Oxidation Of Dye Research Articles

A review of developments in industrial hair colorant actives for oxidative dyes

AbstractThis paper reviews developments in industrial colorants as active ingredients of commercial products that rely on oxidative chemistry for the coloration of human hair. After outlining the regulatory challenges faced by the industry, which are shaping the landscape of colorant usage, the most commercially important actives utilised in oxidative hair colorant formulations are surveyed from the perspective of their chemistry and economics. Some developments in the form of recently introduced actives are also described.

Gallic acid influence on azo dyes oxidation by Fenton processes

ABSTRACT The present work consisted in evaluating the effect of a natural plant reducer, gallic acid (GA), on the discolouration/oxidation of two azo dyes by Fenton processes (Fe3+/H2O2 and Fe2+/H2O2). A kinetic study was performed to better interpret the discolouration data at different temperatures. The 1st-order kinetic model presented the best fit for the experimental data of methyl orange discolouration, while the 2nd-order was better for chromotrope 2R. Due to the addition of GA and the temperature rise, there were increases in discolouration and in the reaction rate constant values. As a highlight, it was possible to verify the reduction of the apparent activation energy (Ea) due to the presence of GA. For example, Ea for discolouring methyl orange corresponded to 81.5 and 53.6 kJ.mol−1 by Fe2+/H2O2 and Fe2+/H2O2/GA, respectively. Thus, it can be inferred that the GA reduces the energy barrier to increase the oxidation of dyes by Fenton processes.

Selective oxidation and direct decolorization of cationic dyes by persulfate without activation

The aim of this work was to investigate the selective oxidation and direct decolorization of selected organic dyes (Methylene Blue (MB), Rhodamine B (RhB) and Orange II (OrgII)) by persulfate (PDS) without activation. Results show that the decolorization rate of MB was up to 58.0% within 10 minutes, while those of RhB and OrgII were only about 29.6% and 3.0% after 80 minutes, respectively. In comparison with the negligible impacts of pH from 2.0 to 9.0 on MB and OrgII decolorization, RhB decolorization rate obviously varied with the pH changes, and acid pH condition was beneficial for RhB decolorization. Quenching tests implied that the decolorization of dyes by PDS without activation was a nonradical oxidation process rather than sulfate radical oxidation. A plausible mechanism is that the decolorization process is attributed to the charged states of the dyes at different pH conditions, and thus direct electron transfer from dyes to PDS may occur, which is responsible for the bleaching of dyes. This study points out the potential bleaching capability of PDS without activation on cationic dyes, which may have important implications for selective oxidation treatment of dye wastewater.

Fenton oxidation of synthetic food dyes by Fe-embedded coffee biochar catalysts prepared at different pyrolysis temperatures: A mechanism study

• Fe-embedded coffee biochar catalysts were synthesized at high pyrolysis temperatures. • Improving catalytic properties was most pronounced for Fe@HCBC prepared at 700 °C. • Fe@HCBC700/H 2 O 2 system showed the highest degradation of synthetic food dyes. • ESR study demonstrated a significant role of •OH in degradation of synthetic food dyes. • Heterogeneous Fenton-like reaction governed the degradation of synthetic food dyes. Fe-embedded biochar catalysts originating from waste coffee grounds (Fe@HCBCs) were developed at different pyrolysis temperatures (500, 600, and 700 °C) for the Fenton oxidation of synthetic food dyes: amaranth (AM) and sunset yellow (SY). Increasing the pyrolysis temperature significantly improved the physicochemical properties of the Fe@HCBCs (i.e., surface area, total pore volume, and Fe content), which led to the highest AM and SY removal in the Fe@HCBC700/H 2 O 2 system. The Fe@HCBC700/H 2 O 2 system showed 19.0 and 14.6 mg(dyes)/g(catalysts)·h of catalytic reaction rate for AM and SY, respectively. The results of the scavenging experiment and electron spin resonance revealed that hydroxyl radicals (•OH) were the dominant reactive oxygen species for the oxidation of AM and SY by the Fe@HCBCs/H 2 O 2 system. The heterogeneous Fenton-like reaction between the Fe content of the Fe@HCBC surfaces and H 2 O 2 was the main contributor to the oxidation of AM and SY compared with the homogeneous Fenton reaction caused by aqueous Fe with H 2 O 2 . The effects of catalyst dosage (0.1–0.5 g/L), H 2 O 2 concentration (0.0–12.5 mM), pH (3.0–9.0), and solution temperature (15–35 °C) on the oxidation of AM and SY by the Fe@HCBCs/H 2 O 2 systems at pH 3.0 were also investigated. The opposite result was obtained in a suspension with pH > 5.0; that is, the removal efficiency gradually increased as the pyrolysis temperature decreased (500 °C > 600 °C > 700 °C) because of the abundance of O-containing functional groups on the surface of the Fe@HCBC500. These observations imply that pyrolysis temperatures might have a strong impact on the catalytic degradation of synthetic food dyes using the Fe@HCBCs/H 2 O 2 systems.

Preparation of porous α-Fe2O3 thin films for efficient photoelectrocatalytic degradation of basic blue 41 dye

A novel method was developed for the preparation of porous hematite (α-Fe2O3) thin films. First, a solution containing iron precursor was spin-coated on fluorine-doped tin oxide substrate and later short heat-treated at 750 °C. The prepared α-Fe2O3 thin films were applied as dual-function catalyst in photoelectrochemical (PEC) water oxidation and textile dye degradation studies. For the first time, α-Fe2O3 thin films were used in efficient PEC degradation of a textile dye (Basic Blue 41 – B41) using in-situ generated reactive chlorine species. In comparison with photocatalytic and electrocatalytic approaches, the PEC technique allows faster degradation of B41 dye at an applied bias potential of 1.5 V versus reversible hydrogen electrode and under visible light illumination. In the presence of Cl− using the PEC approach the degradation of B41 reaches 99.8%. High-performance liquid chromatography coupled with UV–VIS system confirmed the degradation of B41 dye using PEC. Gas-chromatography coupled to mass spectrometry was used to study the by-products obtained during PEC degradation. Chemical oxygen demand analyses confirmed that the mineralization level of B41 is in the order of 68%. The α-Fe2O3 films developed in this study give a higher level of PEC degradation efficiency compared to other iron oxide-based systems.

LignoPhot: Conversion of hydrolysis lignin into the photoactive hybrid lignin/Bi4O5Br2/BiOBr composite for simultaneous dyes oxidation and Co2+ and Ni2+ recycling

Valorization of lignin is still an open question and lignin has therefore remained an underutilized biomaterial. This situation is even more pronounced for hydrolysis lignin, which is characterized by a highly condensed and excessively cross-linked structure. We demonstrate the synthesis of photoactive lignin/Bi4O5Br2/BiOBr bio-inorganic composites consisting of a lignin substrate that is coated by semiconducting nanosheets. The XPS analysis reveals that growing these nanosheets on lignin instead on cellulose prevents the formation of Bi5+ ions at the surface region, yielding thus a modified heterojunction Bi4O5Br2/BiOBr. The material contains 18.9% of Bi4O5Br2/BiOBr and is effective for the photocatalytic degradation of cationic methylene blue (MB) and zwitterionic rhodamine B (RhB) dyes under light irradiation. Lignin/Bi4O5Br2/BiOBr decreases the dye concentration from 80 mg L−1 to 12.3 mg L−1 for RhB (85%) and from 80 mg L−1 to 4.4 mg L−1 for MB (95%). Complementary to the dye degradation, the lignin as a main component of the composite, was found to be efficient and rapid biosorbent for nickel, lead, and cobalt ions. The low cost, stability and ability to simultaneously photo-oxidize organic dyes and adsorb metal ions, make the photoactive lignin/Bi4O5Br2/BiOBr composite a prospective material for textile wastewaters remediation and metal ions recycling.

Visible light responsive TiO2 - graphene oxide nanosheets - Zn phthalocyanine ternary heterojunction assisted photoelectrocatalytic degradation of Orange G

Herein, we report on the successful fabrication of a visible light-responsive TiO2 - graphene oxide nanosheets – Zn phthalocyanine (TiO2@GONS@ZnPc) ternary structure for the photoelectrochemical degradation of Orange G azo dye. The characterization of TiO2@GONS@ZnPc composite was achieved using various spectroscopic and microscopic techniques. Our results show that the TiO2@GONS@ZnPc surface hybrid heterojunction promotes charge separation and electron migration, significantly improving the degradation efficiency with an applied potential. For the first time, we show the existence of a non-radical activation route for persulfate (PS) using such π electron-rich ZnPc-GONS catalysts. The degradation kinetics were found to follow pseudo first order kinetics. Electron spin resonance analyses suggested that neither hydroxyl radicals nor sulfate radicals were produced therein, and therefore were not responsible for the persulfate-driven oxidation of the OG dye. These findings suggest that both which GONS and ZnPc play a critical role in mediating the eventual charge transfer mediated PS activation. The results illustrate the remarkable capacity of the TiO2@GONS@ZnPc composite to rapidly degrade Orange G by a coupled TiO2@GONS@ZnPc-persulfate system.

Synthesis and Properties of Modified Aluminum-Containing Framework Compounds

In this work, nickel- and iron-modified aluminum-containing framework compounds—highly porous stable nanomaterials—have been prepared for the first time using magnetron sputtering, an environmentally friendly method. The materials have been characterized by a variety of physicochemical methods: BET measurements, atomic force microscopy, X-ray diffraction, thermogravimetric analysis, and IR spectroscopy. We have assessed the catalytic activity of the synthesized bimetallic framework compounds for the hydrogen peroxide oxidation of an azo dye. The results demonstrate that the addition of a small amount of these catalysts leads to an increase in reaction rate constant. The nickel- and iron-modified aluminum-containing framework compounds have been shown to retain their performance for at least four cycles (with allowance for regeneration via triple treatment with ethanol). A mechanism has been proposed for the hydrogen peroxide oxidation of the dye in the presence of the synthesized metal complexes, in which hydroxyl radicals act as an oxidizing species.

Detection of Single Nucleotide Polymorphisms by Fluorescence Embedded Dye SYBR Green I Based on Graphene Oxide.

The detection of single nucleotide polymorphisms (SNPs) is of great significance in the early diagnosis of diseases and the rational use of drugs. Thus, a novel biosensor based on the quenching effect of fluorescence-embedded SYBR Green I (SG) dye and graphene oxide (GO) was introduced in this study. The probe DNA forms a double helix structure with perfectly complementary DNA (pcDNA) and 15 single-base mismatch DNA (smDNA) respectively. SG is highly intercalated with perfectly complementary dsDNA (pc-dsDNA) and exhibits strong fluorescence emission. Single-base mismatch dsDNA (SNPs) has a loose double-stranded structure and exhibits poor SG intercalation and low fluorescence sensing. At this time, the sensor still showed poor SNP discrimination. GO has a strong effect on single-stranded DNA (ssDNA), which can reduce the fluorescence response of probe DNA and eliminate background interference. And competitively combined with ssDNA in SNPs, quenching the fluorescence of SG/SNP, while the fluorescence value of pc-dsDNA was retained, increasing the signal-to-noise ratio. At this time, the sensor has obtained excellent SNP resolution. Different SNPs detect different intensities of fluorescence in the near-infrared region to evaluate the sensor's identification of SNPs. The experimental parameters such as incubation time, incubation temperature and salt concentration were optimized. Under optimal conditions, 1 nM DNA with 0–10 nM linear range and differentiate 5% SNP were achieved. The detection method does not require labeling, is low cost, simple in operation, exhibits high SNP discrimination and can be distinguished by SNP at room temperature.

Facile Elaboration of Wet Cellulose Film as Catalyst Support of MnOx Nanoparticles for the Catalytic Oxidation of Dyes in Absence of Light

In the present work a remarkably simple procedure for the elaboration of wet cellulose film containing manganese oxide nanoparticles was developed. The films were produced using a mold made by 3D printing using cellulose dissolved in an ionic liquid, which allows the production of thin and homogeneous films of different shapes, types and designs which cannot be made using conventional techniques. Thanks to this possibility, the final catalytic object can be implemented in specific reactors. Manganese oxide nanoparticles were prepared as a colloidal solution by a redox/sol-gel procedure and then deposited on the cellulose films by wet impregnation. The catalytic film obtained was tested in the decomposition of a dye, indigo carmine (IC), in the absence of light. The influence of the pH of the solution on the decomposition rate was investigated. IC total decomposition was measured after 1-h reaction at pH below 3. At pH = 2, no deactivation of the catalyst was observed even after four decomposition cycles. This work provides a new strategy to design cellulose-based catalysts for dye removal from wastewater.

BiOBr/MoS2 catalyst as heterogenous peroxymonosulfate activator toward organic pollutant removal: Energy band alignment and mechanism insight

Utilization of heterogenous catalysts to trigger peroxymonosulfate (PMS) activation is considered an efficient strategy for environmental decontamination. Herein, a tightly bonded flake-like 2D/2D BiOBr/MoS2 heterojunction was successfully designed through co-precipitation process. By virtue of matched energy levels and intimate interfacial coupling, the Type-II BiOBr/MoS2 heterojunction significantly expedited charge carrier transfer and thereby promoted the catalytic performance for organic dye oxidation and Cr(VI) reduction. The specially designed BiOBr/MoS2 heterojunction is also conducive to split PMS and continuously generated highly active species (SO4−, OH and O2–) in a photo-Fenton system, achieving extraordinary catalytic capacity for various emerging organic pollutants (including phenol, bisphenol A and carbamazepine). The photoexcited electron with prolonged lifetime and exposed Mo sites with multivalence and multiphase nature can effectively activate PMS, which further promotes the oxidation efficiency of holes, as confirmed by scavenging experiments. The excellent stability and oxidative properties could justify scale up using BiOBr/MoS2 to a small pilot test, implementing the potential value in practical applications. This study would provide novel insight and cognition of PMS activation via a superior heterojunction for complex polluted wastewater treatment.

Flavonoid-Decorated Nano-gold for Antimicrobial Therapy Against Gram-negative Bacteria Escherichia coli.

Nano-gold (Aunps) have emerged as promising options that exhibit unique features discrete from traditional materials suited for biomedical applications. Aunps were synthesized using flavonoid quercetin (Q) as reducing agent, and resultant nanoparticles were further conjugated with the flavonoid. The resultant nano-system was expected to perform a dual role as antibacterial and as antioxidant agent. Nano-gold surface plasmon peaks were recorded at 560 nm with size around 62 nm and having slim distribution pattern. Spherical particle with smooth surface was observed under TEM and AFM studies. TEM micrographs confirmed a homogeneous particle population of size around 30 nm. Quercetin association to nano-gold was corroborated through FTIR and EDAX analysis. Antioxidant nature of nano-gold prevented rapid oxidation of brilliant cresyl blue dye, in presence of sodium hypochlorite. Antimicrobial action of QuAunp was tested against Gram-negative bacteria Escherichia coli. Nano-gold designed produced a minimum inhibitory concentration of 7.6 μg/ml and minimum bactericidal concentration 10.5 μg/ml against E. coli. Further TEM analysis and membrane permeability studies revealed the impact of QuAunps on bacterial membrane leading to cell damage.

Construction of two cobalt based bi-functional metal-organic frameworks for enhancing electrocatalytic water oxidation and photocatalytic disposals of hazardous aromatic dyes

Two novel Co-MOFs constructed from aromatic polycarboxylic acid named {[Co(tib)2(bimb)2]·4H2O}n (tib = 3-((4-(1H-1,2,4-triazol-1-yl)benzyl)oxy)benzoic acid, bimb = 1,4-bis(imidazole-1-ylmethy) benzene) and {[Co2(bipa)4(bibp)6]}n (bipa = 2-(4-carboxy-2-nitrophenoxy)-6-nitroterephthalic acid, bibp = 4,4′-bis(imidazolyl) biphenyl), have been synthesized under solvothermal conditions and characterized by single-crystal X-ray diffraction, elemental analysis, IR spectra, powder X-ray diffraction (PXRD), thermogravimetric analysis (TG) as well as electrochemistry. The single-crystal X-ray diffraction analysis indicates that Co-MOF 1 exhibits an uninodal net with a (65·8) topology, whereas Co-MOF 2 exhibits an uninodal 4-connected framework with a (44·62) topology. The electrochemistry studies demonstrate that both of the two Co-MOFs can behave as the efficient electrocatalysts for water oxidation in a mild neutral system at the potential around 1.20 V vs. NHE with comparatively low overpotential (η) for Co-MOF 1 and 2 of 337–541 mV vs. NHE. Moreover, the two Co-MOFs also show good photocatalytic degradation capabilities toward MB/MV dyes under UV irradiation, and the mechanism studies demonstrate that the main active species are ·OH radicals. Therefore, these bi-functional Co-MOFs materials can be treated as convenient and efficient catalysts for the oxygen evolution reaction and aromatic dyes degradation.

The use of basalt powder as a natural heterogeneous catalyst in the Fenton and Photo-Fenton oxidation of cationic dyes

The use of naturally present heterogeneous catalysts has recently been an essential issue in the Fenton and photo-Fenton processes. In this study, the uses of basalt as a catalyst for the Fenton and photo-Fenton reactions for methylene Blue (MB) and Basic Red 18 (BR18) degradations were investigated. Basalt was selected because of the presence of the iron (III) oxide in the structure. Basalt was characterized by X-Ray Fluorescence (XRF) and X-Ray Diffraction (XRD) analysis to obtain the chemical composition and the crystalline phase. The surface charge and the surface area were obtained by zeta potential and Brunauer Emmett-Teller (BET) analysis. Fourier Transform Infrared Spectroscopy (FTIR) and scanning electron microscope (SEM) were utilized to explore the functional group and the surface morphology. Fenton and photo-Fenton processes were applied to explore the best degradation method. Adsorption was also tested and the adsorption process had minimum removal efficiency (12% for MB and 17% for BR18). The removal efficiencies for MB and BR18 by the Fenton process were 87% and 28%, respectively. The photo-Fenton process had maximum removal efficiency with 100% for MB and 70% for BR18. The optimum conditions were 70 mg/L dye concentration, 5 mM H2O2, 1.0 g/L basalt loading and pH 2. Basalt has shown reuse capability as a catalyst for three consecutive cycles.

Immobilization of copper oxide nanoparticles onto chitosan biopolymer: Application to the oxidative degradation of Naphthol blue black

In this study, copper oxide nanoparticles, prepared using pistacia vera hull extract, were immobilized onto chitosan. FT-IR spectrum of copper oxide-chitosan exhibited chemical shifting of the main peaks of the biopolymer indicating that hydroxyl and amino groups were reacted with copper oxide nanoparticles. SEM features showed spherical surface and physical stability of the composite. The shifting of the burning temperature in DTA from 278.5 °C to 212.6 °C in the composite proved the interaction between chitosan and copper oxide nanoparticles. The composite was applied for the oxidative degradation of naphthol blue black in the presence of H2O2. The change of copper oxide nanoparticles loading, time, dye concentration, temperature, and oxidant dose were studied. The degradation yield reached 86 % (C0 = 30 mg/L, T=20 °C, H2O2 = 8 mL/L). The activation energy (Ea), entropy (ΔS*) and enthalpy (ΔH*) were equal to 45.558 KJ. mol−1, −116.203 J mol−1 K−1 and 42.986 kJ mol−1, respectively.

A label-free logic gate hairpin aptasensor for sensitive detection of ATP based on graphene oxide and PicoGreen dye

BackgroundIn this paper, a simple, enzyme-free, label-free fluorescence, high sensitivity logic gate hairpin aptasensor was developed for adenosine triphosphate (ATP) detection based on graphene oxide (GO) and PicoGreen dye.MethodsUsing single-strand deoxyribonucleic acid (DNA) and adenosine triphosphate (ATP) as input signal and fluorescence signal as output signal, if single-strand DNA (DNA-L), single-strand DNA (DNA-S), and ATP were present at the same time, one segment of DNA-L formed a hairpin ring with ATP, and the other segment of DNA-L formed a completely complementary hairpin stem with DNA-S. The hairpin DNA was detached from the GO surface, and PicoGreen dye was embedded into the hairpin stem, and the fluorescence signal was enhanced. The molecular logic gate was constructed through the establishment of logic histogram, logic circuit, truth table, and logic formula. The biosensor-related performances including sensitivity, selectivity, and linearity were investigated, respectively.ResultsWe have successfully constructed a AND logic gate. The detection limit of ATP is 138.0 pmol/L (3σ/slope) with detection range of 50–500 nmol/L (R2 = 0.98951), and its sensitivity is 4.748 × 106–6.875 × 108 a.u. (mol/L)−1.ConclusionsThe logic gate hairpin aptamer sensor has the advantages of high sensitivity, low detection limit, and low cost, and can be successfully applied to the detection of adenosine triphosphate (ATP) in actual human urine samples.

Dyeing Method for Polypropylene Fibers Utilizing Reduction and Oxidation of Cationic Dyes

Dyeing Method for Polypropylene Fibers Utilizing Reduction and Oxidation of Cationic Dyes

The Role of Adsorption in the Photocatalytic Decomposition of Dyes on APTES-Modified TiO2 Nanomaterials

This work investigated for the first time the role of adsorption in the photocatalytic degradation of methylene blue and Orange II dyes in the presence of 3-aminopropyltriethoxysilane (APTES)-modified TiO2 nanomaterials. It has been demonstrated that the decrease in adsorption has a detrimental effect on photocatalytic activity. APTES/TiO2 photocatalysts were successfully prepared by solvothermal modification of TiO2 in a pressure autoclave, followed by heat treatment in an inert gas atmosphere at the temperature range from 300 °C to 900 °C. It was observed that functionalization of TiO2 via APTES effectively suppressed the anatase-to-rutile phase transformation, as well as the growth of crystallites size during calcination, and reduction of specific surface area (APTES modification inhibits sintering of crystallites). The noted alterations in the adsorption properties, observed after the calcination, were generally related to changes in the surface characteristics, mainly surface charges expressed by the zeta potential. Positively charged surface enhances adsorption of anionic dye (Orange II), while negatively charged surface was better for adsorption of cationic dye (methylene blue). The adsorption process substantially affects the efficiency of the photocatalytic oxidation of both dyes. The methylene blue decomposition proceeded according to the pseudo-first and pseudo-second-order kinetic models, while the degradation of Orange II followed the zero, pseudo-first, and pseudo-second order kinetic models.

Brief descriptions of the principles of prominent methods used to study the penetration of materials into human hair and a review of examples of their use.

Consumers are attracted to the latest fashion trends and different looks. This drives the search for novel hair treatments. Some chemicals present in hair treatment products can penetrate the hair shaft. These materials can either nourish or injure the hair cortex. Different techniques have been used to investigate the mechanism of molecule penetration and the conditions under which penetration occurs. This article reviews the techniques applied for this purpose. Various microscopy techniques are used to capture clear and colourful images to determine the diffusion pathways and the exact location of the molecules under study. However, the laborious sample preparation often leads to sample destruction since cross-sectioning is often required. While various other techniques have been successfully used for investigating the penetration methods, most of these require different amounts of work to be put in for sample preparation and instrumentation. Several spectroscopic techniques have been used to study the penetration of the molecules because of the high levels of accuracy and the quick response time of these techniques. Moreover, the samples are not damaged during the investigation.

Reutilization of Fe-containing tailings ore enriched by iron(iii) chloride as a heterogeneous Fenton catalyst for decolorization of organic dyes.

In this study, the Fe-containing tailings (Fe-TO) ore was reutilized and enriched with FeCl3 as a heterogeneous catalyst for the Fenton process to degrade the organic dyes from aqueous solution. The determinants of the heterogeneous catalytic Fenton system which included iron modification ratio, solution pH, catalyst dosage, H2O2 dosage and initial concentration of organic dyes were systematically investigated. The modification ratio of 15% (w/w of iron), pH of 3, MFe-TO15 dosage of 0.5 g L−1 and H2O2 dosage of 840 mg L−1 were chosen as the best operational conditions for Fenton oxidation of organic dyes. The decolorization efficiency of both MB and RhB by MFe-TO15/H2O2 was higher than that of Fe-TO/H2O2 by about two times. The kinetic study showed the degradation of organic dyes well fitted the pseudo-first-order kinetic model with apparent constant rate values (Kd) following the same sequence as the degradation efficiency of organic dyes. The degradation mechanism of dyes could be attributed to adsorption due to the good-development in textural properties of the iron modified catalyst (MFe-TO) with an increase in BET surface area, pore volume and pore diameter of, respectively, 2, 5 and 5 times and leaching iron through homogeneous Fenton reaction. However, the oxidation process occurring on the MFe-TO15's surface by heterogeneous Fenton reaction which enhanced decomposition of H2O2 for continuous generation of hydroxyl radicals was the main mechanism. The key role of *OH radical in oxidation of organic dyes was further ascertained by the remarkable drop in the decolorization of both organic dyes when the various radical-scavengers, including tert-butanol and chloride were supplemented into Fenton systems. A good stability of the catalyst was obtained through leaching test with low leaching iron ratio. The applied modified catalyst remained stable through three consecutive runs. From these findings, it can be concluded that the modified material can be applied as a feasible, inexpensive and highly effective catalyst for removal of persistent organic compounds from wastewater.