餐厨垃圾不同“收集-处理”模式的碳排放估算对比

为明确我国餐厨垃圾不同处理模式下碳排放情况,以中国南方某城市为研究对象,结合实地调研数据,对比研究了集中式好氧堆肥、集中式厌氧发酵和分散式好氧堆肥3种处理模式下的碳排放量。结果表明,集中式好氧堆肥的碳排放总量最高,而集中式厌氧发酵碳排放总量最低。此外,分散式好氧堆肥的主要优势在于可减少收集运输过程的碳排放且可避免其他温室气体的无组织排放;在先进节能手段和控制电耗的措施下,相比于集中式好氧堆肥模式,分散式模式可实现760.91 kg的碳减排(以CO_2计)。然而,餐厨垃圾厌氧发酵模式因其可实现有机质产沼气,总碳减排空间是好氧堆肥的22倍,是一种绿色、低碳的餐厨垃圾处理方式,对实现餐厨垃圾资源化、无害化和减量化具有现实意义。     

2种典型餐厨垃圾资源化处理工艺的环境影响分析

为了评估餐厨垃圾资源化处理工艺对环境的影响,运用生命周期评价的方法,比较了2种典型的资源化处理工艺——好氧堆肥和湿热处理对环境的影响。结果表明,2种餐厨垃圾资源化处理工艺对全球变暖、生态毒性、酸化和富营养化的影响各有不同。其中,好氧堆肥对全球变暖的贡献较大,碳排放为337.7 kg CO_2eq./t。湿热处理为163.1 kg CO_2eq./t。在环境影响负荷方面,湿热处理工艺中的高能耗加重了毒性的影响。但由于其对环境的酸化、富营养化的不利影响较小,湿热处理的环境影响负荷总值是好氧堆肥的62.5%。总体上,湿热处理是一种对环境影响较小的餐厨垃圾处理工艺。     

餐厨垃圾和绿化废弃物换向通风好氧堆肥

以某高校餐厨垃圾和绿化废弃物为原料,利用一种换向通风的堆肥降解装置对其进行好氧堆肥处理,研究了2个进气温度(35℃、45℃)和3个通风速率(1.5、2.5和4 m3/h)6个处理组对堆肥原料理化性质(堆体温度、含水率、pH值、有机质含量、C/N、种子发芽指数)的影响。餐厨垃圾和绿化废弃物进行15 d好氧堆肥后,pH值上升到7左右,有机质含量达到20%~80%,C/N都降到20以下,种子发芽指数均大于50%。经过1个月腐熟,其含水率≤30%。上述指标符合有机肥料标准(NY525-2011)的要求,该堆肥产物可用于园林绿地,具有显著的经济效益和生态效益。本研究结果表明,将城市餐厨垃圾和绿化废弃物混合后进行好氧堆肥是废弃物处理的高效工程,具有良好的发展前景。     

餐厨垃圾连续堆肥处理系统中试研究

餐厨垃圾是影响城市环境重要的污染源,其处理尤其是就地堆肥处理近年来受到重视.为了利用园林绿化基质作为餐厨垃圾堆肥的水分调节材料,按照1:1体积比进行连续堆肥,研究添加园林绿化基质对餐厨垃圾堆肥过程中理化指标的影响,为餐厨垃圾无害化处理提供科学依据和技术指导.结果表明,物料堆肥升温启动迅速,第3天就达到50℃,高温持续10 d以上,达到无害化要求;堆肥最终减容率达到53％以上,减量化效果明显;物料总氮和总磷含量呈升高趋势,总有机质含量降低,肥料营养元素含量在6％以上,符合有机肥国家标准(NY525-2002).总的来说,园林绿化基质作为调理剂与餐厨垃圾联合堆肥方法可行,减量化效果好,品质符合标准.     

基于生命周期分析的餐厨垃圾肥料化利用环境风险评价研究

餐厨垃圾肥料化利用过程的风险因子主要产生于原料运输与存储、预处理、堆肥、废物填埋和肥料化产品施用5个过程,其风险影响包括地表水和地下水污染、恶臭污染、土壤盐碱化和影响作物生长以及由此引起的人体健康损害.基于生命周期全过程分析,以好氧堆肥为代表的餐厨垃圾肥料化利用的环境风险为研究对象,系统地分析了餐厨垃圾堆肥过程中的潜在风险,归纳并提出风险源项估算以及环境风险影响评价的具体方法和相关参数,通过南京市餐厨垃圾示范性项目案例,说明餐厨垃圾肥料化利用风险评价方法的具体应用.     

微生物菌剂强化餐厨垃圾和污泥联合堆肥

为探究微生物菌剂对餐厨垃圾和污泥联合好氧堆肥的影响,以餐厨垃圾和污泥(湿重1∶1)混合原料为堆肥底物,添加底物总湿重30％的废木屑作为膨胀剂,向底物中分别加入微生物菌剂和腐熟堆肥为处理组,并以不添加外源物作为对照,通过测定堆肥过程中的理化性质、腐熟效果和营养元素的变化,考察菌剂和腐熟堆肥对联合堆肥的促进作用.结果表明,...     

接种比对餐厨垃圾干式厌氧发酵启动的影响

针对不同接种比对餐厨垃圾干式厌氧发酵启动的影响,对比分析了VS接种比分别为0.36和0.90两种情况下,餐厨垃圾干式厌氧发酵启动过程中pH、NH4-N、COD、VFA、甲烷含量等指标的变化。实验结果表明,启动初期2组样品pH分别快速降至4.74和5.68,均呈酸化状态,经碱液调整后,接种比为0.36的处理仍无法正常产气,接种比为0.90的处理,pH逐步提高,系统正常运行,经72 d的发酵实验,COD去除率达90.29%,甲烷含量高于60%的沼气产量达255.4 L,分析可见,VS接种比是干式厌氧发酵处理的重要参数;此外,与传统湿式厌氧发酵处理相比,餐厨垃圾干式厌氧发酵在较高的VFA和氨氮浓度下,仍能正常运行,采用干式厌氧发酵技术处理餐厨垃圾是可行的。     

餐厨垃圾厌氧发酵特性的研究

为了实现餐厨垃圾低成本现场能源化处理,利用单相法,采用正交试验法,研究了接种率、温度和含水率对餐厨垃圾厌氧发酵过程中运行特性的影响。结果表明,接种率、含水率、发酵温度以及它们之间的交互作用对餐厨垃圾产气效果影响显著,其中以接种率与温度的交互作用影响最为显著,其次是含水率。采用单相法进行55℃高温厌氧发酵,保证65%左右的接种率和90%以上的含水率,完全可以实现餐厨垃圾现场处理。     

北京市生活垃圾处理的环境影响评价

目前北京市生活垃圾产生量不断增加,处理设施能力日渐不足,生活垃圾管理正面临着减量化与资源化必然趋势。在未来5～10年内,堆肥处理、焚烧处理和综合处理等方式将取代卫生填埋成为北京市垃圾处理的主要方式。本研究采用生命周期评价的方法,对北京市4处垃圾处理设施采用的不同工艺（卫生填埋、好氧堆肥、焚烧处理和综合处理）的环境影响进行比较。评价结果表明4,种处理方式中填埋、堆肥、焚烧和综合处理的环境影响负荷分别为4.82×10-2、1.10×10-21、.31×10-1和2.31×10-2,焚烧处理的总环境影响潜值最大,填埋处理次之,综合处理再次,堆肥处理最小。4种处理方式的资源耗竭系数分别为-2.39×10-51、.11×10-5、-3.45×10-4和-1.04×10-6,焚烧处理的资源耗竭系数最小。     

城市餐厨垃圾前处理的工艺优化

为提高餐厨垃圾资源化,利用自动化分选设备组合处理餐厨垃圾,考察餐厨垃圾快速减量化和资源化的可行性,对自动化分选前后餐厨垃圾成分进行分析,发现分选前其总量为243.05 t·d~(-1),TS为12.69%,VS为93.26%,分选后总量为242.00 t·d~(-1),TS为10.97%,VS为91.93%,其有机物含量稳定,利于厌氧发酵处理的工艺控制;对分选后餐厨垃圾进行厌氧发酵处理,考察其pH和NH_4~+-N变化,发现反应初期pH值出现弱酸性,NH_4~+-N浓度较低;随着反应进行,pH稳定在7.6~7.8,NH_4~+-N浓度约为1 200 mg·L~(-1)左右。最后对厌氧发酵产气量进行考察发现,反应前期受到pH、NH_4~+-N以及温度等反应条件影响,产气量和甲烷含量较低;随着实验趋于稳定,产气量为22 000 m3·d~(-1)左右,甲烷含量范围在65%~72%。结果表明,使用新型餐厨垃圾预处理设备,其分选效率较高,能提高后续厌氧发酵产气量和甲烷含量,较大程度实现餐厨垃圾资源化。     

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.     

Evaluation of trichloroethene recovery processes in heterogeneous aquifer cells flushed with biodegradable surfactants

The ability of two biodegradable surfactants, polyoxyethylene (20) sorbitan monooleate (Tween 80) and sodium dihexyl sulfosuccinate (Aerosol MA), to recover a representative dense non-aqueous-phase liquid (DNAPL), trichloroethene (TCE), from heterogeneous porous media was evaluated through a combination of batch and aquifer cell experiments. An aqueous solution containing 3.3% Aerosol MA, 8% 2-propanol and 6 g/l CaCl(2) yielded a weight solubilization ratio (WSR) of 1.21 g TCE/g surfactant, with a corresponding liquid-liquid interfacial tension (IFT) of 0.19 dyn/cm. Flushing of aquifer cells containing a TCE-DNAPL source zone with approximately two pore volumes of the AMA formulation resulted in substantial (>30%) mobilization of TCE-DNAPL. However, a TCE mass recovery of 81% was achieved when the aqueous-phase flow rate was sufficient to displace the mobile TCE-DNAPL toward the effluent well. Aqueous solutions of Tween 80 exhibited a greater capacity to solubilize TCE (WSR=1.74 g TCE/g surfactant) and exerted markedly less reduction in IFT (10.4 dyn/cm). These data contradict an accepted empirical correlation used to estimate IFT values from solubilization capacity, and indicate a unique capacity of T80 to form concentrated TCE emulsions. Flushing of aquifer cells with less than 2.5 pore volumes of a 4% T80 solution achieved TCE mass recoveries ranging from 66 to 85%, with only slight TCE-DNAPL mobilization (<5%) occurring when the total trapping number exceeded 2 x 10(-5). These findings demonstrate the ability of Tween 80 and Aerosol MA solutions to efficiently recover TCE from a heterogeneous DNAPL source zone, and the utility of the total trapping number as a design parameter for a priori prediction of DNAPL mobilization and bank angle formation when flushing with low-IFT solutions. Given their potential to stimulate microbial reductive dechlorination at low concentrations, these surfactants are well-suited for remedial action plans that couple aggressive mass removal followed by enhanced bioremediation to treat chlorinated solvent source zones.     

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.     

The variation of street air levels of PAH and other mutagenic PAC in relation to regulations of traffic emissions and the impact of atmospheric processes

The occurrence of particle associated PAH and other mutagenic PAC was determined in 1996 in the street air of Copenhagen. In addition, particle extracts were tested for mutagenicity. The measurements were compared with previous measurements in 1992/1993. The levels had decreased in this period. The decrease was caused by an implementation of light diesel fuels for buses and the exchange of older petrol-driven passenger cars with catalystequipped new ones. About 65% of the reduction was caused by the application of the light diesel fuels. Under special conditions, chemical processes in the atmosphere produced many more mutagens than the direct emissions. The concentrations of S-PAC and N-PAC were 10 times lower than those of PAH, while the levels of oxy-PAH were in the same order of magnitude as those of PAH. Benzanthrone, an oxy-PAH, is proposed to be formed in the atmosphere in addition to direct emissions. Benzo(a)pyrene, often applied as an air quality criteria indicator, was photochemically degraded in the atmosphere. A strong increase in the mutagenic activities was observed to coincide with a depletion of benzo(a)pyrene.     

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.     

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.     

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.     

Teratological effects of pesticides in vertebrates: a review

Abstract

In the last decades, the use and misuse of pesticides in the agriculture have increased, having a severe impact on ecosystems and their fauna. Although the various effects of pesticides on biodiversity have been already documented in several studies, to our knowledge no consistent overview of the impact of pesticides in vertebrates, both terrestrial and aquatic, is available. In this review, we try to present a concise compilation of the teratogenic effects of pesticides on the different classes of vertebrates – mammals, birds, reptiles, amphibians and fish.     

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.