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Related Concept Videos

Mass Spectrometry: Molecular Fragmentation Overview01:20

Mass Spectrometry: Molecular Fragmentation Overview

The ionization of a molecule into a molecular ion inside the mass spectrometer causes instability in the molecule's structure due to the loss of an electron. This eventually leads to the fragmentation or breaking of some bonds in the molecule. The fragmentation occurs predominantly at specific bonds to yield relatively stable fragments.
One type of fragmentation pattern is the cleavage of a single bond in the molecular ion. The cleavage leads to a radical and a cation. The cleavage can occur at...
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this species into the...
Mass Spectrometry: Cycloalkane Fragmentation01:05

Mass Spectrometry: Cycloalkane Fragmentation

In mass spectrometry, cycloalkanes exhibit distinct fragmentation patterns due to the inherent stability of their molecular ions compared to linear or branched alkanes. The ring structure of cycloalkanes provides additional stability to the molecular ions, often resulting in prominent ion peaks in the mass spectrum.
For example, cyclohexane molecular ions have a mass-to-charge ratio (m/z) of 84, which tends to produce a stronger signal than linear alkanes like hexane. This stability comes from...
Mass Spectrometry: Branched Alkane Fragmentation01:29

Mass Spectrometry: Branched Alkane Fragmentation

This lesson delves into the mass spectrometry of branched alkane fragmentation. Branched alkanes possess secondary or tertiary carbon atoms, which generate relatively stable carbocations if the cleavage occurs at the branching point. The high stability of carbocations drives the instant fragmentation of branched alkanes. Accordingly, the branched alkane's molecular ion peak is very weak or invisible in the mass spectra, especially in comparison to a linear alkane.
Mass Spectrometry: Long-Chain Alkane Fragmentation01:18

Mass Spectrometry: Long-Chain Alkane Fragmentation

The molecular ions of linear alkanes prefer to fragment at the carbon-carbon bond away from the end of the chain since the cleavage of an inner bond creates a stable carbocation and a stable radical. Consequently, the mass signals of linear alkanes feature intense peaks in the middle of the mass-to-charge ratio plot with weaker peaks on either end. The fragmentation of each carbon-carbon bond with the release of a methyl group in each splitting leads to prominent peaks in the mass spectra...

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Related Experiment Video

Updated: Jun 22, 2026

High-throughput, Microscale Protocol for the Analysis of Processing Parameters and Nutritional Qualities in Maize (Zea mays L.)
05:55

High-throughput, Microscale Protocol for the Analysis of Processing Parameters and Nutritional Qualities in Maize (Zea mays L.)

Published on: June 16, 2018

Structural evolution of maize stalk/char particles during pyrolysis.

Peng Fu1, Song Hu, Lushi Sun

  • 1State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan, PR China. fupengsklcc@gmail.com

Bioresource Technology
|June 2, 2009
PubMed
Summary
This summary is machine-generated.

Maize stalk char becomes more aromatic and carbonaceous with increasing pyrolysis temperature. Structural changes, including pore opening and shrinkage, occur as volatile matter is lost and carbon ordering increases.

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Published on: October 9, 2018

Area of Science:

  • Biomass pyrolysis
  • Materials science
  • Chemical engineering

Background:

  • Maize stalk is a significant agricultural residue.
  • Understanding its pyrolysis behavior is crucial for biomass conversion.
  • Char structural evolution impacts its applications.

Purpose of the Study:

  • To investigate the structural evolution of maize stalk char during pyrolysis.
  • To determine the effects of temperature on char properties.
  • To correlate structural changes with pyrolysis conditions.

Main Methods:

  • Pyrolysis of maize stalk at temperatures from 200 to 900°C.
  • Characterization using thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), helium density measurement, and N(2) adsorption/desorption.
  • Ultimate analysis.

Main Results:

  • Char yield decreased significantly up to 400°C.
  • Aromatization and carbonization increased with temperature, starting around 350°C.
  • Volatile matter removal below 500°C caused pore opening.
  • High temperatures induced softening, melting, fusing, and structural ordering, with shrinkage above 500°C.

Conclusions:

  • Maize stalk char undergoes significant structural transformation during pyrolysis.
  • Temperature is a key factor controlling aromatization, carbonization, and structural ordering.
  • The observed changes suggest potential for tailored char properties through controlled pyrolysis.