Metal nanoparticles decorated mint-cellulose acetate composite as an efficient catalyst for the reduction of methyl orange.

Water contamination caused by toxic compounds has emerged as one of the most severe challenges worldwide. Biomass-based nanocomposites offer a sustainable and renewable alternative to conventional materials. In this study, a nanocomposite of mint and cellulose acetate (Mint-CA) was prepared and employed as a supportive material for Cu nanoparticles (CuNPs) and Ag nanoparticles (AgNPs). The selectivity of CuNPs@mint-CA and AgNPs@mint-CA was assessed by comparing their performance in the reduction reaction of various dyes solutions. AgNPs@mint-CA exhibited superior catalytic performance, with a removal of 95.2 % for methyl orange (MO) compared to 68 % with CuNPs@mint-CA. The absorption spectra of MO exhibited a distinct peak at 464 nm. The reduction reaction of MO by AgNPs@mint-CA followed pseudo-first-order-kinetic with a rate constant of k = 0.0063 min-1 (R2 = 0.928). The highest removal of MO was achieved under the following conditions: a catalyst weight of 40 mg, an initial MO concentration of 0.07 mM, the addition of 0.5 mL of 0.1 M NaBH4, and a temperature of 25 °C. Furthermore, the AgNPs@mint-CA catalyst exhibited exceptional reducibility even after five use cycles, highlighting its potential for efficiently removing MO.

SnAg2O3-Coated Adhesive Tape as a Recyclable Catalyst for Efficient Reduction of Methyl Orange.

Silver oxide-doped tin oxide (SnAg2O3) nanoparticles were synthesized and different spectroscopic techniques were used to structurally identify SnAg2O3 nanoparticles. The reduction of 4-nitrophenol (4-NP), congo red (CR), methylene blue (MB), and methyl orange (MO) was studied using SnAg2O3 as a catalyst. Only 1.0 min was required to reduce 95% MO; thus, SnAg2O3 was found to be effective with a rate constant of 3.0412 min-1. Being a powder, SnAg2O3 is difficult to recover and recycle multiple times. For this reason, SnAg2O3 was coated on adhesive tape (AT) to make it recyclable for large-scale usage. SnAg2O3@AT catalyst was assessed toward MO reduction under various conditions. The amount of SnAg2O3@AT, NaBH4, and MO was optimized for best possible reduction conditions. The catalyst had a positive effect since it speed up the reduction of MO by adding more SnAg2O3@AT and NaBH4 as well as lowering the MO concentration. SnAg2O3@AT totally reduced MO (98%) in 3.0 min with a rate constant of 1.3669 min-1. These findings confirmed that SnAg2O3@AT is an effective and useful catalyst for MO reduction that can even be utilized on a large scale for industrial purposes.

Adsorptive removal of heavy metals and organic dyes by sodium alginate/coffee waste composite hydrogel.

Heavy metals and dyes used in technological applications have a detrimental influence on human health and the environment. The most used methods for removing pollutants depend on high-cost materials. Therefore, this research was conducted on cost-effective alternatives derived from natural resources and food waste. Herein, we designed a composite hydrogel based on sodium alginate/coffee waste (Alg/coffee) as adsorbent for the removal of organic and inorganic pollutants from aquatic solutions. The selectivity study displayed that Alg/coffee is more effective in adsorbing Pb(II) and acridine orange dye (AO). Adsorption of Pb(II) and AO was studied at concentration range of 0-170 mgL-1 and 0-40 mgL-1. Adsorption data of Pb(II) and AO reveals their fitting to Langmuir-isotherm and pseudo-second-order-kinetic models. The findings demonstrated that Alg/coffee hydrogel are more effective than coffee powder itself with an adsorption (%) approaching 98.44 % of Pb(II) and 80.53 % of AO. Real sample analysis reveals the efficiency of Alg/coffee hydrogel beads in Pb(II) adsorption. The adsorption cycle was examined four times providing high efficiency toward Pb(II) and AO. Desorption of Pb(II) and AO was easily performed using HCl eluent. Thus, Alg/coffee hydrogel beads could be promising adsorbent for the removal of organic and inorganic pollutants.

Substantial increase in adsorption efficiency of local clay-alginate beads toward methylene blue impregnated with SDS.

In the current research work, local clay-alginate beads loaded with sodium dodecyl sulfate (SDS) surfactant were prepared for efficient adsorption of methylene blue (MB). FTIR, SEM-EDX, and TGA instruments were used to examine the surface functional groups, morphology, elemental analysis, and thermal stability of beads, respectively. The adsorption efficiency of native clay for MB increases from 124.78 to 247.94 mg/g when loaded in alginate and SDS in beads form. The impacts of adsorbent dosage, initial pH, contact time, initial MB concentration, and temperature were investigated and optimized. The maximum adsorption capacity of beads for MB was 1468.5 mg/g. The process followed a pseudosecond order kinetic and Freundlich adsorption isotherm model. Thermodynamic study confirmed that MB adsorption on beads is endothermic and spontaneous in nature. The beads were recycled and reused for five times. According to the findings, local clay-alginate beads impregnated with SDS proved to be a promising and efficient adsorbent for extracting MB from aqueous solution.

Chitosan@Carboxymethylcellulose/CuO-Co2O3 Nanoadsorbent as a Super Catalyst for the Removal of Water Pollutants.

In this work, an efficient nanocatalyst was developed based on nanoadsorbent beads. Herein, carboxymethyl cellulose-copper oxide-cobalt oxide nanocomposite beads (CMC/CuO-Co2O3) crosslinked by using AlCl3 were successfully prepared. The beads were then coated with chitosan (Cs), Cs@CMC/CuO-Co2O3. The prepared beads, CMC/CuO-Co2O3 and Cs@CMC/CuO-Co2O3, were utilized as adsorbents for heavy metal ions (Ni, Fe, Ag and Zn). By using CMC/CuO-Co2O3 and Cs@CMC/CuO-Co2O3, the distribution coefficients (Kd) for Ni, Fe, Ag and Zn were (41.166 and 6173.6 mLg-1), (136.3 and 1500 mLg-1), (20,739.1 and 1941.1 mLg-1) and (86.9 and 2333.3 mLg-1), respectively. Thus, Ni was highly adsorbed by Cs@CMC/CuO-Co2O3 beads. The metal ion adsorbed on the beads were converted into nanoparticles by treating with reducing agent (NaBH4) and named Ni/Cs@CMC/CuO-Co2O3. Further, the prepared nanoparticles-decorated beads (Ni/Cs@CMC/CuO-Co2O3) were utilized as nanocatalysts for the reduction of organic and inorganic pollutants (4-nitophenol, MO, EY dyes and potassium ferricyanide K3[Fe(CN)6]) in the presence of NaBH4. Among all catalysts, Ni/Cs@CMC/CuO-Co2O3 had the highest catalytic activity toward MO, EY and K3[Fe(CN)6], removing up to 98% in 2.0 min, 90 % in 6.0 min and 91% in 6.0 min, respectively. The reduction rate constants of MO, EY, 4-NP and K3[Fe(CN)6] were 1.06 × 10-1, 4.58 × 10-3, 4.26 × 10-3 and 5.1 × 10-3 s-1, respectively. Additionally, the catalytic activity of the Ni/Cs@CMC/CuO-Co2O3 beads was effectively optimized. The stability and recyclability of the beads were tested up to five times for the catalytic reduction of MO, EY and K3[Fe(CN)6]. It was confirmed that the designed nanocomposite beads are ecofriendly and efficient with high strength and stability as catalysts for the reduction of organic and inorganic pollutants.

Adsorption efficiency of date palm based activated carbon-alginate membrane for methylene blue.

In the current study, activated carbon (AC) was prepared from date palm using single step activation using boric acid as an activating agent. The synthesized AC was incorporated with alginate (AC-alginate (AC-alg)) to prepare membrane for adsorption of methylene blue (MB) in batch adsorption study. The prepared membrane was characterized using different types of analytical techniques such as FTIR, SEM, and TGA analysis. Adsorption of methylene blue dye from aqueous solution was carried out using AC-alg membrane in batch investigation. Various experimental parameters effecting the adsorption of MB on membrane such as initial pH of dye solution, contact time, concentration of dye solution and temperature were optimized to get maximum adsorption efficiency. Kinetics, isotherm and thermodynamics study was performed for dye adsorption. Pseudo-second order kinetic model and Langmuir adsorption isotherm were well fitted to the experimental data. The maximum adsorption capacity for MB adsorption was 666 mg/g found by Langmuir adsorption isotherm. Thermodynamic study revealed that the adsorption of MB on AC-alg membrane is spontaneous and an exothermic process. The experimental result confirmed that AC-alg membrane is a suitable and easily recoverable adsorbent to be used for efficient removal of MB and MB like other dyes.

Synthesis of Activated Carbon from Trachycarpus fortunei Seeds for the Removal of Cationic and Anionic Dyes.

The removal of dyes from industrial effluents is one of the most important industrial processes that is currently on academic demand. In this project, for the first time, Trachycarpus fortunei seeds are used as biosources for the synthesis of activated carbon (AC) using physical as well as acid-base chemical methods. The synthesized AC was initially characterized by different instrumental techniques, such as FTIR, BET isotherm, SEM, EDX and XRD. Then, the prepared activated carbon was used as an economical adsorbent for the removal of xylenol orange and thymol blue from an aqueous solution. Furthermore, the effect of different parameters, i.e., concentration of dye, contact time, pH, adsorbent amount, temperature, adsorbent size and agitation speed, were investigated in batch experiments at room temperature. The analysis of different techniques concluded that the pyrolysis method created a significant change in the chemical composition of the prepared AC and the acid-treated AC offered a high carbon/oxygen composite, which is graphitic in nature. The removal of both dyes (xylenol orange and thymol blue) was increased with the increase in the dye's initial concentration. Isothermal data suggested that the adsorption of both dyes follows the Langmuir model compared to the Freundlich model. The equilibrium time for AC biomass to achieve the removal of xylenol orange and thymol blue dyes was determined to be 60 min, and the kinetic data suggested that the adsorption of both dyes obeyed the pseudo-second order model. The optimal pH for thymol blue adsorption was pH 6, while it was pH 2 for xylenol orange. The adsorption of both dyes increased with the increase in the temperature. The influence of the adsorbent amount indicated that the adsorption capacity (mg/g) of both dyes reduced with the rise in the adsorbent amount. Thus, the current study suggests that AC prepared by an acid treatment from Trachycarpus fortunei seeds is a good, alternative, cost effective, and eco-friendly adsorbent for the effective removal of dyes from polluted water.

Development of alginate@tin oxide-cobalt oxide nanocomposite based catalyst for the treatment of wastewater.

In this study, tin oxide­cobalt oxide nanocatalyst was prepared by a simple method, which grew in spherical particles with an average diameter of 30 nm. Tin oxide-cobalt oxide was further wrapped in alginate polymer hydrogel (Alg@tin oxide-cobalt oxide), and both materials were utilized as nanocatalysts for the catalytic transformation of different pollutants. Tin oxide-cobalt oxide and Alg@tin oxide-cobalt oxide nanocatalysts were tested for the catalytic reduction of 4-nitrophenol, congo red, methyl orange, methylene blue (MB) and potassium ferricyanide in which sodium borohydride was used as a reducing agent. Tin oxide-cobalt oxide and Alg@tin oxide-cobalt oxide nanocatalysts synergistically reduced MB in shorter time (2.0 and 4.0 min) compared to other dyes. The reduction conditions were optimized by changing different parameters. The rate constants for MB reduction were calculated and found to be 1.5714 min-1 and 0.6033 min-1 using tin oxide-cobalt oxide and Alg@tin oxide-cobalt oxide nanocatalysts, respectively. Implementing Alg@tin oxide-cobalt oxide nanocatalyst toward MB reduction in real samples proved its efficacy in sea and well water samples. The catalyst could be easily recovered, recycled and revealed a minimal loss of nanoparticles, which offering a competition and replacement with reputable commercial catalysts.

Alginate/Banana Waste Beads Supported Metal Nanoparticles for Efficient Water Remediation.

Water pollution is considered a perilous issue that requires an immediate solution. This is largely because of the strong correlation between the global population increase and the amount of waste produced (most notably food waste). This project prompts the conversion of food waste into useful materials that can be used with sodium alginate as a catalytic support for metal nanoparticles. Sodium alginate/banana peel (Alg/BP) beads were prepared simply using an eco-friendly method. The prepared materials were modified using nanostructured materials to enhance their characteristics. Alg/BP beads were employed as adsorbents for metals that were then treated with sodium borohydride to produce MNPs@Alg/BP. Different MNPs@Alg/BP (MNPs = Ag, Ni, Co, Fe, and Cu) were used as catalysts for reducing 4-nitrophenol (4-NP) by NaBH4 to evaluate each catalyst performance in a model reaction. The results exhibited that Cu@Alg/BP was most efficient toward complete transformation of 4-NP. Therefore, Cu@Alg/BP was also used as a catalyst for the reduction of potassium ferricyanide, congo red, methyl orange (MO), and methylene blue. It was found that Cu@Alg/BP beads catalytically reduced up to 95-99% of above pollutants within a few minutes. Cu@Alg/BP beads were more selective in reducing MO among the pollutants. The catalytic activity of Cu@Alg/BP was examined by evaluating the impact of numerous parameters on MO reduction. The results are expected to provide a new strategy for the removal of inorganic and organic water contaminants based on efficient and low-cost catalysts.

Sodium alginate nanocomposite based efficient system for the removal of organic and inorganic pollutants from wastewater.

An effective and selective catalytic system based on cerium oxide-stannous oxide (CeO2-SnO) wrapped Na-alginate hydrogel was developed for the selective reduction of potassium ferricyanide (K3[Fe(CN)6]). Na-alginate hydrogel was used as a reacting container for CeO2-SnO nanoparticles. Na-alginate wrapped CeO2-SnO (Alg/CeO2-SnO) was applied as a catalyst and examined toward the reduction of several hazardous pollutants, such as nitrophenols, dyes and K3[Fe(CN)6]. Alg/CeO2-SnO nanocatalyst was mostly selective toward K3[Fe(CN)6] since it was more effective and economical for reduction of K3[Fe(CN)6]. Further different parameters like catalyst amount, reducing agent amount, K3[Fe(CN)6] concentration and recyclability were optimized. The increase in both nanocatalyst amount and NaBH4 concentration resulted in increasing the rate of the catalytic reduction of K3[Fe(CN)6]. Alg/CeO2-SnO nanocatalyst reduced K3[Fe(CN)6] in 4.0 min with a reaction rate constant of 0.9114 min-1. The nanocatalyst can be easily recovered by pulling the hydrogel from the reaction medium up to four cycles. Alg/CeO2-SnO nanocatalyst was also examined in real samples like irrigation water, sea water, well water, university water, which was effective for K3[Fe(CN)6] reduction by 95.16%-96.54%. This novel approach provides a new catalyst for efficient removal of K3[Fe(CN)6] from real samples and can be a time and cost alternative tool for environmental safety.