Why only hydroxy naphthol blue indicator is used for standardisation of 0.05M EDTA solution instead of solochrome Black T or Euriochrome Black T indicator which is used for all sample analysis with 0.05M EDTA solution?

Suppose we prepared pH buffer solution in lab.and calibrate against NIST solution, and same shall going to used upto 30 days. is it possible to stable pH and appearance? suggest?

Meghmani Organics,

How to prepare 1000ppm methylene blue solution

principle of dissolution

Combitic Global Caplet,

How to choose concentration of LOQ solutions for RS analysis? Example.

Abbott, Indoco Remedies,

Question 65 – A differential equation is given as y” + 5y’ + 6y = 0, y(0) = 2 and y’(0) = 3. By using Laplace transform, an engineer has correctly produced the equation L {y} = (2s + 13) / [(s + 2)(s + 3)] = A / (s + 2) + B (s + 3). (a) Find the values of A and B. (b) The inversed Laplace transform of 1 / (s + a) is given by exp (-at) where a is a constant. If the statement : L {y} = 9 L { exp (-2t) } - 7 L { exp (-3t) } is correct, find the equation of y as a function of t as a solution to the differential equation stated in the beginning of this question. When L {d} = 9 L {b} - 7 L {c}, then d = 9b - 7c with b, c and d are unknowns.

How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample

CHEMICAL MATERIAL BALANCE - EXAMPLE 2.3 : A 1.5 weight % aqueous salt solution is concentrated to 4 weight % in a single-effect evaporator. The feed rate to the evaporator is F = 7500 kg / h and the feed is at 85 degree Celsius. The evaporator operates at 1 bar. By assuming that only pure solvent of water exists in the form of vapor from the feed, calculate the flow rate of such vapor V.

Why dissolution test performed on six jar?

Mylan,

How we Can Select Selection Of Dissolution Parameters Like(RPM ,Apparatuses, Sampling Time, Volume of Media)

Question 90 - In the calculation of the growth of bacteria, absorbance, A in spectrophotometry is used. According to Beer-Lambert Law, A = e x l x c where A is the absorbance of the solution (no unit), l is the distance of light travels through the solution (in cm), e is the molar absorptivity or the molar extinction coefficient [ in L / (mol.cm) ]. For a particular solute and fixed path length : As / Ao = Cs / Co where Ao is the observed signal for a known concentration Co, and As is the observed signal for a sample concentration Cs. (a) For a cell concentration of 560 cells / mL, a spectrophotometre gives an absorbance reading of 1.0. A mixture of concentration 3600000 cells / mL can be diluted in several operations, with each operation having a dilution of 1:20. How many dilutions should be made so that the concentration of this mixture can be calculated within a range of A = 0.0 to 1.0. (b) In another experiment, a sample tube of 1 cm in width is used. Let A = 0.06 and e = 0.0012 ml / (cell.cm). Find the cell concentration of the sample.

How we define validity of any Reagent , Indicator and Volumetric Solutions

Question 94 - The resolution of separation, Rs for chromatography is given by the formula Rs = (difference in retention time) / (average width at the base). In a chromatogram, 3 peaks a, b and c are found. Average widths W at the bases of the solutes are : Wa = 20 s, Wb = 40 s, Wc = 30 s. Resolutions of separation, Rs for solutes b and c in comparison to a are 2 and 4 respectively. The differences in retention times T for b and c in comparison to a are (Tb - Ta) and (Tc - Ta), Ta = Tc - Tb : (a) Form 2 equations involving Rs as a function of Wa, Wb, Wc, Ta, Tb and Tc. (b) Find the values of Ta, Tb and Tc.

we have already using static credit check, but for a particular customer we want dynamic credit check from next month how to do this (for one customer only )since it s only for one customer we need to do in master data only, should not go for configuration settings. please provide possible solutions

Accenture,

Question 95 - The following formula is used as a reference : (analyte signal) / (internal standard signal) = (f-factor) x (concentration of analyte) / (concentration of internal standard). A solution containing 3 mM of analyte and 4 mM of internal standard gave peak signals of 2 and 3 mamps respectively. Another similar solution containing 2 mM of analyte and 1 mM of internal standard gave peak signals of 1 and 4 mamps respectively. Find the average f-factor.