季节性城市生活垃圾成分分析及厌氧消化特性研究

城市生活垃圾的成分及特性随着季节和人类在不同季节的生活习惯而变化，针对我国北方城市研究了一年中不同季节的城市生活垃圾成分特点，对影响厌氧发酵过程的相关成分如总有机碳（TOC）、总氮（TN）、蛋白质、脂肪和还原糖等进行了测定分析。通过厌氧消化实验，测得不同季节城市生活垃圾pH值、日产气量、沼气甲烷含量、甲烷累积量、挥发性脂肪酸（VFAs）和氧化还原电位（ORP）等参数的变化规律，分析相应变化的影响因素。结果表明，二、三季度的含水率分别为64．81％和67．50％，高于一、四季度，一季度发酵原料中蛋白质和脂肪含量分别为12．56％和8．86％，明显高于其他3个季度。一季度甲烷累积量最高，达到17616mL，单位发酵原料的产气量为204．8mL／g，也是4个季度中最高的，说明蛋白质、脂肪等有机成分含量对厌氧发酵过程及结果影响比较明显。为进一步的城市生活垃圾厌氧消化制取生物燃气的工艺条件提供依据。     

全日本1987年一般废弃物的排放量

根据厚生省对全日本一般废弃物排放状况的调查和统计,全日本1987年度从家庭和企业中排出的一般废弃物总量约为4650万吨,比1986年增加了162万吨,日平均垃圾排放量约为126956吨,比1986年增加4357吨,人均日排放量为1040克。随着办公自动化(OA)机器的普及,废纸量的增加尤其迅速。     

中国西北典型城市西宁生活垃圾产生及回收

预测了中国西北典型城市西宁的生活垃圾清运量,同时分析了西宁的生活垃圾物料流向,从而估算西宁未来的生活垃圾产生量,为西宁生活垃圾管理规划提供依据。研究发现,西宁未来生活垃圾清运量和产生量均呈增长状态,2025、2035年西宁生活垃圾产生量分别为240.33万、334.04万t,2020—2035年的平均年增长率为3.71%。在考虑分拣率的条件下,2025、2035年西宁生活垃圾人均日产生量分别为1.72、2.21kg/(人·d)。目前,西宁生活垃圾分两级分拣回收,一级分拣率为35.11%,二级分拣率为0.18%,填埋率为64.71%。为提高资源化利用率,建议西宁加强一级分拣能力,特别是加大对纸类和塑料的回收能力;在末端处置上,建议规划考虑建设生活垃圾焚烧发电设施。     

北京市生活垃圾焚烧发电厂温室气体排放及影响因素

以北京高安屯垃圾焚烧发电厂为例,利用《温室气体排放核算指南生活垃圾焚烧企业》(DB 11/T 1416-2017),核算固定设施排放源的直接排放、间接排放和避免排放,并分析影响排放的主要因素。结果表明,2015年高安屯垃圾焚烧发电厂吨垃圾净CO_2排放量为0.165 t,其中生活垃圾中矿物碳焚烧贡献量为0.375 t;燃烧产生的N_2O贡献量为0.015 t;化石燃料燃烧贡献量为0.002 t;发电上网减排量为0.227 t。降低塑料类在入炉生活垃圾中的比例是减少垃圾焚烧发电厂温室气体排放的关键途径之一。     

宁波市废弃物处理温室气体排放特征研究

随着社会经济的快速发展和城市化进程的不断推进,城市废弃物的产生量显著增长,而废弃物的处理过程也成为了产生温室气体的一个不可忽视的排放源。采用《2006年IPCC国家温室气体清单指南》和《浙江省市县温室气体清单编制指南》推荐的方法,估算了2005—2013年宁波市废弃物处理温室气体排放量,主要针对固体废弃物填埋、焚烧和废水处理等过程估算排放总量和强度。结果表明,2005—2013年宁波市温室气体排放总量呈波动上升趋势,2013年比2005年增长了78%,其中,固体废弃物焚烧过程增幅最大,增长了7倍。至2013年,固体废弃物填埋过程仍是占比最大的排放源,其次是固体废弃物焚烧和工业废水处理过程,排放比例分别为40.12%(质量分数,下同)、26.00%、22.53%。最后,提出了减少宁波市废弃物处理领域温室气体排放的有效途径,即开展垃圾分类回收、减少垃圾产生量、增加焚烧处理比例、加大垃圾填埋气回收和适度控制温室气体高排放行业的发展规模等。     

“双碳”目标下城市生活垃圾制氢技术研究进展

在全球碳减排的背景下,中国提出了实现“碳达峰碳中和”的“双碳”目标。利用城市生活垃圾中的生物质能制氢符合“双碳”目标要求。目前,城市生活垃圾制氢技术包括热化学转化、生物转化等直接制氢技术和结合甲烷重整制氢技术与城市生活垃圾厌氧发酵技术的间接制氢技术两大类。间接制氢技术因成熟可靠而成为当下城市生活垃圾制氢的主流工程化应用方向。城市生活垃圾前端分类、中端收运及末端处置系统的完善,将对生活垃圾制氢技术发展起到积极推动作用。     

京津冀地区基础卫生处理设施提升产生的氮素入水削减评估

高强度人为活动排放使得京津冀地区地表水体中氮素浓度一直处于较高水平,而城市、农村地区的人群排泄则是人为氮素排放的重要构成。本研究估算了2006—2014年间,京津冀地区由于城市、农村地区基础卫生处理设施持续改进所带来的水体氮素入水削减量。由于基础卫生设施状况显著提升,即使在人口存在增加的情况下,京津冀地区的氮素入水排放量仍从2006年的305Gg/a下降到2014年的294Gg/a。2014年,京津冀地区河北的人群排泄氮素入水排放量最高,排放量为216Gg/a,而北京单位地表水资源量的氮素排放强度最大,为7.0Gg/(a·亿m~3)。未来进一步通过增加污水处理设施数量来降低城市地区人群排泄的氮素入水排放空间较为有限,京津冀地区人体排泄氮素输入削减空间主要存在于河北的农村地区。     

生物反应器填埋的沉降加速效应

通过实验室填埋柱模拟实验，研究了生物反应器填埋操作方式对填埋层沉降的影响。结果表明：与传统卫生填埋方式相比，回灌经厌氧生物处理后渗滤液的生物反应器填埋方式能够加速填埋层的沉降，140 d内沉降提高比例达10%以上。我国填埋垃圾高含水率、高易腐有机物含量的特性，使得其填埋层的次沉降系数高于文献值。填埋垃圾有机物降解量及其引起的垃圾水分排出量与填埋层沉降有显著相关性，表明有机物降解是引起填埋层沉降的重要因素，也是造成生物反应器填埋与传统卫生填埋方式初期沉降差异的主要原因。     

我国氮氧化物排放因子的修正和排放量计算:2000年

根据我国城市的发展状况 ,采用城市分类的方法 ,将我国 2 6 1个地级市按照人口数量分为 5个类别。每类城市选取一个典型城市进行实地调查 ,对我国燃烧锅炉和机动车的NOx 的排放因子进行了修正 ,提出了适合我国目前排放水平的各类城市的固定源和移动源的排放因子。并依据 2 0 0 0年中国大陆地区的电站锅炉、工业锅炉和民用炉具的燃料消耗量和机动车保有量 ,以地级市为基本单位 ,估算了 2 0 0 0年我国各地区的NOx 排放量 ,分析了分地区、分行业、分燃料类型的NOx 排放特征。 2 0 0 0年我国NOx 排放总量为 11.12Mt,其中固定源占 6 0 .8% ;移动源占 39.2 %。NOx 排放在地域、行业和燃料类型上分布均不平衡。NOx 的排放主要集中在华东和华北地区 ,其排放量占全国排放量的一半以上。燃煤为最重要的NOx 排放源 ,其排放量占燃料型NOx 排放量的 72 .3%左右。     

我国城市的柴油车污染及防治对策探讨

当今城市大气污染物中60％--70％来自机动车的排放，而其中很大部分是柴油车的排放。作者对柴油车在城市生活中的重要地位、对在用柴油车的技术改造措施和城市环境保护的其他举措进行了研究探讨，提出了一些具体方案。     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

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.     

Book review

The Pesticide Manual ‐ A World Compendium, 8th Edition, C.R. Worthing, Editor and S.B. Walker, Assistant Editor, British Crop Protection Council, BCPC Publications Sales, Bear Farm, Binfield, Bracknell, Berkshire RG12 5QE, England. 1987, 1100 pp., UK £50; Overseas £56. ISBN 0–948404–01–9.     

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.     

Observations on the influence of water and soil pH on the persistence of insecticides

Abstract

The pH‐disappearance rate profiles were determined at ca. 25°C for 24 insecticides at 4 or 5 pH values over the range 4.5 to 8.0 in sterile phosphate buffers prepared in water‐ethanol (99: 1 v/v). Half‐lives measured at pH 8 were generally smaller than at lower pH values. Changes in half lives between pH 8.0 and 4.5 were largest (>1000x) for the aryl carbamates, carbofuran and carbaryl, the oxime carbamate, oxamyl, and the organophosphorus insecticide, trichlorfon. In contrast, half lives of phorate, terbufos, heptachlor, fensulfothion and aldicarb were affected only slightly by pH changes. Under the experimental conditions described half lives at pH8 varied from 1–2 days for trichlorfon and oxamyl to >1 year for fensulfothion and cyper‐methrin. Insecticide persistence on alumina (acid, neutral and basic), mineral soils amended with aluminum sulfate or calcium hydroxide to different pH values and four natural soils of different pH was examined. No correlation was observed between the measured pH of these solids and the rate of disappearance of selected insecticides applied to them. These observations demonstrate the difficulty of extrapolating the pH dependent disappearance behaviour observed in homogeneous solution to partially solid heterogeneous systems such as soil.     

The chemical stability of formulations of some hydrolyzable insecticides in aqueous mixtures with hydrolysis catalysts

Abstract

The active ingredients in commercial formulations of malathion, oxamyl, carbaryl, diazinon, and chlorpyrifos diluted to “spray tank”; concentrations with buffered distilled or natural water of pH 4–9 were stable for at least 24 hr. Formulations of trichlorfon were not stable at pH 7 or above but disappearance rates were slower than for the pure chemical in homogeneous solution. Cupric ion was observed to be an effective catalyst for the hydrolysis of a variety of pure organophosphorus insecticides but did not catalyze hydrolysis of the active ingredients of the formulations examined. Increasing the dilution of the formulation increased the susceptibility of malathion, oxamyl, and carbaryl to hydrolysis.     

Organochlorine compounds in a three-step terrestrial food chain

The concentrations of 15 organochlorine chemicals (PCBs and pesticides) were studied in a Central European oak wood food chain system: Great tit (Parus major), caterpillars (Tortrix viridana, Operophtera brumata, Erannis defoliaria), and oak-leaves (Quercus robur). Juvenile tits receive organochlorines from the mother via egg transfer and, eventually to a greater extent, from the caterpillar food source during nestling period. The concentrations of PCB 153 (2,2′,4,4′,5,5′-hexachlorobiphenyl, the most abundant in this study) was found in leaf material at ca. 1 ng/g, in caterpillars 10 ng/g, and in bird eggs 170 ng/g on an average and on a dry mass basis.     

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.     

Radionuclides in pinon pine (Pinus edulis) nuts from los alamos national laboratory lands and the dose from consumption

Abstract

One of the dominant tree species growing within and around the eastern portion of Los Alamos National Laboratory (LANL), Los Alamos, NM, lands is the pinon pine (Pinus edulis). Pinon pine is used for firewood, fence posts, and building materials and is a source of nuts for food—the seeds are consumed by a wide variety of animals and are also gathered by people in the area and eaten raw or roasted. This study investigated the (1) concentration of ³H, ¹³⁷Cs, ⁹⁰Sr, ^totU, ²³⁸Pu, ^{239, 240}Pu, and²⁴¹ Am in soils (0‐ to 12‐in. [31 cm] depth underneath the tree), pinon pine shoots (PPS), and pinon pine nuts (PPN) collected from LANL lands and regional background (BG) locations, (2) committed effective dose equivalent (CEDE) from the ingestion of nuts, and (3) soil to PPS to PPN concentration ratios (CRs). Most radionuclides, with the exception of ³H in soils, were not significantly higher (p < 0.10) in soils, PPS, and PPN collected from LANL as compared to BG locations, and concentrations of most radionuclides in PPN from LANL have decreased over time. The maximum net CEDE (the CEDE plus two sigma minus BG) at the most conservative ingestion rate (10 lb [4.5 kg]) was 0.0018 mrem (0.018 μSv); this is far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem (1000 μSv). Soil‐to‐nut CRs for most radionuclides were within the range of default values in the literature for common fruits and vegetables.     

Degradation and sorption of imidacloprid in dissimilar surface and subsurface soils

Degradation and sorption/desorption are important processes affecting the leaching of pesticides through soil. This research characterized the degradation and sorption of imidacloprid (1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine) in Drummer (silty clay loam) and Exeter (sandy loam) surface soils and their corresponding subsurface soils using sequential extraction methods over 400 days. By the end of the incubation, approximately 55% of imidacloprid applied at a rate of 1.0 mg kg^?1 degraded in the Exeter sandy loam surface and subsurface soils, compared to 40% of applied imidacloprid within 300 days in Drummer surface and subsurface soils. At the 0.1 mg kg^?1 application rate, dissipation was slower for all four soils. Water-extractable imidacloprid in Exeter surface soil decreased from 98% of applied at day 1 to > 70% of the imidacloprid remaining after 400 d, as compared to 55% in the Drummer surface soil at day 1 and 12% at day 400. These data suggest that imidacloprid was bioavailable to degrading soil microorganisms and sorption/desorption was not the limiting factor for biodegradation. In subsurface soils > 40% of ¹⁴C-benzoic acid was mineralized over 21 days, demonstrating an active microbial community. In contrast, cumulative ¹⁴CO₂ was less than 1.5% of applied ¹⁴C-imidacloprid in all soils over 400 d. Qualitative differences in the microbial communities appear to limit the degradation of imidacloprid in the subsurface soils.