FeSO4Ferrous Sulfate
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Hence, FRAP decreased by 20.60% (decrease from 5.68 to 4.51 mM FeSO4) and CUPRAC decreased by 6.45% (decreasing from 1.24 to 1.16 mM trolox).
M3: NaCl 0.8, KCl 0.8, CaCl2 0.1, Na2HPO4 2.0, MgSO40.2, FeSO4 0.1, 8.0 Glucose, NH4 Cl 2.0 [8].
CaCO3 0.02 g, FeSO4.7H20 0.01 g, agar 18 g in one liter) was prepared and sterilized at 121 oC in 15 lbs
The results were expressed as [micro]mol of ferric antioxidant capacity (the FRAP value) and were compared with the standard curve prepared using FeSO4, 7[H.sub.2]O 1 mM in a range of concentrations from 125 to 1000 [micro]M.
Serrano-Lopez et al., "Antioxidant properties of xanthones from Calophyllum brasiliense: prevention of oxidative damage induced by FeSO4," BMC Complementary and Alternative Medicine, vol.
Na3, Fe(NO3)3, FeSO4, folic acid, glucose, H2Se03, HEPES, hypoxanthine, insulin human, KCI, linoleic acid, lipoic acid, MgC12, MnC12, MnSO4, myo-inositol, Na2HPO4, Na2Se03, Na2SiO3, NaC1, NaH2PO4, NaHCO3, sodium pyruvate, sodium acetate, NH4V03, NiC12, nicotinamide, phenol red, polysorbate 80, putrescine, putrescine 2HC1, pyridoxine HO, pyridoxal Ha, riboflavin, SnC12, thiamine HO, thymidine, vitamin B12 and ZnSO4.
Fig 7: Order of preference of various medicaments * Formocresol 60.8% * Ca(OH)2 12.5% * MTA 12.5% * Glutaraldehyde 7.5 % * FeSO4 6.7% Note: Table made from bar graph.
Ether extractable fat ( Percent) = W3/ Sample weight (1.0g) x 100 Crude protein ( Percent): Took 1.0 g of oven dried plant material 30 ml of concentrated H2So4 and 5 g digestion mixture [K2So4; CuSo4; FeSo4 (100g; 10g; 5g)] was added and then digested the material on the gas heater in Kjeldhal digestion flask, cooled it and made up the volume to 100 ml.
The reactive solution composed of 10 [micro]L nicotine (20 ppm), 90 [micro]L [H.sub.2][O.sub.2] (3%), 1890 [micro]L sodium acetate buffer (50 mM, pH 5.6), and 10 [micro]L ferrous sulfate heptahydrate (100 mM) solutions was adjusted to 200 ppb nicotine, 0.135% [H.sub.2][O.sub.2], and 0.5 mM FeSO4. The ultrahigh performance liquid chromatography (UHPLC) gradient was set at 30 mins in one experiment.
The redox initiator system, CHP, sodium pyrophosphate, dextrose, and ferrous sulfate (FeSO4) was used without further purification.
Table 2: Values of Zn, Ni, and Fe amounts in the deposit, total mass of the deposit, % (Zn, Ni, and Fe contents), current efficiencies % (Zn--Ni--Fe deposits) and thickness of the deposit on stainless steel (2 [cm.sup.2]), and electrochemical corrosion measurements of the deposit on steel (0.196 [cm.sup.2]), deposited galvanostatically from a bath containing 0.10 M ZnSO4, 0.10 M FeSO4, 0.10 M NiS[O.sub.