Synthesis of high-performance superabsorbent glycerol acrylate-cross-linked poly (acrylic acid)

Glycerol acrylate (GA) is synthesised by an acryloylation reaction with acryloyl chloride. An ester was used as a cross-linking agent at varying proportions in the synthesis of poly acrylic acid (PAA). The amount of cross-linking density in the product (GA-PAA) and degree of neutralisation determine the absorbency of the polymer samples. A sample of GA-PAA containing 0.8 % GA was discovered to absorb 395 and 66 g/g of water and saline solution, respectively. Different solvent uptakes were tested with the sample showing varying capacity for different solvents. The temperature of the reaction was maintained at 60 °C and a reaction time of 2½ h. FTIR, TGA, SEM and XRD analyses were used to characterise the products.     

Surface reconstruction and the Debye-Waller factor

A recently developed soft-mode theory of surface reconstruction¹ is used to calculate the surface Debye-Waller factor (SDWF) as a function of temperature near a supposed transition temperature (T₀) between two reconstruction patterns. The soft surface mode gives rise to a sharp decrease in the SDWF as T₀ is approached, suggesting that an examination the LEED Bragg intensities may help verify the soft mode theory.     

Doped semiconductors in an inhomogeneous magnetic field

We show that a potential difference is generated across a semiconductor sample containing free carriers when the sample is in a magnetic field gradient in the direction of the field. A measurement of the potential difference can give direct information concerning the effective mass and effective g-factor of the free carriers.     

Generation of 90-nJ pulses with a 4-MHz repetition-rate Kerr-lens mode-locked Ti:Al(2)O(3) laser operating with net positive and negative intracavity dispersion

We demonstrate the generation of high-energy pulses by using a low-repetition-rate Kerr-lens mode-locked laser. Repetition rates as low as 4 MHz were achieved with a long, multiple-pass cavity and a semiconductor saturable Bragg reflector. The laser generated pulses of 55-fs duration with a pulse energy of 48 nJ when it was mode locked in the net negative dispersion regime. Mode locking in the positive dispersion regime reduces instabilities and enables pulses to have durations of 80 fs and energies as high as 90 nJ. This is, to our knowledge, the highest pulse energy and the lowest repetition rate ever generated directly from a femtosecond laser resonator without cavity dumping.     

Superconductivity in dense MgB2 wires

MgB2 becomes superconducting just below 40 K. Whereas porous polycrystalline samples of MgB2 can be synthesized from boron powders, in this Letter we demonstrate that dense wires of MgB2 can be prepared by exposing boron filaments to Mg vapor. The resulting wires have a diameter of 160 microm, are better than 80% dense, and manifest the full chi = -1/4pi shielding in the superconducting state. Temperature-dependent resistivity measurements indicate that MgB2 is a highly conducting metal in the normal state with rho(40 K) = 0.38 microOmega cm. By using this value, an electronic mean-free path, l approximately 600 A can be estimated, indicating that MgB2 wires are well within the clean limit. Tc, Hc2(T), and Jc data indicate that MgB2 manifests comparable or better superconducting properties in dense wire form than it manifests as a sintered pellet.     

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Transference numbers for anhydrous methanol solutions at 10 and 25°C

Transference numbers are reported for LiCl and NaCl in methanol at 25°C and for NaCl, KCl, and Bu₄NBr in methanol at 10°C. The potentiometric moving-boundary method as developed by Kay and Fratiello was employed to give a precision of about 0.05% and an accuracy of at least 0.1% as indicated by two independent determinations of the conductances of the Cl^– and Br^– ions. The data are extrapolated by the Fuoss-Onsager theory, and the magnitude of the electrophoretic effect is calculated as described by Kay and Dye. The agreement with this theory is quite good at both temperatures, although the å value required in the case of Bu₄NBr is considerably larger than that obtained from conductance data. This agreement contrasts with that obtained for ethanol and acetone solutions where the measured electrophoretic effect is considerably larger than the corresponding calculated values. The importance of this fact in the determination of ion-pair association constants is discussed.     

Infrared spectroscopy of closed s-shell gas-phase M+(N2O)n (M = Li,Al) ion-molecule complexes*

ABSTRACT

We present the results of a combined experimental and computational study of the structures of gas-phase M⁺(N₂O)_n (M?=?Li, Al) complexes. Infrared spectra were recorded in the region of the N₂O asymmetric (N?=?N) stretch using photodissociation spectroscopy employing the inert messenger technique. Unlike in our previous studies on M⁺(N₂O)_n (M?=?Cu, Ag, Au and M?=?Co, Rh, Ir) complexes, N– and O–bound isomers in this case are near isoenergetic and are not distinguished spectroscopically at this resolution. In the case of Li⁺ complexes, there is, however, evidence for the presence of bound N₂ moieties, indicating the presence of inserted, OLi⁺N₂(N₂O)_n–type structures. The weak N₂ band lies to the blue of the signature of molecularly N– and O–bound ligands and is well–reproduced in the simulated spectra of energetically low-lying structures computed from density functional theory. No such inserted isomers are observed in the case of Al⁺(N₂O)_n complexes whose infrared spectra can be understood on the basis of molecularly-bound N₂O ligands. The differences in M⁺(N₂O)_n structures observed for these closed–shell, ns², metal centres relative to other metal cations are discussed in terms of the likely bonding motifs.