An Empirical Approach to Spanish Anaphora Resolution

This paper documents the development of an empirically-basedsystem implemented in Prolog that automatically resolves severalkinds of anaphora in Spanish texts. These are pronominalreferences, surface-count anaphora, one-anaphora and ellipticalzero-subject constructions (i.e., sentences that omit theirpronominal subject). The resolution is based onrepresentations resulting from either partial or full parsing. Thesystem developed can also work on the output of a POStagger or with different dictionaries, without changing thegrammar. This grammar represents the syntactic information of eachlanguage by means of the Slot Unification Grammar formalism. The different kinds of information used for anaphora resolution in full and partial parsing are shown, as wellas evaluation results. The system has been adapted toEnglish texts, obtaining encouraging results that prove that itcan be applied with only a very few refinements to other languagesas well as Spanish and English. In addition, the differencesbetween English and Spanish anaphora are noted.     

The effect of ethanol on carbon-catalysed decomposition of methane

Because of its ecological character, the reaction of catalytic decomposition of methane (CDM) is expected to be an important future method of hydrogen generation. However, the main drawback of this technology is a relatively fast deactivation of the catalyst used, as a consequence of its pores blocking by the low-active methane-originated carbon deposit. This paper reports on an attempt of restricting the catalyst deactivation by introducing into the reaction system ethyl alcohol capable of forming in situ a potentially active in this reaction carbonaceous deposit. The catalyst used was activated carbon obtained from the waste material (hazelnut shells). The reactions of methane and ethanol decomposition were performed by the alternate method (for certain time methane was introduced into the reactor, and then it was replaced by ethanol). Three temperatures of the reactions were applied (750, 850 or 950 °C) and another variable was the duration of the ethanol decomposition. As follows from the results, an addition of ethanol has diverse effect on the catalytic activity of activated carbon and the amount of hydrogen formed depends on the temperatures of methane and ethanol decompositions and on the time of the reagent dosing.     

Ethanol reforming over Ni/CeGd catalysts with low Ni content

The catalytic performance of Ni/CeGd SOFC anodes with low Ni content (18%wt) prepared by a hydrothermal method for ethanol conversion reactions was evaluated. Calcination temperature and reaction conditions significantly affected the activity and stability of the samples. Increasing calcination temperature decreased ethanol conversion. This was likely due to the larger CeGd crystallite size. All samples deactivated during reaction under pure ethanol at 773 K. The addition of water or oxygen to the feed and the increase of reaction temperature improved catalyst stability. Scanning electron microscopy and thermogravimetric analysis showed that the deactivation was due to carbon formation. In the presence of oxygen or water, the mechanism of carbon removal was favored. Moreover, carbon formation was not favored at high reaction temperature due to the reverse of the Boudouard reaction as well as the promoting effect of the support on the carbon gasification reaction.     

Facile synthesis of budding yeast a-factor and its use to synchronize cells of α mating type

The ease with which populations of the budding yeast Saccharomyces cerevisiae can be synchronized using the mating pheromone α-factor has been invaluable for studies of the cell cycle. The α-factor response pathway has also remained an important model to study the molecular mechanism of G-protein coupled receptor signalling. α-Factor is a 13 amino acids long peptide that is readily available by automated peptide synthesis. However, only cells of the a mating type respond to α-factor. Cells of the opposite α mating type respond to a-factor, a farnesylated and C-terminally methylated 12 amino acids peptide. Because of its more difficult chemical synthesis, a-factor is not readily available and consequently the a-factor response is less well understood. Here we describe an improved strategy for producing a-factor, based on solid-phase peptide synthesis, followed by two simple steps in solution that show favourable characteristics and good yield. We demonstrate the successful use of the resulting a-factor to synchronize cell cycle progression of α cells. Notably, the a-factor concentrations required for cell synchronization are an order of magnitude lower than typically used α-factor concentrations. Despite a similar cell cycle response, shmoo formation was less pronounced compared to α-factor-treated a cells. Our protocol makes a-factor widely accessible, extending the ease of cell cycle synchronization to budding yeast cells of both mating types and facilitating the study of a-factor signalling.     

Relay Catalysis: Enantioselective Synthesis of Cyclic Benzo‐Fused Homoallylic Alcohols by Chiral Brønsted Acid‐Catalyzed Allylboration/Ring Closing Metathesis

Six‐ and seven‐membered benzo‐fused cyclic homoallylic alcohols can be readily synthesized by a tandem chiral Brønsted acid‐catalyzed allyl (crotyl)boration/ring closing metathesis sequence performed under orthogonal relay catalysis conditions. Excellent enantio‐ and diastereoselectivities are obtained in most of the cases. In addition, the parent crotylboration/RCM process is also described. The required substrates, ortho‐vinylbenzaldehydes, are readily available in one step from commercially available starting materials. Both catalysts and reactants are also available from commercial suppliers. The reaction shows broad functional group compatibility and is also suitable for heteroaromatic substrates. Substitution at any position of the aromatic ring is tolerated; however, substitution at position 6 results in a substantial drop in enantioselectivity.     

Chemical Processes During Energy‐Saving Preparation of Lightweight Ceramics

Lightweight glass‐ceramic material similar to foam glass was obtained at 700°C–800°C directly from alkali‐activated silica clay and zeolitized tuff without preliminary glass preparation. It was characterized by low bulk density of 100–250 kg/m³ and high pore size homogeneity. Chemical processes occurring in alkali‐activated silica clay and zeolitized tuff were studied using X‐ray diffraction, thermal gravimetry, IR‐spectroscopy, and scanning electron microscopy. Pore formation in both compositions is caused by dehydration of hydrated sodium polysilicates (Na₂O·mSiO₂·nH₂O), formed during alkali activation. Additional pore‐forming gas source in alkali‐activated zeolitized tuff is trona, Na₃(CO₃)(HCO₃)·2H₂O, formed during interaction between unbound NaOH and CO₂ and H₂O from air. Influence of mechanical activation of raw materials on chemical processes occurring in alkaline compositions was also studied.     

Silicon‐containing heterocyclic polymers and thin films made therefrom

Thin films, in the range of tens of micrometers thickness, have been prepared by casting onto glass plates the chloroform or N‐methylpyrrolidone solutions of polyimides or poly(imide‐amide)s containing silicon and phenylquinoxaline units in the main chain. The polymers have been synthesized by solution polycondensation reaction of aromatic diamines having preformed phenylquinoxaline rings with bis(3,4‐dicarboxyphenyl)dimethylsilane dianhydride or with a diacid chloride resulting from the reaction of this dianhydride with p‐aminobenzoic acid. The polymers were easily soluble in polar aprotic solvents and showed high thermal stability. The free‐standing films exhibited good mechanical properties with tensile strengths in the range of 48–86 MPa, tensile modulus in the range of 1.25–2.22 GPa and elongation at break in the range of 3–37%. Electrical insulating properties of some polymer films were evaluated on the basis of dielectric constant and dielectric loss and their variation with frequency and temperature. The values of the dielectric constant at 10 kHz were in the range of 2.94–3.08 for polyimides and 3.89–4.49 for poly(imide‐amide)s. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3062–3068, 2006     

Sewage sludge digestion at increased micropollutant content

Research was conducted, which aim was to evaluate quantitative and qualitative PCB changes in sewage sludge during mesophilic digestion, and the influence of those compound concentration above acceptable level (1.9 mg kg⁻¹ of sludge dry matter), also nickel and cadmium ions, on mesophilic digestion process. Before and after the digestion, concentration of seven PCB congeners, Ni and Cd in particular chemical fractions of the sludge was analyzed.     

Structural and photoresponsive behavior of a series of (phenylene)azobenzene‐containing liquid‐crystalline methacrylic copolymers

A series of side‐chain liquid‐crystalline methacrylic copolymers, having various amounts of 4′‐(4‐decyloxyphenyl)‐4‐(hexyloxy)‐azobenzene as the mesogenic group, were synthesized and characterized by differential scanning calorimetry, polarizing optical microscopy and X‐ray diffraction to determine their mesomorphic properties, and by UV?visible spectrometry to elucidate their optical absorption characteristics. Also, birefringence and surface relief gratings were photoinduced in the films using a laser beam of 413 nm. Copolymers with high mesogen contents display a polymorphic behavior of the smectic type. The smectic order tends to disappear as the content of mesogens in the copolymer decreases, going from extended lamellar domains of chromophores packed in a parallel position, typical for smectic liquid crystals, to small aggregates of chromophores dispersed in an amorphous matrix. Important hypsochromic shifts (Δλ_max ≈ 20 nm), associated with π interactions between neighboring aromatic groups, confirm the aggregation of chromophores in lamellar structures. The light‐induced birefringence (0.005 ? 0.06) is not as high as expected but it corroborates that there exists a tight interplay between photoinduced orientation and intrinsic molecular order. Surface relief gratings were recorded in copolymers with low mesogen content (15 ? 30 mol%), showing by atomic force microscopy sinusoidal profiles with an average depth of around 150 nm. © 2013 Society of Chemical Industry