• 공업화학
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• 제29권3호
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• pp.312-317
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• 2018

본 연구에서는 새집증후군 원인가스 중 하나인 벤젠 가스 흡착특성을 향상시키기 위하여 활성탄소섬유에 함산소불소화 처리를 실시하였다. 함산소불소화 처리된 활성탄소섬유 표면특성 및 기공특성은 X-선광전자분광기(XPS)와 Brunauer-Emmett-Teller (BET) 분석을 통해 확인하였으며, 벤젠 가스 흡착 특성은 가스크로마토그래피(GC)로 평가하였다. XPS 결과로부터 불소분압이 증가함에 따라 활성탄소섬유 표면의 불소관능기가 증가함을 알 수 있었다. 함산소불소화 처리 후 모든 샘플의 비표면적은 감소하였으나, 불소 분압이 0.1 bar일 때 그 미세기공 부피비가 증가하였다. 함산소불소화 처리된 활성탄소섬유는 11 h 동안 100 ppm의 벤젠 가스를 모두 흡착하였으며, 이는 미처리 활성탄소섬유와 비교하여 벤젠 가스 흡착효율이 약 2배 향상됨을 알 수 있었다.

• 대한화학회지
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• 제54권1호
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• pp.93-98
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• 2010

본 연구에서는 Urea와 산 처리로 질소 및 산소 관능기가 도입된 다중벽 탄소나노튜브를 각각 제조하였으며, 표면처리에 따른 전기이중층 커패시터 (EDLCs) 특성을 관찰하였다. XPS, zeta-potential, 및 BET 분석방법을 이용하여 구조특성을 확인하였으며, 전기화학적 특성은 1 M 황산용액의 전해질에서 각각 50 $mVs^{-1}$과 100 $mVs^{-1}$의 주사속도로 순환전류 전압곡선 특성 실험을 통해 고찰하였다. 실험 결과로부터 MWNTs의 질소 원소구성비가 늘어날수록 축전용량이 증가하는 것을 확인하였으며, Urea 처리된 MWNTs의 축전용량이 가장 높은 수치를 나타내었다. 이는 전극 표면과 전하 활성종 간의 젖음성이 증가하고, 표면 관능기의 밀도가 증가하기 때문인 것으로 사료된다.

• 공업화학
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• 제26권4호
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• pp.432-438
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• 2015

본 연구에서는 활성탄소섬유(ACFs)에 함산소불화 표면처리를 수행하여 수용액상에 존재하는 저농도 $Cr^{6+}$ 이온의 흡착특성을 조사하였다. ACFs의 기공구조와 표면특성은 BET와 X선 광전자 분광기(XPS)를 통해 각각 확인하였다. ACFs의 함산소불화 처리는 ACFs의 표면에 중금속 흡착 능력에 영향을 미치는 C-O 결합의 비율을 크게 증가시켰으며, 그 결과 $Cr^{6+}$ 흡착이 10 min 이내에 빠르게 평형에 도달할 수 있었다. 또한 초기 $Cr^{6+}$ 농도 20 ppm에서 최대 $Cr^{6+}$ 제거효율은 미처리 ACFs와 비교하여 약 100% 증가하였다. 이러한 결과로부터 ACFs의 함산소불화 반응은 저농도 $Cr^{6+}$의 흡착을 위한 표면처리법으로 응용될 수 있을 것이다.

• 열처리공학회지
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• 제15권5호
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• pp.219-227
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• 2002

This study has been performed to investigate the effect of $CO_2$ content on the growth characteristics of the compound layer, porous layer and corrosion characteristics of carbon steels after gaseous nitrocarburizing in $70%-NH_3-CO_2-N_2$ at $580^{\circ}C$ for 2.5 hrs. The results obtained from the experiment were the thickness of the compound and porous layers increased with increasing $CO_2$ contents. At the same fixed gas composition the thickness of the compound and porous layer increased with increasing carbon content of the specimens. X-ray diffraction analysis showed that compound layer was mainly consisted of ${\varepsilon}-Fe_{2-3}(N,C)$ and ${\gamma}^{\prime}-Fe_4N$ as the increased with $CO_2$ contents in atmosphere, compound layer was chiefly consisted of ${\varepsilon}-Fe_{2-3}(N,C)$ phase. With increasing $CO_2$ content and total flow rate in gaseous nitrocarburizing, the amount of ${\varepsilon}-Fe_{2-3}(N,C)$ phase in the compound layer was increased. The current density of passivity decreased with increasing $CO_2$ content due to the development of porous layer at the out most surface of ${\varepsilon}-Fe_{2-3}(N,C)$.

• 한국재료학회지
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• 제19권11호
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• pp.625-630
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• 2009

Embedding of active devices in a printed circuit board has increasingly been adopted as a future electronic technology due to its promotion of high density, high speed and high performance. One responsible technology is to embedded active device into a dielectric substrate with a build-up process, for example a chipin-substrate (CiS) structure. In this study, desmear treatment was performed before Cu metallization on an FR-4 surface in order to improve interfacial adhesion between electroless-plated Cu and FR-4 substrate in Cu via structures in CiS systems. Surface analyses using atomic force microscopy and x-ray photoemission spectroscopy were systematically performed to understand the fundamental adhesion mechanism; results were correlated with peel strength measured by a 90o peel test. Interfacial bonding mechanism between electrolessplated Cu and FR-4 substrate seems to be dominated by a chemical bonding effect resulting from the selective activation of chemical bonding between carbon and oxygen through a rearrangement of C-C bonding rather than from a mechanical interlocking effect. In fact, desmear wet treatment could result in extensive degradation of FR-4 cohesive strength when compared to dry surface-treated Cu/FR-4 structures.

• Asian Journal of Atmospheric Environment
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• 제10권2호
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• pp.99-113
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• 2016

In order to improve the portability of basic absorbents monoethanolamine (MEA) and glycine (Gly), both were supported on microporous activated carbon (AC). Chemical modification by alkali-metal ion exchange (of Li, Na, K) was carried out on Gly-based absorbents. All supported absorbents were subjected to $CO_2$ absorption capacity (pure $CO_2$) and selectivity (indoor level) tests. Textural and chemical characterizations were carried out on test sorbents. All impregnation brought about significant reduction of specific surface area and microporosity of the adsorbent Depreciation in the textural properties was found to result to reduction in pure $CO_2$ sorption. Contrarily, low-level $CO_2$ removal capacity was enhanced as the absorbent dosage increases, resulting in supported 5 molar MEA in methanol solution. Adsorption capacities were improved from 0.016 and 0.8 in raw ACs to 1.065 mmol/g for MEA's. Surface chemistry via X-ray photoelectron spectroscopy (XPS) of the supported sorbents showed the presence of amine, pyrrole and quaternary-N. In reducing sequence of potency, pyridine, amine and pyrrolic-N were noticed to contribute significantly to $CO_2$ selective adsorption. Furthermore, the adsorption isotherm study confirms the presence of various SNGs heterogeneously distributed on AC. The adsorption mechanism of the present AC adsorbents favored Freundlich and Langmuir isotherm at lower and higher $CO_2$ concentrations respectively.

• 한국재료학회지
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• 제20권4호
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• pp.199-203
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• 2010

Hybridization of semiconductor materials with carbon nanotubes (CNTs) is a recent field of interest in which new nanodevice fabrication and applications are expected. In this work, nanowire type GaAs structures are synthesized on porous single-wall carbon nanotubes (SWCNTs) as templates using the molecular beam epitaxy (MBE) technique. The field emission properties of the as-synthesized products were investigated to suggest their potential applications as cold electron sources, as well. The SWCNT template was synthesized by the arc-discharge method. SWCNT samples were heat-treated at $400^{\circ}C$ under an $N_2/O_2$ atmosphere to remove amorphous carbon. After heat treatment, GaAs was grown on the SWCNT template. The growth conditions of the GaAs in the MBE system were set by changing the growth temperatures from $400^{\circ}C$ to $600^{\circ}C$. The morphology of the GaAs synthesized on the SWCNTs strongly depends on the substrate temperature. Namely, nano-crystalline beads of GaAs are formed on the CNTs under $500^{\circ}C$, while nanowire structures begin to form on the beads above $600^{\circ}C$. The crystal qualities of GaAs and SWCNT were examined by X-ray diffraction and Raman spectra. The field emission properties of the synthesized GaAs nanowires were also investigated and a low turn-on field of $2.0\;V/{\mu}m$ was achieved. But, the turn-on field was increased in the second and third measurements. It is thought that arsenic atoms were evaporated during the measurement of the field emission.

• 한국결정성장학회지
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• 제30권6호
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• pp.226-231
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• 2020

전기방사 공정을 이용하여 니켈, 아연, 철 전구체를 포함하는 Polyvinyl pyrrolidone 나노 섬유를 제조하였다. 이를 전자기파 차폐에 사용할 수 있는 Ni0.5Zn0.5Fe2O4 산화물 나노 섬유로 전환하기 위하여 열처리 조건을 제어하였다. 비정질 카본 블랙이나 의도치 않은 제2상 등을 배제하고 1차원 미세구조를 유지하면서 산화물 나노 섬유로 만들기 위하여 열처리 중 실시간으로 샘플을 채취해 공정 중 샘플 변화를 추적하였다. X-ray diffraction(XRD) 분석 결과 결정화된 Ni0.5Zn0.5Fe2O4의 회절 패턴은 300℃부터 나타나기 시작하였으나, energy dispersive spectroscopy(EDS) 결과 상 카본 블랙이 대부분 사라지기 위해서는 500℃ 이상의 열처리를 필요로 하였다. 650℃ 이상의 온도부터는 본격적으로 결정 핵 성장이 진행되어 섬유 표면 상태가 매끄럽지 않아지므로, 적용 분야에 따라 선택적으로 열처리 조건을 결정해야 함이 확인되었다.

• 한국표면공학회지
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• 제56권6호
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• pp.437-442
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• 2023

This research aims to enhance the efficiency of Pt/C catalysts due to the limited availability and high cost of platinum in contemporary fuel cell catalysts. Nano-sized platinum particles were distributed onto a carbon-based support via the polyol process, utilizing the metal precursor H₂PtCl₆·6H₂O. Key parameters such as pH, temperature, and RPM were carefully regulated. The findings revealed variations in the particle size, distribution, and dispersion of nano-sized Pt particles, influenced by temperature and pH. Following sodium hydroxide treatment, heat treatment procedures were systematically executed at diverse temperatures, specifically 120, 140, and 160 ℃. Notably, the thermal treatment at 140 ℃ facilitated the production of Pt/C catalysts characterized by the smallest platinum particle size, measuring at 1.49 nm. Comparative evaluations between the commercially available Pt/C catalysts and those synthesized in this study were meticulously conducted through cyclic voltammetry, X-ray diffraction (XRD), and field-emission scanning electron microscopy-energy dispersive X-ray spectroscopy (FE-SEM EDS) methodologies. The catalyst synthesized at 160 ℃ demonstrated superior electrochemical performance; however, it is imperative to underscore the necessity for further optimization studies to refine its efficacy.

• Korean Chemical Engineering Research
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• 제43권6호
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• pp.756-760
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• 2005

본 연구에서는 카본블랙을 $N_2$-플라즈마 처리하여 표면 관능기를 변화시킨 후 백금을 담지시켜 전기화학적 활성을 향상시키는 방법에 대하여 고찰하였다. $N_2$-플라즈마 처리된 카본블랙의 표면특성은 FT-IR, XPS 그리고 산-염기도 측정법 등으로 분석하였으며, 전기화학적 특성을 알아보기 위하여 순환전류전압곡선(CV)를 측정하였다. FT-IR과 산-염기도 결과에 의하면 카본블랙을 300 W의 일정한 세기로 $N_2$-플라즈마 처리함으로써, 카본블랙 표면에 생성된 자유라디칼에 의해 새로운 염기성 관능기가 형성되어 처리시간이 증가할수록 염기도가 증가함을 알 수 있었다. C-N, C=N, $-NH_3{^+}$, -NH 그리고 =NH 등과 같은 새로운 염기성 관능기에 의해 염기도 값이 증가하였으나, 일정 반응시간 이후에는 카본블랙 표면에 도입한 약한 결합을 이루는 관능기가 파괴되어 새로운 관능기를 형성하지 못하고 아무런 영향을 미치지 못하는 것으로 판단된다. 결과적으로, 백금/카본블랙 촉매의 전기화학적 활성은 300 W의 세기로 처리하였을 때 최적의 표면처리 시간은 30초이다.