Pathways and products of the degradation of PCBs by the sodium dispersion method

Nine polychlorinated biphenyl (PCB) congeners (2-chlorobiphenyl, 3-chlorobiphenyl, 4-chlorobiphenyl, 2,3,4-trichlorobiphenyl, 2,2',5,5'-tetrachlorobiphenyl, 2,3',4,4',5-pentachlorobiphenyl, 3,3',4,4',5-pentachlorobiphenyl, 2,2',4,4',5,5'-hexachlorobiphenyl, and decachlorobiphenyl) were dechlorinated by the sodium dispersion method (SD) at low temperature (60 degrees C). The dechlorination of 4-chlorobiphenyl was the fastest among the three monochlorobiphenyls. As for the other six congeners, we investigated the major dechlorination pathways. Although reaction selectivity was not very sensitive to the position of the chlorine substituent, the chlorines at the para position were slightly easier to dechlorinate than those at the ortho or meta positions. The decomposition rate increased with the total numbers of chlorine substituents. A chlorine situated between two other chlorines showed a high reactivity. When the numbers of chlorines on each of the phenyl rings were different, the reactions occurred on the more substituted ring. In the degradation of 4-chlorobiphenyl at elevated temperature (160 degrees C), we investigated the structures of the polymerized products and whether all the organic chlorinated compounds degraded finally or not. As for the dimers, p-quarterphenyl (QP) and m,p-QP were detected but not o-QP, m-QP, o,p-QP, o,m-QP, or the mono- to tetra-chlorinated QPs. Compounds with a molecular weight of 534.4183 or 758.6713 were detected. They were considered to have C40H54 or C56H86 as their molecular formula. The compounds were most probably the polymerized products resulting from coupling of hexadecane or two hexadecanes and two phenylcyclohexadienes. It was thought the dechlorination and the polymerization were the main reactions. All of many detected compounds were hydrocarbons without chlorines, and no peaks originating from organic chlorinated compounds were observed by mass spectroscopic (MS) methods.     

Effect of grinding and heating on Ni2+ uptake properties of waste paper sludge

Uptake properties of Ni2+ were examined for unmilled and milled paper sludge calcined at various temperatures to develop a new usage of waste paper sludge. Since paper sludge mainly consists of cellulose ([C6H(10)O5]n) fibers, calcite (CaCO3), kaolinite (Al2Si2O5(OH)4) and talc (Mg3Si(4)O(10)(OH)2), amorphous and crystalline CaO(MgO)-Al(2)O(3)-SiO(2) compounds are formed by calcining paper sludge. Wet and dry milling treatments were performed to accelerate solid-state reaction to form the above mentioned target compounds. The crystalline phases originally present decompose at increasing calcining temperature (up to 800 degrees C) in the order cellulose 相似文献   

Absorption of atmospheric phenol by various tree species and their tolerance to phenol

To assess the effect of tree planting on atmospheric phenol, a study was made on the absorption of phenol by various tree species and the tolerance of these species to phenol. The absorption rates ranged from 21.3 (camellia) to 129 ng dm^‐2h^‐1 ppb^‐1 (Japanese elm) at 1000 μmol of photons m^‐2 s^‐1, and the absorption rate increased in the following order: coniferous tree species ? evergreen broad‐leaved tree species < deciduous broad‐leaved tree species. When the light intensity was varied, a linear relationship between the phenol absorption rate and the transpiration rate was observed for three tree species. In comparison with the absorption rate estimated from a simplified gas diffusive resistance model, we conclude that phenol is absorbed through the stomata and is metabolized fairly rapidly within the leaf tissue, although the absorption rate is less than the estimated potential absorption rate. At phenol concentrations below 200 ppb, the tree can absorb atmospheric phenol for at least 8 h without any visible foliar injury. Trees in general could act as an important sink for atmospheric phenol at phenol concentrations less than 200 ppb, a concentration about twenty times higher than normal ambient levels.     

Studies on the dechlorination and oil-production technology of waste plastics

 Recycle technology for waste plastics containing polyvinyl chloride (PVC) has been developed in the Hokkaido National Industrial Research Institute for the production of solid and liquid fuel, and has established a recycling process which includes a dechlorination process for PVC plastics, and a two-stage catalytic pyrolysis process for plastics using zeolite catalysts. The dechlorination equipment consists of a two-axis screw extruder with a heating element, which can remove chlorine up to 99.9 wt. % from PVC containing plastics as hydrogen chloride. The product had about 44 000 kJ/kg calorific value and was fed into the next oil production process, although it could also be used as a solid fuel. Natural and synthetic zeolite were used as catalysts for the two-stage catalytic process, which produced a light oil with a boiling point which was between those of kerosene and gasoline. The yield of this oil reached 82 wt. %. The chemical type was analyzed using liquid chromatography, and was found to have many aromatic compounds. These technologies make it possible to produce a nonpolluting, high-calorie solid fuel and a liquid fuel very efficiently. Received: July 19, 2000 / Accepted: September 21, 2000     

Universities,government, and industry: An international perspective on developing environmentally conscious technologies

The educational and research roles of universities in environmentally conscious technologies are discussed from a historical perspective. The American university system, and in particular its interactions with government and industry, is compared with that of the United States' main trading partners including Japan, the NAFTA countries, and Western Europe. Examples of federally funded U.S. programs related to green design are also tabulated. The role of universities within the framework of society, politics, and economics is discussed in regard to emerging concepts such as sustainable development, life-cycle analysis, and design for environment, as well as the functioning of local recycling infrastructures. The means by which universities can contribute to environmentally conscious technology are summarized, as are the demands placed on the next generation of engineers.     

Japanese Papilio butterflies puddle using Na+ detected by contact chemosensilla in the proboscis

Many butterflies acquire nutrients from non-nectar sources such as puddles. To better understand how male Papilio butterflies identify suitable sites for puddling, we used behavioral and electrophysiological methods to examine the responses of Japanese Papilio butterflies to Na⁺, K⁺, Ca²⁺, and Mg²⁺. Based on behavioral analyses, these butterflies preferred a 10-mM Na⁺ solution to K⁺, Ca²⁺, and Mg²⁺ solutions of the same concentration and among a tested range of 1?mM to 1?M NaCl. We also measured the ion concentrations of solutions sampled from puddling sites in the field. Na⁺ concentrations of the samples were up to 6?mM, slightly lower than that preferred by butterflies in the behavioral experiments. Butterflies that sipped the 10?mM Na⁺ solution from the experimental trays did not continue to puddle on the ground. Additionally, butterflies puddled at sites where the concentrations of K⁺, Ca²⁺, and/or Mg²⁺ were higher than that of Na⁺. This suggests that K⁺, Ca²⁺, and Mg²⁺ do not interfere with the detection of Na⁺ by the Papilio butterfly. Using an electrophysiological method, tip recordings, receptor neurons in contact chemosensilla inside the proboscis evoked regularly firing impulses to 1, 10, and 100?mM NaCl solutions but not to CaCl₂ or MgCl₂. The dose?Cresponse patterns to the NaCl solutions were different among the neurons, which were classified into three types. These results showed that Japanese Papilio butterflies puddle using Na⁺ detected by the contact chemosensilla in the proboscis, which measure its concentration.     

Influence of combustion-originated dioxins in atmospheric deposition on water quality of an urban river in Japan

Bulk (wet and dry) deposition samples were collected in Saitama Prefecture, Japan throughout a year (February 8, 2012 to February 7, 2013) to estimate the influence of dioxins emitting from waste incinerators on river water quality. The annual deposition flux of dioxins was 3.3 ng-toxic equivalent (TEQ)/m²/year. Source identification using indicative congeners estimated that 82% of dioxin TEQ in the bulk deposition (2.7 ng-TEQ/m²/year) was combustion-originated, indicating that most of the dioxins in the deposition were derived from waste incinerators. In Saitama prefecture the annual flux of combustion-originated dioxins in depositions was apparently consistent with that of dioxin emission into the air from waste incinerators. The TEQ of combustion-originated dioxins in the deposition per rainfall was 2.4 pg-TEQ/L on annual average, exceeding the environmental quality standard (EQS) for water in Japan of 1 pg-TEQ/L. This suggests there is a possibility that dioxins in atmospheric deposition have a significant influence on the water quality of urban rivers which rainwater directly flows into because of many paved areas in the basins. The influence of combustion-originated dioxin in the deposition on the water quality of Ayase River, an urban river heavily polluted with dioxins, was estimated at 0.29 pg-TEQ/L on annual average in 2015. It seems that dioxins in atmospheric deposition from waste incinerators have a significant influence on water quality of some urban rivers via rainwater though the dioxins in the ambient air have achieved the EQS for atmosphere at all monitoring sites in Japan.     

An improved approach for identifying suitable habitat of Sambar Deer (Cervus unicolor Kerr) using ecological niche analysis and environmental categorization: Case study at Phu-Khieo Wildlife Sanctuary,Thailand

To assess habitat suitability (HS) has become an increasingly important component of species/ecosystem management. HS assessment is usually based on presence/absence data related to environmental variables. An exception is Ecological Niche Factor Analysis (ENFA), which uses only presence data and which does not require absence data. Most HS modelling is based on input of all environmental parameters (EnvPs) without environmental categorization, and does not take into account species interaction and human intervention for an assessment of HS. In this study, the EnvPs are arranged into four features: geographical features, consumable features, human-factor features, and species–human interaction features. These features affect species with respect to movement, behavior and activity. The research presented here has used an already existing dataset of wildlife species and human activities/visitations, which was compiled during 2004–2006 in Phu-Khieo Wildlife Sanctuary (PKWS). Data from 2004 to 2005 were used to produce HS maps, while the data of 2006 were used for evaluating these maps. Sambar Deer (SD) was chosen to predict its own HS. Six HS maps of SD were analyzed using ENFA in the following manner: (1) inputting all EnvPs together, (2) inputting each feature, separately and (3) integrating the four resulting HS maps by model averaging. It was found that model averaging was capable of predicting the HS of SD more reliably than the model with all EnvPs put in together. Multiple linear regressions were computed between the HS map with all EnvPs and the HS maps with each feature. The results show that the HS map with only geographical features has the highest coefficient value (0.516) while the coefficient values of other HS maps with the above features are 0.296, 0.53 and −0.006, respectively. This indicates that the geographical features have an influence on the other features and that the predicting power is lower when all EnvPs are computed in the ENFA model. Therefore, in order to generate HS, each feature should at first be put into the model separately. Following that, the average of all features will be combined.     

Fluoride removal studies using virgin and Ti (IV)-modified Musa paradisiaca (plantain pseudo-stem) carbons

The preparation of carbons in virgin and Ti-modified forms under controlled conditions at low temperature from plantain pseudo-stem (Musa paradisiaca) was achieved. These prepared carbons were characterized for instrumental studies such as BET, FTIR, XRD, SEM with EDS and TGA to understand the chemistry and modification. The determination of IEP and pH_ZPC established the presence of positive surface sites on the virgin (VMPC) and Ti-modified (TiMPC) carbons to facilitate the sorption of fluoride. The fluoride removal efficiency as a function of time, pH, dose, initial fluoride concentration, temperature, and co-ion intervention was studied. The maximum fluoride removal of about 81.2 and 97.7% was achievable with VMPC and TiMPC, respectively, after 20 min at the pH of 2.04 and continued for the equilibrium of 60 min. Temperature was found to be influential both by way of initial increase followed by a decrease in the fluoride uptake of MPCs. Regeneration was very consistent up to 7 cycles with the residual fluoride concentration below the WHO guide line of 1.5 mg L^?1. Highest intervention due to hydrogen carbonate ions was observed during the fluoride removal process. Kinetic (pseudo-first-order, pseudo-second-order, and intra-particle diffusion) and isotherm models (Langmuir, Freundlich, and DKR) were checked for their compliance with the present sorption system. These low temperature synthesized MPCs are found to be effective candidates in the process of fluoride abatement in water.

     

Combined biological and photocatalytic treatment for the mineralization of phenol in water

Phenol is degraded by biological treatment, however mineralization requires long time. To decrease the time and operational cost necessary for the mineralization of phenol, an optimum operation condition of the combined biological–photocatalytical treatment was investigated. The mineralization of phenol (50 mg l⁻¹) was conducted in a flow-type biomembrane tank combined with a batch-type TiO₂-suspended photocatalytic reactor. Phenol was degraded biologically to the concentration of 6.8 mg l⁻¹, an effective concentration for further photocatalytic treatment. After the biological treatment, the biotreated phenol was treated photocatalytically to complete the mineralization of phenol. The combined treatment shortened the mineralization time compared to the biological treatment and electric cost compared to the photocatalytic treatment only. The combined treatment may be suitable for a short-time mineralization of phenol in wastewater.