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Cellulose paper, a material that is naturally derived, low cost, lightweight, eco-friendly, and mechanically deformable, plays important roles in producing next-generation flexible electronics. Following the booms in the development of functional electronics, the soft actuators built from cellulose paper have attracted great attention. In this focused review, the milestones and recent achievements of cellulose paper-based actuators are summarized. Electro-, thermal, moisture and magnetic actuation mechanisms are utilized to acquire energy from external stimuli. Corresponding functional materials and available fabrication techniques like film assembly and layer deposition are described. Programmable actions for the emerging applications in bionics, paper grippers and robots are realized by pursuing different strategies to control the responding deformation. Along with a conclusion, the existing challenges and possible solutions in evaluating and improving the performance of cellulose paper are summarized in the final section.

To study the influence of different concentrations of zinc oxide (ZnO)/silicon dioxide (SiO2) composite coating on hydrophobic property and mechanical stability of paper mulch film, three kinds of ZnO/SiO2 composite coating paper mulch films (2%, 4%, 6%) with different coating substance contents were prepared by brush coating method. Through particle size analysis, contact angle, rolling angle and mechanical stability test, combined with scanning electron microscope, three-dimensional morphology and roughness measuring instrument, the optimal concentration of ZnO/SiO2 composite coated paper mulch film was screened out. Through acid-base salt corrosion test, silver mirror reaction and surface self-cleaning, the optimal concentration of composite coated paper mulch film was compared with the original paper mulch film to prove its excellent chemical stability and hydrophobicity. The results show that the paper mulch film with 4% coating material has excellent hydrophobicity and mechanical stability, can effectively reduce the surface roughness of paper mulch film, and has remarkable effects in resisting acid, alkali and salt and self-cleaning.

The pulp and paper industry has been researching different treatments for the degradation of adsorbable organohalogens (AOX). In this work, two agitation processes (mechanical and ultrasound) were analyzed in the AOX degradation of the bleaching wastewater using nano zero valent iron (nZVI). The work used different variables for the AOX removal process, such as pH, time, nZVI, and hydrogen peroxide (H 2 O2) concentration. Results show an increase in AOX degradation when a higher nZVI concentration is used. The optimal combination of variables for the treatment with mechanical agitation was found in the ratio 2:5 (nZVI : H 2 O2), degrading 85% of AOX in 60 min, with acid pH. Ultrasound treatment consisted of half process time and less degradation than mechanical agitation treatment. The 2:5 ratio in ultrasound agitation degraded 55% of AOX within 30 min at the end of the process. Both methods of the homogenization process of zero valent iron nanoparticles in the bleaching wastewater of the paper and cellulose industry are efficient. However, the mechanical stirring process has a more significant potential for AOX degradation. The variables (pH, concentration of nZVI and H 2 O2 and duration of the process) used in the bleaching wastewater treatment process must be considered for future implementation in the pulp and paper industry.

Among the largest producers of waste, the paper industry stands out due to its impact on human health and ecological balance. However, these residues may also contribute to a more environmental friendly brick industry, since the incorporation of fluxing agents may improve the firing process and the induced porosity reduces thermal conductivity of fired bricks. Therefore, this study aims to assess the feasibility of replacing clay with solid paper residue (PPR) from 2.5 to 17.5% in order to reduce resources depletion and improve brick performance. The original clay was characterized as a non-calcareous red clay with high contents of kaolinite. Several samples were made by extrusion and fired at 900 °C in accordance with industrial procedures. The addition of PPR led to increase shrinkage from 5 to 10% due to the effect of fluxing oxides which reduced pores volume and enlarged pores size. In addition, the impervious fraction was slightly reduced while the apparent porosity certainly increased (i.e. approx. 17%) due to the macroscopic pores developed by PPR combustion. This porosity produces lighter bricks (i.e. density decays from 1.76 to 1.39 g dm−3) with lower thermal conductivity (i.e. from 5.53 to 0.41 W m−1 K−1) but also reduces compressive strength (i.e. from 11 to 3 MPa) and increases water absorption (i.e. up to 24%). Nevertheless, toxicity is below the regulatory limits in all cases and fired bricks are easily adaptable to industrial procedures. It must be noticed that this work was supported by the Chilean National Commission on Research and Development (CONICYT) [grant number FONDECYT REGULAR 1180414]. Technical and human support provided by CICT of Universidad de Jaén (UJA, MINECO, Junta de Andalucía, FEDER) and by Centro de Manejo de Residuos y Energía (BIOREN) Universidad de la Frontera (Chile) are gratefully acknowledged.

Detection of mycotoxins by conventional methods such as ELISA or LC-MS can be expensive and time-consuming. Therefore, paper-based biosensors can be effectively used for on-site analysis, due to their low cost and easy detection procedures. Nevertheless, even when the application of colorimetric methods on paper enhance the simplicity and affordability of multiple determinations, the signal intensity and final readout can be affected by a limited color uniformity. In this work, Ellman’s method for the quantification of aflatoxin B1 was utilized as a model colorimetric assay on paper, in which the test zones were modified with chitosan-immobilized enzyme (AChE). A comparison of the cross-linking effect of genipin on two chitosans of varying molar mass and degree of acetylation, exhibited a greater signal enhancement from the sample with a higher degree of acetylation and molecular weight.

The transwell assay is currently the most popular approach to studying cellular invasion due to its ease of use and readout, and the possibility for quantitative measurements. However, it only allows end-point measurements without the possibility for real-time tracking of the dynamics of cell movement during an invasion. Moreover, it requires cell labeling, and construction of customized devices is hampered by the commercial standard membrane inserts, only available in certain designs. Recently, paper has been used as a scaffold for three-dimensional (3D) cell cultures. Because of its microfibrous structure and easy handling, it could be a versatile alternative as a membrane insert in customized devices. Here, we develop a low-cost real-time invasion assay device using paper as an alternative membrane insert. The device was designed for two-electrode impedance measurements and fabricated using CNC micromilling. It also comprised a disposable low-cost stencil-printed working electrode on a poly(methyl methacrylate) substrate below the membrane and glassy carbon counter electrode above the membrane inserted in a specially designed lid. Thus, the impedance measurements during cell invasion addressed the entire membrane. We demonstrated the function of the device by monitoring the invasion of B16 melanoma 4A5 cells from a mouse using insulin growth factor-1 as the chemoattractant. The cell invasion on paper was visualized using scanning electron microscopy and confocal microscopy with Z-stack 3D imaging. Melanoma cell invasion could be observed within 7 h after the chemoattractant treatment, which was faster than the conventional assay and less likely to be influenced by cell proliferation.

Nowadays, there are strong efforts in developing new technology for rapid detection of specific DNA sequences for environmental monitoring, forensic analysis and rapid biomedical diagnosis applications. That is where microfluidic paper-based analytical devices are positioned as suitable platforms for the development of point of care analytical devices, due to their simple fabrication protocols, ease of use and low cost. Herein, a methodology for in situ single strand DNA detection by using a colorimetric assay based on the formation of a DNAzyme within a paper substrate was developed. A DNAzyme that could only be formed in the presence of a specific sequence of the Y human amelogenin gene was designed. The performance of the DNAzyme was followed colorimetrically first in solution and then in paper substrates. The reaction was found to be specific to the Y fragment selected as analyte. The DNAzyme reaction on paper enabled the unequivocal colorimetric identification of the Y single strand DNA fragment both qualitatively, with the naked eye (143 ng), and quantitatively by image analysis (45.7 ng). As a proof of concept, a microfluidic paper-based device, pre-loaded with all DNAzyme reagents, was characterized and implemented for the simultaneous detection of X and Y single strand DNA fragments. This work was supported by Gobierno de España, Ministerio de Economía y Competitividad, with Grant No. BIO2016-80417-P; funding from Basque Government (Grant: IT1271-19) and European Union funds: DNASURF (H2020-MSCA-RISE-778001). E.A.-H. acknowledges funding from the Basque Government, Department of Education, for predoctoral fellowship 2016.

ATP-driven bioluminescence relying on the D-luciferin-luciferase reaction is widely employed for several biosensing applications where bacterial ATP detection allows to verify microbial contamination for hygiene monitoring in hospitals, food processing and in general for cell viability studies. Several ATP kit assays are already commercially available but an user-friendly ATP biosensor characterized by low-cost, portability, and adequate sensitivity would be highly valuable for rapid and facile on site screening. Thanks to an innovative freeze-drying procedure, we developed a user-friendly, ready-to-use and stable ATP sensing paper biosensor that can be combined with smartphone detection. The ATP sensing paper includes a lyophilized “nano-lantern” with reaction components being rapidly reconstituted by 10 μL sample addition, enabling detection of 10−14 mol of ATP within 10 min. We analysed urinary microbial ATP as a biomarker of urinary tract infection (UTI), confirming the capability of the ATP sensing paper to detect the threshold for positivity corresponding to 105 colony-forming units of bacteria per mL of urin, This research was sponsored in part by PRIN 2015 “Multifunctional nanotools for advanced cancer diagnostics” (Prot. 2015TWP83Z) and the NATO Science for Peace and Security Programme under Grant No. 985042. The ICN2 is funded by the CERCA Programme/Generalitat de Catalunya and also supported by the Severo Ochoa program of the Spanish Ministry of Economy, Industry and Competitiveness (MINECO, grants No. SEV-2017-0706 and MAT2017-87202-P).

This work presents a new optical microfluidic paper biosensor for the detection of organophosphate pesticides and carbamate pesticides. The assay strip is composed of a paper support (1 × 17.6 mm) onto which acet- ylcholine esterase (AChE) and acetylcholine chloride (AChCl) are deposited, in such a way that there is a small hole between them that ensures that they only come into contact in the reaction zone when they are carried by a solution of the sample by lateral flow to the reaction zone containing bromocresol purple (BCP) as the pH indicator, immobilized by sol-gel. The sensor operates at room temperature and the rate of the inhibited reaction serves as an analytical signal, which is measured using a camera by quantifying the appropriate colour co- ordinate. Calibration curves were obtained for chlorpyrifos and carbaryl, with a useful concentration range from 0.24 to 20 μg L−1 for carbaryl and from 2.00 to 45 μg L−1 for chlorpyrifos. The detection limits were 0.24 and 2.00 μg L−1, respectively, and with reproducibility around 4.2–5.5%. The method was applied to the de- termination of pesticides in different water samples, with no sample preparation., This study was supported by a project from the Spanish MINECO (CTQ2016-78754-C2-1-R), a project partially supported by European Regional Development Funds (ERDF).

The fluorescence-based detection of biological complexes on solid substrates is widely used in microarrays and lateral flow tests. Here, we investigate thiol-ene micropillar scaffold sheets (“synthetic paper”) as the solid substrate in such assays. Compared to state-of-the-art glass and nitrocellulose substrates, assays on synthetic paper provide a stronger fluorescence signal, similar or better reproducibility, lower limit of detection (LOD), and the possibility of working with lower immunoreagent concentrations. Using synthetic paper, we detected the antibiotic enrofloxacin in whole milk with a LOD of 1.64 nM, which is on par or better than the values obtained with other common tests, and much lower than the maximum level allowed by European Union regulations. The significance of these results lays in that they indicate that synthetically-derived microstructured substrate materials have the potential to improve the performance of diagnostic assays., We gratefully acknowledge the financial support from the European project ND4ID, and Ministry of Science, Innovation and Universities Spain (IMMUNO-QS, SAF2015-67476-R and QS4CF, RTI2018-096278-B-C21). We thank Dr Ana Sanchis from IQAC-CSIC for providing the glass slides and assistance in operating the spotter and scanner, Dr David Santos for the MALDI-TOF tests, and Dr Nuria Pascual for providing the primary antibodies.

A 4D imaging study (3D + time) combining synchrotron tomography with in situ tensile testing has been carried out to observe the fibre and network level micromechanics of paper made from northern bleached softwood kraft (NBSK). Quantitative image analysis and digital volume correlation is used to characterize local deformation, the evolution of fibre-fibre contacts, and fibre straightening in a ”freeze-dried” handsheet as well as standard handsheets low consistency refined at different refining energies. In the freeze-dried handsheet having low fibre conformability, the results show that deformation at the network level occurs because of fibre straightening and possible inter-fibre bond breakage. Further, significant out-of-plane deformation near the failure regions was observed, which led to auxetic behaviour. In the refined handsheets, a strong inverse correlation is seen between refining energy, thickness expansion, and the number of broken fibres. The use of out-of-plane strain norms is proposed as a method to determine network efficiency (i.e. the ratio of the network’s elastic modulus to that of the constituent fibres) as well as the relative contribution of fibre pull-out to the overall failure of the handsheet.

The need for a continuous, real-time monitoring of specific diseases represents an unmet scientific need. Evidently, cancer is one of the most important diseases where it is crucial to increase the rates of patient survival and monitor disease prognosis. Herein, a novel type of immunoassay was developed for detection of cancer biomarkers, using alpha-fetoprotein (AFP) and mucin-16 (MUC16) as model analytes. Using gold nanoparticle (AuNP) bioconjugates as a signal production tool, relevant antibody (Ab)-conjugated AuNPs were prepared on the nitrocellulose (NC) membrane. To construct a spot-like point-of-care (POC) immunoassay, cysteamine conjugated AuNPs (AuNP-Cys) were immobilized on the NC membrane and antibodies were conjugated to the nanoparticle on the detection pad, following a treatment with the samples that contains AFP or MUC16 which are well-known protein biomarkers for liver and ovarian cancer. By using the change in the colorimetric properties of AuNPs, detection of tumor markers was achieved by using a smartphone image and color analysis software at the final stage. Image J application was used for the evaluation of color changes depending on the biomarker concentration in buffer or spiked synthetic serum samples. the linear range was found as 0.1 ng/mL-100 ng/mL for AFP and 0.1-10 ng/mL for MUC16. Limit-of-detection (LOA) was calculated as 1.054 ng/mL and 0.413 ng/mL for AFP and MUC16, respectively. Interferent molecules, Her2, Immunoglobulin G (IgG) and bovine serum albumin (BSA) were tested on the system. Furthermore, synthetic serum samples spiked with selected analyte molecule were applied on the system and measured successfully., COST project of Scientific and Technological Research Council of Turkey (TUBITAK) [117Z609], This work was supported by a COST project of Scientific and Technological Research Council of Turkey (TUBITAK, Project Grant No: 117Z609).

This work is concerned with the electrochemical detection of new psychoactive substances (NPSs), in particular 2,5-dimethoxy-N-(2-methoxybenzyl) phenethylamine structures (NBOMes) and the analogous 2,5-dimethoxy phenethylamine structures (2C-X group) on boron-doped diamond (BDD) electrodes. Fast square-wave voltammetry was used to identify the substances in question. The antifouling properties of the BDD surface resulted in stable, repeatable, sensitive and unique voltammetric responses for these NPSs, producing different voltammetric signatures. Different NBOMes were identified by voltammetric methods in blotting paper seized from the drug market, without any interference from LSD, another psychedelic drug distributed via blotting paper. The proposed method achieved detection limits lower than 0.1μmolL−1 with high precision (RSD

We have previously reported that crystalline samples of 1-acetylaminopyrene (AAPy), 1-octanoylaminopyrene (OAPy), and 1-stearoylaminopyrene (SAPy) exhibited mechanochromic luminescence. In the present study, we have found that these 1-alkanoylaminopyrenes adsorbed onto cellulose papers also exhibited mechanochromic luminescence; however, their behaviors were essentially different from those observed for their crystalline samples. In addition, these cellulose papers were found to exhibit reversible emission color change upon alternate exposure to ethanol and water vapors. It was suggested that 1-alkanoylaminopyrene molecules were dispersed in the paper without aggregation or crystallization and that intermolecular distance of 1-alkanoylaminopyrenes in the paper was reduced by either mechanical stress or exposure to ethanol vapor, resulting in increasing the sites where excimers could be formed and/or in enhancing the efficiencies of energy migration to reach the excimer sites.

Through design hierarchical architectures and interlayer interaction, multifunctional macroscopic graphene oxide papers tend to attain outstanding mechanical properties. Three dimensional architectures functionalized graphene oxide papers are self-assembled with zirconium diboride particles and poly(vinyl alcohol, PVA) using vacuum assisted filtration method. Firstly, ternary graphene oxide micro-scale structures are achieved by the addition of zirconium diboride particles. Then, PVA is introduced to enhance the interface interaction between graphene oxide nanosheets and zirconium diboride particles. The results show significant enhancements in fracture strength (~200%) and tensile modulus (20–100%) are attained through synergistic effect of ternary graphene oxide structures and interlayer interaction between PVA, graphene oxide and zirconium diboride particles. Keywords: Graphene oxide paper, Zirconium diboride, Mechanical behaviors

The deposition of chemical reagent inks on paper is a crucial step in the development and fabrication of microfluidic paper-based analytical devices (mu PADs). A pen-plotting approach, delivering chemical ink deposition using technical pens filled with reagents and inserted into a desktop electronic plotter, is shown herein to be a versatile, low-cost, simple, rapid, reproducible, and high-throughput solution. The volume of the deposited ink was quantified gravimetrically, confirming that nanoliter volumes of reagents can be deposited reproducibly (e.g. 7.55 +/- 0.37 nL/mm for a plotting speed of 10 cm/s) in detection zones of mu PADs, typically spatially defined using wax printing. This approach was further investigated with regard to deposition of reagents in different geometrical forms (circular and linear), so demonstrating its applicability for preparation of mu PADs with flexible design and application. By adjusting the plotting speed for linear deposition, lines with a relatively large range of widths (approximate to 628-1192 mm) were created. Circular deposition was also demonstrated via delivery of reagents within wax printed circular fluidic barriers of a range of diameters (inner diameter = 1.5-7 mm). These capabilities were practically demonstrated via the fabrication of mu PADs, based upon differing detection principles for determination of aluminum in natural waters using Morin as the fluorescent reagent. Traditional mu PADs based on digital image colorimetry (DIC) were produced using circular deposition, whilst distance-based mu PADs exploited linear deposition. Both types of mu PADs developed using this method showed excellent precision for determination of trace concentrations of aluminium (average RSDs = 3.38% and 6.45%, and LODs = 0.5 ng (0.25 ppm) and 2 ng (0.5 ppm), for traditional and distance-based detection, respectively).

Lithium-Sulfur (Li-S) batteries are known for their high energy density and cost-effectiveness. However, the Li-S chemistry is a challenging topic due to the shuttle effect and the use of highly reactive lithium metal anode. To solve these issues, ultra-lightweight multilayered graphene coated paper separator is proposed as an interlayer. The interlayer is firstly coated on nickel foil by Chemical Vapor Deposition (CVD) method followed by transferring to the paper by fishing process. By employing this unique technique, a very light (similar to 8 mu g/cm(2)) graphene coating layer is obtained which does not further imply lowering the entire energy density of the cell. As a whole, the cell with graphene coated paper exhibits 610 mAh/g discharge capacity at C/5 after 100 cycles, while the cell without interlayer exhibits much poorer performance. The improved performance is mostly associated with the interaction between graphene and polysulfide species which is proven by X-Ray Photoelectron Spectroscopy measurement as well as the excellent electronic conductivity of graphene layer which behaves as a secondary current collector resulting the cell resistance decrease. (C) 2018 Elsevier B.V. All rights reserved.

Wireless chemical sensors are increasingly finding use as analytical devices in healthcare diagnostics, wearable sensing (sweat analysis) and in the rapidly emerging area of the Sensor Internet of Things (SIoT). In such wireless scenarios, the application of fluorescence-based sensors is lagging behind other types of transduction mechanisms. In this work a new low-cost and highly portable wireless fluorimeter for optical chemical fluorescence intensity measurements is presented (bill-of-materials approximately €20). The fluorimeter is programmed and communicates wirelessly with mobile devices or personal computers by radio-frequency identification (RFID) or near-field communication (NFC). This novel mobile analytical system is highly adaptable for use with different fluorescent sensor chemistries and analytes. The fluorimeter has been evaluated in the laboratory in two sets of proof-of-concept experiments: firstly fluorimetry in solution, where the fluorescence intensities of fluorescein were recorded, and secondly chloride sensing via a paper-immobilised quinine sulphate fluorescent indicator. The latter represents the first demonstration of wireless (radio-frequency) fluorescence-based chloride sensing. Satisfactory analytical performance was achieved in the entire range of sweat chloride concentrations. The wireless fluorimeter system presented here could make a significant contribution to several emerging areas of mobile chemical sensor research, including wearable sensors for healthcare and sport, mobile point-of-sample diagnostics as well as more generally for the Sensor Internet of Things.

For the first time the feasibility of using an alkaline wastewater coming from the pulp and paper industry as an activator, partially (50 vol%) replacing commercial sodium hydroxide, in the production of cork-based activated carbons was evaluated. The activated carbons showed the highest value of specific surface area ever reported for cork-based activated carbons (1670 m2/g), surpassing several other commercial and waste-based ones. These eco-friendly cork and paper waste-based activated carbons were then evaluated as methylene blue adsorbent materials. The influence of contact time, methylene blue initial concentration and adsorbent amount on the methylene blue removal efficiency by the activated carbons was studied. Extremely fast (>99.9% removal in 5 min) and efficient methylene blue adsorption (uptake of 350 mg/g) by the cork and paper waste-based adsorbents was achieved, which demonstrates the huge potential of these innovative adsorbents. These activated carbons were produced using two unexplored industrial by-products (alkaline wastewater and cork) and, therefore, may be an inexpensive source of activated carbons, which can be used for the effective removal of dyes from wastewaters. Furthermore, despite the very large surface area and high removal efficiency this is not a nano material (being around 30–50 μm in size), its capabilities being due to its unique cork-derived microstructure, and hence it can be handled and removed/filtered much more easily than nanocarbons, and without any associated health or environmental risks. This work was developed within the scope of the project CICECO-Aveiro Institute of Materials, POCI-01-0145-FEDER-007679 (FCT Ref. UID/CTM/50011/2013), financed by national funds through the FCT/MEC and when appropriate co-financed by FEDER under the PT2020 Partnership Agreement. R.C. Pullar wishes to thank FCT grant IF/00681/2015 for supporting this work, and R.M. Novais wishes to thank FCT project H2CORK (PTDC/CTM-ENE/6762/ 2014). published

Understanding the transport processes that occur in carbon-fiber papers (CFPs) used in fuel cells, electrolyzers, and metal-air/redox flow batteries is necessary to help predict cell performance and durability, optimize materials and diagnose problems. The most common technique used to model these thin, heterogeneous, anisotropic porous media is the volume-averaged approximation based on the existence of a representative elementary volume (REV). However, the applicability of the continuum hypothesis to these materials has been questioned many times, and the error incurred in the predictions is yet to be quantified. In this work, the existence of a REV in CFPs is assessed in terms of dry effective transport properties: mass diffusivity, permeability and electrical/thermal conductivity. Multiple sub-samples with different widths and thicknesses are examined by combining the lattice Boltzmann method with X-ray tomography images of four uncompressed CFPs. The results show that a meaningful length scale can be defined in the material plane in the order of 1–2 mm, which is comparable to the rib/channel width used in the aforementioned devices. As for the through-plane direction, no distinctive length scale smaller than the thickness can be identified due to the lack of a well-defined separation between pore and volume-averaged scales in these inherently thin heterogeneous materials. The results also show that the highly porous surface region (amounting up to 20% of the thickness) significantly reduces the through-plane electrical/thermal conductivity. Overall, good agreement is found with previous experimental data of virtually uncompressed CFPs when approximately the full thickness is considered. The authors thank the support team of Calcul Quebec and Compute Canada for their help during the simulation campaign, as well as Dr. Dula Parkinson and Dr. Alastair MacDowell at the Advanced Light Source (ALS) for help in obtaining the tomographic images. This work was funded under the Fuel Cell Performance and Durability Consortium (FC-PAD), by the Fuel Cell Technologies Office (FCTO), Office of Energy Efficiency and Renewable Energy (EERE), of the U.S. Department of Energy under contract number DE-AC02-05CH11231, Project ENE2015-68703-C2-1-R (MINECO/FEDER, UE) and the research grant 'Ayudas a la Investigation en Energia y Medio Ambiente' awarded to the first author by the Spanish lberdrola Foundation. I.V. Zenyuk and A.D. Shum would like to acknowledge support from the National Science Foundation under CBET Award 1605159. X-ray tomography experiments were performed on beamline 8.3.2 at the ALS (Lawrence Berkeley National Laboratory), which is a national user facility funded by the Department of Energy, Office of Basic Energy Sciences under contract DE-ACO2-05CH11231. Numerical calculations were performed on the supercomputing clusters Briaree, Colosse, Guillimin and Mp2, managed by Calcul Quebec and Compute Canada. The operation of these supercomputers is funded by the Canada Foundation for Innovation (CFI), Ministere de l'Economie, de l'Innovation et des Exportations du Quebec (MEIE), RMGA and the Fonds de recherche du Quebec -Nature et technologies (FRQ-NT).

Paper mills yield large volumes of sludge materials which pose an environmental and economic challenge for disposal, despite the fact that they could be a valuable source for cellulose nanofibres (CNF) production. The aim of the study was to evaluate the production process and properties of CNF prepared by mechanical fibrillation of never-dried and dried paper mill sludge (PMS). Atomic force microscopy (AFM) showed that average diameters for both never-dried and dried paper sludge nanofibres (PSNF) were less than 50 nm. The never-dried and dried sludge nanofibres showed no statistical significant difference (p>0.05) in strength ∼92 MPa, and ∼85 MPa and modulus ∼11 GPa and ∼10 GPa. The study concludes that paper mill sludge can be used in a dried state for CNF production to reduce transportation and storage challenges posed on industrial scale.

Zeolite nanostructures were used as hosts for dyes normally used in some bioassays (pH and protein), and applied on microfluidic paper-based analytical devices (PADs). The obtained dye nanomaterials were characterized by several techniques (structural (FTIR and XRD), surface (SEM/EDX), textural (N2 adsorption) analyses and dye loading determination by TGA analysis), to confirm the stability of both host and guest. After their deposition on the papers surface, the color change was studied by analyzing the RGB values, taking into account the lifetime and the results stability of the PADs. These results confirmed that both the lifetime and the color change of the modified devices were stable over one week. It was also demonstrated that the choice of the paper for the PAD as well as the zeolite nanostructures properties influences the colorimetric response. This strategy by encapsulating dyes into zeolites solve current challenges in colorimetric sensors in where long-term stability of the colorimetric results is an issue. The results obtained were promising for the studied assays, and the strategy could also be extended to other bioassays., A.R.B. thanks for the ERASMUS+ program to her grant. This work has been developed under the scope of the projects: BioTecNorte (NORTE-01-0145-FEDER-000004), AIProcMat@N2020 (NORTE-01-0145-FEDER-000006), projects supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). This work also has been funded by ERDF through COMPETE2020–Programa Operacional Competitividade e Internacionalização (POCI), Project POCI-01-0145-FEDER-006984, Associate Laboratory LSRE-LCM and by national funds through FCT, Fundacão para a Ciência e a Tecnologia for project PTDC/AAGTEC/5269/2014 and Centre of Chemistry (UID/QUI/00686/2013 and UID/QUI/0686/2016). The support from the Oslofjordfondet project, «Touchsensor for enklere og raskere urinprøvetaking og analyse (no. 234972)» and NSFC project no. 61650410655 is also acknowledged., info:eu-repo/semantics/publishedVersion

As two important industrial manufacturing materials, ceramics and metals have their own advantages and disadvantages in terms of physical, chemical, and mechanical properties. The field of material manufacturing has witnessed efforts to develop technical processes that can properly combine these two alloys, aiming to effectively use their respective advantages. The welding technology for ceramics and metals, as a research topic with broad prospects, is comprehensively and deeply analyzed in this review. The current research progress in this field is analyzed from different process perspectives such as fusion welding, brazing welding, diffusion welding. By using appropriate intermediate materials between these two materials, the residual stress and brittle intermetallics near the interface of the transition joint can be minimised by solving the thermal expansion mismatch, reducing the bonding temperature and pressure.

An overview of the last trends in lab-on-chip technology highlights the continuous development of biosensing approaches in terms of simplicity, low-cost, and quick response, with a higher sensitivity and selectivity. In this context, electrochemical sensors arrived to overcome the need to develop small, accurate, portable and compact sensing devices, compatible with routine use in loco analysis, especially in point-of-care (POC) assessment. Herein, we have presented the first paper-based electrochemical sensor towards the detection of 3-nitrotyrosine (3-NT), a relevant oxidative stress biomarker. This innovative sensor was designed by, first, modifying paper to become a hydrophobic support and, second applying carbon and silver conductive inks to generate a three electrode-system on a small spot. An intensive voltammetric investigation of the paper-based screen-printed electrodes (SPEs), including the study of different redox-probes, scan-rate values, probe concentrations and supporting electrolyte solutions, confirmed their suitable and reliable electrochemical performance. Square wave voltammetry (SWV) was employed to assess the sensitivity of the proposed sensor at various concentrations of 3-NT, ranging from 500nM to 1mM, enabling a low detection limit (LOD) of 49.2nM. The interference of co-existing species was also tested and good selectivity against 3-NT was accomplished. Overall, this flexible paper-based platform constitutes a promising sensor material towards a quick, sensitive, cost-effective, sustainable and reproducible detection of 3-NT biomarker., European Research Council (ERC) is acknowledged for funding this work through the Starting Grant 3P's (ERC/StG/3P's/GA311086). Portuguese Foundation for Science and Technology (FCT) also supported this work through FEDER funds from COMPETE 2020 Program and National Funds, under the project UID/CTM/50025/2013 and the PhD Grants references SFRH/BD/94159/2013 (GVM) and SFRH/BD/115173/2016 (ACM)., info:eu-repo/semantics/publishedVersion

Electron beam lithography (EBL) was used for preparing nanostructured reduced patterns on the GO paper surface, while preserving its mechanical resistance and flexibility. Different EBL parameters, like dose and time of exposure for patterning were tested. SEM analysis showed the consequent increase of contrast of the reduced stripes on the patterned regions due to the increase of electron beam doses. Moreover, surface potential microscopy experiments also exhibited a clear contrast between the patterned and non-patterned regions. Structural analysis of the patterned paper through X-ray diffraction and nanoindentation showed that the interlayer distance between GO sheets decreases after reduction allowing the increase of the Hardness and Young modulus that makes this material able to be manipulated and integrated on different devices. Furthermore, we also observe that exposed areas to electron beam reduction process show an increase in the electrical conductivity up to 3 × 104 times. The developed flexible GO films can have interesting applications such as biosensors or templates for inducing tissue regeneration, by providing a surface with differently patterned cues with contrasting electron mobility. Preliminary in vitro studies with L929 fibroblasts support the cytocompatible nature of this patterned GO paper., Gil Gonçalves thanks the Fundação para a Ciência e a Tecnologia for the PostDoc grant (SFRH/BDP/84419/2012). P.A.A.P.M. acknowledge the FCT/MCTES for a research contract under the Program Investigator 2013 (IF/00917/2013/CP1162/CT0016) and TEMA – Centre for Mechanical Technology and Automation (UID/EMS/00481/2013), financed by national funds through the FCT/MEC. I.B. wish to acknowledge the Portuguese Foundation for Science and Technology for the financial support (grant IF/00582/2015). H·I·S.N. acknowledges CICECO-Aveiro Institute of Materials, POCI-01-0145-FEDER-007679 (FCT Ref. UID/CTM/50011/2013), financed by national funds through the FCT/MEC and when appropriate co-financed by FEDER under the PT2020 Partnership Agreement. The biological studies of this work have been funded by the Ministerio de Economía y Competitividad and the Fondo Europeo de Desarrollo Regional (MAT2016-78857-R, MINECO/FEDER, UE). AGM and MCS acknowledge ISCIII-MINECO-FEDER for respective contracts. Authors would like to thank Dr M. Teresa Portolés from the Biochemistry and Molecular Biology Department at Universidad Complutense de Madrid for the generous supply of L929 fibroblasts. Dr José Ángel Rodríguez and Dr Javier Mazarío from the Service of Microscopy and Image Analysis at the Hospital Nacional de Parapléjicos are acknowledged for assistance with CLSM studies and Dr Enrique Rodríguez from the Servicio Interdepartamental de Investigación at the Universidad Autónoma de Madrid for SEM studies., info:eu-repo/semantics/acceptedVersion

© 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/, Hydration of a multi-layered graphene oxide (GO) paper in water vapor atmosphere was studied by in-situ X-ray scattering over a wide range of relative humidity (RH). The intercalation of water molecules physically adsorbed between GO layers induces the expansion of the interlayer distance. Two regimes of adsorption are clearly evidenced according to the variation of the interlayer distance as a function of the relative humidity. The expansion of the interlayer distance is limited to ∼1 Å for RH ranging from 6 to 53%, whereas it is ∼3.5 Å for RH 75–100%. The hydration mechanism corresponds to the progressive adsorption of water molecules onto hydrophilic sites at the surface of GO layers in the low-RH regime, then an additional water monolayer is formed in the high-RH regime., EP, SR and PL benefited of a grant from the French Research National Agency under the program Investissements d’Avenir (SEDECO project, ANR-10-LABX-0035: Labex NanoSaclay). AMB and WKM acknowledge funding from the Spanish MINEICO (project ENE2016-79282-C5-1-R), the Gobierno de Aragón (Grupo Reconocido TO3_17R) and associated EU Regional Development Funds.

This study focused on preparation of microfibers from bamboo culms using steam explosion with and without chemical treatments, and utilization of the isolated fibers in formation of bamboo paper fabricated with nanofibrillated cellulose (NFC). Compared with those obtained from the steam explosion alone (S), the bamboo microfibers isolated using the steam explosion followed by bleaching process (S/A) exhibited a significantly reduced fiber width of 7.5 μm and a markedly increased cellulose content of 97.85%. The S/A fiber showed an increased decomposition temperature, corresponding with lower contents of hemicellulose and lignin than those of the S fiber. The S/A microfibers were subsequently proceeded to paper formation. Physical and mechanical properties of the paper with an introduction of different NFC concentrations (0–50 wt%) were investigated. The linear relationship between the density, porosity and mechanical properties of the paper and NFC contents was observed. The more the NFC content, the greater the density and the lower the porosity the paper exhibited. At 50 wt% NFC, the paper density increased to 0.64 g cm−3, and the paper porosity decreased to 57.0% whereas the paper without NFC showed a density of 0.39 g cm−3 and porosity of 73.6%. Tensile strength and strain of the paper composed with 50 wt% NFC were 10-fold and 3-fold, respectively, greater than those of the paper without NFC. The addition of NFC could manifest paper mechanical properties and porosity within the paper structure, which would be useful for scaffold and membrane applications. Keywords: Bamboo, Mechanical properties, Paper, Nanofibrillated cellulose, Steam explosion, Microfibers, Nanofibers

Pulp and paper industry produces massive amounts of sludge from wastewater treatment, which constitute an enormous environmental challenge. A possible management option is the conversion of sludge into carbon-based adsorbents to be applied in water remediation. For such utilization it is important to investigate if sludge is a consistent raw material originating reproducible final materials (either over time or from different manufacturing processes), which is the main goal of this work. For that purpose, different primary (PS) and biological sludge (BS) batches from two factories with different operation modes were sampled and subjected to pyrolysis (P materials) and to pyrolysis followed by acid washing (PW materials). All the materials were characterized by proximate analysis, total organic carbon (TOC) and inorganic carbon (IC), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and N2 adsorption isotherms (specific surface area (SBET)and porosity determination). Sludge from the two factories proved to have distinct physicochemical properties, mainly in what concerns IC. After pyrolysis, the washing step was essential to reduce IC and to considerably increase SBET, yet with high impact in the final production yield. Among the materials here produced, PW materials from PS were those having the highest SBET values (387-488 m2 g-1). Overall, it was found that precursors from different factories might originate final materials with distinct characteristics, being essential to take into account this source of variability when considering paper mill sludge as a raw material. Nevertheless, for PS, low variability was found between batches, which points out to the reliability of such residues to be used as precursors of carbon adsorbents. L'Oreal Portugal published

This work addresses the development of a compact paper-based enzymatic microfluidic glucose/O2 fuel cell that can operate using a very limited sample volume (≈35 µl) and explores the energy generated by glucose at concentrations typically found in blood samples at physiological conditions (pH 7.4). Carbon paper electrodes combined with a paper sample absorption substrate all contained within a plastic microfluidic casing are used to construct the paper-based fuel cell. The anode catalysts consist of glucose dehydrogenase and [Os(4,4′-dimethoxy-2,2′-bipyridine)2(poly-vinylimidazole)10Cl]+ as mediator, while the cathode catalysts were bilirubin oxidase and [Os(2,2′-bipyridine)2(poly-vinylimidazole)10Cl]+ as mediator. The fuel cell delivered a linear power output response to glucose over the range of 2.5–30 mM, with power densities ranging from 20 to 90 µW cm−2. The quantification of the available electrical power as well as the energy density extracted from small synthetic samples allows planning potential uses of this energy to power different sensors and analysis devices in a wide variety of in-vitro applications., Peter Ó Conghaile is thanked for synthesis of the redox polymers. Neus Sabaté acknowledges funding from the European H2020 Framework Programme (Grant Agreement 648518 - SUPERCELL - ERC 2014 CoG). Juan Pablo Esquivel would like to thank the support from Marie Curie International Outgoing Fellowship (APPOCS) within the 7th European Community Framework Programme. F. Javier del Campo acknowledges funding from the Spanish Ministry of Economy through the DADDi2 project (TEC2013-48506-C3). Dónal Leech acknowledges support from Grant number 607793 under the Bioenergy FP7-PEOPLE-2013-ITN Programme.

A simple field method for determination of fluoride in drinking water using handmade fluoride reagent paper impregnated by aluminium quinalizarin complex was developed. Fluoride reacts with the impregnated reagent paper to release the free ligand with new colour, orange different from that of the complex. The change in the colour, which is proportional to the amount of fluoride, was measured by the Arsenator. The functionality of the Arsenator which is based on a photometric measurement of spot on the reagent paper is expanded to analyse fluoride. The method allows a reliable determination of fluoride in the range 0.0–2.0 mg L−1. Further spectrophotometric determinations of fluoride showed that Beer’s law is obeyed in the range of 0.3–5.0 mg L−1 at 553 nm. Sensitivity, detection limit, quantitation limit, and the percentage recovery of 1.5 mg L−1 fluoride were found to be 0.117 μg mL−1, 0.1 mg L−1, 0.3 mg L−1, and 101.2 respectively.

Microfluidic paper-based analytical devices (microPADs) are a relatively new group of analytical tools thatrepresent an innovative low-cost platform technology for fluid handling and analysis. Nonetheless, microPADs lack in the effective handling and controlling of fluids, which leads to a main drawback for their reproducibility in large volumes during manufacturing, their transition from the laboratory into the marketand thus accessibility by end-users. Herein we investigate the applicability of ionogel materials basedon a poly(N-isopropylacrylamide) gel with the 1-ethyl 3-methylimidazolium ethyl sulfate ionic liquidas fluid flow manipulator in microPADs using the ionogel as a negative passive pump to control the flowdirection in the device. A big challenge undertook by this contribution is the integration of the ionogel materials into the microPADs. Finally, the characterisation and the performance of the ionogel as a negative passive pump is demonstrated. The project was carried out with the support of the Ramón y Cajal programme (Ministerio de Economía y Competitividad). FBL thanks to the European Union’s Seventh Framework Programme(FP7) for Research, Technological Development and Demonstration under grant agreement no. 604241 and the Gobierno Vasco, Dpto. Industria, Innovación, Comercio y Turismo under ELKARTEKKK-2015/00088. FBL and TA personally acknowledge Marian M.de Pancorbo for letting them to use her laboratory facilities at UPV/EHU. MCMM acknowledges the Basque Government under theEtortek Program (Grant No. IE14-391) and Dr Seifert for the use ofhis laboratory facilities. NG-G work was supported by a PhD fellowship from the University of Navarra. Authors also acknowledge Adhesive Research for the donation of the PSA samples.

This work demonstrates a stand-alone power source that integrates a paper-based hydrogen fuel cell with a customized chemical heater that produces hydrogen in-situ upon the addition of a liquid. The presented approach operates by capillary action and takes advantage of the hydrogen released as a by-product of an exothermic reaction used in point-of-care diagnostics. The paper-based fuel cell produces a maximum power of 25.8 mW (103.2 mW cm−2), which is suitable for powering a diversity of electrical devices such as commercially available digital pregnancy tests and glucometers. While device shape and dimensions can be customized, here it is shown that the fuel cell can be designed in a compact form factor and footprint comparable to a lateral flow test while providing a remarkable power output. This approach holds great promise for powering portable diagnostics, as the generated electric power could enable device functionalities required for advanced assays, such as device timing, actuation, and signal quantification. Part of the same liquid sample that is to be analyzed (urine, saliva, water, etc) could be used to trigger the hydrogen generation and start the fuel cell operation., J.P. Esquivel acknowledges support from Marie Curie International Outgoing Fellowship (APPOCS - GA.328144) within the 7th European Community Framework Programme. J. Buser and P. Yager were supported by a grant from DARPA DSO/BTO--HR0011-11-2-0007, awarded to Yager at the University of Washington. P. Yager was supported in part by funds from the Department of Bioengineering at the University of Washington. S. Rojas acknowledges financial support from project ENE2013-42322R. N. Sabaté would like to thank financial support received from ERC Consolidator Grant (SUPERCELL - GA.648518).

In this work, several cellulose board grades, including waste board, fluting, and waste milk container board, were pretreated with green choline chloride-urea deep eutectic solvent (DES) and nanofibrillated using a Masuko grinder. DES-treated bleached chemical birch pulp, NaOH-swollen waste board, and bleached chemical birch pulp were used as reference materials. The properties of the nanofibrils after disc grinding were compared with those obtained through microfluidization. Overall, the choline chloride-urea DES pretreatment significantly enhanced the nanofibrillation of the board pulps in both nanofibrillation methods—as compared with NaOH-treated pulps—and resulted in fine and long individual nanofibrils and some larger nanofibril bunches, as determined by field emission scanning electron microscopy and transmission electron microscopy. The nanofibril suspensions obtained from the DES pretreatment had a viscous, gel-like appearance with shear thinning behavior. The nanofibrils maintained their initial crystalline structure with a crystallinity index of 61%–47%. Improved board handsheet properties also showed that DES-treated and Masuko-ground waste board and paper nanocellulose can potentially enhance the strength of the board. Consequently, the DES chemical pretreatment appears to be a promising route to obtain cellulose nanofibrils from waste board and paper.

An organometallic dye, europium tetrakis dibenzoylmethide triethylammonium (EuD4TEA) and gold nanoparticles (Au NPs) impregnated paper based sensor platform have been utilized for development of fluorescence turn-on cyanide assay in aqueous media. The ordinary filter paper with 6 μ m pore size were employed as solid support that facilitates impregnation of EuD4TEA and gold nanoparticles and provides durability. Detection mechanism relying on two processes (i) dissolution of gold nanoparticles causing fluorescence recovery and (ii) ligand exchange of triethyl amine with CN group stimulating cyanide specific fluorescence enhancement. The paper platform exhibit naked eye distinguishable color transition upon CN− addition from 10−2 to 10−12 M. To standardize the methodology a homemade image processing algorithm has been developed that enabling calibration of color change and quantify CN− concentration. The described algorithm is applicable to Android smart phones and facilitate transforming these devices into a quantitative cyanide detector. The overall methodology provides instrument free cyanide detection and therefore rapid control of water quality and safety at off-field conditions.

Herein, we describe a sustainable and inexpensive approach to monitor Zn(II) in biological fluids by fabricating an office paper-based electrochemical sensor. By following two easy steps, consisting of wax patterning and electrode screen-printing, the office paper provides an effective electroanalytical tool that is easily extensible to a broad range of analytes. This approach would be able to develop affordable user-friendly sensing devices, tackling the lack of resources in regions with poor-settings/facilities. In order to provide more details regarding the screen-printed electrodes fabrication, office paper, Whatman #1 chromatrographic paper, and polyester have been characterized with electrochemical, morphological, and mechanical tests and compared. Using office paper, Zn(II) has been detected linearly up to 2 μg/mL with a detection limit equal to 25 ng/mL and a relative standard deviation of 8%. To highlight the feasibility, reliability, and easiness of the proposed electrochemical sensor, Zn(II) has been detected in serum and sweat at physiological level (μg/mL), and the accuracy of the method has been verified by satisfactory recoveries close to 100%.

Aramid fibers exhibit impressive mechanical properties, electrical insulation properties, and chemical stability. However, physical properties of the aramid paper are poor because of the chemical inertness and smooth surface of aramid fibers. This study reports a simple and efficient method for substantially improving the performance of the para-aramid/meta-aramid composite paper by introducing the N,N-dimethylacetamide (DMAc)/LiCl solution to induce partial dissolution or by adding the DMAc/LiCl/para-aramid solution to induce regeneration. Experimental results state that the tensile strength, specific strength, folding resistance, and interlayer bonding strength of the aramid paper are increased by 2.17, 2.13, 34.7, and 9.39 times, respectively, because of the dense and compact structure of the paper. Furthermore, the water resistance of the paper was also considerably improved. After immersing the paper samples in water for 24 h, their moisture absorption rate decreased to approximately 54% from approximately 143% for the original paper. Results indicate that partial dissolution/regeneration welding is a viable method for the efficient reinforcement of the aramid composite paper, providing additional possibilities for manufacturing the high-performance aramid paper-based materials. Keywords: Aramid composites, Partial dissolution, Regeneration welding, Mechanical properties, Reinforcement

The steel-concrete interface is fundamental to many aspects related to the performance of reinforced concrete, particularly for corrosion behavior. A recently published paper by Chen et al. [Effect of design parameters on microstructure of steel-concrete interface in reinforced concrete, Cem. Concr. Res. 119 (2019) 1–10] quantitatively characterized the thickness of the gap observed between the steel and concrete. Considering the low number of available publications, studies documenting the microstructure at the steel-concrete interface are important. However, in our discussion, we think that aspects related to the terminology, the specimen preparation and possible experimental artefacts in the discussed paper can be improved.

Organic heat insulating materials with low density and low thermal conductivity have been widely used in building and domestic appliances. However, their highly flammable and poorly flexible characteristics hamper the application under certain circumstances. In this work, novel nanocomposite paper with low thermal conductivity, flame retardancy and good mechanical property was prepared by employing ultralong hydroxyapatite (HAP) nanowires as scaffolds for silica aerogels. The conductivity of the HAP/silica aerogel nanocomposite paper at room temperature decreased from 0.056 to 0.045 W m−1 K−1 as the amounts of silica aerogels increased from 0 to 50 wt%, indicating the excellent heat insulating performance. Meanwhile, the prepared paper showed remarkable flame retardancy with the peak heat release rate (HRR) of only 33.1 W/g when silica aerogel content was 50 wt%. Thermal stability analysis showed that the weight losses of all the nanocomposite papers with different contents of silica aerogels were

This article reports on the development and validation of a disposable microfluidic paper-based analytical device (μPAD) for on-hand, in-situ, and cheap Fe(III) determination in natural waters complying with World Health Organization guidelines. The developed μPAD used 3-hydroxy-4-pyridinone (3,4-HPO) as a colour reagent due to its considerably lower toxicity than traditionally used iron analytical reagents. It was selected among a group of hydrophilic 3,4-HPO chelators containing ether-derived chains in their structure which were prepared using green methods. The relatively high water solubility of these chelators improved the detection limit and applicability as μPAD reagents. Under optimal conditions, the μPAD is characterised by a quantification range between 0.25 and 2.0 mg/L, a detection limit of 55 μg/L and 15 min of analysis time. The signal stability extends up to 4 h and the device is stable for at least one month. The reagent consumption is below 0.2 mg per analysis and the μPAD method was validated by analysis certified reference materials and by comparison with atomic absorption results (RD < 10%). The newly developed μPAD was successfully applied to the determination of iron in river, well and tap waters with no need of any prior sample pre-treatment.

Metallic lithium (Li) is regarded as the ultimate anode for high-energy-density rechargeable batteries due to its highest theoretical capacity and most electronegative potential. However, there are serious challenges before practical application of Li metal batteries (e. g. Li–air batteries), including the dendritic Li formation and infinite variation of electrode dimension. Herein, nitrogen (N) and sulfur (S) co-doping carbon paper (NS-CP) is synthesized and further modified with a graphite-based layer (GL) by pencil-drawing. The as-prepared GL modified NS-CP (GL/NS-CP) is applied to pre-store Li through the heating-infusion method and Li-GL/NS-CP electrode is obtained. Experimental and theoretical results have demonstrated that N, S co-doping can effectively enhance the lithiophilicity of CP to ensure the uniform Li deposition. In addition, GL presents excellent Li wettability to rapidly syphon molten Li. Moreover, abundant pores in GL/NS-CP can accommodate enough Li to alleviate electrode volume change and lower local current density to restrain Li dendrites. Compared with pure Li anode, Li-GL/NS-CP electrode shows more stable voltage curves with lower overpotential (20 ​mV for 600 cycles). As a result, Li–air batteries with Li-GL/NS-CP anodes also exhibit the satisfying cycling life. These results have shed a new light on the development of Li anodes.

In parallel with the development of nanoparticle coatings for protection of paper substrates, detailed descriptions of the surface topography with micro-to nanoscale roughness features are needed. In this work, papers have been coated with poly(styrene-co-maleic anhydride) nanoparticles including different types of vegetable oils and the surface roughness was evaluated at 2000 x 2000 mu m(2) to 0.2 x 0.2 mu m(2) length scales by combining non-contact optical profilometry (NCP) and atomic force microscopy (AFM). The relationships between roughness data were studied for statistical roughness parameters, spatial roughness parameters and in the frequency domain. In order to compare AFM roughness more accurately, the original images were flattened to remove effects of the underlaying fibrous substrate and highlight features of the nanoparticle coating. More detailed information on the coating topography could be obtained by considering bearing ratio curves and histograms, where it was concluded that the oil-filledcoatings form a rather thin and continuous coating that closely follows the shape of the cellulose fibers. The relation between statistical roughness parameters from NCP and AFM follows an exponential trend with relatively low coefficient of determination. The increase in surface roughness with length scale showed a transition point attributed to short-and long-range surface features. Therefore, the correlation length was used as a spatial roughness parameter that provides a successful extrapolation of the average roughness over different length scales in a double logarithmic diagram with very high coefficient of determination. Based on the power spectral density, it was difficult to exactly distinguish between the different types of SMI/oil coatings, as they include similar nanoscale features. The frequency roughness parameters were better suited for extrapolation than statistical roughness parameters but little less efficient than the spatial roughness parameters. (C) 2015 Elsevier Ltd. All rights reserved.

Electrochemical techniques are attractive for nitrite detection owing to their intrinsic advantages. However, traditional electrochemical sensors often suffer from the effects of fouling due to the adsorption of oxidation products on the electrode surface. In this work, a paper-based, inexpensive, disposable electrochemical sensing platform was developed for nitrite analysis based on a simple and efficient vacuum filtration system. Taking advantage of the physicochemical properties of graphene nanosheets and gold nanoparticles, the mass transport regime of nitrite at the paper-based electrode was thin layer diffusion rather than planar diffusion. In comparison with the electrochemical responses of commercial gold electrodes and glassy carbon electrodes (GCE), a considerably larger current signal was seen at the paper-based sensing interface, which significantly improved its sensitivity for nitrite detection. In particular, the paper-based electrode was a disposable sensing device, so that it effectively avoided the fouling effect arising from the adsorption of oxidation products. Moreover, the paper-based sensing platform made it possible to determine nitrite in environmental and food samples in an accurate, convenient, inexpensive, and reproducible way, indicating that the proposed system is promising for practical applications in environmental monitoring and public health. Keywords: Paper-based electrode, Nitrite, Electrochemical sensing, Graphene

This work presents a novel method for the full fabrication of electrochemical paper-based cells by screen-printing technology. Firstly, a mixture of ultraviolet curable inks was used for patterning hydrophobic barriers into chromatography paper. Afterwards three-electrode systems were coupled for electrochemical detection by printing successively carbon and silver/silver chloride inks over the hydrophilic areas. The resulting electrochemical cells were characterized by cyclic voltammetry in different redox systems and used for amperometric detection of ferricyanide. Keywords: Paper-based device, Screen-printing, Fabrication, Electrode, Voltammetry, Amperometry

International audience; Successful preparation of tungsten oxide thin films on paper substrate, using a novel room temperature deposition method involving the connection of tungsten oxide nanoparticles by UV-irradiation, is reported. WO3 thin films, prepared from synthesized monoclinic WO3 powder as compared to commercial ones, show higher electrochemical activity and good cycling stability in 0.3 M trifluoromethanesulfonimide (HTFSI) in 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (BMITFSI) ionic liquid electrolyte versus Pt as counter electrode. Electrochromic performances of complete devices using Prussian Blue (PB) as complementary counter electrode and 0.3 M Lithium Bis(Trifluoromethanesulfonyl)Imide LiTFSI in BMITFSI plastified with polymethylmetacrylate (PMMA) membrane electrolyte are associated with a contrast in reflectance of 13%, from a yellow to a blue color.

The closure of water circuits within pulp and paper mills has resulted in a higher contamination load of the final mill effluent, which must consequently be further treated in many cases to meet the standards imposed by the legislation in force. Different treatment strategies based on advanced oxidation processes (ozonation and TiO2-photocatalysis), and their combination with biological treatment (MBR), are herein assessed for effluents of a recycled paper mill and a kraft pulp mill. Ozone treatment achieved the highest efficiency of all. The consumption of 2.4 g O3 L−1 resulted in about a 60% COD reduction treating the effluent from the kraft pulp mill at an initial pH = 7; although it only reached about a 35% COD removal for the effluent of the recycled paper mill. Otherwise, photocatalysis achieved about a 20–30% reduction of the COD for both type of effluents. In addition, the effluent from the recycled paper mill showed a higher biodegradability, so combinations of these AOPs with biological treatment were tested. As a result, photocatalysis did not report any significant COD reduction improvement whether being performed as pre- or post-treatment of the biological process; whereas the use of ozonation as post-biological treatment enhanced COD removal a further 10%, summing up a total 90% reduction of the COD for the combined treatment, as well as it also supposed an increase of the presence of volatile fatty acids, which might ultimately enable the resultant wastewater to be recirculated back to further biological treatment.

The vanadium redox flow battery (VRFB) has emerged as a promising technology for large-scale storage of intermittent power generated from renewable energy sources due to its advantages such as scalability, high energy efficiency and low cost. In the current study, a three-dimensional(3D) Lattice Boltzmann model is developed to simulate the transport mechanisms of electrolyte flow, species and charge in the vanadium redox flow battery at the micro pore scale. An electrochemical model using the Butler-Volmer equation is used to provide species and charge coupling at the surface of active electrode. The detailed structure of the carbon paper electrode is obtained using X-ray Computed Tomography(CT). The new model developed in the paper is able to predict the local concentration of different species, over-potential and current density profiles under charge/discharge conditions. The simulated capillary pressure as a function of electrolyte volume fraction for electrolyte wetting process in carbon paper electrode is presented. Different wet surface area of carbon paper electrode correspond to different electrolyte volume fraction in pore space of electrode. The model is then used to investigate the effect of wetting area in carbon paper electrode on the performance of vanadium redox flow battery. It is found that the electrochemical performance of positive half cell is reduced with air bubbles trapped inside the electrode.

The oxygen electrodes in unitized regenerative fuel cells (URFC) must have high activities towards oxygen reduction reaction (ORR) as well as oxygen evolution reaction (OER), thus requiring high loading of noble metal electrocatalysts. In this study, porous Pt/IrO2/carbon paper (CP) electrocatalysts were developed to reduce the metal loading. The Pt/IrO2/CP electrodes were fabricated by sequential formation of IrO2 layers (loading 0.1 mg cm−2) and porous Pt layers (0–0.3 mg cm−2) on CP substrates by electrodeposition and spraying techniques, respectively. The fuel cell (FC) performances increased linearly up to 0.69 A cm−2 with increasing Pt loading (up to ~0.3 mg cm−2) at 0.6 V, whereas the water electrolysis (WE) activity was highest at Pt loading of 0.2 mg cm−2. The current densities in the FC and WE modes and round-trip efficiency of the developed Pt/IrO2/CP electrodes with the oxygen electrocatalysts loadings of 0.3 and 0.4 mg cm−2 were higher or comparable to previously reported values with higher loading (1.5–4.0 mg cm−2). These high performances with low loading are probably due to the facile oxygen and water transport through well-developed macropores originating from the open CP structures, providing effective utilization of the IrO2 and Pt electrocatalysts towards OER and ORR, respectively. Keywords: Unitized regenerative fuel cell, Oxygen electrode, Platinum, Iridium oxide

In the paper [Phys. B 550 (2018) 367–375], Alekberov, Isayev, Mekhtiyeva and Fábián have performed very erroneous calculation on diameter of voids responsible for the first sharp diffraction peak (FSDP) in neutron diffraction patterns of As2Se3-based glasses. The authors used wrong relation for the FSDP position taken from entirely speculative assertion presented by Kavetskyy in [Semicond. Phys. Quantum Electron. Optoelectron. 16 (2013) 136–139], assuming unreasonable equivalence between chemistry of chalcogenide glasses and typical polymers. In this communication, the deep reason for this incorrectness was disclosed, and alternative variant to estimate diameters of interstitial voids responsible for the FSDP in As2Se3-based glasses was presented. Keywords: Chalcogenide glass, Neutron diffraction, First sharp diffraction peak, Interstitial void, Positron annihilation

International audience; A fluorescent chitosan derivative was deposited layer-by-layer onto conventional paper sheets and its distribution, in terms of both spreading and penetration, was assessed by SEM observations and emission measurements. The results showed that, on the one hand the surface distribution was highly homogeneous and, on the other hand, the penetration of chitosan within the paper pores ceased after a three layer deposit, beyond which any additional coating only produced an increase in its overall thickness and film-forming aptitude. These results show that this modified chitosan can be used as probe to optimize and understand the mechanism of the deposition of chitosan onto paper and other substrates.

We introduced a strategic "Kinetic Diffusion Multiple" (KDM) that undergoes interdiffusion annealing followed by realistic thermal treatment. The blended spectra of phases and microstructures subjected to treatment in deeply grooved composition gradients enables the microstructure and micromechanical properties of structural materials to be surveyed by high-spatially resolved micro-analysis along the composition arrays. The KDM was demonstrated as a robust high-throughput methodology that enables rapid screening of the composition-microstructure-micromechanical/properties relationships for different metallic materials. It has also proven great success at elucidating the lasting effects of alloying elements and diffusion flux on microstructure, micromechanical properties, phase transformation, and their interrelationships as a whole., This work was supported by the Natural Science Funds of China [Grant No. 51571113], International S&T cooperation Program of China (2015DFA51430) and the Joint Project of Industry-University-Research of Jiangsu Province [Grant No: BY2016005]. CW, NL and JW are grateful to the China Scholarship Council (grant number: 201406290011; 201506020081; 201506890002) for financial support. Yi Chen would like to thank the Natural Science Foundation of Jiangsu Province (Grant No. BK20160291) and the National Natural Science Foundation of China (Grant No. 51601077) for the financial support. The