Laboratory evaluation of diatomaceous earths, when applied as dry dust and slurries to wooden surfaces, against stored-product insect and mite pests

The efficacy of Silico-sec^® and Diasecticide^™ applied as dry dust and slurry applications to wooden surfaces was assessed in the laboratory against adult Sitophilus granarius, and Lepidoglyphus destructor and against larvae of Ephestia kuehniella. Wood was used as the test substrate as it was considered to present a realistic challenge to efficacy due to its 3-dimensional structure. Against the insects, doses of 10 g/m² Silico-sec^® and 20 g/m² Diasecticide^™ were evaluated. Against the mite 1 and 3 g/m² of the respective Silico-sec^® and Diasecticide^™ dry dusts and 20 g/m² of the slurries were assessed. The effects on the insects and mites were assessed one day, 4 weeks and 12 weeks after treatment of the wood. Mortalities were evaluated after exposure times of 24 h and 7 days for the mite and insects, respectively, at conditions of 15 °C and 80% r.h., chosen to represent typical UK conditions after harvest. Of the four treatments, the Silico-sec^® dry dust was the most effective against all the pest species, producing 80-95, 100 and 93-100% mean mortalities of S. granarius, E. kuehniella and L. destructor, respectively, over the 12-week experimental period. The Diasecticide^™ dry dust produced <11, >99 and 68-93% mortalities of the respective species. The slurry treatments were less effective than the dry dusts with the Silico-sec^® slurry producing 29-46, 83-97 and <8% mortalities of the respective species and the Diasecticide^™ slurry being ineffective against S. granarius and L. destructor and producing 34-61% mortality of E. kuehniella. This study built on information gained from preliminary work and assessed DEs against tolerant pests on a surface where control was expected to be difficult, in order to provide dose recommendations which would encompass a range of infestation situations in the field.     

Organic carbon-water concentration quotients (II(SOC)S and pi(poc)S): measuring apparent chemical disequilibria and exploring the impact of black carbon in Lake Michigan

Chemical concentration quotients measured between water and total organic carbon (TOC) in sediment (II(SOC)) or suspended particulates (pi(poc)) in southern Lake Michigan reveal up to 2 orders of magnitude differences for polychlorinated biphenyl (PCB), dibenzo-p-dioxin (PCDD), dibenzofuran (PCDF), and polycyclic aromatic hydrocarbon (PAH) compounds with similar octanol-water partition coefficients (K(ow)S). Apparent disequilibria for PAHs, PCDDs, and PCDFs, determined as measured II(SOC)S or pi(poc)S divided by their organic carbon equilibrium partitioning values, are significantly greater than disequilibria of PCBs with similar K(ow)S. Apparent disequilibria, when adjusted for black carbon content by using published black carbon nonlinear partition coefficients (K(f,bc)S) and a Freundlich exponent (n(f)) value = 0.7, still exceed equilibrium predictions for the PAHs, PCBs, and PCDDs but with the PCDF disequilibria uniquely below equilibrium. While Monte Carlo analysis of all the variables associated with the black carbon adjusted disequilibria provides wide confidence intervals for individual chemicals, the large class disequilibria differences between PAHs and PCDFs with respect to the PCBs and PCDDs are highly significant. Use of the PCDD K(f,bc)S for calculating both the PCDF and PCDD disequilibria eliminates their extreme divergence. On the basis of the complexity of carbonaceous geosorbent effects and the apparent variable degrees of chemical sequestration in particles, the disequilibria can be adjusted by chemical class to meet expected near equilibrium conditions between suspended particles and water in the hypolimnion. Although these adjustments to the disequilibria calculations produce consistent and plausible values, the complexities of variable carbonaceous geosorbent affinities for these chemicals in Lake Michigan presently favor use of measured, rather than a priori modeled, steady-state total organic carbon-water concentration quotients indexed to TOC as biogenic organic carbon.     

Prompt Shock Initiation of Cased Explosives by Projectile Impact

Experimental results often show that a prompt shock response to projectile impact can be experienced by even relatively heavily cased explosives. This paper will discuss the predictive criteria that can be applied in such circumstances, and in particular will explore the different mechanisms which are present for rod and sphere impacts. Predicted initiation thresholds are shown to give good comparisons with experimental results, using, at most, two empirical shock sensitivity constants obtained from impacts of the uncased explosive.     

Reinvestigation of the antioxidant properties of conjugated linoleic acid

Despite repeated suggestions that antioxidant activity of conjugated linoleic acid (CLA), a collective of conjugated dienoic isomers of linoleic acid, underlies its reported anticarcinogenic and antiatherosclerotic effects, the antioxidant properties of CLA remain ill-defined. Therefore, this study was undertaken to gain more insight into the mechanism of potential CLA antioxidant activity. It was tested whether CLA could protect membranes composed of 1-palmitoyl-2-linoleoyl phosphatidylcholine (PLPC) from oxidative modification under conditions of metal ion-dependent or-independent oxidative stress. Progress of oxidation was determined by direct spectrophotometric measurement of conjugated diene formation and by gas chromatographic/mass spectrometric analysis of fatty acids. The oxidative susceptibility of CLA was higher than that of linoleic acid, and comparable to arachidonic acid. When oxidation of PLPC (1.0 mM) was initiated using the lipid-soluble 2,2′-azobis(2,4-dimethylvaleronitrile) or the water-soluble 2,2′-azobis(2-amidinopropane) hydrochloride, the radical scavengers vitamin E and butylated hydroxytoluene (BHT) at 0.75 μM efficiently inhibited PLPC oxidation, as evident from a clear lagphase. In contrast, 0.75 μM CLA did not have any significant effect on PLPC oxidation. Inhibition of PLPC oxidation by higher concentrations of CLA appeared due to competition, not to an antioxidant effect. When oxidation of PLPC was initiated by hydrogen peroxide/Fe²⁺ (500 μM/0.05–20 μM), both vitamin E (1 μM) and ethylene glycol-bis(aminoethyl ether) tetraacetic acid (50 μM) efficiently inhibited PLPC oxidation. However, CLA (1–50 μM) did not show a clear protective effect under any of the conditions tested. We conclude that CLA, under these test conditions, does not act as an efficient radical scavenger in any way comparable to vitamin E or BHT. CLA also does not appear to be converted into a metal chelator under metal-ion dependent oxidative stress, as had previously been suggested. On the basis of our observations, a role for CLA as an antioxidant does not seem plausible.     

Alumina Agglomerate Effects on Toughness-Curve Behavior of Alumina–Mullite Composites

Toughness-curve ( T -curve) behavior of composites of spherical, polycrystalline, coarse-grained, alumina agglomerates dispersed throughout a constant-toughness, fine-grained, 50–50 vol% alumina–mullite matrix has been evaluated as a function of agglomerate content for the range 15 to 45 vol%. T -curve behavior was evaluated using the indentation-strength method. Increasing alumina agglomerate content resulted in a progressive increase of large indentation load strengths with negligible change of plateau strength levels at small indentation loads. This behavior is consistent with underlying T -curves that rise to greater values and are shifted toward longer crack lengths with increasing agglomerate content, suggesting that both bridge spacing and bridge potency increase with increasing agglomerate content over the range tested. The proposed relationships between bridge spacing and agglomerate content, and bridge potency and agglomerate content, are rationalized in terms of residual stress considerations. The indentation-strength data also demonstrated that the composite containing the greatest alumina agglomerate content, 45 vol%, exhibited the greatest flaw tolerance.     

CFD analysis of low temperature water gas shift reactor

In the design of water gas shift reactors, the performance of catalysts is not known a priori and hence having a general kinetic expression will be of much help. Computational Fluid Dynamic study was carried out to investigate the performance of a packed bed reactor for different feed compositions using five commonly used types of macro kinetic models. User Defined Functions were developed for the reaction rate to predict the CO conversion in the reactor. The effects of temperature and time factor on CO conversion were studied. The Langmuir-Hinshelwood model gave the best prediction for H₂ rich mixtures. The Temkin model was better for higher CO concentrations, whereas the other models gave large deviations for the fixed bed reactor.     

CFD analysis of water gas shift membrane reactor

Fuel cell based modular power generation can be achieved by miniaturization and process intensification of equipments in the process. Fuel cells require hydrogen rich gas which can be generated through reforming and water gas shift reaction. The water gas shift reactor being kinetically limited occupies more volume to achieve the required CO conversion. A membrane reactor integrates the reaction and hydrogen separation stages and hence reduces the volume requirement. Computational Fluid Dynamics offers virtual prototyping of the reactor and thus helps in design, optimization and scale up of reactors. In this study customized User Defined Functions (UDFs) were developed to analyze the performance of low temperature water gas shift membrane reactor. The models were validated using literature data for the parameters – synthesis gas compositions, time factor, sweep flow rate and steam to CO ratio. The effect of all these parameters on the reactor was analyzed for CO conversion, H₂ recovery, DaPe, concentration polarization, concentration profiles and conversion index. The simulations have showed that the UDFs developed were capable of simulating the membrane reactor and this can be used for the design and optimization of the membrane reactor for any process conditions.     

Efficiency of 4,4′‐bis(N,N‐diethylamino) benzophenone for the polymerization of dimethacrylate resins in thick sections

The efficiency of 4,4′‐bis(N,N‐diethylamino)benzophenone (DEABP) for the polymerization of dimethacrylate monomers in thick sections ( 1 – 2 mm) was studied. DEABP (λ_max = 365 nm) represents a complete initiating system as it contains both ketone and amine functional groups. During irradiation, DEABP photobleaches at a fast rate causing deeper penetration of light through the underlying layers, but the photoinitiation efficiency (rate of polymerization per photon absorption rate) is relatively poor. As a result, irradiation of methacrylate monomers at 365 nm results in a slow average polymerization rate and a reduced monomer conversion for thick sections due to the light attenuation caused by the high absorptivity of DEABP and photolysis products. These results highlight the inherent interlinking of light attenuation and photobleaching rate in polymerization of thick sections. Copyright © 2011 Society of Chemical Industry