In this study, copper oxide, manganese oxide and zeolite, clays containing catalysts were prepared to remove hydrogen sulfide emitted in odor of industry. In order to change the heat treatment temperature, a catalyst was prepared 100 degrees from 600 degrees to 1,000 degrees. GC-MS was used to confirm the hydrogen sulfide removal performance. Although the removal performance produced at 600 degrees was maintained by and large, the removal performance decreased as the temperature increased. In particular, the catalyst manufactured at 900 and 1000 degrees had low removal performance. To find out the cause of the decrease in removal performance, the analytical devices XRD, BET, XRF were used. In order to confirm the properties of the catalyst before and after adsorption, SEM-EDS and CS were used. As a result of analyzing the Cu-Mn catalyst, it was confirmed that the material was adsorbed on the surface. To confirm the adsorbent material, SEM-Mapping was employed. And it was verified that the sulfur was adsorbed. Measuring the SEM-EDS 3Point, it was confirmed to be about 25.09%. Another test method CS analyzer (Carbon/Sulfur Detector) was also deployed. As a result of the test, sulfur was confirmed to be about 27.2%. So comparing the two sets of data, it was verified that sulfur was adsorbed on the surface.

체인 형태의 코발트(Co) 메조스피어를 템플레이트로 활용하여 금(Au) 및 팔라듐(Pd) 전구체와의 2단계 갈바닉 치환 반응을 통해 비백금 기반의 AuPd 복합 촉매를 합성하였다. NaAuCl4 전구체로부터 합성된 AuPd-Cl(50) 촉매는 높은 비표면적과 다공성 구조를 통해 산소환원반응(ORR)에서 우수한 촉매 활성을 나타냈으며, 상용화된 Pt-20/C 및 Pd-20/C 촉매 대비 낮은 개시(onset) 전위와 높은 한계 전류 밀도 및 향상된 n 값을 보였다. Koutecky-Levich plot 분 석 결과, ORR이 4-전자 전달 메커니즘에 근접함을 확인하였으며, 메탄올 내성과 안정성 실험에서도 우수한 성능을 보였다. AuPd-Cl(50) 촉매는 경제적이고 효율적인 백금 대체 촉매로서 알칼리 연료전지 및 메탄올 기반 연료전지 응 용 가능성을 제시한다.

황산은 뛰어난 촉매제로서의 특성과 경제성으로 산업현장에서 다양한 화학 반응에 널리 사용되고 있다. 그러나 황산은 사용 후 재활용이 불가능하고 대량의 폐수를 발생시키는 특성이 있어 폐기과정에서 환경오염의 위험이 있으며 폐수 처리 과정에서 추가적인 비용 과 에너지가 소모된다. 본 연구는 황산을 대신할 수 있는 친환경 촉매제를 활용하여 폐수 의 배출을 줄이고 기업의 친환경 경영을 강화할 수 있는 방안을 모색하고자 실시되었다. 연구에서는 아민 산화반응을 위해 사용되는 말레인산 무수물 기반 고분자 촉매인 PIMA 과 POMA을 평가하여 피리딘 유도체의 아민 산화반응을 최적화하였다. POMA 촉매는 아연 피리치온 합성에 적용되었으며, 98% 이상의 선택성과 93% 이상의 합성 수율로 높은 촉매 활성을 보였다. 또한 촉매는 여과 과정을 통해 쉽게 회수되었으며, 회수율은 99.8% 를 초과하였고, 여러 번 사용 후에도 활성을 유지하였다. POMA 촉매는 전통적인 황산 촉매를 대체하여 폐수 발생에 의한 환경 부담을 최소화하고 기업의 ESG 경쟁력을 높이는 데 기여할 것으로 기대한다.

To fabricate intermetallic nanoparticles with high oxygen reduction reaction activity, a high-temperature heat treatment of 700 to 1,000 °C is required. This heat treatment provides energy sufficient to induce an atomic rearrangement inside the alloy nanoparticles, increasing the mobility of particles, making them structurally unstable and causing a sintering phenomenon where they agglomerate together naturally. These problems cannot be avoided using a typical heat treatment process that only controls the gas atmosphere and temperature. In this study, as a strategy to overcome the limitations of the existing heat treatment process for the fabrication of intermetallic nanoparticles, we propose an interesting approach, to design a catalyst material structure for heat treatment rather than the process itself. In particular, we introduce a technology that first creates an intermetallic compound structure through a primary high-temperature heat treatment using random alloy particles coated with a carbon shell, and then establishes catalytic active sites by etching the carbon shell using a secondary heat treatment process. By using a carbon shell as a template, nanoparticles with an intermetallic structure can be kept very small while effectively controlling the catalytically active area, thereby creating an optimal alloy catalyst structure for fuel cells.

바이폴라막은 양이온교환층과 음이온교환층 및 양극접합층으로 이루어진 이온교환막으로 물 분해 특성을 기반으 로 하여 프로톤과 수산화 이온을 생성시키는 막이다. 이러한 특성을 이용하여 화학 산업, 식품 가공, 환경 보호, 에너지 변환 및 저장과 같은 다양한 응용 분야에서 연구가 되고 있다. 본 논문에서는 바이폴라막 기술에 대한 종합적인 이해를 제공하기 위해 바이폴라막의 개념 및 물 분해 메커니즘과 물 분해 촉매에 대한 조사하였다. 마지막으로 최근 에너지 기술에 적용되고 있는 바이폴라막 프로세스를 조사하였다.

Considering the characteristics of aldehydes among volatile organic compounds, a combined process was established by linking an absorbent and a photocatalytic reactor. Experiments to find the optimal operating conditions of the combined process showed that as the amount of photocatalyst coating increases, the wavelength of the ultraviolet lamp used becomes shorter, the photodegradation rate becomes faster, and the removal efficiency increases. It was also demonstrated that by controlling the relative humidity during the connection process of the combined process, the re-evaporation phenomenon at the front end (absorption area) of the hybrid process can be improved and the removal efficiency at the back end (photocatalytic reaction area) can be significantly enhanced. This confirmed the need for a combined process that complements the advantages and disadvantages of each process.

In this study, a THC removal system was developed using an oxidation catalyst to solve the problems of the existing thermal oxidation methods, RTO and RCO. In addition, this system was applied to industrial sites to confirm the VOCs removal efficiency. As a result of testing to remove THC and VOCs by applying the reaction system for THC removal in industrial sites, the THC removal efficiency range is between 99.5% and 99.9%. The treatment efficiency of individual VOCs treated through this system was the lowest at 79.0% for methylethylketone and the highest at 91.3% for acetaldehyde, and the average treatment efficiency was about 85.4%. From these numbers, the performance was superior to the existing RTO and RCO systems that showed THC removal performance. This is due to the fact that the oxidation reaction of the oxidation catalyst is a very fast catalyst surface reaction, and the characteristics of the catalytic oxidation reaction are complete oxidation and oxidation reaction under rarefied conditions. In this study, the catalyst role in the reaction system for THC removal is to process THC simultaneously with the system heat source. This is believed to be because the reaction of the oxidation catalyst is a strongly exothermic reaction and can sufficiently provide the amount of heat necessary for the system. At the same time, an oxidation reaction that breaks the bonds of the THC component also occurs. This reaction is a strong exothermic reaction, which can help the system maintain a high temperature during the reaction, and is considered an effective system for processing high concentrations of THC in actual industrial sites where THC concentrations are high, as in this study.

화학 반응의 수율 향상을 위해 부산물을 제거하는 다양한 방법이 연구되고 있다. 특히 산업적으로 중요한 반응에 서 주로 부산물로 물이 생성되기 때문에 넓은 범위의 온도에서 안정적으로 물을 분리하는 기술이 필요하다. 흡수제의 사용, 탈수 반응의 도입 등 다양한 방법이 제안되었으나 추가적인 에너지 및 시간 소요, 전환율의 지속 가능성 등의 문제로 한계를 가지고 있다. 그에 반해 운전 및 설치가 용이하고, 낮은 유지비용 등의 장점을 가지고 있는 분리막 기술은 다양한 촉매 반응 에 도입되었을 때 안정적으로 부산물을 제거할 수 있어 반응의 효율을 향상시킬 수 있는 좋은 방안이다. 따라서 본 총설에서 는 분리막을 이용한 부산물 제거 및 이를 통한 효과에 대해 논의하였다.