Silk fabric dyed with extract of sophora flower bud

This study analysed the use of sophora flower bud extract for dyeing and the resulting colour character and fastness of dyed silk fabric. The pigment composition on the silk fabric and recycling of this extract were also studied. The results indicated that the dyed silk fabric possessed good washing, rubbing and perspiration fastness, and the pigment composition on the silk fabric was mainly rutin and quercetin. The average recovery rate of the dye was 55.00%. These results demonstrate that the sophora flower bud extract is an effective natural dye.     

Forensic analysis of dyed textile fibers

A rapid, specific, and sensitive method has been developed using molecularly imprinted polymers (MIPs) as solid-phase extraction sorbents for extraction of trace tetracycline antibiotics (TCs) in foodstuffs. MIPs were prepared by precipitation polymerization using tetracycline as the template. Under the optimal condition, the imprinting factors for MIPs were 4.1 (oxytetracycline), 7.0 (tetracycline), 7.4 (chlortetracycline), 7.7 (doxycycline), respectively. Furthermore, the performance of MIPs as solid-phase extraction sorbents was evaluated and high extraction efficiency of molecularly imprinted solid-phase extraction (MISPE) procedure was demonstrated. Compared with commercial sorbents, MISPE gave a better cleanup efficiency than C18 cartridge and a higher recovery than Oasis HLB cartridge. Finally, the method of liquid chromatography–tandem mass spectrometry coupled with molecular-imprinted solid-phase extraction was validated in real samples including lobster, duck, honey, and egg. The spiked recoveries of TCs ranged from 94.51% to 103.0%. The limits of detection were in the range of 0.1–0.3 μg kg⁻¹. Chromatograms obtained by direct injection of the spiked egg extracts (5 × 10^-3 mmol L⁻¹) and purification with MISPE     

Single-molecule orientations in dyed salt crystals

We present single-molecule confocal microscopy studies of orientational distributions for luminophores isolated in potassium hydrogen phthalate (KAP) crystals. The incorporation of dye molecules that bear no size or shape similarity to the host ions is observed, demonstrating that single-molecule studies on mixed crystals need not be restricted to isomorphous host/guest pairs. Violamine R is oriented and overgrown by the fast vicinal slopes of growth hillocks within the symmetry-related {010} growth sectors and DCM deposits in the {11} growth sectors of KAP. Both mixed crystals exhibit modest absorption dichroism relative to basic pyranine-doped K(2)SO(4). The latter was studied to ensure that a range of orientations was sampled in our experiments. Average orientations determined at the single-molecule level were in close agreement to ensemble-averaged measurements for all three systems, and the chromophore orientational distributions were broader than anticipated, indicating that the crystals incorporate guest molecules in a range of orientations outside the measured ensemble average.     

Dyeing of white and indigo dyed cotton fabrics with Mimosa tenuiflora extract

Mimosa tenuiflora extract has been used in food industry as an additive and in textile and leather industry as a colorant. Two types of fabrics, ready to be dyed white and indigo dyed fabrics, were dyed with M. tenuiflora extract. The fabrics were mordanted after dyeing with six different metal salts. Colorimetric evaluations of fabrics were carried out by spectrophotometer. Colour fastness to washing, rubbing and light were performed. Colour strength of fabrics was calculated from Kubelka–Munk formula. Highest vividness (C¹) values were obtained by Ni mordant. Moderate fastness values were observed. However poor wet rubbing fastness values were observed in the case of indigo dyed fabrics due to lack of good wet rubbing fastness of indigo itself.     

Thin-layer gel chromatography of dyed proteins.

Plasma chromatography as a method for ultratrace qualitative and quantitative detection of organic compounds is especially well suited for detection of gas chromatographic effluents. The optimum range of sample quantity is 10(-6) to 10(-12) g for detection and identification of a compound by use of its characteristic positive and negative mobility spectra. The type of reference mobility spectra produced by alkanes, aromatics, esters, halogenated compounds, nitrogenated compounds and organic acids have been previously reported. This study presents the reference mobility spectra produced for lysergic acid diethylamide (LSD), delta9-tetrahydrocannabinol (delta9-THC), digitoxigenin and several biochemical compounds of research significance. LSD and delta9-THC in a mixture can be detected and identified by plasma chromatography positive mobility spectra in quantities of 10(-7) g or less. All the compounds investigated in this study display strong MH+ ions along with other ions primarily of the type (M)NO+, (M)2H+. None of these compounds exhibits negative mobility spectra.     

Photooxidation of dyed styrene-butadiene and natural rubbers

Dyed natural rubber (NR) and styrene-butadiene rubber (SBR) designed for outdoor applications were exposed to accelerated artificial aging in xenon light. The aging results in the deterioration of the properties of the exposed surface material. The ability of dyed polymers to withstand prolonged sunlight exposure without fading or undergoing any physical deterioration is largely determined not only by the photochemical characteristics of the absorbing dyestuff itself but also by the polymer structure and fillers. Results indicate that dyed filled NR and SBR samples behave differently during photooxidation. The photodegradation products were observed by Fourier transform infrared spectroscopy (FTIR) to characterize the changes occurring in the polymer matrix during UV aging. The fading of the dyed polymers was found to be promoted in the NR sample. Moreover, the effects of photooxidation on the dyed SBR and NR materials were assessed by the formation of cracks and the thickness of the degraded area. The degradation thickness is more important for the NR sample than for the SBR one according to environmental scanning electron microscopy (ESEM) observations. For the NR sample, cracks appear initially at the surface and then grow through the thickness of the specimen, while for the SBR sample cracks are small and discontinuous. Published in Russian in Vysokomolekulyarnye Soedineniya, Ser. A, 2008, Vol. 50, No. 6, pp. 1081–1085. This article was submitted by the authors in English.     

UV-sensitive indicators based on bromophenol blue and chloral hydrate dyed poly(vinyl butyral)

UV-sensitive indicators based on dyed poly(vinyl butyral) (PVB) containing acid-sensitive dye (bromophenol blue, BPB) and chloral hydrate have been developed and used successfully to measure the integrated UV irradiance. This flexible film changes colour from blue to green and finally to yellow on exposure to UV irradiation. The radiation-induced change in colour was analysed spectrophotometrically at the absorption band maxima of 421 and 601 nm. The film responds faithfully to UVA, UVB and UVC radiation, showing a maximum sensitivity at 200 nm. Correlations were established between the incident energy of UV radiation and the change in absorbance of BPB/PVB films at 421 and 601 nm using irradiation wavelengths of 248.5, 298.8 and 366 nm. The assessment of the uncertainties, the effect of the irradiation wavelength and chloral hydrate concentration on the performance of BPB/PVB films and the post-irradiation stability in different storage conditions were investigated.     

Orientational dependence of linear dichroism exemplified by dyed spherulites

D-sorbitol forms so-called spherulites from under-cooled melts. These polycrystalline formations have optically uniaxial radii. Melts pressed between glasses crystallize as plane sections of spheres. Dyes that are soluble in molten sorbitol become oriented as the crystallization front passes through the melt so as to form disks with large linear dichroism in the absorption bands of the dyes. The dyeing of spherulites is thus a general method of solute alignment. The linear optical properties of sorbitol spherulites containing the azo dye amaranth were analyzed in detail so as to correct a persistent confusion in the literature regarding the orientational dependence of linear dichroism. In cases involving thin film dichroism of multilayered samples requiring many corrections of intensity data in non-normal incidence, some authors have taken transmittance and others absorbance as having a cosine-squared angular dependence on the plane of the electric vector of linearly polarized light. Plane sections of doped spherulites present all orientations of an electric dipole oscillator in spatially localized region in normal incidence. As such, the samples described herein are ideally suited to resolving this confusion. Images of transmittance of dyed spherulites in polarized light were recorded with a CCD camera and simulated under the assumption that both absorbance and transmittance show a cosine-squared angular dependence but with respect to different angles. Transmittance with a cosine-squared dependence follows azimuthal rotations of the spherulite radii around the wave vector, while absorbance with a cosine-squared dependence follows rotations about axes perpendicular to the wave vector, natural consequences of the properties of the optical indicatrix that are often overlooked. Spherulites obviate the substantial experimental complexities that are engendered in non-normal incidence by sample reorientation. Thus, the principles of anisotropic absorption are given in a complete and intuitive fashion.     

Colouring mechanism of dyed KDP crystal by quantum chemistry

Dye adsorption mechanism, in particular, colouring mechanism of KDP (KH₂PO₄) crystal was investigated by quantum chemistry in this study. Phenomena, such as different preferentially coloured faces of KDP when co-crystallised with different dyes, are explained by the minimum and maximum values of electrostatic potential (ESP). Furthermore, it is found that the ESP distribution of a dye molecule may not necessarily be the single mechanism affecting the dye adsorption in a crystal structure; and that the degree of protonation, crystal surface condition, steric exclusion of dye and the orientation of dye molecules situating on the crystal surface may as well be important factors for the dye adsorption.     

Electrokinetic studies of cellulosic fibres I. Zeta potential of fibres dyed with reactive dyes

Summary The influence of reaction between a reactive dye molecule and cotton cellulose on the zeta potential of the cellulosic fibres has been studied by streaming potential method. As a result of such a reaction the negative value of zeta potential was decreased and the extent of this decrease was proportional to the amount of dye entered into the reaction. With respect to the influence of various structural features of a reactive dye molecule on the zeta potential of dyed fibres, it was observed that the zeta potential was independent of the type of reactive system but was very much dependent on the number of –SO₃H groups in the dye molecule and the chemical constitution of the chromophoric system in the dye structure.A bifunctional reactive dye (Remazol Black B —C. I. Reactive Black 5) has been shown to form crosslinks between cellulose chains and bring about considerable lowering of negative zeta potential of the dyed fibres as compared to the equivalent amount of same dye but in the modified form to act as a monofunctional reactive dye. This bifunctional dye was also observed to induce H-bonding in the vicinity of the sites of cross-links. Trichloropyrimidine type of dyes have been found to be neither completely monofunctional nor fully bifunctional but seem to lie in between the monofunctional and bifunctional types of dyes.

---

Zusammenfassung Der Einfluß der Reaktion zwischen einem reaktiven Farbstoffmolekül und Baumwollzellulose auf das-Potential der Zellulosefasern wurde mit der Strömungspotential-Methode untersucht. Als Ergebnis einer solchen Reaktion sank der negative-Potentialwert ab, und die Abnahme war proportional dem Betrag an Farbstoff, der in Reaktion trat. Im Hinblick auf den Einfluß verschiedener struktureller Eigenschaften eines reaktiven Farbstoffmoleküls auf das-Potential der gefärbten Faser wurde festgestellt, daß letzteres unabhängig vom Typ des Reaktions-systems war, abet sehr abhängig von der Zahl der –SO₃H-Gruppen im Farbstoffmolekül und der Konstitution des chromophoren Systems.Ein zweifunktionaler reaktiver Farbstoff (Remazol Black B — C. I. Reactive Black 5) bildet Vernetzungen zwischen Zelluloseketten und erniedrigt beträchtlich das negative-Potential der gefärbten Fasern, verglichen mit einem Farbstoff in modifizierter Form, so daß er als monofunktioneller Farbstoff wirkt. Dieset zweifunktionale Farbstoff induziert auch Wasserstoffbrücken in der Nachbarschaft der Vernetzungsstellen. Farbstoffe von Trichlorpyrimidin-Typ sind weder streng monofunktionell noch voll bifunktionell. Sie liegen in der Mitte.

---

---

With 11 figures     

Laser addressed thermo-optic effect in a novel dyed liquid-crystalline polysiloxane

Initial experimental evaluation of a novel liquid-crystalline polysiloxane for thermo-optical recording is presented. A versatile system using a single laser source has been used to gather information on the dynamics of laser addressing. To ensure the most stable, highest-contrast pixel the polymer must be heated through its biphasic region and some way into the isotropic phase. It was found that at 60°C using laser pulses of 300μs or less, write-in and selective erasure times were on the submillisecond timescale, and that bulk erasure required 1-2 min. The use of the polymer in an analogue optical store has been demonstrated and an unoptimized sensitivity of 12nJ/μm² for 632°8 nm light was found at 24°C.     

Laboratory and outdoor assessment of UV protection offered by flax and hemp fabrics dyed with natural dyes

The safest protection from UV radiation (UVR) exposure is offered by clothing and its protectiveness depends on fabric composition (natural, artificial or synthetic fibers), fabric parameters (porosity, weight and thickness) and dyeing (natural or synthetic dyes, dye concentration, UV absorbing properties, etc.). In this study the UV protection properties of two fabrics made of natural fibers (flax and hemp) dyed with some of the most common natural dyes were investigated. UVR transmittance of fabrics was measured by two methods: one based on the utilization of a spectrophotometer equipped with an integrating sphere (in vitro test), and the other based on outdoor measurements taken by a spectroradiometer. Transmittance measurements were used to calculate the ultraviolet protection factor (UPF). Experimental results revealed that natural dyes could confer good UV protection, depending mainly on their different UVR-absorbing properties, provided that the fabric construction already guaranteed good cover. An increase in cover factor caused by the dyeing process was also detected. Weld-dyed fabrics gave the highest protection level. The comparison between the two methods applied to measure fabric transmittance pointed out that the UPFs calculated by in vitro measurements were generally lower than those based on outdoor data, indicating an underestimation of the actual protection level of tested fabrics assessed by the in vitro test.     

Structure induced by irradiation of femtosecond laser pulse in dyed polymeric materials

We investigated the structures induced by an irradiation of a near‐infrared (NIR) femtosecond laser pulse in dye‐doped polymeric materials {poly(methyl methacrylate) (PMMA), thermoplastic epoxy resin (Epoxy), and a block copolymer of methyl methacrylate and ethyl acrylate‐butyl acrylate [p(MMA/EA‐BA) block copolymer]}. Dyes used were classified into two types—type 1 with absorption at 400 nm and type 2 with no absorption at 400 nm. The 400‐nm wavelength corresponds to the two‐photon absorption region by the irradiated NIR laser pulse at 800 nm. Type 1 dye‐doped PMMA and p(MMA/EA‐BA) block copolymer showed a peculiar dye additive effect for the structures induced by the line irradiation of a NIR femtosecond laser pulse. On the contrary, dye‐doped Epoxy did not exhibit a dye additive effect. The different results among PMMA, p(MMA/EA‐BA) block copolymer, and Epoxy matrix polymers are supposed to be related to the difference of electron‐acceptor properties. The mechanism of this type 1 dye‐additive‐effect phenomenon for PMMA and p(MMA/EA‐BA) block copolymer is discussed on the basis of two‐photon absorption of type 1 dye at 400 nm by the irradiation of a femtosecond laser pulse with 800 nm wavelength and the dissipation of the absorbed energy to the polymer matrix among various transition processes. Dyes with a low‐fluorescence quantum yield favored the formation of thicker grating structures. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 2800–2806, 2002     

Investigation characteristics of polyvinyl alcohol film dyed methylene blue and irradiated by gamma source

Journal of Radioanalytical and Nuclear Chemistry - The polyvinyl alcohol (PVA) films dyed methylene blue containing different masses of boric acid and PVA powder were investigated. The dyed PVA...     

The application of diffuse reflectance laser photolysis to study photochemistry at interfaces and in dyed fabrics

Recently we have extended to heterogeneous, opaque and often highly scattering systems, the application of flash photolysis by using diffuse reflected light instead of transmitted light as the analysing source on timescales extending from several seconds to picoseconds. Laser-induced transient spectra and decay kinetics have been observed from a wide variety of samples including fractions of monolayers of organic molecules adsorbed on catalytic metal oxide surfaces, within inorganic and organic microcrystals, from dyed fabrics and from paper pulp. The potential of the technique to study photochemical reactions at interfaces is demonstrated with particular reference to ion-electron recombination on porous silica surfaces and to photochemical and photophysical processes occurring in dyed fabrics.     

Production and validation of model iron-tannate dyed textiles for use as historic textile substitutes in stabilisation treatment studies

Adsorption of methylene blue (MB) on agar was investigated as a function of temperature (308-328 K), different concentrations of NaCl and HCl and various weight percentages of binary mixtures of ethanol with water. It was observed that the maximum experimental adsorption capacity, q _{m, exp}, in water is up to 50 mg g^-1 and decreases with increase in weight percentage of ethanol and NaCl and HCl concentration compared to that of water. Analysis of data using ARIAN model showed that MB adsorbs as monomer and dimer on the surface of agar. Binding constants of MB to agar were calculated using the Temkin isotherm. The process is exothermic in water and other solutions. The mean adsorption energy (E) value indicated binding of MB to agar is chemical adsorption. Kinetics of this interaction obeys from the pseudo-second-order model and diffusion of the MB molecules into the agar is the main rate-controlling step.     

Enlightening the influence of mordant, dyeing technique and photodegradation on the colour hue of textiles dyed with madder - A chromatographic and spectrometric approach

Wool samples were dyed with madder and alum, copper, and iron salts at different concentration by pre-mordanting (MD) and simultaneous mordanting (M + D) procedures. Samples were artificially aged to identify the influence of the mordant on the madder chromophores photodegradation. A set of analytical techniques was used for complete characterisation of the dyed fibres before and after light exposure, which included colour and chromophore analysis (colourimetry and LC-ESI-MS/MS analysis), determination of mordant ions amounts in the fibres (FAAS and ICP-OES analysis), morphological characterisation of the fibres and punctual chemical analysis (SEM-EDS studies).Fibre colour hue was found to be dependent on the mordant ion nature, mordant bath concentration and dyeing procedure. Mordant ion quantification showed that the uptake of metal ion by the fibres is relatively small, with the Cu ion presenting the highest affinity for the fibre. MD method yields fibres with higher amounts of metal ions and larger chromophore chromatographic peak areas corresponding, in general, to stronger colour hues. Photodegradation was more severe in alum mordant samples and in the first 480 h of light exposure. Chromophore degradation rates are unequal and dependent on the mordant nature, contributing for colour changes observed after light exposure.