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Timely and rapid detection of antibiotic residues in the environment is conducive to safeguarding human health and promoting an ecological virtuous cycle. A foldable paper-based photoelectrochemical (PEC) sensor was successfully developed for the detection of ampicillin (AMP) based on glutathione/zirconium dioxide hollow nanorods/aptamer (GSH@ZrO 2 HS@apt) modified cellulose paper as a reactive zone with laser direct-writing lead sulfide/cadmium sulfide/graphene (PbS/CdS/LIG) as photoelectrode and cobalt hydroxide (CoOOH) as a photoresist material. Initially, AMP was introduced into the paper-based reaction zone as a biogate aptamer, which specifically recognized the target and then left the ZrO 2 HS surface, releasing glutathione (GSH) encapsulated inside. Subsequently, the introduction of GSH into the reaction region and etching of CoOOH nanosheets to expose the PbS/CdS/LIG photosensitive material increased photocurrent. Under optimal conditions, the paper-based PEC biosensor showed a linear response to AMP in the range of 5.0 - 2 × 10 4 pM with a detection limit of 1.36 pM (S/N = 3). In addition, the constructed PEC sensing platform has excellent selectivity, high stability and favorable reproducibility, and can be used to assess AMP residue levels in various real water samples (milk, tap water, river water), indicating its promising application in environmental antibiotic detection., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Counterfeiting has caused great concern all over the world. What's more, the fluorescent materials play an important role in technological research and development for high-security. In this work, lead-metal-organic framework (Pb-MOF) and perovskite (MAPbBr 3 ) were used in papers to achieving fluorescence counterfeiting. Pb-MOF, as the template or precursor of MAPbBr 3 , were in-situ generated on the surface of cellulose fibers (CFs) to preparing into hand sheets (Pb-MOF@CFs). Through the analysis of experimental results, it was found that ligands, reaction systems, addition sequences of drugs, time, etc. would affect the deposition of Pb-MOF on the surface of CFs. Using CH 3 NH 3 Br (MABr) as the anti-counterfeiting ink to write on Pb-MOF@CFs, the orange writing leaped across the paper, which caused by Pb in Pb-MOF chemically reacting with MABr forming MAPbBr 3 . The orange writing displayed green fluorescence under 365 nm ultraviolet lamp excitation. The orange writing with green fluorescence could be extinguished and reconstructed, which had promise for reuse. In addition, fluorescent security papers (MAPbBr 3 @Pb-MOFs@CFs) were prepared by immersing Pb-MOF@CFs in MABr solution. The fluorescence of MAPbBr 3 @Pb-MOFs@CFs opened when the surface of it was scraped under 365 nm ultraviolet lamp. This unique fluorescence property was very important in improving the security of products. Consequently, the ongoing research on perovskite and MOFs materials is of great significance., Competing Interests: Declaration of competing interest We declare that we have no financial and personal relationships with other people or organizations that can inappropriately influence our work, there is no professional or other personal interest of any nature or kind in any product, service and/or company that could be construed as influencing the position presented in, or the review of, the manuscript entitled., (Copyright © 2024 Elsevier B.V. All rights reserved.)

A simple and rapid distance paper-based analytical device (dPAD) for the detection of lead (Pb) in foods is proposed herein. The assay principle is based on competitive binding between carminic acid (CA) and polyethyleneimine (PEI) to Pb in a food sample. The paper channels were pre-immobilized with PEI, before reacting with a mixture of the sample and CA. Pb can strongly bind to the CA; hence, the length of the red color deposition on the flow channel decreased as a lower amount of free CA bound to PEI. The dPAD exhibited good linear correlation, with ranges of 5-100 µg·mL -1 ( R 2 = 0.974) of Pb. Although, the limit of detection (LOD) of this platform was rather high, at 12.3 µg·mL -1 , a series of standard additions (8.0, 9.0, and 10.0 µg·mL -1 ) can be used to interpret the cutoff of Pb concentrations at higher or lower than 2 µg·mL -1 . The presence of common metal ions such as calcium, magnesium, nickel, and zinc did not interfere with the color distance readout. The validity of the developed dPAD was demonstrated by its applicability to screen the contamination of Pb in century egg samples. The results obtained from the dPAD are in accordance with the concentration measured by atomic absorption spectroscopy (AAS) ( n = 9). In conclusion, this proposed dPAD, combined with the standard addition method, could be applied for screening Pb contamination in food matrices. This platform is, therefore, potentially applicable for field measurements of Pb in developing countries, because it is cheap and rapid, and it requires no significant laborious instruments.

The condensation product (L) of 4,4'-methylenedianiline and p-anisaldehyde acts as colorimetric sensor for Cu 2+ and Pb 2+ ions. On interaction with Cu 2+ , ethanolic solution of L changes its color to brown while it becomes light pink on interaction with Pb 2+ . Interaction of Al 3+ with L coated paper strip emits bright blue fluorescence. Metal ions like Mg 2+ , Cu 2+ , Li + , K + , Na + , Mn 2+ , Al 3+ , Hg 2+ , Co 2+ , Pb 2+ , Ni 2+ , Cd 2+ , Zn 2+ , Fe 3+ do not interfere the paper strip sensor. The fluorescent intensity of L in ethanol is quenched 25 times by Pb 2+ ion. The interaction between L and Pb 2+ is reversible and the detection limit of Pb 2+ is 10 -6  M. The binding constant and stoichiometry of binding between L and Pb 2+ was calculated to be 10 4.8 and 1:2. Theoretical calculations show that the binding of the metal ions to L are favorable and the fluorescence of L is due to π → π* transition.

In this study, a simple paper-based aptasensor has been developed for the ultrasensitive detection of lead (Pb 2+ ) ion within about 10 min. The aptasensor has been successfully designed by taking advantages of the Förster Resonance Energy Transfer (FRET) process and the super fluorescence quenching property of graphene oxide (GO) sheet. The sensing mechanism of the aptasensor is based on the conformational switch of the Pb 2+ -specific aptamer from a random coil to a G-quadruplex structure. An injection of Pb 2+ on the paper-based platform induces the release of the specific aptamer from the GO surface that recovers the fluorescence emission. Under the optimal experimental conditions, there is a good linear relationship between the fluorescence recovery and the Pb 2+ concentration in the ranges of 5-70 pM and 0.07-20 nM. Moreover, the aptasensing array exhibits a high sensitivity to Pb 2+ with an ultra-low detection limit of 0.5 pM. The developed aptasensor has been successfully applied to determine Pb 2+ in tap water, lake water, milk, and human blood serum. The paper-based aptasensor can be efficiently utilized to detect other metal ions and biological molecules by substituting target specific aptamer., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Paper is one of the most commonly used food packaging materials. During the production of packaging paper, it is possible for trace amounts of heavy metals to be incorporated as contaminants. These could migrate into food when packaging paper (food contact paper) is used for cooking, storing and eating. The aim of this study was to determine the migration of lead (Pb) and arsenic (As) from food contact paper into a food simulant and then to assess human safety through the estimated daily intake (EDI) with consumption factor. Migration tests were conducted for 310 samples using 4% acetic acid as a food simulant at 25°C for 10 min and at 95°C for 30 min. Concentrations of Pb and As in a food simulant were quantified by inductively coupled plasma mass spectrometry. LODs for Pb and As were 0.002 and 0.005 µg L -1 , respectively. The migration of Pb from food contact paper ranged from not detected (ND) to 17.5 μg L -1 at 25°C for 10 min and from 0.10 to 25.6 μg L -1 at 95°C for 30 min while As ranged from ND to 0.44 μg L -1 at 25°C for 10 min and from ND to 0.87 μg L -1 at 95°C for 30 min. The migration of Pb and As determined in this study confirm that the human exposure was within safe levels based on the EDI of food contact paper compared with the provisional tolerable weekly intake for Pb of 25 μg kg -1 bw and for As of 15 μg kg -1 bw.

Herein, an easy and effective ratiometric fluorescent nanoprobe for the selective detection of Pb2+ and pyrophosphate (PPi) was developed based on label-free carbon dots (CDs). The CDs showed dual emission bands at 477 and 651 nm under a single-wavelength excitation (391 nm). Pb2+ and PPi were sequentially detected by the sensor with high reliability and accuracy via the exploitation of the fluorescence intensity ratio (F477/F651). The dual emission sensor exhibited high selectivity and excellent sensitivity for Pb2+ and PPi than for other analytes with detection limits as low as 0.055 μM and 0.089 μM, respectively. Moreover, the fluorescent CDs changed from pink to cyan and from cyan to pink and could be used as a fluorescent paper sensor for the visual detection of Pb2+ and PPi. To the best of our knowledge, this is the first report on the ratiometric fluorescence detection of Pb2+ and PPi by CDs; therefore, the as-synthesized CDs show great potential for application in the determination of Pb2+ and PPi in real samples.

This work reports the fabrication of integrated electrochemical fluidic paper-based analytical devices (ePADs) using a marker pen drawing and screen-printing. Electrodes were deposited on paper using screen-printing with conductive carbon ink. Then, the desired fluidic patterns were formed on the paper substrate by drawing with a commercial hydrophobic marker pen using an inexpensive computer-controlled x-y plotter. The working electrode was characterized by cyclic voltammetry and scanning electron microscopy. The analytical utility of the electrochemical PADs is demonstrated through electrochemical determination of Pb(II) and Cd(II) by anodic stripping voltammetry. For this purpose, the sample was mixed with a buffer solution and a Bi(III) solution, applied to the test zone of the PAD, the metals were preconcentrated as a bismuth alloy on the electrode surface and oxidized by applying an anodic potential scan. The proposed manufacturing approach enables the large-scale fabrication of fit-for-purpose disposable PADs at low cost which can be used for rapid on-site environmental monitoring.

A paper-based microfluidic device based on unconventional principle was developed and used to detect lead ions through a two-step process including heated incubation and subsequent mixing. The device was made by generating a superhydrophobic pattern, which defines channel and reservoir barriers, on a water-impermeable paper substrate, followed by loading and drying the reagents in the defined reservoirs. Different from the conventional paper-based devices that are made of water-permeable paper, the as-prepared device holds water drops in discrete reservoirs, and the water drops will not move unless the device is titled along the direction of the predefined channels. In this way, the liquid samples applied onto the device are handled as individual drops and could be stored, transported, and mixed on demand. Different from the conventional paper-based devices that use capillary force to drive liquid, our new device uses wetting and gravity as driving force. We name this operation principle suspending-droplet mode paper-based device (SD-μPAD). The use of a Teflon contact-printing stamp makes the production of such devices rapid, cost efficient, and mass productive. Utilizing a G-quadruplex-based luminescence switch-on assay, we demonstrated rapid, convenient, highly sensitive, and low cost detection of lead(II) ions in water samples, using a custom made battery-powered portable device, and a smart phone as the detector., (Copyright © 2017 Elsevier B.V. All rights reserved.)

A disposable electrochemical lateral flow paper-based sensing device for heavy metal detection is proposed. The quantification of lead and cadmium in aqueous samples is demonstrated in a range from 10 to 100 ppb with a limit of detection of 7 and 11 ppb respectively. Moreover, the platform itself, which is made of paper, served as a sample pretreatment material due to its filtering properties. Real samples, especially in which the matrix is usually turbid and would in principle need a previous filtration, are successfully analyzed. This lab-on-paper device is simple, low cost, easy to fabricate, and portable, being a promising tool for new point-of-care applications in environmental monitoring, public health, and food safety.

A facile and simple paper-based scanometric assay was developed to detect Pb(2+) using GR5-DNAzyme. Magnetic beads (MBs) and gold nanoparticles (AuNPs) were used as a signal collector and a signal indicator, respectively. They were linked together by GR5-DNAzyme, comprising an enzyme and a substrate strand pairing up with each other. In the presence of Pb(2+), the substrate strand is cut into two pieces, resulting in the disassembly of AuNPs from the MBs. These AuNPs were spotted on predefined areas on a chromatography paper, where signal is amplified through silver reduction. This sensing platform exhibits high sensitivity and selectivity toward Pb(2+), giving a detection limit of 0.3 nM and a linear fitting range from 0.1 to 1000 nM. Testing of this biosensor in river water and synthetic urine samples also showed satisfying results. Besides offering simultaneous and multi-sample analysis, this paper-based sensing platform presented here could be potentially applied and served as a general platform for on-site, naked eyes, and low-cost monitoring of other heavy metal ions in environmental and body fluid samples., (Copyright © 2015 Elsevier B.V. All rights reserved.)

A versatile point-of-care assay platform was developed for simultaneous detection of multiple targets based on a microfluidic paper-based analytic device (μPAD) using a target-responsive hydrogel to mediate fluidic flow and signal readout. An aptamer-cross-linked hydrogel was used as a target-responsive flow regulator in the μPAD. In the absence of a target, the hydrogel is formed in the flow channel, stopping the flow in the μPAD and preventing the colored indicator from traveling to the final observation spot, thus yielding a "signal off" readout. In contrast, in the presence of a target, no hydrogel is formed because of the preferential interaction of target and aptamer. This allows free fluidic flow in the μPAD, carrying the indicator to the observation spot and producing a "signal on" readout. The device is inexpensive to fabricate, easy to use, and disposable after detection. Testing results can be obtained within 6 min by the naked eye via a simple loading operation without the need for any auxiliary equipment. Multiple targets, including cocaine, adenosine, and Pb(2+), can be detected simultaneously, even in complex biological matrices such as urine. The reported method offers simple, low cost, rapid, user-friendly, point-of-care testing, which will be useful in many applications.

The scaling up of the intensity of beams of atomic clusters (nanoparticle beams) creates a new route to the fabrication of functional nanostructured materials. A challenge is to present, to the directed beam, high surface areas of the desired support material, for decoration by the clusters at local sub-monolayer densities. Then, the clusters and their properties can be preserved. Here we employ the Matrix Assembly Cluster Source (MACS) to demonstrate and characterise the deposition of lead clusters, with size of order 2 nm, into planar sheets of porous carbon paper, a material employed in electrode fabrication. We find that clusters are deposited to a depth comparable with the pore size of the carbon, ~ 50 μm, giving rise to a metal loading of ~ 0.05 mg cm−2 of carbon paper. The functionality of the nanocomposite film so created is demonstrated by its use as an electrode for the electrochemical generation of oxidising species suitable for water purification. [ABSTRACT FROM AUTHOR]

Lead (Pb) pollution from local mines and industrial use increases risks for human, animal, and plant health. Pectin is an effective chelator of Pb, and it has been shown that a unicellular green alga, Penium margaritaceum, synthesizes pectin in the cell wall. In this study, the ability of P. margaritaceum to remove Pb from an aqueous solution was investigated. Energy dispersive X-ray spectroscopy revealed that two strains of P. margaritaceum accumulated Pb on the cell surface. Hence, P. margaritaceum cells were immobilized on cellulose filter paper. The immobilized algal cells were soaked in 1.0 mg/L Pb solution with gentle shaking for 8 h, and Pb in the solution and on the filter paper was measured by flame atomic absorption spectrometry. The immobilized algal cells continuously decreased the Pb concentration to less than 0.5 mg/L and recovered 31.8–32.7% of added Pb. The specific decrease in Pb and increase in Ca were observed in the presence of 1.0 mg/L each of Ca, Mg, Na, and K. Fourier transform infrared spectra suggested that the carboxylic acid group would be responsible for the adsorption of Pb. This study is the first to demonstrate the effectiveness of the immobilized P. margaritaceum cell in removing Pb from aqueous solutions with simple solid–liquid separation.

A multi-amplified paper-based electrochemical strategy using Pb(2+) dependent DNAzyme as the recognition unit for Pb(2+) detection was developed. In this work, flower-like reduced graphene (FrGO) was prepared utilizing flower-like ZnO as template, which was first one step grown on the gold nanoparticles modified paper working electrode (Au-PWE). After being treated with acid and then modified with Au, a novel sensor platform named Au/FrGO/Au-PWE with large specific surface area and good electrical conductivity was fabricated. The Mn2O3 nanoparticle-assembled hierarchical hollow spheres (H-Mn2O3) was served as nanocarrier to immobilize GOx, HRP and signal strand (S3), resulting to the formation of S3/H-Mn2O3/HRP/GOx bioconjugations. In the presence of Pb(2+), the DNAzyme (S1) was activated and the substrate strand (S2) was cleaved. After the incubation with S3/H-Mn2O3/HRP/GOx in 0.1M HAc-NaAc solution (pH 4.3) containing 30 mM aniline and 15 mM glucose, a readily measurable "turn-on" electrochemical signal could be measured. On the basis of the signal amplification strategy of Au/FrGO/Au-PWE sensing platform and S3/H-Mn2O3/HRP/GOx bioconjugations, the developed biosensor exhibited a good linear response toward over a wide range of concentration from 0.005 to 2000 nM., (Copyright © 2016 Elsevier B.V. All rights reserved.)

Novel miniaturized Pb(II) paper-based potentiometric sensors are described using coumarin derivatives I and II as electroactive ionophores and nano vanadium pentoxide as a solid contact material for the sensitive and selective monitoring of trace lead ions. Density functional theory (DFT) confirms optimum geometries, electronic properties, and charge transfer behaviors of 1:2 Pb(II): coumarin complexes. The sensors are prepared by using two strips of 20 × 5 mm filter paper with two circular orifices. One orifice is coated with vanadium pentoxide (V2O5) nanoparticles in colloidal conductive carbon as a solid-contact, covered by a PVC membrane containing coumarin ionophore to act as a sensing probe. The other orifice is treated with Ag/AgCl in a polyvinyl butyral (PVB) film, to act as a reference electrode. Sensors with ionophores (I) and (II) exhibit Nernstian slopes of 27.7 ± 0.2 and 30.2 ± 0.2 mV/decade over the linear concentration range 4.5 × 10−7 to 6.2 × 10−3 M and 8.5 × 10−8 to 6.2 × 10−3 M, with detection limits of 1.3 × 10−7 M (26.9 ppb) and 2.1 × 10−8 M (4.4 ppb), respectively. The sensors are satisfactorily used for accurate determination of lead ions in drinking water, lead-acid battery wastewater, and electronic waste leachates. The results compare favourably well with data obtained by flameless atomic absorption spectrometry. [ABSTRACT FROM AUTHOR]

Synthetic 11 Å tobermorite (Ca5Si6O16(OH)2.4H2O) and its Al-substituted analogue are layer-lattice ion-exchangers with potential applications in nuclear and hazardous wastewater treatment. The present study reports the facile one-pot hydrothermal synthesis of an Al-tobermorite-rich cation-exchanger from a combination of paper recycling ash, post-consumer container glass, and lime, with compositional ratios of [Ca]/[Si + Al] = 0.81 and [Al]/[Si + Al] = 0.18. The reaction products were characterized by powder X-ray diffraction analysis, 29Si magic angle spinning nuclear magnetic resonance spectroscopy, and scanning electron microscopy. Hydrothermal processing in 4 M NaOH(aq) at 100 °C for 7 days yielded an Al-tobermorite-rich product that also contained katoite (Ca3Al2SiO12H8), portlandite (Ca(OH)2), calcite (CaCO3), and amorphous silicate gel. The hydrothermal product was found to have a Cs+ cation exchange capacity of 59 ± 4 meq 100 g−1 and selective Cs+ distribution coefficients (Kd) of 574 ± 13 and 658 ± 34 cm3 g−1 from solutions with molar ratios [Cs+]:[Na+] and [Cs+]:[Ca2+] of 1:100. In a batch sorption study at 20 °C, the uptakes of Pb2+, Cd2+, and Cs+ were determined to be 1.78 ± 0.04, 0.65 ± 0.06, and 0.36 ± 0.03 mmol g−1, respectively. The kinetics of Pb2+, Cd2+, and Cs+ removal were described by the pseudo-second-order rate model, which gave respective rate constants (k2) of 0.010, 0.027, and 1.635 g mmol−1 min−1, and corresponding correlation coefficients (R2) of 0.997, 0.996, and 0.999. The metal ion sorption properties of the tobermorite-rich product compared favorably with those of other waste-derived tobermorites reported in the literature. Potential strategies to improve the yield, crystallinity, and sorption characteristics of the product are discussed.

Lead (Pb) pollution from local mines and industrial use increases risks for human, animal, and plant health. Pectin is an effective chelator of Pb, and it has been shown that a unicellular green alga, Penium margaritaceum, synthesizes pectin in the cell wall. In this study, the ability of P. margaritaceum to remove Pb from an aqueous solution was investigated. Energy dispersive X-ray spectroscopy revealed that two strains of P. margaritaceum accumulated Pb on the cell surface. Hence, P. margaritaceum cells were immobilized on cellulose filter paper. The immobilized algal cells were soaked in 1.0 mg/L Pb solution with gentle shaking for 8 h, and Pb in the solution and on the filter paper was measured by flame atomic absorption spectrometry. The immobilized algal cells continuously decreased the Pb concentration to less than 0.5 mg/L and recovered 31.8–32.7% of added Pb. The specific decrease in Pb and increase in Ca were observed in the presence of 1.0 mg/L each of Ca, Mg, Na, and K. Fourier transform infrared spectra suggested that the carboxylic acid group would be responsible for the adsorption of Pb. This study is the first to demonstrate the effectiveness of the immobilized P. margaritaceum cell in removing Pb from aqueous solutions with simple solid–liquid separation. [ABSTRACT FROM AUTHOR]

A "turn-on" fluorescent and colorimetric chemosensor (RBS) for Pd(2+) has been designed and synthesized through introduction of sulfur as a ligand atom to Rhodamine B. RBS exhibits high selectivity (freedom from the interference of Hg(2+ )in particular) and sensitivity toward Pd(2+) with a detection limit as low as 2.4 nM. RBS is also a reversible sensor, and it can be made into test paper to detect Pd(2+) in pure water. Compared to the chemosensors that introduced phosphorus to Rhodamine to detect Pd(2+), RBS can be synthesized more simply and economically.

Good drainage of the pulp suspension is vitally important for stable papermaking. Although the addition of lignocellulosic nanofibers (LNFC) in pulp could highly reinforce the end paper sheets, the application of LNFC could diminished the pulp drainage. To solve this problem, the impact of the zeolite-chitosan and bentonite-chitosan microparticle drainage aid systems on the LNFC-reinforced recycled pulp was systematically investigated. Results indicated that the mentioned microparticle systems improved the drainage and retention especially in applying 1% chitosan with 0.3% zeolite. In mechanical properties, applying the microparticle systems, not only did not deteriorate these properties, but also improved most of them, especially in treatment containing zeolitechitosan. It seems that the improved pulp drainage and the mechanical properties of the end papers was due to successful mission of microparticle system and synergistic interactions of pulp fibres, LNFC, chitosan, and zeolite, which could also lead to denser and more uniform structure of handsheets. [ABSTRACT FROM AUTHOR]

A novel electrochemical carbon cloth (CC) analysis device (eCAD) is proposed for the determination of Pb 2+ in environmental water samples, which was assembled using a single-step functional CC as both the sensing and the substrate material. The modified CC was characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, Raman spectra, and electrochemical impedance spectroscopy. The increase in electrochemical activity is due to the increased defective extent and excellent electrochemical activity of CC. Under optimum conditions (viz. a pH value of 4.5, deposition time of 160 s), the sensor is capable of determining Pb 2+ by differential pulse anodic stripping voltammetry (DPASV) at a typical working potential of - 1.0 V (vs. Ag/AgCl). Response is linear from 5.0 × 10 -9 to 3.0 × 10 -6  M Pb 2+ , and the detection limit is 4.8 nM (at S/N = 3). The sensor was successfully applied to the determination of Pb 2+ in real samples, with apparent recoveries from 96.0 to 102.0% and a relative standard deviation of less than 3.4%. In addition, the integration of the sensor with signal collection components has enabled us to realize on-site analysis of Pb 2+ , which is highlighted as a new generation of electrode platform for the development of a portable analysis device.Graphical abstract.

• Adding kaolin reduces the volatility and leachability of heavy metals. • Xerogel with high porosity was successfully synthesized for heavy metal adsorption. • Silica-alumina xerogel can effectively adsorb heavy metals in pyrolysis gas. • Heavy metal species can form ionic or covalent bonds with kaolinite. It is of great significance to reduce the secondary risk of heavy metals during the pyrolysis of paper sludge. This study used kaolin and alumina-silica-based xerogels to control heavy metals released during sludge pyrolysis. Pyrolyzing a mixture of sludge and 7% kaolin at 400 °C achieved high retention rates for Cu (95.85%), Zn (95.97%), Pb (97.15%), Cd (84.23%), and Cr (84.05%) when the pyrolysis tail gas was treated with 9 g of xerogel. The addition of kaolin facilitated the transformation of Cu, Zn, Pb, and Cr from the unstable fraction to the stable fraction in pyrolysis biochar, reducing their leachability. The xerogels also played a crucial role in adsorbing and stabilizing the heavy metals. The results of thermodynamic equilibrium calculations showed that Pb(g), PbS(g), PbCl 2 (g), PbCl(g), Zn(g), ZnCl 2 (g), and Cd(g) were the main gaseous products of Zn, Pb, and Cd during paper sludge pyrolysis. The Pb atoms in PbCl 2 and PbS, and the Zn atoms in ZnCl 2 bond with the oxygen atoms on the kaolin surface by covalent bonds, while the Cl atoms in PbCl and the Pb atoms of elemental lead form ionic bonds with H and O atoms on the kaolinite surface, respectively. These experimental and simulation results offer new ideas for controlling heavy metals during sludge pyrolysis. [ABSTRACT FROM AUTHOR]

Paper-ash is used for remediation of heavily contaminated soils with metals, but remediation efficiency after longer periods has not been reported. To gain insights into the mechanisms of immobilization of cadmium (Cd), lead (Pb), and znic (Zn), a study was performed in the laboratory experiment in uncontaminated, artificially contaminated, and remediated soils, and these soils treated with sulfate, to mimic conditions in contaminated soil from zinc smelter site. Remediation was performed by mixing contaminated soil with paper-ash to immobilize Cd, Pb, and Zn in the geotechnical composite. Partitioning of Cd, Pb, and Zn was studied over one year in seven-time intervals applying the sequential extraction procedure and complementary X-ray diffraction analyses. This methodological approach enabled us to follow the redistribution of Cd, Pb, and Zn over time, thus, to studying immobilization mechanisms and assessing the remediation efficiency and stability of newly formed mineral phases. Cd, Pb, and Zn were effectively immobilized by precipitation of insoluble hydroxides after the addition of paper-ash and by the carbonization process in insoluble carbonate minerals. After remediation, Cd, Pb, and Zn concentrations in the water-soluble fraction were well below the limiting values for inertness: Cd by 100 times, Pb by 125 times, and Zn by 10 times. Sulfate treatment did not influence the remediation efficiency. Experimental data confirmed the high remediation efficiency and stability of insoluble Cd, Pb, and Zn mineral phases in geotechnical composites.

This paper estimates the impacts of cumulative lead exposure on the short-run discipline and academic achievement of elementary school students. An exogenous, heterogeneous shock of lead-in-water levels within classrooms at Flint Community Schools provides the treatment variation used to focus on the understudied, short-run effects of lead on older children. At the mean level of classroom lead exposure disciplinary actions increased by 8 actions per grade within each school, and the share of students proficient in both math and reading declined. These results may help explain observed disparities in both behavior and academic achievement for underprivileged groups., (© 2023 The Authors. Health Economics published by John Wiley & Sons Ltd.)

• The content of potentially toxic metal in KB and PB was low. • Terminal temperature remarkably affected the morphology of potentially toxic metals in biochar. • PB and KB were not hazardous waste with low environmental risk. • PB and KB can fix potentially toxic metal in Tibet soil admirably. This study investigated the morphology and potentially toxic metal concentrations of paper waste-based biochar (PB) and kitchen waste-based biochar (KB) obtained at 500 and 700 °C. The morphology and potentially toxic metals (Cr, Mn, Cu, Cd, Pb, Zn, Ag, and Ba) concentrations in the biochars were determined by SEM and FT-IR analysis. The Cr, Mn, Cu, and Cd concentrations in PB were low, while the Ba content was relatively high at 0.1 mg∙kg−1. An increase in the terminal temperature led to an increase in the concentrations of Fe/Mn oxide-bound potentially toxic metals of PB, and a decrease in the concentrations of organic matter-bound potentially toxic metals. The Fe/Mn oxide-bound Cr, Mn, Cu, Pb, and Zn concentrations of KB decreased with an increase in the terminal temperature. Therefore, increasing the terminal temperature could reduce the bioavailability of potentially toxic metals in PB and KB. The environmental risk of the different biochars when used for soil remediation was assessed by the potential ecological risk index (RI), and a case study of a Tibetan soil was also conducted. The potentially toxic metal concentrations leached from both PB and KB were lower than the relevant standards. The findings showed that both PB and KB can be safely used for soil remediation. [ABSTRACT FROM AUTHOR]

Purpose: This paper aims to present the components' characterization and condition assessment of an important deteriorated Mamluk-illuminated paper manuscript housed in Al-Azhar Library, Egypt. Design/methodology/approach: Different analytical techniques used in this study were the portable digital optical microscope, stereomicroscope, scanning electron microscope with EDX (SEM.EDX), portable X-ray fluorescence (pXRF), X-ray diffraction (XRD), pH measurement and Fourier transform infrared spectroscopy (FTIR). Findings: The results obtained by different microscopes showed that the gilding in the surface of illuminated paper sheets was performed with gold leaves. Additionally, these microscopes revealed that the illuminated paper manuscript has different aspects of deterioration such as adhered dirt, staining, some micro-cracks, cracks and detachment of some parts in some illuminated areas. The results of elemental analysis by EDX, portable XRF and XRD analysis showed that the orange red pigment is red lead (Pb3O4), blue pigment is azurite (2CuCo3.Cu (OH)2), and the gold layer is has consisted of brass alloy (Cu-Zn) with a small amount of gold element (Au). The pH measurement stated that the historical paper in the acidity level. The ATR-FTIR analysis also revealed the oxidation of cellulose. Moreover, it was found from ATR-FTIR that Arabic gum was used as a binder for the pigments. Originality/value: This study presents the important results of analytical methods used for condition assessment and identification of the components of an important Mamluk-illuminated paper manuscript, where these results referred that the studied paper manuscript had different aspects of deterioration. The conservation steps either conservation treatment or preventive conservation are urgently needed in future studies. [ABSTRACT FROM AUTHOR]

A highly sensitive electrochemical (EC) biosensor combined with a 3D origami device for detection of Pb 2+ was developed based on novel Au nanoparticles modified paper working electrode (Au-PWE) as sensor platform and DNA functionalized iron-porphyrinic metal-organic framework ((Fe-P)n-MOF-Au-GR) hybrids as signal probes. In the presence of Pb 2+ , GR could be specifically cleaved at the ribonucleotide (rA) site, which produced the short (Fe-P) n -MOF-linked oligonucleotide fragment to hybridize with hairpin DNA immobilized on the surface of Au-PWE. Because of the mimic peroxidase property of (Fe-P) n -MOF, enzymatically amplified electrochemical signal was obtained to offer the sensitive detection of Pb 2+ . In addition, benefiting from the Pb 2+ dependent GR, the proposed assay could selectively detect Pb 2+ in the presence of other metal ions. This method showed a good linear relationship between the current response and the Pb 2+ concentration ranging from 0.03 to 1000nmolL -1 with a detection limit of 0.02nmolL -1 . The Au-PWE based electrochemical sensor along with the (Fe-P) n -MOF-Au-GR probe exhibited the advantages of low-cost, simple fabrication, high sensitivity and selectivity, providing potential application of real-time Pb 2+ detection both in environmental and biological samples., (Copyright © 2016 Elsevier B.V. All rights reserved.)

Trace metal pollution of soils is a widespread consequence of anthropogenic activity. Land slugs can be used as bio-indicators of the metals' pollution in the soil, so the present study aimed to determine the metal in the soil and Laevicaulis stuhlmanni land slug tissues by studying its effects on different physiological parameters. Slugs and soil samples were collected from fields in Abu-Rawash, Giza, Egypt. Slugs were identified, and the metals were determined in slug tissues and soil samples. On the other hand, slugs were reared in the laboratory and the new generation was fed on lettuce dipped in 0.027 µg/ml lead (Pb) for 10 days. The results revealed that the soil and slug tissues contained copper, manganese, lead, and zinc; the lead metal bioaccumulation factor was the highest. Also, the results showed that the hemocytes' count, testosterone, and estradiol hormones were significantly decreased. At the same time, the phagocytic index was increased considerably, and some morphological alterations in the granulocytes and hyalinocytes were observed after treatment with 0.027 µg/ml lead compared to untreated slugs. On the other hand, all the oxidative stress parameters were significantly increased in the treated slugs compared with the control. Concerning the histopathological studies, lead caused a rupture, vacuolation, or degeneration in the digestive cells of treated slugs. Finally, it can be concluded that the land slugs were sensitive to lead which was reflected by endocrine disruption, immunotoxicity, and increased oxidative stress parameters with histopathological damages. Hence, Laevicaulis stuhlmanni can be used as a metal accumulation bio-indicator to reflect the metal pollution in the soil., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

• A stack-up micro electrochemical device was developed based on the carbon paper electrode. • Cobalt-based MOFs and gold nanoparticles improved the metal ion absorption and electron diffusion. • Sensitive simultaneous determination of Pb2+ and Cd2+ achieved the subnanogram LODs. A portable device is conducive to the on-site detection of heavy metal ions at trace level in food and the prevention of related food safety issues. In this work, an electrochemical device stacked up with flat electrodes was developed for the detection of Pb2+ and Cd2+. The top layer of the device is a carbon paper as working electrode, which is modified with amino functionalized cobalt-based metal-organic framework and gold nanoparticles. The bottom layer was constructed with the carbon counter electrode and Ag/AgCl reference electrode, and a punched sample cell (Φ = 8 mm) was in the middle. The proposed method could simultaneously determinate Pb2+ and Cd2+ via anodic stripping voltammetry with the detection limit of 7.0 × 10−2 ng mL−1 and 1.1 × 10−2 ng mL−1, and was applied in real food samples (drinking water, juice, tea, grain, fruits, vegetables, liver and aquatic products) with the recovery of 91.2–105.4 % and 90.2–111.2 %, respectively. [ABSTRACT FROM AUTHOR]

Synthetic 11 Å tobermorite (Ca5Si6O16(OH)2.4H2O) and its Al-substituted analogue are layer-lattice ion-exchangers with potential applications in nuclear and hazardous wastewater treatment. The present study reports the facile one-pot hydrothermal synthesis of an Al-tobermorite-rich cation-exchanger from a combination of paper recycling ash, post-consumer container glass, and lime, with compositional ratios of [Ca]/[Si + Al] = 0.81 and [Al]/[Si + Al] = 0.18. The reaction products were characterized by powder X-ray diffraction analysis, 29Si magic angle spinning nuclear magnetic resonance spectroscopy, and scanning electron microscopy. Hydrothermal processing in 4 M NaOH(aq) at 100 °C for 7 days yielded an Al-tobermorite-rich product that also contained katoite (Ca3Al2SiO12H8), portlandite (Ca(OH)2), calcite (CaCO3), and amorphous silicate gel. The hydrothermal product was found to have a Cs+ cation exchange capacity of 59 ± 4 meq 100 g−1 and selective Cs+ distribution coefficients (Kd) of 574 ± 13 and 658 ± 34 cm3 g−1 from solutions with molar ratios [Cs+]:[Na+] and [Cs+]:[Ca2+] of 1:100. In a batch sorption study at 20 °C, the uptakes of Pb2+, Cd2+, and Cs+ were determined to be 1.78 ± 0.04, 0.65 ± 0.06, and 0.36 ± 0.03 mmol g−1, respectively. The kinetics of Pb2+, Cd2+, and Cs+ removal were described by the pseudo-second-order rate model, which gave respective rate constants (k2) of 0.010, 0.027, and 1.635 g mmol−1 min−1, and corresponding correlation coefficients (R2) of 0.997, 0.996, and 0.999. The metal ion sorption properties of the tobermorite-rich product compared favorably with those of other waste-derived tobermorites reported in the literature. Potential strategies to improve the yield, crystallinity, and sorption characteristics of the product are discussed. [ABSTRACT FROM AUTHOR]

For the serious situation of heavy metal pollution, the use of cheap, clean, and efficient biochar to immobilize heavy metals is a good treatment method. In this paper, SA@ZIF-8/BC was prepared for the adsorption of Pb 2+ in solution using sodium alginate (SA) and zeolitic imidazolate framework-8 (ZIF-8) modified corn cob biochar. The results showed that the specific surface area of modified biochar was greatly improved, with good adsorption capacity for Pb 2+ , strong anti-interference ability, and good economy. At the optimal adsorption pH of 5, the adsorption model of Pb 2+ by SA@ZIF-8/BC was more consistent with the pseudo-second-order kinetic model and Langmuir isotherm model. This indicates that the adsorption of Pb 2+ by SA@ZIF-8/BC is chemisorption and monolayer adsorption. The maximum adsorption of modified biochar was 300 mg g -1 , which was 2.38 times higher than that of before modified BC (126 mg g -1 ). The shift in binding energy of functional groups before and after adsorption of SA@ZIF-8/BC was studied by XPS, and it was found that hydroxyl and carboxyl groups played an important role in the adsorption of Pb 2+ . It was demonstrated that this novel adsorbent can be effectively used for the treatment of Pb pollution in wastewater., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Various agents, including ethylenediaminetetraacetic acid, oxalic acid, citric acid, and HCl, were applied to remove heavy metals from raw paper incineration ash and render the ash recyclable. Among these prepared agent solutions, ethylenediaminetetraacetic acid showed the highest efficiency for Pb removal, while oxalic acid showed the highest efficiencies for Cu, Cd, and As removal. Additionally, three modes of an advanced removal method, which involved the use of both ethylenediaminetetraacetic acid and oxalic acid, were considered for use at the end of the rendering process. Among these three modes of the advanced removal method, that which involved the simultaneous use of ethylenediaminetetraacetic acid and oxalic acid, i.e., a mixture of both solutions, showed the best heavy metal removal efficiencies. In detail, 11.9% of Cd, 10% of Hg, 28.42% of As, 31.29% of Cu, and 49.19% of Pb were removed when this method was used. Furthermore, the application of these three modes of the advanced removal method resulted in a decrease in the amounts of heavy metals eluted and brought about an increase in the CaO content of the treated incineration ash, while decreasing its Cl content. These combined results enhanced the solidification effect of the treated incineration ash. Thus, it was confirmed that the advanced removal method is a promising strategy by which recyclable paper incineration ash can be obtained. [ABSTRACT FROM AUTHOR]

The possibility of using pyrolyzed paper as disposable working electrodes for trace metals determination is reported for the first time. A small piece of pyrolyzed paper (0.7×0.7 cm) was positioned at the bottom side of the electrochemical cell using a rubber O-ring, which defined the electrode area (0.48 cm; 0.18 cm 2 ). A large number of electrodes can be obtained from a single piece of standard dimensions (2.5 cm×7.5 cm) of paper, therefore minimizing the cost per unit. The electrochemical performance of the pyrolyzed paper was demonstrated by cyclic voltammetry, electrochemical impedance spectroscopy and by the determination of Zn, Cd, and Pb by square-wave anodic stripping voltammetry. The unmodified pyrolyzed paper showed excellent performance for Pb and Cd detection (LOD =0.19 and 0.16 ppb, respectively). In the presence of Bi 3+ (in-situ film formation), the simultaneous determination of Zn, Cd and Pb was also possible (LOD=0.26, 0.25, and 0.39 ppb, respectively). [ABSTRACT FROM AUTHOR]

Rare earth elements (REEs) are widely distributed in low concentrations in all parts of the biosphere. REEs are not at all rare, their concentration in the earth's crust is close to 0.015%. REEs include the elements scandium, yttrium and the lanthanides from lanthanum to lutetium. REEs show similar physical and chemical properties. Today REEs are applied in industries and technologies, in agriculture as microfertilizers and feed additives and they are also used in medicine. REEs are dispersed especially as accessory minerals in pegmatites, granites and associated metamorphic volcanic rocks. Out of more than 250 kinds of minerals containing REEs, only bastnaesite and monazite are of economic importance. Their concentration in the soil varies widely and depends on their presence in parental materials, soil texture, organic matter content, pedogenetic processes and anthropogenic activities. REEs are found in small concentrations in surface stagnant and flowing waters as well as in underground waters. They are found in water in both suspended and dissolved form. REEs enter the atmosphere from various sources, largely owing to human activities. The majority of REEs in the atmosphere are carried by microscopic particles. The uptake and consequently accumulation of REEs in plants are affected by numerous biotic factors, such as plant species and genotype, and abiotic factors such as their concentration in the soil and some chemical and physical soil characteristics. They can enter plants via both root and foliage tissues. There are plant species called hyperaccumulators that are able to accumulate significant amounts of REEs without adverse consequences. RREs are not biogenic for higher plants or for other living organisms, but can influence their life processes. Experiments show that REEs can be beneficial for growth, yield and biochemical composition of cultivated plants. They can also alleviate some ecological stress in plants. It is not clear enough how they affect human and animal health. The wide-spread application of REEs in different industries as well as in agriculture lead to a constant increase of the concentrations of these elements in the environment. Therefore, studies on the uptake, accumulation, distribution of REEs in cultivated plant species and their entrance into the food chain as well as their stimulating or toxic effect on living organisms, can be very significant in the future. [ABSTRACT FROM AUTHOR]

Herein, a simple method to prepare porous carbon that inhibits hydrogen evolution is used, which has enormous advantages for both capacitors and lead‐acid batteries. The quantitative filter paper spongy porous carbon (SQFPC) is successfully synthesized by the two‐step method. SQFPC displays a porous, spongy structure with a large specific surface area (1847 m2 g−1). In electrochemical tests, SQFPC exhibits high specific capacitance (244 F g−1 at 1 A g−1) and a capacitance retention rate of 72.5% at 40 A g−1. In addition, the capacity of the battery with 0.5 wt% SQFPC is improved by 57.6% at a discharge rate of 0.1C, and the cycle life under the high‐rate partial state of charge is 9.3 times that of the blank battery. The enhanced battery performance is related to the unique structure and surface functional groups of carbon, which speed up ion movement inside the battery and provide active sites for lead deposition. [ABSTRACT FROM AUTHOR]

Direct discharge of waste into water bodies and mining are two major sources of lead contamination in ecosystems. Water scarcity promoted the usage of industrial effluent-contaminated waters for crop production, mainly in peri-urban areas. These wastewaters may contain heavy metals and pollute crop ecosystems. These metals can reach the living cell via contaminated raw foodstuffs that grow under these conditions and cause various ill effects in metabolic activities. In this study, graded levels of pressmud (0, 2.5, 5, 10 g/kg) were applied on lead imposed soil with different contamination levels (0, 100, 150, 300 mg/kg) and metal dynamics was studied in spinach crop. Experimental results showed that the addition of pressmud upto 10 mg/kg had decreased different phytoremediation indices in spinach crop. Whereas, increasing Pb level enhanced the indices' values, indicating accumulation of significant amount of Pb in spinach biomass. However, application of pressmud (upto 10 mg/kg) reduced the bioconcentration factor (BCF) from 0.182 to 0.136, transfer factor (TF) from 0.221 to 0.191, translocation efficiency 66.11-59.34%; whereas, Pb removal enhanced from 0.063 to 0.072 over control treatment. These findings suggest that application of pressmud declined Pb concentration, the BCF and the TF in test crop which lead to less chances of adverse effect in human. These information are very useful for effectively managing wastewater irrigated agricultural crop production systems., (© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

A graphene paper-based flexible solid-contact ion-selective electrode (SC-ISE) was developed to detect lead ion sensitively. Graphene paper obtained via a simple vacuum filtration method was used as the electrode substrate for direct coating of an ion-selective membrane. The Nernstian slope of the prepared paper-based potentiometric sensor toward lead ion detection was demonstrated as 29.4 mV per decade. A detection limit as low as 2.5 x 10-7 mol L-1 was achieved. Reversed chronopotentiometry and water layer test revealed that the graphene paper-based SC-ISE possessed excellent potential stability because of the hydrophobicity of graphene paper. Furthermore, reliable data were obtained from the detection of lead ion levels in real water samples using the graphene paper-based potentiometric sensor, which shows great potential in practical application. [ABSTRACT FROM AUTHOR]

Paper is one of the most commonly used food packaging materials. During the production of packaging paper, it is possible for trace amounts of heavy metals to be incorporated as contaminants. These could migrate into food when packaging paper (food contact paper) is used for cooking, storing and eating. The aim of this study was to determine the migration of lead (Pb) and arsenic (As) from food contact paper into a food simulant and then to assess human safety through the estimated daily intake (EDI) with consumption factor. Migration tests were conducted for 310 samples using 4% acetic acid as a food simulant at 25°C for 10 min and at 95°C for 30 min. Concentrations of Pb and As in a food simulant were quantified by inductively coupled plasma mass spectrometry. LODs for Pb and As were 0.002 and 0.005 µg L−1, respectively. The migration of Pb from food contact paper ranged from not detected (ND) to 17.5 μg L−1 at 25°C for 10 min and from 0.10 to 25.6 μg L−1 at 95°C for 30 min while As ranged from ND to 0.44 μg L−1 at 25°C for 10 min and from ND to 0.87 μg L−1 at 95°C for 30 min. The migration of Pb and As determined in this study confirm that the human exposure was within safe levels based on the EDI of food contact paper compared with the provisional tolerable weekly intake for Pb of 25 μg kg−1 bw and for As of 15 μg kg−1 bw. [ABSTRACT FROM AUTHOR]

One of the methods to solve the problem of lead metal in water is adsorption. One of the adsorbents that can be used is cellulose because it has an active group that can bind Pb(II). In this study, cellulose from the HVS wastepaper was used as the adsorbent to adsorb the Pb metal. HVS wastepaper was extracted with 10% w/v NaHCO3 and refluxed with 5% w/v Na2HPO4. Cellulose was characterized using Fourier Transforms Infrared Spectroscopy (FTIR) and Scanning Electron Microscope (SEM). Pb(II) adsorption was carried out by the batch method, and it was evaluated using Atomic Absorption Spectrophotometry (AAS) with varying adsorbent mass, concentration, contact time, and pH. FTIR characterization showed that the presence of O - H, C - H, C = O, and C - O groups played a role in the adsorption process. The surface morphology of cellulose from SEM analysis showed form like a fiber shape with agglomerated fine particles. The optimum conditions for adsorption were 0.100 g of adsorbent mass, Pb(II) concentration of 105 ppm, contact time of 10 minutes, and pH of solution 5. An adsorption isotherm model that is preferable for this adsorption process is the Freundlich isotherm model. From the results of this study, HVS paper waste can be used as an adsorbent to handle Pb(II) metal ions to be an alternative as a lowcost adsorbent. [ABSTRACT FROM AUTHOR]

The lead is poisonous metal and because of its chemical nature it acts as an environmental contaminant through the water or soil and it becomes toxic to humans. The toxicity of Pb occurs as a change in the conformation of nucleic acid and protein, inhibition of enzyme activity, disruption of membrane function and oxidative phosphorylation. For protoplast preparation, the removal of the cell wall and protoplast formation obtained by specific lytic enzyme. In cytoplasmic membrane, the envelope of bacteria consists of overlying cell wall. From hypertonic environment, the complete cell wall removal occurs due to which it maintains the osmotic integrity of the cell and produces the protoplast. In current work, protoplasts were produced by specific lytic enzyme (lysozyme and macerozyme), chemo fused (with the help of Polyethylene Glycol) and regenerated from strains Staphylococcus sp. and Bacillus sp. The fused protoplast was spherical in shape observed under microscopy. Colonies were screened on specific medium supplemented with Pb (Concentration at the rate of 1.5mM). One resistant colony (MICBT-1) was selected and further examined and applied for the transformation of Pb in the broth medium. The strain removed 98% of Pb at 1mM concentration. Next, sucrose containing medium was best which gives maximum protoplast regeneration. From various organisms, fusion technique has been used to combine the genes to create the strains having desired properties. This is a significant technique for engineering of bacterial strains for advantageous applied properties. Further MICBT-1 applied in artificially contaminated soil and removed maximally in exchangeable fraction (remains up to 0.05 mM). An efficient bioremediating agent for lead transformation from soil and water is expected to ease the ever-increasing problem. Further, it is needful to obtain new strain with the help of protoplast technology which can reduce the pollutant. This lead tolerant strain can be applied for bioremediation purposes in the Pb contaminated soil and water environment., (© 2023. The Author(s), under exclusive licence to Springer Nature B.V.)

Lead (Pb) is a widespread heavy metal pollutant that interferes with plant growth. In this study, we investigated the effects of Pb on the mechanical and chemical properties of cell walls and on the growth of coleoptiles of rice (Oryza sativa L.) seedlings grown in the air (on moistened filter paper) and underwater (submerged condition). Coleoptile growth of air-grown seedlings was reduced by 40% by the 3 mM Pb treatment, while that of water-grown ones was reduced by 50% by the 0.5 mM Pb. Although the effective concentration of Pb for growth inhibition of air-grown coleoptiles was much higher than that of water-grown ones, Pb treatment significantly decreased the mechanical extensibility of the cell wall in air- and water-grown coleoptiles, when it inhibited their growth. Among the chemical components of coleoptile cell walls, the amounts of cell wall polysaccharides per unit fresh weight and unit length of coleoptile, which represent the thickness of the cell wall, were significantly increased in response to the Pb treatment (3 mM and 0.5 mM Pb for air- and water-grown seedlings, respectively), while the levels of cell wall-bound diferulic acids (DFAs) and ferulic acids (FAs) slightly decreased. These results indicate that Pb treatment increased the thickness of the cell wall but not the phenolic acid-mediated cross-linking structures within the cell wall in air- and water-grown coleoptiles. The Pb-induced cell wall thickening probably causes the mechanical stiffening of the cell wall and thus decreases cell wall extensibility. Such modifications of cell wall properties may be associated with the inhibition of coleoptile growth. The results of this study provide a new finding that Pb-induced cell wall remodeling contributes to the regulation of plant growth under Pb stress conditions via the modification of the mechanical property of the cell wall. [ABSTRACT FROM AUTHOR]

A novel smartphone-based electrochemical cell sensor was developed to evaluate the toxicity of heavy metal ions, such as cadmium (Cd 2+ ), lead (Pb 2+ ), and mercury (Hg 2+ ) ions on Hep G2 cells. The cell sensor was fabricated with reduced graphene oxide (RGO)/molybdenum sulfide (MoS 2 ) composites to greatly improve the biological adaptability and amplify the electrochemical signals. Differential pulse voltammetry (DPV) was employed to measure the electrical signals induced by the toxicity of heavy metal ions. The results showed that Cd 2+ , Hg 2+ , and Pb 2+ significantly reduced the viability of Hep G2 cells in a dose-dependent manner. The IC 50 values obtained by this method were 49.83, 36.94, and 733.90 μM, respectively. A synergistic effect was observed between Cd 2+ and Pb 2+ and between Hg 2+ and Pb 2+ , and an antagonistic effect was observed between Cd 2+ and Hg 2+ , and an antagonistic effect at low doses and an additive effect at high doses were found in the ternary mixtures of Cd 2+ , Hg 2+ , and Pb 2+ . These electrochemical results were confirmed via MTT assay, SEM and TEM observation, and flow cytometry. Therefore, this new electrochemical cell sensor provided a more convenient, sensitive, and flexible toxicity assessment strategy than traditional cytotoxicity assessment methods.

Paper-ash is used for remediation of heavily contaminated soils with metals, but remediation efficiency after longer periods has not been reported. To gain insights into the mechanisms of immobilization of cadmium (Cd), lead (Pb), and znic (Zn), a study was performed in the laboratory experiment in uncontaminated, artificially contaminated, and remediated soils, and these soils treated with sulfate, to mimic conditions in contaminated soil from zinc smelter site. Remediation was performed by mixing contaminated soil with paper-ash to immobilize Cd, Pb, and Zn in the geotechnical composite. Partitioning of Cd, Pb, and Zn was studied over one year in seven-time intervals applying the sequential extraction procedure and complementary X-ray diffraction analyses. This methodological approach enabled us to follow the redistribution of Cd, Pb, and Zn over time, thus, to studying immobilization mechanisms and assessing the remediation efficiency and stability of newly formed mineral phases. Cd, Pb, and Zn were effectively immobilized by precipitation of insoluble hydroxides after the addition of paper-ash and by the carbonization process in insoluble carbonate minerals. After remediation, Cd, Pb, and Zn concentrations in the water-soluble fraction were well below the limiting values for inertness: Cd by 100 times, Pb by 125 times, and Zn by 10 times. Sulfate treatment did not influence the remediation efficiency. Experimental data confirmed the high remediation efficiency and stability of insoluble Cd, Pb, and Zn mineral phases in geotechnical composites. [ABSTRACT FROM AUTHOR]

Lead (Pb) intoxication is known to damage the proximal tubules of kidney. Autophagy and apoptosis have been shown to be involved in a variety of renal injuries, but the underlying mechanisms remain largely unknown. In this study, we constructed a mice model of Pb intoxication and validated it against lead concentrations in blood and urine. Electron microscopy revealed that Pb promoted the accumulation of autophagosomes. Subsequent immunofluorescence and western blotting revealed that Pb intoxication suppressed the autophagic flux. Next, exosomes were isolated and extracted through ultracentrifugation, and were further identified by diameter analysis and marker detection. We also demonstrated that autophagy and apoptosis were enhanced in renal cells with exosomes of Pb expose. Furthermore, the specific mechanisms were explored by RNA sequencing and it was found that several targeted genes regulated by differential exosomal miRNAs and lncRNAs. Target genes accumulated in several signaling pathways, especially the adenosine 5'-monophosphate-activated protein kinase (AMPK) signaling. We found that Pb intoxication-induced exosomes activated the AMPK signaling in renal proximal tubule cells. Furthermore, autophagy and apoptosis assays showed that GSK-690693, an AMPK inhibitor, significantly alleviated exosome-induced renal injuries by Pb intoxication. In conclusion, Pb-mediated exosome-induced autophagy and apoptosis via activating the AMPK signaling contributing to Pb-induced nephrotoxicity in renal cells., (© 2023 Wiley Periodicals LLC.)

Graphite, an allotrope of carbon, is also a moderately good conductor of electricity. The shading pencil lead consists of graphite mixed with clay and, therefore, can conduct electricity, allowing one to construct and demonstrate different properties and the underlying concepts of circuit elements. The grade displayed on the pencil relates to the graphite-to-clay ratio, with higher B grades indicating a higher graphite-to-clay ratio. In this paper, the main objective is to show the dependence of resistance and capacitors on different physical parameters and to calculate the value of π electrically. The materials used in this activity are readily available, affordable, and suitable for demonstration purposes. The materials used to perform these activities are shading pencils of different grades, A-4 size papers, crocodile clips, and an LCR meter. [ABSTRACT FROM AUTHOR]

A common solid waste - corrugated-paper packaging boxes - was carbonized at 300, 450, and 600ºC to develop low-cost adsorbents (biochars). The resulting adsorbents were characterized and their adsorption performances were evaluated by the batch sorption of aqueous Pb(II), Zn(II), Cd(II), and methylene blue (MB). The biochar obtained at 600ºC exhibited larger specific surface area, higher mineral contents, and pH of zero point charge (pHPZC). Calcium carbonate, lead carbonate/basic, and zinc carbonate were observed in the metal-sorbed biochars by a power X-ray diffractometer (XRD). The biochar of higher pyrolysis temperature (600ºC) had high sorption capacity of aqueous Pb(II), Zn(II), and Cd(II) with the Langmuir maximum sorption capacity of 458, 146, and 10.7 mg g-1, respectively. The pseudo-second-order model gave a better fit for the kinetic data of Pb(II), Zn(II), Cd(II), and MB onto the biochar (600ºC). Moreover, the electrostatic attraction was the dominant mechanism for adsorption of MB while precipitation could be the main mechanisms for adsorption of Pb(II), Zn(II), and Cd(II). Therefore, carbonization can be an efficient and value-addition method for the recycling of waste corrugated paper packaging boxes and for the low-cost wastewater treatment. [ABSTRACT FROM AUTHOR]

The aim of this study was to develop a highly specific electrochemical DNA sensor using functionalized lead sulphide (PbS) quantum dots for hepatitis E virus genotype 3 (HEV3) DNA target detection. Functionalized-PbS quantum dots (QDs) were used as an electrochemical label for the detection of HEV3-DNA target by the technique of square wave anodic stripping voltammetry (SWASV). The functionalized-PbS quantum dots were characterized by UV-vis, FTIR, XRD, TEM and zeta potential techniques. As-prepared, functionalized-PbS quantum dots have an average size of 4.15 ± 1.35 nm. The detection platform exhibited LOD and LOQ values of 1.23 fM and 2.11 fM, respectively. HEV3-DNA target spiked serum is also reported.Graphical abstract.

Stored under optimal conditions, paper can last for hundreds of years; however, paper is also susceptible to numerous agents of deterioration as it is primarily made of cellulose fibre derived from plant cell walls. Paper is especially vulnerable under conditions with high temperature and humidity, which together can encourage mould growth and foster insect pests. Pest infestation is a common type of deterioration responsible for significant damage to paper and books. Endsheets prepared with red lead and sewn into traditional Chinese bookbindings are a historical method used to minimise insect damage to books in southern China. Samples of red-coloured papers from the Fung Ping Shan Library at the University of Hong Kong were assessed. Two types of so called wan nian hong papers (萬年紅紙), (1) damaged and (2) undamaged by insects, were analysed with a scanning electron microscope equipped with an energy dispersive X-ray fluorescence detector. The chemical analyses reveal high concentrations of red lead (lead tetroxide, Pb3O4) in the undamaged papers, and only very few traces of lead in the damaged papers. The orange papers with insect feeding tunnels seem to have been only coloured in orange, and not treated with red lead as a biocide. These results are discussed and compared with modern treatment methods in the integrated pest management of books, archive, and library materials in (a) Europe and (b) Asia. [ABSTRACT FROM AUTHOR]

Paper-based gas sensors represent an emerging important class of devices in flexible electronics. Colloidal nanocrystals unite large surface-to-volume ratio with excellent solution processability, offering avenues to high-performance paper-based gas sensors. One of the factors limiting the performance of paper-based gas sensors is the sphere-like morphology of semiconductor nanocrystals, making it difficult to construct a stable sensing network to ensure efficient carrier transport and mechanical robustness. Here we demonstrated sensitive and flexible gas sensor via the spray coating of PbS nanowires onto paper substrates at room temperature. The pencil-drawn graphite electrode was employed to simplify the sensor design and fabrication. Unlike the sphere-like PbS nanocrystals that usually assemble into compact thin-film solids, the PbS nanowires-on-paper sensor exhibits a porous network microstructure, which not only offers efficient pathway for gas adsorption and diffusion but also possesses inherent flexibility for superior mechanical bendability. The response of the PbS nanowires-on-paper sensor toward 50 ppm of NO2 at room temperature was 17.5, with the response and recovery time being 3 and 148 s, respectively. The sensor shows only a slight decrease in response (6% of the initial value) and identical temporal response when subject to 500 bending and unbending cycles. The competitive adsorption of NO2 with O2 on PbS surfaces is proposed as the sensing mechanism accounts for the high sensitivity and good reversibility at room temperature. Our results highlight the significance of the solution-processable nanowires as the ideal building blocks for the flexible paper-based gas sensors. [ABSTRACT FROM AUTHOR]