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This paper demonstrates a simple-in-struct- ure, cost-effective, and environment-friendly Microfluidic Paper-based Analytical Device for Microbial Biofuel Cell ( $\mu $ PAD-MBFC). It consists of a microchannel with biofuel cell (Escherichia.Coli) and an oxidant (aerated tap water) flowing co-parallelly over Multiwalled Carbon Nanotube (MWCNT)-based Bucky Paper (BP) electrodes using a self-capillary and co-laminar flow mechanism. The electrochemical studies, such as open circuit potential (OCP) and polarization were evaluated using a potentiostat. Various volumetric bacterial studies were also carried out to find out the best suitable optimal bacterial volume. Subsequently, the morphological and detailed element composition study of electrode surface was performed using scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) techniques. This well-designed portable $\mu $ PAD-MBFC yields a maximum power density of 4 $\mu \text{W}$ /cm2 ( $20~\mu \text{A}$ /cm2) at 0.405 V over $200~\mu \text{l}$ of culture and leveraging to its long-lasting potential to operate miniaturized microelectronics sensors and portable devices.

This paper establishes a membraneless, co-laminar flow-based approach to develop a cost-effective microfluidic paper-based analytical device for enzymatic biofuel cell ( $\mu $ PAD-EBFC). The developed $\mu $ PAD-EBFC supporting the self-capillary fluid transport action consists of Y-shaped paper microchannel with the fuel (glucose) and oxidant (O2) streaming in parallel over carbon nanotube-based bucky paper electrodes modified with biocompatible electrocatalytic enzymes, such as glucose oxidase and laccase without any additional redox cofactor. The electrochemical performance for the modified bioelectrodes, i.e., electrocatalytic oxidation and reduction reaction, was carried out using linear sweep voltammetry, cyclic voltammetry, and open circuit potential. The overall performance of $\mu $ PAD-EBFC was evaluated using the polarization studies. Subsequently, the catalytic activity of enzymes on the electrode surface was validated by the scanning electron microscope. This simple and portable $\mu $ PAD-EBFC can generate the maximum power density to the order of $100~\mu \text{W}$ /cm2 ( $600~\mu \text{A}$ /cm2) at 0.505 V over prolonged durations of around 50 h. Hence, the presented $\mu $ PAD-EBFC shows good power density and stability, leading to its strong potential to power miniaturized microelectronics devices and sensors.

The charging/discharging delays in superconducting coils wound without insulation (NI coils) are a major drawback of the technique. While removing the insulation improves safety margins, the increase in the characteristic time constant τ_c can make a coil unfit for a particular purpose. It is widely accepted for instance that NI coils will not be used in ac applications where τ_c ~ 1/f. To decrease τ_c of the NI coils, the same length of superconductor can be wound/connected in parallel rather than in series — decreasing the inductance L, and hence the time constant τ_c, while maintaining the number of amp-turns I_op*N. Here we investigate the effect of parallel connecting coils in a magnet using a 2D axially symmetric model which captures all the necessary electromagnetic properties of the HTS NI coils. These properties include: critical current anisotropy Jc(B, θ), turn-to-turn conductivity, as well as winding parallelism. Our modeling results show that the parallel connected magnet experiences magnet-wide shielding current effects. Whilst these shielding currents affect field homogeneity — the model enables this effect to be quantified. Furthermore, shielding currents are not an issue when running NI coils in saturated mode. The modeling work presented here provides a simple initial example of how magnet designers may approach designing, optimizing, and operating high current, HTS NI coils.

This paper addresses two key challenges toward an integrated forward error-correcting biosensor based on our previously reported self-assembled quick-response (QR) code. The first challenge involves the choice of the paper substrate for printing and self-assembling the QR code. We have compared four different substrates that includes regular printing paper, Whatman filter paper, nitrocellulose membrane and lab synthesized bacterial cellulose. We report that out of the four substrates bacterial cellulose outperforms the others in terms of probe (gold nanorods) and ink retention capability. The second challenge involves remote activation of the analyte sampling and the QR code self-assembly process. In this paper, we use light as a trigger signal and a graphite layer as a light-absorbing material. The resulting change in temperature due to infrared absorption leads to a temperature gradient that then exerts a diffusive force driving the analyte toward the regions of self-assembly. The working principle has been verified in this paper using assembled biosensor prototypes where we demonstrate higher sample flow rate due to light induced thermal gradients.

The applicability of using 2-furfural (2-FAL) and methanol as aging markers for synthetic ester impregnated paper insulation was investigated through laboratory aging experiments at temperatures of 80, 100 and 120 °C. Methanol in the synthetic ester increased linearly with paper aging until degree of polymerisation (DP) reached 400. During this period concentration of methanol in oil was higher than that of 2-FAL, which proved the concept of using methanol to indicate early paper aging in the synthetic ester. However, the rate of methanol increase against the reduction of DP in the synthetic ester was about three times higher than that seen in mineral oil. This is due to a difference in the partitioning of the marker between oil and paper. Since the synthetic ester is more polar than the mineral oil, it attracted more methanol molecules from the paper, resulting in a higher concentration of methanol in oil for the same reduction of DP. In addition, a reduction in methanol was observed at the later stage of paper aging at 120 °C. This could be due to either a change in the partitioning between oil and paper, or an esterification reaction which consumes methanol in the system.

Nowadays, reliability of power system is of great importance. Therefore, the condition of transformers as the expensive and critical components of a power system should be monitored and assessed. The dominant factor that causes limitation in transformers lifetime is the paper insulation. This paper aims to investigate the conspicuous influence of moisture content, especially in low oxygen and temperature on lifetime estimation under constant conditions, based on the results of previous experiments. Degree of polymerization (DP) is employed to quantify the effects of detrimental parameters with respect to their time-varying nature. This paper proposes a novel lifetime estimation-approach considering a yearly moisture growth for transformers. The results indicate different trend of DP profiles, which lead to an accurate lifetime estimation in comparison with DP obtained through ideal conditions. Furthermore, oscillations in the hot-spot temperature of transformers are demonstrated to have a negative effect on the lifetime.

This paper presents a wireless, self-powered, affinity-based biosensor based on the integration of paper-based microfluidics with our previously reported method for self-assembling radio-frequency (RF) antennas. At the core of the proposed approach is a silver-enhancement technique that grows portions of a RF antenna in regions where target antigens hybridize with target specific affinity probes. The hybridization regions are defined by a network of nitrocellulose based microfluidic channels which implement a self-powered approach to sample the reagent and control its flow and mixing. The integration substrate for the biosensor has been constructed using polyethylene and the patterning of the antenna on the substrate has been achieved using a low-cost ink-jet printing technique. The substrate has been integrated with passive radio-frequency identification (RFID) tags to demonstrate that the resulting sensor-tag can be used for continuous monitoring in a food supply-chain where direct measurement of analytes is typically considered to be impractical. We validate the proof-of-concept operation of the proposed sensor-tag using IgG as a model analyte and using a 915 MHz Ultra-high-frequency (UHF) RFID tagging technology.