Optimization of quinacridone magenta,Cu-phthalocyanine cyan,and arylide yellow ink films formulated for maximum color gamut

Investigation of ink formulation options with the purpose to obtain color-gamut-optimal set of Cyan Magenta and Yellow CMY inks is reported. Implementation of the thickness dependent Kubelka-Munk model on multiple ink layers having different and well-defined thicknesses, provides characteristic absorption and scattering (K, S ) spectra of the ink ingredients. These data enable accurate computation of the reflectance spectrum and thus the L*a*b* color coordinates for any given ink thickness or substrate. Pigment materials investigated are quinacridone as magenta, copper-phthalocyanine as cyan, and arylide yellow. Scaling the peak of the absorption band to the number of molecules per unit area for the specific pigments studied in this article provides the molar extinction coefficients, 1.21 × 10⁴ , 4.7 × 10⁴ , and 3.3 × 10⁴ cm²/millimole respectively, regardless of the different ink formulations used, in accord with Avogadro's principle. Having a set of three pairs of K, S spectra is used to compute the color gamut of any CMY color combination in the L*a*b* space as a function of ink layer thickness and formulation. Using an iterative algorithm, a color-gamut-optimal set of CMY inks is obtained.     

Copper phthalocyanine as corrosion inhibitor for ASTM A606-4 steel in 16% hydrochloric acid

A study based on the corrosion inhibition properties of copper phthalocyanine is described. Coverage degrees of copper phthalocyanine (Cu-phcy) on ASTM-A606-4 steel, obtained by weight loss measurements, were fitted to Langmuir, Frumkin, Temkin and Flory–Huggins adsorption isotherms. A better fit to the Langmuir isotherm was obtained. The polarization curves showed that polarization of both the anodic and cathodic reactions were verified for concentrations higher than 10^–4 M, indicating a mixed type action. Only the anodic reactions were polarized for lower concentrations. At high frequencies the Nyquist diagrams showed one capacitive loop attributable to double layer charging and a small one at intermediary frequencies attributable to the faradaic process of hydrogen evolution. The formation of an adsorbed film was characterized by increasing charge transfer resistance values in the low frequency range for increasing inhibitor concentrations. According to the techniques used in this study, copper phthalocyanines showed a high corrosion inhibiting efficiency for all concentrations.     

真空蒸发沉积VOPc薄膜及磁场对薄膜结构与性能的影响

用真空蒸发制备了酞菁氧钒 (VOPc)薄膜 ,并在磁场中进行了热处理。用X光电子能谱、X射线衍射、紫外 可见吸收光谱、原子力显微镜等手段对制备的薄膜进行了表征。结果表明沉积的酞菁氧钒薄膜为α 型 ,成分接近酞菁氧钒的分子式。制备的薄膜在磁场中进行了热处理 ,发现磁场使酞菁氧钒薄膜性质发生改变 :UV VIS吸收谱Q带发生红移 ;XRD谱图衍射峰强度明显增强 ,峰位略有变化 ;原子力显微镜 (AFM)分析发现晶粒大小无明显变化。以上结果说明磁场的存在使得VOPc分子在热处理过程中发生了定向的排列     

Photovoltaic properties of SnCl2Pc films and SnCl2Pc/pentacene heterostructures

The optical and photovoltaic properties of dichlorotin phthalocyanine (SnCl₂Pc) films and SnCl₂Pc/pentacene (Pn) heterostructures (HS) have been studied. Weak bands at 1.35, 1.52 and 2.05 eV have been found in absorption and modulated photoreflectance spectra of SnCl₂Pc films. These bands can be caused by the formation of charge transfer states. The low concentration of recombination centers of charge carriers has been formed on a free surface of SnCl₂Pc films. This concentration essentially decreases at air evacuation before vacuum deposition of a Pn layer. Therefore, interface with an insignificant recombination rate of charge carriers is formed for SnCl₂Pc/Pn HS.     

四异丁氧基镍酞菁的合成及其溶剂效应

4 异丁氧基邻苯二腈与氯化镍在强有机碱 1 ,8 二氮杂双环 (5 ,4,0 )十一碳烯 7催化下反应 ,合成了四异丁氧基镍酞菁 ,产物经FT -IR、元素分析、UV -Vis吸收光谱和1 H NMR表征了结构 ;并研究了其溶剂效应 ,结果表明 :最大吸收峰波数ν与函数 f(n ,ε)存在一定的线性关系 ,线性相关系数为 0 940 2 ,而Bayliss函数项 (n2 - 1 ) /(2n2 +1 )决定了最大吸收波长 (λmax)的位移变化 ;化合物的λmax在不同溶剂中随聚集程度增加 ,发生一定程度的蓝移     

酞菁配合物在光限幅中的应用

酞菁配合物是一种很有前途的光限幅材料,具有特殊的结构和优良的光限幅性能,已引起人们极大的兴趣。综述了近年来酞菁配合物光限幅材料的研究,并展望了今后的研究方向。     

Modeling of solid—liquid adsorption: Effects of adsorbent loads on model parameters

The adsorption of cobalt phthalocyanine dye onto activated carbon in a continuous stirred tank adsorber was studied. The variables investigated were: adsorbent mass, adsorbent particle size and fluid flowrate. Several models based on film, pore and surface diffusion were constructed and fitted to the experimental data. Experimental results showed: (i) the increasing importance of the film mass transfer resistance for increasing adsorbent loads; (ii) the increasing importance of the surface diffusion mechanism for increasing adsorbent loads; and (iii) the better discrimination among different models for higher adsorbent loads and lower flowrate.     

钴酞菁催化氧气氧化邻硝基甲苯制取邻硝基苯甲酸

研究了以钴酞菁为模拟酶催化剂、氧气液相氧化邻硝基甲苯制取邻硝基苯甲酸的最佳工艺条件,考察了温度、氧气压力、溶剂比〔V(甲醇)/V(苯)〕、反应时间、n(NaOH)/n(邻硝基甲苯)等参数对邻硝基苯甲酸收率的影响,发现助催化剂NaOH用量和溶剂体积比影响较大。在温度为40℃、氧气压力为3 0MPa、V(甲醇)/V(苯)=2、n(NaOH)/n(邻硝基甲苯)=11 7时,邻硝基苯甲酸收率可达77 8%。     

近红外敏感的功能分离型有机光接受体系的光导性能研究Ⅱ．CGL／CTL界面能级匹配对体系光导性能的影响

功能分离型光接受体系是由载流子产生层（ＣＧＬ），载流子传输层（ＣＴＬ）和载流子阻挡层（ＵＣｔ）组Ａ成的一种多层光接受体系．本文合成了一系列载流子传输层材料，如吡唑啉、唑和腙的衍生物，并将上述ＣＴＬ材料与酞菁类ＣＧＬ材料，按一定涂布工艺制成近红外敏感（７８０～８３０ｎｍ）的多层光接受体系．通过对样品电照相性能的表征，着重讨论了ＣＧＬｌＣＴＬ界面能级匹配问题及其对体系光导性能的影响。     

The electrochemical behavior of cobalt phthalocyanine/platinum as methanol-resistant oxygen-reduction electrocatalysts for DMFC

The electrochemical behavior of cobalt phthalocyanine/platinum as methanol-resistant oxygen-reduction electrocatalyst for DMFC was investigated. Platinum was chemically deposited on the carbon-supported cobalt phthalocyanine (CoPc), and then it was heat-treated in high purity nitrogen at 300 °C, 635 °C and 980 °C. In order to evaluate the electrocatalytic behavior of CoPc-Pt/C, the PtCo/C and Pt/C as reference catalysts were employed. TGA, XRD, EDAX, XPS and electrochemical experiments were used to study the thermal stability, crystal structure, physical characterization and electrochemical behavior of these catalysts. These catalysts exhibited similar electrocatalytic activity for oxygen reaction in 0.5 M H₂SO₄ solution. In methanol tolerance experiments, Pt/C, PtCo/C and CoPc-Pt/C heated at 980 °C were active for the methanol oxidation reaction (MOR). The presence of Co did not improve resistance to methanol poisoning. However, the CoPc-Pt/C after 300 °C or 635 °C heat-treatment demonstrated significant inactivity for MOR, hence they have a good ability to resist methanol poisoning. The current study indicated that the macrocyclic structure of phthalocyanine is the most important factor to improve the methanol tolerance of CoPc-Pt/C as the oxygen-reduction reaction (ORR) electrocatalyst. The CoPc-Pt based catalyst should be a good alternation for oxygen electro-reduction reaction in DMFC.