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29 protocols using lindberg blue m

1

Activation Protocols for Porous Materials

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For measurements made in the helium pycnometer, activated samples were outgassed in a tube furnace (Lindberg Blue M, Thermo Fisher Scientific Inc., Waltham, MA) attached to an Edwards TIC pumping station (Edwards, West Sussex, UK) that was equipped with a nXDS6i scroll back pump (vacuum level of 10−2 mbar, Edwards, West Sussex, UK) and an EXT-75DX turbo pump (vacuum level of 10 −9 mbar, Edwards, West Sussex, UK). The following activation protocols were used with the porous samples.
After activation, each sample was transferred under air-free conditions from the sealed activator tube to an argon glovebox (Inert Lab Glovebox, Innovative Technology, Port Washington, NY) for storage until helium pycnometry measurements were performed. The percent mass losses for the samples after activation are 7 % mass fraction for ZSM-5, 12 % mass fraction for F400, 6 % mass fraction for MIL-53, and 0.5 % mass fraction for ZIF-8.
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2

Gravimetric Swelling Measurement of Scaffolds

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The swelling percentages of the scaffolds were measured using the gravimetric method. The swelling percentages were evaluated by immersing pre-weighed, in an analytical balance (ES 1255M, Precisa Gravimetrics, Dietikon, Switzerland), dry scaffold sample ( Wd ) of 10 × 10 mm into 4 mL of phosphate-buffered saline solution (PBS, pH 7.4) and incubated at 37 °C, in a vacuum oven (Lindberg/Blue M, Thermo Fisher Scientific, MA, USA), for 3, 7, 14, 21, and 28 days, the buffer was replaced every three days. At certain intervals, the samples were taken out and put on a filter paper to remove the excessive PBS and the weight gain of the swollen film (Ws). This process was continued until reaching the constant weight in three repeating measurements. The swelling percentage (SP) was calculated according to Equation (4) [39 (link)]: SP%=WsWdWd×100
where Ws is the weight of swollen scaffolds samples (mg), and Wd is the weight of dry scaffolds samples (mg). The measurements were repeated three times for each type of scaffold.
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3

Fabricating Hydrophobic Aluminum and Copper Surfaces

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Polished aluminum and copper tabs were first ultra-sonicated in acetone (10 min), followed by IPA (10 min), then thoroughly rinsed in DI water and dried under a clean N2 gas stream. To fabricate the hydrophobic surface, the Al and Cu tabs were functionalized with (heptadecafluoro-1,1,2,2 tetrahydrodecyl)trimethoxysilane (HTMS, TCI America, CAS #: 83048-65−1) using the vapor phase deposition method47 (link). Briefly, the substrates were placed in a glass beaker with a vial of HTMS toluene solution (5% v/v). A glass lid was placed on top to seal the container, followed by heating in atmospheric pressure oven (Thermo Scientific, Lindberg Blue M) at 80 ± 5 °C for 3 h to allow conformal HTMS SAM deposition.
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4

Annealing Graphene Films for Characterization

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Example 17

Annealing Study of Graphene Films.

An ink containing graphene/ethyl cellulose in ethanol/terpineol was prepared for blade-coating films. Graphene/ethyl cellulose powder (˜100 mg) was dispersed in 2 mL of 4:1 ethanol/terpineol v/v by bath sonication. This ink was blade-coated onto glass slides (VWR Micro Slides) into a 15×15 mm2 film defined by a mask of scotch tape. The sample was then annealed in a tube furnace (Thermo Scientific, Lindberg Blue M). The sheet resistance of the resulting film was measured by a 4-point probe technique, employing the appropriate geometric correction factors, while the film thickness was measured by profilometry (Dektak 150 Stylus Surface Profiler). These results were used to calculate the resistivity plotted in FIG. 13A-B.

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5

Non-Isothermal Pretreatment of Wood Flour

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Wood flour and pretreatment liquid (dilute water, acetic or sulphuric acid) were added into reactors at 5% (w/w) solids loading. Reaction vessels with a capacity of 15 mL were stainless steel cylinders with a bolt-screw fitting on either end. Prior to closing the reactors, both fittings were sealed with polytetrafluoroethylene tape. The reactors were vortexed and preincubation at 60 °C for 60 min to ensure impregnation of the wood sample with pretreatment solvent followed. Non-isothermal pretreatment was conducted in a Lindberg Blue M laboratory gravity oven (Thermo Scientific, USA) at 180 °C. At time zero, heating in the oven began. Pressure inside the reactor was measured by attaching a 2000 psi pressure gauge (Ashcroft, USA) to a bolt-screw fitting via 30 cm of stainless steel tubing. All reactions were quenched in an ice bath.
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6

Synthesis of Sulfur-Doped Molybdenum Disulfide

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Solutions of sodium cholate growth promoter (10 mg mL−1) and ammonium heptamolybdate (11 mg mL) were spun onto precleaned 300 nm SiO2/Si substrates. The samples were then inserted into the center of a 1 in. tube furnace (Thermo Scientific Lindberg/Blue M) and were flushed with N2 gas (1000 sccm) at room temperature for 10 min. After flushing, the samples were heated under N2 gas flow (400 sccm) at a rate of 70 °C min−1 and then held at 750 °C for 15 min. Approximately 150 mg of sulfur powder was placed 22 cm away from the target substrates and heated to 180 °C during the growth process. The substrates were rapidly cooled to room temperature by opening the furnace to finish the synthesis.
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7

Pyrolysis of Chromatographic Paper

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Whatman #1 chromatographic
paper was pyrolyzed in a tubular furnace
(Lindberg/Blue M from Thermo Fisher Scientific, USA). First, strips
of paper (10.0 × 2.5 cm) were cut and placed between alumina
plates to avoid wrinkles after thermal treatment. After placing the
substrates inside the tube, a purging step with nitrogen gas (N2) (99.99%) was conducted at 5 L min–1 for
5 min to remove oxygen from the alumina tube. The furnace was heated
from 25 to 1000 °C at a rate of 20 °C min–1. The furnace was kept at 1000 °C for 1h and then it was allowed
to cool at room temperature. During the pyrolysis process, we kept
N2 at a flow rate of 20 L min–1 flowing
through the tube to remove gases produced.
PP strips were functionalized
with PDA using the chemical route32 (link) reported.
Dopamine hydrochloride (Sigma-Aldrich) was dissolved in 10 mM Tris
buffer (Sigma-Aldrich) pH 8.5 to prepare a solution of 2 mg mL–1. PP strips were immersed in this solution for 24
h in a closed bath to minimize evaporation of the solution. After,
the lid was removed, and the solution was allowed to dry in the reservoir.
After the functionalization of PP with PDA (PP + PDA), we performed
a second stage of pyrolysis at different final temperatures of 300,
400, 500, 700, and 1000 °C using the same heating rate in all
cases.
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8

Determining Crude Ash Content

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The crude ash content was determined following Liu’s method (Liu, 2019 (link)). In this method, the porcelain crucible was burnt in an electric furnace (Lindberg/Blue M, Thermo Fisher Scientific, USA) at 600°C for 1 h and cooled in a desiccator for 40 min. Then, 2 g of the sample was placed in an electric furnace at 600°C for 2 h, cooled in a desiccator for 40 min, and measured. The crude ash content was calculated for each treatment as follows:
where a represents the weight of the burnt sample and the porcelain crucible, b represents the weight of the porcelain crucible, and c represents the raw sample weight.
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9

Tin Oxide Nanowires by CVD

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A forest of tin oxide nanowires was initially grown by chemical vapor deposition (CVD). An alumina boat filled with pure tin monoxide was placed as an evaporation source in the center of an oven (Lindberg Blue M, Thermo Fisher Scientific, Waltham, MA, USA) where the temperature is highest. Close to it (1 cm), a silicon substrate of approximately 1 × 2 cm2 was placed, on which a thin gold film (thickness of approximately 5 nm) acted as a catalyst. The quartz tube was then pumped down to 10−2 mbar and purged with high-purity argon (99.999%), repeating these two steps three times, and finally, the system was pumped down to 8 × 10−3 mbar. While the system was in a vacuum, the temperature was increased from room temperature (23 °C) up to 800 °C at a rate of 25 °C/min and then the oven was held at 800 °C for five minutes. At this point, an oxygen flow of 0.35 standard cubic centimeters (sccm) was injected into the system in order to start the growth of the nanowires. The growth of the nanostructures, which follows the gold-catalyzed solid liquid vapor (VLS) mechanism [29 (link)], lasted 30 min, after which the system was shut down and allowed to cool. At the end of the growth process, the sample surface showed a homogeneous white film.
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10

Annealing Study of Graphene Films

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Example 17

Annealing Study of Graphene Films.

An ink containing graphene/ethyl cellulose in ethanol/terpineol was prepared for blade-coating films. Graphene/ethyl cellulose powder (˜100 mg) was dispersed in 2 mL of 4:1 ethanol/terpineol v/v by bath sonication. This ink was blade-coated onto glass slides (VWR Micro Slides) into a 15×15 mm2 film defined by a mask of scotch tape. The sample was then annealed in a tube furnace (Thermo Scientific, Lindberg Blue M). The sheet resistance of the resulting film was measured by a 4-point probe technique, employing the appropriate geometric correction factors, while the film thickness was measured by profilometry (Dektak 150 Stylus Surface Profiler). These results were used to calculate the resistivity plotted in FIG. 13A-B.

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