2021년 기준 4,339개소의 공공하수처리시설에서 발생하는 하수찌꺼기는 년간 4,271,110톤으로 하수처리장 신·증설 등으로 인해 매년 증가하고 있다. 하수찌꺼기 등 유기성폐자원의 처리를 위해서 퇴비화, 혐기성 소화, 열분해, 소각, 매립 등 다양한 방법이 적용되고 있다. 특히 혐기성 소화는 잔류고형물 저감, 자본비와 운영비 절감, 바이오에너지 생산 및 환경에 대한 영향 최소화 등의 장점을 지니고 있어 실행 가능한 방법 중의 하나로 간주되고 있다. 그러나 하수찌꺼기 등과 같이 고형물을 함유한 유기성폐자원의 혐기성 소화 시 가수분해 반응은 율속단계로 알려져 있다. 따라서 혐기성 소화 시 가수분해 효율을 증진하기 위하여 초음파, 마이크로웨이브, 화학적 전처리, 열가수분해 등의 방법이 적용되고 있다. 특히 열가수분해의 경우 지난 20년간 관련 연구가 꾸준히 이루어져 많은 수의 실 규모 시설이 현장에 적용되었다. 그럼에도 불구하고 높은 에너지 소비, 혐기성 소화 저해물질 생성 및 색도로 인한 자외선 소독 효율 저감 등으로 인해 아직도 관련 연구가 지속적으로 진행 중이다 따라서 본 논문에서는 하수찌꺼기의 안정화와 혐기성 소화조의 효율 향상을 위해 가용화 기술 중 대표적이고 상용화가 가장 많이 이루어진 열가수분해에 대해 고찰하고자 한다. 특히 하수처리시설에서 열가수분해와 혐기성 소화조를 연계 하는 경우 예상되는 문제점과 해결방안에 대한 제시를 통해 혐기성 소화조의 안정성 및 메탄 발생량 향상, 하수처리시설 찌꺼기의 효율적 저감 및 에너지 자립화에 기여하고자 한다.

전 세계적으로 배출되는 폐플라스틱을 석유화학제품으로 재활용하는 순환경제가 본격화되고 있다. 따라서, 화학적 재활용 중 하나인 폐플라스틱 열분해유 생산을 위한 파일럿 규모의 시설도 건설되 고 상업적 생산이 시작되고 있다. 본 연구에서는 파일럿 플랜트에서 조건별로 생산된 총 4종의 폐플라 스틱 열분해유를 활용하기 위해 분리된 각각의 유분의 물성 및 구성성분 분석을 통해 나프타, 선박유 및 보일러유 등 다양한 원료‧연료 등으로 사용이 가능한지 확인해보고자 한다. 폐플라스틱 열분해유의 넓은 비점으로 인하여 경질유분은 상압 및 감압증류를 통해 분리하였고, 중질유분은 감압증류를 통해 분 리하였다. 경질유분(fraction 1)은 나프타를 목적으로 물리적 특성, 탄소분포 및 구성성분을 분석하였는 데, 탄소분포, 비점 등은 적합하지만, 초기 폐플라스틱 열분해유에 비해 염소 함량, 올레핀 및 방향족이 높아 전처리공정이 필요하다, 또한 중질유분(fraction 2)은 보일러유 등을 목적으로 할 때, 적합한 밀도, 동점도, 발열량 및 윤활성 등 물리적 특성을 가졌지만, Si 및 전산가 등이 높았다. 분리하고 남은 잔류물 (residue)은 높은 발열량, 낮은 황 함량, 산소 함량 등은 C중유급 연료로서의 사용이 가능할 것으로 판단되었다. 결론적으로, 분리된 폐플라스틱 열분해유에서 분리되는 모든 유분은 전처리만 가능하다면 나프 타 원료뿐만 아니라 저급 연료로도 활용이 가능하리라 판단된다.

Fluorine-doped tin oxide (FTO) has been used as a representative transparent conductive oxide (TCO) in various optoelectronic applications, including light emitting diodes, solar cells, photo-detectors, and electrochromic devices. The FTO plays an important role in providing electron transfer between active layers and external circuits while maintaining high transmittance in the devices. Herein, we report the effects of substrate rotation speed on the electrical and optical properties of FTO films during ultrasonic spray pyrolysis deposition (USPD). The substrate rotation speeds were adjusted to 2, 6, 10, and 14 rpm. As the substrate rotation speed increased from 2 to 14 rpm, the FTO films exhibited different film morphologies, including crystallite size, surface roughness, crystal texture, and film thickness. This FTO film engineering can be attributed to the variable nucleation and growth behaviors of FTO crystallites according to substrate rotation speeds during USPD. Among the FTO films with different substrate rotation speeds, the FTO film fabricated at 6 rpm showed the best optimized TCO characteristics when considering both electrical (sheet resistance of 13.73 Ω/□) and optical (average transmittance of 86.76 % at 400~700 nm) properties with a figure of merit (0.018 Ω-1).

Lithium lanthanum titanium oxide (LLTO) is a promising ceramic electrolyte because of its high ionic conductivity at room temperature, low electrical conductivity, and outstanding physical properties. Several routes for the synthesis of bulk LLTO are known, in particular, solid-state synthesis and sol-gel method. However, the extremely low ionic conductivity of LLTO at grain boundaries is one of the major problems for practical applications. To diminish the grain boundary effect, the structure of LLTO is tuned to nanoscale morphology with structures of different dimensionalities (0D spheres, and 1D tubes and wires); this strategy has great potential to enhance the ion conduction by intensifying Li diffusion and minimizing the grain boundary resistance. Therefore, in this work, 0D spherical LLTO is synthesized using ultrasonic spray pyrolysis (USP). The USP method primarily yields spherical particles from the droplets generated by ultrasonic waves passed through several heating zones. LLTO is synthesized using USP, and the effects of each precursor and their mechanisms as well as synthesis parameters are analyzed and discussed to optimize the synthesis. The phase structure of the obtained materials is analyzed using X-ray diffraction, and their morphology and particle size are analyzed using field-emission scanning electron microscopy.

The object of this study is to feasibility assesment for co-digestion efficiency of food waste recycling wastewater(FWR) with thermal hydrolysis process dehydration cake (THP Sludge). As a result of THP pre-treatment experimental conditions to 160oC and 30 minutes, the solubility rate(conversion rate of TCOD to SCOD) of the THP sludge increased by 34%. And the bio-methane potential in the THP sludge increased by about 1.42 times from 0.230 to 0.328 m3 CH4/kg VS compared to the non-pre-treatment. The substrates of the co-digestion reactor were FWR and THP sludge at a 1:1 ratio. Whereas, only FWR was used as a substrate in the digestion reactor as a control group. The experimental conditions are 28.5 days of hydraulic retention time(HRT) and 3.5 kg VS/m3-day of organic loading rate(OLR). During the 120 days operation period, the co-digestion reactor was able to operate stably in terms of water quality and methane production, but the FWR digestion reactor deteriorated after 90 days, and methane production decreased to 0.233 m3 CH4/kg VS, which is 67% of normal condition. After 120 days of the experiment, organic loading rate(OLR) of co-digestion reactor was gradually increased to 4.5 kg VS/m3-day and operated for 80 days. Methane production during 80 days was evaluated to be good at the level of 0.349 m3 CH4/kg VS. As a result of evaluating the dehydration efficiency of the sludge before/after 150-180oC THP using a filter press, it was confirmed that the moisture content of the sludge treated before THP at 180oC was 75% and improved by 8% from 83-85% level. Therefore, it is expected that the co-digestion reactor of FWR and THP sludge will ensure stable treatment water quality and increase bio-methane production and reduction effect of dehydration sludge volume.

This study demonstrates the effect of the compaction pressure on the microstructure and properties of pressureless-sintered W bodies. W powders are synthesized by ultrasonic spray pyrolysis and hydrogen reduction using ammonium metatungstate hydrate as a precursor. Microstructural investigation reveals that a spherical powder in the form of agglomerated nanosized W particles is successfully synthesized. The W powder synthesized by ultrasonic spray pyrolysis exhibits a relative density of approximately 94% regardless of the compaction pressure, whereas the commercial powder exhibits a relative density of 64% under the same sintering conditions. This change in the relative density of the sintered compact can be explained by the difference in the sizes of the raw powder and the densities of the compacted green body. The grain size increases as the compaction pressure increases, and the sintered compact uniaxially pressed to 50 MPa and then isostatically pressed to 300 MPa exhibits a size of 0.71 m. The Vickers hardness of the sintered W exhibits a high value of 4.7 GPa, mainly due to grain refinement.

아산화질소(N2O, Nitrous Oxide)는 6대 온실가스 중 하나로 대기 중에서 적외선을 흡수하여 온실효과를 유발하는 것으로 알려져 있다. 특히 지구온난화지수(GWP)는 CO2에 비해 310배 높아 국내뿐만 아니라 전 세계적으로 이슈화되고 있으며, 그에 따른 강력한 환경 규 제 강화법들이 발의되고 있다. N2O 저감 기술에는 물리적인 방식에 따라 농축회수, 촉매분해, 그리고 열분해로 구분할 수 있는데, 본 연구 에서는 그 중 가장 효과적인 열분해 처리방식에 대해 논의하고자 일반적인 연소 조건 내 고온 열분해 방식을 이용하여 비용 저감과 함께 질소산화물을 저감시키는 온도 조건 및 반응 시간에 대한 정보를 제공하고자 한다. 열분해 조건으로 선정된 고온 영역은 1073 K부터 1373 K 까지 100 K 간격을 두고 계산을 수행하였다. 1073 K과 1173 K의 온도조건에 경우, N2O 저감율과 일산화질소 농도가 체류시간에 따라 비례관 계를 이루는 것이 관측되었으며, 1273 K에 경우, 체류시간이 증가함에 따라 발생되는 역반응으로 인해 N2O 저감율이 감소되는 것이 관측되 었다. 특히 1373 K에 경우, 모든 체류시간에 대해 정반응과 역반응이 화학 평형상태에 도달하여 N2O 저감에 대한 반응진행율이 오히려 감 소하는 것으로 확인되었다.

Recently, air pollution from fossil fuels is at a serious level, and the IMO proposes to reduce greenhouse gas emissions by about 70% by 2050, and controls greenhouse gas emissions by applying the energy efficiency disign index(EEDI) to each ship type. In this study, the marine fuel oil viscosity of MGO, MDO, HFO and CGO according to the temperature change was compared and measured and the difference was analyzed. As a result, the viscosity of CGO was 3.32mPa·s, which was almost similar to MGO(3.40mPa·s) and MDO(3.51mPa·s) so it was judged that it could be used as a marine fuel, and it was found that there was a significant difference with HFO at P<0.01 there was.

In this study, (GaN)1-x(ZnO)x solid solution nanoparticles with a high zinc content are prepared by ultrasonic spray pyrolysis and subsequent nitridation. The structure and morphology of the samples are investigated by X-ray diffraction (XRD), field-emission scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The characterization results show a phase transition from the Zn and Ga-based oxides (ZnO or ZnGa2O4) to a (GaN)1-x (ZnO)x solid solution under an NH3 atmosphere. The effect of the precursor solution concentration and nitridation temperature on the final products are systematically investigated to obtain (GaN)1-x(ZnO)x nanoparticles with a high Zn concentration. It is confirmed that the powder synthesized from the solution in which the ratio of Zn and Ga was set to 0.8:0.2, as the initial precursor composition was composed of about 0.8-mole fraction of Zn, similar to the initially set one, through nitriding treatment at 700oC. Besides, the synthesized nanoparticles exhibited the typical XRD pattern of (GaN)1-x(ZnO)x, and a strong absorption of visible light with a bandgap energy of approximately 2.78 eV, confirming their potential use as a hydrogen production photocatalyst.

In this study, ultrasonic spray pyrolysis combined with salt-assisted decomposition, a process that adds sodium nitrate (NaNO3) into a titanium precursor solution, is used to synthesize nanosized titanium dioxide (TiO2) particles. The added NaNO3 prevents the agglomeration of the primary nanoparticles in the pyrolysis process. The nanoparticles are obtained after a washing process, removing NaNO3 and NaF from the secondary particles, which consist of the salts and TiO2 nanoparticles. The effects of pyrolysis temperature on the size, crystallographic characteristics, and bandgap energy of the synthesized nanoparticles are systematically investigated. The synthesized TiO2 nanoparticles have a size of approximately 2–10 nm a bandgap energy of 3.1–3.25 eV, depending on the synthetic temperature. These differences in properties affect the photocatalytic activities of the synthesized TiO2 nanoparticles.

Current synthesis processes for titanium dioxide (TiO2) nanoparticles require expensive precursors or templates as well as complex steps and long reaction times. In addition, these processes produce highly agglomerated nanoparticles. In this study, we demonstrate a simple and continuous approach to synthesize TiO2 nanoparticles by a salt-assisted ultrasonic spray pyrolysis method. We also investigate the effect of salt content in a precursor solution on the morphology and size of synthesized products. The synthesized TiO2 nanoparticles are systematically characterized by X-ray diffraction, transmission electron micrograph, and UV-Vis spectroscopy. These nanoparticles appear to have a single anatase phase and a uniform particle-size distribution with an average particle size of approximately 10 nm. By extrapolating the plots of the transformed Kubelka-Munk function versus the absorbed light energy, we determine that the energy band gap of the synthesized TiO2 nanoparticles is 3.25 eV

Despite numerous advances in the preparation and use of GaN, and many leading-edge applications in lighting technologies, the preparation of high-quality GaN powder remains a challenge. Ammonolytic preparations of polycrystalline GaN have been studied using various precursors, but all were time-consuming and required high temperatures. In this study, an efficient and low-temperature method to synthesize high-purity hexagonal GaN powder is developed using sub-micron Ga2O3 powder as a starting material. The sub-micron Ga2O3 powder was prepared by an ultrasonic spray pyrolysis process. The GaN powder is synthesized from the sub-micron Ga2O3 powder through a nitridation treatment in an NH3 flow at 800℃. The characteristics of the synthesized powder are systematically examined by X-ray diffraction, scanning and transmission electron microscopy, and UV-vis spectrophotometer.

본 연구에서는 고수분 음식물 및 농업 폐기물을 재활용한 고형연료 제조에 필요한 열분해장치를 개 발하고 실험을 통해 그 성능을 확인하고자 하였다. 연구를 위해 건조용량 50kg/hr인 실험실용 열분 해장치를 제작하였다. 건조 처리된 농업폐기물과 음식물 폐기물을 열분해처리용 실험 원료로 사용하 였다. 원료종류, 열분해 온도, 열분해 시간에 따른 농업폐기물과 음식물 폐기물의 열분해 특성을 파악 하였다. 농업폐기물 건조물의 열분해 처리 결과, 열분해 처리능력은 평균 55.35kg/hr, 저위발열량은 평균 3,333kcal/kg으로 측정되었다. 열분해처리 하지 않은 농업폐기물의 고위발열량은 3,400kcal/kg, 저위발열량은 3,090kcal/kg으로 측정되어 열분해처리로 발열량이 향상됨을 알 수 있었다. 음식물 폐기 물 건조물의 열분해 처리 결과, 열분해 처리능력은 평균 88.27kg/hr, 저위발열량은 평균 4,016kcal/kg 으로 측정되었다. 열분해처리 하지 않은 음식물 폐기물의 고위발열량은 4,040kcal/kg, 저위발열량은 3,686kcal/kg으로 측정되어 열분해처리로 발열량이 역시 향상됨을 알 수 있다. 열분해 처리능력은 연구목표치인 50kg/hr보다 높게 나타났으며, 저위발열량은 연구목표치인 4,000kcal/kg 보다 다소 높게 나타났다. 다만 저위발열량 측정 기준 함수율이 습량기준으로 약 10%로 추정되는 바 5%로 조절하 고, 열분해 열풍온도를 상승시키면 발열량이 더욱 향상될 것으로 판단되었다.

Copper oxide thin films are deposited using an ultrasonic-assisted spray pyrolysis deposition (SPD) system. To investigate the effect of substrate temperature and incorporation of a chelating agent on the growth of copper oxide thin films, the structural and optical properites of the copper oxide thin films are analyzed by X-ray diffraction (XRD), field-emssion scanning electron microscopy (FE-SEM), and UV-Vis spectrophotometry. At a temperature of less than 350 ℃, threedimensional structures consisting of cube-shaped Cu2O are formed, while spherical small particles of the CuO phase are formed at a temperature higher than 400 ℃ due to a Volmer-Weber growth mode on the silicon substrate. As a chelating agent was added to the source solutions, two-dimensional Cu2O thin films are preferentially deposited at a temperature less than 300 ℃, and the CuO thin film is formed even at a temperature less than 350 ℃. Therefore the structure and crystalline phase of the copper oxide is shown to be controllable.

Li-incorporated ZnO thin films were deposited by using ultrasonic-assisted spray pyrolysis deposition (SPD) system. To investigate the effect of Li-incorporation on the performance of ZnO thin films, the structural, electrical, and optical properites of the ZnO thin films were analyzed by means of X-ray diffraction (XRD), field-emssion scanning electron microscopy (FE-SEM), Hall effect measurement, and UV-Vis spectrophotometry with variation of the Li concentraion in the ZnO sources. Without incorporation of Li element, the ZnO surface showed large spiral domains. As the Li content increases, the size of spiral domains decreased gradually, and finally formed mixed small grain and one-dimensional nanorod-like structures on the surface. This morphological evolution was explained based on an anti-surfactant effect of Li atoms on the ZnO growth surface. In addition, the Li-incorporation changed the optical and electrical properties of the ZnO thin films by modifying the crystalline defect structures by doping effects.

본 연구에서는 자원내 포함된 역청의 경질화 과정에서 배출 및 회수되는 가스상 물질 및 고체상 물질을 활용하기 위한 기초 성상이 조사되었다. 이를 위하여 열분해 온도 별 역청성 오일의 전환에 대한 열분해반응 기초특성이 조사되었다. 또한 실험실 규모의 고정층 반응기를 이용하여 반응온도에 따른 가스 및 고체상 분산물의 특성을 조사하였다. 그 결과 550 ℃에서 약 17%의 오일 수율을 얻었으며, 부산물로는 CH4, CaCO3 및 CaO를 회수할 수 있음을 확인하였다.

We investigated a Leidenfrost effect in the growth of ZnO nanostructures on silicon substrates by ultrasonic-assisted spray pyrolysis deposition(SPD). Structural and optical properties of the ZnO nanostructures grown by varying the growth parameters, such as substrate temperature, source concentration, and suction rate of the mist in the chambers, were investigated using field-emission scanning electron microscopy, X-ray diffraction, and photoluminescence spectrum analysis. Structural investigations of the ZnO nanostructures showed abnormal evolution of the morphologies with variation of the substrate temperatures. The shape of the ZnO nanostructures transformed from nanoplate, nanorod, nanopencil, and nanoprism shapes with increasing of the substrate temperature from 250 to 450 °C; these shapes were significantly different from those seen for the conventional growth mechanisms in SPD. The observed growth behavior showed that a Leidenfrost effect dominantly affected the growth mechanism of the ZnO nanostructures.