본 연구의 목적은 END 금연동기유발 프로그램이 흡연 고등학생의 일산화탄소, 금연자기효능감, 흡연일수, 1일 흡연량에 미치는 효과를 확인하기 위해 실시한 비동등성 대조군 전·후 시차설계를 이용한 유사 실험연구이다. 대상자는 C시에 소재한 고등학생으로 금연에 관심이 있는 흡연학생으로 실험군 27명, 대조군 28명 총 55명이었으며 자료수집은 2018년 7월 12일부터 10월 4일까지였다. 대상자에게 중재한 프로그램은 END 금연동기유발 프로그램으로 주 1회 50분, 총 6주간이었다. 중재결과 실험군은 대조군에 비해 금연 자기효능감(z=110.00, p＜.001), 흡연일수(z=640.00, p＜.001), 1일 흡연량(z=520.50, p＜.016) 이 지지되었다. 따라서 END 금연동기유발 프로그램은 학교 현장에서 흡연 고등학생의 흡연율을 낮추고 금연동기를 유발하여 금연을 유도하기 위한 중재로 본 프로그램의 적용을 제안한다.

Nanofibers(NFs), because of their high surface area and nanosized grains, have appropriate morphologies for use in chemiresistive-type sensors for gas detection applications. In this study, a highly sensitive and selective CO gas sensing material based on Au-decorated SnO2 NFs was fabricated by electrospinning. SnO2 NFs were synthesized by electrospinning and subsequently decorated with various amounts of Au nanoparticles(NPs) by sputtering; this was followed by thermal annealing. Different characterizations showed the successful formation of Au-decorated SnO2 NFs. Gas sensing tests were performed on the fabricated sensors, which showed bell-shaped sensing behavior with respect to the amount of Au decoration. The best CO sensing performance, with a response of ~20 for 10 ppm CO, was obtained at an optimized amount of Au (2.6 at.%). The interplay between Au and SnO2 in terms of the electronic and chemical sensitization by Au NPs is responsible for the great improvement in the CO sensing capability of pure SnO2 NFs, suggesting that Au-decorated SnO2 NFs can be a promising material for fabricating highly sensitive and selective chemiresistive-type CO gas sensors.

동아시아에서 일산화탄소의 지역적 배경 농도 수준을 분석하기 위해, 1991년부터 2004년까지 장기간 중국 Waliguan(WLG), 몽골이아의 Ulaan Uul(UUM), 한국의 태안반도(TAP), 일본의 Ryori(RYO)에서 관측한 일산화탄소 농도를 분석하였다. 연평균 일산화탄소 농도는 WLG(135±22ppb), UUM(155±26ppb), RYO(171±36ppb), TAP(233±41ppb) 순서로 높은 농도를 보이고 있었다. WLG를 제외하고 전체적으로 봄철에 높고 여름철에 낮은 계절 변동의 특징은 동아시아 다른 지점들에서도 공통적으로 나타나고 있다. TAP는 WLG, UUM, RYO와 비교하여 전체 계절에 높은 일산화탄소 농도를 보이고 있으며 히스토그램에서 넓은 농도 분포를 보이는데 동아시아 대륙, 특히 중국의 가까운 풍하측에 위치하고 있어 광역적 대기 오염의 영향이 크기 때문이다. TAP는 중국 동부 지역을 경유하는 RPC가 봄, 가을, 겨울에서 높은 농도를 나타내었고, 여름철에는 저위도 북태평양으로부터의 OBG에 의해 낮은 일산화탄소 농도를 갖고 있는 해양성 기단의 영향을 받고 있다. NOAA 위성 영상과 GEOS-CHEM 모델 시뮬레이션은 중국 남동부 연안으로부터 황해를 거쳐 한반도와 동해로 확산하고 있는 광역적 대기오염 이동 사례를 확인하고 있다.

For pure Molybdenum carburized in mixed gases of argon and carbon monoxide, microstructural observations were carried out. X-ray diffraction analysis for carburized specimens revealed that brittle - layer hardly formed in the case of low carbon monoxide concentration. Fracture strength of the specimen carburized at 1673 K for 16 h is about 550 MPa higher than that of the un-carburized specimen. SEM observation revealed that with increasing carburizing temperature, the region demonstrating a transgranular fracture mode progressed towards the center of specimen. This result means that the grain boundaries were strengthened by the grain boundary diffusion of carbon and the strength of grain boundaries exceeded that of grain itself.

Near-IR H2 emission features in the northern region of the Orion A giant molecular cloud were observed in the CO J = 1 → 0 line in search of CO outflows. Out of the 30 sources surveyed, CO line wings were detected toward 28 positions, suggesting a strong correlation between H2 jets and CO outflows. Blueshifted wings were detected toward 26 positions while redshifted wings were detected toward 15 positions, which suggests that there is a bias in the source selection. The bias is more severe in OMC 3 than in OMC 2. Since the protostars in OMC 3 are younger and more deeply embedded, the bias may be caused by the difference of extinction between blueshifted and redshifted outflows. Some physical parameters of the outflows were derived from the line profiles.

The structure of a carbon monoxide sorption complex of dehydrated fully Ca2+-exchanged zeolite X, |Ca46(CO)27|[Si100Al92O384]-FAU, has been determined in the cubic space group Fd 3 at 21℃ (a = 24.970(4) ) by single-crystal X-ray diffraction techniques. The crystal was prepared by ion exchange in a flowing stream of 0.05 M aqueous Ca(NO3)2 for three days, followed by dehydration at 400℃ and 2×10-6 Torr for two days, and exposure to 100 Torr of zeolitically dry carbon monoxide gas at 21℃. The structure was determined in this atmosphere and was refined, using the 356 reflections for which Fo 〉 4Σ(Fo), to the final error indices R1 = 0.059 and wR2 = 0.087. In this structure, Ca2+ ions occupy three crystallographic sites. Sixteen Ca2+ ions fill the octahedral site I at the centers of hexagonal prisms (Ca-O = 2.415(7) a). The remaining 30 Ca2+ ions are found at two nonequivalent sites II (in the supercages) with occupancies of 3 and 27 ions. Each of these Ca2+ ions coordinates to three framework oxygens, either at 2.276(10) or 2.298(8) a, respectively. Twenty-seven carbon monoxide molecules have been sorbed per unit cell, three per supercage. Each coordinates to one of the latter 16 site-II Ca2+ ions: C-Ca = 2.72(8) a. The imprecisely determined N-C bond length, 1.26(14) a, differs insignificantly from that in carbon monoxide(g), 1.13 a.

Electrochemical promotion of the reaction rate was investigated for CO oxidation in a solid electrolyte catalytic reactor where a thin film of Pt was deposited on the yttria stabilized zirconia as an electrode as well as a catalyst. It was shown under open circuit condition that potential was a mixed potential of O2exchange reaction and electrochemical reaction induced by CO. The effect of electrochemical modification on the CO oxidation rate was studied at various overpotentials and PCOPO2.