• 대한화학회지
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• 제30권2호
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• pp.201-206
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• 1986

새로운 분석시약 N-benzylisonitrosoacetylacetone imine (H-IAA-N-Bz)을 합성하여 원소분석, 적외선흡수스펙트럼, 핵자기공명흡수스펙트럼, 질량스펙트럼 등으로 그 구조를 확인하였다. H-IAA-N-Bz은 알카리 용액(pH = 7.0∼10.0)에서 구리착물을 형성하며, 클로로포름 유기용매층으로 잘 추출된다. 이 구리착물에 대한 분광광도법적 연구의 여러가지의 최적조건은 420nm의 파장에서 구하였으며, 클로로포름 10ml당 구리 $\mu$g이하의 농도 범위에서 Beer법칙이 잘 성립되었다. 구리 착물의 조성은 $Cu(IAA-N-Bz)_2$이며, 착물의 총괄 안정도상수는 $8.55{\times}10^6$이며, 몰흡광계수 $\varepsilon$은 3500l/$cm{\cdot}mol$이다.

• 한국잠사곤충학회지
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• 제38권1호
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• pp.25-30
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• 1996

견 피브로인 섬유에 의한 Cr(VI)의 흡착 특성을 분석하였다. Cr(VI)의 흡착평형은 초기 흡착속도에 큰 영향을 받고 있으며 평형흡착량의 52% 정도에 이르고 있다. 견 피브로인 섬유에 의한 Cr(VI)의 흡착은 크롬염의 산화반응을 일으키는 산성의 pH 범위에서 흡착량이 증가한다. Cr(VI)의 흡착온도에 대한 엔탈피($\Delta$H)의 변화는 39.7KJ.mol-1로 얻어졌다. 이것은 Cr(VI)의 흡착이 착제 화학적 반응이라는 것을 의미하며 IR 스펙트럼의 결과에서도 아미드 형 카르보닐의 배위에 의한 착물형성이 확인되었다. 또한, 견 피브로인 섬유의 크롬 흡착처리에서 물성의 과도한 저하를 고려한 조건은 온도 5$0^{\circ}C$ pH 2.4, 3시간의 처리가 적당하고 5 X 10-3M의 농도에서 흡착평형에 도달하였다.

• 한국펄프종이공학회:학술대회논문집
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• 한국펄프종이공학회 2000년도 추계학술발표논문집
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• pp.83-83
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• 2000

Alkylketene dimer was known as a cellulose reactive or alkaline size because it does not require to fix to the fiber as do the traditional rosin sizes. A proposed sizing mechanism of AKD was the formation of P -ketoester bond between AKD and cellulose which provides the permanent attachment and the orientation of the hydrophobic alkylchains outward. However, some questions about the reaction had arisen and thus, the sizing mechanism of AKD has been a subject of controversy for several decades. The major concern of the controversy is that AKD is really reactive with cellulose or not in the papermaking conditions. In this study, reaction between AKD and pulp fiber was investigated, in order to find out whether AKD forms P-ketoester with pulp fiber during aging under no catalyzed neutral condition with obvious spectroscopic evidence. In addition, effect of aging treatment on the sizing development was studied. It has been disclosed that, in absence of water, AKD reacted with cellulose to form P -ketoester linkage under no catalyzed neutral condition, while, in presence of water, most of AKD was hydrolyzed to a dialkyl ketone or P -ketoacid. In addition, during the aging treatment of AKD-sized paper, its typical IR spectra bands gradually were reduced, completely disappeared after 6hr aging, and formed new absorption bands at 1707cm-' and shoulder peak at 1700cm-' which refer to the typical dialkylketone absorption bands. Therefore, the formation of P -ketoester between AKD and pulp fiber is impossible in the practical papermaking process. It could be suggested that the sizing development of AKD-sized paper is obtained by next two mechanism: 1) formation of a thin-layer of AKD on the fiber surface through melting and spreading of AKD emulsion particles by heat and 2) the hydrolysis of AKD to dialkyl ketone which has higher melting point, during drying and storage of AKD sized papers.

• 한국전기전자재료학회논문지
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• 제30권1호
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• pp.48-53
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• 2017

We report the studies on the red organic phosphor by using perylene bisimide derivatives. Even though perylene bisimide derivatives have excellent thermal stability and luminous efficiency, they have low solubility in organic solvents. In this research, modified perylene bisimide derivative, N,N'-Bis(4-bromo-2, 6-diisopropylphenyl)-1, 6, 7, 12-tetraphenoxyperylene-3, 4, 9, 10-tetracarboxyl bisimide (1C), has been prepared by the reaction of phenol with N,N'-Bis(4-bromo-2, 6-diisopropylphenyl)-1, 6, 7, 12-tetrachloroperylene-3, 4, 9, 10-tetracarboxyl bisimide (1B) in presence of DMF, at $70^{\circ}C$. The synthesized (1C) was characterized by using $^1H-NMR$, FT-IR, UV/V is spectroscopy, and TGA. The absorbtion and emission of (1C) was shown at 576 nm and 610 nm in UV/V is spectrum. In TGA thermogram, (1C) showed good thermal stability without significant weight loss to $220^{\circ}C$. And in the solubility analysis, (1C) with phenoxy group showed the good solubility in general organic solvents. The blended films of (1C) with PMMA (polymethyl methacrylate) at different weight % concentration such as 10, 5, 1 weight % have been prepared. The blended film was shown at 616 nm when monitored at 450 nm in PL emission spectra.

• 대한화학회지
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• 제22권1호
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• pp.19-24
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• 1978

Ambidentate 리간드인 isonitrosobenzoylacetone imine 및 그 N-알킬치환체들의 새로운 니켈(II)착물 Ni(IBA-NH)(IBA-NR)를 합성하였다. 여기서 IBA-NH 및 IBA-NR (R=H, methyl, ethyl, n-propyl, iso-propyl, n-butyl 또는 benzyl)은 각각 isonitrosobenzoylacetone imine 및 그 N-알킬치환체를 표시한다. 합성한 니켈(II)착물들의 적외선, 핵자기공명, 전자스펙트라 및 자기모멘트등을 측정한 결과 이들 착물에서 IBA-NH 리간드는 이소니트로소기의 산소를 통하여 니켈에 배위되어 6각형 고리를 이루고 있으며, 그리고 IBA-NR 리간드는 이소니트로소기의 질소를 통하여 니켈에 배위되어 5각형 고리를 이루고 있음을 확인하였다. 이들 리간드의 배위 구조는 Bose 등에 의해 알려진 isonitrosoacetylacetone imine 및 N-알킬유도체들의 구조와 유사하다.

• 대한화학회지
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• 제26권1호
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• pp.31-35
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• 1982

Amberdentate 리간드인 isonitrosobenzoylacetone imine 및 N-알킬 치환제들의 새로운 팔라듐(Ⅱ) 착물 Pd(IBA-NH)(IBA-NH') 및 Pd(IBA-NR)2를 합성하였다. 여기서 IBA-NH 및 IBA-NR (R: methyl, ethyl, n-propyl, n-butyl, benzyl)은 각각 isonitrosobenzoylacetone imine 및 그 N-알킬 치환제를 표시한다. 합성한 팔라듐(II) 착물들의 적외선, 핵자기 공명, 전자 스펙트라 등을 측정한 결과 이들 착물 중에서 Pd(IBA-NH)(IBA-NH')는 IBA-NH는 이소니트로소기의 산소를 통하여 팔라듐에 배위되어 6각형 고리를 이루며 IBA-NH'는 이소니트로소기의 질소를 통하여 배위되어 5각형 고리를 이루고 있음을 확인하였다. 그리고 Pd$(IBA-NR)_2$는 양쪽의 IBA-NR이 같이 이소니트로소기의 질소를 통하여 배위되어 5각형 고리를 이루고 있음을 확인하였다. 이들 리간드의 배위구조는 $Bose^5$등에 의하여 알려진 isonitrosoacetylacetone imine 및 그 N-알킬 유도체들의 구조와 유사하다.

• 한국재료학회지
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• 제20권5호
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• pp.278-288
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• 2010

High Pressure High Temperature (HPHT) treatment can significantly change the color of diamonds. We studied the variation of the optical properties according to the nitrogen arrangement in natural brown diamonds of various types (type IaAB, type IaB, type IaA > B, type IaA < B, IaA = B) after HPHT treatment. The diamonds with different arrangements of nitrogen were annealed at temperatures in the range $1700-1800^{\circ}C$ under a stabilizing pressure of 5 GPa. HPHT treated samples were analyzed using UV-Vis-NIR, FT-IR, and PL spectroscopy. The absorption and luminescence spectra were measured to compare the variations of nitrogen arrangement in the natural brown diamonds before and after HPHT treatment. After HPHT treatment, the brown coloration in all types of diamonds was reduced and a decrease in the peaks related to the A-aggregate of nitrogen was more predominant than the B-aggregate. Furthermore, the peaks related to N3 (415.4 nm), H4 (496.4 nm), and platelet decreased and the peaks related to H3 (503.2 nm) and G-band increased after HPHT treatment. In conclusion, spectroscopic analysis of natural brown diamonds after HPHT treatment showed that a yellow color was produced by absorption in the H3 centers and a green color was generated by interaction between absorptions of the H3 and H2 centers.

• 폴리머
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• 제29권4호
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• pp.408-412
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• 2005

생체재료로 이용하기 위하여 키토산을 기질로 하여 Bembyx mori로부터 추출한 견 피브로인을 블렌드한 필름에 대한 구조와 특성을 X선 회절분석, 열분석, 적외선 분광분석, 전자현미경 관찰, 접촉각 측정, 흡수율 측정으로 조사하였다. $-\~30wt\%$ 피브로인을 포함하는 블렌드 필름은 리튬이온을 포함하는 초산수용액으로 제조되었다. 키토산/피브로인 블렌드 필름은 키토산의 아미노기와 피브로인의 아미드 카보닐기 사이의 수소결합과 같은 분자간 상호작용의 형성에 의해 결정성이 감소되었다. 피브로인의 비율이 증가할수록 키토산의 무수혈 견정상은 소실되었고, 수화형 결정상은 감소되었으며, 퍼브로인의 P형 결정이 형성되어 혼재된 결정구조를 이루었다. 표면 친수성과 수분 흡수성은 피브로인의 비율이 클수록 증가되었으며, 20 $wt\%$, 이상에서 수화젤 상의 필름을 형성하였다. 전자현미경에 의한 블렌드 필름의 표면과 단면은 균일한 상을 나타내었다.

• 한국수산과학회지
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• 제20권4호
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• pp.273-281
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• 1987

In this work the antioxidant effects of browning reaction products prepared by xylose-tryrtophan reaction system were discussed. The antioxygenic brown pigments were separated by solvent extraction, and column chromatography and isolated by gel filteration. The functional groups of the brown pigments which had antioxidant activity were examined. The brown pigments extracted with methanol showed antioxidant effect and were fractionated in 5portions on DEAE-cellulose column. The elutes with methanol: acetic acid(10:30 v/v sol n(A), methanol: chloroform(95:5 v/v) sol n(C), and chloroform: acetic acid(10:30 v/v) sol n(E) only showed antioxidant activity and their compositions were 22.43, 21.51 and $34.43\%$ respectively. When each fraction on DEAE-cellulose column was reseparated on Sephadex LH-20 column, 2 fractions were obtained from portion A and C respectively. Molecular weights of A, C and E fraction of brown pigments were from 2,600 to 3,700. By elucidation of IR spectra, the pigment fractions which showed a strong antioxidant activity were tearing the indole group. It is suggested that the antioxidant function of the brown pigment is due to hydroxy and amino group. A higher activity of the brown pigment fraction E might be attributed to carboxylic acid or carboxylic ester compounds.

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