过敏性皮肤贴身穿轻薄毛织物的主要医用规格

最新研究表明贴身穿细美利奴羊毛的衣服对敏感型皮肤的皮疹有一定的治疗作用。为了确保这类过敏性皮肤穿着的舒适性,文章利用澳大利亚羊业合作研究中心的穿着试验数据和成衣,借助新近研发的羊毛舒适仪,对过敏性皮肤贴身穿轻薄毛织物的医用规格进行了研究。通过相关性分析发现:纯羊毛织物的刺痒性能很大程度上决定了穿着者的皮肤舒适度。进而通过使用多元变量主成分分析,辨别出人们对羊毛织物刺痒性能在不同的穿着环境和不同的活动强度下的感应模式,从而对织物的刺痒性能进行分类。最后通过对试穿服装的纤维细度和舒适度指数进行测试分析,确定了该类贴身穿毛织物的主要医用规格。包括舒适度指数不高于200,纤维的平均直径不大于17.5μm,直径大于25μm的纤维含量不高于2.0%。     

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.     

Biomagnification of perfluoroalkyl compounds in the bottlenose dolphin (Tursiops truncatus) food web

The environmental distribution and the biomagnification of a suite of perfluoroalkyl compounds (PFCs), including perfluorooctane sulfonate (PFOS) and C8 to C14 perfluorinated carboxylates (PFCAs), was investigated in the food web of the bottlenose dolphin (Tursiops truncatus). Surficial seawater and sediment samples, as well as zooplankton, fish, and bottlenose dolphin tissue samples, were collected at two U.S. locations: Sarasota Bay, FL and Charleston Harbor, SC. Wastewater treatment plant (WWTP) effluents were also collected from the Charleston area (n = 4). A solid-phase extraction was used for seawater and effluent samples and an ion-pairing method was used for sediment and biotic samples. PFCs were detected in seawater (range <1-12 ng/L), sediment (range <0.01-0.4 ng/g wet weight (ww)), and zooplankton (range 0.06-0.3 ng/g ww). The highest PFC concentrations were detected in WWTP effluents, whole fish, and dolphin plasma and tissue samples in which PFOS, C8 and C10-PFCAs predominated in most matrices. Contamination profiles varied with location suggesting different sources of PFC emissions. Biomagnification factors (BMFs) ranged from <1 to 156 at Sarasota Bay and <1 to 30 at Charleston. Trophic magnification factors (TMFs) for PFOS and C8-C11 PFCAs indicated biomagnification in this marine food web. The results indicate that using plasma and liver PFC concentrations as surrogate to whole body burden in a top marine predator overestimates the BMFs and TMFs.     

Structural study of hexane-soluble products from hydroliquefaction of three Yallourn brown coal lithotypes over molten salt catalysts

The hexane-soluble fractions of hydroliquefied products from three Yallourn brown coal lithotypes have been separated into five fractions by combined silica-alumina packed column chromatography. Analyses of various fractions by g.c.-m.s. permitted the identification of ≈50 components in the saturate fraction and 40 components in the diaromatic fraction, together with 30 components in the monoaromatics. The components identified were quite similar among hexane-soluble portions of all three lithotypes. A marked predominance of even carbon number alkane (C₂₃-C₂₉) was observed in the hydrocarbon fractions from pale lithotype over $\text{ZnCl}{}_2\text{KCl}$, and medium light lithotype over both pure ZnCl₂ and $\text{ZnCl}{}_2\text{KCl}$. However, medium dark lithotype over both melt catalysts produced a saturate fraction with an odd carbon number(C₂₂-C₂₈) preference. Based on spectral methods, Soxhlet extracts obtained from untreated lithotypes (hexane and benzene solubles) were characterized as complex mixtures of higher molecular weight(300–1000) aliphatic hydrocarbons, which were supposed to be a precursor of the saturates produced from the corresponding lithotype in the catalytic hydroliquefaction.     

Contributions of Transformation and Microcracking to the Plastic Deformation of Magnesia-Partially-Stabilized Zirconia

The measured plastic deformation of Mg-PSZ under stress contains contributions from both transformation and microcracking. A method is described to separate the contributions from transformation and microcracking for samples deformed in uniaxial tension. Such a separation enables the ratio of the longitudinal to transverse strains arising from the transformation to be estimated. The results are compared to the predictions of the shear–dilatation model of Chen and Reyes-Morel. Serious discrepancies are found between the experimental results and the predictions of the model and the possible reason for this is discussed.     

Fuel cycle analysis of GFR using advanced fuels

The potential benefits of a synergistic light-water reactor (LWR) and gas-cooled fast reactor (GFR) fuel cycle were evaluated for its impact on the front-end and back-end of the fuel cycle. Comparisons were made with conventional once-through cycle (OTC) and MOX fuel cycle. Variations in the synergistic LWR/GFR fuel cycles were based on the degree of recycle in the LWR including both plutonium and reprocessed uranium with concomitant impact on used LWR fuel inventory. This provided a wide range in composition of GFR feed from low to high plutonium content with impact on transmutation/incineration within the GFR fuel cycle. Self-recycle of all actinides was modeled for the GFR with analyses demonstrating that the GFR can be sustained on and consequently accept a wide range of feed materials. Analyses were done using Monteburns along with MCNP and Origen2.2 to model a 60-year period corresponding to the anticipated lifetime of supposed contemporary LWRs and GFRs. All cycles were evaluated based on actinide total mass and isotopic inventory, radiotoxicity, heatload, and resource requirements including natural uranium and SWU. For comparison, all fuel cycles were normalized based on 1 TWHe output. Improvements in fuel cycle performance are dictated by the production and incineration of minor actinides in the GFR and their continued recycle may not be feasible due to the buildup of troublesome isotopes such as ²⁴⁴Cm and ²⁵²Cf. But where uranium and plutonium continue to be recycled beyond the 60-year period, the LWR/GFR cycles demonstrated order of magnitude reductions in used fuel inventories, heatload, and radiotoxicity on a per TWHe basis over LWR only cycles. The full details of the advanced fuel cycle methodology and results are presented.     

Characterisation of the $$chi$$χ-index and the rec-index

Scientometrics - Axiomatic characterisation of a bibliometric index provides insight into the properties that the index satisfies and facilitates the comparison of different indices. A geometric...     

Consistent flavor naming predicts recognition memory in children and young adults

The relationship between flavor naming and recognition memory was evaluated in groups of children and young adults who either self-generated flavor names or chose flavor names from a list of four alternatives. The adults were more successful at naming and remembering the flavors, with the age differences in naming performance tending to be larger than differences in memory performance. Differences in recognition memory among the age groups were modest, ranging from 3% to 12%. Providing flavor labels improved naming accuracy, but not naming consistency or memory for younger children (4-7 years old). Labels improved naming accuracy and consistency for the older children (8-11 years old), and showed a trend toward improving memory. Labels improved naming accuracy, consistency and recognition memory in adults. Consistent naming was a powerful predictor of recognition memory for each age group and test condition. Consistently named flavors were remembered correctly on 88% of the trials while inconsistently named flavors showed no evidence of memory. It was concluded that flavor recognition memory and naming consistency were both rooted in successfully matching flavor percepts to a multi-dimensional flavor representation that includes semantic information.