Analytical techniques for nucleation in studies in lipids: Advantages and disadvantages
Crystallization is generally considered a 2-step process. The 1st step, nucleation, involves the formation of molecular aggregates with a critical size great enough to become stable. During the 2nd step, nuclei grow and develop into crystals. Distinguishing between nucleation and growth constitutes...
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2004
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paper:paper_00221147_v69_n9_pR185_Cerdeira2023-06-08T14:46:21Z Analytical techniques for nucleation in studies in lipids: Advantages and disadvantages Activation-free energy of nucleation Analytical techniques Induction time Nucleation Crystallization is generally considered a 2-step process. The 1st step, nucleation, involves the formation of molecular aggregates with a critical size great enough to become stable. During the 2nd step, nuclei grow and develop into crystals. Distinguishing between nucleation and growth constitutes a major challenge in lipid crystallization studies. Thus, it is of great importance to discuss the information obtained from the different techniques that are usually used to study nucleation behavior such as nuclear magnetic resonance (NMR), differential scanning calorimetry (DSC), rheological techniques, light-scattering techniques such as turbidimetry and scanning diffusive light scattering (SDLS), polarized light microscopy (PLM), and laser polarized optical sets such as laser polarized-light turbidimetry (LPLT). Techniques to describe the nucleation process must be very sensitive to disregard growth. When crystallization is followed by methods such as DSC, NMR, and rheological measurements, at times, small amounts of crystals are present in the melt before any solids are detected. Clearly, at this stage, well beyond the induction time for nucleation (τ), these methods are measuring crystal growth. Techniques of low sensitivity for solid fat contents lower than 0.1% must not be used to evaluate nucleation effects. Sensitive turbidimeters with detectors that saturate below 0.3% solid fat content give good results as do scanning diffusive light-scattering equipment. Although the PLM technique is sensitive enough for these kinds of studies, an understanding of important basic concepts is essential. Laser optical sets are the most appropriated methods to study nucleation in fats systems. 2004 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00221147_v69_n9_pR185_Cerdeira http://hdl.handle.net/20.500.12110/paper_00221147_v69_n9_pR185_Cerdeira |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Activation-free energy of nucleation Analytical techniques Induction time Nucleation |
| spellingShingle |
Activation-free energy of nucleation Analytical techniques Induction time Nucleation Analytical techniques for nucleation in studies in lipids: Advantages and disadvantages |
| topic_facet |
Activation-free energy of nucleation Analytical techniques Induction time Nucleation |
| description |
Crystallization is generally considered a 2-step process. The 1st step, nucleation, involves the formation of molecular aggregates with a critical size great enough to become stable. During the 2nd step, nuclei grow and develop into crystals. Distinguishing between nucleation and growth constitutes a major challenge in lipid crystallization studies. Thus, it is of great importance to discuss the information obtained from the different techniques that are usually used to study nucleation behavior such as nuclear magnetic resonance (NMR), differential scanning calorimetry (DSC), rheological techniques, light-scattering techniques such as turbidimetry and scanning diffusive light scattering (SDLS), polarized light microscopy (PLM), and laser polarized optical sets such as laser polarized-light turbidimetry (LPLT). Techniques to describe the nucleation process must be very sensitive to disregard growth. When crystallization is followed by methods such as DSC, NMR, and rheological measurements, at times, small amounts of crystals are present in the melt before any solids are detected. Clearly, at this stage, well beyond the induction time for nucleation (τ), these methods are measuring crystal growth. Techniques of low sensitivity for solid fat contents lower than 0.1% must not be used to evaluate nucleation effects. Sensitive turbidimeters with detectors that saturate below 0.3% solid fat content give good results as do scanning diffusive light-scattering equipment. Although the PLM technique is sensitive enough for these kinds of studies, an understanding of important basic concepts is essential. Laser optical sets are the most appropriated methods to study nucleation in fats systems. |
| title |
Analytical techniques for nucleation in studies in lipids: Advantages and disadvantages |
| title_short |
Analytical techniques for nucleation in studies in lipids: Advantages and disadvantages |
| title_full |
Analytical techniques for nucleation in studies in lipids: Advantages and disadvantages |
| title_fullStr |
Analytical techniques for nucleation in studies in lipids: Advantages and disadvantages |
| title_full_unstemmed |
Analytical techniques for nucleation in studies in lipids: Advantages and disadvantages |
| title_sort |
analytical techniques for nucleation in studies in lipids: advantages and disadvantages |
| publishDate |
2004 |
| url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00221147_v69_n9_pR185_Cerdeira http://hdl.handle.net/20.500.12110/paper_00221147_v69_n9_pR185_Cerdeira |
| _version_ |
1768543499022499840 |