Performance and efficiency of removal of pharmaceutical compounds from hospital wastewater by lab-scale biological treatment system

The fate of pharmaceuticals after discharged from hospital into wastewater was clarified experimentally by using a new lab-scale conventional activated sludge (CAS) treatment reactor. The 43 target compounds belong to nine therapeutic classes (antivirals, antibacterials, anticancer drugs, psychotropics, antihypertensives, analgesic–antipyretics, contrast media, herbal medicines, and phytoestrogens) were selected with inclusion of 16 newly estimated compounds. The efficiency of the present reactor was estimated by comparing the reaction rate constant of the solid-water partition coefficients (log K_d) between liquid and solid samples and half-life during 48-h experiment obtained by using hospital effluents with those obtained by using STP wastewater. The results that no significant difference in removal efficiency was observed between both water samples (P?>?0.05) indicate high reliability of the present lab-scale reactor. The actual rates of removal when hospital effluent was applied varied widely (mean, 59?±?40%) independent of type of the pharmaceuticals. More than 90% of 17 compounds were removed after 8 h of treatment. However, the values for psychotropics (mean, 19?±?26%) and contrast media (mean, 24?±?17%) were generally low, indicating high stability. The log K_d values ranged from 1.3 to 4.8. Notably, clarithromycin, acridine, and glycitein could be removed in both liquid and solid phases. The dominant removal mechanisms were found to be different for individual pharmaceutical. These results suggest the effectiveness of introduction of the lab-scale biological treatment system for development of a new solution for discharge of pharmaceuticals from hospital.

     

印染污泥无害化处置优化研究及生命周期评价

提出印染污泥的优化处置方案,并通过生命周期评价方法(LCA)对优化方案进行环境影响评价。结果表明:与原处置工艺相比优化后环境负荷降低了11.50%。     

序言

正中国科学院资深院士、中国科学院广州地球化学研究所研究员、著名有机地球化学与沉积学家傅家谟先生离开我们已近一年,我们深沉缅怀他对地球科学、环境科学技术的卓越贡献。傅家谟院士1933年5月生于上海,原籍湖南沅江。1991年当选为中国科学院学部委员(院士)。1956年毕业于北京地质学院地质矿产系。1961年获中国科学院地质研究所硕士学位。曾任中国科学院地球化学研究所副所长、有机地球化学国家重点实验室主任、广东省环境资源利用与保护重点实验室主任,上海大学     

Occurrence of polychlorinated biphenyls (PCBs) together with sediment properties in the surface sediments of the Bering Sea, Chukchi Sea and Canada Basin

The spatial distribution and potential source of polychlorinated biphenyls (PCBs) in surface sediments from Bering Sea, Chukchi Sea, and Canada Basin and the relationship between PCBs and sedimentary properties including grain size, water content, loss on ignition, total organic carbon, and black carbon were explored. ΣPCBs (the sum of the detected PCB congeners) concentrations fluctuated in the study area, ranging from 22-150, 60-640 and 24-600 pg g(-1) dry weight for the Bering Sea, Chukchi Sea, and Canada Basin. A similar homologue pattern was observed at different locations, with tri-chlorinated PCBs being the dominant homologue, implying that the PCBs came mainly from the atmospheric transportation and deposition and ocean current transportation. No apparent co-relationships between PCB concentrations and sediment properties were obtained, indicating that the distribution of PCBs was not only controlled by their source, but also by the multi-factors such as atmospheric transport and depositing, mixing, partitioning and sorption in the water column and sediments.     

Detection of antibiotics in chicken eggs obtained from supermarkets in Ho Chi Minh City,Vietnam

The residual levels of antibiotics in Vietnamese eggs were monitored from 2014 to 2015. A total of 111 egg packages, distributed by 11 different companies, were collected from supermarkets in Ho Chi Minh City and the levels of 28 antibiotics were analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) screening method. Sixteen samples tested positive for antibiotics; a total of eight compounds (enrofloxacin, ciprofloxacin, norfloxacin, sulfadimethoxine, sulfamethazine, sulfamonomethoxine, tilmicosin and trimethoprim) were detected. Enrofloxacin was detected in eight samples, with two samples exhibiting concentrations exceeding 1,000 µg kg^?1. Tilmicosin was detected in three samples at a range of 49–568 µg kg^?1. We observed that two of the 11 companies frequently sold antibiotic-contaminated eggs (detection rates of 56 and 60%), suggesting that a number of companies do not regulate the use of antibiotics in egg-laying hens. Our findings indicate that livestock farmers require instruction regarding antibiotic use and that continual antibiotic monitoring is essential in Vietnam.     

铁炭微电解-Fe2+/K2S2O8降解甲基橙

针对偶氮类有机物废水具有色度大,难降解的特点,以对二甲基氨基偶氮苯磺酸钠(甲基橙)为模拟研究对象,对水体系中铁炭微电解-Fe2+/K2S2O8降解甲基橙的方法进行了研究。通过正交实验确定出该方法各因素的影响程度,进一步通过单因素影响实验确定该方法的最佳条件是:铁炭微电解填料、FeSO4和K2S2O8投加量分别为300 g/L、1.3mmol/L和0.7 mmol/L,初始pH值为7.0。在最佳条件下,甲基橙COD和色度去除率分别能达到64.7%和68.2%。     

The leaching of additive-derived flame retardants (FRs) from plastics in avian digestive fluids: The significant risk of highly lipophilic FRs

The exposure to plastic debris and associated pollutants for wildlife is of urgent concern,but little attention has been paid on the transfer of plastic additives from plastic debris to organisms. In the present study, the leaching of incorporated flame retardants(FRs),including polybrominated diphenyl ethers(PBDEs), alternative brominated FRs(AFRs), and phosphate flame retardants(PFRs), from different sizes of recycled acrylonitrile-butadienestyrene(ABS) polymer were investigated in avian digestive fluids. The impact of co-ingested sediment on the leaching of additive-derived FRs in digestive fluids was also explored. In the recycled ABS, BDE 209(715 μg/g) and 1, 2-bis(2,4,6-tribromophenoxy) ethane(BTBPE,1766 μg/g) had the highest concentrations among all target FRs. The leaching proportions of FRs were higher in finer sizes of ABS. The leaching proportions of FRs from recycled ABS increased with elevated logK OWof FRs. In the tests with coexisted ABS and sediment, hexato deca-BDEs, BTBPE, and decabromodiphenyl ethane(DBDPE) migrated from ABS to sediment, which resulted in the less bioaccessible fractions of these FRs in gut fluids. More lipophilic chemicals tended to be adsorbed by sediment from ABS. The results suggest the migration of additive-derived FRs from plastics to other indigestible materials in digestive fluids. The findings in this study provide insights into the transfer of additive-derived FRs from plastics to birds, and indicate the significant contribution of FR-incorporated plastics to bioaccumulation of highly lipophilic FRs.     

Impact of simulated acid rain on the growth of three species Brassica integrifolia,Brassica rapa,Brassica juncea in Hanoi,Vietnam

Environmental Science and Pollution Research - Over the past decade, the extent and magnitude of acid rain in Vietnam and other Asian countries have become more apparent. In this study, the effect...     

改性粉煤灰催化类Fenton试剂氧化法深度处理造纸废水

采用改性粉煤灰催化类Fenton试剂氧化法处理造纸废水,对COD去除率的各影响因素进行了研究。实验结果表明,在酸改性粉煤灰加入量为34 g/L、H2O2加入量为8.20 mmol/L、FeSO4加入量为8.8 mmol/L、反应时间为45 min、不调节pH的条件下,出水COD为56 mg/L,去除率可达76.45%。该法大大减少了运行费用,是一种有效的造纸废水深度处理方法。     

Polybrominated diphenyl ethers in plastic products,indoor dust,sediment and fish from informal e-waste recycling sites in Vietnam: a comprehensive assessment of contamination,accumulation pattern,emissions, and human exposure

Residue concentrations of polybrominated diphenyl ethers (PBDEs) in different kinds of samples including consumer products, indoor dust, sediment and fish collected from two e-waste recycling sites, and some industrial, urban and suburban areas in Vietnam were determined to provide a comprehensive assessment of the contamination levels, accumulation pattern, emission potential and human exposure through dust ingestion and fish consumption. There was a large variation of PBDE levels in plastic parts of obsolete electronic equipment (from 1730 to 97,300 ng/g), which is a common result observed in consumer plastic products reported elsewhere. PBDE levels in indoor dust samples collected from e-waste recycling sites ranged from 250 to 8740 ng/g, which were markedly higher than those in industrial areas and household offices. Emission rate of PBDEs from plastic parts of disposed electronic equipment to dust was estimated to be in a range from 3.4 × 10^?7 to 1.2 × 10^?5 (year^?1) for total PBDEs and from 2.9 × 10^?7 to 7.2 × 10^?6 (year^?1) for BDE-209. Some fish species collected from ponds in e-waste recycling villages contained elevated levels of PBDEs, especially BDE-209, which were markedly higher than those in fish previously reported. Overall, levels and patterns of PBDE accumulation in different kinds of samples suggest significant emission from e-waste sites and that these areas are potential sources of PBDE contamination. Intakes of PBDEs via fish consumption were generally higher than those estimated through dust ingestion. Intake of BDE-99 and BDE-209 through dust ingestion contributes a large proportion due to higher concentrations in dust and fish. Body weight normalized daily intake through dust ingestion estimated for the e-waste recycling sites (0.10–3.46 ng/day/kg body wt.) were in a high range as compared to those reported in other countries. Our results highlight the potential releases of PBDEs from informal recycling activities and the high degree of human exposure and suggest the need for continuous investigations on environmental pollution and toxic impacts of e-waste-related hazardous chemicals.