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7 protocols using direct q 5 uv water purification system

1

Amphiphilic Copolymer Synthesis and Characterization

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The MPM-GDM amphiphilic random copolymer was provided by NOF Co. The chemical structure of MPM-GDM is shown in Fig. 1. The average molecular weight of the copolymer sample used in this study was 6.35×10 4 , and the polydispersity index was 2.5. The weight ratio of the hydrophilic PEG unit to the hydrophobic diisostearyl unit was set at 7:3. Squalane was purchased from Nikko chemicals Co. The water used in this study was deionized using a reverse osmosis membrane equipped in a Millipore Direct-Q UV 5 water purification system.
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2

Amphiphilic Copolymer Solvent Compatibility

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The amphiphilic random copolymer MPM-GDM was provided by NOF Co. The chemical structure of MPM-GDM is shown in Fig. 1. The average molecular weight of the copolymer sample was 6.35×10 4 , while the weight ratio between the hydrophilic PEG and hydrophobic diisostearyl units was set at 7:3. Xanthan gum was purchased from DSP Gokyo Food & Chemical Co. methanol, ethanol, and 2-propanol were purchased from Wako Pure Chemical Industries, Ltd. 1,3-Butylene glycol (1,3-BG) was purchased from Daicel Co. 1,4-Butylene glycol (1,4-BG) and ethylene glycol were acquired from Tokyo Chemical Industry Co. Glycerin was purchased from Emery Oleochemicals. The water used in this study was deionized using a Millipore Direct-Q UV 5 water purification system equipped with a reverse osmosis membrane.
2.2 Preparation of mixtures 2.2.1 Two/three-component mixtures MPM-GDM and each solvent (water, methanol, ethanol, 2-propanol, 1-butanol, ethylene glycol, 1,3-BG, 1,4-BG, and glycerin) were mixed in a glass test tube using a vortex mixer for several seconds. Spatula mixing was also employed for highly viscous samples. Then, the mixtures were allowed to stand for 2-7 days at 40℃, and finally cooled to room temperature.
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3

Fabrication of PCB Electrodes for Electrochemical Sensors

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Hydrogen peroxide, ammonium hydroxide, potassium hydroxide, potassium ferrocyanide and ferricyanide, phosphate-buffered saline tablets, potassium chloride, and copper etchant (CE-100) were purchased from Sigma-Aldrich (Gillingham, UK), while 1 M sulphuric acid was purchased from Thermo Fisher Scientific (Loughborough, UK). The Ag/AgCl (KCl) reference electrode was purchased from BASi (West Lafayette, IN, USA) and the platinum wire used as the counter-electrode was obtained from ALS (Tokyo, Japan). Milli-Q water was obtained using the Millipore Direct-Q 5 UV Water Purification System and deionised (DI) water. Oxygen plasma Zepto System (Diener electronic, Ebhausen, Germany) was used to perform PCB plasma cleaning.
PCBs were designed using Altium Designer 18 software and fabricated by Lyncolec (Dorset, UK). In short, 1.6 mm FR-4 covered with 1 oz copper was patterned and plated with hard gold by electrodeposition of nickel (3–5 µm) and gold (1 µm) and outlined by the solder mask to make PCB electrodes with 1 mm diameter. PCB boards used in the study are shown in Figure S1. Pictures were taken using a Huawei P10 smartphone.
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4

Microwave-assisted Synthesis of Metal Complexes

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O-salicylaldehyde; 3-amino pyridine; ethanol; nitrate salts of Al(III), Ba(II), Cd(II), Co(II), Cu(II), Fe(III), Mn(II), Ni(II), and Zn(II), and sulfate salt of Fe(II) were all purchased from Sigma-Aldrich (Steinheim, Germany) and dissolved in ultrapure water (Direct-Q 5 UV water purification system, Millipore, Burlington, MA, USA). The microwave reactions were carried out in a Biotage Initiator system (Biotage, Sweden), the temperature and time were preset as required, and the pressure was monitored and indicated. The identity of the products was determined by FTIR and NMR. FTIR analysis was performed on a Spectrum BX FTIR spectrometer (PerkinElmer, Waltham, MA, USA). The 1H- and 13C-NMR spectra were recorded on a JNM-ECZR series 600 MHz spectrometer (JEOL, Tokyo, Japan) operating at 600 and 100 MHz, respectively, using DMSO-d6 as a solvent. The NMR is equipped with a Delta™ NMR data processing software. UV–VIS spectra were carried out using an Agilent 8453 spectrophotometer (Agilent, Santa Clara, CA, USA) in a 1.0 cm quartz cuvette. Fluorescence studies were performed on a PerkinElmer LS 45 Fluorescence spectrometer (PerkinElmer, Waltham, MA, USA) using a 1.0 cm quartz cuvette with a scan speed of 700 nm min−1, and an excitation and emission slit of 10 nm each.
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5

Electrochemical CO2 Reduction Protocol

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AgNO3 (99.8%) and NaOH (99%) were purchased from Aladdin Industrial Co. Ltd. Cs2CO3 (99.9%), isopropyl alcohol (≥99.5%) and ethanol (HPLC, ≥99.8%) were purchased from Macklin Biochemical Co. Ltd. Sodium citrate anhydrous (99%) was purchased from J&K Scientific Ltd. L (+) − Ascorbic acid (≥99.7%) was purchased from Tianjin Kemiou Chemical Reagent Co. Ltd. All chemical reagents were utilized without further purification. Commercially available carbon-based GDLs (AvCarb GDS3250) were purchased from Xima Laya Photo-Electric Technology Co. Ltd., China. PiperION-A5-HCO3 anion exchange resin, Fumion FAA anion exchange resin, PiperION-A15-HCO3 and FAA-3-50 were purchased from SCI Materials Hub. CO2, N2, Ar and H2 were all purchased from Air Liquide (≥99.999%). The ultrapure water (18.25 MΩ·cm) was supplied by a Millipore Direct-Q5 UV water purification system.
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6

Synthesis of N-Methyl-D-glucamine Calixarenes

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N-Methyl-d-glucaminemethylcalix[4]resorcinarenes were synthesized in two steps starting from calix[4]resorcinarenes with sulfonate and methyl groups on the lower rim obtained by a published method [20 (link),21 (link)]. N-Methyl-d-glucamine (99%, Acros Organics, Fair Lawn, NJ, USA) and 1-phenylazo-2-naphthol (Sudan I, Acros Organics) were used as received. Sample solutions were prepared in the deionized water (18.2 MΩ) obtained from a Direct-Q 5 UV water purification system (Millipore, Molsheim, France). The accurate pH was measured with a HI 2110 pH meter (Hanna Instruments, Woonsocket, RI, USA) calibrated using buffers according to the manufacturer’s instructions.
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7

Sophorolipid and β-Glucan Extraction Protocol

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Commercially available sophorolipids (Sopholiance ® S) were obtained from Givaudan (France) . This sample was a mixture of methyl ester, acidic, and lactonic forms, which were estimated to be present in equal proportions. β-(1→3,1→6) -Glucan was purchased from Tokyo Chemical Industry Co., Ltd. (Japan) . Typical chemical structures of sophorolipids and β-glucan are shown in Fig. 1. The samples were used without further purification. Dimethyl sulfoxide (DMSO) and sodium hydroxide solutions were purchased from Fujifilm Wako Chemical Co. (Japan) . The water used in this study was purified using the Millipore Direct-Q 5UV water purification system.
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