Modelling of organic matter dynamics during the composting process

Composting urban organic wastes enables the recycling of their organic fraction in agriculture. The objective of this new composting model was to gain a clearer understanding of the dynamics of organic fractions during composting and to predict the final quality of composts. Organic matter was split into different compartments according to its degradability. The nature and size of these compartments were studied using a biochemical fractionation method. The evolution of each compartment and the microbial biomass were simulated, as was the total organic carbon loss corresponding to organic carbon mineralisation into CO₂. Twelve composting experiments from different feedstocks were used to calibrate and validate our model. We obtained a unique set of estimated parameters. Good agreement was achieved between the simulated and experimental results that described the evolution of different organic fractions, with the exception of some compost because of a poor simulation of the cellulosic and soluble pools. The degradation rate of the cellulosic fraction appeared to be highly variable and dependent on the origin of the feedstocks. The initial soluble fraction could contain some degradable and recalcitrant elements that are not easily accessible experimentally.     

多区域投入产出分析下中国水足迹地区间比较——基于“总量-相关指标-结构”分析框架

在“总量-相关指标-结构”分析框架下,采用中国大陆30省区（除西藏）42经济部门多区域投入产出及伪基尼系数差异成因分解方法,估算、比较各省区水足迹并分析差异成因,衡量省区降低水足迹（即水足迹总量）的紧迫性并识别调整重点,对具体调整提出建议,为构建中国特色水安全保障体系提供依据。研究表明：1）30省区水足迹均方差系数为51.79%,其中新疆、黑龙江水足迹最高,天津、北京对应最低。2）结合相关指标地区间比较,30省区中宁夏、黑龙江、上海降低水足迹紧迫性最强;天津、山西等提高居民生活直接用水效率紧迫性最强。3）根据部门结构地区间比较,列出各省区降低水足迹中须重点关注的部门,可以看到各省区均须重点调整农林牧渔业、食品制造及烟草加工业用水。4）来源结构地区间比较中,青海、宁夏和新疆的水足迹主要靠当地来供给,其余各地区水足迹均主要源于国内其他地区;可得到各省区上述降低水足迹中应重点关注部门的水足迹主要来源地,如黑龙江、天津、海南等地农林牧渔业水足迹主要源自当地。因此,各地区应结合上述紧迫性、重点关注部门及主要来源分析结果,加强节水工作的针对性。     

Decomposing detonation and deflagration properties of ozone/oxygen mixtures

In this study, the decomposing detonation and deflagration properties of ozone/oxygen mixtures of up to 20 vol.% of ozone in oxygen under high pressure of up to 1.0 MPa in a tube were experimentally investigated. The mixtures were ignited by an electric spark at the end of the tube. Flame propagation properties such as flame velocity and pressure were measured with thermocouples and piezo electric transducers mounted along the tube. Slow and constant flame propagation profiles were obtained. We also investigated the quenching ability of a wire gauze as well as the concentration limit for flame propagation. However, in spite of slow flame propagation velocity and easy flame quenching properties under these experimental conditions, direct initiation of detonation by the driver detonation of the stoichiometric oxy-hydrogen mixture was easily achieved at much lower concentrations than the limit of deflagration. The observed detonation properties, such as wave velocity and pressure, agreed fairly well with C–J calculated values. The detonation velocity (900–1200 m/s) and the pressure ratio to initial pressures (5–9.5) were not affected by the initial pressure of the mixtures. Near the detonation limit, typical spinning detonations with oscillatory pressure waves were observed.     

Does hyperaccumulated nickel affect leaf decomposition? A field test using Senecio coronatus (Asteraceae) in South Africa

Summary. Nickel hyperaccumulator plants contain unusually elevated levels of Ni (>1,000 mg Ni kg⁻¹). The high Ni concentration of hyperaccumulator tissues may affect ecosystem processes such as decomposition, but this has yet to be studied under field conditions. We used Senecio coronatus Thunb. (Harv.) from two pairs of serpentine sites: one member of each pair contained a hyperaccumulator population and the other a non-hyperaccumulator population. Our main goal was to determine if leaf Ni status (hyperaccumulator or non-hyperaccumulator) affected leaf decomposition rate on serpentine sites. We also used a non-serpentine site on which leaves from all four S. coronatus populations were placed to compare decomposition at a single location. Dried leaf fragments were put into fine-mesh (0.1 mm) nylon decomposition bags and placed on field sites in mid-summer (early February) 2000. Sets of bags were recovered after 1, 3.5, and 8 months, their contents dried and weighed, and the Ni concentration and total Ni content of high-Ni leaves was measured. For the serpentine sites, there was no significant effect of leaf Ni status or site type on decomposition rates at 1 and 3.5 months. By 8 months, leaf Ni status and site type significantly influenced decomposition on one pair of sites: hyperaccumulator leaves decomposed more slowly than non-hyperaccumulator leaves, and leaves of both types decomposed more slowly on the non-hyperaccumulator site. At the non-serpentine site, the highest-Ni leaves (15,000 mg Ni kg⁻¹) decomposed more slowly than all others, but leaves containing 9,200 mg Ni kg⁻¹ did not decompose more slowly than non-hyperaccumulator leaves. Nickel in decomposing hyperaccumulator leaves was released rapidly: after 1 month 57–68% of biomass was lost and only 9–28% of original Ni content remained. We conclude that very high (>10,000 mg Ni kg⁻¹) leaf Ni concentrations may slow decomposition and that Ni is released at high rates that may impact co-occurring litter- and soil-dwelling organisms.     

Litter decomposition and nitrogen mineralization from an annual to a monthly model

The forest litter decomposition model (FLDM) described in this paper provides an important basis for assessing the impacts of forest management on seasonal stream water quality and export of dissolved organic carbon (DOC). By definition, models with annual time steps are unable to capture seasonal, within-year variation. In order to simulate seasonal variation in litter decomposition and DOC production and export, we have modified an existing annual FLDM to account for monthly dynamics of decomposition and residual mass in experimental litterbags placed in 21 different forests across Canada.The original annual FLDM was formulated with three main litter pools (fast, slow, and very slow decomposing litter) to address the fact that forest litter is naturally composed of a mixture of organic compounds that decompose at different rates. The annual FLDM was shown to provide better simulations than more complex models like CENTURY and SOMM.The revised monthly model retains the original structure of the annual FLDM, but separates litter decomposition from nitrogen (N) mineralization. In the model, monthly soil temperature, soil moisture, and mean January soil temperature are shown to be the most important controlling variables of within-year variation in decomposition. Use of the three variables in a process-based definition of litter decomposition is a significant departure from the empirical definition in the annual model. The revised model is shown to give similar calculations of residual mass and N concentration as the annual model (r² = 0.91, 0.78), despite producing very different timeseries of decomposition over six years. It is shown from a modelling perspective that (i) forest litter decomposition is independent of N mineralization, whereas N mineralization is dependent on litter decomposition, and (ii) mean January soil temperature defines litter decomposition in the summer because of winter-temperatures’ role in modifying forest-floor microorganism community composition and functioning in the following summer.     

Thermal degradation kinetics and mechanisms of Posidonia Oceanica under inert and oxidative atmospheres

The thermal degradation characteristics of Posidonia Oceanica (PO), a marine biomass abundantly available on the coastal zone of the Mediterranean Basin, were investigated using thermogravimetric analysis under inert and oxidative atmospheres. The kinetic parameters of the both thermal degradations conditions were determined using n-reaction order model. Coats–Redfern and Phadnis–Deshpande methods were used to discuss the probable degradation mechanisms. Results showed that PO is an attractive alternative for energy production owing to its elevated heating value. Moreover, PO thermal degradation follows the usual shape of biomass decomposition. Hence, under inert atmosphere, its thermal degradation had two different stages after moisture release. The first stage corresponded to the volatiles release while the second stage corresponded to the char formation. The solid-state decomposition mechanisms followed by the devolatilization step of PO were two or three dimensional diffusion controlled reaction. However, the decomposition mechanism during PO char formation corresponded to a nucleation and growth mechanism. Under oxidative atmosphere, two stages were also observed corresponding to volatiles release and char combustion, respectively. The solid-state mechanism of volatiles release followed three dimensional diffusion controlled reaction while the char combustion mechanism corresponded to a contracting area phase boundary controlled reaction.     

Chlorpyrifos causes decreased organic matter decomposition by suppressing earthworm and termite communities in tropical soil

Effects of pesticides on structural and functional properties of ecosystems are rarely studied under tropical conditions. In this study litterbag and earthworm field tests were performed simultaneously at the same tropical field site sprayed with chlorpyrifos (CPF). The recommended dose of CPF (0.6 kg a.i. ha⁻¹) and two higher doses (4.4-8.8 kg a.i. ha⁻¹) significantly decreased litter decomposition during the first 3 months after application, which could be explained from lower earthworm and termite abundances during this period. Species-specific effects of CPF on organism abundance and biomass were observed, with termites being mostly affected followed by the earthworm Perionyx excavatus; the earthworm Megascolex sp. was least affected. Recovery was completed within 6 months. Decomposition in the controls and lowest two treatments was completed within 4 months, which suggests the need for modification of standard test guidelines to comply with faster litter degradation under tropical conditions.     

Flammability estimation of 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide

Ionic liquids (ILs) are known as room temperature molten salts, which are considered green replacement to traditional organic solvents. The fire hazards of traditional organic solvents mainly depend on the combustibility of their vapors, thus ILs are generally regarded as nonflammable owing to their low volatility. However, recent studies show that ILs may combust due to the potential hazards of thermal decomposition, indicating the issue of fire and explosion of ILs are eager to be evaluated during the applications. In this study, the fire and explosion hazards of IL 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C₆mim][NTf₂]) are explored in different aspects. The traditional definition of the flammability for the common organic solvent is not thoroughly applicable to [C₆mim][NTf₂] due to the low volatility. Furthermore, the common definition of reactivity for traditional organic solvents also fails to apply, because the decomposition reaction is indeed an endothermic reaction. However, the auto-ignition of some decomposition products will result in fire and explosion hazards for [C₆mim][NTf₂]. Therefore the application of such data in safety purposes should be very careful.     

重庆市工业耗能相关碳排放变化驱动因素研究

在构建重庆市工业耗能相关碳排放影响因素分解模型的基础上,采用因素分解方法分析了过去十余年间(1999²011)4种驱动因素对重庆市工业碳排放变化的影响,并识别出关键驱动因素。结果显示:能耗增长的主要原因是工业经济发展;工业能源强度是促进重庆市工业耗能相关碳减排的主要影响因素;产业结构因素对重庆市工业耗能相关碳排放变化的影响存在波动,但其累积效果表现为减排;能源结构因素对重庆市工业耗能相关碳排放变化没有显著影响。最后,结合各关键因素的未来发展趋势,提出重庆市工业未来低碳发展的可行途径为技术进步和产业升级。