An inexact reverse logistics model for municipal solid waste management systems

This paper proposed an inexact reverse logistics model for municipal solid waste management systems (IRWM). Waste managers, suppliers, industries and distributors were involved in strategic planning and operational execution through reverse logistics management. All the parameters were assumed to be intervals to quantify the uncertainties in the optimization process and solutions in IRWM. To solve this model, a piecewise interval programming was developed to deal with Min-Min functions in both objectives and constraints. The application of the model was illustrated through a classical municipal solid waste management case. With different cost parameters for landfill and the WTE, two scenarios were analyzed. The IRWM could reflect the dynamic and uncertain characteristics of MSW management systems, and could facilitate the generation of desired management plans. The model could be further advanced through incorporating methods of stochastic or fuzzy parameters into its framework. Design of multi-waste, multi-echelon, multi-uncertainty reverse logistics model for waste management network would also be preferred.     

固相微萃取-毛细管气相色谱法测定水中的吡啶

用固相微萃取富集水中吡啶,毛细管气相色谱分离分析。通过试验确定了固相微萃取的分析参数。方法的检出限可达0.001mg/L,标准曲线相关系数0.9990,相对标准偏差（RSD）在0.9%~3.1%（n=5）,平均加标回收率在92.4%~104%,已用于饮用水及地表水水中吡啶的测定。     

高效液相色谱-电喷雾电离质谱法测定地表水中微囊藻毒素

采用固相萃取-高效液相色谱-电喷雾电离质谱法测定饮用水源地地表水中痕量微囊藻毒素MC-LR,优化了色谱和质谱条件,以甲醇/水(含0.1％甲酸)混合溶液(体积比60:40)为流动相,选择定量离子质荷比(m/z)996.3.方法在0.100 mg/L-2.00 mg/L范围内线性良好,检出限为0.02 μg/L,空白水样加...     

Correction to: Urban water and food security in this century and beyond: Resource-smart cities and residents

The urban world population will increase from 3 to 8.5 thousand million in the 21st century. Cities become hot spots of both demand for water and global food and for disposed used water and nutrients. Sustainability requires that resource flows through our cities are co-managed and connected to agriculture. Reduced use of harmful chemicals in consumer products facilitates treatment to a quality that allows reuse/recycling of water and nutrients. A solid and liquid waste hierarchy can assist in ordering measures. A novel flexible water balance can guide city infrastructure and keep toilet water separate. New water-saving equipment can substantially reduce water use without losing personal comfort. The combination of these new approaches ascertains access to safe urban water, and that recovered nutrients from cities can substitute half of chemical fertilisers needed in food production. Now, thousands of new cities and suburbs provide unique opportunities to develop resource-smart and sustainable flows.     

Quantifying and managing regional greenhouse gas emissions：Waste sector of Daejeon, Korea

A credible accounting of national and regional inventories for the greenhouse gas （GHG） reduction has emerged as one of the most significant current discussions. This article assessed the regional GHG emissions by three categories of the waste sector in Daejeon Metropolitan City （DMC）, Korea, examined the potential for DMC to reduce GHG emission, and discussed the methodology modified from Intergovernmental Panel on Climate Change and Korea national guidelines. During the last five years, DMC＇s overall GHG emissions were 239 thousand tons C02 eq./year from eleven public environmental infrastructure facilities, with a population of 1.52 million. Of the three categories, solid waste treatment/disposal contributes 68%, whilst wastewater treatment and others contribute 22% and 10% respectively. Among GHG unit emissions per ton of waste treatment, the biggest contributor was waste incineration of 694 kg CO2 eq./ton, followed by waste disposal of 483 kg CO2 eq./ton, biological treatment of solid waste of 209 kg CO2 eq./ton, wastewater treatment of 0.241 kg CO2 eq./m3, and public water supplies of 0.067 kg CO2 eq./m3. Furthermore, it is suggested that the potential in reducing GHG emissions from landfill process can be as high as 47.5% by increasing landfill gas recovery up to 50%. Therefore, it is apparent that reduction strategies for the main contributors of GHG emissions should take precedence over minor contributors and lead to the best practice for managing GHGs abatement.     

Plasma arc welding: Process,sensing, control and modeling

This article introduces the basic principles of plasma arc welding (PAW) and provides a survey of the latest research and applications in the field. The PAW process is compared to gas tungsten arc welding, its process characteristics are listed, the classification is made, and two modes of operation in PAW, i.e., melt-in and keyhole, are explained. The keyhole mechanism and its influencing factors are introduced. The sensing and control methodologies of the PAW process are reviewed. The coupled behaviors of weld pool and keyhole, the heat transfer and fluid flow as well as three-dimensional modeling and simulation in PAW are discussed. Finally, a novel PAW process variant, the controlled pulse keyholing process and the corresponding experimental system are introduced.     

UN test O.1 errors in quantifying the behavior of solid oxidizers

The results of the UN test O.1 for oxidizing solids are shown to be incorrect when specimens contain certain inertant additives, illustrated for the case of oxidizers in the ammonium nitrate fertilizer family. Test results for three different AN-based products containing inertants show that two of the three (including calcium ammonium nitrate, CAN, a long-known safer alternative to AN) would be misranked with the O.1 test. An analogy between the heat release rate of substances containing fire retardant (FR) chemicals is established and several ways by which FR behavior can be achieved are demonstrated. It is shown that the O.1 test implicitly adopts only one model of inertant action, and that chemicals which rely on a differing mode of inertant action are liable to be incorrectly treated. It is further shown that the physical basis of the O.1 test—an intimate mixture of finely-comminuted fuel and oxidizer—misrepresents the most common type of accidents involving oxidizers, and that such test results do not correspond to scenarios of a less extreme nature. The new O.3 test improves the analysis method, but does not resolve the problem of excessive commingling of fuel into oxidizer. It is recommended that the intermediate-scale arrangement used by the Bureau of Explosives be adopted for further development and standardization, in preference to the O.1 or O.3 test arrangements.     

An evaluation of risk assessment framework for industrial accidents in India

Due to rapid industrialization, with high population density and constraints of land, it is expected that level of risks arising from the hazardous industries will increase in India in the coming decades. However, 30 years after the Bhopal accident (1984), except a few discrete regulations, there is as yet no integrated system for assessing and managing risks arising out of these hazardous industries in India. The gravity of aspects related to the management of industrial risk still remains crucially important. In particular, there is no standard guideline on risk analysis methodology, acceptability or tolerability criteria, nor is there an accident database or a risk reduction strategy for the areas where risk levels are already high. On top of this, there are technical and legislative gaps in the institutional framework to implement any of the above mentioned issues. With the backdrop of the Bhopal gas tragedy, the objective of this paper is therefore to evaluate the effectiveness of a comprehensive risk assessment framework for the emerging economy of India, in order to control and/or to reduce the risk level that exists. In this context, regulations and policies pertaining to industrial risk assessment were reviewed.     

Insights into properties of activated carbons prepared from different raw precursors by pyrophosphoric acid activation

Low-cost activated carbons (ACs) were prepared from four kinds of solid wastes: petroleum coke, Enteromorpha prolifera, lignin from papermaking black liquid and hair, by pyrophosphoric acid (H₄P₂O₇) activation. Thermo-gravimetric analysis of the pyrolysis of H₄P₂O₇-precursor mixtures implied that H₄P₂O₇ had different influences on the pyrolysis behavior of the four raw materials. N₂ adsorption/desorption isotherms, scanning electron microscopy, Fourier transform infrared spectroscopy and adsorption capacities for dyes were used to characterize the prepared activated carbons. AC derived from E. prolifera exhibited the highest surface area (1094 m²/g) and maximum monolayer adsorption capacity for malachite green (1250 mg/g). Kinetic studies showed that the experimental data were in agreement with the pseudo-second-order model. The adsorption isotherms were well described by the Langmuir isotherm model, indicating the adsorption of dye onto the ACs proceeded by monolayers.     

Comparison study of phosphorus adsorption on different waste solids: Fly ash, red mud and ferric–alum water treatment residues

The adsorption of phosphorus(P) onto three industrial solid wastes(fly ash, red mud and ferric–alum water treatment residual(FAR)) and their modified materials was studied systematically via batch experiments. Compared with two natural adsorbents(zeolite and diatomite), three solid wastes possessed a higher adsorption capacity for P because of the higher Fe, Al and Ca contents. After modification(i.e., the fly ash and red mud modified by FeCl_3 and FARs modified by HCl), the adsorption capacity increased, especially for the modified red mud, where more Fe bonded P was observed. The P adsorption kinetics can be satisfactorily fitted using the pseudo-second-order model. The Langmuir model can describe well the P adsorption on all of the samples in our study. p H and dissolved organic matter(DOM) are two important factors for P adsorption. Under neutral conditions, the maximum adsorption amount on the modified materials was observed. With the deviation from pH 7, the adsorption amount decreased, which resulted from the change of P species in water and surface charges of the adsorbents. The DOM in water can promote P adsorption, which may be due to the promotion effects of humic-Fe(Al) complexes and the pH buffer function exceeds the depression of competitive adsorption.