Subscriber access provided by University of Colorado Boulder
Article
Envisioning nano release dynamics in a changing world: using dynamic probabilistic modelling to assess future environmental emissions of engineered nanoparticles Tianyin Sun, Denise M. Mitrano, Nikolaus A Bornhöft, Martin Scheringer, Konrad Hungerbuehler, and Bernd Nowack Environ. Sci. Technol., Just Accepted Manuscript • DOI: 10.1021/acs.est.6b05702 • Publication Date (Web): 03 Feb 2017 Downloaded from http://pubs.acs.org on February 6, 2017
Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a free service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are accessible to all readers and citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.
Environmental Science & Technology is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.
Page 1 of 22
Environmental Science & Technology
1
Envisioning nano release dynamics in a changing world: using dynam-
2
ic probabilistic modelling to assess future environmental emissions of
3
engineered nanoparticles
4 5
Tian Yin Sun1,2, Denise M. Mitrano1, Nikolaus A. Bornhöft1,3, Martin Scheringer2,4, Konrad
6
Hungerbühler2 and Bernd Nowack1*
7 8
1)
Empa
–
Swiss
Federal
Laboratories
for
Materials Science
and
Technology,
9
Technology and Society Laboratory, Lerchenfeldstrasse 5, CH-9014 St. Gallen, Switzerland
10
2) Institute for Chemical and Bioengineering, ETH Zürich, CH-8093 Zürich, Switzerland
11
3) Department of Informatics, University of Zurich, Binzmühlestrasse 14, 8050 Zurich, Switzer-
12
land
13
4) RECETOX, Masaryk University, 625 00 Brno, Czech Republic
14 15
* Corresponding author
16
[email protected] 17
Tel: +41 (0)58 765 76 92
18
Fax: +41 (0)58 765 78 62
19 20 21
ACS Paragon Plus Environment
Environmental Science & Technology
22
TOC Art
23 24
ACS Paragon Plus Environment
Page 2 of 22
Page 3 of 22
Environmental Science & Technology
25
Abstract
26
The need for an environmental risk assessment for engineered nanomaterials (ENM) necessi-
27
tates the knowledge about their environmental emissions. Material flow models (MFA) have
28
been used to provide predicted environmental emissions but most current nano-MFA models
29
consider neither the rapid development of ENM production nor the fact that a large proportion
30
of ENM are entering an in-use stock and are released from products over time (i.e. have a lag
31
phase). Here we use dynamic probabilistic material flow modelling to predict scenarios of the
32
future flows of four ENM (nano-TiO2, nano-ZnO, nano-Ag and CNT) to environmental com-
33
partments and to quantify their amounts in (temporary) sinks such as the in-use stock and (“fi-
34
nal”) environmental sinks such as soil and sediment. In these scenarios, we estimate likely fu-
35
ture amounts if the use and distribution of ENM in products continues along current trends (i.e.
36
a business-as-usual approach) and predict the effect of hypothetical trends in the market devel-
37
opment of nanomaterials, such as the emergence of a new widely used product or the ban on
38
certain substances, on the flows of nanomaterials to the environment in years to come. We show
39
that depending on the scenario and the product type affected, significant changes of the flows
40
occur over time, driven by the growth of stocks and delayed release dynamics.
41 42
Introduction
43
The fast-paced growth of the nanotechnology industry brings novel materials into commercially
44
available products on a frequent basis and these engineered nanomaterials (ENM) will be re-
45
leased during the products’ life-cycle. Modelling approaches play an indispensable role in un-
46
derstanding and predicting nanomaterial concentrations in the environment that cannot be re-
47
placed by analytical measurements. Current modelling efforts have approximated the mass
48
flows to and the concentrations of ENM in environmental and technical compartments, allowing
49
researchers from many disciplines to perform more realistic studies concerning environmental
50
health and safety.1-10 The preferred approach follows a life-cycle principle tracking ENM mass-
51
flows (material flow analysis, MFA) from the production of ENM through to their final settling
52
place in environmental or waste streams. Validation of these models proves difficult as analyti-
53
cal measurements in target systems remain largely elusive11. However, all these models were
54
static and did not consider time-dependent processes with respect to the use of nanoproducts and
55
release of ENM, which will become an increasingly important factor in the future.
56
Static MFA models for ENM represent an oversimplification of the system in two respects; 1)
57
only input from production, manufacturing and consumption that occurs in one year is account-
58
ed for and then distributed over the system immediately and 2) the assumption that all ENM
ACS Paragon Plus Environment
Environmental Science & Technology
59
produced and applied in products are released to waste streams and the environment in the same
60
year in which they enter the system. These pitfalls will become increasingly apparent as the
61
number of products that contain nanomaterials begin to increase on the market and the accumu-
62
lation of significant stocks of ENM in the anthroposphere, which currently are not considered,
63
continues. It is particularly important to account for realistic releases into technical and envi-
64
ronmental compartments over a product life-time of many years. The release from these stocks
65
is not necessarily an immediate or linear process but rather one that is dependent on how ENM
66
are used in products and is related to specific releases dictated by their use and disposal path-
67
ways12, 13.
68
While first attempts have been made in considering accumulation in environmental sinks, such
69
as soil, and sediment7, 14, these models cannot predict accurate and realistic emissions into these
70
compartments because the dynamics of production and release from products have not been tak-
71
en into account. For a limited system only involving waste incineration plants, Walser and
72
Gottschalk attempted to adapt older models for dynamic material transfer between compart-
73
ments.15
74
A paradigm shift in the MFA modelling process for ENM is needed to ensure that new models
75
are developed which have a dynamic nature that can encompass the inclusion of ENM stocks.
76
This is an indispensable element of MFA for modelling substance metabolism in the anthropo-
77
sphere16. Conceptually, this modelling approach is different from previous models used to ap-
78
proximate ENM emissions/flows into various environmental compartments in its levels of so-
79
phistication, accuracy and therefore applicability. This step towards a more holistic modelling
80
scheme comes from the convergence of two existing modelling methods: probabilistic materials
81
flow analysis (P-MFA) and dynamic material-flow analysis (D-MFA). With P-MFA, uncertainty
82
in the data used for a given model parameter is addressed as a probability distribution, therefore
83
representing the comprehensive picture of the current understanding. D-MFA17-19 is able to as-
84
sess the past, present and future flows of a material relying on knowledge of how the target sys-
85
tem behaves and does not use the simplified assumption of immediate releases into the system
86
with the additional inclusion of stocks and timed releases. Uncertainty in the system is not usu-
87
ally emphasised in D-MFA20. The dynamic probabilistic MFA (DP-MFA) method recently de-
88
veloped by Bornhöft et al. fills this gap 21. This method provides information about the behav-
89
iour of the system as a function of time while representing all uncertain system parameters as
90
probability distributions. Built on this general DP-MFA framework, Sun et al.22 developed a
91
customised dynamic probabilistic material flow model predicting the mass-flows of four ENM –
92
nano-TiO2, nano-ZnO, nano-Ag, and CNT – to technical and environmental compartments and
93
the resulting concentrations in these compartments over time. One of the main assumptions of
94
Sun et al. is that the share of ENM applied in different products remains constant over time.
ACS Paragon Plus Environment
Page 4 of 22
Page 5 of 22
Environmental Science & Technology
95
However, this is a simplification, especially in a world with a rapid advancement of technology
96
and the appearance and establishment of new products alongside increased regulatory measures
97
that seek to limit facets of this technology.
98
The aims of this work were to predict scenarios of future flows of four ENM (nano-TiO2, nano-
99
ZnO, nano-Ag and CNT) to environmental compartments. In these scenarios, we estimate future
100
amounts if the use of ENM in products continues along current trends and predict the effect of
101
hypothetical trends in the market development of nanomaterials.
102
Methods
103
General principle
104
The general principle of the DP-MFA21 model can be summarised by the following three fea-
105
tures: 1) the use of a life-cycle concept, 2) the application of a probabilistic approach and 3) dy-
106
namic considerations. Following a life-cycle concept, the model tracks the mass-flows of four
107
ENM (nano-Ag, nano-TiO2, nano-ZnO, and CNT) from ENM production to incorporation into
108
commercial products and finally from the products to technical and environmental compart-
109
ments during/after their use and disposal12. We estimated the release of ENM from products as
110
described in Sun et al22. Probabilistic methods were employed for all the parameters used in the
111
modelling processes to address the inherent uncertainty in the raw data used23. The dynamic
112
considerations in this work are comprised of three aspects: the input dynamics, the dynamics of
113
use scenarios and the release dynamics. The input dynamics describe the annual production of
114
ENM as inflows into the system within a given period. The dynamics of the allocation to nano-
115
products address the change of the share of ENM in different products over time. The release
116
dynamics describe the time-dependent ENM release kinetics from a specific product category
117
over its entire lifecycle.
118
DP-MFA is separated into two modules21: the release module and the distribution module, as
119
depicted in Figure 1. The release module addresses the input dynamics, the use scenarios and
120
the (product) release dynamics. It describes the annual ENM production entering the anthropo-
121
sphere system in the European Union (EU) over a period, the changes of the ENM-shares in
122
product categories, and the flows from product categories by immediate release or into in-use
123
stocks and finally the release from in-use stocks. “In-use stocks” in our model represent those
124
ENM that are contained in products or applications during a use-phase that is longer than one
125
year. The total annual release of ENM is then transferred to the compartments of the distribution
126
module. The distribution module is built upon our previous static model3, which describes the
127
ENM transfers within and between technical and environmental compartments.
ACS Paragon Plus Environment
Environmental Science & Technology
128
129 130
Use: Use phase release; EoL: End of Life phase release.
131
Figure 1: Schematic visualization of the release module (input dynamics, mass distribution and
132
the time dependent ENM release dynamics) and the distribution module (movement of ENM
133
to/among technical and environmental compartments after product release). Hourglass symbols
134
represent a phase in the release cycle where product-dependent timed releases occur defined by
135
the life cycle of the given product and the expected yearly releases associated with use and dis-
136
posal over the products lifetime. Stop watches indicate places where releases of ENM are
137
stocked and “stored” for later release in future yearly cycles. In the distribution module, tech-
138
nical systems/compartments include wastewater treatment, waste incineration, landfill and re-
139
cycling; environment indicates compartments of air, soil, surface water and sediment. Releases
140
from production/manufacturing are considered but not depicted in this scheme.
141 142
Input dynamics
143
The estimation of production of ENM over time was determined by multiplying the base year
144
production (2012) with retrospective and prospective scaling factors as described in the Sup-
145
porting Information. The production of the four ENM in 2012 is based on updated probability
146
distributions3, 22. The scaling factors for each individual year were based on ENM market pro-
147
jections, nanotechnology patent analysis and direct information on ENM production when
148
available22. We used the assumption that the development of ENM production is proportional to
149
nanotechnology development.
150 151
Product release dynamics
ACS Paragon Plus Environment
Page 6 of 22
Page 7 of 22
Environmental Science & Technology
152
In our definition, release refers to ENM that leaves the production, manufacturing and consump-
153
tion (use) phase and is subsequently transferred to technical or environmental compartments.
154
ENM that reside in the in-use stock are not yet considered released. The scheme in Figure 1 de-
155
picts how ENM are released in a time-dependent manner from products. Modelling the release
156
of ENM from products to environmental and/or technical compartments proceeds in three steps:
157
1) separation of ENM allocated in one product category into the “Use release” and/or “End of
158
Life (EoL) release”; 2) scheduling of Use and EoL releases, i.e. allocating timed release from
159
each product category in the use phase or product disposal; and 3) distribution of ENM into
160
technical and/or environmental compartment(s) after leaving the Use release and/or EoL release
161
at the specified time. The magnitude of the mass of ENM moving from one stage in a compart-
162
ment to the next takes into account the amount of ENM in the originating compartment but also
163
hinges on the transfer coefficients (TC), where TC values are summarized in our previous stud-
164
ies3, 22. An example of the release parameters is given in Table S2 (Supplementary Information).
165
SI Table S3 provides the new TC values for CNT applied in tyres.
166
The time line of ENM release from products and into the environment or technical compart-
167
ments were established alongside the complete product life times to establish a timed-release
168
schedule. The release kinetics of ENM are specific to which products the ENM are used in,
169
which ENM is applied and how the ENM is bound in a product. Preferably, this information is
170
based on experimental data but it was estimated by expert judgement when no experimental re-
171
sults were available. The EoL release is dictated by the lifetime of the product. Product lifetimes
172
are often independent of ENM application, therefore the period of time a product is used before
173
it is disposed of is either well known or can be easily estimated. A detailed description of the pa-
174
rameters used for the product use schedule and the EoL release schedule is given in the Support-
175
ing Information.
176
The model includes some ENM transformation reactions during release or in technical com-
177
partments3, but no further fate in environmental sinks, such as soils, is considered. Additionally,
178
some transformation processes of ENM may make them inherently loose their “nano” proper-
179
ties, such as when ENM dissolve, become irreversibly complexed to natural particles, or be
180
transformed during some stages of the product life-cycle.24 Therefore, the values given for ENM
181
in environmental sinks represent upper limits for total ENM concentrations.
182 183
Definition of use scenarios
184
We defined six scenarios to explore possible ENM developments. The total ENM production is
185
assigned to different nano-enabled product categories (e.g. cosmetics, textiles, paints, etc.) in
186
shares based on the information provided by our previous work.3 This allocation of ENM to ACS Paragon Plus Environment
Environmental Science & Technology
187
product categories is assumed to remain constant over the timeline considered in this study
188
(1990 to 2020) for the base scenario. For hypothetical scenarios, such as a ban or increase of
189
ENM in a specific application, a gradual change of the share of ENM allocated to a specific
190
product is considered and the timeline is extended to better exemplify the ramifications of the
191
situation. The settings and assumptions of the chosen scenarios are summarised in Table 1.
192 193
Business as usual (Base scenario - BASE)
194
The business as usual approach is based on the production and mass allocation to products of
195
ENM from 1990 to 2020 and assumes that after 2020 the release remains at the same values as
196
in 2020. No realistic market projections after this date are available and thus a conservative ap-
197
proach is adopted and the base scenario is defined as the production value and product distribu-
198
tion with no changes. This scenario serves as a baseline to the product-specific scenarios listed
199
below and is a snapshot of how the situation would develop if current ENM development and
200
usage trends persist.
201 202
Cease nano production and application (ENM Ban - BAN)
203
To better understand the model dynamics, specifically to uncover the importance of in-use
204
stocks and timed releases of ENM into technical and environmental compartments, we supposed
205
a hypothetical ban on the use of nano-enhanced products in the year 2020. Where previous
206
models considered ENM to be immediately released to various system compartments the year
207
after production, the in-use stocks central to the DP-MFA model show more complex release
208
dynamics in the years leading up to and after halting ENM production and incorporation into
209
new products. With production completely halted, we observe the evolution of ENM mass ac-
210
cumulation in various compartments over time until the in-use stocks of ENM have been com-
211
pletely depleted. This thought experiment provides an analysis of how long ENM would remain
212
in the consumer realm and how releases to various system compartments would evolve although
213
there are no new inputs to the system aside from the remaining in-use stock.
214 215
Selective increase or ban of individual nano-enhanced products
216
A more refined approach in understanding more probable ENM dynamics opposed to a simple
217
overarching ban was considered as a next step. The flexibility of the model allows us to amend
218
selected product categories in terms of total production input, release rate, etc. Here we explore
219
the possibilities of innovative products coming to market, which would drastically increase the
ACS Paragon Plus Environment
Page 8 of 22
Page 9 of 22
Environmental Science & Technology
220
production and implementation of a given ENM in a certain product category or, conversely, a
221
legislative ban on ENM in a certain product for e.g. health and safety concerns. In each case, we
222
can observe the dynamic changes one product category can make due to its application volume
223
on the long-term release potential of a specific ENM. This results in a chain reaction affecting
224
the in-use stock and the final releases into environmental and technical compartments in the
225
coming years. In both cases, the hypothetical augmentation of production values was compared
226
to the business as usual (BASE) values. The scenarios put forward in this work include: a ban of
227
nano-TiO2 in cosmetics 25, a ban of nano-Ag in textiles 26, increased use of nano-TiO2 in con-
228
crete in building and road constructions 28, 29
27
and finally the increased production of CNT for use
229
in tyres
. Many of these scenarios have been previously advocated by NGOs, scientists or
230
companies and thus the results presented in this study can help to determine the impact of these
231
calls to ENM management. The detailed transfer factors used for the scenarios are given in the
232
Supporting Information.
233
In the cases of banned items, a new policy to phase out products is not instantaneous from one
234
year to another and therefore the total share of ENM in a certain product category of interest
235
was linearly decreased from the material distribution in the year 2015 until the ban year (2020),
236
thus gradually reaching the target proportion (0%) over a span of five years. Two hypothetical
237
scenarios are shown representing divergent ENM release patterns and product market shares.
238
One product (nano-TiO2 in cosmetics) makes up a dominant fraction (60%) of total use of nano-
239
TiO2 to date and has total, immediate release in one year; thus exemplifying a situation where
240
no in-use stock will be carried over in future years once the ban has taken place. Conversely, the
241
examination of a ban of nano-Ag in textiles constitutes a decidedly smaller market share of Ag
242
products (25%) but the in-use stock has longer viability; thus having smaller yet longer-term
243
impact on total nano-Ag output into various environmental and technical sectors over time.
244
As was the case with banned materials, implementation and adoption of new technology slowly
245
gains popularity and thus a linear increase of ENM in target categories was used. The justifica-
246
tion for increasing nano-TiO2 in concrete from 0% to 10% arose from recent estimates that this
247
use might be one of the main high-volume applications for photocatalytic nano-TiO2 27. This ap-
248
plication serves to illustrate the increased use of a material that has a long life span and there-
249
fore slow releases of large in-use stocks. Currently, CNT usage in polymer nano-composites
250
drives the flow of this material with more than 99% of the annual flows of CNT coming from
251
the in-use stock and only very little immediate release. Given that CNT can improve tyre dura-
252
bility, this technology may come to the market in the future 28, 29 and so we hypothesized an in-
253
creased market share from 0% to 10% of tyres produced which contain CNT. This application
254
serves as an example where the innovation drives a large increase in ENM (CNT) production
255
and causes immediate and steady release over the use phase of the products’ lifetime.
ACS Paragon Plus Environment
Environmental Science & Technology
Page 10 of 22
256
Table 1: Summary of the hypothetical scenarios indicating selective bans or increases in production of various ENM containing products from 2015 to 2030 (or
257
2120 for the BAN scenario); previous studies refer to Sun et al. 20143 and Sun et al. 201622. 2020 was chosen as the year to end the model prediction because this
258
is the year where most of the available trend information ends (e.g. ENM production projections). Scenarios
Abbreviations
Target ENM
Business as usual
BASE
All ENM
Complete ENM ban
BAN
All ENM
Ban of nano-TiO2 in cosmetics
BAN-Cos
nano-TiO2
Ban of nano-Ag in textiles
BAN-Tex
nano-Ag
INC-Concr
nano-TiO2
INC-Tyr
CNT
Increase of nano-TiO2 in concrete Increase of CNT in tyres
Production development and time scope 1990-2020: Real production based on Sun et al. (2016) 2021-2030: Using for each year the value from 2020 1990-2020: Real production based on Sun et al. (2016) 2021-2120: No production 2015-2020: On the basis of real production as modelled in Sun et al. (2016) deducting the smaller amount used in cosmetics 2021-2030: Using for each year the value from 2020 2015-2020: On the basis of real production as modelled in Sun et al. (2016) deducting the smaller amount used in textiles 2021-2030: Using for each year the value from 2020 2015-2020: On the basis of real production as modelled in Sun et al. (2016) adding the increase of application in concrete 2021-2030: Using for each year the value from 2020 2015-2020: On the basis of real production as modelled in Sun et al. (2016) adding the increase of application in tyres 2021-2030: Using for each year the value from 2020
ACS Paragon Plus Environment
Application shares of target ENM Based on Sun et al. 2014 Based on Sun et al. 2014 Based on Sun et al. 2014, the share applied in cosmetics declines from 60% to 0% from 2015 to 2020, mass allocation to other products remains unchanged Based on Sun et al. 2014, the share of application in textiles declines from 25% to 0% from 2015 to 2020, mass allocation to other products remains unchanged, Based on Sun et al. 2014, the share of application in concrete increase from 0% to 10% from 2015 to 2020 mass allocation to other products remains unchanged Based on Sun et al. 2014, the share of application in tyres increases from 0% to 10% from 2015 to 2020, mass allocation to other products remains unchanged
Page 11 of 22
Environmental Science & Technology
259
Results and discussion
260
ENM production over time
261
Figure 2a depicts the modelled production development of nano-TiO2 in the EU between 1990 and
262
2020. Results for nano-TiO2 are demonstrated here as an example because they have the largest pro-
263
duction volume amongst the four ENM considered in this study; the results for other ENM can be
264
found in SI Figures S1. The full probability spectrum of the production development is used as the
265
main input for the dynamic flow modelling. The grey dots represent single model runs with single val-
266
ues randomly selected out of the underlying probability distributions. The denser the grey dots appear,
267
the more likely the modelled value is. The mean value is shown by the red line. The uncertainty is
268
quantified by the width of the gap between the 15% and 85% quantiles (dashed blue lines). The large
269
spread of the values is a consequence of combining a suite of raw data on development of nanotech-
270
nology that diverge quite significantly from each other. The probabilistic modelling is able to synthe-
271
size these data. This approach is needed because no historical data on the actual development of the
272
production of ENM are available (with the exception of CNT)30. We have based our model on the as-
273
sumption that the development of nanotechnology also reflects the trend of the production of ENM,
274
where more research, patents and scientific papers correlate to real increases in production of nano-
275
enhanced products.
276 277
Evolution of ENM in stocks and sinks from realistic estimation and hypothetical extension of produc-
278
tion (BASE scenario)
279
Figure 2b provides a full picture of the likelihood of the distribution of the nano-TiO2 development in
280
in-use stocks of products in the EU from 1990 to 2030, with modelled values from 1990 to 2020 based
281
on real production values and after 2020 the hypothetical BASE scenario is envisioned. This is visual-
282
ized by single simulations (grey lines) of 100,000 iterations with the mean value (red line) and 15%
283
and 85% quantiles (dashed blue lines). Notably, while the total net amount of ENM in the in-use stock
284
is currently increasing because of assumed increased input from new nanomaterials in the BASE sce-
285
nario, other scenarios may not always exhibit sustained growth in all sectors of the in-use stock over
286
time. Figure 2c highlights the mean values of nano-TiO2 accumulated after production and the amount
287
accumulated in the in-use stock, landfills, sludge treated soil and sediment, from which we can deter-
288
mine the dominant fate of nano-TiO2 in a holistic way. In the BASE scenario, all the stocks exhibit an
289
exponential-like increase over time. This is caused by both the primary input increasing yearly (i.e. in-
290
creased stock production) and ENM accumulation in each compartment from year to year; especially
291
in those stocks which are currently considered as final sinks (landfills, soil and sediment).
292
ACS Paragon Plus Environment
Environmental Science & Technology
293 294
Figure 2: a. Estimated annual production development of nano-TiO2 in the EU from 1990 to 2020 with
295
hypothetical extension to 2030 assuming the production after 2020 remains the same. Short grey lines
296
(dots) indicate single modelled values. The red curve is the average trend of all simulated values.
297
Dashed blue lines indicate the 15% and 85% quantile range of the probability density distribution of
298
the production. b. The evolution of nano-TiO2 amount in the in-use stock. Each grey line is a develop-
299
ment trend of a single iteration out of 100 000 simulation runs. The mean (red line) and 15% and
300
85 % quantiles are shown (blue dashed lines). The vertical width of the grey area is indicative of the
301
degree of uncertainty. c. Mean values of the evolution of nano-TiO2 in stocks and sinks as well as the
302
total accumulative production in the EU from 1990 to 2020 with hypothetical extension to 2030 as-
303
suming the production and release after 2020 remain the same. The vertical dashed green lines at year
304
2020 indicate the distinction between the results based on modelled production and release according
305
to Sun et al. (2016) and the hypothetical extension after 2020 using the values from 2020 for each ad-
306
ditional year. “Soil” here indicates the sewage sludge treated soil. Information for nano-ZnO, nano-
307
Ag and CNT are given in SI Figure S1.
308 309
Total cessation of ENM use (BAN Scenario): Understanding memory effects
310
Yearly ENM production inputs to the consumption, release and distribution system are allocated by re-
311
leases into environmental and technical compartments which are split into two fractions: the portion
312
which is immediately released and that which stays in the in-use stock for a pre-determined amount of
313
time depending on the product life-cycle. The differentiation between these two fractions is most evi-
314
dent if we hypothesise a ban of new ENM production in order to visualise the continued release of
315
ENM material from the in-use stock when there is no new production input.
316
In some cases, such as with nano-TiO2, immediate releases dominate the total flow of material, with a
317
lesser fraction being retained in products and released over many years (Figure 3a). This is based on
318
the fact that a significant fraction of products containing nano-TiO2 (e.g. cosmetics, sunscreens at 60%
319
of the total current material distribution) are slated for immediate release whereas a smaller fraction
320
(e.g. paints, consisting of 9% of the total material distribution) have a greater proportion of material al-
ACS Paragon Plus Environment
Page 12 of 22
Page 13 of 22
Environmental Science & Technology
321
located to the in-use stock for releases at later times. Because there is a high amount of initial release
322
in consumer products that have fast releases, when a ban is introduced the amount of product in the
323
market will fall immediately; i.e. the in-use stock from these sources will be fully depleted soon after
324
the ban is enforced. Other uses of nano-TiO2, such as the inclusion in paints and coatings, have a long-
325
er lifespan due to their association with building materials and so a smaller released mass will continue
326
even after the ban is in place as depicted by the small trough in Figure 3a. However, since this use
327
makes up a smaller mass of nano-TiO2, only about 12% of total nano-TiO2 released or produced would
328
be available for release in the longer-term (i.e. approximately around 80 years after its production) in-
329
use stock.
330
In other cases, as with CNT (Figure 3b), the release from the long-term in-use stocks dominates all
331
immediate releases. As the main source of using CNT is currently in polymer composites and only 1%
332
of this material is released in the first year of use, the bulk of the material flow will be dominated by
333
the scheduled in-use stock release. The lifetime of plastic items is distributed around the 8 years and
334
releases of CNT into environmental and technical compartments are scheduled according to the dis-
335
posal of these items. Therefore, even after the ban has come into place, release of CNT from products
336
produced before the ban will continue. Similar to the case of nano-TiO2, due to the fact that a very
337
small fraction (around 3%) of CNT is applied in paints, there is also a much delayed emergence of re-
338
lease after the ban takes place.
339
This hypothetical ban exemplifies how the improved DP-MFA and its possibility to model memory ef-
340
fects can more accurately assess the timeline of ENM releases into environmental and technical sys-
341
tems, because releases are more closely coupled with the life-cycle of individual products and realistic
342
release rates from year to year. Older, static versions of the model did not account for timed releases
343
and so this model memory effect (i.e. the accumulation of ENM in stocks and timed releases) was not
344
considered. As more products reach the market which contain ENM, the in-use stock will become in-
345
creasingly important as essentially an additional, delayed source of particles to environmental and
346
technical systems. In previous models, the production values in one year were completely distributed
347
to the environment in a single year, an assumption that our dynamic modelling has clearly shown to
348
not be representative for the ENM investigated.
349 350
ACS Paragon Plus Environment
Environmental Science & Technology
351 352
Figure 3: Stacked graph of total mass of nano-TiO2 (a.) and CNT (b.) released either immediately
353
(blue sectors) or from in-use stocks (orange sectors) before and after the hypothetical ban of all pro-
354
duction and application in 2020 (BAN scenario). Mass evolution of accumulated productions (orange
355
lines) for nano-TiO2 (c.) and CNT (d.) and the accumulated mass in sink compartments (landfill, soil,
356
sediment and export) until in-use stocks (red trace) are depleted in the BAN scenario.
357 358
Importance of timed release for the accumulation of ENM in sinks
359
The model memory of scheduled releases has further-reaching effects than a simple delayed release to
360
the distribution portion of the model. This also influences the timing of ENM mass that reaches each
361
system compartment and final sink. Following the hypothetical ban of all ENM production in 2020,
362
we can note a few trends differentiating the various ENM and how they are allocated to environmental
363
and technical compartments, even with no further inputs to the system (Figures 3c and 3d.).
364
For example, nano-TiO2 exhibits an initial drop of the in-use stock with a longer tail until it is depleted
365
and this is directly due to the importance of the distribution of the ENM in each of the product sectors
366
(Figure 3c). In this case, the products which dominate the distribution of ENM in products are those
367
where there is a high amount of ENM that are released on a short time scale to one environmental sec-
368
tor (e.g. nanoTiO2 release from cosmetics/sunscreens release to the wastewater treatment system and
369
ultimately to the landfill). This will cause an initial depletion of the in-use stock shortly after the ban in
ACS Paragon Plus Environment
Page 14 of 22
Page 15 of 22
Environmental Science & Technology
370
2020 (Figure 3c), and subsequent distribution of most of the ENM mass amongst the affected sinks.
371
Therefore the accumulation of nano-TiO2 in sediment and soil will not significantly increase a few
372
years after the ban because the in-use stock and flow of ENM contributing to these compartments has
373
been depleted. However, other uses of nano-TiO2, such as the inclusion in paints and coatings associ-
374
ated with building materials, have a longer lifespan (80 years) and so additional releases of ENM to
375
the landfill are anticipated even after the ban is in place. In brief, environmental and technical com-
376
partments remain at a near steady-state condition with no further input into the system almost immedi-
377
ately after the ban is in effect for nearly 80 years until the release of nano-TiO2 from construction
378
waste is scheduled for release, after which the in-use stocks of nano-TiO2 are finally diminished from
379
the pre-ban timeline.
380
Conversely, CNT are currently dominantly used in consumer products such as plastics that have a very
381
low initial release (1%) and thus a longer lagged release from the product into environmental and
382
technical systems. While the in-use stock of CNT is slowly consumed post ban, a continuous addition
383
of CNT to sink compartments will occur several years after the ban due to the delayed releases of CNT
384
from plastics (see from 2020 to 2040 in Figure 3d). It is only when these stocked products are finally
385
disposed of at the end of the life cycle into the landfill (averaging 10 years post-production) that the
386
mass of ENM emitted reaches a steady state; a situation that is directly dictated by the length of prod-
387
uct use and release rates of ENM.
388 389
Influence of variable ENM product incorporation, use and selective ban scenarios on ENM mass flows
390
When hypothetical developments in the use of ENM in products based on selective policy bans or de-
391
velopment and implementation of new technology are considered, the mass of ENM reaching surface
392
water and soil in some instances could change substantially in the near future. Factors influencing the
393
change in the magnitude of release compared to the BASE scenario include 1) share of products af-
394
fected by the change in ENM usage, 2) ENM timed release scheme over the product lifetime (i.e. short
395
vs. long in-use phase), 3) destination of ENM after product release (i.e. environmental or technical
396
compartment) and 4) the transfer parameters over the entire process, both in the release and distribu-
397
tion modules. The development of ENM emissions between 2015 and 2030 in the various scenarios
398
envisioned can be compared to the BASE scenario to better grasp to what extent changes in ENM us-
399
age may affect the mass of ENM reaching the environment (Figure 4).
400
ACS Paragon Plus Environment
Environmental Science & Technology
401 402
Figure 4. Developments of ENM emissions to soil and surface water compartments between 2015 and
403
2030 based on the different scenarios as described in Table 1 compared to the base scenario (BASE).
404
For surface water (panels a. and d., shown in blue and green colours), which is a flow-through com-
405
partment, the annual emissions are shown; for soil (both natural, urban and sewage sludge treated
406
soils, shown in red and grey colours), which is a sink-compartment, panels b. and e. show the annual
407
emissions and panels c. and f. the accumulated mass. The average evolution of emissions and cumula-
408
tive mass in each scenario is indicated by darker lines with yearly markers (dots). Corresponding col-
409
oured bands express the range between the 15% and 85% quantiles, which delineates the uncertainty
410
in the results. The small year-to-year fluctuations of the annual emission are derived from random var-
411
iations of the stochastic simulations.
412 413
Given that cosmetics constitute up to a 60% share of all nano-TiO2 uses3 and the majority of this frac-
414
tion is released immediately to surface water after the product use phase, once the mass of this fraction
415
of the nano-TiO2 product distribution decreases there will be a significant reduction of total nano-TiO2
416
emitted to the surface water (Figure 4a). In the BASE scenario, the evolution of emissions into surface
417
water has a positive correlation with annual nano-TiO2 input, as noted by the steady increase in nano-
418
TiO2 to surface water between 2015 and 2020, but remains constant thereafter because the input mass
419
was fixed to the 2020 value in future projections. The discrepancy between nano-TiO2 emissions of the
420
BASE and BAN-Cos scenarios demonstrate the effect of this cosmetics ban, where the annual emis-
ACS Paragon Plus Environment
Page 16 of 22
Page 17 of 22
Environmental Science & Technology
421
sions of nano-TiO2 to surface water would be projected to decrease by nearly three quarters. From
422
2020 onwards, the difference between the BASE and BAN-COS remains steady because the total in-
423
put into both modelled systems remains constant due to steady inputs from other product sectors using
424
nano-TiO2, for example cleaning agents and consumer appliances.
425
Conversely, little difference in both the annual emission to and the accumulation of nano-TiO2 in soil
426
between the BASE scenario and INC-Concr were observed between 2015 and 2030 (Figure 4b and
427
4c). This result stems from two sources. Firstly, the transfer data for nano-TiO2 applied in concrete
428
were the same as those used for paints, where only 1% is released during use and 99% is defined as
429
EoL release. Because emissions to natural and urban soils account for only 25% of the total use re-
430
lease, a mere 0.25% additional yearly increase derives from the increased use of nano-TiO2 in con-
431
crete. Secondly, because the bulk of the release is slated to occur at the EoL phase, averaging 80 years
432
post-production, we would only expect the in-use stocks of our hypothetical system to deviate from
433
the BASE scenario on a longer time frame. However, even then low emissions to soil are expected
434
given that after building demolition, as 30% of concrete goes to landfill and 70% is recycled. There-
435
fore the addition of nano-TiO2 to concrete appears to not expose soils to a large increase of ENM when
436
compared to all other uses of nano-TiO2 and the accompanying releases.
437
There is approximately a 20% reduction in nano-Ag emissions to surface water when the BASE and
438
BAN-Tex scenarios are compared (Figure 4d). The mass of Ag released from the textile during the use
439
phase, which has shown to be variable under different use conditions31, 32, has significant ramifications
440
both on the initial release to water but also on the mass of Ag remaining on the textile that will further
441
be distributed during the EoL phase. Secondly, releases to the surface water from nano-textiles first
442
must pass through the wastewater treatment plant, and so any variations in this transfer factor would
443
directly affect the calculated amount of nano-Ag emitted to surface water.
444
A significant difference between the BASE scenario and a hypothetical change to ENM use is found in
445
the case of increased CNT application in tyres (INC-Tyr) and the subsequent annual emission to and
446
accumulation of CNT in soil (Figure 4e and 4f). Approximately 9% of the total mass of the tyre is ex-
447
pected to be lost during the use phase (Table S2), which corresponds to the 9% out of the 10% (Table
448
1) of CNT applied in tyres being released during the use phase. Out of this fraction, approximately
449
half is estimated to be destined for the soil environmental compartment. This application accounts for
450
up to 0.5% of the total share of CNT consumption in all product categories. By the year 2030, the an-
451
nual CNT emission to soil rises to 40 tonnes in contrast to approximately 20 tonnes for the BASE sce-
452
nario; for the accumulated CNT mass in soil, the value of the INC-Tyr scenario is projected to rise to
453
approximately 500 tonnes by 2030.
ACS Paragon Plus Environment
Environmental Science & Technology
454
Calculating the ratio of the accumulated mass in the soil to the annual emission to this compartment,
455
we see that in the early stages of increased CNT use (e.g. 2015), the annual flow accounts for approx-
456
imately one fifth of the accumulated mass, by 2020 this value drops to less than one tenth.
457 458
Implications of the model results
459
For all the scenarios developed in this work and the flows quantified for extended periods of time, we
460
did not include any transformation reactions of the ENM after they end up in environmental compart-
461
ments. We have only taken into account some specific and well-studied transformations of ENM dur-
462
ing wastewater treatment (sulfidation of nano-Ag and ZnO) and incineration processes (combustion of
463
CNT), of which the transformed fraction is represented by the virtual compartment “elimination”. The
464
emissions to landfill, soil, surface water, sediment that we provide therefore constitute a likely upper
465
bound for material flows depending on the ENM investigated. The mass flows given in Figure 4 may
466
therefore be lower for a reactive material, such as nano-Ag, which can dissolve or undergo chemical
467
transformation reactions. These mass flows are also one of the primary input data for environmental
468
fate models that describe mechanistically the fate of ENM in natural systems33-36. In these models the
469
further dissolution/transformation over time of the deposited masses can be predicted.
470
The ability to predict the dynamic flows of ENM to several environmental and technical compartments
471
based on prospective changes in materials development is an important development for the risk as-
472
sessment of ENM. The risk, comprised of the combination of hazard and exposure, of using nano-
473
enhanced products can change over time depending on the flow of ENM to the environment. The
474
emissions data generated from our previous (static) modelling efforts3, 7 have long stood as bench-
475
marks for the likely exposure values in the risk equation and therefore were used as realistic ENM
476
concentrations when evaluating the fate of ENM in the environment33, 37, 38 or to assess environmental
477
risks of ENM39, 40. A more refined, time-resolved analysis of this emissions data assists in more realis-
478
tic risk assessments as well as provides improved input data for environmental fate models, such as to
479
follow the heteroagglomeration in natural waters38. By better assessing the relative impact of the use
480
of given nano-enabled products over time both researchers and regulators may be able to better assess
481
the pros and cons of implementing new products and the potential for far reaching affects that curbing
482
ENM usage may have on various environmental sectors.
483 484
Acknowledgements
485
Tian Yin Sun was supported by project 406440_131241 of the Swiss National Science Foundation
486
within the National Research Program 64. Nikolaus A. Bornhöft was supported by the European
487
Commission within the Seventh Framework Programme (FP7; MARINA project - Grant Agreement ACS Paragon Plus Environment
Page 18 of 22
Page 19 of 22
Environmental Science & Technology
488
n° 263215). Martin Scheringer acknowledges financial support by the Czech Ministry of Education,
489
Youth, and Sports (LM2015051) and Masaryk University (CETOCOEN PLUS project).
490 491
Supporting Information
492
Description of input dynamics; raw data for production volume; data used for parameterization; trans-
493
fer coefficients; Figure with dynamic evolution of production and amounts in stocks for nano-ZnO,
494
nano-Ag and CNT; product use release schedule, EOL release schedule.
495
ACS Paragon Plus Environment
Environmental Science & Technology
496
References
497 498 499
1. Liu, H. H.; Bilal, M.; Lazareva, A.; Keller, A.; Cohen, Y., Simulation tool for assessing the release and environmental distribution of nanomaterials. Beilstein Journal of Nanotechnology 2015, 6, 938-951.
500 501
2. Keller, A. A.; Lazareva, A., Predicted Releases of Engineered Nanomaterials: From Global to Regional to Local. Environmental Science & Technology Letters 2013, 1, (1), 65-70.
502 503 504
3. Sun, T. Y.; Gottschalk, F.; Hungerbühler, K.; Nowack, B., Comprehensive probabilistic modelling of environmental emissions of engineered nanomaterials. Environmental Pollution 2014, 185, (0), 69-76.
505 506
4. Arvidsson, R.; Molander, S.; Sandén, B. A., Particle Flow Analysis. Journal of Industrial Ecology 2012, 16, (3), 343-351.
507 508 509
5. Blaser, S.; Scheringer, M.; MacLeod, M.; Hungerb¸hler, K., Estimation of cumulative aquatic exposure and risk due to silver: Contribution of nano-functionalized plastics and textiles. Science of the total environment 2008, 390, (2-3), 396-409.
510 511
6. Boxall, A.; Tiede, K.; Chaudhry, Q., Engineered nanomaterials in soils and water: how do they behave and could they pose a risk to human health? Nanomedicine 2007, 2, (6), 919-927.
512 513 514
7. Gottschalk, F.; Sonderer, T.; Scholz, R.; Nowack, B., Modeled environmental concentrations of engineered nanomaterials (TiO2, ZnO, Ag, CNT, fullerenes) for different regions. Environmental Science and Technology 2009, 43, (24), 9216-9222.
515 516 517
8. Johnson, A.; Cisowska, I.; Jurgens, M.; Keller, V.; Lawlor, A.; Williams, R., Exposure assessment for engineered silver nanoparticles throughout the rivers of England and Wales (CB0433). Centre for Ecology and Hydrology, UK 2011.
518 519
9. Keller, A. A.; McFerran, S.; Lazareva, A.; Suh, S., Global life cycle releases of engineered nanomaterials. Journal of Nanoparticle Research 2013, 15, (6), 1-17.
520 521
10. O'Brien, N.; Cummins, E., Nano-Scale Pollutants: Fate in Irish Surface and Drinking Water Regulatory Systems. Human and Ecological Risk Assessment 2010, 16, (4), 847-872.
522 523 524 525
11. Nowack, B.; Baalousha, M.; Bornhoft, N.; Chaudhry, Q.; Cornelis, G.; Cotterill, J.; Gondikas, A.; Hassellov, M.; Lead, J.; Mitrano, D. M.; von der Kammer, F.; Wontner-Smith, T., Progress towards the validation of modeled environmental concentrations of engineered nanomaterials by analytical measurements. Environmental Science: Nano 2015, 2, (5), 421-428.
526 527 528
12. Mitrano, D. M.; Motellier, S.; Clavaguera, S.; Nowack, B., Review of nanomaterial aging and transformations through the life cycle of nano-enhanced products. Environment international 2015, 77, 132-147.
529 530 531
13. Froggett, S.; Clancy, S.; Boverhof, D.; Canady, R., A review and perspective of existing research on the release of nanomaterials from solid nanocomposites. Particle and FibreToxicology 2014, 11, 17.
532 533 534
14. Sun, T. Y.; Conroy, G.; Donner, E.; Hungerbuhler, K.; Lombi, E.; Nowack, B., Probabilistic modelling of engineered nanomaterial emissions to the environment: a spatio-temporal approach. Environmental Science: Nano 2015, 2, (4), 340-351.
535 536
15. Walser, T.; Gottschalk, F., Stochastic fate analysis of engineered nanoparticles in incineration plants. Journal of Cleaner Production 2014, 80, 241-251.
537 538
16. Baccini, P.; Brunner, P. H., Metabolism of the Anthroposphere: Analysis, Evaluation, Design. Second ed.; The MIT Press: Cambridge, MA, USA, 2012; p 408.
539 540 541
17. Spatari, S.; Bertram, M.; Gordon, R. B.; Henderson, K.; Graedel, T. E., Twentieth century copper stocks and flows in North America: A dynamic analysis. Ecological Economics 2005, 54, (1), 37-51.
ACS Paragon Plus Environment
Page 20 of 22
Page 21 of 22
Environmental Science & Technology
542 543
18. Tabayashi, H.; Daigo, I.; Matsuno, Y.; Adachi, Y., Development of a Dynamic Substance Flow Model of Zinc in Japan. ISIJ International 2009, 49, (8), 1265-1271.
544 545
19. Hatayama, H.; Yamada, H.; Daigo, I.; Matsuno, Y.; Adachi, Y., Dynamic substance flow analysis of aluminum and its alloying elements. Mater Trans 2007, 48, (9), 2518-2524.
546 547 548
20. Müller, E.; Hilty, L. M.; Widmer, R.; Schluep, M.; Faulstich, M., Modeling Metal Stocks and Flows: A Review of Dynamic Material Flow Analysis Methods. Environ Sci Technol 2014, 48, (4), 2102-2113.
549 550
21. Bornhöft, N. A.; Sun, T. Y.; Hilty, L. M.; Nowack, B., A dynamic probabilistic material flow modeling method. Environmental Modelling & Software 2016, 76, 69-80.
551 552 553
22. Sun, T. Y.; Bornhöft, N. A.; Hungerbühler, K.; Nowack, B., Dynamic Probabilistic Modeling of Environmental Emissions of Engineered Nanomaterials. Environ Sci Technol 2016, 50, (9), 47014711.
554 555 556
23. Gottschalk, F.; Scholz, R. W.; Nowack, B., Probabilistic material flow modeling for assessing the environmental exposure to compounds: Methodology and an application to engineered nano-TiO2 particles. Environ. Modeling Software 2010, 25, 320-332.
557 558 559
24. Mitrano, D. M.; Nowack, B., The need for a life-cycle based aging paradigm for nanomaterials: Importance of real-world test systems to identify realistic particle transformations. Nanotechnology 2017.
560 561
25. Friends of the Earth Nanomaterials, sunscreen and cosmetics: small ingredients big risks; 2006.
562
26.
563 564 565
27. Bossa, N. Nanotechnologies et matériaux de construction: Mécanismes de relargage des nanomatériaux durant l’utilisation et la dégradation des ciments photocatalytiques. Université d’AixMarseille, 2015.
566 567
28. Kim, Y. N., Rubber composition comprising carbon nanotubes as reinforcing agent and preparation thereof. In Google Patents: 2003.
568 569
29. OCSIAL TUBALL — http://ocsial.com/en/product/tuball/
570 571
30. Piccinno, F.; Gottschalk, F.; Seeger, S.; Nowack, B., Industrial production quantities and uses of ten engineered nanomaterials in Europe and the world. J Nanopart Res 2012, 14, (9), 1-11.
572 573 574 575
31. Mitrano, D. M.; Lombi, E.; Arroyo Rojas Dasilva, Y.; Nowack, B., Unraveling the Complexity in the Aging of Nanoenhanced Textiles: A Comprehensive Sequential Study on the Effects of Sunlight and Washing on Silver Nanoparticles. Environmental Science & Technology 2016, 50, (11), 57905799.
576 577 578 579
32. Reed, R. B.; Zaikova, T.; Barber, A.; Simonich, M.; Lankone, R.; Marco, M.; Hristovski, K.; Herckes, P.; Passantino, L.; Fairbrother, D. H.; Tanguay, R.; Ranville, J. F.; Hutchison, J. E.; Westerhoff, P. K., Potential Environmental Impacts and Antimicrobial Efficacy of Silver- and Nanosilver-Containing Textiles. Environmental Science & Technology 2016, 50, (7), 4018-4026.
580 581 582
33. Meesters, J. A. J.; Koelmans, A. A.; Quik, J. T. K.; Hendriks, A. J.; van de Meent, D., Multimedia Modeling of Engineered Nanoparticles with SimpleBox4nano: Model Definition and Evaluation. Environ Sci Technol 2014, 48, (10), 5726-5736.
583 584 585
34. Dale, A. L.; Casman, E. A.; Lowry, G. V.; Lead, J. R.; Viparelli, E.; Baalousha, M., Modeling nanomaterial environmental fate in aquatic systems. Environmental science & technology 2015, 49, (5), 2587-2593.
586 587 588
35. Praetorius, A.; Labille, J.; Scheringer, M.; Thill, A.; Hungerbühler, K.; Bottero, J.-Y., Heteroaggregation of Titanium Dioxide Nanoparticles with Model Natural Colloids under Environmentally Relevant Conditions. Environ Sci Technol 2014, 48, (18), 10690-10698.
Hansen, S. F.; Baun, A., When enough is enough. Nat Nano 2012, 7, (7), 409-411.
the
universal
nanomodifier
ACS Paragon Plus Environment
for
materials.
Environmental Science & Technology
589 590 591
36. Meesters, J. A. J.; Quik, J. T. K.; Koelmans, A. A.; Hendriks, A. J.; van de Meent, D., Multimedia environmental fate and speciation of engineered nanoparticles: a probabilistic modeling approach. Environmental Science: Nano 2016, 3, (4), 715-727.
592 593 594
37. Dale, A. L.; Lowry, G. V.; Casman, E. A., Stream dynamics and chemical transformations control the environmental fate of silver and zinc oxide nanoparticles in a watershed-scale model. Environ Sci Technol 2015, 49, (12), 7285-7293.
595 596 597
38. Praetorius, A.; Scheringer, M.; Hungerbühler, K., Development of Environmental Fate Models for Engineered Nanoparticles—A Case Study of TiO2 Nanoparticles in the Rhine River. Environ Sci Technol 2012, 46, (12), 6705-6713.
598 599 600
39. Gottschalk, F.; Kost, E.; Nowack, B., Engineered nanomaterials (ENM) in waters and soils: a risk quantification based on probabilistic exposure and effect modeling. Environ. Toxicol. Chem. 2013, 32, 1278–1287.
601 602
40. Garner, K. L.; Suh, S.; Lenihan, H. S.; Keller, A. A., Species Sensitivity Distributions for Engineered Nanomaterials. Environmental Science & Technology 2015, 49, (9), 5753-5759.
603
ACS Paragon Plus Environment
Page 22 of 22