• Title/Summary/Keyword: 촉매 열분해

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Study of Hydrotreating and Hydrocracking Catalysts for Conversion of Waste Plastic Pyrolysis Oil to Naphtha (폐플라스틱 열분해유의 납사 전환을 위한 수첨처리 및 수첨분해 촉매연구)

  • Ki-Duk Kim;Eun Hee Kwon;Kwang Ho Kim;Suk Hyun Lim;Hai Hung Pham;Kang Seok Go;Sang Goo Jeon;Nam Sun Nho
    • Applied Chemistry for Engineering
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    • v.34 no.2
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    • pp.126-130
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    • 2023
  • In response to environmental demands, pyrolysis is one of the practical methods for obtaining reusable oils from waste plastics. However, the waste plastic pyrolysis oils (WPPO) are consumed as low-grade fuel oil due to their impurities. Thus, this study focused on the upgrading method to obtain naphtha catalytic cracking feedstocks from WPPO by the hydroprocessing, including hydrotreating and hydrocracking reaction. Especially, various transition metal sulfides supported catalysts were investigated as hydrotreating and hydrocracking catalysts. The catalytic performance was evaluated with a 250 ml-batch reactor at 370~400 ℃ and 6.0 MPa H2. Sulfur-, nitrogen-, and chlorine-compounds in WPPO were well eliminated with nickel-molybdenum/alumina catalysts. The NiMo/ZSM-5 catalyst has the highest naphtha yield.

Viscosity Reduction by Catalytic Aquathermolysis Reaction of Vacuum Residues (접촉식 가수열분해 반응에 의한 감압잔사유의 점도 강하에 대한 연구)

  • Ko, Jin Young;Park, Seung-Kyu
    • Applied Chemistry for Engineering
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    • v.29 no.4
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    • pp.468-473
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    • 2018
  • In this study, the reforming reaction of vacuum residues (VR), high viscosity oil residues produced from vacuum distillation process of petroleum oil, was carried out using catalytic aquathermolysis reaction. VR showed a prone to decrease the amount of resins and asphaltenes in the constituents, and to increase saturates and aromatics when reacting with steam at 30 bar and above $300^{\circ}C$ for 24 h. When the amount of steam is not enough at this reaction, the asphaltene content in the products was rather increased after the reaction. As a result of the catalytic aquathermolysis using the metal oxide-zeolite catalyst with the decaline as a hydrogen donor, a 10% decrease in resin and asphaltene as well as a 10% increase in the aromatic hydrocarbon were observed. Consequently, the viscosity of VR decreased by 70% after the reaction. GC-Mass spectroscopy showed that the aquathermolysis of VR resulted in the decomposition of the resins and asphaltens into a low molecular weight material.

Effects of Reaction Conditions on the Performance of Catalytic Pyrolysis of LDPE in a Semi-Batch Reactor (LDPE 반회분식 촉매열분해에서 조업조건이 반응 특성에 미치는 영향)

  • Na, Jeong-Geol;Leem, Chel-Hyen;Choi, Hwi-Kyoung;Chung, Soo-Hyun
    • 한국신재생에너지학회:학술대회논문집
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    • 2006.11a
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    • pp.79-82
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    • 2006
  • Fueled by ballooning oil prices, waste plastics are now regarded as being cheap and abundant renewable sources, removing their stigma of dirty wastes Catalytic pryolysis of plastics in liquid phase allows recovery of light fuel oil as well as green treatment of polymerics wastes, and therefore significant efforts have been devoted to this research field. In this study, catalytic Pyrolysis of LDPE was carl ied out in semi-batch reactor which equipped a unit of separation and recirculation. The effect of react ion conditions were examined by analyzing liquid oil yield and carbon number distribution of products

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Effect of temperature in the distribution of production by catalytic decomposition on the carbon based catalyst (탄소계 촉매상에서 부탄 분해에 따른 생성물 분포에 미치는 온도의 영향)

  • Yoon, Suk-Hoon;Han, Gi-Bo;Park, No-Kuk;Ryu, Si-Ok;Lee, Tae-Jin;Yoon, Ki-June;Han, Gui-Young
    • 한국신재생에너지학회:학술대회논문집
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    • 2006.06a
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    • pp.89-92
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    • 2006
  • 수소에너지는 화석연료 사용의 증가로 인한 환경오염 및 자원고갈의 문제점을 해결해 줄 수 있는 미래의 청정한 에너지이다. 현재 주 에너지원인 화석연료의 사용에 의하여 배출된 오염물질이 지구온난화와 같은 문제점들을 일으킨다. 이러한 문제점들을 없애줄 수 있는 대안 중 하나가 수소에너지이다. 수소에너지는 자원이 풍부하며 연소시에 오염물질이 배출되지 않는 장점이 있다. 수소에너지는 수소를 연소시켜서 얻는 에너지로써, 수소를 태우면 같은 무게의 가솔린 보다 3배나 많은 에너지를 방출한다. 수소를 생산하는 방법 중 가장 이상적인 방법은 물을 분해하는 방법이다. 그러나 이 방법은 수소를 대량으로 생산하기에는 아직 기술에 대한 확보가 되어있질 않으며, 경제성도 떨어진다는 단점이 있다. 현재 많이 쓰이는 방법 중 탄화수소류의 메탄을 수증기 개질하는 방법이 있다. 메탄 수증기 개질방법은 환경오염물질인 CO나 $CO_2$를 배출한다는 것과 높은 열원이 필요하다 본 연구에서는 C-H결합에너지가 낮아 메탄보다 분해하기 쉬운 부탄의 직접분해로 수소를 생산하고자 한다. 부탄 직접분해는 환경오염물질인 CO나 $CO_2$가 발생되지 않는 장점이 있다. 부탄 분해반응은 $500{\sim}1100^{\circ}C$의 범위에서 이루어 졌으며, 촉매는 탄소계인 카본블랙을 사용하였고, 촉매의 성능을 비교하기 위하여 열분해반응이 동시에 수행되었다.

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Thermal Decomposition of PVB(polyvinyl butyral) and Ni Green Sheet (PVB와 니켈 그린 시트의 열분해)

  • Seo, Jung Ju;Kuk, Seung Taek;Kim, Keon
    • Journal of the Korean Chemical Society
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    • v.40 no.3
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    • pp.180-186
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    • 1996
  • To determine burn-out condition of polyvinyl butyral as binder, TGA and GC/MS were used to analyze decomposed products of PVB and Ni green sheet during binder pyrolysis. The produced gases are similar in kind each other but the relative amount of produced gases was different. When the atmosphere air contains water, relatively larger amount of carboxylic acids and aromatic compounds were detected, and the amount of the decomposed products were larger in Ni green sheet than PVB alone. And Ni acted as a catalyst in the thermal decomposition of PVB.

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Effect of MCM-41 Preparation Methods on the Kinetics of Catalytic Pyrolysis of Linear Low Density Polyethylene (MCM-41 촉매 합성법이 선형 저밀도 폴리에틸렌의 촉매 열분해 동역학에 미치는 영향)

  • Park Young-Kwon;Kim Joo-Sik;Jeon Jong-Ki;Lim Jung Eun;Kim Ji Man;Yoo Kyung-Seun
    • Polymer(Korea)
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    • v.29 no.2
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    • pp.122-126
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    • 2005
  • The effect of Al-MCM-41 preparation methods on the catalytic degradation of linear low density polyethylene (LLDPE) was investigated. Al-MCM-41 catalysts were synthesized by direct method (Al-MCM-41-D) and post treatment method (Al-MCM-41-P) and their characteristics were elucidated by XRD, BET, $NH_3\;TPD,\;^{27}Al$ MAS NMR. TGA kinetic analysis showed that the catalytic activation energies of Al-MCM-41-D and Al-MCM-41-P were 191.54 and 114.26 kJ/mol, respectively. The higher catalytic activity of Al-MCM-41-P would be attributed to its smaller pore size as well as higher number of acid sites that are accessible.

Analysis of Catalytic Cracking and Steam Reforming Technologies for Improving Endothermic Reaction Performance of Hydrocarbon Aviation Fuels (탄화수소 항공유의 흡열반응 성능향상을 위한 촉매 분해 및 수증기 개질 기술분석)

  • Lee, Hyung Ju
    • Journal of the Korean Society of Propulsion Engineers
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    • v.25 no.2
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    • pp.98-109
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    • 2021
  • Fundamental parameters describing overall operational characteristics of active cooling systems of a hypersonic flight vehicle are mainly classified into endothermic hydrocarbon fuels, regenerative cooling channels, and materials and system structures. Of primary importance is the improvement of endothermic performance of hydrocarbon aviation fuels in a series of studies developing efficient regenerative cooling systems. In a previous study, therefore, an extensive technical analysis has been carried out on thermal decomposition characteristics of liquid hydrocarbon fuels. As a subsequent study, catalytic cracking and steam reforming technologies have been reviewed to find a way for the improvement of endothermic reaction performance of hydrocarbon aviation fuels.

Carbon Dioxide-based Plastic Pyrolysis for Hydrogen Production Process: Sustainable Recycling of Waste Fishing Nets (이산화탄소 기반 플라스틱 열분해 수소 생산 공정: 지속가능한 폐어망 재활용)

  • Yurim Kim;Seulgi Lee;Sungyup Jung;Jaewon Lee;Hyungtae Cho
    • Korean Chemical Engineering Research
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    • v.62 no.1
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    • pp.36-43
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    • 2024
  • Fishing net waste (FNW) constitutes over half of all marine plastic waste and is a major contributor to the degradation of marine ecosystems. While current treatment options for FNW include incineration, landfilling, and mechanical recycling, these methods often result in low-value products and pollutant emissions. Importantly, FNWs, comprised of plastic polymers, can be converted into valuable resources like syngas and pyrolysis oil through pyrolysis. Thus, this study presents a process for generating high-purity hydrogen (H2) by catalytically pyrolyzing FNW in a CO2 environment. The proposed process comprises of three stages: First, the pretreated FNW undergoes Ni/SiO2 catalytic pyrolysis under CO2 conditions to produce syngas and pyrolysis oil. Second, the produced pyrolysis oil is incinerated and repurposed as an energy source for the pyrolysis reaction. Lastly, the syngas is transformed into high-purity H2 via the Water-Gas-Shift (WGS) reaction and Pressure Swing Adsorption (PSA). This study compares the results of the proposed process with those of traditional pyrolysis conducted under N2 conditions. Simulation results show that pyrolyzing 500 kg/h of FNW produced 2.933 kmol/h of high-purity H2 under N2 conditions and 3.605 kmol/h of high-purity H2 under CO2 conditions. Furthermore, pyrolysis under CO2 conditions improved CO production, increasing H2 output. Additionally, the CO2 emissions were reduced by 89.8% compared to N2 conditions due to the capture and utilization of CO2 released during the process. Therefore, the proposed process under CO2 conditions can efficiently recycle FNW and generate eco-friendly hydrogen product.

An experimental study on methanol decomposition catalysts for long distance-heat transportation (장거리 열수송을 위한 메탄올 분해 촉매에 대한 실험적 연구)

  • 문승현;박성룡;윤형기;윤기준
    • Korean Journal of Air-Conditioning and Refrigeration Engineering
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    • v.10 no.3
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    • pp.334-342
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    • 1998
  • In this experimental study, methanol was chosen as a system material for a long -distance heat transportation. Not only transition metals but also noble metals were investigated as an active component, and several metal oxides, such as ${\gamma}$-$Al_2$,$O_3$, $SiO_2$, etc. as a support. In general, transition metal catalysts absorbed more heat than noble metal catalysts. The amount of heat absorption and CO selectivity depends on temperature and methanol partial pressure, and 25$0^{\circ}C$ Ni/$SiO_2$ catalyst showed the best result for methanol decomposition reaction.

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