Formula:
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Definition: This calculation determines column efficiency in chromatography by relating retention time to peak width (as standard deviation).
Purpose: It helps analytical chemists evaluate the performance of chromatographic columns and separation efficiency.
The calculator uses the formula:
Where:
Explanation: The number of theoretical plates is proportional to the square of retention time and inversely proportional to the square of peak standard deviation.
Details: Higher plate numbers indicate better column efficiency and sharper peaks, leading to improved resolution between analytes.
Tips: Enter the retention time in seconds and standard deviation (both must be > 0). Standard deviation can be determined from peak width at baseline (W = 4σ).
Q1: What is a good number of theoretical plates?
A: Values vary by column type, but generally >10,000 plates/meter is good for HPLC, >5,000 for GC.
Q2: How is standard deviation related to peak width?
A: For Gaussian peaks, baseline width (W) ≈ 4σ, and half-width ≈ 2.355σ.
Q3: Does this formula work for asymmetric peaks?
A: This formula assumes Gaussian peaks. For tailing peaks, other methods may be more accurate.
Q4: Why square both terms in the formula?
A: The squaring accounts for the relationship between peak variance (σ²) and retention.
Q5: How does this relate to resolution?
A: Resolution between peaks improves with the square root of plate number (√N).