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18 protocols using mwcnts

1

Intracranial Electrophysiology in Insomnia Rats

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The surface modification of the sites was performed using 3,4-Ethylenedioxythiophene (EDOT) (Aladdin, Shanghai, China), polystyrene sulfonate (PSS) (HEROCHEM, Shanghai, China), and short multi-walled carbon nanotubes (MWCNTs) (XFNANO, Nanjing, China). Reference 600 (Gamry Instruments, Warminster, PA, USA) evaluated the MEA site impedance. P-chlorophenylalanine (PCPA) (Sigma–Aldrich, Shanghai, China) and phosphate-buffered saline (PBS) (Sigma–Aldrich, Shanghai, China) were used to induce insomnia in rats. R520IP (RWD Life Science, Shenzhen, China) was used to anesthetize the rats. KeyGEN BioTECH (Nanjing, China) provided cell membrane orange fluorescent dye (DiI). Brain slices were manufactured by leica1950 (Leica Biosystems, Deer Park, IL, USA). The brain slices were imaged by ZEISS Axio Observer (ZEISS, Jena, Germany). The 128-channel neural data recording system (Blackrock Microsystems, Tampa, FL, USA), micropositioner (model 2662, David KOPF instrument, Los Angeles, CA, USA), and a classic stereotaxic instrument for rats (Stoelting, Wood Dale, IL, USA) were used to capture intracranial electrophysiological signals in rats.
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2

Physico-chemical Characterization of Nanoparticles

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Al2O3 NPs, TiO2 NPs, SiO2 NPs, MWCNTs, BCs, and GOs were purchased from XFNANO Materials Tech Co., Ltd. (Nanjing, China), and graphenes were provided by Strem Chemicals, Inc (Newburyport, MA, USA). FeOx NPs were synthesized using iron (III) chloride hexahydrate (FeCl3·6H2O) according to a mechanochemical method with a few modifications (three times KCl addition) [14 (link)]. The urban particulate matter sample (SRM 1648a), obtained from the National Institute of Standards and Technology (NIST), was used as a standard for comparative toxicity evaluation between PM and NPs.
All particles were subjected to the same procedure for characterization. After dispersion in the culture medium by ultrasonication (5 min), number-weighted hydrodynamic diameters and zeta potentials were characterized by dynamic light scattering (DLS, Brookhaven NanoBrook 90Plus PALS, Holtsville, NY, USA) and zeta potential analyzer (Malvern, Zetasizer Nano ZS90, Worcestershire, UK), respectively. The shape, size, and agglomeration status of NP/PM samples were then determined using a field emission scanning electron microscope (FESEM, Hitachi SU8220, Tokyo, Japan).
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3

Synthesis of MWCNT Conductive Ink

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MWCNTs (diameter: 30–50 nm, length: <10 μm) and the MWCNTs conductive ink were purchased from Nanjing XFNANO Materials Tech. Co. Ltd and used without further purification. All the chemicals were purchased from Sinopharm Chemical Reagent Co. Ltd.
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4

MWCNT Surface Functionalization Protocol

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MWCNTs with average outer/inner diameters of 15 nm/8 nm and lengths of 50 μm were purchased from XF Nano, Ltd (Nanjing, CN). To improve the hydrophilicity of the nanotube substrate, the MWCNT surface was functionalized prior to MoS2 deposition. First, 100 mg of MWCNTs was sonicated in 500 mL of concentrated HNO3 solution (70% w/w) at a temperature of 60 °C for 1 h. After that, the MWCNT sample was washed with deionized (DI) water and dried at 60 °C in a vacuum oven for 6 h.
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5

Analytical Standards Preparation and Characterization

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Standards of chlorantraniliprole, bromoantraniliprole, flubendiamide, tetrachlorantraniliprole, cyclaniliprole, flonicamid, cyantraniliprole and tolfenpyrad were bought from Tianjin Alta Scientific Ltd. (Tianjin, China), and all those compounds were dissolved in methanol to 100 µg/mL. Methanol and acetonitrile of HPLC grade were obtained from Merck KGaA. (Darmstadt, Germany). Highly purified water was prepared by a Milli-Q water purification system (Bedford, MA). Ammonium formate (≥ 99.995%) was purchased from MilliporeSigma Company (St Louis, MO). Analytical reagent grade including anhydrous sodium chloride (NaCl) and magnesium sulfate (MgSO4) were obtained from Sinopharm Chemical Reagent (Beijing, China). MWCNTs (10–30 µm length, 10–20 nm diameter) were provided by Nanjing XFNANO Materials Tech Co., Ltd. (Nanjing, China). PSA with diameter of 50 μm were bought from Dikma Technologies Inc. (Beijing, China).
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6

Sensitive Pesticide Detection Assay

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CdSe QDs were purchased from BEIDA JUBANG Science & Technology Co., Ltd. (Beijing, China). The MWCNTs were supplied by XFNANO Materials Tech Co., Ltd. (Nanjing, China). Nafion (≥98.0%) was obtained from Sigma–Aldrich Trading Co., Ltd. (Shanghai, China). CYF, bifenthrin (BIF), deltamethrin (DEL), cypermethrin (CYP), and fenvalerate (FEN) were obtained from the Shanghai Pesticide Research Institute Co., Ltd. (Shanghai, China). 3-Aminopropyl-triethoxysilane (APTES), tetraethoxysilane (TEOS) and Triton X-100 were purchased from Sigma–Aldrich (Steinheim, Germany). H2O2 (AR, 30 wt. % in H2O) was obtained from Aladdin (Shanghai, China). All other reagents were of analytical grade and used with ultrapure water (resistivity ≥ 18.25 Ω).
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7

Fabrication of Cathode Materials

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Lead oxide (PbO) powder (oxidation degree = 72%) and vanisperse A were provided by Zhaoqing Leoch Battery Technology Co. Ltd. (Zhaoqing, China). Vulcan carbon XC-72R (VC-72) was purchased from Cabot Co. Ltd. (Shanghai, China). MWCNTs were purchased from Nanjing XFNANO Materials Tech Co. Ltd. (Nanjing, China). Barium sulfate (BaSO4) and sulfuric acid (H2SO4, 98%) were procured from Sinopharm Chemical Reagent Co. Ltd. (Shanghai, China). Unless otherwise specified, reagents were used as received without further purification. Ultrapure water is adopted as water source if necessary in all experiments.
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8

Synthesis of Reinforced Epoxy Composites

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MWCNTs with a diameter of 20–30 nm and a purity of more than 95% were provided by Nanjing XFNANO Materials Tech Co., Ltd, China. Graphite powder (4000 mesh) was supplied by Shanghai Aladdin Reagent Co., Ltd, China. The epoxy resin used in this study was a bisphenol A epoxy resin (WSR618) with an epoxy equivalent of 185–192 g eq−1 from Bluestar Wuxi Petrochemical Co., Ltd, China. The curing agents were QS-1622 supplied by Beijing Qingda-QS Materials Co., Ltd, China, which was modified aromatic amine. The mixing ratio of QS-1622 and WSR618 used in this study was 1 : 2.
Sodium nitrate, potassium permanganate, sulfuric acid, hydrogen peroxide, hydrochloric acid, triphenyl phosphine (TPP), tetrahydrofuran (THF), N,N-dimethylformamide ethanol (DMF) and ethanol were supplied by Shanghai Aladdin Reagent Co., Ltd, China, and used without further purification.
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9

Characterization of Multiwalled Carbon Nanotubes

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MWCNTs with > 95% purity were purchased from XFNANO Materials Tech Co. Ltd (Nanjing, Jiangsu, China). MWCNTs were dissolved in 1% DMSO and MWCNTs suspension was prepared by sonication machine. The ultraviolet (UV) visible spectra of MWCNTs was measured by UV visible light absorption spectroscopy (Biochrom, Cambridge, UK). The morphology of MWCNTs was observed by transmission electron microscopy (TEM; HT7700; Hitachi, Japan).
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10

Fabrication of Flexible Conductive PU Composite

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Thermoplastic PU (Elastollan 1185A) was purchased from BASF Company, Germany. The MWCNTs were purchased from XFNANO Materials Tech Co., Ltd., China. Sodium dodecyl benzene sulfonate (SDBS, 99.5%, AR) and N,N-dimethylformamide (DMF, 99.5%, AR) were purchased from Sigma Aldrich, United States. Ethanol (99.5%, AR), acetone (99.5%, AR), isopropyl alcohol (IPA, 99.5%, AR), ferric chloride (FeCl3, 98%) and ethyl dioxythiophene (EDOT, 99%) were purchased from Aladdin Biochemical Technology Co., LTD, China. PU adhesive was purchased from Hongsheng Medical Technology Co., LTD, China. The interdigital electrodes were commercially customized by Shenya Precision Circuit Company.
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