Авторы

  • N.B. Ruzikulova
    Navoi State University
  • H.M. Vapoev
    Navoi State Mining and Technological University

DOI:

https://doi.org/10.71337/inlibrary.uz.arims.115478

Ключевые слова:

Acetylene water acetaldehyde acetone CCF (cadmium calcium phosphate) CaO CdO P2O5 MgO.

Аннотация

The composition of the raw materials used in the synthesis of acetaldehyde, the catalyst CCF (cadmium calcium phosphate), was analyzed and determined. Based on the analysis results, active cadmium oxide was isolated from the KKF catalyst and new catalysts were prepared. Acetaldehyde and acetone were synthesized from the prepared catalysts. 


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ACADEMIC RESEARCH IN MODERN SCIENCE

International scientific-online conference

144

CHROMATO-MASS-SPECTRAL ANALYSIS OF THE SYNTHESIZED

SUBSTANCES

Ruzikulova N.B.

Vapoev H.M.

Navoi State University

Navoi State Mining and Technological University

Email: ruziqulovagina4@gmail.com

https://doi.org/10.5281/zenodo.15752834

Annotation.

The composition of the raw materials used in the synthesis of

acetaldehyde, the catalyst CCF (cadmium calcium phosphate), was analyzed and
determined. Based on the analysis results, active cadmium oxide was isolated
from the KKF catalyst and new catalysts were prepared. Acetaldehyde and
acetone were synthesized from the prepared catalysts.

The qualitative and quantitative properties of the synthesized substances

were analyzed and confirmed by chromato-mass spectrometry methods.

Keywords:

Acetylene, water, acetaldehyde, acetone, CCF (cadmium calcium

phosphate), CaO, CdO, P

2

O

5

, MgO.

A mass spectrometer determines the mass and structure of a substance.

This step works as follows:

Each molecule ionizes (loses or gains electrons).
Ions move through an electric/magnetic field.
The device determines the mass-to-charge ratio (m/z) of ions.
The result is a mass spectrum - a graph showing the intensity and mass of

each ion.

In this method, each substance separated by chromatography is

sequentially sent to a mass spectrometer where it is detected. These two stages
are connected sequentially in one system.

Pharmaceutical - in the determination of pure or mixtures of medicinal

products,

criminalistics - in the detection of narcotic drugs or poisons,
ecology - determination of pollutants in air, water, soil,
food industry - used to detect preservatives or pesticides in food.
The obtained spectra were identified using the i-NIST standard library. The

composition of the studied sample was calculated based on TIC (Total Ion
Chromatogram) - total ion chromatogram data.


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ACADEMIC RESEARCH IN MODERN SCIENCE

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145

Figure 1. Chromato-mass spectrum of acetaldehyde

Figure 2. Chromato-mass spectrum of acetone

The mass spectrum of acetaldehyde (Fig. 1) is characterized by the

following main peaks:

~29 -100% (main peak) [CHO]

+

fragment - most stable and widespread;

~44 - average peak, molecular ion [C

2

H

4

O]

+

- ionic form of the entire

molecule;


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ACADEMIC RESEARCH IN MODERN SCIENCE

International scientific-online conference

146

~43 - upper peak [CH

3

CO]

+

- simple fragment, often found in ketones and

aldehydes;

~15 - Low [CH

3

]

+

- methyl group fragment.

The strongest peak in this spectrum is at m/z = 29, representing the [CHO]

+

fragment of the acetaldehyde molecule.

At the same time, the molecular ion peak at m/z = 44 confirms the total

mass of the substance.

The mass spectrum of acetone (Fig. 2) is characterized by the following

main peaks:

~43 - 100% (main peak) [CH

3

CO]

+

- this fragment is very characteristic of

ketones;

~58 - approximately 80%, molecular ion [C

3

H

6

O]

+

- whole acetone

molecule;

~15 - low [CH

3

]

+

- methyl fragment;

~29 - less intense [C

2

H

5

]

+

- ethyl fragment.

The peak at m/z = 58 indicates the molecular ion of acetone.
m/z = 43 is the main fragment, which is the most intense and stable

[CH

3

CO]+ ion in the spectrum.

Chromatography-mass spectrometry is a highly accurate, cost-effective, and

versatile technology for chemical analysis. It is one of the most reliable tools in
chemistry for structural, qualitative, and quantitative analysis of substances.

References:

1.

Vinarskiy V.A. Chromatography // Course of Lectures in Two Parts: Part 1.

Gas chromatography. Scientific and Methodological. Moscow 2003.- P. 172.
2.

Nifantev I.E., Ivchenko P.V. Practical Course of Nuclear Magnetic

Resonance Spectroscopy. Methodological development. Moscow. 2006.
- P. 13-197.

Библиографические ссылки

Vinarskiy V.A. Chromatography // Course of Lectures in Two Parts: Part 1. Gas chromatography. Scientific and Methodological. Moscow 2003.- P. 172.

Nifantev I.E., Ivchenko P.V. Practical Course of Nuclear Magnetic Resonance Spectroscopy. Methodological development. Moscow. 2006.

- P. 13-197.