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10 1016@j Seppur 2018 09 074
10 1016@j Seppur 2018 09 074
PII: S1383-5866(18)31324-8
DOI: https://doi.org/10.1016/j.seppur.2018.09.074
Reference: SEPPUR 14972
Please cite this article as: O. Yıldırım GÜLSOY, E. GÜLCAN, A new method for gravity separation: Vibrating
table gravity concentrator, Separation and Purification Technology (2018), doi: https://doi.org/10.1016/j.seppur.
2018.09.074
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A new method for gravity separation: Vibrating table gravity concentrator
a
Hacettepe University, Mining Engineering Department, Mineral Processing Division, 06800, Beytepe,
Ankara, Turkey
Abstract
This paper discusses recently developed gravity concentration equipment, namely vibrating
table, and reports detailed descriptions of the equipment in terms of principles of design and
their effects on operational parameters. Vibrating table originally combines the known
physical phenomena of a teetered bed, resistance to water flow, vibration, and density
differences. The resulting effect of these combined forces can also be manipulated by
integrated settings of feed rate, solid %, plate inclination, and water rate. Following the
detailed description of the equipment, mineral separation tests with two different chromite
ores obtained from industrial applications were performed in order to investigate the
performance of the laboratory scale vibrating table. While former chromite ore had low grade
with complex mineralogy and inadequate liberation, the latter had high grade consisting of
liberated lumpy chromite particles. Experimental studies were focused on investigating the
effect of plate inclination, removal of slimes, ore type, size classification, and particle size on
separation performance. Within the tests performed with -600 µm, -800 µm, and -1000 µm
high grade chromite ores under certain conditions, it was observed that increase in particle
size results in a dramatic increase in recovery, while % grade decreases slightly. In another
test with high grade chromite ore, sustainable product qualities were achieved up to a
recovery of 93.22% in comparison with the 66.08% achieved with a conventional shaking
table, within and approx. 47-48% final grade level. Additionally, product grades and
recoveries up to 50.20%-58.36% with deslimed -400 µm low grade chromite feed and
53.68%-67.45% with deslimed -200 µm low grade chromite feed were obtained, respectively.
chromite ore
1. Introduction
In its simplest definition, gravity concentration is a class of methods which take advantage of
the density differences among mineral particles [1-3]. As a result, particles of which densities
are different from each other have their own relative movement against the forces of the
gravity depending on the factors such as viscosity of the environment, resistance to the
motion in viscous environment, density, weight, particle size, and shape or a relevant
combination of them [4]. Although interest in gravity concentration dates back to Homer's
Odyssey according to Wills’ [5], cultivating for modern methods and technologies for the
equipment and application have been reviewed successfully. Some of the most popular
examples and successful applications are the ones with jigs or centrifugal jigs (gold bearing
sulfide minerals, tin, mineral sands, chromite, iron, coal, etc. [9-12]), centrifugal gravity
concentrators such as Knelson and Falcon (gold, copper, platinum, chromite ore, coal, etc.
[13-17]), teetered bed separators (coal, chromite, manganese, etc., [18-20]), FGX dry
separators (coal [21, 22]), air table separators (coal [23, 24]), dense medium separators such
as dense medium cyclone (coal and minerals [25, 26]), spiral concentrators (chromite, sand,
coal, iron, etc. [27-29]), shaking tables (chromite, gold, rare earth minerals [30-33]), and
multi-gravity separators (chromite, coal, graphite, rare earth minerals [34-37]). Among the
afore mentioned methods and equipment, shaking tables are one of the oldest yet the most
effective appliances allowing to process a wide range of minerals and coal having various
particle size ranges from 15 millimeters down to 10-15 microns [38] [5] [31]. Capacity of a
shaking table is in the range between 0.5 tons per hour and approx. 1.5-2 tons per hour
depending on the particle size processed. Therefore, it is usually a standard in the industry to
install tens of shaking tables in series or parallel in order to process excessive tonnages,
especially in chromite processing. Hence, new problems arise due to the required space for
Besides the wide range of use, easiness, and effectiveness of gravity concentration without
the need for any chemical intervention, low capacities of the equipment and increasing
demand for better production always made it the last resort to be considered when all other
methods fail. Therefore, search for enhanced gravity concentration methods are all in
progress either by investigating the better versions of current setups or attempting to invent
totally new perspectives based on gravity differences in order to achieve possible alterations
The purpose of this study is to investigate the performance of a recently developed gravity
concentration system, namely “vibrating table” [39], and highlight the effect of operational
parameters in altering the product qualities. Therefore, configured new system was revealed
in detail and exemplary chromite processing studies had been performed. Within the
experimental studies, vibrating table performance was investigated at various particle sizes
under different equipment specific parameters. For this purpose, either vibrating table was
integrated into some basic mineral processing flowsheets or used solely. Effect of size
classification and desliming prior to the operation was also investigated. Finally, performance
of a vibrating table in comparison with the shaking table had been tested under similar
conditions. Following the data collection, product qualities of each test and their possible
2. Equipment descriptions
The recently developed gravity concentration system namely “vibrating table” shown in
Figure 1 allows the particles to be separated from each other due to density differences [39].
A heterogeneous mixture of particles is fed to the inclined chute1 either dry or wet with a
substantial solid percent. Sample particles17 are contained in a teetered bed12, within of which
volume the denser particles14 move downwards at relatively higher velocities in comparison
with lighter particles13. Consequently, the submerged dense particles14 are transported
horizontally upward from the teetered bed through the serrated surface of the groove10 of the
inclined chute1 by linear vibration. Vibration frequency9 is controlled by a unit9 which can be
adjusted depending on the sample characteristics. Meanwhile, the light particles13 and those
above the layer of the teetered bed drag to the tailing stream by the water3&4 through the
inclination direction, and they are separated. Water within the process is supplied via wash
water4 (WW) and teetering water (TW) jets3. While WW4 cleans the concentrate from by-
passing lighter particles13, TW3 helps form the fluidized bed where the actual separation takes
place. TW rate3, and WW flow4 are the most important operational parameters which are
adjusted by a water rate adjustment unit, and solenoid valve control unit7, respectively.
Additionally, the water level of the teetered bed is also critical. Denser particles14 are drawn
away from the bed, travel horizontally upwards on the serrated surface of the groove10, and
leave the system through product discharge16. Inclination of the chute is set via a tilt
adjustment bar11 placed under the chute, which also effects water level cut point18 of the
teetered bed. Meanwhile, lighter particles13 having lower specific gravity tend to layer on the
top of the denser particles14. Consequently, with the effect of drag force of the water flow,
lighter particles13 leave the system from tail discharge15. It is important to note that, gravity
powered separation process is started after a steady state fluidized bed is formed. Therefore,
after reaching the steady state, properties of the bed forming material are constant unless
The inclined chute1 is vibrated via one or two magnetic vibration device(s) depending on the
width of the chute. This unit provides single-directional vibrations. The chute can be
manufactured to have a width of 20 cm to 100 cm and a length of 50 cm to 150 cm. The chute
is fixed to the magnetic vibration unit2 which is a ready-to-use system with amplitude and
frequency control. The unit is mounted on a horizontal steel plate5 whose inclination is
adjustable. The steel plate5 is mounted on the main frame6 (a table with four legs) to fix the
The groove10 on the inclined chute1 can be made of stainless steel, painted normal steel,
fiberglass, etc., a sufficiently hard and durable material. The serrated groove surface10 may
be smooth, rough or saw-toothed as the sandpaper surface. The surface of the groove10 can be
3. Experimental studies
In the experimental work, run of mine samples from two different operating chromite
processing plants in Sivas and Denizli regions of Turkey were studied. In order to evaluate
the method from different angles, dissimilar chromite samples had been selected according to
mineralogical, grade, liberation and lithological considerations. Chromite ore of Sivas region
had low initial grade and insufficient liberation degree in comparison with the Denizli
region’s ore. Therefore, characterization studies had been performed individually for each ore
as follows.
3.1.1. Characterization of the low grade chromite ore
Detailed characterization studies of the relatively problematic low grade chromite ore were
carried out on physical, chemical and mineralogical bases. Hence, particle size distribution,
specific gravity, mineralogy, and basic mineralization related to grain sizes were determined.
The brief mineralogy of the ore was determined by optical microscopy and XRD method,
while quantitative mineralogy and liberation analysis were carried out with scanning electron
microscopy. Specific gravity (SG) of the as-received sample was measured as 2.69 with a
pycnometer of which top particle size was 14.47 mm (f80=12.3 mm). Fe2+Cr2O4, Fe2O3, SiO2,
CaCO3, Mg2SiO4 (lizardite), and Mg(OH)2 contents of the low grade chromite ore were
5.48%, respectively. Previous studies and visual observations showed that chromite
liberation of this particular ore was starting below 600 μm [40] and reaches up to approx.
80% below 212 μm. Accordingly, sample preparation efforts were focused on crushing the
original sample down to 400 µm (f80=348 μm) and 200 µm (f80=151 μm), respectively.
X-ray Diffraction (XRD) analysis had also been performed with the main batch to determine
primary minerals along with the chromite [40]. Chromite ore showed reasonable peaks
related with the contents observed in chemical analysis. In the analysis of the XRD patterns,
Lizardite (Mg3Si2O5.OH), Brusit (Mg.OH) and chromite (Fe+2Cr2O4) minerals were primarily
determined.
Mineralogical analysis showed that the main mineral in the ore is forsterite, which is a
magnesium silicate mineral, and it is present in a very high amount such as 86%. Other major
minerals are brucite and chromite. Both minerals are found in approximately 5-5.5% of the
ore. The percentages of Cr and Fe in chromite were 46.46% and 24.94%, respectively.
Forsterite and brucite have lower density values than chromite concentration, which
About 15% of chromite is bonded with other minerals. Additionally, 13.46% of this amount
is originated from forsterite mineral. Forsterite is more free than chromite, with a total of
High grade chromite ore delivered to the laboratory was below 300 mm in size, having a
significant number of lumpy and high quality chromite particles within. Cr2O3, Fe2O3, SiO2,
Al2O3, and MgO contents of the high grade chromite ore were determined by chemical
analysis as approx. 33-38%, 24.30%, 4.63%, 13.38%, and 18.33%, respectively. Chromite
liberation of high grade ore was starting below 1000 μm and reaching up to approx. 75-80%
below 425 μm. Majority of the chromite (Cr2O3) was reported as free and liberated from the
host minerals providing a more convenient angle for concentration methodology design.
Therefore, lump particles in the original sample batch were initially classified into two
different grade batch by hand-picking. Hence, two distinct groups of sample batches having
approx. 32-33% and 37-38% chromite content were obtained, respectively. Due to the high
liberation tendency and % chromite grade, each sample group was ground below 1 mm
(f80=825 μm for the former and f80=812 μm for the latter). For more detailed examination,
additional size reduction had been performed with high grade chromite ore batches depending
on the application.
Following the sample preparation via subsequent crushing and grinding, various chromite
processing flowsheets either to apply solely using vibrating table or in combination with
other gravity type equipment were designed based on the properties of the sample batch.
Brief summary of the experimental methodology is given in Table 1. Initially, vibrating table
tests were performed with -400 µm and -200 µm low grade chromite samples under varying
plate inclinations of 9°, 7°, and 5° for the former and 4°, 3°, and 2° for the latter particle sizes
(Figure 2a). Following, same plate inclinations were applied to process -400 µm and -200
µm low grade chromite samples right after removing the slimes with hydrocyclone (Figure
2b). TW was kept constant in order to keep the solid ratio of the feed around 30% by weight.
WW was also set constant to 0.75 liters per minute (for a 20 cm chute opening) of water for a
clear observation of recovery changes related with the change in plate inclination.
In the experimental work with two distinct high grade chromite samples, while the former
one with approx. 32-33% chromite was directly fed to the vibrating table in three distinct size
fractions (namely -1000, -800, and -600 µm) (Figure 2a), latter with approx. 37-38%
chromite content was first classified with hydrosizer. 1st reservoir and a combination of 2nd,
3rd, and 4th reservoirs of hydrosizer were separately fed to the both vibrating table (Figure
3a) and shaking table (Figure 3b) in order to conduct a reasonable comparison between
sibling instruments. In the tests applied to hydrosizer products, two different quality product
were collected through the surface ending line of the shaking table along with a middling
product which is usually reprocessed (Figure 3b). Considering that the vibrating table
outputs consist of a concentrate and a tailing, an additional cleaner stage was applied to the
1st stage vibrating table tail which enabled a convenient comparison with shaking table
(Figure 3a). Nevertheless, combined products were also compared in terms of grade and
Finally, -600 µm high grade (approx. 37-38%) chromite sample was fed to the hydrocyclone
for the removal of the fines (d50=-75 µm) and clayey content (Figure 4). After
representatively sampling from the underflow (U/F) stream of the hydrocyclone, -600+75 µm
product was wet classified with a 212 µm screen forming two narrowly sized fractions
namely -600+212 µm and -212+75 µm samples. Then, -600+75 µm, -600+212 µm, and -
212+75 µm samples were fed to the vibrating table, separately. After first stage vibrating
table tests of three size fractions, each chromite concentrate and tail of each operation was
subjected to subsequent cleaner and scavenger stages in order to further increase final product
Within the tests performed with -1000, -800, and -600 µm fractions of 32-33% grade
chromite samples, concentrates of the first stage cleaning was re-processed through a second
stage. While plate inclination, TW, and feed rates were kept constant in both cleaning stages,
WW was increased from 0.5 to 1 lpm (for a 20 cm chute opening) in order to investigate if
further increase in final product quality could be achieved. In other words, while adjusting
WW rate, plate inclination was set to a moderate 8°, TW was controlled maintaining a solid
ratio of the feed around 30% by weight, and feed rate was set to a constant of approx. 0.25 t/h
Additionally, within each test, approx. 4.5-5 kg sample batches were used. Bed forming
inclined chute after reaching the steady state. It was also collected and evaluated separately
after each test to be used within the recovery calculations in order to better reflect the mass
balance of laboratory scale tests. In a real life-continuous vibrating table operation, bed
forming material can be neglected by directly sampling from products. Final chromite
Equation 1
where
Following the experimental studies, products of each test was collected, weighed, and %
Cr2O3 contents were analyzed. Vibrating table test parameters of low grade chromite sample
and product qualities were reviewed in Table 2. Also, change in chromite recoveries and
grades of final products depending on the particle size, plate inclination, and desliming were
presented in Figure 5a-d. Results showed that vibrating table performed best especially at
finer particle sizes and when the slime was fairly removed. These findings also corroborate
the mineralogical analysis results of low grade chromite ore. On the other hand, at higher
plate inclinations fine particles were also removed with the help of teetering and washing
water resulting with the highest recovery achievement with -200 µm feed (at plate inclination
of 4°). Even so, -200 µm deslimed feed at 4° plate inclination ensured the highest grade
(Figure 5d). Based on Figure 5a-d, it is safe to conclude that both grade and recovery
increase as the inclination of the plate of the vibrating table is increased. Although desliming
has positive effects on overall recovery, lower grades were observed with -200 µm deslimed
feed samples in comparison with -200 µm feed samples (Figure 5b and 5d). The only
exception to this behavior was observed with -400 µm deslimed feed (plate inclination=9°) at
which coarser than expected particles was presumably reported to the tailings provoking a
4.1.2. Effect of feed particle size and WW (wash water) rate on separation performance
All three -1000 µm, -800 µm, and -600 µm size fractions of the high grade chromite sample
having approx. 32-33% chromite were fed to the vibrating table under similar operating
parameters other than particle size and WW rate in order to observe their effects on
separation performance. In all tests, a second stage cleaning operation was applied to
chromite concentrate at relatively higher WW rates while keeping other operating parameters
constant. 1st and 2nd stage cleaning concentrates obtained under two different WW rates were
combined forming a single chromite product. Results of the separation tests were given in
combined products were presented in Figure 6a. Additionally, the effect of WW rate on %
chromite recoveries and % chromite grades of final products were given in Figure 6b and
Figure 6c, respectively. In Figure 6a, effect of particle size on Cr2O3 grade and recovery
were discussed on the basis of combined 1st and 2nd stage products. Results showed that
sufficient liberation at -600 µm particle size provoked a slightly higher grade. On the other
hand, loses were also higher resulting with the lack of the resistance to the WW and low G-
force action. With -1000 µm feed, grade of final product decreased down to 37.63 % Cr2O3,
while chromite recovery in the final product was increased up to 81.63% within a single stage
operation. In Figure 6b-c, effect of increasing solely the WW rate was presented while
keeping plate inclination (8°) and feed rate (0.15 t/h) constant (for a 20 cm chute opening) for
given particle sizes. Results showed that under WW rate of 1 lpm, although chromite
recovery was significantly lower at finer sizes in comparison with 0.5 lpm WW rate, %
chromite grades were higher due to obtaining a cleaner product. Similarly, higher WW rate
increased the % grade of final product of coarse size fraction (-1000 µm) slightly without any
significant decrease in % recovery of final product in comparison with 0.5 lpm WW rate.
The WW jet pipe of the equipment extends along the bed and stands perpendicular to the
flow. The diameter of WW pipe is less than 0.5 mm with holes drilled along at every 0.5-1
cm width, thus the water can be sprayed smoothly. The rate of WW should be set according
to plate inclination and feed particle size. WW is an important separation parameter and
should be provided intermittently, ideally with an opening and closing time interval in
between 0.5 seconds and 20 seconds resulting with a WW rate of 0.5 and 1.25 lpm,
respectively. When processing finer particle sizes, lower WW rates result in higher % grade
and % recoveries in final products, and vice versa while processing coarser sizes due to the
4.1.3. Effect of TW (teetering water), feed rate and solid % on separation performance
Chute of the laboratory scale experimental setup manufactured with the dimensions of 20 cm
in width ×5 cm in height ×50 cm in length. Due to the design principle, effective separation
takes place in teetered zone and flowing water film carry low density particles through tail
discharge while denser particles move down through product discharge (Figure 7). In order
to determine the solid percent within the system, water and material supplies of the operation
was instantly shut down after the steady state was reached. Solid % determination tests were
performed with -1000 µm high grade chromite sample under constant feed rate of 0.25 t/h at
varying TW rates. Plate inclinations of 11° and 5° were applied for each test separately.
Following, solid % measurements were carried out with the remaining material in chute and
results were presented in Table 4. It was observed that, although plate inclination and TW
have primary importance, solid % within chute does not change significantly with feed rate
after steady state is reached. It is also important to note that higher feed rates would only
increase loses to the tailings due to the chute’s effective volume limited by plate inclination
and TW rate. Additionally, higher TW rates also decrease the performance by over-teetering
the bed in separation zone resulting with the material loses through tailing discharge with
The ore to be separated within the device is fed dry from the water level cut point.
Considering the addition of water via TW and WW jets, a value in the range of approx. 11-
58% solids by weight was observed for the feed having 1000 µm top size. Outside these
limits of solid %, an efficient teetered bed could not be constructed. Therefore, an average
30% solids by weight was preferred throughout the experimental studies. In case of feeding a
Within the experimental studies, an inclined chute having a 20 cm product discharge width
was used. Under the conditions of 30 % feed solid by weight, 7° plate inclination, approx. 5
lpm TW rate, 0.75 lpm WW rate, and with a chute supposedly having 100 cm opening,
capacities for -1000 µm and -200 µm feeds was calculated as 0.25 t/h and 0.12 t/h,
respectively. It is important to note that these values are representative and collected
approximately from the laboratory scale equipment. Also, these throughput values of the
operations were measured without any classification or slime removal prior to the
application. Considering the fact that for a sustainable process control within most of the
operations in mineral processing, properly classified and deslimed narrow size fractions are
preferred. Hence, capacity values may momentously increase for a single vibrating table unit
due to the use of sufficiently classified feed. While an industrial scale up would presumably
increase the capacity, given values are only monitored and circumscribed representing a
equipment used specifically for chromite processing in the industry and the vibrating table,
classified identical high grade chromite samples were fed to both equipment, separately. At
the outset, -1000 µm high grade chromite (approx. 37-38%) sample was fed to the hydrosizer
at optimum vertical water velocities decreasing through the reservoirs. Although hydrosizer is
principally a classifier, relatively higher water rate at first reservoir ensured a slightly higher
grade product (41.96%) and coarser particles to accumulate within. Due to the mass pull
amounts of each reservoir, 2nd, 3rd, and 4th reservoirs were merged forming a single
hydrosizer product along with the 1 st reservoir (Table 5). Additionally, 12.90% weight of the
initial sample having 33.89% Cr2O3 was lost as slimes during hydrosizer operation.
Following, “Hydrosizer 1st reservoir” and combination of the “Hydrosizer 2 nd, 3rd, and 4th
resevoirs” were fed to the shaking table and vibrating table, separately. Shaking table tests
were presented in Table 6. In response to two different product qualities achieved within a
shaking table, an additional scavenger stage was applied to the 1 st stage tailings with
vibrating table and results were given in Table 7. Additionally, step by step comparisons
between product qualities of shaking table and vibrating table operations were rendered in
Figure 8. Considering the tests with “Hydrosizer 1st reservoir”, although individual and
combined product grades achieved with shaking table are slightly higher, recoveries were
evidently elevated with vibrating table reaching up to 93.22% in comparison with the 66.08%
recovery of shaking table’s combined products (Figure 8a). When combined 2 nd+3rd+4th
reservoirs of hydrosizer was processed, overall product recoveries were reported as 59.18%
and 52.88% for shaking table and vibrating table, respectively (Figure 8b). Moreover, grades
of the final products of both equipment were approx. at 48-49% Cr2O3 level. It is important to
note that, these tests were performed under optimum conditions with simplest possible
analogous flowsheets. Considering the operational differences of both vibrating table and
shaking table, linking additional cleaning stages up to the process, applying more advanced
equipment settings such as varying water speeds and different inclinations, and feeding
In the fashion of real life operations, use of the shaking tables are favorable when sample to
be fed has adequate liberation and is classified prior to processing [30]. These universal rules
for the success of gravity concentration are also considered to be valid for vibrating table as
discussed in afore experimental sections. It was observed that capacities of vibrating table for
-1000 µm and -200 µm original feeds was calculated as 0.25 t/h and 0.12 t/h with a chute
supposedly having 100 cm opening. The capacity of an average shaking table (1.5-2.5 m×3.0-
4.0 m) varies according to size of feed particles and the concentration criteria, and reportedly
they can handle up to 2 t/h of 1.5 mm sand and perhaps 1 t/h of fine sand [5]. These figures
may decrease down to 0.2-0.5 t/h when fine size fractions were processed.
An average feed rate of 30% solid by weight could be accepted as optimum for a vibrating
table operation due to the experimental results. On the other hand, although the quantity of
water used in the feed pulp varies, shaking table’s normal feed dilution in comparison with
the vibrating table were reported as 20-25% solids by weight for ores, and 33-40% solids for
Shaking tables are used in a variety of applications, and depending on the application an
industrial shaking table is approx. 2-5 meters long and 1-3 meters wide. Hence, single
shaking table occupies a large area and most operations require tens of tables in order to
handle excessive tonnages. In contrary, although an industrial scale vibrating table operation
has not been undertaken yet, installation space required for vibrating table is predicted to be
was observed that vibrating table either caught up or outperformed the performance of the
shaking table under the given conditions. Considering the factors such as capacity, space
required for installation, etc., vibrating table was proved to be a strong alternative to
Final tests were solely performed with high grade chromite (approx. 37-38%) sample. Slimes
(approx. -75 µm) of -600 µm sample batch was removed with hydrocyclone and
(Table 8). Consequently, a deslimed -600+75 µm batch along with the classified -600+212
µm and -212+75 µm sample batches. These size fractions were fed to the vibrating table
separately. Subsequent cleaner and scavenger stages were also applied to each product and
tail. Overall and combined results of the vibrating table tests of classified hydrocyclone
products were given in Table 9. Additionally, product grade and recovery comparisons of
three distinct sample batches were compared in Figure 9. Plate inclinations, WW rates, and
feed rates were chosen optimum and constant specifically for processing each sample batch.
Results showed that relatively coarser -600+212 µm sample batch provided highest recovery.
Addition of the finer -212+75 µm fraction decreased the overall recovery of Cr 2O3 due to the
increasing loses. Contributing to these observation, overall product grades of -600+212 µm, -
600+75 µm, and -212+75 µm operations were observed in the range of 47-49% Cr2O3 with
higher loses in finer particle sizes. Consequently, it was observed that feeding narrow and
relatively coarser size fractions ensure more distinct operational stability resulting with
5. Conclusions
A gravity concentrator namely “vibrating table” has been developed with the objective of
increasing the product quality of density based physical separation processes. The system is
mainly composed of a vibration unit, an inclined chute, TW and WW jets. The principle idea
of the separation is to combine the involved forces of a teetered bed, resistance to water flow,
vibration, and density differences in order to benefit best from gravitational separation.
Influence of the operating parameters on vibrating table performance had been investigated
by performing separation tests with mineralogically distinct chromite ore samples. In the
experimental studies effect of particle size and chute inclination, effect of removing slimes,
and effect of combining with other physical separation and classification equipment on
performances of the vibrating table and a shaking table had been tested under similar
Both grade and recovery increase as plate inclination of the vibrating table is fairly
Desliming predictably decreased the chromite loses. In addition to the positive effects
of removing the slimes prior to operation, overall performance is also highly effected
by the equipment settings applied whether slime is removed or not. For instance,
Liberation has great importance on determining feed particle size. Vibrating table test
results of -1000 µm, -800 µm, and -600 µm high grade (approx. 32-33%) chromite
samples at similar plate inclinations showed that mass pulls to the tailings increase
underflow provided the highest recovery. Therefore, it was concluded that size
classification prior to vibrating table operation result with better performance values.
Results suggest that industrial application of the vibrating table could be used for processing
distinct chromite samples having a specific liberation degree and typical mineralogy.
Vibrating table was proved to be a strong alternative to the gravity concentration equipment
used for similar tasks due to the experimental results, thanks to the design ability of using
equipment is very new, studies on gold and rare earth mineral processing will be evaluated in
future studies.
Acknowledgements
The authors kindly acknowledge the financial support of Hacettepe University Scientific
Research Projects Coordination Unit (HU BAP) and Hacettepe University Technology
Transfer Center (HT-TTM) for providing technical assistance during patent process.
Conflict of interest
There is not a potential conflict of interest, including any personal or other relationships with
other people or organizations within the three years of beginning the submitted work, which
could inappropriately influence or be perceived to influence their work. All credits on this
study belong to its authors. Acknowledging the financial support from Hacettepe University
Scientific Research Projects Coordination Unit is the only condition that was deemed
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10 3
15
8 1. Inclined chute
1
7 2. Magnetic vibration unit
3. Teetering water jet
4 2 9 4. Wash water jet
5 5. Vertical steel plate
11 6. Main frame
7. Solenoid valve control unit
8. Solenoid valve
6 9. Vibrator frequency control unit
10. Serrated groove surface
11. Tilt adjustment bar
17 1 14 4 12. Teethered bed
18 13. Lighter particles
15 13 14. Denser particles
16
15. Tail discharge
16. Product discharge
12 17 16 17. Sample particles (ore)
18. Water level cut point
3
2
Side view 15
Side perspective view
(a)
(b)
Figure 1. Vibrating table gravity separator schematical representation (a) and actual views
(b)
Feed Over flow
(Slimes)
Chromite Feed
product Hydrocyclone
Under
Vibrating table flow Chromite
Tail product
Vibrating table
Tail
(a) (b)
Figure 2. Schematic view of the tests in which feed samples were either directly fed to the
vibrating table or after removal of slimes via hydrocyclone (a; applied to -400 µm and -200
µm low grade chromite samples; and -1000 µm, -800 µm, and -600 µm high grade chromite
samples. b; desliming was applied to -400 µm and -200 µm low grade chromite ores)
Hydrosizer
Feed Slime
To Cleaner and
Scavenger steps
Chromite
Product to Cleaner product
Vibrating table
Scavenger
(a)
Hydrosizer
Feed Slime
Shaking table
1st product
2nd product Tail Shaking table
Midling
1st product
2nd product Tail
Midling
(b)
Figure 3. Schematic view of the -1000 µm high grade chromite sample tests in which feed
samples were primarily classified via hydrosizer (a: vibrating table tests, b: shaking table
tests)
Over
flow
Feed
Hydrocyclone
to cleaner step
Tail
to scavenger step
to cleaner step
Tail
Chromite to scavenger step
Vibrating table
product
to cleaner step
Figure 4. Schematic view of the vibrating table tests with -600 µm high grade chromite
samples in which feed samples were primarily classified via hydrocyclone
100
90 Mass pull, % Weight
Cr₂O₃, %
80 Cr₂O₃ Recovery, %
70
60
%
50
40
30
20
10
0
4 6 8 10
Plate inclination, °
(a)
100
90 Mass pull, % Weight
80 Cr₂O₃, %
Cr₂O₃ Recovery, %
70
60
%
50
40
30
20
10
0
1 2 3 4 5
Plate inclination, °
(b)
100
90 Mass pull, % Weight
Cr₂O₃, %
80 Cr₂O₃ Recovery, %
70
60
%
50
40
30
20
10
0
4 6 8 10
Plate inclination, °
(c)
100
90 Mass pull, % Weight
Cr₂O₃, %
80
Cr₂O₃ Recovery, %
70
60
%
50
40
30
20
10
0
1 2 3 4 5
Plate inclination, °
(d)
Figure 5. % grade and % recovery comparison of the low grade chromite sample vibrating
table test products (a: 400µm, b: 200µm, c: 400µm deslimed, d: 200µm deslimed)
100
80
60
%
40
20 Cr₂O₃, %
Cr₂O₃ Recovery, %
0
500 600 700 800 900 1000 1100
Feed top size, microns
(a)
70
Cr₂O₃ Recovery, % (WW=0.5 lpm)
60 Cr₂O₃ Recovery, % (WW=1 lpm)
50
40
%
30
20
10
0
500 600 700 800 900 1000 1100
Feed top size, microns
(b)
60
Cr₂O₃, % (WW=0.5 lpm)
Cr₂O₃, % (WW=1 lpm)
50
%
40
30
500 600 700 800 900 1000 1100
Feed top size, microns
(c)
Figure 6. % grade and % recovery change in of the -1000 µm, -800 µm, and -600 µm high
grade chromite (approx. 32-33%) sample vibrating table test products (a: combined product
qualities, b: % recovery change due to change in WW rate and particle size, c: % grade
change due to change in WW rate and particle size)
water level
teetered bed
Ѳ - plate inclination
tail discharge product discharge
Figure 7. Schematical representation of the separation zones within a vibrating table
0 20 40 60 80 100
(a)
0 10 20 30 40 50 60 70
(b)
Figure 8. Comparison of the high grade chromite (approx. 37-38%) sample shaking table and
vibrating table test results applied to classified products obtained from hydrosizer reservoirs
(a, 1st reservoir; b, combination of 2 nd, 3rd, and 4th reservoirs) (ST, shaking table; VT,
vibrating table)
100
90
80
70
60
%
50
40
30
20
10
0
-600+75 µm -600+212 µm -212+75 µm
Figure 9. Comparison of the high grade chromite (approx. 37-38%) sample vibrating table
test results applied to classified products obtained from hydrocyclone underflow
A new method for gravity separation: Vibrating table gravity concentrator
Table 2. Low grade chromite sample vibrating table test parameters and product qualities
Test Feed top size, Desliming Plate Vibration Mass pull, Cr₂ O₃ in Cr/Fe in
notation µm inclination frequency % product, % product
1 400 µm not applied 9° max. 4.27 45.87 1.22
2 400 µm not applied 7° moderate 7.36 44.55 1.19
3 400 µm not applied 5° moderate 8.93 38.77 1.02
4 400 µm with hydrocyclone 9° max. 7.53 50.20 1.34
5 400 µm with hydrocyclone 7° moderate 8.88 41.15 1.10
6 400 µm with hydrocyclone 5° moderate 12.68 36.22 1.07
7 200 µm not applied 4° moderate 8.37 42.67 1.30
8 200 µm not applied 3° low 7.09 33.23 1.01
9 200 µm not applied 2° low 7.87 25.00 0.98
10 200 µm with hydrocyclone 4° moderate 10.34 53.68 1.51
11 200 µm with hydrocyclone 3° low 7.43 39.10 1.10
12 200 µm with hydrocyclone 2° low 4.44 29.77 1.02
Feed 5.04 0.33
Table 3. Vibrating table test results of -1000 µm, -800 µm, and -600 µm high grade chromite
(approx. 32-33%) samples
-1000 µm feed -800 µm feed -600 µm feed
8° plate inclination Weight Cr₂ Cr₂ O₃ Weight Cr₂ Cr₂ O₃ Weight Cr₂ Cr₂ O₃
% O₃ Recovery % O₃ Recovery % O₃ Recovery
% % % % % %
1st stage Cr2O3 47.02 36.42 51.46 37.28 39.88 44.44 37.22 44.86 49.46
product
2nd stage Cr2O3 25.17 39.88 30.16 15.21 45.68 20.77 5.28 46.74 7.31
product
Combined chromite 72.19 37.63 81.63 52.49 41.56 65.20 42.50 45.09 56.77
product
Bed forming 12.31 16.22 6.00 23.62 20.35 14.37 12.64 21.44 8.03
material
Tailing 15.50 26.55 12.37 23.89 28.61 20.43 44.86 26.49 35.20
Feed 100.00 33.28 100.00 100.00 33.46 100.00 100.00 33.76 100.00
Table 4. Change in separation solid % due to TW rate, WW rate, and feed rate
Feed rate, kg/h* TW rate, lpm* Plate inclination,° Measured solid %**
24 8 11 11.69
24 2 11 23.80
24 8 5 37.84
24 2 5 51.40
50 8 11 18.03
50 2 11 35.33
50 8 5 49.35
50 2 5 58.26
*Values calculated for laboratory scale vibrating table with a 20cm chute opening. **2.7 g/cm3 bulk density
value for the chromite ore sample was used within calculations.
Table 5. Hydrosizer test results of -1000 µm high grade chromite (approx. 37-38%) samples
Table 6. High grade chromite (approx. 37-38%) sample shaking table test results applied to
classified products obtained from hydrosizer reservoirs
Feed from hydrosizer 1st reservoir hydrosizer 2nd+3rd+4th reservoirs
Weight Cr₂ O₃ Cr₂ O₃ Weight Cr₂ O₃ Cr₂ O₃
% % Recovery % % Recovery
% %
1st stage chromite product 20.53 49.00 23.99 13.12 49.68 17.22
2nd stage chromite product 37.03 47.66 42.09 32.54 48.79 41.96
Middling 41.14 33.79 33.16 46.39 29.08 35.66
Tailing 1.31 24.45 0.76 7.96 24.54 5.16
Feed 100.00 41.92 100.00 100.00 37.83 100.00
1st+2nd stage chromite product 57.55 48.13 66.08 45.65 49.04 59.18
Table 7. High grade chromite (approx. 37-38%) sample vibrating table test results applied to
classified products obtained from hydrosizer reservoirs
Feed from hydrosizer 1st reservoir hydrosizer 2nd+3rd+4th reservoirs
Weight Cr₂ O₃ Cr₂ O₃ Weight Cr₂ O₃ Cr₂ O₃
% % Recovery % % Recovery
% %
Cleaner 1 chromite product 80.64 47.26 91.57 23.08 48.38 30.93
Scavenger 1 chromite product 2.22 30.91 1.65 16.31 48.57 21.94
(1st stage tail cleaned)
Cleaner 1 bed forming material 6.86 15.58 2.57 4.43 17.55 2.15
Scavenger 1 tail 9.00 13.70 2.96 54.53 28.33 42.80
Cleaner 1 tail 1.28 40.63 1.25 1.66 47.20 2.17
Feed 100.00 41.62 100.00 100.00 36.10 100.00
Cleaner 1 + Scavenger 1 82.86 46.83 93.22 27.36 48.41 52.88
chromite product
Table 8. Hydrocyclone test results of -600 µm high grade chromite (approx. 37-38%)
samples
Table 9. High grade chromite (approx. 37-38%) sample vibrating table test results applied to
classified products obtained from hydrocyclone underflow
Feed from Hydrocyclone U/F -600+75 Hydrocyclone U/F -600+212 Hydrocyclone U/F -212+75
Weight Cr₂ O₃ Cr₂ O₃ Weight Cr₂ O₃ Cr₂ O₃ Weight Cr₂ O₃ Cr₂ O₃
% % Recovery % % Recovery % % Recovery
% % %
Rougher chromite product 57.62 48.83 69.98 33.73 50.06 41.21
Scavenger chromite product 7.09 32.56 5.74 3.91 37.56 3.58
Scavenger bed forming material+tail 35.30 27.66 24.28 27.30 9.97 7.08 62.36 36.27 55.20
Feed 100.00 40.21 100.00 100.00 38.43 100.00 100.00 40.97 100.00
Rougher+scavenger chromite product 64.70 47.05 75.72 72.70 49.12 92.92 37.64 48.76 44.80