Elimination of Carbamazepine,Diclofenac and Naproxen from Treated Wastewater by Nanofiltration

Most conventional wastewater treatment plants remove very small amounts of micropollutants, such as pharmaceuticals. Here, the ability of two different types of submerged nanofiltration flat sheet modules to remove pharmaceuticals from wastewater is analyzed. The two nanofiltration membranes were used at relatively low pressures of only 0.3 and 0.7 bar. At such low pressures, the membranes did not retain salts to a great extent. This is advantageous in wastewater treatment because no salt concentrate is produced. Carbamazepine was retained only slightly by the nanofiltration membranes, whereas approximately 60% of diclofenac and naproxen were retained by both membranes. This level of effectiveness might not be enough to justify the use of such a system as an additional treatment step in wastewater treatment plants.     

Satellite estimates and subpixel variability of rainfall in a semi-arid grassland

卫星估雨精度的不确定性受到当地降雨类型和像元内降雨非均匀性影响,而结合这两个关键因素开展半干旱草原卫星估雨的研究有限.2009年夏,我们在中国锡林郭勒半干旱草原用多部微雨雷达和雨量计构建了9 km卫星像元降雨观测网,观测了像元内降雨非均匀性(空间变异系数CV),并评估了卫星估雨精度.结果表明:(1)CV值受像元内平均降雨量,降雨类型,降雨云面积及移向等影响,如高Cv值的降雨过程大多为平均降雨量小,对流性降雨过程,降雨云边缘像元CV值较高;(2)TRMM 3B42V7卫星估雨产品适用性较好,CMORPH和PERSIANN次之,但TRMM 3B42V7易在半干旱草原湖泊处高估降雨.     

Heavily fractionated noble gases in an acid residue from the Klein Glacier 98300 EH3 chondrite

Noble gases were measured both in bulk samples (stepped pyrolysis and total extraction) and in a HF/HCl residue (stepped pyrolysis and combustion) from the Klein Glacier (KLE) 98300 EH3 chondrite. Like the bulk meteorite and as seen in previous studies of bulk type 3 E chondrites (“sub-Q”), the acid residue contains elementally fractionated primordial noble gases. As we show here, isotopically these are like those in phase-Q of primitive meteorites, but elementally they are heavily fractionated relative to these. The observed noble gases are different from “normal” Q noble gases also with respect to release patterns, which are similar to those of Ar-rich noble gases in anhydrous carbonaceous chondrites and unequilibrated ordinary chondrites (with also similar isotopic compositions). While we cannot completely rule out a role for parent body processes such as thermal and shock metamorphism (including a later thermal event) in creating the fractionated elemental compositions, parent body processes in general seem not be able to account for the distinct release patterns from those of normal Q noble gases. The fractionated gases may have originated from ion implantation from a nebular plasma as has been suggested for other types of primordial noble gases, including Q, Ar-rich, and ureilite noble gases. With solar starting composition, the corresponding effective electron temperature is about 5000 K. This is lower than inferred for other primordial noble gases (10,000-6000 K). Thus, if ion implantation from a solar composition reservoir was a common process for the acquisition of primordial gas, electron temperatures in the early solar system must have varied spatially or temporally between 10,000 and 5000 K.Neon and xenon isotopic ratios of the residue suggest the presence of presolar silicon carbide and diamond in abundances lower than in the Qingzhen EH3 and Indarch EH4 chondrites. Parent body processes including thermal and shock metamorphism and a late thermal event also cannot be responsible for the low abundances of presolar grains. KLE 98300 may have started out with smaller amounts of presolar grains than Qingzhen and Indarch.     

Noble gas adsorption with and without mechanical stress: Not Martian signatures but fractionated air

Abstract– Sample preparation, involving physical and chemical methods, is an unavoidable step in geochemical analysis. From a noble gas perspective, the two important effects are loss of sample gas and/or incorporation of air, which are significant sources of analytical artifacts. This article reports on the effects of sample exposure to laboratory air without mechanical influence and during sample grinding. The experiments include pure adsorption on terrestrial analog materials (gibbsite and olivine) and grinding of Martian meteorites. A consistent observation is the presence of an elementally fractionated air component in the samples studied. This is a critical form of terrestrial contamination in meteorites as it often mimics the heavy noble gas signatures of known extra‐terrestrial end‐members that are the basis of important conclusions about the origin and evolution of a meteorite. Although the effects of such contamination can be minimized by avoiding elaborate sample preparation protocols, caution should be exercised in interpreting the elemental ratios (Ar/Xe, Kr/Xe), especially in the low‐temperature step extractions. The experiments can also be transferred to the investigation of Martian meteorites with long terrestrial residence times, and to Mars, where the Mars Science Laboratory mission will be able to measure noble gas signatures in the current atmosphere and in rocks and soils collected on the surface in Gale crater.     

Catalyzed Reactions on Mineral Plaster Materials Used for Indoor Air Purification

Zeolites have been used for a long time for purification and catalytical purposes. Recently, first products appeared on the market using zeolites also for improving the indoor air quality so far volatile organic compounds (VOC) are concerned. However, porous compounds like zeolites can be found also in plaster material. Therefore, it was manifest to evaluate the capability of plaster with regard to air cleaning. In this article, the contribution of plaster compounds toward adsorption and catalytical decomposition of VOCs is evaluated using α‐pinene, chlorobenzene, 2‐ethoxyethylacetate, and pentanal as target substances under standard conditions (23°C, 50% r.H.). These compounds were chosen because of their VOC typical physicochemical properties like molecular dimensions, density, boiling point, vapor pressure, and octanol–water distribution coefficient (logk_ow). Hydrated lime and metakaolin were found out to have good adsorption properties under these circumstances. Also natural zeolites showed good results especially on pentanal. By investigations in environmental chambers the reduction potential of test plasters on chlorobenzene and 2‐ethoxyethylacetate concentrations could be shown. Application of coatings had no or only temporary influence on the performance of the plaster. Additional tests in small chambers demonstrated the possibility to improve the properties of plasters with help of FAU‐ or MFI‐type zeolites but the experiments also showed that α‐pinene and pentanal undergo chemical reactions. Further effort should be made on investigations also toward other compounds, especially more volatile ones like formaldehyde. Also additional building materials like insulation material or boards should be taken into account.     

Coesite in suevite from the Ries impact structure (Germany): From formation to postshock evolution

Coesite is one of the most common and abundant high‐pressure phases occurring in impactites. The mechanism of formation of coesite and its postshock evolution is revisited in this paper based on Raman microspectroscopy, and scanning and transmission electron microscopy of a coesite‐bearing suevite from the Ries impact structure. Our data indicate that coesite forms through a single process, i.e., by crystallization from high‐pressure silica melt, and that its formation is related to fluid inclusions in precursor quartz. During the postshock phase, coesite aggregates are partially modified by annealing and interactions with fluids. In an early stage of the postshock evolution, coesite is back‐transformed to quartz and the surrounding diaplectic glass devitrifies into β‐cristobalite, which transforms into α‐cristobalite and then into microcrystalline quartz during subsequent stages of the postshock evolution. Altogether these postshock modifications result in a significant volume loss and extensional fracturing. During a late postshock stage, the fractures are filled with clay minerals due to circulation of hydrothermal fluids.     

Über die Vertikalverteilung und jahreszeitliche Entwicklung der Larvendichte vonDreissena polymorpha Pallas im Pelagial des unteren Zürichseebeckens im Jahre 1974

The freshwater musselDreissena polymorpha Pallas was sighted for the first time in Lake Zürich about 1969. This meant a real problem for the water treatment of lake water. By means of a pump and vertical net hauls it was tried to add more information to the scarce results on Lake Zürich. Additional dates about temperature, depth of Secchi disk visibility and beam transmittance were collected. There was a first appearance of the larvae ofD. polymorpha at the beginning of June. Following the mean temperature of the epilimnion the number of individuals/m² reached max. 210,000. The greatest concentration measured in 1974 of larvae/m³ was 54,375 at a depth of 4 m. The last appearance ofD. polymorpha was observed at the end of October.