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A simple electrochemical approach has been strategically developed for in situ generations of ZnO nanoparticles using Zn rods as electrodes and hydrogen peroxide as the oxidant without the formation of any by-product. These ZnO nanoparticles were extended for remediation of pollutants present in paper mill effluents, and separation efficiency was found to be above 90% for hydrocarbons, 92% for lignin, 99% for phenol, and 93% of chemical oxygen demand (COD), as confirmed by gas chromatography-mass spectrometry and COD analysis. It was also observed that the experimental setup could successfully remove 99% of the color from the sample. These ZnO nanoparticles have been proven in the past to be antibacterial and were explored for its ability to inhibit the growth of both Gram-positive and Gram-negative bacteria in the effluent samples after the removal of toxic pollutants. Therefore, we proposed an electrochemical reaction for the in situ synthesis of ZnO nanoparticles for remediation of paper mill effluent as well as inhibit the bacterial growth in the treated effluent sample.

The salivary glands are closely associated with stress conditions and the neuroendocrine system. The concentrations of these salivary biomarkers fluctuate with a person’s disease status. Until now, salivary diagnostics have been promising; however, the analytical tools for detecting salivary biomarkers have remained burdensome due to the lack of user-friendly and cost-effective equipment. In this study, we used a microfluidic starch-coated paper-based chip to isolate ɑ-amylase from human saliva. The concentration of ɑ-amylase on the head and tail sections of the paper-based chip was compared in the presence or absence of starch. We found that ɑ-amylase was highly concentrated only in the head section of the starch-coated paper-based chip through Western blotting (WB) and enzyme-linked immunosorbent assay (ELISA). We expect our designed paper-based chip will aid in α-amylase detection technologies using saliva and small amounts of other biofluids including blood, tears, pancreatic juice, and urine.

In this elucidation, we synthesized novel molecularly imprinted polymers (MIPOH1-4) that were used as organic fillers on bagasse pulp to form cellulosic paper sheets, the formation of MIPOH1-4 from the reaction of enaminone 3 with methyl methacrylate monomer in the presence of ethylene glycol dimethyl acrylate and 2,2’-azobisisobutyronitrile. The obtained MIPOH1-4 was confirmed via FT-IR and SEM with different pore sizes. And we noticed that the increase of template 3 increases the hydrogen bond between monomer and template and gave sponge surface of MIPOH4. Furthermore, the computational energies of the template with different monomers utilize DFT/B3LYP/6-31G (d) level to know the stability of polymers and hydrogen bonding between them. So that we applied that in paper manufacture through the adsorption of MIPOH4 as an organic filler on bagasse pulp to form novel cellulosic paper sheets with different concentrations and these sheets which characteristic through FT-IR, SEM, sizing test, tensile strength, and elucidation their antimicrobial activity with theoretical and docking studies. The MIPOH4 and cellulosic paper sheets showed the thermal stability and high tendency of sizability of these paper sheets and concluded the interaction between cellulose fibers of pulp with MIPOH polymer with physical hydrogen bonding.

A high-barrier, strong, and antibacterial paper was fabricated by coating the acetylated cellulose solution with different contents of cinnamaldehyde (CIN) on Kraft paper. The antibacterial, antioxidant, mechanical, and barrier properties of coated paper were investigated. When the amount of CIN added in coating reached 6% v/v, the coated paper exhibited excellent antioxidant activity and antibacterial activity against Escherichia coli and Staphylococcus aureus. Notably, the dry and wet tensile strength of paper after coating was increased by 26.4 and 10.6 MPa, respectively. Furthermore, the coated papers' barrier properties against oil, water, water vapor, and oxygen were dramatically improved, especially for the water barrier rate up to 96.4%. Our coated papers with over 6% v/v CIN could extend beef's shelf-life for at least 4 days, which exhibited a promising prospect in eco-friendly antibacterial packaging.

All-cellulose paper-based composites with underwater superoleophobicity and high-wet-strength were developed by casting a barrier layer of bacterial cellulose (BC) on a filter paper substrate. To optimize the pore structure of barrier layer, slow gel process of BC dispersion was conducted via acidification and solvent exchange. 1,2,3,4-butanetetracarboxylic acid was used to improve the wet strength and surface hydrophilicity through the crosslinking reaction between fibers. The underwater oil contact angles are higher than 150° in neutral environment, and slightly decrease under acid and alkali conditions. Combined with the micron-sized pore structure of BC barrier layer, the composite papers show good separation performance of oil-in-water emulsion. A denser BC layer can significantly improve the separation efficiency, but also lead to the reduction of flux. During the gelation of BC barrier layer, the increase in the ethanol/water ratio of the dispersion medium is able to increase the flux without obvious negative impact on the separation efficiency. When the ethanol/water ratio is 80%, the separation efficiency and water flux reach 99.2% and 1320 L m−2 h−1·bar−1 for the emulsified soybean oil with the average size of 13 μm, respectively. This type of all-cellulose composite papers provides a new idea for the fabrication of membrane materials for oil–water separation.

A paper-based membrane coated by graphitic carbon nitride (g-C3N4) is prepared via a dip-coating method and used as a separator for sodium metal batteries with merits of low cost and environment-friendliness. Introduction of g-C3N4 effectively improves the ionic conductivity and the structural stability of the separator. Compared with traditional polyethylene separators and Al2O3-coated separators, the g-C3N4-coated separators show better electrolyte wettability, thermal stability, and electrochemical stability. Therefore, Na||Na3V2(PO4)3 battery using the g-C3N4-coated separator exhibits better cycling stability and higher rate capability. These results prove that the g-C3N4-coated paper-based separator is expected to become the next generation of low-cost and high-safety separator in sodium metal batteries.

Natural cellulose paper is flame retarded using ammonium polyphosphate/montmorillonite (APP/MMT) nanocompound through coating method. Their morphologies are assessed by scanning electron microscopy, chemical components by energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy, chemical structure by Fourier transform infrared, thermal stability by thermo-gravimetric analysis and fire retardancy by 45° horizontal burning test. The results show that the thermal stability and flame retardancy of coated paper samples are enhanced obviously, and all samples are self-extinguishing during the tests due to the char formation reaction between APP/MMT and cellulose. Then the treated paper, AM-18.3, as surface flame retardant treatment for low specific surface area (SSA) polypropylene (PP) specimens (PP@AM-18.3) also is investigated using cone calorimeter. Compared with two controlled samples, PP@AM-18.3 shows significantly increased time to ignition, the lowest fire growth index and highest fire performance index. This may give a new flame retarded approach for low SSA polymer materials with little amount flame retardants.

An industry compatible chemo-refining approach was tested for preparation of micro-nanofibrillated cellulose (MNFC) from bleached softwood pulp using sodium meta-periodate and sodium chlorite as oxidizers followed by refining in Valley beater. SEM and FTIR analyses confirmed micro-nano scale fibrillation and chemical functional group modification in laboratory prepared MNFC, respectively. The water retention value, carboxyl content and viscosity of MNFC were found comparable with imported NFC as reference (R-NFC). To evaluate MNFC as strength enhancer for paper properties, 5% MNFC addition to bleached mixed hardwood pulp showed 6% reduction in bulk with 36%, 24% and 97% increment in breaking length, burst index and double fold of the handsheets, respectively without affecting tear index and optical properties than the control. Surface properties were also improved. Pulp drainability (37°SR) after MNFC addition was found suitable for papermaking. These laboratory results confirmed the potential of MNFC as a suitable strength additive for paper quality improvement.

In this study, a microfluidic paper-based analytical device (mu PAD) was integrated with a smartphone app capable of offline (without internet access) image processing and analysis for the rapid colorimetric detection of glucose. A self-inking stamp was used to form hydrophobic channels on a piece of paper-towel due to its superior water absorption efficiency. As demonstrated, the developed sensor was employed for the colorimetric detection of glucose in artificial saliva in the linear scope of 0 - 1 mM with a calculated detection limit of 29.65 mu M. The experimental results show that the quantitative analysis of glucose with the proposed smartphone platform could be completed in less than one minute. The app developed for the smartphone platform is capable of extracting the color-changing area with an embedded image processing tool which could address the problem of color uniformity in the detection zones of mu PAD. The integrated platform has great potential to be used for non-invasive measurements of glucose in body fluids, like tears, sweat and saliva.

Lightweight yet strong paper with high toughness is desirable especially for impact protection. Herein we demonstrated electrically conductive and mechanically robust paper (AP/PB-GP) made of reduced graphene oxide via interfacial crosslinking with 1-aminopyrene (AP) and 1-pyrenebutyrat (PB) small molecules. The AP/PB-GP with thickness of over ten micrometer delivers a record-high toughness (∼69.67 ± 15.3 MJ m−3 in average), simultaneously with superior strength (close to 1 GPa), allowing an impressive specific penetration energy absorption (∼0.17 MJ kg−1) at high impact velocities when used for ballistic impact protection. Detailed interfacial and structural analysis reveals that the reinforcement is synergistically determined by π-π interaction and H-bonding linkage between adjacent graphene lamellae. Especially, the defective pores within the graphene platelets benefit the favorable adsorption of the pyrene-containing molecules, which imperatively maximizes the interfacial binding, facilitating deflecting crack and plastic deformation under loading. Density functional theory simulation suggests that the coupling between the polar functional groups, e.g., −COOH, at the edges of graphene platelets and −NH2 and −COOH of AP/PB are critical to the formation of hydrogen bonding network.

Pathogen detection is crucial for human, animal, and environmental health; crop protection; and biosafety. Current culture-based methods have long turnaround times and lack sensitivity. Nucleic acid amplification tests offer high specificity and sensitivity. However, their cost and complexity remain a significant hurdle to their applications in resource-limited settings. Thus, point-of-need molecular diagnostic platforms that can be used by minimally trained personnel are needed. The nuclease protection assay (NPA) is a nucleic acid hybridization-based technique that does not rely on amplification, can be paired with other methods to improve specificity, and has the potential to be developed into a point-of-need device. In traditional NPAs, hybridization of an anti-sense probe to the target sequence is followed by single-strand nuclease digestion. The double-stranded target-probe hybrids are protected from nuclease digestion, precipitated, and visualized using autoradiography or other methods. We have developed a paper-based nuclease protection assay (PB-NPA) that can be implemented in field settings as the detection approach requires limited equipment and technical expertise. The PB-NPA uses a lateral flow format to capture the labeled target-probe hybrids onto a nitrocellulose membrane modified with an anti-label antibody. A colorimetric enzyme-substrate pair is used for signal visualization, producing a test line. The nuclease digestion of non-target and mismatched DNA provides high specificity while signal amplification with the reporter enzyme-substrate provides high sensitivity. We have also developed an on-chip sample pretreatment step utilizing chitosan-modified paper to eliminate possible interferents from the reaction and preconcentrate nucleic acids, thereby significantly reducing the need for auxiliary equipment. Graphical abstract.

The study describes the preparation of pulp and nanocellulose from non-wood plant materials, as well as an improved properties of paper and cardboard for mass production. The pulps from wheat straw, kenaf and flax fibers were prepared by the environmentally friendly organosolv method—cooking in a solution of isobutanol or peracetic acid. The organosolv pulps used to prepare nanocellulose had traces of lignin and mineral substances. The process of hydrolysis of the investigated organosolv pulps was optimal when carried out under the following conditions: 43% sulfuric acid, temperature 60 °C, hydrolysis time 90 min and ultrasonic treatment 60 min. Using the methods of SEM, XRD, TEM, AFM and TGA, the structure and properties of organosolv pulps and nanocellulose were studied. The use of nanocellulose in bulk and on the surface of mass types of paper and cardboard—paper for corrugation, offset paper, recycled containerboard and cardboard for flat layers of corrugated cardboard were investigated. We established the positive effect of nanocellulose application on the physical and mechanical properties of paper and cardboard. Low consumption of nanocellulose allows production of the paper and cardboard with properties that meet the requirements to appropriate standards and replacement of synthetic reinforcing materials.

Propofol is a widely used intravenous anesthetic agent in sedation and general anesthesia. To improve the safety and maintain the depth of anesthesia, it is important to develop a rapid, sensitive, and reliable method to monitor the concentration of propofol in blood during anesthesia continuously. Here, we present a novel strategy based on paper spray ionization-mass spectrometry (PSI-MS) to detect propofol. Samples (in 10 μL) were mixed with methanol as protein precipitation solvent and 2,6-dimethylphenol as internal standard. Protein micro-precipitation was achieved with methanol by vortexing and centrifuging for 5 s each, and propofol was extracted to the supernatant. PSI-MS was performed in negative ionization mode, and MS signal lasted for 1 min. The analysis of a single sample was completed within 2 min. The area ratios of propofol to internal standard were calculated for quantification. Limit of detection of 5.5 ng mL−1 and limit of quantification of 18.2 ng mL−1 were achieved for propofol in whole blood. Calibration curve was linear in the range of 0.02–10 μg mL−1. The developed method was used successfully in monitoring the propofol concentration in 3 patients’ whole blood during anesthesia, showing its further application in controlling and feeding-back target concentration infusion.

Microfluidic paper-based analytical devices (μ-PADs) fabricated in Japan were employed for the determination of total chromium (Cr) in water, soil, and lettuce irrigated with wastewater in Ethiopia. The μ-PADs, which were printed by wax printing in Japan, were transported to Ethiopia and prepared for the determination of total Cr by adding appropriate reagents to the pretreatment and detection zones. Soil and lettuce samples were determined by the μ-PADs and a UV-Vis spectrophotometer in Ethiopia. A paired t-test showed that the mean total Cr concentrations determined in the soil and lettuce samples were not significantly different between μ-PADs and UV-Vis spectrophotometric analysis at the 5% level of significance. This implies that the μ-PADs have good accuracy and reliability, and could be employed to monitor Cr in environmental samples. We found that the total Cr concentrations in all soil and lettuce samples were above the permissible limit. Moreover, evaluating Cr contamination level using the geo-accumulation index indicated that the soils were contaminated with Cr moderately to heavily. Thus, the present work successfully demonstrated the potential of remote investigations of pollution in a less-equipped laboratory by transporting the μ-PADs fabricated in another laboratory.

This study demonstrates a method for patterning paper-based microfluidic devices. An octadecyltrichlorosilane (OTS) solution is used to coat a chromatography paper to make it hydrophobic. A low-temperature (~ 32.9 °C) atmospheric-pressure dielectric-barrier-discharge jet with a shadow mask is then used to pattern hydrophilic stripes on the OTS-coated hydrophobic paper. In this manner, 1-mm-wide hydrophilic stripes are patterned successfully. Liquids are demonstrated to be transported and mixed in the hydrophilic stripes. Water contact angle measurement, X-ray photoelectron spectroscopy, surface profiler, optical emission spectroscopy, and scanning electron microscopy are used to characterize effect of pattering.

In this paper hemicellulose was separated by using 1-ethyl-3-methylimidazolium acetate (EmimAc, an ionic liquid) -water mixtures from a paper grade market bleached hardwood kraft pulp to produce dissolving pulp. Pure EmimAc dissolves pulp fibers completely in 30 min at ambient temperatures. By adding water (as an antisolvent to EmimAc system) the cellulose dissolution decreases and by optimizing the conditions, hemicellulose is largely removed while cellulose remains as the solid residue (dissolving pulp). At optimal conditions: molar ratio of water to EmimAc of 2, 60 °C, an alpha-cellulose content of 92.2%, with a high yield (78 wt%) was obtained. The viscosity of the solvent mixture decreases by increasing water to EmimAc molar ratio, which improves the mobility of ions, thus, facilitating their penetration into pores and lumens of the fibers during the dissolution process. Cellulose purity increases and purified cellulose yield decreases with the increases in temperature and water content (up to 2 wt%) in the mixture. This study implies that the optimal EmimAc/water mixture is an effective system to separate hemicellulose from hemicellulose/cellulose matrix.

A method for treating cellulose paper using the ionic liquid 1-butyl-3-methylimidazolium chloride ([BMIM]Cl) was developed. The treatment was intended to reform the paper structure. Filter paper was immersed in 20 g of molten [BMIM]Cl at 80 °C for 20–80 s and then washed with ethanol and distilled water. The treated paper was then immersed in tert-butyl alcohol before drying in a freeze dryer for 30 min. Next, polyethylene glycol (PG) and trichloromethylsilane were fixed to freeze-dried paper. The paper treated with [BMIM]Cl had a higher specific surface area than that not treated with [BMIM]Cl, and the specific surface area increased as the treatment time increased. The amount of PG fixed to the paper increased as the specific surface area of the paper increased, and PG improved moisture retention. The degree to which the moisture retention was improved was therefore related to the increase in the specific surface area caused by [BMIM]Cl treatment. Addition of trichloromethylsilane to the paper treated with [BMIM]Cl improved the hydrophobicity, and this was caused by the [BMIM]Cl treatment. Overall, [BMIM]Cl treatment was effective for reforming the paper structure and this improved the amount of functional material that could be fixed to the paper.

Water–oil separation from their emulsions and mixtures has been a prominent topic in fundamental research and in industries. A superhydrophobic/oleophilic membrane (SHP) was obtained by dipping a cellulose filter paper in an acetonitrile solution of toluene diisocyanate (TDI) and in that of N-(2,4-diaminophenyl) maleimide, alternatively and repeatedly for three times, to make the paper coated by maleimide-containing polyurea (PU), which was then reacted with n-dodecanethiol (DAT) through Michael addition to obtain the superhydrophobic porous membrane (SHP). All the involved reactions were confirmed by different techniques. SHP membrane as prepared was demonstrated to be superhydrophobic and oleophilic and of high performance in separation of oil and water from their emulsions and mixtures. This study provides a new route to the fabrication of new materials of high superhydrophobicity and oleophilicity, featured by ease of fabrication, low-cost and versatile availability of the starting materials, both synthetic and natural.

Fluorine-free cellulosic paper was successfully obtained by coating the glassine base paper with eco-friendly cellulosic coating, which was made from dissolving cellulose in 8 wt% NaOH/12 wt% urea aqueous solution. Then the coated paper was severally immersed into CH3COOH, Na2SO4, and H2O solution to coagulate and regenerate. Benefiting from the compact matrix and fully covered surface, the resultant cellulosic paper exhibited favorable barrier properties and mechanical performance. Notably, the paper coagulated with CH3COOH displayed the reduction in water–vapor transmission rate, air permeability, and uptake of organic solvents due to its low porosity (26.8%) and narrow pore size distribution (0.1–0.36 µm). The tensile strength and elongation at break of papers treated by CH3COOH at coating weight of 5 g/m2 were increased by 72.1% and 34.0%, respectively. In summary, the fluorine-free cellulosic paper with high oil and grease resistance is attractive for the development of high-performance materials for food packing applications. Fluorine-free paper was obtained from the glassine base paper coated with eco-friendly, non-fluorinated, and degradable cellulosic coating, then coagulated with CH3COOH, Na2SO4, and H2O solution, respectively. The resultant functional papers displayed enhanced barrier properties (oil, organic solvent, vapor, and gas) and mechanical performance.

The use of nanocelluloses is being conducted for the most diverse applications. Their performance as coating agent has been mainly explored to improve barrier properties, as they emerge as perfect candidate for plastic substitution, but it is also important to explore their potential to improve printing quality. In the present work, the influence of different nanocelluloses, obtained through mechanical, enzymatic, TEMPO-mediated oxidation and carboxymethylation treatments, in the coating process and inkjet printability of office papers was assessed. The results revealed that the cellulose nanofibrils are better for printability than the microfibrils. But the size and charge of the former must be taken into account, since fibrils of very small size penetrate the paper structure, dragging the pigments from the surface, and very anionic nanofibrils can also have negative influence on the optical density. Besides, an interesting synergy between surface-sizing starch and the cellulose nanofibrils was found to occur as the latter closed the paper structure, which prevented starch from penetrating, while potentiating both of their positive effects on ink pigment entrapment. An additional study of characterization of inkjet pigments was also performed.

Chitosan is a biopolymer that has shown promising results for surface treatment of paper to enhance barrier and mechanical properties. Commercially, chitosan is available with a wide range of degree of deacetylation (DD). Herein, effect of DD on performance of chitosan in surface application of paper is investigated. Surface application of chitosan of different DD (77%, 84% and 94%) was done at a dose of 1.0 ± 0.2 g/m2 on kraft paper and comparison in terms of strength, structural, surface and barrier properties of paper was performed. Different DD of chitosan was confirmed by FTIR analysis. Results showed that breaking length of paper maximally increased by 15.2%/26.6% in machine direction (MD)/cross direction (CD), respectively after surface application of 94% DD chitosan followed by 77% DD and 84% DD. The maximum increase in burst index, stretch in MD and TEA in both directions of paper was found after surface application of 94% DD chitosan. Results attained by 77% DD and 84% DD chitosan for improvement in burst index, stretch and tensile energy absorption of paper were also encouraging. Maximum increase in stiffness was observed in CD with application of 84% DD chitosan. Double fold of paper also increased the maximum after surface application of 84% DD chitosan. The best results of contact angle, surface energy, Cobb60 and water vapor transmission rate were attained after surface application with 94% DD chitosan whereas the results attained by 77% DD and 84% DD chitosan for contact angle, surface energy, Cobb60 were also encouraging.

Gas chromatography is commonly employed to detect gaseous pollutants. However, gaseous pollutants in paper mills are multicomponent and difficult to be detected and analyzed by gas chromatography. Therefore, we developed a novel autoanalyzer with an embedded supervisory system, with which multicomponent gaseous pollutants in paper mills can be detected in real time. The autoanalyzer was applied in two paper mills for the detections of the total volatile organic compounds (TVOC) and benzene at five sampling sites. The detection results show that the TVOC concentrations in two mills exceed the standard severely, especially in mill A, which can be attributed to the application of pulping and bleaching chemicals. In addition, benzene is also detected in Mill A due to benzene release from the fluorescent brighteners in the papermaking section. The large amounts of TVOC detected in the sequencing batch reactor (SBR) equalization tank of Mill A are explained by their release from the biodegradation of wastewater.

In this study, different methods for incorporating mixed or laminar copper microparticles (CuMPs) during papermaking were evaluated to determine the optimum paper-making process and correlate particle concentration and shape with antimicrobial activity. The addition of CuMPs during the disintegration of dry pulp stage was observed to produce a paper with uniformly distributed CuMPs, as determined through optical microscopy and UV–Vis spectroscopy analyses by measuring absorbance spectra in different areas of papers. Determination of two indices related to the concentration and distribution of copper will allow to predict the copper content in other papers. CuMP-paper samples were evaluated for structural, optical, and mechanical strength properties according to paper industry standards. Quantitative analyses by atomic absorption showed that between 24 and 39% of CuMPs were embedded in the paper fibre, independent of particle type. Finally, antibacterial activity analyses were performed according to ISO 20645 and ISO 20743. The results showed that papers with 0.30 g of incorporated CuMPs have antimicrobial activity, independent of particle morphology, with effects observed towards Gram (+) and Gram (−) bacteria and fungus. Furthermore, the evaluation of antimicrobial activity at different times of exposure to the microorganisms showed differences in effects that were dependent on the shape of the CuMPs incorporated into paper, where laminar particles exerted a sufficient effect, while no or a slight effect was observed for mixed CuMPs against Aspergillus niger.

Mixed office waste paper (MOWP) is a low cost, high quality and easily collected fiber source for the papermaking industry. Unfortunately, limits in the application of traditional deinking are related to the negative environmental impacts of using chemicals during the deinking process. Hence, enzymatic deinking has received growing attention in the last decade. This study investigates the effect of using the effective enzymes produced from Rhizopus microspores AH3 which is grown on watermelon peel waste (WPW) extract, as a bio-deinking method in the deinking of MOWP, which is difficult to recycle because of their ink type and printing process. The methodology involves preparation of samples, impregnation with water, enzymatic treatment, washing, papermaking, evaluation of the produced paper sheets. The evaluation includes determination of the optical and mechanical properties as well as topographic investigation via scanning electron microscope of produced paper sheets. The results showed that there is an improvement in both optical and mechanical properties of all paper sheets produced in this study. The best enhancement was for medium B30 which was extracted by boiling of WPW for 30 min. This treatment gave high enhancement because of the effect of the produced enzymes from Rhizopus microspores AH3, where cellulase, xylanase, lignin peroxidase, poly phenol oxidase and laccase were 1.62, 1.49, 1.38, 1.2 and 1.5 U/ml, respectively. Moreover, the tensile strain (maximum load) increased by about 77% as well as the brightness percentage achieved about 86.78% and the deinking ability was increased approximately 16%.

Green/sustainable cellulose paper-based platforms at point-of-care testing have received much interest in biomedical fields at resource-limited settings. In such platforms, biomolecules would have to be immobilized onto paper substrate to achieve detection. Therefore, effective molecule immobilization is critical for the performance of paper-based testing, especially the detection sensitivity. Although various methods have been developed to improve the detection sensitivity, the immobilization capacity of biomolecules has not been considered yet. In this study, we developed a facile method for modifying paper materials by incorporating chitosan into NC membrane, which has positive effect on the pore size, porosity, and surface groups of NC membrane, hence, enhancing the immobilization capacity of biomolecules on paper substrate. We demonstrated the effectiveness of the above mentioned approach by using nucleic acid lateral flow assay (NALFAs) as a model paper-based platform; in comparison with the unmodified NALFAs, the results showed ten-fold increase in the detection sensitivity for HBV. We envision that this facile modification method will have a great potential for developing other highly sensitive paper-based detecting platforms.

We report a smartphone–paper-based sensor impregnated with cetyltrimethylammonium bromide modified silver nanoparticles (AgNPs/CTAB) for determination of Fe3+ in water and blood plasma samples. The methodology for determination of Fe3+ is based on the change in signal intensity of AgNPs/CTAB fabricated on a paper substrate after the deposition of analyte, using a smartphone followed by processing with ImageJ software. The mechanism of sensing for detection and determination of Fe3+ is based on the discoloration of AgNPs which impregnated the paper substrate. The discoloration is attributed to the electron transfer reaction taking place on the surface of NPs in the presence of CTAB. Fe3+ was determined when the paper was impregnated with 1 mM AgNPs for 5 min of reaction time and the substrate was kept under acidic conditions. The linear range for determination of total iron in terms of Fe3+ was 50–900 μg L−1 with a limit of determination (LOD) of 20 μg L−1 and coefficient of variation (CV) of 3.2%. The good relative recovery of 91.3–95.0% and interference studies showed the selectivity of the method for determination of total iron in water and blood plasma samples. Smartphone–paper-based sensors have advantages of simplicity, rapidity, user-friendliness, low cost, and miniaturization of the method for on-site determination of total iron compared to methods that require sophisticated analytical instruments.

Cellulose is the main component of transformer insulating paper. In this paper, the pyrolysis mechanism of cellulose is studied by means of computational chemistry. This study is aimed at exploring the generation process of the methanol from cellulosic insulating paper at the atomic level. A simulation scheme of cellulose pyrolysis with detailed reaction pathways for methanol production has been obtained that is not readily accessible by experiments. The molecular dynamics method based on reactive force field (ReaxFF) is adopted to simulate the pyrolysis of cellobiose. A model composed of 40 cellobioses simulated at 500–3000 K was established, and the force biased monte-carlo is mixed into ReaxFF to make it closer to the actual situation and ensure the reliability. The result reveals that the –CH2– group from the C5 (or $${\text{C}}_{ 5}^{{\prime }}$$) group in cellobioses grabbed the nearby H atom to form methanol. In the pyrolysis process of cellobioses, methanol is stable at the early stage but unstable even disappeared in the later stage. The pre-exponential factor A and activation energy Ea of the ReaxFF-MD simulation are consistent with previous experimental results. Thus, this study provides an effective theory of the methanol as an indicator to evaluate the aging condition of cellulosic insulating paper in the early stage at the atomic level.

The utilization of nitrophenols as raw materials for the synthesis of dyes, explosives, pesticides, and pharmaceuticals has increased the presence of nitrophenols as pollutants in industrial and agricultural wastewater. Similarly, the wide application range of rhodamine 6G and methylene blue enable their potential as pollutants of surface and ground waters. Both classes of chemicals can change water ecosystems dangerously. In this study, filter paper-based silver nanoparticles are prepared as catalysts for reduction of 4-nitrophenol to 4-aminophenol and for degradation of rhodamine 6G and methylene blue. This method avoids utilization of toxic reagents and is simple and inexpensive. The formation of the silver nanoparticles on filter paper was characterized using different techniques, such as scanning electron microscopy, X-ray diffraction, and surface-enhanced Raman spectroscopy. In the presence of sodium borohydride, the silver nanoparticles coated filter paper was able to reduce 4-nitophenol to 4-aminophenol within a short period of time. It has been found that, the nanocatalyst can be recycled and recovered from the reaction solutions easily without losing its high efficiency. Additionally, we demonstrated the potential of the substrate to study the in situ reduction reaction via surface-enhanced Raman spectroscopy.

In this study, we developed a simple, inexpensive and easily fabricable paper-based SERS substrate with high sensitivity and reproducibility. The filter paper has natural pleats and small pores that allow the metal nanoparticles to be deposited and arranged on the paper to form large area SERS ‘active sites’. Silver nanoparticles can be embedded and grown on cellulose nanocrystals framework through the in situ reduction to form cellulose nanocrystal–silver (CNC–Ag) composites, which are coated on the filter paper to form composite paper-based substrates. The CNC–Ag composites further filled the pores on the surface of the filter paper and improved the adhesive rate of metal nanoparticles, thus the reproducibility of the SERS sensor has been improved. At the same time, because it has the agglomerating effect on samples, the hydrophobic dodecyl mercaptan covered on paper-based substrates can improve detection limit of analyte. Furthermore, we demonstrate that paper-based SERS substrates can efficiently detect two substances, including phenylethanolamine A and metronidazole. The limits of detection for phenylethanolamine A and metronidazole were found to as low as 5 × 10−9 M and 2 × 10−7 M, respectively. The paper-based SERS substrates offer great potential for label-free and on-site detection of trace substances.

Effective separation of oil and water has always been a long-term challenge. Here we introduce a facile and fluorine-free method to fabricate superhydrophobic and superoleophilic filter paper without the decoration of solid particles for robust oil/water separation. After chemically bonding octadecanoyl and α-bromoisobutyryl groups on the surface of filter paper through simultaneous esterification with stearoyl chloride and α-bromoisobutyryl bromide (BiBB) to obtain C18-FP-g-Br, superhydrophobic poly(styrene-co-acrylonitrile) (SAN) grafted filter paper (C18-FP-g-SAN) was fabricated via surface-initiated atom transfer radical polymerization. The obtained C18-FP-g-SAN showed a water contact angle of 153° and achieved a separation efficiency exceeding 98.5% after ten different typical oil/water separation processes due to the synergistically combined contributions of bonded octadecanoyl chain and grafted SAN. C18-FP-g-SAN remained high separation efficiency after 10 cycles of use and treatment with strong acidic or basic solution. The excellent reusability and chemical stability of C18-FP-g-SAN promise its practical applications of continuous oil/water separation and oil spillage cleanup.

The use of dielectric nanofluids has been recently proposed as a method to improve the insulation system of transformers. It has been widely reported that these liquids present superior dielectric properties than conventional dielectric liquids and have a better behavior as cooling agents. Nevertheless some aspects need to be addressed before these materials are applicable to real equipment. This paper analyzes the interaction between dielectric nanofluids and the cellulose materials that constitute the solid insulation of transformers. The impregnation process of a transformer has been emulated in order to obtain samples of solid insulation impregnated with a Fe3O4 based nanofluid. The samples have been subjected to ICP testing and CryoSEM observation, complemented with the determination of the EDX sprectrum. The interaction between the nanoparticles and the cellulose fibers has been investigated finding that bonds are established between them when cellulose is impregnated with nanofluids. This research was funded by the Spanish Ministry of Economy and Competitiveness. Grant Number DPI2015-71219-C2-2-R and Spanish Ministry of Innovation. Grant Number PID2019-107126RB-C21.

Polyhedral oligomeric silsesquioxane (POSS) has eight substituent groups, which can be substituted with various substances to obtain different modification effects. In order to study the effect of different substituents on the modification of cellulose by POSS and its internal mechanism, the pure cellulose model and the modified cellulose with three kinds of POSS derivatives, polyoctamethyl silsesquioxane (PMSQ), polyoctaphenyl silsesquioxane (PPSQ) and polyoctaaminophenyl silsesquioxane (OAPS), were established by molecular dynamics method. The thermal stability parameters and polarizability were calculated. The simulation results showed that different POSS derivatives can improve the thermal stability of insulating paper cellulose, and the modified effect of OAPS is the best. Compared with the unmodified model, the glass transition temperatures of the modified cellulose models of PMSQ, PPSQ and OAPS increased by 58 K, 63 K and 71 K, respectively. The mean square displacement of the modified models is significantly reduced, and the free volume is increased. The addition of POSS derivatives increase the entanglement between the cellulose chains, and compresses the gap between the cellulose molecular chains to suppress the movement of the cellulose chain. It is also found that the addition of POSS derivatives can effectively reduce the polarizability of cellulose, even the electric field distribution in oil paper insulation system, so as to enhance the insulation of transformer.

Cellulose-based material has been increasingly used as a suitable substrate for depositing metal–organic frameworks (MOFs) in recent years. In this work, MOFs (Cu-BTC) were deposited onto carboxymethylated filter paper (CMP) using four different preparation procedures: one-pot, two-step, layer-by-layer-organic (LbL-org), and layer-by-layer-water-organic (LbL-wtr-org). The products (Cu-BTC@CMP) were comparatively characterized by SEM, ATR FT-IR, XRD, and BET specific surface area analyses. The Cu-BTC crystals were immobilized on the CMP surface, where different deposit ratios (1.31% for one-pot, 4.23% for two-step, 31.49% for LbL-org, and 39.38% for LbL-wtr-org, respectively) were obtained when different preparation procedures were used under the precondition of the same chemical dosage and reaction time. The Cu-BTC crystals were found to grow in the main solution rather than on the substrate surface and the layer-by-layer method would contribute to a remarkable quantity of MOFs depositing onto the substrate surface. The crystals on Cu-BTC@CMP surface prepared by LbL-wtr-org procedure presented a much larger particle size and rougher surface compared to those prepared by the LbL-org procedure due to the aqueous solution of copper precursor. Depositing more Cu-BTC onto CMP surface also endowed the composite prepared by LbL-wtr-org procedure with the highest gas adsorption capacity (1.59 × 102 m2/g of BET specific surface area). Hence, the LbL-wtr-org procedure will be an optimal pathway for depositing metal–organic frameworks onto cellulose-based materials with the advantages of saving organic solvents and best gas adsorption ability.

In this work, the mechanical properties of Kraft paper (KP) coated with a coating formulated with recycled polystyrene dissolved in the solvent lime limonene (rEPS/LL) are investigated. These mechanical properties are compared with those of KP coated with three different commercial coatings: oil-based alkyd coating (ALKY), oil-based phenolic coating (PHEN) and water-based acrylic coating (ACRY). The morphology characterization via scanning electron microscopy showed the KP coated with rEPS/LL resembles a layered structure, in which, part of the coating remained on the surface and part of the coating was absorbed by the KP. The KP coated with rEPS/LL exhibited the highest tensile stiffness and compression strength when compared to the uncoated KP and KP coated with commercial coatings. The remarkable compression properties of the KP coated with rEPS/LL coating may be explained by the bending and crushing mechanisms observed during the ring crush test. The excellent mechanical performance of rEPS/LL combined with an environmentally friendly process to obtain recycled EPS using a bio-based solvent presents several advantages for coating applications. These results warrant further research to fully understand the properties of KP coated with rEPS/LL.

Infections caused by foodborne microorganisms are a great threat to the global environment and public healthcare today. Thus, rapid, portable and sensitive assays that can realize the identification of foodborne bacteria are highly desired. In this study, a smart fluorescent and colorimetric dual-readout sensing system has been established for simple and rapid E. coli determination by utilizing the Cu2+-triggered oxidation of o-phenylenediamine (OPD). Initially, Cu2+ can oxidize OPD to OPDox, resulting in an orange-yellow fluorescence and visible pale-yellow color. However, E. coli can effectively reduce Cu2+ into Cu+, inhibiting the Cu2+-triggered oxidation of OPD to OPDox. Consequently, the introduction of E. coli can turn off both the fluorescence and the UV-vis absorbance signals of the OPD-Cu2+ system, illustrating an original mechanism for fluorescent and colorimetric dual-channel detection of E. coli. Moreover, a filter paper-based visual sensor was built and coupled with OPD-Cu2+ solution under the assistance of a UV lamp. The as-prepared sensor can detect E. coli quantitatively with the help of a typical smartphone color-scanning application (APP). Thus, this study offers a valid dual-mode assay for sensitive and on-site visible detection of E. coli, guaranteeing the reliability of the results and is more attractive for practical use. Graphical Abstract Schematic illustration of the smartphone-integrated sensing system for fluorescent and colorimetric dual-channel detection of E. coli based on the Cu2+-OPD system.

构建基于有机材料的高性能柔性储钠电极面临诸多挑战. 本 工作通过可控组装及还原的方式, 实现了铁基配位聚合物纳米线/还原氧化石墨烯柔性薄膜的构筑. 多维复合薄膜可直接用作钠离 子电池自支撑负极, 且具有较高的储钠容量(200 mA g−1电流密度 下可逆容量为319 mA h g−1)和优异的倍率性能(3000 mA g−1大电 流密度下比容量可保持在∼120 mA h g−1). 研究表明有机配体(氨 三乙酸)中的羧基及氨基为储钠活性位点, 而配位金属离子(Fe2+)不 参与电化学反应.

Owing to the increasing amount of industrial wastewater and ocean pollution, separation of water and oil from their mixtures and emulsions has been an active area in water treatment industry and in academic research. Using cellulose filter paper as the substrate, a porous superoleophobic membrane (OP) was easily prepared by immersing the paper in an acetonitrile solution of toluene diisocyanate and that of N-(2,4-diaminophenyl) maleimide, alternatively and repeatedly, coating the paper with maleimide-containing polyurea (PU). PU coated paper was then functionalized by 2-[(tris(hydroxymethyl)methyl)amino]-1-ethanesulfonic acid through aza-Michael addition. The formation of PU coating and the subsequent functionalization were confirmed by FTIR, NMR and XPS analyses. The produced OP paper was shown to be superoleophobic and had excellent performance for oil–water separation from their mixtures and emulsions. This study provides therefore a novel protocol for preparation of superoleophobic materials, featuring easy operation, low cost, and in particular, versatile applicability to different natural and synthetic materials.

Tissue paper that is prepared from bamboo has a very promising future in the world, especially in China, thanks to the various merits of bamboo fibers. However, the water absorption behavior and mechanical properties of bamboo pulp based tissue paper need to be improved due to the inherent drawbacks of bamboo fiber, such as high stiffness, weak interaction between bamboo fibers etc. Hence, cellulose nanofibers (CNFs) were combined with bamboo fibers before the tissue paper-making process, to improve the water absorption behavior and mechanical properties of tissue paper. The hypotheses are that: (1) CNFs themselves possess large specific surface area and abundant hydroxyl groups as well, thus enhancing the hydrophilicity of tissue paper; and (2) the added CNFs can form 3D structures in tissue paper, thus providing abundant pores with uniform small size, which would facilitate the capillary effect for water absorption; and (3) more hydrogen bonds will be formed between CNF and bamboo fibers, thus improving the strength properties of tissue paper, thanks to the excellent mechanical and physical properties of CNF. The results from water absorption and tensile strength tests of bamboo handsheets indicated that the addition of CNFs can increase the water absorption capacity from 6.6 to 8.7 g/g when the CNF dosage was 10 wt% (based on the dried pulp). The water retention value of prepared bamboo fibers increased from 163 to 190% at the same CNF dosage, the tensile index increased from 18.5 to 24.5 N m/g as well. The results from the bulk and pore size analyses, FTIR, as well as SEM images of tissue paper also evidenced the conclusions above. Cellulose nanofiber (CNF) as a versatile filler for the preparation of bamboo pulp based tissue paper with improved water absorption behavior and mechanical properties

Recycled paper and some hardwood paper often display poorer mechanical properties, which hinder its practical applications and need to be addressed. In this work, cellulose nanofibrils (CNFs) obtained by a combined process of enzymatic hydrolysis and grinding (EG-CNFs), grinding and microfluidization (GH-CNFs) or TEMPO-mediated oxidation and grinding (TE-CNFs) were characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Moreover, CNFs were made into films on which some characterizations including X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and UV–Vis transmittance spectroscopy were implemented. Results showed that CNF fibrillation was promoted as times of passes increased in microfluidization, and CNFs pretreated by enzyme possessed shorter length. Crystallinity of CNFs was related to CNF manufacturing methods, while CNF films’ transparency was correlated to CNF diameter distributions. Moreover, CNFs were applied with different dosages on recycled and hardwood paper. Lengths of CNFs, strength of CNF network, and pulp properties were critical factors affecting the mechanical strength of CNFs-enhanced paper. GH-CNFs showed better strengthened effect on tensile strength of paper than TE-CNFs and EG-CNFs. The best overall improvement was achieved at GH-CNF10 dosage of 5.0 wt% on hardwood paper. The increment of tensile index, burst index, and folding endurance were 108.32%, 104.65%, and 600%, respectively. This work aims to find out the relationship between production methods and morphologies of CNFs and how the morphological characteristics of CNFs affecting the mechanical performance of paper when they are added as strength additives.

Tissue furnish optimization plays a key role in enhancing tissue properties, making the process cost-effective. Typically, this furnish is composed of a mixture of hardwood eucalyptus fibers (HW) and softwood (SW) fibers, which ensure strength and tissue machine runnability. However, the tissue paper production with the maximization of eucalyptus fibers achieves softer papers at less cost, since SW fibers are often more expensive than HW fibers. From this perspective, this study aims to investigate the effect of micro/nano-fibrillated cellulose (MFC/NFC) as an additive, on structural, softness, strength, and water absorption properties of tissue papers, promoting partial or total removal of SW fibers to produce 100% eucalyptus materials. MFC/NFC was characterized in terms of morphological, chemical, and water interaction properties. The results showed that MFC/NFC presents a high bonding surface area, high carboxyl group content and, when incorporated into tissue furnishes, it promotes strong inter-fiber bonds. This evidence was also supported by SEM image analysis methods and FTIR. Additionally, laboratory tissue handsheets with low basis weight were produced and used in the characterization assays. Overall, the results indicated that MFC/NFC improved strength, at the expense of bulk, porosity, softness, and absorption properties. Compared to typical industrial furnish mixtures (75%HW + 25%SW), MFC/NFC enhanced the production of bulkier, porous, and softer structures, but with reduced strength and absorption. It was possible to optimize the furnish composition by using fiber modeling to obtain 3D structure computation simulations with predictive capability. The MFC/NFC proved to be a high-quality additive to improve softness and strength properties.

This paper describes the design and development of miniaturized microfluidic paper-based analytical devices (μPADs) for biological assays and enzyme storage instruments. Here, a glucose assay utilizing glucose oxidase (GOx), horseradish peroxidase (HRP), and potassium iodide (KI) is used as the model system. The efficacy of the miniaturized devices is further examined by assessing the activity of acetylcholinesterase (AChE). Two types of μPADs were developed: one, "strip" chips of detection zones of area 0.5, 0.1 cm2 and, two, "grid" chips of detection zone 0.05 cm2. The devices are easily fabricated via a wax printing process whereby lines of wax are deposited onto chromatographic paper and heated to create rows of hydrophobic barriers. The "strip" chips were subjected to three different temperature environments (-20, 0, and 20°C) over 30 days and glucose assays conducted at intermittent times yielding a correlation between corrected average inverse yellow intensity, days, and glucose concentration. Calculated and experimentally derived color intensity values for 1, 4, and 9 mM glucose concentrations after a 7-day storage study showed a good correlation (0.89 - 15.76% error). Both types of μPADs are effective platforms as potential point-of-care (POC) diagnostic devices and display minimal enzyme denaturation. μPADs of this size show promise as alternative devices for resource-limited regions and especially those areas where materials and instrumentation are not always available.

Respiratory viral infections often mimic the symptoms of infections caused by bacteria; however, restricted and targeted administration of antibiotics is needed to combat growing antimicrobial resistance. This is particularly relevant in low-income settings. In this work, we describe the use of isothermal amplification of viral DNA at 37 °C coupled to a paper-based vertical flow microarray (VFM) setup that utilizes a colorimetric detection of amplicons using functionalized gold nanoparticles. Two oligonucleotide probes, one in-house designed and one known adenoviral probe were tested and validated for microarray detection down to 50 nM using a synthetic target template. Furthermore, primers were shown to function in a recombinase polymerase amplification reaction using both synthetic template and viral DNA. As a proof-of-concept, we demonstrate adenoviral detection with four different adenoviral species associated with respiratory infections using the paper-based VFM format. The presented assay was validated with selected adenoviral species using the in-house probe, enabling detection at 1 ng of starting material with intra- and inter-assay %CV of ≤ 9% and ≤ 13%. Finally, we validate our overall method using clinical samples. Based on the results, the combination of recombinase polymerase amplification, paper microarray analysis, and nanoparticle-based colorimetric detection could thus be a useful strategy towards rapid and affordable multiplexed viral diagnostics. Electronic supplementary material The online version of this article (10.1007/s00216-018-1503-y) contains supplementary material, which is available to authorized users.

The copper(II) ion (Cu2+) has played an indispensable role in diverse kinds of functional physiological processes of organisms, which has become of growing interest. Despite the fact that numerous Cu2+ test papers using fluorescent probes have been fabricated, sensors featuring the ratiometric property that integrates quenched probes and an inner standard dye are rarely reported. Herein, a two-component ratiometric sensor in a paper-based device is proposed to realize highly selective Cu2+ detection. To overcome shortcomings such as low signal-to-noise ratio and incorrect response of the quenching probe, a novel BODIPY-based turn-off probe (P2017) is designed and introduced into the paper-based device with better water solubility and selectivity for Cu2+ detection. Furthermore, a reference dye (B001), exhibiting an emission at 690 nm when the excitation wavelength is 480 nm, is also introduced into the paper-based device. These two components can enhance the quality of the signal as P2017 is sensitively quenched by Cu2+, while B001 with a photostable property, serving as an internal benchmark, is unable to react with Cu2+. The results indicated that the two components provided a new concept for optimizing paper-based device fabrication and developing accurate, simple, and inexpensive Cu2+ detection methods, which could be potentially applied to monitor human health and the environment in remote areas.

Paper industry being a mature mega-scale industry is focusing on process oriented technical modifications to reduce dependency on wood fibers and resource utilization. In this research study, conventional chlorine dioxide (D0) bleaching method was modified to hot chlorine dioxide (DHT) with an aim of reducing the effluent load with special concern to chlorolignin compounds. These compounds were measured by gas chromatograph equipped with ECD detector. The chlorophenols, chlorocatechols, chloroguaiacols, chlorovanillins, chlorosyringols and bromophenols were reduced by 9%, 50%, 34%, 47%, 17% and 31%, respectively under DHT based sequence at same dose of chemicals. The general environmental parameters i.e. COD, BOD, TS, colour, lignin and AOX also got reduced in DHT based sequence. The modification of D0 to DHT was found to be effective as effluent quality was enhanced without compromising the optical and strength properties of cellulosic paper even at low dose of chlorine dioxide.

This study aims to decrease the dielectric constant of cellulose insulating paper by octa(aminophenyl)silsesquioxane (OAPS) grafting. OAPS was grafted onto the primary hydroxyl group of cellulose molecules via amino groups and epichlorohydrin. The dielectric constant and dielectric loss of insulating paper before and after modification were investigated. Relative to the unmodified paper, the dielectric constant of 15 wt% OAPS-grafted paper decreased from 5.27 to 4.28, and the dielectric loss decreased by 37.5% at 50 Hz. The movement and orientation polarization of the cellulose chains could be restricted due to the porous macromolecular structure and nano quantum interface effect produced by OAPS, thereby resulting in the reduction of cellulose polarizability. Moreover, the OAPS grafting modification does not degrade the other properties of cellulose insulation, i.e., its thermal stability, mechanical performance, fire-resistant properties, and electrical strength. OAPS grafting has promising potential application for preparing low dielectric constant insulating paper.

Hairy cellulose nanocrystalloids (HNC) are a brand new family of nanocellulose characterized by having functionalized amorphous poles joined by a crystalline shaft. In this paper we hypothesize that cationic HNC (CNCC) could be used as an effective retention agent in papermaking. To investigate this, we first flocculated a suspension of only fillers, namely kaolinite and CaCO3, and second, a suspension of recycled fibers, with CNCC. It was monitored by photometric dispersion analysis and laser focused beam reflectance. The flocculation mechanism was assessed by means of zeta potential, reflocculation efficiency, flocculation stability and optical microscopy. Finally, the effect of CNCC on drainage, retention and paper mechanical properties was studied. CNCC were found to heteroflocculate fillers at a wide range of dosages, finding a maximum floc size at a dosage of 30 mg/g. On the other hand, the maximum floc size when flocculating the pulp suspension, was found at a lower CNCC dosage (20 mg/g). In this case, fillers were being attached to the exterior surface of the fibers. In both systems, the maximum size increment was observed at the isoelectric point, so a charge neutralization mechanism was proposed. The addition of CNCC not only improved filler retention, but also pulp drainage by reducing these times. Moreover, although mechanical properties of the handsheets were affected by the presence of CNCC, this effect was much lighter than that caused by traditionally used retention systems. Hence, CNCC could replace many additives used in the wet-end of a paper machine, thus simplifying its operation.

We investigated treatment of cellulose paper with a phosphoric acid–urea solution for increasing the wet strength. First, a filter paper was immersed in a phosphoric acid–urea solution (phosphoric acid: urea mole ratio = 1:0, 3:1, 1:1, or 1:3). Next, the filter paper was put between glass plates and heated at 80–140 °C for 15 min to 3 h. Then, the filter paper was washed for 1 h in distilled water. After washing, the filter paper was dried in a hot press at 110 °C and 1.1 MPa for 1 h. We investigated disintegration by immersing the prepared filter papers in distilled water. The paper treated with the 1:3 phosphoric acid–urea solution did not disintegrate. The optimum concentrations for developing the wet strength of the paper were 1.2–2.5 M phosphoric acid and 3.7–7.5 M urea. The optimum treatment time and temperature were 1.5 h and 140 °C, respectively. The wet strength of the paper increased after treatment with the phosphoric acid–urea solution. This method is a viable alternative to treatment with chemicals such as polyamidoamine epichlorohydrin.

The development of point-of-care (POC) devices for the detection of environmental contaminants and the early monitoring of disease outbreaks in the health and food sectors has steadily grown in recent times. The real-time analysis offered by POC devices is pivotal in developing areas where access to skilled labor is often lacking. Chelating agent–based signal amplification methods have previously been employed in conjunction with electroplated metallic films to improve electrode sensitivity in trace metal analysis. Here, we describe a method for the dry storage of electrochemical reagents: ammonia/ammonium chloride (NH3/NH4Cl) buffer as a supporting electrolyte, dimethylglyoxime (DMG) as a chelating agent, and mercury in paper-based electrochemical cells (PECs), fabricated from commercial filter paper. The stored PECs were applied to the trace, microliter analysis of nickel in water samples by adsorptive cathodic stripping voltammetry (AdCSV) in conjunction with screen-printed electrodes. The method relies on the single-step accumulation/adsorption of microvolumes of the metallic analyte onto stored DMG ligands to form [Ni(dmgH)2] complexes in the presence of mercury films. By integrating the AdCSV techniques with paper-based analytical devices, detection of Ni2+ in water samples with good resolution was achieved at 20 μL sample volumes in the low parts per billion range. The mechanism for pre-concentration and its subsequent reduction was demonstrated as it differs from bulk electroanalysis. Instrumental parameters of the PECs, accumulation time, and deposition potential were optimized along with reagent storage introduction and concentrations. Further, the PECs were investigated in the absence and presence of mercury and had shown good possibility for metal-free sensors in future work. The prepared PECs showed good reproducibility (4.36%, n = 4) and no intermetallic interferences in the presence of 100 μg L−1 Zn2+, Cd2+, Pb2+, Co2+, and In2+. Detection and quantitation limits were calculated and recorded as 6.27 μg L−1 and 18.8 μg L−1, respectively, for Ni2+ determination and 13.1 μg L−1 and 39.3 μg L−1 for the Hg-free derivative at the 90-s accumulation time. The pre-stored paper-based electrochemical cells were then applied to the detection of Ni2+ in real tap water samples and showed good recovery values of ± 94%. Further, the infusion of PECs with a range of chelating agents (dimethylglyoxime, nioxime, and morin hydrate) demonstrates the possibility for tuning PECs to specific applications and improving selectivity in metal analysis applications.

Superamphiphobic surfaces generally need a specific combination of low surface energy and re-entrant surface structure. Herein, we have created a hexane suspension of trichloro(1H,1H,2H,2H-tridecafluoro-n-octyl) silane, tetraethyl orthosilicate, silicon dioxide and titanium dioxide nanoparticles and modify a series of filter papers by one-step immersion in 10 min. Superhydrophobic and quasi-superoleophobic properties are obtained for the optimal filter papers, which repel both of polar and non-polar liquids such as water, glycerol, 1,4-butanediol, soybean oil and 1-octadecene with the contact angles of 168°, 158°, 154°, 145° and 121°, respectively. More importantly, the respective contribution of each component to the superhydrophobic and oleophobical property is explicated through a series of comparative experiments based on the optimal suspension prescription. The wettability transformation from quasi-superamphiphobicity to superhydrophilicity after UV irradiation is evaluated and illustrated. What’s more, the patterned paper is successfully used for the colorimetric detection of glucose using a simple paper-based analytical device. A linear correlation between gray intensity (GI) and glucose concentration (C), GI = − 10.7C + 161.8 is achieved with a correlation coefficient of 0.991, indicating the potential for semi-quantitative analysis of real sample in the field.

The aim of this research was to design a model for simulating the degradation of paper in various environmental conditions by taking into consideration all the parameters (exogenous and endogenous) that influence the overall process of the acid catalyzed hydrolysis of cellulose. Three kinetic equations (Ekenstam, Calvini, and Ding and Wang) for determining the degradation rate coefficient (k) were compared. For this purpose, previously published and new experimental data on the degradation of pure and unsized cotton linter papers (neutral and acidic) upon ageing were used. The frequency factor parameter (A) in the Arrhenius formula was adjusted with additional input factors in the expression of A proposed by Zou et al. (Cellulose 3:243–267, 1996a). The model takes into account the increase of the acidity and the decrease of the moisture content induced during paper degradation. Besides the temperature and humidity, external gaseous pollutants (NO2, formic and acetic acids) were also taken into account as degradation factors. The model can be used to simulate cellulose depolymerisation of cotton papers exposed to single pollutants, but reached a limit for simulating with confidence the degradation of papers exposed simultaneously to multiple volatile compounds, due to the lack of available data, especially concerning certain volatile compounds counter-degradation effects. Future adjustments can be done when more experimental data becomes available.