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Development of a Calibration Methodology for the SDS011 Low-Cost PM-Sensor with respect to Professional Reference Instrumentation

Authors:
  • Independent Citizen Scientist Stuttgart
1
Development of a Calibration Methodology for the SDS011 Low-Cost
PM-Sensor with respect to Professional Reference Instrumentation
Bernd Laquai, Antonia Saur, December 28th 2017
Introduction
When low-cost laser-scattering PM-sensors came up, mainly targeted for use in commodity devices,
scientific researchers and citizen scientists also became interested. The idea that popped up was to
deploy them for the investigation of the outside air pollution instead of using expensive professional
equipment. It was mainly the fact, that air quality in the outdoor environment is not just an issue
occurring only at a single spot but it is a spatial problem. For an in-depth investigation of particulate
matter concentrations in the air and its meteorological dependencies it is required to perform
simultaneous distributed measurements to obtain 3D spatial data, or at least 2D areal data, instead of
collecting data solely from a few hot spots. Since professional PM-measurement equipment is still
extremely costly, the idea to equip the nodes of a sensor network distributed across a large city or
even larger regions with professional equipment is simply infeasible. However, when a sensor for such
a network node is available for several tens of Euro, then it becomes a highly attractive option to really
implement such a network based measurement system.
Many studies were carried out to compare low-cost PM sensors with professional equipment. Many
of these studies simply positioned the sensors together with professional equipment in the outdoor
environment and compared the results. The particle spectra changed with meteorology and the
location where the sensors where positioned. Since the computation of a PM value such as PM10
actually means to integrate the particle mass distribution from the lower detection limit up to the
10um size (to be correct, a certain fractional efficiency characteristic should be also taken into
account), the specific influence of a certain particle mass distribution on the result is lost. Therefore,
such comparisons weren’t really able to state the accuracy of the sensors in dependence of different
particle spectra. As a result, the sensors performed reasonable under very typical conditions where
the mass distribution was comparable to conditions assumed by the manufacturers but failed for
conditions where the particle mass was distributed in an unexpected way.
However, as soon as more detailed lab investigations were published, the envisioned area of
application narrowed down. Several significant deficiencies and sources of measurement errors for
low-cost PM sensors become apparent. The very low-cost PM sensors mostly designed and
manufactured in China are PM2.5 sensors. Often, they also provide an additional PM10 or even a PM1
value output without providing specifications of accuracy differently for each PM class. During lab
measurements, it became clear that these sensors aren’t really able to measure particle sizes larger
than 5um. The size limitation also became pretty obvious when artificial light pulses of different
intensity and frequency were injected into the measurement chamber to simulate scattering pulses of
particles of different size and concentration or when the pulses at the transimpedance amplifier output
are substituted by precisely controlled pulses from a pulse generator. Therefore, it must be assumed,
that at least the values for PM10 are simply extrapolations from particle sizes between 0.3 and 2.5um,
the low-cost sensor is still able to detect.
It also became evident, that most of these very low-cost devices do not calculate a PM value from a
multi-bin histogram but either average the signal from the scattering light detector or do a simple two
or three threshold comparison to determine a PM value. Since in such a case, only a coarse average
mass can be assigned to the counted number of scattering light pulses, the sensor overestimates the
mass of smaller particles and underestimates the mass of larger particles. The actual relationship
between mass and size, which according to the ideal spherical theory is a function of the third power
of the particle size, is rarely reflected correctly by low-cost sensors. However, at least one of the
investigated sensors really does a histogram based PM calculation and outputs PM1, PM2.5 and PM10
values calculated from 16 bins in a comprehensible way (Alphasense OPC-N2).
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Finally, a severe issue that became apparent when using low-cost PM sensors for environmental
investigations is related to humidity: Most governmental regulations require the PM concentrations
to be measured using gravimetric methods in laboratory. In order to match these laboratory results
with laser scattering equipment measuring online, the air taken in from the measurement device must
be dried to remove humidity. A low-cost PM sensor based on laser scattering however sees the
particles under the influence of hygroscopic growth. Particles released in the urban environment often
contains hygroscopic salts that start to grow in volume when being exposed to relative humidity
already at 60-70%. Since dust prone meteorological situations in winter often correlate with high
relative humidity, the particle growth factors related to particle mass is in the range of 2-5 leading to
heavily overestimated PM values when not being corrected for the humidity influence. For
professional laser scattering PM-measurement equipment it was shown that a humidity correction is
possible when no air dryer is used and finally yields comparable results to the measurement with an
air dryer or with gravimetric measurements as requested by regulation authorities.
The issues described above raise the question, if it is possible to calibrate a low cost-sensor to
professional reference equipment in order to overcome the measurement deficiencies. Theoretically,
a calibration measurement in the lab or in the field should be possible, comparing a low-cost sensor to
the reference equipment from which a calibration factor or function is obtained. Then it can be
expected that during the application of the low-cost sensor the calibration data can be used to
compensate the differences to a reference instrument to a certain degree, such that the final
measurement accuracy after calibration is improved compared to the accuracy without the calibration.
Assumed the humidity effect is treated separately, the challenge for the design of a calibration
algorithm is the dependency of the measurement error on the shape of the particle mass distribution
versus size. It seems to be obvious that the absence of binning the particles into size classes for many
low-cost PM sensors results in strong deviations when the measured particle spectrum does not match
the one for which the sensor was designed. Typically, a mass distribution determined at the curbside
of a road in an area heavily loaded with traffic is dominated by large particles. This means that the
center of gravity in such a particle spectrum is located at a size larger than 5um. On the other hand, in
urban residential areas with low traffic load the mass distribution is normally dominated by small
particles. Therefore, the center of gravity in such a particle spectrum is located below 5um. As a result,
the ratio between the PM values of the low-cost sensor and the reference equipment will be different
in both locations. As a consequence, a calibration should take into account any information available
on the shape of the particle mass distribution and has to be designed rather as a calibration function
than as a simple fitting factor.
Particle Generation Experiments
In most cases where comparative measurements were taken in the field yielding simultaneous PM
data from low-cost sensors and the reference instrument the influence of the mass distribution on the
PM results couldn’t be analyzed in a controlled way. Therefore, in this study the idea was to investigate
this dependency in a measurement chamber of a particle generator in laboratory where particle
spectra could be generated with a controlled distribution.
For this purpose, a particle generator was developed that is able to disperse very small particles from
a smoke generator as well as large particles from a powder disperser. The smoke generator is
constructed from a heater that nebulizes a smoke liquids as used by model railways (paraffin, glycol).
The powder disperser is constructed from a bass loudspeaker driven from a low-frequency AC source.
The powder is loaded on the speaker membrane and is dispersed by the oscillating movement of the
membrane. Both particle sources are electronically controlled. The heating element of the smoke
generator is controlled from a PWM modulated microcontroller via a MOSFET power switch and the
powder disperser is driven from a sinusoidal AC source with controlled frequency and amplitude.
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Both particle sources are arranged in the upper portion of a measurement chamber whereas the
device under test and the reference instrument are arranged in the lower portion of the chamber to
ensure enough homogenization of the particle concentration in the air when the particle sediment
under the influence of gravity (see fig. 1).
Fig. 1: Conceptual drawing and implementation of the particle generator used for the calibration
measurements
Several smoke liquids as well as powders were tested to generate distinct particle distributions that
result in different PM10/PM2.5 ratios. With respect to the goal of developing a calibration scheme, it
turned out that with the two dispersing methods two extreme particle distributions can be generated
in a complementing way. Whereas the smoke generator typically generates a particle spectrum with
particle mass distributed between the lower detection limit of the reference instrument (0.3um) up to
1um, the powder disperser typically generates a particle spectrum where the mass is distributed
between 2um and 15um. The powder that is used for such a spectrum is either milled mineral powder
available as pharmaceutical product (Luvos Heilerde) or pastry flower (type 405).
PM-measurement observations for different particle spectra
When particles with a broadly distributed mass spectrum are released into the measurement chamber,
the sedimentation process induces a change of the mass distribution of the particle spectrum during
the subsequent measurement time. Since larger particles sediment faster than small particles, the
center of gravity shifts towards smaller sizes over time. As a consequence of this shift and due to the
fact that the low-cost sensors typically underestimate the large particle mass concentrations, it can be
observed that the ratio between the low-cost sensor values and the professional equipment values
also changes. With a particle spectrum where the mass is initially dominated by large particles, the
ratio of low-cost PM values and professional PM values typically starts significantly below 1 and then
shifts towards a ratio of 1 after a certain amount of time. Towards the end of the measurement, the
large particles are already settled to the ground and only small particles are left in the air volume. A
requirement to clearly observe this behavior is an overall mass concentration that is small enough with
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respect to the maximum range of the low-cost sensor to avoid non-linearity issues due to coincidence
effects during particle counting.
Fig. 2a: Typical particle mass distribution generated by the smoke generator (paraffin liquid)
Fig. 2b: Typical particle mass distribution generated by the powder disperser (pastry flower type 405)
In this study a SDS011 sensor from Nova Fitness Co., Ltd. (China) was used as a low-cost sensor and a
Grimm 1.108 aerosol spectrometer was used as reference equipment. The SDS011 device is a PM2.5
laser-scattering sensor developed mainly for air conditioning and air cleaning equipment. It also
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provides a PM10 output. However, dedicated tests have clearly shown that the device is not able to
detect particles larger than 5um when no small particles are contained in the particle spectrum. From
previous investigations, it is also assumed that the device does not calculate a multi-bin histogram for
PM-calculation. The datasheet does not provide a separate accuracy specification different for PM2.5
and PM10.
Fig. 3a: Particle mass distribution for mineral dust at the beginning of the measurement
Fig. 3b: Particle mass distribution for mineral dust at the end of the measurement
A situation as described above is shown in the following first measurement example. Mineral dust with
a typical mass distribution between 0.3 and 10um was released to a measurement chamber. At the
beginning of the measurement, the reference instrument shows a mass distribution between 0.3 and
15um. In the course of sedimentation, the mass distribution changed and the center of gravity in the
distribution shifted from about 3um towards less than 1um.
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This behavior can be observed even better when a 3D color graded contour plot is generated from the
particle mass distribution across the time. From this plot, it can be seen that the large particles vanish
quickly and then a shift of the center of gravity in the distribution occurs towards smaller particle sizes.
Fig. 4: Color graded contour plot of the particle mass distribution (logarithmic scale) versus size and
measurement time for the mineral dust experiment
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In fig. 5a and b the PM10 and PM2.5 measurement result for both the SDS device and the Grimm
reference instrument are shown. From the reference instrument results that is supposed to be correct,
it can clearly be seen that initially, a distinct peak appears where PM10 is significantly larger than
PM2.5. During this initial peak the mass is dominated by particles larger than 2.5um. When the ratio
of PM10/PM2.5 is evaluated, the reference instrument shows an initial PM10 value that is by a factor
of 4 larger than PM2.5. After a certain amount of time the large particles are settled to the ground and
the PM10/PM2.5 ratio tends towards 1, since only small particles still remain in the air and the PM10
and the PM2.5 values become almost equal. The SDS011 device however, reports a large initial
PM10/PM2.5 ratio of about 6.5, mainly because PM2.5 was measured much smaller during this phase.
For the rest of the measurement the ratio PM10/P2.5 remains between 5 and 4. During this phase, the
PM10 values estimated by the SDS011 are much larger than that of the reference instrument (see fig.
6 and 7).
Fig. 5a: PM measurement result of the reference instrument (Grimm 1.108) for the mineral dust
experiment
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Grimm
PM10 PM2.5 PM1
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Fig. 5b: PM measurement result of the SDS011 low-cost sensor for the mineral dust experiment
Fig. 6: PM10/PM2.5 ratios for low-cost sensor and reference instrument
When comparing the results of both devices it becomes obvious that the ratio SDS/Grimm initially is
smaller than 1 for PM10 (and PM2.5) and after the large particles have settled, this ratio approaches
2 for PM10. In contrast, for PM2.5, the SDS/Grimm ratio stays between 0.3 and 0.6.
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SDS 5001-0DB9
PM10 PM2.5
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Fig. 7: The ratio of PM results for low-cost sensor versus reference instrument (averaged), a strong
deviation of the low-cost sensor becomes visible
These observations are repeatable and can also be reproduced with other types of dust as long as the
mass is distributed broadly. There is also only minimal variation when different low-cost sensor devices
of the same manufacturing batch are used. It clearly shows that for such a particle spectrum the
SDS011 low-cost device shows a large measurement inaccuracy. Other devices similar in cost from
different manufacturers (Plantower, Bjhike) were also investigated and even showed a worse
behavior.
In the following second measurement example, the smoke generator was used with a paraffin liquid
to generate a particle spectrum. Fig. 7 shows the mass distribution versus time indicating that the
particle mass is initially distributed across diameters < 5um and at the end of the measurement the
particles contributing to the mass are smaller than 2um. Therefore, with respect to the particle mass
distribution, this spectrum complements the previous spectrum.
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Fig. 8: Color graded contour plot of the particle mass distribution (logarithmic scale) versus size and
measurement time for the paraffin smoke experiment
As a consequence of the missing mass contribution from particles > 2.5um (except during start of the
measurement), the reference instrument reports a PM10 value almost equal to PM2.5. The low-cost
sensor however shows a PM10 value that remains much larger than PM2.5 throughout the whole
measurement. The reason for this behavior is the fact, that the low-cost sensor actually is a PM2.5
sensor and does not measure PM10 but estimates it from smaller particle sizes. As it can be seen,
under this conditions of the given particle spectrum, the low-cost sensor performs a fairly wrong
estimation of PM10 with a PM10/PM2.5 ratio between 1.5 and 2.5 instead of ideally 1 after the larger
particles have settled (fig. 9a, b).
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Fig. 9a: PM measurement result of the reference instrument (Grimm 1.108) for the paraffin smoke
experiment
Fig. 9b: PM measurement result of the SDS011 low-cost sensor for the paraffin smoke experiment
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SDS 5001-0DB9
PM10 PM2.5
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Fig. 10: PM10/PM2.5 ratios for low-cost sensor and reference instrument
Fig. 11: The ratio of PM results for low-cost sensor versus reference instrument; PM2.5 of the low-cost
sensor is close to the reference, PM10 of the low-cost sensor shows a strong deviation from the
reference
Since it is known that the SDS011 device is marketed as a PM2.5 sensor and the PM10 values of the
SDS011 device are just extrapolations from measurements in the PM2.5 size range, there is no
expectation that PM10 can be calibrated to the reference instrument in a meaningful way. Therefore,
in this study the development of a calibration method was restricted to PM2.5. The PM2.5 values
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PM10
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however, seem to be based on real measurements and show results that are not too far away from
the reference instrument. Therefore, a calibration of the PM2.5 measurement with the low-cost sensor
seems to be feasible.
Calibration Methodology
During the above type of measurements, it becomes obvious that not only the difference in the type
of the individual mass distribution for each of the two particle dispersion systems cause major
differences in the results of the PM2.5 measurement of low-cost sensor and reference instrument.
Also, the shift of the center of gravity in each mass distribution during a measurement causes a varying
deviation of the low-cost sensor from the reference instrument. When the ratio between the PM2.5
values of low-cost sensor versus reference instrument is formed, it becomes clearly visible that it is not
possible to just use a constant correction factor for the compensation of the low-cost sensor results
with respect to the reference instrument. In case of the mineral dust for example, the PM2.5 ratio
between both sensors varies between 0.25 and 0.65 (fig. 12a) and in the case of the smoke aerosol the
ratio varies between 0.6 at the release time of the particles (relative time 00:20:42) and 1.1 at the end
of the measurement (fig. 12b). As a consequence, a compensation function must be found that yields
values between 0.25 and 1.1 to correct the low-cost sensor results with respect to the reference
instrument for the whole variability seen in both types of particle spectra including the intra-spectral
shifts.
Fig. 12a: Variability of the ratio in the PM2.5 results for low-cost sensor versus reference instrument
for the mineral dust experiment
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PM2.5 SDS vs. Grimm
SDS/Grimm
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Fig. 12b: Variability of the ratio in the PM2.5 results for low-cost sensor versus reference instrument
for the paraffin smoke experiment
The design of a compensation function requires the identification of a measurable dependency that is
linked to the change in the compensation factor. Since the low-cost sensor only outputs a PM2.5 and
a PM10 value, the PM10/PM2.5 ratio is the most obvious value that provides information about the
shape of the particle mass spectrum, even though it remains unclear how the PM10 value is actually
calculated from the firmware of the sensor.
A very surprising observation in this respect is the effect that the ratio in the PM2.5 values between
low cost sensor and reference instrument is visibly correlated in an almost linear way to the
PM10/PM2.5 ratio reported by the low-cost sensor. This correlation was visible for both types of
particle sources, however, the slope of the linear regression curve was different.
Fig. 13a: Correlation between the ratio of the PM2.5 values of low-cost sensor and reference and the
PM10/PM2.5 ratio of the low-cost sensor for the mineral dust example
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PM2.5 SDS vs. Grimm
SDS/Grimm
y = -0,0759x + 0,8218
R² = 0,4138
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SDS/Grimm
PM10/PM2.5 SDS
SDS/Grimm vs. PM10/PM2.5 SDS
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Fig. 13b: Correlation between the ratio of the PM2.5 values of low-cost sensor and reference and the
PM10/PM2.5 ratio of the low-cost sensor for the paraffin smoke example
For further investigation, several measurements were run with particle spectra from dispersing other
aerosols and powders with either the smoke generator or the powder disperser. In each case the
dependency between the ratio in the PM2.5 values between low cost sensor and reference instrument
as well as the PM10/PM2.5 ratio reported by the low-cost sensor was analyzed and a linear regression
curve was fitted through the data points over the range covered by the measurement. Only a few data
points were calculated on each regression curve and plotted into an overall graph for further
decimation of the data (fig. 14).
Fig. 14: Correlation results for different measurements and different particle sources
The resulting graph visualizes the overall dependency including the variability of the different particle
sources and the individual shifts within each particle spectrum. Clearly a distinct behavior for particle
spectra dispersed from the smoke generator and the powder dispenser can be recognized. The spectra
generated from the smoke generator covers a SDS/Grimm ratio for PM2.5 of 0.8 to 1.1 while the
spectra from the powder disperser cover larger ranges of ratios SDS/Grimm of 2 to 8 due to the much
larger particle sizes.
y = -0,2244x + 1,4335
R² = 0,611
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SDS/Grimm
PM10/PM2.5 SDS
SDS/Grimm vs. PM10/PM2.5 SDS
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Smoke 3sds
Powder16
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smoke19
16
Nevertheless, a clear trend is visible when a trend line is fitted through the supporting points from the
individual measurements from both particle sources (fig. 15). This trend line gives a best regression
performance (r2) when a logarithmic dependency is assumed. This characteristic also makes sense with
respect to the construction related difficulty of the low-cost sensor to detect large particles on one
hand and the tendency to overestimate the mass of very small particles on the other hand.
Fig. 15: Logarithmic regression into the overall dependency visible from all measurements
The actual calibration function for the SDS011 low cost sensor was finally taken from the fitting of a
logarithmic regression curve:
PM2.5SDS calibrated/PM2.5Grimm = -0.509*ln(PM10 SDS /PM2.5SDS)+1.2203
For compensation, the actual ratio PM10 SDS /PM2.5SDS measured by the low-cost sensor was taken to
correct the measured PM2.5SDS value:
PM2.5SDS calibrated = PM2.5SDS / (PM2.5SDS calibrated/PM2.5Grimm)
The resulting PM2.5 measurement values for the SDS011 that is now calibrated for the reference
instrument are shown in fig. 16 for the mineral dust particle spectrum generated from the powder
disperser. For this type of particle spectrum, the deviation of the low-cost sensor was particularly
strong due to the dominance of large particles.
y = -0,509ln(x) + 1,2203
R² = 0,8158
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PM10/PM2.5 SDS
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Fig.16: Result of the calibrated low-cost sensor (red) with respect to the uncalibrated low-cost sensor
and the reference instrument for the mineral dust experiment
Fig. 17: Ratio of PM2.5 values between the low-cost sensor and the reference before and after
calibration for the mineral dust experiment
During the initial spike where larger particles appear in the particle spectrum a close fit of the
calibrated sensor can now be observed. The same is the case for the end of the measurement when
the small particles dominate the spectrum. The fit is less perfect for the midrange. However, the ratio
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PM2.5 Calibration Result
Grimm SDS SDS calibrated
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PM2.5 SDS vs. Grimm
SDS/Grimm SDScalib/Grimm
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between low-cost sensor and reference is now much closer to the reference instrument (factor 1.2)
than without calibration (factor 0.45). The overall RMS-error was 59.93µg/m3 before calibration and is
now 16.00µg/m3 after calibration. Assuming an average measurement value of 200ug/m3 this means
an accuracy improvement from 30% before calibration and 8% after calibration.
For the particle spectra generated with the smoke generator the deviation of the uncalibrated SDS011
low-cost sensor with respect to the reference instrument was less pronounced particularly at the end
of the measurement when almost only small particles dominated the spectrum. Therefore, the
expectation for the calibrated sensor was that the application of the compensation will not worsen the
match between both instruments. Fortunately, the calibrated SDS011 shows even a small
improvement at the beginning of the measurement (factor 1.15 instead of 0.8 with respect to the
reference instrument). At the end of the measurement the perfect match (factor 1) indeed remained
even after the calibration. In this experiment the overall RMS-error was 33.98µg/m3 before calibration
and is now 30.27µg/m3 after calibration (fig. 18 and 19).
Fig. 18: Result of the calibrated low-cost sensor (red) with respect to the uncalibrated low-cost sensor
and the reference instrument for the paraffin smoke experiment
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PM2.5 Calibration Result
Grimm SDS SDS calibrated
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Fig. 19: Ratio of PM2.5 values between the low-cost sensor and the reference before and after
calibration for the paraffin smoke experiment
Conclusion
Low-cost PM2.5 sensors that also provide a PM10 measurement output such as the SDS011
manufactured by Nova Fitness Inc. may significantly deviate in their measurement results compared
to reference equipment due to their cost-efficient construction. This deviation may be large for PM10
since the device is actually not able to measure PM10 correctly but simply does an extrapolation from
a measurement of particle sizes much smaller than 10µm. However, for PM2.5 this deviation is
moderate and a calibration of the PM2.5 with respect to the reference instrumentation is feasible and
makes sense. Even though the PM10 measurement output often does not reflect the value measured
with reference instrumentation correctly, it still provides additional information that can be used for
calibration of the PM2.5 output.
In this study a calibration concept was developed that is based on the finding that the PM10/PM2.5
ratio of the low-cost sensor gives an indication for the particle mass distribution that significantly
influences the PM2.5 measurement inaccuracies. Therefore, the PM10/PM2.5 value ratio of the low-
cost sensor was used to describe the dependency of the match between the low-cost sensor results
and a reference instrument. The dependency was measured for different conditions and different
particle spectra during a calibration measurement. A special particle generator was constructed for
the purpose of calibration to cover a wide range of particle sizes for different and complementing
particle mass distributions.
Based on the dependency of the measurement inaccuracy of the low-cost sensor on its own
PM10/PM2.5 value ratio a compensation function was derived that in turn helps to correct the PM2.5
values of the low-cost device such that it matches the result of the reference instrument with higher
accuracy. For particle spectra dominated by small particles such as smoke from paraffin generated by
a smoke generator the match of the low-cost sensor was already good without calibration and could
be slightly improved by the calibration method. For particle spectra that contained large particles such
as mineral dust, the improvement achieved with the present method was significant.
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PM2.5 SDS vs. Grimm
SDS/Grimm SDScalib/Grimm
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Literature
/1/ Laser PM2.5Sensor specification Product model SDS011 V1.3; Nova Fitness Co.,Ltd, China,
2015-10-9
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... Although both sensors are marketed as "factory calibrated", the results observed during the research would suggest a different calibration of the two sensors or a lack of calibration of one or both sensors. Before conducting field measurements, it would be essential to verify the calibration of these low-cost sensors by making measurements in controlled atmosphere chambers (with known concentrations of particulate matter in the air) or by comparison with professional instruments whose calibration is known [31]. Additionally, the poor linear correlation between the measurements made Sensors 2024, 24, 6621 9 of 16 by the two instruments throughout the monitoring period meant that one or both sensors used could not measure the true concentration of the two fractions of particulate matter. ...
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The paper discusses the results of the concentrations of atmospheric particulate matter, in the PM2.5 and PM10 fractions, acquired by two low-cost sensors. The research was carried out from 1 July 2023 to 30 June 2024, in Palermo, Sicily. The results obtained from two systems equipped with the same sensor model were compared. Excellent linear correlation was observed between the results, with differences in measurements falling within instrumental accuracy. Two instruments equipped with different sensors, models Novasense SDS011 and Plantower PMSA003, were placed at the same site. These were complemented by a weather station to measure meteorological parameters. Upon comparing the atmospheric particulate matter concentrations measured by the two instruments, it was observed that there was a good linear correlation for PM2.5 and a poor linear correlation for PM10. Additionally, the PMSA003 sensor appeared to consistently record higher concentrations than the SDS011 sensor. During periods influenced by natural sources and/or anthropogenic activities at the regional and/or local scale, i.e., the dispersal of Saharan sands, forest fires, and local events using fireworks, abnormal concentrations of atmospheric particulate matter were detected. Despite the inherent limitations in precision and accuracy, both low-cost instruments were able to identify periods with abnormal concentrations of atmospheric particulate matter, regardless of their source or type.
... Laquai and Saur (2017) [55] explain a calibration strategy for PM2.5 measured using the SDS011 sensor and using the Grimm 1.108 as a reference instrument. Based on an experimental setup, it is found that the PM10/PM2.5 ...
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Over the last decade, manufacturers have come forth with cost-effective sensors for measuring ambient and indoor particulate matter concentration. What these sensors make up for in cost efficiency, they lack in reliability of the measured data due to their sensitivities to temperature and relative humidity. These weaknesses are especially evident when it comes to portable or mobile measurement setups. In recent years many studies have been conducted to assess the possibilities and limitations of these sensors, however mostly restricted to stationary measurements. This study reviews the published literature until 2020 on cost-effective sensors, summarizes the recommendations of experts in the field based on their experiences, and outlines the quantile-mapping methodology to calibrate low-cost sensors in mobile applications. Compared to the commonly used linear regression method, quantile mapping retains the spatial characteristics of the measurements, although a common correction factor cannot be determined. We conclude that quantile mapping can be a useful calibration methodology for mobile measurements given a well-elaborated measurement plan assures providing the necessary data.
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During the last decade, extensive research has been carried out on the subject of low-cost sensor platforms for air quality monitoring. A key aspect when deploying such systems is the quality of the measured data. Calibration is especially important to improve the data quality of low-cost air monitoring devices. The measured data quality must comply with regulations issued by national or international authorities in order to be used for regulatory purposes. This work discusses the challenges and methods suitable for calibrating a low-cost sensor platform developed by our group, Airify, that has a unit cost five times less expensive than the state-of-the-art solutions (approximately €1000). The evaluated platform can integrate a wide variety of sensors capable of measuring up to 12 parameters, including the regulatory pollutants defined in the European Directive. In this work, we developed new calibration models (multivariate linear regression and random forest) and evaluated their effectiveness in meeting the data quality objective (DQO) for the following parameters: carbon monoxide (CO), ozone (O3), and nitrogen dioxide (NO2). The experimental results show that the proposed calibration managed an improvement of 12% for the CO and O3 gases and a similar accuracy for the NO2 gas compared to similar state-of-the-art studies. The evaluated parameters had different calibration accuracies due to the non-identical levels of gas concentration at which the sensors were exposed during the model’s training phase. After the calibration algorithms were applied to the evaluated platform, its performance met the DQO criteria despite the overall low price level of the platform.
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The use of low-cost air quality sensors has proliferated among non-profits and citizen scientists, due to their portability, affordability, and ease of use. Researchers are examining the sensors for their potential use in a wide range of applications, including the examination of the spatial and temporal variability of particulate matter (PM). However, few studies have quantified the performance (e.g., accuracy, precision, and reliability) of the sensors under real-world conditions. This study examined the performance of two models of PM sensors, the AirBeam and the Alphasense Optical Particle Counter (OPC-N2), over a 12-week period in the Cuyama Valley of California, where PM concentrations are impacted by wind-blown dust events and regional transport. The sensor measurements were compared with observations from two well-characterized instruments: the GRIMM 11-R optical particle counter, and the Met One beta attenuation monitor (BAM). Both sensor models demonstrated a high degree of collocated precision (R² = 0.8–0.99), and a moderate degree of correlation against the reference instruments (R² = 0.6–0.76). Sensor measurements were influenced by the meteorological environment and the aerosol size distribution. Quantifying the performance of sensors in real-world conditions is a requisite step to ensuring that sensors will be used in ways commensurate with their data quality.
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Health effects attributed to ambient fine particulate matter (PM2.5) now rank it among the risk factors with the highest health burdens in the world, but existing monitoring infrastructure cannot adequately characterize spatial and temporal variability in urban PM2.5 concentrations, nor in human population exposures. The development and evaluation of more portable and affordable monitoring instruments based on low-cost sensors may offer a means to supplement and extend existing infrastructure, increasing the density and coverage of empirical measurements and thereby improving exposure science and control. Here, we report on field calibrations of a custom-built, battery-operated aerosol monitoring instrument we developed using low-cost, off-the-shelf optical aerosol sensors. We calibrated our instruments using 1 h and 24 h PM2.5 data from a class III US EPA Federal Equivalent Method (FEM) PM2.5 β-attenuation monitor in continuous operation at a regulatory monitoring site in Oakland, California. We observed negligible associations with ambient humidity and temperature; linear corrections were sufficient to explain 60% of the variance in 1 h reference PM2.5 data and 72% of the variance in 24 h data. Performance at 1 h integration times was comparable to commercially available optical instruments costing considerably more. These findings warrant further exploration of the circumstances under which this class of aerosol sensors may profitably be deployed to generate improved PM2.5 datasets.