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High-capacity electrode materials are critical for portable electronic equipment that requires a high-energy density from lithium ion batteries (LIBs). Many different materials and fabrication methods for such electrodes have been developed for this purpose. Carbon paper coated with recycled silicon powder (CP-RSP) was prepared by coating silicon and pitch powder on the carbon paper, followed by stabilization at 250 °C in air and carbonization at 1000 °C in N2. The CP-RSP acted as both the current-collector and the active material for the anodes of LIBs. Electrodes with 2.5, 5, and 10 wt.% silicon exhibited capacity increases of 94, 129 and 41%, respectively, compared with the silicon-free electrode. The electrode for the CP-RSP with 5 wt. % silicon exhibited an optimal balance between discharge capacity and stability in long-cycle tests under various charging rates.

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.

The present study was conducted to form polysaccharide-based multilayers of cationic starch (CS)/anionic starch (AS), and CS/carboxymethyl cellulose (CMC) on broke chemi-mechanical pulp (BCMP) fibers. It aimed to examine the buildup of CS/AS and CS/CMC polyelectrolyte multilayers (PEM) on the fibers surface, and explore the effects of PEM formation on the properties of the resulting papers. The assembly of PEM was analyzed by using zeta (ζ-) potential, water retention value (WRV), SEM micrographs, and paper properties such as thickness and strength. The results of ζ-potential inversions indicated successful constitution of PEM on the BCMP fiber surface by assembling CS/AS or CS/CMC multilayers. Further, larger ζ-potential variations occurred in depositing CS/CMC PEM, due to more charge of CMC, which presumably formed a layer with greater potential of absorption. Based on the SEM images, the surface of PEM-treated fibers was rougher, compared to the untreated fibers due to the coating with starch. Furthermore, the PEM fabrication resulted in creating fibers with higher degree of WRV, which was consistent with the significant improvement of the sheet strengths. Finally, the strength enhanced papers made from PEM-treated fibers with tensile index of about 37.33 ± 1.47 N m/g vs 22.24 ± 1.23 N m/g or 11.60 ± 0.57 N m/g for the papers made from original CMP and untreated BCMP fibers, respectively, may diminish the challenges related to web breaks in the paper machine conveying BCMP broke fibers.

The development of point-of-care (POC) devices for the detection of environmental contaminants and the early monitoring of disease outbreaks in the health and food sectors has steadily grown in recent times. The real-time analysis offered by POC devices is pivotal in developing areas where access to skilled labor is often lacking. Chelating agent–based signal amplification methods have previously been employed in conjunction with electroplated metallic films to improve electrode sensitivity in trace metal analysis. Here, we describe a method for the dry storage of electrochemical reagents: ammonia/ammonium chloride (NH3/NH4Cl) buffer as a supporting electrolyte, dimethylglyoxime (DMG) as a chelating agent, and mercury in paper-based electrochemical cells (PECs), fabricated from commercial filter paper. The stored PECs were applied to the trace, microliter analysis of nickel in water samples by adsorptive cathodic stripping voltammetry (AdCSV) in conjunction with screen-printed electrodes. The method relies on the single-step accumulation/adsorption of microvolumes of the metallic analyte onto stored DMG ligands to form [Ni(dmgH)2] complexes in the presence of mercury films. By integrating the AdCSV techniques with paper-based analytical devices, detection of Ni2+ in water samples with good resolution was achieved at 20 μL sample volumes in the low parts per billion range. The mechanism for pre-concentration and its subsequent reduction was demonstrated as it differs from bulk electroanalysis. Instrumental parameters of the PECs, accumulation time, and deposition potential were optimized along with reagent storage introduction and concentrations. Further, the PECs were investigated in the absence and presence of mercury and had shown good possibility for metal-free sensors in future work. The prepared PECs showed good reproducibility (4.36%, n = 4) and no intermetallic interferences in the presence of 100 μg L−1 Zn2+, Cd2+, Pb2+, Co2+, and In2+. Detection and quantitation limits were calculated and recorded as 6.27 μg L−1 and 18.8 μg L−1, respectively, for Ni2+ determination and 13.1 μg L−1 and 39.3 μg L−1 for the Hg-free derivative at the 90-s accumulation time. The pre-stored paper-based electrochemical cells were then applied to the detection of Ni2+ in real tap water samples and showed good recovery values of ± 94%. Further, the infusion of PECs with a range of chelating agents (dimethylglyoxime, nioxime, and morin hydrate) demonstrates the possibility for tuning PECs to specific applications and improving selectivity in metal analysis applications.

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.

Superamphiphobic surfaces generally need a specific combination of low surface energy and re-entrant surface structure. Herein, we have created a hexane suspension of trichloro(1H,1H,2H,2H-tridecafluoro-n-octyl) silane, tetraethyl orthosilicate, silicon dioxide and titanium dioxide nanoparticles and modify a series of filter papers by one-step immersion in 10 min. Superhydrophobic and quasi-superoleophobic properties are obtained for the optimal filter papers, which repel both of polar and non-polar liquids such as water, glycerol, 1,4-butanediol, soybean oil and 1-octadecene with the contact angles of 168°, 158°, 154°, 145° and 121°, respectively. More importantly, the respective contribution of each component to the superhydrophobic and oleophobical property is explicated through a series of comparative experiments based on the optimal suspension prescription. The wettability transformation from quasi-superamphiphobicity to superhydrophilicity after UV irradiation is evaluated and illustrated. What’s more, the patterned paper is successfully used for the colorimetric detection of glucose using a simple paper-based analytical device. A linear correlation between gray intensity (GI) and glucose concentration (C), GI = − 10.7C + 161.8 is achieved with a correlation coefficient of 0.991, indicating the potential for semi-quantitative analysis of real sample in the field.

Paper-based microfluidics is a rapidly developing field with applications for point-of-care disease and environmental diagnostics. In parallel, printed electronics has grown swiftly, particularly for wearable technologies. By combining these fields, fluidic sample processing and control, as well as automated sensing and readout can be integrated on a single device. Towards this goal, this work highlights the design, manufacture, and testing of paper-based electrochemical sensors, with focus on photo paper and chromatography paper substrates. These substrates are typically used for printed electronics and paper-based fluidics, respectively. The electrochemical sensors were screen printed using manual techniques. For chromatography paper sensors, wax-printed fluidic barriers were used to illustrate the potential integration of the sensors with typical paper-based microfluidic device formats. As an initial example, the detection of heavy metals (Cd(II) and Pb(II)) in buffer solution was demonstrated. Commercial DropSens sensors were used as reference with the limit of detection (LOD) of Cd(II) and Pb(II) on chromatography sensors showing comparable results to commercial DropSens sensors. It is worth noting that the chromatography paper sensors showed a higher repeatability than the commercial DropSens sensors. Tap water samples spiked with Cd(II) and Pb(II) were also tested and showed promising results. Future work will include sensor optimization and exploration of scale-up to provide low-cost solutions for effective point-of-need diagnostics—ranging from environmental monitoring to healthcare applications.

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.

A new kind of environmentally friendly filter paper based on ultralong hydroxyapatite nanowires (HAPNWs) and cellulose fibers (CFs) with excellent filtration and adsorption properties has been developed for the application in high-performance water purification. The use of polyamidoamine-epichlorohydrin (PAE) resin increases the wet mechanical strength of the as-prepared HAPNW/CF filter paper. The addition of CFs enhances the mechanical strength of the HAPNW/CF filter paper. Owing to the porous structure and superhydrophilicity of the as-prepared HAPNW/CF filter paper, the pure water flux is as high as 287.28 L m-2 h-1 bar-1 under cross-flow conditions, which is about 3200 times higher than that of the cellulose fiber paper with addition of PAE. More importantly, the as-prepared HAPNW/CF filter paper shows superior performance in the removal of TiO2 nanoparticles (>98.61%) and bacteria (up to 100%) in water by the size exclusion and blocking effect. In addition, the HAPNW/CF filter paper also exhibits high adsorption capacities for methyl blue (273.97 mg g-1) and Pb2+ ions (508.16 mg g-1). The adsorption mechanism of the HAPNW/CF filter paper is investigated. The as-prepared environmentally friendly HAPNW/CF filter paper with both excellent filtration and adsorption properties has promising application in high-performance water purification to tackle the worldwide water scarcity problem.

The increasing demand for high-specific-energy batteries drives researchers to revisit Li metal anode. However, the formation and growth of Li-dendrite possibly leads to short-circuit of the battery, causing safety hazard of Li metal batteries. Therefore, it is quite necessary to regulate the plating/stripping behaviors of Li metal anodes to address this long-standing issue. Herein, we report the regulation of Li plating/striping behavior via manipulating the ratio of oxygen containing groups on reduced graphene oxide papers. It has been revealed that the electrochemical properties are highly dependent on the amount of carbonyl C O groups, which could associate Li+ and serve as a uniform nucleation site to guide Li plating. Furthermore, a high lithium ion diffusion coefficient of ∼2.09 × 10−14 m2 s−1 was enabled, around one magnitude higher than that of the Li lattice self-diffusivity (∼2 × 10−15 m2 s−1). As a result, stable dendrite-free Li metal anode is realized on the reduced graphene oxide paper with high C O group content (8.4%), which exhibits a low and stable overpotential of 50 mV for a long lifetime of 400 h. Our studies provide a fresh insight into the Li ion diffusion and its critical role in the regulation of the Li plating/stripping behaviors.

Nowadays quantitative chemical analysis is usually costly, instrument-dependent, and time-consuming, which limits its implementation for remote locations and resource-limited regions. Inspired by the ancient papercutting art (kirigami), we herein introduce a novel cut-and-paste protocol to fabricate 3D microfluidic paper-based analytical devices (μPADs) that are suitable for on-site quantitative assay applications. The preparation of the device is fast, simple, and independent of any lithographic devices or masks. Particularly designed reaction “channels” were pre-cut from a piece of filter paper, then assembled back to the silanized, superhydrophobic paper pads. The different layers of the device were assembled using a chemically-inert adhesive spray. The fabricated device has high efficiency of liquid handling (up to 60 times faster than conventional methods) and it is particularly inexpensive. Beyond the benchtop fabrication advantage, in conjunction with a custom mobile app developed for colorimetric analysis, we were able to quantify representative environmental contaminants (i.e., the amount of Cr(VI) and nitrite ions) in various water samples with the cut-and-paste μPADs (namely kPADs). Their detection limits (0.7 μg mL−1 for Cr(VI) and 0.4 μg mL−1 for nitrite ions, respectively) are comparable with conventional spectrophotometric methods, which confirm the potential of kPADs for on-site environmental/sanitary monitoring and food toxin pre-screening.

Free-standing graphene-based composite paper electrodes with various active materials have attracted tremendous interest for next-generation lithium-ion batteries (LIBs) due to advantages such as their light weight, excellent mechanical flexibility, and superior electrochemical performance. However, despite its high theoretical energy density, SnS2 is rather difficult to composite with the graphene paper, because conventional reduction procedures for graphene oxide (GO) induce either decomposition or oxidation of SnS2. Herein, a novel solid/gas two-phase interface hydrothermal process is reported to fabricate flexible free-standing SnS2/graphene nanocomposite papers (SGP) assisted by a reducing and stabilizing agent thioacetamide aqueous solution. Such hydrothermal process not only successfully reduces SnS2/graphene oxide paper (SGOP) to SGP, but more importantly, keeps intact the paper configuration as well as the phase stability of SnS2. The as-prepared SGP electrode exhibits high reversible discharge capacity, outstanding cyclic stability and rate capability, which can be attributed to the synergistic effect of the conductive and flexible graphene matrix for accommodation of the volumetric changes of SnS2 upon cycling and the planar SnS2 nanospacers between the graphene layers introducing nanopores for penetration of electrolyte and inhibition of graphene nanosheets restacking. This report demonstrates a new strategy for more active materials with promising lithium storage properties joining the flexible graphene-based paper electrode family.

Wearable electrochemical sensors have attracted tremendous attention in recent years. Here, a three-dimensional paper-based microfluidic electrochemical integrated device (3D-PMED) was demonstrated for real-time monitoring of sweat metabolites. The 3D-PMED was fabricated by wax screen-printing patterns on cellulose paper and then folding the pre-patterned paper four times to form five stacked layers: the sweat collector, vertical channel, transverse channel, electrode layer and sweat evaporator. A sweat monitoring device was realized by integrating a screen-printed glucose sensor on polyethylene terephthalate (PET) substrate with the fabricated 3D-PMED. The sweat flow process in 3D-PMED was modelled with red ink to demonstrate the capability of collecting, analyzing and evaporating sweat, due to the capillary action of filter paper and hydrophobicity of wax. The glucose sensor was designed with a high sensitivity (35.7 μA mM−1 cm−2) and low detection limit (5 μM), considering the low concentration of glucose in sweat. An on-body experiment was carried out to validate the practicability of the three-dimensional sweat monitoring device. Such a 3D-PMED can be readily expanded for the simultaneous monitoring of alternative sweat electrolytes and metabolites.

Free-standing graphene (FSG) paper plays a vital role in a wide variety of applications as an electrode material. Specifically, the electrical properties of FSG are the most important factor affecting its use as an electrode material. Herein, the vacuum filtration technique is utilized to fabricate GO paper, which is then reductively treated with HI. Initially, the electrical conductivity is measured for GO papers with different thicknesses by varying the concentration of GO precursor as well as the reduction time. The FSG paper with a thickness of 3 microns exhibits the lowest sheet resistance and further characterization is carried out to reveal the origin of this enhancement of electrical properties. The low resistance is attributed to its crystalline nature, stacking height (Lc), in-plane crystallite size (La) and defect density (nD). Meanwhile, iodide ions intercalated into the graphene layers act as hole-carriers, and their intercalation is favoured over adsorption at the surface.

In this study, optical microfluidic paper analytical devices (μPADs) for glucose detection from whole blood samples with a small sample volume (2 μL) have been developed on a single paper. In the proposed method, a mushroom-shaped analytical device contains a sample inlet zone and a detection zone. When blood is dripped onto the inlet region of a μPAD, the plasma diffuses to the detection region. The detection region is implanted with a metallic three-dimensional (3D) polymer hydrogel vehicle. The gel vehicle consists of a copper complex that responds to oxygen changes and glucose oxidase (GOx) immobilized inside the gel as a bioactivity preservative. The phosphorescence of the copper complex is enhanced by oxygen consumed by detection of glucose with a limit of detection (S/N = 3) of 0.44 mM, and the total analysis of the sample is completed within 1 min. The validity of the proposed research is demonstrated using control samples and real-world whole blood samples of glucose concentrations ranging from 3 to 200 mM, and the detection results are shown to be in agreement with those obtained using a glucometer. Attaining a simple device for analysing glucose in human whole blood without any pretreatment procedures and having a broad sensing range while consuming a small sample volume remain challenging; thus, our new analytical device is of great interest.

Herein, a new colorimetric paper sensor based on the layer-by-layer assembled multilayers of a cationic surfactant, tetrabutylammonium bromide (TBABr), and an anionic surfactant, sodium dodecyl sulfate (SDS), modified on filter paper was developed for the determination of total antioxidant capacity (TAC). In this study, gallic acid (GA) was used as the antioxidant standard. The fabricated (TBABr/SDS)3/PAD was loaded with Fe3+ ions to obtain Fe3+/(TBABr/SDS)3/PAD, exhibiting high selectivity for the detection of GA when compared with the case of other metal ions. The interaction between GA and the Fe3+/(TBABr/SDS)3/PAD sensor occurred rapidly, and the colorimetric paper sensor changed from yellow to purple immediately. The quantitative detection of GA was enabled by taking an image using an ordinary smartphone and applying the ImageJ software based on the change in color. Under optimum conditions, a linear response was obtained between the change in the color of the sensor and the TAC value expressed in terms of gallic acid equivalents. The linear range was from 0.50 μM to 6.50 mM with the detection limit of 0.35 μM. The colorimetric paper sensor was applied to detect the TAC in three kinds of green tea and vegetable samples, which provided the good recoveries of 86.0–109.9%. The proposed sensor is simple, cheap, equipment-free, rapid and environmentally friendly. In addition, the colorimetric sensor Fe3+/(TBABr/SDS)3/PAD has potential applicability for TAC detection in real food samples.

Cellulose is a promising biomass material suitable for high volume applications. Its potential lies in sustainability, which is becoming one of the leading trends in industry. However, there are certain drawbacks of cellulose materials which limit their use, especially their high wettability and low barrier properties, which can be overcome by applying thin coatings. Plasma technologies present a high potential for deposition of thin environmentally friendly and recyclable coatings. In this paper, two different plasma reactors were used for coating two types of cellulose-based substrates with hexamethyldisiloxane (HMDSO). The changes in surface characteristics were measured by atomic force microscopy (AFM), scanning electron microscopy (SEM), surface free energy and contact angles measurements, X-ray photoelectron spectroscopy (XPS), and secondary ion mass spectrometry (SIMS). Successful oleofobization was observed for an industrial scale reactor where pure HMDSO was used in the absence of oxygen.

Airflow sensor is a crucial component for monitoring environmental airflow conditions in many engineering fields, especially in the field of aerospace engineering. However, conventional airflow sensors have been suffering from issues such as complexity and bulk in structures, high cost in fabrication and maintenance, and low stability and durability. In this work, we developed a facile direct-writing method for fabricating a low-cost piezoresistive element aiming at high-performance airflow sensing, in which a commercial pen was utilized to drop solutions of single-walled carbon nanotubes onto tissue paper to form a piezoresistive sensing element. The encapsulated piezoresistive element was tested for electromechanical properties under two loading modes: one loading mode is the so-called pressure mode in which the piezoresistive element is pressed by a normal pressure, and another mode is the so-called bending mode in which the piezoresistive element is bended as a cantilever beam. Unlike many other developed airflow sensors among which the sensing elements are normally employed as cantilever beams for facing winds, we designed a fin structure to be incorporated with the piezoresistive element for airflow sensing, the main function of the fin is to face winds instead of the piezoresistive element, and subsequently transfer and enlarge the airflow pressure to the piezoresistive element for the normal pressure loading mode. With this design, the piezoresistive element can also be protected by avoiding experiencing large strains and direct contact with external airflows so that the stability and durability of the sensor can be maintained. Moreover, we experimentally found that the performance parameters of the airflow sensor could be effectively tuned by varying the size of the fin structure. When the fin sizes of the airflow sensors were 20 mm, 30 mm, and 40 mm, the detection limits and sensitivities of the fabricated airflow sensors were measured as 8.2 m/s, 6.2 m/s, 3.2 m/s, 0.0121 (m/s)−2, 0.01657 (m/s)−2, and 0.02264 (m/s)−2, respectively. Therefore, the design of the fin structure could pave an easy way for adjusting the sensor performance without changing the sensor itself toward different application scenarios.

The combination of the selective catalytic reduction technology with catalytic filters constitutes one of the most efficient ways for diesel engine exhaust treatment. In this paper, the development of catalytic ceramic papers as structured systems for the abatement of diesel soot particles is addressed. Ceramic papers were prepared by the dual-polyelectrolyte papermaking method, which is based on the conventional papermaking technique used for cellulosic papers, in which a portion of cellulosic fibers is replaced by ceramic ones. The deposition of Co and Ce as catalytic materials by the wet spray method on ceramic papers was studied for the development of structured catalysts using an ultrasonic nebulizer and different solvents. The use of alcohol-water solutions for the impregnation of cobalt generated smaller particles and a high dispersion of them on the ceramic fibers, greater than that obtained when pure water was employed. Temperature programmed oxidation (TPO) assays showed that the best catalytic performance was acquired with the catalysts generated with alcohol solvents, showing a maximum rate for soot combustion at a temperature close to 400 °C. The adequate soot combustion performance and the high thermal and catalytic stability make catalytic ceramic papers impregnated by the wet spray method, promising systems for their application as diesel particulate filters. Fil: Sacco, Nicolás Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Banus, Ezequiel David. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Bortolozzi, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Milt, Viviana Guadalupe. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Miro, Eduardo Ernesto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina

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.

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.

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.

In this work, we constructed a sensing system on Janus paper with hydrophilic side and hydrophobic side via depositing polymer precursor onto one side of qualitative filter paper. Water in humid environment (including liquid water, condensed moisture airflow and gaseous humid atmosphere) will be captured and gathered in the hydrophilic region of Janus paper due to the asymmetric hydrophobicity and hygroscopicity, which can induce the novel directional deformation. Additionally, MWCNTs (multiwalled carbon nanotubes) were loaded onto hydrophobic region beforehand to construct conductive network. The resistance of the conductive network changes synergistically as the Janus paper deforms in humid environment. Thus, the novel Janus paper realized the induction of environment humid factors, and conversion from the deformation signals to the desirable electric signals. The Janus paper also shows excellent stability in cycle use.

In this paper, we characterized the behavior of polymer jet from near-field electrospinning onto the inkjet patterned paper with conductive Ag nanoparticles in order to form the controlled three-dimensional nanostructures. Using inkjet patterned paper with conductive ink as a collector, the polymer jet is induced to the pre-patterned shape through the concentrated electric field caused by singularity between the spinneret and the printed patterns. Due to the electric field enhancement of the deposited electrospun fiber, an additionally spun fiber can be stacked on the deposited fibers directly. Therefore, the controlled three-dimensional nano/micro structures can be successfully realized by the proposed method. We characterized the deposition of the electrospun fiber according to the distance between the inkjet printed pattern and the spinneret. In addition, the sharp edged three-dimensional microstructures were fabricated by carrying out the electrospinning on the patterns with various angled edges. A CCD camera was used to observe the behavior of the polymer jet, and the SEM image was analyzed to confirm that the fibers are stacked as desired.

Inspired by the robust and durable adhesion of mussels, highly hydrophobic filter paper was fabricated by a polydopamine (PDA)-assisted one-pot procedure using silica nanoparticles and silane coupling agent (hexadecyltrimethoxysilane, HDTMS) as coating materials at ambient temperature. The surface chemistry, morphology, and hydrophobicity of the coated filter paper were measured by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, atomic force microscope, scanning electron microscopy, and water contact angle. The capacity, durability, and recyclability of the coated filter paper were evaluated by the separation of oil–water mixtures and emulsions. The coated filter paper is highly hydrophobic with a water contact angle of > 130°. The coatings with enhanced adhesion to the substrate resisted mechanical abrasion without significant loss of hydrophobicity, which suggested that PDA plays a crucial role in improving the adhesion of silica nanoparticles to the paper surface. The coated filter paper showed high oil–water separation efficiency up to 95%, and maintained high hydrophobicity after recycling over 10 cycles. The coated filter paper that is based on a simple, low cost, and environmentally friendly procedure exhibits potential for applications in oil-recovery and oil–water separation materials.

In this work, a novel holey graphene oxide bonded with sulfonic acid groups (S-HGO) was developed using a facile and eco-friendly strategy: erosion and oxidation of graphene oxide (GO) by H2O2 and sulfonation by 4-benzenediazoniumsulfonate. The freestanding paper fabricated by S-HGO shows a high proton conductivity of 4.97 × 10−2 S cm−1 at 60 °C and 100% relative humidity (RH), which is comparable to Nafion 115 (7.67 × 10−2 S cm−1) at the same condition. The holes on S-HGO provide shortcut channels for proton transfer across the GO nanosheet. The chemical-linked sulfonic acid groups afford additional hop sites for proton conduction and endow itself an enhanced thermostability. Under 100% RH and ambient pressure, the freestanding S-HGO deliver a peak power density of 103 mW cm−2 at a load current density of 273 mA cm−2, which is about three times more than that of GO at 35 °C. The results demonstrate that this S-HGO paper is a promising nanoscale inorganic material for proton exchange membranes.

A layer deposition method was developed to prepare a series of nanocellulose/filter paper (NC/FP) composite filtration membranes by vacuum filtration of an aqueous nanocellulose dispersion on a filter paper substrate. The deposited NC networks and the final pore structure of the NC/FP composite were affected by the size and the amount of the nanocellulose. Drying methods further influenced the filtration performance of the membranes. With a greater NC aspect ratio and an increasing amount of added NC, NC/FP composite membranes exhibited better rejection rates with lower water flux. Two types of NC were chosen with different sizes as follows: (1) cellulose nanocrystals prepared from microcrystalline cellulose, which are characterized by their small size, and (2) cellulose nanofibers (CNFs) prepared from hardwood bleached Kraft pulp, which are characterized by their large size. Varying filtration performance was also achieved by altering the drying conditions (temperature, pressure and solvents) during the manufacturing process of NC/FP composite filtration membranes. In particular, NC/FP composite membranes obtained by vacuum drying at 60 °C with 0.1% CNFs demonstrated excellent ultrafiltration properties with retention rates as high as 97.14% and an acceptable flux (46,279 L m−2 h−1). Furthermore, NC/FP composite membranes demonstrated good tolerance to acidic and alkaline conditions, but their performance was weakened when treated with high or low temperatures. NC/FP composite membranes have promising potential for use as advanced separation membranes for water purification.

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.

The construction of a photoelectrochemical (PEC) strategy for multi-component detection represents a great challenge in the field of sensing. To address these challenges, herein we presented a hollow-channel paper-based PEC analytical platform based on chemiluminescence (CL) addressable strategies excited PEC strategy for multiplexed sensing application. Sandwich-structured CdS quantum dots (QDs)/reduced graphene oxide (RGO)/ZnO nanorods arrays (NRAs) heterostructure where CdS serves as visible light sensitizers, RGO acts as an electron relay between ZnO NRAs and CdS QDs, were simply assembled on the gold nanoparticles modified paper working photoelectrode (Au-PWE). The PEC performance of the CdS/RGO/ZnO can be greatly improved benefiting from the formation of type II band alignment between CdS QDs and ZnO NR as well as the super charge collection and shuttling property of RGO. Multiplexed CL emission could be achieved through controlling the CL co-reagents transport. By the virtue of CL addressable technique and the excellent PEC activity of CdS/RGO/ZnO, a highly sensitive, and selective multiple microRNAs (miRNAs) quantification method was achieved. Such a tailored strategy would break the bottleneck of the current PEC detection techniques in multiplex tracing, as well as serve as a novel concept for designing multi-channel PEC sensing method.

A simple formulation of an organic-inorganic composite for spray-coating was adopted toward photoluminescent paper sheets. The coating composite layer was composed of a synthetic organic adhesive binder mixed with an inorganic lanthanide-doped strontium aluminate pigment. Such pigment-binder formula was applied effectively onto paper sheets via spray-coating followed by thermal fixation. The applied transparent photoluminescent coated layer exhibited optimal excitation wavelength at 365 nm and emission band at 517 nm resulting in phosphorescence of the paper surface with a substantial development of green-yellow, bright white, turquoise, and off-white colors as indicated by CIE Lab color coordinates under ultraviolet irradiation. The mechanical, decay and lifetime properties of the composite photoluminescent coated layer were described. The standard techniques of morphological properties and elemental analysis were explored by scanning electron microscope (SEM), wavelength dispersive X-ray fluorescence (WDXRF), and energy dispersive X-ray spectroscopic analysis (EDX). The spray-coated paper sheets demonstrated good fastness to light and reversible phosphorescence without fatigue.

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.

Rewritable paper based on switchable molecules has attracted great attention in both academic research and marketplace. However, most available switchable dyes have single switchable color state only, which cannot meet the long-awaited multicolor reversible displays. Herein, through simple introduction of phenolic hydroxyl group, we develop a series of new oxazolidines with one switch unit, which could reversibly display two different as well as their mix-gradient colors by treating with water and mild acid, respectively, both in solution and solid substrate. The structures and mechanism for the formation of two colors had been studied in detail via UV-vis/NMR spectroscopy, skillfully designing contrast molecules, and kinetics experiments. This multiple switchable colors of the dyes have been further applied to construct a rewritable paper for ink-free printing with multi/gradient-color display.

Inspired by the well-known "Wheel of Fortune", a rotatable paper-photocontrollable switch (RPPS) was designed to form an addressable paper-based photoelectrochemical (PEC) cyto-sensor for ultrasensitive detection of a cell-surface protein. By simply rotating the RPPS, a light source can selectively activate the desired working zones of the cyto-sensor. To realize the high-performance paper-based PEC cyto-sensor, a cascaded photoactive interface consisting of neat TiO2 nanotubes arrays, Pt nanoparticles (NPs), and nitrogen-carbon dots was introduced into paper fibers, gaining signal-on PEC state (NTPP for short). Then the NTPP fixed with a hairpin probe H1 allowed the hybridization chain reaction (HCR) to happen with CuS NPs-labeled hairpin probe H2 by the free primer strand (PS) triggering; hence, the CuS NPs as the emulative sensitizers were introduced onto the NTPP with the photocurrent intensity decrement for signal-off PEC state. During this process, the PS carefully designed with specific sequences can recognize the target strand (TS) of MCF-7 cells and stimulate HCR by its trigger zone. The presence of MCF-7 cells destroyed the interaction between PS and ZnFe2O4 functionalized TS, causing the PS release from the mixture of PS and TS under the help of a magnet. Then, the released PS, acting as a primer probe, realized ultrasensitive detection of a cell-surface protein. On the basis of this novel protocol, multiple-signal amplification was skillfully imported into the addressable paper PEC chip, resulting in ultrasensitive quantification of carcinoembryonic antigen in the surface of MCF-7 cells. Given the fascinating analytical performances of the developed cyto-sensor, ultralow expression of antigens for MCF-7, A549, and PC 3 cells was discriminated effectively.

Fast supercapacitors that can be charged and discharged at tens of hertz high frequency are reported using binder-free electrodes of MoS2 nanosheets grown on plasma pyrolyzed cellulose microfiber (pCMF) paper. Rapid plasma pyrolysis was applied to obtain highly conductive carbon fiber sheet from conventional cellulose filter paper to be used as a scaffold, on which MoS2 nanosheets were grown vertically wrapped around carbon microfibers in a hydrothermal reaction. Such binder-free MoS2-pCMF electrode based supercapacitor demonstrated fast-rate performance in an aqueous electrolyte with a cutoff frequency of 103 Hz. A large specific capacitance density of 125 mF cm−2 was also measured. The organic electrolyte cell of these electrodes exhibited a power density of 12.05 W cm-3 at a rate of 15 V s−1. These MoS2-pCMF electrodes were highly stable. In a cycling test at a current density of 10 mA cm−2, the cell maintained its capacitance with trivial degradation in 50,000 cycles.

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.

Paper is a perfect example of the circular economy as it remains the furthermost recycled product in Europe, creating significant environmental benefits and raw materials resources to the industry. Indeed, maintaining a consistent level of quality whilst limiting the environmental footprint of the product has become a major challenge for the industry. In this direction, paper is proving to be the promising feedstock for biorefinery and biomaterials. The future of paper recycling is slowly going beyond fibre recovery to address the needs of other industries because for the earth's environmental well-being various paper products need to be recycled and reused persistently. In this article, we outline the ambitious use of wastepaper (WP) for high-value applications such as; production of cellulose nanocrystals (CNC), composite reinforcement, high performance electrical components and biofuels.

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.

Hypotheses (1) The equilibrium size and characteristics of a radially wicked fluid on porous material such as paper is expected to be dependent on the fluid properties and therefore could serve as a diagnostic tool. (2) The change in wicked stain size between biological fluids is dependent on a change in solid-liquid surface interfacial energy due to protein adsorption. Experiments Sessile droplets of increasing volume of blood, its components, and model fluids were deposited onto paper and the equilibrium stain size after coming to a halt was recorded. The contact angle of fluid droplets on model cellulose surfaces was measured to quantify the effect that blood protein adsorption at the solid-liquid interface has on radially wicked equilibrium size. Finally the significance of droplet evaporation for the time scale of interest was analysed. Findings The final stain area of all fluids tested on paper scales remarkably linearly with droplet volume. Different fluids were compared and the gradient of this linear relation was measured. Model fluids varying in surface tension and viscosity all behave similarly and exhibit a constant gradient. Blood and its components produce smaller stains, demonstrated by lower gradients. The gradient is a function of protein concentration, thus the mechanism of this phenomenon was identified as protein adsorption at the cellulose-liquid interface. The slope of the area/volume relationship for droplets is an important quantitative mechanistic variable.

The growing socio-economic burden of chronic skin wounds requires the development of new automated and non-invasive analytical systems capable of wirelessly monitoring wound status. This work describes the low-cost fabrication of single-use, omniphobic paper-based smart bandages (OPSBs) designed to monitor the status of open chronic wounds and to detect the formation of pressure ulcers. OPSBs are lightweight, flexible, breathable, easy to apply, and disposable by burning. A reusable wearable potentiostat was fabricated to interface with the OPSB simply by attaching it to the back of the bandage. The wearable potentiostat and the OPSB can be used to simultaneously quantify pH and uric acid levels at the wound site, and wirelessly report wound status to the user or medical personnel. Additionally, the wearable potentiostat and the OPSBs can be used to detect, in an in-vivo mouse model, the formation of pressure ulcers even before the pressure-induced tissue damage becomes visible, using impedance spectroscopy. Our results demonstrate the feasibility of using inexpensive single-use OPSBs and a reusable, wearable potentiostat that can be easily sterilized and attached to a new OPSB during the dressing change, to provide long term wound progression data to guide treatment decisions.

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.

As a cost-effective approach for detecting trace amounts of pesticides, filter paper-based SERS sensors have been the subject of intensive research. One of the hurdles to overcome is the difficulty of retaining nanoparticles on the surface of the paper because of the hydrophilic nature of the cellulose fibers in paper. This reduces the sensitivity and reproducibility of paper-based SERS sensors due to the low density of nanoparticles and short retention time of analytes on the paper surface. In this study, filter paper was treated with alkyl ketene dimer (AKD) to modify its property from hydrophilic to hydrophobic. AKD treatment increased the contact angle of the aqueous silver nanoparticle (AgNP) dispersion, which consequently increased the density of AgNPs. The retention time of the analyte was also increased by preventing its rapid absorption into the filter paper. The SERS signal was strongly enhanced by the increased number of SERS hot spots owing to the increased density of AgNPs on a small contact area of the filter surface. The reproducibility and sensitivity of the SERS signal were optimized by controlling the distribution of AgNPs on the surface of the filter paper by adjusting the concentration of the AgNP solution. Using this SERS sensor with a hydrophobicity-modified filter paper, the spot-to-spot variation of the SERS intensity of 25 spots of 4-aminothiophenol was 6.19%, and the limits of detection of thiram and ferbam as test pesticides were measured to be 0.46 nM and 0.49 nM, respectively. These proof-of-concept results indicate that this paper-based SERS sensor can serve for highly sensitive pesticide detection with low cost and easy fabrication.

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.

The printability properties of the paper can be increased by some processes applied to the surface. The use of non-recyclable materials derived from petroleum is decreasing day by day, and the demand for recyclable materials obtained from renewable sources is increasing. These materials include cellulose derivatives, starch types and polyvinyl alcohol. The materials ratios, sizes, physical and chemical properties of these materials used in the processes applied to the paper and the content of the paper will affect the strength of the paper as well as change the surface properties and significantly affect the printability. The aim of this study is to obtain better printability properties by improving the paper surface with CNF/CNF-OX coating. In this study, fluting and core board papers coated with different amounts of cellulose nanofiber (CNF)/cellulose nanofiber-oxidized (CNF-OX) were produced. Surface properties, contact angle, surface energy, color and gloss of the produced papers were measured by optical microscope, goniometer, spectrophotometer and glossmeter. The papers were printed with the IGT C1 offset printability tester. As a result, in terms of printability, it was determined that CNF/CNF-OX coated papers have smoother surfaces and give better results in terms of both gloss properties and printability. [GRAPHICS] . WOS:000637661300003 2-s2.0-85103957996

With the extensive use of palladium derivatives in the industry, their environmental pollution has become more and more serious. Herein, allyl functionalized hydrazone 2D COFs (XB-COFs) were found for selective fluorescent detection of Pd2+ (detection concentration of 0.29 μM) in water. The stable structure of the hydrazone bond and the complexation ability of allyl to Pd2+ cause XB-COF to have a good fluorescence sensing effect in both acid and alkaline solutions, and its adsorption capacity for Pd2+ is up to 120 mg g-1. During the interaction between XB-COF and Pd2+, a part of Pd2+ can be reduced to Pd nanoparticles with a diameter of about 10 nm. A fluorescent test paper was prepared by the in situ growth of XB-COF onto a filter paper, which can realize visualization detection of Pd2+ in 10 s with the naked eye or under a 365 nm UV lamp. This is the first time a fluorescent test paper based on in the situ growth of COFs has been applied for the detection of heavy metal ions, which provides a new platform for the application of COF materials in the medical health field, food safety, and environmental protection.

A simple and cheap filter paper-based SERS substrate has been developed for the sensing of tetracycline (TC) traces. In fact, antibiotics could represent a danger for environment and human health and TC is, in detail, one of the most wide-spread antibiotics entering the food chain and as water contaminant. According to this aim, Ag nanodisks (AgNDs) synthesis procedure was designed for tailoring the plasmonic peak position and, so, the SERS effect. Synthetized AgNDs were then used to simply decorate the surface of common filter paper, chosen because of its biocompatible, porosity and cheapness features. The obtained substrates based on filter paper and AgNDs allow the fast and easy analysis of aqueous solution containing first methylene blue used as standard and then TC samples. Fixed volume (20 μL) of TC solutions at different concentrations was simply dropped on the SERS support. The SERS spectrum was acquired before the complete water evaporation allowing TC detection down to the concentration of 10−9 M in aqueous solution. The results demonstrated that the SERS substrate obtained with the proposed facile, low-cost and relatively green fabrication process and the possibility to tune the plasmon excitation can be implemented for TC low concentration samples.

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.