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With the increased awareness of reusing solid wastes for higher sustainability and the concern of water pollution associated with phosphorus over-emission, there are strong interests in developing solid waste based adsorbents for purifying phosphorus-containing wastewater. As a rich calcium resource, paper mill sludge (i.e., a major solid waste from pulping industry) can be used as phosphorus removal adsorbent after calcination. Thus, in this work, a simple and clean thermally treating route has been proposed for preparing calcium-containing biochar from paper mill sludge. The effect of the physicochemical properties of paper mill sludge and its carbonization condition on phosphorus adsorption has been analyzed. Moreover, the influence of some key adsorption parameters, e.g., biochar dosage, initial pH of solution, co-existing anions, initial phosphorus concentration and contact time has also been investigated. The results showed that the phosphorus adsorption data could be fitted well with pseudo-second-order kinetic and Langmuir isothermal models. The calculated maximum adsorption capacity of the as-prepared optimal calcium-containing biochar could reach to 68.49 mg·g−1 at 25 °C. Combined with the characterization results, it can be reasonably inferred that the adsorption process was chemisorption-dominated. Lastly, the application of this spent adsorbent in agriculture field has also been discussed. In brief, this work provided a feasible strategy for converting paper mill solid waste to an environmental functional material (i.e., calcium-rich biochar) for remediation of eutrophic water.

Graphene-based nanomaterials possess broad applications because of their excellent multi-functional properties. In this work, a facile self-assembling method was presented for preparing one kind of graphene oxide-based paper/hollow microspheres hybrid. It was found that most of the hollow microspheres can strongly anchored on the surface of graphene oxide paper (GOP) by an in-situ scanning electron microscope peeling testing combining with molecular dynamics (MD) simulation. In addition, the uniform distribution of hollow microspheres on the surface of GOP cannot only provide a better surface wettability, but also can effectively improve the interfacial stress-transfer capability between such hybrid and polymer matrix. Our work provides a guidance for the structural designs of graphene-based nanomaterials and broaden their applications.

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.

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

Photocatalytic materials have been widely used to remove dyes from printing and dyeing wastewater. However, difficulty in recycling of photocatalysts is the great concern in the real catalytic applications, which significantly raises the application cost. This study developed a low-cost catalyst by loading magnetic Ni onto filter paper (FP) via an easy going in-situ reaction. The characterization results displayed that the Ni particles were uniformly anchored onto the FP. The Ni@FP material presented a strong magnetic ability which was evidenced by a saturation magnetization (Ms) of 5.014 emu·g−1, a remanent magnetization (Mr) of 2.067 emu·g−1 and a coercivity (Hc) of 133.868 Oe. Meanwhile, the magnetic Ni@FP material displayed a recyclable advantage in photocatalytic degradation of methyl orange (MO) via an external magnetic field. There existed an optimal photocatalytic degradation rate of 93.40% within 5 min when MO concentration was 15 mg·L−1 at pH 8.0. Three cycle experiments confirmed that the Ni@FP possessed a satisfied stability and recycling ability. Moreover, the Ni@FP material presented a strong antibacterial activity which can prevent it from being contaminated by microorganisms. The versatility of the newly proposed photocatalyst in this study demonstrated its great application prospect in dyeing wastewater treatment.

The growing need for reliable analytical tools to perform measurements at the point-of-need has prompted the development of novel sensors that are low cost, portable, sensitive, easy to use, and capable of multiplexed analysis. Miniaturization of the sensors into microfluidic platforms has become a promising approach to achieve these self-contained sensors. However, traditional microfluidics often require relatively expensive and complicated pumping mechanisms that increase the cost and limit the portability of the sensors. From a material perspective, paper is an attractive substrate for constructing point-of-need sensors because of its affordability, vast availability, and self-pumping ability, particularly when combined with electrochemical detection. In this mini-review, we discuss various strategies to achieve multiplexing or simultaneous detection of multiple analytes in electrochemical paper-based devices and provide a brief guide on selecting the detection strategy based on the electrochemical property of the analytes.

A novel nacre-like flame-retardant paper based on graphene oxide (GO), and phytic acid (PTA) is fabricated via evaporation-induced self-assembly. This facile method is time saving and low energy consuming. A facile approach is proposed to improve thermal oxidative stability of GO paper by in situ phosphorus doping during flame exposure. Then fire-alarm system is designed based on the high-temperature thermal reduction characteristic of GO. The GO paper functionalized with PTA (GO-PTA) can provide ultrasensitive, reliable and longtime fire early-warning signal. Fire alarm can be triggered at approximately 0.50 s when GO-PTA samples are attacked by fire. Phosphorus atoms are in situ doped into graphene layers during fire exposure, endowing GO-PTA paper with outstanding thermal oxidative stability, and thus alarm duration time of GO is greatly improved. The work develops advanced fire detection and early-warning sensors that provide reliable and continuous signals, which provide more available time for fire evacuation.

Simultaneous enhancement in water flux and removal efficiency during the filtration process remains a big challenge for separation membranes. The porous structure of the filter paper can provide many channels for water transportation, but the separation performance is generally poor. The purpose of this study is to develop a new kind of filter paper consisting of ultralong hydroxyapatite (HAP) nanowires, cellulose fibers (CFs) and double metal oxide (LDO) nanosheets, and to achieve the simultaneous enhancement of both water flux and removal efficiency for high-performance dye separation. In this work, a novel kind of LDO/HAP/CF nanocomposite filter paper consisting of ultralong HAP nanowires and CFs and LDO nanosheets has been developed for rapid water filtration and highly efficient dye adsorption. Positively charged LDO nanosheets can adsorb on the surface of negatively charged ultralong HAP nanowires and embed in the porous networked structure of the LDO/HAP/CF nanocomposite filter paper, which can provide a porous structure for rapid water transportation and can adjust the pore size of the nanocomposite filter paper. As a result, the pure water flux of the LDO/HAP/CF nanocomposite filter paper can be adjusted. The optimized pure water flux of the LDO/HAP/CF nanocomposite filter paper can reach 783.6 L m-2 h-1 bar-1, which is 1.51 times that of the HAP/CF filter paper without LDO nanosheets (518.6 L m-2 h-1 bar-1). More importantly, the adsorption capacity of LDO nanosheets is high for dye molecules, the rejection percentage of Congo red (CR) by the as-prepared HAP/CF filter paper is only 59.8%, and its water flux is 534.7 L m-2 h-1 bar-1. The optimized rejection percentage and water flux of the LDO/HAP/CF nanocomposite filter paper for CR are significantly enhanced (98.3% and 736.8 L m-2 h-1 bar-1, respectively) compared to those of the HAP/CF filter paper. The size of LDO nanosheets has a significant effect on the water flux and dye rejection percentage of the LDO/HAP/CF nanocomposite filter paper. The as-prepared LDO/HAP/CF nanocomposite filter paper is promising for the applications in highly efficient purification of wastewater containing dye molecules.

With the rapid emergence of wearable devices, flexible lithium-ion batteries (LIBs) are much more needed than ever. Free-standing graphene-based composite paper electrodes with various active materials have appealed wide applications in flexible LIBs. However, due to the prone-to-restacking feature of graphene layers, a long cycle life at high current densities is rather difficult to be achieved. Herein, a unique three-dimensional (3D) hierarchically porous NiO micro-flowers/graphene paper (fNiO/GP) electrode is successfully fabricated. The resulting fNiO/GP electrode shows superior long-term cycling stability at high rates (e.g., storage capacity of 359 mAh/g after 600 cycles at a high current density of 1 A/g). The facile 3D porous structure combines both the advantages of the graphene that is highly conductive and flexible to ensure rapid electrons/ions transfer and buffer the volume expansion of NiO during charge/discharge, and of the micro-sized NiO flowers that induces hierarchical between-layer pores ranging from nano-micro meters to promote the penetration of the electrolyte and prevent the re-stacking of graphene layers. Such structural design will inspire future manufacture of a wide range of active materials/graphene composite electrodes for high performance flexible LIBs.

Rapid and simultaneous in situ detection of multi-components is extremely crucial for the real-time monitoring of nutrients in fruits. Herein, a facile and user-friendly poly(carboxybetaine methacrylate)-coated paper-based microfluidic device (pCBMA-μPAD) has been exploited to synchronously identify and semi-quantify vitamin C, glucose, sucrose and fructose in fruits. The pCBMA was successfully grafted from the surface of paper sensor using a convenient and robust method, which was confirmed by Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectrometry (XPS). The superior hydrophilicity and ultra-low fouling of pCBMA endowed the pCBMA-μPAD with remarkably rapid response (3 min), high sensitivity, good linear relationship and low detection limit (LOD) (vitamin C: y = 33.809 + 5.175x, R2 = 0.993, LOD = 0.179 mmol/L; glucose: y = −0.113 + 30.066lg(x), R2 = 0.988, LOD = 0.095 mmol/L; sucrose: y = −5.334 + 34.858lg(x), R2 = 0.996, LOD = 0.097 mmol/L; fructose: y = 4.996 + 23.325lg(x), R2 = 0.994, LOD = 0.140 mmol/L). Furthermore, satisfactory results were yielded in the detection of these nutrients in 9 fruits, which were much agreed well with those obtained by spectrophotometry. Such a portable and versatile pCBMA-μPAD will profoundly shape the future of food analysis, especially for the assessment of food quality and nutrition in the process of agricultural production and marketing.

Filter paper, as a widely used and low-cost lab consumable, can serve as template for the synthesis of one-dimensional (1D) materials since it is composed of 1D cellulosic fiber. In this work, 1D NiO/NiCo2O4 composite was simply fabricated by adsorption of Ni and Co acetate on the filter paper and subsequent calcination process. The precursors were obtained without further treatment to filter paper or chemical reaction between metal salts. Calcination process leads to the removal of template and formation of binary NiO/NiCo2O4 composite. Electromagnetic (EM) wave absorption performance of NiO/NiCo2O4 composite could be tuned by adjusting the calcination temperatures and dosage of metal salts. For the optimized absorber (calcination temperature of 600 °C and dosage of Ni and Co acetate with 2 mmol and 4 mmol), a wide absorption bandwidth of 6.08 GHz could be achieved with thickness of 1.88 mm and minimum reflection loss value was up to −57.4 dB by changing the thickness. The facile synthetic route may also inspire the preparation of other high-performance one-dimensional EM wave absorbing materials.

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

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.

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

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.

This study reports on eco-friendly graft polymerization approach for the modification of a cellulosic material via combination between enzymatic catalysis and reversible addition-fragmentation chain transfer polymerization (RAFT). Polyacrylamide (PAM) was polymerized on a cellulosic filter paper via horseradish peroxidase (HRP)-initiated RAFT polymerization. The results of grafting ratio, conversion, and pseudo-first-order kinetics were proved that the PAM graft polymerization on the filter paper followed RAFT rules. The results of Attenuated total reflection (ATR-FTIR), elemental analysis, and X-ray photoelectron spectroscopy (XPS) confirmed the presence of PAM in PAM-grafted filter paper. The results of water contact angle and Thermogravimetric analysis (TG) evidenced the change in the wetting properties and thermal performance, respectively of the treated filter paper. This work provides a new environmentally approach to graft polymerization on cellulosic materials.

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

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.

The development of renewable energy sources minimizes the burning of fossil fuels for clean and green environment. Electrochemical energy storage/conversion device pays a way towards sustainable development that concludes an emerging field in the trends of the research community. Prominently, the functional materials with suitable structure and property determine the performance and durability of the devices. In recent times, graphene with its tremendous properties play a major role in electrochemical energy device applications. Meanwhile, the graphene-based electrodes were fabricated by various coating techniques on existing electrodes that utilized for energy device fabrication. Apart from these, it is also fabricated in a paper like a form (self-supported or free-standing) with its remarkable high conductivity, flexibility, robustness and electrochemical behavior which have been nominated for fabrication of flexible energy devices. Paper-like electrodes become an emerging field to fabricate a light-weight and flexible electronic devices for future prospects. Thus, we have summarized a synthetic strategy of graphene paper and its properties that potentially focused on flexible device fabrication in both the energy storage and conversion system. Hence, this review boosts up the forthcoming researchers to enhance the device performance with interrelating free-standing graphene and other host material.

Fluoro-functionalized paper was prepared and applied in solid phase extraction (SPE) for the analysis of trace-level perfluorinated compounds (PFCs). The proposed fluoro-functionalized paper-based solid-phase extraction (Fp-SPE) exhibits significant advantages for sample preparation, such as the biodegradability of paper-based adsorbent, simple manipulation and low cost. Owing to the fluorous affinity, the Fp-SPE technique with high sensitivity and high selectivity is more suitable for the selective enrichment of fluorine-containing molecules from the background of non-fluorinated organic compounds in a real water sample. Combined with high-performance liquid chromatography coupled with electrospray ionization-tandem mass spectrometry analysis (HPLC-MS/MS), the linear range of the PFCs, including perfluorobutyric acid (PFBA), perfluorooctanic acid (PFOA), perfluorooctane sulfonic acid (PFOS), and perfluorodecanoic acid (PFDA), was 0.20–5.0 ng/L with the limits of detection (LOD) ranging from 0.04–0.05 ng/L and the limits of quantification (LOQ) ranging from 0.15-0.20 ng/L. The method was then applied to the analysis of tap water, river water and waste water samples. The results of the actual sample analysis are consistent with that by reverse phase SPE (RP-SPE).

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.

Great attention has been drawn to flexible and portable electronic devices, so it is important to develop flexible energy-storage devices. In this study, the porous Ni-Co-N nanosheets on flexible graphene paper (GP) are prepared by surface nitridation of NiCo2O4 nanosheets. Compared with NiCo2O4/GP, Ni3N/GP and CoN/GP, Ni-Co-N/GP shows superior performance in terms of specific capacitance of 960 F/g (48.1 mF/cm2) at 4 A/g, rate performance (86% capacitance retention) and cycle life (the capacitance retention reaches 95% over 5000 cycles). The paper-based all-solid-state asymmetric supercapacitors (SCs) are manufactured based on Ni-Co-N/GP and chemical oxidized GP (graphene oxide paper, GOP), which exhibits excellent bendability, flexibility, editability. The flexible energy device shows an outstanding specific energy of 4.78 mWh/cm3 and excellent cycle life (89% capacitance retention after 8000 cycles).

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.

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.

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.

Development of recoverable and sustainable catalysts for environmental remediation still remains a great challenge. Here, we report a simple approach to immobilizing polyethylenimine (PEI)-templated silver nanoparticles (Ag PTNPs) onto the surface of cellulose filter paper for catalytic applications. First, branched PEI was utilized as a template to complex Ag(I) ions, then, sodium borohydride was applied as a reducing agent to generate Ag PTNPs. Thereafter, the formed Ag PTNPs were assembled onto filter paper via electrostatic interaction. The developed Ag PTNP-immobilized filter paper was characterized through different methods. We show that Ag PTNPs with a mean diameter of 4.6 ± 1.3 nm are able to be immobilized onto the surface of filter paper, and the Ag paper displays a remarkable catalytic activity and reusability towards the catalytic transformation of 4-nitrophenol to 4-aminophenol. The developed approach may be extended for the production of different kinds of NP-immobilized filter paper for the applications in sensing, environmental remediation, and biomedicine.

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 direct coating of graphene sheets obtained by electrochemical exfoliation on commercial paper renders the preparation of highly conductive flexible paper substrate for subsequent deposition of polyaniline (PANi) nanorods via electrochemical polymerization. The deposition of PANi can be well-controlled by adjusting the electrochemical polymerization time, leading to the formation of PANi coated graphene paper (PANi-GP). The as-prepared electrode exhibited high areal capacitance of 176 mF cm−2 in three-electrode system at a current density of 0.2 mA cm−2, which is around 10 times larger than that of pristine graphene paper due to the pseudocapacitive behavior of PANi. In-situ Raman test was used to determine the molecular changes during redox process of PANi. More importantly, all-solid-state symmetric capacitor assembled with two PANi-GP electrodes in a polymer electrolyte delivered an areal capacitance of 123 mF cm−2, corresponding to an areal energy density of 17.1 µWh cm−2 and an areal power density of 0.25 mW cm−2. The symmetric capacitor held a capacitive retention of 74.8% after 500 bending tests from 0 to 120°, suggesting the good flexibility and mechanical stability. These results showed the great promising application in flexible energy-storage devices.

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.

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 paper, a simple and effective ratiometric fluorescent nanoprobe for visual detection of hypochlorous acid (HOCl) has been developed by loading silicon coated rhodamine B (RBDS) nanospheres on the surface of amino-modified graphene oxide (GO-NH2) nanosheets. The fabricated nanoprobe exhibits dual-emissions peaked at 427 and 585 nm, under a single excitation wavelength of 365 nm. The blue fluorescence of GO-NH2 can be selectively quenched by oxidation of HOCl, while the red fluorescence of RBDS remain unchanged, resulting in a distinguishable fluorescent color change from blue to pink under a UV lamp. Nanoprobes present high selective and sensitive for HOCl determination with a limit of detection (LOD) of 2.92 μM. Moreover, potable paper sensor has been prepared by coating the ratiometric fluorescent probe on filter paper, which provides a convenient and simple approach for HOCl visual detection.

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.

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.

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 negative effect of solid waste on the environment is a topical issue effecting the global population. Waste paper is a major component of organic solid waste and cellulose a structural component of waste paper is a suitable biopolymer that could be resolved into glucose, a fermentable sugar. Also of concern to many sections of the farming community is the negative effect of garden snails on plants and fruits. When consumed by snails the cellulose section of plant materials can be hydrolysed by an enzyme system called cellulase into glucose which then is utilized as a resource of energy. Cellulase enzymes extracted from garden snails were incubated with seven different waste paper materials during ten successive incubating periods. Different sugar releasing patterns were constructed during the saccharification of the various paper materials indicating the different structural compositions of these paper materials. Foolscap paper showed the highest relative susceptibility for snail cellulase catalysed saccharification followed by brown envelope paper. The lowest amount of sugar was released during the degradation of newspaper and Pick n Pay advertising paper.

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.

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.

The recently emergent laser induced graphene paper (LIGP) has endowed the large-scale assembly of 2D electronics with freestanding and multifunctional natures. Liquid sensors, a crucial component in next-generation smart devices, were developed in this report through LIGP technology. Attributed to the one-step process of computer-aided laser scribing, the new sensor was fulfilled easily with arbitrary 2D shapes, sizes and array modalities. In comparison to indirect sensing manners existed majorly in polymer binder/substrate enabled carbon devices, the novel LIGP sensors with self-supported graphitic structures evidently showed multiple superiorities, including faster response, greater reproducibility, and higher sensitivity for micro-volume liquid detections. Benefiting from the laser-process dependent structures, we further proved the tunable sensing characteristics relying dominantly on specific surface area, a critical factor for introducing capillary pressure to facilitate liquid infiltration and electrical disruption. Additionally, a dual-mode liquid-recognition strategy based on both time and speed was creatively proposed for identification of various liquids. With successful utilization of 5 × 5 LIGP array for mapping the distribution of different fluid emissions on composite structures, we highly anticipate the escalation of LIGP sensors for commercialization, roll-to-roll manufacturing, and multimodal safety-assurance applications.

Contaminated water contains various types of pollutants, the removal of which requires two or more technologies. It is imperative but challenging to develop water purifier for simultaneous removal of multiple pollutants for the sake of easy operation, low cost, and etc. Previously reported multifunctional purifiers are normally nanoparticles which require caution during use. Here, we describe a design of paper-like multifunctional purifier, which has biomass-based structure by grafting polyethylenimine derived quaternary ammonium compounds onto three-dimensional bacterial cellulose substrate. Compared to similar materials reported previously, our product exhibited strikingly higher adsorption capacities towards various metal ions including Pb2+, Cu2+, and Cr6+, anionic organic dyes including congo red, methyl orange and methyl red, and excellent disinfection efficiency towards both Gram-negative and Gram-positive bacteria. Remarkably, this purifier also demonstrated effective removal of the three contaminative species simultaneously from both simulated and local polluted water. With more virtues of superior reusability and extreme handy convenience, we hope our molecular design could inspire further efforts on the rational construction of multifunctional water purifier with easy operation. We reckon our material to have strong potential for the possible use in water treatment, especially in regions that are short of environmental infrastructures.

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.

The electrochemical oxidation of organics in paper mill wastewater belonging to Halfa industries (Tunisia) was performed by galvanostatic electrolyses using electro-Fenton (EF) process. The effect of several operating parameters, such as applied current density, electrodes material, air pressure and the presence of sodium chloride (NaCl) was evaluated. In particular, carbon felt (CF), modified carbon felt (MCF) and gas diffusion electrode (GDE) were used as cathode while Ti/IrO2-Ta2O5 and Boron Doped Diamond (BDD) as anode. Total Organic Carbon (TOC) measure was chosen as reference parameter to assess the extent of the treatment. The experimental results show that, by adopting the optimal set of operative conditions, EF can allow a high removal of TOC. It was shown that better performances can be achieved increasing the complexity of the treatment, by using sufficiently long electrolysis time or BDD as anode, MCF or GDE as cathode or the addition of NaCl.

Focusing on eco-friendly materials, cellulose nanocrystal (CNC) extracted from office waste paper was used to reinforce waterborne polyurethane (WPU) with varying content by two incorporation routes including blending method by sonication after WPU synthesis (BCNC/WPU) and the alternative in-situ during the WPU synthesis process (CNC/WPU). The results showed that new interaction between CNC and WPU through hydrogen bonds in the interfacial area was formed and CNC reinforced hard segments effectively. However, the interaction in BCNC/WPU was not as stronger as that in CNC/WPU. Besides, CNC improved thermal stability of WPU remarkably, especially BCNC/WPU. The addition of CNC caused a delay around 50 °C in the start of the degradation process, and a delay of 5–18 °C and 2–20 °C in the temperatures at 10 and 50 wt% weight loss, respectively. These eco-friendly and biodegradable novel materials have potential applications in medical and biologic fields.

In this work, the effect of liquid evaporation on electrochemical measurements with electrochemical paper-based devices (ePADs) is studied. The time evolution of cyclic voltammograms of ferricyanide is used to study the effect of liquid evaporation under different conditions of relative humidity and air currents. Moreover, the enclosure of ePAD channels with adhesive tape is evaluated in terms of minimising the evaporation, as well as increasing the sensitivity in the electrochemical determination of horseradish peroxidase in long-term assays. This project has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement No 760876.