Tar and soot generation behaviors from ABS,PC and PE pyrolysis

In this study we performed a non-isothermal thermogravimetric analysis on three thermoplastics—ABS, PC and PE. The Coats and Redfern method (Nature 201:68–69, 1964) was then used to approximate the kinetic parameters of each material. In addition, we performed a series of pyrolysis experiments in a batch reactor, for each plastic. The experiments were performed over the temperature range of 600–1000 °C at a constant residence time. The liquid and solid products of the pyrolysis, were collected, separated and weighted. Those products were categorized as soot, tar and char (PC only), and their relative weight to initial sample weight (DAF) was plotted against the temperature. The tar measured was exclusively medium to high molecular weight (>80 g/mol). Results revealed that relative tar and soot production, for all three materials, first increases and then decreases with temperature increase. The maximum achieved tar yields for ABS, PC and PE were at 700, 650 and 800 °C, respectively; and the maximum soot yields were at 1000, 1000, 950 °C, respectively.     

Effect of dietary fluoride derived from Antarctic krill (Euphausia superba) meal on growth of yellowtail (Seriola quinqueradiata)

Yellowtail (Seriola quinqueradiata) is the most important cultured marine fish in Japan. Dietary fish meal for yellowtail in aquaculture was replaced with 0.0%, 15.4% and 100.0% Antarctic krill meal (KM0, KM15, and KM100) and with 0.0%, 15.4%, and 100.0% low-fluoride krill meal (LFK0, LFK15 and LFK100). The fish was fed to duplicate fish groups for 92 d (KM trial) or 75 d (LFK trial), and fish growth was monitored.Dietary fluoride (F⁻) concentrations (mg kg⁻¹) were 110, 160, and 580 (KM0, KM15, and KM100, respectively) and 98, 120, and 190 (LFK0, LFK15, and LFK100, respectively). The growth during the experimental period, weight gain, feed intake, specific growth rate, and feed efficiency in fish fed the KM100 diet were markedly lower than the other experimental groups, which showed no marked differences in growth performance.After the experiment, dorsal muscle fluoride concentrations in each group were below the detectable limit (1 mg kg⁻¹), but vertebral bone fluoride concentrations increased with increasing proportion of KM to 655 (KM0), 870 (KM15), and 2150 (KM100) mg kg⁻¹. With increasing LFK in the feed, vertebral bone fluoride concentrations (mg kg⁻¹) increased slightly from 500 (LFK0) to 655 (LFK15), and 695 (LFK100). No histopathological changes were detected in the liver tissue in any experimental group.It has been reported that the fluoride bioavailability was reduced with increasing water hardness, however, the dietary fluoride derived from KM exoskeleton accumulates in vertebral bones of marine fish with growth inhibition, as has already been shown for freshwater fish. Vertebral bone fluoride concentrations in two krill-eating Antarctic marine fish in the wild were 33 000 mg kg⁻¹ (Champsocephalus gunnari) and 15 000 mg kg⁻¹ (Notothenia rossii), but they did not show any adverse effect of growth. Therefore, fish bone fluoride accumulation apparently depends on fish species rather than the salinity of the habitat. Consequently, krill exoskeleton must be removed during the processing of Antarctic krill if indeed these krill are to be used as fish feed. However, LFK can completely replace dietary fish meal without apparent adverse effects.     

Comparison of Surface Organic Compound Mass Spectrum Patterns by LD-TOFMS for Megalopolis Atmospheric Particles and Diesel Exhaust Particles (DEP)

PM_2.5 and PM₁₀ samples for megalopolis atmospheric particles were collected at Shinjuku, Tokyo in December 1998–January 1999 and August 1999, for two weeks both in winter and summer, with a 24 hr sampling interval. Sampling of PM_2.5 and PM₁₀ in diesel exhaust particles (DEP) was carried out using an automobile exhaust testing system, with a diesel truck placed on a chassis dynamometer. Sampling conditions included idling, constant speed of 40 km hr^-1, M-15 test pattern and 60%-revolution/40%-load of maximum power. Mass spectrums of organic compounds adhering to the surface of the PM_2.5 and PM₁₀ samples were analyzed by laser desorption time-of-flight mass spectrometry (LD-TOFMS, analytical mass range: m/z 1–m/z 380 000). LD-TOFMS analysis of those samples revealed consistently the detection of low-mass organic compounds up to m/z 800. For the megalopolis atmospheric particles, the mass spectrum pattern of wintertime samples was almost the same as that of the summertime samples for both PM_2.5 and PM₁₀. The major peak was m/z 177, and the minor peaks were m/z 84, 94, 101, 163, 189 and 235. The mass spectrum pattern of DEP was the same for all samples under all test conditions. The major peak was m/z 101, and other detected peaks were small.     

Study of Asian Dust Phenomena in 2001–2003 Using A Network of Continuously Operated Polarization Lidars

We have conducted dust observations at a number of locations including Beijing, Hefei, Suwon, Fukue, Nagasaki, Tsukuba, and Sapporo using automated two-wavelength polarization lidars o study Asian dust phenomena, including generation, transport, and change during transport. We developed a method using the depolarization ratio for estimating the contributions of Asian dust and spherical air-pollution aerosols in observed aerosol mixtures. We analyzed the dust profiles statistically to derive climatological characteristics and year-on-year variations. We also studied dust source and transport path for each dust event using the regional chemical transport model CFORS. The statistical analysis clearly demonstrated the year-on-year variation of dust phenomena and the characteristics depending on the locations of the observational sites. Most major dust events in 2001 and 2002 originated in Inner Mongolia and/or Mongolia at the southern edge of a low-pressure area located in Siberia and were transported by strong westerlies. In 2003, the typical meteorological pattern for heavy dust cases accompanying a strong low in Siberia was not seen, except for one case in April. Furthermore, the lidar observation in Beijing suggests that less dust was generated in the source regions in Inner Mongolia and/or Mongolia, probably due to higher precipitation in 2003.     

PnET-CN模型对东亚森林生态系统碳通量模拟的适用性和不确定性分析

东亚地区森林类型多样,开展区域生态系统碳循环模拟时应考虑森林类型的差异。论文利用基于叶氮浓度-最大净光合作用速率关系的PnET-CN模型,对东亚地区8 个森林生态系统通量观测站点的总生态系统碳交换（GEE）和生态系统呼吸（RE）进行模拟,以探讨模型的适用性并对不确定性来源进行分析。研究结果表明：①PnET-CN模型能较为准确地模拟东亚地区大部分森林生态系统站点的GEE和RE;②模型的适用性排序依次为温带、寒温带、亚热带、 热带,模型未能很好地模拟热带湿地森林GEE和RE 的季节与年际变异;③在同一气候区中,PnET-CN模型更加适用于针叶林碳交换的模拟;④PnET-CN模型比较准确地反映了东亚森林生态系统GEE、RE对气候因子（例如,温度或辐射）的响应,但在低温、较弱辐射条件下模型低估了GEE,在高温或较强辐射条件下高估了GEE;在低温条件下模型低估了RE,在高温条件下模型高估了RE。针对东亚多个森林通量站点的模拟情况,论文提出模型应在以下方面进行改进：①PnET-CN模型计算物候时除了考虑温度之外还应加入土壤湿度的影响,并对不同气候区森林生态系统赋予不同叶片凋落时长;②PnET-CN模型中温度对GEE的限制以及光合最适温度应该根据不同站点设置;③PnET-CN模型应该考虑森林生态系统对环境胁迫的适应性,加强对干旱等干扰的模拟;④同时对于拥有复杂水文条件的森林生态系统应该改进土壤含水量的算法,以准确反映该类型森林生态系统GEE和RE的季节变化。     

Prenatal diagnosis of infantile hypophosphatasia

Prenatal diagnosis was attempted in a pregnant Japanese woman whose son had died of infantile hypophosphatasia, using chorionic villi sampled at 10 weeks of gestation. Southern blot analysis of restriction fragment length polymorphism was used as a guide, with cDNA for the human liver-type alkaline phosphatase as a probe, and BclI as a restriction enzyme. The fetus was found to be a heterozygote; the pregnancy was allowed to continue; and the baby born was phenotypically normal.     

Sintering characteristics of CaO-rich municipal solid waste incineration fly ash through the addition of Si/Al-rich ash residues

Thermal treatment is a promising technology for the fast disposal of hazardous municipal solid waste incineration (MSWI) fly ash in China. However, fly ash produced in grate incinerator (GFA) is rich in CaO and chlorides, which promote the formation of toxic hexavalent chromium [Cr(VI)] and ash agglomeration during the thermal process, inhibiting the thermal disposal of GFA. In this study, sintering characteristics of CaO-rich GFA were improved by adding Si/Al-rich MSWI ash residues. According to the results, ash agglomeration was well suppressed during thermal treatment of the mixed ash. Si/Al/Fe-compounds competed with un-oxidized Cr-compounds to react with CaO and suppressed Cr(VI) formation. Meanwhile, chlorides in GFA facilitated heavy metal volatilization from added ashes to the secondary fly ash, favoring the recovery of these metals. Ca-aluminosilicates was found as the main mineral phase in the thermally treated mixed ash, which has attractive potential for applications. The formation of the aluminosilicates made the heavy metals that remained in the treated mixed ash more stable than the thermally treated single ash.     

A case study on identification of airborne organic compounds and time courses of their concentrations in the cabin of a new car for private use

The cabin of an automobile can be considered to be a part of the living environment because many people spend long periods of time during business, shopping, recreation or travel activities. However, little is known about the interior air contamination due to organic compounds diffusing from the interior materials used in the interior of automobiles. In the present study, the compounds in the interior air of a new car were identified, and the time courses of their concentrations were examined for over 3 years after the delivery (July, 1999). A total of 162 organic compounds, involving many aliphatic hydrocarbons and aromatic hydrocarbons, were identified. High concentrations of n-nonane (458 microg/m(3) on the day following delivery), n-decane (1301 microg/m(3)), n-undecane (1616 microg/m(3)), n-dodecane (716 microg/m(3)), n-tridecane (320 microg/m(3)), 1-hexadecene (768 microg/m(3)), ethylbenzene (361 microg/m(3)), xylene (4003 microg/m(3)) and 2,2'-azobis(isobutyronitrile) (429 microg/m(3)) were detected, and the sum of the concentrations determined for all compounds excluding formaldehyde (TVOC) was approximately 14 mg/m(3) on the day after the delivery. The concentrations of most compounds decreased with time, but increased with a rise of the interior temperature. The TVOC concentration in the next summer (July, 2000) was approximately one-tenth of the initial concentration. During the 3-year study period, the TVOC concentrations in summer exceeded the indoor guideline value (300 mug/m(3)) proposed by [Seifert B. Volatile organic compounds. In: Maroni M, Seifert B, Lindvall T, editors. Indoor air quality. A comprehensive reference book. Air quality monographs, vol. 3. Netherlands: Elsevier Science; 1995. p. 819-21]. The interior temperature and days lapsed after delivery were the main factors affecting the interior concentrations of most compounds according to multiple linear regression analysis. The results of this study offer useful fundamental data for investigations on air pollution in automotive cabins due to the organic compounds diffusing from the interior materials.