Toward maximizing the recycling rate in a Sapporo waste plastics liquefaction plant

Sapporo Plastics Recycling Co., Ltd., (SPR) started its commercial operation of waste plastics liquefaction in 2000. At first only hydrocarbon oil was reclaimed, this being derived from the waste plastics liquefaction process under the Japanese Containers and Packaging Recycling Law. Presently, thermal degradation residue and hydrochloric acid are being produced as by-products in addition to the hydrocarbon oil. As a result, the SPR plastics liquefaction plant has achieved a high reclamation rate of 96%, and 93% of the recycled products have been reused in Hokkaido, where SPR is located. The technical problems caused by corrosion and clogging have been solved. Chemical Feedstock Recycling & Other Innovative Recycling Techniques 6     

Aromatization of waste polyolefin pyrolysate over H-ZSM-5 zeolite-supported gallium oxide catalysts

H-ZSM-5 zeolite-supported gallium oxides were studied as aromatization catalysts for polyolefin pyrolysate. The catalysts were prepared by a conventional physical mixing method with a gallium content of 1.0 and 4.5 wt% and were reduced in flowing hydrogen at 585°C. To test their activity, a polyolefin sample was pyrolyzed and passed over a heated catalyst layer; the product was analyzed by gas chromatography/mass spectrometry. A continuous-flow fixed-bed reactor was used for aromatization of a model gas of polyolefin pyrolysate. For chlorine-free sources at 450°C, the catalyst with only 1.0 wt% gallium exhibited activity comparable to a gallium silicate catalyst. For chlorine-contaminated sources, the catalyst with 4.5 wt% gallium sustained catalytic activity for long periods. From the activity test results, it was found that zeolite-supported gallium catalysts prepared by the physical mixing method are suitable for converting polyolefin into aromatic hydrocarbons.     

Photodegradation fates of cis-chlordane, trans-chlordane, and heptachlor in ethanol

cis-Chlordane, trans-chlordane, and heptachlor were photodegraded in ethanol, and their degradation fates and degradation products were determined by a computational chemical method. The most degradable material was heptachlor (first-order reaction constant k=0.13 min(-1)). Chlorine balances changed during UV irradiation, and the chlorine atoms in chlordane and heptachlor were eventually mineralized. cis-Chlordane, trans-chlordane and heptachlor each generated two di-dechlorinated products. Reactivities at various positions in these compounds were predicted on the basis of bond dissociation energies calculated by nonempirical molecular orbital calculation (Gaussian 98W).     

Polychlorinated dibenzothiophenes in Japanese environmental samples and their photodegradability and dioxin-like endocrine-disruption potential

Polychlorinated dibenzothiophenes (PCDTs) in sediment, soil, and fly ash samples collected in Japan were analyzed and their dioxin-like endocrine-disruption potential and photodegradability investigated. PCDTs were detected in all three types of sample, although the concentrations were lower than those of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs). An Ah-immunoassay confirmed that 2,3,7,8-TeCDT, 1,2,3,7,8-PeCDT, 1,2,3,7,8,9-HxCDT, and 1,2,3,4,7,8,9-HpCDT had Ah receptor-binding activities, which means that these PCDTs have the potential to cause dioxin-like endocrine-disruption. Photodegradation of PCDTs by UV irradiation was accompanied by dechlorination. The photodegradation rates of 2,3,7,8-TeCDT and OCDT were lower than the rates for the corresponding PCDF isomers (2,3,7,8-TeCDF and OCDF), which indicates that PCDTs are more stable than PCDFs to photodegradation.     

Release of phosphorus from lake sediments

The relationship between the content of various forms of phosphorus in lakesediments and the amount of phosphorus released under aerobic and anaerobic conditions was studied. Total phosphorus content in the sediment of Lake Kasumigaura was highest at the 0–5 cm surface layer and decreased with depth. The constant value below 15 cm was consistent with the decrease of iron-bound phosphorus conent (FeP). The amount of phosphorus released from the sediments was proportional to the decrease of FeP under both aerobic and anaerobic conditions. Under anaerobic conditions, 90% of the FeP initially held in the sediments was released in 55 days. Using dialysis apparatus, maximum growth yield of algae was shown to be linearly dependent on the amount of phosphorus released under aerobic conditions.     

Viral Interference as a Factor of False-Negative in the Infectious Adenovirus Detection Using Integrated Cell Culture-PCR with a BGM Cell Line

Food and Environmental Virology - This study investigated the influence of viral interference on the detection of enteric viruses using the integrated cell culture (ICC)-PCR with a BGM cell line....     

Pathway of 17��-estradiol degradation by Nitrosomonas europaea and reduction in 17��-estradiol-derived estrogenic activity

In recent years, natural and synthetic estrogens have been recognized as endocrine disruptors in aquatic organisms. Although natural and synthetic estrogens are known to be degraded by microbes, only limited information about their degradation pathways is available. Here, we studied the degradation pathways of a natural estrogen, 17β-estradiol, by the nitrifying microorganism Nitrosomonas europaea, and we determined whether the degradation products of 17β-estradiol had estrogenic activity. To identify the degradation products, we subjected the culture solution to solid-phase extraction, and the extract was analyzed by gas chromatography–mass spectrometry. The potential estrogenic activity of the degradation products was investigated by means of a yeast two-hybrid assay. 1,3,5(10),16-Estratetraen-3-ol (estratetraenol) was newly identified as a degradation intermediate produced by dehydration of 17β-estradiol. Estratetraenol was also degraded by N. europaea, and its degradation rate was faster than that of 17β-estradiol. The two-hybrid assay confirmed that estratetraenol acted as a ligand for the estrogen receptor; estratetraenol thus has potential estrogenic activity. N. europaea eliminated the estrogenic activity derived from 17β-estradiol. This paper is the first to report dehydration as a mechanism of microbial estrogen degradation.     

Occurrence of Viruses and Protozoa in Drinking Water Sources of Japan and Their Relationship to Indicator Microorganisms

A nationwide survey of viruses, protozoa, and indicator microorganisms in drinking water sources of Japan was conducted. Among 64 surface water samples collected from 16 drinking water treatment plants, 51 (80?%) samples were positive for at least one of the 11 pathogen types tested, including noroviruses of genogroups I (positive rate, 13?%) and II (2?%), human sapoviruses (5?%), human adenoviruses of serotypes 40 and 41 (39?%), Cryptosporidium oocysts (41?%), and Giardia cysts (36?%). Total coliforms, Escherichia coli, and F-specific coliphages were detected in 63 (98?%), 33 (52?%), and 17 (27?%) samples, respectively, and E. coli was judged to be the most suitable indicator of pathogen contamination of drinking water sources. Genogroup-specific real-time PCR for F-specific coliphages revealed the presence of F-specific RNA coliphages of animal genogroup I and human genogroups II and III in 13 (41?%), 12 (39?%), and 1 (3?%), respectively, of 31 plaques isolated.     

Behavior of flames propagating through lycopodium dust clouds in a vertical duct

The structure of flame propagating through lycopodium dust clouds has been investigated experimentally. Upward propagating laminar flames in a vertical duct of 1800 mm height and 150×150 mm square cross-section are observed, and the leading flame front is also visualized using by a high-speed video camera. Although the dust concentration decreases slightly along the height of duct, the leading flame edge propagates upwards at a constant velocity. The maximum upward propagating velocity is 0.50 m/s at a dust concentration of 170 g/m³. Behind the upward propagating flame, some downward propagating flames are also observed. Despite the employment of nearly equal sized particles and its good dispersability and flowability, the reaction zone in lycopodium particles cloud shows the double flame structure in which isolated individual burning particles (0.5–1.0 mm in diameter) and the ball-shaped flames (2–4 mm in diameter; the combustion time of 4–6 ms) surrounding several particles are included. The ball-shaped flame appears as a faint flame in which several luminous spots are distributed, and then it turns into a luminous flame before disappearance. In order to distinguish these ball-shaped flames from others with some exceptions for merged flames, they are defined as independent flames in this study. The flame thickness in a lycopodium dust flame is observed to be 20 mm, about several orders of magnitude higher than that of a premixed gaseous flame. From the microscopic visualization, it was found that the flame front propagating through lycopodium particles is discontinuous and not smooth.