Beer-Lambert Law:
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The Beer-Lambert Law describes the relationship between the absorption of light and the properties of the material through which the light is traveling. It is fundamental to quantitative spectroscopy and analytical chemistry.
The calculator uses the Beer-Lambert Law equation:
Where:
Explanation: The law states that absorbance is directly proportional to the concentration of the absorbing species and the path length of the light through the sample.
Details: Accurate concentration determination is crucial for quantitative analysis in chemistry, biochemistry, pharmaceutical sciences, and environmental monitoring. It enables precise measurement of solute concentrations in solutions.
Tips: Enter absorbance (typically between 0.1-1.0 for best accuracy), extinction coefficient (specific to the compound and wavelength), and path length (usually 1 cm for standard cuvettes). All values must be positive.
Q1: What is the valid absorbance range for Beer-Lambert Law?
A: The law is typically valid for absorbance values between 0.1 and 1.0. Values outside this range may show deviations due to instrumental limitations or non-linear effects.
Q2: How do I find the extinction coefficient for my compound?
A: Extinction coefficients are compound-specific and wavelength-dependent. They can be found in chemical databases, literature references, or determined experimentally using standards of known concentration.
Q3: Why is path length important?
A: Path length affects the amount of light absorbed. Longer path lengths result in greater absorption for the same concentration, making the measurement more sensitive.
Q4: What are common sources of error?
A: Common errors include stray light, improper blank correction, sample turbidity, chemical reactions during measurement, and deviations from ideal Beer-Lambert behavior at high concentrations.
Q5: Can this be used for mixtures?
A: For mixtures, the total absorbance is the sum of individual absorbances. Multiple wavelength measurements and matrix algebra are typically required to determine individual concentrations.