why KBr is used in FTIR SPECTROSCOPY and why is it necessary
to triturate KBr during FTIR analysis?

Answer Posted / bem nyax

This method exploits the property that alkali halides become plastic when subjected to pressure and form a sheet that is transparent in the infrared region. Potassium bromide (KBr) is the commonest alkali halide used in the pellets. Cesium iodide (CsI) may also be used to measure the infrared spectrum in the 400 to 250 cm-1 low-wavenumber region. 
The preparation method for 13 mm-diameter pellets is described below. Approximately 0.1 to 1.0 % sample is well mixed into 200 to 250 mg fine alkali halide (the example of KBr is used below) powder and then finely pulverized and put into a pellet-forming die. A force of approximately 8 tons is applied under a vacuum of several mm Hg for several minutes form transparent pellets. Degassing is performed to eliminate air and moisture from the KBr powder. Inadequate vacuum may result in easily broken pellets that scatter light. Before forming the KBr powder into pellets, pulverize it to 200 mesh max. and then dry at approximately 110 °C for two to three hours. Note that rapid heating can oxidize some of the KBr powder to KBrO3, causing a brown discoloration. After drying the powder, store it in a desiccator. 
When performing measurements, the background can be measured with an empty pellet holder inserted into the sample chamber. However, background measurements on a pellet holder with a pellet of KBr only, that contains no sample, can correct for infrared light scattering losses in the pellet and for moisture adsorbed on the KBr.

Reference >> http://www.shimadzu.com/an/ftir/support/ftirtalk/talk8/intro.html

Is This Answer Correct ?    14 Yes 0 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development

1106


i want model written test paper for the post of analyst in IOCL(indian oil corporation ltd) any one pls help me

2189


4. Describe the operation of the Craig apparatus. Chapter.3 Equilibrium Processes in Separations

2164


in dissolution if one bowl got 70 percent 2nd bowl got 80 percent and 3rd bowl got 90 percent then how proceed?

340


What is the difference between chromatographic purity and related substances?

794






Why we select scan range from higer wavelength to lower wavelength in uv visible spectroscopy and ftir spectroscopy ? .

463


What is the formula for relative diffrence for standard solution in solution stability in validation?

312


Which products will produce when acetic anhydride reacts with Ter-butanol, Sec-butanol, Iso butanol, Dimethylamine etc.

2397


we can use expired sample for validation and analyst qualification?

307


What is viod volume and peak purity in HPLC?

2347


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?

2217


we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion

1361


analytical method validation require to with respect to release specification or shelf life specification?

285


If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?

532


What is the requirement for brazil in the analytical method vslidation comparr to ich?

276