Bias Testing of Cross-Belt Samplers
Bias Testing of Cross-Belt Samplers
Bias Testing of Cross-Belt Samplers
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Introduction
The cross-belt sampler has been a contentious
machine for many years. The first testing of
the device was carried out by Siebtechnik in
Germany in 1989 (Reiners and Mohrhauer1).
This test was carried out on coal which was
such that the ash content of the coal was
almost constant as a function of particle size,
and the bias test was carried out using ash
content as the test analyte. Consequently, the
machine was given a clean bill of health and
the cross-belt or hammer sampler became a
well-known piece of equipment. The original
machine had a cutter head with parallel side
plates which were perpendicular to the motion
of the belt. The design concept for the sampler
was that it should cut a swath of solids off the
belt, of a width determined by the aperture of
the cutter, and propel these solids into a chute
at the side of the belt from where they would
be collected as a sample increment. These
machines are still common in the mineral
industry. They have the advantage of being
relatively cheap to manufacture and can be
retrofitted to an existing conveyor at low cost.
No transfer point is needed for installation as
would be needed for a cross-stream sampler.
Subsequent to the development of the first
cross-belt sampler, a machine was designed in
South Africa which came to be known as a
go-belt sampler. This design was patented by
JCI (van der Merwe and English2) and had
parallel plates that were angled with respect to
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Synopsis
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Test system
The product belt at Thabazimbi has a run of 27.7 m where
the belt is accessible downstream of the second installed
cross-belt sampler (the go-belt type). There is a belt end
sampler of the Vezin type which was refurbished by Multotec.
This last machine is mechanically correct. The belt speed is
1.47 m/s and the belt width 0.75 m with 35 degree idlers.
Figure 1 shows the layout of the samples on the belt. The
sampling was initiated by taking three sets of increments
with the cross-belt samplers at 2 second intervals; a belt end
sample cut was initiated at the same time as the last crossbelt cut. The belt was then stopped as quickly as possible. A
stopped belt increment of nominally 0.4 m was taken, as
shown in Figure 1. The belt was then started and a second
belt end cut taken about 8.7 seconds after the start, giving
the sampling pattern as shown. Care was taken to reject any
sample sets where there was any overlap of the sample
increments; this could be verified visually.
The full set of samples was taken in a 19 m length of belt.
Close spacing of the samples was used to avoid, as far as
possible, the introduction of variance between the samples
due to distributional heterogeneity. Three cross-belt cuts
were taken for every stopped belt sample to match the sample
volumes and a stopped belt increment was about 3 times the
mass of each cross-belt increment. Two belt end samples
were taken to bracket the other samples and these samples
were split in half by rotary sample division, after drying, to
approximately match the sample mass of the other samples.
Samples from each stop of the belt were combined (3 to 6
stops) to make up a sample of nominally 100 kg, which was
then sized on 25, 20, 16, 12.5, 9.5, 8.0, 6.3 mm sieves. The
results of the sizings are provided in Appendix 1.
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VOLUME 110
stopped belt samples, the belt end samples, and the two
samples from the cross-belt samplers. These samples are all
paired and so should all have the same expected value of the
size distribution. The sample masses are all similar so the
variance of the size analysis should be similar for all
samples. There should be only two sources of variance
attached to a single sample: the difference between the
100 kg samples due to the intrinsic heterogeneity with
respect to particle size and the uncertainty associated with
the sizing procedure itself. The careful pairing of the samples
should eliminate the uncertainty due to distributional heterogeneity along the belt as far as possible.
In making a statistical comparison between two measured
size distributions, it must be recognized that the mass
fraction reporting to a given size fraction is statistically
correlated with the mass fraction reporting to any other size
fraction. The correlation comes about as a result of having
added up the masses in each size fraction and then dividing
each mass by the total to arrive at the mass fraction in the
size fraction. Therefore, it is incorrect to treat the amounts in
each size fraction (or the amounts passing or retained on a
given sieve) as independent random variables.
Treating them as such is, however, a common practice.
This practice is justified only when a single measure of bias
is involved (e.g a single analyte assay). When more than one
analyte and particularly when sizings are involved in making
paired comparisons, the covariance structure of the data must
be taken into account. The temptation to carry out individual
t-tests on the mean differences derived from n independent
measures of the difference should be avoided.
There are three problems associated with such a
procedure. First, working only with mean differences ignores
that fact that the bias in the sampler may be a bias of scale
which is not discovered using mean differences (see
Lyman3). Secondly, covariance in the data set is ignored, and
thirdly, one has to decide how many of the t-tests must fail
in order for the sampler to be deemed biased.
Does it suffice that one t test fail at the 95% level? Or
must a certain fraction of all possible t-tests fail at the 95%
level. With p size fractions defined, it is possible to carry out
p 1 t-tests (the pth test is not independent due to the
correlations of the mass fractions). Appendix 3 deals with
this problem comparing t-testing to the Hotelling T-squared
test, which fully accounts for the correlation between the size
fractions and provides a single test statistic for the entire
group of size fractions. It is shown there that determination
of the number of t-tests that should fail before deciding is not
trivial and that deciding, for example, that three tests must
fail for the sizing to be different may be too strong a
criterion, whereas deciding that two failures are sufficient
may be too weak a criterion. Use of the Hotelling statistic
entirely circumvents this problem.
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Rosin-Rammler coordinate
0.8
0.6
0.4
0.2
0
-0.2
-0.4
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-0.8
-1
1
10
100
Results
It is instructive to note that based on the aperture of the
hammer samplers, the actual sample masses were 83 and
85% of the expected masses for samplers H1 and H2. This
suggests that both hammer samplers were leaving material
on the belt (or that the usual method of estimating the
hammer sample increment mass is in error).
The increment masses were checked after drying of the
samples to ensure that the samples had not been corrupted.
The expected increment masses were compared with the
actual increment masses. For a given sampler, these ratios
The Journal of The Southern African Institute of Mining and Metallurgy
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t-test results (significant results shown in red). Differences correspond to test reference sample. Size
fractions run from + 25 mm to 6.3 mm
Mean
difference
(% abs)
Belt end
SD mean
Rel
difference difference
(%)
0.649
-0.482
-0.086
-0.194
-0.616
-0.188
0.029
0.160
0.318
0.394
0.257
0.484
0.313
0.274
0.279
0.250
5.41
-3.82
-0.73
-1.27
-3.15
-1.64
0.26
2.68
t stat
Mean
difference
(% abs)
2.04
-1.22
-0.33
-0.40
-1.97
-0.69
0.10
0.64
2.481
1.819
-0.287
-1.058
-1.750
-0.811
-0.211
-0.050
Hammer 1
SD mean
Rel
difference difference
(%)
0.483
0.496
0.169
0.343
0.336
0.227
0.350
0.267
Table II
BE
H1
H2
8.71
0.0053
7.47
0.0083
9.60
0.0040
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VOLUME 110
20.71
14.42
-2.44
-6.93
-8.95
-7.10
-1.85
-0.84
t stat
Mean
difference
(% abs)
5.14
3.67
-1.70
-3.08
-5.21
-3.57
-0.60
-0.19
2.450
-1.241
-2.877
0.194
1.667
-0.012
-0.150
0.101
Hammer 2
SD mean
Rel
difference difference
(%)
0.490
0.391
0.313
0.496
0.536
0.303
0.319
0.310
20.45
-9.83
-24.45
1.27
8.53
-0.11
-1.31
1.68
t stat
5.00
-3.17
-9.18
0.39
3.11
-0.04
-0.47
0.33
Conclusions
Bias testing of a sampler is a critical factor in the testing of a
machine. Beyond the collection of the magical 30 pairs of
samples suggested by some Standards, it is rare to see any
statistically rigorous discussion of the level of detectable bias
that will be achieved in the bias test. It is obvious that the
detectable bias is a figure of economic significance.
The application of individual t-tests to the results of
testing a sampler on size distribution is incorrect as such
testing ignores correlation between the amounts in size
fractions. t-testing when more than one analyte is used is
also incorrect when the analyte contents in samples are
correlated (as they usually are).
The Hotelling T squared test, correctly, takes correlation
in the data into account when tests on simple differences are
used. However, as apparently illustrated by the results in this
paper, the Hotelling test is sensitive to outliers and general
non normality of the data. A robustified version of the
Hotelling test can be devised based on the signed rank of the
differences observed. Having replaced the actual differences
by their signed ranks, the calculations for the robustified
method do not differ from the method described in here. The
critical value of the robustified statistic must be determined
by permutation tests.
The important point to note is that replicate analyses are
necessary to assess the accuracy of the size analysis or
analyte analyses carried out. In spite of working many years
The Journal of The Southern African Institute of Mining and Metallurgy
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Figure 3Box plots for samplers: Top left: belt end; top right: hammer 1; bottom, hammer 2. Size fraction 1 is +25 mm and fraction 8 is -6.3 mm. Note the
difference in vertical scales on the plots
Acknowledgements
Thabazimbi mineThe authors would like to
acknowledge Thabazimbi Mine, in particular Cornelia
Holtzhausen, for allowing the mine to be used as a test
facility.
The Journal of The Southern African Institute of Mining and Metallurgy
References
1. REINERS, E. and MOHRHAUER, P. Hammer Samplera proven sampling unit,
Aufbereitungs-Technik, vol. 30, no. 4. pp. 218225.
2. VAN DER MERWE, E. English; Ralph H, Device for sampling material from a
moving belt conveyor, US Patent No. 5,115,688, filed 1990.
3. LYMAN, G.J. Determination of Bias in Sampling Systems, Minerals
Engineering, vol. 6. pp. 99105.
VOLUME 110
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295
Table A1-I
H1 Sample 1
H2 Sample 1
BE Sample 1
BC Sample 1
H1 Sample 2
H2 Sample 2
BE Sample 2
BC Sample 2
H1 Sample 3
H2 Sample 3
BE Sample 3
BC Sample 3
H1 Sample 4
H2 Sample 4
BE Sample 4
BC Sample 4
H1 Sample 5
H2 Sample 5
BE Sample 5
BC Sample 5
H1 Sample 6
H2 Sample 6
BE Sample 6
BC Sample 6
H1 Sample 7
H2 Sample 7
BE Sample 7
BC Sample 7
H1 Sample 8
H2 Sample 8
BE Sample 8
BC Sample 8
H1 Sample 9
H2 Sample 9
BE Sample 9
BC Sample 9
H1 Sample 10
H2 Sample 10
BE Sample 10
BC Sample 10
H1 Sample 11
H2 Sample 11
BE Sample 11
BC Sample 11
H1 Sample 12
H2 Sample 12
BE Sample 12
BC Sample 12
H1 Sample 13
H2 Sample 13
BE Sample 13
BC Sample 13
H1 Sample 14
H2 Sample 14
BE Sample 14
BC Sample 14
296
Initial
mass
(g)
+25
25 x 20
16 x 20
12.5 x 16
9.5 x 12.5
8 x 9.5
6.3 x 8
-6.3
106890.7
96893.6
122211.4
131795.2
116468.7
107837.8
129272
151180.6
63533.6
92819.7
107154
119238.9
80191.7
96437.1
111628.5
105801.8
95208.5
97659.5
108957.2
118741
80443.7
93998.4
110978.6
113439.8
101970.7
110455
118381.2
120593.7
96406.8
106661.3
119804.4
122111.3
73585.5
98025.6
107699.7
112416.7
75343.8
103269.6
116373.3
117126.8
77859.4
104637
118804.5
129356.5
59259.5
95509.2
95468.5
113510.4
102442.6
112105.7
129651.8
132705.7
116895.2
107281.2
128267.2
139238.4
9.182651
9.620759
7.983216
7.007691
9.180664
9.418404
7.643186
6.729567
13.29722
13.56005
10.85802
11.41934
10.08758
8.774424
7.796127
6.677864
13.05923
13.64138
11.11813
10.55086
23.98808
23.9652
21.62372
22.05355
15.92889
18.22561
16.01175
15.74875
13.25166
16.47917
12.34562
11.88948
11.61003
12.82451
11.46224
10.00101
11.45482
12.07974
9.90442
9.956048
13.99934
13.42948
11.75275
9.756139
17.46555
15.06808
12.75363
13.67593
17.9318
14.84037
17.22876
17.54537
22.02879
20.10324
18.33087
14.719
13.80045
12.10317
11.48379
13.87979
14.11761
11.02025
11.15145
11.78438
18.56608
12.81862
13.96607
14.18354
14.99557
10.64217
12.11232
10.44103
12.94412
11.41589
12.7328
12.05321
18.1517
16.39539
18.09862
19.17325
16.97664
15.86447
14.28419
15.38463
17.58932
10.15176
13.09676
13.94416
14.42703
12.79635
11.65351
10.89509
12.9716
9.81189
10.73537
10.76568
10.84609
9.466154
10.44304
11.10729
11.21761
7.451324
11.01777
8.808444
13.98412
9.613963
9.531067
11.92616
11.51809
9.71736
9.580158
12.29029
13.01778
11.486
13.11072
13.16315
13.22973
10.07365
13.84646
12.92679
12.31726
7.972984
11.38558
12.75129
13.12243
9.684447
13.49593
13.24221
12.10092
7.838357
12.61569
12.64391
12.17671
10.05751
11.08313
12.30194
11.37954
9.741343
11.18328
12.29815
11.46071
8.901917
12.48819
12.65952
11.08112
8.645293
12.37153
11.21631
10.66936
9.004392
11.29898
10.04569
11.26184
9.431081
11.67464
10.45537
9.152963
7.680098
9.285052
10.47957
9.529336
6.479064
9.593388
9.562815
10.24045
7.490781
10.12792
11.01729
16.95077
19.34173
16.53864
15.93283
17.38922
18.29831
16.28419
16.70472
14.04312
14.46708
15.56097
13.96549
13.70616
15.13277
14.60765
16.93884
17.38847
18.96969
15.89101
19.90635
11.54447
11.8202
12.45051
11.78043
12.15388
12.88733
14.57715
14.7686
13.05582
14.80481
13.7818
14.65827
13.34652
13.9078
14.35909
14.66401
16.68034
16.50447
15.71314
18.0226
15.25031
13.44763
14.89211
14.90965
12.36392
17.36775
14.887
13.80587
14.25559
18.11139
19.02434
15.81711
10.64475
11.24148
12.30237
11.7069
20.31739
22.55536
20.79912
20.37146
19.04486
22.62574
20.89927
21.61607
16.99762
21.70035
19.11277
18.55217
18.13679
25.26165
19.97859
20.69747
19.87669
23.00903
20.23629
20.60527
14.27433
15.85101
14.45774
13.8707
16.4409
17.05835
15.40388
17.736
16.54406
19.91866
17.68975
18.92601
19.19563
20.03864
19.43432
21.12782
18.95591
22.1863
21.13045
23.45108
18.18997
20.29942
21.25551
20.70735
17.96134
23.43575
19.02586
19.30396
18.28985
23.55563
20.1391
19.10204
15.02962
19.60754
15.57935
17.69332
11.681
9.946787
12.404
12.72854
10.68244
12.23078
11.54225
12.36878
9.533381
11.95393
11.35123
11.23291
11.1529
11.78219
11.9723
12.45366
10.60231
11.29445
11.46312
10.75366
8.095103
8.94079
8.550117
8.328118
10.02965
9.69182
11.89902
9.74769
11.35646
12.13055
11.09183
10.75879
12.78078
12.23282
11.17905
13.15481
10.73134
11.89314
12.10742
12.19593
10.67591
13.21378
9.945415
11.76617
11.50432
11.8041
11.5349
12.0196
9.729741
11.18016
9.506308
9.997008
9.922991
11.36583
12.65904
12.32663
10.16693
9.824178
11.29723
11.51195
10.76032
10.80706
11.54643
11.77115
9.210717
10.79361
10.63544
10.45892
12.43346
12.68132
13.03941
13.59249
9.890609
9.522371
10.35875
9.530491
7.751135
8.263864
8.019384
8.226566
11.05602
10.76022
10.64358
9.456547
10.96614
11.77831
12.06049
11.2621
10.97716
12.80614
12.34005
12.5541
12.26471
12.17735
12.04108
9.884672
12.52283
13.2672
11.93246
13.9533
13.40241
11.48549
13.91328
14.01246
10.63991
10.74361
9.234812
10.69901
14.7912
12.77726
13.13368
12.87454
4.883025
5.12201
6.383283
5.404597
5.595151
5.525799
7.086763
6.098534
6.034602
6.733377
7.129925
7.436332
6.365123
6.041036
6.997675
5.95642
4.137656
4.308849
5.584211
3.956258
4.018463
4.706038
5.716778
4.265434
6.034479
5.770857
5.997152
4.859624
5.775837
5.834825
7.445553
5.901665
6.581731
6.748441
7.200206
6.386862
6.271916
6.342718
7.069147
5.678291
7.253716
7.445263
8.10407
7.344741
6.931884
5.707408
7.582501
7.894167
5.639646
5.475814
5.742226
5.350486
5.824106
7.696502
8.286608
7.372032
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Mass % in fraction
VOLUME 110
Table A1-II
+25
2.960
2.985
3.112
3.023
2.772
2.856
2.479
2.955
3.161
3.112
3.510
2.849
3.080
3.261
3.284
3.027
0.243
8.028
13.250
20 x 25
16 x 20
12.5 x 16
9.5 x 12.5
8 x 9.5
14.057
14.073
14.719
14.905
14.376
14.308
15.018
14.966
14.689
15.155
14.583
15.233
15.020
14.717
14.957
14.719
0.373
2.534
3.811
12.489
11.945
11.212
11.091
12.330
12.123
12.220
12.537
11.625
11.897
10.088
12.177
11.871
12.100
11.835
11.836
0.635
5.363
3.208
12.095
12.745
12.484
11.971
13.310
12.681
12.499
12.126
11.546
11.634
12.201
12.416
11.447
11.770
11.818
12.183
0.513
4.213
2.332
14.350
14.309
14.333
14.568
15.449
14.213
14.000
14.342
14.754
14.669
14.545
14.104
14.788
14.025
14.073
14.435
0.381
2.637
1.611
9.298
8.634
8.936
8.969
8.381
8.784
8.703
8.770
8.778
8.748
8.574
8.656
8.990
8.657
8.970
8.790
0.218
2.485
1.573
-8
34.751
35.307
35.204
35.473
33.382
35.035
35.081
34.303
35.447
34.785
36.499
34.565
34.805
35.471
35.063
35.011
0.680
1.943
0.992
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*Based only on the Poisson distribution of particle numbers in the size fractions
Methodology
To illustrate the concepts behind the comparison of the
methods, a particular size distribution will be chosen and the
tendency to collect more coarse particles will be modelled by
choosing a size distribution that plots linearly on RosinRammler coordinates and pivoting the cumulative passing
curve at a particular point. It is convenient to choose the 40%
passing point. One sampler will sample from the true size
distribution and the second sampler will sample from the
distorted distribution.
The sampling and sizing of the samples from the two
samplers will be simulated by allowing for a Poisson error in
the numbers of particles in each size fraction and a random
The Journal of The Southern African Institute of Mining and Metallurgy
Results
Figure A2-1 shows the statistical results for the base size
distribution of A2-I.
The results were collected by simulation of 5 000 datasets and using 10 pairs of samples. There are 7 size fractions
that can be t-tested and 6 size fractions used in the Hotelling
test. The Hotelling test uses one less size fraction than is
present as the last size fraction is linearly dependent on the
other and provides no additional statistical information.
When there is no difference in size distribution between
the two samples (slope factor = 1.00), the critical F value for
the Hotelling test is chosen as the 95% point for 6 and 4
degrees of freedom corresponding to the test of 6 size
fractions and using 10 pairs of samples. The covariance
matrix in the test is estimated from the data. At this stage,
the probablility that there will be no t-test failures out of the
7 is 0.826, but the probability that one t-test will fail is
0.168. If the criterion for the detection of bias is a failed ttest, then there is a probability of 0.168 (16.8%) of failing
the sampler when it is perfect.
VOLUME 110
JUNE 2010
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Mass %
25
20
16
12.5
9.5
8
0.5
31.5
25
20
16
12.5
9.5
8
Figure A2-2Biased and unbiased distributions and difference in distributions at the critical point for detection of bias by the Hotelling T
squared test
8.86
8.77
11.22
13.50
14.21
7.80
35.65
Table A2-II
Results of Monte Carlo simulation for statistical evaluation of the individual t-test method and the Hotelling T
squared test method
Rosin-Rammler slope
Probability of Hotelling
test failing
1.00
1.02
1.04
1.05
1.06
1.07
0.0494
0.1950
0.6210
0.8162
0.9280
0.9766
0.8258
0.4326
0.0178
0.002
0
0
298
JUNE 2010
VOLUME 110
0.1678
0.5278
0.803
0.7504
0.6622
0.5764
0.0064
0.0396
0.1762
0.243
0.3196
0.3926
3
0
0
0.003
0.0046
0.0182
0.031