Grain boundary diffusion of Cu in TiN film by X-ray photoelectron spectroscopy

In this study, the grain boundary diffusion of Cu through a TiN layer with columnar structure was investigated by X-ray photoelectron spectroscopy (XPS). It was observed that Cu atoms diffuse from the Cu layer to the surface along the grain boundaries in the TiN layer at elevated temperature. In order to estimate the grain boundary diffusion constants, we used the surface accumulation method. The diffusivity of Cu through TiN layer with columnar structure from 400 °C to 650 °C is D_b≈6×10⁻¹¹exp(−0.29/(k_BT )) cm²/s. Received: 18 May 1999 / Accepted: 8 September 1999 / Published online: 23 February 2000     

Application of nonionic surfactants combining hydrophobic and hydrophilic cholelitholytic solvents on dissolution of gallstones

Application of nonionic surfactants in chemolitholysis was developed to combine two immiscible cholelitholytic solvents, MTBE and EDTA, into a homogeneous solution to increase the efficiency of gallstone dissolution. Eight kinds of Sinopol were employed to investigate and prepare the homogeneous solution, which included MTBE, EDTA (2wt.%) aqueous solution and the Sinopol, thereby, an in vitro study of chemolitholysis was carried out. Three kinds of gallstones were characterized by FTIR and SEM. The dissolution percentage of three kinds of gallstones in the homogeneous (Sinopol mixed) solution was evaluated and a comparison of the average dissolution percentage between these Sinopol mixed solutions and traditional cholelitholytic solvents was made. The composition of gallstones was classified into oil-soluble and water-soluble groups. Furthermore, the hydrophobic and hydrophilic properties of solvents corresponding to oil-soluble and water-soluble gallstone components were analysed and discussed with a phase diagram.     

The Effect of MoO3 Addition to V2O5/Al2O3 Catalysts for the Selective Catalytic Reduction of NO by NH3

The effect of MoO₃ addition to alumina supported vanadia catalysts on the catalytic activity for the selective catlaytic reduction of NO is investigated. Upon the addition of MoO₃, catalytic activity is enhanced and the particle size of V₂O₅ which is shown by the results of XRD and Raman spectroscopy is decreased. The MoO₃-V₂O₅/Al₂O₃ catalyst also exhibits more resistance to SO₂ deactivation than V₂O₅/Al₂O₃ does.     

Soft gluons in logarithmic summations

We demonstrate that all the known single- and double-logarithm summations for a parton distribution function can be unified in the Collins–Soper resummation technique by applying soft approximations appropriate in different kinematic regions to real gluon emissions. Neglecting the gluon longitudinal momentum, we obtain the (double-logarithm) resummation for two-scale QCD processes, and the Balitsky–Fadin–Kuraev–Lipatov (single-logarithm) equation for one-scale processes. Neglecting the transverse momentum, we obtain the threshold (double-logarithm) resummation for two-scale processes, and the Dokshitzer–Gribov–Lipatov–Altarelli–Parisi (single-logarithm) equation for one-scale processes. If we keep the longitudinal and transverse momenta simultaneously, we derive a unified resummation for a large Bjorken variable x, and a unified evolution equation appropriate for both intermediate and small x. Received: 9 March 1999 / Revised version: 12 April 1999 / Published online: 3 August 1999     

Miniemulsion polymerization of styrene with a block copolymer surfactant

A series of miniemulsion systems based on styrene/azobisisobutyronitrile in the presence of poly(methyl methacrylate‐b‐2‐(dimethylamino)ethyl methacrylate) as a surfactant and hexadecane (HD) as a cosurfactant were developed. For comparison, a series of pseudoconventional emulsions also were carried out with the same procedure used for the aforementioned series but without the cosurfactant (HD). Both the droplet size and shelf life were also measured. Experimental results indicate that it is possible to slow the effect of Ostwald ripening and thereby produce a stable miniemulsion with the block copolymer as the surfactant and HD as the cosurfactant. In addition, the extent to which varying the surfactant concentration and copolymer composition could affect both the polymer particle size during the polymerization and the polymerization rate was examined. Variation in the polymer particle sizes during polymerization indicates that droplet and aqueous (micellar or both homogeneous) nucleation occurs in the miniemulsion polymerization. With the same concentration of the surfactant used in the miniemulsion polymerization, the polymerization rates of systems with M₁₂B₃₆ are faster than those of systems with M₁₂B₁₂. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 1818–1827, 2000     

Conjugated vinyl derivatives of chitooligosaccharide: Synthesis and characterization

The introduction of a conjugated vinyl group to chitooligosaccharide (COS) has been easily accomplished by the coupling of glycidyl methacrylate (GMA) to COS in aqueous solution without an additional catalyst. Depolymerization of chitosan was carried out by deaminative cleavage using sodium nitrite. The average degree of polymerization of COS could be controlled by varying the molar ratio of sodium nitrite and the amino group of chitosan. The degree of substitution (percentage), as determined by ¹H NMR, of GMA to COS increased up to 60% at a reaction time of 48 h. The structure of products (COS‐GMAs) were identified by Fourier transform infrared spectroscopy, ¹H NMR, and ¹³C NMR. The resulting COS‐GMAs were readily soluble in neutral water, like the original COS, and exhibited an excellent antimicrobial activity. The reactivity of COS‐GMA was investigated by the reaction with poly(vinyl alcohol) (PVA). The reaction products were found to have a lower crystallinity than PVA because of the introduction of the COS‐GMA units. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 880–887, 2001