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Some disadvantages of wet chemical analysis include the potential for human error in manual handling of reagents, limitations in detecting trace amounts of substances, and the time-consuming nature of the techniques involved. Additionally, wet analysis may require specialized equipment and trained personnel, making it costly and less accessible compared to other analytical methods.

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Why orsat analysis is a dry analysis?

Orsat analysis is considered a dry analysis because it measures the composition of a gas sample without any moisture present. The gas sample is dried before analysis to ensure accurate results and to eliminate the presence of water vapor, which can affect the readings of the analysis.


What is wet ashing and dry?

Wet ashing involves heating a sample with a nitric acid solution to decompose organic material into ash. Dry ashing involves heating a sample in a furnace to completely combust organic material to ash without the use of acid. Both methods are used for preparing samples for further analysis, such as inorganic elemental analysis.


What is wet chemical method?

The wet chemical method is a technique used in chemical analysis that involves dissolving a sample in a liquid reagent to perform a chemical reaction. It is commonly used for qualitative and quantitative analysis of chemical compounds in various industries such as pharmaceuticals, environmental monitoring, and food testing. The results obtained from the wet chemical method help in determining the composition and properties of a sample.


What are the advantages and disadvantages of modacrylic?

Advantages of modacrylic: flame retardant, soft texture, quick drying, and resistant to chemicals. Disadvantages of modacrylic: prone to pilling, low melting point, can be stiff if not properly treated, and may lose shape over time.


What are the disadvantages of an internal standard in gas chromatography?

Disadvantages of using an internal standard in gas chromatography include the need for additional sample processing steps, the potential for introducing errors during the mixing of the internal standard with the sample, and the possibility of the internal standard not behaving identically to the target analyte during the analysis.