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Nitric acid

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Nitric acid is a colorless to slightly yellow, fuming, and highly corrosive liquid chemical. It is commonly used in laboratories for various analytical and synthetic applications.

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193 protocols using nitric acid

1

Quantification of Lead in Blood

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The BLL was quantified by using an inductively coupled plasma mass spectrometry with triple quadrupole technology (iCAP™ TQ ICP-MS, Thermo Fisher Scientific, Bremen, Germany). The EDTA blood was homogenized for 10 min by mechanical shaking; thereafter blood plasma (1.0 ml) was gravimetrically diluted (in precleaned polypropylene bottles kept in 2% nitric acid for 72 h) with 0.5% m/m nitric acid (Fisher Scientific) and 2% m/m tetramethylammonium hydroxide (Merck, Sigma Aldrich) in ultrapure water. A calibration blank, a series of standards, and a quality control were prepared by using the same procedure. All samples and standards were spiked with an internal standard mix (10 μg/L of 209Bi). The sample digests were filtered with Wattman paper several times to obtain a clear solution. The diluted digests were measured directly by ICP-MS, and the concentration of Pb in blood was quantified as μg/dl.
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2

Measuring Cellular Copper Concentration

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YST cells were transfected with 2 µg of the ATP7B plasmids as described above. After 16 h of transfection, the cells were treated with 100 μM CuCl2 for 24 h and then collected by centrifugation at 10,000 rpm for 10 min. Approximately 106 cells were collected from each well and then washed once with ultrapure water. The cell pellets were resuspended in 100 µL of concentrated nitric acid (trace element grade, Fisher Scientific) and heated at 90 °C for 2 h. The samples were cooled to RT and then diluted in 1.4 mL of 1% nitric acid. The volume of the sample was determined before ICP-MS measurements were taken. The concentration of Cu was normalized to cell count.
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3

Elemental Analysis of Wine Samples

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For determination of the elemental content in wine (see Table 2), samples were diluted 10 times with water containing 2% (v/v) nitric acid (Merck, Germany). Standards were prepared with 1% (v/v) ethanol and 2% (v/v) nitric acid in order to provide the same concentrations of ethanol and nitric acid as the samples [14 (link),15 (link),16 (link),17 (link),18 ,19 (link)].
The elements were determined using inductively coupled plasma with optical emission spectrometry (ICP-OES, iCAP 6500 Duo Thermo Scientific, Llanthony Rd, Gloucester GL2 8DN, Highnam, UK) and inductively coupled plasma quadrupole mass spectrometry (ICP-QMS, Thermo Scientific, Xseries 2, Hemel Hempstead, UK). ICP-OES was applied for K, Na, Mg, Ca, Rb, and Fe examination, while the remaining 14 elements were analyzed using ICP-QMS. For elemental determination, a multi-element plasma standard solution 4, Specpure, containing 1 g/L of 22 elements were used for calibration [19 (link)].
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4

Trace Metal Enrichment Membrane Fabrication

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Polyethersulfone (PES) microfiltration membranes (0.45 μm pore diameter, 47 mm diameter) were purchased from MilliporeSigma (Burlington, USA). Glycidyl methacrylate (≥97.0%), lanthanum(III) nitrate hexahydrate (99.999% trace metal basis), cerium(III) chloride heptahydrate (99.9% trace metal basis), neodymium(III) nitrate hexahydrate (99.9% trace metal basis), zinc perchlorate hexahydrate, calcium chloride (anhydrous, Redi-Dri, ≥97%), sodium standard for ICP (1,000 mg/L ± 2 mg/L), calcium standard for ICP (1,000 mg/L ± 2 mg/L), and magnesium standard for ICP (1,000 mg/L ± 2 mg/L) were purchased from Sigma-Aldrich. Magnesium chloride hexahydrate (99–102%, ACS grade) was purchased from VWR Life Science. L-lysine (98%, powder) was purchased from Alfa Aesar. Ethyl alcohol (absolute, 200 proof, ≥99.5%, ACS Reagent grade) was purchased from Acros Organics. Denatured Ethyl alcohol (88–91%), sodium chloride (≥99%, certified ACS grade, crystalline), nitric acid (68–70%, certified ACS plus grade), and hydrochloric acid (36.5–38%, certified ACS plus grade) were purchased from Fisher Chemical. Arsenazo (III) was purchased from Pointe Scientific. Sodium hydroxide (10 N, biotech reagent grade) was purchased from Avantor. Deionized water (DI water) was made from a RiOS-DI 3 water purification system (MilliporeSigma, Burlington, MA, USA).
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5

Antibiotic Sensitivity of Multidrug-Resistant Salmonella

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Multidrug-resistant Salmonella (ATCC 700408) was obtained from the American Type Culture Collection (Manassas, VA). Silver nitrate, sodium borohydride, sodium citrate, NaOH, tetracycline hydrochloride (TET), neomycin sulfate (NEO), kanamycin sulfate (KAN), tryptic soy broth (TSB), and tryptic soy agar (TSA) were purchased from Sigma-Aldrich (St. Louis, MO). Penicillin G sodium salt (PEN) and nitric acid (trace metal grade, 67%–70%) were from Fisher Scientific (Houston, TX). Ampicillin sodium salt (AMP) was from Research Products International Corp (Prospect, IL), and enoxacin hydrochloride (ENO) was from MP Biomedicals LLC (Solon, OH). The structures of the antibiotics are shown in Figure SI 1.
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6

Synthesis and Characterization of Iron Nanoparticles

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Iron (II) chloride tetrahydrate
(FeCl2·4H2O) 99%, iron (III) chloride
hexahydrate (FeCl3·6H2O) 99%,
tetramethylammonium hydroxide (TMAOH) 25% w/v, agarose high melting
point, hydroxylamine hydrochloride, sodium acetate, 1,10-phenantroline
monohydrate and iron standard (Cat. #56209) were purchased from
Sigma-Aldrich. Ammonium hydroxide (NH4OH) 29% v/v and nitric
acid 70% v/v (Optima Grade) were purchased from Fisher Scientific. All
reagents were used as received.
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7

Assessing Metal Levels in Bone Broths

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Three animal bone broth-based street foods were obtained from local stores in Douliu city (central Taiwan) to evaluate the levels of essential and toxic metals in broths, and the health risks that would be associated with their ingestion. These foods included pork rib chops that had been stewed in Chinese medicinal herb broth (PR, n = 7), beef noodle (Chinese-style noodle with stewed beef in bovine bone broth, BN, n = 6) and tonkotsu ramen (Japanese-style noodle in pork bone broth, TR, n = 6), all of which are readily available. For simplicity, only the liquid portion (broth) of the foods was assessed. After the samples were cool, the soups were filtered using a 20-mesh gauze; the volume and pH level were recorded, and any grease was removed. The remaining contents were acidified by adding 3 ml of diluted (1:1) nitric acid (~67%, Fisher) per litre of broth, and kept at 4°C until analysis.
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8

Quantifying Stent Encrustation Composition

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All experimental containers were prewashed with
1% nitric acid (Fisher Scientific, Hampton, NH) before ultra-trace
elemental analysis via inductively coupled plasma mass spectrometry
(ICP-MS). 11 week dried, encrusted stent specimens were submerged
in 1 mL of 1% HNO3 (v/v), followed by ultrasonication for
1 h using a Branson ultrasonic cleaner (Branson Ultrasonics Corp.,
Danbury, CT) to agitate, extract, and dissolve the encrusted minerals
on the stents. Each sonicated sample was further diluted 100-fold
in 1% HNO3 to achieve a total dissolved solid of <1
weight percent (wt %) and a final volume of 10 mL before ICP-MS analysis.
The presence of magnesium (Mg), calcium (Ca), and phosphorus (P) was
measured by using an iCAP RQ inductively coupled plasma mass spectrometer
with a Teledyne laser ablation (LA) system (Thermo Scientific, Waltham,
MA, USA). Standard solutions of Mg, Ca, and P (Inorganic Ventures,
Christiansburg, VA, USA) were used to generate a standard curve (100,
50, 20, and 0 ppm). One-way ANOVA was performed using GraphPad Prism
(Dotmatics, Boston, MA, USA) to compare the amount of encrusted deposit
on each stent material.
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9

Synthesis and Characterization of Potassium Ferrate

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Ultrapure water (18.2 MΩ•cm) was obtained from a Milli-Q Element A10 water purification system. Suwannee River NOM (SRNOM, 2R101N) and Suwannee River humic acid (SRHA, 3S101H) were purchased from the International Humic Substances Society. Solid potassium ferrate (K2FeO4) was chemically prepared based on previous studies (Yang et al., 2015 ; Dong et al., 2019 (link)). Stock solutions of Fe(VI) were freshly prepared by dissolving K2FeO4 in ultrapure water before each experiment, and Fe(VI) concentration was quantified with the absorbance at 510 nm (absorption coefficient 1150 M−1 cm−1). HF Mega Bond Elut C18 cartridges (1 g, 6 mL) were ordered from Agilent Technologies. Lead(IV) oxide (> 97%, extra pure, ACROS Organics) were ordered from Fisher Chemical (Hampton, NH, USA), and it has been identified as pure plattnerite (β-PbO2) by X-ray Diffraction in a previous study (Xie et al., 2010 (link)). Other chemicals and reagents, including potassium iodide (KI, 99+%, ACS reagent), potassium bromide (KBr, 99+%, for spectroscopy, IR grade), nitric acid (trace metal grade), and methanol (Optima LC/MS grade) were purchased from Fisher Chemical (Hampton, NH, USA).
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10

Copper Nanoparticle Synthesis Protocols

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Copper nitrate (Cu(NO3)2·2.5H2O) and chloroform were purchased from Fisher. Copper(II) chloride (97%), oleylamine (70%), 1-octadecene(90%), sulfur powder (99.99%), and copper ICP standard were purchased from Sigma-Aldrich. Ethanol (200 proof) was purchased form Goldshield Chemical. Poly(ethylene glycol) methyl ether thiol (PEG-thiol, Mw=5000) was purchased from Laysan Bio. Dulbecco’s modified eagle medium (DMEM), fetal bovine serum, antibiotic-antimycotic (100X), and AlamarBlue® assay were purchased from Thermo Fisher Scientific. The internal standard for ICP was purchased from Inorganic Ventures. The nitric acid (70%) and hydrochloric acid (36.5–38%) was purchased from Fisher Scientific and J.T. Baker, respectively. Laboratory polyethylene tubing (OD: 1.27 mm, ID: 0.85 mm) was purchased from Harvard Apparatus, and 0.2 μm polyethersulfone syringe filters (Puradisc 25AS) were purchased from Whatman.
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