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Nanozymes are nanomaterials that possess intrinsic enzyme mimicking activity. In this study, the application of silver nanoparticles coated filter paper (AgNPs/FP) that exhibits a peroxidase-like catalytic activity as a potential sensor is reported. A simple chemical reduction method was used to produce AgNPs/FP. The formation of the particles on filter paper were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and surface-enhanced Raman spectroscopy (SERS). In the presence of hydrogen peroxide, AgNPs/FP oxidized the colorless o-phenylenediamine (OPD) and 3,3′,5,5′-tetramethylbenzidine (TMB) solutions to a yellow colored 2,3-diaminophenazine (DAP) and deep blue colored oxidized TMB (oxTMB), respectively. In the presence of thiocyanate, however, the peroxidase-like activity was inhibited in a concentration dependent manner. This makes the AgNPs/FP a promising catalyst and employed for colorimetric detection of thiocyanate via inhibition of the peroxidase-like activity. The application can be further extended to other environmentally and biologically important analytes.

The adsorption of locust bean gum (LBG) onto Northern Bleached Softwood Kraft (NBSK) pulp improved paper tensile and burst strength and lowered refining energy by strengthening inter-fibre bonding. Adsorption kinetics and isotherms were investigated to develop a fundamental understanding of the adsorption mechanism. The adsorption rate followed pseudo-second-order kinetics and the activation energy was 99.34 kJ·mol−1, suggesting chemisorption. The adsorption rate constant increased rapidly with temperature from 25 to 45 °C (k = 1.93 to 24.03 g·mg−1·min−1), but the amount adsorbed at equilibrium decreased (qe = 1.91 to 0.48 mg·g−1 o.d. fibre). LBG adsorption to NBSK at 25 °C was consistent with the Langmuir adsorption model for LBG n = 5.00, and the equilibrium constant Kf = 2.57 mg·g−1·(mg·L−1)−1/n at 25 °C. Favorable adsorption conditions for negatively charged LBG were identified: 25 °C for 10 min, low dosage level ( 150 r.p.m.), acidic or neutral conditions (pH 2–7) without salt addition. Graphic abstract

Hydrophobic substrates for surface-enhanced Raman scattering (SERS) of adsorbate species are of great interest in chemical analysis because they can concentrate the analyte molecules in a small area of the surface, thereby improving the SERS sensitivity. Here, we propose a general strategy to fabricate hydrophobic paper-based substrates for SERS applications. The paper substrates have been manufactured by inkjet printing of aqueous emulsions containing Ag and polystyrene (PS) colloidal nanoparticles. In a first stage, the SERS performance of the substrates was optimized by varying the relative amounts of polymer/metal colloidal nanoparticles, the number of printing layers, and the degree of hydrophobicity of the substrates, using crystal violet as a molecular probe, which is well known for its strong SERS activity. In these conditions, the strongest surface Raman enhancement was observed for the highest water contact angle (146°) achieved. The selected Ag/PS-coated paper substrates showed wide applicability for several analytes, but in this study, a detailed analysis is provided for the pesticide thiram as a proof of concept. Several samples spiked with thiram have been analyzed by SERS, giving a detection limit of 0.024 ppm thiram in mineral water and apple juice, while in apple peel, the detection limit achieved for the same pesticide was 600 ng/cm2. We suggest that this one-step fabrication method produces a hydrophobic coating whose nanoscale features improve the SERS performance of the paper substrates. published

In order to obtain a lignin-based adsorbent with low cost, simple operation and no further modification, a calcium lignin adsorbent was prepared from chemical mechanical pulping (CMP) waste liquor by directly calcification from lime. The calcium lignin was characterized by BET, SEM, TEM, FT-IR and solid-state NMR analyses. The results showed that the molecular structure of the calcium lignin particles did not change when compared to sodium lignin, the formation mechanism of calcium lignin was revealed. The initial COD and lignin contents of CMP waste liquid were 54858 mg/L and 24.39 g/L, the conversion rate of lignin can reach 71.36% when was deal with lime. Thus, most of the lignin resources in the waste liquid were recovered. The middle-stage wastewater (MSWW) of pulping and papermaking was dealt with calcium lignin, the COD removal rate was up to 85.83%. The adsorption isotherms and kinetics were well fitted by the Langmuir model and pseudo-second-order kinetic model, respectively. Lime was regenerated from the used calcium lignin with high-temperature calcination, the conversion rate of calcium ions can reach 83.56%. Overall, the calcium lignin prepared by the one-step method exhibited great potential for effectively removing COD from middle-stage wastewater.

Thermochemical parameters of A4-sized printing paper (AP), filter paper (FP), newspaper (NP), writing paper (WP), and reed pith (RP) samples were estimated using standard protocol to identify its fuel characteristics, and thermal degradation of the same was studied using thermogravimetric analysis (TGA) and differential thermogravimetric (DTG) techniques in the temperature range of 30–800 °C at the heating rates of 10, 15, and 20 °C/min under nitrogen atmosphere. The curves of TGA and DTG exhibited four significant stages. Maximum weight loss was found to be in the second stage. Kinetic analysis was carried out in the conversion range of 0.1 to 0.7 using iso-conversational models of Flynn-Wall-Ozawa (FWO), Kissinger-Akahira-Sunose (KAS), Vyazovkin, and Vyazovkin AIC (V.AIC). The average activation energies were found to be 139.90, 115.93, 212.52, 257.41, and 241.63 kJ/mol using FWO; 129.73, 103.06, 202.46, 248.38, and 231.55 kJ/mol using KAS; 145.57, 134.00, 195.29, 256, and 241.63 kJ/mol using Vyazovkin; and 140.71, 133.86, 193.14, 247.57, and 190.14 kJ/mol using Vyazovkin AIC model. Thermodynamic parameters (enthalpy change (ΔH), Gibbs free energy change (ΔG), and entropy change (ΔS)) using these models have been evaluated.

This work investigates the influence of blending waste paper and cement at fixed proportion with varying proportions of chicken feather fiber (CFF) and wood saw dust (WSD) as reinforcements. Samples produced were tested for flexural properties and water absorption potentials. The outcome showed that with increasing CFF content and reducing WSD content, water absorption reduced while flexural strength, modulus of ruptures (MOR) and modulus of elasticity (MOE) increases. MOR and MOE were at peaked when the ratio of CFF to WSD was 3:2 while flexural strength reached it crescendo at 4:1 of CFF to WSD. It was noticed that higher CCF content from 3 to 5 wt% gave better results in most of the investigated properties compared to WSD. Therefore, it was concluded that low quantity of WSD is needed to form a synergy with CFF in order to achieve optimum results. Well dispersed CFF-WSD phase in waste paper-cement based composites was observed to be responsible for the enhancement in the investigated properties.

This paper focused on the studying of adsorption properties of Fe3O4-waste paper activated carbon composites for the removal of methylene blue dyes from water. The various parameters were carried out for the adsorption test of the composites, namely; contact time, adsorbent dose, initial MB concentration, pH solution, and temperature. The adsorption of isotherm, thermodynamics and kinetic was used to determine the characteristics of methylene blue adsorption onto the prepared adsorbent. The result indicates that the optimum adsorption capacity has occurred at pH = 6 in water solution. The adsorption capacity increase as the temperature increase until at 315K (45oC). The Langmuir isotherm is more appropriate to be applied as the adsorption model with the maximum adsorption capacity (qm) value of 101 and 93 mg/g for KA HCl-Fe3O4 and KA-Fe3O4 composites, respectively. The value of adsorption thermodynamic parameters was positive for ΔH, negative for ΔGo and positive for ΔSo, meaning the process adsorptions were endothermic, feasibility and spontaneity and randomness, respectively. The pseudo-second-order model was appropriate to predict the kinetic models for methylene blue adsorption onto the composites. The obtained adsorbent composites possess high adsorption efficiency and rapid magnetic separation. They were a promising for practical wastewater treatment for dyes removal from water.

Process-monitoring laboratories in the pulp and paper industry generally use a combination of wet chemical analyses and physical measurements to certify the fitness of a production pulp for a specific end-use. These laboratory tests require time and the effort of trained personnel, limiting their utility for real-time process control. Here we show that Raman probes of unrefined cellulosic pulps, well-suited to the online measurement of in-process materials, can predict the quality attributes of manufactured papers. The accuracy of prediction improves when the covariance is modelled in a reduced measurement space selected by a data-driven, feature-selection technique referred to as a Template Oriented Genetic Algorithm (TOGA). TOGA, combined with discrete wavelet transform (DWT), isolates functional-group features that correlate best with mechanical properties paper derived from refined pulp. Paper makers refine market pulps to build sheet strength using a beating process that decreases freeness as it increases fibre-fibre bonding. Methods demonstrated here predict manufactured sheet properties obtainable after any specified degree of refining from the Raman spectrum of an unrefined pulp. This analysis capacity will enable both vendors of market pulp and makers of sheet paper to specify in advance the amount of beating required to produce a desired product, thereby saving cost and conserving resources.

Background Surface enhanced Raman scattering (SERS) based on highly sensitive, flexible, solid-state sensors can provide molecular vibrational fingerprints of targeted substances in point-of-care (POC) analysis. Cellulose paper offers many advantages for the build-up of silver and gold nanostructures on a three-dimensional scaffold. Such composites can be made to contain SERS hot spots required for sensitive SERS detection in an active solid-state sensor. Scope and approach In this review, we discuss the key technical issues involved in the fabrication of SERS sensors combining a metallic SERS substrate and a cellulose paper support. We then survey recent literature for methods designed to address these issues with applications to support food safety where POC analysis serves as a valuable tool. Key findings and conclusions Sensitivity of detection is a primal challenge in the development of a paper-based SERS substrate. The fibril structures of paper materials, a suitable modification for improved bonding at the paper-metal interface, and the surface conditions of metal nanostructures all contribute to sensitive SERS performance on paper. Continuing expansion of spectrum collection in a database format, diverse methods for the statistical analyses of Raman spectra, and advanced integration of portable Raman instruments with the mobile tele-networks are critical in the further development of flexible SERS sensor in POC testing of food-borne substances.

Detecting microRNA (miRNA) biomarkers expression is of great significance for the diagnosis and treatment of lung cancer. Surface-enhanced Raman scattering (SERS) has achieved microRNA sensing for the diagnosis of primary liver cancers. In this work, we developed a SERS technology for the rapid detection of lung cancers-related miRNA (miR-196a) using bimetallic Au-Ag nanowire (AgNW@AuNPs) substrates coupled with the target hairpin DNA. The finite-difference time-domain simulation proved that a large number of “hot spots” were generated between the AgNW and AuNPs, which resulted in a huge enhancement of the signal of Raman reporters. Filter paper treated by hexadecenyl succinic anhydride hydrophobic and modified with AgNWs@AuNPs was used as capturing substrate. The detection limits of miR-196a in PBS and serum were as low as 96.58 aM and 130 aM, respectively. Studies on nonspecific sequence and single-base mismatch of miRNA demonstrated that SERS-based platform was highly selective, excellent uniform, and reproducible. Finally, the platform was used to show that the miR-196a expression in the serum of lung cancer patients was much higher than that in healthy people. The detection results indicated that the SERS platform had potential applications in cancer diagnosis and might be a viable alternative to the conventional miRNA detection method, the real-time polymerase chain reaction (RT-PCR) technology.

The application of microfluidics for largescale rapid analytics holds great promise in the pharmaceutical diagnostics and analytical chemistry. Here we report a paper based microfluidic substrate designed by the impregnation of Silver nanoparticles. This study demonstrates the achievement of a thousand-fold increase in the successful detection level up to 10 ppb (90.8 nM) by employing Surface Enhanced Raman Spectroscopy (SERS) for the detection of Catechol. The presented sensor exhibits the following main features: (i) high specificity of enzyme (Hemocyanin)-based sensing, (ii) effective SERS sensitivity, (iii) easiness and cost-effectiveness of a paper-based platform. We rationalize these findings using the ab initio DFT simulations using Gaussian 09 whose theoretical calculations reflect the observed experimental Raman peaks.

Graphene oxide (GO) paper is an attracting structural material because of its high stiffness and light-weight. In order to exploit the high strength and stiffness of individual GO nanosheet into GO paper, the fabrication process must be optimized. In this study we fabricated ultra-stiff and strong GO paper by directed-flow vacuum filtration and compared its mechanical properties under different loading conditions. We also explored the effect of cross-linking with borax, thermal annealing and sonication to further enhance mechanical properties. The stiffest GO paper reported here has a tensile modulus of 109.9 GPa and a flexural modulus of 45.7 GPa. We also found that the flexural modulus of GO paper is significantly lower than the tensile modulus because of interlayer shearing, micro-buckling and delamination during flexural deformation. The properties of GO papers therefore need to be carefully selected for mechanical structures where flexion is the major deformation. This study provides significant insights about improving mechanical properties of GO paper and selecting GO paper for different loading conditions.

Real-time monitoring of neonicotinoid pesticide residues is of great significance for food security and sustainable development of the ecological environment. Herein, a paper-based surface-enhanced Raman scattering (SERS) amplified approach was proposed by virtue of multilayered plasmonic coupling amplification. The unique plasmonic SERS multilayer was constructed using three-dimensional (3D) silver dendrite (SD)/electropolymerized molecular identifier (EMI)/silver nanoparticle (AgNP) sandwich hybrids with multiple hotspots and a strong electromagnetic field in nanogaps. Dendritelike 3D silver materials with remarkably high accessible surface areas and the lightning rod effect constituted the first-order enhancement of paper-based sensors. Molecular identifiers coated upon an SD layer as the interlayer were used for target capture and enrichment. Subsequently, AgNPs featuring rough surface and local plasma resonance decorated as the top layer formed the secondary enhancement of the amplification strategy. As the most brilliant part, dendritelike 3D silver coupled with AgNPs has established double Ag layers to accomplish a multistage enhancement of SERS signals based on the superposition of their electromagnetic fields. Owning to the distinctive design of the multiple coupling amplification strategy, the fabricated SERS paper chips demonstrated impressive specificity and ultrahigh sensitivity in the detection of imidacloprid (IMI), with a detection limit as low as 0.02811 ng mL-1. More importantly, the multiple SERS enhancement paper chip holds great potential for automated screening of a variety of contaminants.

The utilization of nitrophenols as raw materials for the synthesis of dyes, explosives, pesticides, and pharmaceuticals has increased the presence of nitrophenols as pollutants in industrial and agricultural wastewater. Similarly, the wide application range of rhodamine 6G and methylene blue enable their potential as pollutants of surface and ground waters. Both classes of chemicals can change water ecosystems dangerously. In this study, filter paper-based silver nanoparticles are prepared as catalysts for reduction of 4-nitrophenol to 4-aminophenol and for degradation of rhodamine 6G and methylene blue. This method avoids utilization of toxic reagents and is simple and inexpensive. The formation of the silver nanoparticles on filter paper was characterized using different techniques, such as scanning electron microscopy, X-ray diffraction, and surface-enhanced Raman spectroscopy. In the presence of sodium borohydride, the silver nanoparticles coated filter paper was able to reduce 4-nitophenol to 4-aminophenol within a short period of time. It has been found that, the nanocatalyst can be recycled and recovered from the reaction solutions easily without losing its high efficiency. Additionally, we demonstrated the potential of the substrate to study the in situ reduction reaction via surface-enhanced Raman spectroscopy.

Paper-based flexible surface-enhanced Raman scattering (SERS) chips have been demonstrated to have great potential for future practical applications in point-of-care testing (POCT) due to the potentials of massive fabrication, low cost, efficient sample collection and short signal acquisition time. In this work, common filter paper and Ag@SiO2core-shell nanoparticles (NP) have been utilized to fabricate SERS chips based on shell‐isolated nanoparticle‐enhanced Raman spectroscopy (SHINERS). The SERS performance of the chips for POCT applications was systematically investigated. We used crystal violet as the model molecule to study the influence of the size of the Ag core and the thickness of the SiO2coating layer on the SERS activity and then the morphology optimized Ag@SiO2core-shell NPs was employed to detect thiram. By utilizing the smartphone as a miniaturized Raman spectral analyzer, high SERS sensitivity of thiram with a detection limit of 10−9M was obtained. The study on the stability of the SERS chips shows that a SiO2shell of 3 nm can effectively protect the as-prepared SERS chips against oxidation in ambient atmosphere without seriously weakening the SERS sensitivity. Our results indicated that the SERS chips by SHINERS had great potential of practical application, such as pesticide residues detection in POCT.

Removing benzene from indoor space plays an important role in indoor air purification. A novel filter with vegetal fiber paper (VFP) as matrix hosting silica gel is proposed in this paper for benzene removal. In order to investigate the feasibility and performance of this idea, firstly, three pieces of VFP samples impregnated with different amounts of silica gel are fabricated and their benzene adsorption quantities are tested. The results show that three times is recommended as the optimal number for impregnating. The VFP sample impregnated with silica gel after the third impregnating exhibits commendable coating stability and good benzene adsorption performance. Additionally, at low relative pressure (Pb /Ps ≤ 0.05), the experimental data of benzene adsorption isotherms fit well with the Langmuir model with R2 greater than 0.97. Then, two actual filters made of VFP impregnated with silica gel after the third impregnating were fabricated. It is found that the pressure drop of the actual filter is only 1200 Pa/m when the air velocity is 2 m/s. Besides, the one-pass efficiency of the filter can reach to 19.44%. It is expected that the silica gel coated on the filter can be modified to improve the purification performance of the filter.

Food safety issues, especially those related to drug residues, have caused concern in recent years. Malachite green (MG), which is frequently used as ectoparasiticide, fungicide, and antiseptic in fish farming, is poisonous and carcinogenic. Several technologies and methods have been developed to accurately detect MG, but they can be time-consuming and expensive. Herein, we prepared a glass fiber paper as a surface-enhanced Raman scattering substrate for rapid and convenient detection of MG residues in fish. Uniform silver nanoparticles were deposited on the glass fiber paper by two in situ reduction steps of silver nitrate. The Raman signal of MG was detected and recorded using a portable Raman spectrometer in 10 s. There was a good linear relationship between the surface-enhanced Raman scattering signal intensity and the concentration of MG between 1 × 10−7 and 1 × 10−5 mol/L and the limit of detection was 5 × 10−10 mol/L. Residual MG in fish samples was extracted and detected with a recovery rate range of 98.9–119.4%. This method provides a novel way to detect MG in fish.

We introduce a facile and low-cost method for fabricating gold nanostructures on cellulose filter paper (CFP) to prepare a paper-based surface-enhanced Raman scattering (SERS) sensor for label-free molecular detection. Polymerized dopamine (PD) was used as an adhesive layer on the CFP and simultaneously functioned as a reducing agent for gold nanoparticle (AuNP) nucleation. The size of the AuNPs was dependent on the pH of the gold precursor solution, and nanoparticles with an average size of 102 nm were formed on the PD-coated CFP at a pH 3, exhibiting high SERS activity. Finite-difference time-domain (FDTD) simulations of the electromagnetic field enhancement of AuNPs with different sizes and interparticle distances were performed to identify the origin of the SERS effect. The developed paper-based SERS substrate showed uniform and excellent molecular sensitivity with a limit of detection (LOD) of 10−7 M for methylene blue, as measured by a portable Raman spectrometer. Furthermore, as a field application test, surfaces of apples were pretreated with diquat (DQ) and paraquat (PQ) pesticides, which were then detected down to a concentration of 1 ppm after simple attachment of the sensor on the apple peels and performing a SERS measurement. The developed paper-based SERS sensor is expected to be applicable as a label-free sensor for a variety of chemical and biological molecules.

A classical result of K. L. Chung and W. Feller deals with the partial sums S k S_k arising in a fair coin-tossing game. If N n N_n is the number of “positive” terms among S 1 S_1 , S 2 S_2 , …, S n S_n then the quantity P ( N 2 n = 2 r ) P(N_{2n} = 2r) takes an elegant form. We lift the restriction on an even number of tosses and give a simple expression for P ( N 2 n + 1 = r ) P(N_{2n+1} = r) , r = 0 r = 0 , 1 1 , 2 2 , …, 2 n + 1 2n+1 . We get to this ansatz by adaptating the Feynman–Kac methodology.

There is a growing interest on recycling of waste fibres as an alternative to landfill disposal. The aim of the study was to investigate the durability and mechanical properties of waste paper–cement composite panels reinforced with varying kenaf fibre content (FC, 2–10%). The panels produced were evaluated for properties including modulus of rupture (MOR) and apparent modulus of elasticity (MOE). The resistance of the panels was tested in the field for both termite damage and fungi decay for a period of 24 weeks. Accelerated decay test was also performed on selected samples. The results showed that the mean MOR ranged from 3.17 MPa for samples with 10% FC to 4.84 MPa for samples with 8% FC. The mean MOE ranged from 248 MPa for samples with 10% FC to 1298.1 MPa for samples with 8% FC. Statistical analysis showed that the effect of the fibre content was significant on the properties evaluated (p

Rising concern about the use of non-permitted colourants, in common food items such as dals and green vegetables sold in Indian markets, have led to a demand for low-cost point-of-use chemical analysis tools. Conventional food-analysis techniques involving tedious sample preparation protocols are not suited for in-field applications. Surface Enhanced Raman Spectroscopy (SERS) is an analytical technique that is well-suited for point-of-use chemical analysis with molecular level detection capability, which can also serve as a quality assurance tool for businesses. Effective and rapid signal collection from a large-area sample within a field-setting using disposable, low-cost SERS substrates is a key challenge in implementing such a solution. Herein, we demonstrate the use of inkjet-printed thin films comprising of robust nanostructured-silver as flexible, paper-based SERS (P-SERS) swabs for the direct detection of Metanil Yellow (MY) from toor dal (yellow split pigeon peas) samples and Malachite Green (MG) from green peas and green chillies. The macroscopic uniformity of these thin-films in combination with a portable Raman spectrometer equipped with orbital raster scanning (ORS™) technology for signal collection results in an unprecedented precision (RSD ∼ 1.6%) upon characterizing samples saturated with Rhodamine-6G (R6G), a standard Raman probe. As several food-cleansing products have appeared in the marketplace, the adulterant removal efficacy of some commercially available ‘washes’ as well as products such as ‘ozoniser’, which was determined by SERS characterization of swabs before and after use, is also reported.

Oil-paper insulation is the key insulation structure of the transformers, whose aging condition is closely related to the operations of the equipment. The degree of polymerization (DP) is the direct parameter characterizing the aging condition of oil-paper insulation. Recently, the near infrared spectroscopy (NIRS) measurement powered by quantitative analysis is used to evaluate DP of the insulating papers mainly. While the applications of NIRS for DP evaluation is constrained because the present spectral quantitative analysis method is not accurate and stable enough, especially for onsite tests. In this paper, we propose a Gaussian process regression (GPR) method to predict DP of the oil- paper insulation in laboratory as well as in field. Firstly, the basic principles of GPR algorithm are illustrated. A GPR model for DP prediction is established based on the spectra of differently aged insulating paper samples which are prepared in laboratory. The GPR model show a high prediction accuracy both for training set and testing set. The established GPR model is finally applied on the DP prediction of insulating papers originating from a de-tanked transformer. The accurate predicted DP and the reliable aging assessment results indicate that the established model can be implemented on site.

Oil-paper insulation is an important component of the oil-immersed power transformer, and its insulation life is directly related to the operating life of the transformer. Therefore, it is particularly important to accurately assess the life of the oil-paper insulation system. In this paper, aging insulation paper samples with different mechanical stresses were prepared in an aging vibration chamber under laboratory conditions, and the activation energy under the synergistic machine-thermal action was obtained using the translation factor. The Arrhenius equation was then combined with the Ekenstam equation to derive an equation that can accurately determine the degree of polymerization of the oil-paper insulation system. It is proved that this equation can predict the degree of polymerization of the paper under the synergistic action of machine and heat, and can provide theoretical support for the evaluation of paper life.

In this paper, we obtain samples of thermal aging transformer insulation paper at 6 time points through an accelerated thermal aging test that simulates the actual operating state of the transformer. The Raman spectroscopy diagnosis model of transformer insulating paper aging is proposed. The model combines an autoencoder and a linear discriminant analysis algorithm to extract the characteristics of the Raman spectrum, and uses a Naive Bayes classification method to divide the aging stage of the insulating paper. Through the Raman spectroscopy diagnosis model of transformer insulation paper aging designed in this paper, the Raman spectroscopy characteristic quantity extracted by the AE-LDA method can effectively reflect the aging characteristic information of the insulating paper, and the Naive Bayes classification algorithm is used to predict. Research shows that the model has a high predictive accuracy for the assessment of the aging state of insulating paper, and can effectively diagnose the aging state of transformer oil-paper insulation. The Raman spectroscopy used in the diagnosis of the aging of insulating paper has good aging discrimination ability and good application prospects, and provides a new idea for the diagnosis of the aging state of transformer oil-paper insulation.

Minimally invasive devices to detect molecules in dermal interstitial fluid (ISF) are desirable for point-of-care diagnostic and monitoring applications. In this study, we developed a microneedle (MN) patch that collects ISF for on-patch biomarker analysis by surface-enhanced Raman scattering (SERS). The micrometer-scale MNs create micropores in the skin surface, through which microliter quantities of ISF are collected onto plasmonic paper on the patch backing. The plasmonic paper was prepared by immobilizing poly(styrenesulfonate) (PSS) coated gold nanorods (AuNRs) on a thin strip of filter paper using plasmonic calligraphy. Negatively charged PSS was used to bind positively charged rhodamine 6G (R6G), which served as a model compound, and thereby localize R6G on AuNR surface. R6G bound on the AuNR surface was detected and quantified by acquiring SERS spectra from the plasmonic paper MN patch. This approach was used to measure pharmacokinetic profiles of R6G in ISF and serum from rats in vivo. This proof-of-concept study indicates that a plasmonic paper MN patch has the potential to enable on-patch measurement of molecules in ISF for research and future medical applications.

Highlights • Numerical simulations of acoustophoresis in pulp flow is conducted. • Parametric study of fiber characteristics, pulp flow regimes and acoustic parameters are conducted. • A feasibility study of industrial acoustophoresis for pulp concentration is performed. • A potential concentration gain of 15% is obtained experimentally., In pulp and paper mills, mechanical processes such as screening and washing are commonly used to remove accumulated solid suspensions and concentrate the pulp. For environmental reasons and to optimize paper production, an emerging challenge is to develop alternative methods to concentrate paper pulp between 3 % and 6 % consistency for which the mixed pulp-water flow is complex. Among the proposed solutions in the literature, solutions based on acoustic levitation, also referred as acoustophoresis, of low-consistency pulp have been demonstrated as a potential solution for efficient pulp concentration and water recirculation. However, no sensitivity analysis on the ultrasound and physical parameters was proposed, limiting the extension to a realistic application. Thus, this paper presents a numerical modeling of acoustophoresis for pulp flow concentration in a pipe. For this purpose, the pulp flow is defined as a pseudo-homogenous fluid with a turbulent Low Re k- ∊ formalism, and the pulp particles are considered spherical and deflected by two acoustic forces, namely the acoustic radiation force and the Stokes drag force, both induced by an ultrasound wave generated along the walls of a circular pipe. The combined action of these two forces in the pulp flow enables to concentrate the particles at the center of the pipe. The influences of particle size and mechanical properties, fluid properties and ultrasound parameters are analyzed within a parametric study to optimize the particle deflection and the pulp concentration. The experimental feasibility of the industrial use of acoustophoresis for the concentration of paper pulp is demonstrated with a concentration gain up to 15 %.

Conventional paper lateral flow assays have low sensitivity and suffer from severe interference from complex human fluid sample matrices, which prevents their practical application in the testing of whole blood samples in the point-of-care settings. To solve this problem, gold nanostar@Raman reporter@silica-sandwiched nanoparticles have been developed as the surface-enhanced Raman scattering (SERS) probes for sensing transduction; and a functionalized filter membrane assembly has been designed and constructed in the paper-based lateral flow strip (PLFS) as a built-in plasma separation unit. In this "on-strip" plasma separation unit, three layers of filter membranes are stacked and surface-modified to maximize the separation efficiency and the plasma yield. As a result, the integrated PLFS has been successfully used for the detection of carcinoembryonic antigen (CEA) in 30 μL of whole blood with the assistance of a portable Raman reader, achieving a limit of detection of 1.0 ng mL-1. In short, this report presents an inexpensive, disposable, portable, and field-deployable paper-based device as a general point-of-care testing tool for protein biomarker detection in a drop of whole blood.

Raman spectroscopy has been widely used to measure thermophysical properties of 2D materials. The local intense photon heating induces strong thermal nonequilibrium between optical and acoustic phonons. Both first principle calculations and recent indirect Raman measurements prove this phenomenon. To date, no direct measurement of the thermal nonequilibrium between optical and acoustic phonons has been reported. Here, this physical phenomenon is directly characterized for the first time through a novel approach combining both electrothermal and optothermal techniques. While the optical phonon temperature is determined from Raman wavenumber, the acoustic phonon temperature is precisely determined using high‐precision thermal conductivity and laser power absorption that are measured with negligible nonequilibrium among energy carriers. For graphene paper, the energy coupling factor between in‐plane optical and overall acoustic phonons is found at (1.59–3.10) × 1015 W m−3 K−1, agreeing well with the quantum mechanical modeling result of 4.1 × 1015 W m−3 K−1. Under ≈1 µm diameter laser heating, the optical phonon temperature rise is over 80% higher than that of the acoustic phonons. This observation points out the importance of subtracting optical–acoustic phonon thermal nonequilibrium in Raman‐based thermal characterization., The optical–acoustic phonon thermal nonequilibrium is first probed through novel electrothermal and optothermal techniques. For graphene paper, the optical‐acoustic phonon energy coupling factor is found at (1.59–3.10) × 1015 W m−3 K−1, agreeing well with theoretical predictions. Under ≈1 µm laser heating, the optical phonon temperature rise is over 80% higher than that of the acoustic phonons.

We studied the production and electrochemical performance of NiCo2S4 electrodeposited reduced graphene oxide (rGO) paper for use as a freestanding flexible electrode for the simultaneous determination of folic acid (FA) and ascorbic acid (AA). Production of rGO paper was achieved through vacuum filtration of the aqueous dispersion of graphene oxide, followed by chemical reduction in hydrogen iodide solution. NiCo2S4/rGO paper material was fabricated with a simple approach using electrodeposition of hydrothermal synthesized NiCo2S4 nanoparticles directly on rGO paper. The physicochemical properties of as-prepared flexible NiCo2S4/rGO paper were characterized by means of field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, and X-ray powder diffraction patterns. This freestanding paper electrode demonstrated high sensitivity, a wide linear range, and a low detection limit towards the simultaneous detection of FA and AA. NiCo2S4/rGO paper sensor, possessing easy preparation, low cost, and high flexibility, was tested in real samples with promising recoveries. This study exhibited that the approach of the electrodeposition of bimetallic sulfides on freestanding graphene paper substrates has great potential to develop high-performance flexible electrochemical sensors.

Improper storage and transportation of non-alcoholic beverages can, over longer periods, induce Maillard reaction, degrading nutritional components and generating genotoxic and carcinogenic by-products such as furfural and 5-hydroxymethylfurfural (HMF), rendering products unsafe for human consumption. Here, we describe a rapid quantitative solution-based method and test-strips for detection of furfural and HMF. The standard spectroscopic method indicated an LOD of 0.006 ± 0.003 % (v/v) and 0.005 ± 0.002 % (v/v) for furfural and HMF, respectively in fruit juice samples. The novel chromogenic test-strip has sensitivity of 0.008 % (v/v) and 0.004 % (v/v) for furfural and HMF, respectively in the same samples of fruit juice. Thus, the developed method and test-strips were specific for furfural and HMF and can be used to help ensure food safety and quality in various industrial applications.

Organic-rich pulp and paper mill sludge (PPMS) has the potential to become a renewable carbon source for producing alternatives to fossil-based product. In this work, PPMS treated by hydrothermal carbonization (HTC) was investigated based on its pyrolysis properties. The pyrolytic mechanism, kinetics data and product of the sample were studied using TG as well as pyrolysis tests in Py-GC/MS and a bench-scale reactor at 450, 550, and 650 °C. The results show that the thermal decomposition of feedstock is a two-stage reaction. The mean activation energy of the pyrolysis of HTC treated PPMS was estimated as 233.08 kJ/mol, which is higher than that of the pyrolysis of paper sludge reported before. The changes in enthalpies, entropies and Gibbs free energies from the reactants to the activated complex were estimated. The concentration of monocyclic aromatic hydrocarbons in the derived organic liquid fraction shows a positive correlation with the pyrolysis temperature. At 550 °C, the organic liquid fraction reached its highest yield at 13.7% with an oxygen level of 10.7 wt% and a higher heating value of 35.9 MJ/kg. The pyrolytic chars show that a molar ratio of O:C is less than 0.2, which shows potential for use as a carbon sink.

This work is devoted to the study of the composition of such a characteristic object for the 17–19 centuries as wafers, which were used to join sheets of paper in documents or to seal letters. Owing to the limited information in the literature and possible degradation processes that may occur with them in this paper, the modern optical techniques were applied to gain information about them. As the object of the investigation the wafers found in the hand-written documents of Academician Friedrich Georg Wilhelm von Struve (Vasily Yakovlevich Struve 1793–1864) were chosen (Fund number 721, the RAS Archive, Saint-Petersburg branch, Struve V.). Besides the common way it was found that a large number of colored wafers were used to join several sheets in one composite elongated document and also to make correction on top of what was written. As the part of a major task aimed at maintaining the fund documents dated 19th century and the stability of the used joining wafers in particular the Raman and UV–Vis absorbance spectroscopies were applied in order to investigate wafers chemical composition. It was found the use of two different types of pigments for orange hues. One of them is cinnabar and another one is made up of red lead and massicot mixture. The Prussian blue was used for wafers with dark blue hue and as a mixture with massicot for green hue. According to UV–Vis absorbance spectroscopy it was found the use of anthraquinone type pigment for the red, rose and purple hues. The presence of the wafers with different base materials were determined by means of the Raman spectroscopy, namely of the vegetable (presumably starch) and protein (presumably gelatin) origin. The obtained results were compared with the data available in the previous researches, including the recipes given in the publications of the 19th century.

A new method was performed to prepare silver-coated cellophane paper substrates, and the influence of reaction time on the morphology and performance of the substrates were studied via SEM and Raman scattering techniques. The SERS activity including sensitivity, uniformity, reproducibility and stability of the cellophane paper-based substrates were analyzed. The cellophane paper-based substrates were applied for detecting Rhodamine 6G (R6G) in tap water, lake water, rain water and chili powders. Using the prepared SERS substrates, as low as 10−11 M R6G in water samples and 10−10 M R6G in chili powders can be detected respectively. The results proved that the as-prepared cellophane paper-based substrates were suitable for detection of R6G with low concentrations in real samples.

Early and precise diagnosis of cancer is critical for a better prognosis. Here, we describe a simple and cost-effective plasmonic paper as a surface enhanced Raman scattering (SERS) substrate in combination with magnetic separation for cancer screening. The plasmonic paper was fabricated by immersing plain filter paper into gold nanorod solution and the SERS property of the paper was evaluated using 4-mercaptobenzoic acid (4-MBA) and rhodamine 6 G (R6 G), which showed an enhancement factor (EF) in the range of 106–108. HT-29, a colorectal cancer cell line that highly expresses epithelial cell adhesion molecule (EpCAM), served as the target cells; non-EpCAM-expressing cells, namely fibroblasts and red blood cells (RBCs), were used as negative controls. Intrinsic SERS spectra of the target and control cells showed distinctive patterns on the plasmonic paper due to differences in their structure and components. A combination of principal component analysis (PCA) and k-nearest-neighbor algorithm (k-NN) was employed to analyze and distinguish the acquired HT-29 and fibroblast SERS spectra, demonstrating a diagnostic sensitivity and specificity of 84.8% and 82.6%, respectively, whereas the differentiation between HT-29 and RBCs SERS spectra showed a sensitivity and specificity of 96.4% and 100%, respectively. The magnetic separation was applied to capture the target cells from cell mixtures followed by PCA and k-NN analysis. The identification of the captured cells as cancerous cells from the HT-29 and fibroblast mixture indicated an accuracy of 83.7%, while that from a mixture of HT-29 and RBCs was 98.2%. Thus, the simple paper-based SERS substrate with the assistance of magnetic enrichment and multivariate analysis offers a potent new platform for cancer cell detection and screening.

Graphene paper is a promising electrode material for use in flexible supercapacitors due to its good electronic conductivity and excellent mechanical characteristics. However, layers of graphene paper have a strong tendency to restack, resulting in a seriously reduced specific surface area and limited electrochemical performance. In this paper, restacked layers of graphene paper are reopened by a vacuum-assisted method, and carbon nanotubes (CNTs) are directly deposited on the enlarged space between the opened graphene layers. Consequently, an ordered carbon composite structure with alternately arranged graphene sheets and CNTs is constructed and exhibits increased specific surface area and a 3D conductive network. The structure and morphology of the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy and N2 adsorption/desorption measurements. The electrochemical performance was tested by galvanostatic charge-discharge test (GDC), electrochemical impedance spectroscopy (EIS) and cyclic voltammograms (CV). The obtained graphene/CNT paper exhibits a remarkably improved capacity of 170.8 F g−1, which is nearly two times higher than that obtained for a regular graphene paper.

Methylene blue removal by adsorption method had been done in batch method using adsorbent of used paper powder. Adsorption parameters covering adsorbent doses, contact times, pH, adsorbate concentrations and adsorption isotherm as well as desorption study of the absorbed methylene blue were evaluated. The results showed the highest adsorption of methylene blue was obtained at an optimum adsorbent dose, for 30 min at pH > 9. The maximum adsorption capacity of 30.77 mg/g was obtained with Langmuir isotherm model. While the effective methylene blue desorption on the used paper powder adsorbent was obtained c.a. 0.27 mg/g at pH 1.

The issue of operation of submersible vortex flowmeters used in the systems of monitoring of circulating and waste waters of pulp and paper production is considered. It is shown that in the event of an error in the installation of these instruments, an additional error appears due to the angle between the axis of the flow body (TO) of the flowmeter and the axis of the pipeline. This error is related to the measurement method, which in turn leads to a change in the Strouhal number (Sh). The influence of this error leads to a change in the geometry of the flow part of the submerged flowmeter (the appearance of the angle β), which in turn leads to a change in the vortex formation process. Variants of finding this error are considered, from which the method of numerical modeling of hydrodynamic processes with subsequent processing by the method of experiment planning was chosen. For each investigated velocity of the fiber suspension and the angle of deflection of the TO axis, a graph of the frequency spectrum of the vortex formation process was obtained. Which was later used to find the number Sh. The dependence of the installation error ΔSh,% is presented. in the form of a response surface. It is revealed that the error in the installation of the TO, which is estimated by the angle β, is relatively small and varies linearly with increasing β. If the angle β = ± 3 ° is accepted as an allowable value, then the error in measuring the flow rate of the suspension will not exceed 0.25% over the entire range of velocities under consideration., Рассматривается вопрос особенностей эксплуатации погружных вихревых расходомеров, применяемых в системах мониторинга оборотных и сточных вод целлюлозно-бумажного производства. Показано, что при ошибке монтажа данных приборов может появляться дополнительная погрешность, появляющаяся вследствие угла между осью тело обтекания (ТО) расходомера и осью трубопровода. Данная погрешность связана с методом измерения, которая в свою очередь ведет к изменению числа Струхаля (Sh). Влияние данной погрешности приводит к изменению геометрии проточной части погружного расходомера (появление угла β), что способствует изменению процесса вихреобразования. Рассмотрены варианты нахождения данной погрешности из которых был выбран метод численного моделирования гидродинамических процессов с последующей обработкой методом планирования эксперимента. Для каждой исследуемой скорости волокнистой суспензии и угле отклонения оси ТО был получен график частотного спектра процесса вихреобразования на ТО, который впоследствии использовался для нахождения числа Sh. Представлена зависимость погрешности монтажа ΔSh,% в виде поверхности отклика. Выявлено, что погрешность монтажа ТО, которая оценивается углом β, является относительно небольшой иизменяется сувеличением β линейно. Если принять в качестве допустимой величины угла β=±3°, то погрешность измерения расхода суспензии не будет превосходить 0,25% во всем диапазоне рассматриваемых скоростей.

The aim of this research was to design a model for simulating the degradation of paper in various environmental conditions by taking into consideration all the parameters (exogenous and endogenous) that influence the overall process of the acid catalyzed hydrolysis of cellulose. Three kinetic equations (Ekenstam, Calvini, and Ding and Wang) for determining the degradation rate coefficient (k) were compared. For this purpose, previously published and new experimental data on the degradation of pure and unsized cotton linter papers (neutral and acidic) upon ageing were used. The frequency factor parameter (A) in the Arrhenius formula was adjusted with additional input factors in the expression of A proposed by Zou et al. (Cellulose 3:243–267, 1996a). The model takes into account the increase of the acidity and the decrease of the moisture content induced during paper degradation. Besides the temperature and humidity, external gaseous pollutants (NO2, formic and acetic acids) were also taken into account as degradation factors. The model can be used to simulate cellulose depolymerisation of cotton papers exposed to single pollutants, but reached a limit for simulating with confidence the degradation of papers exposed simultaneously to multiple volatile compounds, due to the lack of available data, especially concerning certain volatile compounds counter-degradation effects. Future adjustments can be done when more experimental data becomes available.

We proposed a new type of freestanding Catalase (EC 1.11.1.6) (Cat) modified paper electrode based on Fe3O4 crystals decorated freestanding reduced graphene oxide (rGO) paper (Cat-Fe3O4/rGO) using a facile electrodeposition method. This enzyme modified paper electrode was used for the specific determination of hydrogen peroxide (H2O2). Structural, chemical, and morphological characterization of the Fe3O4 crystals formed on rGO paper was investigated by (i) using scanning electron microscopy (SEM), (ii) energy-dispersive X-ray spectroscopy (EDS), (iii) X-ray photoelectron spectroscopy (XPS), (iv) X-ray diffraction spectroscopy (XRD), (v) Raman spectroscopy, (vi) electrochemical impedance spectroscopy (EIS) and (vii) cyclic voltammetry (CV) techniques. The Cat enzyme was successfully adsorbed on the Fe3O4 nanocrystals surface which was demonstrated by fluorescence microscopy. The Cat-Fe3O4/rGO paper electrode showed excellent electrocatalytic activity toward H2O2. It is found that Cat-Fe3O4/rGO paper electrode shows a wide linear range, high sensitivity, and a low detection limit for H2O2 detection.

We report the development of a surface-enhanced Raman spectroscopy sensor chip by decorating gold nanoparticles (AuNPs) on ZnO nanorod (ZnO NR) arrays vertically grown on cellulose paper (C). We show that these chips can enhance the Raman signal by 1.25 × 107 with an excellent reproducibility of 92% clinical sensitivity and specificity. Our technology has the potential to be used for the early detection of prenatal diseases and can be adapted for point-of-care applications.

Paper‐based sensors, microfluidic platforms, and electronics have attracted attention in the past couple of decades because they are flexible, can be recycled easily, environmentally friendly, and inexpensive. Here we report a paper‐based potentiometric sensor to detect the whole Zika virus with a minimum sensitivity of 0.26 nV/Zika and a minimum detectable signal (MDS) of 2.4x107 Zika. Our paper sensor works very similar to a P‐N junction where a junction is formed between two different regions with different electrochemical potentials on the paper. These two regions with slightly different ionic contents, ionic species and concentrations, produce a potential difference given by the Nernst equation. Our paper sensor consists of 2‐3 mm x 10 mm segments of paper with conducting silver paint contact patches on two ends. The paper is dipped in a buffer solution containing aptamers designed to bind to the capsid proteins on Zika. We then added the Zika (in its own buffer) to the region close to one of the silver‐paint contacts. The Zika virus (40 nm diameter with 43 kDa or 7.1x10‐20 gm weight) became immobilized in the paper’s pores and bonded with the resident aptamers creating a concentration gradient. Atomic force microscopy and Raman spectroscopy were carried out to verify that both the aptamer and Zika become immobilized in the paper. The potential measured between the two silver paint contacts reproducibly became more negative upon adding the Zika. We also showed that a Liquid Crystalline Display (LCD) powered by the sensor can be used to read the sensor output.

In this paper, a method based on Raman spectroscopy to diagnose the aging degree of oil-paper insulation is discussed. According to IEEE guidelines, oil-paper insulation samples were prepared in the laboratory, and the degree of polymerization values of the samples were measured to obtain the exact aging states. Raman detections of the samples were carried out based on the Raman experimental platform. T-S fuzzy neural network was used to analyze the Raman spectrum data of insulating oil. By using the experimental data to train the diagnosis model, constantly modifying the membership function, and mining the internal mathematical relationship between the Raman spectrum characteristics of oil paper insulation and the degree of polymerization of insulating paper, this paper managed to use the Raman spectrum data of insulating oil to predict the aging degree of oil paper insulation. Finally, the deviations between the predicted and the measured degree of polymerization values of the five test samples in this experiment are both less than 150.

A graphene oxide paper (GOP) was irradiated with 500 keV proton for total fluence of 2 × 1013 cm−2 to 2 × 1015 cm−2 in a ground-based irradiation simulator. The spacing of layer, surface chemical composition, structural defects, thermal conductivity and electrical property of the GOP before and after irradiation was measured. The results indicated that the spacing of layer decreased after irradiation. The ratio of total carbon atom and total oxygen atom increased from 2.40 to 4.31 as well as the sp2 hybridized carbons obviously increased after 2 × 1015 cm−2 irradiation. The XPS analysis suggested the occurrence of reduction, and the Raman spectra indicated that the defects were produced after proton irradiation. Furthermore, the thermal conductivity of GOP decreased, and then increased smoothly as the irradiation fluences were increased, and the electrical property showed the similar trend. The change in the thermal and electrical properties for GOP could be attributed to the defects and the removal of oxygen-containing functional groups, which lead to the phonon conduct path and scattering centers changed under proton irradiation. This study could promote the application of GOP in future space expeditions.

We report on a corroborative study of the structural, morphological and electrical property alterations of free-standing graphene oxide (GO) papers subject to thermal reduction. Structural analysis performed using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Raman techniques prove that the onset of major structural changes, characterized by removal of oxygen functionalities, occur in the 200–300 °C temperature range. The results are corroborated with related morphological changes observed using Scanning electron microscopy (SEM) and Atomic force microscopy (AFM) imaging. Elemental analysis shows the GO paper reduced at 600 °C to contain an 85 wt. % carbon content and a remnant oxygen level of 13.31 wt. %. At the highest reduction temperatures, we see evidence of vacancy-type defects impeding the overall effectiveness of the reduction process. Detailed electrical resistance measurements and current–voltage (I-V) profiling conducted using four-point probe method reveals a several orders of magnitude drop in the sample resistance once the reduction temperature exceeds 200 °C, in good agreement with the structural and morphological changes. The fundamental insights revealed through these studies will be important for future applications where the electrical and mechanical properties of free-standing GO and reduced graphene oxide (rGO) are exploited in practical devices. Graphical abstract

A miniaturized paper-based disposable pH sensor has been developed for the measurement of urine pH. The proposed sensor requires $2~\mu \text{l}$ of analyte solution for rapid detection of the analyte pH with a response time of 3.07 sec and 36.04 sec for acidic and basic pH, respectively. The sensor is fabricated via in situ deposition of polyaniline over the paper substrate by chemical oxidative synthesis. The sensitivity of the sensor is 1.6 $\text{k}\Omega $ /pH for acidic pH and 6.2 $\text{K}\Omega $ /pH for basic pH, at a frequency of 1kHz. The sensor has been characterized using scanning electron microscopy, Raman spectroscopy, and UV-vis spectroscopy to validate the formation of emeraldine salt and emeraldine base state of polyaniline. The varying optical band gap values of the in-situ deposited paper sensor in the acidic and basic region also validates the presence of polaron in acidic pH and formation of emeraldine base in basic pH. DC conductivity measurement reveals that the conductivity of the polyaniline coated paper substrate decreases at a higher pH value. For an in-depth understanding, a novel electrical equivalent model is proposed, and the electrical parameters extracted from the Bode impedance and phase plot. The fabricated sensor exhibits an average accuracy of 95.53% when tested with urine sample of healthy subjects and patients suffering from urinary tract infection (UTI).

We examine the trends in the studies published in international trade journals indexed in Web of Science (WoS) before and after the 2008 Global Financial Crisis (GFC). This study investigates the 5001 abstracts of trade articles starting from the post-millennium period by addressing issues in WoS database trade journals using the Latent Dirichlet Allocation (LDA) topic model. The purpose of the study is to evaluate whether topics and words differ that have been discussed in international trade literature before and after GFC. Mostly, contain topics differ when two periods are compared, although trade agreements and disputes, stock markets, and growth issues are frequently mentioned in both periods. In the post-crisis period, volatility, banks, and firm-specific issues are more popular. It is also among the findings that Asian economies gained importance after GFC. Generally, it has been revealed that the topics and titles in the trade literature can reflect current developments in international economics. Therefore, probably for next years, advances in technology as blockchain, emerging economies –especially China and India – and firm-based micro-scale papers will dominate the trade journals.

Background This work investigated adsorption behaviors of NH4+ onto H2O2 modified paper waste sludge-derived hydrochar (HPSH). Methods Effect of various operational parameters, including modification ratio, solution pH, adsorbent dosage, initial NH4+ concentration and contact time on NH4+ adsorption was studied. Besides, the NH4+ adsorption isotherms, kinetics and thermodynamics at different operational temperatures were systematically investigated. The textural, morphology, crystalline structure and surface chemistry characteristics of hydrochars were analyzed. Specially, NH4+ adsorption mechanisms controlled by enriched oxygen-containing surface functional groups by treatment of H2O2 onto hydrochars were deeply discussed. Significant findings The results showed that the optimal treatment ratio between H2O2 and PPSH was 40. Characterization data indicated H2O2 modification increased the oxygen-containing functional groups on the hydrochar surface. The maximum adsorption capacity of HPSH-40 was 7.941 mg/g which was higher that of PPSH about double. NH4+ adsorption onto hydrochars was well described by the pseudo-second-order model and Langmuir isotherm. The thermodynamic studies showed NH4+ adsorption onto hydrochars was endothermic in nature. The mechanisms of NH4+ adsorption onto hydrochars included π-cation interaction, cation exchange, surface complexation and electrostatic attraction which were attributed to the vital role of enriched oxygen-containing surface functional groups on hydrochar's surface.

A free-standing palladium/reduced graphene oxide paper (Pd/rGOP) based on one-pot co-reduction was prepared. The as-prepared Pd/rGOPs contain evenly distributed Pd particles interposing between the rGOP layers. The structure and composition of Pd/rGOP were characterized by SEM, EDX, XRD and Raman spectra. We investigated the glucose sensing performance of Pd/rGOP by chronoamperometry, the sensitivity reach as high as 6.70 µA mM−1 cm−2 with the linear range between 0.5 mM and 8 mM. The sensor also exhibits a good anti-interference ability and detection selectivity toward the interference. The proposed sensor has great potential to become a reliable tool in point-of-care medical devices.