Remote magnetically stimulated xanthan-biochar-Fe3O4-molecularly imprinted biopolymer hydrogel toward electrochemical enantioselection of l-tryptophan.

Monitoring the levels of L-Tryptophan (L-Trp) in body fluids is crucial due to its significant role in metabolism and protein synthesis, which ultimately affects neurological health. Herein, we have developed a novel magneto-responsive electrochemical enantioselective sensor for the recognition of L-Trp based on oriented biochar derived from Loofah, Fe3O4 nanoparticles, and molecularly imprinted polydopamine (MIPDA) in xanthan hydrogel. The successful synthesis of these materials has been confirmed through physicochemical and electrochemical characterization. Various operational factors such as pH, response time, loading sample volume, and loading of active materials were optimized. As a result, the sensor exhibited an affordable linear range of 1.0-60.0 µM, with a desirable limit of detection of 0.44 µM. Furthermore, the proposed electrochemical sensor demonstrated good reproducibility and desirable selectivity for the determination of L-Trp, making it suitable for analyzing L-Trp levels in human plasma and serum samples. The development presented offers an appealing, easily accessible, and efficient strategy. It utilizes xanthan hydrogel to improve mass transfer and adhesion, biochar-stabilized Fe3O4 to facilitate magnetic orientation and accelerate mass transfer and sensitivity, and polydopamine MIP to enhance selectivity. This approach enables on-site evaluation of L-Trp levels, which holds significant value for healthcare monitoring and early detection of related conditions.

Prussian Blue Analogues-Derived Molecularly Imprinted Nanozyme Array for Septicemia Detection.

Septicemia, a severe bacterial infection, poses significant risks to human health. Early detection of septicemia by tracking specific biomarkers is crucial for a timely intervention. Herein, we developed a molecularly imprinted (MI) TiO2-Fe-CeO2 nanozyme array derived from Ce[Fe(CN)6] Prussian blue analogues (PBA), specifically targeting valine, leucine, and isoleucine, as potential indicators of septicemia. The synthesized nanozyme arrays were thoroughly characterized using various analytical techniques, including Fourier transform infrared spectroscopy, X-ray diffraction, field-emission scanning electron microscope, and energy-dispersive X-ray. The results confirmed their desirable physical and chemical properties, indicating their suitability for the oxidation of 3,3',5,5'-tetramethylbenzidine serving as a colorimetric probe in the presence of a persulfate oxidizing agent, further highlighting the potential of these arrays for sensitive and accurate detection applications. The MITiO2 shell selectively captures valine, leucine, and isoleucine, partially blocking the cavities for substrate access and thereby hindering the catalyzed TMB chromogenic reaction. The nanozyme array demonstrated excellent performance with linear detection ranges of 5 µM to 1 mM, 10-450 µM, and 10-450 µM for valine, leucine, and isoleucine, respectively. Notably, the corresponding limit of detection values were 0.69, 1.46, and 2.76 µM, respectively. The colorimetric assay exhibited outstanding selectivity, reproducibility, and performance in the detection of analytes in blood samples, including C-reactive protein at a concentration of 61 mg/L, procalcitonin at 870 ng/dL, and the presence of Pseudomonas aeruginosa bacteria. The utilization of Ce[Fe(CN)6]-derived MITiO2-Fe-CeO2 nanozyme arrays holds considerable potential in the field of septicemia detection. This approach offers a sensitive and specific method for early diagnosis and intervention, thereby contributing to improved patient outcomes.

Eco-friendly and sustainable basil seed hydrogel-loaded copper hydroxide-based catalyst for the synthesis of propargylamines and tetrazoles.

The broad use of propargyl amines and tetrazoles in pharmaceutical applications presents a well-established challenge. Their synthesis relies heavily on catalysis, which, in turn, has been hindered by the scarcity of stable and practical catalysts. In response to this issue, we have developed an environmentally friendly and sustainable catalyst by infusing copper hydroxide into basil seed hydrogel (Cu(OH)2-BSH), creating a 3D nanoreactor support structure. To verify the structural, physical, chemical, and morphological properties of the prepared samples, a comprehensive analysis using various techniques, including FT-IR, EDX, FE-SEM, TEM, XRD, BET, TGA, and XPS, were conducted. The results not only confirmed the presence of Cu(OH)2 but also revealed a porous structure, facilitating faster diffusion and providing a substantial number of active sites. This catalyst boasts a high surface area and can be easily recovered, making it a cost-effective, safe, and readily available option. This catalyst was applied to the synthesis of propargyl amines and tetrazoles through multi-component reactions (MCRs), achieving excellent results under mild conditions and in a remarkably short timeframe. Consequently, this work offers a straightforward and practical approach for designing and synthesizing metal hydroxides and 3D hydrogels for use in heterogeneous catalysis during organic syntheses. This can be achieved using basic and affordable starting materials at the molecular level.

Paper-based microfluidic system and chiroptical functionalized gold nano-oval for colorimetric detection of L-Tryptophan.

"The development and deployment of a practical and portable technology for on-site chiral identification of enantiomers hold immense significance in the fields of medical and biological sciences. Among the essential amino acids, Tryptophan (Trp) plays a crucial role in human metabolism and serves as a diagnostic marker for various metabolic disorders. In this study, we introduce an innovative approach that combines an enantio-selective ZIF-8-His MOF-MIPs packed-bed centrifugal microfluidic system with an enantioselective colorimetric sensor probe. This system is further integrated with smartphone-based on-site data recording. The basis of this colorimetric sensor's operation lies in the controlled morphology and surface passivation of gold nano-ovals (Au-NOs) through DL-Alanine. To confirm the successful synthesis of the chiral recognition elements, we employed various characterization techniques, including FE-SEM, TEM, FTIR, CD, UV-Vis, zeta potential, DLS, and XRD. Our focus was on optimizing operational parameters for the effective separation and determination of L-chiral tryptophan on-site. The sensor exhibited two linear ranges for L-Trp detection: 0-5.42 and 5.42-80.47 mM, with a detection limit of 0.5 mM. The integrated system possesses advantages such as ease of availability, preparation, high stability, desirable selectivity even in the presence of similar biomolecules, and rapid detection capabilities. Furthermore, our method demonstrated successful enantioselective sensing of L-Trp in various biological samples, including human blood plasma, urine, milk, and bovine serum albumin (BSA), yielding promising results. The integrated microfluidic platform follows a "sample-in and answer-out" approach, making it highly applicable in healthcare, environmental monitoring, food safety analysis, and point-of-care testing. The chiral recognition pretreatment assay and self-contained, automated colorimetric detection on the microfluidic disc represent a promising avenue for cutting-edge research in these domains".

Enhancing On-Skin Analysis: A Microfluidic Device and Smartphone Imaging Module for Real-Time Quantitative Detection of Multianalytes in Sweat.

Wearable sweat sensors present exciting opportunities for advancing personal health monitoring and noninvasive biomarker measurements. However, existing sensors often fall short in accurate detection of low analyte volumes and concentrations and lack multimodal sensing capabilities. Herein, we present a highly portable four-channel microfluidic device capable of conducting simultaneous sweat sampling and fluorometric sensing of potential biomarkers, such as l-Tyr, l-Trp, Crt, and NH4+, specifically designed for kidney disease monitoring. Our microfluidic device seamlessly integrates with smartphones, facilitating easy data retrieval and analysis. The core of the sensing array is a novel fluorometric solid-state mechanism utilizing carbon polymer dots derived from dopamine, catechol, and o-phenylenediamine monomers embedded in gelatin hydrogels. The sensors exhibit exceptional performance, offering linear ranges of 5-275, 6-170, 4-220, and 5-170 µM, with impressively low detection limits of 1.5, 1.2, 1.3, and 1.4 µM for l-Tyr, l-Trp, Crt, and NH4+, respectively. Through meticulous optimization of operational variables, comprising the temperature, sample volume, and assay time, we achieved the best performance of the device. Furthermore, the sensors exhibited remarkable selectivity, effectively distinguishing between biologically similar species and other potential biological compounds found in sweat. Our evaluation also extended to monitoring kidney diseases in patients and healthy individuals, showcasing the device's utility in world scenarios. Promising results showcase the potential of low-cost, multidiagnostic microfluidic sensor arrays, especially with synthetic skin integration, for enhanced disease detection and healthcare outcomes.

Cellulose acetate/MOF film-based colorimetric ammonia sensor for non-destructive remote monitoring of meat product spoilage.

Herein, we designed an on-site and portable colorimetric assay using cellulose acetate polymeric films incorporated with HKUST-1 metal-organic framework while immersed in a solution of methyl red and brilliant cresyl blue organic dyes as an indicator for monitoring ammonia levels. Ammonia serves as a significant biomarker of food spoilage which falls under the category of volatile organic compounds (VOCs). The designed colorimetric solid-state sensor was comprehensively characterized using FE-SEM, EDS-mapping, XRD, FTIR, and contact angle analyses. The results confirmed the superior stability, water permeability, good crystallinity and desirable morphology of the prepared sensor platform. Additionally, customized smartphone was developed and applied for online signaling and colorimetric analysis. The findings demonstrated two linear ranges: 1-100 ppb and 0.1-1340 ppm with a detection limit of 0.02 ppm. The solid-state sensor exhibited high selectivity in the presence of other VOCs such as methanol, ethanol, acetone, 2-propanol, toluene, humidity, and hexane. It displayed acceptable repeatability in both inter-day (RSD = 3.38 %) and intraday (RSD = 3.86 %), long-term stability over 4 days as well as reusability over 3 cycles. We successfully applied this sensing platform for ammonia monitoring in spoiled meat foods including veal, fish and chicken. The results indicated favorable percentage recovery and repeatability, confirming the feasibility and potential applicability of this intelligent packaging system for monitoring freshness. The platform allows for real-time monitoring and data analysis via smartphone-based online signaling, providing a convenient and effective method for ensuring food quality.

Red-emissive carbon nanostructure-anchored molecularly imprinted Er-BTC MOF: a biosensor for visual anthrax monitoring.

Investigating effective fluorescence strategies for real-time monitoring of dipicolinic acid (DPA) is of paramount importance in safeguarding human health. Herein, we present the design of a desirable red-emissive carbon nanostructure anchoring a molecularly imprinted Er-BTC MOF as a fluorescence biosensor for the visual determination of DPA. DPA is a biomarker of Bacillus anthracis, a subcategory of serious infectious diseases and bioweapons. We introduce a paper test strip sensitized with the aforementioned nanostructure, which is integrated with online UV excitation and smartphone digital imaging, resulting in a DPA signal-off sensing platform. The proposed fluorometric visual paper-based biosensor demonstrates wide linear ranges for DPA (10-125 µM) with a LOQ and LOD of 4.32 and 1.28 µM, respectively. The designed platform exhibits impressive emission properties and adaptable surface functional groups, which confirm its desirable selective sensing capabilities against other biological molecules and DPA isomers. As a proof of concept, DPA monitoring is successfully applied to real samples of tap water and urine. This integrated selective paper-based nano-biosensor, coupled with smartphone signal recording, holds great promise for state-of-the-art practical applications including fluorometric/colorimetric detection in healthcare and environmental monitoring, food safety analysis, and point-of-care testing.

Ruthenium-Encapsulated Porphyrinic Organic Polymer as a Photoresponsive Oxidoreductase Mimetic Nanozyme for Colorimetric Sensing.

The advantages of porosity and stable unpaired electrons of porphyrinic organic polymers (POPs) with free radicals are exclusive and potentially practical functionalities and combining the semiconductor-like characteristics of these materials and metal ions has been an effective way to assemble an efficient photocatalytic system. Herein, a new ruthenium (Ru) ion-encapsulated porphyrinic organic polymer (POP/Ru) is facilely synthesized as a proper photoresponsive nanozyme with unique photo-oxidase properties. Surprisingly, the proposed POP/Ru revealed outstanding photoresponsive oxidase-mimicking activity due to the synergetic effect of the integration of Ru and π-electrons of POP, which boosts charge separation and transport. POP/Ru was applied to the oxidation of o-phenylenediamine (o-PDA) as a chromogenic probe for producing a colorimetric signal. The kinetic study reveals that these photo-oxidase mimics have a significant affinity for the o-PDA chromogenic agent owing to a lower Km and superior Vmax. Further findings demonstrate that the presence of the l-arginine (l-Arg) target causes an inhibition effect on the photo-nanozymatic colorimetry of POP/Ru. This research develops the applications of the comprehensive colorimetric strategy for ultrasensitive l-Arg monitoring with a limit of detection (LOD) of 15.2 nM in the dynamic range of 4.0 nM-340 µM and illuminates that the proposed photo-oxidase nanozyme as a visual strategy is feasible in l-Arg environmentally friendly colorimetric detection in juice samples.

Biomass derived reduced-graphene-oxide supported α-Fe2O3/ZnO S-scheme heterostructure: Robust photocatalytic wastewater remediation.

The emergence of new diseases and the unplanned industrialization of cities have led to new diseases and the subsequent use of antibiotics. Hence the remediation of wastewater containing antibiotics and their severe pollution has raised serious concerns in recent years. Herein coral-shaped α-Fe2O3/ZnO/reduced graphene oxide (r-GO)-like carbon heterojunction in-situ were prepared from basil seed as a sustainable biomass resource and applied for the photodegradation of the oxytetracycline (OTC) as a typical antibiotic in a helical plug flow photoreactor (HPFPR) via persulfate activation under visible light irradiation. Spectroscopy and electrochemical results confirmed the tunable band structure and quick light absorption, superior charge separation and transfer, satisfactory charge carrier lifetime, and long-term stability for the prepared photocatalyst. The 98% degradation efficiency was achieved for OTC within 90 min fitted by a first-order kinetic model with the rate constant of 0.1248 min-1. The finding proves that HPFPR exhibited a higher degradation rate of OTC by 2.3 times compared to the batch reactor. The 3D computational fluid dynamics (CFD) model confirmed the outstanding performance of the HPFPR. Scavenging experiments integrated with mott Schottky and DRS results revealed that rGO intensifies the S-scheme charge carrier transfer and built-in electric field and reduces the recombination. Finally, this work has substantial potential for the in-situ synthesis of environmental-friendly and large-scale metal oxide heterojunctions in natural carbon supports as well as scale-up and gives novel insights from molecular and engineering points of view into the wastewater remediation processes and clean water production.

Photo-responsive oxidase-like nanozyme based on a vanadium-docked porphyrinic covalent organic framework for colorimetric L-Arginine sensing.

This study reports the development of a vanadium-docked porphyrinic covalent organic framework as a novel class of highly polar photoactive materials. Thanks to its extended π-electron conjugation and high chemical stabilities, this framework can serve as an oxidase-Like photo-nanozyme for photocatalytic oxidation of o-phenylenediamine (o-PDA) and a colorimetric substrate for the production of the yellow-colored oxidized o-PDA (o-PDAox). The physicochemical properties of the as-prepared photo-nanozyme were characterized by several analytical techniques. Its enhanced light harvesting and charge separation and transfer were also verified by electrochemical and spectroscopic analysis. This photo-nonenzymatic colorimetric assay was applied for the sensitive L-Arginine (L-Arg) detection as a typical amino acid in the linear range of 8.1 nM-330 µM with a limit of detection (LOD) of 3.5 nM. The findings of this research confirmed the safety and feasibility of the proposed photo-nonenzymatic colorimetric sensing strategy for the detection of L-Arg and other similar biomolecules in food samples. Kinetic investigation revealed that the photo-responsive oxidase mimic exhibits satisfactory Km (0.47 mM) and Vmax (42.0 µM/s) values. This work broadened our insight into the development of modified porphyrinic-COF-based visible light-responsive oxidase-like photo-nanozyme for environmentally friendly colorimetric biosensing.

Development of peptide impregnated V/Fe bimetal Prussian blue analogue as Robust nanozyme for colorimetric fish freshness assessment.

Colorimetric sensing is a low-cost and visual method for food freshness monitoring. We prepared a Vanadium-Iron Prussian blue analogue (V1/5Fe(CN)6 PBA) impregnated with insulin (INS), as a peroxidase-like mimetic probe toward 3,3'5,5'-tetramethylbenzidine (TMB) oxidation and colorimetric monitoring of fish freshness. A specific chemical reaction between putrescine as spoilage marker and the Vanadium-Iron V1/5Fe(CN)6PBA impregnated with insulin (V1/5Fe(CN)6PBA/INS) induces a decreasing peroxidase-like activity of the V1/5Fe(CN)6PBA/INS, generating lower amounts of oxidized products of TMB. The proposed bio-strategy achieved highly sensitive responses in the range of 30 nM to 12 µM toward putrescine with a detection limit of 9.0 nM and outstanding stability, reproducibility, and selectivity. The freshness of five different types of fish samples determined and produces a noticeable color change consistent with the stale fish around the 10 µM, which can warn the oldness of the fish. This new strategy of integration between peptide and multi-metal PBA with intensified enzyme-like mimetics activity may be highly meaningful for thoroughly monitoring the amount of fish freshness.

Visible light-responsive vanadium-based metal-organic framework supported pepsin with high oxidase mimic activity for food spoilage monitoring.

A photo-induced metal-organic framework-enzyme hybrid nanosystem was developed via a controllable physical embedding method that displays dual enzymatic and photo-non-enzymatic strategy which cause high stability and cascade catalytic performance to oxidation of o-phenylenediamine and generate a UV-Vis signal at 450 nm for the tracing and sensitive detection of putrescine (Put). Under optimal conditions, the present bioassay provides a wide detection range from 0.02 to 10 µM and 20-80 µM with a detection limit of 5.5 nM, which is more desirable than numerous previous reports. In addition, the established colorimetric photo-bioassay can selectively and accurately identify Put in the presence of other distributing species. The present work provides an elegant strategy to merged photo-nanozymes' and enzyme capabilities and also broadened the sensing strategies of photo-nanozymes with promising potential in the realm of cancer diagnosis and food quality monitoring as well as its potential in various bioassays and heterogeneous catalysis fields.

Molecular Imprinted Poly(2,5-benzimidazole)-Modified VO2-CuWO4 Homotype Heterojunction for Photoelectrochemical Dopamine Sensing.

A photoactive molecularly imprinted poly(2,5-benzimidazole)-modified vanadium dioxide-cupric tungstate (VO2-CuWO4) as an efficient photosensitive n-n type-II heterojunction thin film was electrochemically deposited on Ti substrate for the selective and robust photoelectrochemical (PEC) bioanalysis of dopamine (DA). The optical absorption of n-VO2/n-CuWO4 type-II heterojunction was capably broadened toward the visible region, which permitted superior light-harvesting and robust carriers generation, separation, and transfer processes significantly enhancing the anodic photocurrent, as confirmed by a series of PEC analyses. Findings revealed that the as-prepared label-free MIP-PEC sensor can quantitatively monitor DA in a linear range of 1 nM to 200 µM with a detection limit of 0.15 nM. This MIP-PEC sensor showed robust selectivity under conditions with high concentrations of interfering substances, which can be recovered in the real samples of urine, cocoa chocolate, and diluted yogurt, indicating its promising potential applications in biological and food samples. This work not only featured the use of photoelectrically active MIP/VO2-CuWO4 for PEC detection of DA, but also provided a new horizon for the design and implementation of functional polymers/metal oxides heterojunction materials in the field of PEC sensors and biosensors.

Hydrophilic magnetic molecularly imprinted resin in PVDF membrane for efficient selective removal of dye.

Selective removal of contaminants from water by membranes is of practical importance for water purification and environmental protection. In the present study, through an in-situ polymerization process, a novel composite of Fe3O4/molecularly imprinted resorcinol -formaldehyde-melamine resin (Fe3O4/MIRFMR) was synthesized. Then, the novel membrane was prepared from a tea filter bag (TFB) as a base substrate which was subsequently coated by a casting solution containing polyvinylidene fluoride (PVDF) matrix, Prunus scoparia gum as a hydrophilic agent and Fe3O4/MIRFMR as selective filler by phase inversion technique. Resorcinol as functional monomers with multiple hydrophilic groups such as -OH, -NH2 and -NH-, were used for selective removal of Rhodamine B (RhB) as target molecule. The Fe3O4/MIRFMR/PVDF/TFB membranes were characterized by FE-SEM, XRD, FTIR, BET, VSM, water contact angle (WCA) and mechanical analysis. The filtration and adsorption of RhB on the prepared membrane was investigated parameters in a cross-module filtration setup. Casting solution containing 0.01 g of Fe3O4/MIRFMR as optimum value showed good wettability, high water flux (42.5 L/m2 h), flux recovery ratio (88.9%), RhB removal efficiency (95.8%). The selectivity of 4.9, 3.3, 2.1 and 2.5 was found to be for RhB compared to AB, MG, EB, and TB dye. It seems that the fabricated membrane could be an effective and selective option for wastewater containing pollutants. The high removal efficiency, fouling resistance, good wettability and stability of the fabricated membrane are promising for use in practical water filtration, especially for selective removal of dyes.

An asymmetric Schiff base-functionalized gold nanoparticle-based colorimetric sensor for Hg2+ ion determination: experimental and DFT studies.

We report a colorimetric sensor for the detection of Hg2+ ions utilizing surface-modified gold nanoparticles. Gold nanoparticles (GNPs) were synthesized by direct reduction and were subsequently functionalized using Schiff base ligands. Schiff base ligands as electron transfer agents have been frequently used for the determination of heavy metal ions. From the spectroscopic analysis, it was found that the mechanism could be defined as coordination between azomethine nitrogen and the carbonyl oxygen of the ligand with Hg2+ ions. The affinity of Hg2+ ions towards the bidentate Schiff base on the GNPs result from their self-aggregation and investigated to be a powerful asset for the development of Hg2+ ion-selective sensors, which is accompanied by a visible color change from pink to purple or can be detect by UV-Vis spectroscopy. The optimized structures and binding mechanisms were supported with a high correlation and agreement via spectroscopy and DFT calculations. These simple colorimetric tests can be extended for the rapid pre-screening of a wide variety of heavy metal ions for onsite detection and mitigation.

Application of magnetic nanomaterials in electroanalytical methods: A review.

Magnetic nanomaterials (MNMs) have gained high attention in different fields of studies due to their ferromagnetic/superparamagnetic properties and their low toxicity and high biocompatibility. MNMs contain magnetic elements such as iron and nickel in metallic, bimetallic, metal oxide, and mixed metal oxide. In electroanalytical methods, MNMs have been applied as sorbents for sample preparation before the electrochemical detection (sorbent role), as the electrode modifier (catalytic role), and the integration of the above two roles (as both sorbent and catalytic agent). In this paper, the application of MNMs in electroanalytical methods have been classified based on the main role of the nanomaterial and discussed separately. Furthermore, catalytic activities of MNMs in electroanalytical methods such as redox electrocatalytic, nanozymes catalytic (peroxidase, catalase activity, oxidase activity, superoxide dismutase activity), catalyst gate, and nanocontainer have been discussed.

Processing Guar Gum into polyester fabric based promising mixed matrix membrane for water treatment.

A reactive and mechano-chemically stable support was prepared from Ag-nanoparticles decorated polyester fabric which was subsequently coated by a casting solution containing polyvinylidene fluoride matrix, guar gum (GG) exo-polysaccharide hydrophilic agent, and UiO-66 filler. FE-SEM, XRD, FT-IR, water contact angle technique, and mechanical stability tests were applied to characterize the prepared membranes. The water contact angle measurements indicated the hydrophilicity of the prepared membrane which can be attributed to the nature of bio-GG and UiO-66. The prepared membrane was employed for purifying contaminated waters containing N-cetyl-N,N,N-trimethylammonium bromide (CTAB) and congo-red (CR) dye through a cross-module set-up. The central composite design was also exploited to study the effect of operational parameters such as CTAB and CR concentration, pH solution, and pressure on the removal efficiency. Particularly, the bio-based GG/UiO-66 dispersion showed excellent self-healing properties, which enabled an effective pollutant separation ability and facilitated the recyclability/sustainability of the as-prepared membrane.

Ce/Eu redox couple functionalized HKUST-1 MOF insight to sono-photodegradation of malathion.

The Ce/Eu redox pair-functionalized HKUST-1 MOF, as an innovative environmentally friendly and recyclable sono-photocatalyst, was hydrothermally mixed and fully characterized by XRD, PL, EIS, FE-SEM, EDS, Mott-Schottky, chronoamperometry, and DRS techniques. The obtained chemical and optical characteristics of the n-type Ce/Eu-HKUST-1 MOF showed that the transfer of additional 4f orbital electrons in the Ce/Eu redox pair improves the sono-photocatalytic activity. The performance of Ce/Eu-HKUST-1 MOF for the sono-photodegradation of Malathion (MA) was evaluated in the aqueous media in the simultaneous presence of blue light and ultrasonic irradiation. The optimization of the process was cross-examined using the response surface methodology as a function of the MA concentration (15-35 mg·L-1), Ce/Eu-HKUST-1 mass (10-30 mg), pH (4-12), and ultrasonic wave irradiation duration (10-30 min). The maximum sono-photocatalytic degradation capacity was found to be 99.99% under the optimum conditions set as 25 mg·L-1, 20 mg, 8, and 25 min for the concentration of Malathion, photocatalyst mass, pH, and irradiation duration, respectively. These findings were attributed to the suppression of electron-hole pair recombination, increased life-time of charge carriers, enhanced visible light absorption, and prominent proportion of hydroxyl and peroxide radicals formed.

Fe3O4-FeMoS4: Promise magnetite LDH-based adsorbent for simultaneous removal of Pb (II), Cd (II), and Cu (II) heavy metal ions.

There have always been numerous challenges to designing a cost-effectiveness, reusable and robust adsorbents for simultaneous heavy metal ion remediations from wastewaters. Herein, a novel kind of nanocomposite relying on the synergic impact of magnetic Fe3O4, FeMoS4-2, and magnesium-aluminum layered double hydroxide (MgAl-LDH) using loading the FeMoS4-2 on protonated Fe3O4 and adhered to the surface of Mg/Al-LDH (Fe3O4/FeMoS4/MgAl-LDH). The nanocage structures adsorbent was characterized via FT-IR, XRD, FE-SEM, EDX, and VSM techniques and demonstrated having an efficient adsorption capability to common cationic pollutants (Pb (II), Cd (II) and Cu (II) by batch experiments. Disparate chief parameters affecting adsorption performance, including Fe3O4/FeMoS4/MgAl-LDH mass, metal ion concentrations, solution pH, and contact time were considered and optimized through central composite design (CCD) in detail. Its supreme adsorption efficiency toward Pb (II), Cd (II), and Cu (II) accounted for 190.75, 140.50, and 110.25 mg g-1, respectively, which acquired by the Langmuir model under the parameter set at 60 min contact time, solution pH at 5, 0.03 g the Fe3O4/FeMoS4/MgAl-LDH and metal ion concentrations ranging from 10 to 300 mg L-1. Such enhancement stemmed from the coordinated complexes in the LDH interlayer region and electrostatic attraction between Fe3O4/FeMoS4/MgAl-LDH and metal ions. Furthermore, the adsorption conducts were more consistent with the pseudo-second-order model and the Langmuir isotherm model, respectively. Likewise, the features such as the superior regeneration and reusability allow the Fe3O4/FeMoS4/MgAl-LDH nanocomposite to constitute as one of the promising materials for heavy metals remediation in wastewater.

L-phenylalanine-imprinted polydopamine-coated CdS/CdSe n-n type II heterojunction as an ultrasensitive photoelectrochemical biosensor for the PKU monitoring.

A simple and highly sensitive photoelectrochemical biosensor towards L-phenylalanine, as a kind of typical essential amino acid and phenylketonuria biomarker was developed on a surface molecular imprinted (MIP) polydopamine-coated CdS/CdSe/Zn heterojunction. Hierarchical marigold flower-like Zn layer decorated by n-type dichalcogenides interfacial heterojunction was successfully designed and synthesized on Ti foil for PEC converter by in situ electrodeposition. A visible-light-driven molecular imprinting film was prepared through the electropolymerization of dopamine in the presence of L-Phe as biomarker. The combination of bio-MIP and photoelectrochemistry overcomes the defects of the PEC method, which is the absence of selectivity, and offers a new PEC sensor with high sensitivity and selectivity based on visible-light-driven heterojunction and biopolymer-enhanced strategy. The unique interfacial between the Zn marigold flower layer as low work function support and CdS/CdSe n-n heterojunction as well as n-type characteristics of polydopamine imprinted by L-Phe biomarker drastically increase the light trapping and absorption in the visible range, and dramatically inhibit the charge carrier recombination, which is crucial for boosting the Bio-PEC activity. Photocatalytic, electrocatalytic and physicochemical properties of the above-mentioned layers were fully characterized. As-prepared PEC biosensor displayed superb performance for the detection of L-Phe biomarker in the optimized condition obtained from central composite design modeling, showing two linear range 0.005-2.5 and 2.5-130 µM and a low detection limit of 0.9 nM. This work suggests that such L-Phe-imprinted polydopamine-coated Zn/CdS/CdSe heterojunction is greatly promising for being applied in photoelectrochemical biosensing with high photo-electron conversion efficiency.