• 폴리머
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• 제36권1호
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• pp.65-70
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• 2012

글리시딜메타크릴레이트(GMA)의 플라즈마 유도 그래프트 공중합을 통해 기재로 사용한 평판형 폴리프로필렌 위에 에폭시 그룹을 도입하였다. 그래프트 공중합은 에멀젼 공중합법을 적용하였고, 기존의 용액 공중합과 비교하여 그 효과를 확인하고자 하였다. 대기압 플라즈마 처리 조건은 RF power 200 W, 처리시간 30초, Ar 기체 유속 6 LPM으로 고정하였고, 처리 후의 대기 중 노출시간 역시 5분으로 고정하였다. 중합반응에서는 GMA의 농도, 반응온도, 반응시간에 따라 표면 그래프트도의 변화를 최적화하였다. 그 결과, GMA 농도 12%, 반응온도 $90^{\circ}C$, 반응시간 5시간으로 중합하였을 때 가장 높은 그래프트도를 나타내었다. 분석 결과, 같은 반응조건 하에서 에멀젼 중합이 용액 중합에 비하여 더 많은 에폭시 그롭 도입에 효과적임을 확인하였다.

• 폴리머
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• 제35권1호
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• pp.66-71
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• 2011

현탁중합에 이은 프리델 크래프츠 촉매에 의한 hyper crosslinking 반응 및 hydrolysis반응으로 hydroxyl 반응 관능기를 포함하는 hyper crosslinked polymer particle(HCPP)을 합성할 시, 1) 각 단량체의 함량 변화에 따른 HCPP의 표면 모폴로지, 기공 크기 및 분포도의 변화, 2) hyper crosslinking 반응조건 변화에 따른 HCPP의 BET 비표면적 값의 변화 및 3) $CO_2$ 초임계 건조공정을 이용한 HCPP에서의 미반응 잔류 단량체, 올리고머 및 촉매의 제거 등에 관해 연구하였다. 이번 연구를 통해 초기 HCPP의 합성 시 관찰되었던 고분자 입자 표면의 균열 및 파괴현상은 hyper crosslinking 과정 중에 진행되는 microphase separated domain간의 반응과 깊은 관계가 있음을 관찰하였고, 또한 hyper crosslinking 반응 시 반응온도 반응시간 및 사용 용매의 증가는 HCPP의 BET 비표면적 값의 증가에 기여함을 관찰하였다. 그리고 hyper crosslinking을 유발하는 단량체의 함량변화는 다른 단량체에 비해 HCPP의 BET 비표면적, 기공 크기 및 분포도에 상대적으로 큰 영향을 미침을 확인하였다. 또한 HCPP에서의 미반응 잔류 단량체, 올리고머 등의 제거에 $CO_2$ 초임계 건조공정이 매우 효과적임을 확인할 수 있었고 특히 이 과정에서의 보조용매(메탄올)의 첨가는 잔류촉매(Fe)의 제거에 있어 탁월한 효과를 나타내었다.

• Bulletin of the Korean Chemical Society
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• 제33권1호
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• pp.215-220
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• 2012

ZnO nanoparticles were synthesized through a facile route and were used as ozonation catalysts. With the increase of calcination temperature ($150-300^{\circ}C$), surface hydroxyl groups and catalytic efficiency of asobtained ZnO decreased remarkably, and the ZnO obtained at $150^{\circ}C$ showed the best catalytic activity. Compared with ozonation alone, the degradation efficiency of phenol increased above 50% due to the catalysis of ZnO-150. In the reaction temperatures range from $5^{\circ}C$ to $35^{\circ}C$, ZnO nanocatalyst revealed remarkable catalytic properties, and the catalytic effect of ZnO was better at lower temperature. Through the effect of tertbutanol on degradation of phenol and the catalytic properties of ZnO on degradation of nitrobenzene, it was proposed that the degradation of phenol was ascribed to the direct oxidation by ozone molecules based on solidliquid interface reaction.

• 한국진공학회지
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• 제4권S1호
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• pp.92-96
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• 1995

• Bulletin of the Korean Chemical Society
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• 제32권1호
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• pp.196-200
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• 2011

In this work, poly(methyl methacrylate) (PMMA) was grafted onto amine treated graphite nanosheets ($NH_2$-GNs) and the surface characteristics and physical properties of the $NH_2$-GNs-g-PMMA films were investigated. The graft reaction of $NH_2$-GNs and PMMA was confirmed from the shift of the $N_{1S}$ peak, including amine oxygen and amide oxygen, by X-ray photoelectron spectroscopy (XPS). The surface characteristics of the $NH_2$-GNs-g-PMMA films were measured as a function of the $NH_2$-GN content using the contact angle method. It was revealed that the specific component of the surface free energy (${\gamma}s$) of the films was slightly increased as the $NH_2$-GN content increased. Also, the thermal and mechanical properties of the $NH_2$-GNs-g-PMMA films were enhanced with the addition of $NH_2$-GNs. This can be attributed to the chemical bonding caused by the graft reaction between the $NH_2$-GNs and the PMMA matrix.

• Korean Chemical Engineering Research
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• 제50권4호
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• pp.678-683
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• 2012

세리아 미세입자는 자동차, 석유공정, 폐수처리 등 다양한 분야에서 촉매로서 널리 쓰이고 있는 중요한 물질이다. 이제까지, 세리아 미세입자를 제조하기 위한 다양한 제조법이 연구되었는데, 본 연구에서는 짧은 반응시간과 간단한 공정이 가능한 초임계 메탄올을 이용하는 입자 제조 공정을 통해 세리아 나노입자를 제조하였다. 회분식 반응기를 이용하여 짧은 시간 안에 세리아 나노입자를 제조하는데 성공하였다. 초임계 메탄올을 이용하여 세리아 나노입자를 제조하는 경우, 다른 첨가제 없이도 약 6 nm의 크기를 갖는 나노입자를 합성할 수 있었다. 이 크기는 같은 온도와 압력조건의 초임계수를 이용하여 표면개질제 없이 합성한 입자보다 훨씬 작은 크기이다. 이는 초임계수와 초임계 메탄올의 밀도 차이와, 초임계 메탄올에서의 세리아 표면에서 일어나는 결정성장을 제한하는 반응, 그리고 초임계 메탄올과 초임계수의 임계점의 차이에서 기인하는 것이다. 또한 여러 가지 유기물을 표면개질제로 첨가하여 표면을 개질한 세리아 나노입자를 제조하였으며, FT-IR과 HR-TEM, TGA를 통해 이를 확인할 수 있었다. 표면을 개질한 세리아 나노입자는 표면개질을 하지 않은 세리아 나노입자와는 다르게, 유기용매에 대한 분산성이 뛰어났으며, 표면개질제로 사용하는 유기물의 양과 종류를 조절함으로써 세리아 나노입자의 크기와 모양을 조절할 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제31권11호
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• pp.3145-3150
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• 2010

Ruthenium catalysts modified by selenium have been introduced as alternative materials to Pt in Direct methanol fuel cells (DMFCs). RuSe nano-particles were synthesized on the Vulcan XC72R carbon supports via polyol method. The prepared catalysts were electrochemically and physically characterized by cyclic voltammetry (CV,) linear sweep voltammetry, methanol tolerance test, X-ray diffraction (XRD), Transmission electron microscopy (TEM), Energydispersive Spectrometer (EDS) and X-ray photoelectron spectroscopy (XPS). Increasing the Se concentration up to 20 at % increased the electro-catalytic activity for the oxygen reduction. By increasing Se amount, Ru metallic form on the surface was increased. The $Ru_{80}Se_{20}$/C catalysts showed the highest oxygen reduction reaction (ORR) activity and outstanding methanol tolerant property in half cell tests as well as single cell test.

• Bulletin of the Korean Chemical Society
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• 제18권11호
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• pp.1186-1191
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• 1997

Solvolyses of methanesulfonyl chloride (CH3SO2Cl) in water and methanol have been studied theoretically using ab initio self-consistent reaction field (SCRF) molecular orbital method. All stationary structures including transition state on the potential energy surface in solution have been found and compared with the gas phase structures. The overall reaction occurs via a concerted SN2 mechanism with a non-cyclic trigonal bipyramidal transition state, and the activation barrier is lowered significantly in solution. The transition state for the hydrolysis reaction is looser than that for the methanolysis reaction, and this is in accord with the experimental findings that an SN2 type mechanism, which is shifted toward an SN1 process or an SAN process in the hydrolysis and alcoholysis reaction, respectively, takes place. The catalytic role of additional solvent molecules appears to be a purely general-base catalysis based on the linear transition structures. Experimental barrier can be estimated by taking into account the desolvation energy of nucleophile in the reaction of methanesulfonyl chloride with bulk solvent cluster as a nucleophile.

• 소성∙가공
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• 제12권7호
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• pp.623-630
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• 2003

Nanomachining process, static nanoplowing, is one of the most promising lithographic technologies in terms of the low cost of operation and variety of workable materials. In nanomachining process, chemical effects are more dominant factor compared with those by physical deformation or fracture. For example, during the nanoscratch on a silicon surface in the atmosphere, micro protuberances are formed due to the mechanochemical reaction between diamond tip and the surfaces. On the contrary, in case of chemically stable materials, such as ceramic or glass, surface protuberances are not formed. The purpose of this study is to understand effects of the mechanochemical reaction between tip and surfaces on deformation behaviors of hard-brittle materials. Nanometerscale elasoplastic deformation behavior of single crystal silicon (100) was characterized with micro protuberance phenomena, and compared with that of borosilicate (Pyrex glass 7740). In addition, effects of the silicon protuberances on nanoscratch test results were discussed.

• Bulletin of the Korean Chemical Society
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• 제27권12호
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• pp.1976-1980
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• 2006

We have calculated the reaction probability and the reaction cross-section of the $N(^4S)+O_2(X^3\sum_{g}^{-})\;\rightarrow\;NO(X^2\Pi)+O(^3P)$ reaction by the quasiclassical trajectory method with the 6th-order explicit symplectic algorithm, based on a new ground potential energy surface. The advantage of the 6th-order explicit symplectic algorithm, conserving both the total energy and the total angular momentum of the reaction system during the numerical integration of canonical equations, has firstly analyzed in this work, which make the calculation of the reaction probability more reliable. The variation of the reaction probability with the impact parameter and the influence of the relative translational energy on the reaction cross-section of the reaction have been discussed in detail. And the fact is found by the comparison that the reaction probability and the reaction cross-section of the reaction estimated in this work are more reasonable than the theoretical ones determined by Gilibert et al.