Low-Power and Eco-Friendly Temperature Sensor Based on Gelatin Nanocomposite.
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ABSTRACT: An environmentally-friendly temperature sensor has been fabricated by using a low-cost water-processable nanocomposite material based on gelatin and graphene. The temperature dependence of the electrochemical properties has been investigated by using cyclic voltammetry, chronopotentiometry and impedance spectroscopy measurements. The simple symmetric device, composed of a sandwich structure between two metal foils and a printable graphene-gelatin blend, exhibits a dependence on the open-circuit voltage in a range between 260 and 310 K. Additionally, at subzero temperature, the device is able to detect the ice/frost formation. The thermally-induced phenomena occur at the electrode/gel interface with a bias current of a few tens of μA. The occurrence of dissociation reactions within the sensor causes limiting-current phenomena in the gelatin electrolyte. A detailed model describing the charge carrier accumulation, the faradaic charge transfer and diffusion processes within the device under the current-controlled has been proposed. In order to increase the cycle stability of the temperature sensor and reduce its voltage drift and offset of the output electrical signal, a driving circuit has been designed. The eco-friendly sensor shows a temperature sensitivity of about -19 mV/K, long-term stability, fast response and low-power consumption in the range of microwatts suitable for environmental monitoring for indoor applications.
Project description:Now the wide use of nanooxides is attributed to their remarkable collection of properties. Nanocomposites have an impressive variety of important applications. A thermal decomposition approach provides a more optimistic method for nanocrystal synthesis due to the low cost, high efficiency, and expectations for large-scale production. Therefore, in this study a new eco-friendly nanooxide composite with sorption characteristics for europium (Eu(III)) and strontium (Sr(II)) was synthesized by a one-step thermal treatment process using earth-abundant tafla clay as a starting material to prepare a modified tafla (M-Taf) nanocomposite. The synthesized nancomposite was characterized by different techniques before and after sorption processes. Different factors that affected the sorption behavior of Eu(III) and Sr(II) in aqueous media by the M-Taf nanocomposite were studied. The results obtained illustrated that the kinetics of sorption of Eu(III) and Sr(II) by the M-Taf nanocomposite are obeyed according to the pseudo-second order and controlled by a Langmuir isotherm model with maximum sorption capacities (Q max) of 25.5 and 23.36 mg/g for Eu(III) and Sr(II), respectively. Also, this novel low-cost and eco-friendly sorbent has promising properties and can be used to separate and retain some radionuclides in different applications.
Project description:One of the frontier research areas in the field of gas sensing is high-performance room temperature-based novel sensing materials, and new family of low-cost and eco-friendly carbon nanomaterials with a unique structure has attracted significant attention. In this work, we propose a novel low-cost flexible room temperature ammonia gas sensor based on nitrogen-doped carbon nano-onions/polypyrrole (NCNO-PPy) composite material mounted low-cost membrane substrate was synthesized by combining hydrothermal and in-situ chemical polymerization methods. The proposed flexible sensor revealed high sensing performance when employed as the sensing material for ammonia detection at room temperature. The NCNO-PPy ammonia sensor exhibited 17.32% response for 100 ppm ammonia concentration with a low response time of 26 s. The NCNO-PPy based flexible sensor displays high selectivity, good repeatability, and long-term durability with 1 ppm as the lower detection limit. The proposed flexible sensor also demonstrated remarkable mechanical robustness under extreme bending conditions, i.e., up to 90° bending angle and 500 bending cycles. This enhanced sensing performance can be related to the potential bonding and synergistic interaction between nitrogen-doped CNOs and PPy, the formation of defects from nitrogen doping, and the presence of high reactive sites on the surface of NCNO-PPy composites. Additionally, the computational study was performed on optimized NCNO-PPy nanocomposite for both with and without NH3 interaction. A deeper understanding of the sensing phenomena was proposed by the computation of several electronic characteristics, such as band gap, electron affinity, and ionization potential, for the optimized composite.
Project description:In the context of imminent threats concerning biological and chemical warfare agents, the aim of this study was the development of a new method for biological and chemical decontamination, employing non-toxic, film-forming, water-based biodegradable solutions, using a nano sized reagent together with bentonite as trapping agents for the biological and chemical contaminants. Bentonite-supported nanoparticles of Cu, TiO2, and Ag were successfully synthesized and dispersed in a polyvinyl alcohol (PVA)/glycerol (GLY) aqueous solution. The decontamination effectiveness of the proposed solutions was evaluated by qualitative and quantitative analytical techniques on various micro-organisms, with sulfur mustard (HD) and dimethyl methylphosphonate (DMMP) as contaminants. The results indicate that the peelable active nanocomposite films can be successfully used on contaminated surfaces to neutralize and entrap the hazardous materials and their degradation products. Mechanical and thermal characterization of the polymeric films was also performed to validate the decontamination solution's potential as peelable-film generating materials. The removal efficacy from the contaminated surfaces for the tested micro-organisms varied between 93% and 97%, while for the chemical agent HD, the highest decontamination factor obtained was 90.89%. DMMP was almost completely removed from the contaminated surfaces, and a decontamination factor of 99.97% was obtained.
Project description:Reduced graphene oxide (rGO) was synthesized from a simple, cost-effective, and eco-friendly method by using Capsicum annuum (CA) as reducing agent. The rGO was mixed with SnO2 to synthesize a nanocomposite. The synthesized materials were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, and UV-visible spectroscopy techniques. The SnO2-C. annuum reduced graphene oxide (CRGO) nanocomposite exhibited a photodegradation efficiency of 97.4% when employed to remove methylene green (MG) dye. The synthesized nanocomposite showed improved photodegradation ability due to its high charge transfer and separation and owing to the presence of the large surface area of the CRGO network system. Degraded water was used in the plant and animal survival study, in which the dye solution treated with CRGO nanocomposite exhibited better growth compared to that of untreated MG solution. Likewise, in the ecotoxicity study, Artemia salina and zebra fish (Danio rerio) survival was found to be enhanced with CRGO nanocomposite-treated dye solution. This finding supports the effectiveness of CRGO/SnO2 nanocomposite for the treatment of MG dye-contaminated effluent samples.
Project description:Fluorescent carbon nanomaterials, especially zero-dimensional (0D) carbon nanodots (CDs), are widely used in broad biological and optoelectronic applications. CDs have unique characteristics such as strong fluorescence, biocompatibility, sun-light response, and capability of mass-production. Beyond the previous green CD obtained from harmful natural substances, we report a new type of fluid-based fluorescent CD paints (C-paints) derived from polyethylene glycol (PEG; via simple ultrasound irradiation at room temperatures) and produced in quantum yields of up to ~14%. Additionally, C-paints possess a strong, UV- and visible-light-responsive photoluminescent (PL) property. Most especially, C-paints, by incorporation into a photocatalytic system, show additional roles in the emission of fluorescent light for activation of TiO2 nanoparticles (NPs) and the resultant detoxification of most organic dyes, thus further enabling embarkation in advanced water purification.
Project description:The civil construction industry consumes huge amounts of raw materials and energy, especially infrastructure. Thus, the use of eco-friendly materials is indispensable to promote sustainable development. In this context, the present work investigated low-carbon concrete to produce eco-friendly paving blocks. The binder was defined according to two approaches. In the first, a binary binder developed with eucalyptus biomass ash (EBA) and silica fume (SF) was used, in total replacement for Portland cement. In the second, the mixture of residues was used as a precursor in alkali-activation reactions, forming alkali-activated binder. The experimental approach was carried out using five different mixtures, obtained by varying the amount of water or sodium hydroxide solution. The characterization of this new material was carried out using compressive strength, expandability, water absorption, deep abrasion, microstructural investigation, and organic matter degradation potential. The results showed that the EBA-SF system has a performance compatible with Portland cement when used as an alternative binder, in addition to functioning as a precursor to alkali-activated concrete. The blocks produced degraded organic matter, and this degradation is more intense with the incidence of UV. In this way, the EBA-SF binder can be successfully used for the manufacture of ecological paving blocks with low carbon emissions.
Project description:A series of novel superabsorbent composites of poly(acrylic acid)/semicoke were prepared by polymerization of acrylic acid using ammonium persulphate as initiator, N,N'-methylenebisacrylamide as crosslinker and semicoke which was the by-product of coal carbonizing as the inorganic components. FTIR and SEM analysis indicated that the superabsorbent composites had been successfully polymerized and the semicoke participated in construction of the 3D polymeric network. Meanwhile, the effects of initiator, crosslinker, semicoke, and neutralization degree, as well as the pH value, were investigated, and the results showed that superabsorbent composites containing 10% of semicoke possessed the maximum water absorbency of 584 g/g in distilled water and 75 g/g in 0.9% NaCl solution. The superabsorbent composites kept the high water absorbency within a wide pH range of 4-11, and still exhibited better re-swelling capability even after seven times. The superabsorbent composite with its excellent performance is a potential water-retaining agent used in agriculture.
Project description:Epoxy resin plays a key role in composite matrices and DGEBA is the major precursor used. With the aim of favouring the use of bio resources, epoxy resins can be prepared from lignin. In particular, diglycidyl ether of isoeugenol derivatives are good candidates for the replacement of DGEBA. This article presents an effective and eco-friendly way to prepare epoxy resin derived from isoeugenol (BioIgenox), making its upscale possible. BioIgenox has been totally characterized by NMR, FTIR, MS and elemental analyses. Curing of BioIgenox and camphoric anhydride with varying epoxide function/anhydride molar ratios has allowed determining an optimum ratio near 1/0.9 based on DMA and DSC analyses and swelling behaviours. This thermoset exhibits a Tg measured by DMA of 165 °C, a tensile storage modulus at 40 °C of 2.2 GPa and mean 3-point bending stiffness, strength and strain at failure of 3.2 GPa, 120 MPa and 6.6%, respectively. Transposed to BioIgenox/hexahydrophtalic anhydride, this optimized formulation gives a thermoset with a Tg determined by DMA of 140 °C and a storage modulus at 40 °C of 2.6 GPa. The thermal and mechanical properties of these two thermosets are consistent with their use as matrices for structural or semi-structural composites.
Project description:The sensing of volatile organic compounds by composites containing metal oxide semiconductors is typically explained via adsorption-desorption and surface electrochemical reactions changing the sensor's resistance. The analysis of molecular processes on chemiresistive gas sensors is often based on indirect evidence, whereas in situ or operando studies monitoring the gas/surface interactions enable a direct insight. Here we report a cross-disciplinary approach employing spectroscopy of working sensors to investigate room temperature methanol detection, contrasting well-characterized nanocomposite (TiO2@rGO-NC) and reduced-graphene oxide (rGO) sensors. Methanol interactions with the sensors were examined by (quasi) operando-DRIFTS and in situ-ATR-FTIR spectroscopy, the first paralleled by simultaneous measurements of resistance. The sensing mechanism was also studied by mass spectroscopy (MS), revealing the surface electrochemical reactions. The operando and in situ spectroscopy techniques demonstrated that the sensing mechanism on the nanocomposite relies on the combined effect of methanol reversible physisorption and irreversible chemisorption, sensor modification over time, and electron/O2 depletion-restoration due to a surface electrochemical reaction forming CO2 and H2O.
Project description:CeO2/ZnO-heterojunction-nanorod-array-based chemiresistive sensors were studied for their low-operating-temperature and gas-detecting characteristics. Arrays of CeO2/ZnO heterojunction nanorods were synthesized using anodic electrodeposition coating followed by hydrothermal treatment. The sensor based on this CeO2/ZnO heterojunction demonstrated a much higher sensitivity to NO2 at a low operating temperature (120 °C) than the pure-ZnO-based sensor. Moreover, even at room temperature (RT, 25 °C) the CeO2/ZnO-heterojunction-based sensor responds linearly and rapidly to NO2. This sensor's reaction to interfering gases was substantially less than that of NO2, suggesting exceptional selectivity. Experimental results revealed that the enhanced gas-sensing performance at the low operating temperature of the CeO2/ZnO heterojunction due to the built-in field formed after the construction of heterojunctions provides additional carriers for ZnO. Thanks to more carriers in the ZnO conduction band, more oxygen and target gases can be adsorbed. This explains the enhanced gas sensitivity of the CeO2/ZnO heterojunction at low operating temperatures.