Cooperative inclusion of sodium 1-pyrenesulfonate by γ-cyclodextrin

Summary The interaction of -cyclodextrin(-CD) with sodium 1-pyrenesulfonate(PS) was studied spectrophotometrically. -CD was found to cause much larger decrease in the absorption maxima of PS than -CD. The fluorescence spectra of PS in the presence of -CD showed excimer emission, while those of PS with -CD showed only monomer emission, indicating that -CD forms 12 (-CDPS) complexes in which two PS molecules are included in the -CD cavity in a face-to-face fashion. The binding isotherm showed a sigmoidal curve. The association constants were estimated by computer simulation of the binding curve. The 12 (CDPS) complex was found to be much more stable (K=10⁶ M^–1) than the 11 complex (K=1 M^–1). At high concentration of -CD another -CD cooperates in binding two PS molecules, resulting in the formation of a 22 complex.     

Sex pheromone components of corn stalk borerSesamia nonagriodes (Lef.) isolation,identification, and field tests

Z-11-Hexadecenyl acetate (Z11–16OAc), dodecyl acetate (12OAc),Z-11-hexadecenal (Z11–16Aid), andZ-11-hexadecenol (Z11– 16OH), were found in pheromone gland extracts of femaleSesamia nonagriodes (Lef.) [Lepidoptera: Noctuidae]. These four components were also present in airborne volatiles collected from calling virgin females in a 651889 ratio. Hexadecyl acetate (16OAc) was also detected but found to be inactive. The identification was based on multicolumn GC analysis, mass spectrometry, and field activity.Z11–16OAc is the major sex pheromone component; the addition of the secondary components individually decreased male captures. The blend of the four synthetic components in 691588 ratio was highly attractive to males; 200 g per trap was the most effective concentration in field tests.Lepidoptera: Noctuidae     

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.     

Sex pheromone ofEupoecilia ambiguella female: Analysis and male response to ternary blend

Sex gland extracts and washes ofEupoecilia ambiguella contain 10–20 ng/female of the primary sex pheromone componentZ-9-dodecenyl acetate (Z9–12Ac), accompanied by a number of related compounds. These areE-9-dodecenyl acetate (E9–12Ac),Z-9-dodecen-1-ol (Z9–12OH), saturated acetates of 12, 16, 18, and 20 carbons, and traces of a doubly unsaturated acetate, tentatively identified as a 9,11-dodecadienyl acetate. Octadecyl acetate predominates among the pheromone-related components, making up 1–2, occasionally 20–30 times the amount ofZ9–12Ac. The same compounds were also found in field-collected females and in effluvia.Z-9-Undecenyl acetate, which is a male attractant on its own, was also found in a sample of female effluvia. A hierarchy is observed in the ethological function of the pheromone components.Z9–12Ac is an attractant forE. ambiguella males. Dodecyl acetate (12Ac) is not attractive on its own but augments male catch when added to the main attractant. Addition of 18Ac augments attraction only when bothZ9–12Ac and 12Ac are present. Windtunnel tests demonstrate that 18Ac also raises the disorientation threshold, as previously shown for 12Ac. Other compounds, with the possible exception of additional saturated acetates, had either no effect on trap catch or, in the case ofE9–12Ac,Z9–12OH, andE-9,11-dodecadienyl acetate, were inhibitory above a certain level. A blend of roughly equal parts ofZ9–12Ac, 12Ac, and 18Ac provides the best attractant blend forE. ambiguella known to date.     

Field response ofDendroctonus brevicomis toexo-brevicomin,frontalin, and myrcene released at two proportions and three levels

Racemicezo-brevicomin, racemic frontalin, and myrcene were released at two proportions (51400 and 111), each at three levels (1 ×, 10 ×, and 100 ×) in a ponderosa pine forest in central California. The 51400 mix was based on an estimate of the relative amounts released from a ponderosa pine under attack by the western pine beetle,Dendroctonus brevicomis. MoreD. brevicomis were trapped at a source of the three compounds released at 51400 than were trapped at a source released at 111, at all three levels, but this difference was statistically significant only at the 1 × and 10 × levels. Sex ratio of trapped beetles and distribution of catch at the source of attractant and 5 m away apparently did not differ between relative release rates.Coleoptera: Scolytidae.Trade names are mentioned solely for information. No endorsement by the U.S. Department of Agriculture is implied.     

High resolution transmission electron microscopic (HRTEM) determination of the preferentially exposed faces onγ-Al2O3 andη-Al2O3

High resolution transmission electron microscopy has been used to examine the crystallites in -Al₂O₃ and -Al₂O₃. -Al₂O₃ has been found to be nearly hexagonally shaped crystallites whose identity distances and angles of fringe patterns indicate that (110) planes are preferentially exposed. -Al₂O₃ showed preferentially exposed surfaces of (100), (110) and super imposed (111)/(211). This information is valuable to the catalyst researcher trying to model the surfaces of these two supports.     

Sex attractants and sex pheromone components of noctuid mothsEuclidea cuspidea,Caenurgina distincta,and geometrid mothEupithecia annulata

Pheromone components and sex attractant blends consisting of 3Z,6Z,9Z-triene hydrocarbons and racemic and chiral forms of3Z,6Z-cis-9, 10-epoxydienes have been elucidated for two noctuid and one geometrid moth species. MaleEuclidea cuspidea moths were attracted to blends of 3Z,6Z,9Z-heneicosatriene (3Z,6Z,9Z-21H) with 3Z,6Z-cis-9,10-epoxyheneicosadiene (3Z,6Z-cis-9,10-epoxy-21H). In addition to these compounds, 3Z,6Z,9Z-20H, and two regioisomeric C₂₁ epoxides were tentatively identified in pheromone gland extracts.Caenurgina distincta moths were attracted by an 81 blend of 3Z,6Z,9Z-20H with3Z,6Z-cis- 9,10-epoxy-20H.Eupithecia annulata moths were attracted by either 3Z,6Z-cis-9,10-epoxy-20H or 3Z,6Z-cis-9,10-epoxy-21H, and by the 95,10R enantiomer of each epoxide. 3Z,6Z,9Z-21H and 3Z,6Z-cis-9,10-epoxy-21H were tentatively identified from pheromone glands. Pheromone components were identified by a combination of coupled gas chromatography-electroantennography, gas chromatography-mass spectrometry, and field bioassays.Issued as NRCC #32477.     

Properties ofSrMO 3-δ(M=Fe,Co) as oxygen electrodes in alkaline solution

Strontium ferrates and cobaltates with compositions SrFeO_3- (0.060.40) and SrCoO_3- (0.040.30) were synthesized. The dependence of the oxygen electrode properties on the value was examined in 1 mol dm^–3 KOH solution. In the SrFeO_3- series, the samples with 0.24<<0.29, showed the highest activity in both oxygen evolution and reduction reactions. In contrast, no strong dependence on the value was observed in SrCoO_3-, which also showed a high catalytic activity for oxygen evolution.     

Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N, N′-bis (2-hydroxy-1-naphthalidene) Thiosemicarbazone

The oxidative polycondenzation reaction conditions of N, N-bis (2-hydroxy-1-naphthalidene) thiosemicarbazone (HNTSC) using air oxygen, H₂O₂ and NaOCl were studied in an aqueous alkaline medium between 50–90°C. Oligo-N, N-bis (2-hydroxy-1-naphthalidene) thiosemicarbazone was characterized by ¹H-NMR, FT-IR, UV-Vis, size exclusion chromatography (SEC) and elemental analysis techniques. Solubility testing of oligomer was investigated using organic solvents such as DMF, THF, DMSO, methanol, ethanol, CHCl₃, CCl₄, toluene acetonitrile, ethyl acetate, concentrated H₂SO₄ and an aqueous alkaline solution. Using NaOCl, H₂O₂ and air O₂ oxidants, conversion to oligo-N, N-bis (2-hydroxy-1-naphthalidene) thiosemicarbazone (OHNTSC) of N, N-bis (2-hydroxy-1-naphthalidene) thiosemicarbazone was found to be 85, 80 and 76%, respectively, in an aqueous alkaline medium. According to the SEC analyses, the number-average molecular weight, weight-average molecular weight and polydispersity index values of OHNTSC synthesized were found to be 1050 gmol^–1 1715 gmol^–1 and 1.63, using NaOCl, and 2137, 2957 gmol^–1 and 1.38, using air O₂ and 2155 gmol^–1 4164 gmol^–1 and 1.93, using air H₂O₂, respectively. Also, TG analysis was shown to be unstable of oligo-N, N-bis (2-hydroxy-1-naphthalidene) thiosemicarbazone against thermo-oxidative decomposition. The weight loss of OHNTSC was found to be 97.29% at 900°C.     

Composition of Pd-La/α-Al2O3 catalysts

The objective of this study is to investigate the structure of the Pd-La/-Al₂O₃ catalyst. X-ray diffraction (XRD) and temperature-programmed reduction (TPRd) were used as characterization techniques. Contrary to the assertions in the literature, XRD studies conducted on La/-Al₂O₃ composite oxides and Pd-La/-Al₂O₃ catalysts show that Pd catalyzes the solid state reaction between A1₂O₃ and Al₂O₃ to form LaAlO₃. TPRd studies conducted on Pd/-Al₂O₃, Pd/La₂O₃, Pd/LaAlO₃, and Pd-La/-Al₂O₃ catalysts suggest that Pd in the Pd-La/-Al₂O₃ catalyst interacts more strongly with LaAlO₃ than with -Al₂O₃. Reaction studies were conducted to investigate the activity of Pd/-Al₂O₃, Pd/La₂O₃, Pd/LaA10₃, and Pd-La/-Al₂O₃ catalysts for nitric oxide (NO) reduction. These studies show that Pd/LaAlO₃ catalysts are most active for NO removal at stoichiometric and under net reducing conditions.     

Partial oxidation of methane over platinum metal gauze

The partial oxidation of methane to synthesis gas has been studied over a platinum gauze catalyst. The experiments were carried out at atmospheric pressure with a single gauze in a quartz reactor heated in an electric furnace. The furnace temperature was varied in the range 200–900°C and the space time in the range 0.00021–0.00042 s. The feed consisted of a mixture of CH₄O₂Ar2110 and carbon oxides and water were the main products. Oxygen was only partly consumed and relatively small amounts of hydrogen were formed.     

Preparation of nanosize Pt clusters using ion exchange of Pt(NH3) 4 2+ inside mesoporous channel of MCM-41

Mesoporous molecular sieve MCM-41 with a Si/Al ratio of 35 was obtained by hydrothermal synthesis using a gel mixture with a molar composition of 6 SiO₂0.1 Al₂O₃1 hexadecyltrimethylammonium chloride 0.25 dodecyltrimethylammonium bromide 0.25 tetrapropylammonium bromide0.15 (NH₄)₂O1.5 Na₂O300 H₂O. The MCM-41 sample was calcined in O₂ flow at 813 K and subsequently ion exchanged with Ca²⁺. A small Pt cluster has been supported on the MCM-41 sample following a procedure using ion exchange of Pt(NH₃) ₄ ²⁺ . The Pt(NH₃) ₄ ²⁺ ion supported on MCM-41 has been activated in O₂ flow at 593 K and subsequently reduced with Fh flow at 573 K, in the same way used for the preparation of a Pt cluster entrapped inside the supercage of zeolite NaY. The resulting Pt cluster supported on the MCM-41 shows hydrogen chemisorption oftotal two H atoms per Pt at 296 K (based on the total amount of Pt) and high catalytic activity for hydrogenolysis of ethane. The chemical shift in¹²⁹Xe NMR spectroscopy of adsorbed xenon indicates that the Pt cluster is located inside the mesoporous molecular sieve.     

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.     

ß-Al2O3 synthesis from m-Al2O3

-Al₂O₃ formation fromm-Al₂O₃ was found by a new convenient technique. By thermal decomposition of a complex compound, trioxalatoaluminate Na _x (NH₄)_3–x [Al(C₂O₄)₃]yH₂O(0.091 x 0.333;y= 3), a very fine powder ofm-Al₂O₃ was formed. The decomposition process was examined by thermal analysis and X-ray diffraction and the phase relation of the system Na₂O-Al₂O₃ in the midtemperature region between 600 and 1200° C is discussed briefly. The tablet ofm-Al₂O₃ was fired at 1600° C for 30 min to prepare dense-Al₂O₃ ceramics, the apparent density of which was greater than 95% of the theoretical value. The sintered tablet was examined from the structural point of view and the electrical conductivity was measured by an a.c. method to verify that the procedure of the complex decomposition is a suitable technique for-Al₂O₃ synthesis.     

Attraction ofCacoecimorpha pronubana male moths to synthetic sex pheromone blends in the wind tunnel

Attraction ofCacoecimorpha pronubana male moths to blends of four sex pheromone components was studied in the wind tunnel.Z11–14Ac alone did not elicit upwind flight, admixture of 10%Z11–14OH or more led to successful attraction of males to the source. Attractivity of these binary blends was further enhanced by addition ofE11–14Ac orZ9–14Ac; the optimum was a blend ofZ11–14Ac,Z11–14OH,E11–14Ac, andZ9–14Ac at the proportion of 1003033. In ternary and quaternary blends, the effect ofZ11–14OH andE11–14Ac was strongest at 30% and 3%, respectively. By contrast,Z9–14Ac increased behavioral responses over a wide range.     

Zirconium tetra-n-butylate modified with different organic acids: Hydrolysis and polymerization of the products

In this work; (a) complexation reaction of zirconium tetra-n-butylate, Zr(OBu ⁿ )₄, with MAc and different organic acids. (b) the hydrolysis reaction of modified Zr species, and (c) the polymerization reaction of complex products are studied. Zr(OBu ⁿ )₄ was reacted with different mole ratios of methacrylic acid (MAc) at room temperature and the maximum combination ratio was found to be 12 [Zr(OBu ⁿ )₄MAc] by FT IR. The modification of zirconium tetra-n-butylate with the acid mixtures [methacrylic acid-acetic acid (MeCOOH), methacrylic acid-propionic acid (EtCOOH), methacrylic acidbutyric acid (PrCOOH)] was made for a combination ratio of 111 [MAcRCOOHZr(OBu ⁿ )₄RMe. Et, Pr] and the products were characterized by¹H-NMR, FT-IR, and UV-spectroscopies. Following their synthesis, hydrolysis of the complexes with various amounts of water and polymerization with benzoyl peroxide were realized. The hydrolysis and polymerization products of the complexes were studied by Karl-Fischer Coulometric titration and thermal analysis respectively. Methyl-ethyl-ketone (MEK) and chloroform were chosen as solvents.     

Temporal patterns of sex pheromone titers and release rates inHolomelina lamae (Lepidoptera: Arctiidae)

Six hydrocarbon components (2-methylhexadecane,n-heptadecane, 2-methylheptadecane, 2-methyloctadecane,n-nonadecane, and 2-methylnonadecane) were identified in sex-pheromone gland extracts and in airborne collections ofHolomelina lamae. Low variability in the ratio of components among individuals indicates tight regulation of blend composition. Minor changes were evident in the quantity and ratio of the blend as a function of time of day. Based on gland extracts, the total quantity of the six components increased from day 1 (X = 6299 ng) to day 4 (X = 7498 ng) and subsequently decreased. No significant correlations were found between total gland contents and wet or dry weights of moths. Emission rates ofH. lamae females were determined from pheromone adsorbed onto Porapak Q. Quantities released peaked shortly after the onset of calling and decreased rapidly as calling continued. Peak release rates ranged from 13 to 350 ng/10 min, and from 37 to 835 ng/60 min. Noncalling females did not emit detectable quantities of pheromone. Based on release rates and the rate of pulsation of the abdominal tip, the average amount released per pulse is not constant. The mean ratio of components released (0.787.45 84.802.842.591.53) was not very different from the ratio of components in gland extracts of 2-day-old females (0.704.1990.12 1.651.911.42). We propose that the blend is atomized rather than volatilized from the gland, thus retaining nearly the same ratios in the female's effluvium as in her gland.     

Catalytic oxidation of methanol to methyl formate over silver – a new purpose of a traditional catalysis system

Catalytic reaction was performed in the unregarded temperature region over silver catalysts with long catalytic lifetime for the conversion of methanol to methyl formate. O-saturated or O-saturated silver catalysts were studied individually to identify the roles of O, O in the oxidative esterification of methanol over an unsupported polycrystalline silver catalyst. A synergic process is proposed based on the coexistence of -oxygen species and -oxygen species on the surface of polycrystalline silver at about 573 K.     

Temperature programmed oxidation of Cu/ZnO catalysts with N2O: an attempt for characterization of copper catalysts

For characterization of the surface structure of metallic copper formed on the support, temperature programmed oxidation (TPO) with N₂O was carried out over various Cu/ZnO catalysts. Four peaks of the N₂ formation (, , and ) were observed at 223, 400, 545 and 600 K in the TPO runs. The average copper crystallite size estimated from the sum of the amount of - and -peaks agreed fairly with those determined by X-ray diffraction and transmission electron microscopy. It was concluded that - and -peaks resulted from the oxidation of metallic copper atoms on the steps, corners and/ or defect sites, and on the flat sites of the surface of copper crystallites, respectively, while - and -peaks resulted from the bulk oxidation of copper.     

Unsteady mass transfer in turbulent flow close to a rotating cylinder

Electrodiffusional methods of studying unsteady turbulent mass transfer involved measurement of a transient current characteristicI() after step polarization of a rotating annular cylindrical 46 mm dia electrode at a fixed rotational velocity atRe=(2–9)×10⁴ andSc=2.4×10³. The potassium ferri-ferrocyanide system with NaOH background electrolyte was used. An initial asymptote at 0 served as a test. The similarity of the normalized transfer coefficientK ₊=/u _* with respect to the Reynolds number demonstrated turbulent flow development. Tests were aimed at determining the powern in the approximate law of attenuation of turbulent diffusionD _t in they-direction normal to the wallD _t/v=by ₊ ⁿ .A numerical solution of the unsteady turbulent diffusion equation obtained as a set of lg ()=f() curves for 3n4 with an interval 0.2, where ()=I/I()_#x2212;1 has been achieved.Notation I diffusion current - C C ₀ andC _p concentration, concentration in the bulk liquid and polymer concentration, respectively - C _f drag of a Newtonian fluid - time - U linear velocity - v kinematic viscosity - angular velocity - j flow - y ₊ yu _*/v, ₊ = u _* ² and =(1-C/C ₀), dimensionless quantities This paper was presented at the Workshop on Electrodiffusion Flow Diagnostics, CHISA, Prague, August 1990.