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68 protocols using h2so4

1

Characterization of Fruit and Vegetable Samples

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‘Jonagold’ apples (Malus domestica), yellow onions (Allium cepa), ‘Nerac’ carrots (Daucus carota) and ‘Hokkaido’ pumpkins (Cucurbita maxima) were bought at a local shop.
Technical ethanol (99%), technical acetone, Na2CO3 and NaOH pellets were bought from VWR (Leuven, Belgium). HCl, NaOH (0.1 M), H2SO4 (concentration ≥ 95% w/w) and disodium tetraborate decahydrate were obtained from Fisher Scientific (Merelbeke, Belgium). Rhamnose monohydrate, 3-phenylphenol and HNO3 were bought from Acros Organics (Geel, Belgium). H2SO4 (72% w/w) and NaOH (50% w/w) were obtained from Alfa Aesar (Kandel, Germany) and J.T. Baker (Gliwice, Poland), respectively. Galacturonic acid monohydrate and fucose were bought from Sigma-Aldrich (Diegem, Belgium), arabinose from Fluka Biochemika (Buchs, Switzerland), galactose from Merck (Darmstadt, Germany), glucose monohydrate from Riedel-de-Haën (Seelze, Germany), xylose from UCB (Leuven, Belgium) and mannose from Fluka Analytical (Buchs, Switzerland). The ultrapure water (organic free, 18.2 MΩ·cm resistance) was provided by a SimplicityTM 150 system. Unless otherwise mentioned, all chemicals used were of analytical grade.
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2

Characterization of Gypsum-Based Construction Materials

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Mineral gypsum (MG) and commercial stucco (CS) currently used in plasterboard manufacturing were provided as fine powders by a UK plasterboard supplier. MG was used for comparison purposes and to define the criterion for the calculation of the chemical purity of the samples through X-ray fluorescence. CS was produced in a continuous calciner at 150 °C and was used as reference to evaluate stuccos obtained from gypsum from post-consumer plasterboard waste before and after acid leaching purification. Sulfuric acid (H
2SO
4, Fisher Chemicals, certified analytical reagent, minimum purity 95 vol%) and distilled or purified water were used to prepare the H
2SO
4 solutions to carry out the acid leaching tests. Calcium hydroxide powder (Ca(OH)
2, Acros Organics, ACS reagent, purity > 95 wt%) was used in neutralization and wastewater treatment tests.
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3

Electrolytes for Bulk CO2 Reduction

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The following chemicals were used to prepare the electrolytes for bulk CO2 electrolysis: Cs2SO4 (Sigma Aldrich, 98%), Li2SO4 (Sigma Aldrich, 98%), KHCO3 (Acros Organics, 99.5%), H2SO4 (Acros Organics, for analysis ACS, 95% solution in water).
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4

Adsorption Experiments Using Sulfuric and Phosphoric Acids

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For the adsorption experiments, H2SO4 (Acros, 96% in H2O) and H3PO4 (Sigma-Aldrich, München, Germany, 85% in H2O) were used as received without further purification.
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5

BoNT/A Detection Assay Protocol

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NaCl (Sigma),
HEPES (Sigma),
EDTA (Sigma), CaCl2 (Sigma), NaCN (Sigma), NaOH (Sigma),
H2SO4 (Acros Organics), 2-mercaptoethylamine-HCl
(2-MEA, Thermo Scientific), sulfosuccinimidyl 4-[N-maleimidomethyl]cyclohexane-1-carboxylate (sulfo-SMCC, Thermo Scientific),
BupH Phosphate Buffered Saline Packs (Fisher Scientific), 3-cyanopropyldimethylchlorosilane
(Gelest), and 3-aminopropyldimethylethoxysilane (Gelest) were used
as received. Acetonitrile (Sigma) was stored over a 3 Å molecular
sieve. Cleaved SNAP-25 (cSNAP-25, Antibodies-Online) was received
as a lyophilized powder, diluted to 1 mg/mL in H2O, and
stored at −20 °C when not in use. Monoclonal antibody
(IgG) specific to the cleaved form of SNAP-25 (anti-cSNAP-25, Antibodies-Online)
from a murine host was received as a cell supernatant, stored at −20
°C when not in use, and purified (Antibody Clean-up Kit, Pierce)
prior to use. Interferent species (used for control experiments) include
TCEP (Sigma) and monoclonal antibody specific to BoNT/A LC (R&D
Antibodies), which were used as received, and uncleaved SNAP-25 (Creative
BioMart), BoNT/A LC (List Laboratories), and BoNT/A (Metabiologics)
were filtered via centrifugation prior to use. All aqueous solutions
were prepared using H2O (18 MΩ·cm) from a Barnstead
E-pure water purification system.
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6

Synthesis of TiO2-Aniline Composites

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TiO2 (P-25, Aeroxide) from Evonik (Degussa, Essen, Germany), aniline (An, 99%), ammonium persulfate (APS) and H2SO4 (96%) from Acros Organics (Morris Plains, NJ, USA) were used to synthesize samples. The chemicals were used as received, without any additional pre-treatment.
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7

Mechanically Activated Cellulose Characterization

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The following inorganic and organic chemicals were used in this work without any preliminary purification: H 2 SO 4 (96%, extra pure, Acros Organics), NaOH (high purity, Ekros), HNO 3 (high purity, 18-4, Reakhim, Russia), acetic acid (Acros Organics), formic acid (98%, Panreac), D-glucose (99%, Fisher Chemical), D-fructose (> 99%, Sigma-Aldrich), D-mannose (> 99%, Sigma-Aldrich), D-cellobiose (> 99%, Alfa Aesar), 5-hydoxymethylfurfural (> 98%, Sigma-Aldrich), levulinic acid (98%, Acros Organics) and furfural (> 99%, Sigma-Aldrich). Milli-Q water (Millipore, France) was used for preparing all the solutions.
Mechanically activated microcrystalline cellulose (13 ± 6 μm, crystallinity ca. 37%, Vekton, Russia) was used in all the experiments. Cellulose activation and characterization techniques were the same as discussed previously (Gromov et al. 2016 (link)(Gromov et al. , 2017 (link)(Gromov et al. , 2018;; (link)Pestunov et al. 2015) (link).
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8

Trichoderma reesei Bioprocess for HFBI Production

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Production of HFBI was performed using a native strain of Trichoderma reesei. The strain MUCL 44908 (BCCM/MUCL Agro-Food & Environmental Fungal Collection, Belgium) was purchased and maintained on potato dextrose agar (Merck, Germany) at 25 °C. Inoculum and cultivation medium was prepared as previously described [18] . The strain was cultivated in fed-batch mode using a 5 l bioreactor (BIOFLO 3000, New Brunswick). Bioproduction was started at a working volume of 2.5 l and after 30 hours of cultivation, the feed containing 40% glucose was initiated. The feed was added at a rate of 0.25 ml.min -1 for 90 hours. During cultivation, temperature and pH were automatically controlled. Temperature was set at 30 °C and pH was kept at 4.75 using 2.6 M NH 4 OH (Brenntag, Belgium) and 0.5 M H 2 SO 4 (Acros Organics, Belgium). Agitation was set at 400 rpm and aeration was kept constant at 2.5 l.min -1 . The cell concentration during production was determined as previously described [18] . The bioproduction was stopped after 120 hours.
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9

Comprehensive Chemical Reagents Procurement

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MgCl2•6H2O (98%), NaCl (98%), NaClO4•H2O (98%), NaF (99%), Mg(NO3)2•6H2O, KSCN (99%), LiNO3 (99%) and D2O (99.9 atom% D) were obtained from Sigma-Aldrich (Diegem, Belgium). CaCl2•2H2O (99.5%), NaNO3 (99%), Na2SO4 (99%), Ca(NO3)2•4H2O (99%), KNO3 (99%), NH4NO3 (99%) and HNO3 (65%) were purchased from Chem-Lab (Zedelgem, Belgium). KCl (99.5%) and NaI (99.5%) were purchased from AppliChem (Darmstadt, Germany) and LiCl (99%) from Fisher Chemical (Loughborough, UK). CsCl (99%), NaBr (99.5%), NH4Cl (99.5%), H2SO4 (96%), HClO4 (70%), HCl (37%) and 1,4-dioxane (99.9%) were obtained from Acros Organics (Geel, Belgium). The silicone solution in isopropanol was purchased from SERVA Electrophoresis GmbH (Heidelberg, Germany). All chemicals were used as received without further purification.
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10

Synthesis and Characterization of Metallic Nanoparticles

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NaNO3 (>99.0% pure, Sigma Aldrich), NaClO4 (>98.0% pure, Sigma Aldrich), NaCl (biological grade, Fischer Scientific), H2SO4 (99.9999% pure, Alfa Aesar), and Na2SO4 (99.9955% pure, Alfa Aesar) were used as received and diluted in Millipore water (>1 MΩ resistivity). NaNO3 and H2SO4 were used as scavengers, NaClO4 for electrochemical roughening and as a background electrolyte, and NaCl and Na2SO4 as background electrolytes. Colloidally synthesized nanoparticles (100 nm BioPure Silver Nanospheres, Nanocomposix, and 100 nm BioPure Gold, Nanocomposix) were concentrated by centrifuging 1.5 mL of nanosphere solution at 10,000 rpm for 10 min. 1 mL of supernatant was decanted off and the nanoparticles were redispersed in the remaining supernatant by sonication for 2 min. SEM revealed that the actual sizes were 95 nm and 94 nm for the silver and gold nanospheres, respectively (SI Appendix, Fig. S16).
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