Carbon nanotube aging process and spectroscopic characterization

BT Brittany Twibell
KS Kalie Somerville
GM Geoffrey Manani
MD Molly Duszynski
AW Adam Wanekaya
PS Paul Schweiger
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To simulate environmental weathering, pristine CNTRENE material was aged as supplied in distilled water in a QUV Accelerated Weathering chamber (Q-Lab Corp, Cleveland, OH, USA) as previously described (Woodman et al., 2016). Briefly, 14 mL pristine CNTRENE material was exposed to 3–4 h alternating ultraviolet and condensation cycles for 12 days. The UV cycle and condensation cycle temperatures were 68 ± 0.5 °C and 47 ± 0.5 °C, respectively. The current of the lamps were 0.5–0.6 amperes and the condensation cooling fan set point was 15. Distilled water was used to provide moisture and served as temperature control bath. The Raman, FTIR, and UV-vis spectra of both pristine and aged CNT material were quantified after sonication for one minute to disperse the CNTs. For Raman spectroscopy, 2–10 µL of the sample was dropped onto an aluminum foil wrapped around a microscope glass slide. The sample was air-dried in a clean environment free from any dust or other contaminants. A Horiba LabRAM HR800 spectrometer equipped with a 50 mW 532 nm excitation laser with a detection capability in the range of 200 to 4,000 nm was used for Raman Photoluminescence spectroscopy at ambient temperature. For FTIR spectroscopy, 20 µL of the CNTs were put into separate pre-cleaned dry mortars preheated at 80 °C. The sample was dried on the mortar and approximately 400 µg of dry potassium bromide was added and ground into fine powder to make a KBr pellet. The pellet was used for IR measurements using a Bruker IR spectrophotometer. The background data was obtained using a KBr pellet without CNTs. For UV-Vis analysis, CNTs were diluted 10-fold with deionized water and spectra taken with a PerkinElmer Lambda 650 UV-Vis spectrometer at room temperature.

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