Surface Modification of Bamboo-based Activated Carbon for Methylene Blue Removal

The feasibility of biomass-based activated carbon has received tremendous attention owing to its excellent properties,such as insensitivity,good adsorption performance,and potential to reduce the strong dependence on non-reproducible precursors.In this study,bamboo-based activated carbon(BAC)was used as the raw material for methylene blue(MB)removal.Cetyltrimethylammonium bromide(CTAB),sodium dodecyl sulfate(SDS),and sodium dodecylbenzene sulfonate(SDBS)were used as BAC surface modifiers.The morphologies and structures of the samples were characterized.In addition,the effects of the surfactant type and concentration on the adsorption-based removal of MB from aqueous solutions by the modified BAC were systematically investigated.For the 0.2 g/L MB solution,the MB removal rate reached 99.7%when the concentration of CTAB was 0.25 g/L.Moreover,the kinetic model curve of 0.25 g/L CTAB-modified BAC(CAC)was consistent with the Freundlich isotherm model.This research work enriches the technical pathway of modification and application of activated carbon,which is not only beneficial for realizing the high-value utilization of biomass bamboo resources but also can play an active role in guiding the treatment of MB-containing wastewater.

ZnO/V_(2)C/Fe_(2)O_(3)三元复合材料的制备及其对MB的光降解性能

采用高效催化剂技术可以处理工业废水中的污染物,而单相催化剂存在可见光响应范围窄的问题。通过静电自组装的方法制备ZnO/V_(2)C/Fe_(2)O_(3)三元光催化复合材料,利用X射线衍射(XRD)、扫描电子显微镜(SEM)、X射线光电子能谱(XPS)等分析技术对复合材料进行表征,并以亚甲基蓝(MB)染料为目标污染物,研究三元复合物的光催化性能。在紫外光和可见光分别照射120 min后,ZnO/V_(2)C/Fe_(2)O_(3)三元复合材料对MB染料的降解速率分别是纯ZnO的19.68倍和21.76倍。在复合Fe_(2)O_(3)和V_(2)C后,缩短了ZnO禁带宽度,激发响应范围到可见光区域,有更大的比表面积和更多的反应活性位点,从而使ZnO的光催化性能增强。

Optimizing Methylene Blue Removal from Textile Effluents: Comparative Study of Adsorption Efficiency Using Raw and Activated Carbon Derived from Gmelina Wood Wastes

This research investigates the efficacy of activated Gmelina Wood Sawdust (GWS) as an adsorbent for the removal of methylene blue (MB) dye from aqueous solutions, in comparison with raw GWS. The study employs laboratory experiments to assess the percentage of dye removal across various temperature and pH conditions. The adsorption process is scrutinized under different parameters, encompassing contact time, initial dye concentration, adsorbent dosage, temperature, and pH. Results demonstrate that activated GWS surpasses its raw counterpart, showcasing superior MB dye removal percentages. Extended contact times increased initial dye concentrations, and higher adsorbent dosages contribute positively to removal efficiency, while temperature exhibits an inverse relationship with dye removal. Optimal adsorption occurs at a pH of 7.0, aligning with the adsorbent’s zero-point charge (pHzpc), underscoring the role of surface charge in the adsorption process. This study underscores the potential of activated GWS as an economical and promising adsorbent material for addressing pollutants. Furthermore, the utilization of activated carbon derived from abundant agricultural waste underscores an environmentally conscious approach to adsorption applications. The ability to tailor the size and properties of activated carbon particles opens avenues for optimizing adsorption capabilities, thereby presenting opportunities for enhanced water treatment solutions.

Effect of Methylene Blue (MB)-value of Manufactured Sand on the Durability of Concretes

The relation between the methylene blue （MB） value of MS and its limestone powder content and clay content was investigated. The effects of MB values ranging from 0.35 to 2.5 on the workability of fresh concrete, the mechanical properties, the resistance to freezing as well as the resistance to chlorine ion permeation of the hardened concrete were all investigated. The experimental results showed that the MB value had no correlation with the limestone powder content of MS, while it was directly related to the clay content. With an increase of MB value, concrete workability decreased, as did the flexural and 7-day compressive strengths, however, the 28-day compressive strength was not affected. Furthermore, influence of MB value on concretes of different strength levels was different. For low-strength concretes, an increase of MB value could improve its impermeability, but this was not the case for high-strength concretes. Instead, their resistance to chloride ion permeability decreased slightly. However, even a slight increase in MB value remarkably accelerated freeze-thaw damage of MS concrete. It was thus concluded that the critical MB value of 1.4 would not cause significant deterioration in the performance of MS concretes.

Silicalite-1 zeolite encapsulated Fe nanocatalyst for Fenton-like degradation of methylene blue

Encapsulation of Fe nanoparticles in zeolite is a promising way to significantly improve the catalytic activity and stability of Fe-based catalysts during the degradation process of organic pollutants.Herein,Fe nanocatalysts were encapsulated into silicalite-1(S-1)zeolite by using a ligand-protected method(with dicyandiamide(DCD)as a organic ligand)under direct hydrothermal synthesis condition.High-resolution transmission electron microscopy(HRTEM)results confirmed the high dispersion of Fe nanocatalysts which were successfully encapsulated within the voids among the primary particles of the S-1 zeolite.The developed S-1 zeolite encapsulated Fe nanocatalyst(Fe@S-1)exhibited significantly improved catalytic activity and reusability in the catalytic degradation process of methylene blue(MB).Specifically,the developed Fe0.021@S-1 catalyst showed high catalytic degradation activity,giving a high MB degradation efficiency of 100%in 30 min,outperformed the conventional impregnated catalyst(Fe/S-1).Moreover,the Fe@S-1 catalyst afforded an outstanding stability,showing only ca.7.9%activity loss after five cycling tests,while the Fe/S-1 catalyst presented a significantly activity loss of 50.9%after only three cycles.Notably,the encapsulation strategy enabled a relatively lower Fe loading in the Fe@S-1 catalyst in comparison with that of the Fe/S-1 catalyst,i.e.,0.35%vs.0.81%(mass).Radical scavenging experiments along with electron spin resonance(ESR)measurements confirmed that the major role of
OH in the MB degradation process.Specifically,Fe@S-1 catalyst with high molar ratio of[Fe(DCD)]Cl3 is beneficial to form Fe complexes/nanoclusters in the voids(which has large pore size of 1–2 nm)among the primary particles of the zeolite,and thus improving the diffusion and accessibility of reactants to Fe active sites,and thus exhibiting a relatively higher degradation efficiency.This work demonstrates that zeolite-encapsulated Fe nanocatalysts present potential applications in the advanced oxidation of wastewater treatment.

Understanding association between methylene blue dye and biosorbent: Palmyrah sprout casing in adsorption process in aqueous phase

Water pollution caused by industrial dyes has become a severe problem in the modern world. Biosorbents can be used in an eco-friendly manner to remove industrial dyes. In this study, five biosorbents were selected: palmyrah sprout casing (PSC), manioc peel, lime peel, king coconut husk, and coconut kernel. Batch adsorption experiments were conducted to identify the best biosorbent with the highest ability to adsorb methylene blue (MB) from wastewater. The detailed mechanisms of PSC used in the adsorptive removal of MB in aqueous phase were investigated. Of the five biosorbents, PSC exhibited the best removal performance with an adsorption capacity at equilibrium (qe) of 27.67 mg/g. The qe values of lime peel, king coconut husk, manioc peel, and coconut kernel were 24.25 mg/g, 15.29 mg/g, 10.84 mg/g, and 7.06 mg/g, respectively. To explain the mechanisms of MB adsorption with the selected biosorbents, the Fourier transform infrared (FTIR) spectrometry and X-ray diffraction (XRD) analyses were performed to characterize functional properties, and isotherm, kinetic, rate-limiting, and thermodynamic analyses were conducted. The FTIR analysis revealed that different biosorbents had different functional properties on their adsorptive surfaces. The FTIR and XRD results obtained before and after MB adsorption with PSC indicated that the surface functional groups of carbonyl and hydroxyl actively participated in the removal process. According to the isotherm analysis, monolayer adsorption was observed with the Langmuir model with a determination coefficient of 0.998. The duration to reach the maximum adsorption capacity for MB adsorption with PSC was 120 min, and the adsorption process was exothermic due to the negative enthalpy change (-9.950 kJ/mol). Moreover, the boundary layer thickness and intraparticle diffusion were the rate-limiting factors in the adsorption process. As a new biosorbent for MB adsorption, PSC could be used in activated carbon production to enhance the performance of dye removal.

Enhanced photocatalytic performance of iron oxides@HTCC fabricated from zinc extraction tailings for methylene blue degradation:Investigation of the photocatalytic mechanism

Photocatalytic processes are efficient methods to solve water contamination problems,especially considering dyeing wastewater disposal.However,high-efficiency photocatalysts are usually very expensive and have the risk of heavy metal pollution.Recently,an iron oxides@hydrothermal carbonation carbon(HTCC)heterogeneous catalyst was prepared by our group through co-hydrothermal treatment of carbohydrates and zinc extraction tailings of converter dust.Herein,the catalytic performance of the iron oxides@HTCC was verified by a nonbiodegradable dye,methylene blue(MB),and the catalytic mechanism was deduced from theoretical simulations and spectroscopic measurements.The iron oxides@HTCC showed an excellent synergy between photocatalysis and Fenton-like reactions.Under visible-light illumination,the iron oxides@HTCC could be excited to generate electrons and holes,reacting with H_(2)O_(2)to produce·OH radicals to oxidize and decompose organic pollutants.The removal efficiency of methylene blue over iron oxides@HTCC at 140 min was 2.86 times that of HTCC.The enhanced catalytic performance was attributed to the advantages of iron oxides modification:(1)promoting the excitation induced by photons;(2)improving the charge transfer.Furthermore,the iron oxides@HTCC showed high catalytic activity in a wide pH value range of 2.3-10.4,and the MB removal efficiency remained higher than 95% after the iron oxides@HTCC was recycled 4 times.The magnetically recyclable iron oxides@HTCC may provide a solution for the treatment of wastewater from the textile industry.

Methylene blue intercalated vanadium oxide with synergistic energy storage mechanism for highly efficient aqueous zinc ion batteries

With the rise of aqueous multivalent rechargeable batteries,inorganic-organic hybrid cathodes have attracted more and more attention due to the complement of each other’s advantages.Herein,a strategy of designing hybrid cathode is adopted for high efficient aqueous zinc-ion batteries(AZIBs).Methylene blue(MB)intercalated vanadium oxide(HVO-MB)was synthesized through sol-gel and ion exchange method.Compared with other organic-inorganic intercalation cathode,not only can the MB intercalation enlarge the HVO interlayer spacing to improve ion mobility,but also provide coordination reactions with the Zn^(2+)to enhance the intrinsic electrochemical reaction kinetics of the hybrid electrode.As a key component for the cathode of AZIBs,HVO-MB contributes a specific capacity of 418 mA h g^(-1) at 0.1 A g^(-1),high rate capability(243 mA h g^(-1) at 5 A g^(-1))and extraordinary stability(88%of capacity retention after 2000cycles at a high current density of 5 A g^(-1))in 3 M Zn(CF_(3)SO_(3))_(2) aqueous electrolyte.The electrochemical kinetics reveals HVO-MB characterized with large pseudocapacitance charge storage behavior due to the fast ion migration provided by the coordination reaction and expanded interlayer distance.Furthermore,a mixed energy storage mechanism involving Zn^(2+)insertion and coordination reaction is confirmed by various ex-situ characterization.Thus,this work opens up a new path for constructing the high performance cathode of AZIBs through organic-inorganic hybridization.

Silica Gel from Chemical Glass Bottle Waste as Adsorbent for Methylene Blue:Optimization Using BBD

This research focuses on the effective removal of methylene blue dye using silica gel synthesized from chemical glass bottle waste as an environmentally friendly and cost-effective adsorbent.The adsorption process was optimized using Box-Behnken Design(BBD)and Response Surface Methodology(RSM)to investigate the influence of pH(6;8 and 10),contact time(15;30 and 45 min),adsorbent mass(30;50 and 70 mg),and initial concentration(20;50 and 80 mg/L)of the adsorbate on the adsorption efficiency.The BBD was conducted using Google Colaboratory software,which encompassed 27 experiments with randomly assigned combinations.The silica gel synthesized from chemical glass bottle was characterized by XRD,FTIR,SEM-EDX and TEM.The adsorption result was measured by spectrophotometer UV-Vis.The optimized conditions resulted in a remarkable methylene blue removal efficiency of 99.41%.Characterization of the silica gel demonstrated amorphous morphology and prominent absorption bands characteristic of silica.The Langmuir isotherm model best described the adsorption behavior,revealing chemisorption with a monolayer coverage of methylene blue on the adsorbent surface,and a maximum adsorption capacity of 82.02 mg/g.Additionally,the pseudo-second-order kinetics model indicated a chemisorption mechanism during the adsorption process.The findings highlight the potential of silica gel from chemical glass bottle waste as a promising adsorbent for wastewater treatment,offering economic and environmental benefits.Further investigations can explore its scalability,regenerability,and reusability for industrial-scale applications.

Enhanced photocatalytic activity of methylene blue using heterojunction Ag@TiO_(2)nanocomposite:Mechanistic and optimization study

The objective in this study is to investigate the adsorption-degradation of the methylene blue(MB)dye using a fabricated heterojunction Ag@TiO_(2)nanocomposite.The batch factors used in photo catalytic reactions were pH,UV-irradiation time,temperature,catalytic dosage,and concentration of MB.The results showed that 0.2×10^(3) g·ml^(-1))of the catalytic dose caused the Ag@TiO_(2)adsorption to degrade by 96.67%with darks and UV exposure.Using the Langmuir-Hinshelwood model to determine the kinetic,the Ag@TiO_(2)displays a greater kinetic rate than TiO_(2)and silver nanoparticle(AgNPs).The photocatalytic degradation of MB,which is an endothermic reaction involving all catalysts,is shown by the thermodynamic parameter to have the positive value of enthalpy(ΔH°).The enthalpies observed were Ag@TiO_(2)(126.80 kJ·mol^(-1))<AgNPs(354.47 kJ·mol^(-1))<TiO_(2)(430.04 kJ·mol^(-1)).Ascorbic acid(·OH scavenger),2-propanol(·O_(2)scavenger),and ammonium oxalate(AO)(hole h+scavenger)were employed to conduct the scavenger effects.The Ag@TiO_(2)demonstrated a reduction in MB degradation when combined with 2-propanol,and this clearly demonstrated that,in contrast to hydroxyl radicals(·OH)and holeh scavengers,superoxide radical anion(O_(2)scavenger)plays a significant role in MB degradation.Utilizing density functional theory(DFT)to elucidate the mechanism and B3LYP/6-311+G(d,p)level optimization,the degradation-adsorption process was explained.When the N-N,C-N or C-C bonds were severed,the Fukui faction was demonstrated for nucleophilic,electrophilic,and radical attack.

Investigation of photoelectrocatalytic degradation mechanism of methylene blue by a-Fe_(2)O_(3) nanorods array

Efficiently and thoroughly degrading organic dyes in wastewater is of great importance and challenge.Herein,vertically oriented mesoporous a-Fe_(2)O_(3)nanorods array(a-Fe_(2)O_(3)-NA)is directly grown on fluorine-doped tin oxide(FTO)glass and employed as the photoanode for photoelectrocatalytic degradation of methylene blue simulated dye wastewater.The Ovsites on the a-Fe_(2)O_(3)-NA surface are the active sites for methylene blue(MB)adsorption.Electrons transfer from the adsorbed MB to Fe-O is detected.Compared with electrocatalytic and photocatalytic degradation processes,the photoelectrocatalytic(PEC)process exhibited the best degrading performance and the largest kinetic constant.Hydroxyl,superoxide free radicals,and photo-generated holes play a jointly leading role in the PEC degradation.A possible degrading pathway is suggested by liquid chromatography-mass spectroscopy analysis.This work demonstrates that photoelectrocatalysis by a-Fe_(2)O_(3)-NA has a remarkable superiority over photocatalysis and electrocatalysis in MB degradation.The in-depth investigation of photoelectrocatalytic degradation mechanism in this study is meaningful for organic wastewater treatment.

Desorption of Methylene Blue Adsorbed on Activated Carbon from Cocoa Pod Shell

Environmental protection has become a concern for the world. For this reason, the objective of this work is to remove methylene blue adsorbed on activated carbon. The coal used comes from cocoa pod shells. Before pyrolysis, the shells were ground, sieved and impregnated with orthophosphoric acid. Before desorption, the activated carbons were initially saturated with MB. These saturated coals were brought into contact with a sodium chloride (NaCl) solution and then stirred. The evolution of the resorbed MB concentration was monitored by spectrophotometry. The desorption tests showed a remarkable elimination from the first 10 minutes. The desorption kinetics comprises two phases: a rapid kinetics between 0 and 30 minutes and a slow kinetics between 30 and 60 minutes. The desorption of the dye reaches a concentration aqual to 0.84 mg/l at pH = 4 at temperature = 80°C. For modeling, the coefficient of the Langmuir II model is greater than or equal to O.9893. The model of Langmuir III is less than or equal to 0.9373. The Freundlich model coefficient is 0.9842 or less. The desorption is thefore carried out on energy-homogeneous adsorption sites and without any interaction between the adsorbed cations of the dye. Experimental parameters such as pH, temperature and concentration of sodium chloride (NaCl) solution influence the desorption of MB. And the model of Langmuir II describes well the process of desorption of the MB.

Percutaneous transhepatic cholangial drainage-guided methylene blue for fistulotomy using dual-knife for bile duct intubation: A case report

BACKGROUND Difficult bile duct intubation is a big challenge for endoscopists during endoscopic retrograde cholangiopancreatography(ERCP)procedure.We report a case of percutaneous transhepatic cholangial drainage(PTCD)-guided methylene blue for fistulotomy using dual-knife for bile duct intubation.CASE SUMMARY A 50-year-old male patient had developed obstructive jaundice,and ERCP procedure need to be performed to treat the obstructive jaundice.But intubation cannot be performed if the duodenal papilla cannot be identified because of previous surgery for a perforated descending duodenal diverticulum.We used PTCD-guided methylene blue to identify the intramural common bile duct before dual-knife fistulotomy,and bile duct intubation was successfully completed.CONCLUSION The method that combing methylene blue and dual-knife fistulotomy to achieve bile duct intubation during difficult ERCP is safe and effective.

Multifunctional catalytic sites regulation of atomic-scale iridium on orthorhombic-CoSe_(2)for high efficiency dual-functional alkaline hydrogen evolution and organic degradation

The earth-abundant and high-performance catalysts are crucial for commercial implementation of hydrogen evolution reaction(HER).Herein,a multifunctional site strategy to construct excellent HER catalysts by incorporating iridium(Ir)ions on the atomic scale into orthorhombic-CoSe2(Ir-CoSe_(2))was reported.Outstanding hydrogen evolution activity in alkaline media such as a low overpotential of 48.7 mV at a current density of 10 mA cm^(-2)and better performance than commercial Pt/C catalysts at high current densities were found in the Ir-CoSe_(2) samples.In the experiments and theoretical calculations,it was revealed that Ir enabled CoSe_(2)to form multifunctional sites to synergistically catalyze alkaline HER by promoting the adsorption and dissociation of H_(2)O(Ir sites)and optimizing the binding energy for H^(*)on Co sites.It was noticeable that the electrolytic system comprising the Ir-CoSe_(2)electrode not only produced hydrogen efficiently via HER,but also degraded organic pollutants(Methylene blue).The cell voltage of the dual-function electrolytic system was 1.58 V at the benchmark current density of 50 mA cm^(-2),which was significantly lower than the conventional water splitting voltage.It was indicated that this method was a novel strategy for designing advanced HER electrocatalysts by constructing multifunctional catalytic sites for hydrogen production and organic degradation.

Removal of the Methylene Blue Dye (MB) with Catalysts of Au-TiO₂: Kinetic and Degradation Pathway

Au-TiO2 catalysts were used in the photocatalytic degradation of the methylene blue dye (MB). The synthesis of titanium oxide (TiO2) was carried out by sol-gel method. Subsequently, particles of Au were deposited on the surface of the semiconductor by photo-deposition, thus modifying the surface of the semiconductor. For the characterization of the catalyst obtained, the techniques of X-ray Diffraction (DRX), Scanning Electron Microscopy (SEM), Spectroscopy with Diffuse Reflectance (DR) and Surface Area by the BET (Brunauer, Emmett y Teller) were used. The solid obtained was tested experimentally as a catalyst in the photocatalytic degradation of a solution of MB. The data obtained were analyzed by UV-vis Spectroscopy and Total Organic Carbon (TOC) and the results indicated conversions were greater than 80%. The intermediate products were evaluated by mass coupled gas chromatography (GC-MS) and the MB decomposition route was by hydroxylation, obtaining aromatic intermediates, esters and products of the chemical degradation of the molecule.

石灰岩机制砂MB值测定方法研究与改进

为了简化实验步骤,确保实验数据准确可靠,本文基于GB/T14684-2022《建设用砂》亚甲蓝值测定实验及GB/T35164-2017《用于水泥砂浆、混凝土中的石灰石粉》中石灰石粉的亚甲蓝值测定方法,采用石灰岩机制砂中石粉进行粉碎处理后,分级进行了亚甲蓝值的测定,选用石灰岩机制砂中粒径小于0.075mm的颗粒直接进行吸附实验,并将该方法与GB/T14684-2022标准方法进行对比实验,由此可为标准方法提供数据参考,进而对标准方法进行改进。本文重点阐述了TPZ防水卷材湿铺技术的操作要点及关键节点做法总结,可供类似项目借鉴。

Enhanced adsorption of Methylene Blue from aqueous solution by chitosan-g-poly(acrylic acid)/vermiculite hydrogel composites

A series of chitosan-g-poly （acrylic acid）/vermiculite hydrogel composites were synthesized and used as adsorbents for the investigation of the effect of process parameters such as vermiculite content, pH of dye solution, contact time, initial concentration of dye solution, temperature, ionic strength and concentration of surfactant sodium dodecyl sulfate on the removal of Methylene Blue （MB） from aqueous solution. The results showed that the adsorption capacity for dye increased with increasing pH, contact time and initial dye concentration, but decreased with increasing temperature, ionic strength and sodium dodecyl sulfate concentration in the present of the surfactant. The adsorption kinetics of MB onto the hydrogel composite followed pseudo second-order kinetics and the adsorption equilibrium data obeyed Langmuir isotherm. By introducing 10 wt.% vermiculite into chitosan-g-poly （acrylic acid） polymeric network, the obtaining hydrogel composite showed the highest adsorption capacity for MB, and then could be regarded as a potential adsorbent for cationic dye removal in a wastewater treatment process.

TiO_2/polyaniline composites:An efficient photocatalyst for the degradation of methylene blue under natural light

Polyaniline （PAn） sensitized nanocrystalline TiO2 composites （TiO2/PAn） were successfully prepared and used as an efficient photocatalyst for the degradation of dye methylene blue （MB）. The results showed that PAn was able to sensitize TiO2 efficiently and the composite photocatalyst could be activated by absorbing both the ultraviolet and visible light （λ： 190 ～ 800 nm）, whereas pure TiO2 absorbed ultraviolet light only （λ 〈 380 nm）. Under the irradiation of natural light, MB could be degraded more efficiently on the TiO2/PAn composites than on the TiO2 Furthermore, it could be easily separated from the solution by simple sedimentation.

Adsorption Kinetics of Methylene Blue from Aqueous Solutions onto Palygorskite

The adsorption kinetics of methylene blue from aqueous solutions on purified palygorskite was investigated. The kinetics data related to the adsorption of methylene blue from aqueous solutions are in good agreement with the pseudo-second order equation in ranges of initial concentration of 120-210 mg/L, oscillation speed of 100-200 r/min and temperature of 298-328K. The experimental results show that methylene blue is only adsorbed onto the external surface of purified palygorskite, and the apparent adsorption activation energy is 13.92 kJ/mol. The relatively low apparent adsorption activation energy suggests that the adsorption of methylene blue involves in not only a chemical, but also a physical adsorption process, and it is controlled by the combination of chemical adsorption and fiquid-film diffusion.