Studies of the Formation and Stability of Ezetimibe-Cyclodextrin Inclusion Complexes

In the presented studies, the interactions between ezetimibe (EZE) and selected cyclodextrins were investigated. α-Cyclodextrin (αCD), β-cyclodextrin (βCD) and its modified derivatives, hydroxypropyl-β-cyclodextrin (HPβCD) and sulfobutylether-β-cyclodextrin (SBEβCD), were selected for the research. Measurements were carried out using calorimetric and spectroscopic methods. Additionally, the Hirshfeld surface and biochemical analysis were achieved. As a result of the study, the inclusion complexes with 1:1 stoichiometry were obtained. The most stable are the complexes of β-cyclodextrin and its derivatives. The comparison of βCD with its derivatives shows that the modifications have an affect on the formation of more durable and stable complexes.     

Heterocyclic azo dyes. II. Azo Dyes Containing the Benzotriazole and/or benzimidazole nucleus

The synthesis, some dyeing, and fastness properties of several new dispersed and acid dyes derived from the amino-benzotriazoles 1 & 3 and the aminobenzimidazoles 2a , 2b & 4 are described. The suitability of the amino derivatives 1 , 2a , 2b , 3 & 4 as bases for azoic dyeing has also been studied. Several interesting observations between the properties of some synthesised dyes and the corresponding benzene or naphthalene analogues are cited.     

不同修饰剂对β-环糊精微球吸附性能的影响

以β-环糊精为原料,通过传统的反相乳液聚合法合成β-环糊精微球,选择壳聚糖和四甲基氢氧化铵分别对其进行修饰,考察溶液的搅拌时间、吸附体系的温度、pH等条件对β-环糊精微球及其衍生物吸附甲基橙的影响。结果显示,β-环糊精微球对甲基橙吸附效果较好,修饰改性后,吸附效果增强,四甲基氢氧化铵修饰的β-环糊精微球吸附效果优于壳聚糖修饰后β-环糊精微球。     

New catalytic systems for selective oxidation of aromatic compounds by hydrogen peroxide

Some new water-soluble catalytic systems based on iron complexes of polyethylene oxide and block copolymers of ethylene oxide and propylene oxide functionalized by catechol or β-cyclodextrin have been developed. These complexes were examined as catalysts for biomimetic hydroxylation of benzene and phenol by hydrogen peroxide. It is shown that the introduction of β-cyclodextrin into the polyethylene oxide molecule is favourable for rate and selectivity of hydroxylation of aromatic compounds in a two-phase system.     

Effect of blending β-cyclodextrin with poly(vinyl chloride) on the leaching of phthalate ester to hydrophilic medium

β-Cyclodextrin was blended with poly(vinyl chloride) to study the influence of β-cyclodextrin on the leaching of phthalate ester from PVC. β-Cyclodextrin was found to reduce the migration of phthalate ester. The considerable effect of β-cyclodextrin on the leaching of phthalate ester was traced to the formation of an inclusion complex formation between the two components. © 1996 John Wiley & Sons, Inc.     

Synthesis and characterization of a β-CD-alginate conjugate

Selective chemical modification of both β-cyclodextrin (β-CD) and sodium alginate (alg) was performed in order to produce an alginate derivative possessing pendant β-CD cavities along the chain. The latter was then fully characterized in terms of chemical integrity and purity, complexation properties and ability to form hydrogels. Thus, a sodium alginate derivative modified with adipic dihydrazide (alg-ADH) and a β-cyclodextrin derivative possessing an aldehyde function on the primary face were synthesized, and both were selectively coupled by a reductive amination-type reaction. Comparison of the complexation properties of the grafted and natural β-CDs by isothermal titration calorimetry using sodium adamantane acetate as a model guest gave similar enthalpy values suggesting similar mechanisms of binding. However, the association constant for the grafted CD is slightly lower as a result of a less favorable change in the binding entropy. Investigation of the gelation ability in the presence of calcium ions led to the following order: alg > alg-ADH > alg-CD. The decrease of gelation efficiency for the modified alginate samples reflected the reduction of ionic interchain bonds as a result of the unavailability or non-accessibility of G units on the alginate backbone, due to the chemical modification and steric effect of the CD molecule for alg-CD.     

Synthesis of acid dyes containing polyetheramine moieties and their low‐temperature dyeing properties on wool fiber

To realize the low‐temperature dyeing of wool fibers, the use of auxiliaries and wool modification are common methods. Low‐temperature auxiliaries may cause water‐pollution problems, and wool modification is a costly and uncontrollable process. In this study, new acid dyes, named D1–D3, containing polyetheramine groups were synthesized and applied to wool fiber by conventional and low‐temperature exhaust dyeing procedures. The results indicate that the new acid dyes could interact with wool‐fiber‐like auxiliaries and render a high exhaustion rate to the wool fiber at a dyeing temperature of 80 °C. In comparison with Acid Blue 25, the D1–D3 dyes showed an increased dyeing rate, especially under a dyeing temperature of 80 °C. Despite the bigger relative molecular masses of D1–D3, the exhaustion rates of D1–D3 were still higher, and the times of half‐dyeing were shorter than that of Acid Blue 25. The color differences between the wool fabrics dyed with the four dyes at 80 and 98 °C, respectively, were compared. We found that the color differences of D1–D3 between 80 and 98 °C were smaller than that of Acid Blue 25. The interactions between the dyes and wool fiber were analyzed and manifested by the measurement of the ζ potential of the dyes and wool fiber. The leveling and transfer properties of the D1–D3 dyes were also investigated, and the color differences of the wool fabrics dyed with Acid Blue 25, D1, and D2 were very low at all measured pH values and temperatures. The fastnesses of D1–D3 on wool fabric were almost the same as that of Acid Blue 25. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45793.     

Use of γ-cyclodextrin/epichlorohydrin polymer in merging fabric formation and coloration processes

A candidate polymeric size was synthesised by the polymerisation of γ -cyclodextrin with epichlorohydrin under alkaline conditions. The motivation for the synthesis was to produce a polymer that could not only function as a warp size for fabric formation, but also serve as a host for dye molecules that could subsequently be released after the weaving process, ultimately promoting the merging of fabric formation and coloration processes. The γ -cyclodextrin/epichlorohydrin polymer has been found to promote the dissolution of textile dyes, such as CI Disperse Blue 3, CI Disperse Yellow 82 and CI Disperse Red 91 to yield pad baths capable of evenly coating polyester fabric. Upon padding and subsequent drying, the dye– γ -cyclodextrin/epichlorohydrin polymer pad baths have been used for dyeing the fabric upon thermofixation. Furthermore, cross-sections of fibre dyed in the same manner indicate dye penetration into the fibre.     

Dyeing transition temperature of wools treated with low temperature plasma,liquid ammonia,and high‐pressure steam in dyeing with acid and disperse dyes

Wool fibers treated with oxygen low‐temperature plasma, liquid ammonia (NH₃), and high‐pressure (HP) steam were dyed with two acid and three disperse dyes. Rate of dyeing, saturation dye uptake, and dyeing transition temperature were measured. Rate of dyeing of the O₂ plasma, NH₃, and HP steam‐treated wools increased with acid dyes, whereas it did not increase with disperse dyes. Although dyeing transition temperature for acid dyes was decreased by the plasma, NH₃, and HP steam treatments, the temperature for disperse dyes was not changed by the treatments. Therefore, it seems that acid dyes penetrate by the intercellular diffusion through the interscale Cell Membrane Complex (CMC) of wool, whereas disperse dyes penetrate by the intracellular diffusion through the intrascale cuticle surface independently with CMC relaxation by the treatments. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1058–1062, 2001     

Effect of microencapsulation on dyeing behaviors of disperse dyes without auxiliary solubilization

Microencapsulated disperse dye can be used to dye hydrophobic fabric in the absence of auxiliaries and without reduction clearing. However, little available information for dyeing practice is provided with respect to the effect of microencapsulation on the dyeing behaviors of disperse dyes. In this research, disperse dyes were microencapsulated under different conditions. The dyeing behaviors and dyeing kinetic parameters of microencapsulated disperse dye on PET fiber, e.g., dyeing curves, build up properties, equilibrium adsorption capacity C_∞, dyeing rate constant K, half dyeing time t_1/2, and diffusion coefficient D were investigated without auxiliary solubilization and compared with those of commercial disperse dyes with auxiliary solubilization. The results show that the dyeing behaviors of disperse dye are influenced greatly by microencapsulation. The diffusion of disperse dyes from microcapsule onto fibers can be adjusted by the reactivity of shell materials and mass ratios of core to shell. The disparity of diffusibility between two disperse dyes can be reduced by microencapsulation. In addition, the microencapsulation improves the utilization of disperse dyes due to no auxiliary solubilization. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

The Effect of Pressure and Temperature on Supercritical CO2 Dyeing of PET-Dyeing with Mixtures of Dyes

Abstract

Dyeing is supercritical CO2 is one of the most advanced dyeing technologies. The dyeing medium is not water but carbon dioxide in the supercritical state (temperatures above 31°C and pressures above 74 bar).

The effect of pressure and temperature on dyeing of PET in supercritical CO₂ with only one dye and with mixtures of two or three dyes has been investigated.

The variations of pressure (250 in 300 bar) and temperature (70 in 130°C) cause differences in colour, especially when mixtures of dyes are used. The dyed samples were evaluated using colorimetry and the extraction of dyes from the fabric.

The amount of all dyes on the fabric rises with the rising temperature due to the accelerated motion of molecular chains and the formation of the free volume in the fibre, so important for the diffusion of dyes. The change of pressure does not after the amount of fixed dyes significantly, but the ratio between the dyes is changed when dyeing with mixtures of dyes.     

Synthesis,spectral properties and dyeing on polyester of monoazo dyes from indol‐2‐one derivatives

Three series of phenylazo disperse dyes were prepared by coupling diazotised 4‐aniline dyes with 5‐indol‐2‐one dyes. The structures of these dyes were determined by proton nuclear magnetic resonance, Fourier Transform–infrared and elemental analysis. The effects of solvent on the ultraviolet–visible absorption spectra of these dyes were studied. The dyes displayed a λ_max shift of between 399 and 438 nm. The dyes were finally applied in the dyeing of polyester fibres in order to investigate their colour range and dyeing properties. Most of the dyes displayed high rubbing fastness and good washing and sublimation fastnesses on polyester fibres.     

FLAVOR ENCAPSULATION AND RELEASE CHARACTERISTICS OF SPRAY-DRIED POWDER BY THE BLENDED ENCAPSULANT OF CYCLODEXTRIN AND GUM ARABIC

The flavor inclusion powder was prepared by spray drying, using the combined encapsulation method of inclusion by β-cyclodextrin (β-CD) and emulsified by gum arabic (GA). d-Limonene and ethyl n-hexanoate were used as model flavors. The application of high pressure by Microfluidizer to the mixture of flavors and β-CD slurry was an effective means of forming inclusion complex. Flavor retention during spray drying under various compositions of the encapsulants was investigated. The flavor retention using the blended encapsulant was increased by adding GA in the encapsulant. The characteristics of release of encapsulated flavor during storage were evaluated at 50°C and 75% of relative humidity. The release rate of flavor in spray-dried powder depended on kinds of the flavors and composition of the encapsulant. The blending MD and β-CD in the feed liquid decreased the release rate of flavors. The rate of release of flavor was analyzed by Avrami's Equation.     

β-环糊精促进环己酮肟水解脱保护生成环己酮

利用β-环糊精对有机物的增溶和活化性能将β-环糊精应用于环己酮肟水解脱保护反应,系统地研究了β-环糊精催化性能、反应温度、β-环糊精的量、酸的用量和种类等对环己酮肟水解脱保护反应的影响。实验结果表明,β-环糊精通过和酸共同作用,可以显著地催化环己酮肟脱保护反应,在60℃ β-环糊精加入时,反应的收率从73％提高到92％。酸及其添加的量对反应也具有明显作用,强酸对脱保护反应的效果明显优于弱酸。     

世界染料与染整工艺科技创新

根据染料母体的生物相容性论述了非诱变性染料和仿生染料在纺织纤维着色中的发展方向；论述了实现高固色率活性染料的有效途径以及通过交联染色方法实现染料与纤维近100％化学结合的可行性；介绍了环境友好染色新工艺，活性染料无盐染色，还原染料和硫化染料生化法还原或电还原法染色，非水溶剂染色以及喷墨印染技术。     

Synthesis and properties of acid dye derivatives of arylsulphonanilides

Thirty-five acid dyes suitable for dyeing wool and polyamide fibres were synthesized, using derivatives of arylsulphonanilides prepared from o-nitrotoluene or chloronitrotoluene. As coupling components, derivatives of 1-phenyl-3-methylpyrazolone-5 and 2-naphthol were used. Fastness and colour properties of the prepared dyes were determined. It was found that some of the prepared dyes on polyamide fibres show batho- and hypso-chromic effects as well as hypo- and hyper-chromic effects during testing of their fastness to washing and to acid and alkaline perspiration. Spectroscopic examinations and determination of pK_a of the sulphonamide and hydroxyl groups of the dyes showed that the observed changes are associated with aggregation or disaggregation of the dyes on fibres or with a change in the azo-hydrazone equilibrium. Some of the prepared dyes are characterized by very good dyeing and fastness properties.     

槐米染色棉织物工艺及其抗紫外性能研究

为实现槐米染料的工业化应用及提高棉织物的功能性,分析了使用壳聚糖、Al3+、Fe2+媒染剂预媒染色法对棉织物染色效果的影响,重点研究了铝预媒染方法染色温度、染色时间、pH值等工艺参数对染色棉织物K/S值的影响,并测试了槐米染色棉织物的抗紫外性能。结果表明:直接使用槐米染色的效果较差;壳聚糖媒染对上染效果影响不大,使用铝、铁媒染剂,可得到不同颜色的棉织物;铝媒染剂染色棉织物为鲜艳的黄色,为较好的媒染方法;铝预媒染染色方法染色优化条件为:温度为80℃,染色时间120分钟,染浴pH值为6.8;铝预媒染染色棉织物具有较好的抗紫外性能。     

酸性金属络合染料上染锦氨织物的色牢度探讨

采用酸性金属络合染料对锦氨织物进行染色,从染料、染色工艺、助剂三个角度探讨了对染色牢度的影响。结果表明:酸性金属络合染料对锦氨织物染浅、中及中深色的牢度较好;染深色时,需通过工艺调整及助剂辅助。其优化的工艺条件为:染色温度93℃,保温时间30 min,染浴p H值在3~4,配合1.0 g/L氨纶防沾色剂,2%(omf)酸性固色剂DM-2539G及2.0 g/L增进剂CIBAFIX ECO后处理,各项牢度指标能提升到3-4级及以上。     

β-环糊精接枝壳聚糖-黄连素包合物抑菌性能的研究

通过壳聚糖席夫碱反应合成了β-环糊精接枝壳聚糖,用合成产物对黄连素进行了包合.研究了合成产物、包合物对大肠杆菌、金黄色葡萄球菌和黑曲霉的抑菌作用.结果表明,β-环糊精接枝壳聚糖和包合物的抑菌活性较壳聚糖有显著提高.     

锌金属和镀锌染色(一)

介绍了锌金属和镀锌层染色的特点,选择染料的原则及适用的染料类型(包括媒介染料、直接染料、酸性染料、活性染料和可溶性还原染料)。从染料的表面活性,染料与铬酸盐转化膜之间的作用力,染色过程及染色层的位置等方面阐述了锌金属和镀锌层染色的机理。