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11 protocols using orion star a111 benchtop ph meter

1

Generating Plasma-Activated Water (PAW)

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The schematic diagram for generating PAW from cold atmospheric pressure plasma (CAPP) is shown in Figure 1. CAPP equipment consisted of an Openair Plasmajet technology (Plasma Treat Inc., IL), where the plasma was released through a rotating nozzle (RD1004) into a discharge chamber. The plasma generator (FG5001) was operated at an air pressure of 1990 mBar, at 295 V, and a frequency of 22.5 kHz. Dry, filtered air was used as feed gas in the production of plasma.

Schematic of PAW generation and PAW egg washing.

Figure 1
Sterilized DW (300 mL) in a 1,000 mL sterile glass beaker was exposed to the plasma jet for 5 min to generate PAW. The distance between the plasma nozzle and the water surface was maintained at 7.7 cm to avoid excessive heating of the water. The final temperature of PAW was ∼50°C, and it was allowed to cool to room temperature. The pH of PAW was measured to be 2.95 ± 0.02 while the oxidation-reduction potential (ORP) was 575.8 RmV. Both the pH and the ORP values were measured using Orion Star A111 pH Benchtop Meter (Thermo Fisher Scientific, Waltham, MA) equipped with Orion 9157BNMD Triode 3-in-1 pH/ATC Probe (Thermo Fisher Scientific, Waltham, MA) and 9678BNWP Orion Metallic Combination Electrode (Redox/ORP model with Epoxy body) probe.
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2

Peptide Self-Assembly and Disassembly

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To eliminate the preformed peptide seeds during the purification, concentration and drying process, the peptide powder was pre-treated with HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) on ice for 1 h, followed by the evaporation of HFIP in the fume hood to generate peptide film. For peptide self-assembly, the treated peptide film was dissolved in ddH2O and the pH was adjusted with buffer of different pHs (acidic acetate buffer of pH 5.0, neutral HEPES buffer of pH 7.4 and CHES basic buffer of pH 9.5).
The nanofibril disassembly was carried out by the pH adjustment of the mature peptide nanofibrils from pH 9.5 to pH 5.0 with the addition of 1 M HCl. The mature peptide assemblies was prepared under basic pH (pH 9.5) and incubated at room temperature for two weeks. The pH adjustment was preformed by the addition of 1 M HCl and the sample pH was measured with micro pH probe (Orion™ 9810BN Micro pH Electrode. Thermo Fisher Scientific Inc.), connected to a pH meter (Orion Star™ A111 pH Benchtop Meter, Thermo Fisher Scientific Inc.).
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3

Acetaminophen Impacts on Calf Abomasal Health

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Calf BW was measured on arrival and on d 9. Acetaminophen (50 mg/kg; 4-acetamidophenol; ACROS Organics) was mixed into each OES on d 9 to indirectly assess AER. Jugular venous blood samples (6 mL potassium-citrate, Vacutainer, Becton, Dickinson and Company) were collected -0.5, 0, 1, 2, 3, 4, 6, and 8 h relative to the OES administration at 0700 h. Following centrifugation (1,500 × g for 15 min at 23°C), plasma was isolated and stored at -80°C for later analyses. Aseptic abomasal fluid sampling occurred at -0.5, 0, 1, 2, 4, and 6 h after OES supplementation. Volume and pH (Orion Star A111 pH Benchtop Meter, Thermo-Fisher Scientific) were measured immediately following collection. A sample from 6 h post-OES supplementation was immediately stored at -80°C for subsequent analysis of bacterial communities.
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4

pH Measurement of Extracts

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The pH of extracts was assessed using an Orion Star A111 Benchtop pH Meter (ThermoFisher Scientific) under room temperature conditions (20 °C).
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5

Grape Juice pH Measurement

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The pH value of grape juices was measured at room temperature using a pH meter (Thermo Scientific Orion Star A111 Benchtop pH Meter, USA).
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6

Characterization of Surface Properties

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Surface tension, interfacial
tension and contact angle were characterized using a standard pendant
drop method on commercial tensiometer, Biolin Scientific, Theta Flex.
Optical power was measured by using optical power meter (Newport,
843-R) connected with a thermopile Sensor (Newport 919P-003–10,
3 W, 10 mm, 0.19–11 μm). Optical images and videos were
taken by a Canon EOS 80D camera. IR images were recorded by a high-performance
Telops M3K infrared camera. UV–Vis absorption spectra were
recorded on an Agilent 8453 UV–Vis spectrometer from 200 to
1200 nm wavelengths. 1H and 13C NMR spectra
were recorded on a Bruker 500 MHz NMR spectrometer. The pH of the
solutions was measured by using a Thermo Scientific Orion StarA111
Benchtop pH Meter. The scanning electron microscope (SEM) image was
obtained from a FEI Sirion SEM.
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7

Analytical Methods for Water Quality

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Dissolved organic carbon (DOC) was measured based on Standard Method 5310 D using an O-I Corporation Model 1010 Analytical TOC Analyzer (College Station, TX, USA) equipped with a Model 1051 Vial Multi-Sampler [44 ]. Ultraviolet absorbance at 254 nm (UV254) was measured using an Agilent 8453 UV–VIS spectrophotometer (Agilent Technologies, Mississauga, ON, Canada) with a 1 cm quartz cuvette (Hewlett Packard, Mississauga, ON, Canada). pH was measured using an Orion Star A111 Benchtop pH Meter (Thermo Scientific, Mississauga, ON, Canada). Turbidity was measured using a HACH 2100N Turbidimeter (Loveland, CO, USA). Temperature was recorded at 10-min intervals during in situ trials using an OM-EL-USB-TP-LCD temperature probe data logger (Omega Engineering, Stamford, CT, USA). All parameters mentioned above, except water temperatures, were measured in triplicate.
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8

Phosphate Buffer Preparation and Modification

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The phosphate buffer of pH 8 was prepared by dissolving 0.19 M MOH (M+ = K+, Na+, Cs+, TMA+, TEA+) and 0.1 M H3PO4 in Milli-Q water and titrated with MOH or H3PO4 to achieve pH of 8 measured with an Orion Star™ A111 Benchtop pH Meter (Thermo Fisher Scientific). For electrolyte containing Li+, lithium carbonate buffer solution was used due to the low solubility of lithium phosphate. Lithium carbonate buffer was prepared by dissolving 0.19 M LiOH in Milli-Q water and purging with CO2 to achieve pH of 8. For the experiments with crown ether, 18-Crown-6 was directly added to the potassium phosphate electrolyte with a pre-determined molar ratio of 18-Crown-6 to K+.
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9

Measuring Testicular Fluid Osmolality and pH

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Osmolality of testicular fluid (n = 5 males) was determined in triplicate for each sample using a Vapor Pressure Osmometer (Model 5600 Wescor, Inc, Logan, Utah, USA). The pH of testicular fluid (n = 5 males) was measured using a benchtop pH meter (Orion Star™ A111 Benchtop pH Meter, Thermo Fischer Scientific, Madison, WI, USA) and an electrode (Orion™ PerpHecT™ ROSS™ Combination pH Micro Electrode, Thermo Fischer Scientific, Madison, WI, USA). Osmolality and pH were also measured for all activation media.
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10

Purification of Hydroxide Electrolytes

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Lithium hydroxide monohydrate (99.995% metals basis) was purchased from Alfa Aesar. Sodium hydroxide (semiconductor grade, 99.99% trace metals basis) was purchased from Sigma-Aldrich. Potassium hydroxide (semiconductor grade, 99.99% trace metals basis) was purchased from Sigma-Aldrich. Rubidium hydroxide hydrate (15 to 20% H2O, 99% metals basis) was purchased from Alfa Aesar. Cesium hydroxide monohydrate (99.95% trace metals basis) was purchased from Sigma-Aldrich. The electrolytes used for all reactivity studies were purified with Chelex resin (Sigma-Aldrich, Chelex 100 sodium form). To further remove the trace metal contamination in 0.1 M RbOH, preelectrolysis of the electrolyte in an Ar atmosphere was carried out for 2 hours using electropolished Cu foil electrodes at a constant current density of −5 mA cm−2. The electrolyte pH, which was detected using the Orion Star A111 Benchtop pH Meter (Thermo Fisher Scientific), showed no significant change after the electrolysis.
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