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8 protocols using boron nitride

1

Nanosuspension Formulation Protocols

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Boron nitride, medium molecular weight (MW) chitosan, Tween 20, acetic acid, Poloxamer 407, sodium lauryl sulphate (SLS), polyvinyl alcohol (PVA, high MW), and dimethyl sulphoxide (DMSO) used in the preparation of nanosuspensions were purchased from Sigma-Aldrich (USA). Tween 60 and PVA (low MW) were purchased from Merck (Germany). Gibco™ DMEM/F12 and Gibco™ FBS used for cell culture studies were purchased from ThermoFisher Scientific (USA). Penicillin/Streptomycin, PBS, Trypsin/EDTA, MTT Cell Growth Assay Kit CT-02, and Triton™ X-100 were purchased from Sigma-Aldrich (USA). Deionized water (Direct-Q® 3 UV Millipore, Merck) was used in all formulations (18.2 MΩ·cm, TOC ≤ 4 ppb).
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2

Synthesis of Lithium-ion Battery Electrolyte

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Lithium hydroxide (LiOH, 98%), lithium chloride (LiCl, 99.0%), phytic acid (70%), epoxy chloropropane (ECH, 99.5%), and urea (99.0%) were obtained from Aladdin Reagent Co., Ltd. Cotton linter pulp was obtained from Jilin Chemical Fiber Group Co., Ltd. These chemicals were used as received without further purification. Boron nitride (99.9%, 12 μm) was obtained from Sigma-Aldrich Co., Ltd and was exfoliated according to our previous study.
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3

PHBV Biocomposites with Cellulosic Fillers

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Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) with 3% HV (molar content) was purchased from Natureplast under the grade PHI003, in the form of a fine and electrostatic powder (d50 = 19.9 ± 2.3 µm). Boron nitride was purchased from Sigma Aldrich (reference 255475) and used as nucleating agent. Three different grades of (ligno-)cellulosic fibres were supplied by J. Rettenmaier & Söhne (JRS), i.e., Arbocel B00, Arbocel BE 600 30 PU and Filtracel EFC 950. Their intrinsic characteristics are fully detailed in the Section 3. Results and Discussion, e.g., Section 3.2.1. Description of (ligno-)cellulosic fillers.
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4

Synthesis of Magnetic Nanoparticles

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Iron(III)
chloride hexahydrate (reagent grade,
≥98%), iron(II) chloride tetrahydrate (p.a. ACS reagent), cobalt(II)
chloride hexahydrate (reagent grade, ≥98%), ethylene glycol
(anhydrous 98%), HMTA (reagent grade, 99%), methylene blue (reagent
grade), ethanol (HPLC grade), and boron nitride (reagent grade) were
supplied by Sigma-Aldrich. Sodium acetate (extra pure >99%) and
Durapore
0.45 μm PVDF membrane were supplied by Merck. Ethylenediamine
(>99%) was supplied by Merck-Schuchardt. Sodium hydroxide (reagent
grade) was supplied by Fisher Scientific. MP H2O (Millipore
water) was obtained using a Synergy 185 Millipore filtration system
equipped with a 0.22 μM filter that was filtering distilled
water. Technical grade solvents (>99%; ethanol, methanol, and acetone)
supplied by Lennox were used for washing and storage.
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5

Synthesis of Magnetic Nanocomposite Materials

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Iron(lll) chloride hexahydrate,
reagent grade ≥98%; manganese(ll) chloride tetrahydrate, reagent
grade ≥98%; ethylene glycol, anhydrous 98%; methylene blue,
reagent grade; ethanol, HPLC grade; and boron nitride, reagent grade
were supplied by Sigma-Aldrich. The Durapore 0.45 μm PVDF membrane
was supplied by Merck. Ethylenediamine, >99% was supplied by Merck-Schuchardt.
Sodium hydroxide, reagent grade was supplied by Fisher Scientific.
MP H2O (Millipore water) was acquired through a Synergy
185 Millipore filtration system employing a 0.22 μM filter designed
for purifying distilled water. Technical-grade solvents, >99% pure
(ethanol, Methanol, and Acetone), provided by Lennox, were utilized
for washing and storage purposes.
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6

Synthesis of Inorganic Nanocomposite Materials

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β-Nickel hydroxide powder (>95% 283622), magnesium hydroxide (95% 310093), copper hydroxide (289787), talc (243604), boron nitride (255475) and sodium cholate were purchased from Sigma Aldrich. gallium sulphide was purchased from American Elements (99.999% GaS-05-P). De-ionized water was prepared in house and all solvents used were purchased with the highest available purity.
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7

Boron Nitride and Ionic Liquid Composites

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Boron nitride (BN) and an ionic liquid ([EMIM][BF4]) were purchased from Sigma Aldrich (USA). A ~3 wt % CNF aqueous dispersion was purchased from the University of Maine (Orono, ME, USA). The width and length of the CNF were ~50 nm and several μm, respectively.
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8

Thermally Conductive Epoxy-PCM Composites

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The fabrication steps for the formulations employed and the rationale for their use can be found elsewhere [8 (link)]. The PCM (n-Nonadecane, Sigma-Aldrich, St. Louis, MO, United States) was melted using a water bath and then mixed with Part A (resin) of EpoFix (Struers Inc., Cleveland, OH, United States) using a dual asymmetric speed mixer (Flacktek, Landrum, SC, United States). The thickening agent (Carbopol, Sigma-Aldrich, St. Louis, MO, United States) was then added, followed by the thermally conducting fillers, carbon nanofibers (CNF, 2 wt.%) and boron nitride (BN, 10 wt.%) particles, both of which were procured from Sigma Aldrich. Part B (hardener) of the EpoFix was finally added to the mixture, and the formulation was left to cure at room temperature in flexiform molds for 24 h (Struers, Inc. Cleveland, OH, United States). The samples containing CNF and BN powders were designated as EC-PCM40-CNF2 and EC-PCM40-BN10, respectively. The sample preparation steps for the specimen without thermally conductive fillers, designated as EC-PCM40, were identical than for the other formulations except the filler addition. Detailed sample formulations are presented in Table 1.
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