• 펄프종이기술
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• 제47권1호
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• pp.24-34
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• 2015

Domestic companies supplying electricity must increase obligatory duty to use renewable energy annually. If not met with obligatory allotment, the electricity-supply companies must pay RPS (Renewable Portfolio Standards) penalty. Although the power plants using a pulverizing coal firing boiler could co-fire up to around 3 per cent with wood pellets mixed in with coal feedstock without any major equipment revamps, they recorded only about 60 per cent fulfillment of RPS. Consequently, USD 46 million of RPS penalty was imposed on the six power supplying subsidiaries of GENCOs in 2014. One of the solutions to reduce the RPS penalty is that the power supply companies adopt the co-firing of torrefied lignocellulosic biomass in coal plants, which may contribute to the use of over 30 per cent of torrefied biomass mixed with bituminous coals. Extra binder was required to form pellets using torrefied biomass such as wood chips, PKS (Palm Kernel Shell) and EFB (Empty Fruit Bunch). Instead of corn starch, 30, 50 and 70 per cent of Larix saw dusts were respectively added to the torrefied feedstocks such as Pinus densiflora chips, PKS and EFB. The addition of saw dusts led to the decrease of the calorific values of the pellets but the forming ability of the pelletizer was exceedingly improved. Another advantage from the addition of saw dusts stemmed from the reduction of ash contents of the pellets. Finally, it was confirmed that torrefied oil palm biomass such as PKS and EFB could be valuable feedstocks in making pellets through improved binding ability.

• 한국산학기술학회논문지
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• 제21권8호
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• pp.248-255
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• 2020

경사화 두께를 갖는 열차폐 코팅의 열적 내구성과 열적 안정성에 대한 코팅층 두께의 영향을 화염 열피로 시험과 열충격 시험을 통해서 조사하였다. Bond 층과 top 층은 각각 Ni-Cr계 상용 MCrAlY 분말과 상용 이트리아 안정화 지르코니아 (YSZ) 분말을 사용하여 니켈기지의 초내열합금 모재 (GTD-111)에 대기 플라즈마 용사법 (APS)으로 코팅층을 형성하였다. 1100 ℃의 화염으로 1429회 열피로 시험 후 bond 층이 일부 산화되고 top 층과 bond 층 계면에서 열화에 의한 산화층 (TGO)이 관찰되었으나, 코팅층 부위와 관계없이 균열이나 박리현상 없는 양호한 미세구조를 나타내었다. 1100 ℃ 열충격 시험결과, 37회 열충격 테스트 후 코팅층의 얇은 부위에서 박리가 시작되어 98회 시험 후 코팅층의 50% 이상이 박리되었으며, 코팅층의 두께가 얇게 형성된 부위는 코팅층이 두껍게 형성된 부위에 비해, top 층의 박리와 함께 bond 층의 산화가 많이 진행되었으며, 코팅층 두께가 상대적으로 두껍게 형성된 부위에서 열차폐 효과의 증가로 인해 bond 층의 내산화성과 열적 안정성이 우수한 것으로 나타났다.

• 한국광물학회지
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• 제20권3호
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• pp.223-229
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• 2007

포항부근에 널리 분포하는 제3기 퇴적암인 규질이암(siliceous mudstone)으로부터 $Na_2O/SiO_2 =0.6,\;SiO_2/Al_2O_3 = 2.0,\;H_2O/Na_2O=119$ 몰 비의 수열조건에서 반응시간($10{\sim}70$시간)을 변화시켜 Na-A형 제올라이트를 합성하는 반응기구에 대한 연구를 수행하였다. 각 조건에서의 합성상은 X-선회절분석을 통하여 확인하였고, 적외선 분광분석, 열분석 및 주사전자현미경에 의한 특성분석을 수행하였다. 이러한 결과를 토대로, 규질이암으로부터 Na-A형 제올라이트의 단계별 반응기구는 초기에 규산 소다와 알루민산 소다의 반응에 의해 Na-A형 제올라이트가 1차적인 핵생성이 이루어진 후, 반응시간이 증가됨에 따라 잔여 알루민산 소다와 용해된 규질이암의 반응에 의해 Na-A형 제올라이트의 결정이 성장하였고 또한 하이드록시 소달라이트가 생성되었다. 그리고 반응 시간이 50시간의 장시간이 되면 Na-A형 제올라이트로부터 용해되면서 빠져나온 성분은 하이드록시 소달라이트와 반응에 의해 새로운 상인 Na-P형 제올라이트가 생성되는 일련의 과정으로 해석될 수 있다.

• Korean Chemical Engineering Research
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• 제46권3호
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• pp.585-597
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• 2008

본 연구의 목적은 가동 시간과 생산량에 있어서 무작위 변동을 일으키는 공정 시스템에서 최종 제품의 수요를 만족하는 공정-저장조 망구조의 최적용량을 결정하는 문제의 해석적인 해를 유도하는 것이다. 여기서 논의되는 공장의 구조는 회분식 공정과 저장조가 병렬 또는 직렬로 연결된 망구조를 구성하고 있다. 생산공정은 다수의 원료물질을 다수의 제품으로 일정 비율로 전환한다. 최종제품의 수요는 주문주기와 물량이 무작위 변동을 일으킨다. 일부 생산공정은 생산량에 있어서 무작위 변동을 일으키며, 오염된 물질은 재생공정이나 폐기과정을 거쳐서 처리된다. 다른 공정들은 모두 가동시간이 무작위로 변한다. 최적화의 목적함수는 총비용을 최소화하는 것인데, 여기서 총비용은 준비비와 재고 유지비 그리고 공정과 저장조의 자본비용으로 구성되어 있다. 새로운 생산 재고 분석도구인 사각파 모형은 무작위 흐름의 상한값과 하한값을 계산하는 도형적 방법을 제공한다. 이 모형의 장점은 공정과 저장조 사이의 무작위 흐름을 사실적으로 묘사하면서도 간단한 해석적인 해를 제공하는데 있다. 결과적으로 계산량이 획기적으로 줄어든다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2010년도 하계학술대회 논문집
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• pp.264-264
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• 2010

Single-walled carbon nanotubes (SWCNTs) were grown on a Si wafer by using thermal chemical vapor deposition (t-CVD). We investigated the effect of the catalyst deposition rate on the types of CNTs grown on the substrate. In general, smaller islands of catalyst occur by agglomeration of a catalyst layer upon annealing as the catalyst layer becomes thinner, which results in the growth of CNTs with smaller diameters. For the same thickness of catalyst, a slower deposition rate will cause a more uniformly thin catalyst layer, which will be agglomerated during annealing, producing smaller catalyst islands. Thus, we can expect that the smaller-diameter CNTs will grow on the catalyst deposited with a lower rate even for the same thickness of catalyst. The 0.5-nm-thick Fe served as a catalyst, underneath which Al was coated as a catalyst support as well as a diffusion barrier on the Si substrate. The catalyst layers were. coated by using thermal evaporation. The deposition rates of the Al and Fe layers varied to be 90, 180 sec/nm and 70, 140 sec/nm, respectively. We prepared the four different combinations of the deposition rates of the AI and Fe layers. CNTs were synthesized for 10 min by flowing 60 sccm of Ar and 60 sccm of $H_2$ as a carrier gas and 20 sccm of $C_2H_2$ as a feedstock at 95 torr and $810^{\circ}C$. The substrates were subject to annealing for 20 sec for every case to form small catalyst islands prior to CNT growth. As-grown CNTs were characterized by using field emission scanning electron microscopy, high resolution transmission electron microscopy, Raman spectroscopy, UV-Vis NIR spectroscopy, and atomic force microscopy. The fast deposition of both the Al and Fe layers gave rise to the growth of thin multiwalled CNTs with the height of ${\sim}680\;{\mu}m$ for 10 min while the slow deposition caused the growth of ${\sim}800\;{\mu}m$ high SWCNTs. Several radial breathing mode (RBM) peaks in the Raman spectra were observed at the Raman shifts of $113.3{\sim}281.3\;cm^{-1}$, implying the presence of SWCNTs (or double-walled CNTs) with the tube diameters 2.07~0.83 nm. The Raman spectra of the as-grown SWCNTs showed very low G/D peak intensity ratios, indicating their low defect concentrations.

• Journal of Plant Biotechnology
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• 제38권4호
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• pp.241-250
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• 2011

식물유의 거의 대부분은 triacylglycerol (TAG) 형태로 종자에 축적되어있으며 이는 종자가 발아할 때에 필수적인 에너지공급원이자 동물과 인간들에게 필수지방산과 중요한 에너지원이다. 최근 식용유의 건강기능성으로 수요증가와 더불어 바이오디젤과 산업원료 등의 산업적 수요도 증가함에 따라 더욱 중요한 자원이 되고 있다. 그래서 생명공학기술로 종자유의 함량을 증진하고자 하면 지질 생합성에 탄소의 유입에 관여하는 조절 유전자를 과발현 또는 억제하는 것이 결정적으로 중요하다. 본 총설에서는 지질함량에 영향을 미치는 것으로 여겨지는 후보 유전자들에 대해 기술하고 이들의 지방 함량 증대 가능성을 조사하였다. 식물의 지방산의 생합성과 종자유의 축적에 관여하는 유전자들은 크게 구분하자면 첫째, TAG가 생합성되기 위해 필요한 전구체를 합성하는 유전자, 둘째, 지방산합성과 TAG 축적에 관여하는 유전자, 셋째, 종자 발달과 종자유 축적에 관여하는 전사인자 유전자가 있다. 종자유 함량을 결정하는 대사들은 앞에서 언급했듯이 매우 복잡하기 때문에 최근에 전사인자의 조절이 다수의 지방생산 대사 유전자를 동시 조작하여 형질전환 식물에서 종자유 함량이 증진하는 것보다 더 바람직한 접근법으로 여겨지고 있다. 그러나 전사조절유전자의 과발현에 의해 나쁜 농업형질의 유도 같은 문제점도 해결해야 한다.

• Tribology and Lubricants
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• 제30권5호
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• pp.256-264
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• 2014

Enhancing the value of fine chemicals based on biomass resources is an important objective for addressing environmental and other concerns such as demand for renewable or green products, as well as from the political perspective to reduce dependence on fossil feedstock associated with the use of petroleum-based products. Based on these considerations, we studied the synthesis of estolide using waste plant-based oil materials and their application as lubricants and pour point depressants. Five estolides were prepared by varying molar ratio of palmitic acid (PA) to oleic acid (OA) using a reaction time of 48 h. The estolides were characterized by size exclusion chromatography (SEC) and nuclear magnetic resonance (NMR). The isolated yields were in the range of 57-78 % and purity was 93-97%, showing iodine values of 18.2-37.8, total acid numbers (TANs) of 75.6-94.2 mg KOH/g and estolide numbers (ENs) of 1.2-1.8. Increasing the ratio of OA to PA in the synthesis decreased the kinematic viscosity and clouding point of the estolides. Four ball wear test of the estolides as a base oil demonstrated that the wear scar diameter (WSD) of the estolides was significantly lower (0.320-0.495 mm) than the WSD of general base oils such as 150N and Yubase (0.735 and 0.810 mm, respectively), indicating better wear resistance of the estolides. However, the lubricant property was found to be independent of the amount of OA in the estolides. These new materials are prospective candidates for application as a lubricant base oil.

• 상하수도학회지
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• 제25권6호
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• pp.893-906
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• 2011

The effect of ultrasound pretreatment on sludge degragability was investigated at different condotions: ultrasonic frequency(28, 40, 50kHz), intensity(10, 25, 50W), sonication time(10, 20, 30, 60min). Total suspended solid(TSS) and soluble chemical oxygen demand(SCOD) concentration were measured for the evaluation of pretreatment efficiency. The pretreated sludge was used as the feedstock for anaerobic digestion process. Biogas production and volatile suspended solid(VSS) removal were determined for evaluating the process performance. 1. TSS concentration of the sludge decreased at a constant rate as sonication operation was applied. The degradation rate of TSS increased when ultrasound frequency was decreased from 50kHz to 28kHz and intensity was increased from 10W to 50W. Efficiency of TSS degradation per input energy increased as ultrasonic frequency and intensity were decreased. At the frequency of 28 and 40kHz, SCOD concentration rapidly increased during the initial 30min of sonication time, and then it gradually increased. At 50kHz, SCOD concentration constantly increased for 60min of the sonication time. The SCOD production rate increased with increasing intensity under all ultrasound frequencies. 2. The optimum condition of ultrasound treatment was 28kHz, 50W and 60min for maximizing the biogas production, methane fraction, VSS removal. The highest values in biogas production, methane fraction in biogas, VSS removal were 370ml, 70%, 2.45g, respectively. Methane production rate per input energy increased at ultrasonic frequency and intensity decreased. 3. When raw sludge was pretreated at the condition of ultrasonic frequency of 28 and 40kHz in series, sequential-frequency sonication, intensity of 50W and 60min, biogas production, methane fraction, VSS removal were about the same that of 28kHz single-frequency sonication. When sequential-frequency sonication of 28 and 50kHz was applied in series, biogas production, methane fraction, VSS removal were 356 ~ 423ml, 69 ~ 71%, 2.41 ~ 2.78g, respectively. The pretreatment efficiency of 28-50kHz sequential-frequency sonication which sonication time of 28kHz and 50kHz was 40min and 20min was higher than that of 28kHz single-frequency sonication.

• 한국응용과학기술학회지
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• 제32권1호
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• pp.136-147
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• 2015

신재생에너지 공급 의무화제도(Renewable Portfolio Standard(RPS))가 시행됨에 따라, 발전 사업자들은 의무공급량 이행을 위해 발전용 바이오중유를 사용하고 있다. 본 연구에서는 발전용 바이오중유의 원료물질별 물성과 원료 조성에 따른 발전용 바이오중유의 품질특성을 알아보았다. 발전용 바이오중유와 원료유지의 연료특성은 전산가, 동점도, 금속분 등 고시 상 품질기준 항목을 분석하였으며, 적외선 분광광도계와 고성능 액체크로마토그래피를 이용하여 조성분포를 분석하였다. 팜유계열의 저가의 고산가 유지는 유리지방산 함량이 높아 전산가가 높고, 금속분에 의한 회분함량이 높았으며, 바이오디젤 공정부산물은 점도가 높았다. 동점도, 전산가, 금속분과 같은 발전용 바이오중유의 연료특성은 원료물질 의 조성 및 혼합비와 관련이 깊다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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• pp.181.2-181.2
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• 2014

A single-layer graphene has been uniformly grown on a Cu surface at elevated temperatures by thermally processing a poly (methyl methacrylate) (PMMA) film in a rapid thermal annealing (RTA) system under vacuum. The detailed chemistry of the transition from solid-state carbon to graphene on the catalytic Cu surface was investigated by performing in-situ residual gas analysis while PMMA/Cu-foil samples being heated, in conjunction with interrupted growth studies to reconstruct ex-situ the heating process. We found that the gas species of mass/charge (m/e) ratio of 15 ($CH_3{^+}$) was mainly originated from the thermal decomposition of PMMA, indicating that the formation of graphene occurs with hydrocarbon molecules vaporized from PMMA, such as methane and/or methyl radicals, as precursors rather than by the direct graphitization of solid-state carbon. We also found that the temperature for dominantly vaporizing hydrocarbon molecules from PMMA and the length of time, the gaseous hydrocarbon atmosphere is maintained, are dependent on both the heating temperature profile and the amount of a solid carbon feedstock. From those results, we strongly suggest that the heating rate and the amount of solid carbon are the dominant factors to determine the crystalline quality of the resulting graphene film. Under optimal growth conditions, the PMMA-derived graphene was found to have a carrier (hole) mobility as high as ${\sim}2,700cm^2V^{-1}s^{-1}$ at room temperature, which is superior to common graphene converted from solid carbon.