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3.1. SOIL PHYSICS 125<br />

3.1.4 Near Infrared Imaging Spectroscopy of Water States in Porous Silicate<br />

Media<br />

Participating scientist Nadiya Smolyar, Kurt Roth, Bernd Jähne<br />

Abstract We have examined capillary and adsorbed water in porous silicates (quartz sand, clay,<br />

silica gel) by using of Near Infrared Image Spectroscopy, NIRIS. The interaction of water with the<br />

porous media, the spatial distribution of water content, and the physics of different water states, as<br />

well as their transformation will be studied.<br />

Figure 3.4: Spectral transmission images of capillary water in sand at different times t1(a) < t2(b),<br />

showing the distribution of water content and state.<br />

Background NIRIS examinations are important<br />

for understanding the molecular mechanisms<br />

of water interacting with porous silicate media.<br />

Even today, the role water plays in the quality of<br />

soils and in further environmental effects is not<br />

unterstood in many aspects.<br />

Methods and results Capillary and adsorbed<br />

water is examined spectrally in both dry and<br />

saturated silica specimens. The frequency spectra<br />

are measured in near infrared (ν = 3300 −<br />

11000cm −1 ; λ = 700 − 3000nm) with a UV-NIR<br />

spectrometer Scan 500 (Varian,USA).<br />

The frequency values, the characteristic intensities,<br />

and appearance of new spectral bands of water<br />

in SiO2 media yield numerous data as elasticity<br />

constants, bond geometries, and adsorption<br />

mechanisms. The analysis of OH vibration<br />

modi permits the determination of water content<br />

along with changes of water states in the silicate<br />

medium. We have found that the water content<br />

can be determined best by using the intensive<br />

bands 2νOH and νOH + ν2, and the water state<br />

according to the bands 3νOH and 2νOH+ν2.<br />

A new innovative NIRIS method has been developed<br />

for investigations on the spectral optical<br />

qualities of water in porous specimens with spatial<br />

resolution. To this end, an imaging multispectral<br />

32-channel CCD spectrometer has been set up.<br />

The corresponding CCD camera takes sequences<br />

of spectral images at certain wavelengths using<br />

band pass filters. The images are by spectral digital<br />

image processing analyzed.<br />

Outlook/Future work The NIRIS concept<br />

permits the determination of molecular interaction<br />

forces of water on solid boundaries and micro<br />

pores together with the physics of water states and<br />

measuring the water distribution on porous silicates.<br />

The results will aid in gaining deeper understanding<br />

of the thermodynamical, structural,<br />

and dynamic characteristics of water in silicate<br />

media. We are planning the following investigations<br />

of water in porous silicate media:<br />

-Relation of multiple light scattering for determination<br />

of true values of water absorption; -<br />

Investigation of different water states, their spatial<br />

distribution and concentration; -Investigation<br />

of the stationary and dynamic water regimes; -<br />

Spectral analysis of the influence of physical factors<br />

on the interaction of water and medium; -<br />

Investigation of multi-phase systems with various<br />

kinds of intermolecular interaction.<br />

Main publication Smolyar N., M. Korniyenko<br />

and K. Roth (2005) Near Infrared imaging spectroscopy:<br />

A new tool for studying water states<br />

and movement in porous media, ’Geophysical Research<br />

Abstracts’, EGU05-A-07910.<br />

Smolyar N. (2003) Bildgebende Spektroskopie<br />

an Pflanzenblättern. Dissertation, <strong>Universität</strong><br />

Heidelberg, Interdisziplinäres Zentrum <strong>für</strong> Wissenschaftliches<br />

Rechnen (IWR), 195 S.<br />

Garbe C., N. Smolyar, M. Korniyenko and<br />

U. Schurr (2003) Water relations in plant leaves,<br />

Springer Verlag. Lecture Notes in Computer Science,<br />

LNCS 19: 377-401.

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