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Graphical abstract Enzyme-linked immunosorbent assay (ELISA) is widely used for the detection of disease biomarkers. However, it utilizes time-consuming procedures and expensive instruments, making it infeasible for point-of-care (POC) analysis especially in resource-limited settings. In this work, a multicolorimetric ELISA biosensor integrated on a paper/polymer hybrid microfluidic device was developed for rapid visual detection of disease biomarkers at point of care, without using costly equipment. This multicolormetric ELISA platform was built on multiple distinct color variants resulted from the catalytic oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) and the etching of gold nanorods (AuNRs). The vivid color changes could be easily distinguished by the naked eye, and their red mean values allowed quantitative biomarker detection, without using any sophisticated instruments. When this multicolorimetric ELISA was integrated on a paper/polymer hybrid analytical device, it not only provided integrated processing and high portability but also enabled fast assays in about 50 min due to the unique advantages of paper/polymer hybrid devices. The limit of detection of 9.1 ng/μL of the hepatitis C virus core antigen, a biomarker for hepatitis C, was achieved using this multicolorimetric ELISA platform. This multicolor ELISA analytical device provides a new versatile, user-friendly, affordable, and portable immunosensing platform with high potential for on-site detections of various viruses, proteins, and biomarkers for low-resource settings such as at home, public venues, rural areas, and developing nations. Supplementary Information The online version contains supplementary material available at 10.1007/s00216-021-03359-8.

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.

In this research, simultaneous quantification of cysteine (Cys) and histidine (His) using a paper-based sensor was investigated for the first time. A microfluidic paper-based sensor is a promising amino acid determination tool due to its low cost, low sample consumption, and fast analysis and is easy to make. We used SBA-15 as porous materials that are crystalline compounds formed with surfactants and TEOS as a silica source. The SBA-15 sample was characterized by X-ray diffraction, Fourier transform infrared, and scanning electron microscope techniques. The microfluidic paper-based sensors were fabricated using a wax pen, and the mesoporous SBA-15 modified filter paper. The fabricated sensors for Cys and His determination are operated based on an indicator-displacement assay. A comparative determination study of Cys and His on the sensors was carried out. The results illustrated that the addition of silica nanoporous material led to an immediate and uniform color change. The sensors were successfully exploited in the simultaneous determination of urinary Cys and His levels, thus providing the potential opportunity for clinical diagnosis. The linear range of 1.0 to 90.0 μM and 1.0 to 100 μM for His and Cys was obtained from the calibration data. The detection limits were also calculated (S/N = 3) for His and Cys of 0.5 μM and 1.5 μM, respectively. The proposed method showed a good agreement with the results achieved by a standard method.

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.

The present study reports the characterization of reverse osmosis (RO) technology at water treatment plant Cogen-2 in paper and Board mills, Pakistan. RO is a commonly used process to obtain de-mineralized water for high-pressure boiler operation in thermal power plants. Scaling and fouling in three-stage RO plants is a major challenge in chemical industry due to the use of raw brackish water in the power plant of paper and board mills. In our study, the feed water quality of RO was changed from soft water to raw water to make it economical. The cleaning frequency was increased three times than normal, which was unsafe for operation and it was required to control scaling and fouling to achieve the desired result. Differential pressures behavior of all stages for 2-month data was observed without acid treatment, and the results of Langelier Saturation Index (LSI) control parameters (temperature, pH, total dissolved solids, calcium hardness, and alkalinity) clearly showed the abnormality. To optimize scaling and fouling of RO, the LSI factor was controlled in total reject water for the next 2 months by acid treatment in feed water. Duration of chemical cleaning and membranes’ life has been extended by fouling and scaling control. Understanding the effect of operational parameters in RO membranes is essential in water process engineering due to its broad applications in drinking water, sanitation, seawater, desalination process, wastewater treatment, and boiler feed water operation. The product flow increased from 18.3 to 19.9 m3/h, and this was due to a decrease in the rejection flow from 8.2 to 6.7 m3/h. The total reject stream pressure also increased from 8.1 to 9 bar. A lower value of LSI of 1.6 is obtained in the reject water stream after the acid treatment.

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.

Microfluidic paper-based analytical devices (μPADs) have developed rapidly in recent years, because of their advantages, such as small sample volume, rapid detection rates, low cost, and portability. Due to these characteristics, they can be used for in vitro diagnostics in the laboratory, or in the field, for a variety of applications, including food evaluation, disease screening, environmental monitoring, and drug testing. This review will present various detection methods employed by μPADs and their respective applications for the detection of target analytes. These include colorimetry, electrochemistry, chemiluminescence (CL), electrochemiluminescence (ECL), and fluorescence-based methodologies. At the same time, the choice of labeling material and the design of microfluidic channels are also important for detection results. The construction of novel nanocomponents and different smart structures of paper-based devices have improved the performance of μPADs and we will also highlight some of these in this manuscript. Additionally, some key challenges and future prospects for the use of μPADs are briefly discussed.

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.

Currently, most of the collected waste medium-density fiberboards (MDF) is incinerated or landfilled, as economically viable recycling methods are yet to be developed. By steam refining waste medium-density fiberboards (MDF), it is possible to hydrolyze the incorporated resins and isolate a high yield fiber fraction. Further refining of the steam treated fibers might enable the fibers to be utilized in applications such as paper packaging, facilitating a cascading use of the waste material stream. To this end, intimate knowledge of the material is needed. In this study, the steam refined fibers of two waste MDF samples containing differing amounts of softwood and hardwood underwent refining and beating. The resulting fibers were characterized regarding their morphology and paper test sheets were produced to evaluate their strength (compression-, tensile- and tear-strength). Distinct differences in response to refining between the MDF samples were apparent. For the sample with the higher hardwood share an increase in strength properties with increasing steam treatment severities could be observed and it was possible to produce test sheets with comparable compression strength to recycled pulp for industrial corrugated paperboard. For the sample with a higher share of softwood, the steam treatment severity did not show any influence on fiber morphology or paper properties, and the resulting paper strength was low in comparison to the other steam refined waste MDF sample. Graphic Abstract

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.

Compared with a single chemical indicator, the use of multivariate chemical indicators in aging status assessment of transformer cellulose paper insulation can improve the reliability of the evaluation. In this study, a non-destructive method based on multivariate chemical indicators was proposed to evaluate the remaining life of cellulosic paper insulation. The selected chemical indicators closely related to the aging of the insulating paper were analyzed. Additionally, by applying the subjective and objective weighting method, the evaluation information of each indicator was fully extracted to obtain reasonable comprehensive evaluation weights. Besides, the comprehensive evaluation index of multivariate chemical indicators was obtained by using the technique for order preference by similarity to ideal solution method, which is consistent with the deterioration law of paper insulation. Then, the correlation lifespan model between the comprehensive evaluation index of multivariate chemical indicators and the degree of polymerization of insulating paper under different aging stages was established. The effectiveness of the proposed model was verified by experiments. This promising model can increase the accuracy of the condition assessment for the transformer cellulosic paper insulation.

Gelatine sizing was used extensively for western papermaking before the nineteenth century and this technique is still applied nowadays for restoration purposes. Despite its wide use, the relationships between gelatine types, the strength of the size and its distribution inside the paper sheet are still unclear. Different concentrations of three gelatines of various origins and types (A/B) were used to size model papers. The gelatine uptake, the strength of the size and the presence of gelatine at the papers surface were investigated by using a water drop test method and ATR-FTIR spectroscopy. At a given concentration, similar uptakes were found for all gelatines but great variations were observed in terms of size strength and of gelatine ability to cover the surface of paper sheets. In addition, Scanning transmission X-ray microscopy was performed on paper fibres cross sections to map the distribution of the organic compounds (both cellulosic and proteinaceous) on a nanometer scale. This showed that gelatine coats but does not penetrate the fibres. It can be inferred that the different size strengths observed between the tested gelatines are mainly due to different ways of filling holes between fibres inside the paper mat, some gelatines being more prone to go inside the sheet than others which remain mostly distributed near the surface.

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.

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.

In China, Xuan paper has been the paper of choice as artwork support and for conservation, for several centuries. However, little is known about its material properties, especially given the many grades of sized and unsized Xuan paper. In addition, there is a lack of information on its degradation. In this research, a selection of contemporary unsized Xuan papers was investigated, representing diverse raw materials. Seven out of twelve contemporary unsized Xuan papers were determined to be approximately neutral and contain > 2% alkaline reserve, indicating good durability. Viscometry was used to determine the degree of polymerisation (DP) as none of the samples gave significant reactions to the phloroglucinol spot test. The average DP of ten contemporary unsized Xuan papers is ~ 1700, excluding two papers that have presumably been sun-bleached, and that exhibit significantly lower DP. Using X-ray fluorescence, it can be demonstrated that Ca and Si are the dominant elements and interestingly, Ca content is directly correlated with ash content and with alkaline reserve. Accelerated degradation was performed at two sets of environmental conditions, i.e. 90 °C, 30% RH and 60 °C, 70% RH, and the established degradation rates agreed with the Collections Demography model of paper degradation meaning that degradation of Xuan papers proceeds in the same way as other types of paper. This research gives fundamental insights into contemporary unsized Xuan papers, which exhibit good stability during accelerated degradation despite the low starting DP in the context of the samples used in this study. Our findings may inform methods of Xuan paper production, selection of Xuan paper for conservation purposes, as well as preventive conservation of Xuan paper-based artefacts.

Process-monitoring laboratories in the pulp and paper industry generally use a combination of wet chemical analyses and physical measurements to certify the fitness of a production pulp for a specific end-use. These laboratory tests require time and the effort of trained personnel, limiting their utility for real-time process control. Here we show that Raman probes of unrefined cellulosic pulps, well-suited to the online measurement of in-process materials, can predict the quality attributes of manufactured papers. The accuracy of prediction improves when the covariance is modelled in a reduced measurement space selected by a data-driven, feature-selection technique referred to as a Template Oriented Genetic Algorithm (TOGA). TOGA, combined with discrete wavelet transform (DWT), isolates functional-group features that correlate best with mechanical properties paper derived from refined pulp. Paper makers refine market pulps to build sheet strength using a beating process that decreases freeness as it increases fibre-fibre bonding. Methods demonstrated here predict manufactured sheet properties obtainable after any specified degree of refining from the Raman spectrum of an unrefined pulp. This analysis capacity will enable both vendors of market pulp and makers of sheet paper to specify in advance the amount of beating required to produce a desired product, thereby saving cost and conserving resources.

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.

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.

The sensitive quantitative analysis of trace heavy metallic elements (Cd, Mn, Cr, and Cu) in aqueous solutions was achieved successfully through the combination of filter paper enrichment with laser-induced breakdown spectroscopy. Filter paper was enriched with 0.4 mL aqueous solutions to form a homogeneous sample layer on the surface of the metallic target. Considering the limits of detection, the values deduced with calibration curves already exhibited the high performance of the proposed method at several hundred or 10 μg/L (Cd 0.165, Mn 0.035, Cr 0.012, and Cu 0.078 mg/L), lower than or comparable to those using other similar methods. The LIBS results agreed reasonably well with those from ICP-MS for real samples. All results showed that our method was suitable and accurate for rapid on-site detection of trace metals in aqueous solutions. This indicates that filter paper enrichment combined with laser-induced breakdown spectroscopy is a feasible approach to wastewater quality monitoring.

Abstract Tissue paper softness relies on two major factors, the bulk softness, which can be indicated by the elasticity of the sheet, and surface softness. Measurement of surface softness is complicated and often requires a multi-step process. A key parameter defining surface softness is the topography of the surface, particularly the crepe structure and its periodicity. Herein, we present a novel approach to measure and quantify the tissue paper surface crepe structure and periodicity based on the detection of waviness along the sample using laser scanning confocal microscopy (LSM) and X-ray tomography (XRT). In addition, field emission scanning electron microscope (FESEM) was used to characterize the tissue paper surface. We demonstrate that surface topography is directly correlated to the erosion of the doctor blade, which is used to remove the dry tissue paper from the Yankee cylinder. Because of its accuracy and simplicity, the laser confocal microscopy method has the potential to be used directly on the production line to monitor the production process of the tissue paper. XRT revealed more structural details of the tissue paper structure in 3D, and it allowed for the reconstruction of the surface and the internal structure of the tissue paper. Graphic abstract

A superhydrophobic paper with excellent robustness was fabricated by roll coating with modified nano-TiO2. First, nano-TiO2 particles were hydrophobically modified by γ-aminopropyltriethoxysilane and 1H, 1H, 2H, 2H-perfluorooctyltriethoxysilane (POTS). Then the paper coating composed of modified nano-TiO2 particles as pigments and epoxy resin (EP) as adhesives was coated on a paper surface to create the desired surface morphology and surface energy. Compared with the uncoated filter paper, the prepared paper showed an improved rough surface morphology owing to the uniform layer of TiO2 microclusters deposited on the fiber network. The superhydrophobic paper exhibited water contact angles (WCA) about 153° ± 1.5°, and water sliding angles (WSA) about 3.5° ± 0.5°, low surface adhesion and excellent bounce ability. The superhydrophobic paper can withstand a variety of wear and tear, such as tape stripping and knife scraping. The as-prepared superhydrophobic paper showed mechanical durability even after 20 wear cycles with sandpaper,thus sustaining excellent superhydrophobicity on the filter paper surface. Moreover, it remains fully functional even in environments with high concentrations of acid and alkali for 96 h. The superhydrophobicity was not affected after storage for 6 months in a natural environment. It was confirmed that the superhydrophobic paper surface exhibited excellent chemical stability, long-term stability and self-cleaning properties. The entire production process was operated under normal environment, without complex equipment; and, as such, has the possibility for large-scale production and application in industry.

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.

We present a high resolution, ultra-frugal printing of paper microfluidic devices using in-house paraffin formulation on a simple filter paper. The patterns printed using an office inkjet printer formed a selective hydrophobic barrier of 4 ± 1 µm thickness with a hydrophilic channel width of 275 µm. These printed patterns effectively confine common aqueous solutions and solvents, which was verified by solvent compatibility studies. SEM analysis reveals that the solvent confinement is due to pore blockage in the filter paper. The fabricated paper-based device was validated for qualitative assessment of Candida albicans (pathogenic fungi) by using a combination of L-proline β-naphthylamide as the substrate and cinnamaldehyde as an indicator. Our studies reveal that the pathogenic fungi can be detected within 10 min with the limit of detection (LOD) of 0.86 × 106 cfu/mL. Owing to its simplicity, this facile method shows high potential and can be scaled up for developing robust paper-based devices for biomarker detection in resource-limited settings. Graphic abstract

In order to improve the efficiency of disease diagnosis and environmental monitoring, it is desirable to detect the concentration of proteins and metal ions simultaneously, since the current popular diagnostic platform can only detect proteins or metal ions independently. In this work, we developed a colorimetric microfluidic paper-based analytical device (µPAD) for simultaneous determination of protein (bovine serum albumin, BSA) and metal ions [Fe(III) and Ni(II)]. The µPAD consisted of one central zone, ten reaction zones and ten detection zones in one device, in which reaction solutions were effectively optimized for different types of chromogenic reactions. Fe(III), Ni(II) and BSA can be easily identified by the colored products, and their concentrations are in good accordance with color depth based on the established standard curves. The detection limits are 0.1 mM for Fe(III), 0.5 mM for Ni(II) and 1µM for BSA, respectively. Best of all, we demonstrated the efficiency of the µPAD with accurate detection of Fe(III), Ni (II) and BSA from river water samples within 15 minutes. The µPAD detection is efficient, instrument-free, and easy-to-use, holding great potential for simultaneous detection of cross type analytes in numerous diagnostic fields.

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.

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.

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.

Korean hand papermaking is a renowned cultural tradition in the Korean peninsula. It is still practiced while scientific analysis of paper itself from a large data set is rare. In this study, a set of more than three hundred Korean handmade papers, collected in a reference collection book Hanji: Korean handmade paper, were chemically investigated, and their property data such as colour, pH, grammage, thickness, tensile strength, folding endurance were statistically analysed in order to determine general features for Korean papers. The influence of different paper sheet formation methods (Heullimtteugi vs Gadumtteugi) were revealed by multivariate data analysis and the chemical profiles of raw materials were studied by pyrolysis–gas chromatography/mass spectrometry (Py-GC/MS). The Korean handmade paper samples display colour gamut in the colour space L* (69.9–95.9), a* [(−3)-3], b* (0–20), most have neutral/alkaline pH values. Paper density, fiber orientation and physical properties are influenced by the sheet formation techniques. For instance, Gadumtteugi tends to produce papers with strong fiber orientation while Heullimtteugi produces papers with more evenly distribution of fibers. In addition, Py-GC/MS analysis results show that paper mulberry fibers contain less intensity lignin monomers and more terpenic compounds in comparison with gampi and mitsumata fibers. This study provides paper analysis from large sample set, statistics reveal that the material preparing and making craft determined the paper structure which reflected in their physical properties. These properties influenced paper performance and applications in art creations as well as relics conservation and restoration. The characterized paper sample database could be used for handmade paper studies in East Asian region. Consequently, this study contributes to a better understanding of contemporary Hanji properties as well as improves knowledge on handmade papers from the Korean peninsula.

Background Microfluidic chip detection technology is considered a potent tool for many bioanalytic applications. Rapid detection of foodborne pathogens in the early stages is imperative to prevent the outbreak of foodborne diseases, known as a severe threat to human health. Conventional bacterial culture methods for detecting foodborne pathogens are time-consuming, laborious, and lacking in pathogen diagnosis. To overcome this problem, we have created an embedded paper-based microchip based on isothermal loop amplification (LAMP), which can rapidly and sensitively detect foodborne pathogens. Results We embed paper impregnated with LAMP reagent and specific primers in multiple reaction chambers of the microchip. The solution containing the target pathogen was injected into the center chamber and uniformly distributed into the reaction chamber by centrifugal force. The purified DNA of Escherichia coli O157:H7, Salmonella spp., Staphylococcus aureus, and Vibrio parahaemolyticus has been successfully amplified and directly detected on the microchip. The E. coli O157:H7 DNA was identified as low as 0.0134 ng μL− 1. Besides, the potential of this microchip in point-of-care testing was further tested by combining the on-chip sample purification module and using milk spiked with Salmonella spp.. The pyrolyzed milk sample was filtered through a polydopamine-coated paper embedded in the inside of the sample chamber. It was transported to the reaction chamber by centrifugal force for LAMP amplification. Then direct chip detection was performed in the reaction chamber embedded with calcein-soaked paper. The detection limit of Salmonella spp. in the sample measured by the microchip was approximately 12 CFU mL− 1. Conclusion The paper embedded LAMP microchip offers inexpensive, user-friendly, and highly selective pathogen detection capabilities. It is expected to have great potential as a quick, efficient, and cost-effective solution for future foodborne pathogen detection.

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.

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.

The diagnosis of dengue infection is still a critical factor determining success in the clinical management and treatment of patients. Here, the development of microfluidic paper-based analytical devices (μPADs) utilizing a sandwich immunoassay on wax patterned paper functionalized with anti-dengue NS1 monoclonal antibodies for point-of-care detection of dengue NS1 (DEN-NS1-PAD) is reported. Various assay conditions, including the length of the channel and diluent, were optimized, and the response detected by the naked eye and digitized images within 20–30 min. The DEN-NS1-PAD was successfully tested in the field for detecting dengue NS1 in buffer, cell culture media, and human serum. The limit of detection (LoD) of the DEN-NS1-PAD obtained with the naked eye, scanner, and a smartphone camera was 200, 46.7, and 74.8 ng mL−1, respectively. The repeatability, reproducibility, and stability of the DEN-NS1-PAD were also evaluated. High true specificity and sensitivity in the serum of pediatric patients were observed. These evaluation results confirm that the DEN-NS1-PAD can potentially be used in point-of-care dengue diagnostics, which can significantly impact on the spreading of mosquito-borne diseases, which are likely to become more prevalent with the effects of global warming.

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.