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260 J. GALVAN-MIYOSHI AND R. CASTILLO<br />

and<br />

where<br />

U(L) + CL<br />

C0 = 2 (1 + R)<br />

3 (1 − R)<br />

∂U<br />

(L) = 0, (11)<br />

∂z<br />

and CL = 2 (1 + Ref )<br />

3 (1 − Ref ) .<br />

Now, us<strong>in</strong>g Eqs. 8, 9, and J± expressions, we obta<strong>in</strong> the<br />

follow<strong>in</strong>g expressions for the fluxes:<br />

J−(0) = v Al<br />

2 C0l∗ �<br />

C0l∗ �<br />

l∗<br />

+ =<br />

2 3<br />

vAl<br />

(3C0 + 2) , (12)<br />

12C0<br />

and<br />

∗ vAll<br />

J+(L) = −<br />

12C0<br />

(C0 + α∗ ) (3CL + 2)<br />

(L + CLl∗ , (13)<br />

− zo)<br />

JT = |J−(0)| + |J+(L)| = vAl<br />

12C0<br />

�<br />

(3C0+2) (y+CL−α<br />

×<br />

∗ ) + (C0+α∗ ) (3CL+2)<br />

(y+CL−α∗ �<br />

, (14)<br />

)<br />

where y = L/l ∗ . F<strong>in</strong>ally, the static transmission coefficient<br />

is given by:<br />

T ∗ =<br />

(C0+α ∗ ) (3CL+2)<br />

(3C0+2) (y+CL−α ∗ ) + (C0+α ∗ ) (3CL+2)<br />

. (15)<br />

This f<strong>in</strong>al expression for T ∗ depends on α ∗ , L, and l ∗ as well<br />

as on R and on Ref through C0 and CL. As we shall show<br />

below, all variables <strong>in</strong>volved <strong>in</strong> this equation can be measured<br />

to obta<strong>in</strong> l ∗ . α ∗ can be obta<strong>in</strong>ed through a backscatter<strong>in</strong>g experiment,<br />

as described <strong>in</strong> Appendix C, while R is calculated<br />

with the procedure given by Kaplan et al. [10], us<strong>in</strong>g:<br />

l ∗ =<br />

This expression is our basic work<strong>in</strong>g equation to obta<strong>in</strong> l ∗<br />

from experimental data.<br />

2. Experimental section<br />

Materials. Polystyrene microspheres (Bangs Labs Inc,<br />

USA) <strong>of</strong> different diameters were used to prepare the water<br />

suspensions and also functioned as microsphere tracers <strong>in</strong> the<br />

DWS experiments to measure l ∗ . Glass cells were supplied<br />

by Hellma GmbH (Germany) and by Starna Cells Inc (USA)<br />

with different optical <strong>path</strong>s (2 mm to 4 mm) and different<br />

cross sections (3.0 × 4.2 mm and 2.8 × 3.7 mm). Water was<br />

milli-Q water (Nanopure-UV, USA; 18.3MΩ). Microspheres<br />

were added to water while stirr<strong>in</strong>g. Water suspensions were<br />

usually prepared with volume fractions < 0.04.<br />

Integrat<strong>in</strong>g sphere throughput. An <strong>in</strong>tegrat<strong>in</strong>g sphere<br />

(Oriel Newport, USA) was used to obta<strong>in</strong> l ∗ <strong>in</strong> the colloidal<br />

suspensions. Here, <strong>light</strong> detection was carried out by a photo<br />

multiplier tube (Hamamatsu Ltd, Japan) attached at the wall<br />

sphere. We obta<strong>in</strong>ed the <strong>in</strong>tegrat<strong>in</strong>g sphere throughput by<br />

where<br />

and<br />

R = 3C2 + 2C1<br />

. (16)<br />

3C2 − 2C1 + 2<br />

�<br />

C1 =<br />

π/2<br />

0<br />

�<br />

C2 =<br />

π/2<br />

0<br />

R(θ) cos θ s<strong>in</strong> θdθ<br />

R(θ) cos 2 θ s<strong>in</strong> θdθ.<br />

Ref can be calculated us<strong>in</strong>g the procedure presented <strong>in</strong> Appendix<br />

A, where the follow<strong>in</strong>g formula is obta<strong>in</strong>ed:<br />

with<br />

and<br />

D1 = −C1 + RspTwb<br />

D2 = C2 + RspTwb<br />

Ref = 3D2 − 2D1<br />

, (17)<br />

3D2 + 2D1 + 2<br />

�π<br />

π/2<br />

�π<br />

π/2<br />

Two(θ) cos θ s<strong>in</strong> θdθ,<br />

Two(θ) cos 2 θ s<strong>in</strong> θdθ.<br />

F<strong>in</strong>ally, solv<strong>in</strong>g for l ∗ <strong>in</strong> Eq. 15 and tak<strong>in</strong>g <strong>in</strong>to account the<br />

transmittance along the wall cells, we obta<strong>in</strong>:<br />

(3C0 + 2) TcdL<br />

(C0 + α ∗ ) (3CL + 2) (T1T0 − Tcd) + (CL − α ∗ ) (3C0 + 2) Tcd<br />

. (18)<br />

measur<strong>in</strong>g the <strong>in</strong>cident power, P 0 , at the front entrance port<br />

<strong>of</strong> the <strong>in</strong>tegrat<strong>in</strong>g sphere, and then ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g the laser <strong>light</strong><br />

power; constant the <strong>light</strong> power at the detection port <strong>of</strong> the<br />

<strong>in</strong>tegrat<strong>in</strong>g sphere, P 0 d<br />

Rev. Mex. Fís. 54 (3) (2008) 257–264<br />

, was measured. The throughput is<br />

b = P 0 d /P 0 . The <strong>in</strong>tegrat<strong>in</strong>g sphere is part <strong>of</strong> the <strong>in</strong>strument<br />

described below.<br />

Transport <strong>mean</strong> <strong>free</strong> <strong>path</strong>, l ∗ . We measured transmittance<br />

and reflectance for the suspensions under study with an<br />

<strong>in</strong>tegrat<strong>in</strong>g sphere as shown <strong>in</strong> Figs. 1 and 2, where a laser<br />

beam (λ = 514.5 nm) expanded and collimated with a 2<br />

mm p<strong>in</strong>hole was sent at normal <strong>in</strong>cidence <strong>in</strong>to the entrance<br />

port <strong>of</strong> the sphere. To measure l ∗ , we followed Eq. (18),<br />

where the total transmittance Tcd for a sample-cell system<br />

was measured, as described <strong>in</strong> Eq. (6), us<strong>in</strong>g the <strong>light</strong> power<br />

collected by the sphere detector <strong>in</strong> three different cases: when<br />

the sample is placed at the entrance port (transmission geom-<br />

), when it is placed at the reflection port (reflection<br />

etry, P T d<br />

geometry, P R d ), and when there is no sample on any port, P 0 d .

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