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Abstract
Until now, the choice of materials for seed pelleting has been mostly empirical. We have analysed coating materials
(silicate powder A, clay B and hydrophobic clay C ) and their water-transfer properties. Seed-pelleting materials were
studied with conventional soil-analysis techniques. An original device for studying water transfer through a thin layer
of powder was designed to simulate the transfer of water from the soil to the seed, through the pelleting material.
Different parameters were studied: particle-size distribution, water-retention curve of materials, thickness of powder,
influence of concentration of adhesive in pelleting, etc. The sintered glass on which the powders were placed in the
device constituted a limiting factor. The major component, a silicate powder (A), consisting of large particles, is
responsible for the general structure of the pelleting. Introduction of clay (B) gave intermediate properties between
A and C to water-transfer capacity. Hydrophobic clay (C ) can be used to control the incoming flow. The particle-
size distribution and wettability of materials have a direct impact on the transfer capacity of the powder. High
adhesive concentration had a negative effect on water transfer. These parameters and the formulation have a direct
impact on imbibition of pelleting materials. Objective tools, like the analytical methods used in this study, enable
water-transfer parameters and consequences on imbibition of coated seed to be understood. © 1999 Elsevier Science
B.V. All rights reserved.
Keywords: Pelleting materials; Water flow measurement; Porosity; Wettability; Seed; Thickness; Adhesive
1161-0301/99/$ – see front matter © 1999 Elsevier Science B.V. All rights reserved.
PII S 11 6 1 -0 3 0 1 ( 9 8 ) 0 0 0 50 - 1
58 P. Grellier et al. / European Journal of Agronomy 10 (1999) 57–65
L.) with clay acted as a barrier to oxygen transfer found nothing in the literature related to their
and to the opening of the radicule. water-transfer properties.
Pelleting modifies the germination of seeds,
according to their thickness and the nature of
these components. Pelleting thickness, like tegu- 2. Materials and methods
ment thickness, acts directly on the oxygen made
available to the embryo. Thus, it may be preferable For industrial reasons, it is not possible to give
that the pelleting is as thin as possible and that it the exact nature of the pelleting. The materials
does not absorb too much water ( Tonkin, 1979). used in the different experiments were (1) silicate
The nature of the components is important for powder A, (2) clay B, (3) clay C with a special
water transfer within the pelleting material. For a treatment, and (4) adhesive agent D. Clay C
given thickness, the structure influences the germi- received a hydrophobic treatment. Different com-
nation. Durrant and Loads (1986) showed that positions of the pelleting were produced by mass:
the heavy clay pelleting, used for sugarbeet seeds AB (A 94.5% and B 5.5%); ABB (A 85%, B 15%);
in England until 1984, delayed and reduced the ABC (A 85%, B 5% and C 10%) and ABCD (A
germination in humid soil. A lighter and more 85%, B 5%, C 10% and D). The purpose of the
porous structure gave 5–10% more plants, com- experiment was to describe the effects of elements
pared to clay pelleting, in humid conditions. with different properties on the pelleting. The
Direct application of a supplementary granular coating process used the pelleting technique with
layer of active charcoal (Sharples, 1981) around the adhesive agent D (Schiffers and Fraselle, 1988).
the lettuce seed (Lactuca sativa L.) gave more The particle-size distributions of the different
rapid, complete and uniform seedling emergence materials were studied by means of a particle
than coatings made from standard materials. A counter (Coulter Multisizer, Miami, FL).
more porous structure seemed to allow a better The water retention curve was obtained using
the classical sand-box method (Stakman et al.,
distribution of oxygen. Active charcoal absorbed
1969) for water potentials higher than −10 kPa,
the endogenous growth inhibitors secreted by the
and using Richards’ apparatus (Richards, 1947)
seed.
for water potentials between −50 kPa and
Most studies on soil-water flow have been car-
−1.6 MPa.
ried out under saturated conditions (Prost, 1984;
A novel device was designed to study the influ-
Tamari et al., 1993) and on a centimetre or metre
ence of the pelleting material on water transfer
scale. Some of them dealt with gaseous exchange under steady-state conditions. Two closed cham-
(Reyzabal and Bazan, 1992). The in-situ water- bers that simulated the soil and seed were separated
transfer properties of coated seeds are difficult to by the pelleting material ( Fig. 1). Communication
study since the seeds only measure a few mil- was established between the chambers through
limetres, and the flow is low. sintered glass (porosity: 40–100 mm in diameter;
We studied pelleted materials using standard soil thickness: 4 mm; diameter: 36 mm). The upper
analysis techniques of a specific pelleting, designed chamber represented the soil-water potential, Y ,
to represent the components of a commercial 1
and the lower chamber represented the seed-water
pelleting. Mixes were made to observe influences potential of the seeds. A saturated CaCl , 6H O
on structure and water transfer. Our first aim was 2 2
solution was used to set this lower potential, Y
to completely characterize the structure of materi- 2
(relative humidity: 33%). These conditions cor-
als. To take this characterization further, we responded to the best seed-storage conditions
designed a device whose physical structure imitated commonly used (Ashton, 1992; Grabe, 1992).
real conditions (from gaseous phase flow to satu- Preliminary tests were carried out in order to
rated flow), enabling the parameters of water detect a limiting sorption ability of the saturated
transfer through pelleted seed to be analysed. salt solution. The sorption capacity of the satu-
The pelleting materials used for this study were rated salt solution was at least twice the maximum
not specific to the seed coating. Nevertheless, we total outflow observed.
P. Grellier et al. / European Journal of Agronomy 10 (1999) 57–65 59
The different pelleting materials presented a 3.2. Water flow through the pelleting materials
unimodal distribution (Fig. 4). The silicate powder
A was composed of various particles a few tens of The curves of water flow as a function of water
micrometres and above, whereas clay B had a potential in the soil are shown in Fig. 5. The results
smaller range of a few micrometres. were obtained after a steady-state regime had been
P. Grellier et al. / European Journal of Agronomy 10 (1999) 57–65 61
Fig. 5. Water flow after the steady state obtained through the sintered glass and pelleting material. A (silicate powder), B (clay), C
(clay-treated ), AB (mixed powder 94.5%, B/5.5%), ABC (mixed powder A/85%, B/5% and C/10%) and ABCD (mixed powder
ABC+adhesive coming from the pelleting).
established. They ranged from a few hours (silicate tial above −70 kPa. In contrast, the addition of
powder A, clay B) to 1 day (mixture ABC ). C led to a large shift in the water-flow curve
(Fig. 5). For ABC, a steady-state regime was
3.2.1. Flow through basic materials observed after only 30 h for a thickness of 16 mm
The water flow through silicate powder (A) and a soil-water potential of −10 kPa. The intro-
increased dramatically until a threshold value of duction of C delayed the establishment of a steady-
around −50 kPa was reached (Fig. 5). The flow state regime.
observed for clay B showed a progressive increase The final mixed powder ABCD (ABC+
in transfer conductivity from −1000 kPa and was adhesive) had a similar threshold but had a smaller
stabilized at around −50 kPa. A clay shrinkage, shift than the silicate powder A. The mixture
which broke up the continuity of the soil–powder showed a relative decrease in flow at a high
system, relative to material like silicate powder A, potential (−10 kPa), due to shrinkage.
was observed. This explains the decrease in flow
of B from −30 kPa. 3.3. Other flow parameters
The water flow for clay C was constant, irrespec-
tive of the soil-water potential applied. Only clay 3.3.1. Influence on thickness
C represented a barrier to water transfer when An increase in thickness of materials led to a
large differences in water potential existed. decrease in water transfer ( Fig. 6). This influence
was only observed under extreme conditions, i.e.
3.2.2. Flow through mixed powder at a low soil-water content (15% water by weight;
In the mixed powder AB, the introduction of B water potential Y =−1.5 MPa) and high poten-
soil
(5.5% of mass) contributed to a significant increase tial differences (water content 40%;
in flow ( Fig. 5) as observed at a soil-water poten- Y =−4.2 kPa).
soil
62 P. Grellier et al. / European Journal of Agronomy 10 (1999) 57–65
Table 1
Influence of the thickness on the water transfer
Conditions: saturated salt solution CaCl , 6H O (RH 33% −152 MPa); powdered materials in powder (thickness ranging from 4 to
2 2
16 mm) on the sintered glass (4 mm).
P. Grellier et al. / European Journal of Agronomy 10 (1999) 57–65 63
4. Discussion
understand the parameters and consequences on At low soil humidity, the flow and resistance
the pelleting structure and properties. results indicated that water was transferred in the
The majority of materials presented a similar gaseous phase. With the increase in water potential
sigmoid curve between flow and soil-water poten- difference, and when the material was not purely
tial (Fig. 5). At high water potential, flow through hydrophobic, the filling of the pore network ena-
the various materials approached that of the bled a continuity of water film and an increase in
system alone. As the sorption capacity of the water flow. The material presented no further
saturated salt solution increased, the sintered glass obstacle to transfers, and its hydraulic resistance
restricted water transfer. A clear change in the decreased to near zero. The system consisted solely
properties of water transfer was observed once a of the sintered glass and the sorption capacity of
threshold value was reached. The transfer proper- the saturated solution, which then became the
ties of materials increased rapidly as a function of factors that limited water transfer.
potential. The variations in transfer rate may be explained
These observations are related to the wettability by the intrinsic properties of the adhesive or the
of materials and the porosity induced by the induced structure. The adhesive facilitated the
powder. The comparison with the water-retention water transfer (ABCD with 1 and 2.5% of D),
curve (Fig. 3) shows that for the wettable material for a soil-water potential of −200 kPa (Fig. 6).
(A, B and A+B combined ), pore filling corres- The adhesive was apparently not hydrophobic.
ponded to the increase in conductivity. Silicate However, we observed a decrease in flow with
powder A is a typical example of this behaviour higher concentrations (5% of D). Thus, it is reason-
(Fig. 10). If the material is hydrophilic, the pore able to assume that the induced structure may
distribution of powder has a direct impact on the alter the water flow inside the blocks. In the case
flow. Clay B was characterized by small particles, of the mixed powder ABC, which was non-wetta-
which resulted in a low porosity. The filling of ble, the local deformation of the network with
pores by capillarity was easier since they were capillary forces during imbibition enabled a higher
smaller. Silicate powder A, composed of large capacity transfer than in the presence of adhesive.
particles and having a coarse narrow porosity, This was more noticeable at stronger water poten-
became highly conductive as soon as water connec- tial differences with an increase in adhesive concen-
tivity was performed. The hydrophobic nature of tration. In contrast, too much adhesive filled the
the treated clay C prevents the material from being network porosity and hindered the establishment
imbibed and limited the water transfer in the of a continuous film by capillary forces and thus
liquid phase. affected the water-transfer capacity.
5. Conclusion