소종을 제거하는 항산화 능력이 높아져 한발 스트레스 대한 내성을 높여 수수의 생육과 수량성 저하가 억제되는 것을 확인할 수 있었다.