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4 protocols using potassium nitrate

1

Preparation and Characterization of Ion Exchange Membranes

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Sodium hypochlorite (NaClO, 14%), sodium hydrogen phosphate (NaH2PO4), sodium chloride (NaCl), calcium chloride dihydrate (CaCl2∙2H2O), magnesium sulfate heptahydrate (MgSO4∙7H2O), sodium hydrogen carbonate (NaHCO3), potassium nitrate (KNO3), sodium nitrate (NaNO3), calcium carbonate (CaCO3), magnesium chloride hexahydrate (MgCl2∙6H2O), potassium sulfate (K2SO4), sodium sulfate (Na2SO4), calcium sulfate dihydrate (CaSO4∙2H2O), boric acid (H3BO3, 0.5%), hydrogen peroxide (H2O2, 30%), and chloride acid (HCl, 0.1 M) were purchased from Scharlab S.L., Barcelona, Spain. The ultrapure water (Milli-Q) used in the experiments was obtained from Millipore, Molsheim, France, equipment (conductivity less than 0.055 µS cm−1).
Polyvinyl chloride (PVC, Mw 112,000 g mol−1) was supplied by ATOCHEM, Madrid, Spain. Tetrahydrofuran (THF) was purchased from Scharlab S.L. Amberlite® IRA-402 (Cl form, total exchange capacity ≥ 1.0 mol L−1) was supplied by Merck Life Science, Darmstadt, Germany, S.L.U.
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2

Trace Metal Analysis Procedure

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All reagents were analytical-reagent grade unless otherwise stated. Potassium nitrate (99%) and sodium chloride (99.5%) were obtained from Scharlau (Barcelona, Spain). Kerosene and ammonia (30%) were obtained from Panreac (Barcelona, Spain). Sodium thiosulfate (100%) was purchased from Merck (Darmstadt, Germany). Tri-isobutylphosphine sulfide (TIBPS) was provided by Cytec Industries Inc (Saddle Brook, NJ, USA), and humic acids were obtained from Aldrich (Steinheim, Germany). Aqueous solutions of silver were prepared from a 1000 mg L−1 standard solution obtained from Merck (Darmstadt, Germany). Deionized water of resistivity lower than 18.2 MΩ cm was obtained by a Millipore Quantum Ultrapure water supplier (Millipore, Bedford, Ma, USA). Acetylene for atomic spectrometry was obtained from Air Liquide (Madrid, Spain).
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3

TEMPO-Oxidized Nanocellulose Production

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Bleached eucalyptus kraft
pulp, unrefined (15 °SR), was provided by Ence (Navia, Spain).
2,2,6,6-Tetramethylpiperidine-1-oxy radical (TEMPO), NaBr, NaOH, NaClO
(15%), copper(II) ethylenediamine, and DTZ (≥98%) were purchased
from Sigma-Aldrich (Schnelldorf, Germany). Glacial acetic acid was
purchased from Scharlab (Sentmenat, Barcelona, Spain). All organic
solvents (reagent grade) were received from Thermo Fisher Scientific
(Loughborough, U.K.). Preliminary results indicated that amylene-stabilized
chloroform is preferred over ethanol-stabilized chloroform.
Distilled water was used for nanocellulose production, but metal
salts were dissolved in Milli-Q water. These metal salts were lead(II)
nitrate, lead(II) chloride, cadmium(II) nitrate, cadmium(II) chloride,
copper(II) chloride, nickel(II) chloride, chromium(III) chloride,
chromium(III) nitrate, and magnesium chloride from Panreac Applichem
(Castellar del Vallès, Barcelona, Spain); potassium nitrate,
iron(III) chloride, and manganese(II) chloride from Scharlab; and
mercury(II) nitrate 1-hydrate, mercury(II) chloride, silver nitrate,
and zinc chloride from Sigma-Aldrich.
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4

Swelling Quantification of Nanohybrid Materials

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Swelling of the nanohybrid materials was quantified at equilibrium, by weighing the dry samples, m, and after equilibration at 37ºC in two different ambients: at 97% relative humidity (RH), and immersed in water. The first swelling medium was prepared with a potassium nitrate (Scharlab) supersaturated solution in a closed moisture chamber [25] .
The samples were withdrawn from the moisture chamber after different times and immediately weighed, until no weight change was further observed; this value was taken for each nanohybrid as the equilibrium value, mw. The equilibrium water content, EWC, was calculated as: 𝐸𝐸𝐸𝐸𝐸𝐸 = 𝑚𝑚 𝑤𝑤 -𝑚𝑚 𝑚𝑚 . Three replicates per composition were measured. A Mettler-Toledo XS105DU balance (Columbus, OH, USA) was used for this purpose.
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