scholarly journals Improving Linear Range Limitation of Non-Enzymatic Glucose Sensor by OH− Concentration

Crystals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 186
Author(s):  
Lory Wenjuan Yang ◽  
Elton Enchong Liu ◽  
Alex Fan Xu ◽  
Jason Yuanzhe Chen ◽  
Ryan Taoran Wang ◽  
...  
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Glucose Oxidation ◽  
Glucose Sensor ◽  
Linear Range ◽  
Diabetic Patients ◽  
Current Response ◽  
Effective Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Naoh Solution

The linear range of the non-enzymatic glucose sensor is usually much smaller than the glucose level of diabetic patients, calling for an effective solution. Despite many previous attempts, none have solved the problem. Such a challenge has now been conquered by raising the NaOH concentration in the electrolyte, where amperometry, X-ray diffraction, Fourier-transform infrared spectroscopy, and Nuclear magnetic resonance measurements have been conducted. The linear range has been successfully enhanced to 40 mM in 1000 mM NaOH solution, and it was also found that NaOH affected the degree of glucose oxidation, which influenced the current response during sensing. It was expected that the alkaline concentration must be 25 times higher than the glucose concentration to enhance the linear range, much contrary to prior understanding.

scholarly journals Non-enzymatic Glucose Sensor Based on CuO Nanoplates

2020 ◽  
Vol 30 (7) ◽  
pp. 54-57
Author(s):  
Thi Xuan Chu
Keyword(s):  
Electrochemical Method ◽  
Glucose Sensor ◽  
Glucose Measurement ◽  
Glucose Detection ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
Promising Candidate ◽  
Facile Hydrothermal Method ◽  
X Ray ◽  
Naoh Solution

We have successfully fabricated an electrochemical sensor for non-enzymatic glucose measurement based on copper oxide (CuO) nanoplates. CuO nanoplates were synthesized by a facile hydrothermal method at 180 oC for 23 h without using any surfactants. Filed-emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD) were used to characterize morphologies and crystal structures of synthesized CuO nanoplates. A mixture of CuO nanoplates and polytetrafluoroethylene with mass ratio 0.15:1 was compressed at 9800 kPa onto platinum (Pt) to form Pt/CuO disk and it has been used as a working electrode for glucose measurement following non-enzymatic approach. Glucose concentration was evaluated by cyclic voltammetry in 0.1M NaOH solution. This enzyme-free electrochemical method was able to detect glucose with a concentration as low as 0.1 mM. These results show that CuO nanoplates are a promising candidate for non-enzymatic glucose detection.

scholarly journals Exploring the Structural Chemistry of Pyrophosphoramides: N,N′,N″,N‴-Tetraisopropylpyrophosphoramide

Chemistry ◽  
2021 ◽  
Vol 3 (1) ◽  
pp. 149-163
Author(s):  
Duncan Micallef ◽  
Liana Vella-Zarb ◽  
Ulrich Baisch
Keyword(s):  
Crystal Structure ◽  
Mass Spectrometry ◽  
Nuclear Magnetic Resonance ◽  
Hydrogen Bonding ◽  
Nmr Spectroscopy ◽  
Ir Spectroscopy ◽  
Room Temperature ◽  
Intermolecular Hydrogen Bonding ◽  
X Ray Diffraction ◽  
X Ray

N,N′,N″,N‴-Tetraisopropylpyrophosphoramide 1 is a pyrophosphoramide with documented butyrylcholinesterase inhibition, a property shared with the more widely studied octamethylphosphoramide (Schradan). Unlike Schradan, 1 is a solid at room temperature making it one of a few known pyrophosphoramide solids. The crystal structure of 1 was determined by single-crystal X-ray diffraction and compared with that of other previously described solid pyrophosphoramides. The pyrophosphoramide discussed in this study was synthesised by reacting iso-propyl amine with pyrophosphoryl tetrachloride under anhydrous conditions. A unique supramolecular motif was observed when compared with previously published pyrophosphoramide structures having two different intermolecular hydrogen bonding synthons. Furthermore, the potential of a wider variety of supramolecular structures in which similar pyrophosphoramides can crystallise was recognised. Proton (1H) and Phosphorus 31 (31P) Nuclear Magnetic Resonance (NMR) spectroscopy, infrared (IR) spectroscopy, mass spectrometry (MS) were carried out to complete the analysis of the compound.

Effect of Yttria-Stabilized Zirconia Concentration in an Electroless Bath on Microstructure and Composition of Ni/Yttria-Stabilized Zirconia Nanocomposite

2021 ◽  
Vol 21 (11) ◽  
pp. 5592-5602
Author(s):  
Samira Almasi ◽  
Ali Mohammad Rashidi
Keyword(s):  
High Performance ◽  
Yttria Stabilized Zirconia ◽  
X Ray Diffraction ◽  
Stabilized Zirconia ◽  
Nickel Ion ◽  
Nanocomposite Particles ◽  
X Ray ◽  
Ni Content ◽  
Naoh Solution ◽  
Average Size

The effect of the yttria-stabilized zirconia (YSZ) nanoparticle loading in an electro-less bath was considered as one of the vital synthesis variables for control Ni content and microstructure of prepared nanocomposite particles, which are two crucial factors to achieving high-performance SOFC anode. Nanocomposite particles were prepared using a simple electroless method without any expensive pretreatment of sensitizing by Sn2+ ions as well as activating by Pd2+ ions that are usually used to apply nickel coating on the surface of a non-conductive substrate. The process was performed by adding YSZ nanoparticles into NaOH solution, separating them from the solution by the centrifugal method, then providing several water-based nanofluids with different concentrations of activated YSZ nanoparticles, mixing them with NiCI2 solution, followed by adding the hydrazine and then NaOH solution. X-ray diffraction and scanning electron microscopy coupled with energy dispersive X-ray analysis were used to analyze the prepared nanocomposite particles. It is observed that after adding YSZ nanoparticles into the NaOH solution, the pH of the solution varied gradually from a starting pH of 10.2 to 9. Also, by increasing the YSZ nanoparticles loading in the electroless bath from 76 mg/l to 126 mg/l, the grain size of Ni deposits, the Ni content and the average size of the prepared nanocomposite particles decreased. The electrochemical mechanism previously proposed for the nickel ion reduction was modified, and a novel analytical model was proposed for variation of the efficiency of Ni deposition with YSZ nanoparticles loading.

A new stacking variant of Na2Pt(OH)6

2018 ◽  
Vol 73 (11) ◽  
pp. 831-836 ◽  
Author(s):  
Gohil S. Thakur ◽  
Hans Reuter ◽  
Claudia Felser ◽  
Martin Jansen
Keyword(s):  
Oxygen Pressure ◽  
Title Compound ◽  
Structure Type ◽  
Direct Reaction ◽  
Solid Residue ◽  
X Ray Diffraction ◽  
X Ray ◽  
Edge Distance ◽  
Naoh Solution

AbstractA new stacking variant of sodium hexa-hydroxo platinate(IV), Na2Pt(OH)6, was synthesized and its structure elucidated through X-ray diffraction. The new polymorph was prepared by direct reaction of PtO2 with an excess of NaOH solution applying elevated oxygen pressure at 300°C. The structure consists of layers of edge sharing Pt(OH)6 and Na(OH)6 octahedra. These layers are separated by an edge-to-edge distance of ~2.4 Å. The packing of the hydroxide ions corresponds to the hcp sequence, the title compound thus may be regarded a cation ordered variant of the Brucite structure type. During heating above T~300°C all constitutional water is released, and anhydrous Na2PtO3 remains as the solid residue.

CoO-Co2P composite nanosheets as highly active catalysts for sodium borohydride hydrolysis to generate hydrogen

2020 ◽  
Vol 13 (06) ◽  
pp. 2051025
Author(s):  
Hongyan Liu ◽  
Qianyu Shi ◽  
Yumei Yang ◽  
Ya-Na Yu ◽  
Yan Zhang ◽  
...  
Keyword(s):  
Sodium Borohydride ◽  
Hydrogen Generation ◽  
Sodium Hypophosphite ◽  
X Ray Diffraction ◽  
Water Displacement ◽  
X Ray ◽  
Highly Active ◽  
Naoh Solution ◽  
Adsorption Desorption ◽  
Hydrolysis Of

In this paper, CoO[Formula: see text]Co2P composite nanocatalysts as highly active catalysts were successfully prepared for catalytic hydrolysis of sodium borohydride (NaBH[Formula: see text] to generate hydrogen. For catalyst preparation, pre-synthesized Co(OH)2 nanosheets were uniformly mixed with sodium hypophosphite (NaH2PO[Formula: see text] and then treated through vapor-phase phosphorization process. For characterization, field-emission scanning electron microscopy (FE-SEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD), N2 adsorption–desorption measurement and X-ray photoelectric spectroscopy (XPS) were carried out, and traditional water-displacement method was performed to measure the hydrogen generation rate (HGR). It was found that component and catalytic activity of the composites were greatly affected by the ratio of Co(OH)2 to NaH2PO2. When the ratio was 2:1, the obtained catalyst composed of CoO and Co2P presented the highest HGR up to 3.94[Formula: see text]L min[Formula: see text] g[Formula: see text] using a 2[Formula: see text]wt.% NaBH[Formula: see text][Formula: see text]wt.% NaOH solution at [Formula: see text]C, and the apparent activation energy was detected as low as 27.4[Formula: see text]kJ mol[Formula: see text]. Additionally, the optimum CoO[Formula: see text]Co2P catalyst still retains 60% of the initial activity after recycling four times.

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