Identification and field testing of female-produced sex pheromone components of the spring cankerworm,Paleacrita vernata Peck (Lepidoptera: Geometridae)

Two sex pheromone components, 3(Z),6(Z),9(Z)-nonadecatriene (3Z,6Z,9Z-19 H), and 3(Z),6(Z),9(Z)-eicosatriene (3Z,6Z,9Z-20 H), have been positively identified, and a third component, 6(Z),9(Z)-nonadecadiene (6(Z),9(Z)-19 H) has been tentatively identified from abdominal tip extracts of female spring cankerworm moths,Paleacrita vernata Peck (Lepidoptera Geometridae). The pheromone components were identified by a combination of gas chromatography, electroantennography, mass spectrometry, chemical tests, comparison with standards, and field testing. Only 3Z,6Z,9Z-20 H exhibited significant attractant activity when tested alone, and it was potentiated by the other two components. The attractive blend was an 821 ratio of 3Z,6Z,9Z-20H/3Z,6Z,9Z-19H/6Z,9Z-19H. However, the two-component blend of 3Z,6Z,9Z-20 H and 6Z,9Z-19 H (81 ratio) was as attractive as the three-component blend in further field tests. A series of related compounds, the diene monoepoxides available from epoxidation of C₁₉ and C₂₀ 3Z,6Z,9Z-trienes, some of which have been found in the pheromone blends of other moth species, were tested as behavioral antagonists. The attraction of male moths to synthetic lures was suppressed by the addition of 6Z,9Z-cis-3,4-epoxy-nonadecadiene to the lures. Additional experiments were performed to determine the effects of lure dosage, trap height, and trap design on the numbers of male moths captured.Issued as NRCC 30711.     

Synthesis of poly[(silanylene)thiophene]s

Poly[(silanylene)thiopene]s, copolymers with alternating thiophene, 2,2-bithiophene, or 2,2:5,5-terthiophene and mono-, di-, or tetrasilanylene units, were prepared by condensation of the dilithium salts of the thiophenes or the bis(2-thienyl)silanes with ,-dichlorosilanes in diethylether. The polymers were characterized with¹H,¹³C, and²⁹Si NMR, UV, IR, GPC, TGA, and elemental analyses. UV absorption maxima of these polymers all show a red shift with increasing length of the polymer backbone, suggesting that conjugation occurs through the combined -Si and -thiophene backbone.This paper was presented at the Second International Topical Workshop, Advances in Silicon-Based Polymer Science.     

Mass transfer in an annular electrodialysis cell in pulsating flow

The effect of pulsating flow on the mass transfer in an annular electrodialysis cell has been studied in terms of the limiting current. The results indicate that the limiting current is influenced by the fluid velocity, the pulsation amplitude and the pulsation frequency, giving an increase of 400% with respect to the steady state. For a given amplitude, the dimensionless velocity, 0 (0 = a/v), can be taken as a representative parameter of the pulsation effect on the mass transfer. The fractional increase in the Sherwood number in pulsating flow with respect to the steady state has been correlated in terms of the dimensionless velocity, 0, and the Stokes number, 1 (1 = Deq (/)1/2), giving the correlation:     

Studies on the response of ‘Tifblue’ and ‘Woodard’ rabbiteye blueberries to fertilizers

A field study was conducted to investigate the effects of three fertilizer placement methods and 11 fertilizer formulations on plant survival, economics of replanting, yield, and fruit size of two rabbiteye blueberry (Vaccinium ashei Reade) cultivars Tifblue and Woodard. Fertilizer rates were either mixed with the soil under plants (before planting), sidedressed, or half-rate was placed under plants with the other half sidedressed. Fertilizers at planting caused a total of 34% Woodard and 12% Tifblue plants to die as compared to 6% for Woodard and none for Tifblue when no fertilizer was applied. Fertilizer formulas 2-1-1 and 5-10-10 oxide ratios placed under Woodard plants caused 100% mortality whereas Tifblue fertilized with oxide ratios 2-2-2 and 5-10-10 under plants reached the maximum 50% mortality. Splitting fertilizer placement under the side of the plants resulted in less Woodard plant mortality (30%) than placing all the fertilizer under plants (54%). However, plant mortality for the side/under group was not different than sidedressing all fertilizer (23%). A planted hectare in this experiment consisted of 1852 Tifblue and 926 Woodard plants, providing one Woodard plant to pollinate two Tifblue plants. Based on the results obtained, the 5-10-10 fertilizer placed under plants would be expected to cause half the Tifblue (926 plants) and all the Woodard (926 plants) to be replanted. Plant costs alone was estimated to be $2315 with additional replanting costs of $93 for Tifblue and much higher for Woodard. Sidedressing 5-10-10 fertilizer eight weeks after planting would have prevented plant mortality. Placement of various fertilizers under Woodard or Tifblue plants resulted in a significant increase in plant mortality as compared to side placement of fertilizers. Yield loss due to plant mortality increased linearly with the N level of the fertilizers (ranging from 0 to 2) for both cultivars. Woodard fruit size was not affected by fertilizer placement but placing fertilizers under Tifblue plants produced smaller yields with larger fruit than sidedressed plants. Blueberry plants in a virgin acidic soil may experience no reduction in yield if fertilization is completely eliminated.     

Synthesis and polymerization of 2-(β-N-3′-halogencarbazolylethyl)-2-oxazolines

Summary The synthesis of three novel oxazoline monomers,all of which contain 3-halogen substituted carbazolyl groups [i.e., 2-(-N-3 chlorocarbazolylethyl)-2-oxazoline, 2-(-N-3 bromocarbazolylethyl)-2-oxazoline and 2-(-N-3 iodocarbazolylethyl)-2-oxazoline]and their polymerization is described.     

The relationship between the growth rate of hydrogen bubbles and the duration of the ‘induction period’ in the electrowinning of zinc from sulphate electrolytes

As a result of detailed polarization, volumetric and optical,in situ investigations of the growth rate of hydrogen bubbles during the electrowinning of zinc from Ni²⁺-containing sulphate electrolytes and in the presence of an inhibitor, a relationship has been established between the shape of the hydrogen bubbles and the duration of the induction period. It has been found that during the induction period hydrogen bubbles alter their shape from spherical at the beginning to cupola-shaped at the end, thus increasing by 10–12 times the extent of the screening of the cathode surface beneath. Experimental confirmation is presented for the validity of the previously proposed [1] physical model for the nature of the induction period.     

Critical solution point and chain dimension of branched-polystyrene solutions

Summary Critical solution point and chain dimension were measured for branched polystyrene(BPS) in solution as a function of molecular weight(M) and compared with those for linear polystyrene(LPS). The critical concentration _c of BPS was quite different from that of LPS at a fixed M, but the same at a fixed overlap-concentration ^*, i.e., plots of _c vs. ^* fall on a single straight line for both BPS and LPS (gf_c ^*). Reduced critical temperature _c defined by gt_c=(–T_c)/ [T_c: critical temperature, : the -temperature] was related to _c as _{c c} ² for BPS, whereas _{c c} for LPS.     

Study of the β — α solid-solid transition of isotactic polypropylene by synchrotron radiation

Synopsis The transformation of the -modification into -modification in isotactic polypropylene was investigated by WAXS, DSC and dilatometric methods. The temperature and time dependent WAXS spectra were made by using high-intensity synchrotron radiation. The - transformation was followed by short time exposures. The transformation of the -modification was found to act toward the increase in the total crystallinity.     

Identification of sex pheromones of two sibling species in dingy cutworm complex,Feltia jaculifera (GN.) (Lepidoptera: Noctuidae)

The sex pheromone components of the two sibling species of the dingy cutworm that occur on the prairies of western Canada were identified in abdomen-tip extracts from calling female moths. Three monounsaturated acetates, (Z)-7-dodecenyl acetate, (Z)-9-tetradecenyl acetate, and (Z)-11-hexadecenyl acetate, are common to both species in ratios of 100133 for species A and 0.30.5100 for species B. The most effective synthetic blends for the attraction of male moths in the field consisted of these three components in ratios of 1010 at 8.8g/lure for species A and 112000 at 500g/lure for species B. The addition of Z5-12Ac to either blend reduced the catches and the addition of Z7-12OH orZ11-16OH to the three-component blend reduced the catches of species B males. The species are morphologically indistinguishable, but the identity of the males attracted to the synthetic blends could be confirmed by their antennal responses to a test blend of the three components using a GC-EAD system. Both synthetic attractant blends are competitive with females and will be useful for studying the distribution, biology, and relative abundances of the two species.Contribution no. 3879005 of the Lethbridge Research Station.     

Blackheaded fireworm: Laboratory and field studies of its sex pheromone

Electroantennogram (EAG) responses of maleRhopobota naevana (Hübner), the blackheaded fireworm, to all of the monoene straightchain 12- and 14-carbon alcohols and acetates implicated (Z)-11-tetradecenl-1-ol (Z11–14OH) and its acetate (Z11–14Ac) as sex pheromone components.Z11–14Ac produced the strongest EAG response of all compounds tested. Gas chromatography-mass spectrometry (GC-MS) analysis of extract of female sex pheromone glands (SPG) confirmed the presence ofZ11–14OH (125 pg/female) andZ11–14Ac (600 pg/female) (all other monoenes had different retention times). In field tests, traps baited withZ11–14OH alone captured males, but traps baited withZ11–14Ac alone did not. Traps baited with a combination ofZ11–14OH andZ11–14Ac in various ratios did not produce better trap catches thanZ11–14OH alone. (Z)-9-Dodecen-1-ol acetate (Z9–12Ac), reported by others to be a field attractant, did not produce trap catch in our tests, but in combination withZ11–14 OH (982 in septa corresponding to 95:5 in vapor,Z11–14OH toZ9–12AC) produced a sevenfold increase in catch overZ11–14OH alone. IfZ9–12AC had been present in extract of SPG at 2–5% ofZ11–14OH, it would not have been detected in our GC-MS experiment. Rhopobota naevana (Hübner) Lepidoptera: Tortricidae: Olethreutinae.     

Dynamic mechanical properties of crosslinked polyisoprene under deformation

Summary Molecular motions of elastomers under deformations were observed through dynamic mechanical measurements. Composite master curves of dynamic moduli E and E and loss tangent tan over a wide range of frequency and in a state of elongation were obtained by the time-temperature superposition procedure. It is found that both moduli increase with strain, . The slope of the dispersion curve of E become more gradual with the increase in , while that of E is almost unchanged. The increment of E is generally larger than that of E, which does not agree with the N. W. Tschoegl prediction, E ^* ()=f() E _o ^* (), where E ^* () and E _o ^* () are complex moduli at the strain of and O, respectively, and f() is the function of only . The difference in the strain dependence of E from E was found to correspond to the strain dependence of the equilibrium modulus.     

Studies concerning charged nickel hydroxide electrodes I. Measurement of reversible potentials

Reversible potentials (E _R) have been measured for nickel hydroxide/oxyhydroxide couples over a range of KOH concentrations from 0·01–10 M. It is shown that the couples derived from the parent- and-Ni(OH)₂ systems can be distinguished by the relative change in KOH level on oxidation and reduction. In the case of couples derived from the-class of materials a dependence of 0·470 moles of KOH per 2e change is found compared with 0·102 moles of KOH per 2e change for the-class of materials. Couples derived from the- and-Ni(OH)₂ systems can be encountered in a series of activated and de-activated forms having a range of formal potentialsE ₀ . Activated. and de-activated-Ni(OH)₂/-NiOOH couples are found to lie in the range 0·443–0·470 V whilst-Ni(OH)₂/-NiOOH couples lie in the range 0·392–0·440 V w.r.t. Hg/HgO/KOH. It is demonstrated for de-activated,-Ni(OH)₂/-NiOOH couples thatE _R is independent of the degree of oxidation of the nickel cation between states of charge of 25% and 70%. SimilarlyE _R is constant for states of charge between 12% and 60% for activated-Ni(OH)₂/-NiOOH couples. The constant potential regions are considered to be derived from heterogeneous equilibria between pairs of co-existing phases both containing nickel in upper and lower states of oxidation. Differences inE ₀ between the activated and de-activated couples are considered to be related to the degree of order/disorder in the crystal lattice.     

Preparation of poly(alkylvinylether)s for nonlinear optical applications

Summary 3,5-Dimethoxy-4-(2-vinyloxyethoxy)-4-nitrostilbene 2 and 3,5-dimethoxy-4-(2-vinyloxyethoxy)-2,4-dinitrostilbene 5 were prepared by the reactions of 2-iodoethyl vinyl ether with 3,5-dimethoxy-4-hydroxy-4-dinitrostilbene 1 and 3,5-dimethoxy-4-hydroxy-2,4-dinitrostilbene 4, respectively. Monomers 2 and 5 were polymerized with cationic initiators to obtain polymers with the NLO-phores 3,5-dimethoxy-4-oxy-4-nitrostilbene and 3,5-dimethoxy-4-oxy-2,4-nitrostilbene in the side chain. The resulting polymer 3 and 6 were soluble in DMSO and DMF. The inherent viscosities of polymers were in the range of 0.28–0.33 dL/g in DMSO. Polymers 3 and 6 showed good thermal stabilities in their TGA thermograms, and the T_g values from DSC thermograms were in the range of 81–87°C.     

Condensation polymerization of α,α′-dimethoxycarbonyl-p-xylylenedicyanide (α,α’) and oxidation to a quinodimethane polymer

Summary , -di(methoxycarbonyl)-p-xylylenedicyanide and oxydiethanol were treated with Ti(OBu)₄ to produce a linear soluble polyester. Long reaction times led to the formation of an insoluble cross-linked polymer by reaction of the cyano groups.Treatment of the soluble polyester with N-cholrosuccinimide and Et₃N resulted in oxidation to a quinodimethane polymer.     

Studies on electrical conductivity of gamma irradiated polyaniline

Summary de electrical conductivity at surface of -irradiated polyaniline (PAn) has been studied. EPR spectroscopic results indicate that the variation of spin concentration is consistent with the increase of _de. Electrical conductivity (_de) versus temperature (T) characteristics of unirradiated and irradiated PAn were performed, which demonstrate that the unirradiated curve can fit to ln_deT₁, while the irradiated curve fit to ln_deT_1/4.     

Convective Regime of Filtration Combustion of Energetic Materials in a Cocurrent Flow of Their Combustion Products

The convective regime of filtration combustion of energetic materials in a cocurrent flow of their combustion products is studied using a model with extremely simplified kinetics and heat transfer, which shows instability of the process. It is shown that the more accurate twotemperature model describes a steadystate regime. In this regime, the gas temperature on the hot boundary of the heating zone is well below the combustion temperature, and the solidphase temperature is well below the temperature proposed in recent studies on this topic. It is pointed out that the twotemperature approach is unjustified and intragranular nonisothermicity must be taken into account for convective regimes. It is shown that the threetemperature model, which takes into account this effect, does not give a stable steadystate solution.     

Preparation of crimped synthetic fibres directly in the spinning process

Conclusions In the preparation of crimped polyamide yarns without the use of texturing devices, it has been found that in yarns of complex profile, of the head-tail type, the two parts of the yarn cross-section interact in accordance with the bimetallic plate rule. The crimp can be described satisfactorily by the Brand-Backer equation.Dependences of the degree of crimp on the ratio of the head and tail lengths, birefringence, and spinning speed have been obtained for selected variants of yarn profile; this makes it possible to find an optimum regime for yarn preparation.Translated from Khimicheskie Volokna, No. 3, pp. 32–33, May–June, 1985.     

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.     

The electrochemical properties of polyaniline derivatives: poly(4,4′-diphenylamine methylenes) and poly(4,4′-diphenylimine methines)

Summary The electrochemical properties of poly(4,4-diphenylamine methylenes) and poly(4,4-diphenylimine methines) were investigated by cyclic voltammetry. A dehydrogenation reaction occured when poly(4,4-diphenylamine methylenes) underwent a electrochemical reaction and transformed to poly(4,4-diphenylimine methines). The fully oxidized poly(4,4-diphenylimine methines) had the electrochemical band gaps of 1.60–1.72 eV, which were found to significantly smaller than those of the fully reduced poly(4,4-diphenylamine methylenes).     

Stress and recovery maxima in LDPE melt elongation

Summary By means of a new tensile rheometer for polymer melts, stress-strain curves () and the elastic recovery _R() of a low density polyethylene melt were measured up to total strains =7, i.e. stretch =1097, at 150°C and two strain rates, =0.03 and 0.1 s^–1. Tensile tests up to very high strains e give relevant results only if the test performance is characterized by quality parameters which are defined and given in this paper. The test results show a maximum in a as well as in _R at about =5.5. Hence, in the range of investigated, a rheologically steady-state of flow does not exist.