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Chloroform

Manufactured by Agilent Technologies
Sourced in United States

Chloroform is a colorless, dense liquid commonly used as a solvent in various laboratory applications. It has a high boiling point and is miscible with a wide range of organic solvents. Chloroform is often employed in extraction and purification processes in analytical chemistry and organic synthesis.

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4 protocols using chloroform

1

Quantification of Fecal Phenols and Indoles

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After centrifuging the fecal and slurry samples at 3134× g for 20 min at 20 °C, 4 mL of supernatant was collected. The supernatant was placed in a 20-mL glass vial, and then 4 mL of chloroform (Merck, Darmstadt, Germany) and 60 μL of 4 M sodium hydroxide solution (Sigma-Aldrich, St. Louis, MO, USA) were also added to the glass vial and mixed with supernatant. The mixture in the glass vial was centrifuged at 3134× g for 20 min at 20 °C, and the chloroform layer was collected and placed into a 2.0-mL gas chromatography vial (Agilent, Santa Clara, CA, USA). Phenols and indoles in the chloroform layer were determined using a gas chromatograph (6890N, Agilent, Santa Clara, CA, USA) that was equipped with a DB-1 column (30 m × 0.25 mm × 0.25 μm, Agilent, Santa Clara, CA, USA) and a flame ionization detector. A sample of 2.0 μL was injected at a 5-to-1 split ratio. The gas chromatography oven was initially set at 40 °C for 5 min, increased to 230 °C at a rate of 10 °C per min, and finally held at 230 °C for 2 min. The injection and detection ports of gas chromatography were maintained at 250 °C.
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2

Characterization of PLA and PHB Polymers

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PLA granulate was supplied from Fillamentum Manufacturing Czech s.r.o., Hulín, Czech Republic. Measured polymer parameters were as follows: number-average molecular weight (Mn), 123,500 g/mol; weight-average molecular weight (MW), 235,300 g/mol; dispersity, 1.90. PHB powder was acquired from NAFIGATE Corporation a.s., Prague, Czech Republic. Measured polymer parameters were as follows: number-average molecular weight (Mn), 85,040 g/mol; weight-average molecular weight (MW), 211,400 g/mol; dispersity, 2.49. All measurements of polymer properties were measured via GPC (Agilent 1100, Santa Clara, CA, USA) in chloroform (CHCl3) and the analysis parameters were as follows: mobile phase flow 1 mL/min; column temperature 30 °C, used column: PLgel 5 μm MIXED-C (300 × 7.5 mm). Aliphatic alcohols for depolymerization (methanol 99%, ethanol 99%) were supplied by Honeywell Research Chemicals, Charlotte, NC, USA (used alcohols were not claimed either synthetic or bio-source by the supplier). The catalyst for alcoholyses (p-toluensulphonic acid monohydrate), methacrylic anhydride (94%), potassium hydroxide (p.a.), d-chloroform (CDCl3; 99.8%), and 2-ethylhexanoic acid (for synthesis) were all acquired from Sigma-Aldrich, Prague, Czech Republic.
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3

GC Analysis of Phenols and Indoles in Slurry Samples

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Slurry samples were centrifuged at 4,000 rpm for 20 min at 20°C. The 4 mL of supernatant was mixed with 4 mL of chloroform (Merck, Darmstadt, Germany) and 60 μL of 4 M sodium hydroxide (Sigma-aldrich, USA) solution in 20 mL glass vial. The mixed solution was centrifuged at 4,000 rpm for 20 min at 20°C, and chloroform layer was transferred to 2.0 mL GC vial (Agilent, USA). Phenols and indoles were analyzed using a GC (6890N, Agilent, USA) equipped with DB-1 column (30 m×0.25 mm×0.25 μm, Agilent, USA) and FID. The oven temperature was programmed to initial temperature of 40°C for 5 min, increasing to 230°C at a rate of 10°C/min, and holding at 230°C for 2 min. The injection and detection ports were maintained at 250°C. The sample injection volume was 2.0 μL with a 5:1 split ratio.
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4

Extraction and Analysis of Phenols and Indoles

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Slurry samples were centrifuged at 3,134 × ɡ for 20 min at 20°C, and then 4 mL of supernatant was mixed with 4 mL of chloroform (Merck, Darmstadt, Germany) and 60 μL of 4M sodium hydroxide solution (Sigma-Aldrich, St. Louis, MO, USA) in a 20 mL glass vial. The mixture was centrifuged at 3,134 × ɡ for 20 min at 20°C, and the chloroform layer was transferred to a 2.0 mL GC vial (Agilent, Santa Clara, CA, USA). Phenols and indoles were analyzed using a GC (6890N, Agilent, Santa Clara, CA, USA) equipped with a DB-1 column (30 m × 0.25 mm × 0.25 μm, Agilent, Santa Clara, CA, USA) and a FID. The sample injection volume was 2.0 μL with a 5:1 split ratio. The oven temperature was initially 40°C for 5 min, increasing to 230°C at 10°C/min, which was then held at 230°C for 2 min. The injection and detection ports were maintained at 250°C.
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