I'm studying the adsorption of scale inhibitors onto nanoparticles and rock formation. My blank solution is brine (Si and Mg brine) + scale inhibitors. The wavelength is somewhere around 250 to 260 nm.
Negative absorbance values in UV-VIS analysis can occur due to several reasons, including errors in sample preparation, instrumental issues, or chemical interactions. Here are a few potential reasons why you might be getting negative absorbance in your experiment:
Instrumental Issues: Negative absorbance can occur if the baseline is not properly set or if there is an issue with the instrument's detector. You can try recalibrating your instrument or checking for any hardware issues.
Sample Preparation Errors: If your blank solution is not correctly prepared, you may observe negative absorbance values. Make sure that your reagents are correctly measured and mixed.
Chemical Interactions: The scale inhibitors you are using may be reacting with other components in the solution, leading to negative absorbance values. You can try changing the pH or solvent of your sample to see if this changes the absorbance values.
Wavelength Selection: The wavelength you have chosen might not be optimal for your analysis. You may want to try scanning a wider range of wavelengths to identify the peak absorbance and then focus your analysis on that range.
It is essential to troubleshoot the issue to determine the cause of the negative absorbance values. Once the source of the problem is identified, you can take appropriate steps to rectify it.
you can use X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM), can be used to analyze the surface chemistry and morphology of nanoparticles and rock formations before and after adsorption of scale inhibitors. These techniques can provide information on the chemical bonding between the scale inhibitors and the surface of the nanoparticles or rock formations, as well as the changes in surface morphology induced by adsorption.