微波联合酸预处理对厨余垃圾酶水解糖化的影响

酶水解糖化是厨余垃圾制造燃料乙醇的关键步骤,对厨余垃圾进行预处理以促进糖化过程,具有重要意义.以学生食堂厨余垃圾为原料,以常规、微波为加热手段,比较不同预处理方式对厨余垃圾酶水解的影响.结果表明,微波加热结合酸性溶剂的预处理方式最有利于厨余垃圾酶水解糖化.考察微波联合酸预处理的影响因素,得到最佳的预处理条件为:溶剂为H2SO4、溶剂浓度3％、微波功率80 W,预处理时间40 min,固液比1∶8,该条件预处理后,与未经预处理的厨余垃圾酶水解糖产量相比,提高46.1％.     

辅料添加对厨余垃圾生物干化产品燃烧热特性的影响

为达到降低厨余垃圾含水率,使其可作为垃圾衍生燃料进行燃烧的目的,选择玉米秸秆和木本泥炭2种辅料与厨余垃圾进行联合生物干化,研究了辅料添加对厨余垃圾生物干化产品燃烧热特性的影响,以不添加任何辅料的厨余垃圾单独进行生物干化作为对照处理,生物干化周期为21 d。结果表明:单独进行厨余垃圾生物干化时挥发性固体(VS)降解率最高,添加木本泥炭处理时VS降解率最低;对照处理对VS降解损失主要的贡献组分为淀粉、纤维素和脂肪,然而,对于添加玉米秸秆和木本泥炭的处理,纤维素、半纤维素和淀粉是VS降解损失主要的贡献组分。随着生物干化反应的进行,物料的燃烧速率和燃烧率均降低,同时燃烬点推后,但燃点基本保持不变。其中,添加木本泥炭的处理燃点最高,燃烬点最低,燃烧率最高。各处理物料燃烧一级动力学方程拟合效果较好(R~2=0.86～0.97)。生物干化过程使厨余垃圾单独处理第2失重段反应变难,第3失重段反应变易。然而,对于添加辅料的处理,生物干化过程使第2失重段反应变易,第3失重段反应变更难。总体而言,生物干化过程使各处理的表观活化能(E_m)降低了15.9%～29.4%,使得厨余垃圾的燃烧更加容易。以上研究结果可为厨余垃圾燃料化处理提供参考。     

采用正交实验优化湿热法处理厨余垃圾的工艺条件

实验采用3因素3水平的正交实验设计方法,研究了湿热法处理厨余垃圾并使其饲料化的加工工艺中,时间、温度、加水量对厨余垃圾饲用价值的影响,选取粗蛋白、粗脂肪、粗纤维、粗灰分、钙和盐分为评价指标,确定反应的最佳工艺条件。实验结果表明,反应的最佳工艺条件为温度100℃、加水量50%、反应时间30 m in。     

采用正交实验优化湿热法处理厨余垃圾的工艺条件

实验采用3因素3水平的正交实验设计方法,研究了湿热法处理厨余垃圾并使其饲料化的加工工艺中,时间、温度、加水量对厨余垃圾饲用价值的影响,选取粗蛋白、粗脂肪、粗纤维、粗灰分、钙和盐分为评价指标,确定反应的最佳工艺条件.实验结果表明,反应的最佳工艺条件为温度100℃、加水量50%、反应时间30 min.     

两段式热解厨余垃圾实验研究

通过厨余垃圾的工业分析，发现其挥发分比例较高，适合热解利用；采用热重分析方法分析了不同条件下厨余垃圾的热解特性，提出了厨余垃圾两段式热解转化利用的思路，得出了厨余垃圾热解的合适工艺条件。在自行设计建造的一段回转炉、二段焦化罐中对厨余垃圾热解，并分析了产物的组成和性质。     

塔式矿化垃圾生物反应床处理垃圾填埋场渗滤液的效能研究

通过正交试验研究了固液比、进水COD和运行周期对塔式矿化垃圾生物反应床处理垃圾渗滤液的性能影响.小试试验结果表明,在温度为10～37 ℃条件下,固液比是影响污染物去除性能的关键因素.现场中试研究表明,在水力负荷为0.267～0.444 m3/d(以每立方米矿化垃圾计)条件下,出水COD和出水氨氮基本满足国家二级排放标准.塔式矿化垃圾生物反应床是一种高效低耗的垃圾渗滤液处理工艺.     

低强度超声波预处理对厨余垃圾厌氧消化的影响

以厨余垃圾为研究对象,实验研究产气效率、pH、SCOD、甲烷浓度及生物降解率5个参数的变化趋势,比较低强度超声波处理对厨余垃圾厌氧消化产气特性的影响,结果表明:(1)低强度超声波处理对厨余垃圾厌氧消化产生明显效果,在不同的超声波强度(100、175和250 W)或处理时间(20和40 min)下,产气效率、累计产气量、pH下降幅度、SCOD增加幅度随处理时间和超声功率增加而增加;在超声波强度250 W和处理时间60 min下出现抑制作用;(2)在超声波强度250 W和处理时间40 min条件下,超声波对厨余垃圾厌氧消化增强效果最明显,累计产气量由未处理的3 513 mL提高至5 007 mL,提高42.6%,甲烷气体浓度由51.25%提高至58.8%,生物降解率由58.11%提高至73.5%.     

基于响应面法的新型餐厨垃圾菌剂制备

设计三因素三水平实验并采用响应面优化法对反应适宜的实验参数进行了优化.选择温度、供氧条件和反应时间作为菌剂制备的可控因素,选择温度、菌剂投加量和木屑投加量(水分调节)作为菌剂处理厨余垃圾的可控因素,研究菌剂制备与处理垃圾的优化工艺参数.研究结果表明,菌剂的最优制备条件为:温度35℃、间歇震荡、培养108 h,按重量百分比为碎花生壳∶刨花∶鱼骨粉∶麸皮∶菌体=2∶1∶1∶1∶1比例制得的固体菌剂具有较高的活性.菌剂处理厨余垃圾的响应面优化法分析结果表明,当温度为45℃,菌剂投加量为6％,木屑投加量为30％时,厨余垃圾的减量率最大,2d降解率可达40％.     

以废渣磷石膏为原料水热法制备硫酸钙晶须

以磷石膏为原料,采用水热法制备硫酸钙晶须。借助X射线衍射仪(XRD)、扫描电子显微镜(SEM)及红外光谱仪(FT-IR)等仪器对产物进行表征,研究了反应温度和时间、料浆初始固液比及不同添加剂等因素对产物形貌及可溶磷含量等的影响。结果表明,最佳反应条件为:反应温度140℃,反应时间2 h,料浆固液比为1∶10,最佳添加剂及剂量为丙三醇(V醇/V总液为50%)。所得产物为六方晶系的CaSO4.0.5H2O,直径1～3μm,晶须长径比为45左右,合成率约95%,产物可溶磷含量由原样的0.41%降至0.21%。     

基于活性污泥的厨余垃圾厌氧发酵产酸研究

以厨余垃圾和活性污泥为原料,考察了不同接种比例对厌氧发酵产物的挥发性脂肪酸产量、pH值和COD去除率的影响.结果表明,当厨余垃圾和活性污泥接种比例为4∶1时,挥发性脂肪酸产量在第3天达到最大值为42.7 g/L,产率提高了40%,COD去除率达到了35.6%,pH值没有发生较大的差异,其变化幅度在4～6之间.     

Patterns of volatile metabolites and nonvolatile trichothecenes produced by isolates of <Emphasis Type="Italic">Stachybotrys,Fusarium, Trichoderma,Trichothecium</Emphasis> and <Emphasis Type="Italic">Memnoniella</Emphasis>

We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.     

Radionuclides and trace elements in fish collected upstream and downstream of Los Alamos national laboratory and the doses to humans from the consumption of muscle and bone

Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for ³H, ⁹⁰Sr, ¹³⁷Cs, ^totU, ²³⁸Pu, ^239,240Pu, and ²⁴¹Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of ⁹⁰Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g^‐1 [126E‐02 Bq kg^‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g^‐1 [518E‐02 Bq kg^‐1]). The differences in ⁹⁰Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y^‐1 (1.0 ± 1.0 μSv y^‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y^‐1 (1000 μSv y^‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.     

A History of Dry Cleaners and Sources of Solvent Releases from Dry Cleaning Equipment

Approximately 25, 000-35, 000 dry cleaning facilities currently operate in the U.S. The release of perchloroethylene and other solvents from these establishments represents a major source of soil and groundwater contamination. The manner in which dry cleaning solvents escape from dry cleaning plants is, for all practical purposes, identical for chlorinated and petroleum hydrocarbon solvents and is related to one of the following events: the catastrophic failure of a component of the dry cleaning system, the improper installation, operation or maintenance of the dry cleaning equipment or a combination of all of these causes. Acceptable customs, codes and regulations can also dictate what is authorized for operation of a dry cleaning facility in a particular community, geographic area during a particular time frame. Environmental litigation dealing with the origin of a solvent release from dry cleaners tends to focus on the design and manufacture of dry cleaning industry machines such as washers, washer extractors, tumblers, solvent filters, water separators, stills and spotting boards. A thorough analysis of the daily operations of dry cleaners often reveals that poor maintenance, failure to follow the manufacturer's instructions and the actions of the operator are the most likely causes of soil and groundwater pollution. In order to forensically evaluate the most probable origins of a solvent release and to examine issues regarding liability, a thorough understanding of the history of dry cleaning and a detailed analysis of the operation and maintenance of the dry cleaning equipment are necessary. The discovery of solvent plumes in the vicinity of dry cleaning plants may suggest that the solvent source is the dry cleaning plant; however, the presence of these plumes does not necessarily indicate that the dry cleaning equipment was defectively designed or manufactured. A thorough review of the type of equipment used over the life of the dry cleaning plant and verifiable solvent mileage records frequently indicates that operators of the plant have disposed of solvent and contaminated solids into the municipal sewer or on ground surfaces.     

Radionuclides in deer and elk from Los Alamos national laboratory and the doses to humans from the ingestion of muscle and bone

Abstract

This paper summarizes radionuclide concentrations (³H, ⁹⁰Sr, ¹³⁷Cs, ²³⁸Pu, ^239,240Pu, ²⁴¹Am, and ^totU) in muscle and bone tissue of mule deer (Odocoileus hemionus) and Rocky Mountain elk (Cervus elaphus) collected from Los Alamos National Laboratory (LANL), Los Alamos, New Mexico, lands from 1991 through 1998. Also, the committed effective dose equivalent (CEDE) and the risk of excess cancer fatalities (RECF) to people who ingest muscle and bone from deer and elk collected from LANL lands were estimated. Most radionuclide concentrations in muscle and bone from individual deer (n = 11) and elk (n = 22) collected from LANL lands were either at less than detectable quantities (where the analytical result was smaller than two counting uncertainties) and/or within upper (95%) level background (BG) concentrations. As a group, most radionuclides in muscle and bone of deer and elk from LANL lands were not significantly higher (p<0.10) than in similar tissues from deer (n = 3) and elk (n = 7) collected from BG locations. Also, elk that had been radio collared and tracked for two years and spent an average time of 50% on LANL lands were not significantly different in most radionuclides from road kill elk that have been collected as part of the environmental surveillance program. Overall, the upper (95%) level net CEDEs (the CEDE plus two sigma for each radioisotope minus background) at the most conservative ingestion rate (50 lbs of muscle and 13 lbs of bone) were as follows: deer muscle = 0.22 mrem y^‐1 (2.2 μSv y^‐1), deer bone = 3.8 mrem y^‐1 (38 μSv y^‐1), elk muscle = 0.12 mrem y^‐1 (1.2 μSv y^‐1), and elk bone = 1.7 mrem y^‐1 (17 μSv y^‐1). All CEDEs were far below the International Commission on Radiological Protection guideline of 100 mrem y^‐1 (1000 μSv y^‐1), and the highest muscle plus bone net CEDE corresponded to a RECF of 2E‐06, which is far below the Environmental Protection Agency upper level guideline of 1E‐04.     

Leaching of seven pesticides currently used in cotton crop in Mato Grosso State—Brazil

This study aimed to evaluate the leaching of pesticides and the applicability of the Attenuation Factor (AF) Model to predict their leaching. The leaching of carbofuran, carbendazim, diuron, metolachlor, α and β endosulfan and chlorpyrifos was studied in an Oxisol using a field experiment lysimeter located in Dom Aquino – Mato Grosso. The samples of percolated water were collected by rain event and analyzed. Chemical and physical soil attributes were determined before pesticide application to the plots. The results showed that carbofuran was the pesticide that presented a higher leaching rate in the studied soil, so was the one representing the highest contamination potential. From the total carbofuran applied in the soil surface, around 6 % leached below 50 cm. The other pesticides showed lower mobility in the studied soil. The calculated values to AF were 7.06E-12 (carbendazim), 5.08E-03 (carbofuran), 3.12E-17 (diuron), 6.66E-345 (α-endosulfan), 1.47E-162 (β-endosulfan), 1.50E-06 (metolachlor), 3.51E-155 (chlorpyrifos). AF Model was useful to classify the pesticides' potential for contamination; however, that model underestimated pesticide leaching.     

Endosulfan in China 2—emissions and residues

Background, aim, and scope  Endosulfan is one of the organochlorine pesticides (OCPs) and also a candidate to be included in a group of new persistent organic pollutants (UNEP 2007). The first national endosulfan usage inventories in China with 1/4° longitude by 1/6° latitude resolution has been reported in an accompanying paper. In the second part of the paper, we compiled the gridded historical emissions and soil residues of endosulfan in China from the usage inventories. Based on the residue/emission data, gridded concentrations of endosulfan in Chinese soil and air have been calculated. These inventories will provide valuable data for the further study of endosulfan. Methods  Emission and residue of endosulfan were calculated from endosulfan usage by using a simplified gridded pesticide emission and residue model—SGPERM, which is an integrated modeling system combining mathematical model, database management system, and geographic information system. By using the emission and residue inventories, annual air and soil concentrations of endosulfan in each cell were determined. Results and discussion  Historical gridded emission and residue inventories of α- and β-endosulfan in agricultural soil in China with 1/4° longitude by 1/6° latitude resolution have been created. Total emissions were around 10,800 t, with α-endosulfan at 7,400 t and β-endosulfan at 3,400 t from 1994 to 2004. The highest residues were 140 t for α-endosulfan and 390 t for β-endosulfan, and the lowest residues were 0.7 t for α-endosulfan and 170 t for β-endosulfan in 2004 in Chinese agricultural soil where endosulfan was applied. Based on the emission and residue inventories, concentrations of α- and β-endosulfan in Chinese air and agricultural surface soil were also calculated for each grid cell. We have estimated annual averaged air concentrations and the annual minimum and maximum soil concentrations across China. The real concentrations will be different from season to season. Although our model does not consider the transport of the insecticide in the atmosphere, which could be very important in some areas during some special time, the estimated concentrations of endosulfan in Chinese air and soil derived from the endosulfan emission and residue inventories are in general consistent with the published monitoring data. Conclusions  To our knowledge, this work is the first inventory of this kind for endosulfan published on a national scale. Concentrations of the chemical in Chinese air and agricultural surface soil were calculated for each grid cell. Results show that the estimated concentrations of endosulfan in Chinese air and soil agree reasonably well with the monitoring data in general. Recommendations and perspectives  The gridded endosulfan emission/residue inventories and also the air and soil concentration inventories created in this study will be updated upon availability of new information, including usage and monitoring data. The establishment of these inventories for the OCP is important for both scientific communities and policy makers.     

Impact of spiked concentrations of Cd,Pb, As and Zn in growth medium on elemental uptake of Nasturtium officinale (Watercress)

This study is aimed at investigating the impact of water quality on the uptake and distribution of three non-essential and toxic elements, namely, As, Cd and Pb in the watercress plant to assess for metal toxicity. The plant was hydroponically cultivated under greenhouse conditions, with the growth medium being spiked with varying concentrations of As, Cd and Pb. Plants that were harvested weekly for elemental analysis showed physiological and morphological symptoms of toxicity on exposure to high concentrations of Cd and Pb. Plants exposed to high concentrations of As did not survive and the threshold for As uptake in watercress was established at 5 ppm. Translocation factors were low in all cases as the toxic elements accumulated more in the roots of the plant than the edible leaves. The impact of Zn on the uptake of toxic elements was also evaluated and Zn was found to have an antagonistic effect on uptake of both Cd and Pb with no notable effect on uptake of As. The findings indicate that phytotoxicity or death of the watercress plant would prevent it from being a route of human exposure to high concentrations of As, Cd and Pb in the environment.     

Butyltin compounds in sediment and fish from the Polish Coast of the Baltic Sea

Concentrations of mono- (MBT), di- (DBT), and tri-(TBT) butyltin compounds were measured in eggs, liver, and muscle of nine species of fish from four regions of the Baltic Sea - the Firth of Vistula, the Gulf of Gdańsk, Puck Bay, and the mouth of the Vistula River. The overall concentration ranges among all the fish sampled from the four sites were: < 7 to 79 ng/g for MBT, 6 to 1100 ng/g for DBT, 7 to 3600 ng/g for TBT, and 16 to 4800 ng/g for total BTs, on a wet wt basis. The highest concentration of total BTs was found in herring liver from the Firth of Vistula (4800 ng/g, wet wt) and in roach muscle from Puck Bay (3300 ng/g, wet wt), while the least concentration was found in burbot eggs and liver from the Vistula River (39 and 32 ng/g, wet wt, respectively). TBT was the major form of BTs present in most samples analyzed. Sediment samples collected from shipyards in the Gulf of Gdańsk contained butyltin concentrations ranging from 1.2 to 46 μg/g (dry wt) for MBT, 2.0 to 42 μg/g for DBT, and 2.6 to 40 μg/g for TBT. As with the fish, the majority of the BTs in sediment were present as TBT, which suggested recent exposure of the aquatic environment of the region to TBT.     

Malathion-induced sublethal toxicity on the intestine of cricket frog (Fejervarya limnocharis)

The effect of malathion [diethyl(dimethoxythiophosphorylthio)succinate] at sublethal concentration (0.006 ppm) on intestinal parameters of cricket frog (Fejervarya limnocharis) was studied for 24 hrs to 240 hrs of exposure and remarkable histopathological alterations were observed. The study on intestinal parameters revealed acute pathological conditions in the intestinal wall. The toxic effect became evident as the cytoplasm of the cells disintegrated and the cells became empty and vacuolated. The cell membranes were also ruptured. Degenerative changes of the absorptive surface (villi) of the intestine in the different periods of exposure were pronounced. Severe atrophic nature (necrotic mucosa) of the intestine began from 48 hrs onwards to 96 hrs of exposure.