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31 protocols using hydrofluoric acid hf

1

Synthesis of InCl3 Nanocrystals

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Indium chloride (InCl3, 98%), tris(dimethylamino)phosphine ((Me2N)3P), 97%), oleylamine (70%), lithium bis(trimethylsilyl)amide (or lithium hexamethyldisilazide, LiHMDS, 97%), diisobutylaluminum hydride (DIBAL-H, 1.0 M in toluene), and hydrofluoric acid (HF, 48 wt% in H2O) were purchased from Sigma-Aldrich. Tris(dimethylamino)arsine ((Me2N)3As), 99%) was purchased from Strem. Unless otherwise stated, all chemicals were used without further purification. Degassed oleylamine (D-OLA) was prepared by degassing under vacuum (~1.0 Torr) at 90 °C for 60 min.
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2

PMMA Slide Fabrication and Characterization

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Polymethylmethacrylate (PMMA) slides, methylene chloride, and the microscope slides were obtained at the local market; 99.9% lead pellets and 99.9% platinum wire were purchased from Kurt J. Lesker (Jefferson Hills, PA, USA); 1 inch double-sided tape and 1 inch copper tape were acquired from 3M (USA), ultra-high purity (>99.9%) nitrogen was purchased from Linde (Bogota, Colombia), 99.9% and potassium hydroxide (KOH) and 99.9% hydrofluoric acid (HF) were obtained from Sigma–Aldrich (Saint Louis, MO, USA).
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3

Synthesis and Characterization of Ti2AlC

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All the reagents were of analytical grade and used without further purification. Absolute ethanol (99.8%) was purchased from POCH. Hydrofluoric acid (HF) (48%), phosphoric acid (≥99%) and titanium carbide (98%) (325 mesh) were obtained from Sigma-Aldrich. Maxthal 211—Ti2AlC (325 mesh) was purchased from Kanthal (Hallstahammar, Sweden). The N2 (5.0), Ar (5.0) and O2 (5.0) were purchased from Linde (Kraków, Poland). All solutions were prepared on the basis of MilliQ (13.6 MΩ/cm) type 1 water (T1-H2O).
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4

Solvothermal Synthesis of Titanium Fluoride

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Titanium butoxide (TNBT) or Ti(OBu)4 (Bu = CH2CH2CH2CH3) (Molar mass = 340.32 g/mol) (97%), sodium fluoride (NaF) (99%), hydrofluoric acid [HF] (40 wt%), and anhydrous ethanol (99.8%) were purchased from Sigma-Aldrich. All chemicals were used directly without further processing. Additionally, Teflon-lined stainless-steel autoclave (Parr Instrument Co., Moline, IL, USA) with a capacity of 45 mL was used.
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5

In Vitro Nanoparticle Toxicity Assay

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Analytical grade chemicals sodium hydrogenphosphate (Na2HPO4), di-potassium hydrogen phosphate trihydrate (K2HPO4·3H2O), calcium chloride (CaCl2), sodium chloride (NaCl), potassium chloride (KCl), magnesium chloride hexahydrate (MgCl2·6H2O), sodium hydrogencarbonate (NaHCO3), sodium sulfate (Na2SO4), Tris-hydroxymethyl aminomethane ((HOCH2)3CNH2, Tris), hydrochloric acid (HCl), sodium hydroxide (NaOH), TiO2 nanoparticles, TiO2 P25 Degussa (75% anatase, 25% rutile), titanium tetraisopropoxide (TIIP), hydrofluoric acid (HF), 2′,7′-dichlorodihydrofluoresin diacetate (DCFH2-DA), methanol, Triton X-100, Polyethylene glycol 600 and Hemoglobin (Hb) standard were obtained from Sigma Aldrich, Darmstadt, Germany. In addition, 3-morpholinosydnonimine hydrochloride (SIN-1 hydrochloride) was obtained from Abcam, Cambridge, UK, Gibco DPBS from Thermofisher Scientific, Waltham, MA, USA, and Drabkin’s reagent from Randox, Crumlin, County Antrim, UK. Ultrapure water (UPW, conductivity 0.5 μS cm−1, Hydrolab HLP 10 UV, Straszyn, Poland) was used throughout.
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6

Fabrication of Hydrophobic Aluminum Surfaces

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Commercially available hot rolled aluminum plates EN AW-6082 T6 (30 mm × 24 mm × 2 mm) were used as substrates. Hydrochloric acid (HCl, 37%) was purchased from Fluka (Buchs, Switzerland). Nitric acid (HNO3, 60%) was purchased from Carlo Erba (Cornaredo, MI, Italy). Hydrofluoric acid (HF, 48%) and octadecyltrimethoxysilane (OTMS) (C21H46O3Si, 90%) were procured from Sigma-Aldrich (St. Louis, MI, USA). Toluene was obtained from Riedel-de Haën (Seelze, Germany). Ethanol and acetone were purchased from J.T. Baker (Phillipsburg, NJ, USA). Ultra-pure water from Best Chemical (Vairano Patenora, CE, Italy) was used throughout the experiment.
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7

Nanomaterial Synthesis and Characterization

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Hydrofluoric acid (HF, 40%), N,N-dymethylformamide (DMF), buffered hydrofluoric acid (BHF) and tetramethylammonium hydroxide (TMAH, 25%), PAH (Mw 58,000) and PSS (Mw 70,000) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Acetate buffer (ABS) pH 5.2 and phosphate buffer (PBS) pH 7.4 solutions were also obtained from Sigma-Aldrich. Doxorubicin hydrochloride was obtained from the European Pharmacopoeia (Strasbourg, France). All other chemicals used in the experiments were obtained from commercial sources as analytical reagents without further purification. Milli-Q water (Millipore, Billerica, MA, USA) with a resistivity of 18.2 MΩ cm was used throughout the study. Boron-doped (p-type) silicon wafers (1 0 0) and resistivity 10 to 20 Ω cm were supplied by Si-Mat (Kaufering, Germany).
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8

Wet Chemical Synthesis of Nanostructures

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All chemicals were used as received: Potassium hydroxide pellets (KOH, Alfa Aesar, 85%), hydrogen peroxide (H2O2, 30% (w/w) in H2O, contains stabilizer, Sigma-Aldrich), sulfuric acid (H2SO4, 99.999%, Sigma-Aldrich), hydrofluoric acid (HF, ACS reagent 48%, Sigma-Aldrich), hydrochloric acid (HCl, reagent grade, 37%, Sigma-Aldrich), potassium hexacyanoferrate(II) trihydrate (K4Fe(CN)6. 3H2O, ≥99% puriss. p.a., ACS reagent, Sigma-Aldrich), potassium hexacyanoferrate(III) (K3Fe(CN)6, ≥99% puriss. p.a., ACS reagent, Sigma-Aldrich). Water with resistivity 18.2 MΩ cm from Milli-Q integral ultrapure water (Merck Millipore).
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9

Synthesis of Metal Hexacyanoferrates

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All chemicals were used as received: potassium
hydroxide pellets (KOH, Alfa Aesar, 85%), hydrogen peroxide (H2O2, 30% (w/w) in H2O, contains stabilizer,
Sigma-Aldrich), sulfuric acid (H2SO4, 99.999%,
Sigma-Aldrich), hydrofluoric acid (HF, ACS reagent 48%, Sigma-Aldrich),
hydrochloric acid (HCl, reagent grade, 37%, Sigma-Aldrich), potassium
hexacyanoferrate(II) trihydrate (K4Fe(CN)6·3H2O, ≥99% puriss. p.a., ACS reagent, Sigma-Aldrich),
potassium hexacyanoferrate(III) (K3Fe(CN)6,
≥99% puriss. p.a., ACS reagent, Sigma-Aldrich). Water with
resistivity of 18.2 MΩ cm from Milli-Q integral ultrapure water
(Merck Millipore).
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10

Anatase and Rutile n-TiO2 Powder Preparation

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Uncoated n-TiO2 powders of anatase (10–30 nm, 99.5%) and rutile (10–30 nm, 99.5%) polymorphs and mixture of anatase/rutile (10–30 nm, 30% rutile and 70% anatase) were purchased from Skyspring Nanomaterials Inc., Houston, TX USA. Some physical properties of these nanopowders are summarized in Table 1. Aqueous suspensions were prepared as described elsewhere (Ates et al., 2013a (link)). Briefly, 1% (m/v) n-TiO2 (e.g., 10,000 mg/mL) stocks were prepared by dispersing appropriate amount of each n-TiO2 powder in 100 mL deionized water. These suspensions were vortexed for 20 s, and then sonicated in an ultrasonic bath for about 10 min for maximum dispersion. Then, appropriate volumes were immediately transferred into the exposure tanks containing Artemia salina larvae in seawater.
Artemia cysts (The Great Salt Lake, Utah harvest) were purchased from Artemia International LLC, Houston TX, and were kept in a refrigerator at 4°C. High purity acids were used for instrumental chemical analyses. Hydrofluoric acid (HF, 99.999%) was purchased from Sigma Aldrich. Trace metal grade nitric acid (HNO3) was procured from Fisher Scientific. Carbon coated Cu TEM grids (300 mesh) were purchased for Electron Microscopy Sciences (EMS), Hatfield, PA and used in measurement of particle size of n-TiO2 in stocks and experimental colloids.
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