The low-temperature heat capacity and standard entropy of synthetic huttonite ThSiO4

The low-temperature heat capacity of synthetic huttonite ThSiO₄ has been measured from T = (2 to 300) K. The sample was synthesised successfully from SiO₂ and ThO₂ by solid-state reaction at T = 1873 K at atmospheric pressure. From the calorimetric results, the value for the standard entropy $S_{\text{m}}^{°}$ (ThSiO₄, huttonite, 298.15 K) = (104.3 ± 2.0) J · K^?1 · mol^?1 has been obtained. This value indicates that the entropy of reaction from SiO₂ and ThO₂ is negative, giving a positive entropy term (?T · Δ_rS) of the Gibbs free energy of reaction. The implications of this finding are discussed extensively.     

Well‐Balanced Designs for Data Placement

The problem we consider in this article is motivated by data placement, in particular data replication in distributed storage and retrieval systems. We are given a set V of v servers along with b files (data, documents). Each file is replicated on exactly k servers. A placement consists in finding a family of b subsets of V (representing the files) called blocks, each of size k. Each server has some probability to fail and we want to find a placement that minimizes the variance of the number of available files. It was conjectured that there always exists an optimal placement (with variance better than any other placement for any value of the probability of failure). We show that the conjecture is true, if there exists a well‐balanced design—that is, a family of blocks—each of size k, such that each j‐element subset of V, , belongs to the same or almost the same number of blocks (difference at most one). The existence of well‐balanced designs is a difficult problem as it contains, as a subproblem, the existence of Steiner systems. We completely solve the case and give bounds and constructions for and some values of v and b.     

New di-(beta-chloroethyl)-alpha-amides on N-(meta-acylamino-benzoyl)- D,L-aminoacid supports with antitumoral activity

In order to obtain new compounds with antitumoural action the N-(meta-acylaminobenzoyl)-alpha-acylaminobenzoyl)-alpha-aminoacids 4-9 were prepared. These compounds were subsequently converted into the corresponding Delta(2)-oxazolin-5-ones 10-15, which in turn were submitted to a ring opening reaction with di-(beta-chloroethyl)amine to afford the peptide supported N-mustards 16-21, which showed low toxicity and cytostatic activity similar to that of sarcolisine against the Ehrlich ascite and Walker 253 carcinosarcoma.     

Synthesis of the silaisocyanoacetylene molecule

The hitherto elusive silaisocyanoacetylene molecule (HCCNSi)-a member of the silaisocyanide family-has been synthesized for the first time through the reaction of the silicon nitride radical (SiN) with acetylene (C(2)H(2)) in the gas phase under single collision conditions. Compared to the isoelectronic reaction of the cyano radical (CN) with acetylene, the replacement of the carbon atom in the cyano group by an isovalent silicon atom has a pronounced effect on the reactivity. Whereas the silicon nitride radical was found to pass an entrance barrier and adds with the nitrogen atom to the acetylene molecule, the cyano radical adds barrierlessly with the carbon atom forming the HCCH(NSi) and HCCH(CN) intermediates, respectively. These structures undergo hydrogen loss to form the linear silaisocyanoacetylene (HCCNSi) and cyanoacetylene molecules (HCCCN), respectively. Therefore, the isovalency of the silicon atom was found to bear little resemblance with the carbon atom having a dramatic effect not only on the reactivity, but also on the reaction mechanism, thermochemistry, and chemical bonding of the isoelectronic silaisocyanoacetylene and cyanoacetylene products, effectively reversing the thermodynamical stability of the nitrile versus isonitrile and silanitrile versus isosilanitrile isomer pairs.     

Crossed beam study of the atom-radical reaction of ground state carbon atoms (C(3P)) with the vinyl radical (C2H3(X2A'))

The atom-radical reaction of ground state carbon atoms (C((3)P)) with the vinyl radical (C(2)H(3)(X(2)A')) was conducted under single collision conditions at a collision energy of 32.3 ± 2.9 kJ mol(-1). The reaction dynamics were found to involve a complex forming reaction mechanism, which is initiated by the barrier-less addition of atomic carbon to the carbon-carbon-double bond of the vinyl radical forming a cyclic C(3)H(3) radical intermediate. The latter has a lifetime of at least 1.5 times its rotational period and decomposes via a tight exit transition state located about 45 kJ mol(-1) above the separated products through atomic hydrogen loss to the cyclopropenylidene isomer (c-C(3)H(2)) as detected toward cold molecular clouds and in star forming regions.     

Enhanced Ammonia Content in Compost Leachate Processed by Black Soldier Fly Larvae

Black soldier fly (BSF) larvae (Hermetia illucens), feeding on leachate from decaying vegetable and food scrap waste, increase ammonia (NH₄⁺) concentration five- to sixfold relative to leachate unprocessed by larvae. NH₄⁺ in larva-processed leachate reached levels as high as ∼100 mM. Most of this NH₄⁺ appears to have come from organic nitrogen within the frass produced by the larvae as they fed on leachate. In nitrate-enriched solutions, BSF larvae also facilitate dissimilatory nitrate reduction to ammonia. The markedly higher concentration of NH₄⁺ recovered in leachates processed with BSF larvae and concomitant diversion of nutrients into insect biomass (itself a valuable feedstock) indicate that the use of BSF larvae in processing leachate of decaying organic waste could be advantageous in offsetting capital and environmental costs incurred in composting.     

Design,synthesis and structure of new dendritic melamines. First use of a tandem C-2-substituted serinol—O,O-masked 4-piperidone as a peripheral unit in iterative synthesis

The iterative chemoselective amination of cyanuric chloride to dimers of new G-2 dendritic N-substituted-2,4,6-triamino-s-triazines (melamines) having C-2-substituted 2-aminopropane-1,3-diols (‘serinols’) in tandem with the ethylene ketal of 4-piperidone as peripheral units is reported. The structure as a function of increasing molecular size was studied by NMR spectroscopy, DFT calculation and AFM imaging. A concise nomenclature defining the restricted rotational phenomena about the newly created C(s-triazine)–N(exocyclic) partial double bonds, seen as axes of (pro)diastereomerism, is used. We propose a new form of frontier rotamerism for the dendrimer surface, which operates over a long range.     

Underwater psychophysical audiogram of a young male California sea lion (Zalophus californianus)

Auditory evoked potential (AEP) data are commonly obtained in air while sea lions are under gas anesthesia; a procedure that precludes the measurement of underwater hearing sensitivity. This is a substantial limitation considering the importance of underwater hearing data in designing criteria aimed at mitigating the effects of anthropogenic noise exposure. To determine if some aspects of underwater hearing sensitivity can be predicted using rapid aerial AEP methods, this study measured underwater psychophysical thresholds for a young male California sea lion (Zalophus californianus) for which previously published aerial AEP thresholds exist. Underwater thresholds were measured in an aboveground pool at frequencies between 1 and 38 kHz. The underwater audiogram was very similar to those previously published for California sea lions, suggesting that the current and previously obtained psychophysical data are representative for this species. The psychophysical and previously measured AEP audiograms were most similar in terms of high-frequency hearing limit (HFHL), although the underwater HFHL was sharper and occurred at a higher frequency. Aerial AEP methods are useful for predicting reductions in the HFHL that are potentially independent of the testing medium, such as those due to age-related sensorineural hearing loss.     

A simplified Time Reversal method used to localize vibrations sources in a complex structure

The main issue while dealing with problems due to structural vibrations is the identification of the sources that create annoyance. One of the experimental processes that permit to tackle this reverse problem uses Time Reversal method to localize the origin of the vibration detected on the surface of a structure.The Time Reversal experiment is based on a principle of time symmetry of waves propagation in a media. Using transceivers located on the structure, one can record its state of vibration. If all the signals recorded by the transceivers are reversed in time and reemitted from the position where they have been recorded, the resulting vibration will converge back to the point where it was originally emitted. In the standard approach, localization is observed both in time and space. We propose here a simplified localization process based on space localization only. We will apply this method on a complex industrial structure, stimulated with bursts. We shall show in the article the influence of certain parameters such as the number of transceivers or the structure complexity. Finally, all the tests presented hereby will allow us showing that the Time Reversal method is a very efficient and very easy to use method.