Characteristics investigation on heat transfer growth of sonochemically synthesized ZnO-DW based nanofluids inside square heat exchanger

Journal of Thermal Analysis and Calorimetry - In recent decades, the growth of heat transfer using nanomaterials in the conventional base fluid has caught the attention of researchers...     

One cannot hear orbifold isotropy type

We show that the isotropy types of the singularities of Riemannian orbifolds are not determined by the Laplace spectrum. Indeed, we construct arbitrarily large families of mutually isospectral orbifolds with different isotropy types. Finally, we show that the corresponding singular strata of two isospectral orbifolds may not be homeomorphic. Received: 6 October 2005     

Acyl vs sulfonyl transfer in N-acyl beta-sultams and 3-oxo-beta-sultams

[reaction: see text] N-Acylsulfonamides usually react with nucleophiles by acyl transfer and C-N bond fission. However, the hydrolysis of N-acyl beta-sultams is a sulfonyl transfer reaction that occurs with S-N fission and opening of the four-membered ring. Similar to other beta-sultams, the N-acyl derivatives are at least 10(6)-fold more reactive than N-acyl sulfonamides. 3-Oxo-beta-sultams are both beta-lactams and beta-sultams but also hydrolyze with preferential S-N bond fission.     

Effect of Dissolved Oxygen Tension and Agitation Rates on Sulfur-Utilizing Autotrophic Denitrification: Batch Tests

The effect of dissolved oxygen (DO) and agitation rate in open and closed reactors was examined for sulfur-utilizing autotrophic denitrification. The reaction rate constants were determined based on a half-order kinetic model. Declining denitrification rate constants obtained for open reactors those of 8.46, 8.03, and 2.18 for 50 mg NO₃ ^?-N/L, while 11.12, 9.14, and 0.12 mg^1/2/L^1/2?h were for 100 mg NO₃ ^?-N/L at agitation speeds of 0, 100, and 200 rpm. In closed reactors, the ever-increasing denitrification rates were 10.13, 22.56, and 37.03, whereas for the same nitrate concentrations and speeds the rates were 13.17, 15.63, and 26.67 mg^1/2/L^1/2?h. The rate constants correlated well (r ² ?=?0.89–0.99) with a half-order kinetic model. In open reactors, high SO₄ ^2?/N ratios (8.02–75.10) while in closed reactors comparatively low SO₄ ^2?/N ratios (6.10–13.39) were obtained. Sulfur oxidation occurred continuously in the presence of DO, resulting in mixed cultures acclimated to sulfur and nitrate. SO₄ ^2? was produced as an end product, which reduced alkalinity and lowered pH over time. Furthermore, DO inhibited sulfur denitrification in open reactors, while agitation in closed reactors increased the rate of denitrification.     

Mechanistic Insights into a Sustainable Mechanochemical Synthesis of Ettringite

Mechanochemistry offers an environmentally benign and facile synthesis method for a variety of cement paste constituents. In addition, these methods can be used to selectively tune the properties of cement components. The mineral ettringite is an important component of cementitious materials and has additional technological potential due to its ion exchange properties. Synthesis of ettringite via mechanochemistry is an environmentally friendly alternative to conventional wet-chemical synthesis established in industry. This contribution explores the mechanism of a two-step mechanochemical synthesis of ettringite, which was previously found to greatly improve the reaction conversion as compared with one-pot synthesis. The crystallinity of Al(OH)₃ was found to decrease during the first stage of this mechanochemical synthesis. This was correlated to a significant decrease in the particle size of Al(OH)₃ in this stage. No other significant changes were found for the other components, suggesting that mechanochemical activation of Al(OH)₃ is responsible for the enhanced formation of ettringite by the two-step approach. The environmentally friendly approach developed for ettringite synthesis offers a versatile synthetic strategy, which can be applied to synthesise further cementitious materials.     

Study of the interfacial charge transfer in bismuth vanadate/reduce graphene oxide (BiVO4/rGO) composite and evaluation of its photocatalytic activity

Research on Chemical Intermediates - We prepared unique BiVO4/reduce graphene oxide (BiVO4/rGO) nanocomposite with enhanced photocatalytic ability by hydrothermal method applying...     

Distance in stratified graphs

A graph G is stratified if its vertex set is partitioned into classes, called strata. If there are k strata, then G is k-stratified. These graphs were introduced to study problems in VLSI design. The strata in a stratified graph are also referred to as color classes. For a color X in a stratified graph G, the X-eccentricity e _X(v) of a vertex v of G is the distance between v and an X-colored vertex furthest from v. The minimum X-eccentricity among the vertices of G is the X-radius rad_X G of G and the maximum X-eccentricity is the X-diameter diam_X G. It is shown that for every three positive integers a, b and k with ab, there exist a k-stratified graph G with rad_X G = a and diam_X G = b. The number s _X denotes the minimum X-eccetricity among the X-colored vertices of G. It is shown that for every integer t with rad_X G t diam_X G, there exist at least one vertex v with e _X(v) = t; while if rad_X G t s _X, then there are at least two such vertices. The X-center C _X(G) is the subgraph induced by those vertices v with e _X(v) = rad_X G and the X-periphery P _X (G) is the subgraph induced by those vertices v with e _X(G) = diam_X G. It is shown that for k-stratified graphs H ₁, H ₂,..., H _k with colors X ₁, X ₂,..., X _k and a positive integer n, there exists a k-stratified graph G such that C X _i(G) H _i (1 ; i ; k1) and for i j. Those k-stratified graphs that are peripheries of k-stratified graphs are characterized. Other distance-related topics in stratified graphs are also discussed.     

Mechanical response of proton beam irradiated nitinol

The present investigation deals with the study of mechanical behavior of proton beam irradiated nitinol at room temperature. The specimens in austenitic phase were irradiated over periods of 15, 30, 45 and 60 min at room temperature using 2 MeV proton beam obtained from Pelletron accelerator. The stress-strain curves of both unirradiated and irradiated specimens were obtained using a universal testing machine at room temperature. The results of the experiment show that an intermediate rhombohedral (R) phase has been introduced between austenite and martensite phase, which resulted in the suppression of direct transformation from austenite to martensite (A-M). Stresses required to start R-phase (σ_RS) and martensitic phase (σ_MS) were observed to decrease with increase in exposure time. The hardness tests of samples before and after irradiation were also carried out using Vickers hardness tester. The comparison reveals that the hardness is higher in irradiated specimens than that of the unirradiated one. The increase in hardness is quite sharp in specimens irradiated for 15 min, which then increases linearly as the exposure time is increased up to 60 min. The generation of R-phase, variations in the transformation stresses σ_RS and σ_MS and increase in hardness of irradiated nitinol may be attributed to lattice disorder and associated changes in crystal structure induced by proton beam irradiation.     

Application of homomorphism to secure image sharing

In this paper, we present a new approach for sharing images between l players by exploiting the additive and multiplicative homomorphic properties of two well-known public key cryptosystems, i.e. RSA and Paillier. Contrary to the traditional schemes, the proposed approach employs secret sharing in a way that limits the influence of the dealer over the protocol and allows each player to participate with the help of his key-image. With the proposed approach, during the encryption step, each player encrypts his own key-image using the dealer's public key. The dealer encrypts the secret-to-be-shared image with the same public key and then, the l encrypted key-images plus the encrypted to-be shared image are multiplied homomorphically to get another encrypted image. After this step, the dealer can safely get a scrambled image which corresponds to the addition or multiplication of the l + 1 original images (l key-images plus the secret image) because of the additive homomorphic property of the Paillier algorithm or multiplicative homomorphic property of the RSA algorithm. When the l players want to extract the secret image, they do not need to use keys and the dealer has no role. Indeed, with our approach, to extract the secret image, the l players need only to subtract their own key-image with no specific order from the scrambled image. Thus, the proposed approach provides an opportunity to use operators like multiplication on encrypted images for the development of a secure privacy preserving protocol in the image domain. We show that it is still possible to extract a visible version of the secret image with only l-1 key-images (when one key-image is missing) or when the l key-images used for the extraction are different from the l original key-images due to a lossy compression for example. Experimental results and security analysis verify and prove that the proposed approach is secure from cryptographic viewpoint.