Concentration and distribution of platinum group elements (Pt, Pd, Rh) in airborne particulate matter in Frankfurt am Main, Germany

The concentrations and distribution of platinum group elements (Pt, Pd, Rh) in airborne particulate matter were studied in a period of one year from August 2001 to July 2002 in urban and in nonurban areas. Airborne dust samples were collected as a total amount (particles with an aerodynamic diameter <22 microm) and classified using an eight-stage Andersen impactor (<10 microm) at three locations with different traffic density roads in the Frankfurt am Main and nonurban areas. Sampling at the three locations was performed simultaneously for total airborne dust and fractionated airborne dust. Pd was determined by total reflection X-ray fluorescence after Hg coprecipitation. Pt and Rh were analyzed by adsorptive striping voltammetry after HPA digestion. The results show that the PGE concentrations in airborne samples depend on the traffic density. The highest PGE concentrations in air were found in the vicinity of major roads with heavy traffic, and the lowest ones were found in the nonurban area. The presence of PGE at the sampling station relatively free of traffic in a nonurban area hints to a transport of some of the emitted PGE from the city to this station by wind. At all three sampling locations, a heterogeneous distribution of the Pd, Pt, and Rh concentrations during the sampling year can be observed. The sum of PGE concentrations in total airborne dust is comparable with the sum of impactor samples. However, the concentration of Pt and Rh in total airborne dust (<22 microm) is on average higher than in impactor samples (<10 microm). On the contrary, Pd concentration is higher in impactor samples in most cases. The airborne PGE distribution is dominated by Pt, followed by Pd and Rh. The impactor samples are dominated by Pd, followed by Pt and Rh. This fact indicates that palladium occurs mainly in relatively fine airborne particles. The main fraction of PGE is found on average in particle sizes between 1.1 and 4.7 microm. Knowledge of the size distribution of particles containing PGE is important with respect to risk assessment of human inhalation.     

无反作用力的摇振器--DuoShake

无反作用力的摇振器-DuoShake,已应用于低速机至1200m/min高速纸机,定量范围18～550g/m2,已在中国、欧洲、北美和南美的70台纸机上应用.     

Survival analysis methodology to predict the shelf-life of probiotic flavored yogurt

The feasibility of survival analysis methodology was used to determine the shelf-life of probiotic strawberry flavored yogurt supplemented with Bifidobacteirum animalis DN 173010 W was investigated. The quality parameters of probiotic yogurts were related to storage conditions which they are submitted. The consumers were shown sensitive to changes towards sensory characteristics introduced into the products. Using the survival analysis and considering 25% and 50% probability of consumer rejection, the shelf-life of the probiotic yogurt was estimated at 38 and 53 days, respectively. The findings of this research highlighted the feasibility this technique to determine the shelf-life of foods, in particular, functional foods, as probiotic yogurts.     

Hydraulic/partitioning tracer tomography for DNAPL source zone characterization: small-scale sandbox experiments

Dense nonaqueous phase liquids (DNAPL) are prevalent at a large number of sites throughout the world. The variable release history, unstable flow, and geologic heterogeneity make the spatial distribution of DNAPLs complex. This causes difficulties in site remediation contributing to long-term groundwater contamination for decades to centuries. We present laboratory experiments to demonstrate the efficacy of Sequential Successive Linear Estimator (SSLE) algorithm that images DNAPL source zones. The algorithm relies on the fusion of hydraulic and partitioning tracer tomography (HPTT) to derive the best estimate of the K heterogeneity, DNAPL saturation (S(N)) distribution, and their uncertainty. The approach is nondestructive and can be applied repeatedly. Results from our laboratory experiments show that S(N) distributions compare favorably with DNAPL distributions observed in the sandbox but not so with local saturation estimates from core samples. We also found that the delineation of K heterogeneity can have a large impact on computed S(N) distributions emphasizing the importance of accurate delineation of hydraulic heterogeneity.     

Temporal trends, congener patterns, and sources of octa-, nona-, and decabromodiphenyl ethers (PBDE) and hexabromocyclododecanes (HBCD) in Swiss lake sediments

With the recent ban of pentabromodiphenyl ether (technical PentaBDE) and octabromodiphenyl ether (technical OctaBDE) mixtures in the European Union (EU) and in parts of the United States, decabromodiphenyl ether (technical DecaBDE) remains as the only polybrominated diphenyl ether (PBDE) based flame retardant available, today. The EU risk assessment report for DecaBDE identified a high level of uncertainty associated with the suitability of the current risk assessment approach for secondary poisoning by debromination of DecaBDE to toxic lower brominated diphenylethers. Addressing this still open question, we investigated concentrations and temporal trends of DecaBDE, NonaBDE, and OctaBDE congeners in the sediments of Greifensee, a small lake located in an urban area close to Zürich, Switzerland. PBDE appeared first in sediment layers corresponding to the mid 1970s. While total Tri-HeptaBDE (BDE-28, -47, -99, -100, -153, -154 and -183) concentrations leveled off in the mid 1990s to about 1.6 ng/g dw (dry weight), DecaBDE levels increased steadily to 7.4 ng/g dw in 2001 with a doubling time of 9 years. Hexabromocyclododecanes (HBCD) appeared in Greifensee sediments in the mid 1980s. They are an important class of flame retardants that are being used in increasing amounts, today. As was observed for DecaBDE, HBCD concentrations were continuously increasing to reach 2.5 ng/g dw in 2001. Next to DecaBDE, all 3 NonaBDE congeners (BDE-208, BDE-207, and BDE-206) and at least 7 out of the 12 possible OctaBDE congeners (BDE-202, BDE-201, BDE-197/204, BDE-198/203, BDE-196/200, BDE-205, and BDE-194) were detected in the sediments of Greifensee. Highest concentrations were found in the surface sediments with 7.2, 0.26, 0.14, and 1.6 ng/g dw for Deca-, Nona-, Octa-, and the sum of Tri-HeptaBDE, respectively. While DecaBDE and NonaBDE were found to increase rapidly, the increase of OctaBDE was slower. Congener patterns of Octa- and NonaBDE present in sediments of Greifensee did not change with time. Consequently, there was no evidence for sediment mediated long-term transformation of PBDE within the observed time span of almost 30 years. Despite the high persistence of DecaBDE, environmental debromination occurs, as shown by the detection of a shift in congener patterns of Octa- and NonaBDE in sediments, compared to the respective congener patterns in technical PBDE products. The OctaBDE congener BDE-202 was detected in sediments, representing a transformation product that is not reported in any of the technical PBDE products. Comparison of OctaBDE congener patterns in sediments with OctaBDE congener patterns from known sources reveals that (i) they were distinctively different from the congener patterns in technical PBDE products and (ii) that they were similar to the OctaBDE patterns in house dust and photodegradation products of DecaBDE, suggesting contributions from these sources.     

On the mechanism of transfer enhancement by eddy promoters

Mass transfer rates in a rectangular duct of low aspect ratio containing semicircular cylindrical inserts attached alternately on opposite walls and perpendicular to the flow direction were measured with the electrochemical diffusion-limited current technique. Local and average mass transfer coefficients determined with arrays of strip electrodes indicate the existence of at least two transfer regimes. In the laminar regime the exponent on the Reynolds number depends on the eddy promoter spacing. In the turbulent regime the data correlate well according to j_D = 0.57 Re^?0.35(d_h/p)^0.40.The local transfer distributions reveal the existence of separated flow regions downstream of, as well as opposite to, turbulence promoters. The flow in the reattachment region is very unstable and this results in earlier transition to turbulence.The local transfer distributions also suggest that boundary layer disruption at, and redevelopment downstream of, separated regions is the dominant mechanism of transfer enhancement in the turbulent regime. An idealized model based on this assumption, and making use, of results obtained for turbulent transfer to a flat plate in an infinite medium predicts a relationship in approximate agreement with the experimental correlation given above.The mass transfer results for fully developed turbulent flow also correlate well according to a mass transfer similarity law.     

Heme-dependent and heme-independent nitrite reduction by lactic acid bacteria results in different N-containing products

Seventy strains of lactic acid bacteria were investigated for nitrite reductase activity. Two types of this activity were detected. Type I was found in Lactobacillus plantarum, L. pentosus and Pediococcus pentosaceus. This activity is heme-dependent with ammonia as the sole product. Type II mechanism is heme-independent and reduces nitrite to NO and N₂O.     

Bestimmung niedermolekular gebundener Purin- und Pyrimidinbasen in Lebensmitteln nach gelchromatographischer Isolierung und hydrolytischem Druckaufschlu?

Zusammenfassung Die gelchromatographisch abgetrennten und isolierten niedermolekularen Purin- und Pyrimidinverbindungen wurden nach hydrolytischem Druckaufschluß an einem Kationenaustauscher als freie Basen bestimmt. Diese Daten werden auch im Verhältnis zu den Gesamtgehalten der Basen des Substrates mitgeteilt. Es zeigte sich, daß bei unbehandelten Proben der Anteil der niedermolekular gebundenen Basen 5–15% (je nach Base und Lebensmittel) der jeweiligen Gesamtbasenmenge beträgt. Bei frischen, nicht erhitzten Lebensmittelproben findet ein schneller Abbau von Adeninnucleotiden zu Inosinnucleotiden und zu Hypoxanthin statt, so daß nur geringe Adeningehalte aus niedermolekularen Verbindungen angetroffen werden. Bei erhitzten Lebensmitteln ist der Anteil niedermolekular gebundener Purin- und Pyrimidinbasen durch Teilhydrolyse von Nucleinsüren höher. Er beträgt dann 30–50% (je nach Base und Lebensmittel) der jeweiligen Gesamtbasenmenge.

---

Determination of purine and pyrimidine bases, bound in compounds of low-molecular weight after isolation by gelpermeation-chromatography and hydrolytic digestion under pressure

Summary Compounds with purine and pyrimidine bases of low-molecular weight were separated and isolated by gelpermeation-chromatography. After acid hydrolysis of nucleotides to free bases in a pressure digestion vessel the bases were separated on cation exchange resins. The data obtained are also reported in relation to the total base content of the substrate. It could be demonstrated that in untreated samples the portion of combined bases of low-molecular weight results in 5 to 15% of the corresponding total base content, depending on base and kind of food. In fresh unheated food samples adenine nucleotides are con verted rapidly to inosine nucleotides and hypoxanthine; therefore only a small share of adenine is found from compounds of low-molecular weight. In heated food the portion of combined low-molecular weight purine and pyrimidine bases proves to be much higher, due to partial hydrolysis of nucleic acids. It amounts to 30 to 50% of the total base content, depending on base and kind of food.

     

Up-cycling of PET (polyethylene terephthalate) to the biodegradable plastic PHA (polyhydroxyalkanoate)

The conversion of the petrochemical polymer polyethylene terephthalate (PET) to a biodegradable plastic polyhydroxyal-kanoate (PHA) is described here. PET was pyrolised at 450 degrees C resulting in the production of a solid, liquid, and gaseous fraction. The liquid and gaseous fractions were burnt for energy recovery, whereas the solid fraction terephthalic acid (TA) was used as the feedstock for bacterial production of PHA. Strains previously reported to grow on TA were unable to accumulate PHA. We therefore isolated bacteria from soil exposed to PET granules at a PET bottle processing plant From the 32 strains isolated, three strains capable of accumulation of medium chain length PHA (mclPHA) from TA as a sole source of carbon and energy were selected for further study. These isolates were identified using 16S rDNA techniques as P. putida (GO16), P. putida (GO19), and P. frederiksbergensis (GO23). P. putida GO16 and GO19 accumulate PHA composed predominantly of a 3-hydroxydecanoic acid monomer while P. frederiksbergensis GO23 accumulates 3-hydroxydecanoic acid as the predominant monomer with increased amounts of 3-hydroxydodecanoic acid and 3-hydroxydodecenoic acid compared to the other two strains. PHA was detected in all three strains when nitrogen depleted below detectable levels in the growth medium. Strains GO16 and GO19 accumulate PHA at a maximal rate of approximately 8.4 mg PHA/l/h for 12 h before the rate of PHA accumulation decreased dramatically. Strain GO23 accumulates PHA at a lower maximal rate of 4.4 mg PHA/l/h but there was no slow down in the rate of PHA accumulation over time. Each of the PHA polymers is a thermoplastic with the onset of thermal degradation occurring around 308 degrees C with the complete degradation occurring by 370 degrees C. The molecular weight ranged from 74 to 123 kDa. X-ray diffraction indicated crystallinity of the order of 18-31%. Thermal analysis shows a low glass transition (-53 degrees C) with a broad melting endotherm between 0 and 45 degrees C.     

Platinum particle size and support effects in NO(x) mediated carbon oxidation over platinum catalysts

Platinum metal was dispersed on microporous, mesoporous, and nonporous support materials including the zeolites Na-Y, Ba-Y, Ferrierite, ZSM-22, ETS-10, and AIPO-11, alumina, and titania. The oxidation of carbon black loosely mixed with catalyst powder was monitored gravimetrically in a gas stream containing nitric oxide, oxygen, and water. The carbon oxidation activity of the catalysts was found to be uniquely related to the Pt dispersion and little influenced by support type. The optimum dispersion is around 3-4% corresponding to relatively large Pt particle sizes of 20-40 nm. The carbon oxidation activity reflects the NO oxidation activity of the platinum catalyst, which reaches an optimum in the 20-40 nm Pt particle size range. The lowest carbon oxidation temperatures were achieved with platinum loaded ZSM-22 and AIPO-11 zeolite crystallites bearing platinum of optimum dispersion on their external surfaces.