Biomass explosion testing: Accounting for the post-test residue and implications on the results

This work uses the ISO 1 m³ dust explosion equipment to study the explosion properties and combustion characteristics of pulverized biomass dust clouds. An unreported feature of this apparatus is that in rich concentrations only about half the dust injected is burned in the explosion, while the overpressures remain high. This work was undertaken to try to understand the mechanisms of these phenomena, through the accounting of the debris at the end of the explosion, some of which was found in the form of impacted “cake” against the vessel wall. One possible explanation is that the residue material was biomass dust blown ahead of the flame by the explosion induced wind, impacted on the walls where then the flame side underwent flame impingement pyrolysis and the metal (wall) side material was compacted but largely chemically unchanged. The results also show that the heat transfer insulation provided by the powder wall layer contributes to the higher observed pressures. The risk of explosion with significant overpressures remains at 100% in very rich environments (equivalence ratios of up to 6) although these environments are leaner than thought due to material sequestration within the “cake”. There was little indication that a rich combustion limit was approached, this was determined in standard testing equipment that has been modified and calibrated to handle larger quantities of powder than normal.     

Dehydration of ethanol with different salts in a packed distillation column

This work aimed the evaluation of a saline extractive distillation for the ethanol production. A thermodynamic model was used to predict the influence of the salts in the liquid–vapor equilibrium of the system water–ethanol and inside the packed column. The experiments were done in a distillation unit, with an internal diameter of 5.9 cm and a packing section with 37 cm of height, packed with raschig rings with 0.73 cm of characteristic inner made of glass. All the bottom and top samples were analyzed by refractive index. Two synthetic charges with the same composition of ethanol that are produced in the refinery (0.02 and 0.25 mol.L^-1) were distilled under atmospheric pressure. Sodium chloride, calcium chloride, potassium acetate, calcium nitrate and a mixture of sodium and potassium acetates were added to the synthetic charges and the results were compared to the experiments already done without the presence of the salts, revealing the ethanol enrichment in the top product of the distillation unit, for all the systems analyzed. Another charge from the refinery, known as load of wine without yeast, was evaluated and the results indicated the same behavior, enriching the ethanol with the application of the saline extractive distillation.     

生物化学法净化低浓度甲苯废气的传质研究

通过试验和理论分析,研究生物化学法净化低浓度甲苯废气这一传质一生化反应过程的控制因素,结果表明生物化学法净化低学本废气为传播控制过程,并以气膜控制为主,研究为工业化装置的设计和操作提供了理论依据。     

Single- and dual-porosity modelling of flow in reclaimed mine soil cores with embedded lignitic fragments

Lignitic mine soils represent a typical two-scale dual-porosity medium consisting of a technogenic mixture of overburden sediments that include lignitic components as dust and as porous fragments embedded within a mostly coarse-textured matrix. Flow and transport processes in such soils are not sufficiently understood to predict the course of soil reclamation or of mine drainage. The objective of this contribution is to identify the most appropriate conceptual model for describing small-scale heterogeneity effects on flow on the basis of the physical structure of the system. Multistep flow experiments on soil cores are analyzed using either mobile–immobile or mobile–mobile type 1D dual-porosity models, and a 3D numerical model that considers a local-scale distribution of fragments. Simulations are compared with time series' of upward infiltration and matric potential heads measured at two depths using miniature tensiometers. The 3D and the 1D dual-permeability models yielded comparable results as long as pressure heads are in local equilibrium; however, could describe either the upward infiltration or the matric potential curves but not both at the same time. The mobile–immobile type dual-porosity model failed to describe the data. A simultaneous match with pressure heads and upward infiltration data could only be obtained with the 1D dual-permeability model (i.e., mobile–mobile) by assuming an additional restriction of the inter-domain water transfer. These results indicate that for unsaturated flow conditions at higher matric potential heads (i.e., here >− 40 hPa), water in a restricted part of the fragment domain must be more mobile as compared to water in the sandy matrix domain. Closer inspections of the pore system and first neutron radiographic imaging support the hypothesis that a more continuous pore region exists at these pressure heads in the vicinity of the lignitic fragments possibly formed by fragment contacts and a lignitic dust interface-region between the two domains. The results suggest that the small-scale structure is too complex as to be represented by weighted contributions of individual components alone.     

Organochlorine pesticides and polychlorinated biphenyls in riverine runoff of the Pearl River Delta, China: assessment of mass loading, input source and environmental fate

A large-scale sampling program was conducted to simultaneously collect water samples at the eight major riverine runoff outlets of the Pearl River Delta (PRD), South China to assess the importance of riverine runoff in transporting anthropogenic pollutants from terrestrial sources to the coastal ocean. The concentrations of ∑₂₁OCPs (sum of 21 OCP components) and ∑₂₀PCBs (sum of 20 PCB congeners) were 2.57-41.2 and 0.12-1.47 ng/L, respectively. Compositional distributions of DDTs suggested the possibility of new input sources in the study area, but contributions from dicofol seemed considerably low. The annual inputs of ∑₂₁OCPs and ∑₂₀PCBs were 3090 and 215 kg, with those of total HCHs and DDTs being 1110 and 1020 kg, respectively. A mass balance consideration indicated that riverine runoff is the major mode carrying OCPs from the PRD to the coastal ocean, and the majority of OCPs is further dissipated to open seas.     

Fate of polybrominated diphenyl ethers in the environment of the Pearl River Estuary, South China

Ninety-six riverine runoff samples collected at eight major outlets in the Pearl River Delta (PRD), South China, during 2005-2006 were analyzed for 17 brominated diphenyl ether (BDE) congeners (defined as Σ₁₇PBDE). Fourteen and 15 congeners were detected, respectively, in the dissolved and particulate phases. These data were further used to elucidate the partitioning behavior of BDE congeners in riverine runoff. Several related fate processes, i.e. air-water exchange, dry and wet deposition, degradation, and sedimentation, within the Pearl River Estuary (PRE), were examined to estimate the inputs of Σ₁₀PBDE (sum of the target BDE congeners, BDE-28, -47, -66, -85, -99, -100, -138, -153, -154, and -183) and BDE-209 from the PRD to the coastal ocean based on mass balance considerations. The results showed that annual outflows of Σ₁₀PBDE and BDE-209 were estimated at 126 and 940 kg/year, respectively from the PRE to coastal ocean. Besides sedimentation and degradation, the majority of Σ₁₀PBDE and BDE-209 discharged into the PRE via riverine runoff was transported to the coastal ocean.     

Secondary ozonides of substituted cyclohexenes: a new class of pollutants characterized by collision-induced dissociation mass spectrometry using negative chemical ionization

Recent studies indicate that secondary ozonides of cyclic alkenes are formed in atmospheric reactions and may be relatively stable. The secondary ozonides (SOZs) of cyclohexene (1), 1-methylcyclohexene (2), 4-isopropyl-1-methylcyclohexene (3) and 4-isopropenyl-1-methylcyclohexene (limonene) (4) have been characterized by rapid gas chromatography electron ionization (EI), negative and positive chemical ionization (CI: ammonia, isobutane and methane) and collision-induced dissociation (CID) mass spectrometry. Both EI and positive CI spectra were found unsuitable for reproducible analysis. However, negative CI showed stable (M−H)⁻ ions with minor fragmentation. CID of the (M−H)⁻ ions resulted in simple and reproducible fragmentation patterns for all four SOZs with loss of m/z 18, 44 and 60, tentatively assigned as H₂O, CO₂ and C₂H₄O₂ or CO₃, respectively. Thus, negative CI-MS–MS in combination with rapid gas chromatography is the preferred method for identification of secondary ozonides of cyclohexenes.     

Characterization of humic substances of different origin by means of mass spectrometry and neural networks

Mass spectrometry fingerprinting of humic acids extracted from different soils has been carried out using laser desorption/ionization mass spectrometry (LDI-TOF MS). LDI-TOF MS provides characteristic mass spectra fingerprints for the humic acids of different origin. The information given in the fingerprints was evaluated for natural grouping trends in the samples by neural networks computing tools, such as self-organizing feature map (SOFM). This approach is efficient for recognizing patterns in the humic acids samples independently of their characteristic variability; variability characterizing natural products such as humic substances. The use of multi-layer perceptron artificial neural networks gave a successful classification of the samples.     

质谱技术在环境突发性事故中的应用

介绍了质谱技术在环境突发性事故应急监测中的应用,通过分析化工仓库爆炸应急监测和水厂污染事故调查监测两个实际案例,指出质谱技术能提供准确的定性定量结果,是环境突发性事故应急监测强有力的手段和工具.     

Emission modelling and validation of VOCs' source strengths in air-conditioned office premises

An emission model for indoor volatile organic compounds (VOCs) based on mass balance considerations has been presented and validated under steady state conditions. Comparison were made for the measured and predicted concentrations of 37 selected VOCs and TVOC through a case intervention study on the filters of the ventilation system in a new commercial air-conditioned office building. The intervention involved replacing media filters with electronic and carbon filtration. TVOC and 37 compounds selected for their health and comfort impact, representation of major chemical classes that occur in indoor air and their utility as markers of pollution sources were studied. The concentration levels predicted by the model were compared with actual measurements. Twenty-five target compounds and the TVOC were adequately described by the model where the measured concentrations were in agreement with the predicted concentrations. Modeling of the remaining 12 compounds was found to be affected by the emission rates that were occupant related.