添加剂对炭黑颗粒润湿和沉降性能的影响

为提高湿式除尘装置对炭黑颗粒物的去除效率,通过向吸收液中添加复配表面活性剂以提高吸收液对炭黑的润湿性,投加絮凝剂使进入吸收液的炭黑颗粒发生凝聚和沉降,从而使吸收液得以循环利用。其中表面活性剂的复配以非离子表面活性剂月桂醇聚氧乙烯（9）醚（AEO-9）为主,与十二烷基苯磺酸钠（SDBS）、十六烷基三甲基溴化胺（CTAB）和壬酚基聚氧乙烯醚（TX-10）分别复配,筛选出复配效果最好的一组复配液;然后投加絮凝剂,探讨絮凝剂的加入对吸收液中炭黑颗粒物絮凝沉降的影响。结果表明,在AEO-9浓度为0．05mmol／L,TX-10浓度为0．09mmol／L时,吸收液的表面张力最小,为36．75mN／m;投加无机絮凝剂聚合氯化铝（PAC）浓度为100mg／L时,经15min沉降,炭黑的沉降率可达88．1％,上清液中悬浮颗粒的平均粒径为6．36μm。     

Spatial distribution of perfluoroalkyl acids in the Pearl River of Southern China

An intensive campaign was conducted in September 2012 to collect surface water samples along the tributaries of the Pearl River in southern China. Thirteen perfluoroalkyl acids (PFAAs), including perfluorocarboxylates (PFCAs, C4–C11) and perfluorosulfonates (PFSAs, C4, C6–C8, and C10), were determined using high-performance liquid chromatography/negative electrospray ionization–tandem mass spectrometry (HPLC/(-)ESI–MS/MS). The concentrations of total PFAAs (ΣPFAAs) ranged from 3.0 to 52 ng L⁻¹, with an average of 19 ± 12 ng L⁻¹. The highest concentrations of ΣPFAAs were detected in the surface water of the Dong Jiang tributary (17–52 ng L⁻¹), followed by the main stream (13–26 ng L⁻¹) and the Sha Wan stream (3.0–4.5 ng L⁻¹). Perfluorooctanoate (PFOA), perfluorobutane sulfonate (PFBS), and perfluorooctane sulfonate (PFOS) were the three most abundant PFAAs and on average accounted for 20%, 24%, and 19% of ΣPFAAs, respectively. PFBS was the most abundant PFAA in the Dong Jiang tributary, and PFOA was the highest PFAA in the samples from the main stream of the Pearl River. A correlation was found between PFBS and PFOA, which suggests that both of these PFAAs originate from common source(s) in the region. Nevertheless, the slope of PFBS/PFOA was different in the different tributaries sampled, which indicates a spatial difference in the source profiles of the PFAAs.     

Hexabromocyclododecanes in limnic and marine organisms and terrestrial plants from Tianjin,China: Diastereomer- and enantiomer-specific profiles,biomagnification, and human exposure

To interpret the distribution of hexabromocyclododecanes (HBCDs) in various organisms, we measured the concentrations and diastereomer and enantiomer profiles of HBCDs in 21 different species of limnic and marine cohorts from Tianjin, China. The concentration ranges of HBCDs in limnic and marine organisms were 64.3–1111 ng g⁻¹ lw and 85.5–989 ng g⁻¹ lw, respectively. Living habitat and feeding habits had important impacts on HBCD diastereomer distribution. Most of the species appeared to preferentially select (+)-α-, (−)-β- and (−)-γ-HBCD. There is a tendency that the total and α-HBCDs were magnified as trophic level increased with trophic magnification factors (TMFs) around 2. The concentrations of HBCDs in the limnic and marine fishes were highest in the liver, followed by the gill, skin, and muscle. In terrestrial plants, the highest concentrations of HBCDs were observed in the leaf, followed by the root and the rhizosphere soil. Plants showed enantioselectivity for HBCD enantiomers, which varied with plant species and organs (leaf vs. root) of the same plant. Higher estimated daily intakes (EDIs) of HBCDs were observed from fish than from wheat.     

Photo-dissociation of dimethylamine by KrBr excilamp

A study of dimethylamine photo-dissociation in the gas phase has been conducted using UV radiation delivered from a KrBr^* excilamp, driven by a sinusoidal electronic control gear with maximum emission at wavelength of 207 nm. The electrical input power and radiant power of the lamp were measured to determine their effects on the degradation. The influence of flow velocity and initial concentration of dimethylamine were also examined. In order to evaluate the photo-dissociation process comprehensively, several parameters were investigated, including removal efficiency, energy yield, carbon balance and CO₂ selectivity. It is shown that the removal efficiency increases with enhanced input power and decreased gas flow rate. A high removal efficiency of 68% is achieved for lamp power 102 W and flow velocity 15 m³ h⁻¹. The optimum dimethylamine initial concentration is around 3520 mg m⁻³, for which the energy yield reaches up to 442 g kW h⁻¹ when the input power is 65 W. In addition, two chain compounds (1,3-bis-dimethylamino-2-propanol; 3-penten-2-one, 4-amino) and three ring organic matters (1-azetidinecarboxaldehyde, 2,2,4,4-tetramethyl; N-m-tolyl-succinamic acid; p-acetoacetanisidide), were identified by GC–MS as secondary products, in order to demonstrate the pathways of the dimethylamine degradation.     

Acute and chronic toxicity of organophosphate monocrotophos to Daphnia magna

The acute and chronic toxicity of monocrotophos (MCP), the binary joint toxicity of MCP and bifenthrin (BF), and sodium dodecyl benzene sulfonate (SDBS) to Daphnia magna (D. magna) was evaluated. The 24 h-median effective concentration (24 h-EC₅₀) and 48 h-median lethal concentration (48 h-LC₅₀) of MCP towards D. magna were 161 and 388 μ g/L, respectively. In addition, the lowest-observed effective concentration (LOEC) and non-observed effective concentration (NOEC) of MCP to D. magna were 10 and 5 μ g/L, respectively. Furthermore, the chronic value (ChV) of MCP against D. magna was 7 μ g/L and the acute chronic ratio (ACR) was 55. The number of offspring per female and the intrinsic rate of natural increase (r) were identified as the parameters that were most sensitive to MCP. In addition, toxic unit (TU) analysis was employed to evaluate the joint toxicities. The calculated TU_mix values of binary equitoxic mixtures of MCP + BF and MCP + SDBS were 1.47 and 1.63, respectively, which suggests that both equitoxic mixtures exert a limited antagonistic effect. The results of this study revealed that the toxic threshold of MCP towards D. magna is higher than its reported highest residue (4 μ g/L) in the ordinary aquatic environment, and that concurrent exposure to BF or SDBS may exert a slight antagonistic effect.     

Methyl Tertiary Hexyl Ether and Methyl Tertiary Octyl Ether as Gasoline Oxygenates: Assessing Risks from Atmospheric Dispersion and Deposition

Abstract

Methyl tertiary hexyl ether (MtHxE) and methyl tertiary octyl ether (MtOcE) are currently being developed as replacement oxygenates for methyl tertiary butyl ether (MtBE) in gasoline. As was the case with MtBE, the introduction of these ethers into fuel supplies guarantees their introduction into the environment as well. In this study, a screening-level risk assessment was performed by comparing predicted environmental concentrations (PEC) of these ethers to concentrations that might cause adverse effects to humans or ecosystems. A simple box model that has successfully estimated urban air concentrations of MtBE was adapted to predict atmospheric concentrations of MtHxE and MtOcE. Expected atmospheric concentrations of these ethers were also estimated using the European Union System for the Evaluation of Substances (EUSES) multimedia fate model, which simultaneously calculates PECs in the various environmental compartments of air, water, soil, and sediment. Because little or no data are available on the physicochemical, environmental, and toxicological properties of MtHxE and MtOcE, estimation methods were used in conjunction with EUSES to predict both the PECs and the concentrations at which these ethers might pose a threat. The results suggest that these ethers would contaminate the air of a moderately sized U.S. city (Boston, MA) at levels similar to those found previously for MtBE. The risk assessment module in EUSES predicted risk characterization ratios of 10^?3 and 10^?2 for MtHxE and MtOcE, respectively, in Boston, and 10^?2 and 10^?1 in very large urban centers, suggesting that these ethers pose only a minimal threat to ecosystems at the anticipated environmental concentrations. The assessment also indicates that these compounds are possible human carcinogens and that they may be present in urban air at concentrations that pose an unacceptable cancer risk. Therefore, testing of the toxicological properties of these compounds is recommended before they replace MtBE in gasoline.     

Fluorine distribution in aquatic environment and its health effect in the Western Region of the Songnen Plain, Northeast China

Endemic fluorosis was investigated and studied in the west region of the Songnen plain, Northeast China in 2001–2002. The results showed that the fluorine distribution in aquatic environment was that the fluorine concentrations in the lake water and unconfined ground water were higher than that in the river water and confined ground water. The lake water (Alkali lake) is connected with unconfined ground water. In unconfined ground water, from the east and southeast areas to the west and the northwest areas of the plain, fluorine concentration fluctuated with high and low alternatively. The fluorine in the water comes from the weathering of rocks and minerals in the mountains and hills around the Songnen Plain. The main influence factors of the fluorine distribution in aquatic environment are discussed. Unconfined ground water containing high fluorine is used as drinking water. In this region, the fluorine concentration in drinking water is evidently correlated to the morbidity of dental and skeletal fluorosis. High fluorine concentration in drinking water has endangered human health.     

Estimation of the temporal and spatial distribution of dust concentration over China by combining PM10 and conventional meteorological observations

In this paper, we will present a simple algorithm to estimate the temporal and spatial distribution of dust mass concentration by combining PM10 and conventional meteorological observations. The efficiency of the algorithm has been demonstrated by applying it to analyze the dust source, transport, and dissipation of the dust storm which occurred in the west region of Pa-tan-chi-lin Desert at 0200 BST 27 March, 2004.     

Effects of crude oil residuals on soil chemical properties in oil sites, Momoge Wetland, China

Crude oil exploration and production has been the largest anthropogenic factor contributing to the degradation of Momoge Wetland, China. To study the effects of crude oil on wetland soils, we examined the total petroleum hydrocarbon (TPH), total organic carbon (TOC), total nitrogen (TN), and total phosphorus (TP), as well as pH and electricity conductivity (EC) from oil sites and uncontaminated areas in the Momoge Wetland. All contaminated areas had significantly higher (p < 0.05) contents of TPH and TOC, but significantly lower (p < 0.05) TN contents than those of the uncontaminated areas. Contaminated sites also exhibited significantly higher (p < 0.05) pH values, C/N and C/P ratios. For TP contents and EC, no significant changes were detected. The level of soil contamination and impact of oil residuals on soil quality greatly depended on the length of time the oil well was in production. Oil residuals had caused some major changes in the soils’ chemical properties in the Momoge Wetland.