Synthesis Characterization of Nanostructured ZnCo2O4 with High Sensitivity to CO Gas

In this work, nanostructured ZnCo2O4 was synthesized via a microwave-assisted colloidal method, and its application as gas sensor for the detection of CO was studied. Typical diffraction peaks corresponding to the cubic ZnCo2O4 spinel structure were identified at calcination temperature of 500°C by X-ray powder diffraction. A high degree of porosity in the surface of the nanostructured powder of ZnCo2O4 was observed by scanning electron microscopy and transmission electron microscopy, faceted nanoparticles with a pockmarked structure were clearly identified. The estimated average particle size was approximately 75 nm. The formation of ZnCo2O4 material was also confirmed by Raman characterization. Pellets fabricated with nanostructured powder of ZnCo2O4 were tested as sensors using CO gas at different concentrations and temperatures. A high sensitivity value of 305–300 ppm of CO was measured at 300°C, indicating that nanostructured ZnCo2O4 had a high performance in the detection of CO

CO and C 3

ZnSb2O6 has been synthesized by a microwave-assisted solution method in order to test its possible application as a gas sensor. Zinc nitrate, antimony trichloride, and ethylenediamine were used as precursors and deionized water as solvent. Microwave radiation, with a power of ~350 W, was applied for solvent evaporation. The thermal decomposition of the precursors leads to the formation of ZnSb2O6 at 600°C. This oxide crystallized in a tetragonal structure with cell parameters a=4.66 Å, c=9.26 Å and space group P42/mnm. Microwires and microrods formed by nanocrystals were observed by means of scanning and transmission electron microscopies (SEM and TEM, resp.). Pellets of the oxide were tested as gas sensors in flowing atmospheres of carbon monoxide (CO) and propane (C3H8). Sensitivity increased with the gas concentration (0–300 ppm) and working temperatures (ambient, 150 and 250°C) increase. The results indicate high sensitivity of ZnSb2O6 in both gases at different concentrations and operating temperatures

Reducing the environmental impact of surgery on a global scale: systematic review and co-prioritization with healthcare workers in 132 countries

Abstract Background Healthcare cannot achieve net-zero carbon without addressing operating theatres. The aim of this study was to prioritize feasible interventions to reduce the environmental impact of operating theatres. Methods This study adopted a four-phase Delphi consensus co-prioritization methodology. In phase 1, a systematic review of published interventions and global consultation of perioperative healthcare professionals were used to longlist interventions. In phase 2, iterative thematic analysis consolidated comparable interventions into a shortlist. In phase 3, the shortlist was co-prioritized based on patient and clinician views on acceptability, feasibility, and safety. In phase 4, ranked lists of interventions were presented by their relevance to high-income countries and low–middle-income countries. Results In phase 1, 43 interventions were identified, which had low uptake in practice according to 3042 professionals globally. In phase 2, a shortlist of 15 intervention domains was generated. In phase 3, interventions were deemed acceptable for more than 90 per cent of patients except for reducing general anaesthesia (84 per cent) and re-sterilization of ‘single-use’ consumables (86 per cent). In phase 4, the top three shortlisted interventions for high-income countries were: introducing recycling; reducing use of anaesthetic gases; and appropriate clinical waste processing. In phase 4, the top three shortlisted interventions for low–middle-income countries were: introducing reusable surgical devices; reducing use of consumables; and reducing the use of general anaesthesia. Conclusion This is a step toward environmentally sustainable operating environments with actionable interventions applicable to both high– and low–middle–income countries

A Novel Gas Sensor Based on MgSb2O6 Nanorods to Indicate Variations in Carbon Monoxide and Propane Concentrations

Bystromite (MgSb2O6) nanorods were prepared using a colloidal method in the presence of ethylenediamine, after a calcination step at 800 °C in static air. From X-ray powder diffraction analyses, a trirutile-type structure with lattice parameters a = 4.64 Å and c = 9.25 Å and space group P42/mnm was identified. Using scanning electron microscopy (SEM), microrods with sizes from 0.2 to 1.6 μm were observed. Transmission electron microscopy (TEM) analyses revealed that the nanorods had a length of ~86 nm and a diameter ~23.8 nm. The gas-sensing properties of these nanostructures were tested using pellets elaborated with powders of the MgSb2O6 oxide (calcined at 800 °C) at temperatures 23, 150, 200, 250 and 300 °C. The pellets were exposed to different concentrations of carbon monoxide (CO) and propane (C3H8) at these temperatures. The results showed that the MgSb2O6 nanorods possess excellent stability and high sensitivity in these atmospheres

A simple route for the preparation of nanostructured GdCoO3 via the solution method, as well as its characterization and its response to certain gases

This work presents the synthesis of perovskite GdCoO3 by a microwave-assisted solution method in order to test its possible application as a gas sensor. The crystal evolution, structure, composition, texture, morphology, and particle size were analyzed by X-ray diffraction, scanning and transmission electron microscopies, and nitrogen physisorption. Our synthesis route allowed to obtain GdCoO3 at lower temperatures and shorter reaction times than conventional methods. Measurements confirmed the formation of porous GdCoO3 microbases with a thickness of 7–13 μm. The GdCoO3 microbases were constituted by nanoparticles of size 10–20 nm. Additionally, crystallites of size 85–130 nm were observed distributed on the surface of the microbases, covering a surface area of around 19 m2/g. Pellets elaborated from GdCoO3 powders were tested as sensors in carbon monoxide and propane gaseous atmospheres at different temperatures and gas concentrations. The GdCoO3 showed a good performance as a gas sensor compared to other similar oxides. The oxide was clearly sensitive to the studied gases even at concentrations as low as 5 ppm at a temperature of 100 °C. The response of the material was homogeneous and increased with both the increase in temperature and gas concentration. Keywords: GdCoO3, Perovskites, Nanoparticles, Gas sensor

Synthesis of ZnAl2O4 and Evaluation of the Response in Propane Atmospheres of Pellets and Thick Films Manufactured with Powders of the Oxide

ZnAl2O4 nanoparticles were synthesized employing a colloidal method. The oxide powders were obtained at 300 °C, and their crystalline phase was corroborated by X-ray diffraction. The composition and chemical structure of the ZnAl2O4 was carried out by X-ray and photoelectron spectroscopy (XPS). The optical properties were studied by UV-vis spectroscopy, confirming that the ZnAl2O4 nanoparticles had a direct transition with bandgap energy of 3.2 eV. The oxide’s microstructures were microbars of ~18.2 nm in size (on average), as analyzed by scanning (SEM) and transmission (TEM) electron microscopies. Dynamic and stationary gas detection tests were performed in controlled propane atmospheres, obtaining variations concerning the concentration of the test gas and the operating temperature. The optimum temperatures for detecting propane concentrations were 200 and 300 °C. In the static test results, the ZnAl2O4 showed increases in propane response since changes in the material’s electrical conductance were recorded (conductance = 1/electrical resistance, Ω). The increases were ~2.8 at 200 °C and ~7.8 at 300 °C. The yield shown by the ZnAl2O4 nanoparticles for detecting propane concentrations was optimal compared to other similar oxides categorized as potential gas sensors

Preparation of Powders Containing Sb, Ni, and O for the Design of a Novel CO and C3H8 Sensor

In this work, powders of NiSb2O6 were synthesized using a simple and economical microwave-assisted wet chemistry method, and calcined at 700, 800, and 900 °C. It was identified through X-ray diffraction that the oxide is a nanomaterial with a trirutile-type structure and space group P42/mnm (136). UV–Vis spectroscopy measurements showed that the bandgap values were at ~3.10, ~3.14, and ~3.23 eV at 700, 800, and 900 °C, respectively. Using scanning electron microscopy (SEM), irregularly shaped polyhedral microstructures with a size of ~154.78 nm were observed on the entire material’s surface. The particle size was estimated to average ~92.30 nm at the calcination temperature of 900 °C. Sensing tests in static atmospheres containing 300 ppm of CO at 300 °C showed a maximum sensitivity of ~72.67. On the other hand, in dynamic atmospheres at different CO flows and at an operating temperature of 200 °C, changes with time in electrical resistance were recorded, showing a high response, stability, and repeatability, and good sensor efficiency during several operation cycles. The response times were ~2.77 and ~2.10 min to 150 and 200 cm3/min of CO, respectively. Dynamic tests in propane (C3H8) atmospheres revealed that the material improved its response in alternating current signals at two different frequencies (0.1 and 1 kHz). It was also observed that at 360 °C, the ability to detect propane flows increased considerably. As in the case of CO, NiSb2O6’s response in propane atmospheres showed very good thermal stability, efficiency, a high capacity to detect C3H8, and short response and recovery times at both frequencies. Considering the great performance in propane flows, a sensor prototype was developed that modulates the electrical signals at 360 °C, verifying the excellent functionality of NiSb2O6

Gas Sensing Properties of NiSb 2

Micro- and nanoparticles of NiSb2O6 were synthesized by the microwave-assisted colloidal method. Nickel nitrate, antimony chloride, ethylenediamine, and ethyl alcohol were used. The oxide was obtained at 600°C and was analyzed by X-ray diffraction (XRD) and Raman spectroscopy, showing a trirutile-type structure with cell parameters a = 4.641 Å, c = 9.223 Å, and a space group P42/mnm (136). Average crystal size was estimated at ~31.19 nm, according to the XRD-peaks. The microstructure was scrutinized by scanning electron microscopy (SEM), observing microrods measuring ~3.32 μm long and ~2.71 μm wide, and microspheres with an average diameter of ~8 μm; the size of the particles shaping the microspheres was measured in the range of ~0.22 to 1.8 μm. Transmission electron microscopy (TEM) revealed that nanoparticles were obtained with sizes in the range of 2 to 20 nm (~10.7 nm on average). Pellets made of oxide’s powders were tested in propane (C3H8) and carbon monoxide (CO) atmospheres at different concentrations and temperatures. The response of the material increased significantly as the temperature and the concentration of the test gases rose. These results show that NiSb2O6 may be a good candidate for gas sensing applications

Facile Synthesis, Microstructure, and Gas Sensing Properties of NdCoO3 Nanoparticles

NdCoO3 nanoparticles were successfully synthesized by a simple, inexpensive, and reproducible solution method for gas sensing applications. Cobalt nitrate, neodymium nitrate, and ethylenediamine were used as precursors and distilled water as solvent. The solvent was evaporated later by means of noncontinuous microwave radiation at 290 W. The obtained precursor powders were calcined at 200, 500, 600, and 700°C in a standard atmosphere. The oxide crystallized in an orthorhombic crystal system with space group Pnma (62) and cell parameters a=5.33 Å, b=7.52 Å, and c=5.34 Å. The nanoparticles showed a diffusional growth to form a network-like structure and porous adsorption configuration. Pellets prepared from NdCoO3 were tested as gas sensors in atmospheres of carbon monoxide and propane at different temperatures. The oxide nanoparticles were clearly sensitive to changes in gas concentrations (0–300 ppm). The sensitivity increased with increasing concentration of the gases and operating temperatures (25, 100, 200, and 300°C)

Synthesis of ZnMn2O4 Nanoparticles by a Microwave-Assisted Colloidal Method and their Evaluation as a Gas Sensor of Propane and Carbon Monoxide

Spinel-type ZnMn2O4 nanoparticles were synthesized via a simple and inexpensive microwave-assisted colloidal route. Structural studies by X-ray diffraction showed that a spinel crystal phase of ZnMn2O4 was obtained at a calcination temperature of 500 °C, which was confirmed by Raman and UV-vis characterizations. Spinel-type ZnMn2O4 nanoparticles with a size of 41 nm were identified by transmission electron microscopy. Pellet-type sensors were fabricated using ZnMn2O4 nanoparticles as sensing material. Sensing measurements were performed by exposing the sensor to different concentrations of propane or carbon monoxide at temperatures in the range from 100 to 300 °C. Measurements performed at an operating temperature of 300 °C revealed a good response to 500 ppm of propane and 300 ppm of carbon monoxide. Hence, ZnMn2O4 nanoparticles possess a promising potential in the gas sensors field