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Electronic paper displays rely on electrokinetic effects in nonpolar solvents to drive the displacement of colloidal particles within a fluidic cell. While Electrophoresis (EP) is a well-established and frequently employed phenomenon, electro-osmosis (EO), which drives fluid flow along charged solid surfaces, has not been studied as extensively. We hypothesize that by exploiting the interplay between these effects, an enhanced particle transport can be achieved. In this study, we experimentally investigate the combined effects of EP and EO for colloidal particles in non-polar solvents, driven by an electric field. We use astigmatism micro-particle tracking velocimetry (A- μ PTV) to measure the motion of charged particles within model fluidic cells. Using a simple approach that relies on basic fluid flow properties we extract the contributions due to EP and EO, finding that EO contributes significantly to particle transport. The validity of our approach is confirmed by measurements on particles with different magnitudes of charge, and by comparison to numerical simulations. We find that EO flows can play a dominant role in the transport of particles in electrokinetic display devices. This can be exploited to speed up particle transport, potentially yielding displays with significantly faster switching times. Interplay of electrokinetic effects : Driven by the applied electric field, both electro-osmosis (EO, top left), which drives a flow along the surfaces of the fluidic cell, and electrophoresis (EP, top right), which drives a migration of particles relative to the background liquid, occur in our system. A typical example of the resultant particle velocity field (bottom) illustrates the important role of EO on particle transport in the fluidic cell. • Studied electrokinetics of particles in nonpolar solvent using astigmatism micro-PTV. • Both electrophoresis (EP) and electro-osmosis (EO) play important roles. • Combination of EO and EP could be exploited in faster switching e-paper displays. [ABSTRACT FROM AUTHOR]

A bilayer photothermal paper-based 3D cone flowing evaporator with high solar light absorption, low water evaporation enthalpy and excellent salt-rejecting performance is fabricated using multilayered MXene, ultralong hydroxyapatite nanowires, and hydrophilic polymers. The 3D cone flowing evaporator cooperates with a siphon effect-driven unidirectional fluid transportation unit to guide concentrated saline flows out from the evaporating surface, leading to high water evaporation rate and salt-rejecting stable seawater desalination performance. [Display omitted] • A bilayer photothermal paper-based cone flowing water evaporator is reported. • The evaporator exhibits excellent properties for solar seawater desalination. • The evaporator exhibits much higher water evaporation rate than most reported values. • The evaporator can effectively prevent salt accumulation on the evaporating surface. Solar energy-driven water evaporation technology is a promising, low-cost and sustainable approach to alleviate the global clean water shortage, but usually suffers from low water evaporation rate and severe salt deposition on the water evaporation surface. In this work, a hydrophilic bilayer photothermal paper-based three-dimensional (3D) cone flowing evaporator was designed and prepared for stable high-performance seawater desalination with excellent salt-rejecting ability. The as-prepared bilayer photothermal paper consisted of MXene (Ti 3 C 2 T x) and HAA (ultralong hydroxyapatite nanowires, poly(acrylic acid), and poly(acrylic acid-2-hydroxyethyl ester)). The accordion-like multilayered MXene acted as the efficient solar light absorber, and ultralong hydroxyapatite (HAP) nanowires served as the thermally insulating and supporting skeleton with a porous networked structure. A siphon effect-driven unidirectional fluid transportation unit in the 3D cone flowing evaporator could guide the concentrated saline flowing away from the evaporating surface to prevent salt deposition on the evaporation surface, avoiding severe deterioration of the performance in solar water evaporation. Furthermore, combining high solar light absorption and high photothermal conversion efficiencies, low water evaporation enthalpy (1838 ± 11 J g−1), and additional energy taken from the ambient environment, the as-prepared cone flowing evaporator exhibited a high water evaporation rate of 3.22 ± 0.20 kg m−2 h−1 for real seawater under one sun illumination (1 kW m−2), which was significantly higher than many values reported in the literature. This study provides an effective approach for designing high-performance solar energy-driven water evaporators for sustainable seawater desalination and wastewater purification. [ABSTRACT FROM AUTHOR]

[Display omitted] • Bilayered V 2 O 5 nH 2 O xerogel constructed 2D nanopapers were synthesized. • The V 2 O 5 nH 2 O Xerogel combines oxygen defect engineering. • Oxygen defect improves Zn2+/Mg2+ insertion/extraction kinetics. Aqueous zinc ion batteries (AZIBs) and aqueous magnesium ion batteries (AMIBs) offer powerful alternatives for large-scale energy storage because of their high safety and low cost. Consequently, the design of high-performance cathode materials is essential. In this paper, we present a simple strategy that combines oxygen defect (O d) engineering with a 2D-on-2D homogeneous nanopape-like bilayer V 2 O 5 nH 2 O xerogel (BL-HVO d NPS). This strategy employs O d to improve Zn2+/Mg2+insertion/extraction kinetics and reduce irreversible processes for high-performance AZIBs/AMIBs. And interlayer water molecules serve as an effective spacer to stabilize the expanded interlayer gap in BL-HVO d NPS, thereby providing extended diffusion channels for Zn2+/Mg2+ during insertion/extraction. The interlayer water molecules help shield the electrostatic interaction between Zn2+/Mg2+ and BL-HVO d NPS lattice, which improves diffusion kinetics during repeated. In addition, electrochemical characterization results indicate that the BL-HVO d NPS can effectively the surface adsorption and internal diffusion of Zn2+/Mg2+. More importantly, the successfully prepared unique 2D-on-2D homogenous nanopaper structure enhances electrolyte/electrode contact and reduces the migration/diffusion path of electrons/Zn2+ and Mg2+, thus greatly improving rate performance. As a result, the BL-HVO d NPS as AZIBs/AMIBs electrodes offer better reversible capacity of 361.8 and 162.8 mA h g−1 (at 0.2 A g−1), while displaying impressively long cycle lifes. This method provides a way to prepare advanced xerogel cathode materials for AZIBs and AMIBs. [ABSTRACT FROM AUTHOR]

The MXene-modified papers with high-uniform loading of polypyrrole and excellent conductivity have been fabricated via a multiple self-assembly and in-situ polymerization strategy, which achieves boosting areal capacitance. [Display omitted] • Multiple self-assembly and in-situ polymerization strategy is proposed tofabricate paper-based supercapacitors. • Alternate adsorption of MXene and polypyrrole on paper yields an ultra-high polypyrrole loading of 10.0 mg/cm2. • The paper-based supercapacitor shows a boosting areal capacitance of 2316 mF/cm2. Despite the intriguing features of freestanding flexible electronic devices, such as their binder-free nature and cost-effectiveness, the limited loading capacity of active material poses a challenge to achieving practical high-performance flexible electrodes. We propose a novel approach that integrates multiple self-assembly and in-situ polymerization techniques to fabricate a high-loading paper-based flexible electrode (MXene/Polypyrrole/Paper) with exceptional areal capacitance. The approach enables polypyrrole to form a porous conductive network structure on the surface of paper fiber through MXene grafting via hydrogen bonding and electrostatic interaction, resulting in an exceptionally high polypyrrole loading of 10.0 mg/cm2 and a conductivity of 2.03 S/cm. Moreover, MXene-modified polypyrrole paper exhibits a more homogeneous pore size distribution ranging from 5 to 50 μm and an increased specific surface area of 3.11 m2/g. Additionally, we have optimized in-situ polymerization cycles for paper-based supercapacitors, resulting in a remarkable areal capacitance of 2316 mF/cm2 (at 2 mA/cm2). The capacitance retention rate and conductivity rate maintain over 90 % after undergoing 100 bends.The maximum energy density and cycling stability are characterized to be 83.6 μWh/cm2 and up to 96 % retention after 10,000 cycles. These results significantly outperform those previously reported for paper-based counterparts. Overall, our work presents a facile and versatile strategy for assembling high-loading, paper-based flexible supercapacitors network architecture that can be employed in developing large-scale energy storage devices. [ABSTRACT FROM AUTHOR]

[Display omitted] The complex spreading dynamics of blood on paper matrix is likely to be quantitatively altered with variations in the fractional occupancy of red blood cells in the whole blood (haematocrit). Here, we presented an apparently surprising observation that a finite volume blood drop undergoes a universal time-dependent spreading on a filter paper strip that is virtually invariant with its hematocrit level within physiologically healthy regime, though distinctively distinguishable from the spreading laws of blood plasma and water. Our hypothesis was ascertained by performing controlled wicking experiments on filter papers of different grades. Spreading of human blood samples of different haematocrit levels ranging between 15% and 51% and the plasma separated from therein were traced by combined high-speed imaging and microscopy. These experiments were complemented with a semi-analytical theory to decipher the key physics of interest. Our results unveiled the exclusive influence of the obstructing cellular aggregates in the randomly distributed hierarchically structured porous pathways and deciphered the role of the networked structures of the various plasma proteins that induced hindered diffusion. The resulting universal signatures of spontaneous dynamic spreading, delving centrally on the fractional reduction in the interlaced porous passages, provide novel design basis for paper-microfluidic kits in medical diagnostics and beyond. [ABSTRACT FROM AUTHOR]

[Display omitted] Solar interfacial evaporation is one of the most efficient and environmentally-friendly clean freshwater production technologies. Plasma metal nanoparticles are excellent optical absorption materials, but their high cost and inherent resonance narrow bandwidth absorption limit their application. In this work, commercial cellulose papers are used as substrates to synthesize Ag-Ni/cellulose paper by the seed-mediated method. The Ag-Ni/cellulose paper exhibits high light absorption at the full wavelength (200–2500 nm) resulting from the synergistic effect of localized surface plasmon resonance (LSPR) of Ag NPs and the interband transitions (IBTs) of Ni. Under one-sun irradiation (1 kW m−2), the energy utilization efficiency of Ag-Ni/cellulose paper is as high as 93.8%, and the water evaporation rate is 1.87 kg m−2 h−1. Diffusion inhibition experiment results show that the Ag-Ni/cellulose paper exhibits excellent antibacterial performance, and the antibacterial performance is highly related with Ag NPs content. These provide new opportunities for commercial production of competitive cost, green, and portable solar evaporators for different application sceneries. [ABSTRACT FROM AUTHOR]

[Display omitted] Lithium metal is deemed a promising anode material for the next-generation batteries with high specific energy. Unfortunately, the growth of Li dendrites and infinite volume change during cycling, caused by the "hostless" feature of metallic Li, have posed a great challenge to the commercialization of Li metal anode. The introduction of appropriate host materials for Li metal is highly desirable. In this work, a N, P dual-doped 3D carbon derived from low-cost quantitative filter paper (NPCQP) is designed and fabricated for direct using as a host for Li metal anode. The resulting NPCQP host achieves a high deposition/stripping Coulombic efficiency of above 97.5 % with a low nucleation overpotential. Moreover, the NPCQP@Li symmetric cells enable an excellent long-term cycling performance (1000 h) with an ultralow voltage hysteresis (12 mV) and stable interface behavior. When paired with the commercial LiFePO 4 cathode, the full cell with NPCQP@Li anode displays impressive long-term cyclic stability and rate capability, outperforming the counter cell with bare Li anode. This contribution sheds light on the rational design of viable host for practical lithium metal anodes. [ABSTRACT FROM AUTHOR]

[Display omitted] • A flexible rechargeable Ag 2 O-Zn battery was in situ constructed on the filter paper. • The tree-root-like interfacial design was achieved between Ag 2 O and filter paper. • The interlocking interface favored high mechanical stability for the Ag 2 O-Zn battery. Flexible zinc–silver oxide (Zn–Ag 2 O) batteries have attracted extensive attention for comfortable wearable electronics owing to their stable output voltage, inherent safety, and environmental benignity. However, they suffer from inferior specific capacity and poor mechanical stability due to the low utilization of Ag 2 O cathodic material and weak interfacial adhesion of active material/substrate. Inspired by the nature of the tree root system, we develop an interface-engineered cathode, in which Ag 2 O nanoparticles are rooted on an Au, Ni co-modified filter paper substrate (CFP) through an electroless plating followed by an in situ electrochemical oxidation. The staggered-stacked Ag 2 O nanoparticles provide abundant electrochemically active sites and convenient ion diffusion paths, and the unique biological tree-root-like structure of the electrode material creates robust interlocking interfaces. A quasi-solid-state Zn–Ag 2 O battery assembled with a tree-root-like Ag 2 O/CFP cathode delivers a high areal specific capacity of 1.08 mAh cm−2 and long-term cycling durability with a capacity retention of 77.3% even after 100 cycles. Moreover, the device presents good mechanical stability under various flexural deformations, including bending, folding, and twisting, and exhibits minimal capacity changes after 1000 bending cycles. These findings suggest that the bio-inspired interface-engineered electrode structure is an efficient approach for developing flexible batteries with excellent electrochemical performance and mechanical properties. [ABSTRACT FROM AUTHOR]

[Display omitted] An abundance of early warning graphene-based nano-materials and sensors have been developed to avoid and prevent the critical fire risk of combustible materials. However, there are still some limitations that should be addressed, such as the black color, high-cost and single fire warning response of graphene-based fire warning materials. Herein, we report an unexpected montmorillonite (MMT)-based intelligent fire warning materials that have excellent fire cyclic warning performance and reliable flame retardancy. Combining phenyltriethoxysilane (PTES) molecules, poly(p-phenylene benzobisoxazole) nanofiber (PBONF), and layers of MMT to form a silane crosslinked 3D nanonetwork system, the homologous PTES decorated MMT-PBONF nanocomposites are designed and fabricated via a sol–gel process and low temperature self-assembly method. The optimized nanocomposite paper shows good mechanical flexibility (good recovery after kneading or bending process), high tensile strength of ∼81 MPa and good water resistance. Furthermore, the nanocomposite paper exhibits high-temperature flame resistance (almost unchanged structure and size after 120 s combustion), sensitive flame alarm response (∼0.3 s response once exposure onto a flame), cyclic fire warning performance (>40 cycles), and adaptability to complex fire situations (several fire attack and evacuation scenarios), showing promising applications for monitoring the critical fire risk of combustible materials. Therefore, this work paves a rational way for design and fabrication of MMT-based smart fire warning materials that combine excellent flame shielding and sensitive fire alarm functions. [ABSTRACT FROM AUTHOR]

Industrial processes and municipal wastes largely contribute to the fluctuations in iron (Fe) content in soils. Fe, when present in unfavorable amount, causes harmful effects on human, flora, and fauna. The present study is an attempt to evaluate the composition of Fe in surface soils from paper mill and municipal landfill sites and assess their potential ecological and human health risks. Geochemical fractionation was conducted to explore the chemical bonding of Fe across different fractions, i.e., water-soluble (F1) to residual (F6). Different contamination factors and pollution indices were evaluated to comprehend Fe contamination extent across the study area. Results indicated the preference for less mobile forms in the paper mill and landfill, with 26.66% and 43.46% of Fe associated with the Fe–Mn oxide bound fraction (F4), and 57.22% and 24.78% in the residual fraction (F6). Maximum mobility factor (MF) of 30.65% was observed in the paper mill, and 80.37% in the landfill. The enrichment factor (EF) varied within the range of 20 < EF < 40, signifying a high level of enrichment in the soil. The individual contamination factor (ICF) ranged from 0 to >6, highlighting low to high contamination. Adults were found to be more vulnerable towards Fe associated health risks compared to children. The Hazard Quotient (HQ) index showed the highest risk potential pathways as dermal contact > ingestion > inhalation. The study offers insights into potential Fe contamination risks in comparable environments, underscoring the crucial role of thorough soil assessments in shaping land use and waste management policies. [Display omitted] • Geochemical fractionation unveils less bioavailable Fe in contaminated soil. • EF, ICF, and I geo indicate high Fe contamination. • Adults are more susceptible to potential health risks from surplus Fe exposure. • HQ analysis pinpoints dermal contact as the primary pathway for Fe exposure risks. [ABSTRACT FROM AUTHOR]

The use of microalgae and bacteria as a strategy for the startup of bioreactors for the treatment of industrial wastewater can be a sustainable and economically viable alternative. This technology model provides satisfactory results in the nitrification and denitrification process for nitrogen removal, organic matter removal, biomass growth, sedimentation, and byproducts recovery for added-value product production. The objective of this work was to evaluate the performance of microalgae and bacteria in their symbiotic process when used in the treatment of paper pulp industry wastewater. The experiment, lasting fourteen days, utilized four bioreactors with varying concentrations in mgVSS/L of microalgae to bacteria ratio (R1-100:100, R2-100:300, R3-100:500, R4-300:100) in the startup process. Regarding the sludge volumetric index (SVI), the results show that the R1 and R2 reactors developed SVI30/SVI10 biomass in the range of 85.57 ± 7.33% and 84.72 ± 8.19%, respectively. The lipid content in the biomass of reactors R1, R2, R3 e R4 was 13%, 7%, 19%, and 22%, respectively. This high oil content at the end of the batch, may be related to the nutritional stress that the species underwent during this feeding regime. In terms of chlorophyll, the bioreactor with an initial inoculation of 100:100 showed better symbiotic growth of microalgae and bacteria, allowing exponential growth of microalgae. The total chlorophyll value for this bioreactor was 801.46 ± 196.96 μg/L. Biological removal of nitrogen from wastewater from the paper pulp industry is a challenge due to the characteristics of the effluent, but the four reactors operated in a single batch obtained good nitrogen removal. Ammonia nitrogen removal performances were 91.55 ± 9.99%, 72.13 ± 19.18%, 64.04 ± 21.34%, and 86.15 ± 30.10% in R1, R2, R3, and R4, respectively. [Display omitted] • Microalgae and bacteria symbiotically initiated bioreactor start-up. • Initial inoculation concentrations were critical for photogranule development. • High total nitrogen removal efficiency in all bioreactor configurations. • Optimal setup boosts biomass and pigment. • Microalgae-bacteria consortium facilitated the production of valuable bioproducts. [ABSTRACT FROM AUTHOR]

Biomass can be used as an energy source to thermochemical conversion processes to biocrude production. However, the supply and dependence on only one biomass for biocrude production can be an obstacle due to its seasonality, availability, and logistics costs. In this way, biomass waste and agroindustrial residues can be mixture and used as feedstock to the hydrothermal co-liquefaction (co-HTL) process as an alternative to obtaining biocrude. In this sense, the present paper analyzed the biocrude yield influence of the co-HTL from a quaternary unprecedented blend of different biomasses, such as sugarcane bagasse, brewer's spent grain (BSG), sludge from a paper recycling mill (PRM), and microalgae (Chlorella vulgaris). In this way, a simplex lattice design was employed and co-HTL experiments were carried out in a 2000 mL high-pressure stirred autoclave reactor under 275 °C for 60 min, considering 15% of feedstock/water ratio. Significant effects in each feedstock and their blends were analyzed aiming to increase biocrude and biochar yield. It was found that the addition of microalgae is only significant when considered more than 50% into the blend with BSG and PRM sludge to increase biocrude yield. • Unprecedented blend (microalgae, sugarcane bagasse, BSG, and PRM sludge) in co-HTL. • Highest biocrude yield of 51.7% using microalgae as the only feedstock. • Second-highest biocrude yield (29%) for BSG and PRM sludge (synergetic interaction). • BSG and PRM sludge can complement co-HTL feedstock in low microalgae availability. • E RoI higher than one for 50% of microalgae, 25.8% of BSG, and 24.2% of PRM sludge. [ABSTRACT FROM AUTHOR]

[Display omitted] • Paper mill sludge-based calcium-containing biochar was cleanly prepared. • The maximum phosphorus adsorption capacity of an as-prepared biochar could be up to 68.49 mg·g−1. • Phosphorus was immobilized onto the as-prepared biochar in the forms of CaHPO 4 and Ca 5 (PO 4) 3 (OH). With the increased awareness of reusing solid wastes for higher sustainability and the concern of water pollution associated with phosphorus over-emission, there are strong interests in developing solid waste based adsorbents for purifying phosphorus-containing wastewater. As a rich calcium resource, paper mill sludge (i.e., a major solid waste from pulping industry) can be used as phosphorus removal adsorbent after calcination. Thus, in this work, a simple and clean thermally treating route has been proposed for preparing calcium-containing biochar from paper mill sludge. The effect of the physicochemical properties of paper mill sludge and its carbonization condition on phosphorus adsorption has been analyzed. Moreover, the influence of some key adsorption parameters, e.g., biochar dosage, initial pH of solution, co-existing anions, initial phosphorus concentration and contact time has also been investigated. The results showed that the phosphorus adsorption data could be fitted well with pseudo-second-order kinetic and Langmuir isothermal models. The calculated maximum adsorption capacity of the as-prepared optimal calcium-containing biochar could reach to 68.49 mg·g−1 at 25 °C. Combined with the characterization results, it can be reasonably inferred that the adsorption process was chemisorption-dominated. Lastly, the application of this spent adsorbent in agriculture field has also been discussed. In brief, this work provided a feasible strategy for converting paper mill solid waste to an environmental functional material (i.e., calcium-rich biochar) for remediation of eutrophic water. [ABSTRACT FROM AUTHOR]

[Display omitted] The pulp and paper sectors are thriving yet pose significant environmental threats to water bodies, mainly due to the substantial release of pollutants. Lignin-derived compounds are among the most problematic of these contaminants. To address this issue, we present our initial results on utilizing organic semiconductor photocatalysis under visible light for treating lignin-derived compounds. Our investigation has been centered around creating a green and cost-effective organic semiconductor photocatalyst. This catalyst is designed using a structure of bagasse cellulose spheres to support PM6 (poly[(2,6-(4,8-bis(5-(2-ethylhexyl)-4-fluorothiophen-2-yl)benzo[1,2- b :4,5- b' ]dithiophene))– co -(1,3-di(5-thiophene-2-yl)-5,7-bis(2-ethylhexyl)-benzo[1,2- c :4,5- c' ]dithiophene-4,8-dione))]: MeIC (3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-cyclopentane-1,3-dione[ c ]-1-methyl-thiophe))-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3- d:2′ , 3′-d' ]-s-indaceno[1,2- b :5,6- b' ]-dithiophene)). This photocatalyst demonstrates remarkable efficiency, achieving over 91 % degradation of lignin-derived compounds. The superior photocatalytic performance is attributed to three main factors: (1) The ability of PM6 to broaden MeIC's absorption range from 300 to 800 nm, allowing for effective utilization of visible light; (2) the synergistic interaction between PM6 and MeIC, which ensures compatible energy levels and a vast, evenly spread surface area, promoting charge mobility and extensive donor/acceptor interfaces. This synergy significantly enhances the generation and transport of carriers, resulting in a high production of free radicals that accelerate the decomposition of organic materials; (3) The deployment of PM6:MeIC on biomass-based carriers increases the interaction surface with the organic substances. Notably, PM6: MeIC showcases outstanding durability, with its degradation efficiency remaining between 84 % and 91 % across 100 cycles. This study presents a promising approach for designing advanced photocatalysts aimed at degrading common pollutants in papermaking wastewater. [ABSTRACT FROM AUTHOR]

[Display omitted] • A novel route to carbon quantum dots (CQDs) of customized surface functionality. • CQDs with amine functionality obtained from modified paper precursors. • Amine functionalized CQDs demonstrated as efficient probes for DNA binding studies. We report a novel synthesis route for preparing carbon quantum dots (CQDs) of customized surface functionality from readily available precursors. The synthetic strategy is based on the chemical modification of paper precursors prior to preparing CQDs from them. The pre-synthesis modification of paper precursors with (3-Aminopropyl) triethoxy silane (APTES) enabled us to synthesize CQDs with amine functional groups on the surface. The silane coupling via condensation between the ethoxy group of APTES and the cellulose hydroxyl group on the paper resulted in the tethering of amine groups on the paper substrates, which are retained as surface-bound species during the synthesis of CQDs from the modified paper. Amine functionalization on the surface of CQDs helped us use them in applications such as DNA binding. We analyzed the interaction of CQDs with calf thymus DNA (CT-DNA), and the results imply their propensity as an efficient biological probe. The synthetic strategy presented here can also be extended to other functional groups. [ABSTRACT FROM AUTHOR]

[Display omitted] Energy consumption from air cooling systems in summer, water scarcity in hot regions, and the functional reusability of waste paper are emerging environmental problems. Finding solutions to these problems simultaneously remains a significant challenge. Herein, a superhydrophobic passive cooling Cellulose-CaCO 3 film with hierarchical nano-sheets was fabricated to realize daytime radiative cooling with a temperature drop of 15–20 °C in summer and water harvesting with harvesting efficiency of 387 mg cm−2h−1 bd utilization of recycled waste paper. The superhydrophobic Cellulose-CaCO 3 film demonstrates its self-cleaning properties against inorganic and organic pollutants. Furthermore, the superhydrophobicity of the film was maintained after base/acid corrosions, dynamic water flushing, and thermal treatment at 100 °C for 7 h, exhibiting good durability of the superhydrophobicity. Moreover, the superhydrophobic Cellulose-CaCO 3 film is nonflammable after exposure to fire combustion for 1 min. In addition to waste paper, waste maize straws, and pasteboards were also collected to produce superhydrophobic passive cooling films. Results indicate that the above three cellulose-based raw materials can be well used to prepare durable superhydrophobic passive cooling materials. Environmental toxicology assessments confirm the safety of the material. This study not only provides a protocol for preparing superhydrophobic materials; but also demonstrates their potential for passive cooling and water harvesting. [ABSTRACT FROM AUTHOR]

Over time, the risk assessment of dermal exposure to pollutants in print paper products has received considerable attention. Most studies have focused on organic pollutants, especially bisphenol A (BPA). However, little is known about the levels of trace elements in print paper products, despite the knowledge that these elements are components of printing inks and toners. This study was aimed at determining the concentrations of trace elements in 5 types of paper products, namely bulletins, magazines, special events program booklets, handbills, and newspapers. The average daily intake (ADI) of each element was subsequently estimated through dermal exposure to the papers. The detection frequency of the elements of interest was high (nearly 100%) in most paper products, with the exception of chromium, whose detection was low. In contrast, Ag was not detected in any sample. The levels of the elements in the paper products were low and comparable to those found in other personal and consumer products with the potential for skin contact. The range values of estimated ADIs were 1.70–3.90E-08, 2.30–18.2E-10, 2.60–16.4E-09, 3.65–5.75E-08, 1.29–4.38E-08, 6.23–15.6E-10, 1.51–2.80E-10, 1.43–9.16E-09, 0.00–9.47E-09, and 4.68–220E-08 mg/kg bw/day for Mn, Co, Ni, Cu, Zn, As, Cd, Pb, Cr and Fe respectively. These values were well below the dermal standard reference doses (R f D) for each element. The present results indicate that dermal exposure to trace elements from print paper products was low and does not pose significant risks for toxic (non-carcinogenic) effects on humans. • Previous efforts have focused on the risk assessment of organic contaminants in print paper products. • Limited attention accorded to risk assessment of trace elements in print paper products • Human dermal exposure to trace elements via print paper products was low • Exposure to trace elements via print paper products has low risks of non-carcinogenic events. [ABSTRACT FROM AUTHOR]

Three specific catalysts, namely ZIF-67 (zeolitic imidazolate framework-67), Co@NCF (Co@Nitrogen-Doped Carbon Framework), and 3D NCF (Three-Dimensional Nitrogen-Doped Carbon Framework), were prepared and studied for pulp and paper mill effluent degradation using heterogeneous activation of peroxymonosulfate (PMS). Numerous characterizations, including scanning electron microscopy (SEM), X-ray diffraction (XRD), and N 2 adsorption, were used to characterize the properties of three different catalysts. 3D NCF is remarkably effective at heterogeneous activation of PMS to generate sulfate radicals to degrade pulp and paper mill effluent (PPME) compared to the other as-prepared catalysts. The catalytic activity reveals a sequence of 3D NCF > Co@NCF > ZIF-67.3D NCF could degrade organic pollutants in 30 min at an initial COD concentration of 1146 mg/L of PPME, 0.2 g/L catalysts, 2 g/L PMS, and 50 °C. Consequently, it was observed that the degradation of PPME using 3D NCF followed first-order kinetics, with an activation energy of 40.54 kJ mol−1. Overall, 3D NCF/PMS system reveals promising performance for PPME removal. • 3D NCF synthesized via calcining and etching a zeolitic imidazolate framework (ZIF-67). • 3D NCF presented the highest activity in the pulp and paper mill effluent degradation. • 3D NCF proved to be a promising catalyst and has superior stability. • Pulp and paper mill effluent degradation on 3D NCF followed pseudo-first-order kinetics. [ABSTRACT FROM AUTHOR]

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

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

[Display omitted] The O-vacancy Bi 2 WO 6 /SrTiO 3 heterojunction photocatalyst with Z scheme photogenerated electron transfer mechanism was loaded on cellulose fibers to construct a visible light-responsive photocatalytic composite paper for efficient and recyclable degradation of organic dyes in water. The introduction of O vacancies in Bi 2 WO 6 by alkali etching increased the utilization rate of Bi 2 WO 6 for visible light and achieved effective regulation of the energy band structure and Fermi level, which transformed Bi 2 WO 6 /SrTiO 3 type-II heterojunction into Z scheme heterojunction. The light-excited electrons in the conduction band of O-vacancy Bi 2 WO 6 directly migrated to the valence band of SrTiO 3 , which improved the separation efficiency of photogenerated carriers and maximized the redox capability of semiconductors. Compared with other control papers, O-vacancy Bi 2 WO 6 /SrTiO 3 paper exhibited the best photocatalytic performance, and its degradation rate for rhodamine B could reach 71.1% under 100 min of Xe lamp irradiation. The O-vacancy Bi 2 WO 6 /SrTiO 3 paper also showed good photocatalytic cycle stability. Loading heterojunction on the cellulose fibers solved the problem of poor reusability and difficult in recovery for powder semiconductor photocatalyst in practical applications. This study provides a novel strategy for constructing Z scheme heterogeneity on cellulose fibers to prepare composite paper with high photocatalytic activity and good reusability. [ABSTRACT FROM AUTHOR]

Novel multifunctional hard core/soft shell colloidal nanoparticles have been developed by introducing the elastic compounds into the shell and the rigid compounds into the core via Semi-continuous seed emulsion polymer method. these core/shell nanoparticles can facile self-assemble into large-scale dense ordered structure film via dried at room temperature due to the relatively low glass transition temperature (Tg) of the shell layers. The as-formed papers not only possess the capacity to solvent (water/ethanol) rewritable and multicolor painting, but also can rapidly reversible mechanochromic. With these outstanding features, it can be concluded that this kind of novel multifunctional PCs papers can be served as a promising candidate for next-generation rewriteable and environment-friendly papers, anti-counterfeiting tags and smart tunable bio-sensors, etc. [Display omitted] Photonic crystals film that possesses periodic dielectric structure have shown great prospect in developing environmentally friendly paper alternatives due to the unique properties of dye free and non-photobleaching, but their practical application is limited by the weak interaction between colloidal particles. Although some progress has been obtained, it is still a challenge to develop photonic paper with the desired mechanical and optical properties. Herein, multifunctional hard core/soft shell nanoparticles with controlled size are fabricated by semi-continuous seed emulsion polymerization method. Compared with convention colloidal particles, these core/shell nanoparticles can facile self-assemble into large-scale dense ordered structure film via dried at room temperature due to the relatively low glass transition temperature (Tg) of the shell layers. The facile fabrication route enables the continuous high-through put production of the photonic papers. The as-formed papers not only possess the capacity to solvent (water/ethanol) rewritable and multicolor painting, but also can rapidly reversible mechanochromic. Moreover, due to the good compatibility of core/shell interface, these photonic films possess excellent mechanical properties, demonstrating that this multifunctional film makes the fabrication of novel robust rewritable papers possible and enables visual monitoring of deformation degree. [ABSTRACT FROM AUTHOR]

Accompanying China's accession to the World Trade Organization, the rapid development of the Chinese economy has led to increasingly serious environmental issues. However, the inherent mechanisms underlying the impact of Environmental Information Disclosure (EID) policy and trade on the environmental effects of Chinese paper enterprises remain unclear in the context of the era's requirement for a resource-conserving and environmentally-friendly society. The pollution problem in the papermaking industry has received attention worldwide, and how to balance the environmental and development issues of papermaking enterprises is an urgent issue that needs to be solved in the academic community. This study explores the impact mechanisms of EID policy and trade on the environmental effects of enterprises from the perspective of financial constraints. Utilizing the PSM-DID model, the study investigates the moderating effects of financial constraints on the EID policy and import-export trade. The findings reveal that both external and internal financial constraints have negative, detrimental effects on the environmental effects of the EID policy and trade. These constraints impede research and development investment and technological upgrades, hinder productivity improvement, and hamper the realization of "regulatory and trade innovation effects". This study enriches our understanding of the mechanisms by which trade affects the environmental effects of Chinese paper enterprises and further identifies the impacts of Chinese EID policy and trade on pollution emissions by enterprises, providing a theoretical basis and practical foundation for the government in formulating financial, environmental, and trade policies. • Analyzing the environmental effects of Chinese paper enterprises from the perspective of financing constraints. • This study validated the research hypothesis using three micro databases. • This study decomposes the impact mechanism into three aspects: scale effects, technical effects, and structural effects. [ABSTRACT FROM AUTHOR]

Agro-based pulp and paper mills (PPMs) inevitably produce numerous refractory pollutants in their wastewater, including chlorolignin, chlorophenols, chlorocatechols, chloroguaiacol, cyanide, furan, dioxins, and other organic compounds, as well as various heavy metals, such as nickel (Ni), zinc (Zn), chromium (Cr), iron (Fe), lead (Pb), arsenic (As), etc. These pollutants pose significant threats to aquatic and terrestrial life due to their cytogenotoxicity, mutagenicity, impact on sexual organs, hormonal interference, endocrine disruption, and allergenic response. Consequently, it is crucial to reclaim pulp paper mill wastewater (PPMW) with high loads of refractory pollutants through effective and environmentally sustainable practices to minimize the presence of these chemicals and ensure environmental safety. However, there is currently no comprehensive published review providing up-to-date knowledge on the fate of refractory pollutants from PPMW in soil and aquatic environments, along with valuable insights into the associated health hazards and remediation methods. This critical review aims to shed light on the potential adverse effects of refractory pollutants from PPMW on natural ecosystems and living organisms. It explores existing effective treatment technologies for remediating these pollutants from wastewater, highlighting the advantages and disadvantages of each approach, all in pursuit of environmental safety. Special emphasis is placed on emerging technologies used to decontaminate wastewater discharged from PPMs, ensuring the preservation of the environment. Additionally, this review addresses the major challenges and proposes future research directions for the proper disposal of PPMW. It serves as a comprehensive source of knowledge on the environmental toxicity and risks associated with refractory pollutants in PPMW, making it a valuable reference for policymakers and researchers when selecting appropriate technologies for remediation. The scientific community, concerned with mitigating the widespread risks posed by refractory pollutants from PPMs, is expected to take a keen interest in this review. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] The commercialization of lithium metal batteries (LMBs) is encountering significant challenges due to the electrolyte incompatibility and poor mechanical properties of polyolefin separators, as well as the hazardous growth of lithium dendrites at the anode. Simultaneously, the development of safe and environmentally-friendly separators has become a central focus in rechargeable battery technology. In this study, we introduce a novel Janus separator (CP@SiO 2), featuring a composite structure with cellulose paper (CP) as the base layer and electrospun polyvinylidene fluoride (PVDF) nanofibers as the top layer. The nanofibers are uniformly coated with mesoporous SiO 2 nanoparticles through hydrogen bonding. The CP@SiO 2 separator leverages its three-dimensional lithium-ion channels and rigid ceramic particles to enhance electrolyte retention and stabilize lithium metal anodes (LMA). Shielded by this separator, LMA exhibits an impressive cycling performance, enduring a current density of 2 mA cm−2 for 350 h without short-circuiting, effectively doubling the cycle life compared to conventional PP separators. Furthermore, the Li/LiFePO 4 cell utilizing the CP@SiO 2 separator demonstrates a high capacity of 101 mAh·g−1 at 5C, with 90 % capacity retention after 1000 cycles. This outstanding electrochemical performance is attributed to the compatible anode/separator interface and the effective inhibition of lithium dendrite growth. The research presented in this work capitalizes on a synergistic configuration design, offering a promising pathway towards the development of high-safety and advanced lithium-ion separators. [ABSTRACT FROM AUTHOR]

Waste paper disposed in landfills notably contributes to greenhouse gas (GHG) emissions and impedes more sustainable, circular alternatives, such as recycling. In Hong Kong, this unsustainable approach is currently dominant as 68% of waste paper products are treated in landfills in 2020. To contextualize the impact of local waste paper management and explore mitigation potentials of circular alternatives, this paper develops a quantitative assessment framework around GHG emissions development trajectories. Combining guidelines of the Intergovernmental Panel on Climate Change (IPCC), national GHG inventories, and local parameters from life cycle analysis, five GHG emissions projections were simulated along the Shared Socioeconomic Pathways (SSPs) until 2060. Most recent baselines indicate that Hong Kong's current waste paper treatment generated 638,360 tons CO 2 -eq in 2020, comprising 1,821,040 tons CO 2 -eq from landfill and 671,320 tons CO 2 -eq from recycling, and −1,854,000 tons CO 2 -eq from primary material replacement. Proceeding along a Business-as-Usual scenario under SSP5, GHG emissions will dramatically increase to a net 1,072,270 tons CO 2 -eq by 2060, whereas a recycling-intensive scenario will lead to a net saving of −4,323,190 tons CO 2 -eq. To complement the quantitative evidence on the benefits of waste paper recycling, field research was conducted to explore the feasibility of circular policy innovation from the perspective of recycling stakeholders. These empirical qualitative and quantitative findings from stakeholders' business routines and material transactions provide crucial indications for policy and institutional innovation: Essentially, for Hong Kong to improve waste paper recycling capacities and facilitate a circular economy (CE), local stakeholders require support via fiscal policy measures (financial subsidies or tax reductions) and infrastructure improvements (delivery access and material storage). In sum, this study employs a novel analytical framework combining original qualitative and quantitative evidence to provide policy innovation towards circular, GHG emission-saving waste paper management. [Display omitted] • A new framework assessing greenhouse gas emissions from waste paper treatment. • Exploring long-term carbon neutrality pathways for managing waste paper. • Using empirical evidence from recycling stakeholders for circular policy innovation. [ABSTRACT FROM AUTHOR]

[Display omitted] Investigation of sluggish redox kinetics and polysulfide shuttling is crucial to design advanced lithium sulfur battery. Cerium oxide (CeO 2) has remarkable polysulfide adsorption capability and has been recently investigated in lithium sulfur battery application. With the goal of bridging towards commercialization of lithium sulfur battery, cellulose paper derived carbon fiber decorated with CeO 2 nanorods using hydrothermal method has been fabricated and used as interlayer material for lithium sulfur battery. In this novel design, the carbon fiber provides physical confinement with its 3-D interconnected conductive structure and CeO 2 adsorbs lithium polysulfides chemically to reduce shuttle effect to achieve long lifetime and high capacity for lithium sulfur battery. With a sulfur content of 2 mg, a high capacity of 1177 mAhg−1 was achieved at 0.2C with an excellent stability of only 0.11% capacity decay per cycle over 300 cycles. The improved performance is attributed to the binding of lithium polysulfides by CeO 2 and the blocking of polysulfides physically by the compact conducting carbon fiber. [ABSTRACT FROM AUTHOR]

[Display omitted] Enhancing the interfacial dispersion and suspension stability is crucial for magnesium hydroxide (Mg(OH) 2) nanomaterials in the long-term deacidification of paper-based cultural relics. However, because of the low specific surface area and the poor solvent compatibility of as-prepared large-sized Mg(OH) 2 , it often tends to agglomerate and settle down during the usage and storage, that is harmful for paper protection due to its unevenly deacidification and nonuniformly distribution on paper cellulose. Herein, we propose a feasible preparation of colloidal Mg(OH) 2 ultrathin nanoflakes with high dispersion stability via a simple one-step surfactant-assisted strategy. The surfactant acts as both a structure-direct agent to confine the growth of Mg(OH) 2 with rich active sites and a surface modifier to enhance its solvent adaptability and dispersion stability, avoiding the common fussy procedure with additional steric stabilizer. Owing to the evenly interaction with free acid species therein and the uniformly distribution on the paper fiber as alkaline reserve, the as-obtained Mg(OH) 2 presents the superior paper protection performance characterized by its safer pH of 7.29 for the original aged paper (pH = 5.03) and the excellent long-term anti-acidification effect with competitive pH of 5.47 after accelerated-aging at 105 °C for 5 months. Furthermore, Mg(OH) 2 nanoflakes with surfactant-modified structure also endue them as an improved flame retardant for multifunctional paper protection. The protection with Mg(OH) 2 has little effect on the paper surface properties and cellulose crystallinity, in line with the principle of least intervention. This work will put forward a feasible way toward colloidal Mg(OH) 2 nanoflakes with excellent paper protection performance, shedding light on the development of emerging protection materials for paper-based cultural relics. [ABSTRACT FROM AUTHOR]

Effective packaging solutions are pivotal in addressing sustainability challenges associated with food consumption. Sustainable packaging must not only reduce ecological impact but also ensure food quality preservation, minimize the risk of foodborne diseases, and contribute to mitigating the accumulation of plastic waste. While paper-based food packaging is environmentally friendly, it is susceptible to mold growth when exposed to specific humidity and temperatures, potentially leading to spoilage and safety concerns. This study introduces an innovative modeling approach employing survival analysis to estimate time to visible mold growth on paper-based materials used in food-contact packaging under varying environmental conditions. The objective is to establish an alternative statistical framework for assessing the impact of relative humidity and temperature on mold proliferation. This approach is particularly relevant to novel sustainable packaging materials in the food industry, especially when dealing with censored data. Survival heatmaps are developed to simplify the visualization of spoilage likelihood, measured by time to visible growth at a given confidence level. Although the survival model is proposed for paper-based materials, there are no theoretical limitations to its extension for use with other materials within and beyond the food industry. • Proposed survival heatmaps to simplify spoilage likelihood visualization. • Investigated spoilage characteristics of novel paper-based packaging. • Addressed challenges of censored data in mold growth modeling. • Proposed a conservative predictive model to assess spoilage timelines. [ABSTRACT FROM AUTHOR]

[Display omitted] Soybean-oil-based polymer is a promising bio-based water barrier coating on paper packaging but the application is challenged due to its poor water dispersibility. In this present study, 3-aminopropyltriethoxysilane (APTES) modified nanocrystalline cellulose (NCC) was used to implement a stable dispersion of acrylated epoxidized soybean oil (AESO) in water and thus synergistically improved the water vapor barrier properties after coating on paper. APTES-NCC was successfully prepared, and displayed a better interface compatibility with AESO through the Michael addition reaction. Compared with NCC, APTES-NCC displayed an improved hydrophobicity and wettability with AESO, with an increase of contact angle from 38.0° to 76.4°, and a decrease of interfacial tension from 91.5 ± 3.5 mN/m to 82.9 ± 1.8 mN/m. As an emulsifier, APTES-NCC can be more effectively adsorbed on the oil–water interface to form a more stable emulsion than NCC, with a decrease of AESO droplets size from 4.8 µm to 3.1 µm, and a remarkable improvement in static and centrifugal stability. In rheological measurement, the APTES-NCC/AESO emulsion showed a wider linear viscoelastic region (3.4%), better viscoelasticity and thermal curing properties than that of NCC/AESO emulsion, which further explained that the stability of APTES-NCC/AESO emulsion were improved. Therefore, APTES-NCC/AESO emulsion as a coating on paper cured into a continuous barrier film can effectively improve the water vapor barrier properties of paper, and the water vapor transmission rate (WVTR) of paper can be reduced from 1392.8 g/m2•24 h (NCC/AESO emulsion-coated) to 1286.3 g/m2 24 h (APTES-NCC/AESO emulsion-coated), both are significantly lower than that of base paper (1926.7 g/m2•24 h). CLSM testing showed that APTES-NCC could interact effectively with AESO to forming a tight barrier on paper surface and at the same time, sealing the pores inside the paper to resist water vapor penetration. The high-stable AESO emulsion prepared by APTES-NCC is expected to facilitate the utilization of NCC and AESO as a value-added material in making sustainable barrier packaging. [ABSTRACT FROM AUTHOR]

The pulp-paper industry is one of the main industrial sectors that produce massive amounts of residual sludge, constituting an enormous environmental burden for the industries. Traditional sludge management practices, such as landfilling and incineration, are restricted due to mounting environmental pressures, complex regulatory frameworks, land availability, high costs, and public opinion. Valorization of pulp-paper industry sludge (PPS) to produce high-value products is a promising substitute for traditional sludge management practices, promoting their reuse and recycling. Valorization of PPIS for biorefinery beneficiation includes biomethane, biohydrogen, bioethanol, biobutanol, and biodiesel production for renewable energy generation. Additionally, the various thermo-chemical technologies can be utilized to synthesize bio-oil, hydrochar, biochar, adsorbent, and activated carbon, signifying potential for value-added generation. Moreover, PPIS can be recycled as a byproduct by incorporating it into nanocomposites, cardboard, and construction materials development. This paper aims to deliver a comprehensive overview of PPIS management approaches and thermo-chemical technologies utilized for the development of platform chemicals in industry. Substitute uses of PPIS, such as making building materials, developing supercapacitors, and making cardboard, are also discussed. In addition, this article deeply discusses recent developments in biotechnologies for valorizing PPIS to yield an array of valuable products, such as biofuels, lactic acids, cellulose, nanocellulose, and so on. This review serves as a roadmap for future research endeavors in the effective handling of PPIS. [Display omitted] • Valorization of pulp-paper industry sludge is a sustainable option for getting waste to wealth. • Pre-treatment of pulp-paper industry sludge helps in yielding platform chemicals in the biorefinery scenario. • Pulp-paper industry sludge is a sustainable feedstock for renewable energy production. • Biochars derived from pulp-paper industry sludge exhibited excellent adsorption performance for metals removal. [ABSTRACT FROM AUTHOR]

The carbonization of lignocellulosic biomass with ionic liquids (ILs) are considered as an advantageous approach for the preparation of carbonaceous materials. The commonly used imidazolium and pyridinium based ILs have drawbacks such as toxicity, resistance to biodegradation, high cost and viscosity. These issues can be mitigated by diluting ILs with water, although excessive water content above 1 wt% can reduce the solubility of biomass. This research aims to investigate the potential of pretreating wastepaper with a "fully green" ILs, amino acid-based IL with high water content, followed by pyrolysis without IL, in enhancing the properties of biochar. For this purpose, the paper was treated with an aqueous solution of IL cysteine nitrate ([Cys][NO 3 ]), and the IL was not involved in the pyrolysis process to prevent the formation of secondary gaseous pollutants. The findings revealed that the hemicellulose and mineral filler in the paper were eliminated during pretreatment, leading to higher carbon content but lower oxygen content. As a result, the biochar exhibited micropores of 0.42 cm3g-1 and a specific surface area of 1011.21 m2 g−1. The biochar demonstrated high adsorption capacities for Cd2+, enrofloxacin, bisphenol A, ciprofloxacin, and tetracycline, with values of 45.20 mg g−1, 49.82 mg g−1, 49.90 mg g−1, 49.88 mg g−1, and 49.65 mg g−1, respectively. The proposed mechanism for the adsorption of enrofloxacin by the biochar primarily involves physical adsorption such as pore filling and electrostatic interactions, along with chemical adsorption facilitated by graphitic nitrogen. [Display omitted] • Amino acid-based IL with high water content removed the hemicellulose and minerals. • The specific surface area was four times of that of biochar without pretreatment. • More nitrogen was retained in the biochar and provided adsorption sites. [ABSTRACT FROM AUTHOR]

Abstract As promising energy storage equipment, Zn-air battery exhibits the advantage of high energy density, lightweight and compact structure over other rechargeable batteries, which is an ideal choice for electric vehicles. For Zn-air battery, the activity of air cathode plays an important role in its performance. Here, we report the fabrication of Co 3 O 4 based bulky electrode with three-dimensional mesoporous carbon as matrix, which originates from cheap filter paper precursor. This electrode exhibits excellent activity and durability in oxygen reduction (ORR) and oxygen evolution reaction (OER) process, which possesses small half-wave potential (ORR 1/2 = 0.811 V) and low overpotential (OER 10 = 1.518 V) for ORR and OER, respectively. With this electrode as air cathode directly, a rechargeable Zn-air battery is assembled successfully. During discharge process, the maximum power density of this Zn-air battery achieves 71 mW cm−2. Furthermore, it also exhibits high specific capacity (828 mAh g−1 at 20 mA cm−2, 544 mAh g−1 at 50 mA cm−2) and small voltage gap (0.91 V at 10 mA cm−2) in charge and discharge process. As a rechargeable battery, it also shows promising stability after long time charge-discharge experiments. Thus, we find out a simple and convenient method to fabricate cheap and effective bi-functional air cathode for rechargeable Zn-air battery. Graphical abstract A Co 3 O 4 electrode was fabricated with Co(NO 3) 2 ·6H 2 O and filter paper as precursors, which exhibits excellent ORR and OER activities. It was employed as air cathode in Zn-air battery. fx1 Highlights • Filter paper was employed as precursor to fabricate Co 3 O 4 electrode. • 3D mesoporous electrode with N-doped carbon as matrix is obtained. • The electrode exhibits excellent ORR and OER activities. • The electrode is employed as air cathode in Zn-air battery directly. [ABSTRACT FROM AUTHOR]

Abstract Many paper products are coated with plastic to improve their quality and stability. However, this limits recycling and recovery options and the plastic-coated waste paper is mostly disposed in landfills. Such practices are uneconomical and contrary to sustainable waste management. In this work enzymes of the white rot fungus Dichomitus squalens were investigated for possible delamination of plastic-coated waste paper. Enzymes were found capable to release the polyethylene foil from plastic-coated paper which resulted in 88.6–91.5% mass loss. The delamination rate, however, was depended on the ratio between plastic-coated paper and volume of enzyme filtrate. Results of a consequent experiment showed that enzymes are also efficient when plastic-coated paper is treated in a sequencing batch reactor resulting in 88.2–90.6% mass loss. The system was fully functional up to the 5th cycle; afterwards, the delamination rate reduced due to high thickness of the waste paper sludge. The enzyme activity, however, was still very high; with the laccase activity at the end of the experiment above 900 U/L and manganese peroxidase above 250 U/L. Our results demonstrated, that plastic-coated waste paper has the potential to be efficiently recovered instead of being disposed in landfills. Graphical abstract Image 1 Highlights • Enzymatic delamination of waste paper was investigated. • Enzymes were capable to release the polyethylene foil from the plastic-coated paper. • Treatment in a sequencing batch reactor is also possible. [ABSTRACT FROM AUTHOR]

Abstract Using waste paper as fuel for domestic heating is a beneficial recycling option for small island developing states where there are lacks of resources for energy and waste treatment. However, there are concerns about the impact of air pollutants emitted from the burning of the self-made paper briquettes as household air pollution is recognised as the greatest environmental risk for human. In this study, combustion tests were carried out for paper briquettes made in one Pacific island and three commercial fuels in Australia including wood briquettes, kindling firewood and coal briquettes in order to: 1) characterise the emissions of three criteria air pollutants including particulate matters, CO and NO x including their emission factors (EF) from the tested fuels; and 2) compare the EFs among the tested fuels and with others reported in the literature. The results showed that waste paper briquettes burned quickly and generated high temperature but the heat value is relatively low. Paper briquettes and coal briquettes produced higher CO concentration than the others while paper briquettes generated the highest NO x level. Only PM 2.5 concentration emitted from paper briquettes was similar to kindling firewood and lower than wood briquettes. Burning of paper briquettes and wood briquettes produced particulate matter with large average count median diameter (72 and 68 nm) than coal briquette and kindling firewood (45 and 51 nm). The EFs for CO, NO x and PM 2.5 of paper briquettes were within the range of EFs reported in this study as well as in the literature. Overall, the results suggested that using paper briquettes as fuel for domestic heating will not likely to generate higher level of three major air pollutants compared to other traditional fuels. Highlights • The first attempt to report emission of key air pollutants from waste paper briquettes. • Burning of paper briquettes emitted relatively high CO and NO x concentration. • Burning of paper briquettes emitted PM with large average particle size. • Waste paper could be recycled as briquettes for domestic use like other common fuels. [ABSTRACT FROM AUTHOR]

Paper mill Electrostatic Precipitator (ESP) ash contains a mixture of alkali metal chloride (34.2 %) and sulfate (84.2 %) which has serious negative effects on the environment and makes it more expensive and constrained to dispose ESP ash. Therefore, handling and recycling ESP ash demands extra thought when disposing of it. Present study, aimed to separate chloride and sulfate from ESP ash using electrochemical membrane technology. Three different concentrations of ESP ash solution such as 200 g L-1, 320 g L-1 and 450 g L-1 were used as the electrolyte. Ti/TiO 2 –IrO 2 –RuO 2 and titanium (Ti) are used as anode and cathode respectively. Caustic and sulfate solutions were recovered at the respective compartments. The collected sulfate solution was dried by solar light to convert 99 % sulfate salts as confirmed by Energy-dispersive X-ray analysis (EDAX) analysis. Recovered sulfate salt was used for the dye fixing process, in which the colour fixing difference of ΔE value was about 2.10 and the strength of the dye was about 86.72 %. Therefore, the textile industry can repurpose the recovered sulfate salt for the dye fixing process. [Display omitted] • An electrochemical membrane process was adopted to treat the ESP ash slat. • Na2SO4, Cl2 and alkali were recovered in a single electrochemical process. • Double layer cation exchange membrane provided good current efficiency. • Recovered Na2SO4 was used in the dyeing process and ΔE is 2.10 and dye strength is 86.72 %. • Sulfate concentration does not affect the CEM in the electrochemical process. [ABSTRACT FROM AUTHOR]

[Display omitted] • Trimetallic NiCoFe PBAs are electrodeposited homogeneously on CFP as precursors. • The NiCoFe-Se NCs grown on CFP as self-supported electrode for OER. • The NiCoFe-Se/CFP exhibits remarkable OER activity and desirable stability. • Trimetallic element regulation effectively improves the OER activity of selenides. The progress of inexpensive, high-efficiency, and steady oxygen evolution reaction (OER) electrocatalysts is of great importance to promoting water splitting for green hydrogen production. Herein, tri-metallic NiCoFe selenide catalyst backed up by carbon fiber paper (CFP) was synthesized by a facile selenization of NiCoFe Prussian blue analogues (PBAs) for OER in alkaline solutions. The NiCoFe-Se/CFP inherited the porous nanostructure of the metal-organic frameworks (MOFs) precursors prepared by rapid cyclic voltammetry electrodeposition. Benefiting from the 3D hierarchical porous structure, optimized electronic structure of NiCoFe selenides and high conductivity, the synthesized electrocatalyst exhibits outstanding catalytic activity to the corresponding mono-metallic or bi-metallic selenides. Specifically, the NiCoFe-Se/CFP electrode demands an overpotential of 221 mV to attain the 10 mA cm−2 current density in 1.0 M KOH solution and a low Tafel slope of 38.6 mV dec-1. The prepared catalyst also displays good stability and durability. These findings prove a feasible strategy to further improve the catalytic activities of non-precious metal based OER electrocatalysts by the cooperation of structure design and chemical component modification. [ABSTRACT FROM AUTHOR]

The research aimed to develop a paper box with 10–300 μl of cardamom oil to improve rambutan storage, reduce waste, and explore reuse possibilities. The experiment investigated the delay in mold growth caused by the post-harvest disease, Pestalotiopsis sp., both on the medium and on rambutan fruit under storage conditions of 10 ± 2 °C and approximately 80% RH. The results showed that CM at 300 μl significantly inhibited Pestalotiopsis sp. mycelium and spore germination on the medium, while a lower volume of 30 μl effectively delayed mold incidence on rambutan during the 14-day storage period. The confirmed antifungal mode of action indicated that CM disrupted Pestalotiopsis sp. ergosterol and cell membrane integrity, resulting in mycelium lysis and damaged morphology, thereby inhibiting its growth. The active fruit box can be reused for at least 2 or 3 storage cycles, effectively delaying rambutan decay and preserving its color change parameters. By using the box with 30 μl of CM, rambutan's shelf-life was extended to 14 days compared to the control's shelf-life of around 7 days. Active paper boxes offer a valuable solution for improving post-harvest fruit storage and transportation, benefiting both farmers and consumers. • A paper box with a CM paper pad effectively delayed the growth of Pestalotiopsis sp. • CM vapor released from packaging damaged the conidia and mycelium of Pestalotiopsis sp. • The paper box with CM can be reused at least twice to preserve the quality of rambutans. • CM showed destructive potential in the cell membrane of the fungi. • CM could maintain the quality of rambutan during storage seven to 14 days of storage. [ABSTRACT FROM AUTHOR]

The research assessed waste-based briquettes consumption compared to conventional fuels in the Andes. Laboratory tests were conducted together with on-field analysis in Colquencha (Bolivia). The laboratory study shows that the performances of briquettes are better in terms of PM2.5 (933.4 ± 50.8 mg kg−1) and CO emissions (22.89 ± 2.40 g kg−1) compared to animal dung (6265.7 ± 1273.5 mgPM2.5 kg−1 and 48.10 ± 12.50 gCO kg−1), although the boiling time increased due to the lower fuel consumption rate and firepower compared to shrubs. The social survey organized with 150 Bolivian citizens suggested that low-income households are not able to pay for an alternative fuel: about 40% would pay less than 4 USD per month, while methane use for cooking is positively correlated with the income level (r = 0.244, p < 0.05). On field analysis suggested that local cookstoves are not appropriate for briquettes combustion since indoor air pollution overcomes 30 ppm of CO and 10 mgPM2.5 m-3. On balance, local small manufactures can be the main target for selling waste-based briquettes to reduce shrubs and wood consumption. However, briquettes production costs seem not yet competitive to natural easy-to-obtain fuels (i.e., animal dung). The research encourages the use of cellulosic and biomass waste-based briquettes in the Andean area for cooking, heating, or manufacturing and strongly advises policy-makers to introduce economic incentives for the recovery of secondary raw materials. • Analysis of waste-based briquettes use in Andean areas were conducted. • Laboratory analysis, social surveys, and on field evaluations are the methods. • Briquettes can be employed for reducing about 30% of the conventional fuels. • The research encourages the employment of waste-based briquettes in the Andes. • Incentives to briquettes production and consumption should be introduced. [ABSTRACT FROM AUTHOR]

Novel Carbon quantum dots-graphite composite ink-based Screen-printed electrodes (CQDs/SPEs) were used to assemble a highly sensitive electrochemical aptasensor against chlorpyrifos (CPF). The aptasensor showed a broad linear range from 1 pM (0.445 ng/ml) to 500 nM (0.22 mg/ml) with a detection limit (LOD) 0.834 pM (0.37 ng/ml); sensitivity 21.39 μA pM−1 cm− 2 and with good linearity of R2 = 0.973. Moreover, the aptasensor's showed better selectivity among few other pesticides. Further, the aptasensor electrode showed high stability for five months when stored at 4 °C. In the final step, the aptasensor's ability to identify CPF in real samples was evaluated on spiked potato (Solanum tuberosum) extract samples. Potato extract spiked with CPF in the electrochemical aptasensing platform showed excellent linearity of R2 = 0.981. The developed aptasensor showed good response to without spiked potato extract with increasing volumes. Hence, the developed aptasensor demonstrated reasonable applicability in real food and agriculture samples. • Chlorpyrifos (CPF), an organophosphate pesticide, is known for detrimental effects on environment raising global health concern. • Electrochemical based disposable screen printed aptasensor is developed for the detection of chlorpyrifos pesticide. • The CQDs/SPE aptasensor was fabricated using carbon quantum dots (CQDs) through drop cast method. • The aptasensor exhibited a wide linear range (1 pM-500 nM) with LOD (0.834 pM) and high sensitivity (21.39 μA pM−1 cm− 2). [ABSTRACT FROM AUTHOR]

Flexible and conductive polypyrrole (PPy) paper shows the potential use in electromagnetic shielding, antistatic packaging, and electrochemical materials due to its low cost and facile manufacturing procedure. However, the poor mechanical strength and relatively low electrical stability of PPy paper is still challenging. In this study, we use horseradish peroxidase polymerized sulfonated alkaline lignin (HSAL) as a dispersant and dopant for PPy and demonstrate mechanically strong and electrically stable PPy paper by a combination of multiple impregnations and in-situ polymerization. The abundant sulfonic, carboxyl, and phenolic hydroxyl groups of HSAL could significantly improve the interfacial interaction between cellulose fibers and PPy. Meanwhile, its high molecular weight facilitated the uniform distribution of pyrrole along the fiber axial direction during in-situ polymerization. As a result, the resulting PPy paper exhibits enhanced mechanical properties and electrical stability, as well as high conductivity (24.84 S cm−1). More significantly, we investigated the influences of the dosage of HSAL and the cycles of multilayer impregnations on the electrical and mechanical properties of PPy paper. This work sheds light on the design and fabrication of flexible and conductive PPy paper with superior mechanical robustness and stable electrical performance. [ABSTRACT FROM AUTHOR]

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

An ultrafast and efficient strategy is developed to produce homogeneous GQDs through instantaneous photothermal gasification and recrystallization, revealing the promising potential for large-scale production. [Display omitted] Graphene quantum dots (GQDs) are attractive fluorescent nanoparticles that have wide applicability, are inexpensive, nontoxic, photostable, water-dispersible, biocompatible and environmental-friendly. Various strategies for the synthesis of GQDs have been reported. However, simple and efficient methods of producing GQDs with control over the size of the GQDs, and hence their optical properties, are sorely needed. Herein, an ultra-fast and efficient laser writing technique is presented as a means to produce GQDs with homogeneous size from graphene produced by the instantaneous photothermal gasification and recrystallization mechanism. Controlling the laser scan speed and output power, the yield of GQDs can reach to be about 31.458 mg/s, which shows promising potential for large-scale production. The entire process eliminates the need for chemical solvents or any other reagents. Notably, the prepared laser writing produced GQDs (LWP-GQDs) exhibit blue fluorescence under UV irradiation of 365 nm and the Commission Internationale de L'Eclairage (CIE) chromaticity coordinates is measured at (0.1721, 0.123). Overall, this method exhibits superior advantages over the complex procedures and low yields required by other existing methods, and thus has great potential for the commercial applications. [ABSTRACT FROM AUTHOR]

In this study, hydrogen harvesting from fermentation of sugarcane bagasse (SCB) was promoted by maintaining synergism between sulfonated graphene (SGR) catalyst and paper mill sludge (PMS). The sulfonic acid (–SO 3 H) groups in the catalyst played a major role in destructing the β-1,4 glycosidic bonds of sugarcane bagasse, releasing readily biodegradable sugars into the fermentation medium. The cellulose, hemicellulose, and lignin conversion efficiency were improved by 127.5%, 495.0%, and 109.2%, respectively with 20 mgSGR/gVS catalyst addition, compared with the control samples. These values were also higher than those obtained by non-sulfonated graphene catalyst. The hydrogenation of sugarcane bagasse was maximized at a sulfonated graphene catalyst dosage of 60 mgSGR/gVS, providing the highest hydrogen harvesting of 4104 ± 321 mL. This was associated with an increase of the Proteobacteria phyla up to 52.0%, Firmicutes phyla to 13.9%, and Acinetobacter sp. to 39.8% compared with only 37.0%, 11.3% and 11.1% in the control assay respectively. Moreover, sulfonated graphene catalyst supplementation promoted the acetate fermentation reaction pathway by increasing the acetate/butyrate ratio up to 4.1. Nevertheless, elevating the catalyst dosage up to 120 mgSGR/gVS reduced the hydrogen harvesting (1190 ± 92 mL) due to the release of furfural (1.76 ± 0.02 g/L) in the fermentation cultures, deteriorating the microbes' internal composition and metabolism bioactivities. Finally maximizing the hydrogen productivity from sugarcane bagasse is feasible by incorporation of paper mill sludge and sulfonated graphene catalyst at dosage not exceeding 60 mgSGR/gVS. However, investigating the recyclability and disposal of digestate containing sulfonated graphene catalyst and the associated economic feasibility needs more attention in the future. [Display omitted] • Sugarcane bagasse was fermented by paper mill sludge supported on sulfonated graphene. • Synergism between paper mill sludge/sulfonated graphene improved bio-H 2 by 4.8 times. • Sulfonated graphene promoted acetate fermentation (HAc/HBu of 4.1) and inhibited HPr. • Acinetobacter degrading phenol increased by 3.6 folds with sulfonated graphene catalyst. • MolDock visualized H-bonding in hydrogenase protein/sulfonated graphene interaction. [ABSTRACT FROM AUTHOR]

[Display omitted] From environmental waste to energy storage, waste boxes converted into conductive electrodes to further grow active materials has been an interesting way of upcycling. In this study, we transformed waste boxes of KIMTECH Kimwipes® into conductive f-MWCNTs light and flexible substrate (LFS) as current collectors. Then, undoped and P-doped active materials consisting of layered quadruple hydroxides (LQH) was successfully grown on the conductive f-MWCNTs/LFS. Specifically, P-doped f-MWCNTs/LQH demonstrates 1.8 times the capacitance of an undoped f-MWCNTs/LQH. Such conversion of waste boxes not only offers a useful way of reusing waste papers which commonly ends in landfills, but the inexpensive method also offers an extreme way of cutting cost in developing conductive substrates. Also, the effective strategy of synthesizing active materials on the conductive f-MWCNTs/LFS paves its way as potential cheap electrodes of the future generation. [ABSTRACT FROM AUTHOR]

The heteroatoms and transition metal co-doped carbon-based catalysts are an important way to improve the catalytic activity of oxygen reduction reaction (ORR). Herein, we reported a facile method to obtain iron, nitrogen, and sulfur co-doped cellulose paper carbon fibers as catalysts (Fe–N–S/CFs) for ORR in microbial fuel cells (MFCs) with the adsorption recovery of Congo red molecules from dye wastewater. The thermal treatment promoted the etching of carbon surface by ferric ions, resulting in increased surface roughness for forming the defective carbon structure. The rich active species and defective carbon formed on the etched surface to enhance the electroactive surface area and effective sites. Fe–N–S/CFs catalysts achieved high half-wave potential due to the synergy effect between chemical components and defect structures. The assembled single-chamber air cathode MFC gained a high maximum power density of 1773 ± 40 mW m−2 versus Pt/C MFC of 1325 ± 94 mW m−2. This work provides a strategy for recovering dye molecules from wastewater to prepare non-precious metal catalysts for enhancing ORR activity. • Mg(OH) 2 @PF was employed to efficiently adsorb Congo red from the dye wastewater. • Congo red/Mg(OH) 2 @PF co-calcined with iron nitrate to fabricate Fe–N–S/FCs catalyst. • The Fe–N–S/CFs showed the excellent ORR performance with the active specie of FeN x. • The assembled air cathode MFCs achieved high maximum power density (1773 ± 40 mW m−2). [ABSTRACT FROM AUTHOR]