Search Results (20)

Wastewater contains dyes originating from textile industries, and above a certain concentration, they can become dangerous due to their high toxicity. Divalent and trivalent metal coagulants, usually aluminum- or iron-based, have been studied worldwide. However, tetravalent coagulants, such as tin chloride, have not yet been extensively studied for application in wastewater treatment. Therefore, in this study, three types of coagulants were examined: SnCl₄, Cs, and a hybrid composite (CS@Sn) in two different mass ratios, abbreviated hereafter as CS@Sn_5% and CS@Sn_50%. The formation of the suggested CS@Sn hybrid coagulants was confirmed by applying SEM, XRD, and FTIR techniques. The results showed that the optimum conditions for RB5 removal was the addition of 20 mg Sn/L SnCl₄ (97.8%) and 50 mg Sn/L of CS@Sn_50% (64.8%) at pH 3.0. In addition, SnCl₄ was found to be an effective coagulant for all the examined anionic dyes, but it was not as effective for cationic dyes. Moreover, the coagulants were then tested in two mixed-dye solutions, both anionic dyes (RB5/RR120) and anionic/cationic (RB5/MV), resulting in a synergistic effect in the first one and a competitive effect in the secon. Finally, the proposed coagulants were successfully tested on real wastewater samples from an untreated textile dyeing industry. Therefore, the coagulants presented in this work for the removal of several dyes are also capable of being used for wastewater treatment. Full article

Diaryldithiocarbamate complexes, [Fe(S₂CNAr₂)₃], have been prepared and their structure, reactivity, and thermal degradation to afford iron sulfide nanomaterials have been investigated. The addition of three equivalents of LiS₂CNAr₂ to FeCl₂·4H₂O in water-air affords dark red [Fe(S₂CNAr₂)₃] in high yields. All show magnetic measurements consistent with a predominantly high-spin electronic arrangement at room temperature. The molecular structure of [Fe{S₂C(N-p-MeOC₆H₄)₂}₃] reveals the expected distorted octahedral geometry, but Fe-S distances are more consistent with a low-spin electronic configuration, likely a result of the low temperature (120 K) of the data collection. The thermal stability of [Fe{S₂C(N-p-MeC₆H₄)₂}₃] has been investigated. TGA shows that it begins to decompose at a significantly lower temperature (ca. 160 °C) than previously observed for [Fe(S₂CNEt₂)₃], and this is further lowered (to ca. 100 °C) in oleylamine. The decomposition of [Fe{S₂C(N-p-MeC₆H₄)₂}₃] in oleylamine, via either a heat-up or hot injection process, affords nanoparticles of Fe₃S₄ (greigite), while in contrast, dry heating at 450 °C affords FeS (troilite) as large agglomerates. Full article

The adsorption of copper ions and Reactive Red 120 azo dye (RR-120) as models of water pollutants on unmodified halloysite (H-NM), as well as halloysites modified with sulfuric acid (H-SA) and (3-aminopropyl)triethoxysilane (H-APTES), was investigated. The results showed that adsorption of both the adsorbates was pH-dependent and increased with the increase in halloysite dosage. The adsorption kinetics were evaluated and the results demonstrated that the adsorption followed the pseudo-second-order model. The adsorption isotherms of Cu(II) ions and RR-120 dye on the halloysites were described satisfactorily by the Langmuir model. The maximum adsorption capacities for the Cu(II) ions were 0.169, 0.236, and 0.507 mmol/g, respectively, for H-NM, H-SA, and H-APTES indicating that the NH₂-functionalization rather than the surface area of the adsorbents was responsible for the enhanced adsorption. The adsorption capacities for RR-120 dye were found to be 9.64 μmol/g for H-NM, 75.76 μmol/g for H-SA, and 29.33 μmol/g for H-APTES. The results demonstrated that APTES-functionalization and sulfuric acid activation are promising modifications, and both modified halloysites have good application potential for heavy metals as well as for azo dye removal. Full article

Photodynamic therapy (PDT) is a non-invasive anticancer treatment that uses special photosensitizer molecules (PS) to generate singlet oxygen and other reactive oxygen species (ROS) in a tissue under excitation with red or infrared light. Though the method has been known for decades, it has become more popular recently with the development of new efficient organic dyes and LED light sources. Here we introduce a ternary nanocomposite: water-soluble star-like polymer/gold nanoparticles (AuNP)/temoporfin PS, which can be considered as a third-generation PDT system. AuNPs were synthesized in situ inside the polymer molecules, and the latter were then loaded with PS molecules in an aqueous solution. The applied method of synthesis allows precise control of the size and architecture of polymer nanoparticles as well as the concentration of the components. Dynamic light scattering confirmed the formation of isolated particles (120 nm diameter) with AuNPs and PS molecules incorporated inside the polymer shell. Absorption and photoluminescence spectroscopies revealed optimal concentrations of the components that can simultaneously reduce the side effects of dark toxicity and enhance singlet oxygen generation to increase cancer cell mortality. Here, we report on the optical properties of the system and detailed mechanisms of the observed enhancement of the phototherapeutic effect. Combinations of organic dyes with gold nanoparticles allow significant enhancement of the effect of ROS generation due to surface plasmonic resonance in the latter, while the application of a biocompatible star-like polymer vehicle with a dextran core and anionic polyacrylamide arms allows better local integration of the components and targeted delivery of the PS molecules to cancer cells. In this study, we demonstrate, as proof of concept, a successful application of the developed PDT system for in vitro treatment of triple-negative breast cancer cells under irradiation with a low-power LED lamp (660 nm). We consider the developed nanocomposite to be a promising PDT system for application to other types of cancer. Full article

The objective of this study was to evaluate the viability and performance of nitric oxide modified-atmosphere packaging (MAP) as a novel alternative to high oxygen and carbon monoxide MAP for ground beef. Packages of ground beef under high oxygen (HI-OX), carbon monoxide (CO), and nitric oxide (NO) atmospheres were evaluated for descriptive and instrumental color every 12 h during a 120 h display period. Surface myoglobin percentages, internal cooked color, thiobarbituric acid reactive substances (TBARS), and residual nitrite and nitrate were also evaluated. There were gas × time interactions for descriptive color, discoloration, a* values, b* values, deoxymyoglobin percentages, and metmyoglobin percentages (p < 0.05). There were also gas-type main effects for cooked color and TBARS (p < 0.05). Carbon monoxide maintained the most redness and least discoloration throughout the display period, while HI-OX started with a bright red color but rapidly browned (p < 0.05). Nitric oxide started as dark red to tannish-red but transitioned to a dull red (p < 0.05). However, NO had increased redness and a* values for internal cooked color (p < 0.05). Although CO outperformed NO packages, NO exhibited a unique color cycle warranting further research to optimize its use. Full article

This study investigates the biodegradation of Reactive Red 141 (RR 141), an azo dye prevalent in the textile industry, by bacteria isolated from activated sludge in a textile effluent treatment plant. RR 141, characterized by nitrogen–nitrogen double bonds (-N=N-), contributes to environmental issues when improperly disposed of in textile effluents, leading to reduced oxygen levels in water bodies, diminished sunlight penetration, and the formation of potentially carcinogenic and mutagenic aromatic amines. This research focuses on identifying bacteria from activated sludge with the potential to decolorize RR 141. Microbiological identification employs MALDI-TOF-MS, known for its precision and rapid identification of environmental bacteria, enhancing treatment efficiency. Results highlight Bacillus thuringiensis and Kosakonia radicincitans as the most promising strains for RR 141 decolorization. Analysis of micro-organisms in activated sludge and database exploration suggests a correlation between these strains and the decolorization process. It is worth noting that this is the first report on the potential use of K. radicincitans for azo dye decolorization. Three distinct culture media—BHI, MSG, and MS—were assessed to investigate their impact on RR 141 decolorization. Notably, BHI and MSG media, incorporating a carbon source, facilitated the bacterial growth of both tested species (B. thuringiensis and K. radicincitans), a phenomenon absent in the MS medium. This observation suggests that the bacteria exhibit limited capability to utilize RR 141 dye as a carbon source, pointing towards the influence of the culture medium on the discoloration process. The study evaluates performance kinetics, decolorization capacity through UV-VIS spectrophotometry, potential degradation pathways via HPLC-MS analysis, phytotoxicity, and enzymatic activity identification. B. thuringiensis and K. radicincitans exhibit potential in decolorizing RR141, with 38% and 26% removal individually in 120 h. As a consortium, they achieved 36% removal in 12 h, primarily through biosorption rather than biodegradation, as indicated by HPLC-MS analyses. In conclusion, the research emphasizes the importance of exploring bacteria from activated sludge to optimize azo dye degradation in textile effluents. B. thuringiensis and K. radicincitans emerge as promising candidates for bioremediation, and the application of MALDI-TOF-MS proves invaluable for rapid and precise bacteria identification. Full article

The present study explores the solar-induced photocatalytic degradation of reactive red (RR) and reactive turquoise (RT) dyes in a single system using TiO₂ immobilized in xanthan gum (TiO₂/XG), synthesized using the sol–gel dip-coating technique for direct precipitation. SEM-EDX, XRD, FTIR, and UV–Vis were used to assess the characteristics of the resulting catalyst. Moreover, the effects of different operating parameters, specifically pH, dye concentration, TiO₂/XG concentration, H₂O₂ concentration, and contact time, were also investigated in a batch photocatalytic reactor. The immobilized TiO₂/XG catalyst showed a slight adsorption degradation efficiency and then improved the RR and RT dye degradation activity (92.5 and 90.8% in 120 min) under solar light with a remarkable Langmuir–Hinshelwood pseudo-first-order degradation rate of 0.0183 and 0.0151 min⁻¹, respectively, under optimum conditions of pH 5, dye concentration of 25 mg/L, TiO₂/XG concentration of 25 mg/L, H₂O₂ concentration of 400 mg/L, and reaction time of 120 min. The improved photocatalytic ability was ascribed to the impact of TiO₂/XG nanoparticles with a high surface area, and lower band gap energy. Solar light energy has significant potential for addressing energy deficit and water pollution concerns. Full article

Metallic iron (Fe⁰) is a reactive material for treating polluted water. The effect of water salinity on the efficiency of Fe⁰-based remediation systems is not yet established. This work aims to clarify the reasons why Cl⁻ ions are often reported to improve the efficiency of Fe⁰/H₂O remediation systems. Quiescent batch experiments were carried out to characterize the effect of chloride (Cl⁻) ions on the efficiency of methylene blue (MB) discoloration in the presence of Fe⁰. Cl⁻ was used in the form of NaCl at concentrations ranging from 0 to 40 g L⁻¹. The MB concentration was 10 mg L⁻¹, the Fe⁰ loading was 5 g L⁻¹, and the duration of the experiment varied from 2 to 46 days. Four different Fe⁰ materials were tested in parallel experiments. Tests with different NaCl levels were performed in parallel with three other organic dyes: Methyl orange (MO), orange II (OII), and reactive red 120 (RR 120). The results clearly show that the presence of Cl⁻ reduces the extent of dye discoloration in all systems investigated. The efficiency of the dyes increased in the order MB < MO < RR 120 < OII. In systems with varying NaCl concentrations, dye discoloration initially decreases with increasing NaCl and slightly increases for [NaCl] > 30 g L⁻¹. However, the extent of dye discoloration for [NaCl] = 40 g L⁻¹ remains much lower than for the system with [NaCl] = 0 g L⁻¹. The results clearly demonstrate that the presence of Cl⁻ fundamentally delays the process of contaminant removal in Fe⁰/H₂O systems, thus improving the understanding of the contaminant interactions in Fe⁰-based remediation systems. These results also suggest that the effects of other inorganic anions on the efficiency of Fe⁰/H₂O systems should be revisited for the design of field applications. Full article

In this work, we investigated the effect of various adsorption parameters (solution pH, temperature, contact time, and the presence of phosphate and nitrate ions) on the adsorption of Reactive Red 120 (RR120) dye by Polyamide Nylon 6 (PN6) microplastics (MPs). Maximum uptake was achieved at pH 2.0, and the temperature rise from 295 to 313 K resulted in the decrease of the RR120 sorption by PN6. Equilibrium was achieved after 7 h, and the adsorption kinetic data obeyed the pseudo-second-order kinetic model. The experimental adsorption data were better fitted by the Langmuir isotherm model, and the q_m was found to be 3.96 mg/g at pH 2.0 and 295 K. Thermodynamic studies pointed out that the adsorption was spontaneous and exothermic, with decreasing entropy at the solution/solid interface. Future work will focus on the effect of aging on the adsorptive properties of PN6 toward RR120 dye. Full article

Traditional dyeing usually consumes a significant amount of water and salts, thus causing environmental pollution. Salt-free and low-water dyeing has become an important research direction in the cotton fabric dyeing industry. The non-aqueous media dyeing technology, using decamethylcyclopentasiloxane (D5) as the dyeing medium, has achieved energy saving and emission reduction in this industry. To investigate the influence of inorganic salts on the dyeing properties of reactive dyes in a non-aqueous medium dyeing system, the adsorption kinetics and level dyeing property of C.I. Reactive Red 120 were investigated at various concentrations of sodium sulfate. When no salts were included in the siloxane non-aqueous dyeing system, 80% of the reactive dye could diffuse onto the cotton fabric surface after 10 min. However, if 13% salts were added during dyeing, 87% of the reactive dye could diffuse to cotton fabric surface over the same amount of time. Moreover, the adsorption rate of dye was increased from 3.85 mg/g·min to 5.04 mg/g·min when the quantity of salts was increased from 0% to 13%. However, the concentration of sodium sulfate had minimal effect on the color depth of the dyed fabric and the final uptake of dye. But, when the concentration of sodium sulfate was significant, the level dyeing property of the dye became poor as the Sγ(λ) value was increased from 0.020 to 0.042. The adsorption kinetic of C.I. Reactive Red 120 in D5 dyeing solution may be best described by the pseudo-second-order kinetic model. As the sodium sulfate concentration increases, the half-dyeing time gradually decreases and the adsorption rate of dye increases. The repulsive force between the dye and the cotton fiber was lowered by the addition of sodium sulfate. Consequently, in the D5 dyeing system, the level dyeing property of reactive dye may be affected by the adsorption rate. Therefore, the formula of reactive dyes that do not contain salts can be applied successfully in non-aqueous dyeing systems. Full article

This research investigates the potential use of pyrite cinder (PC) as an efficient Fenton-like catalyst for the removal of the reactive azo dye Reactive Red 120 (RR120) from aqueous solutions. The characterization of its PC structure and composition confirmed its great potential to act as catalytic iron source in a heterogeneous Fenton system. Dye removal optimization was performed in terms of PC dosage (0.4–8 g/L), H₂O₂ concentration (2–25 mM), pH value (2–4.6), initial dye concentration (50–200 mg/L), and mixing time. The highest decolorization efficiency (92%) was achieved after a reaction time of 480 min under following conditions: RR120 = 50 mg/L, PC = 4 g/L, H₂O₂ = 10 mM, and pH = 3. After decolorization, an extensive analysis of the generated effluent was performed regarding metal leaching, mineralization, toxicity, and degradation product formation. The metal leaching indicated the necessity for a pH increase in order to remove the settled metal hydroxides. The mineralization efficiency was satisfactory, reaching 85% and 62% of the COD and TOC removal, respectively. The respirometry measurements and bioluminescence tests indicated the detoxification of the treated solution. The absorption spectra and GC/MS analysis confirmed the changes in the molecular structure in the form of the destruction of the azo bond, with a simpler aromatic and aliphatic intermediates formation. This study provides an effective method for removing azo dye in polluted water by employing waste tailings as alternative Fenton-like catalysts, while also using waste tailings as the secondary resource. Full article

Non-protein nitrogen (NPN) is abundant in stingray (Himantura signifier) muscle, which also has in vitro antioxidant activity. In this study, NPN from stingray muscle was further investigated for its antioxidant properties in lecithin liposome and oxymyoglobin model systems to validate its protective impact against lipid and myoglobin oxidations during storage for 120 min at various temperatures (4, 25, and 60 °C). NPN solution (10 ppm nitrogen) was added to the lecithin liposome system at different concentrations (0, 0.5, 1, 5, and 10% (v/v)) to investigate its effects on lipid stability by measuring the conjugated diene (CD), peroxide value (PV), and thiobarbituric acid reactive substances (TBARS) contents. In the oxymyoglobin system, NPN solution (10 ppm nitrogen) was also added at different concentrations (0, 0.5, 1, 5, and 10% (v/v)) to the oxymyoglobin solution in order to examine its effect on the stability of myoglobin by determining the contents of oxymyoglobin, metmyoglobin, and protein carbonyl. According to the findings, in all NPN concentrations, the system incubated at 4 °C had the lowest levels of lipid oxidation as measured by CD, PV, and TBARS values, and the lowest levels of myoglobin oxidation. At all incubating temperatures, the oxymyoglobin and lipid oxidation of all model systems tended to rise with the lengthening of the incubation duration. With the addition of 5% NPN, however, the lowest CD, PV, TBARS, oxymyoglobin oxidation, metmyoglobin formation, and protein carbonyl content were all observable, and the remarkable result was discovered during incubation at 4 °C. The results indicate that stingray NPN, especially at 5%, can be used to delay lipid and myoglobin oxidation, particularly at 4 °C. In order to prolong the shelf life of products with dark-fleshed fish and red meat, stingray NPN might be used as an alternative antioxidant to delay the oxidation of lipid and myoglobin during cold chain storage. Full article

Herein, we present an original report on chlorine activation by ultrasound (US: 600 kHz, 120 W) for intensifying the sonochemical treatment of hazardous organic materials. The coupling of US/chlorine produced synergy via the involvement of reactive chlorine species (RCSs: Cl^•, ClO^• and Cl₂^•−), resulting from the sono-activation of chlorine. The degradation of Allura Red AC (ARAC) textile dye, as a contaminant model, was drastically improved by the US/chlorine process as compared to the separated techniques. A synergy index of 1.74 was obtained by the US/chlorine process for the degradation of ARAC (C₀ = 5 mg·L⁻¹) at pH 5.5 and [chlorine]₀ = 250 mM. The synergistic index increased by up to 2.2 when chlorine concentration was 300 µM. Additionally, the synergetic effect was only obtained at pH 4–6, where HOCl is the sole chlorine species. Additionally, the effect of combining US and chlorine for ARAC degradation was additive for the argon atmosphere, synergistic for air and negative for N₂. An air atmosphere could provide the best synergy as it generates a relatively moderate concentration of reactive species as compared to argon, which marginalizes radical–radical reactions compared to radical–organic ones. Finally, the US/chlorine process was more synergistic for low pollutant concentrations (C₀ ≤ 10 mg·L⁻¹); the coupling effect was additive for moderate concentrations (C₀~20–30 mg·L⁻¹) and negative for higher C₀ (>30 mg·L⁻¹). Consequently, the US/chlorine process was efficiently operable under typical water treatment conditions, although complete by-product analysis and toxicity assessment may still be necessary to establish process viability. Full article

The design and development of novel photocatalysts for treating toxic substances such as industrial waste, dyes, pesticides, and pharmaceutical wastes remain a challenging task even today. To this end, a biowaste pistachio-shell-derived activated carbon (AC) loaded TiO₂ (AC-TiO₂) nanocomposite was fabricated and effectively utilized towards the photocatalytic degradation of toxic azo dye Reactive Red 120 (RR 120) and ofloxacin (OFL) under UV-A light. The synthesized materials were characterized for their structural and surface morphology features through various spectroscopic and microscopic techniques, including high-resolution transmission electron microscope (HR-TEM), field emission scanning electron microscope (FE-SEM) along with energy dispersive spectra (EDS), diffuse reflectance spectra (DRS), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, photoluminescence spectra (PL) and BET surface area measurements. AC-TiO₂ shows enhanced photocatalytic activity compared to bare TiO₂ due to the change in the bandgap energy and effective charge separation. The degradation rate of dyes was affected by the bandgap of the semiconductor, which was the result of the deposition weight percentage of AC onto the TiO₂. The presence of AC influences the photocatalytic activity of AC-TiO₂ composite towards RR 120 and OFL degradation. The presence of heteroatoms-enriched AC enhances the charge mobility and suppresses the electron-hole recombination in AC-TiO₂ composite, which enhances the photocatalytic activity of the composite. The hybrid material AC-TiO₂ composite displayed a higher photocatalytic activity against Reactive Red 120 and ofloxacin. The stability of the AC-TiO₂ was tested against RR 120 dye degradation with multiple runs. GC-MS analyzed the degradation intermediates, and a suitable degradation pathway was also proposed. These results demonstrate that AC-TiO₂ composite could be effectively used as an ecofriendly, cost-effective, stable, and highly efficient photocatalyst. Full article

This paper presents an estimation of the adsorptive potential of multiwalled carbon nanotubes (MWCNTs) and modified poly (acrylonitrile-co-styrene) with activated carbon for the uptake of reactive red 35 (RR35) dye from aqueous solution by a batch system. MWCNT adsorbent was synthesized by encapsulation via in situ polymerization. The copolymer material of poly (acrylonitrile-styrene) P (AN-co-ST) was prepared in a ratio of 2:1 V/V by the precipitation polymerization process. The prepared composites’ properties were characterized by FTIR, SEM, Raman, mean particle size (PSA), and XRD analysis. The PSA of the copolymeric material was determined to be 450.5 and 994 nm for MWCNTs and P(AN-co-St)/AC, respectively. Moreover, the influences of different factors, for example pH (2–10), adsorbents dosage (0.005–0.04 g), contact time (5–120 min), initial dye concentration (10–50 mg L⁻¹), and temperature (25–55 °C). The optimum values were determined to be 2 and 4 pH, 10 mg L⁻¹ of RR35 dye, and 0.04 g of adsorbents at early contact time. Furthermore, the adsorption isotherm was studied using Langmuir, Freundlich, Tempkin, and Halsey models. Maximum capacity q_max for MWCNT_S and P (AN-co-St)/AC was 256.41 and 30.30 mg g⁻¹, respectively. The investigational kinetic study was appropriated well via a pseudo second-order model with a correlation coefficient around 0.99. Thermodynamic study displayed that the removal of RR35 is exothermic, a spontaneous and physisorption system. The adsorption efficiency reduced to around 54–55% of the RR35 after four cycles of reuse of the adsorbents at 120 min. Full article