The spectrum of the B[e] star BAL224

We present optical spectroscopy of the emission line star BAL 224 (V=17.3, B-V=0.46). This star also named KWBBE 485, [MA93]906 is located at the periphery of the young SMC cluster NGC 330; it is known as a photometric variable with a possible period around 1 day (Balona 1992). Furthermore it was reported as the optical counterpart of the prominent mid-infrared source (MIR1) by Kucinskas et al. (2000), indicating the presence of a dust shell. The star was included in a sample of B-type stars observed using the ESO VLT-FLAMES facilities. The presence of emission lines such as Fe II,[Fe II], [S II] make this object like a B[e] star. The H$alpha$, H$gamma$ and H$delta$ lines show an asymmetrical double-peaked emission profile suggesting the presence of an accretion disk. Moreover the MACHO and OGLE light curves were analyzed; in addition to a long-term variability ($simeq$ 2300d), a short period very close to 1 day has been detected using different methods, confirming the variability previously reported by Balona (1992). Finally the nature of this object is reconsidered.Comment: 4 page

Fuel versus Food

Many countries are actively encouraging the supply of biofuels as a low carbon alternative to the use of fossil fuels for transportation. To what extent do these trends imply a reallocation of scarce land away from food to fuel production? This paper critically reviews the small but growing literature in this area. We find that an increase in biofuel production may have a significant effect on food prices and in certain parts of the world, in speeding up deforestation through land conversion. However, more work needs to be done to examine the effect of newer generation biofuel technologies that are less land-intensive as well as the effect of environmental regulation and trade policies on land allocation between fuel and food.agricultural production; biofuel economics; climate policy; environmental regulation; land allocation

Oxidation of nitrobenzene by ozone in the presence of faujasite zeolite in a continuous flow gas–liquid–solid reactor

This work investigates the oxidation of nitrobenzene (NB) by ozone in the presence of faujasite zeolite. Experiments were carried out in a gas–liquid–solid reactor were ozone transfer and NB oxidation took place at the same time. Three configurations of the reactor were compared: empty, filled with inert glass beads and filled with faujasite pellets. First, ozone transfer coefficient (kLa) and decomposition rate constant (kC) were determined for each configuration. In presence of solid, kLa was 2.0 to 2.6 times higher and kC was 5.0 to 6.4 times higher compared to the empty reactor. Then, the various configurations were evaluated in terms of NB removal and chemical oxygen demand (COD) decrease. The faujasite reactor showed higher removal of NB and decrease of COD compared to other configurations under the same conditions suggesting that the faujasite increases the oxidation rate of NB. Oxidation of NB in presence of faujasite also proved to be limited by the transfer of ozone from the gas to the liquid phase

Adsorption of Nitrobenzene from Water onto High Silica Zeolites and Regeneration by Ozone

This work investigates the removal of nitrobenzene (NB), a model pollutant from water, by combining adsorption onto zeolites and regeneration with ozone. The adsorption equilibrium isotherms of NB onto zeolites enabled the best adsorbent to be selected and zeolites with a high Si/Al ratio were the most efficient. The adsorption capacity depended on the Si/Al ratio and on the pore size. In a sequential process coupling adsorption and oxidation by ozone, NB was completely removed from water and the initial adsorption capacity of the zeolite was totally restored. Although no catalytic effect was noticed, the adsorption produced locally high concentrations, thus enhancing the oxidation rate for NB

Telegram from Marie to Hubert Creekmore

Marie writes from New York City to Creekmore in Pacific Palisades, California, regarding travel expenses for Clifford. Includes envelope.https://egrove.olemiss.edu/creekmore/1094/thumbnail.jp

The use of ozone and high silica zeolites to enhance refractory compounds removal

This work investigates the removal of organic pollutants from water through a three-phase process combining adsorption onto hydrophobic zeolites and in situ oxidation by ozone gas. Zeolites are aluminosilicates with various crystalline structures – and especially different pore sizes - which offer a great selectivity, profitable to organic pollutants separation in a complex matrix like natural water. They are highly resistant to chemical agents as acids, bases or oxidising agents such as ozone. Moreover, high silica zeolites have a high adsorption capacity for organics. Ozone is known to be a powerful oxidising agent able to react with various organic compounds. Its action – either direct or indirect - leads to the decomposition of organics into smaller molecules that are generally biodegradable. Previous studies have shown that organics adsorbed onto zeolites could be oxidised by ozonated water faster than in bulk water because of a micropore concentration effect (Fujita et al, 2004 and Sagehashi et al, 2005). In the gas phase, Monneyron et al (2003) showed that high silica zeolites could catalyse ozone decomposition into radical species and that adsorption properties were not significantly modified after exposition to ozone. Hence it is expected that zeolites saturated with organics could undergo regeneration by ozone without degradation of their structures or decrease of their adsorption capacities. The present work showed that high silica zeolites could efficiently adsorb nitrobenzene from water although their capacity stayed beyond that of activated carbon, except at low concentrations. The adsorption capacity depended on the zeolite structure and the Si/Al ratio. Adsorption isotherms could be well described by Langmuir or Freundlich models. As regards the three phase coupled process, the adsorbent could be efficiently regenerated during an ozonation step consisting in bubbling ozone through a suspension of saturated zeolite in a nitrobenzene solution at equilibrium. The initial adsorption capacity was quickly recovered and, continuing the treatment, the adsorption capacity of the zeolite was even increased. This may be due to the cleaning of zeolites pores by ozone (Pic et al, 2005). Yet traces of template molecules could probably remain from the zeolite synthesis process. Until now the catalytic effect of the zeolites has not been evidenced in the liquid phase. Therefore future work will focus on the conditions in which the oxidation kinetics can be enhanced in the presence of zeolites through a concentration effect, and to what extent

Enhanced bio-recalcitrant organics removal by combined adsorption and ozonation

Removal of bio-recalcitrant and toxic compounds from wastewaters has been a major objective of industrial manufacturers for a few years. Due to the potential risk toward public health,regulations are becoming increasingly strict and classical treatments like biological treatments are not efficient. Other techniques such as incineration, oxidation or adsorption provide higher levels of removal but with a high energy and capital cost. A coupled process involving adsorption and oxidation is studied. Four adsorbents are tested and compared according to two objectives,their adsorption capacity and their capability to decompose ozone into powerful hydroxyl radicals. Two model compounds were chosen: 2,4-dichlorophenol and nitrobenzene.Experimental results allow comparing coupled process with results obtained during ozonation alone. Zeolite (Faujasite Y) gave disappointing results in term of both adsorption kinetics and ozone decomposition. On the contrary, activated carbons showed fast adsorptions and important capabilites to decompose ozone into radicals, almost in nitrobenzene experiments. S-23 activated carbon proved to be the most interesting adsorbent for better mechanical and chemical stabilities over time. Sequential adsorption/ozonation experiments were conducted,showing a strong loss of adsorption efficiency after the first operation, but the positive point is that the adsorption capacity remains almost constant during further cycles