In this study, an Co/Fe coated porcelain using a cobalt and ferrous sulfate was sintered at 1,250 oC. The specimens were investigated by HR-XRD, FE-SEM (EDS), Dilatometer, and UV-vis spectrophotometer. The surface of the porcelain was uniformly fused with the pigment, and white ware and celadon body specimens were densely fused to a certain thickness from the surface. Other new compounds were produced by the chemical reaction of cobalt/ferrous sulfate with the porcelain body during the sintering process. These compounds were identified as cobalt ferrite spinel phases for white ware and white mixed ware, and an andradite phase for the celadon body, and the amorphous phase, respectively. As for the color of the specimens coated with cobalt and ferrous mixed pigments, it was found that the L* value was greatly affected by the white ware, and the a* and b* values were significantly changed in the celadon body. The L* values of the specimens fired with pure white ware, celadon body, and white mix ware were 72.1, 60.92, 82.34, respectively. The C7F3 pigment coated porcelain fired at 1,250 oC had L* values of 39.91, 50.17, and 40.53 for the white ware, celadon body, and white mixed ware, respectively; with a* values of -1.07, -2.04, and -0.19, and at b* values of 0.46 and 6.01, it was found to be 4.03. As a new cobalt ferrite spinel phase was formed, it seemed to have had a great influence on the color change of the ceramic surface.

본 연구는 정원 장미에서 화색과 향기의 상관관계를 분석하기 위해 개화단계 동안 화색소와 향기물질 구성의 변화를 조사하였 다. 화색과 향기 특성이 다른 세 품종의 정원 장미를 식물재료로 이용하였다. ‘Faustinia’는 황색 꽃잎과 tea-type향을 가지며, ‘Liparfum’은 적색 꽃과 sweet-type향을, ‘Tchaikovsky Meichibon’ 은 약한 향의 백색 꽃을 피운다. 개화과정을 S1에서 S5까지 5단 계로 나뉘어 설정하였다. 세 품종에서 꽃과 꽃잎의 크기, 꽃잎의 생체중과 같은 형태적 특성은 S1에서 S4로 개화가 진행됨에 따 라 증가했다. ‘Faustinia’와 ‘Liparfum’은 S3까지 화색이 선명하고 밝아지고 이후 퇴색되어 a*와 b*값이 감소하였다. 세 품종 모두 향기는 S3~S4에서 가장 강했다가 S5에서 감소하였다. ‘Faustinia’ 의 총 카로티노이드와 ‘Liparfum’의 총 안토시아닌 함량은 S1대 비 S3에서 약 7.2~40.5배 증가하였고 S5에서 약 30.6%까지 현저 하게 감소하였다. 백색 계열 ‘Tchaikovsky Meichibon’의 화색소 함량은 개화 과정 중 큰 변화를 보이지 않았으나 S5에서 2.3배 감소하였다. 향기물질은 화색소 변화와 유사한 패턴을 보였다. 2-phenylethanol과 3,5-dimethoxytholuene은 모든 품종 ‘Faustinia’ (84.2%), ‘Liparfum’(89.6%), ‘Tchaikovsky Meichibon’(94.8%) 에서 높은 함량비율을 보였고, 테르펜 향기물질 구성비율은 역순 으로 높았다. ‘Liparfum’의 안토시아닌은 향기물질 2-phenylethanol (r=-0.51), 3,5-dimethoxytoluene(r=-0.72**), eugenol(r=-0.58*),neral(r=-0.48), geranial(r=-0.42)과 음의 상관관계를 보였으나, 카로티노이드는 명확한 상관성을 갖지 않았다

A high NIR-reflective black pigment is developed by Mn doping of Fe2O3. The pigment powders are prepared by spray pyrolysis, and the effect of the Mn concentration on the blackness and optical properties is investigated. Mn doping into the crystal lattice of -Fe2O3 is found to effectively change the powder color from red to black, lowering the NIR reflectance compared to that of pure Fe2O3. The pigment doped with 10% Mn, i.e., Fe1.8Mn0.2O3, exhibits a black color with an optical bandgap of 1.3 eV and a Chroma value of 1.14. The NIR reflectance of the prepared Fe1.8Mn0.2O3 black pigment is 2.2 times higher than that of commercially available carbon black, and this material is proven to effectively work as a cool pigment in a temperature rise experiment under near-infrared illumination.

섬진강 및 영산강 하구의 환경변화에 따른 식물플랑크톤의 상관성을 조사하기 위해, 2016년 4월부터 11월까지 매월 현장조사를 수행하였다. 조사 정점에서 용존무기질소(DIN, dissolved inorganic nitrogen)와 규산염(DSi, dissolved silicate)은 강으로부터 유입되는 담수의 영향을 강하 게 받았다. 특히 섬진강하구에서는 DIN과 DSi가 내측에서 점차적으로 외해로 확산되는 특성 을 보였으나, 영산강 하구는 복잡한 지형학적 특징으로 내측과 외해와 잘 섞이지 않았다. 식 물플랑크톤 분류군별 지표색소를 활용하여 분류군별 분포를 조사하였다. 규조류 지표색소인 fucoxanthin은 섬진강, 영산강 하구에서 각각 평균 0.61±1.00 μg l-1, 0.76±1.22 μg l-1로 나타나, chlorophyll a 이외 다른 색소에 비해 2배 이상 높은 농도를 나타내었다. 와편모조류 지시색소 peridinin은 현미경 검경결과와 와편모조류의 출현양상과 유사한 경향을 보였다. 소형 녹조류, 은편모조류, 남조류는 현미경으로 관찰되지 않았으나, 각각의 지표색소 chlorophyll b, alloxanthin, zeaxanthin은 일정하게 검출되어, 하구역 내 상기와 같은 종의 출현가능성을 시사하였다. 결과 적으로 본 연구의 색소분석을 통하여, 하구역 상류의 환경 특성이 연안내만생태에 영향을 미 칠 수 있다는 것을 밝혔다. 특히 영산강 하구는 인공적인 배수갑문의 독특한 특성으로, 대량방 류되는 담수에 의하여 연안내만에서 관찰되는 담수종이 일시적으로 분포하였다.

지구 온난화에 따른 기온 상승, 보나 댐의 건설로 인한 체류시간의 변화는 식물플랑크톤의 이상증식을 일으키며 이로 인한 수계의 부영양화, 녹조 현상은 상수원 수질 악화에 영향을 미쳐 심각한 사회적 문제로 대두되고 있다. 본 연구와 같이 일차생산력과 환경요인들의 상관관계를 확인하는 것은 일차생산력의 조절인자 파악에 매우 효과적이다. 또한 HPLC-CHEMTAX 분석 방법은 간편하며 짧은 시간 안에 식물플랑크톤의 색소 비 값을 기반으로 각 군집의 상대적인 기여도 추정이 가능하다. 이러한 연구 방법들을 적용할 경우 수 생태 건강성 평가 및 식물플랑크톤 이상증식에 영향을 주는 군집조성을 빠르게 파악할 수 있어 조류 예보제 및 수계관리에 있어 효과적으로 활용될 수 있을 것으로 판단된다.

Carotene, xanthophyll, carotenoid anthocyan, phycopyrine, chlorophyll, and monascus pigments are used as natural coloring agents since they are more stable to human body than synthetic coloring agents. Among them, monascus pigments are a natural red pigment produced by the Monascus purpureus. For the development of edible paint using natural pigment, Monascus purpureus strain was cultured at a temperature of 35℃ for 15 days on a PDYA plate and liquid medium to produce a red pigment. In addition, a large amount of the red pigment was extracted from Hongkuk Koji in parallel with water extraction and ultrasonic wave extraction. At this time, the yield of ultrasonic extract was 2~4 times higher. Thus, Monascus purpureus strains, etc. were prepared by freeze-drying powder. In conclusion, natural paints made with red pigments have enabled the development of been edible paints that can be used as eco-friendly materials with good viscosity, enhanced spread ability and coloration.

전통회화에 사용된 각종 색 재료 즉 유기, 무기안료나 염료는 온도, 습도, 빛, 그리고 대기 오염에 의한 각종 화학 물질 등과 직접 반응하여 탈․변색을 유도하기도 하고, 안료와 결합된 각종 수지의 열화에 의해 손상되기도 한다. 본 연구에서는 조선종이라고 불리는 한지에 석록, 석청 무기 안료를 사용해 인위적인 노화시험을 시행하면서, 동시에 전시 관에 전시를 통해 환경 요인으로 인한 자연적 노화시험을 수행하였다. 인위적인 노화와 자연적인 환경시험에 의해 일어 난 화학적인 변화는 자외선-가시광선 분광기와 FT-IR, TGA, XRD을 통해 측정하였고, 전통회화의 변색은 색차계와 video microscope로 관찰하였다. 이를 통해 석록이 포함된 전통회화의 변색은 대기 중의 산도와 자외선에 의해 일어났음을 알 수 있었다.

천연색소는 색을 발현할 수 있는 물질로서 식품, 화장품, 의약품 등에 사용된다. 천연색소는 동・식물에서 추출하여 만들기 때문에 크기가 균일하지 않으며 특히 적색색소의 경우, 다른 색의 색소 에 비해 친유성이 강해 수용액 상태에서 쉽게 응집이 되는 경향이 있다. 또한 응집에 의한 크기변화로 인해 색의 재현이 어려운 문제점이 있다. 적색색소로 기존에 사용했던 동물성 색소인 코치닐 추출 색 소는 알레르기를 유발하고 식용으로서의 거부감이 있는 등의 문제점으로 인하여 사용이 기피되는 추 세이다. 본 연구에서는 적색의 식물성 색소인 라이코펜 추출물과 치자황색소를 사용하였고 Ball-milling을 이용하여 색소의 크기를 균일하게 만든 후 Asymmetrical flow field-flow fractionation(AsFlFFF), Dynamic light scattering(DLS)를 이용하여 크기를 분석하고 색차계를 이용하 여 색을 확인하는 연구를 진행하였다. 실험결과 milling 전에는 색소 입자의 크기가 크고 크기분포가 넓었으나, milling 후에는 크기가 감소하고 크기분포가 좁아짐을 확인하였다. 색차계 측정 결과, milling 시간이 증가함에 따라 밝기, 적색도, 황색도가 높아져서 밝은 적색을 나타내었다.

Ink-jet printing techniques with ceramic ink, which contains ceramic pigments as colorant, are in increasingly use in the ceramic industry. Generally, ceramic pigments that are produced by conventional method show diameters of several micrometers; these micrometer sized particles in the ink-jet printing process can cause undesirable behavior such as print head nozzle clogging. To prevent this problem, a particle size reduction process is required. In this study, CMYK (cyan, magenta, yellow, black) pigments were synthesized via solid state method. Each pigment particle was milled to submicron size by an attrition mill. The effects of micronizing on the morphology, mechanical property, crystal structure and color property of the CMYK ceramic pigments were investigated by field emission scanning electron microscopy (FE-SEM), particle size analysis (PSA), X-ray diffraction (XRD) and CIE L*a*b*.

In this work, we synthesize brilliant yellow color α-FeOOH by controlling the rod length and core-shell structure. The characteristics of α-FeOOH nanorods are controlled by the reaction conditions. In particular, the length of the α-FeOOH rods depends on the concentration of the raw materials, such as the alkali solution. The length of the nanorods is adjusted from 68 nm to 1435 nm. Their yellowness gradually increases, with the highest b* value of 57 based on the International Commission on Illumination (CIE) Lab system, by controlling the nanorod length. A high quality yellow color is obtained after formation of a silica coating on the α-FeOOH structure. The morphology and the coloration of the nal products are investigated in detail by X-ray diffraction, scanning electron microscopy, UV-vis spectroscopy, and the CIE Lab color parameter measurements.

Serratia marcescens (S. marcescens)는 Gram-음성 박테리아로 soytone과 에탄올이 함유된 Cang’s soytone (CS) 배지에서 28 °C, pH 7.5의 조건으로 배양할 때 가장 많은 붉은 색소를 생성하였 다. S. marcescens 균주로부터 붉은 색소를 분리, 정제하기 위하여 여러 가지 유기용매를 사용하였다. 분리 정제한 붉은 색소는 가시광선 영역의 537 nm에서 λmax를 가지고 있었고, HPLC-Mass로 분석한 결과 분자량 537과 565 g을 가지는 두 가지 물질로 구성되어 있음을 확인하였다. 또한 상온과 pH 6 이하의 산성조건에서는 태양광에도 안정함을 확인하였다.

NiO-doped hibonite pigments were synthesized by the solid state method to get stabilized blue color pigment inboth oxidation and reduction atmospheres. Optimum substitution condition with NiO for hibonite blue pigment was investigated.Experimental results were comparable to those of previous cobalt-minimization studies performed with other phosphate- oroxide-based cobalt-containing ceramic pigments (having olivine (Co2SiO4), spinel (CoAl2O4), or with co-doped willemite((Co,Zn)2SiO4) structures). Composition was designed varying the NiO molar ratio increasing with SnO2. The optimumsubstitution content is 0.93mole NiO with 0.75mole SnO2. The characteristics of the synthesized pigment were analyzed byXRD, Raman spectroscopy, SEM, and UV-vis. Synthesized pigment was applied to a lime-barium glaze with 10wt% each andfired at an oxidation atmosphere of 1250oC/1h and a reducing atmosphere 1240oC/1h. Blue color was obtained with L*a*b*values at 43.39, −6.78, −18.20 under a reducing atmosphere and 41.66, −6.36, −14.7 under and oxidation atmosphere, respectively.

Fe4[Fe(CN)6]3 coated on a mica or TiO2/mica surface as infrared reflective blue pigment was prepared by a hydrothermal method. Fe4[Fe(CN)6]3, used as coloring agent, was uniformly coated on mica or TiO2/mica under the optimized condition of a 1.2 : 1 weight ratio between iron(III) chloride hexahydrate and potassium ferrocyanidetrihydrate at the initial pH level of 4.5 at 70˚C. The infrared (IR)-reflective pigments were characterized by SEM, Zeta-potenial, FT-IR, and UV-VIS NIR spectrophotometry. Especially the CIE color coordinate and total solar reflectance(TSR) properties of the pigments were investigated in relation to variation of the coating and coated substrate thicknesses. Isolation-heat paint was prepared with 20 wt% blue pigments fully dispersed in acryl-urethane resin and several additives to coat the film uniformly. The films were also measured with CIE color coordinate, TSR, and the surface temperature was recorded by an isolation-heat measuring system. The pigments and films of Fe4[Fe(CN)6]3 coated on mica and TiO2/mica showed high TSR values compared with the TSR value of Fe4[Fe(CN)6]3 itself. According to the increase of TSR value, the property of isolation-heat is effective. To realize the optimal blue color, we applied the the pigment to TiO2 coated mica(TM(b)) which has blueish interference color. The pigment of Fe4[Fe(CN)6]3 coated on TM(b) shows a strong blue color compared with that of Fe4[Fe(CN)6]3 coated on TiO2/Mmca(TM(w)), which has a whitish interference color.

Abstract This manuscript reports on compared color evolution about phase transformation of α-FeOOH@SiO₂ and β-FeOOH@SiO2 pigments. Prepared α-FeOOH and β-FeOOH were coated with silica for enhancing thermal properties and coloration of both samples. To study phase and color of α-FeOOH and β-FeOOH, we prepared nano sized iron oxide hydroxide pigments which were coated with SiO2 using tetraethylorthosilicate and cetyltrimethyl-ammonium bro- mide as a surface modifier. The silica-coated both samples were calcined at high temperatures (300, 700 and 1000°C) and characterized by scanning electron microscopy, CIE L*a*b* color parameter measurements, transmission electron microscopy and UV-vis spectroscopy. The yellow α-FeOOH and β-FeOOH was transformed to α-Fe2O3 with red, brown at 300, 700°C, respectively.

This manuscript reports on compared color evolution about phase transformation of α-FeOOH@SiO2 and β-FeOOH@SiO2 pigments. Prepared α-FeOOH and β-FeOOH were coated with silica for enhancing thermal properties and coloration of both samples. To study phase and color of α-FeOOH and β-FeOOH, we prepared nano sized iron oxide hydroxide pigments which were coated with SiO2 using tetraethylorthosilicate and cetyltrimethyl-ammonium bro- mide as a surface modifier. The silica-coated both samples were calcined at high temperatures (300, 700 and 1000°C) and characterized by scanning electron microscopy, CIE L*a*b* color parameter measurements, transmission electron microscopy and UV-vis spectroscopy. The yellow α-FeOOH and β-FeOOH was transformed to α-Fe2O3 with red, brown at 300, 700°C, respectively.

작은 고체 분체들은 피커링 유화 체계에서 안정화제로 작용하는 것은 이미 알려진 사실이다. 이 연구에서 우리는 알킬실란 처리 TiO2와 n-헥실알코올, 수계로 안정한 피커링 에멀젼을 제조하였다. TiO2 입자에 의해 안정화된 피커링 에멀젼을 제조하기 위한 최적의 조건은 TiO2 입자의 양과 수상/유상의 비에 의해 결정된다. 피커링 에멀젼의 형태는 물과 n-헥실알코올에 대한 입자들의 젖음성에 의존된다. 피커링 에멀젼은 TiO2가 5.00 wt%, 오일과 수상의 비가 3 : 7인 경우에 가장 안정하였다. 피커링 에멀젼을 형판으로 하여 무기 전조체를 졸-겔 공정에 의해 다공성 분체들이 합성되었다. 합성된 다공성 분체들은 광학 현미경, SEM, BET, XRD 및 EDS에 의해 확인되었다.

The purpose of this study was to determine the optimal firing condition and composition for Al2TiO5 crystal, which is suitable for stable coloration in glazes at high temperatures, using Cr2O3 as chromophore for the synthesis of Al2TiO5 system pigments. Al2TiO5 has a high refractive index and good solubility of chromophore in the Al2TiO5 lattice, making this structure a good candidate for the development of new ceramic pigments. Pigments were synthesized by using Al2O3 and TiO2 mainly. Various amounts of Cr2O3 such as 0.01, 0.02, 0.03, 0.04 and 0.05 mole were also added. Each compound was synthesized at 1300˚C, 1400˚C, and 1500˚C for 2 hours and cooled naturally. The crystal structure, solubility limit, and color of the synthesized pigments were analyzed by XRD, SEM, Raman spectroscopy, UV and UV-vis. The changes in color as the result of applying 6 wt% of the synthesized pigments to lime barium glaze were expressed as CIE-L*a*b* values. A Cr2O3 0.03 mole doped Al2TiO5 brown pigment was successfully synthesize at 1400˚C, and the values of CIE-L*a*b* parameters were L* = 44.62, a* = 3.10, and b* = 17.25. In the case of the pigment synthesized at 1500˚C, the brown color was obtained at 0.01 mole and 0.02 mole Cr2O3, and the CIE-L*a*b* values were 55.34, 1.73, 28.64, and 49.39, 0.51, 21.33, respectively. At 1500˚C, the maximum limit of solid solution was 0.03 mole Cr2O3. The glazed sample showed green color, and the values of the CIEL* a*b* parameters were L* = 45.69, a* = -0.98, and b* = 20.38.

The pearlesent pigment has received attention in a diversity of fields like cosmetics, inks, paints and so on. Ferric Ferrocyanide, one of the nano sized pearlescent pigment, is a kind of surface modification pigment that covers a metal oxidized substance or a coloring agent with uniform thickness. Characteristics of pearlescent pigment are various interference color, intense gloss effect and a three-dimensional effect. We synthesised the pearlesent pigment that ferric ferrocyanide can be deposited on the titania/mica surface by hydrothermal synthesis method. The process parameters are concentration of precursor, controlling pH and reaction temperature. The optimun conditions is that amount of iron(III) chloride hexahydrate is 3.1 wt% and amount of potassim ferrocynide trihydrate is 3.6 wt% in the started pH 4.5 at 70℃. The coating rate and coating efficiency of ferric ferrocyanide was about 1.47 % and 96.7 %, respectively. The synthesised pearlesent pigment was characterized by SEM, XRD, FT-IR and EDS.

A greening phenomenon has been observed in some plant foods such as chestnut, sweet potato,burdock, and others during processing. The formation of the pigments was postulated as reactions of primary amino compounds with chlorogenic acid or caffeic acid ester, yielding acridine derivatives. Acridine derivatives have been regarded as mutagenetic agents. For the reason, the bacterial reverse mutation test was carried out to evaluate the genotoxicity of green pigment using Salmonella typhimurium TA98 and TA100. Alanine, arginine, aspartic acid, glycine,lysine, and phenylalanine were reacted repectively with chlorogenic acid to synthesize model compound. Green pigment was extracted from sweet potato. Maximum concentration of 2 and 50 mg/plate was tested for the synthetic green pigments and extracted green pigment respectively, taking bacterial survival, solubility, and color intensity into consideration. There was no signigicant increase in the reverse mutation either with or without S9 activation system by any test material. Though further studies with other genotoxicity test system are necessary, both synthetic and sweet potato green pigments seemed not to cause mutation despite the acridine moiety in their structures.