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This study optimizes a novel surfactant-assisted green liquor dregs (GLD) pretreatment of paper mill sludge (PMS), both of which are wastes from the kraft pulping industry, using a combined Response Surface Methodology (RSM) design. Optimized conditions give a maximal reducing sugar release of 16.38 g/L. A substantial reduction in heavy metals aluminum, chromium, cobalt, arsenic, lead, and copper after pretreatment illustrates the enhancement of substrate digestibility by reducing toxic elements. Separate hydrolysis and fermentation (SHF) and simultaneous saccharification and fermentation (SSF) for hydrogen production are assessed. SSF produced a hydrogen yield of 3.72 mL/g, displaying a 36.26% increase from pretreated PMS compared to SHF. These findings provide insights into possible methods of reducing process duration, energy input, and costs incurred with waste disposal within the paper industry. Furthermore, improved hydrogen yield using an SSF process demonstrates the potential beneficiation of pulp and paper GLD and PMS wastes.

In this elucidation, we synthesized novel molecularly imprinted polymers (MIPOH1-4) that were used as organic fillers on bagasse pulp to form cellulosic paper sheets, the formation of MIPOH1-4 from the reaction of enaminone 3 with methyl methacrylate monomer in the presence of ethylene glycol dimethyl acrylate and 2,2’-azobisisobutyronitrile. The obtained MIPOH1-4 was confirmed via FT-IR and SEM with different pore sizes. And we noticed that the increase of template 3 increases the hydrogen bond between monomer and template and gave sponge surface of MIPOH4. Furthermore, the computational energies of the template with different monomers utilize DFT/B3LYP/6-31G (d) level to know the stability of polymers and hydrogen bonding between them. So that we applied that in paper manufacture through the adsorption of MIPOH4 as an organic filler on bagasse pulp to form novel cellulosic paper sheets with different concentrations and these sheets which characteristic through FT-IR, SEM, sizing test, tensile strength, and elucidation their antimicrobial activity with theoretical and docking studies. The MIPOH4 and cellulosic paper sheets showed the thermal stability and high tendency of sizability of these paper sheets and concluded the interaction between cellulose fibers of pulp with MIPOH polymer with physical hydrogen bonding.

Paper and pulp mills generate substantial quantities of cellulose-rich sludge materials that are disposed in landfills at a large scale. For sustainability purposes, sludge materials can be bioprocessed to produce renewable fuels and useful chemicals. The enzymatic hydrolysis of cellulose is the process bottleneck that affects the conversion economics directly by using zero-cost raw materials. In order to study and optimize the process, the characteristics of the sludge raw materials should be first evaluated. In this work, sludge samples were obtained from paper mills located at different locations in Wisconsin and Minnesota. Part of the sludge samples was washed (de-ashed) with hydrochloric acid while the other part remained unwashed. The samples were subjected to multiple spectroscopic analyses techniques to evaluate the morphological properties of cellulose fibers and to estimate the total structural carbohydrate content. The results showed that the de-ashing process changed some fiber characteristics and cellulose crystallinity structure in all sludge samples. Sludge sample A (obtained from Kraft pulp and recycled paper mill region) showed a high percentage of fiber, with crystalline cellulose, compared to the other two sludge samples suggesting that sludge A is a valuable source to make value-added products. Aspen Plus mass and energy calculations performed in view of the ‘zero’ cost and the reliable supply of sludge raw materials producing 2 mol H2/mol glucose. Moreover, the results showed that extracting crystalline cellulose from these sludge samples is more profitable than crystalline cellulose made from the other lignocellulosic feedstocks. The results reported here showed that the utilization of these sludge materials would be an economically attractive and promising alternative for the production of hydrogen.

By continuously varying the structure of graphene oxide paper (PRGP) using Joule heating annealing, we are able to tune its electrical conductivity (σ) and thermal diffusivity (α) in a very wide range: more than three orders of magnitude for σ (186–503009 S/m) and 10-fold for α (8.31 × 10−7 m2/s to 9.31 × 10−6 m2/s). Excellent coherency-linear relationship between σ and α is discovered although they are sustained by different carriers: electrons and phonons. Such coherency exists over two sections: σ > 2 × 104 S/m, and 103

A paper-based membrane coated by graphitic carbon nitride (g-C3N4) is prepared via a dip-coating method and used as a separator for sodium metal batteries with merits of low cost and environment-friendliness. Introduction of g-C3N4 effectively improves the ionic conductivity and the structural stability of the separator. Compared with traditional polyethylene separators and Al2O3-coated separators, the g-C3N4-coated separators show better electrolyte wettability, thermal stability, and electrochemical stability. Therefore, Na||Na3V2(PO4)3 battery using the g-C3N4-coated separator exhibits better cycling stability and higher rate capability. These results prove that the g-C3N4-coated paper-based separator is expected to become the next generation of low-cost and high-safety separator in sodium metal batteries.

Neotame is an artificial sweetener with increasing consumption in recent years, excessive intake of it may bring potential health risk. In this work, a rapid method was developed to detect neotame in instant grain beverages, which was based on surface-enhanced Raman scattering (SERS) technique and filter paper-based silver nanoparticles (AgNPs@FP) substrates. The designed substrate exhibits good SERS activity with an enhancement factor of 105 because of the synergistic effect of the concentrated silver nanoparticles and filter paper. Meanwhile, the stability and repeatability of this fabricated substrate have been investigated with the relative standard deviation of 6.1%. In addition, it shows an excellent linear relationship (R 2 = 0.997) between the SERS signal and the logarithm concentration of neotame with a wide concentration range (0.05–5 g/kg) in the quantitative analysis. The limit of detection of neotame can be as low as 0.01 g/kg in instant grain beverages, which is below the maximum allowable addition level for neotame in instant grain beverages set in China (GB2760-2014, 0.16 g/kg). The proposed method has great potential for the identification and quantification of neotame in food safety applications with high sensitivity.

Flexible thin-film solar cells with high weight-specific power density are highly desired in the emerging portable/wearable electronic devices, solar-powered vehicles, etc. The conventional flexible metallic or plastic substrates are encountered either overweight or thermal and mechanical mismatch with deposited films. In this work, we proposed a novel substrate for flexible solar cells based on graphene paper, which possesses the advantages of being lightweight and having a high-temperature tolerance and high mechanical flexibility. Thin-film amorphous silicon (a-Si:H) solar cells were constructed on such graphene paper, whose power density is 4.5 times higher than that on plastic polyimide substrates. In addition, the a-Si:H solar cells present notable flexibility whose power conversion efficiencies show little degradation when the solar cells are bent to a radius as small as 14 mm for more than 100 times. The application of this unique flexible substrate can be extended to CuInGaSe and CdTe solar cells and other thin-film devices requiring high-temperature processing.

Inorganic salt modified paper substrates were developed and utilized in microfluidic paper based sampling coupled with potentiometric ion sensors for the determination of heavy metals, such as Cd2+ and Pb2+. The application of paper based sampling without any paper substrate pre-treatment were characterized with super Nernstian response, while the paper substrates with inorganic salt pre-treatment were characterized with standard Nernstian response. The application of inorganic salt modified paper substrates was found advantageous when the cation of the salt in the conditioning solution was the same as the primary cations of the ion-selective electrodes (ISEs). A relatively high concentration of inorganic salts during pre-treatment of the paper substrates, namely Cd(NO3)2 or Pb(NO3)2 with subsequent measurement of cadmium(II) and lead(II), by Cd2+- and Pb2+-ISEs, respectively was needed to sustain Nernstian response of sensors. It was also found that paper substrates facilitate sorption of metal ions onto the paper substrates, with stronger binding strength given to Pb2+ over Cd2+. Moreover, the metal-paper interactions suggest concentration dependent sorption-desorption of metal ion, which can have direct limitations of the use of paper based analytics for the determination of low analyte concentration of heavy metals. Nanyang Technological University The authors would like to thank NTU-India Connect Research Internship Program for financial support of Ms Tharini Saravana Sundaram from Coimbatore Institute of Technology, India.

A simple process of commercial paper functionalisation via in situ polymerisation of conductive polymers onto cellulose fibres was investigated and applied as electrodes in paper-based batteries. The functionalisation involved polypyrrole (PPy) and Poly (3,4-ethylenedioxythiophene) (PEDOT) as conductive polymers with the process of functionalisation optimised for each polymer individually with respect to oxidant-to-monomer ratios and polymerisation times and temperature. Paper with conductivity values of 44 mS/cm was obtained by exposing the samples to pyrrole vapour for a period of 30 min at room temperature; however, polymerisation at temperatures of 40 °C lead to higher conductivity values to up 141 mS/cm. Consequently, functionalised PPy and PEDOT papers were applied as cathodes in batteries with Al foil anodes and commercial paper soaked in an electrolyte solution of NaCl.

In this study, fabrication of microfluidic paper based analytical devices (μPADs) by microembossing was proposed. Different from the embossing methods described in the literature, the filter paper was embossed such that a protruded structure was formed, which subsequently became the channel after heating the wax at the backside of the filter paper. It was found that, when using the Whatman No. 3 filter paper, the embossing pressure needed to be larger than 50 kg/cm2 in conjunction with using a minimal 2-mm wide channel, and the wax heating time ranged from 15 to 45 s in order to obtain a reliable μPAD with repetitive and consistent results. In addition, there was no need of a hydrophobic material as the backside support. The glucose detection was demonstrated using the μPADs as fabricated and a linear relationship was obtained between 5 and 50 mM glucose concentrations. With the proposed method, the processing time of fabricating μPADs can be reduced within approximately 1 min.

Paper-based devices are always more gaining a relevant position in the field of sensors. The continuous demand for affordable, simple, sustainable, and portable devices, is making paper as the ideal basis towards the realization of analytical tools for the easy self-testing. In this work, we demonstrate, for the first time, the development of a disposable paper-based printed electroanalytical strip for reliable, rapid, and high-throughput detection of glutathione in blood. The detection is based on the thiol-disulfide exchange reaction, which produces a detectable compound easily oxidizable at a Prussian Blue/carbon black nanocomposite involving a favorable low-interference overpotential. This nanocomposite is mixed within a carbon-based conductive ink and successively screen-printed onto a wax-patterned filter paper. The employment of paper provides a reagent-free device, as a consequence of the reagents pre-loading within the testing area. After the experimental conditions have been optimized, glutathione has been detected up to 10 mM, with a detection limit of 60 μM, and a sensitivity of (0.102 ± 0.005) μA/mM. This sensor showed satisfactory repeatability (relative standard deviation equal to 10%, for detection of glutathione 1 mM), especially by considering the hand-made manufacturing process. The “real-world” applicability of this strip has been evaluated by quantifying blood glutathione at physiological levels and by recovery studies achieving satisfactory values.

A facile and feasible method for decoration of iron oxide (Fe3O4) submicron-sized particles on carbon paper at room temperature in a short time of 10 min is demonstrated in this work. The Fe3O4-particles decorated carbon papers were used as the negative electrode for an Fe-air rechargeable battery in both an alkaline aqueous solution system and an all-solid-state system. As for the all-solid-state Fe-air rechargeable battery, KOH-ZrO2 electrolyte powder developed by our group was used in the battery fabrication. In the alkaline aqueous solution based Fe-air rechargeable battery, a high initial discharge capacity of 460 mAh g−1(Fe) was achieved. Meanwhile, in the novel all-solid-state Fe-air rechargeable battery system, an initial discharge capacity of 70 mAh g−1(Fe) was obtained demonstrating the feasibility of this system that could be further developed towards a practical Fe-air rechargeable battery for portable and lightweight device application.

Selective detection of different explosive materials is essential to the current world scenario from the perspective of health, safety, and environment. Here, we have developed and characterized a couple of bio-based conjugated systems, viz. cholesterol-tryptophan and cholesterol-cysteine for the detection of nitroaromatic explosive chemicals. The presence of tryptophan moiety introduces fluorescence property to the non-fluorescence cholesterol backbone, and hence it was used as a tag molecule to prepare photoluminescent filter papers which serve as indicators for picric acid and dinitrosalicylic acid. These paper strips undergo instant quenching in the presence of the experimental analytes under the UV irradiation, which could be visualized through the naked eye. The amount of quenching is found to be proportional to the concentration of the analytes. The limit of detection for picric acid and dinitrosalicylic acid was estimated to be about 33 nM and 48.7 nM respectively, and the mechanism of this quenching is mainly due to fluorescence resonance energy transfer between the fluorophore and the quencher. Also, the vapor of picric acid completely diminishes the photoluminescence of the filter papers. Such an easy, selective and instant detection of nitroaromatic chemicals is in high demand due to increasing health and security concern worldwide.

One of the most important problems in dark fermentative hydrogen production is the need for the regulation of the ambient pH due to the formation of volatile fatty acids. For this purpose, alkaline chemicals are usually used; however, alkaline addition to the media increases salt formation, which negatively affects microbial activity. In this study, pH adjustment was performed by providing direct current as an alternative to alkali addition. Experiments were carried out batchwise and electricity was only applied to neutralize the acidic pH value. The waste paper hydrolysate was used as a substrate and the effects of applied voltage (0.25-3 V), substrate concentration (4.8-41.2 g/L at 1 V) and electrode distance (0.3-1.3 cm at 1 V) on hydrogen production performance was investigated. Voltages less than 1 V required too much time to keep the pH convenient and voltages more than 1.5 V adversely affected hydrogen production performance. Providing direct current to the fermentation media significantly reduced the adaptation phase. Conditions for optimal pH adjustment and hydrogen production were obtained at 1 V, 20 g glucose/L and 0.5 cm electrode distance. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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.

There is a high interest in nanomaterials that effectively deactivate different types of bacteria and provide alternatives to chemical substances and antibiotics. This research is reporting the antibacterial performance in contaminated water of flexible structures consisting of thin metallic films deposited on water filter paper. Coatings were performed at low temperatures using high vacuum direct current (DC) magnetron sputtering deposition. The effectiveness of different metallic nanoparticles in functionalizing the fibrous surfaces and deactivating bacteria from water was tested during the experiment. The surface morphology of coated filter paper was characterized using digital optical microscopy and scanning electron microscopy (SEM). The fibrous substrates provided large area of exposure for metals to bacteria. X-ray diffraction and Energy Dispersive X-ray Spectrometer (EDS) were used to identify the chemical composition of the structures. The antibacterial performance was evaluated against Escherichia coli (E-coli) and total coliforms using the standardized membrane filtering technique for water and wastewater examination. Silver and copper effectively deactivate coliforms from water with copper providing higher performance. The antibacterial effect of copper and silver coatings with different thicknesses as well as the nanolayered combination of the two metals was also investigated. It was observed that coatings remained adherent to substrates and the antibacterial performance was maintained over consecutive exposures.

In the last years, the imprinting technology has raised attention and different polymers with artificial recognition sites towards a target molecule have been developed. In this article, a polymerization-free method ―which only requires the dissolution of nylon-6 polymer and its subsequent incubation with the template molecule― has been employed for the preparation of a molecularly imprinted polymer directly immobilized on filter paper, thus increasing the versatility and manageability of the new material. The molecularly imprinted paper-based analytical device (MIP PAD) has been coupled to a fluorimeter via a custom-built platform, which enables direct measurement of the fluorescence at the surface of the MIP PAD. Extraction efficiency of the MIP PAD was evaluated using quinine as model analyte, measuring the fluorescence directly at the MIP PAD surface after incubation on aqueous standards of quinine and soda drink, showing that the performance of the imprinted material was superior to that of the non-imprinted polymer. In addition, the selectivity of the MIP PAD versus analogous organic fluorescent molecules has been further evaluated using norfloxacin, observing that the molecular imprinting results in selective extraction of quinine. The performance of the method has been evaluated for quantitative analysis, achieving limits of detection (LOD) and quantification (LOQ) for aqueous standards of 0.37 and 1.24 mg L−1, respectively, while in the case of spiked soda drink the LOD and LOQ were 0.63 and 2.11 mg L−1, respectively. The reproducibility of the measurements was also evaluated, observing values within range 2.30 and 9.07% measured as relative standard deviation.

The present work focused in assessing the hydrogen production from pretreated wastes of the paper industry (PIW) by simultaneous saccharification and fermentation (SSF) using anaerobic biofilms developed in natural fibers (ixtle) at different conditions. Anaerobic sludge from brewery wastewater treatment was used for biofilms and they were developed in plastic spheres covered with fiber cord from ixtle. The solid wastes of paper industry were previously pretreated with H2SO4 at 2.5% (v/v) at 120 °C by 30 min. The solids pretreated were hydrolyzed and fermented in batch reactors. All reactors were kept at an initial pH of 5.0 and three levels of enzyme loadings (10, 40 and 70 FPU/mL) and temperatures (35, 45, 55 °C) were assessed. The maximum hydrogen obtained (60.75 mmol/h*g volatile solids) was at 45 °C and 70 FPU/mL, moreover, no methane was detected in all cases.

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.

In this communication, a novel surface modification method of the paper surface using 3-aminopropyltriethoxysilane (APTES) and gold nanoparticles is reported. This functionalized paper (flower-shaped paper-based microfluidic devices (F-PMD) for simultaneous assay of multiple analytes) is used for determination of total lipid profiling (TLP) in a single device. Here, we have determined total cholesterol along with low-density lipoprotein (LDL), high-density lipoprotein (HDL) and triglycerides (TGL). The LDL and HDL were estimated by erasing the non-HDL and non-LDL components with a help of precipitating reagents. Standard graphs prepared by the present paper-based method nicely correlates with the conventional method (calculated by Roche- COBAS C111 autoanalyzer) with Pearson Correlation Coefficient (R) of 0.903, 0.9727, 0.9939 and 0.9866 respectively for total cholesterol, LDL, HDL and triglycerides. The present assay device is intended to assist in the screening of individual’s lipid level for diagnosis of disorders involving high cholesterol level in the blood or for metabolic disorders associated with lipid and lipoprotein. As this is affordable, miniaturized, easily portable, self-testing and rapid, the present assay device can be used easily by pre-clinical, non-professionals, children in schools, labs, etc as a point-of-care diagnostics.

In this study, we designed a rapid colorimetric sensing system using competitive ELISA test on a microfluidic paper-based analytical device for the detection of ketamine, a frequently abused drug. Oral fluid was selected for the test to facilitate the collection of samples based on its advantages of low infection risk, noninvasiveness of sample collection, and decreased chance of sample adulteration. After optimization of the operation parameters, including reaction temperature, vibration washing time, reaction time, and antibody concentration, the resulting assay can be completed in as little as 6 min with a detection limit of 0.03 ng/mL. Moreover, we developed an Android smartphone app to analyze and measure the results of the test, further enhancing the test’s portability, and image recording and data transmission capabilities. In order to test the feasibility and performance of the optimized colorimetric assay, 90 oral fluid samples from drug abuse patients were tested. The paper-based platform features 90% sensitivity (confidence interval (CI): 76.34–97.21%) and 92% specificity (CI: 80.77–97.78%) for ketamine analysis. This competitive paper-based ELISA sensing system provides a rapid, convenient, sensitive, and high-throughput approach for drug monitoring.

Free-standing hierarchical polyaniline/graphene/MnO2 (PANI/G/MnO2) paper is well constructed using low-cost printing paper by a simple layer-by-layer in situ growth and vacuum filtration method. The PANI nanofiber was polymerized on cellulose fibers, and then the pristine graphene sheet was introduced to generate the polyaniline/graphene paper, whose surface was subsequently scattered with the formed MnO2 nanoflowers through oxidation of the cellulose fiber and graphene. The PANI/G/MnO2 paper possessing a mass loading of 11.75 mg cm−2 is of high flexibility and could serve as a working electrode without using any binder and conductive additives. The electrode shows a sizeable areal capacitance of 3.5 F cm-2 at 5 mA cm−2 and excellent cycling stability of 90% after 1000 bending cycles. All-solid-state supercapacitor assembled with the PANI/G/MnO2 paper exhibits a high energy density of 5.2 mW h cm-3 at 8.4 mW cm-3. Eight supercapacitors connected in series can light a green light-emitting diode of 3 V.

A novel visual and fluorometric-sensor paper is prepared for the monitoring of atmospheric humidity and ethanol. The paper contains a combination of copper nanoclusters (CuNCs) and carbon dots (CDs), immobilized on a filter paper. This makes it a dual-emission system. The visual sensor shows bright fluorescence and has a diameter of ∼8 cm with uniform and homogeneous surface. The detection mechanism of the sensing paper is based on the fluorescence intensity variation of CuNCs in different environments. Desirable linear relationship is observed between fluorescence intensity ratio (red/blue) and humidity. Visible color transformation of this sensor paper is observed in the humidity range ∼40-80%, implying utility for easy and facile atmospheric humidity determination. Furthermore, due to the water and ethanol have different impacts on the spectrum, this paper-based fluorescent probe shows excellent response to ethanol. Therefore dual-emitting sensing paper, when suitably calibrated, shows promise for visual and fluorometric sensing platforms aimed at humidity or ethanol detection.

The separation of oil and water mixtures is an important issue in acidic and alkaline conditions. In this paper, the chitosan (CS)-coated filter paper was successfully fabricated for application in the field of oil/water separation by crosslinking filter paper with hydrophilic chitosan through a simple Schiff’s base reaction. The surface of the prepared CS-coated filter paper maintains superhydrophilic and low adhesive ability to oil in water. Besides, this filter paper can resist highly acidic erosion even concentrated sulfuric acid. Surprisingly, CS-coated filter paper can be efficiently applied on the separation of different types of oil/water mixtures in wide pH range conditions and exhibits excellent recyclability and antibacterial property. The antibacterial rate of CS fiber pure textile can reach 99%. The antibacterial rate of blended fabric is about 75%. This separation process has high potential for industrial oilfield wastewater treatment and separation in extreme environments.

Zn/Ce redox flow battery (ZRFB) is emerging as a promising technology to store large amount of energy economically and efficiently, wherein a highly efficient positive electrode with a continuous and fast electronic and ionic transportation path is urgently desired. The unique nanostructure of reduced graphene oxide (RGO) paper electrode is prepared by a simply chemical reduction method, which facilitates transference of the electron and Ce3+/Ce4+ at the electrolyte/electrode interface. Thus ZRFB exhibits superior extent of charge (81.0%) and energy efficiency (71.3%). The results show RGO paper is a good candidate for positive electrode of ZRFB.

Since hydrophobicity can improve the usability and functionality of materials in humid condition, enhancing the hydrophobic behavior of starch films or papers is of importance. In this work, ZnO nanoparticles (NPs) were introduced into the starch solution under ultrasonic and magnetic-stirring, followed by cast filming and paper coating. The contact angles of resulting film and coated paper containing 2% (wt) NPs were increased from 85.73° to 121.45°, 64.47° to 103.94°, respectively. The results from comprehensive characterizations confirmed the hierarchical structure created by ZnO nanoparticles on the surface of starch film as well as the formation of intact layers on coated paper. The excellent miscibility between starch and ZnO NPs was also achieved. The approach developed is promising and facilitates the hydrophobic modification of green-based materials.

Developing high-performance electrode is crucial to energy storage performance of vanadium redox battery. Herein, TiO 2 decorated carbon paper was developed by hydrothermal route with various treatment time, and employed as negative electrode for vanadium redox battery. TiO 2 can be in situ covered on carbon paper by hydrothermal route. Wetting performance of carbon paper is markedly enhanced by introduction of TiO 2 . Compared with raw carbon paper, TiO 2 decorated carbon paper demonstrates excellent electrochemical performance towards V 3+ /V 2+ couple. The sample treated for 6 h (CP-H06) exhibits the best electrochemical properties. The enhanced performance comes from the accelerated transfer of vanadium ions and electrons. The single cell testing indicates that the cell performances are improved significantly by using CP-H06 as negative electrode in terms of increased discharge capacity and energy efficiency. Discharge capacity and energy efficiency increase by 17.8% and 6.4% by using CP-H06 at 100 mA cm −2 , respectively. Our study reveals that TiO 2 decorated carbon paper with outstanding electrochemical performance exhibits a promising prospect in the energy storage system of vanadium redox battery.

Pressure sensor, as one of the most common components in the sensing systems, has attracted plenty of attention in recent years with urgent needs. Herein, a highly sensitive flexible pressure sensor based on conducting polymer (CP)-coated paper is developed via an ultra-simple approach of synthesis and fabrication. This paper-based sensor displays an ultra-low detection limit as low as 0.3 Pa level, and outstanding sensitivity (∼2 kPa−1, P ≤ 75 Pa), which can rank the top among that of the reported pressure sensors. The advantages based on paper framework such as low cost, portability, and easy disposability further enhance its feasibility. Meanwhile, combining its rapid and precise response at room temperature and the recognized stability of PPy in the ambient environment, the sensor would ensure direct and continuous environment monitoring with low energy consumption.

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.

In this study, a facile method was applied to modify the hydrophobicity of filter paper, and the application of the filter paper in water-oil separation was investigated. The modification was accomplished by immersing the filter paper into the modifier solution containing poly(methylhydrosiloxane) (PMHS) for only 2 min at room temperature. PMHS was found to be covalently grafted onto the surface of filter paper. After PMHS modification, the hydrophobicity of filter paper was significantly improved, as indicated by the increase of the water contact angle from 19.0° to 131.8°. Because PMHS has very low surface energy, after modification, the wettability of filter paper was transformed from hydrophilic to very hydrophobic and subsequently to oleophilic; therefore, the modified filter paper presented excellent performance in water-oil separation. The separation efficiency of diesel and n-hexane from water was more than 94.3% and 80.0%, respectively. This method is simple and based on commercially available materials; moreover, it can be applied to the hydrophobic modification of not only filter paper but also any materials containing hydroxyl groups.

Control over the mechanical properties of cellulose-based artifacts (e.g. paper) is highly important in cultural heritage science. Especially, a non-aqueous method that does not cause swelling but can be applied to either single paper sheets or bound cellulose items (e.g., books) without any preselection is currently needed. Herein, we present a new multilayer deposition method that can simultaneously deposit alkaline reserve and improve the mechanical properties of historic wood pulp (HWP) paper, which often suffers from high fragility and brittleness. Alkaline nanoparticles (magnesium hydroxide Mg(OH) 2 NPs) stabilized by hydrophobic cellulose derivative i.e., trimethylsilyl cellulose (TMSC) in hexamethyldisiloxane (HMDSO) are prepared and deposited in the form of multiple layers on HWP paper by a technically effortless dip coating procedure. An enhanced and irreversible deposition of Mg(OH)2 NPs–TMSC and an alkaline reserve (AR) up to 4% (139 meq[OH − ]/100g) are achieved as revealed by infrared spectroscopy and back-titration measurement. The tensile strength of uncoated HWP paper (1.6 MPa) is increased to 5.5 MPa after coating with Mg(OH) 2 NPs/TMSC (before aging) and then to ca 9 MP (after accelerated aging). In the latter case, the TMSC is transformed to cellulose by cleaving of O–Si bonds. The surfaces are evenly covered with thin and transparent coatings of hydrophobized nanoparticles as demonstrated by electron scanning microscopy and contact angle measurements.

Paper cup composed of crude cellulose is a common waste in daily life. In this paper, hierarchical porous carbons have been successfully prepared by an initial hydrothermal treatment and subsequent activation route from abandoned paper cup, and then paper cup derived carbons are used as scaffolds to fabricate serial carbon/Se composites. The optimal composite presents unique 3D porous structure, with amorphous selenium uniformly confined into the micropores of carbon. As the cathode materials of Li-Se battery, this composite reveals an initial reversible discharge capacity of 517.2 mAh g−1 at 0.2C, and a capacity value of 431.9 mAh g−1 can be retained after 60 cycles. Even at a high rate of 4C, a capacity value of 295.8 mAh g−1 can be obtained. By comparison, the improved electrochemical performance of the optimal composite should be attributed to reasonable porous structure and effective encapsulation of amorphous selenium.

Graphical abstract, Highlights • Detection of cytokine storm biomarkers with mobile biosensors. • Immunosensors are made solely of cellulose modified with antibody-decorated nanoparticles. • Turnaround time under 10 min. • Detection of biomarkers in respiratory samples allows monitoring local inflammation. • Compatible with decentralized health care schemes., Decentralizing COVID-19 care reduces contagions and affords a better use of hospital resources. We introduce biosensors aimed at detecting severe cases of COVID-19 in decentralized healthcare settings. They consist of a paper immunosensor interfaced with a smartphone. The immunosensors have been designed to generate intense colorimetric signals when the sample contains ultralow concentrations of IL-6, which has been proposed as a prognosis biomarker of COVID-19. This is achieved by combining a paper-based signal amplification mechanism with polymer-filled reservoirs for dispensing antibody-decorated nanoparticles and a bespoken app for color quantification. With this design we achieved a low limit of detection (LOD) of 10−3 pg mL-1 and semi-quantitative measurements in a wide dynamic range between 10−3 and 102 pg mL-1 in PBS. The assay time is under 10 min. The low LOD allowed us to dilute blood samples and detect IL-6 with an LOD of 1.3 pg mL-1 and a dynamic range up to 102 pg mL-1. Following this protocol, we were able to stratify COVID-19 patients according to different blood levels of IL-6. We also report on the detection of IL-6 in respiratory samples (bronchial aspirate, BAS) from COVID-19 patients. The test could be easily adapted to detect other cytokines such as TNF-α and IL-8 by changing the antibodies decorating the nanoparticles accordingly. The ability of detecting cytokines in blood and respiratory samples paves the way for monitoring local inflammation in the lungs as well as systemic inflammation levels in the body.

Paper has the potential to dramatically reduce the cost of electronic components. In fact, paper is 10 000 times cheaper than crystalline silicon, motivating the research to integrate electronic materials on paper substrates. Among the different electronic materials, van der Waals materials are attracting the interest of the scientific community working on paper-based electronics because of the combination of high electrical performance and mechanical flexibility. Up to now, different methods have been developed to pattern conducting, semiconducting and insulating van der Waals materials on paper but the integration of superconductors remains elusive. Here, the deposition of NbSe2, an illustrative van der Waals superconductor, on standard copy paper is demonstrated. The deposited NbSe2 films on paper display superconducting properties (e.g. observation of Meissner effect and resistance drop to zero-resistance state when cooled down below its critical temperature) similar to those of bulk NbSe2., Paper has the potential to dramatically reduce the cost of electronic components but the integration of electronic materials is challenging. Here the integration of NbSe2, a van der Waals superconductor, on paper is demonstrated.

International audience; The durability of paper documents treated with aminoalkylalkoxysilane copolymer (co-AAAS) flexible networks, as deacidifying and strengthenening agents, was studied. To this end, a 1922 lignocellulos ic newsprint paper was treated with co-AAASs and characterized. Physico-chemical properties such as pH, chromatism, opacity and mechanical strength were measured shortly upon treatment and several years after. In order to better understand the role of the initial degradation state of the paper and the impact of its constituents other than cellulose (lignin, alum-rosin sizing) on the treatment efficiency, several laboratory papers were added as models. It was shown that alum-rosin sizing contributed to a decrease in pH of the most degraded treated paper over the monitoring time, whereas the strengthening effect was mostly affected by the presence of lignin. In particular, for most papers, after several years, the gain in folding endurance was the lowest in the lignin-rich ones. The breaking length of all the papers increased post-treatment and over time, independently of the paper constituents. This was attributed to the slowly progressing aminoalkylalkoxysilanes polycondensation, on the scale of years, as evidenced by Cross Polarisation-Mass Angle Spinning 29 Si solid-state Nuclear Magnetic Resonance.

Cost-effective, simple and flexible hydrogen gas sensors operating at room temperature were demonstrated based on DC magnetron sputtered palladium thin films. The main idea is to use commercial microfiber filtration paper as a cheap, fibrous and flexible substrate for palladium. With this objective, Pd thin films with 21, 38 and 54 nm thicknesses were deposited and characterized by grazing incident X-ray diffraction (GIXRD) and scanning electron microscope (SEM). The gas sensing behavior was tested by hydrogen gas in the concentration rang of 0.5–10%. GIXRD showed a PdX/Pd phase and SEM revealed existing of many structural nanocracks. An activation process was needed where sensors were heated up to 110 °C in the presence of 10% H2. Then a desirable hydrogen sensitivity with good stability based on hydrogen induced lattice expansion (HILE) effect in which conductance increases was observed. However, for low Pd thicknesses (21 and 38 nm) and at below 4% H2, an inverse effect was observed in which the conductance decreased instead of increasing. For all samples the response time is incremental in the range of 0.5–4% and declining for 4–10%. Moreover, the deposited Pd sensors operate well when they are bent inward or outward. The governed physical mechanism was expressed and discussed.

Here we report the construction of CoFe2O4 coating on carbon fiber and the coated paper was used as the interlayer between the separator and cathode of Li-S batteries. The amorphous CoFe2O4 coating was deposited by the industry-oriented spray pyrolysis technique and carbon fiber was completely enwrapped by the coating. Compared to the non-coated carbon fiber, the coated carbon fiber as the interlayer exhibits a superior reversible capacity of 1086 mA h g−1 at moderate current of 0.1C and a low decay rate in the capacity of 0.043% per cycle after 1000 cycles at 1C. Excellent long-term cycling life and rate capacity were also achieved through the coated interlayer. The specially designed interlayer showed remarkable capability to trap effectively the intermediate LPS (lithium polysulfide). The significantly inhibited “shuttle effect” of LPS would give insight into designing and making the interlayer by using new coating materials for enhanced performances of the Li-S batteries.

A simple, low cost, and lightweight three-dimensional (3D) primary alkaline Zn/Fe3O4 origami-battery fabricated from Whatman 1 paper was developed. The battery was created using printed wax to define the hydrophobic and hydrophilic barriers and active electrocatalytic materials for fabricating the electrodes. The boat-shaped 3D-battery consisted of two screen-printed Zn/Fe3O4 batteries connected in series that were activated with a small volume of aqueous KOH solution. The metallic electrodes were first characterized outside the folded battery using electrochemical techniques. Subsequently, the electrodes and separator were assembled together in a triangle-shaped battery resembling the main structure of the boat-shaped 3D-device and this triangle-shaped battery was further optimized. The addition of water triggered the activation of the 3D battery delivering a maximum current and power of 7 mA and 3 mW, respectively. The 3D-Zn/Fe3O4-battery displayed an OCP of 2.2 V and a maximum current and power of 22 mA and 7.5 mW, respectively, in the presence of 6 M KOH electrolyte. These results demonstrate the potential of 3D origami-based structures and Zn/Fe3O4 batteries as an alternative low cost energy source to power portable devices.

Filter paper (FP) with superhydrophobicity and high water adhesion was prepared by adsorption and simple immersion process. The surface morphologies displayed the micro-nano structure of FP. The surfaces composition was investigated by Fourier transform IR, X-ray photoelectron spectrum and X-ray diffractometer. The superhydrophobic surfaces with a water contact angle of 153° benefited from the Fe(OH)3 nanostructure formed on FP and subsequent stearic acid (STA) modification. The as-prepared superhydrophobic surfaces could firmly pin the water droplet even when the surfaces turned upside down. The wettability properties of the FP surfaces could be repaired by immersing the damaged samples into the solution again.

A recent commentary by Santhosh and Ravindran on our paper (Int. J. Hydrogen Energy 2014, 39:10606) demonstrated that the interaction between H2 and MXene (Sc2C and Ti2C) phases are not Kubas-type and should be of weak physisorption, and thus made a conclusion that 2D Sc2C and Ti2C are not suitable for practical hydrogen storage applications. In this responses, we recalculated hydrogen adsorption on 2D Sc2C and Ti2C by using different exchange-correlation functionals. And based on the calculated results, bare MXenes (especially the Ti2C) are suitable as hydrogen storage materials at temperatures of several tens degrees lower than room temperature. And the hydrogen adsorptions on the MXenes terminated with oxygen group were also investigated. Among the Ti2C, Sc2C and their oxygen-functional counterparts, the binding energy of H2 on Sc2CO2 surface is the closest to the ideal range of 0.16–0.42 eV/H2 at ambient conditions, and thus the Sc2C with oxygen group is expected to be more suitable as hydrogen storage materials.

Palladium in the form of G-Pd nanocomposite possesses multiple enzyme mimicking activity. It catalyzes the oxidation of dopamine, glutamate, H2O2 and NADH through dopamine oxidase, glutamate oxidase, peroxidase and NADH oxidoreductase biomimetic activity. Kinetic studies were performed to calculate the catalytic parameters of G-Pd nanocomposite towards the substrates for a potential heterogeneous catalyst. Among them, glutamate oxidase activity was coupled with peroxidase activity of G-Pd for the detection of glutamate, in the form of a paper based sensor. Analytical performance of G-Pd nanocomposite catalyzed glutamate detection was characterized, and found to be linear in the range 0–400 μM and 400–8000 μM with limit of detection and quantification of 49.4 μM and 117.9 μM respectively. Results from the present study provides substantial progress in the practical application of nanomaterials as heterogeneous catalysts with multi enzyme mimicking property. G-Pd nanocomposite overcomes the complexity of enzyme based biosensors due to less number of reagents, better stability due to the absence of enzymes with mild storage conditions. Multi-mimetic catalytic activity of Pd will find applications in the field of analytical chemistry, biosensors, energy, environment and food safety.

Sandwich-type hybrid structure consisting of etched nitrogen-doped graphene paper (ENGP) and flower-like MnO2 are fabricated through a three-step method. The ENGP were synthesized by vacuum assisted flow-filtration of the dicyandiamide (DCD) and graphene oxide (GO) aqueous solution through filter membrane, followed by a carbonization process, and then by an electrochemical etching method to improve the surface active-sites and wettability. The MnO2 nanoflowers consisting of multiple thin MnO2 nanosheets were anchored on both side of ENGP by electrodeposition techniques. The optimized hybrid electrodes exhibited a high specific capacitance of 368.3 F/g at 0.2 A/g, and excellent cycling performance of 98.4% capacitance retention over 3000 cycles.

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.

A bacterial “systematic evolution of ligands by exponential enrichment” protocol was developed herein to identify nucleic acid aptamers capable of binding molecules from three common nosocomial and antibiotic-resistant bacteria: Acinetobacter baumannii, Escherichia coli, and multidrug-resistant Staphylococcus aureus. This high-affinity and high-specificity process featured three selection stages for screening of bacteria-specific aptamers, and the aptamers identified were integrated into a microfluidic system. The biotin-labeled aptamers were first bound to nitrocellulose membranes housed within the chip and then incubated with bacteria; a tetramethyl benzidine (TMB)-streptavidin (blue) color reaction was next exploited upon binding of secondary aptamers to primary ones, thereby permitting bacterial detection. This new dual-aptamer microfluidic chip possesses many advantages over its traditional-scale counterparts, such as faster detection times (35 min), smaller size (7.0 cm × 5.0 cm × 1.2 cm), higher specificity, and the capability to detect multiple pathogens simultaneously; it may therefore be promising for point-of-care bacterial diagnostics.

High polyphenols levels are one of the main quality characters of Extra Virgin Olive Oil (EVOO), leading to high antioxidant activity and contributing to the EVOO health beneficial effects. Analytical methods for the rapid assessment of EVOO polyphenols content, possibly directly at the place of production or distribution, are therefore important for the commercial enhancement of this product. Unfortunately, most analytical methods for quantification of polyphenols in EVOO require laboratory instrumentation and preliminary sample extraction procedures. In this paper we describe a paper-based chemosensor based on the well-known Folin-Ciocalteu colorimetric assay for the rapid (assay time 15 min) quantitative detection of polyphenols in EVOO without any preliminary sample extraction. Use of n-propanol for diluting the EVOO sample allows its direct analysis on paper supports loaded with the Folin-Ciocalteu reagent. The color change of the paper supports is measured using a smartphone camera. A disposable analytical cartridge containing all necessary reagents, including calibration standards, and accessories for performing the assay using a Samsung S8 smartphone have been developed to perform on-site analysis. Measurement of total polyphenol content of EVOO samples gave results in good agreement with the conventional Folin-Ciocalteu assay, and the limit of detection was 30 μg gallic acid equivalents g−1 EVOO. The same approach can be employed to measure polyphenols in other oils of vegetal origin.

A new concept of a solid reference electrode integrated with microfluidic paper-based sampling was introduced and applied in potentiometric ion sensing. The new reference electrode consisted of an Ag/AgCl reference element (reusable) that is in contact with a disposable paper substrate (DPS) containing solid KCl. Thus, no KCl reference solution was applied during the analysis step, but the applied sample solution dissolved the solid KCl in the paper providing the electrolyte for the Ag/AgCl reference element. Such reference electrode was found to give a relatively constant potential after less than ca 1 min of equilibration. Moreover, the response of the reference electrode was not affected by concentrations of background electrolytes in the sample. Thus the proposed reference electrode was integrated with a paper-based microfluidic device and solid-contact ion-selective electrodes (ISEs) sensitive to K+, Na+ and Cl−. The optimized systems were characterized with near-Nernstian sensitivities (59.1 ± 1.5, 57.5 ± 0.5 and –56.4 ± 0.6 mV dec−1) and detection limits (10−4.1 ± 0.1, 10−3.3 ± 0.1 and 10−4.1 ± 0.1 mol dm−3) for K+, Na+ and Cl− ions, respectively. The paper-based measurement setup was favourably used for potentiometric determination of ions in environmental (wastewater sludge) and clinically relevant (sweat) samples.

A simple, scalable approach is developed to fabricate a flexible hybrid paper electrode composed of the polyaniline/graphene and the carbon fiber (CF)-reinforced bacterial cellulose. The prepared hybrid paper presents high areal capacitance of 4.145 F cm−2 at 5 mA cm−2 and an extremely low sheet resistance of 29.7 Ω sq.−1. The CF endows the paper electrode remarkable foldability with no mechanical destruction. Even after being repeatedly bent 180° up to 1000 times, the initial capacitance can be retained up to 98%. A fabricated all-solid-state supercapacitor based on the resulting paper electrode has an excellent areal capacitance of 630 mF cm−2 and energy density of 2.8 mWh cm−3. The results confirm that this approach can fabricate the highly foldable and shape-tailorable energy storage devices and may have wide potential applications.

The oil pollution is an increasing threat to nature and human health. Therefore, effective separation of oil from the oily wastewater is a challenging task. Through the nonsolvent vapor method, a superhydrophobic paper can be self-assembled by dropping the conjugated poly-p-phenylenes solution on the commercial filter paper in a nonsolvent vapor atmosphere. The numerous nano-mircostructral particles composed of polymer nanowires covered on the filter paper, just like the morphology of lotus leaves, lead to the excellent superhydrophobic effect. Moreover, the polymer-coated filter paper not only exhibits good mechanical stability, long-term durability, self-cleaning, but also has superhydrophobicity and superoleophilicity. The as-prepared paper possess remarkable oil/water separation ability for a variety of oil/water mixtures, including bromoethane, hexane, cyclohexane, petroleum ether, gasoline, dodecane, and the mixed oil of gasoline and diesel, demonstrating that it can be a good candidate for the treatment of industrial oil-polluted water.

Flexible and lightweight shielding materials recently have attracted increasing attention for terahertz wave due to the deteriorated performance of electronic equipment interferenced by electromagnetic yielding. Herein, flexible reduced graphene oxide (rGO) papers were prepared by solution evaporation method to attenuate the electromagnetic wave in terahertz field. They exhibited excellent electrical conductivity and remarkable electromagnetic interference shielding effectiveness. The electrical conductivity of the rGO papers was improved from 54.07 to 78.67 S/cm after annealing at 400 °C. The rGO paper annealed at 400 °C was only ~ 370 µm in thickness and particularly exhibited an outstanding absorption performance of 17.6 dB at 0.7 THz. It has been found that the maximum absorption performance of rGO papers was basically equivalent to that of the metamaterials. Moreover, electromagnetic interference shielding effectiveness of 72.1 dB of the rGO papers was obtained at 0.6 THz, which indicated that ~ 99.99% of the power was shielded. Thus, the flexible rGO papers maybe a promising candidate for optimized electromagnetic shielding materials in the terahertz band.

In analytical science, it is always of great scientific and practical significances to explore convenient, rapid, and reliable methods/devices to trace the H2O2 level in various matrices. Herein, we fabricated a ready-to-use paper-based chemosensor by using mesoporous carbon-dispersed Pd nanoparticles (Pd NPs/meso-C) as a promising peroxidase mimic for the visual determination of H2O2. Thanks to the large exposed surface of the meso-C support and the highly dispersed active Pd NPs, the synthesized Pd NPs/meso-C exhibited favorable catalytic performance to trigger the chromogenic reaction of colorless TMB to blue TMBox mediated by H2O2, providing a Kcat of 326.67 s−1 for H2O2 and 0.55 s−1 for TMB, larger than the bare Pd NPs and even comparable to the activity of natural horse radish peroxidase. As demonstrated, this principle could be employed to colorimetrically detect H2O2 in the linear scope of 5–300 μM. By simply immobilizing the Pd NPs/meso-C mimic and the TMB substrate onto a common filter paper, ready-to-use paper-based sensors were further prepared. By combining these test strips with a smartphone and an easy-to-access color-scanning APP together, the integrated platform could be used for the quantitative analysis of H2O2 with advantages of simple operation, fast response, low cost, and good selectivity and repeatability. Furthermore, reliable sensing of the target in milk matrices suggested great promise of the integrated platform in practical applications.