• 헤리티지:역사와 과학
• /
• 제54권4호
• /
• pp.22-35
• /
• 2021

최근 기후가 급격히 변하고 미세 먼지가 증가하는 등 대기 환경 오염 물질의 양상도 변하고 있다. 이에 따라 채색 문화재에 사용되는 안료의 안정성 연구에 대한 필요성이 대두되고 있다. 회청은 전통 인공 무기 안료로 스몰트(Smalt)라고 불리는 청색의 유리 안료이다. 포타쉬 유리에 코발트를 녹여 만드는데 벽화, 회화 등의 채색 문화재에 사용되어왔다. 본 연구에서는 시판되는 회청 안료 3종을 수집하여 안료의 특성을 분석하였다. 회청은 제조사에 따라 발색 원소인 Co와 융제인 K의 함량에 차이를 보였는데 Smalt-3의 경우 Co 함량이 15.1 wt.%로 가장 적았고, K 함량은 29.6 wt.%로 가장 많았다. 채색 시편을 제작하여 안료의 보존에 영향을 미치는 것으로 알려진 자외선, CO₂/NO₂ 등의 대기 오염 가스, 그리고 미세 먼지에 이온 상태로 존재하는 염(NaCl) 등 주요 환경 인자에 대한 안정성을 평가하였다. 색 안정성에 영향을 미친 인자는 NO₂ 가스, 자외선, 수용성 염(NaCl)이며 이 중 NO₂ 가스가 색 변화에 가장 큰 영향을 미친 것으로 나타났다. 성분 분석 결과, 안료의 색 변화에 K와 Co의 함량이 영향을 미치는 것을 확인할 수 있었으며, Smalt-3은 NO₂와 수용성 염(NaCl)에서 색의 안정성이 가장 취약하였다. 특히 수용성 염(NaCl)은 색 변화에도 작용하지만 이보다 채색층 표면 물성을 약화시켜 채색층 도막 안정성에 악영향을 미치는 것을 본 연구를 통해 확인하였다. 반면 CO₂ 가스에 노출된 시편들은 색상 및 성분에 큰 변화가 없었다. 따라서 CO₂를 제외하고 시험에 적용된 모든 환경 인자가 회청의 색상을 변화시키고 도막의 안정성도 저해한다는 것을 알 수 있었다.

• Bulletin of the Korean Chemical Society
• /
• 제26권10호
• /
• pp.1525-1528
• /
• 2005

The synthesis and characterization of ${K_3[Ru(C_2O_4)3]{\cdot}4H_2O\;(C_2O_4}^{2-}$ = oxalato anoin) complex are described, and its redox properties (in buffer solution of pH = 12) have been investigated. This complex is used for in situ generation of oxoruthenates complexes which have been characterized by electronic spectroscopy. Reaction of ${K_3[Ru(C_2O_4)3]{\cdot}4H_2O$ with excess ${S_2O_8}^{2-}$ in molar KOH generates trans-${[RuO_3(OH)_2]^{2-}/S_2O_8}^{2-}$ reagent while with excess ${BrO_3}^-$ in molar $Na_2CO_3$ generates ${[RuO_4]^-/BrO_3}^-$ reagent. Avoiding the direct use of [$RuO_4$] the organic-soluble $(n-Pr_4N)^+[RuO_4]^-$, (TPAP) has been isolated by reaction of $K_3[Ru(C_2O_4)3]{\cdot}4H_2O$ with excess ${BrO_3}^-$ in molar carbonate and n-$Pr_4$NOH. In a mixture of $H_2O/CCl_4$ ruthenium tetraoxide can be generated by reaction of $K_3[Ru(C_2O_4)3]{\cdot}4H_2O$ with excess ${IO_4}^-$. The catalytic activities of oxoruthenates that have been made from $K_3[Ru(C_2O_4)3]{\cdot}4H_2O$ towards the oxidation of benzyl alcohol, piperonyl alcohol, benzaldehyde and benzyl amine at room temperature have been studied.

• The Korean Journal of Physiology and Pharmacology
• /
• 제26권1호
• /
• pp.25-36
• /
• 2022

To identify the effect and mechanism of carbon monoxide (CO) on delayed rectifier K⁺ currents (I_K) of human cardiac fibroblasts (HCFs), we used the wholecell mode patch-clamp technique. Application of CO delivered by carbon monoxidereleasing molecule-3 (CORM3) increased the amplitude of outward K⁺ currents, and diphenyl phosphine oxide-1 (a specific I_K blocker) inhibited the currents. CORM3-induced augmentation was blocked by pretreatment with nitric oxide synthase blockers (L-NG-monomethyl arginine citrate and L-NG-nitro arginine methyl ester). Pretreatment with KT5823 (a protein kinas G blocker), 1H-[1,-2,-4] oxadiazolo-[4,-3-a] quinoxalin-1-on (ODQ, a soluble guanylate cyclase blocker), KT5720 (a protein kinase A blocker), and SQ22536 (an adenylate cyclase blocker) blocked the CORM3 stimulating effect on I_K. In addition, pretreatment with SB239063 (a p38 mitogen-activated protein kinase [MAPK] blocker) and PD98059 (a p44/42 MAPK blocker) also blocked the CORM3's effect on the currents. When testing the involvement of S-nitrosylation, pretreatment of N-ethylmaleimide (a thiol-alkylating reagent) blocked CO-induced I_K activation and DL-dithiothreitol (a reducing agent) reversed this effect. Pretreatment with 5,10,15,20-tetrakis(1-methylpyridinium-4-yl)-21H,23H porphyrin manganese (III) pentachloride and manganese (III) tetrakis (4-benzoic acid) porphyrin chloride (superoxide dismutase mimetics), diphenyleneiodonium chloride (an NADPH oxidase blocker), or allopurinol (a xanthine oxidase blocker) also inhibited CO-induced I_K activation. These results suggest that CO enhances I_K in HCFs through the nitric oxide, phosphorylation by protein kinase G, protein kinase A, and MAPK, S-nitrosylation and reduction/oxidation (redox) signaling pathways.

• 한국산업융합학회 논문집
• /
• 제25권2_2호
• /
• pp.289-297
• /
• 2022

Deterioration in durability of structures due to the steel corrosion is difficult to determine whether or not corrosion is initiated and how much propagated, and moreover, repair and maintenance are not easy to deal with. Therefore, preventive treatments can be the best option to avoid the deterioration. Various methods for preventing corrosion of steel, such as electrochemical treatments, anti-corrosion agents and steel surface coatings, are being developed, but economic and environmental aspects make it difficult to apply them to in-situ field. Thus, the purpose of this study was to improve corrosion resistance by using CA-based clinker that are relatively simple and expected to be economically profitable Existing CA-based clinkers had problems such as flash setting and low strength development during the initial hydration process, but in order to solve this problem, CA clinker with low initial reactivity were used as binder in this study. The cement paste used in the experiments was replaced with CA₂ clinker for 0%, 10%, 20%, and 30% in OPC. And the mixture used in the chloride binding test for the extraction of water-soluble chloride was intermixed with Cl- 0.5%, 1%, 2%, and 3% by weight of binder content. To evaluate characteristic of hydration heat evolution, calorimetry analysis was performed and simultaneously chloride binding capacity and acid neutralization capacity were carried out. The identification of hydration products with curing ages was verified by X-ray diffraction analysis. The free chloride extraction test showed that the chlorine ion holding ability improved in order OC 10 > OC 30 > OC 20 > OC 0 and the pH drop resistance test showed that the resistance capability in pH 12 was OC 0 > OA 10 > OA 20 > OA 30. The XRD analyses showed that AFm phase, which can affect the ability to hold chlorine ions, tended to increase when CA₂ was mixed, and that in pH12 the content of calcium hydroxide (Ca(OH)₂), which indicates pH-low resistance, decreased as CA₂ was mixed

• 한국환경농학회지
• /
• 제35권2호
• /
• pp.121-127
• /
• 2016

BACKGROUND: Anaerobic digestion is the most feasible technology because not only the energy embedded in organic matters can be recovered, but also they are stabilized while being degraded. This study carried out to improve methane yield of slaughterhouse wastewater treatment sludge cake by the thermal pre-treatment prior to anaerobic digestion.METHODS AND RESULTS: Slaughterhouse wastewater treatment sludge cake was pre-treated by the closed hydrothermal reactor at reaction temperature of 190℃. BMPs (Biochemical methane potential) of the thermal hydrolysate was tested in the different S(Substrate)/I(Inoculum) ratio conditions. COD(Chemical oxygen demand) and SCOD(Soluble chemical oxygen demand) contents of thermal hydrolysate were 10.99% and 10.55%, respectively, then, the 96.00% of COD was remained as a soluble form. The theoretical methane potential of thermal hydrolysate was 0.51 Nm³ kg^-1-VS_added. And BMPs were decreased from 0.56 to 0.22 Nm³ kg^-1-VS_added when S/I ratio were increased from 0.1 to 2.0 in the VS content basis. Those were decreased from 0.32 to 0.13 Nm³ kg^-1-COD_added when S/I ratio were increased from 0.1 to 2.0 based on COD content. The anaerobic degradability of VS basis have showed 196.9%, 102.2%, 80.7%, 67.4%, and 39.4% in S/I ratios of 0.1, 0.3, 0.5, 1.0, and 2.0, respectively. Also the COD of 119.6%, 76.3%, 70.1%, 69.0%, and 43.1% were degraded anaerobically in S/I ratios of 0.1, 0.3, 0.5, 1.0, and 2.0, respectively.CONCLUSION: BMPs obtained in the S/I ratios of 0.1 and 0.3 was overestimated by the residual organic matters remaining at the inoculum. And inhibitory effect was observed in the highest S/I ratio of 2.0. The optimum S/I ratios giving reasonable BMPs might be in the range of 0.5 and 1.0 in S/I ratio. Therefore VS biodegradability of thermal hydrolysate was in 67.4-80.7% and COD biodegradability showed 69.0-70.1%.

• 한국대기환경학회지
• /
• 제21권4호
• /
• pp.439-458
• /
• 2005

An automated analysis system for water soluble constituents in $PM_{2.5}$ has been developed. The system consists of a high capacity multi tube diffusion scrubber (MTDS), a low temperature particle impactor (LTPI), and two ion (anion and cation) chromatography (IC) systems. Atmospheric particles have been collected by passing sample air through a thermostated MTDS followed by a LTPI. This system allows simultaneous measurements of soluble ions in $PM_{2.5}$ at 30 minutes interval. At the air sampling flow rate of 1.0L/min, the detection limits of the overall system are in the order of tens of $ng/m^3$. This system has been successfully used for the measurement of particulate components of Seoul air from April 2003 to January 2004. $SO_4^{2-},\;NO_3^-,\;NH_4^+,\;NO_2^-,\;Cl^-,\;Na^+,\;K^+,\;Ca^{2+},\;and\;Mg^{2+}$ are the major ionic species for $PM_{2.5}$ at Seoul. Among them, $SO_4^{2-},\;NO_3^-\;and\;NH_4^+$ are the most abundant ions, contributed up to $86\%$ of the total and the concentrations were higher than those in any other urban sites in the world except for Chinese cities. There are high pollutant episodes which contribute about $15\~20\%$ of annual average values of the major ions. During the episode, the all parcels were transported from the asian continent and $PM_{2.5}$ were significantly neutralized. This suggests that aged and long range transported pollutants caused the high pollutant episodes. They showed a distinct daily and seasonal variations:they showed a peak in the early morning caused by the night-time accumulation of particulate matters. Atmospheric reactions including gas-to-particle reactions and inter-particle reactions and meteorological parameters including relative humidity and ambient temperature were described with related to the $PM_{2.5}$ 5 concentrations. All of the ionic species showed higher concentrations during the spring than those for summer and winter.

• 한국환경농학회지
• /
• 제40권4호
• /
• pp.313-321
• /
• 2021

비가림 시설에서 'Beni Balad' 포도재배 시 부숙유기질비료 및 Urea를 토양 시용에 의한 암모니아 배출량 산정과 과실품질에 미치는 영향은 다음과 같다. Urea는 처리 1일째부터 암모니아 배출량이 급격히 증가하기 시작하여 15일째에 peak를 이루다가 점차 감소하였으며 그 이후에는 다른 처리와 큰 차이는 없었다. COF2 처리는 처리 후 1일째 peak를 보이다가 점차 감소하였으며, 그 이후는 대조구와 비슷한 발생량을 나타내었다. COF1 처리는 1일째 증가하여 완만한 곡선을 이루다가 15일째에 peak를 이루고 점차 감소하여 그 이후 대조구와 비슷하였다. 140일간 암모니아 누적 배출량은 대조구 2.63, Urea 12.95, COF1 2.05, COF2 3.97 kg NH₃-N ha^-1 day^-1 이었다. 토양내 무기성분 함량이 COF2에서 암모니아태 질소는 유의하게 높았으며 수확시 엽병의 T-N 농도는 COF1 처리보다 COF2 처리가 0.1% 감소하였다. P와 K 농도는 COF1 처리로 인하여 증가하였으나 Ca와 Mg 농도는 차이가 없었다. 과실품질은 Urea 처리는 과피의 경도, 가용성 고형물 및 안토시아닌 함량은 증가하였고, COF1 처리는 가용성고형물 및 안토시아닌 함량은 증가하였으며, 산 함량은 전 처리 모두 증가하였다. 그러나 과중, 과방크기, Hunter L, a, b값에는 차이가 없었다. 이상의 결과는 포도나무 Beni Balad 품종에서 Urea, 부숙유기질비료의 토양 시용 시 암모니아 배출량 산정에 기초자료가 될 것으로 판단되었다.

• Tribology and Lubricants
• /
• 제32권5호
• /
• pp.141-146
• /
• 2016

The diketopyrrolopyrrole (DPP) pigment is a bicyclic 8-π-electron system containing two lactam units. Typical DPP derivative pigments have melting points of over 350°C and very low solubility in most solvents, and show absorption in the visible region with a molar extinction coefficient of 33,000 dm²mol⁻¹ and strong photoluminescence with maxima in the range 500–600 nm. X-ray structure analyses of DPP show that the whole molecule is almost in one plane. The phenyl rings are twisted out of the heterocyclic plane and the intermolecular hydrogen bonding between neighboring lactam NH and carbonyl units influences the structure of the DPP pigment in the solid state. In this study, mono-N-alkylation and mono-N-arylation were undertaken for Pigment Red 264 or Pigment Orange 73 with alkyl halide and aryl halide, respectively, in the presence of sodium tert-butoxide as a base catalyst to improve the solubility of DPP pigments and their application as CO₂ indicators. The synthetic yield was in the range 11–88%. The indicator dyes are highly soluble in organic solvents and shows pH-dependent absorption (λ_max 501 and 572 nm for the protonated and deprotonated forms, respectively) and emission (λ_max 524 and 605 nm for the protonated and deprotonated forms, respectively) spectra. The mono-N-alkylated and mono-N-arylated DPP pigment was identified by ¹H-NMR (¹H-Nuclear Magnetic Resonance Spectrometer), FT-IR (Fourier Transform Infrared Spectroscopy), and MS (Mass Spectrometry). According to the results of color and hue properties obtained by a color matching analyzer, the synthesized DPP pigment material can be used as a CO₂ indicator.

• 현장농수산연구지
• /
• 제17권1호
• /
• pp.133-144
• /
• 2015

포도 '캠벨얼리'에서 적립의 노동력을 절감하기 위한 지베렐린(GA₃)의 처리 방법, 적정농도 및 처리시기를 구명하기 위하여 실시하였다. 지베렐린 처리에 의한 적립의 노동력은 만개 5일 전 40ppm, 만개기 10, 20, 40ppm에서 14.27~19.15 분/주 절약 할 수 있었다. GA3 40ppm 과방 침지는 탄립현상이 심하게 나타났으며 가용성고형물이 감소하여 실용화에는 문제가 있었다. GA3 처리에 의한 적립의 노동력 절감은 만개기 GA3 10 및 20ppm 과방 침지 처리에서 가장 좋았다.

• Journal of Electrochemical Science and Technology
• /
• 제13권2호
• /
• pp.269-278
• /
• 2022

Utilization of high-voltage electrolyte additive(s) at a small fraction is a cost-effective strategy for a good solid electrolyte interphase (SEI) formation and performance improvement of a lithium-rich layered oxide-based high-energy lithium-ion cell by avoiding the occurrence of metal-dissolution that is one of the failure modes. To mitigate metal-dissolution, we explored fluorinated dual-additives of fluoroethylene carbonate (FEC) and di(2,2,2-trifluoroethyl)carbonate (DFDEC) for building-up of a good SEI in a 4.7 V full-cell that consists of high-capacity silicon-graphite composite (15 wt% Si/C/CF/C-graphite) anode and Li_1.13Mn_0.463Ni_0.203Co_0.203O₂ (LMNC) cathode. The full-cell including optimum fractions of dual-additives shows increased capacity to 228 mAhg^-1 at 0.2C and improved performance from the one in the base electrolyte. Surface analysis results find that the SEI stabilization of LMNC cathode induced by dual-additives leads to a suppression of soluble Mn²⁺-O formation at cathode surface, mitigating metal-dissolution event and crack formation as well as structural degradation. The SEI and structure of Si/C/CF/C-graphite anode is also stabilized by the effects of dual-additives, contributing to performance improvement. The data give insight into a basic understanding of cathode-electrolyte and anode-electrolyte interfacial processes and cathode-anode interaction that are critical factors affecting full-cell performance.