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PubMed2001

Dye removal from textile dye wastewater using recycled alum sludge.

The removal of dyes from textile dying wastewater by recycled alum sludge (RAS) generated by the coagulation process itself was studied and optimized. One hydrophobic and one hydrophilic dye were used as probes to examine the performance of this process. It was found that RAS is a good way of removing hydrophobic dye in wastewater, while simultaneously reducing the fresh alum dosage, of which one third of the fresh alum can be saved. The back-diffusion of residued dye from the recycling sludge is detected but is easily controlled as long as a small amount of fresh alum is added to the system. The use of RAS is not recommended for the removal of hydrophilic dyes, since the high solubility characteristics of such dyes can cause deterioration in the water quality during recycling.

Alum Compounds↗
PubMedDate not supplied

Comparative molecular surface analysis (CoMSA) for modeling dye-fiber affinities of the azo and anthraquinone dyes.

Despite recent investigations aimed at modeling 3D QSAR for dye molecules a controversy still exists: can a pharamacophore hypothesis be used for such purposes. In the present publication we reported on the application of the CoMSA method for modeling 3D QSAR of azo and anthraquinone dyes. We obtained very predictive models, which significantly outperform those reported in the previous CoMFA studies, especially for the azo dyes. Our results proved the previous conclusion that steric requirements are far less pronounced for the cellulose cavities than for the classical drug receptor. Moreover, our results indicate that all molecular surface segments are important for dye-fiber interactions, which also makes an important difference in relation to the classical drug pharmacophore. On the other hand, high predictivity of the CoMSA models indicates that a pharmacophore concept is suitable for the description of the dye-fiber interactions. However, this pharmacophore must substantially differ from the drug pharmacophore used for the illustration of the drug-receptor interactions. From a theoretical point of view dye-cellulose interactions can be an interesting case in which shape decides the activity rules not by the steric repulsion but as a cofactor determining the electrostatic potential distribution.

Journal Article↗
PubMed2005

Luminescence properties of the mixed J-aggregate of oxacyanine dye and thiacyanine dye. Formation of a persistence-type aggregate.

The monolayer assemblies incorporating the J-aggregates of oxacyanine dye, N,N'-dioctadecyloxacyanine perchlorate (S9), and thiacyanine dye, N,N'-dioctadecylthiacyanine perchlorate (S11), S9(J) + S11(J), have been fabricated by the Langmuir-Blodgett (LB) technique. The mole fraction X of S11, X = [S11]/([S9] + [S11]), was varied from 0 to 1. Steady-state absorption spectra, fluorescence spectra, and picosecond fluorescence decay curves of the monolayer assemblies have been measured. Spectroscopic properties of the monolayer assemblies incorporating the individual dye aggregates, S9 J-aggregate (S9(J), X = 0) or S11 J-aggregate (S11(J), X = 1), are characterized by a distinct J-band and resonance fluorescence at lambda(ab) = 403 nm and lambda(em) = 403 nm for S9(J) and lambda(ab) = 456 nm and lambda(em) = 463 nm for S11(J). On the other hand, absorption spectra of the S9(J) + S11(J) assemblies for X = 0.1-0.9 display two absorption bands, a shorter wavelength one and a longer wavelength one, whose peak positions are blue-shifted from those of the corresponding J-bands of the S9 J-aggregate and the S11 J-aggregate, respectively. Furthermore, fluorescence spectra are characterized by a single band (longer wavelength fluorescence) which is somewhat blue-shifted from the resonance fluorescence of the S11 J-aggregate. The fluorescence lifetimes of the S11 J-aggregate and isolated S11 molecules in LB films appear to be tau = 110 and 1900 ps, respectively, while the fluorescence lifetime of the longer wavelength fluorescence of the S9(J) + S11(J) assemblies takes practically a constant value of tau = 170-180 ps for X = 0.2-0.8. These observations would indicate that S9 and S11 molecules in the S9(J) + S11(J) assembly can form a specific mixed aggregate distinct from the individual S9 and S11 J-aggregates. From detailed considerations of the former works on luminescence properties of the S9 J-aggregate doped with isolated S11 molecules, as well as the mosaic-type mixed J-aggregate (M-aggregate) composed of a certain thiacyanine dye, 3,3'-disulfopropyl- 5,5'-dichlorothiacyanine sodium salt, and thiacarbocyanine dye, meso-substituted 3,3'-disulfopropyl-5,5'-dichlorothiacarbocyanine potassium salt, it is suggested that S9 and S11 can form a homogeneous aggregate of the persistence type (HP-aggregate). The HP-aggregate is distinguished from the M-aggregate because it is characterized by homogeneous mixing of two component dyes and persistence of two absorption bands.

Carbocyanines↗
PubMed2005

A strategy to increase the efficiency of the dye-sensitized TiO2 solar cells operated by photoexcitation of dye-to-TiO2 charge-transfer bands.

Dye-sensitized nanoporous TiO2 solar cells (DSSCs) can be classified into two types, namely, Type-I and Type-II. Type-I DSSCs are the DSSCs in which electrons are injected from the adsorbed dyes by photoexcitation of the dyes followed by electron injection from the excited dyes to TiO2 (pathway A). Type-II DSSCs are the DSSCs in which electrons are injected not only by pathway A but also by direct one-step electron injection from the dyes to TiO2 by photoexcitation of the dye-to-TiO2 charge-transfer (DTCT) bands (pathway B). The DSSCs employing catechol (Cat) or its derivatives as the sensitizers have been the typical examples of Type-II DSSCs. However, their solar energy-to-electricity conversion efficiencies (eta) have never exceeded 0.7%, and the external quantum efficiencies (EQE) at the absorption maximums of the DTCT bands have never exceeded 10%. We found that the attachment of electron-donating compounds such as (pyridin-4-yl)vinyl and (quinolin-4-yl)vinyl, respectively, to Cat (designated as Cat-v-P and Cat-v-Q, respectively) leads to 2- and 2.7-fold increases, respectively, in eta, driven by large increases in short circuit current (Jsc). The EQE increased from 8.5 to 30% at 400 nm upon changing from Cat to Cat-v-P, at which only the DTCT band absorbs. In the case of the Cat-v-Q-sensitized DSSC, even the eta obtained by exciting only the DTCT band was higher than 1%. Interestingly, the illumination of only the DTCT band resulted in the increase of fill factor from 62.6% to 72.3%. This paper provides for the first time an insight into the strategy to increase the eta values of Type-II DSSCs.

Adsorption↗
PubMed2003

Highly-efficient metal-free organic dyes for dye-sensitized solar cells.

A solar-to-electric conversion efficiency of 6.1% is achieved with this new dye, compared to 6.3% for N3 dye under the same experimental conditions. Although these indoline dyes are slightly less efficient than N3 dye, the cost of indoline dye is much less than for N3 due to ease of preparation. Furthermore, indoline dyes are shown to be highly stable to photoredox processes by cyclic voltammogram.

Journal Article↗
PubMed1983

Cloning and insertional inactivation of the dye (sfrA) gene, mutation of which affects sex factor F expression and dye sensitivity of Escherichia coli K-12.

Deletions of the Escherichia coli K-12 chromosome between trpR and thr render the bacterium sensitive to the dye toluidine blue (Dye-), and if male (Hfr or F'), the strain is sterile (Fex-), failing to donate F' or chromosomal markers and resistant to male-specific phages as a consequence of its inability to elaborate F pili. A 6-kilobase SalI fragment of E. coli chromosomal DNA cloned into the plasmid pBR322 has been shown to complement both the Dye- and Fex- phenotypes. Insertion of the transposon gamma delta (Tn1000) into a specific part of this plasmid invariably results in both the Dye- and Fex- phenotypes, indicating that these phenotypes derive from mutation in a single gene. Complementation tests between such insertions and sfrA4, a previously isolated mutation resulting in a Fex- phenotype and reported to code for a transcriptional control factor for F (L. Beutin, P. A. Manning, M. Achtman, and N. Willetts, J. Bacteriol. 145:840-844, 1981), indicated that dye and sfrA4 were mutations in a single cistron. It is proposed that the dye (sfrA) gene product is necessary not only for efficient transcription of the F factor genes, but also for some component(s) of the bacterial envelope, loss of which results in sensitivity to toluidine blue.

Cloning, Molecular↗
PubMed2002

Dye purity and dye standardization for biological staining.

This review starts with a short discussion of what is meant by a pure dye and a brief description of how dyes are produced. A listing of the types of impurities encountered in dyes is made, followed by technical investigations and assessments of dyes and their impurities including methods for separating, identifying and assaying dye components. In the second part of the review, descriptions are given of the standardized staining method approach using standard staining methods for assessing stains, and practical responses to stain impurity including commercial quality control, third-party quality control and standardization of reagents, protocols and documentation. Finally, reference is made to the current state of affairs in the dye field.

Coloring Agents↗
PubMed1990

[Genotoxicity of synthetic dyes in the umu test using Salmonella typhimurium TA1535/pSK1002 (II). Results of examination of basic dyes].

In the present study, SOS-inducing activity of 76 basic dyes was investigated by umu test using Salmonella typhimurium TA1535/pSK1002 under the condition of absence and presence of rat liver microsomal fraction. The test was carried out with five doses of basic dyes (400, 120, 40, 12, and 4 micrograms/ml). The samples showing beta-galactosidase activity more than 1.5-fold over the background level were reexamined and the dose-response curves were prepared at various doses. Thereafter, samples showing beta-galactosidase activity unit more than 1.5-fold of the background level were defined as genotoxic. Among the basic dyes examined, 13 compounds induced umu gene expression. The potent genotoxic compounds without metabolic activation were Blue 40, Blue 47, Brown 14, Orange 30, Red 24, Violet 30, Violet 31, Yellow 13(h), Yellow 19, Yellow 25, Yellow 67, and Yellow 73 and in the presence of S9, Orange 47 was judged as genotoxic in addition to the aforementioned dyes. An evident dose-response relationship between the doses of the dye and umu gene expression was observed in these 13 dyes.

Coloring Agents↗
PubMed2000

Dye- and gamma probe-guided sentinel lymph node biopsy in breast cancer patients: using patent blue dye and technetium-99m-labeled human serum albumin.

BACKGROUND: Sentinel lymph node (SLN) biopsy is a promising method for the diagnosis of the axillary nodal status. We examined the availability of the SLN biopsy using two mapping procedures: the dye- and gamma probe-guided method, and preoperative lymphoscintigraphy by gamma camera imaging. METHODS: We enrolled 48 patients with breast cancer. Technetium-99m-labeled human serum albumin was injected into the subdermal tissue above the primary tumor or biopsy cavity, and preoperative gamma camera imaging was performed. After induction of general anesthesia, patent blue dye was injected into the peritumoral area prior to the surgical procedure. A handheld gamma-detection probe was used to assist in SLN detection. Careful dissection was performed to identify blue-stained afferent lymphatic vessels and nodes. An SLN was defined as any blue and/or radioactive node, and was excised. After SLN biopsy, axillary lymph node dissection of level I, II, and III was completed, in order to confirm the diagnostic ability of the SLN biopsy. RESULTS: Intraoperative SLN identification of axillary lesions was successful in 43 of 48 patients (90%). The dye- and gamma probe-guided method was successful in 25 patients (52%), the dye-guided method alone succeeded in 11 patients (23%), and the gamma probe-guided method alone succeeded in 7 patients (15%). Preoperative lymphoscintigraphy revealed axillary focal accumulations in 29 of 48 patients (60%). All patients who underwent successful preoperative SLN identification by lymphoscintigraphy had successful intraoperative SLN identification. A diagnostic accuracy of 95%, a sensitivity of 89%, and a specificity of 100% were achieved in the diagnosis of axillary metastasis. Internal mammary SLNs were identified in four patients intraoperatively, but we could not detect cancer metastasis in the internal mammary SLNs. CONCLUSIONS: The dye-guided and gamma probe-guided methods were complementary. Preoperative lymphoscintigraphy was useful to predict intraoperative SLN identification. Further study is necessary to assess the role of SLN biopsy of the internal mammary lymph nodes.

Adult↗
PubMed2005

Evaluation of an integrated anaerobic/aerobic SBR system for the treatment of wool dyeing effluents. Purification of wool dyeing effluent in a SBR.

This work examined the performance of a sequencing batch reactor treating dyeing effluents from a factory that processes mainly wool and wool/polyester blends. Different operational conditions were evaluated, namely the influence of the anaerobic and the subsequent aerobic phase on the organic load removal, as well as the effect of the length of the aeration period (from 8 to 12 h) on process efficiency. A comparison between a fill stage in fast and slow modes was carried out. Results indicate that the cycle 2 conditions (fast fill and 12 h aeration time) improved the overall efficiency (85+/-6% soluble COD and 95+/-4% BOD5 removal yields) with a predominant COD uptake occurring in the aerobic stage. Slow, linear COD removal was observed in the anaerobic phase, in contrast with an exponential COD decrease in the oxic phase. For SS a level under 100 mg/l was general achieved in the exit of the reactor. With respect to dye degradation, a noticeable decrease of the absorbance measured in the UV-visible range was observed. This could be explained by the reduction of the azo bonds of some of the present dyes in the anaerobic step, in which ORP values lower than -400 mV were attained. Some oxidation of anthraquinone sulphonate dyes and of the aromatic amines resulting from azo bond cleavage could also have been taken place, as well as bioelimination mechanisms such as dye sorption.

Aerobiosis↗
PubMed1990

A simple dye-coupling assay for evaluating gap junctional communication: the importance of transcription and translation on the establishment of dye-coupling.

A simple dye-coupling assay has been developed to study gap junctional communication using a uterine cell line. The new dye-coupling assay was found to be of comparable sensitivity to an autoradiographic assay for transfer of radiolabelled nucleotide. To investigate the importance of protein synthesis in the establishment of dye-coupling under the conditions of this assay, cultures were treated with actinomycin-D and cycloheximide to inhibit transcription and translation, respectively. Inhibition of transcription had no significant effect on dye-coupling. The protein synthesis inhibitor, cycloheximide, also had no significant effect on dye-coupling at concentrations up to 1 uM, even though protein synthesis was inhibited to 19% of control.

Cell Communication↗
PubMed2006

Comparison of dye adsorption by mesoporous hybrid gels: understanding the interactions between dyes and gel surfaces.

Without using any templating agents, mesoporous hybrid gels were prepared using mixtures of tetraethoxysilane (TEOS) with n-propyltriethoxysilane (PTES), bis(trimethoxysilyl)hexane (TSH), or bis(trimethoxysilylpropyl)amine (TSPA) as precursors. Fourier transform infrared (FTIR), N2 adsorption/desorption, thermogravimetry (TG), point of zero charge (PZC), and water vapor adsorption measurements were used to characterize the gels. The adsorption of methyl orange (MO), methyl red (MR), bromocresol purple (BP), phenol red (PR), neutral red (NR), and brilliant blue FCF (BBF) by the gels in both 0.01 M HCl and 0.01 M NaOH solutions was compared comprehensively. The gel derived from TEOS/TSH (with -(CH2)6- groups, Gel 2) has the largest specific surface area (695 m2 g(-1)), the smallest pore volume (0.564 cm3 g(-1)), and the smallest average pore size (3.7 nm). The gels derived form TEOS/PTES (with -(CH2)2CH3 groups, Gel 1), and TEOS/TSPA (with -(CH2)3NH(CH2)3- groups, Gel 3) have similar textual properties. The PZC of Gels 1, 2, and 3 was estimated to be 6.28, 6.20, and 6.88, respectively. Gel 3 has the highest PZC due to the presence of -NH- groups. In general, Gel 2 shows the highest dye adsorption among all the gels in both acidic and basic solutions. All the dyes except NR have much lower adsorption in basic solutions than in acidic solutions. In acidic solutions Gels 1 and 2 have similar adsorption trends for the dyes, except for BP, with NR having the highest adsorption, and PR the lowest adsorption. Gel 3 presents a different trend from Gels 1 and 2, with BBF having the highest adsorption, and MR the lowest adsorption. In basic solutions the order of dye adsorption by all the gels is shown to follow the sequence NR>>MR approximately BBF>MO>BP approximately PR. The adsorption results can be explained by considering the textural properties of the gels and the interactions between the gel surfaces and the dyes, which include hydrogen bonding, electrostatic, and hydrophobic interactions.

Journal Article↗
PubMed2003

Development of a rapid, sensitive, dye immunoassay for schistosomiasis diagnosis: a colloidal dye immunofiltration assay.

The colloidal dye immunofiltration assay (CDIFA) combines the concepts of the double-antigen sandwich assay, the Dot immunofiltration assay, and colloidal dye-linked antigen technique to produce a new dye immunoassay for antibody detection in schistosomiasis. The CDIFA consisted of soluble egg antigen (SEA) of Schistosoma japonicum coated onto nitrocellulose membrane, mounted on a flow-through test device to provide the assay capture matrix. SEA absorbed to a red colloidal dye, R-3, produced in China, served as the antigen-antibody complex detecting reagents. The results showed that the sensitivity of the CDIFA was 100% in 35 cases of acute schistosomiasis (35/35), 98% in 50 cases of chronic schistosomiasis (49/50). The specificity of the assay was 99.4% in 180 healthy individuals (179/180). The cross-reaction was 13.3% in 30 cases of paragonimiasis, 2.6% in 38 cases of clonorchiasis sinensis and 0% in 20 cases of hookworm infection, 20 cases of fasciolopsiasis and 16 cases of ascariasis. The results were similar to those detected by routine enzyme-linked immunosorbent assay (ELISA). In a field evaluation of the CDIFA kit, the positivity rate of the CDIFA was 97.5% in 157 cases of schistosomiasis, compared with 91.1% with the circumoval precipitin test (COPT). The dye-labeled SEA conjugate was stable at room temperature for at least 6 months. The results indicated that the CDIFA provided an economic, simple, rapid, robust test for the detection of schistosome infection, suitable for a wide variety of field applications without any instrumentation.

Acute Disease↗
PubMed1998

MALDI mass spectrometry of dye-peptide and dye-protein complexes.

Immobilized sulfonate dyes are widely used for protein separation and purification, but the mode of interaction between the dye molecules and the proteins is largely unknown. Here we show that specific noncovalent dye-protein and dye-peptide complexes can be observed using MALDI mass spectrometry. We prove that the interaction is prodominantly electrostatic and that it involves protonated sites of the peptides and proteins, including the NH2 terminus, and deprotonated SO3 groups of the dyes. Furthermore, we show that MALDI-MS of such complexes with a nonacidic matrix, p-nitro-aniline, can be used to determine the number of accessible basic sites of a protein or peptide in its folded structure. Our results are in good agreement with measurements of the same property done with electrospray ionization.

Adrenocorticotropic Hormone↗
PubMed1981

Synthesis and properties of acrylamide-substituted base pair specific dyes for deoxyribonucleic acid template mediated synthesis of dye polymers.

We have tried to construct synthetic polymers for sequence-specific recognition and complexation of longer deoxynucleotide sequences. For this purpose, we developed a method of template-directed polymerization of basic pair specific DNA ligands such as basic dyes. The template-directed polymerization consists in a copolymerization of various dyes of different specificities staying simultaneously in a binding equilibrium with DNA. In the present paper, we describe the synthesis and the properties of base pair specific monomers especially designed for performance of radical chain polymerization reactions in aqueous medium at room temperature. Different acrylamide derivatives of well-known dyes, such as AT-specific malachite green and GC-specific phenyl neutral red, were synthesized and studied for their ability of base pair specific complex formation with DNA of different base composition. Partition equilibrium dialysis and dye titration agarose gel electrophoresis were used to ensure for several dyes that they may be incorporated into different polymers via copolymerization of their acrylamido derivatives with various small base-unspecific monomers without substantial change of their binding parameters. Furthermore, we demonstrate that acrylamide and other small acrylamide derivatives can be used as building blocks for the synthesis of polymeric links between base pair specific monomers. The results and their consequences for template polymerization reactions are discussed.

Acrylamides↗
PubMedDate not supplied

Spectroscopic characterization of SC-NTR: a subsidiary dye of allura red AC dye (FD&C red no. 40).

A major subsidiary dye in US certified Allura Red AC dye (FD&C Red No. 40) has been isolated by preparative high performance liquid chromatography. The paper chromatographic properties of the isolated dye indicate that it is the dye designated as SC-NTR in a previous paper (Marmion 1971). Spectroscopic analysis of the isolated dye is consistent with the disodium salt of 6-hydroxy-5-(2-methoxy-5-methyl-3-sulphophenylazo)-2-naphthalen esulphonic acid, which is an azo-coupling product between the meta-isomer of cresidine-p-sulphonic acid (CSA) and Schaeffer's salt (SS).

Azo Compounds↗
PubMed1979

Studies on the toxicity of coal-tar dyes. I. Photodecomposed products of four xanthene dyes and their acute toxicity to fish.

The acute toxicity of photodecomposed products of Erythrosine, Eosine, Phloxine and Rose Bengale were studied, since it was found that toxicity of these dyes to fish increased after the dyes had been photoirradiated. Photodecomposed products of the dyes were isolated and identified with UV, IR, NMR spectra and the acute toxicity of those compounds were determined by TLm test. As results of these studies, it became clear that the toxicity of photodecomposed organic products (dehalogenated compounds of dyes) were lower than the mother compounds. The increases in toxicity of the xanthene dyes by photo-irradiation were attributed to the liberated halogens by irradiation.

Animals↗
PubMed2001

A new technology for harnessing the dye polluted water and dye collection in a chemical factory.

A new technology for harnessing the dye polluted water and dye collection was developed. It is based on the enhanced evaporation by using solar, wind and air temperature energy and additional heat-electric energy. It consists of four parts: (1) evaporation carrier system (evaporation carrier and frame for evaporation carrier) for polluted water; (2) polluted water circulating system (pumping-spraying-collecting); (3) heating system; (4) workshop with polluted water reservoir-tanks and rainfall prevention roof. The polluted water was (heated in case necessary) sprayed to the evaporation carrier system and the water was evaporated when it moved in the space and downward along the carrier mainly by using natural (solar, wind and air temperature energy). In case, when there is no roof for the carrier system, the polluted water can be stored in the reservoirs (storage volume for about 20 days). The first 10-25 mm rainfall also need to be stored in the reservoirs to meet the state standard for discharging wastewater. The dye may be collected at the surface in the reservoir-tanks and the crystallized salt may be collected at the bottom plate. The black-color wastewater released by the factory is no more discharged to the surface water system of Taihu Lake Basin. About 2 kg dye and 200 kg industrial salt may be collected from each tone of the polluted water. The non-pollution production of dye may be realized by using this technology with environmental, economical and social benefits.

Chemical Precipitation↗