Search

In this paper, the mechanical properties of nano-silica modified insulating paper under the combined action of mechanical vibration and temperature conditions are studied. Unmodified and nano-silica modified cellulose insulating paper with 2 wt% and 4 wt% were prepared, respectively, and a series of mechanical-thermal synergy experiments were carried out. With the same mechanical stress and temperature, and with the same aging duration of 144 h (6d), the tensile strength of modified insulating paper with 4 wt% nano-silica, increased 0.99 kN/m and 0.55 kN/m, respectively, compared with those of the unmodified and the 2 wt% nano-silica modified insulating paper. The experiments indicate that the nano-silica modification can effectively improve the mechanical properties of insulating paper. In this work, the modified mechanism of nano-silica is analyzed from the interface effect of modified polymer and the quantum effect of the modified polymer interface two aspects. It is shown that the interface formed in the modified insulating paper can transfer the mechanical stress acted on the insulating paper and prevent the cracks formed in the aging process of the test sample from further expansion, while the quantum effect discretizes the electron energy level, which can restrict the motion of the molecular chain segment to some extent. The conclusion can be used for reference to improve the performance of insulating paper.

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

Free-standing reduced graphene oxide (rGO) papers were prepared by chemical reduction, thermal reduction and combined chemical-thermal reduction, respectively. Four-point probe and nanoindentation experiments were conducted to investigate the electrical and mechanical properties of rGO papers. The rGO paper prepared by soaking in L-ascorbic acid and thermal annealing in argon at 1000 °C (labeled rGO-AsA-T) showed superior electrical and mechanical properties when compared with rGO papers prepared merely by chemical reduction or thermal reduction. The as-prepared rGO-AsA-T paper exhibited an electrical conductivity of 5.7 × 104 S/m, showing an increase of 90% compared to that in the thermally annealed rGO paper and nearly 40 times that of rGO paper reduced by L-ascorbic acid. It was also found that the rGO-AsA-T paper had the lowest elastic modulus of 288 MPa, showing enhanced flexibility. The nearly free voids in rGO-AsA-T paper proved by scanning electron microscopy (SEM) were due to the capillary action in chemical reduction and were significant in improving the electrical conductivity and flexibility of the paper. The rGO-AsA-T paper with high conductivity and flexibility has a promising application in flexible electronics.

We demonstrated the thermally robust reduced graphene oxide (rGO)/boron nitride nanotube (BNNT) papers and their application in electromagnetic interference shielding. In order to overcome the thermal durability shortcomings of electromagnetic wave shielding paper based on rGO nanomaterial, rGO/BNNT electromagnetic interference (EMI) shielding paper having excellent thermal durability could be manufactured using BNNT nanomaterials having excellent chemical and thermal stability at high temperature. With the addition of a little BNNT, the durability against temperature can be increased by more than two times while there is little reduction in EMI performance.

We report a paper-based photodetector made from mixed cation organic perovskite halide MA1–xFAxPbI3 (MA = methylammonium (CH3NH3); FA = formamidium CH(NH2)2). The detector shows a substantial photo...

This research presents a solar-blind (UVC) office paper-based photodetector that is self-biased, superflexible, nonwettable, high-performance, and high-voltage stable. In contrast to the traditiona...

Lithium metal is deemed a promising anode material for the next-generation batteries with high specific energy. Unfortunately, the growth of Li dendrites and infinite volume change during cycling, caused by the "hostless" feature of metallic Li, have posed a great challenge to the commercialization of Li metal anode. The introduction of appropriate host materials for Li metal is highly desirable. In this work, a N, P dual-doped 3D carbon derived from low-cost quantitative filter paper (NPCQP) is designed and fabricated for direct using as a host for Li metal anode. The resulting NPCQP host achieves a high deposition/stripping Coulombic efficiency of above 97.5 % with a low nucleation overpotential. Moreover, the NPCQP@Li symmetric cells enable an excellent long-term cycling performance (1000 h) with an ultralow voltage hysteresis (12 mV) and stable interface behavior. When paired with the commercial LiFePO

A simple system to control the selectivities of C2 products in electrochemical CO2 reduction with copper phenanthroline on carbon paper.

We breathe in a world where growing electronic wastages are a serious threat to our ecosystem, and therefore biodegradable devices are more in demand. We have unprecedentedly demonstrated broad-ban...

The oil-paper insulation of high-frequency (HF) transformers frequently withstands high-frequency over-voltages at frequencies of several kHz and above. This leads to the occurrence of partial discharge (PD), which causes premature insulation failure in HF transformers. In order to investigate the effect of PD under high-frequency stresses on oil-impregnated Nomex paper, this paper analyzes the surface morphology, bond-broken types of the molecular chain, and product types formed for oil paper after PD degradation. Then, the damage mechanism of oil-immersed Nomex paper between high-frequency and AC stress is explored. The experimental results show that the branches of creepage do not exist in the oil-paper insulation during the entire discharge process under high-frequency stresses, and that their damage degree is higher than that of AC stress. This is mainly because the benzene ring of oil-impregnated Nomex paper is destroyed and opened caused by high-energy particles, the heating effect in HF discharge, and the bulk effect. These results help to improve the design theory of insulation structures and to develop PD-resistant insulation materials in HF transformers.

Photocatalytic materials have been widely used to remove dyes from printing and dyeing wastewater. However, difficulty in recycling of photocatalysts is the great concern in the real catalytic applications, which significantly raises the application cost. This study developed a low-cost catalyst by loading magnetic Ni onto filter paper (FP) via an easy going in-situ reaction. The characterization results displayed that the Ni particles were uniformly anchored onto the FP. The Ni@FP material presented a strong magnetic ability which was evidenced by a saturation magnetization (Ms) of 5.014 emu·g−1, a remanent magnetization (Mr) of 2.067 emu·g−1 and a coercivity (Hc) of 133.868 Oe. Meanwhile, the magnetic Ni@FP material displayed a recyclable advantage in photocatalytic degradation of methyl orange (MO) via an external magnetic field. There existed an optimal photocatalytic degradation rate of 93.40% within 5 min when MO concentration was 15 mg·L−1 at pH 8.0. Three cycle experiments confirmed that the Ni@FP possessed a satisfied stability and recycling ability. Moreover, the Ni@FP material presented a strong antibacterial activity which can prevent it from being contaminated by microorganisms. The versatility of the newly proposed photocatalyst in this study demonstrated its great application prospect in dyeing wastewater treatment.

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

Detection and characterization of DNA damage plays a critical role in genotoxicity testing, drug screening, and environmental health. We developed a fully integrated origami paper-based analytical device (oPAD) for measuring DNA damage. This simple device allows on-paper cell lysis, DNA extraction, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) reaction and signal readout with simple operation steps, enabling rapid (within 30 min) and high throughput assessment of multiple DNA damages induced by exogenous chemical agents.

Organic electrochemical transistors (OECTs) have attracted great interest in the last few years as biochemical sensors due to their outstanding analytical performance, versatility, stability, and e...

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

Paper-based electronics are gaining increasing attention because of their merits of low cost, degradability, and foldability. However, the roughness and porosity of paper are not conducive to the d...

Filter paper, as a widely used and low-cost lab consumable, can serve as template for the synthesis of one-dimensional (1D) materials since it is composed of 1D cellulosic fiber. In this work, 1D NiO/NiCo2O4 composite was simply fabricated by adsorption of Ni and Co acetate on the filter paper and subsequent calcination process. The precursors were obtained without further treatment to filter paper or chemical reaction between metal salts. Calcination process leads to the removal of template and formation of binary NiO/NiCo2O4 composite. Electromagnetic (EM) wave absorption performance of NiO/NiCo2O4 composite could be tuned by adjusting the calcination temperatures and dosage of metal salts. For the optimized absorber (calcination temperature of 600 °C and dosage of Ni and Co acetate with 2 mmol and 4 mmol), a wide absorption bandwidth of 6.08 GHz could be achieved with thickness of 1.88 mm and minimum reflection loss value was up to −57.4 dB by changing the thickness. The facile synthetic route may also inspire the preparation of other high-performance one-dimensional EM wave absorbing materials.

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

Recent advances in the design and preparation of electroactive materials, particularly semiconducting and conductive polymers, have resulted in the creation of novel organic electronics with advanced functionality and performance competitive with that of devices made of silicon. With an increasing number of organic and printed electronics being engineered and produced at a larger scale, the environmental cost of the final organic electronic devices (life cycle, environmental impact, etc.) needs to be considered. While e-waste is already a growing global problem, improving the sustainability of emerging electronics through a careful materials selection is highly desirable. In this work, we explore the use of shellac as a sustainable greener dielectric material in organic field-effect transistors (OFET). A careful examination of shellac in combination with diketopyrrolopyrrole-based semiconducting polymers was performed on rigid substrates through AFM and the fabrication of thin film transistors. All devices made from this green dielectric showed good performance and device characteristics. Building from this investigation, shellac was further integrated with paper substrates to fabricate paper-based thin film transistors. Thin film samples based on shellac on both silicon wafer and paper substrates were characterized by atomic force microscopy to investigate solid-state morphology of shellac and selected semiconducting materials. Through careful optimization of the device architecture and processing time, device characteristics and performances on paper substrates (average charge mobilities and on/off current ratios) were comparable to those of devices prepared on silicon wafers, confirming that shellac, in combination with organic semiconducting polymers, can be an advantageous dielectric material to be used for the fabrication of greener and sustainable thin film electronics from renewable feedstocks and components.

A bio-inspired cellulose paper–poly(amidoxime) composite hydrogel is explored via UV-polymerization. This hydrogel has a highly efficient uranium capture capacity of up to 6.21 mg g−1 for WU/Wdry gel and 12.9 mg g−1 for WU/Wpoly(amidoxime) in seawater for 6 weeks, due to its enhanced hydrophilicity, good hydraulic/ionic conductivity and broad-spectrum antibacterial performance.

A novel, simple and low-cost method for fabricating paper-based microfluidic device was presented. A soldering wire was used for making a template with specific pattern, and transfer printing to a ...

It is important to develop green and sustainable approaches to enhance electrochemical charge storage efficiencies. Herein, a two-step in-situ growth process was developed to fabricate carbon fiber paper-supported CeO2/MnO2 composite (CeO2/MnO2—CFP) as a binder-free photo-electrode for the photo-assisted electrochemical charge storage. The formation of CeO2/MnO2 type II heterojunction largely enhanced the separation efficiency of photo-generated charge carriers, resulting in a substantially enhanced photo-assisted charging capability of ∼20%. Furthermore, it retained a large part of its photo-enhanced capacitance (∼56%) in dark even after the illumination was off for 12 h, which could be attributed to its slow release of stored photo-generated electrons from its specific band structure to avoid their reaction with O2 in dark. This study proposed the design principles for supercapacitors with both the photo-assisted charging capability and its long-lasting retainment in dark, which may be readily applied to other pseudocapacitive materials to better utilize solar energy.

Developing highly efficient and stable non-precious metal catalysts for water splitting is urgently required. In this work, we report a facile one-step molten salt method for the preparation of self-supporting Ni-doped Mo2C on carbon fiber paper (Ni-Mo2CCB/CFP) for hydrogen evolution reaction (HER). The effects of nickel nitrate concentration on the phase composition, morphology, and electrocatalytic HER performance of Ni-doped Mo2C@CFP electrocatalysts was investigated. With the continuous increase of Ni(NO3)2 concentration, the morphology of Mo2C gradually changes from granular to flower-like, providing larger specific surface area and more active sites. Doping nickel (Ni) into the crystal lattice of Mo2C largely reduces the impedance of the electrocatalysts and enhances their electrocatalytic activity. The as-developed Mo2C-3 M Ni(NO3)2/CFP electrocatalyst exhibits high catalytic activity with a small overpotential of 56 mV at a current density of 10 mA·cm−2. This catalyst has a fast HER kinetics, as demonstrated by a very small Tafel slope of 27.4 mV·dec−1, and persistent long-term stability. A further higher Ni concentration had an adverse effect on the electrocatalytic performance. Density functional theory (DFT) calculations further verified the experimental results. Ni doping could reduce the binding energy of Mo-H, facilitating the desorption of the adsorbed hydrogen (Hads) on the surface, thereby improving the intrinsic catalytic activity of Ni-doped Mo2C-based catalysts. Nevertheless, excessive Ni doping would inhibit the catalytic activity of the electrocatalysts. This work not only provides a simple strategy for the facile preparation of non-precious metal electrocatalysts with high catalytic activity, but also unveils the influence mechanism of the Ni doping concentration on the HER performance of the electrocatalysts from the theoretical perspective.

Inorganic salt modified paper substrates were developed and utilized in microfluidic paper based sampling coupled with potentiometric ion sensors for the determination of heavy metals, such as Cd2+ and Pb2+. The application of paper based sampling without any paper substrate pre-treatment were characterized with super Nernstian response, while the paper substrates with inorganic salt pre-treatment were characterized with standard Nernstian response. The application of inorganic salt modified paper substrates was found advantageous when the cation of the salt in the conditioning solution was the same as the primary cations of the ion-selective electrodes (ISEs). A relatively high concentration of inorganic salts during pre-treatment of the paper substrates, namely Cd(NO3)2 or Pb(NO3)2 with subsequent measurement of cadmium(II) and lead(II), by Cd2+- and Pb2+-ISEs, respectively was needed to sustain Nernstian response of sensors. It was also found that paper substrates facilitate sorption of metal ions onto the paper substrates, with stronger binding strength given to Pb2+ over Cd2+. Moreover, the metal-paper interactions suggest concentration dependent sorption-desorption of metal ion, which can have direct limitations of the use of paper based analytics for the determination of low analyte concentration of heavy metals. Nanyang Technological University The authors would like to thank NTU-India Connect Research Internship Program for financial support of Ms Tharini Saravana Sundaram from Coimbatore Institute of Technology, India.

In this article, we report the development and optimization of a cost-effective, biodegradable, disposable, and lightweight conductive polymer deposited on exfoliated graphite paper battery. The anode is made of aluminum foil and the cathode using electrochemically deposited anthraquinone conductive polymers on exfoliated graphite paper. Concentrated sodium chloride salt is used as the electrolyte. The battery shows a maximum capacity of 235 mA h g−1 and a superior cyclability of up to 500 cycles at 50.0 mA cm−2 current density.

The first discrete bimetallic europium(iii)/copper(ii) complex for the fast, sensitive and selective luminescent detection of both aqueous and gaseous hydrogen sulfide has been developed. The chemosensor displayed an impressive response time of 30 seconds and a low theoretical limit of detection (100 ppb) for gaseous hydrogen sulfide.

A simple process of commercial paper functionalisation via in situ polymerisation of conductive polymers onto cellulose fibres was investigated and applied as electrodes in paper-based batteries. The functionalisation involved polypyrrole (PPy) and Poly (3,4-ethylenedioxythiophene) (PEDOT) as conductive polymers with the process of functionalisation optimised for each polymer individually with respect to oxidant-to-monomer ratios and polymerisation times and temperature. Paper with conductivity values of 44 mS/cm was obtained by exposing the samples to pyrrole vapour for a period of 30 min at room temperature; however, polymerisation at temperatures of 40 °C lead to higher conductivity values to up 141 mS/cm. Consequently, functionalised PPy and PEDOT papers were applied as cathodes in batteries with Al foil anodes and commercial paper soaked in an electrolyte solution of NaCl.

Because of the rapid evolution of wearable devices, great effort has been devoted to widely developing flexible strain sensors, as one of the most important components. However, realizing the low-c...

Purpose The purpose of this paper is to predict a suitable paper substrate which has high capillary pressure with the tendency of subsequent fluid wrenching in onward direction for the fabrication of microfluidics device application. Design/methodology/approach The experiment has been done on the WhatmanTM grade 1, WhatmanTM chromatography and nitrocellulose paper samples which are made by GE Healthcare Life Sciences. The structural characterization of paper samples for surface properties has been done by scanning electron microscope and ImageJ software. Identification of functional groups on the surface of samples has been done by Fourier transform infrared analysis. A finite elemental analysis has also been performed by using the “Multiphase Flow in Porous Media” module of the COMSOL Multiphysics tool which combines Darcy’s law and Phase Transport in Porous Media interface. Findings Experimentally, it has been concluded that the paper substrate for flexible microfluidic device application must have large number of internal (intra- and interfiber) pores with fewer void spaces (external pores) that have high capillary pressure to propel the fluid in onward direction with narrow paper fiber channel. Originality/value Surface structure has a dynamic impact in paper substrate utilization in multiple applications such as paper manufacturing, printing process and microfluidics applications.