Facile and not facile reactions for the production of maleic and phthalic anhydrides with vanadium mixed oxides based catalysts

Vanadium is a key element in the formulation of catalysts for the production of anhydrides by selective vapor oxidation with molecular oxygen. A study of the oxidations ofo-xylene,n-butane and benzene on V-P, V-Mo and V-Ti mixed oxides, the commercial catalysts for the synthesis of anhydrides, was carried out. The oxidation ofo-xylene on the three catalysts was the most facile reaction leading to high yields in phthalic anhydride; on the contrary in the oxidation ofn-butane only V-P mixed oxide was active and selective. V-P mixed oxide is active and selective in the oxidation of all the feedstocks and can be identified as the most polyfunctional catalyst. V-Mo is active and selective in botho-xylene and benzene oxidation and V-Ti only ino-xylene oxidation. Moreover the lesser selectivity in phthalic anhydride observed with V-P and V-Mo mixed oxides has been attributed to parallel oxidation reactions to the formation of phthalic anhydride, evidenced by a higher amount of phthalide.     

Computer tracking as a behavioral GC detector: Nematode responses to vapor of host roots

A computer tracking system previously developed for studying the behavioral responses of nematodes to volatile stimuli was modified so that the effluent of a gas chromatograph passed over the nematodes while their behavior was analyzed. Since the behavior of several hundred nematodes can be analyzed simultaneously, this technique has the potential to provide a sensitive assay for behaviorally active fractions from the GC. This potential was tested with infective juveniles of the root-knot nematodeMeloidogyne incognita and vapor from the roots of host tomato plants. Direct injection of 1 ml of vapor led to reproducible responses at times corresponding to nitrogen plus oxygen elution and to carbon dioxide elution. Experiments with pure gases demonstrated responses to oxygen and to carbon dioxide. Attempts were made to find less volatile and less active components by pulling large volumes of vapor through a trap of Tenax GC and subsequently eluting them onto the GC. This approach did not lead to the detection of other activities. We conclude that, other than carbon dioxide, there are no volatile stimuli released from host roots in effective quantities.     

Influence of calcination procedure on the catalytic property of sulfated zirconia

Calcination parameters, such as atmosphere, duration and catalyst bed depth have a marked influence on the catalytic and spectroscopic properties of sulfated zirconia. Sulfated zirconia calcined in nitrogen or synthetic airflow, in deep bed, exhibited comparable activity in n-butane isomerization at 373 K, which suggests that oxygen is not necessary for formation of active sites. Catalysts calcined in shallow bed are catalytically inactive. Thus, the bed depth is concluded to be crucial for the formation of active sites. The samples calcined in shallow bed possessed lower sulfate content and the S=O stretching vibration was located at lower frequency. Calcination in the presence of water vapor also led to lower catalytic activity, sulfate content, and BET area. Extended calcination reduced gradually the activity and the sulfate content, which underlines the labile property of the active sites. A new interpretation of the function of the calcination step is proposed and compared with models described in the literature.     

On the Substrate Binding of Linoleate 9-Lipoxygenases

Lipoxygenases (LOX; linoleate:oxygen oxidoreductase EC 1.13.11.12) consist of a class of enzymes that catalyze the regio- and stereo specific dioxygenation of polyunsaturated fatty acids. Here we characterize two proteins that belong to the less studied class of 9-LOXs, Solanum tuberosum StLOX1 and Arabidopsis thaliana AtLOX1. The proteins were recombinantly expressed in E. coli and the product specificity of the enzymes was tested against different fatty acid substrates. Both enzymes showed high specificity against all tested C18 fatty acids and produced (9S)-hydroperoxides. However, incubation of the C20 fatty acid arachidonic acid with AtLOX1 gave a mixture of racemic hydroperoxides. On the other hand, with StLOX1 we observed the formation of a mixture of products among which the (5S)-hydroperoxy eicosatetraenoic acid (5S-H(P)ETE) was the most abundant. Esterified fatty acids were no substrates. We used site directed mutagenesis to modify a conserved valine residue in the active site of StLOX1 and examine the importance of space within the active site, which has been shown to play a role in determining the positional specificity. The Val576Phe mutant still catalyzed the formation of (9S)-hydroperoxides with C18 fatty acids, while it exhibited altered specificity against arachidonic acid and produced mainly (11S)-H(P)ETE. These data confirm the model that in case of linoleate 9-LOX binding of the substrate takes place with the carboxyl-group first. Sequence data: The nucleotide sequences reported in this paper are annotated in the GenBank/EMBL data bank under the accession numbers Q06327 and S73865.     

Catalytic Properties of Ag/Al2O3 Catalysts for Lean NOx Reduction Processes and Characterisation of Active Silver Species

A study of the lean NO _x reduction activity employing different reductants over Ag/Al₂O₃ samples prepared from reverse microemulsions or impregnation with EDTA-complexes is presented. A multitechnique approach is employed for characterisation of the samples and/or processes taking place in the course of the NO _x -SCR reaction with propene and propane. Results by in situ-DRIFTS reveal that, for the propene reductant, silver provides a new path for hydrocarbon activation involving generation of adsorbed acrylate species as a partially oxidised active intermediate, in line with previous proposals for other non-noble metal systems. It is shown, mainly on the basis of XAFS studies, that active silver species are related to well dispersed silver aluminate-like phases with tetrahedral local symmetry and a relatively high disorder in the oxygen first shell.     

Neural networks modeling signal responses and taxol production of cultured Taxus chinensis cells induced by bio-elicitor

Quantitatively describing the signal transduction process is important for understanding the mechanism of signal regulation in cells, and thus, poses both a challenge and an opportunity for chemical and biochemical engineers. An artificial neural network (ANN), in which we took the signal molecules as neural nodes, was constructed to simulate the generation of active oxygen species (AOS) in Taxus chinensis cells induced by a bio-elicitor. The relative contents of AOS in cells predicted by the ANN model agreed well with the experimental data and three notable stages of AOS increase were observed from the 3D figure of AOS generation. The robustness of AOS trajectories indicated that signal regulation in vivo was an integral feedback control model that ensured the adaptation of Taxus chinensis to environmental stress. The artificial neural network was able to predict taxol production as well as determine the optimal concentration of oligosaccharides needed for it.     

Comparative Metabolism of Dietary Terpene, p-Cymene, in Generalist and Specialist Folivorous Marsupials

The urinary metabolites of the monoterpene, p-cymene, were studied in three marsupial species: a generalist herbivore, the brushtail possum (Trichosurus vulpecula), and two specialist folivores, the greater glider (Petauroides volans) and the ringtail possum (Pseudocheirus peregrinus), as well as in the laboratory rat (Rattus norvegicus). Each animal was dosed, intragastrically, with single doses of p-cymene (0.37 mmol/kg and/or 1.49 mmol/kg). Urine and feces were collected for two 24-hr periods. Quantitative analysis of urinary metabolites by extraction, gas chromatography, and mass spectrometry gave a mean recovery of 64% (range 52–74%) of the administered dose in 48 hr for the four species. No fecal metabolites were found. A species-specific pattern of metabolite excretion was evident and reflected the natural occurrence of p-cymene (and terpenes in general) in the diet. If the metabolites excreted are grouped according to the total number of oxygen atoms added (one to four), then the rat excreted metabolites encompassing all degrees of oxidation, but predominantly a monooxygenated metabolite. The brushtail possum excreted metabolites having two, three, and four oxygen atoms added. The ringtail possum and greater glider only excreted metabolites with three or four oxygen atoms. Conjugation played a significant role in the excretion of oxidized metabolites in only the brushtail possums and the rat. These findings indicate that species encountering terpenes, such as p-cymene, in their normal diet have developed efficient oxidation pathways to eliminate them. This oxidative efficiency could also reduce the necessity for subsequent conjugation of metabolites which minimizes further demands on a nutritionally limited diet.     

Structure-activity relationships among maytansinoids in their effect on the European corn borer,Ostrinia nubilalis (Hübner)

Five maytansinoids fromMaytenus (Celastraceae) andPutterlickia (Rhamnaceae) species were tested for biological activity against the European corn borerOstrinia nubilalis. Maytanbutine, maytansine, and maytanvaline, all of which contain an amino acid residue at C-3, were active and comparable in their effect on larvae to trewiasine, a known active, amino acid-containing maytansinoid fromTrewia nudiflora. Maytanacine, which has an acetate group at C-3, was not as active as maytansine, maytanvaline, maytanbutine, or trewiasine, but significantly retarded the development of the larvae. Normaysine, which has no oxygen substituent at C-3, had no significant effect on mortality and only moderate effect on development of the larvae. The presence of the amino acid moiety at C-3 appears to be an important factor for the biological activity of maytansinoids.Lepidoptera: Pyralidae.The mention of firm names or trade products does not imply that they are endorsed or recommended by the U.S. Department of Agriculture over other firms or similar products not mentioned.     

Aggregation pheromones of the flat grain beetle,Cryptolestes pusillus (Coleoptera: Cucujidae)

Aggregation pheromones were isolated fromCryptolestes pusillus (Schönherr), a coleopteran pest of stored products. Porapak Q-captured beetle and frass volatiles were fractionated by preparative gas-liquid chromatography. The fractions were bioassayed with an arena olfactometer and/or with a two-choice, pitfall olfactometer. Three biologically active, male-produced compounds eliciting aggregation behavior from adultC. pusillus were isolated and identified by spectroscopic methods as (Z)-3-dodecenolide (I), (Z)-5-tetradecen-13-olide (II), and (Z,Z)-3,6-dodecadienolide (III). Compound I was the major volatile produced and was active alone. Compound II was not active alone, but synergized the response to I. Compound III was active alone at higher concentrations, but did not significantly increase the response when added to the most active mixture of I and II, and so it is probably not part of the aggregation pheromone. Pheromone production increased dramatically when the insects were aerated on a food source.Research supported in part by the Natural Sciences and Engineering Research Council of Canada, Operating Grants A3881 and A3785, Strategic Grant 60958, and a Graduate Scholarship to J. G. Millar.     

Vermiculites intercalated with Al2O3 pillars and modified with transition metals as catalysts of DeNOx process

Vermiculites intercalated with alumina pillars and modified with transition metals (Cu, Fe) were studied as catalysts of selective reduction of NO with ammonia. Prior to the pillaring process, a raw vermiculite was treated with a solution of nitric acid and then citric or oxalic acid in order to reduce the overall charge of layers. This modification was necessary for a successful pillaring of the clay. Transition metals (Fe, Cu) were deposited on the surface of the modified vermiculites by an ion-exchange method. The obtained samples were characterized with respect to composition (EPMA), structure (XRD), texture (BET) and chemical nature of deposited transition metal species (UV–vis–DRS). The vermiculite based materials have been found to be active and selective catalysts of the DeNOx process. The Cu-containing samples were catalytically active at lower temperatures than the pillared clays modified with iron. A side reaction of ammonia oxidation by oxygen decreased the effectiveness of the DeNOx process in the high temperature range.     

Attractancy and species specificity of 6-acetoxy-5-hexadecanolide,a mosquito oviposition attractant pheromone

Four stereoisomers of 6-acetoxy-5-hexadecanolide, a mosquito oviposition attractant pheromone, were bioassayed for their activity on mosquitoes. Only (–)-(5R,6S) isomer was active in attractingCulex quinquefasciatus Say females for oviposition at dosages of 0.5 g/100 ml water and above with the floating-cap method. The activity of this isomer increased 50-fold when it was applied directly to the water surface. The other three isomers, (+)-(5S,6R), (+)-(5R,6R), and (–)-(5s, 6s), were not active. The active isomer was ovipositionally attractive not only toC. quinquefasciatus but also toC. tarsalis Coquillett; however, it was 100 times more active in the former than in the latter species.Aedes aegypti (L.) andAnopheles quadrimaculatus Say were not attracted to the pheromone, thus suggesting that the pheromone is genus-specific.     

Investigation of Ammonia Oxidation over Copper with In Situ NEXAFS in the Soft X-Ray Range: Influence of Pressure on the Catalyst Performance

The oxidation of ammonia over polycrystalline copper was investigated by means of in situ NEXAFS (near-edge X-ray absorption fine structure) spectroscopy in the soft X-ray range. The reaction, carried out in a 1:12 excess of oxygen, was observed by mass spectrometry. The simultaneous detection of the surface electronic structure and its catalytic performance allows correlation of different reaction products to the current surface structure of the catalyst. It is shown that a change in total pressure from 0.4 to 1.2 mbar severely affects the reaction path. Copper(I) nitride was identified as poison and a copper oxide was found to be the active phase for the selective oxidation of ammonia to nitrogen.     

Mechanistic Study of Selective Oxidation of Dimethyl Ether to Formaldehyde over Alumina-supported Molybdenum Oxide Catalyst

XPS and IR spectroscopies were used to investigate the surface intermediates of dimethyl ether (DME) oxidation to formaldehyde over MoOx/Al₂O₃ catalyst. The reaction performances were tested by employing three typical reaction conditions, depending on the O₂/DME ratio and the reaction temperature. When there was sufficient oxygen present in the reaction media, a terminal or bridged CH₃O* species formed by DME dissociation was highly active and rapidly reacted with lattice oxygen to produce formaldehyde, leading to higher selectivity of HCHO. When oxygen was consumed completely or only DME was present in the reaction media, CH₃O species bonded to more than two Mo atoms (μ-OCH₃) and CH_x (x=1–3) species attached to the Mo atoms were observed and the relative ratio of (μ-OCH₃) /Mo–CH_x was significantly dependent on the reduction degree of MoO_x domains. The (μCH₃O) species was related to the formation of CH₃OH or CO_x, and the Mo–CH_x species led to the formation of CH₄.     

Laboratory and field tests with the synthetic sex pheromone of threeMatsucoccus 1 pine bast scales

Matsunone, (2E,4E)-4.6,10,12-tetramethyl-2,4-tridecadien-7-one, is the primary sex pheromone ofMatsucoccus resinosae, M. thunbergianae, andM. matsumurae. The synthetic compound was tested in the laboratory and in field tests with all three species, and significantly more males responded to synthetic matsuone than to controls. The attraction of synthetic matsuone to males in field tests was not significantly different from that of virgin females at the same matsuone release rate. An analog of matsuone previously shown to be biologically active was also tested in the laboratory withM. resinosae andM. thunbergianae, and field tested withM. resinosae. The active analog required a dose approximately 100 times greater than matsuone to yield maximum laboratory bioassay response, and in field tests, attraction was not significantly different from controls at doses at which matsuone was significantly attractive.Homoptera: Coccoidea: Margarodidae.Deceased.     

Inhibition of growth ofPhytophthora parasitica var.nicotianae by aromatic acids and coumarins in a laboratory bioassay

Hydroxy-, dihydroxy-, trihydroxy-, methoxy-, dimethoxy-, hydroxy-+methoxy-, amino-, chloro-, and nitro-substituted benzoic, phenylacetic, phenylpropanoic, and phenylpropenoic (cinnamic) acids were evaluated for activity against the growth ofPhytophthora parasitica var.Nicotianae, Races 0 and 1, in a laboratory bioassay. Several substituted coumarins were also tested. In general, for Race 0, the phenylpropenoic acids were more active (on a millimolar basis), than the corresponding benzoic, phenylacetic, or phenylpropionic acids (9 of 14 series). Among the most active acids wereo-hydroxycinnamic and the chloro- and methoxycinnamic acids. The activities of unsubstituted benzoic and phenylpropionic acids were comparable to the most active compounds tested. Monohydroxyaromatic acids were more active than most dihydroxy acids of the same chain length. Dihydro-3,4-dihydroxycinnamic acid was slightly more active than the corresponding cinnamic acid, while the reverse was true for the mono-p-hydroxycinnamic acid versusp-hydroxyphenylpropionic acid. Coumarin was more active than its hydroxy, methyl, hydroxymethyl, or methoxy derivatives. In general, Race 1 was even more significantly affected by the aromatic acids. Glycosylated coumarins were inactive in the bioassay, compared to their aglycones.     

Cu,Co, Ag-Containing Pillared Clays as Catalysts for the Selective Reduction of NOx by Hydrocarbons in an Excess of Oxygen

Thermally stable Al- and Zr-PILC loaded with copper and cobalt cations and silver nanoparticles were synthesized. The structural and surface features of these nanosystems were studied and compared with those of bulk analogs – partially stabilized ZrO₂ loaded with the same active components. Specificity of the catalytic properties of nanocomposites in SCR of NO _x by propane, propylene and decane in the excess of oxygen appears to be determined both by distribution of active components on the catalytic surface and degree of their interaction with supports. Formation of ads.-NO _x , nitroxyl-hydrocarbon C _x H _y NO₂ and isocyanate NCO intermediates was observed by ESR and IR spectroscopy in situ.     

NO Oxidation Kinetics on Iron Zeolites: Influence of Framework Type and Iron Speciation

Zeolites having MFI, FER and *BEA topology were loaded with iron using solid state cation exchange method. The Fe:Al atomic ratio was 1:4. The zeolites were characterized using nitrogen adsorption, FTIR and DR UV–Vis–NIR spectroscopy. The catalytic activity in NO oxidation and the occurrence of NO _x adsorption was determined in a fixed-bed mini reactor using gas mixtures containing oxygen and water in addition to NO and NO₂ and temperatures of 200–350 °C. Under these reaction conditions, the NO _x adsorption capacity of these iron zeolites was negligible. The kinetic data could be fitted with a LHHW rate expression assuming a surface reaction between adsorbed NO and adsorbed O₂. The kinetic analysis revealed the occurrence of strong reaction inhibition by adsorbed NO₂. FER and MFI zeolites were more active than *BEA type zeolite. MFI zeolite is most active but suffers most from NO₂ inhibition of the reaction rate. FTIR and UV–Vis spectra suggest that isolated Fe³⁺ cations and binuclear Fe³⁺ complexes are active NO oxidation sites. Compared to the isolated Fe³⁺ species, the binuclear complexes abundantly present in the MFI zeolite seem to be most sensitive to poisoning by NO₂.     

Components of Honeybee Royal Jelly as Deterrents of the Parasitic <Emphasis Type="Italic">Varroa</Emphasis> Mite, <Emphasis Type="Italic">Varroa destructor</Emphasis>

The parasitic mite Varroa destructor Anderson & Trueman reproduces on the immature stage of the honeybee, Apis mellifera L. Mites are found more often on drone brood than worker brood and only infrequently on queen brood. We investigated the chemical basis for the low incidence of mites on queen brood. V. destructor mites were deterred by a crude extract of royal jelly, a glandular secretion produced by nurse bees and fed to queen larvae. Bioassay-driven fractionation of the crude extract via column chromatography resulted in one active fraction that was as active as the crude extract. Compounds in the active fraction were identified using gas chromatography (GC) and coupled gas chromatography/mass spectrometry (GC-MS). Before injection, compounds were esterified with MeOH/sulfuric acid, followed by silylation of any hydroxyl groups present. The active fraction contained at least 22 compounds, all fatty acids, several of which contained an additional hydroxyl group on the alkyl chain. Synthesis of some of these compounds that are not commercially available is described. A synthetic mixture containing most of the compounds in the active fraction was as active as the active fraction in the bioassay.     

Aggregation pheromones of the grain beetle,cryptolestes turcicus (Coleoptera: Cucujidae)

Two biologically active macrolides were isolated from Porapak Q-captured beetle and frass volatiles ofCryptolestes turcicus (Grouvelle) and identified spectroscopically as (Z,Z)-5,8-tetradecadien-13-olide (I) and (Z)-5-tetradecen-13-olide (II). Natural I was active alone and was synergized by inactive II. The pheromones were male-produced but attractive to both sexes. Pheromone production increased dramatically when insects were aerated on a food source. Pure (R)- and (S)-I were inactive, but mixtures of (R)- and (S)-I were active, the first reported instance of enantiomeric synergism in the Cucujidae.     

Molecular design and characterization of catalysts for NO x selective reduction by hydrocarbons in the oxygen excess based upon ultramicroporous zirconia pillared clays

Approaches to design of zirconia pillared clays via control of the properties of pillaring species in solutions were elaborated. Structural features of pillars and Pt + Cu active components fixed at these nanoparticles were shown to determine catalytic properties of pillared clays in NO_x selective reduction by hydrocarbons in the oxygen excess.