Analysis and Modeling of the Hydroisomerization Process for <Emphasis Type="Italic">n</Emphasis>-Hexane

A stage six-path mechanism for the reaction of n-hexane hydroisomerization on a BEA Pt-zeolite catalyst has been proposed. The mass flow rate of n-hexane in the feed stream varies in the range of 0.7?2.8 h^?1; the mole ratio of hydrogen to the n-hexane range of 2.7–14.6; the reactor temperature falls in the range from 453 to 573 K; and the gas flow pressure varies in the range of 1.0–10.0 atm. Thirty experiments have been carried out. In the product stream, the concentrations of n-hexane, 2-methylpentane, 3-methylpentane, 2,2-dimethylbutane, 2,3-dimethylbutane, propane, C₁-alkanes, and C₂-alkanes are analyzed by gas chromatography. A kinetic model has been constructed for the six-path mechanism of the reaction of n-hexane hydroisomerization, which contains 15 kinetic constants. Based on the results of laboratory experiments, the kinetic constants of the model have been estimated by the method of nonlinear least squares. The model has been shown to correspond with the experiment in the selected field of experimentation.     

Female Sex Pheromone in Trails of the Minute Pirate Bug, <Emphasis Type="Italic">Orius minutus</Emphasis> (L)

Orius minutus (L.) (Heteroptera: Anthocoridae) is a natural enemy of agricultural pests such as thrips, aphids, and various newly hatched insect juveniles. In this study, we conducted 1) behavioral assays for evidence of contact sex pheromone activity in trails of O. minutus, and 2) chemical analysis to identify the essential chemical components of the trails. Males showed arrestment to trails of mature virgin females but not to trails from either conspecific nymphs or immature females. Females also showed arrestment to trails from conspecific males, although the response was weaker than that exhibited by males. The activity of female trails lasted for at least 46 h after deposition. Males showed a response irrespective of mating experience. Following confirmation that a contact sex pheromone was present in the trails of female O. minutus, we used a bioassay-driven approach to isolate the active chemicals. After fractionation on silica gel, the n-hexane fraction was found to be biologically active to males. A major compound in the active fraction was (Z)-9-nonacosene; this compound was found only in trail extracts of mature virgin females. Synthetic (Z)-9-nonacosene arrested O. minutus males, indicating that it is the major active component of the contact sex pheromone in the trails of female O. minutus.     

Partition of <Emphasis Type="Italic">n</Emphasis>-Butanol Among Phases and Solubilization Ability of Winsor type III Microemulsions

The partition of n-butanol in Winsor type III (W-III) microemulsions was investigated in this work. Three kinds of anionic surfactants (sodium dodecyl sulfate (SDS), sodium dodecyl sulfonate (DSS), and sodium dodecyl benzene sulfonate (SDBS)) and two kinds of anionic/cationic surfactant mixtures (SDS/octadecyl trimethyl ammonium chloride (OTAC) mixtures and DSS/OTAC mixtures) were studied. Internal standard gas chromatography was employed in n-butanol content analysis. The results showed that no water exists in the excess oil (EO) phase and no oil exists in the excess water (EW) phase. For the W-III microemulsions obtained by salinity scanning, relatively constant n-butanol content in the EO (11–12 v%) and EW (1–4 v%) was found under different salinities. Accurate measurement of n-butanol content in each phase is important for those systems having low solubilization ability. For the W-III microemulsions prepared using SDS/OTAC surfactant mixture, the percentage of n-butanol distributed into the interfacial layer decreased while the fraction of n-butanol in the interfacial layer first increased sharply and then tended to be stable with the addition of n-butanol. For the different optimum W-III microemulsion systems tested, most of the surfactant-to-alcohol molar ratio data are near 1:3, but obvious deviation could be observed for some data. On the basis of the accurate measurement of n-butanol content in the EO and EW phases, the standard free energy, ΔG _o→in ^* (T = 298.15 K) of n-butanol transferring from the EO phase to the interfacial region was calculated. The results show negative ΔG _o→in ^* values. For microemulsions with the same components, n-butanol content is an important factor influencing the ΔG _o→in ^* value, and a high absolute value of ΔG _o→in ^* leads to high solubilization ability.     

<Emphasis Type="Italic">n</Emphasis>-Pentacosane Acts as both Contact and Volatile Pheromone in the tea Weevil, <Emphasis Type="Italic">Myllocerinus aurolineatus</Emphasis>

Insect cuticular hydrocarbons (CHCs) play important roles in chemical communication, as well as having ecological and physiological roles. The use of CHCs for mate recognition has been shown in many insect genera, but little is known about their use in the tea weevil Myllocerinus aurolineatus. Here, we provide evidence that CHCs on the surface of sexually mature M. aurolineatus females act as contact sex pheromones, facilitating mate recognition and eliciting copulatory behavior in male weevils. Using gas chromatography-mass spectrometry, we identify n-pentacosane and n-heptacosane as two potential contact pheromone components. Results from arena bioassays showed that n-pentacosane is a component of a contact pheromone of M. aurolineatus. Further results from the Y-tube olfactometer bioassays showed that n-pentacosane also acts as a volatile attractant. Our results greatly improve our understanding of the chemical ecology of M. aurolineatus.     

Optimization of controlled ring-opening polymerization of <Emphasis Type="SmallCaps">l</Emphasis>-lactide to hydroxyl terminated polylactides using zinc acetate catalyst

Hydroxyl terminated polylactide polymers with number of average molecular weights (M _n ) varying from 1625 to 3459 g mol^?1 were synthesized by ring opening bulk polymerization of lactide in the presence of zinc acetate being a potent catalyst. The use of 1,4 butanediol (BDO) initiator leads to hydroxyl terminated polylactides, thus excellent precursors for shape-memory biodegradable polyurethanes. Different reaction conditions employed for the synthesis of hydroxyl terminated polylactide polymers via activated monomer mechanism may result in differences in M _n , percentage mass conversion and percentage degree of crystallinity (%χ _c ) of the product. Influence of process parameters, i.e. catalyst concentration, initiator concentration, reaction temperature and time on characteristics of hydroxyl terminated polylactides was studied. These polymers were characterized by Nuclear Magnetic Resonance (¹H-NMR) spectroscopy, Fourier transforms infrared (FTIR) spectroscopy, gel permeation chromatography (GPC) and X-ray diffraction (XRD) techniques. FTIR and ¹H-NMR confirmed the formation of hydroxyl terminated polylactides. M _n was determined by ¹H-NMR, GPC and end group analysis. %χ _c was calculated from XRD spectra. Maximum mass conversion, M _n and %χ _c were observed at 5 mol% SnOct₂ and 5 mol% BDO concentration. At optimum temperature of 145 °C, these characteristics improved linearly with polymerization time up to 6 h and declined thereafter.     

Sexual Isolation and Cuticular Hydrocarbon Differences between <Emphasis Type="Italic">Drosophila santomea</Emphasis> and <Emphasis Type="Italic">Drosophila yakuba</Emphasis>

Drosophila santomea and Drosophila yakuba are two sister species inhabiting Saõ Tomé island. Previous studies showed that both species display strong reproductive isolation, although they can produce a few viable hybrids. Our study tried to understand the mechanism of this ethological isolation between two allopatric strains. A strong sexual isolation was confirmed, with a marked asymmetry. Comparisons of latency times to either courtship or copulation suggest that males do not discriminate females, whereas D. yakuba females, but not D. santomea females, accept their homospecifics more quickly. Cuticular hydrocarbon compositions of both species and sexes were also established with gas chromatography (GC) and GC/mass spectrometry analysis. All have (Z)-7-tricosene as their major compound. There are several quantitative differences between species for few minor compounds. The largest difference concerns n-heneicosane, which is more abundant in D. santomea than in D. yakuba flies (up to seven times more between males). A similar quantitative difference was also found in a pair of sympatric strains. Furthermore, D. yakuba males artificially perfumed with n-heneicosane were discriminated negatively by D. yakuba females, suggesting a role for this compound in the sexual isolation between these two species.     

<Emphasis Type="Italic">Tetramorium tsushimae</Emphasis> Ants Use Methyl Branched Hydrocarbons of Aphids for Partner Recognition

In mutualisms, partner discrimination is often the most important challenge for interacting organisms. The interaction between ants and aphids is a model system for studying mutualisms; ants are provided with honeydew by aphids and, in turn, the ants offer beneficial services to the aphids. To establish and maintain this system, ants must discriminate mutualistic aphid species correctly. Although recent studies have shown that ants recognize aphids as mutualistic partners based on their cuticular hydrocarbons (CHCs), it was unclear which CHCs are involved in recognition. Here, we tested whether the n-alkane or methylalkane fraction, or both, of aphid CHCs were utilized as partner recognition cues by measuring ant aggressiveness toward these fractions. When workers of Tetramorium tsushimae ants were presented with dummies coated with n-alkanes of their mutualistic aphid Aphis craccivora, ants displayed higher levels of aggression than to dummies treated with total CHCs or methyl alkanes of A. craccivora; responses to dummies treated with n-alkanes of A. craccivora were similar to those to control dummies or dummies treated with the CHCs of the non-mutualistic aphid Acyrthosiphon pisum. By contrast, ants exhibited lower aggression to dummies treated with either total CHCs or the methylalkane fraction of the mutualistic aphid than to control dummies or dummies treated with CHCs of the non-mutualistic aphid. These results suggest that T. tsushimae ants use methylalkanes of the mutualistic aphid’s CHCs to recognize partners, and that these ants do not recognize aphids as partners on the basis of n-alkanes.     

Synthesis and crystal structure of the low-temperature modification of Li<Subscript>12</Subscript>Zn<Subscript>4</Subscript>(P<Subscript>2</Subscript>O<Subscript>7</Subscript>)<Subscript>5</Subscript>

The crystal structure of a low-temperature modification of the Li₁₂Zn₄(P₂O₇)₅ compound has been determined by full-profile analysis from the X-ray powder diffraction data. The compound crystallizes in the monoclinic crystal system (a = 5.130(1) Å, b = 13.454(1) Å, c = 8.205(1) Å, β = 90.36(1)°, space group P2₁/n, Z = 4) and has a framework structure in which the zinc and lithium atoms statistically occupy equivalent positions.     

Probing the Structural,Electronic, and Magnetic Properties of Ag<Subscript><Emphasis Type="Italic">n</Emphasis></Subscript>V (<Emphasis Type="Italic">n</Emphasis> = 1–12) Clusters

The structural, electronic, and magnetic properties of Ag _n V (n?=?1–12) clusters have been studied using density functional theory and CALYPSO structure searching method. Geometry optimizations manifest that a vanadium atom in low-energy Ag_nV clusters favors the most highly coordinated location. The substitution of one V atom for an Ag atom in Ag _n?+?1 (n ≥ 5) cluster modifies the lowest energy structure of the host cluster. The infrared spectra, Raman spectra, and photoelectron spectra of Ag _n V (n?=?1–12) clusters are simulated and can be used to determine the most stable structure in the future. The relative stability, dissociation channel, and chemical activity of the ground states are analyzed through atomic averaged binding energy, dissociation energy, and energy gap. It is found that V atom can improve the stability of the host cluster, Ag₂ excepted. The most possible dissociation channels are Ag _n V?=?Ag?+?Ag _n???1V for n?=?1 and 4–12 and Ag _n V?=?Ag₂?+?Ag _n???2V for n?=?2 and 3. The energy gap of Ag _n V cluster with odd n is much smaller than that of Ag _n?+?1 cluster. Analyses of magnetic property indicate that the total magnetic moment of Ag _n V cluster mostly comes from V atom and varies from 1 to 5 μ _B. The charge transfer between V and Ag atoms should be responsible for the change of magnetic moment.     

One Pot Synthesis and Properties of Cationic Surfactants: <Emphasis Type="Italic">n</Emphasis>-Alkyl-3-Methylpyridinium Bromide

Three new amphiphilic compounds i.e., n-decyl-3-methylpyridinium bromide (a), n-dodecyl-3-methylpyridinium bromide (b), and n-tetradecyl-3-methylpyridinium bromide (c), have been synthesized by condensation reaction and characterized by NMR (¹H, ¹³C) and FTIR spectroscopic techniques. The micellization behavior of the compounds has been studied in ethanol employing conductometry and UV/visible spectroscopy. The critical micellization concentration (CMC) values for compound a, b and c was found to be 0.31, 0.29 and 0.27 m mol L^?1, respectively. Effect of temperature on the CMC was checked in the range of 298-318 K. The thermodynamic parameters such as ΔG, ΔH and ΔS of the micellization process of these surfactants were computed. The negative values of ΔG and positive values of ΔH indicated the spontaneous and endothermic nature of the micellization process. Antimicrobial activities of these amphiphiles showed significant activity against different bacterial strains.     

A Comprehensive Study on the Synthesis and Micellization of Disymmetric Gemini Imidazolium Surfactants

Two groups of disymmetric Gemini imidazolium surfactants, [C₁₄C₄C _m im]Br₂ (m = 10, 12, 14) and [C _m C₄C _n im]Br₂ (m + n = 24, m = 12, 14, 16, 18) surfactants, were synthesized and their structures were confirmed by ¹H NMR and ESI–MS spectroscopy. Their adsorption at the air/water interface, thermodynamic parameters and aggregation behavior were explored by means of surface tension, electrical conductivity and steady-state fluorescence. A series of surface activity parameters, including cmc, γ _cmc, π _cmc, pC ₂₀, cmc/C ₂₀, Γ _max and A _min, were obtained from surface tension measurements. The results revealed that the overall hydrophobic chain length (N _c) for [C₁₄C₄C _m im]Br₂ and the disymmetry (m/n) for [C _m C₄C _n im]Br₂ had a significant effect on the surface activity. The cmc values decreased with an increase of N _c or m/n. The thermodynamic parameters of micellization (ΔG _m ^θ , ΔH _m ^θ , ΔS _m ^θ ) derived from the electrical conductivity indicated that the micellization process of [C₁₄C₄C _m im]Br₂ and [C _m C₄C _n im]Br₂ was entropy-driven at different temperatures, but the contribution of ΔH _m ^θ to ΔG _m ^θ was enhanced by increasing N _c or m/n. The micropolarity and micellar aggregation number (N _agg) were estimated by steady-state fluorescence measurements. The results showed that the surfactant with higher N _c or m/n can form larger micelles, due to a tighter micellar structure.     

Unsaturated Cuticular Hydrocarbons Enhance Responses to Sex Pheromone in Spruce Budworm, <Emphasis Type="Italic">Choristoneura fumiferana</Emphasis>

The primary sex pheromone components of the female spruce budworm, Choristoneura fumiferana (Clem.) (Lepidoptera: Tortricidae), are (E)- and (Z)-11-tetradecenal, produced in 95:5 ratio. However, male flight responses to calling females in a wind tunnel were faster and maintained longer than responses to any synthetic aldehyde blend. Analyses of cuticular extracts from spruce budworm adults revealed series of n-alkanes and n-monoalkenes with predominantly odd numbers of carbon atoms from C₂₃- C₂₉ in both sexes. (Z,Z,Z)-3,6,9-tricosatriene and (Z,Z,Z)-3,6,9-pentacosatriene were identified only in cuticular extracts from females. Pheromonally naïve males showed wing fanning and circling responses to forewing scales from females but not to scales from males. Males also exhibited the same strong responses to scales excised from pharate females, indicating that the pheromone components are produced by females prior to emergence. (Z)-11-hexadecenal and (Z)-5-tricosene enhanced male responses to the primary sex pheromone aldehydes in wind tunnel bioassays, including higher proportions of in-flight and copulatory responses by males and increased time on the source. Addition of (Z,Z,Z)-3,6,9-tricosatriene to the 95/5 blend of (E)- and (Z)-11-tetradecenal released close-range copulatory responses including abdomen curling on treated septa. We propose that the sex pheromone blend of C. fumiferana is composed of the 95/5 blend of (E)- and (Z)-11-tetradecenal as primary components, with (Z)-11-hexadecenal, (Z)-5-tricosene and (Z,Z,Z)-3,6,9-tricosatriene fulfilling secondary roles in orientation and close-range courtship.     

Optimization of biodiesel production process in a continuous microchannel using response surface methodology

We assessed the biodiesel production process in a continuous microchannel through preparation of a heterogeneous catalyst (CaO/MgO) from demineralized water plant sediment. This mixed oxide catalyst was used for transesterification of rapeseed oil as feedstock by methanol to produce biodiesel fuel at various conditions. A microchannel, utilized as a novel reactor, was applied to convert rapeseed oil into biodiesel in multiple steps. The effects of the process variables, such as catalyst concentration, methanol to oil volume ratio, n-hexane to oil volume ratio, and reaction temperature on the purity of biodiesel, were carefully investigated. Box-Behnken experimental design was employed to obtain the maximum purity of biodiesel response surface methodology. The optimum condition for the production of biodiesel was the following: catalyst concentration of 7.875 wt%, methanol to oil volume ratio of 1.75: 3, n-hexane to oil volume ratio of 0.575: 1, and reaction temperature of 70 °C.     

Effect of the 3<Subscript>d</Subscript>-Transition Metal Oxides on the Surface Tension of the Sodium Silicate Melt

The effect of 3d-transition metal oxides on the surface tension of the 17.5Na₂O · 82.5SiO₂ · nRO (R = Mn, Fe, Co, Ni, Cu; n = 0.1–10) melt is revealed in the temperature range 1250–1450°C. It is found that cobalt oxide in the range of low concentrations (0.1–1.0 mol %) is characterized by anomalously low values of the surface tension. In the case of CoO oxide, the surface tension increases as the temperature increases and the melts containing MnO, FeO, NiO, and CuO oxides have negative temperature coefficients. In the range of high concentrations of the studied oxides (n = 10 mol %), the surface tension of melts decreases with an increase in the atomic number of cation in the sequence Mn → Fe → Co → Ni → Cu.     

Attractiveness of Host Plant Volatile Extracts to the Asian Citrus Psyllid, <Emphasis Type="Italic">Diaphorina citri,</Emphasis> is Reduced by Terpenoids from the Non-Host Cashew

Diaphorina citri is a vector of the bacterial causative agent of Huanglongbing (HLB?=?Citrus greening), a severe disease affecting citrus crops. As there is no known control for HLB, manipulating insect behaviour through deployment of semiochemicals offers a promising opportunity for protecting citrus crops. The behavioural responses of D. citri to plant volatiles, and the identity of these plant volatiles were investigated. Volatiles were collected from host plants Murraya paniculata, Citrus sinensis, C. reshni, C. limettioides, Poncirus trifoliata, and from non-host plants Psidium guajava, Mangifera indica, Anacardium occidentale. In behavioural assays, female D. citri spent more time in the arms containing volatiles from either M. paniculata or C. sinensis compared to the control arms. When D. citri was exposed to volatiles collected from A. occidentale, they preferred the control arm. Volatiles emitted from the other studied plants did not influence the foraging behaviour of D. citri. Chemical analyses of volatile extracts from C. sinensis, M. paniculata, and A. occidentale revealed the presence of the terpenoids (E)-4,8-dimethylnona-1,3,7–triene (DMNT) and (E,E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene (TMTT) in higher amounts in A. occidentale. In further behavioural bioassays, female D. citri spent less time in arms containing a synthetic blend of DMNT and TMTT compared to the control arms. Female D. citri also spent less time in arms containing the synthetic blend in combination with volatile extracts from either M. paniculata or C. sinensis compared to the control arms. Results suggest that higher release of the two terpenoids by A. occidentale make this species unattractive to D. citri, and that the terpenoids could be used in reducing colonisation of citrus plants and therefore HLB infection.     

Structure of an <Emphasis Type="Italic">n</Emphasis>-heptane/toluene flame: Molecular beam mass spectrometry and computer simulation investigations

Molecular beam mass spectrometry was used to measure mole fraction profiles of the reactants, major reaction products and intermediates, including precursors of polycyclic aromatic hydrocarbons, in a premixed fuel-rich (equivalence ratio of 1.75) n-heptane/toluene/O₂/Ar flame stabilized on a flat burner at atmospheric pressure. The ratio of the liquid volumes in the n-heptane/toluene mixture was 7: 3. The chemical structure of the flame was modeled using a detailed mechanism of chemical reactions tested against experimental data of other authors on n-heptane/toluene flames and comprising the reactions of formation of polycyclic aromatic hydrocarbons. The mechanism was extended with cross-reactions involving derivatives of n-heptane and toluene. Overall, the new experimental data are in satisfactory agreement with the numerical simulation results; however, there are differences between the measured and calculated mole fraction profiles of some species. Analysis shows that in the n-heptane/toluene flame, the main reactions leading to the formation of low-aromatic compounds (benzene and phenyl) are reactions typical of the pure toluene flame.     

Parameters of luminescence and the local structure of Eu<Superscript>3+</Superscript> centers in fluorogermanate glasses

The influence of the chemical nature of the local environment of Eu³⁺ ions on the parameters of luminescence of these centers in glasses of the (BaGeO₃)_{1 ? x ? y} (Al₂O₃) _x (0.45CaF₂ · 0.55MgF₂) _y (x = 0.25, y = 0; x = 0.17, y = 0.17; x = 0.15, y = 0.22; x = 0.07, y = 37.00; x = 0, y = 0.45) system is investigated. The oxidation state of europium atoms and the degree of homogeneity of their local environment in the glasses are determined using ¹⁵¹Eu Mössbauer spectroscopy.     

Density and microhardness of glasses in the SrO-B<Subscript>2</Subscript>O<Subscript>3</Subscript>-SiO<Subscript>2</Subscript> system

The density d at a temperature of 25°C is measured by the hydrostatic weighing method, the Vickers microhardness H _V is determined, and the fluctuation free volume fraction f _g is calculated for glasses in the SrO-B₂O₃-SiO₂ system with a constant strontium oxide content in the range from 35 to 45 mol %. It is demonstrated that the quantities H _V and f _g decrease and the density d increases with an increase in the SrO content.     

Effect of the zeolite modulus of Pt/MOR/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> catalysts on the <Emphasis Type="Italic">n</Emphasis>-heptane isomerization reaction

The effect of the mordenite acidic modulus (SiO₂/Al₂O₃, 20 and 30) of Pt/MOR/Al2O3 catalysts on the heptane isomerization reaction is investigated. The content of zeolite in the catalysts is varied from 10 to 50 wt %, with platinum applied to the samples from solutions of different precursors: H₂PtCl₆ and [Pt(NH₃)₄]Cl₂. It is established via the TPD of ammonia and FTIR spectroscopy (the adsorption of NH₃ and СО) that the total acidity of zeolite falls as the modulus grows: the number of Brønsted (BAC) and Lewis (LAC) acidic sites is reduced, accompanied by an increase in the strength of their acidity. The catalysts are tested in the n-heptane isomerization reaction. It is shown that the selectivity of n-heptane isomerization falls substantially when the acidic mordenite modulus is increased from 20 to 30.     

Role of Plant Volatiles in Host Plant Recognition by <Emphasis Type="Italic">Listronotus maculicollis</Emphasis> (Coleoptera: Curculionidae)

The annual bluegrass weevil (ABW), Listronotus maculicollis Kirby, is an economically important pest of short cut turfgrass. Annual bluegrass, Poa annua L., is the most preferred and suitable host for ABW oviposition, larval survival and development. We investigated the involvement of grass volatiles in ABW host plant preference under laboratory and field conditions. First, ovipositional and feeding preferences of ABW adults were studied in a sensory deprivation experiment. Clear evidence of involvement of olfaction in host recognition by ABW was demonstrated. Poa annua was preferred for oviposition over three bentgrasses, Agrostis spp., but weevils with blocked antennae did not exhibit significant preferences. ABW behavioral responses to volatiles emitted by Agrostis spp. and P. annua were examined in Y-tube olfactometer assays. Poa annua was attractive to ABW females and preferred to Agrostis spp. cultivars in Y-tube assays. Headspace volatiles emitted by P. annua and four cultivars of Agrostis stolonifera L. and two each of A. capillaris L. and A. canina L. were extracted, identified and compared. No P. annua specific volatiles were found, but Agrostis spp. tended to have larger quantities of terpenoids than P. annua. (Z)-3-hexenyl acetate, phenyl ethyl alcohol and their combination were the most attractive compounds to ABW females in laboratory Y-tube assays. The combination of these compounds as a trap bait in field experiments attracted adults during the spring migration, but was ineffective once the adults were on the short-mown turfgrass. Hence, their usefulness for monitoring weevil populations needs further investigation.