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• Pulp and paper mill sludge (PPMS) landfill sites have GHG assessment challenges. • GHG fluxes measured by chambers with (F +) and without (F-) a frame were compared. • Flux relationships up to 80 % were shown between F- and F + chambers (the standard) • Correction factors for F- chambers were built to estimate fluxes from F + chambers. • The approach can refine GHG inventories on PPMS landfill sites. Assessments of greenhouse gas (GHG) emissions in managed areas are facing various challenges. A non-flow-through, non-steady-state (NFT-NSS) chamber coupled to a frame permanently inserted into the landfilled substrates is a standard method for quantifying GHG emissions in managed areas, such as pulp and paper mill sludge (PPMS) landfill sites. Frequent measurements are needed to minimize uncertainties on GHG emission factors at the landfill site scale. However, maintaining a frame inserted into the substrates for a long time period is often impossible due to landfilling management operations. Therefore, GHG measurements using NFT-NSS chambers placed directly on substrates' surface could be an interesting option. Our objectives were to determine the relationships between CO 2 , CH 4 , and N 2 O fluxes measured with (F +) and without (F-) a frame inserted in the substrates' surface and to develop correction factors for fluxes measured without a frame. Measurements were made at different PPMS landfill sites in the province of Québec, Canada. Stronger GHG flux relationships were observed at the provincial (across sites) than the specific site scale: the variance in GHG fluxes from F- chambers explained up to 80 % of variance in fluxes from F + chambers. The measured CO 2 , CH 4 , and N 2 O fluxes in F- chambers were on average 53, 78, and 63 % lower, respectively, than those estimated by the models at provincial scale. The correction factors developed with this approach could greatly extend the number of sites where in situ GHG measurements can be done and would help refining GHG inventories at the provincial and national levels. [ABSTRACT FROM AUTHOR]

Carbon paper is one of the most widely used gas diffusion layer substrate materials due to its stable performance, relatively low cost, and easy for subsequent processing. Water-soluble phenolic resin, which is more ecologically friendly than alcohol-soluble phenolic resin, was used to prepare carbon paper as the precursor of the carbon matrix. And the effect of different resin solution concentrations on the properties of carbon paper was explored. The results showed that the graphitization, electrical conductivity and mechanical properties of carbon paper increased with the increase of resin solution concentration. When the concentration of resin solution was 20 wt%, the performance of carbon paper was relatively optimal. The graphitization of the carbon paper reached 65.45%, the porosity reached 80.74%, the resistance value at 1 MPa pressure was only 7.61 mΩ cm2, the tensile strength was 1.57 MPa, and the elastic modulus was 1210.98 MPa. [ABSTRACT FROM AUTHOR]

Carbon paper as a macroporous substrate of gas diffusion layer in proton exchange membrane fuel cells directly impacts the output performance of cells. In this study, we present a straightforward strategy to improve the overall performance of carbon paper by mixing short/long (6mm/10 mm) chopped carbon fibers at an optimal concentration of phenolic resin. The results show that incorporating longer carbon fibers can increase the porosity, conductivity, gas flux, and mechanical properties of carbon paper. The membrane electrode assembly achieved a peak power density of 1182.61 mW cm−2 at 60% RH using carbon paper with a long carbon fiber content of 40 wt% and an impregnation concentration of 10 wt%. This outperforms commercially available carbon paper. Based on electrochemical impedance spectroscopy results, it was confirmed that our carbon paper had a lower mass transfer resistance of only 32.17 mΩ cm−2 under conditions of 2 A cm−2 and 60% RH. This was due to its sparser three−dimensional network-like pore structure which was created by mixing different lengths (6mm/10 mm) of carbon fibers. This work provides new insights into preparing high−performance carbon papers. • The nature of carbon paper is regulated by mixing short/long (6mm/10 mm) CFs ratio. • The long carbon fiber contents of 20–40 wt% present better physical properties. • The optimal carbon papers can mitigate mass transfer resistance. • MEA composed of the optimal CP shows a higher power density than commercial CP. [ABSTRACT FROM AUTHOR]

A facile method is proposed in this work to prepare a carbon paper (CP) with outstanding properties by doping boron to catalyze graphitization at lower temperature. Boron was introduced into CP by impregnating carbon fiber preform into a boron/phenolic resin/ethanol solution, and then CP was obtained after the consecutive procedures of hot pressing, carbonization, and graphitization. Morphology, microstructure, composition, and physical properties of the doped and undoped CPs were thoroughly investigated via various techniques to exam the effects of boron concentration and graphitization temperature. Furthermore, the boron doped CP was fabricated into fuel cell gas diffusion layer (GDL) and membrane electrode assembly (MEA) to evaluate its performance through the single cell performance. The findings indicated CP doping with 2 wt% boron could lower the graphitization temperature by at least 200 °C. The B-doped GDL had a higher power density in comparison with the undoped GDLs made in our lab or from the commercial brands. • The innovative preparation method for carbon paper with high conductivity. • The effect of boron concentration and graphitization temperature on carbon paper. • The single cell performance of B-doped gas diffusion layer. [ABSTRACT FROM AUTHOR]

Development of low-cost, efficient, and stable oxygen evolution electrocatalysts is crucial for the conversion and storage of renewable energy. Therefore, an effective integrated heterostructure catalyst is needed to achieve a lower overpotential during oxygen evolution process. In this paper, cobalt-zinc bimetallic MOF precursors are used as templates to prepare bimetallic cobalt-based selenides with good oxygen evolution catalytic activity and stability on carbon fiber paper. Due to the high specific surface area and porous structure of the coupling structure of nanorods and polyhedra, and the strong electronic coupling between CoSe 2 and ZnSe on nanorods. CoSe 2 -ZnSe/CP exhibits excellent electrocatalytic activity in 1 M KOH solution. It only requires an overpotential of 275 mV to reach the current density of 10 mA cm-2, and the Tafel slope is 68.9 mV dec-1. In addition, after 12 h of continuous operation of CoSe 2 -ZnSe/CP, the activity decay of the catalyst is negligible. This work provides a method for the design of heterogeneous bimetallic selenide integrated oxygen evolution electrocatalysts. [Display omitted] • The CoSe 2 -ZnSe/CP catalyst is obtained by selenization of MOF precursor at high temperature. • The catalyst has unique nanorod-coupled polyhedral morphology and high specific surface area. • The strong electron coupling between CoSe 2 and ZnSe improves the oxygen evolution activity. • CoSe 2 -ZnSe/CP exhibits low overpotential, high exchange current density and fast kinetics. [ABSTRACT FROM AUTHOR]

The solar photocatalytic degradation of pulp and paper mill wastewater has been reported by several scientists. However, this is the first time we are reporting for solar photocatalytic hydrogen production from pulp and paper mill wastewater and simultaneous degradation of pollutants. In this work, CuO based photocatalysts and novel square type photocatalytic reactor of 5 L capacity were used. The result shows that the prepared photocatalysts are solar active, efficient in hydrogen recovery and pollutant degradation from the pulp and paper wastewater. The effects of catalyst loading, sacrificial agent, pollutant removal efficiency and stability check were investigated. At 0.25 g/L of CuO/Fe 2 O 3 , 0.2 M of sacrificial agent (Na 2 SO 3 2−) and hydrogen yield of 1000 mL from 1000 mL of wastewater was achieved. The removal efficiency of TSS, TDS, BOD, COD, turbidity and TOC are around 70, 50, 60, 65, 70 and 45% respectively. Reusability study revealed that CuO/Fe 2 O 3 was chemically stable and could be reused successively (five cycles) without significant changes in its photoactivity and intrinsic properties. [Display omitted] • Visible light active CuO mixed with novel metal oxides were employed. • Hydrogen recovery from black liquor, paper mill wastewater were 1000 mL/h/L and 850 mL/h/L. • Efficiency of degradation of pulp & paper wastewater chemicals were around 50–70%. • AcHieved high recovery of hydrogen from pulp & paper wastewater. [ABSTRACT FROM AUTHOR]

Enzymes derived from microbial sources have gained increasing popularity in industrial applications over the past decades. Despite the high production cost, alkaline proteases have wide applications in industries such as tanneries, food production, and detergents. In recent years, there has been a shift towards utilizing natural carbon sources for cultivating microorganisms and extracting proteases in order to reduce production costs. This study aimed to investigate the biochemical and kinetic properties of protease enzymes obtained from Aspergillus niger cultivated in a paper waste medium and compare with the enzyme produced in a basal medium. Glucose is a more favorable carbon source compared to cellulose, so paper waste was pretreated with cellulose-degrading bacteria to convert cellulose into smaller carbohydrates. After the growth of A. niger in basal and combinational media, the enzymatic properties were compared between the extracted enzymes by using casein as substrate. The results demonstrated that A. niger could produce protease enzymes in the paper waste medium similar to the basal medium with more than 5-fold cost saving. The specific activity of the enzymes isolated from the basal and paper waste media was calculated to be 184.95 ± 10.56 U ml−1 and 169.88 ± 11.05 U ml−1, respectively. Carbon sources did not affect the optimum pH and temperature of the protease enzyme, which were found to be 8 and 37 °C, respectively. This study provides valuable insights into the production of alkaline protease from A. niger using a combinational medium (paper waste pretreated by cellulose-degrading bacteria), offering a cost-effective approach for industrial applications. [ABSTRACT FROM AUTHOR]

The Proton Exchange Membrane Fuel Cell (PEMFC) performances are strongly impacted by the compression of the Gas Diffusion Layer (GDL). Despite its fibrous microstructure, this material is usually considered as a continuous medium and characterized with uniform loading. However, the GDL is subjected to a heterogeneous compression onto rib/channel patterns in the fuel cell assembly. In the present study, a complex behavior of the GDL response is experimentally revealed when the material is loaded with a rib/channel pattern, compared to uniform compression. The tests are simulated by finite element modeling using a classical strain-dependent elastic law, using parameters fitted from uniform compression experiments. It is shown that the numerical results do not reproduce the effect of pattern observed experimentally. Hypotheses to interpret these results involve mechanisms at the fiber microscale including fiber fracture, cross-link breakage and fiber rearrangement, which are exacerbated by larger material deformation caused by the heterogeneous loading. • Unexpected impact of rib/channel patterns on GDL compression. • Experimental investigation of the effect of rib/channel width on GDL deformation. • Numerical study with classical model unable to reproduce experimental results. • Interpretations based on mechanisms at the fiber microscale. [ABSTRACT FROM AUTHOR]

• The PBAT/PLA coated paper shows high methane yield under AD condition. • Plastic film residues remain after the digestion of PBAT/PLA coated paper. • The decrease of hydrophobicity for PBAT/PLA bags is due to the formation of PLA monomers. • The bacterial community shows difference between PBAT/PLA coated paper and bags. • Methanoculleus is enriched on the plastic surface under mesophilic AD. Poly (lactic acid) (PLA) and Poly(butylene adipate-co-terephthalate) (PBAT) are two of biodegradable plastics with the highest production capacities in 2021. Bioplastic waste management can be easily integrated with organic waste management, especially when bioplastics are used as food packaging material, since they are potentially biodegradable. The aim of this study was to assess the biodegradability of biodegradable polymer-coated paper (BPCP) and bioplastic bags made from PBAT/PLA blend during mesophilic and thermophilic anaerobic digestion (AD) and to reveal the changes in the physicochemical properties of the bioplastics. BPCP obtained 155 NmL-CH 4 /g VS and 307.3 NmL-CH 4 /g VS under mesophilic and thermophilic conditions, respectively, but left bioplastic film residues. The bioplastic bags did not exhibit significant biodegradation during the AD processes. 1H NMR results indicated that the ratio of PLA to PBAT decreased significantly after AD of the BPCP film and that PLA monomers were formed from the bioplastic bags, leading to a decrease in the hydrophobicity on the surfaces of the materials. Methanoculleus was found to be enriched on the bioplastic surface after mesophilic AD. From the perspective of coupling bioplastic waste management with the food waste management, the incorporation of BPCP into the AD reactor not only enhances system stability and methane production to a greater extent than biodegradable plastic bags but also raises concerns regarding the residual biofilm when utilizing the digestate for direct land applications. [ABSTRACT FROM AUTHOR]

This paper describes the fabrication and characterization of porous SiC ceramics derived from highly-filled preceramic papers. The SiC ceramics were obtained by spark plasma sintering of stacked preceramic papers at temperatures of 2100 and 2200 °C under pressures of 5–60 MPa for 10 min. The microstructure and phase composition were analyzed by scanning electron microscopy and X-ray diffraction, respectively. Gas permeation tests were performed using hydrogen permeation cell at room temperature. It is revealed that the porosity of sintered SiC can be varied from 9 to 45 % depending on the sintering parameters. The shrinkage of the materials during spark plasma sintering occurs in four stages. The linear shrinkage value of the material increases from 7 to 47 % at 2100 °C and from 20 to 50 % for the samples sintered at 2100 and 2200 °C, respectively. Correlation dependencies between porosity and mechanical properties of the fabricated SiC were established. The obtained porous SiC ceramics exhibit high bending strength of 165 MPa and gas permeation flux of 78 molH 2 /m2/s at the porosity of 36 % that make it suitable for ceramic-based membranes. [ABSTRACT FROM AUTHOR]

As a H 2 O 2 electrochemical biomimetic enzyme sensor, the stability, repeatability and sensitivity of hemin-based composites are closely connected with the loading of hemin on high-performance matrix. Herein, polypyrrole/paper-derived carbon (PPy/PC) nanocomposite was used for the construction of a hemin-based non-enzymatic sensor to detect H 2 O 2. Where the poplar wood is used to obtain crude cellulose through a straightforward paper-making process. This crude cellulose is then subjected to pyrolysis to yield the desired paper-based carbon material. The hemin-decorated PPy/PC was demonstrated possessing remarkable electrocatalytic activity for H 2 O 2 reduction, and the possible mechanism of the reactions was discussed. The electrochemical sensor, utilizing the H-PPy/PC composite, achieved a low detection limit of 30 ​nM, along with enhanced selectivity and stability under optimized conditions. The favorable results observed can primarily be attributed to the superior electrochemical performance of PPy/PC, as well as its unique 3D interconnected structure. This structure effectively impedes the self-dimerization of hemin, thereby ensuring the generation of active catalytic species. [ABSTRACT FROM AUTHOR]

The large-scale development of flexible electrode is urgently needed for water electrosplitting. Herein, the common and low-cost filter paper (FP) is utilized as the substrate to adjust the flexible property of the catalytic electrode. Through an electroless plating method, the NiFeP alloys were deposited onto the filter paper, which acted as the flexible and self-supported electrode for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The resultant NiFeP@FPs require low overpotentials of 158 mV for HER and 282 mV for OER to deliver a current density of 10 mA cm−2, and exhibit a good stability of 30 h in 1 M KOH. The synergistic effect of Fe–Ni sites regulates electron structure and boosts the catalytic activity. Benefited from good hydrophilicity and interlaced fiber structure of filter paper, electrolyte penetration and electron transfer in the sample are promoted. The assembled two-electrode electrolyzer only requires 1.814 V to achieve 100 mA cm−2 for overall water splitting and shows excellent stability. This work provides a new strategy for the development of flexible and efficient electrodes for water splitting, which advances the development of wearable electronic devices. [Display omitted] • The flexible filter paper-based electrode was successfully synthesized. • The good hydrophilicity and porous structure facilitated electrolyte permeation. • The sample required low overpotentials of 158 mV for HER and 282 mV for OER. • The two-electrode electrolyzer provided 100 mA cm−2 at a low voltage of 1.814 V. [ABSTRACT FROM AUTHOR]

Aerogel composites reinforced by fibers have found extensive applications in the field of thermal insulation and energy conservation. However, the composites are hindered by their high infrared radiation transmittance and weak interface adhesion in practical applications. Herein, we designed and prepared a novel thin composite called 'fiber/whisker/aerogel paper' (SWAP) with a thickness of less than 1 mm. The SWAP integrated SiC nanowhiskers (SiC nw) as opacifiers and ultrafine SiO 2 fibers as reinforcement, fabricated through wet manufacturing and sol-gel process. The 'fiber/aerogel paper' (SAP) and SWAP exhibited low thermal conductivity at room temperature, measuring 0.025 W/(m·K) and 0.033 W/(m·K), respectively. Additionally, they exhibited low densities of 0.195 g/cm3 and 0.225 g/cm3, respectively. Notably, SWAP exhibited excellent high-temperature insulation performance, primarily due to its low infrared transmittance (50% at 3 μm). The incorporation of SiC nw and ultrafine SiO 2 fibers collectively enhanced the interfacial adhesion with the aerogel matrix even amidst rigorous testing (weight loss less than 3%). SWAP also demonstrated flexibility, high thermal stability, hydrophobicity, and flame resistance. Furthermore, a comprehensive investigation into the performance variations and influencing g factors of the material was conducted under different heat treatment conditions. This research provides guidance for the application of such materials under high temperatures. [ABSTRACT FROM AUTHOR]

The ZrO 2 fiber paper exhibits excellent thermal insulation properties, however, its limited mechanical strength and insufficient thermal stability hinder its widespread applications. The composite fiber papers, using mullite fibers possessing a high aspect ratio and exceptional thermal stability combined with ZrO 2 fibers, were fabricated via a vacuum-assisted filtration method. This method involved the successive stacking of composite fibers with alumina sol, using vacuum-induced directed water flow to create a layered structure reminiscent of nacre. The layered structure of the nacre, which demonstrates remarkable strength and hardness, has also served as a source of inspiration for the architectural design of the fiber paper. The tensile strength of pure ZrO 2 fiber paper was significantly enhanced by the addition of 7 wt% mullite fibers, resulting in a remarkable increase to 0.1805 kN/m. The paper exhibited exceptional resistance to bending, maintaining 96 % of its bending strength even after undergoing 100 cycles. The thermal shrinkage of the composite paper, containing 15 wt% mullite fibers, was reduced from 17.75 % observed in pure ZrO 2 fiber paper to a mere 1.32 % after undergoing heat treatment at a temperature of 1300 °C for 2 h. The composite paper, measuring 5 mm in thickness and consisting of 7 wt% compositions, displayed exceptional thermal insulation properties when exposed to a hot side temperature of 1370 °C. It effectively insulated temperatures up to approximately 1000 °C. [ABSTRACT FROM AUTHOR]

Black liquor (BL) bioconversion into valuable by-products is essential to develop a bioeconomy strategy; however, its furfural content hinders microbial fermentation activities. Hence, this study utilizes paper mill sludge (PMS) to provide extracellular enzymes, furfural-degrading microbial consortia, and electron donor required for promoting the BL hydrogenesis potential. Three up-flow anaerobic sequential batch reactors (UASBRs) are fed with PMS (UASBR1), BL (UASBR2), and PMS + BL (UASBR3) and operated in parallel at 15 min fill, 72 h reaction, and 4 h settling. The UASBR3 achieves the maximum volumetric H 2 of 1.483 ± 0.088 L/L/d and H 2 yield of 2.06 ± 0.12 mol/mol glucose, which drops by 88% in UASBR2 and 24% in UASBR1. The insufficient H 2 productivity values in UASBR2 could be due to a lack of nutrients availability (C:N = 440:1 and C:P = 19:1), higher furfural concentration (2116 ± 422 mg/L), and involvement of the butyrate fermentation pathway. The synergetic effect between PMS and BL overcomes these limitations and enriches the fermentation medium with Proteobacteria phyla (22.8%) and Acinetobacter sp. degrading furfural (6.1%). The microbial community at the phylum level (e.g., Proteobacteria , Firmicutes , and Actinobacteria) in UASBR3 maximizes the migration of electrons (e−eq = 9.34 ± 0.54%) towards efficient H 2 formation. [Display omitted] • Paper mill sludge (PMS) mitigated inhibitory effect of furfural in black liquor (BL). • PMS improved H 2 yield from the BL by 8.3-folds and accounted for 2.1 mol/mol glucose. • e– eq transferred to H 2 was 9.3% in the PMS:BL, 7.4% in PMS, and 1.27% in BL. • Acinetobacter degrading furfural (6.1%) was abundant with PMS addition. • Bacilli (8.9%) and Clostridia (5.4%) was dominant in the hydrogenesis of PMS:BL. [ABSTRACT FROM AUTHOR]

This research investigated the hydrogen production and energy conversion from automobile shredder residues (ASRs) and paper mill sludge (PMS) co-gasified in a full-scale fluidized bed gasification plant. The results obtained from full-scale tests provided important information on the feasible assessment of ASRs-to-energy and the selection of alternative technologies for ASRs. Based on the analysis results of produced gas composition, H 2 , CO, and CH 4 composition produced from paper-mill sludge gasified were 4.17%–6.01%, 3.08%–4.32%, 1.71%–2.4%, respectively. Another C 2 gas composition ranged from 2.9% to 3.59%. The heating value of produced gas ranged between 1.64 MJ/Nm3 and 2.18 MJ/Nm3. In the case of 10% ASR addition, the heating value of produced gas was slightly increased to 1.84 MJ/Nm3-2.34 MJ/Nm3. The dioxin emission concentration of flue gas was approximately 0.064 ng I-TEQ/Nm3. It can comply with Taiwan regulation thresholds. The dioxin leaching concentrations of residues derived from gasification were also in compliance with regulation limits by the TCLP test. Meanwhile, in the case of 10% ASRs addition, the dioxin equivalence concentration of gasified residue was nearly 0.002 ng I-TEQ/Nm3. It was far below the current regulation standard limit. In summary, the results of this research have proved the performance of ASRs-to-energy by co-gasified with paper mill sludge using a full-scale gasification plant. The results obtained from this research also provided the information for selecting ASRs alternative technologies and operating full-scale gasifiers in the future. [Display omitted] • This study has confirmed the feasibility of co-gasification of calcium-rich PMS and chlorine-rich ASRs. • Adding 5%–15% of ASRs can maintain the regular operation of the full-scale commercial gasifier. • The synthesis gas has a composition of 4.91 vol% H 2 and 2.06 vol% CO, with a LHV of 1.93 MJ/Nm3. • The HCl emission could comply with regulation thresholds in co-gasification. • Dioxin reformation reduced significantly in co-gasification of PMS and ASRs. [ABSTRACT FROM AUTHOR]

Lower-limb strength measures can enhance falls risk assessment but due to the lack of clinically applicable methods, such measures are not included in current screening. The enhanced paper grip test (EPGT) is a simple-to-use and cost-effective test that could fill this gap. However, its outcome measure (EPGT force) has not yet been directly linked to the risk of falling. Is the EPGT a good candidate for falls risk screening in older people in the community? Seventy-one older people living independently in the community were recruited for this prospective observational study (median age 69 y, range 65y-79y). Lower-limb and whole-body strength were assessed at baseline using the EPGT and a standardised hand-grip method respectively. Incident falls were recorded monthly for a year through follow-up telephone conversations. The capacity of individual strength measures to predict falls and to enhance an established falls risk assessment tool (FRAT) commonly used by UK's national health service (NHS) was assessed using binomial logistic regression. The analysis was repeated for the subset of participants without history of falling at baseline (prediction of first-ever falls). Increased EPGT force and increased symmetry in strength between limbs were significantly associated with reduced risk of falling. Compared to the NHS-FRAT, the EPGT correctly classified more people (73% vs 69%), it achieved higher sensitivity (56% vs 26%) and higher negative predictive value (76% vs 68%). Complementing the NHS-FRAT with the EPGT produced a more comprehensive model that correctly classified 91% of participants and achieved 98% specificity, 81% sensitivity, 89% negative and 96% positive predictive value. Replacing the EPGT with hand-grip strength consistently undermined prediction accuracy. The EPGT remained highly accurate when focused on the prediction of first-ever falls. The EPGT can substantially enhance falls screening in the community. These results can also inform effective personalised strength exercise interventions. • The enhanced paper grip test (EPGT) accurately predicted the risk of falling. • The EPGT can enhance community screening for falls (recurrent and first-ever). • Higher EPGT force is significantly associated with reduced risk of falling. • Higher strength asymmetry between limbs also decreases the risk of falling. • These results can guide effective personalised strength exercise interventions. [ABSTRACT FROM AUTHOR]

Pen-on-paper pain drawing are an easily administered self-reported measure that enables patients to report the spatial distribution of their pain. The digitalization of pain drawings has facilitated the extraction of quantitative metrics, such as pain extent and location. This study aimed to assess the reliability of pen-on-paper pain drawing analysis conducted by an automated pain-spot recognition algorithm using various scanning procedures. One hundred pain drawings, completed by patients experiencing somatic pain, were repeatedly scanned using diverse technologies and devices. Seven datasets were created, enabling reliability assessments including inter-device, inter-scanner, inter-mobile, inter-software, intra- and inter-operator. Subsequently, the automated pain-spot recognition algorithm estimated pain extent and location values for each digitized pain drawing. The relative reliability of pain extent analysis was determined using the intraclass correlation coefficient, while absolute reliability was evaluated through the standard error of measurement and minimum detectable change. The reliability of pain location analysis was computed using the Jaccard similarity index. The reliability analysis of pain extent consistently yielded intraclass correlation coefficient values above 0.90 for all scanning procedures, with standard error of measurement ranging from 0.03% to 0.13% and minimum detectable change from 0.08% to 0.38%. The mean Jaccard index scores across all dataset comparisons exceeded 0.90. The analysis of pen-on-paper pain drawings demonstrated excellent reliability, suggesting that the automated pain-spot recognition algorithm is unaffected by scanning procedures. These findings support the algorithm's applicability in both research and clinical practice. [ABSTRACT FROM AUTHOR]

In this study, practical application for the industrial-scale hydrogen evolution reaction (HER) process is established using sustainable Cu 2 CoSnS 4 embedded in paper-working electrodes. The Cu 2 CoSnS 4 is produced using a solvent-free solid-phase approach. The effect of a wide pH range of electrolytes on working electrodes for hydrogen evolution reactions is also investigated. The Cu 2 CoSnS 4 embedded paper-working electrodes exhibit goodelectrocatalytic activity for hydrogen evolution reaction with low overpotential values of 233, 310, and 261 mV vs RHE at 10 mA/cm 2 in 0.5 M H 2 SO 4 ,1 M KOH, and 1 M PBS, respectively. These designed electrodes exhibit high double-layer capacitance and electrochemical surface area for a wide pH range. In acidic, alkaline and neutral environments, the catalyst-embedded paper electrodes explicit high turnover frequencies of 2.15 s−1, 2.75 s−1, and 2.11 s−1, respectively. The temperature-dependent hydrogen evolution reaction is studied to calculate the activation energy of the cathodic electrode. Utilising chrono-amperometry for about 118 h in an acidic media, which shows that electrodes have a high degree of stability. In comparison to other previously reported work on catalyst-embedded electrodes, the Cu 2 CoSnS 4 embedded paper-working electrodes offer excellentpotential for HER activity across a wide pH range and are suitable for industrial application. • Cu 2 CoSnS 4 embedded paper working electrodes are developed for hydrogen generation. • The electrodes exhibit universal pH hydrogen evolution reaction. • Electrodes shows excellent stability upto 40hr for continuous hydrogen generation. • The electrode displays good stability at current density more than 200 mA/cm2. [ABSTRACT FROM AUTHOR]

A variety of real-world situations take the form of repeated principal-agent problems with binary evaluation. I evaluate the principal's optimal evaluation effort and quality threshold for acceptance in the setting of dynamic agency with binary evaluation, focusing specifically on the evaluation by a top academic journal of papers submitted by economists. In the baseline model, the journal should statistically discriminate in favour of high-status economists, by setting an acceptance threshold that declines with their prior estimate of the economist's quality, while evaluation effort should likely increase with perceived author quality, as this provides incentives for authors to exert more effort, which is particularly valuable from the highest-quality authors. However, if a first good publication is more valuable than subsequent publications by the same economist, acceptance thresholds will tend to increase after publication success, relative to the threshold that would have followed a rejection. • Considers repeated principal-agent problem with binary evaluation. • Specifically, evaluation by a top academic journal of papers submitted by economists. • Journal should statistically discriminate in favour of high-status economists. • Acceptance threshold declines with prior estimate of economist's quality. • But threshold could increase after publication if first publication is most valuable. [ABSTRACT FROM AUTHOR]

The concern over plastic contamination has led to bans on plastic shopping bags, often replaced by paper ones. However, logos painted or printed on paper bags may still contain plastics, as investigated herein. In some logos, for example, white pigment of titanium dioxide (TiO 2) nanoparticles are bound with plastic binder onto the cellulose surface of the paper. This hybrid of plastic and nanoparticle is examined using scanning electron microscope (SEM) to characterise morphology physically, and Raman imaging to identify and visualise them chemically. Raman imaging scans the sample to separate images and identify not only plastic but also the co-formulated pigment. The scan generates a hyperspectral matrix containing hundreds to thousands of spectra, and subsequent analysis can enhance the signal-to-noise ratio. Decoding the hyperspectral matrix using chemometrics like principal component analysis (PCA) can effectively map plastic and pigment separately with increased certainty. The image can be further refined through 3-dimensional surface fitting for deconvolution, providing direct visualisation of the plastic-nanoparticle hybrid at a density of approximately 7.3 million particles per square millimetre. Overall, caution should be exercised when using paper bags, as they may not be entirely free of plastics. Raman imaging proves to be an effective method for identifying and visualising complex components, including plastics and nanoparticles. The concern over plastic contamination has led to bans on plastic shopping bags, replaced by paper alternatives. However, some logos on paper bags may still contain plastics, which is investigated to confirm the presence of plastic-nanoparticle hybrid using SEM and Raman imaging. By employing decoding algorithms such as PCA to separately map plastic and pigment, and utilising 3D surface fitting to deconvolute the image, the hybrid plastic-nanoparticle is estimated at a density of approximately 7.3 million particles per square millimetre. It's important to exercise caution and not assume these items are plastic-free. This aspect of plastics may have been overlooked as another potential source of contamination. [Display omitted] • paper bags might be not plastic-free at logo area. • hybrid structures of plastic-nanoparticle of TiO 2 is estimated at ∼7.3 million/mm2. • Raman imaging via hyperspectral matrix can increase signal-to-noise ratio. • principal component analysis (PCA) can separately map the plastic and pigment. • Gaussian surface fitting towards deconvolution can further increase signal-to-noise ratio. [ABSTRACT FROM AUTHOR]

• Preparation of ZIF-67/PEDOT/CP self-supporting electrodes using simple in situ hydrothermal. • The addition of PEDOT to ZIF-67 helps to achieve high electrical conductivity and large specific surface area. • The sensor has a high detection performance for CGA. • ZIF-67/PEDOT/CP provided a new sensor for the detection of CGA in real sample. The design of efficient electrocatalysts for the determination of chlorogenic acids (CGA) is crucial in the biological and medical fields. In this paper, ZIF-67/poly(3,4-ethylenedioxythiophene) (PEDOT) nanocomposites were synthesised. The introduction of PEDOT increased the electrical conductivity of the ZIF-67/PEDOT composites, inhibited the Co atom agglomeration, led to the exposure of more active sites and increased the transport channels. An ultrasensitive CGA sensor based on ZIF-67/PEDOT nanocomposite modified carbon paper (CP) electrode was developed. The nanomaterials were characterised using scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction spectroscopy (XRD). Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used to study the electrochemical properties of the modified CP electrode. In addition, the effects of different experimental conditions such as pH, scan rate and concentration on the peak current of CGA were investigated. Under the optimised conditions, the linear range of ZIF-67/PEDOT/CP for the determination of CGA was 0.1 ∼ 40 μM, and the limit of detection (LOD) was as low as 0.003 μM (S/N = 3). Furthermore, the sensor was successfully used for the quantitative analysis of CGA in real samples. [ABSTRACT FROM AUTHOR]

[Display omitted] • Designing materials using rice-leaf-mimetic paper as a substrate. • Engineering rice-leaf-mimetic paper with hydrochromic dyes or biolubricants. • Processes based on mass-producible papermaking unit operations. Biomimetics has revolutionized materials innovation by drawing inspiration from biological systems. Cellulosic paper, a sustainable biomaterial, offers immense potential for biomimetic research. Paper-based biomimetic materials, which replicate the structures and functionalities of natural materials by utilizing the cellulosic fiber network as a substrate or skeleton, provide customizable functional properties, thereby enabling advanced applications. Here, we introduce rice-leaf-mimetic paper, inspired by the leaf's microstructure and biowax-based cuticle. This paper exhibits self-cleaning superhydrophobicity and showcases possibilities for additional functionalities, including antibacterial properties and food preservation, as evidenced in our prior research. We propose its utilization as a substrate for rewritable and biolubricant-infused surfaces. These somehow distinct surfaces draw inspiration from the chemistry and microstructure of the rice leaf. Although incorporating hydrochromic dyes enables rewritability, controlling the retention time of colors remains challenging. The biowaxy structure of the paper prolongs color maintenance by inhibiting water evaporation. Moreover, the hierarchically rough microstructure of rice-leaf-mimetic paper effectively stores biolubricant molecules, reducing friction and enhancing slipperiness. Surface microcavity ratio analysis provides insights into the paper's biolubricant-storability. The surface engineering of rice-leaf-mimetic paper using hydrochromic dyes or biolubricants holds potential for designing novel materials. Unveiling the vast potential of easily scalable papermaking processes alongside biomimetics and surface engineering opens new avenues for materials innovation. [ABSTRACT FROM AUTHOR]

• Liquid water saturation in carbon paper is measured • Quantifies the capillary trapping effect of isolated water drops in carbon papers • Proposes a model describing liquid water drops transport In previous macroscopic average models of proton exchange membrane fuel cells (PEMFCs), liquid water was assumed to be continuous throughout the carbon paper. The transport of disconnected water drops in carbon paper has long been neglected in these models, which tend to underestimate water saturation in carbon paper. This study proposes a two-phase flow model that considers the transport of disconnected water drops to simulate the air-water transport in carbon paper. The proposed model was established based on the relationship between capillary force and liquid water saturation, and this relationship was obtained by conducting centrifuge experiments. In the centrifuge experiment, initially, the water saturation inside the carbon paper sample was one, and the centrifugal acceleration was zero. As the centrifugal acceleration increased, the water saturation decreased owing to the centrifugal force. After twenty seconds, the water saturation no longer decreases because the centrifugal force on the liquid water is balanced by the capillary force. Centrifugal acceleration was used to evaluate the capillary force. When the centrifugal acceleration was 185 m s − 2 , the saturation of the water drops in the balanced state was 32.0%. As the centrifugal acceleration increases to 739 m s − 2 , the saturation decreases to 6.5%. According to the experimental results, a function correlating the saturation and centrifugal acceleration, that is, the capillary force, was established. Finally, the results show that the centrifugal acceleration is more than 18.5 times that of the gravitational acceleration, indicating that the effect of gravity on the motion of water drops is negligible. [Display omitted] [ABSTRACT FROM AUTHOR]

The catalytic ozonation processes with continuous-flow reactors were used for pulp and paper mill wastewater treatment. [Display omitted] • The pulp and paper wastewater is treated effectively by catalytic ozonation with continuous-flow reactor. • The porous ceramsite catalytic ozonation can be used for continuous-flow process. • The porous ceramsite catalyst is continuously and stably operated for 30 days. • The lowest E EO value is reached at the O 3 dosage of 15 g/L. • The degraded or transformed organic pollutants present in PPMW by O 3 alone system and catalytic ozonation system were identified. The pollutants in wastewater can be degraded effectively by heterogeneous catalytic ozonation due to the production of hydroxyl radical (•OH) with strong oxidation power. For the natures of low weight, large specific surface area, excellent physical strength and stable chemical characteristics, the porous ceramsite was chosen for catalytic ozonation of wastewater in the present study, and the practical application parameters of the system were investigated for the actual pulp and paper mill wastewater (PPMW) in the continuous-flow reactor including temperatures, feeding flow rate, O 3 flow rate and O 3 dosage. The optimum experimental conditions were obtained (T = 25 ℃, feeding flow rate = 0.25 L/min, O 3 flow rate = 0.5 L/min, O 3 dosage = 15 g/L) for the process of catalytic ozonation. The results show that the effluent concentration of COD decreases from about 200 mg/L to 10 mg/L, namely the removal efficiency is about 95 %. The stability of the catalyst over time was tested in the continuous-flow reactor for 48 days, confirming that the porous ceramsite exhibits good performance in 30 days. The reusability of the catalyst was studied after the used catalyst was washed with Milli-Q water and ethanol, exhibiting good catalytic activity of the regenerated catalyst in three cycles. The fluorescent excitation-emission matrix (EEM), UV–vis analysis and GC–MS analysis were used for analyzing the organic pollutants in raw PPMW and after treatment. These results indicate that the process of catalytic ozonation with porous ceramsite has a high treatment efficiency on PPMW, and the continuous-flow reactor can be more practically used for a full-scale community PPMW application at a mill level. [ABSTRACT FROM AUTHOR]

Natural rubber latex (NRL) and cellulosic fibre are promising additives for improving the performance and sustainability of cement composite. This study investigated the optimised inclusion of NRL into waste paper pulp (WPP)-ordinary Portland cement (OPC) composites to enhance mechanical and durability properties. Three mixing methods were compared, revealing pre-mixing WPP with OPC before adding diluted NRL as the most effective. Both high-ammonia NRL (HA-NRL) and prevulcanised NRL (PV-NRL) significantly reduced water absorption, with PV-NRL slightly outperforming HA-NRL. Flexural properties were optimised at an NRL/OPC/WPP ratio of 10/700/300 parts by dry weight, although excessive NRL content reduced modulus. NRL also enhanced fire resistance through a synergistic effect, forming an ash-char layer, with HA-NRL exhibiting superior performance due to chemical distinctions. Failure modes and crystal formation were analysed using FE-SEM. Overall, optimised NRL and WPP incorporation improved water resistance, flexural performance, and fire resistance, suggesting their potential for sustainable construction. Further research could explore additional performance aspects and optimise NRL and WPP dosages for broader applications. • NRL incorporation significantly enhances flexural strength and modulus, promising structural applications. • Optimised composite formulations with natural rubber latex and waste paper pulp offer sustainable construction materials. • Synergy between NRL and waste paper pulp enhances fire resistance, resulting in the formation of a ash-char layer, suggesting suitability for fire-prone environments. • Exceptional water resistance ensures durability and resilience against moisture-induced degradation. [ABSTRACT FROM AUTHOR]

Electrochemical approaches to water desalination show promise for processing brackish water, but continued progress relies on developing scalable electrode architectures with competitive capacity and uptake dynamics for ion capture. Binder-free, device-ready carbon nanofoam papers (CNFPs) are one such candidate, where intermingled nanoscale networks of conductive carbon and pores balance the transport of electrons and ions throughout the electrified interior. Microwave-assisted electroless deposition of conformal nanoscale manganese oxide (MnO x) at the CNFP surface amplifies the ion-capture capacity to technologically relevant levels via faradaic pseudocapacitance. We take advantage of the design flexibility of these electrode architectures to vary CNFP pore size (5 to >100 nm) and thickness (100–300 μm), and then characterize the resulting MnO x @CNFP electrode series for their respective desalination performance in 20 mM NaCl using automated recirculating-batch protocols. The combination of CNFP conductivity and facile ion/electrolyte transport through the pore network with the faradaic ion-capture capability of the MnO x coating enables effective desalination. Using 0.3 mm-thick electrodes and MnO x loadings over 16 mg cm−2, we obtain desalination productivity of 6.8 L m−2 at 4.4 L m−2 h−1 for 90 % salt removal at only 0.13 Wh L−1 energy consumption. [Display omitted] • Well-plumbed/wired electrode architectures deliver superior desalination performance. • Areal ion-capture capacity is a more critical performance benchmark vs gravimetric. • Computer-controlled recirculating-batch testing enables practical evaluation. • Throughput productivity and capacity reported at standard concentration reduction [ABSTRACT FROM AUTHOR]

Pickering emulsions consisting of nanochitin/nanocellulose and cinnamon essential oil were synthesized and utilized as a water-based coating for filter paper, resulting in improved oxygen barrier and vapor barrier characteristics. The incorporation of cinnamon essential oil within Pickering emulsion facilitated a delayed release of the oil, thereby imparting antibacterial properties against E. coli on the coated filter paper. Moreover, the Pickering emulsion coating technique not only formed a uniform film that covered the fibers and pores of the filter paper, which enhanced the oxygen barrier properties (oxygen permeability reached 0.00285 ± 1.69967E-5 cm3/m2·d·Pa, 0.02937 ± 1.71335E-14 cm3/m2·d·Pa and 0.2283 ± 4.18994E-14 cm3/m2·d·Pa for DEChN, ChNC and CNC treated sample, respectively), but also reduced filter hydrophilicity performance (contact angles of DEChN, ChNC and CNC coated samples increased from 10.93 ± 0.89° to 81.10 ± 0.89°, 65.57 ± 1.09° and 58.93 ± 0.95°, respectively) and water vapor barrier performance (moisture permeability of DEChN, ChNC and CNC coated samples increased from 2530.9346 ± 20.3587 g/m2·day to 90.2211 ± 11.3913 g/m2·day, 153.547 ± 3.9448 g/m2·day and 350.5407 ± 0.24364 g/m2·day, respectively) of the filter paper. This work investigated the coating performance of nanochitin/nanocellulose based Pickering emulsion, and would provide a green route for preparing all biomass-base packing materials. [Display omitted] • Nano-chitin/cellulose can stabilize cinnamon essential oil-based Pickering emulsion. • Pickering emulsions possess water-based coating for paper-based packaging. • Pickering emulsion coating leads antibacterial, barrier and hydrophobic performance. [ABSTRACT FROM AUTHOR]

Developing environmentally friendly barrier coatings as an alternative to petroleum-based polymer packaging is a challenge. Cellulose nanofibres (CNF) films have exhibited great potential as water and gas barrier layers. Recycled paper was multi-layer coated with three commercial CNF (mechanical (M-CNF), TEMPO (T-CNF) and carboxymethylated (C-CNF)) using two metering systems (wound rod and blade micrometer) and two drying methods (tension-free contact drying and air drying). The coatability and rheological behaviour of the CNF suspensions were analysed. The gas, water and grease barrier properties of the CNF coated papers were determined and compared with the results of paper coated with cationic starch. The three CNF suspensions and the starch suspension were successfully coated using both metering systems. In the multi-layer coating, air drying yielded higher coat weights than contact drying, and the difference was more noticeable in M-CNF and T-CNF coated samples. A lack of uniformity observed in CNF coatings increased with the number of coating layers. M-CNF coated samples had a whitish surface with a uniform appearance, but coating was insufficiently compact to provide barrier properties. T-CNF coating exhibited a cracked surface and consequently provided no barrier properties. Drying stresses caused breakage of T-CNF coating, which could be explained by the drop in apparent viscosity at much lower rheological shear stresses in the T-CNF suspension. C-CNF showed successful coatability and provided barrier properties to paper with both metering systems and drying methods. Air permeance decreased considerably and the water wettability of the paper decreased by 60% compared to the reference paper, even with a single coating layer (about 1 g·m−2). In addition, a greaseproof paper (grease resistance >1800 s and kit no >10) was obtained with multi-layer C-CNF coating. Although water vapour permeability at 90 % RH and 20 °C decreased slightly with a single layer of CNF coating, higher amounts of CNF did not improve this parameter. • Evaluation of CNF coatability in metering and drying systems employed in papermaking • Air stream drying led higher CNF coat weights in multi-layer application. • Cracked coating under drying stresses was related to rheological behaviour of CNF. • Carboxymethylated CNF can be used as pre-coating to improve paper barrier properties in papermaking. • A greaseproof paper by multi-layer carboxylated CNFs coating could achieved [ABSTRACT FROM AUTHOR]

Novel photoelectrochemical ultraviolet detection technologies based on semiconductor/electrolyte heterojunctions have attracted significant attention due to their cost-effective fabrication and self-powered characteristic. In this study, ZnO films were deposited on three-dimensional carbon fiber paper (3D CFP) using a one-step sputtering method, resulting in the preparation of 3D ZnO/CFP composites as photoanodes for photoelectrochemical (PEC) type photodetectors (PDs). The fabricated device demonstrates outstanding photoelectrochemical performance, showcasing a remarkable responsivity of approximately 31.76 mA/W, a detectivity of 3.06 × 1012 jones, and a rapid photoresponse time of 76.51/48.51 ms. Furthermore, the device exhibits exceptional photoresponse stability during cycling tests. The unique structure of 3D CFP, composed of intertwined carbon fiber in three dimensions, offers an enlarged specific surface area and efficient carrier transport pathways for the photoanode in self-powered PEC-PDs. This characteristic facilitates effective electrolyte diffusion throughout the entire film, as well as efficient transport of photo-generated charge carriers, thereby significantly enhancing the overall performance of the PEC-PDs. This study affirms the effectiveness of the synergistic interaction between 3D CFP and ZnO film for advanced UV photodetectors, demonstrating both mass production viability and promise for the future of photoelectrochemical detection technology. [Display omitted] • Preparation of three-dimensional ZnO/CFP composites as photoanodes for self-powered UV photodetectors by one-step sputtering. • The 3D ZnO/CFP photochemical photodetector has a remarkable response rate and outstanding photoresponse stability. • Demonstration of the effectiveness of synergy between 3D CFP and ZnO films for advanced UV photodetectors. [ABSTRACT FROM AUTHOR]

This study investigates the impact of incorporating lime mud (LM) as a filler material to develop sustainable, cementless ultra-high performance concrete (UHPC) by replacing silica powder (SP) and silica sand (SS) at varying percentages. Flowability analysis reveals that LM, with its distinctive particle size, influences flow characteristics differently at different replacement levels. Compressive strength was improved by 5.4% with 30% SP replacement, showcasing the role of LM in nucleation, as well as its particle size advantage. The heat of hydration analysis indicates that LM likely influences the early curing stages, enhancing reactivity and nucleation. TGA analysis also confirms that LM plays a role in hydration reaction, influencing weight loss and hydration peaks. The mercury intrusion porosimeter results show the impact of LM on pore distribution, with 30% for SP and 50% for SS replacements, favoring denser matrices. Life cycle assessment (LCA) demonstrates reduced CO 2 emissions and favorable environmental performance, highlighting the sustainability potential of LM replacements. Overall, the incorporation of LM in UHPC shows promise in terms of enhancing its mechanical properties and environmental sustainability. [Display omitted] • Lime mud (LM) in UHPC boosts material strength, leading to denser, more effective concrete. • LM enhances hydration, flowability, and refines pore structure. • High LM ratios in UHPC increase sustainability and reduce CO 2 emissions. • LM's use in UHPC significantly advances its mechanical properties and eco-friendliness. [ABSTRACT FROM AUTHOR]

Paper-based composite materials exhibit a marked tendency towards thinner and lighter profiles in the context of electromagnetic interference (EMI) shielding. Carbon fiber paper (CFP) has excellent electrical conductivity and Lightweight base characteristics. However, its single electrical loss characteristic and uncontrollable EMI shielding performance are limited in application. Therefore, we prepared CFP@ graphene oxide (GO)/ZIF-67 composites by chemical bonding and in-situ polymerization, and then prepared CFP@rGO/Co/C composites with integrated structure and function by heat treatment. Layer-by-layer assembly technology was employed to develop composite materials with tunable EMI shielding performance. The composite material has excellent high conductivity (2475.86 S/m) and excellent EMI shielding performance (average X-band EMI efficiency (SE)38.46 dB, absolute shielding effectiveness (SSE/t) = 14388.56 dB cm2 g−1). Through the layer-by-layer assembly technology, the EMI SE performance of the 7-layer assembled material reached 85.83 dB, and the EMI SSE/t reached 32110.51 dB cm2 g−1. Through simulation verification, the EMI shielding performance of the materials is compared, and ideas for EMI material design are provided. In addition, the material also has excellent Joule heating performance, fast electrothermal response and good temperature controllability. The material exhibits remarkable resilience against harsh environmental conditions, including strong acids, bases, organic reagents, ultrasonic waves, combustive processes, and extremely low temperatures. Despite these severe treatments, its performance remains above 90 % intact. This study proposes a magnetic-dielectric synergistic, performance-adjustable CFP-based shielding material, which has great application potential in the future wearable, defense, and aerospace fields. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] • Facile and scalable self-assembly of perylene diimide polymer with carbon paper. • Effective facilitation of carrier separation by π-π built-in electric field. • Narrowed band gap and low VB due to the VB tail states induced by π-π interactions. • Enhanced photocatalytic water oxidation activity of the PDIP/CP photocatalyst sheet. • Suitability of the PDIP/CP photocatalyst sheet for large-scale applications. Photocatalytic water splitting is a highly promising future energy technology. In contrast to the extensive work on particulate photocatalysts, there is still a lack of sufficient investigation for regularized photocatalysts. Here, from perylene diimide polymer (PDIP) and commercial carbon paper (CP), we develop a self-assembled PDIP/CP photocatalyst sheet that is easily scalable and can be used for photocatalytic water oxidation. Driven by strong interfacial π-π interactions, the PDIP spontaneously adsorbs onto the CP, which leads to a narrowed band gap, down-shifted VB edge, and enhanced separation of the photogenerated charge carriers of the PDIP. Under visible light, the PDIP/CP photocatalyst sheet shows significantly enhanced photocatalytic water oxidation activity (4 h cumulative oxygen evolution is 1.7 times higher than that of the powder-suspended system) and considerable cycling stability. The PDIP/CP photocatalyst sheet has the potential for large-scale device applications. [ABSTRACT FROM AUTHOR]

[Display omitted] • Office paper waste is processed using physiochemical and enzymatic hydrolysis. • The yeast is isolated from rotten banana for the fermentation process. • Box-Behnken analysis was used to determine optimal conditions for key variables. • A blended membrane was applied for the purification process. • Amicon cell and polymeric membrane dehydrate ethanol–water combinations. One potential replacement for fossil fuels is the generation of biofuel from biomass feedstock. To reach the global sustainability goals, it is also necessary to address a number of issues, such as reducing environmental pollution, climate change, and carbon emissions. This work was aimed to convert the office paper waste as biomass feedstock into bioethanol through a sustainable pathway. The office paper waste was hydrolyzed via physiochemical and enzymatic hydrolysis, the liberated glucose was estimated at 15.72 g/L using the optimum conditions of 15 % HCl and 6 % office paper waste followed by enzymatic hydrolysis. The yeast isolate B2 that was applied for the fermentation process was isolated from rotten banana, identified as Hanseniaspora uvarum (STDF-B2) and submitted to GenBank with accession number (OP800106). The Box-Behnken design was applied to estimate the optimal conditions for the three most significant variables depending on the one variable at a time results. A blended membrane of sulphonated polyvinyl chloride with poly(2-acrylamido-2-methyl-1-propanesulfonic acid) (SPVC-PAMPS) was applied for the purification of both standard ethanol and produced bioethanol via pervaporation technique (PV). The morphology, chemical composition, mechanical properties and permeability of the membrane were all analyzed in various ways. Following purification using a membrane-integrated amicon cell, the total permeate flows of the laboratory-prepared ethanol and generated bioethanol were 289.54 and 253.06 (g/m2 h), respectively. [ABSTRACT FROM AUTHOR]

[Display omitted] • A novel combination of aptasensing platform and speckle pattern analysis was introduced. • PDA@CNTs mussel chemistry was used to immobilize aptamer on cellulose paper matrix. • A label free aptasensor was designed for detection of breast cancer biomarker mucin 1. • Aptasensor was characterized with very good analytical figure of merits. Herein, we have developed a cellulose paper-based aptasensing protocol by employing dynamic laser speckle (DLS) analysis for direct and label-free probing of the binding interface. Cellulose filter paper surface was modified by using the mussel adhesion chemistry of polydopamine modified carbon nanotubes (PDA@CNTS). The mussel chemistry resulted in strong adhesion and binding of PDA@CNTs on cellulose paper surface. The modified surface was subsequently employed in the construction of label free aptasensor for detection of cancer biomarker mucin 1 (MUC1). Taking advantage of DLS technique, it provided us with sensitive and accurate analysis of target biomarker MUC1 by the intrinsic randomness of patterns generated from cellulose based paper surface. The developed aptasensor was evaluated using DLS at various fabrication steps, where the scattered laser beams from these samples were collected and analyzed based on the obtained speckle patterns. Under the optimal experimental conditions, paper-based aptasensor achieved sensitive and selective detection of MUC1, exhibiting excellent linear range (15–100) µM with a limit of detection of 1 µM. This work presents a novel study of promising laser speckle paper-based aptasensor, providing new insights for the development of low-cost, sensitive, and portable paper-based analytical tools for biological applications. [ABSTRACT FROM AUTHOR]

Phase II metabolites play an important role in diazepam-related cases. The study aimed to assess the stability of diazepam's phase II metabolites in dried blood spots on filter paper. A piece of filter paper was spotted with 100 µL of whole blood (added 1% sodium fluoride as needed) obtained from participant who received 5 mg diazepam orally, air dried for 2 h at room temperature, and then stored at different conditions. Whole spots were cut at 0.1 cm from the outer edge of blood spots at post-consumption time-points of prior (zero), 5, 16, 35, 61, 120 days and 1, 1.5 years. Analytes were extracted with methanol/water mixture (8:2, v/v) and determined using HPLC-MS/MS. Decomposition rules were analyzed by a statistical software "SPSS". Temazepam glucuronide remained stable (0.5–18.6% loss) at 20 ℃ and at 20 ℃ with 1% sodium fluoride for 16 days, while it was unstable after 5 days at 4 ℃ (21.1–26.2% loss) and − 20 ℃ (28.9 - 34.4% loss). After 35 days, temazepam glucuronide concentrations began to fluctuate significantly under all conditions, and an obvious increase (290.4–355.1%) was observed in 1.5 years. Oxazepam glucuronide was always unstable after 5 days, the percentage loss was even 100% when it was stored for 61 days and 1.5 years. Dried blood spots on ordinary filter paper are recommended to be stored at 20 ℃ or 20 ℃ with 1% sodium fluoride within 16 days. Samples should be analyzed immediately or stored in sterile and dry media. • TG was stable on filter paper at 20 ℃ with or without 1 % NaF within 16 days, and it is a more reliable marker in real cases. • OG was always unstable after 5 days, the percentage loss was even 100% when it was stored for 61 days and 1.5 years. • DBS on filter paper in diazepam-related cases are recommended to be stored at 20 ℃ with or without 1 % NaF within 16 days. [ABSTRACT FROM AUTHOR]

Given its superior structure, the abundance of surface functional groups, and low cost, cotton fiber filtration paper can be used as the support for hydrogen evolution reaction (HER) and oxygen evolution reaction catalysts (OER) instead of copper foam (CF), nickel foam (NF), or carbon cloth (CC). Herein, the chemical plating method was used to create thin self-supporting electrodes based on cotton fiber filtration paper (FP). The Co-Ni-P amorphous nanospheres can be uniformly dispersed on the self-supporting FP due to its porous structure and oxygen functional groups. The Co-Ni-P/FP electrode has an overpotential as low as 125 mV for HER and 320 mV for OER at the current density of 10 mA cm−2. Additionally, according to density functional theory (DFT) calculations, the Co atom added to the Ni-P nanosphere can lead to considerably more charge accumulation around the Co and Ni active sites, which greatly encourages the HER and OER processes. The novel porous support, FP, provides a fresh way the preparation of self-supporting electrodes. [Display omitted] • Filter paper is used to prepare the self-supporting electrode as the substrate. • The preparation method is simple and the properties are stable. • Rich oxygen-containing functional groups of FP promote deposition and dispersion. • Explore the excellent electrochemical performance of amorphous Co-Ni-P/FP by DFT. [ABSTRACT FROM AUTHOR]

Rewritable paper (RP) which takes advantages of stimuli-responsive color-changing materials/smart materials and can be used multiple times has been demonstrated to hold potential to reduce human waste of paper and alleviate the increasingly severe environmental issues. To make the RP closer to the way that people are accustomed to reading and more practical for daily life, interest and effort toward smart materials with clearly visible or naked-eye color-switching properties are particularly important. In this review, depending upon the stimulation protocol, five types of stimuli (thermo-, water-related-, light-, stress-, and electric-field-) smart chromogenic materials and systems with visible color switching applied in light absorptive display for RP are focused on. In each section, different stimulus-chromic molecules and their corresponding systems are discussed to explore the design concepts, methodologies, working mechanisms, and pros and cons of various chromogenic materials used in light absorptive RP. In addition, the challenges and prospects are sketched to provide strategies to explore more smart materials for high-performance RP and its relative techniques. [ABSTRACT FROM AUTHOR]

The challenge of global climate change has drawn people's attention to the issue of carbon emissions. Reducing the use of petroleum-derived materials and increasing the use of biodegradable materials is a current focus of research, especially in the packaging materials industry. This study focused on the use of environmentally friendly plastics and waste paper as the main materials for packaging films. Poly(butylene succinate- co -lactate) (PBSL) was modified with maleic anhydride (MA) to form a biobased compatibilizer (MPBSL), which was then blended with a mixture (WPS) of waste-paper powder (WP) and silica aerogel powder (SP) to form the designed composite (MPBSL/WPS). The modification of PBSL with MA improved interfacial adhesion between PBSL and WPS. The structure, thermal, and mechanical properties, water vapor/oxygen barrier, toxicity, freshness, and biodegradability of MPBSL/WPS films were evaluated. Compared with the PBSL/WP film, the MPBSL/WPS film exhibited increased tensile strength at break of 4–13.5 MPa, increased initial decomposition loss at 5 wt% of 14–35 °C, and decreased water/oxygen permeabilities of 18–105 cm3/m2·d·Pa. In the water absorption test, the MPBSL/WPS film displayed about 2–6 % lower water absorption than that of the PBSL/WP film. In the cytocompatibility test, both MPBSL/WPS and PBSL/WP membrane were nontoxic. In addition, compared with PBSL/WP film and the control, the MPBSL/WPS film significantly reduced moisture loss, extended the shelf life, and prevented microbial growth in vegetable and meat preservation tests. Both MPBSL/WPS and PBSL/WP films were biodegradable in a 60-day soil biodegradation test; the degradation rate was 50 % when the WP or WPS content was 40 wt%. Our findings indicate that the composites would be suitable for environmentally sustainable packaging materials. [Display omitted] • An environmentally friendly PBSL/WPS film for packing material is successfully fabricated. • Increase of recycling waste paper and PBSL utilization can reduce carbon emissions. • MPBSL/WPS films have comparable properties to pure PBSL. • A formula of MPBSL/WPS products are sustainable and economic. [ABSTRACT FROM AUTHOR]

[Display omitted] • Plasmonic filter paper was prepared via electroless immobilization Ag NPs on filter paper. • The fluid flow in cellulose fiber could concentrate and separate analyte on the SERS substrate. • The plasmonic filter paper were used for preconcentration, separation and detection of Sudan dye in chili powder. We proposed a triple functional SERS substrate by immobilized Ag nanoparticles on the surface of filter paper. The high dense Ag nanoparticles were distributed on the SERS substrate via in-situ growth process. By optimizing the parameter in preparation process, the optimal filter paper SERS substrate was fabricated by using 30 mM of AgNO 3 with 20 S growth time. Due to capillary-effect wicking of cellulose fiber, the paper SERS substrate provide simple, fast and pump-free function for transferring analyte onto sharp tip through development of fluid. The fluid flow also brings target concentrate effect within the tip area. Furthermore, the separation feasibility was obtained during the development process of fluid. The preconcentrated effects not only enhanced the SERS signal of analyte, but also improve the fluorescence visible effect. The filter paper SERS substrate was successfully used for separating, concentrating and detecting Sudan dye from chili product, the detection limit could achieve 10−6 M. This study developed a portable, cost-effective and eco-friendly SERS substrate for separating and detecting trace chemical in food. [ABSTRACT FROM AUTHOR]

Several lignocellulosic wastes are generated in the pulp and paper industry (PPI), such as small wood chips (pinchips) and paper sludge, presenting a high cellulose content suitable to be converted into biofuels or bio-products in a forest biorefinery scheme. In this work, two schemes of biorefinery were proposed for their valorization, processing small eucalyptus wood pinchips in two different strategies: (i) autohydrolysis at 230ºC, and (ii) autohydrolysis at 195ºC followed by organosolv process (47.7% ethanol-water, 198ºC for 60 min). More than 95% of cellulose was recovered in both schemes. In the combined process, 76% of delignification was achieved and 78% of xylan was solubilized as xylooligosaccharides. To reduce operational cost of lignocellulosic biomass-to-ethanol fermentation, the mixture of the treated eucalyptus pinchips from two processes with sludge was also proposed to increase the initial glucan content and to supply a rich source of nitrogen (present in the sludge). For that, two experimental designs were carried out for ethanol production by simultaneous saccharification and fermentation (SSF) process. Ethanol from SSF assays using sludge as co-substrate at 0.6 g of sludge/g of treated wood pinchips and 16 FPU/g of pretreated solids allowed to obtain 59 g/L (90% of conversion) and 46 g/L (96% of conversion) when blended with the wood from autohydrolysis and with the wood from autohydrolysis followed by organosolv, respectively. Overall, this study shows an alternative process valorization of biomasses derived from PPI for production of advanced biofuels and bio-products (such as xylooligosaccharides and lignin) contributing to achieving a circular economy. • Multi-waste valorization approach was proposed to produce biofuel and bioproducts. • Autohydrolysis and organosolv processes allowed > 90% glucan recoveries. • Higher than 40 g/L of ethanol and 90% of yield were obtained in both schemes developed. • Blending with sludge improve ethanol production from pretreated eucalyptus wood. [ABSTRACT FROM AUTHOR]

[Display omitted] • Three industrial yeast strains compared in high-solids paper sludge fermentation. • Highest ethanol titre of 101.8 g/L achieved using paper sludge from virgin pulping. • Xylose utilisation by engineered strain Cellusec® 1.0 improved ethanol titre by 10.3%. • Required enzyme dosage reduced by 50% using cellulase-secreting strain Cellusec® 2.0. Reported ethanol titres from hydrolysis-fermentation of the degraded fibres in paper sludge (PS) waste, generally obtained under fed-batch submerged conditions, can be improved through fermentation processes at high solids loadings, as demonstrated in the present study with two industrial PS wastes at enzyme dosages appropriate for solids loadings up to 40% (w/w). The industrial yeast, Saccharomyces cerevisiae strain Ethanol Red®, was compared to two genetically engineered S. cerevisiae strains, namely Cellusec® 1.0 and Cellusec® 2.0, capable of xylose utilisation, and xylose utilisation and cellulase production, respectively. High-solids batch fermentations were conducted in 3 L horizontal rotating reactors and ethanol titres of 100.8 and 73.3 g/L were obtained for virgin pulp and corrugated recycle PS, respectively, at 40% (w/w) solids loading using Ethanol Red®. Xylose utilisation by Cellusec® 1.0 improved ethanol titres by up to 10.3%, while exogenous cellulolytic enzyme requirements were reduced by up to 50% using cellulase-producing Cellusec® 2.0. [ABSTRACT FROM AUTHOR]

A large number of fresh fruits are wasted in the supply chain due to spoilage, so it is crucial to develop fruit preservation materials. Herein, two novel Ag-MOFs/carboxymethyl filter paper (Ag-MOFs/CMFP) composites were successfully synthesized by in situ facile synthesis, which can be used as packaging materials to delay fruit spoilage. The synthesis process is simple and environmentally friendly, and the reaction conditions are mild. The mechanical property, water stability, and antibacterial activity of the as-synthesized Ag-MOFs/CMFP composites were investigated. Specifically, the composites exhibited high mechanical performance and the tensile strength was >10.00 MPa. Moreover, the composites displayed good water stability and can remain stable in water environment for >7 days, which can be attributed to the strong interaction between Ag-MOFs and CMFP. Significantly, Ag-MOF particles endow the composite papers with excellent antibacterial activity, which can inactivate 99.9 % of the bacteria. Attributed to these characteristics, these composite papers were used as fruit fresh-keeping materials and can prolong the shelf-life of cherry tomatoes and peaches for >10 days. This research not only provides a facile synthesis strategy for the flexible MOFs paper, but also provides instructive guidance for related research on fruit preservation materials. [Display omitted] • Two novel Ag-MOFs/CMFP composites are prepared by in facile situ synthesis. • Ag-MOFs can grow uniformly and tightly on the fibers surface of CMFP. • The composites exhibited good mechanical performance and water stability. • The composites showed excellent antibacterial activity and low toxicity. • The composite papers as preservation material can extend the shelf life of fruit. [ABSTRACT FROM AUTHOR]

An active chitosan-based coating with an addition of a natural antioxidant and a natural crosslinker has been applied to improve the performance of Kraft paper. Coatings, including chitosan (CS), CS crosslinked with 1.5 % genipin (CS-1.5G), CS containing 1 % astaxanthin (CSA) and CSA crosslinked with 1 % genipin (CSA-1G) were coated on Kraft paper. Uncoated and coated papers were then evaluated for water content (WC), water vapor permeability (WVP), contact angle, oxygen permeability (OP), tensile strength (TS), bursting strength and elongation at break (EAB). Results indicated that the coating improved the properties of Kraft paper. When compared with CS-coated paper, WC and WVP of CSA-1G-coated paper decreased significantly by 40 % and 24 %, respectively. The lowest OP was also observed in CSA-1G-coated paper. CSA- and CSA-1G-coated paper had contact angle values >100°, indicating hydrophobic nature of coated paper surface. All coatings largely improved TS of the paper (by 182–224 %) whereas CS-1.5G and CSA-1G significantly improved the bursting strength of the paper. The developed genipin-crosslinked chitosan-based coating enriched with astaxanthin can improve the functional properties of Kraft paper and thus will facilitate the usage of the paper for food packaging applications. [Display omitted] [ABSTRACT FROM AUTHOR]

The reuse of waste papers by conversion into valuable carbon materials has received considerable attention for diverse applications such as energy storage and water purification. However, traditional methods for converting waste papers into materials with suitable properties for specific applications are often complex and ineffective, involving consecutive carbonization and activation steps. Herein, we propose a simple one-step microwave (MW)-assisted synthesis for preparing waste paper-derived porous carbons (WPCs) for energy storage and water purification. Through a 30-min synthesis, WPCs with graphitic structure and high specific surface area were successfully produced. The fabricated WPCs exhibited outstanding charge storage capability with a maximum specific capacitance of 237.7 F g−1. Additionally, the WPC demonstrates a high removal efficiency for various dyes, achieving a maximum removal efficiency of 95.0% for methylene blue. The developed one-step MW synthesis not only enables the production of porous carbon from waste paper, but also offers a viable approach to address solid waste management challenges while simultaneously yielding valuable materials. [Display omitted] • Waste paper-derived porous carbons were synthesized by one-step microwave synthesis. • Within 30-min MW synthesis, graphitic and high-surface area WPCs were produced. • WPC exhibits outstanding electrochemical capacitance of 237.7 F g−1. • WPC exhibits high removal of various dyes, with maximum of 95.0% for methylene blue. [ABSTRACT FROM AUTHOR]

[Display omitted] • The alcohol yields achieved were 41.3 wt% and 48.5 wt% from the corrugated box and A4 paper. • Cellulose exhibited the conversion rate of 100 %, with alcohol substances achieving a yield of 71.2 wt% and a selectivity of 89.4 % within 6 h. • The mechanism of cellulose hydrolysis and the catalytic effect of CuMgAlO x were explored. • Multiple techniques were utilized to analyze the alcoholysis pathways and mechanisms of cellulose in waste paper. In an effort to valorize under-exploited cellulose sources like waste paper for sustainable energy production, this study investigates a catalytic process to convert these materials into low-carbon alcohols. We explored the conversion efficiency of various cellulose materials, including corrugated box, A4 paper, and pure cellulose, under the influence of a CuMgAlO x catalyst. Our findings indicate that at 360 °C for 6 h, the conversion rates were substantial, yielding 70.1 % for corrugated box, 85.2 % for A4 paper, and 100 % for cellulose. The respective alcohol selectivities achieved were 54.7 %, 83.0 %, and 89.4 %, with alcohol yields of 41.3 wt%, 48.5 wt%, and 71.2 wt%. Notably, the absence of the catalyst led predominantly to the production of sugars and lipids, whereas the catalytic conditions facilitated the formation of alcohols. The study also examined the effects of temperature and reaction time on cellulose conversion. It was found that a complete conversion was possible at 320 °C within 1 h, with extended temperature and time improving the alcohol yield. The development of a kinetic model for the cellulose conversion process has allowed for accurate predictions of the transformations under varied conditions, which offers a strategic framework for reaction optimization. Furthermore, the role of the CuMgAlO x catalyst was elucidated through the examination of model compounds, demonstrating its capability in converting cellulose intermediates such as sugars, lipids, and ketones into alcohols. This research highlights a potent strategy for the production of high-value, eco-friendly green fuels from readily available paper products and cellulose biomass, marking a significant advancement in chemical engineering and sustainable energy resources. [ABSTRACT FROM AUTHOR]

[Display omitted] • Chromatography paper was used to develop an analytical device to detect salt. • Chloride ions reacted with silver nanoparticles and carboxymethyl cellulose. • Stability and interference against Cl− detection were good. • The device detected salt in twenty-five food samples. Using silver nanoparticles (AgNPs) and carboxymethyl cellulose (CMC), a simple distance-based paper analytical device (dPAD) was developed for the determination of chloride ions in food products. The determination of chloride ions was based on the Mohr argentometric method without the chromium compound. A hydrophobic barrier was created on chromatography paper using a wax-printing technique. The barrier protected a channel that was impregnated with AgNPs and CMC. In the presence of chloride, chloride ions moved along the channel, reacting with AgNPs, and forming an AgNPs-Cl sediment deposited as a white/gray precipitation in the orange-colored channel. The chloride ion concentration was interpreted from the length of the color change visualized with the naked eye without external equipment. The amount and volume of AgNPs and CMC impregnated on the chromatography paper were optimized. The response of the AgNPs-CMC/dPAD to the chloride ion was linear from 0.01 to 1.00 % w/v (r = 0.9931). In addition, the proposed device was stable for more than 28 days, with a relative response of 105 ± 3 % compared to day one, resulting in consistent and precise results. Intra-day (6 measurements) and inter-day (over 6 days) precision were excellent with RSDs less than 6 %. The developed dPAD was used to detect salt in twenty-five real samples, including instant noodles, condiments and sauces, and snacks. Recoveries ranged from 96 ± 5 to 105 ± 5 %. The proposed method showed acceptable accuracy, precision and good shelf life for monitoring chloride in food products at the point of need and demonstrated potential for commercial development. [ABSTRACT FROM AUTHOR]

[Display omitted] • Paper mill sludge ash (pm SA) was used as catalysts to activate PMS. • Aerobic calcination was conducive to the exposure/formation of octahedral FeIII. • The O O bond fracture was the root pathway for FeIV O production. • The release of solid calcium in pm SA could inhibit the active decay of FeIV O. • The pm SA could effectively degrade similar pollutants in near-neutral water. The excellent performance of high-valent iron-oxo species (FeIV O) in the degradation of pollutants by activating peroxymonosulfate (PMS) had attracted much attention. However, the generation and reaction mechanisms were still unclear. In this study, iron-rich paper mill sludge was used as a raw material for the first time to prepare iron-based catalysts with abundant octahedral FeIII sites (Fe oct III). The results showed that the highest content of Fe oct III was found in the paper mill sludge ash obtained by aerobic calcination at 800 °C (pm SA800), and the pm SA800 could exhibit excellent catalytic activity (0.4785 min−1) and stability during the oxytetracycline (OTC) degradation process. The characterization and density functional theory (DFT) calculations further indicated that the Fe oct III was the dominant active site for FeIV O production. PMS tended to be adsorbed on two adjacent Fe oct III sites to form a [Fe oct III-OSO 2 OO(H)-Fe oct III] complex with a two-site adsorption configuration. Subsequently, the O O and O H bonds in [Fe oct III-OSO 2 OO(H)-Fe oct III] broken by absorbing energy, generating FeIV O. It's worth noting that the Ca species of pm SA800 effectively stabilized the pH of the reaction solution, which ensured the stable and continuous production of FeIV O. This work provides a new idea and insight for preparing catalysts that could produce FeIV O active species. [ABSTRACT FROM AUTHOR]

Waste paper and tyre are typical solid wastes with distinct composition. Their pyrolysis could generate varied volatiles that may interact with each other or with resulting char. In this study, the co-pyrolysis of waste paper and tyre was investigated at 400 and 600 ºC, with the focus on understanding the interaction of the volatiles on evolution of the products. The results show that the interaction of the volatiles at 400 ºC forms more gaseous products like CO and CO 2 , while the interactions of the heavier organics at 600 ºC forms more oil (49.3% vs 42.6%). The interaction of the volatiles also affects the generation of sulfur-containing organics and diminishes the paper-derived aldehydes and ketones or the heavy organics with the π-conjugated structures in the oil. In addition, the volatile-char interactions exist and form the char of higher carbon content through promoting carbonization and deoxygenation reactions, generating char of higher thermal stability and higher hydrophilicity via tailoring functional group, pore structures and morphologies of the char. [Display omitted] • Interaction of volatiles in co-pyrolysis of waste paper and tyre exists. • Co-pyrolysis promotes formation of gases at 400 ℃ while oil at 600 ℃ via condensation. • Paper-derived intermediates capture CH x * /H* radicals, minimizing CH 4 /H 2 formation. • Volatiles interactions interfere formation of S-containing organics and aldehydes/ketones. • Co-pyrolysis affects composition, stability, functionality and morphologies of char. [ABSTRACT FROM AUTHOR]