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Objectives. Dimensional changes occur in set dental alginate impression materials when
immersed in disinfecting solutions. In this contribution the dimensional changes of two algi-
nates in two disinfecting solutions, and for two specimen thicknesses, have been studied.
20 November 2011
Methods. The dimensional changes of two commercial alginates (Blueprint Cremix and
Hydrogum), have been measured, in distilled water and two disinfecting solutions (Perform
ID/sodium hypochlorite), using a traveling microscope, at 5 min intervals over a period of 1 h.
Keywords:
Samples of simple geometry have been studied, namely rectangular strips with thicknesses
Cross contamination
Immersion disinfection
Results. In all cases, both alginates continuously shrank with time, in the three immersion
Alginates
liquids, over the hour of measurement, indicating transfer of water from the alginate into
Shrinkage
the external water or disinfecting solution. The t1/2 shrinkage plots were generally linear,
Expansion
but with an intercept on the t1/2 axis, indicating the possibility of an initial expansion at
Diffusion
very short times. In most cases, the ratios of slopes for both thicknesses were 1.331.54, in
Disinfectants
contrast to the theoretical value of 2. Perform ID however gave anomalous results for the
1.5 mm thick samples. At 10 min their shrinkage was 1.341.72%, compared with 0.42% to
0.67% in the other two media.
Signicance. The effects of thickness observed were not in accord with simple Fickian theory
because of the various ions diffusing into and out of the alginate. Moreover, the water content
of the alginate decreased consequent on the cross-linking process.
2012 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.
1.
Introduction
have been reported, for example, by Jennings and Samaranayake [2], and Look et al. [3].
There are generally two disinfecting methods available,
namely the use of aerosols or immersion in disinfecting solutions [4]. Clearly, either method should not compromise the
dimensional stability of the impression material. With alginate impression materials, dimensional changes are known
Corresponding author at: Dental Physical Sciences (Oral Growth and Development), Francis Bancroft Building (2nd Floor), Queen Mary,
University of London, Mile End Road, London E1 4NS, United Kingdom. Tel.: +44 020 7882 5982; fax: +44 020 7882 7089.
E-mail address: M.Patel@qmul.ac.uk (M.P. Patel).
1
Faculty of Dentistry, SEGi UniversityCollege, Malaysia.
0109-5641/$ see front matter 2012 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.
doi:10.1016/j.dental.2012.03.013
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2.
2.1.
Materials
2.2.
Methods
2.2.1.
Sample preparation
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d e n t a l m a t e r i a l s 2 8 ( 2 0 1 2 ) 749755
2.2.2.
As soon as a given sample was set, it was placed in a atbottomed polytetrauoroethylene (PTFE) mold. The sample
was anchored on a xed pin at one end of the trough, and
a second pin was carefully inserted into the other end of the
sample, taking care not to penetrate the sample completely.
Then the sample was covered with the appropriate liquid
(30 ml).
Dimensional changes were measured with a traveling
microscope (Chesterman) to 0.001 cm, for each material in
DW and the two disinfecting solutions. First a reading was
obtained for the xed pin. Then the microscope was focussed
on the opposite edge of the sample, closest to the movable
pin, and the second reading was taken, to obtain a baseline
reading. The subsequent readings were taken every 5 min up
to 1 h, on the sample edge closest to the movable pin.
Initially the data were plotted as percentage linear shrinkage against time, followed by percentage linear shrinkage
against the square root of time (t1/2 min1/2 ); the latter was to
establish the role of diffusion in the samples.
2.3.
1.5 mm
3.0 mm
Air
Distilled water
Sodium hypochlorite
Perform ID
NS
S1
S2
NS
NS
NS
NS
NS
Statistical analysis
3.
Results
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1.5 mm
Blueprint
Hydrogum
NS (NS)
S2 (NS)
3 mm
S1 (S1 )
S3 (S3 )
Thickness (mm)
Hydrogum
Na hypochlorite (%)
0.42 (0.2)
0.20 (0.7)
0.66 (2.0)
0.32 (1.3)
*
1.5
3.0
1.5
3.0
Blueprint
Perform ID (%)
0.25 (1.6)
0.42 (1.3)
0.67 (2.4)
0.42 (1.7)
1.72 (3)
0.06 (0.5)
1.34 (2.3)
0.12 (0.6)
Signies expansion.
Table 4 Analysis of graphical data giving the slope, slope ratio and intercept on t1/2 axis, for the 1.5 and 3 mm alginate
samples (derived from % linear shrinkage versus t1/2 plots).
Figure
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Material
Blueprint (DW)
Hydrogum (DW)
Hydrogum (NaOCl)
Blueprint (NaOCl)
Hydrogum (PID)
Slope
1.5 mm
3.0 mm
Ratio, S
1.5 mm
0.33
0.14
0.20
0.40
0.50
0.23
0.10
0.15
0.26
0.10
1.44
1.40
1.33
1.54
5.00
0.90
6.40
1.70
1.21
0.00
3 mm
1.94
0.86
1.90
1.21
1.92
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alginates (of two thicknesses) in the three media. Table 4 summarizes the slopes and intercepts of the data in Figs. 25, that
is the gures where there is a major linear region (Fig. 6, for
Hydrogum in Perform ID, has markedly different proles). The
following equation applies to these linear regions:
L
1/2
(%) = S(t1/2 t0 )
L
(1)
4.
Discussion
Dt 1/2
L2
(2)
D 1/2 1
2L
(3)
(4)
where S1.5 is the slope of the 1.5 mm samples and S3.0 the
slope of the 3 mm samples. Hence the ratio of the 1.5 mm samples slope is predicted to be twice that of the 3.0 mm samples.
However, in this contribution (Table 4), although the t1/2 plots
were generally linear in Figs. 26, the ratios of the slopes of
the two plots, for the two alginates immersed in NaOCl and
DW, were between 1.33 and 1.54 and 5 for Hydrogum in Perform ID, compared with the theoretical value of 2. Clearly in
most cases, simple Fickian Diffusion Theory cannot explain
the anomalous results seen in Figs. 26. Therefore further factors need to be taken into consideration, as highlighted below,
in order to attempt to explain the anomalous results obtained.
It is worth noting in this context, that Nallamuthu et al. [6]
studied alginate weight loss in air, which gave linear t1/2 plots,
but for the two thicknesses studied, the slope ratios were 1.2,
and again the thickness ratios were 2:1. Hence, the effects of
thickness on dimensional changes in air were similar in character to those studied here, in DW and disinfecting solutions.
This indicates that the relationship between linear shrinkage
and mass uptake is not a simple one.
One further factor that should be considered is the entropy
change consequent on cross-linking as the material sets. This
will reduce the equilibrium water content of the alginate, and
needs incorporation into the theoretical approach, as follows:
an extension of the Fickian diffusion theory is given by Gibbs
modication of the diffusion theory, which replaces Ficks Law
[16] by:
F=
c
RT x
(5)
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where is the chemical potential, F is the ux and c, the concentration at point x, measured for example, from one of the
surfaces or the center plane; c will equal v1 , if concentration
is measured as the volume of diffusant (water) as a fraction
of the volume of the whole polymer system, v2 = 1 v1 = 1 c.
This has been studied by Muniandy and Thomas [17] to analyze the water uptake of hydrophobic elastomers containing
water soluble moieties.
The Flory Huggins Theory [18,19] is a possible model for the
current system, where:
(2 V1 v2 1/3 )
= RT ln(1 v2 ) + v2 + v2 +
Mc
(6)
where is the chemical potential, R is the universal gas constant, T is the temperature (K), v2 the volume fraction of
polymer (alginate), v1 the volume fraction of the liquid, the
solvent parameter, V1 the molar volume of the solvent (water),
2 the density of the polymer, and Mc the molecular weight
between cross-links. In Eq. (6), considering the four terms
within the square brackets, terms 1, 2 and 4 give the entropy
for a given v2 value; the third term (containing ) gives the
corresponding enthalpy (H) value.
It must be stressed Eq. (6) is being used as a guide. It is not
known whether it is quantitatively valid for the alginate-water
system; furthermore the alginate formulations studied here
contain a considerable quantity of ller. Nevertheless it should
be a useful guide. If the nal term in Eq. (5) (i.e. [2 V1 v2 3 ]/Mc ) is
omitted, the equation is for the interaction between the polymer and liquid. In this case if < 0.5, is negative for all values
of v2 , and the polymer and liquid are miscible in all proportions (i.e. the polymer is soluble in the liquid). If the polymer
is cross-linked, it will swell until = 0.
The case of the alginate impression material is interesting
in that on mixing the powder and water, the alginate dissolves
(partially) in water to give a paste, which then sets (cross-links)
later. When cross-linked, Eq. (6) applies, and it is suggested,
becomes positive (i.e. the system now has more water than
is compatible, and it is expelled from the sample, resulting in
shrinkage). This process is diffusion controlled, but not necessarily governed by simple Fickian equations.
It is presumed in this work that the dimensional changes
observed for the two commercial alginate materials are consequent on weight changes; Nallamuthu et al. [6] have shown
this to be the case with water and articial saliva, who
demonstrated an initial expansion in water with some alginate materials, followed by shrinkage. They suggested that
on immersion of the alginate in water, there is some uptake
due to the presence of soluble ions in the set alginate matrix.
However on the entry of water, these ions diffuse out, thus
reversing the chemical potential, so that water then diffuses out with consequent shrinkage. In this contribution, the
shrinkage on immersion in water has been explained by the
fact that when the alginate sets (cross-links), this decreases
the entropy of mixing, resulting in the equilibrium concentration of water in the alginate decreasing, so that excess water
is expelled from the alginate, albeit diffusion controlled.
The implication for the current work is clear; standard
Fickian Theory does not necessarily apply, and explains why
simple Fickian prediction of thickness dependence of t1/2 is not
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5.
Conclusions
references
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