This document discusses applications of UV-visible spectroscopy. It provides examples of UV-visible spectroscopy applications in food analysis for quality control, food color analysis, antioxidant analysis, flavor and aroma analysis, and nutrient analysis. It also discusses using online UV-visible spectrophotometers for drinking water quality monitoring and process control. Finally, it outlines five steps for reading and interpreting UV-visible spectrophotometric results to determine the structure of chemical compounds, including observing spectrum patterns, absorption bands, absorbance values, identifying possible chromophores, and observing band shifting.
UV-Visible spectroscopy is considered as an important tool in the analytical chemistry.
Most powerful tool available for the study of atomic and molecular structure.
- Most commonly used techniques in clinical as well as chemical laboratories.
- Used for the qualitative analysis and identification of chemicals.
ain use is for quantitative determination of different organic and inorganic compounds in solution.
Basically, spectroscopy is related to the interaction of light with matter.
As light is absorbed by matter, the result is an increase in the energy content of the atoms or molecules.
The absorption of visible or ultraviolet light by a chemical compound will produce a distinct spectrum.
UV-Visible light range- 200-800 nm
Visible range: 400-800 nm
UV range: 200-400 nm
UV-Visible spectroscopy is considered as an important tool in the analytical chemistry.
Most powerful tool available for the study of atomic and molecular structure.
- Most commonly used techniques in clinical as well as chemical laboratories.
- Used for the qualitative analysis and identification of chemicals.
ain use is for quantitative determination of different organic and inorganic compounds in solution.
Basically, spectroscopy is related to the interaction of light with matter.
As light is absorbed by matter, the result is an increase in the energy content of the atoms or molecules.
The absorption of visible or ultraviolet light by a chemical compound will produce a distinct spectrum.
UV-Visible light range- 200-800 nm
Visible range: 400-800 nm
UV range: 200-400 nm
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2. APPLICATIONS IN FOOD ANALYSIS
Quality control
Food color analysis
Antioxidant analysis
Flavor aroma analysis
Nutrient analysis
3. Application#11.6. Application 1:
Applications of Online UV-Vis
Spectrophotometer for Drinking Water
Quality Monitoring and Process Control
Online UV-Vis spectrophotometers can be effective and practical for
measuring water quality parameters continuously and without the need for
physical filtration using software particle compensation techniques. The
water industry has deployed more online instruments to monitor water quality
from catchment to tap for online and in-situ measurements as well as the
treatment process control. However, the reputation of lacking reliability of
the measurements is the general restriction of these instruments to expand to
a wider range of water quality management applications. This section
discusses those issues and limitations.
4. Conclusion:
This research paper covers the practical aspects of the employment of online
UV-Vis spectrophotometers for water quality monitoring and process control,
particularly techniques for industrial applications. The use of online UV-Vis
spectrophotometers for drinking water quality management in the literature
has been discussed. Commonly employed online UV-Vis instruments for
drinking water have been discussed. Water quality parameters, including
UV254, color, DOC, turbidity and nitrate, can be directly generated from the
built-in algorithms of the online UV-Vis instruments. Site-specific calibrations
can be conducted to improve the accuracies of the measurements if the
generic built-in algorithms are under-performing for a water source.
5. 1.7. Application 2: How to Read and
Interpret UV-VIS Spectrophotometric
Results in Determining the Structure of
Chemical Compounds
Step 1: The overall spectrum pattern is observed. Usually for each spectrum
each compound has a distinctive band pattern, and can be easily recognized.
Several peaks will appear in the UV-VIS spectrum. Figure 3 shows an
absorption band at 217 nm with ε = 17.900 indicating an unsaturated
aldehyde or ketone-α, β (Pavia, D et al. 2022).
Step 2: The number and intensity of each absorption band that appears is
observed. The number of absorption bands indicates the number of
chromophore contained in the sample compound. It is possible that there is
more than one absorption band for one type of chromophore. The second
step: The number and intensity of each absorption band that appears is
observed. The number of absorption bands indicates the number of
chromophore contained in the sample compound. It is possible that there is
more than one absorption band for one type of chromophore.
6. Step 3: The absorbance magnitude and wavelength for the emerging
absorption band are identified. The value of ε is important in
determining the structure associated with the allowed electron
transitions. This value also affects the chromophore would be
expected of the compound to be analyzed. The amount of ε and the
wavelength range is typical for any chromophore.
Step 4: Possible chromophore can be identified based on the data
amount, the identity, the magnitude of ε, and wavelength for each
absorption band that appears. Each identified chromophore has its
own characteristic UV-VIS spectrum band. Based on the existing
literature (Kristianingrum, 2013; Pavia et al., 2008; Skoog et al.
2016), there are several characteristic bands produced in the UV-Vis
spectrum for various chromophore and compounds.
7. Step 5: Shifting / shifting in the absorption band is observed. Substituents bound to
the chromophore structure can change the position and intensity of the absorption
band of the chromophore. Ausochrome is a substituent that can increase the
absorption intensity and wavelength of a chromophore. Common ausochromes are
methyl, hydroxyl, alloxy, halogen, and amino groups. There are four types of
shifting that can affect the absorption of a chromophore, namely bathochromic (the
maximum transfer of absorption to a longer wavelength or lower energy from blue
to red), hypsochromic (the maximum transfer of absorption from red to ultraviolet
occurs at shorter wavelengths or higher energy), hyperchromic (wavelength shift
that occurs due to an increase in absorption intensity), hypochromic (wavelength
shift that occurs due to a decrease in absorption intensity). Changes in the shift in
wavelength or absorption intensity can be illustrated in Figure (below) (Suhaimi, H
et al. 2021)
8. Conclusion:
Determination of the structure of chemical compounds can be done by
analyzing the resulting UV-VIS spectrum pattern. The analysis can be carried
out based on the steps described above.