Facile Synthesis of Polyaniline/Carbon-Coated Hollow Indium Oxide Nanofiber Composite with Highly Sensitive Ammonia Gas Sensor at the Room Temperature.

Hollow carbon-coated In2O3 (C#In2O3) nanofibers were prepared using an efficiently combined approach of electrospinning, high-temperature calcination, and hydrothermal process. The polyaniline (PANI)/hollow C#In2O3 nanofiber composites were synthesized used hollow C#In2O3 nanofibers worked as a core through the in situ chemical oxidative polymerization. The morphology and crystalline structure of the PANI/hollow C#In2O3 nanofiber composite were identified using wide-angle X-ray diffraction and transmission electron microscopy. The gas-sensing performances of the fabricated PANI/hollow C#In2O3 nanofiber composite sensor were estimated at room temperature, and the response value of the composite sensor with an exposure of 1 ppm NH3 was 18.2, which was about 5.74 times larger than that of the pure PANI sensor. The PANI/hollow C#In2O3 nanofiber composite sensor was demonstrated to be highly sensitive to the detection of NH3 in the concentration range of 0.6~2.0 ppm, which is critical for kidney or hepatic disease detection from the human breath. This composite sensor also displayed superior repeatability and selectivity at room temperature with exposures of 1.0 and 2.0 ppm NH3. Because of the outstanding repeatability and selectivity to the detection of NH3 at 1.0 and 2.0 ppm confirmed in this investigation, the PANI/hollow C#In2O3 nanofiber composite sensor will be considered as a favorable gas-sensing material for kidney or hepatic disease detection from human breath.

The Room Temperature Highly Sensitive Ammonia Gas Sensor Based on Polyaniline and Nitrogen-Doped Graphene Quantum Dot-Coated Hollow Indium Oxide Nanofiber Composite.

Hollow indium trioxide (In2O3) nanofibers fabricated via an effectively combined method of electrospinning and high-temperature calcination were coated with nitrogen-doped graphene quantum dots (N-GQDs) prepared by a hydrothermal process through electrostatic interaction. The N-GQD-coated hollow In2O3 nanofibers served as a core for the synthesis of polyaniline (PANI)/N-GQD/hollow In2O3 nanofiber ternary composites using in situ chemical oxidative polymerization. The chemical structure and morphology of the fabricated ternary composites were characterized using Fourier transform infrared, field-emission scanning electron microscopy, and transmission electron microscopy. The gas-sensing performances of the ternary composites were estimated by a homemade dynamic test system which was supplied with a real-time resistance acquisition platform at room temperature. The response value of the PANI/N-GQD/hollow In2O3 nanofiber sensor with a loading of 20 wt% N-GQD-coated hollow In2O3 nanofiber and an exposure of 1 ppm NH3 was 15.2, which was approximately more than 4.4 times higher than that of the PANI sensor. This ternary composite sensor was proved to be very sensitive in the detection of NH3 at a range of concentration between 0.6 ppm and 2.0 ppm at room temperature, which is crucial in the detection of hepatic or kidney disease in human breath. The PANI/N-GQD/hollow In2O3 nanofiber sensor also revealed higher selectivity and repeatability when exposed to 1.0 and 2.0 ppm NH3 at room temperature. Because of the excellent selectivity and repeatability in the detection of 1.0 and 2.0 ppm NH3 at room temperature achieved in this study, it is considered that the PANI/N-GQD/hollow In2O3 nanofiber composite sensor will be a favored gas-sensing material applied on human breath for the detection of hepatic or kidney disease.

Optimal Performance of Thin-Film Composite Nanofiltration-Like Forward Osmosis Membranes Set Off by Changing the Chemical Structure of Diamine Reacted with Trimesoyl Chloride through Interfacial Polymerization.

Thin-film composite (TFC) polyamide membranes formed through interfacial polymerization can function more efficiently by tuning the chemical structure of participating monomers. Accordingly, three kinds of diamine monomers were considered to take part in interfacial polymerization. Each diamine was reacted with trimesoyl chloride (TMC) to manufacture TFC polyamide nanofiltration (NF)-like forward osmosis (FO) membranes. The diamines differed in chemical structure; the functional group present between the terminal amines was classified as follows: aliphatic group of 1,3-diaminopropane (DAPE); cyclohexane in 1,3-cyclohexanediamine (CHDA); and aromatic or benzene ring in m-phenylenediamine (MPD). For FO tests, deionized water and 1 M aqueous sodium sulfate solution were used as feed and draw solution, respectively. Interfacial polymerization conditions were also varied: concentrations of water and oil phases, time of contact between the water-phase solution and the membrane substrate, and polymerization reaction time. The resultant membranes were characterized using attenuated total reflectance-Fourier transform infrared spectroscopy, field emission scanning electron microscopy, atomic force microscopy, and surface contact angle measurement to identify the chemical structure, morphology, roughness, and hydrophilicity of the polyamide layer, respectively. The results of FO experiments revealed that among the three diamine monomers, CHDA turned out to be the most effective, as it led to the production of TFC NF-like FO membrane with optimal performance. Then, the following optimum conditions were established for the CHDA-based membrane: contact between 2.5 wt.% aqueous CHDA solution and polysulfone (PSf) substrate for 2 min, and polymerization reaction between 1 wt.% TMC solution and 2.5 wt.% CHDA solution for 30 s. The composite CHDA-TMC/PSf membrane delivered a water flux (Jw) of 18.24 ± 1.33 LMH and a reverse salt flux (Js) of 5.75 ± 1.12 gMH; therefore, Js/Jw was evaluated to be 0.32 ± 0.07 (g/L).