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• White acrylic paint pigment is slightly alkaline and foxing-resistant. • Acrylic-gesso-coated watercolor paper can be used as an anti-foxing backing. • Acrylic gesso coating is simple & cost-effective against foxing. One of the concerns of watercolor artworks on paper is the natural oxidation process of the paper, leading to the development of unsightly yellow-brown spots referred to as foxing. Historically, efforts to preserve watercolor pieces in museums, institutions, and private collections have relied on intricate and expensive techniques. Unfortunately, these methods are not practical for the broader community of artists and less affluent collectors. Furthermore, the introduction of foreign preservation materials, which can interact with the artwork's components, poses a risk to the original visual appeal. Consequently, watercolor art collections have lost some of their appeal compared to oil paintings on canvases. This study endeavors to offer an alternative, straightforward, and cost-efficient approach to safeguarding watercolor artworks created on high-quality watercolor paper, a type commonly used by typical watercolorists, making it a suitable candidate for this investigation. This approach also avoids introducing additional substances to the artwork. The protective technique involves the application of commercially available acrylic gesso to a fresh sheet of watercolor paper. This gesso-coated paper serves as a backing for framing and displaying the original watercolor artwork, without the need for any foreign preservation materials to be added to the artwork itself. To assess the effectiveness of this protection method, a comparison was made between the foxing tendencies of protected and unprotected paper artworks stored for a decade. These samples were subjected to various analytical techniques, including optical microscopy (OM), confocal laser scanning microscopy (CLSM), field emission scanning electron microscopy with energy dispersive X-ray spectroscopy (FESEM-EDX), X-ray diffraction (XRD), attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), and thermogravimetric analysis (TGA). The results revealed that, when compared to untreated samples, rarely any foxing spots were observed on any of the treated samples, and both the oxidation and degradation of cellulose fibers were diminished. Additionally, the analysis showed that the acrylic gesso comprised inorganic components such as calcium carbonate (CaCO 3), dolomite (CaMg(CO 3) 2), rutile (TiO 2), and organic acrylics. The carbonates created a mildly alkaline environment, neutralizing the acidity in the paper. The titanium dioxides exhibited biocidal and fungicidal properties due to their photocatalytic characteristics. The acrylic component bound and dispersed the inorganic constituents, and the coating formed a less impenetrable barrier layer as indicated by the scanning electron microscopy (SEM) results. In addition to significantly improving the resistance of the paper to foxing, the methods outlined in this study are highly cost-effective and readily accessible to artists and collectors. Importantly, they do not involve the addition of any restoration materials to the original artworks. [ABSTRACT FROM AUTHOR]

[Display omitted] • Food delivery boxes are tested for aerobic disintegration and anaerobic degradation. • Boxes made of paper only or with coatings (including polylactic acid) are analysed. • Paper is highly suitable for biological treatments behaving similarly to food waste. • Aerobic disintegration of coated boxes is much slower than that of paper only boxes. • Undigested polylactic acid coating is found in anaerobic semi-continuous tests. This study evaluated the fate of food delivery boxes when subjected to biological treatments, reproducing at the lab-scale the conditions of full-scale plants. Four paper-based boxes were composted: two made of paper only, one coupled with polylactic acid (PLA), and one with a barrier coating. One paper only box and the box with PLA were also investigated for their anaerobic degradability with biochemical methane potential (BMP) and semi-continuous tests. During composting, the boxes were not recognisable inside the compost after four (paper only boxes), eight (box with PLA), and twelve (box with barrier coating) weeks. In BMP tests, the paper only box showed a degradability similar to that of food waste (92 %), while the box with PLA degraded only at 76 %. Furthermore, undigested pieces of PLA were found in semi-continuous tests. Accordingly, paper resulted suitable for biological treatments, while the presence of PLA or other barrier coatings can be critical. [ABSTRACT FROM AUTHOR]

• Silk and sensitive paper was deteriorated by UV-radiation, NO 2 , and O 3 in museums. • Sensitive paper was also deteriorated by SO 2 at 4 µgm−3 and HCOOH at 50 µgm−3. • Intolerable degradation happened 6–7 times earlier in galleries than in enclosures. This paper reports 1 year of data of the environments and changes in the molecular weight of silk and the degree of polymerization of sensitive paper measured externally and indoors in 10 European museums, and the dose-response functions that were obtained by statistical analysis of this data. The measurements were performed in the EU FP5 project Master (EVK-CT-2002-00093). The work provides documentation of deterioration of silk by NO 2 and O 3 , and alternatively in combination with UV radiation. The indoor deterioration of the silk was only observed in one location with high UV radiation. The indoor deterioration of sensitive paper correlated with the UV radiation, the concentrations of NO 2 and O 3 , and in addition with an SO 2 concentration of 4 µgm−3 and a formic acid concentration of 50 µgm−3 in two different locations. If the observed dose-response effects are linear to lower doses and longer exposure times, then the lifetime to intolerable deterioration of the paper and silk would be 6–7 times longer overall in the enclosures than in the galleries. [ABSTRACT FROM AUTHOR]

• A cost-effective and eco-friendly polyDOPA@paper was prepared for DNA extraction. • The adsorption capacity of polyDOPA@paper for DNA was 20.7 μg cm−2. • An automated extraction system was designed to ensure results consistency. • The DNA extraction platform averts the need for specialized training of operators. • The platform combined with qPCR realized the detection of E. coli in milk samples. The success of polymerase chain reaction (PCR) depends on the quality of deoxyribonucleic acid (DNA) templates. This study developed a cost-effective and eco-friendly DNA extraction system utilizing poly(3,4-dihydroxyphenylalanine)-modified cellulose paper (polyDOPA@paper). PolyDOPA@paper was prepared by oxidatively self-polymerizing DOPA under weak alkaline conditions and utilizing the adhesive property of polyDOPA on different materials. Compared to the uncoated cellulose paper, polyDOPA coating significantly enhances DNA adsorption owing to its abundant amino, carboxyl, and hydroxyl moieties. The DNA extraction mechanism using polyDOPA@paper was discussed. The maximum adsorption capacity of polyDOPA@paper for DNA was 20.7 μg cm−2. Moreover, an automated extraction system was designed and fabricated using 3D printing technology. The device simplifies the operation and ensures the reproducibility and consistency of the results. More importantly, it eliminates the need for specialized training of operators. The feasibility of the polyDOPA@paper-based automated extraction system was evaluated by quantitatively detecting Escherichia coli in spiked milk samples via a real-time PCR. The detection limit was 102 cfu mL−1. The results suggest that the system would have significant potential in detecting pathogens. [ABSTRACT FROM AUTHOR]

Cellulose microspheres (CMS) are a type of spherical regenerated cellulose particles with versatile properties which have been used as carrier materials in medical and technical applications. The integration of CMS into paper products opens up novel application scenarios for paper products in a wide range of fields. However, the incorporation of CMS carriers into paper products is challenging and hitherto no reports do exist in literature. Here, we present a feasibility study to incorporate up to 50 w.% CMS in paper hand sheets using retention aids. Our primary observations highlight the successful formation of uniform paper hand sheets retaining its tensile strengths at elevated CMS concentrations. Sheets with high CMS contents exhibit an increase in density and display enhanced surface smoothness — an outcome of a CMS layer forming atop the fiber base — which effectively bridges voids and rectifies surface irregularities as supported by Gurley testing, infinite focus microscopy and scanning electron microscopy. While our primary objective centered on the general feasibility to manufacture CMS-containing papers, the resulting composite scaffold carries significant potential as a platform for innovative, functional paper-based materials. [Display omitted] [ABSTRACT FROM AUTHOR]

• Hydroxyapatite (HAP) composite paper with biocompatibility and hygroscopicity was prepared. • HAP composite paper has better hygroscopic and triboelectric properties than pure paper, making it more suitable for wearable sensing applications. • The HAP composite paper-based triboelectric nanogenerator can detect and distinguish different joint movements. • Hemostatic and disposable HAP composite paper can be degraded in the natural environment without harm. Wearable triboelectric nanogenerators (TENGs) have attracted considerable attention in the field of self-powered sensors that can be worn on the skin directly without packaging because of their breathability, conformability, and sensitivity to collect biomechanical energy. However, high humidity on the skin can affect the wearable TENG output performance, substantially affecting the sensor performance and stability. When worn for a long time, humidity can even cause skin inflammation. Thus, for a wearable TENG, moisture control and biocompatibility are also key factors that need to be addressed. Herein, we report a hygroscopic and biocompatible paper-based TENG using a hydroxyapatite (HAP) mineral coating to enhance the paper fiber. The mineral coating can maintain the surface of the paper fiber, which will not cause large external deformation of the paper fiber under a force, avoid squeezing out excess water, and keep the friction surface dry, avoiding humidity affecting the output performance. Without interfering with the performance of the TENG, the maximum water absorption of the HAP composite paper is ∼8 μL. The HAP composite paper–based TENG (4 cm2) has an open-circuit voltage and short-circuit current 5.8 times and 4.2 times that of pure paper, respectively, and can obtain 80.4 mW/m2 output and directly light 117 LEDs. At relative humidity values of 25.7 %, 43.1 %, and 58.8 %, the performance retained the peak values of 80.2 %, 68 %, and 63.7 %, respectively. Even at a high relative humidity of 71.7 %, the triboelectric performance of HAP composite paper is retained 59.3 %, and the stability under humidity is better than that of pure paper (45.6 %). In addition, the mineral paper can even work with tissue fluid and output performance decreases by 43.8 %. The mineral-enhanced paper TENG with high power generation performance, hygroscopicity, biocompatibility, and degradability provides a new perspective for disposable wearable sensors, even in medical treatment. [ABSTRACT FROM AUTHOR]

Paper-based packaging is experiencing a resurgence due to its inherent biodegradability and recyclability. To meet the barrier properties required for certain applications, a coating is necessary. This coating must enhance functionality without compromising the environmental sustainability of the substrate. With this goal in mind, we prepared waterborne dispersions of biodegradable poly(lactic acid) (PLA) using a PEG-PLA-PEG triblock copolymer as the main surfactant. We achieved formulations with good stability over a 6-month period and high solids content (∼40 wt%). The waterborne dispersions underwent analysis by dynamic light scattering (DLS), size exclusion chromatography (SEC), gravimetric tests, and rotational rheology with and without xanthan gum (0.2–0.8 wt%) as a thickener. Subsequently, the thickened dispersions were coated at 60 °C onto a paper substrate. SEM analyses revealed the formation of a polymer layer on the paper surface with thickness and morphology dependent on the processing conditions. Partial interpenetration between the coating and the paper fibers was observed, resulting in excellent adhesion between the layers. The coated paper exhibited good barriers to liquid and water vapor, with Cobb60 < 5 g/m2 and water vapor transmission rate (WVTR) < 100 g/(m2∙day) for coating weights ≤15 g/m2, comparable to the performance of solvent-based PLA paper coatings. The surface energy of the coating was approximately 50 dyne/cm, higher than that of neat PLA, making it suitable for printing with common inks. Furthermore, the coated paper can be fully pulped in water, indicating that it can still be recycled in the paper stream, albeit with potentially increased processing time due to the coating weight. [Display omitted] • A PEG-PLA-PEG block copolymer was proven to stabilize waterborne PLA dispersions. • Dispersions with 40 % solid content were obtained. • The dispersions thickened with xanthan gum were successfully coated on paper at 60 °C. • PLA-coated paper had similar water barrier properties to its oil-based counterpart. • Repulping of PLA-coated paper is possible but slower than for uncoated paper. [ABSTRACT FROM AUTHOR]

Sensor arrays, which draw inspiration from the mammalian olfactory system, are fundamental concepts in high-throughput analysis based on pattern recognition. Although numerous optical sensor arrays for various targets in aqueous media have demonstrated their diverse applications in a wide range of research fields, practical device platforms for on-site analysis have not been satisfactorily established. The significant limitations of these sensor arrays lie in their solution-based platforms, which require stationary spectrophotometers to record the optical responses in chemical sensing. To address this, this review focuses on paper substrates as device components for solid-state sensor arrays. Paper-based sensor arrays (PSADs) embedded with multiple detection sites having cross-reactivity allow rapid and simultaneous chemical sensing using portable recording apparatuses and powerful data-processing techniques. The applicability of office printing technologies has promoted the realization of PSADs in real-world scenarios, including environmental monitoring, healthcare diagnostics, food safety, and other relevant fields. In this review, we discuss the methodologies of device fabrication and imaging analysis technologies for pattern recognition-driven chemical sensing in aqueous media. [Display omitted] • Cross-reactive sensors are applied to paper-based arrays for simultaneous detection. • Portable digital recorders can be used for detecting various responses. • Imaging analysis techniques can accelerate accurate data processing. [ABSTRACT FROM AUTHOR]

[Display omitted] • PVC-diphenylamine modified cellulose was proposed as sorptive phase. • The synthesis, using the dip-coating technique, is simple and cost-effective. • Opioids interact with the membrane by a mixed-mode interaction. • Direct infusion mass spectrometry allows to reduce the time of analysis. • The approach was successfully applied to real saliva samples containing codeine and tramadol. This article evaluates the potential of cellulose paper as a substrate for preparing a polyvinylchloride (PVC)-diphenylamine sorptive phase that can be used under the thin film microextraction (TFME) format. This phase was easily synthesized using the dip-coating technique to coat the filter paper with PVC, followed by the covalent bonding of diphenylamine. As a result, aromatics rings are available on paper surface to isolate the target analytes by a mixed-mode interaction at physiological pH. The resulting material was characterized by infrared spectroscopy, UV–Vis diffuse reflection spectroscopy, and scanning electron microscopy. As analytical problem, three opioids (methadone, codeine, and tramadol) were determined in saliva samples by direct infusion mass spectrometry. Different variables involved in the extraction procedure have been optimized (e.g. sample pH, extraction time, and sample dilution). The proposed method provides good linearity (R2 > 0.9817) and sensitivity (detection limits in the range from 1.5 µg L−1 to 15 µg L−1). The intra-day and inter-day precision, expressed as relative standard deviation, were better than 16.4 % and 18.5 % respectively. The accuracy, expressed as relative recovery, provides values in the interval from 82 % to 105 %. Finally, the proposed approach has been successfully applied to real saliva samples of patients under codeine and tramadol medical prescription. [ABSTRACT FROM AUTHOR]

The paper-based triboelectric nanogenerators (PB-TENGs) satisfied the requirement of sustainability and aroused great research interests, however how to improve their outputs still remains as a huge challenge. Most of the reported strategies to enhance the performance of PB-TENG focused on the chemical modification of the friction layers (FL), which may be restricted by the high-cost and cumbersome protocols being required. In this work, a general strategy of interface engineering to boost the outputs of the PB-TENG was proposed and validated by employing graphene composite paper (GC-paper) as electrodes. At the beginning, the hydroxyethyl cellulose (HEC) and Ecoflex were cured as separated films and used as friction layers, which were adhered with copper or GC-paper electrodes. The PB-TENG device can be obtained and possesses acceptable performance. Subsequently, we were surprised to find that the outputs of the PB-TENG largely increased by coating the FLs on the GC-paper rather than adhering. The maximum open-circuit voltage jumped from 300 V to 734 V, and the maximum short-circuit current boosted from 3.4 µA to 8.7 µA. This phenomenon may be ascribed to an interface effect between the FLs and electrodes, which enhanced the electrostatic induction. The strategy of this interface engineering was also proved to be general for other PB-TENG devices with various friction materials. Therefore, it may pave a way for the development of sustainable TENG devices with high performance. [Display omitted] • The output of the paper-based triboelectric nanogenerator (PB-TENG) was boosted. • A general strategy of interface fusion was demonstrated for the high performance. • The interface fusion was realized by coating frication layers on graphene-paper. • The PB-TENG was successfully used for energy harvesting and self-powered sensing. [ABSTRACT FROM AUTHOR]

[Display omitted] • Multi-layer forming technology can integrate triboelectric material with electrode. • The all CPTENGs can exhibit excellent humidity, acid and alkali resistance. • The CPTENGs can yield a V OC , I SC and power density of 227.1 V, 6.9 μA and 520 mW/m2. • Matching CPTENGs with P-ZISC can obtain a self-charging power system (PSCPS). • The PSCPS can drive some miniaturized electronics for a long time. Triboelectric nanogenerators (TENGs) are regarded as a promising technology to drive the development of flexible/wearable electronics and self-powering sensor. Application of cellulose paper as the triboelectric positive materials makes TENGs more environmentally friendly. However, the limited output performance and stability in harsh environments and oxidation and corrosion of the metal electrodes have limited the practical application of cellulose paper based triboelectric nanogenerators (CPTENGs). Here, we have integrated cellulose paper-based triboelectric material and electrode in one sheet by using multi-layer forming technology in paper industry; the upper triboelectric layer shows excellent triboelectric positive performance, hydrophobicity and acid and alkali resistance, while the bottom electrode exhibits promise conductivity. The all CPTENGs can yield a maximum open-circuit voltage (V OC) of 227.1 V, a short-circuit current (I SC) of 6.9 μA. Furthermore, the V OC values of the all CPTENGs increase from 0.02 V to 225.1 V at the load resistance of 100 Ω∼10 GΩ; and a power density of 520 mW·m−2 is also obtained at a load resistance of 30 MΩ. Moreover, the V OC of CPTENGs not only retains up to 78 % of its initial value at a high relative humidity of 90 %, but also almost maintains unchanged in a wide range of the pH environment (pH = 1∼13). More importantly, the CPTENGs can be readily matched with paper-based zinc supercapacitor (P-ZISC) to act as an all paper based self-charging power system (PSCPS). The PSCPS is capable of driving various miniaturized electronics, such as electronic watch, temperature/humidity indicator, demonstrating its potential application in a sustainable power source for portable and green electronics. [ABSTRACT FROM AUTHOR]

Cu2+ contamination and food spoilage raise food and drinking water safety issues, posing a serious threat to human health. Besides, Cu2+ and H 2 S levels indicate excess Cu2+-caused diseases and protein-containing food spoilage. Herein, a coumarin-containing bifunctional paper-based fluorescent platform integrated with a straightforward smartphone color recognition app is developed by an all-in-one strategy. The proposed fluorescent materials can simultaneously detect Cu2+ and H 2 S for on-demand food and drinking water safety monitoring at home. Specifically, a coumarin-derived fluorescence sensor (referred to as CMIA) with a low detection limit (0.430 μM) and high-selectivity/-sensitivity for Cu2+ is synthesized through a simple one-step route and then loaded onto commercially used cellulose fiber filter paper to engineer a biomass-based fluorescent material (CMIA-FP). The CMIA-FP offers user-friendly, high-precision, fast-responsive, and real-time visual monitoring of Cu2+. Moreover, CMIA forms a chemically stable complex with Cu2+, loaded onto filter paper to prepare another biomass-based fluorescent platform (CMIA-CU-FP) for visual real-time monitoring of H 2 S. Based on the exquisite composition design, the proposed dual-function paper-based fluorescent materials equipped with a smartphone color recognition program concurrently realize fast, accurate, and easy real-time monitoring of Cu2+ in drinking water and H 2 S in chicken breast-/shrimp-spoilage, demonstrating an effective detection strategy for the Cu2+ and H 2 S monitoring and presenting the new type of biomass-based platforms for concentrated reflection of drinking water and food safety. [Display omitted] • On-demand platform enabling simultaneously home-detecting Cu2+/H 2 S was proposed. • The platform realizes user-friendly, low-cost, fast-response detecting of Cu2+/H 2 S. • The platform achieves real-time monitoring of drinking-water and meat-storage safety. • The study provides effective tactics for the integrated Cu2+ and H 2 S home-detecting. [ABSTRACT FROM AUTHOR]

• Efforts to enhance PMFC performance are reviewed. • Both exciting advancements and current limitations are discussed. • An innovative strategy of multi-scale simultaneous optimization is proposed. Paper-based microfluidic fuel cell (PMFC) has attracted great attention in the microfluidic fuel cell field in recent years. It utilizes the spontaneous capillary flow of reactant solutions in paper-based porous substrate to achieve passive transportations of fuel and oxidant, solving the fluid driving issue encountered in traditional microfluidic fuel cells and thus having broad application prospects in medical detection, wearable devices, micro sensors, environmental monitoring, and many other fields. However, the commercialization of this technology is impeded by the low output performance caused by the limited mass and energy transfer in PMFCs. To enhance the mass and energy transfer in PMFCs, numerous research studies have been conducted via experimental optimization of the cell materials and structures. Numerical analyses focusing on the structure–activity relationship of PMFCs were also performed recently. To provide a comprehensive and thorough review about the efforts devoted to improving performance of PMFC, research papers relevant to PMFC since its invention in 2014 have been extracted in this work and significant works were filtered to highlight the exciting advancements. The experimental studies were classified and discussed based on the key components involved in the PMFC system, followed by a critical review of the limited computational models. Potential directions for future research were also provided, aimed at overcoming the current technological challenges in PMFCs. Importantly, an innovative strategy of multi-scale simultaneous optimization of the cell properties is proposed considering the typical multi-scale feature of the PMFC system, which could inspire the designing of advanced cell materials with optimal multi-scale structures for applications of PMFCs. [ABSTRACT FROM AUTHOR]

Frequent oceanic oil spill incidents and the discharge of industrial oily wastewaters have caused serious threats to environments, food chains and human beings. Lignin wastes with many reactive groups exist as the byproducts from bioethanol and pulping processing industries, and they are either discarded as wastes or directly consumed as a fuel. To make full use of lignin wastes and simultaneously deal with oily wastewaters, porous lignin-based composites have been rationally designed and prepared. In this review, recent advances in the preparation of porous lignin-based composites are summarized in terms of aerogels, sponges, foams, papers, and membranes, respectively. Then, the mechanisms and the application of porous lignin-based adsorbents and filtration materials for oil/water separation are discussed. Finally, the challenges and perspectives of porous lignin-based composites are proposed in the field of oil/water separation. The utilization of abundant lignin wastes can replace fossil resources, and meanwhile porous lignin-based composites can be used to efficiently treat with oily wastewaters. The above utilization strategy opens an avenue to the rational design and preparation of lignin wastes with high-added value, and gives a possible solution to use lignin wastes in a sustainable and environmentally friendly way. [ABSTRACT FROM AUTHOR]

Predictive models for the transport of volatile organic compounds in paper need to consider the complex interplay of diffusion, adsorption, desorption, or chemical reactions. The relative importance of each of these processes is determined by the polarity of the volatile. Hence, it is challenging to pick a valid theoretical model that correctly predicts transport regardless of the polarity. Here, physics-informed neural networks (PINNs) assess which of five different models correctly describe transport of DMSO as polar and n-tetradecane as apolar model compound: (i) a pseudo first-order adsorption model for an irreversible sorption process, (ii) a first-order kinetics model allowing reversible sorption, (iii) a second-order model with a reversible process, and an effective diffusion model accounting for a constant (iv) and for a variable effective diffusivity (v). Each tested model is given as set of partial differential equations (PDE). Considering the model under testing and experimentally obtained spatially and temporally resolved concentration profiles through stacks of paper sheets, PINNs predict concentration of the volatiles and associated material constants such as sorption constants and effective diffusion coefficients by solving the inverse problem. Our PINNs revealed two models, pseudo first-order sorption and second-order reversible sorption, that correctly predict concentration profiles and polarity-driven differences in sorption times. While a PINN-based picking of valid transport models has important implications for the development of effective methods for controlling emission of volatiles from paper materials, PINNs represent a versatile mathematical tool to validate or refute the capability of PDE-based theoretical models to describe experimental data. • PINNs evaluate sorption kinetics in porous materials. • Focus: Transport of organic volatiles in cellulose. • Pseudo first-order model suits organic volatiles. • Predicting transport of volatiles through paper. [ABSTRACT FROM AUTHOR]

[Display omitted] • Honeycomb panels with discrete arranged block reinforcements were numerically designed. • The elastic moduli of the new honeycomb panels are higher than those of heavier panels with slatted. • Tables with new cellular panels are characterized by a stiffness of 85 % of the stiffness of heavier tables with slats. Furniture manufacturers indicate they know the benefits of lightweight honeycomb panels but still expect their higher mechanical properties. This work presents a numerical and experimental approach to designing new tables manufactured of paper honeycomb panels with discreetly arranged reinforcing blocks in the core. The main goal was to determine whether the discrete arrangement of the blocks affects the strength and amount of energy absorbed by the newly designed tables and stiffness of honeycomb panels. Optimization reduced the weight of the panels by up to 30 %. At the same time, their linear elastic modulus was increased from 1579 MPa to 1771 MPa. After ten load cycles, tables with discrete reinforcements have a stiffness up 86.85–87.20 % of the stiffness of the reference table. After destructive tests up 89.96–91.16 %. Ultimately, the test results demonstrate the effectiveness of replacing wide slats with discreetly placed reinforcing blocks in the core structure. [ABSTRACT FROM AUTHOR]

Liquid penetration in porous cellulosic materials is crucial in many technological fields. The complex geometry, small pore size, and often fast timescale of liquid uptake makes the process hard to capture. Effects such as swelling, vapor transport, film flow and water transport within cellulosic material makes transport deviate from well-known relations such as Lucas-Washburn and Darcy's Law. In this work it is demonstrated how Ultra-Fast Imaging NMR can be used to simultaneously monitor the liquid distribution and swelling during capillary uptake of water with a temporal- and spatial resolution of 10 ms and 14.5–18 μm respectively. The measurements show that in a cellulose fiber sheet, within the first 65 ms, liquid first penetrates the whole sheet before swelling takes place for another 30 s. Furthermore, it was observed that the liquid front traps 15 v% of air which is slowly replaced by water during the final stage of liquid uptake. Our method makes it possible to simultaneously quantify the concentration of all three phases (solid, liquid and air) within porous materials during processes exceeding 50 ms (5 times the temporal resolution). We hence believe that the proposed method should also be useful to study liquid penetration, or water diffusion, into other porous cellulosic materials like foams, membranes, nonwovens, textiles and films. [Display omitted] [ABSTRACT FROM AUTHOR]

• An attempt to characterize thin, low impedance paper at various high strain-rates. • The creation of a digital twin of the physical Split Hopkinson Test bench. • To demonstrate that there can be distortions of the transmitted measuring signal. This work deals with the high strain-rate characterization of paper under uniaxial tension using a Split Hopkinson test bench. An aluminum bar system featuring a highly sensitive hollow transmission bar was used. Paper tests were performed in a strain-rate range between approximately 60 s−1 and 210 s−1. The experimental tests showed that the breaking strength appears to decrease with increasing strain-rate. To verify these results, a digital twin of both the paper specimen and the entire test rig was created in an explicit Finite Element method environment. The numerical model was then used to perform a parameter study with different types of transmission bars. It was shown that the system is quite sensitive to additional masses caused by the specimen fixtures, as well as to drastic reductions in the cross section of the transmission bar. As a result, the transmitted measuring signal can be distorted and may need to be corrected using the digital twin. [ABSTRACT FROM AUTHOR]

[Display omitted] • Molecular-level light-emitting origins were strategically imparted to paper. • The morphology of AIE self-assembly can be adjusted on demand. • AFP-FP exhibited high selectivity, sensitivity and repeatable recognition of NH 3. • AFP-FP integrated with smartphone realized the visual food spoilage monitoring. Biogenic amines containing NH 3 are important indicators for conducting full-scale appraisal of food spoilage and disease diagnosis. However, the currently-used detection methods of NH 3 have several limitations such as time-consuming high cost, and inability to provide visual real-time monitoring. Therefore, researchers have attempted to explore strategies for quantitative real-time monitoring of NH 3 for food spoilage has attracted widespread attentions. Herein, we developed sustainable, fast response, hypersensitized, user-friendly and molecular-level light-emitting biomass-based materials (AFP-FP) containing on-demand nanostructured brain-cells-inspired aggregation-induced-emission (AIE) self-assembles for real-time visual monitoring of seafood spoilage. The 2-hydroxy-5-methyl-isophthalaldehyde-based AIE probe (AFP) was synthesized using a simple "one-step" route. AFP-FP exhibited high selectivity, sensitivity, repeatable and quantitative recognition (y = 7.292×103x + 7.621×104, R = 0.990) of NH 3 with a low detection limit (246 ppb) and fast response (<1 s). Furthermore, we integrated AFP-FP into a user-friendly smartphone color recognition app, enabling its practical application in visual, real-time daylight monitoring of food spoilage. [ABSTRACT FROM AUTHOR]

[Display omitted] • An visual distance-based paper analytical device has been developed for on-site detection of Pb(II). • Pb(II) can inhibit the catalytic activity of G4/hemin DNAzyme induced by K+. • The biosensor can sensitively detect Pb(II) with a lowest detection limit of 1 nM. • The biosensor can be applied to detect Pb(II) in real samples. A simple, inexpensive, fast, and visual distance-based paper analytical device has been developed for on-site detection of Pb(II). Pb(II) can inhibit the catalytic activity of G-quadruplex/hemin (G4/hemin) DNAzyme induced by K+, which catalyzes 3,3,5,5-tetramethyl benzidine (TMB) immobilized on paper to produce a visible blue band. The factors affecting Pb(II) detection have been optimized with PS concentration of 3 μM, K+ concentration of 10 mM, and hemin concentration of 10 μM, as well as the straight channel width of 2.0 mm. It can be well found that the formed length correlates with the concentration of Pb(II) with a linear detection range of 0.02 μM − 50 μM. A fitting linear equation of Y = 20.793–5.391Log C (R2 = 0.9788) can be obtained with a lowest detection limit of 1 nM. Additionally, the method is capable of selectively detecting Pb(II) and works well for Pb(II) detection in real samples. Overall, the visual distance-based paper analytical device offers an ideal platform for on-site detection of heavy metal ions, especially in resource-limited areas. [ABSTRACT FROM AUTHOR]

Deoxyribonuclease I (DNase I) is a biomarker which has important applications in various biological processes. Thus, it is highly important to develop a user-friendly method for the detection of DNase I. Here, we present a paper-based distance sensor for the rapid detection of DNase I based on changes in the viscosity of DNA mucus. The viscosity of DNA mucus varies with different concentrations of DNase I, showing different water flow lengths on the pH test papers, this makes the quantification of DNase I possible. This method has a wide linear range (0.01–10 U/mL), excellent sensitivity, remarkable specificity and excellent reproducibility. The detection limit reaches 0.003 U/mL. Additionally, it can be well applied to detection of DNase I inhibitors, assay of DNase I in human serum and quality evaluation of nucleic acid scavengers. In general, this study offers a brief, convenient, label-free, and economical method to construct paper-based distance sensors using DNA mucus, which is very promising in the detection of DNase I in various applications. [Display omitted] • The paper-based sensor detects DNase I by distance signal. • The new method for detecting DNase I based on viscosity changes. • The detection limit for DNase I is 0.003 U/mL. • The sensor shows excellent specificity, remarkable practicality and portability. [ABSTRACT FROM AUTHOR]

An effective strategy was demonstrated to design an electromagnetic interference (EMI) shielding paper via a facile surface treatment on paper. TEMPO-oxidized cellulose nanofibers (TOCN) were first integrated with Ti 3 C 2 T x MXene, and subsequently cast onto a filter paper with cationic guar gum (CGG) in a sequential way. TOCN and CGG generated a self-assembling hydrogel and formed a MXene-containing hydrogel film on top of the filter paper. The hydrogel film enhanced the tensile strength (9.49 MPa) of composite paper, and resulted in a 17 % increase as compared to the control. The composite paper containing 80 mg MXene (namely, 2.07 mg·cm−2) showed a conductivity of 3843 S·m−1 and EMI shielding effectiveness (EMI SE) of 49.37 dB. Furthermore, the 2-layer assembled TC-M 80 hydrogel composite paper achieved an EMI SE of 73.99 dB. Importantly, this composite paper showed higher EMI SE and lower thickness than a lot of reported materials. The presence of TOCN and CGG also protected MXene against several solvents and the incorporation of polydimethylsiloxane (PDMS) further improved the durability of the composite paper. This work provides a novel and simple strategy to design robust, ultrathin and flexible EMI shielding materials, and it might also inspire other work in paper-based functional materials. [Display omitted] [ABSTRACT FROM AUTHOR]

Xylan is primarily found in the secondary cell wall of plants providing strength and integrity. To take advantage of the reinforcing effect of xylan in papermaking, it is crucial to understand its role in pulp fibers, as it undergoes substantial changes during pulping. However, the contributions of xylan that is added afterwards (extrinsic) and xylan present after pulping (intrinsic) remain largely unexplored. Here, we partially degraded xylan from refined bleached softwood kraft pulp (BSKP) and adsorbed xylan onto BSKP. Enzymatic degradation of 1 % xylan resulted in an open hand sheet structure, while adsorption of 3 % xylan created a denser fiber network. The mechanical properties improved with adsorbed xylan, but decreased more significantly after enzymatic treatment. We propose that the enhancement in mechanical properties by adsorbed extrinsic xylan is due to increased fiber-fiber bonds and sheet density, while the deterioration in mechanical properties of the enzyme treated pulp is caused by the opposite effect. These findings suggest that xylan is decisive for fiber network strength. However, intrinsic xylan is more critical, and the same properties cannot be achieved by readsorbing xylan onto the fibers. Therefore, pulping parameters should be selected to preserve intrinsic xylan within the fibers to maintain paper strength. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] • For the first time the root cause for paper curl developing over days and weeks is described. • The curl of the paper sheets is caused by migration of co-solvents (e.g., glycerol) from the inkjet ink. • A 2D-laser scanner is utilized to investigate short- and long-term paper curl. • Glycerol migration in paper sheets is monitored using a combination of sheet splitting and subsequent HPLC analysis. The dimensional stability of paper during printing is crucial for ensuring production quality and runnability. However, inkjet printing faces inherent challenges due to the hygroscopic nature of paper and the use of water-based inks. Despite freshly printed sheets are flat, a considerable development of paper curl is often observed during storage. In this study, we establish the link between the migration of ink co-solvents and the long-term curl development of printed paper. A4 paper sheets were sprayed with a water-glycerol model ink and changes in the sheet's curvature were monitored using a 2D-laser sensor. We also investigated glycerol migration by splitting the sheets into layers and determining the glycerol distribution using high-performance liquid chromatography. Our results demonstrate the development of curl during storage as well as glycerol migration in thickness direction of the sheet, both on a comparable timescale. We thus propose that long term curl in inkjet printing can be caused by z-directional migration of the co-solvent (glycerol) over time. This study enhances understanding of the physical mechanisms that drive the long-term curl phenomenon in inkjet-printed sheets. The results can be used to optimize printing processes, allowing for the production of higher quality printed products with greater dimensional stability. [ABSTRACT FROM AUTHOR]