Effect of the naturally occurring salt ‘Kanwa’ as a fertilizer on the productivity ofStylosanthes in the subhumid zone of Nigeria

Soil nutrient deficiencies pose a serious limitation to higher crop and forage yields in the Nigerian subhumid zone. Some of the deficiencies may be alleviated by using as a fertilizer a salt mined locally called Kanwa which is traditionally used as a cattle lick. Yields ofStylosanthes hamata cv Verano andS. guianensis cv Cook seed and dry matter increased with Kanwa application at different locations. The effect of Kanwa was enhanced when phosphorus was adequately supplied. Improvements to soil physical properties were proportional to the yield of the legume. The implications of good quality fodder and improved soil conditions in Agro-pastoral Systems in the Nigerian SHZ are discussed.     

Electrosynthesis of 4,4′-dinitroazobenzene on PbO2 electrodes

Parameters which affect the electrosynthesis of 4,4-dinitroazobenzene from p-nitroaniline on platinum and PbO₂ electrodes were investigated and optimum conditions were determined. Maximum conversion efficiency for electrosynthesis was 95% with a pure -PbO₂ electrode. It was found that the electrocatalytic activity of a PbO₂ electrode depends upon its / ratio and its degree of crystallinity. The effects of the added base and water on the conversion efficiency were also elucidated.     

Mechanisms of Iron Activation on Fe-Containing Zeolites and the Charge of α-Oxygen

According to previous Mössbauer data [1] -sites formation at the activation of Fe-containing zeolites is accompanied by irreversible self-reduction of the iron, proceeding without participation of an external reducing agent. Reduced Fe²⁺ ions are inert to O₂ but are reversibly oxidized to Fe³⁺ by N₂O, generating the -oxygen species, O, which provide selective oxidation of hydrocarbons.In this work, the mechanism of -sites formation was studied via quantitative measurement of the dioxygen amount desorbed into the gas phase at the step of self-reduction. A prominent role of the zeolite matrix chemical composition has been revealed. For example, with zeolites of Al–Si composition (FeZSM-5 and Fe-), heating to 900 °C in a closed vacuum space leads to irreversible evolution of O₂, which is accompanied by the immediate formation of -sites. Similar heating of B–Si and Ti–Si zeolites also leads to dioxygen evolution; however, this evolution is reversible and is not accompanied by formation of -sites. Activation of these zeolites occurs only in the presence of water vapor. Stoichiometric measurements showed that in terms of charge one regular O^2- ion, removed at the activation, is equivalent to two -oxygen atoms. So, -oxygen is identified as an ion-radical species O ^-., whose unique oxidation properties still distinguish it from the generally observed O^-. radicals.The mechanism of -sites formation is proposed, in which the process of strong chemical stabilization of reduced Fe²⁺ atoms in the zeolite structure is a key step, making impossible the reoxidation of the iron with O₂.     

Hydrosilylation catalysts derived from cyclodextrin organometallic platinum inclusion compounds and their use in command-cure applications

Beta-cyclodextrin (-CD) complexes of CODPtX ₂ (COD=1.5-cyclooctadiene.X=Cl, Br, and I) have been prepared and employed as hydrosilylation catalysts. When used in cross-linkable, silicone-containing systems, these catalysts provide a long shelf stability at ambient temperature but cure rapidly at elevated temperature. These systems thus have the property of command-cure. Extensive analytical investigations were undertaken to develop reproducible synthetic methodology for the preparation of inclusion compounds free of surface contamination of the guest platinum compound. Water plays a key role in the synthesis of such platinum inclusion compounds. Dried -CD CODPtX ₂ compounds can be washed with organic solvent to remove residual uncomplexed CODPtX ₂, while organic solvent washing of wet inclusion compounds results in removal of the guest from the -CD cavity. Examination of these catalysts in curable silicone systems is described.     

Chemical effects in commercial and laboratory mixtures of ‘reactive’ phosphate rock and acidulated fertilisers

The chemical analyses of different size fractions of a variety of commerical and laboratory prepared samples of partially acidulated phophate rocks and mixtures of reactive phosphate rock and single superphosphate (called LONGLIFE in New Zealand) have been studied. Whereas only minor chemical segregation effects have been observed for partially acidulated products quite a large bias has been established for LONGLIFE materials, and more especially commercial samples, where larger proportions of phosphate rock were found in the lower size fractions. This inhomogeneity was considered to arise from poor mixing of components and subsequent inconsistent granulation; more stringent rejection criteria for undersize material would greatly assist in improving the product quality. Chemical deactivation of the phosphate rock residue in LONGLIFE materials was also observed; this can be partially explained by a selective reaction of the reactive phosphate rock component with acid still present at the time of mixing with the single superphosphate component.     

High-Performance Directional Metallopolyamides. II. Optical Spectroscopic Studies of Metal Chelation

The chelating interaction between metal ions and 4,4-disubstituted-2,2-bipyridyl-containing high-performance polymeric ligands prepared from 2,2-bipyridyl-4,4-dicarboxylic acid and a series of primary aromatic diamines was investigated by optical spectroscopy. Optical spectroscopic studies of the chelation of ruthenium ions by the 2,2-bipyridyl-containing polyamides revealed the formation of distinct ruthenium(II) complexes [Ru^II(poly)L₄] ( _max=530 nm), [Ru^II(poly)₂L₂] ( _max=584 nm), and [Ru^II(poly)₃]²⁺ ( _max=476 nm), while iron(II) ions formed only one complex ( _max=569 nm). The diverse functional features of the polymer repeat unit directly influences the chelation of metal ions.     

Isolation and identification of cotton synomones mediating searching behavior by parasitoidCampoletis sonorensis

In laboratory bioassays, the parasitoidCampoletis sonorensis was attracted to the following sesquiterpenes isolated from cotton essential oil: -humulene, -bisabolene, -caryophyllene oxide, spathulenol, -bisabolol, and a new, naturally occurring bisabolene-related alcohol, (2-p-tolyl-6-methylhept-5-en-2-ol) which we name gossonorol. This is the first report of spathulenol in cotton. -Caryophyllene, a major component of cotton, was not attractive to the parasitoids. The response of the parasitoids to these compounds and the possibility of augmenting parasitoid activity in the field by manipulating plant secondary metabolites is discussed.Synomone: A chemical produced or acquired by an organism that benefits both the emitting and receiving organisms (Nordlund and Lewis, 1976).     

Heterogeneous asymmetric reactions. 23. Enantioselective hydrogenation of ethyl pyruvate over cinchonine- and α-isocinchonine-modified platinum catalysts

The enantioselective hydrogenation of ethyl pyruvate to (S)-ethyl lactate over cinchonine- and -isocinchonine-modified Pt/Al₂O₃ catalysts was studied as a function of modifier concentration and reaction temperature. The maximum enantioselectivities obtained under the applied mild conditions were 89% ee using cinchonine (0.014 mmoldm^–3, 1 bar H₂, 23°C, 6% AcOH in toluene), and 76% ee in the case of -isocinchonine (0.14 mmoldm^–3, 1 bar H₂, –10°C, 6% AcOH in toluene). Since -isocinchonine of rigid structure exists only in anti-open conformation these data provide additional experimental evidence to support the former suggestion concerning the dominating role of anti-open conformation in these cinchona-modified enantioselective hydrogenations.     

Lean NOx catalysis over alumina‐supported catalysts

aluminasupported catalysts show promise as lean NO_x catalysts. The role of alumina in influencing the structural and chemical properties of the active phase supported on it is discussed using some effective aluminabased lean NO_x catalysts. These include Ag/Al₂O₃, CoO_x/Al₂O₃ and SnO₂/Al₂O₃. Alumina plays an important role in stabilizing Ag in the oxidic phase and cobalt in the 2+ oxidation state. For SnO₂/Al₂O₃, alumina increases the SnO₂ surface area. On both Ag/Al₂O₃ and SnO₂/Al₂O₃, alumina also participates actively in the NO_x reduction reaction. An active organic intermediate is formed on Ag or Sn oxide which reacts with NO_x subsequently on alumina to form N₂.     

Catalytic Combustion of Model Carbon Particles (CPs) over Pt/β-SiC Catalyst

Platinum catalyst supported on a medium surface area -SiC was successfully used for the catalytic combustion of model carbon particles and compared to a catalyst supported on a low surface area -SiC. The -SiC-based catalyst showed no deactivation as a function of cycling tests while a strong deactivation was observed on the -SiC-based catalyst. This deactivation was attributed to the progressive encapsulation of the platinum particles by a layer of silica which built up during the combustion cycle. These results render possible the use of Pt/-SiC catalyst as a diesel carbon particle catalytic filter with continuous regeneration.     

High-Performance Directional Metallopolyamides. I. Synthesis and Thermal Analysis

High-performance polyamides containing the 4,4-disubstituted-2,2-bipyridyl moiety were synthesized by phosphorylation polycondensation from 2,2-bipyridyl-4,4-dicarboxylic acid and a series of primary aromatic diamines with triphenylphosphite and pyridine as the agents to facilitate condensation. Polyamides exhibiting improved solubility in organic solvents and strong acids, melting transitions at low temperatures, and good thermal properties were prepared by introducing bulking methyl and fluoro groups and flexible ether and propyl linkages and by using monomers with reduced symmetry. Solutions of the polyamides with rigid main chains (III, IV, V, VI, and VIII) showed birefringence (colorful spherulites) at concentrations of 5, 10, and 15% (w/v) polymer/solvent. The chelation of ruthenium(II) ions resulted in the preparation of directional metallopolyamide systems based on the geometrically favorable tris(2,2-bipyridyl)ruthenium(II) complex. The three-dimensional polyamides, which absorbed at a _max of 476 mm and emitted at a _max of 620 nm, exhibited a high thermal stability and improved solubility, making them suitable candidates for compressive strength studies and cyclic voltammetry studies as part of an effort to address the corrosion of graphite fiber-reinforced composites.     

Phase transitions and dimensional and morphological changes in an “Aluminum Hydroxide-Alumina” system under a shock-wave action

A method is proposed to study the sequence of phase transitions in powdered materials under a shock-wave action. It is shown that the aluminum hydroxide-alumina system has the following sequence of phase transformations under a shock-wave action: bayerite boehmite -Al₂O₃ -Al₂O₃. It is found that there are no transitional high-temperature modifications of alumina. A method is developed for obtaining a submicron alumina powder, which allows obtaining materials with a controlled phase composition, including a thermodynamically stable -modification of Al₂O₃. The specific features of the morphological structure and the phase and structural characteristics of powders after a shock-wave action are considered.Translated from Fizika Goreniya i Vzryva, Vol. 41, No. 1, pp. 110–119, January–February, 2005.     

Synthesis and properties of aromatic polyesters and brominated polyesters derived from α,α′-bis(4-hydroxyphenyl)-1,4(or 1,3)-diisopropylbenzene

The interfacial polycondensation technique was used for the preparation of polyarylates and brominated polyarylates. Polyarylates and brominated polyarylates were prepared by mixing a solution of diacid chloride such as terephthaloyl chloride, isophthaloyl chloride, or their mixture in dichloromethane with an aqueous alkaline solution of ,-bis(4-hydroxyphenyl)-1,4(or 1,3)-diisopropylbenzene or ,-bis(4-hydroxy-3,5-dibromophenyl)-1,4(or 1,3)-diisopropylbenzene using triethylbenzylammonium chloride as the phase transfer agent. Moderate to high molecular weight polyarylates with _inh up to 1.27 dL/g were obtained, and most of them could be cast into tough and flexible films depending on the polymer composition. In general, polymers containing more 1,3-isomer or isophthaloyl chloride moieties gave transparent and flexible films and had lower glass transition temperatures and higher solubility. Although these polymers have two isopropylidene linkages in their repeating units, they still exhibit moderately high thermal stability and show no obvious weight loss before 400 °C. The introduction of bromine on the polymer backbone caused a decrease of inherent viscosity, crystallinity, and thermal stability of the polyarylates, while causing an increase in glass transition temperature and a great enhancement of fire retardancy.     

Synergistic Effect of Ethanol to α-Pinene in Primary Attraction of the Larger Pine Shoot Beetle, Tomicus piniperda

-Pinene and ethanol were released in the approximate proportions 1:0.1, 1:0.9 and 1:9 (at 21°C). Ethanol, released in the range of 3–279 mg/day, generally synergized the attraction of T. piniperda to -pinene (30 mg/day at 21°C), although attraction to the mixtures varied within and between years. The low release rate of ethanol together with -pinene attracted a significantly higher number of beetles than -pinene alone in 1995, April of 1996, and in 1997. Lures with the medium release rate of ethanol were the most attractive only in March of 1996. The high dose of ethanol significantly synergized attraction to -pinene in 1995 and 1997. The variable attraction of T. pinipeda to ethanol and -pinene at various release rates and proportions may be due to the temperature dependent nature of beetle antennal sensitivity. At ambient temperatures of 10–13°C. T. piniperda was most attracted to the lures with -pinene and high release rates of ethanol, at 14–17°C it was most attracted to those with medium release rates of ethanol, and at 18°C and higher it was most attraacted to those with low release rates of ethanol.     

Chiral specificity in responses by the bark beetleDendroctonus valens to host kairomones

The attraction of the red turpentine beetle,Dendroctonus valens, to the resin volatiles of its host,Pinus ponderosa, is elicited by three chiral monoterpenes. In field assays response was greatest to (S)-(–)--pinene; 92% (S)-(–)--pinene found inP ponderosa resin was not attractive. However, 75% (R)-(+)--pinene, which occurs inPinus lambertiana, a sympatric host ofD. valens, was attractive. (S)-(–)--Pinene interrupted response to (R)-(+)--pinene. (S)-(+)-3-Carene from both hosts was attractive at the (R)-(+)--pinene level. Three sympatric coniferous nonhosts each have the same attractive monoterpenes but produce less resin. These studies demonstrate the importance of chirality of host compounds in the host finding behavior of this bark beetle.     

Location of Mn in MnAPO‐11: influence of synthesis from aqueous and non‐aqueous media

MnAPO11 samples were synthesized from aqueous (MnAPO11(A)) and ethylene glycol (MnAPO11(NA)) media. The crystallinity of the samples was more when the synthesis was carried out in ethylene glycol. Chemical and thermogravimetric analyses reveal greater incorporation of Mn in the framework of MnAPO11(NA) than in MnAPO11(A). At least five different types of Mn(II) species are detected in the samples by ESR. The studies suggest that Mn is more homogeneously distributed in MnAPO11(NA) than in MnAPO11(A).     

Kinetics and Mechanism of Copolymerization of α-terpineol with Methylmethacrylate in Presence of Azobisisobutyronitrile as an Initiator

The radical copolymerization of -terpineol with methyl-methacrylate in xylene at 80±0.1C for 50 minutes in the presence of azobisisobutyronitrile (AIBN) follows ideal kinetics and results in the formation of a functional and random copolymer. The activation energy is 33 KJ/mole. The IR spectrum and NMR spectra of the copolymer(s) shows the bands at 1750 and 3400 cm^–1 for ester group of methylmethacrylate and alcoholic group of -terpineol and peaks at 3 to 4 for methoxy group and at 6.5 to 7.5 due to alcoholic group of methylmethacrylate and -terpineol repectively. The values of reactivity ratios, calculated by Kelen–Tüdos method, are r ₁ (MMA) = 0.18 and r ₂ (-terpineol) = 0.046. The Alfrey-Price; Q–e parameters for -terpineol has been calculated as 0.149 and 2.486. The mechanism of copolymerization has been elucidated and it is concluded that the double bond present in the monocyclic ring of -terpineol is an active site for copolymerization and the alcoholic group of -terpineol remain to give functional copolymer.     

Alleviation of α-tomatine-induced toxicity to the parasitoid,Hyposoter exiguae,by phytosterols in the diet of the host,Heliothis zea

The solitary, endoparasitic ichneumonid,Hyposoter exiguae (Viereck) is a parasitoid of the tomato fruitworm,Heliothis zea (Boddie). However, the parasitoid is deleteriously affected by the tomato glycoalkaloid, -tomatine, ingested from hosts (H. zea) fed on artificial diets or semipurified extracts of tomato plants that contained -tomatine. -Tomatine causes prolonged larval development; disruption or prevention of pupal eclosion; deformation of antennal, abdominal, and genital structures; and reduction in adult weight and longevity of the parasitoid. These toxic effects are exacerbated when the dietary dose of -tomatine is increased from 12 mol to 20 mol/g dry wt of diet. However, the toxicity of -tomatine is attenuated in parasitoids reared from hosts fed on artificial diets that contain equimolar or supramolar amounts of 3-OH-sterols admixed with -tomatine. Further, the toxicity of extracts from the foliage of different cultivars of tomatoes toH. exiguae is contingent upon the composite levels of -tomatine and total phytosterol (free and esterified). Cultivars with a low total sterol-tomatine ratio are more toxic toH. exiguae. The possible mode of action of -tomatine toxicity toH. exiguae by disruption of sterol metabolism is discussed.     

High‐activity catalyst of SO 4 2− /ZrO2 supported on γ‐Al2O3 for n‐butane isomerization

A series of Al₂O₃supported SO ₄ ^2– /ZrO₂ superacid catalysts (named SZ/Al₂O₃) were prepared by a precipitation method and their catalytic behavior for nbutane isomerization at low temperature in the absence of H₂ and at high temperature in the presence of H₂ was studied in this paper. The catalytic activities of some of these catalysts were enhanced significantly at both low and high temperatures. At 250°C after 6 h on stream, the steady activity of the most active sample, 60%SZ/Al₂O₃, is about two times higher than that of conventional SZ. The texture properties of catalysts were studied by the methods of XRD and the adsorption of N₂. Experimental evidence of IR of adsorbed pyridine indicates that the significant activity enhancements of SZ/Al₂O₃ catalysts are caused by the increasing of the amount of strong acid sites.     

Investigation of sex pheromone components of female asian corn borer,Ostrinia furnacalis (Hübner) (Lepidoptera: Pyralidae) in Taiwan

(E)-12-Tetradecenyl acetate (E12–14OAc), (Z)-12-tetradecenyl acetate (Z12–143nOAc), and tetradecanyl acetate (14OAc) were extracted and identified as major chemical components from female tips of the Asian corn borer,Ostrinia furnacalis (Hübner) (Lepidoptera: Pyralidae) in Taiwan, with a combined wash ratio of 483715 and an individual female ratio of 453916. The average amount ofE12-,Z12–14OAc and 14OAc in each female gland was 6.6±4.6, 5.8±3.5, and 2.4±1.7 ng/female, respectively. The mixture of these three synthetic chemicals not only gave strong activities in male antennae but also could catch significantly more males than virgin females in field-trapping tests. The field test also showed no significant difference in trapping ability among the three-component Taiwan formulations, the two-component Taiwan formulation (Z12–14OAc andZ1214OAc, 5347), and the Japan formulation (Z12–14 OAc andE 12–14OAc, 3:2).