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Carbon suspension cement

Manufactured by SPI Supplies
Sourced in United States, United Kingdom

Carbon suspension cement is a specialized laboratory product used for suspending and dispersing carbon particles in various liquid media. It serves as a binding agent, facilitating the creation of stable carbon suspensions for analytical, research, or industrial applications.

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2 protocols using carbon suspension cement

1

Morphological Characterization of PLA Blends

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SEM was used to investigate the morphology of the samples. Bar specimens of PLA-c, PLA-g-TPCS, PLA-GRH, and PLA-g-TPCS-GRH blends were produced by compression molding using pellets from the twin-screw extruder. Bars of PLA-g-TPCS and PLA-g-TPCS-GRH were immersed in liquid nitrogen for ~3 min, then fractured by hand, treated with hydrochloric acid (6 N) for 6 h to remove the TPCS phase, and air dried for 12 h in a fume hood [17 (link)]. Finally, the samples were mounted on aluminum stubs using carbon suspension cement (SPI Supplies, West Chester, PA, USA). Samples of films evaluated before and after tensile testing were also mounted on aluminum stubs with high vacuum carbon tabs (SPI Supplies) and coated with iridium at a thickness of ~2.7 nm. Samples were examined in a JEOL 6610LV (tungsten hairpin emitter) and a JEOL 7500F (field emission emitter) scanning electron microscope (JEOL Ltd., Tokyo, Japan) at various magnifications at 10 and 3.0 kV, respectively.
AFM was conducted using a Cypher™ atomic force microscope (Oxford Instruments Asylum Research, Inc., Santa Barbara, CA, USA) in the contact mode. Roughness parameters, calculated as the root mean square (Rq) and average roughness (Ra), were determined for each type of film and were calculated from the Htr mode image. Images were obtained in the Dfr mode. The film area for the determination of roughness was 900 μm2.
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2

Newt Skin Ultrastructural Analysis

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3 × 3 mm skin samples were dissected from the dorsal region of a euthanized newt. Each sample was fixed in 4% glutaraldehyde in 0.1 M sodium phosphate buffer (pH 7.4) overnight at 4°C. Following fixation, samples were briefly rinsed in 0.1 M sodium phosphate buffer and dehydrated in an ethanol gradient (25, 50, 75, 95, 100, 100, 100%) for 10 min each. Any remaining liquid in the samples was removed by critical point drying in a Balzers Model 010 critical point dryer (Balzers Union Ltd., Balzers, Liechtenstein) using carbon dioxide as the transitional fluid. Each skin sample was then mounted on an aluminum stub using carbon suspension cement (SPI Supplies, West Chester, PA) and coated with platinum (8 nm thickness) using a Q150T turbo pumped sputter coater (Quorum Technologies, Laughton, East Sussex, England) purged with argon gas. Samples were examined and images obtained using a JEOL JSM-7500F cold field emission scanning electron microscope (JEOL Ltd, Tokyo, Japan).
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