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37 protocols using pc 420d

1

Synthesis of High Molecular Weight Polyphosphazene

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Example 6

High molecular weight polyphosphazene was prepared via crosslinking allyl phenoxyphosphazene (SPV-100) (SPV-100 from Otsuka Chemical Co., 11.4% P, viscous liquid at room temperature) with 7-8% methylhydrosiloxane-dimethylsiloxane copolymer (HMS-082, Mn=5000-7000 g/mol, viscosity=110-150 cSt, Gelest Inc) under the influence of catalyst platinum carbonyl complex (1.85-2.1% platinum concentration).

3.0065 g SPV-100, 0.4928 g HMS-082 and 0.0034 g platinum carbonyl complex (1.85-2.1% platinum concentration) were mixed in a Fisherbrand Aluminum Weighing Dish (40 ml) and heated on a 250° C. Corning® PC-420D stirring hot plate with manual physical stirring. The white mixture increase viscosity significantly in 1 minute. The reaction was stopped after 15 minutes. The product is a white solid.

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Synthesis of High Molecular Weight Polyphosphazene

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Example 11

High molecular weight polyphosphazene was prepared via crosslinking allyl phenoxyphosphazene (SPV-100) (SPV-100 from Otsuka Chemical Co., 11.4% P, viscous liquid at room temperature) with poly(methylhydrosiloxane) (DF 1040, viscosity=15-40 cSt, Gelest GE Bayer Silicone) under the influence of catalyst platinum carbonyl complex (1.85-2.1% platinum concentration).

2.9241 g SPV-100, 0.4807 g DF 1040 and 0.0053 g platinum carbonyl complex (1.85-2.1% platinum concentration) were mixed in a Fisherbrand Aluminum Weighing Dish (40 ml) and heated on a 250° C. Corning® PC-420D stirring hot plate with manual physical stirring. The white mixture increase viscosity significantly in 1 minute, and then started to form gel and solid. The reaction was stopped after 5 minutes. The product is a rubbery white solid.

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3

Headspace GC-MS Analysis of Volatile Compounds

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Volatile compounds were analyzed as described by Piao et al [26 (link)]. Briefly, LT samples were grilled on a hot plate (PC-420D; Corning, NY, USA) until they reached an internal temperature of 72°C and transferred to glass vials (N9306078; PerkinElmer, Boston, MA, USA). The vials were placed in the oven of a headspace sampler, and extraction of the volatile compounds of the samples was performed using a headspace auto-sampler. The transfer line from the headspace sampler was directly connected to the injector for the gas chromatograph (GC). A Perkin Elmer 680 gas chromatograph equipped with a 600T mass spectrometry detector was used to analyze the volatile compounds. The compounds were separated using an HP-PLOT Q column (Agilent, Wilmington, DE, USA; 30 m×0.53 mm×0.25-μm film thickness). The resolved mass spectrometry spectra obtained from custom scripts were matched against reference mass spectra using the National Institute of Standards and Technology (NIST) mass spectral search program and the NIST/US Environmental Protection Agency (EPA)/National Institutes of Health (NIH) mass spectral library (ver. 2.0). A GC chromatogram was used to quantify the volatile compounds, and mass spectrometry was used to identify the volatile compounds. Results of the analyses are expressed as percentages of the total chromatographic area.
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Synthesis and Characterization of SPAs

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SB (1.0 g), PA (6.0 or 8.0 g), and anhydrous Py (15 mL) were added to a 100 mL round-bottomed flask to give a solid-to-liquid ratio of 1:15 (w/v). A reflux condenser with a drying tube filled with anhydrous calcium chloride was attached to the flask. The suspensions were heated at 100 • C in an oil bath placed on a heating plate (Corning ® , model PC-420D) under constant magnetic stirring at 300 rpm. The reaction times studied for 6.0 g of PA were 3 and 6 h and for 8.0 g they were 1, 3, 6, 12, 18, and 24 h. The purification and characterization of the SPAs followed the procedures described in Section 2.2.1.
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5

Preparation of PVA Solution for Liquid Ejection

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The solution was prepared
following the protocol described in our previous publications.33 (link),37 (link),38 (link),40 (link) Briefly, a 6 wt % PVA solution in a water/ethanol mixture (water
mass fraction, χw = 0.35) was prepared by adding
a weighted mass of polymer powder to the solvent followed by stirring
using a hot plate (Corning PC-420D) until a transparent solution was
obtained. The stirring was carried out in a water bath by applying
mild heating to facilitate mixing. Other relevant parameters of the
polymer solution are surface tension, σ, and density, ρl, which in this case are 0.0324 N/m and 885.3 kg/m3, respectively. The solution was allowed to cool to room temperature
before liquid ejection experiments.
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6

Synthesis and Characterization of Chitosan Nanoparticles

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Blank CSNPs were prepared by adding 1 mL of a 1% sodium tripolyphosphate solution dropwise to a chitosan solution under constant stirring over 3–4 hours. The blank nanoparticles were designated as BNP. Prior to any testing, the CSNP-containing solution was stirred with a magnetic stirrer (Corning PC-420D, Seoul, South Korea) for 15 min at room temperature to ensure the homogenous dispersion of nanoparticles. The drops of nanoparticles spread uniformly on the glass slide and were left to dry [27 (link)]. The dried nanoparticles were inspected with a scanning electron microscope (JEOL JSM-6390 LA, Tokyo, Japan) at a resolution of 10kV and 5,000–50,000 x.
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7

Encapsulation of Probiotic Lactobacillus rhamnosus

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The preparation of the encapsulating matrix and the encapsulation process was carried out following the methodology of Ding and Shah [17] (link) with modifications in the amount of vegetable oil added to the mixture, the rpm used in the homogenization, and the dosage of the alginate in the calcium chloride solution. The encapsulating alginate matrix (Sigma-Aldrich ® , St Louis, MO, USA) (ALG) consisted of 25 mL of bacterial suspension with a concentration greater than 1 × 10 10 CFU/mL of Lacticaseibacillus rhamnosus GG in combination with 100 mL of 3% sodium alginate (w/v). Subsequently, 1 mL of Tween ® 80 (Sigma-Aldrich ® , St Louis, MO, USA) and 100 mL of vegetable oil (Selecto BRAND ® , Xalapa, Mexico) were added. The pretreatments to which the mixture was subjected were ultra-turrax homogenizer (UT) (model T-25 digital Ultraturrax ® , IKA, Staufen, Germany) set at 4000 rpm for 7.5 min and magnetic stirring (Corning PC-420D, NY) (AM) at 1150 rpm for 10 min. The emulsified mixture was dispersed in a 0.1 M calcium chloride solution by dripping at 15 cm of the solution with a flow of 2.5 mL/min with the help of a peristaltic pump (Ecoshell ® RD100-01, Pharr, TX, USA) with YZ1515 head and silicone hose #19 (Qilipump, Hebei, China). Once the capsules were formed, they were stored at 4 • C for 12 h before being used for further analysis [17] (link)[18] (link)[19] (link).
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8

Facile Growth of CuO Nanowires

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A copper foil was cut into 1 cm2 square substrates. First, the Cu substrates were cleaned with dilute HCl to remove the surface oxide layer and adsorbed impurities. Then, the Cu substrates were cleaned with acetone, de-ionized water, and ethanol in an ultrasonic bath for 10 min and dried in the air. The thermal oxidation method can be used to directly grow CuO nanowires on the Cu foil with a facile hotplate (Corning, PC-420D, Corning, New York, NY, USA). The reaction temperatures are 550 °C for 6 h under ambient conditions.
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9

Thermal Injury Wound Creation in Pigs

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To create full-thickness wounds, 1 × 1 in stainless steel blocks were placed onto pig skin to create a thermal injury. Two different burn devices were utilized. The first was a standard burn stylus consisting of a stainless steel block (1 in.3) connected to a metal rod and handle (Fig. 1A), which can be heated using a hot water bath or using a hot plate. A hot plate (Corning PC-420D, Tewksbury, MA) was used in this study to heat the block to 200 °C (Fig. 1A). The second device was a custom burner fabricated in house that consisted of a stainless steel block (2.5 cm3) connected to a metal stylus, an electronic microstat (JUMO GmbH and Co. KG, Fulda, Germany) and electronic scale (Guangzhou WeiHeng Electronics Co. Ltd., Guangdong, China) (Fig. 1B). The custom burn device was electronically heated internally, and the electronic scale allowed for precise measurements of pressure applied to the skin surface. The housing surrounding the heating element and pressure gauge was constructed from aluminum to keep the added weight to a minimum (custom unit was 2.5 lbs heavier than the commercial unit). The housing unit can be handled without the use of thermally insulated gloves during operation.
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10

Crosslinked Polyphosphazene Synthesis

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Example 7

High molecular weight polyphosphazene was prepared via crosslinking allyl phenoxyphosphazene (SPV-100) (SPV-100 from Otsuka Chemical Co., 11.4% P, viscous liquid at room temperature) with 7-8% methylhydrosiloxane-dimethylsiloxane copolymer (HMS-082, Mn=5000-7000 g/mol, viscosity=110-150 cSt, Gelest Inc) under the influence of catalyst platinum carbonyl complex (1.85-2.1% platinum concentration).

3.1274 g SPV-100, 3.1240 g HMS-082 and 0.0067 g platinum carbonyl complex (1.85-2.1% platinum concentration) were mixed in a Fisherbrand Aluminum Weighing Dish (40 ml) and heated on a 250° C. Corning® PC-420D stirring hot plate with manual physical stirring. The white mixture increase viscosity significantly in 1 minute, and then started to form gel and solid. The reaction was stopped after 15 minutes. The product is a rubbery white solid. It does not burn and drip.

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