1 / 14

Dynamic Light Scattering

Dynamic Light Scattering. S. Ramanathan, Dept. Chem. Engg., IIT-Madras. Simplified theoretical background. Theory. Problems faced during experiments. Issues. Suggested solutions. Soln. Theory.

verlee
Download Presentation

Dynamic Light Scattering

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Dynamic Light Scattering S. Ramanathan, Dept. Chem. Engg., IIT-Madras Simplifiedtheoretical background Theory Problems faced during experiments Issues Suggested solutions Soln

  2. Theory Small, spherical particles (less than 3 micron size) in liquid undergo brownian motion. Smaller particle move faster. Motion Light passing through the suspension (particle + liquid) will be scattered by the particles. This happens when the refractive index of the particles are different from that of the liquid Scatter Intensity vs angle is called static light scattering. Here, light detector is placed at some angle, and the intensity of scattered light is measured for some time and the average value is used Static Scattering

  3. Theory Many detectors are placed at various angles and the “intensity vs angle” data is analysed. This is useful for particles over 1 micron size Static Intensity vs time is measured at a fixed angle (usually 90 degrees). The scattered light fluctuates because of movement of particle scattering it. Think of doppler effect. This is not the same, but somewhat similar in idea. A fast response detector, at a fixed angle, is used. This is useful for particles less than 3 micron size Dynamic

  4. Measurement Auto correlation vs time is meaured. Don’t ask what this is (i.e. if you want to know, please google). Using a model, the particle size distribution is calculated Measured Particle Size Distribution Correlation curve Model

  5. Measurement The number of signals (counts per second) is also given. Usually it will be in kcps (kilo cps) or Mcps. More is better. Counts

  6. Model Assumptions Single particle scattering effects can be compard with analytical solutions. Multi particle scattering (i.e. high concentration) give incorrect results Single Non spherical particles can not be compared with analytical solutions. So only a ‘sort of’ diameter can be calculated. This is the diameter of spherical particle that will give similar fluctuations. Spherical

  7. Issues Too high a concentration gives very nice looking correlation curves, but incorrect (usually less than actual) diameter. If particle dia is 200 nm, the diameter given by the instrument may be 20 or 50 nm! X Single Non spherical particles can not be compared with analytical solutions. So only a ‘sort of’ diameter can be calculated. This is the diameter of spherical particle that will give similar fluctuations. X Spherical

  8. Issues Too low a concentration gives very noisy correlation curves, and possibly incorrect diameter. Counts will be low and decrease (or remain stable) with dilution Single X Particles settling over time give ‘unstable’ suspension. The correlation curves may look OK, but the diameter measured over time will change Unstable

  9. Issues Correlation curve should go to zero on the right side, for good samples. If not, it means that the solution is dirty (i.e.large particles are present) Dust Correlation curve (good sample) Correlation curve (BAD sample)

  10. Solution Identify concentration effects. A general rule of thumb is “dilute 5 times and measure”. Repeat (i.e. dilute 25 times and measure). Counts should DECREASE with dilution. If they increase, you have too much concentration. Note : Counts may appear to be low to begin with! Dilute and remeasure. Conc Dilute Until “counts vs dilution” remains stable OR counts decrease with dilution. If you can’t dilute (e.g. some sample property of interest depends on dilution), then you can’t use our DLS. You can try other DLS instrument which claim to handle concentrated solutions, but I don’t have any experience with them. Soln

  11. Solution Non spherical particles can not be compared with analytical solutions. So only a ‘sort of’ diameter can be calculated. This is the diameter of spherical particle that will give similar fluctuations. X Spherical No Solution. The best that can be done is to estimate the spherical particle(s) that will give similar correlation curve. There is no DLS model for non spherical particles, in our software Soln

  12. Solution Too low a concentration gives very noisy correlation curves, and possibly incorrect diameter. Counts will be very low (10 or 20 kcps) and will decrease (or remain stable) with dilution. Single X Concentrate the suspension, perhaps by centrifugation. One can use a more sensitive detector (avalance photo diode) for low concentrations, but we don’t have it at present. Soln

  13. Solution Repeat the experiments. A general rule of thumb is “1 min” experiments, repeated 5 times, at a given concentration. If data (dia and counts) change over time, then… Unstable No Solution If your sample is inherently unstable. Our DLS can’t handle it. Soln

  14. Solution Correlation curve should go to zero on the right side, for good samples. If not, it means that the solution is dirty (i.e.large particles are present) Dust Use clean water to make the samples. Millipore water with 0.2 micron filter is good. If sample inherently has large particles, you can’t use DLS. If other liquids (e.g. acetone) are present, then use semiconductor grade materials Soln

More Related