Recent Progress on Potentiometric Sensor Applications Based on Nanoscale Metal Oxides: A Comprehensive Review.

Electrochemical sensors have been the subject of much research and development as of late, with several publications detailing new designs boasting enhanced performance metrics. That is, without a doubt, because such sensors stand out from other analytical tools thanks to their excellent analytical characteristics, low cost, and ease of use. Their progress has shown a trend toward seeking out novel useful nano structure materials. A variety of nanostructure metal oxides have been utilized in the creation of potentiometric sensors, which are the subject of this article. For screen-printed pH sensors, metal oxides have been utilized as sensing layers due to their mixed ion-electron conductivity and as paste-ion-selective electrode components and in solid-contact electrodes. Further significant uses include solid-contact layers. All the metal oxide uses mentioned are within the purview of this article. Nanoscale metal oxides have several potential uses in the potentiometry method, and this paper summarizes such uses, including hybrid materials and single-component layers. Potentiometric sensors with outstanding analytical properties can be manufactured entirely from metal oxides. These novel sensors outperform the more traditional, conventional electrodes in terms of useful characteristics. In this review, we looked at the potentiometric analytical properties of different building solutions with various nanoscale metal oxides.

Assessment of heavy metals accumulation by vegetables irrigated with different stages of textile wastewater for evaluation of food and health risk.

Wastewater irrigation for vegetable cultivation is greatly concerned about the presence of toxic metals in irrigated soil and vegetables which causes possible threats to human health. This study aimed to ascertain the accumulation of heavy metals (HMs) in edible parts of vegetables irrigated with different stages of textile dyeing wastewater (TDW). Bio-concentration factor (BCF), Estimated daily intake (EDI), and target hazard quotient (THQ) were computed to estimate human health risks and speculate the hazard index (HI) of adults and children with the consumption of HMs contaminated vegetables at recommended doses. Five vegetables (red amaranth, Indian spinach, cauliflower, tomato, and radish) in a pot experiment were irrigated with groundwater (T1) and seven stages of TDW (T2∼T8) following a randomized complete block design (RCBD) with three replications. Among the TDW stages, T8, T7, T4, and T5 exhibited elevated BCF, EDI, THQ, and HI due to a rising trend in the accumulation of Pb, Cd, Cr, and Ni heavy metals in the edible portion of the red amaranth, followed by radish, Indian spinach, cauliflower, and tomato. The general patterns of heavy metal (HM) accumulation, regarded as vital nutrients for plants, were detected in the following sequence: Zn > Mn/Cu > Fe. Conversely, toxic metals were found to be Cd/Cr > Ni > Pb, regardless of the type of vegetables. Principal Component Analysis (PCA) identified T8, T7, and T4 of TDW as the primary contributors to the accumulation of heavy metals in the vegetables examined. Furthermore, the analysis of the heavy metals revealed that the BCF, THQ, and HI values for all studied metals were below 1, except for Pb. This suggests that the present consumption rates of different leafy and non-leafy vegetables, whether consumed individually or together, provide a low risk in terms of heavy metal exposure. Nevertheless, the consumption of T8, T7, and T4 irrigated vegetables, specifically Indian spinach alone or in combination with red amaranth and radish, by both adults and children, at the recommended rate, was found to pose potential health risks. On the other hand, T2, T3, and T6 irrigated vegetables were deemed safe for consumption. These findings indicated that the practice of irrigating the vegetables with T8, T7, and T4 stages of TDW has resulted in a significant buildup of heavy metals in the soils and edible parts of vegetables which are posing health risks to adults and children. Hence, it is imperative to discharge the T8, T7, and T4 stages of TDW after ETP to prevent the contamination of vegetables and mitigate potential health risks.

Healthcare waste in Bangladesh: Current status, the impact of Covid-19 and sustainable management with life cycle and circular economy framework.

COVID-19 has accelerated the generation of healthcare (medical) waste throughout the world. Developing countries are the most affected by this hazardous and toxic medical waste due to poor management systems. In recent years, Bangladesh has experienced increasing medical waste generation with estimated growth of 3 % per year. The existing healthcare waste management in Bangladesh is far behind the sustainable waste management concept. To achieve an effective waste management structure, Bangladesh has to implement life cycle assessment (LCA) and circular economy (CE) concepts in this area. However, inadequate data and insufficient research in this field are the primary barriers to the establishment of an efficient medical waste management systen in Bangladesh. This study is introduced as a guidebook containing a comprehensive overview of the medical waste generation scenario, management techniques, Covid-19 impact from treatment to testing and vaccination, and the circular economy concept for sustainable waste management in Bangladesh. The estimated generation of medical waste in Bangladesh without considering the surge due to Covid-19 and other unusual medical emergencies would be approximately 50,000 tons (1.25 kg/bed/day) in 2025, out of which 12,435 tons were predicted to be hazardous waste. However, our calculation estimated that a total of 82,553, 168.4, and 2300 tons of medical waste was generated only from handling of Covid patients, test kits, and vaccination from March 2021 to May 2022. Applicability of existing guidelines, and legislation to handle the current situation and feasibility of LCA on medical waste management system to minimize environmental impact were scrutinized. Incineration with energy recovery and microwave sterilization were found to be the best treatment techniques with minimal environmental impact. A circular economy model with the concept of waste minimizaton, and value recovery was proposed for sustainable medical waste management. This study suggests proper training on healthcare waste management, proposing strict regulations, structured research allocation, and implementation of public-private partnerships to reduce, and control medical waste generation for creating a sustainable medical waste management system in Bangladesh.

Sustainable futures in agricultural heritage: Geospatial exploration and predicting groundwater-level variations in Barind tract of Bangladesh.

Groundwater resources are one of the essential aspects of achieving self-sufficiency in a country's agricultural production, poverty alleviation, and socioeconomic development, particularly in agricultural heritage management and practices. In the Barind Tract in Bangladesh, groundwater levels have steadily declined due to growing irrigation demand. Surface water sources become scarce during the dry season, and groundwater levels fall to levels that make minimum cultivation challenging. In these circumstances, determining the current status of groundwater is key to any action in the future. This study investigated the existing geospatial pattern and critical zone of groundwater level in Chapainawabganj District, a significant area of the Barind Tract of Bangladesh, and predicted future groundwater levels considering multiple factors. Kriging, a sophisticated geostatistical method, was performed to examine the geographical pattern and groundwater variations, and time series analysis was employed to determine data trends and make future projections. The current study used groundwater level data from 23 monitoring stations over 10 years (2009-2018). Exponential, Gaussian, and Spherical models were cross-matched here for the best predictor model in four fitness measures to determine groundwater concentrations (RMSE, ME, RMSS, ASE), and Box-Jenkins ARIMA (3,1,0) was found best-fit for predictions, and variance estimation. Likewise, cross-validation has been assessed for the accuracy of anticipated results across spatial scales. Although more research is needed to identify the underlying mechanisms, critical zones, and their pattern of modification, possible recharge zones and their locations have been identified. Future groundwater levels, critical zones, and recharge locations have been indicated for the research area and potential recommendations.

The Utilization of Algae and Seaweed Biomass for Bioremediation of Heavy Metal-Contaminated Wastewater.

The presence of heavy metals in water bodies is linked to the increasing number of industries and populations. This has serious consequences for the quality of human health and the environment. In accordance with this issue, water and wastewater treatment technologies including ion exchange, chemical extraction, and hydrolysis should be conducted as a first water purification stage. However, the sequestration of these toxic substances tends to be expensive, especially for large scale treatment methods that require tedious control and have limited efficiency. Therefore, adsorption methods using adsorbents derived from biomass represent a promising alternative due to their great efficiency and abundance. Algal and seaweed biomass has appeared as a sustainable solution for environmentally friendly adsorbent production. This review further discusses recent developments in the use of algal and seaweed biomass as potential sorbent for heavy metal bioremediation. In addition, relevant aspects like metal toxicity, adsorption mechanism, and parameters affecting the completion of adsorption process are also highlighted. Overall, the critical conclusion drawn is that algae and seaweed biomass can be used to sustainably eliminate heavy metals from wastewater.

Generation of novel n-p-n (CeO2-PPy-ZnO) heterojunction for photocatalytic degradation of micro-organic pollutants.

Recently, hetero junction materials (p-n-p and n-p-n) have been developed for uplifting the visible light activity to destroy the harmful pollutants in wastewater. This manuscript presents a vivid description of novel n-p-n junction materials namely CeO2-PPy-ZnO. This novel n-p-n junction was applied as the photocatalyst in drifting the mobility of charge carriers and hence obtaining the better photocatalytic activity when compared with p-n and pure system. Such catalyst's syntheses were successful via the copolymerization method. The structural, morphological and optical characterization techniques were applied to identify the physio-chemical properties of the prepared materials. Additionally, the superior performance of this n-p-n nanostructured material was demonstrated in the destruction of micro organic (chlorophenol) toxic wastes under visible light. The accomplished ability of the prepared catalysts (up to 92% degradation of chlorophenol after 180 min of irradiation) and their profound degradation mechanism was explained in detail.

Functionalized layered double hydroxides composite bio-adsorbent for efficient copper(II) ion encapsulation from wastewater.

In this study, naturally abundant and inexpensive bamboo was used to make cheaper activated charcoal for efficient encapsulation of toxic copper (Cu(II)) ion from wastewater. The functionalized bamboo charcoal-Layered double hydroxides (BC-LDHs) composite bio-adsorbent was prepared using co-precipitation method. The composite bio-adsorbent was exploited to eliminate Cu(II) ion with high sensitivity and selectivity from contaminated water. The adsorption parameters including the effect of pH, contact time, adsorbent dose, and effect of initial concentration were optimized in systematic way and the adsorption kinetics and isotherms were investigated for potential use in real sample treatment. The physicochemical properties and morphological structure of the adsorbent were examined using X-ray Diffraction, Scanning Electronic Microscopy, Fourier Transform Infrared Spectroscopy and Thermogravimetric Analysis to understand the Cu(II) ion adsorption mechanism. The adsorption results revealed that the BC-LDH could remove almost 100% of Cu(II) ion from aqueous solution at pH range between 3.0 and 6.0 within 30 min. The maximum monolayer adsorption capacity was determined to be 85.47 mg/g based on the Langmuir isotherm. The adsorption equilibrium data were well-fitted by the Langmuir isotherm model (R2 = 0.998) and the experimental kinetic data were supported by the pseudo-second order model (R2 = 0.999). The BC-LDH could be reused without losing its adsorption performance in several cycles after successful regeneration with 0.10 M HCl. The Cu(II) ion removal mechanism was postulated with intercalated ion exchange, surface precipitation and interaction between BC-LDH and surface functionalities. Therefore, the highly functional BC-LDH composite could be a promising adsorbent for efficient Cu(II) ion removal from wastewater.

Efficient cesium encapsulation from contaminated water by cellulosic biomass based activated wood charcoal.

In this study, cost-effective cellulosic biomass based activated wood charcoal was developed from Japanese Sugi tree (Cryptomeria japonica) by concentrated nitric acid modification for adsorption of Cs from contaminated water. The physicochemical properties of specimens were investigated using N2 adsorption-desorption isotherms (BET method), FESEM, FTIR, and XPS spectra analysis. The experimental results revealed that the surface area of the raw wood charcoal was significantly decreased after boiling nitric acid modification. However, several oxygen-containing acidic function groups (-COOH, -CO) were introduced on the surface. The adsorption study confirmed that the equilibrium contact time was 1 h, the optimum adsorption pH was neutral to alkaline and the suitable adsorbent dose was 1:100 (solid: liquid). The maximum Cs was removed when the concentration of Na and K were lower (5.0 mM) with Cs in solution. The Cs adsorption processes well approved by the Langmuir isotherm and pseudo-second-order kinetic models and the maximum adsorption capacity was 35.46 mgg-1. The Cs adsorption mechanism was clearly described and it was assumed that the adsorption was strongly followed by chemisorptions mechanism based on the adsorbent surface properties, kinetic model and Langmuir isotherm model. Most importantly, about 98% of volume reduction was obtained by burning (500 °C) the Cs adsorbed charcoal, which ensured safe storage and disposal of radioactive waste. Therefore, this study can offer a guideline to produce a functional adsorbent for effective Cs removal and safe radioactive waste disposal.

Assessing of cesium removal from wastewater using functionalized wood cellulosic adsorbent.

Sustainable materials are urgently desired for treatment of radioactive cesium (Cs) contaminated water to safe-guard the public health. Apart from the synthetic ligand-based materials, the Mangrove charcoal modified adsorbent was fabricated for assessing of Cs removal from waste sample. The raw charcoal was oxidized using nitrification approach and diverse oxygen containing carboxyl, carbonyl and hydroxyl functional groups were introduced. After modification, the adsorbent characteristics were drastically changed as compared to the charcoal during the measurement of FTIR, N2 adsorption-desorption isotherms and SEM micrographs. The data clarified that charcoal modified adsorbent was exhibited high Cs transport through the inner surface of the adsorbent based on bonding ability. The adsorbent was shown comparatively slow kinetics to Cs ion; however, the adsorption capacity was high as 133.54 mg/g, which was higher than the crown ether based conjugate materials. The adsorption data were followed to the Langmuir adsorption isotherms and the monolayer coverage was possible due to the data presentation. The presence of high amount of Na and K were slightly interfered to the Cs adsorption by the charcoal modified adsorbent, however; the Na and K concentration was 350-600 folds higher than the Cs concentration. Then the proposed adsorbent was selective to Cs for the potential real radioactive Cs contaminated water. The volume reduction was established rather than desorption and reuses advantages. More than 99% volume reduction was measured by burning of Cs adsorbed adsorbent at 500 °C for ensuring the safe storage and disposal of used adsorbent. Therefore, the charcoal modified adsorbent may open the new door to treat the Cs containing wastewater.

Ultrathin Assembles of Porous Array for Enhanced H2 Evolution.

Since the complexity of photocatalyst synthesis process and high cost of noble cocatalyst leftovers a major hurdle to producing hydrogen (H2) from water, a noble metal-free Ni-Si/MgO photocatalyst was realized for the first time to generate H2 effectively under illumination with visible light. The catalyst was produced by means of simple one-pot solid reaction using self-designed metal reactor. The physiochemical properties of photocatalyst were identified by XRD, FESEM, HRTEM, EDX, UV-visible, XPS, GC and PL. The photocatalytic activities of Ni-Si/MgO photocatalyst at different nickel concentrations were evaluated without adjusting pH, applied voltage, sacrificial agent or electron donor. The ultrathin-nanosheet with hierarchically porous structure of catalyst was found to exhibit higher photocatalytic H2 production than hexagonal nanorods structured catalyst, which suggests that the randomly branched nanosheets are more active surface to increase the light-harvesting efficiency due to its short electron diffusion path. The catalyst exhibited remarkable performance reaching up to 714 µmolh-1 which is higher among the predominant semiconductor catalyst. The results demonstrated that the photocatalytic reaction irradiated under visible light illumination through the production of hydrogen and hydroxyl radicals on metals. The outcome indicates an important step forward one-pot facile approach to prepare noble ultrathin photocatalyst for hydrogen production from water.

Novel conjugated hybrid material for efficient lead(II) capturing from contaminated wastewater.

An efficient material is always welcoming for the water treatment due to the need of clean water to safe the human health. The conjugate adsorbent (CJA) was fabricated by functional ligand embedded onto the highly porous silica material for selective lead (Pb(II)) ion monitoring and removal from wastewater. The study was achieved not only investigating the beginning material but also the performing extrusion as novel conjugate material, this defining the material novelty of this study considers to the modern state-of-art. The fabricated material was characterized in all aspects and then the experimental works for Pb(II) ion assessing were carried in batch mode. The CJA was exposed the color and signal intensity upon addition of Pb(II) ion from low to high concentrations. The optimum pH was considered at 5.50 based on the sensitivity, the color formation ability and high adsorption of Pb(II) ion. The determined limit of low detection was 0.18 µg/L, which was the extraordinary performance for the Pb(II) ion monitoring ability by the CJA. The adsorption efficiency, specific attention was remunerated to the influence of solution pH, reaction time, foreign ion, initial Pb(II) amounts and regeneration. The CJA was exhibited high kinetic performances and showed high adsorption Pb(II) ion compared with the different forms of material. The adsorption was completely fitted with the Langmuir adsorption as defining the monolayer coverage as expected of the homogeneous porosity of the CJA. The maximum adsorption was determined as high as 175.16 mg/g. In addition, the foreign ions were not affected in the Pb(II) adsorption by the CJA, and the adsorbent was regenerated using 0.20 M HCl for several cycles used without significant loss of the initial performance. Considering these advantages, the CJA demonstrated the potential low-cost material for competitive use in wastewater remediation, especially in the developing countries.

Composite nanofibers membranes of poly(vinyl alcohol)/chitosan for selective lead(II) and cadmium(II) ions removal from wastewater.

The nanofibers membranes were fabricated by poly(vinyl alcohol)/chitosan (PVA/Chi) using an electro-spun technique for selective and high adsorption of lead (Pb(II)) and cadmium (Cd(II)) ions based on the solution acidity. The PVA/Chi NFs membranes were characterized systematically using several instrumentations. In addition, several experimental parameters such as initial metal ions concentration, interaction time, adsorbent dosage, solution pH and the effects of competing ions on Pb(II) and Cd(II) adsorption were evaluated. The adsorption data were also clarified that the PVA/Chi NFs membranes were exhibited high kinetic performances towards the both toxic ions at the optimum conditions. The adsorption data were manipulated using different kinetics models, and it was confirmed that only pseudo-second-order model obeyed the adsorption kinetics for Pb(II) and Cd(II) ions. Similarly, the equilibrium data were well fitted with the Langmuir adsorption isotherms model, and the maximum adsorption capacity was 266.12 and 148.79 mg/g for Pb(II) and Cd(II) ions, respectively. The Pb(II) and Cd(II) ions adsorptions were also measured to know the selectivity with simulated environmental solution, and the data were confirmed the high selectivity to Pb(II) and Cd(II) ions at the optimum condition and the nanofibers membrane shown the potentiality for possible use in efficient removal of the selected toxic ions from waste samples. Thus, the PVA/Chi NFs are considered to be effective and promising materials for Pb(II) and Cd(II) ions from wastewaters with high efficiency.

Investigation of novel nanomaterial for the removal of toxic substances from contaminated water.

Ligand-functionalized nanomaterials exhibit great potential for the removal of hazardous substances from the environment and industrial wastewater. In this work, a composite nanosphere material was fabricated using mesoporous silica and organic ligand, and employed for the efficient detection and subsequent removal of toxic sulfanilamide (SNA) from waste samples. The organic ligand 2-naphthol was successfully conjugated onto the mesoporous nanospheres, which then captured SNA under suitable conditions. A naked-eye color change was observed even when a trace amount of SNA interacted with the material, which is the most promising advantage of the fabricated material. A low limit of detection and quantification limit were also determined, and the new nanosphere material revealed the ultra-trace detection performance of 0.27 µg L-1 of SNA in aqueous media. The effect of solution pH, competing ions, color optimization and initial concentration of SNA on the nanosphere material was investigated under the optimum conditions. The nanosphere material exhibited rapid adsorption properties, and its maximum adsorption capability approached 79.20 mg g-1. Several compounds were examined as common interfering substances including vanillin, glucose, lactose, starch and sucrose, which did not adversely interfere in both the detection and adsorption systems using the proposed nanosphere material. The data emphasized that the proposed material is highly suitable for the capture of SNA from contaminated water based on its selectivity, sensitivity, cost-effectiveness and eco-friendly approach. The results also indicate that this nanosphere material will attract attention from researchers for the efficient and selective capture of the toxic SNA.

A Reliable Hybrid Adsorbent for Efficient Radioactive Cesium Accumulation from Contaminated Wastewater.

Cesium (Cs) removal from nuclear liquid wastewater has become an emerging issue for safeguarding public health after the accident at the Fukushima Daiichi Nuclear Power Plant. A novel macrocyclic ligand of o-benzo-p-xylyl-22-crown-6-ether (OBPX22C6) was developed and successfully immobilized onto mesoporous silica for the preparation of hybrid adsorbent. The benzene ring π electron is the part of crown ether of OBPX22C6 for easy orientation of the macrocyclic compound for making the π electron donation with Cs complexation. The potential and feasibility of the hybrid adsorbent as being Cs selective was evaluated in terms of sensitivity, selectivity and reusability. The results clarified that the Cs removal process was rapid and reached saturation within a short time. Considering the effect of competitive ions, sodium (Na) did not markedly affect the Cs adsorption whereas potassium (K) was slightly affected due to the similar ionic radii. However, the oxygen in long ethylene glycol chain in OBPX22C6 was expected to show strong coordination, including Cs-π interaction with Cs even in the presence of the high amount of K and Na. Due to its high selectivity and reusability, significant volume reduction is expected as this promising hybrid adsorbent is used for Cs removal in Fukushima wastewater.

Ultimate selenium(IV) monitoring and removal from water using a new class of organic ligand based composite adsorbent.

This work reports the selenium (Se(IV)) detection and removal from water by ligand functionalized organic-inorganic based novel composite adsorbent. The composite adsorbent was prepared by direct immobilization of N,N'-di(3-carboxysalicylidene)-3,4-diamino-5-hydroxypyrazole onto the mesoporous silica monolith. The adsorbent exhibited distinct color change in the presence of various concentrations of Se(IV). This was characterized by UV-vis spectroscopy, and the color change was observed by naked-eye observation. The detection limit was determined to be 1.14 µg/L. The effect of solution pH, interferential metal ions, contact time, initial Se(IV) concentration, and adsorbent regeneration were evaluated. The maximum sorption capacity was determined based on the initial concentration. The data fitted well to the Langmuir isotherm model, and the maximum Se(IV) sorption capacity was 111.12 mg/g. The presence of diverse competing ions did not affect the Se(IV) sorption capacity, and the adsorbent had almost no sorption capacity for these coexisting ions, which suggests the high selectivity to Se(IV) ions. The adsorbed Se(IV) was eluted with suitable eluent (0.10 M NaOH) and simultaneously regenerated into the initial form for the next operation. The excellent reusability of the adsorbent was justified after eight consecutive sorption-elution-regeneration cycles. The proposed adsorbent is cost-effective and environmentally friendly and a potential candidate for treatment of water containing Se(IV).

Selective cesium removal from radioactive liquid waste by crown ether immobilized new class conjugate adsorbent.

Conjugate materials can provide chemical functionality, enabling an assembly of the ligand complexation ability to metal ions that are important for applications, such as separation and removal devices. In this study, we developed ligand immobilized conjugate adsorbent for selective cesium (Cs) removal from wastewater. The adsorbent was synthesized by direct immobilization of dibenzo-24-crown-8 ether onto inorganic mesoporous silica. The effective parameters such as solution pH, contact time, initial Cs concentration and ionic strength of Na and K ion concentrations were evaluated and optimized systematically. This adsorbent was exhibited the high surface area-to-volume ratios and uniformly shaped pores in case cavities, and its active sites kept open functionality to taking up Cs. The obtained results revealed that adsorbent had higher selectivity toward Cs even in the presence of a high concentration of Na and K and this is probably due to the Cs-π interaction of the benzene ring. The proposed adsorbent was successfully applied for radioactive Cs removal to be used as the potential candidate in Fukushima nuclear wastewater treatment. The adsorbed Cs was eluted with suitable eluent and simultaneously regenerated into the initial form for the next removal operation after rinsing with water. The adsorbent retained functionality despite several cycles during sorption-elution-regeneration operations.

Selective lanthanide sorption and mechanism using novel hybrid Lewis base (N-methyl-N-phenyl-1,10-phenanthroline-2-carboxamide) ligand modified adsorbent.

This study aims to develop a highly selective Lewis base adsorbent to investigate the selective sorption and recovery of Eu(III) and Sm(III) from wastewater. The oxygen and nitrogen donor atoms containing Lewis base N-methyl-N-phenyl-1,10-phenanthroline-2-carboxamide (MePhPTA) ligand was synthesized and subsequently an adsorbent was prepared by direct immobilization onto mesoporous silica. Determined maximum adsorption capacities were 125.63 and 124.38 mg/g for Eu(III) and Sm(III), respectively. Experiments with mixed-cations solutions showed that the sequence of preferential adsorption was Eu(III)>Sm(III). The lanthanide sorption by hybrid Lewis base adsorbent (HyLBA) was not adversely affected by the presence of sodium, potassium, calcium, magnesium, chloride, sulfate and nitrate ions due to strong affinity between hard Lewis acid lanthanide and hard Lewis base adsorbent. The crystallography for the Sm-MePhPTA complex suggested that MePhPTA was strongly coordinated to Sm(III) with oxygen and nitrogen by forming a stable complex with two 5-membered rings. The data clarified that bond lengths between Sm(III) and amide oxygen (2.475Å) were shorter than SmN (2.662Å) in phenanthroline moiety indicating strong oxygen driven HyLBA. The results suggested that HyLBA has a good prospect of promising applications for separation/sorption of lanthanide ions from effluents.

Efficient arsenic(V) removal from water by ligand exchange fibrous adsorbent.

This study is an efficient arsenic(V) removal from contaminated waters used as drinking water in adsorption process by zirconium(IV) loaded ligand exchange fibrous adsorbent. The bifunctional fibers contained both phosphonate and sulfonate groups. The bifunctional fiber was synthesised by graft polymerization of chloromethylstyrene onto polyethylene coated polypropylene fiber by means of electron irradiation graft polymerization technique and then desired phosphonate and sulfonate groups were introduced by Arbusov reaction followed by phosphorylation and sulfonation. Arsenic(V) adsorption was clarified in column methods with continuous flow operation in order to assess the arsenic(V) removal capacity in various conditions. The adsorption efficiency was evaluated in several parameters such as competing ions (chloride and sulfate), feed solution acidity, feed flow rate, feed concentration and kinetic performances at high feed flow rate of trace concentration arsenic(V). Arsenic(V) adsorption was not greatly changed when feed solutions pH at 3.0-7.0 and high breakthrough capacity was observed in strong acidic area below pH 2.2. Increasing the flow rate brings a decrease both breakthrough capacity and total adsorption. Trace level of arsenic(V) (0.015 mM) in presence of competing ions was also removed at high flow rate (750 h(-1)) with high removal efficiency. Therefore, the adsorbent is highly selective to arsenic(V) even in the presence of high concentration competing ions. The adsorbent is reversible and reusable in many cycles without any deterioration in its original performances. Therefore, Zr(IV) loaded ligand exchange adsorbent is to be an effective means to treat arsenic(V) contaminated water efficiently and able to safeguard the human health.

Enhanced trace phosphate removal from water by zirconium(IV) loaded fibrous adsorbent.

This study was investigated for the trace phosphate removal at high feed flow rate by ligand exchange fibrous adsorbent. The zirconium(IV) loaded bifunctional fibers containing both phosphonate and sulfonate were used as a highly selective ligand exchange adsorbent for trace phosphate removal from water. The precursory fiber of the bifunctional fibers was co-grafted by polymerization of chloromethylstyrene and styrene onto polyethylene coated polypropylene fiber and then bifunctional fibers were prepared by Arbusov reaction followed by phosphorylation and sulfonation. Phosphate adsorption experimental work was carried out in column approach. Phosphate adsorption increased with decreasing the pH of feed solutions. An increase in the feeds flow rate brings a decrease in both breakthrough capacity and total adsorption. The effect of competing anions on phosphate adsorption systems was investigated. The experimental findings reveal that the phosphate adsorption was not affected in the presence of competing anions such as chloride and sulfate despite the enhancement of the breakthrough points and total adsorption. Due to high selectivity to phosphate species, low concentration level of phosphate (0.22 mg/L) was removed at high feed flow rate of 450 h(-1) in space velocity. The adsorbed phosphate on the Zr(IV) loaded fibrous column was quantitatively eluted with 0.1 M NaOH solution and then the column was regenerated by 0.5M H2SO4 for the next adsorption operation. During many adsorption-elution-regeneration cycles, no measurable Zr(IV) was found in the column effluents. Therefore, the Zr(IV) loaded bifunctional fibrous adsorbent is to be an effective means to treat wastewater to prevent eutrophication in the receiving water bodies for long time without any deterioration.

Efficient adsorbents of nanoporous aluminosilicate monoliths for organic dyes from aqueous solution.

Growing public awareness on the potential risk to humans of toxic chemicals in the environment has generated demand for new and improved methods for toxicity assessment and removal, rational means for health risk estimation. With the aim of controlling nanoscale adsorbents for functionality in molecular sieving of organic pollutants, we fabricated cubic Im3m mesocages with uniform entrance and large cavity pores of aluminosilicates as highly promising candidates for the colorimetric monitoring of organic dyes in an aqueous solution. However, a feasible control over engineering of three-dimensional (3D) mesopore cage structures with uniform entrance (~5 nm) and large cavity (~10 nm) allowed the development of nanoadsorbent membranes as a powerful tool for large-quantity and high-speed (in minutes) adsorption/removal of bulk molecules such as organic dyes. Incorporation of high aluminum contents (Si/Al=1) into 3D cubic Im3m cage mesoporous silica monoliths resulted in small, easy-to-use optical adsorbent strips. In such adsorption systems, natural surfaces of active acid sites of aluminosilicate strips strongly induced both physical adsorption of chemically responsive dyes and intraparticle diffusion into cubic Im3m mesocage monoliths. Results likewise indicated that although aluminosilicate strips with low Si/Al ratios exhibit distortion in pore ordering and decrease in surface area and pore volume, enhancement of both molecular converges and intraparticle diffusion onto the network surfaces and into the pore architectures of adsorbent membranes was achieved. Moreover, 3D mesopore cage adsorbents are reversible, offering potential for multiple adsorption assays.