TY - JOUR
T1 - Evaluating the environmental impact of artificial sweeteners
T2 - A study of their distributions, photodegradation and toxicities
AU - Sang, Ziye
AU - Jiang, Yanan
AU - Tsoi, Yeuk Ki
AU - Leung, Kelvin Sze Yin
N1 - Funding Information:
This work has been supported by a General Research Fund (GRF) grant (Project No. HKBU 201210) from the Research Grants Council of Hong Kong Special Administrative Region, PR China . Z.Y.Sang and Y.N.Jiang gratefully acknowledge their receipts of postgraduate studentship from the University Grants Committee. We acknowledge Dr Patrick Y K Yue for his technical assistance in the toxicity test.
PY - 2014/4/1
Y1 - 2014/4/1
N2 - While having a long tradition as safe food additives, artificial sweeteners are a newly recognized class of environmental contaminants due to their extreme persistence and ubiquitous occurrence in various aquatic ecosystems. Resistant to wastewater treatment processes, they are continuously introduced into the water environments. To date however, their environmental behavior, fate as well as long term ecotoxicological contributions in our water resources still remain largely unknown. As a first step in the comprehensive study of artificial sweeteners, this work elucidates the geographical/seasonal/hydrological interactions of acesulfame, cyclamate, saccharin and sucralose in an open coast system at an estuarine/marine junction. Higher occurrence of acesulfame (seasonal average: 0.22μgL-1) and sucralose (0.05μgL-1) was found in summer while saccharin (0.11μgL-1) and cyclamate (0.10μgL-1) were predominantly detected in winter. Seasonal observations of the four sweeteners suggest strong connections with the variable chemical resistance among different sweeteners. Our photodegradation investigation further projected the potential impact of persistent acesulfame and sucralose compounds under prolonged exposure to intensive solar irradiation. Real-time observation by UPLC-ESI/MS of the degradation profile in both sweeteners illustrated that formation of new photo by-products under prolonged UV irradiation is highly viable. Interestingly, two groups of kinetically behaved photodegradates were identified for acesulfame, one of which was at least six times more persistent than the parent compound. For the first time, acute toxicity for the degradates of both sweeteners were arbitrarily measured, revealing photo-enhancement factors of 575 and 17.1 for acesulfame and sucralose, respectively. Direct comparison of photodegradation results suggests that the phototoxicity of acesulfame degradation products may impact aquatic ecosystems. In an attempt to neutralize this prolonged environmental threat, the feasibility of UV/TiO2 as an effective mineralization process in wastewater treatment was evaluated for both sweeteners. Under an environmental and technical relevant condition, a >84% removal rate recorded within 30min and complete photomineralization was achieved within 2h and delivering the best cost efficiency comparing to existing removal methods. A compilation of distribution, degradation, toxicity and attenuation results presented in this paper will go through critical discussions to explore some current issues and to pinpoint solutions for a better control in the emergent contamination of artificial sweeteners.
AB - While having a long tradition as safe food additives, artificial sweeteners are a newly recognized class of environmental contaminants due to their extreme persistence and ubiquitous occurrence in various aquatic ecosystems. Resistant to wastewater treatment processes, they are continuously introduced into the water environments. To date however, their environmental behavior, fate as well as long term ecotoxicological contributions in our water resources still remain largely unknown. As a first step in the comprehensive study of artificial sweeteners, this work elucidates the geographical/seasonal/hydrological interactions of acesulfame, cyclamate, saccharin and sucralose in an open coast system at an estuarine/marine junction. Higher occurrence of acesulfame (seasonal average: 0.22μgL-1) and sucralose (0.05μgL-1) was found in summer while saccharin (0.11μgL-1) and cyclamate (0.10μgL-1) were predominantly detected in winter. Seasonal observations of the four sweeteners suggest strong connections with the variable chemical resistance among different sweeteners. Our photodegradation investigation further projected the potential impact of persistent acesulfame and sucralose compounds under prolonged exposure to intensive solar irradiation. Real-time observation by UPLC-ESI/MS of the degradation profile in both sweeteners illustrated that formation of new photo by-products under prolonged UV irradiation is highly viable. Interestingly, two groups of kinetically behaved photodegradates were identified for acesulfame, one of which was at least six times more persistent than the parent compound. For the first time, acute toxicity for the degradates of both sweeteners were arbitrarily measured, revealing photo-enhancement factors of 575 and 17.1 for acesulfame and sucralose, respectively. Direct comparison of photodegradation results suggests that the phototoxicity of acesulfame degradation products may impact aquatic ecosystems. In an attempt to neutralize this prolonged environmental threat, the feasibility of UV/TiO2 as an effective mineralization process in wastewater treatment was evaluated for both sweeteners. Under an environmental and technical relevant condition, a >84% removal rate recorded within 30min and complete photomineralization was achieved within 2h and delivering the best cost efficiency comparing to existing removal methods. A compilation of distribution, degradation, toxicity and attenuation results presented in this paper will go through critical discussions to explore some current issues and to pinpoint solutions for a better control in the emergent contamination of artificial sweeteners.
KW - Artificial sweetener
KW - Emerging environmental contaminant
KW - Photodegradation
KW - Phototoxicity
KW - Wastewater treatment
UR - http://www.scopus.com/inward/record.url?scp=84897631998&partnerID=8YFLogxK
U2 - 10.1016/j.watres.2013.11.002
DO - 10.1016/j.watres.2013.11.002
M3 - Journal article
C2 - 24289948
AN - SCOPUS:84897631998
SN - 0043-1354
VL - 52
SP - 260
EP - 274
JO - Water Research
JF - Water Research
ER -