Elevated expression of epidermal ornithine decarboxylase mRNA in scleroderma

Using in situ hybridization techniques, we examined the expression of ornithine decarboxylase (ODC) mRNA in the skin of five patients with systemic sclerosis (SSc) and five normal controls. Sections treated with an anti-sense probe showed concentrated grains exclusively in the epidermis of SSc patients, but not in that of normal controls. Because our subcloned anti-sense probe specifically hybridizes with ODC mRNA, these findings indicate that the expression of ODC mRNA is elevated in SSc epidermis. Possibly polyamines have an important part to play in the skin changes of SSc.     

Large magnetoresistivity of sputtered Al-(O or N)-Bi alloys

Application of the sputtering technique to (Al₂O₃)_xBi_100–x and (AIN)_x Bi_100–x (x = 0 to 100%) has been found to result in the formation of a duplex material consisting of hexagonal bismuth particles dispersed finely and homogeneously in amorphous Al_xO_y and Al_xN_y matrices. The particle size and interparticle distance of the bismuth phase were about 5 to 140nm and 5 to 35 nm. The duplex alloys have high electrical resistivities ranging from 1.82 × 10³ to 3.16 × 10⁵ cm combined with a negative temperature-dependent resistivity of 148 to 342% of ₂₇₃. Furthermore, all the Al-O-Bi and Al-N-Bi alloys have been found to exhibit a positive magnetoresistive change and the maximum value, (H), at 4.2 K and 7.5T reaches 5.85 × 10⁴ cm for (Al-O)_65.7Bi_34.3 and 1.99 × 10⁵ cm for (Al-N)_69.7 Bi_30.3. The large magnetoresistivities are probably due to the unique sputtered structure consisting of metallic bismuth particles with a long mean free path of electrons embedded finely and homogeneously in amorphous Al_xO_y or Al_xN_y matrix, resulting in the large difference of the relaxation times (different mobilities) of electron carriers. It has thus been demonstrated that the oxide- or nitride-based composite materials exhibiting large magnetoresistivities, which cannot be achieved in metallic composite materials, are obtained by sputtering simultaneously Al₂O₃ or AIN and bismuth which is immiscible to aluminium.     

Co-crosslinking blend of incompatible polymers VI: Poly(vinyl chloride) toughened with polyethylene via a co-crosslinking technique

A binary blend which consists of two incompatible polymers such as poly(vinyl chloride) and polyethylene has been performed through a partial co-crosslinking reaction with peroxide to give a co-crosslinked blend with a uniform dispersion of small polyethylene particles and with an improved mechanical property. The results are obtained through the formation of a co-crosslinked product which acts as a potential solid phase dispersant as well as a well-bonded reinforcing interlayer on polyethylene particles uniformly dispersed in poly(vinyl chloride) matrix. The resulting blends (PVC/PE=10/90 wt) give carbon spherules of 0.5 to 1m diameter through pressure-carbonization at 650° C for 1 h.     

High-field superconductivity in Al-O-Pb and Al-O-Pb-Bi sputtered films

The sputter-quenched Al _x O _y alloys containing lead and bismuth elements, which are insoluble to aluminium; have been found to exhibit a remarkably enhanced upper critical field,H _c2, which is higher by about 6 to 66 times than those of pure lead metal and Pb₆₀Bi₄₀ alloy. The sputtered structure consists of amorphous Al _x O _y and f c c lead or h c p (lead-bismuth) phases. The lead and phases disperse homogeneously in the amorphous matrix and their particle sizes and interparticle distances are about 10 to 20 nm and 5 to 20 nm, respectively, for lead and particles. The superconducting transition temperature,T _c, upper critical magnetic field,H _c2, at 4.3 K, and residual resistivity at 10 K are 7.74 K, 3.3 T and 2.09 × 105cm, respectively, for (Al-O)_92.8 Pb_7.2 and 7.45 K, 8.2 T and 1.70 × 106 cm, respectively, for (Al-O)_86.2(Pb_0.6 Bi_0.4)_13.8. The remarkable enhancement ofH _c2 is interpreted as being mainly due to a remarkable decrease of the coherence length resulting from a large reduction of the effective mean free path of electrons. Additionally, the fluxoid pinning force under applied field has also been markedly enhanced for the duplex structure films than for sputtered lead film, probably because of the change of the dispersed lead phase into a type-II superconductor and an effective fluxoid pinning action at the interface between Al _x O _y and fine lead particles.     

PbTiO3–PbO–SiO2 Glass-Ceramic Thin Film by a Sol–Gel Process

PbTiO₃(PT)-PbO-SiO₂ glass-ceramic thin films were pro-duced by a sol-gel process. The crystallization of PT oc-curred at ∼700°C and was higher than that in PT-PbO-B₂ O₃ sol-gel glass-ceramics. A pinhole-free thin film was obtained by a rapid thermal annealing process when the designed glass-forming phase content in the thin film was >24 vol%. The measured dielectric constants of the films fairly agreed with the predicted values, based on a parallel mixing model. The dielectric constant was 219 and the di-electric loss was 0.04 in the 0.6PT-0.4(PbO-SiO₂) film that was fired at 700°C.     

New amphoteric surfactants containing a phosphoric acid group: I. syntheses and physicochemical properties of sodium 2-(n-2-hydroxyalkyl-n-methylamino)ethyl hydrogen phosphate

A series of new amphoteric surfactants having a phosphoric acid group, a tertiary amino group and a 2-hydroxyalkyl group, sodium 2-(N-2-hydroxyalkyl-N-methyl-amino)ethyl hydrogen phosphates (alkyl: n-tetradecyl, n-hexadecyl, n-octadecyl), were prepared by an addition reaction of 1,2-epoxyalkanes to N-methylaminoethanol, followed by the introduction of a phosphoric acid group and neutralization with sodium hydroxide. The structures of these compounds were confirmed by spectroscopy and elemental analysis. The solubility in solvents, Krafft point, surface tension, critical micelle concentration (CMC), occupation area of the molecule at the surface of aqueous solutions and foaming power were measured. It was shown that a 2-hydroxyethyl group in a long alkyl chain seemed to behave as a hydrophobic part.     

The Roles of 3- and 4-Isopropylbiphenyls in the Isopropylation of Biphenyl over a H-Mordenite

The isopropylation of mixtures of 3- and 4-isopropylbiphenyls (3- and 4-IPBPs) was examined over a dealuminated H-mordenite (HM) to elucidate the role of 3- and 4-IPBPs in the isopropylation of biphenyl (BP). 4-IPBP was consumed much faster than 3-IPBP in all cases. 4-IPBP was an exclusive precursor to diisopropylbiphenyls (DIPBs), particularly 4,4-DIPB, and 4,4-DIPB was found in encapsulated products during the reaction. These results show that 4-IPBP can allow establishment of an active complex with propylene and acid site in HM pores, whereas 3-IPBP cannot. It is concluded that the isopropylation of BP over HM occurs through a reactant selectivity mechanism, and through a restricted transition state mechanism, but not through a product selectivity mechanism.     

The degradation of polystyrene during extrusion

An investigation was made of the magnitude and mechanism of shear degradation of a narrow distribution, high molecular weight (M_w = 670,000) polystyrene. An Instron rheometer was used to perform the extrusion at temperatures from 164° to 250°C. The change in molecular weight distribution was studied by gel permeation chromatography. The maximum shear stress employed was 5.83 kg/cm². It was found that degradation could be induced at high stress at temperatures of 50°C lower than degradation of polystyrene would occur exclusively due to thermal forces. An activation energy for the degradation, calculated at constant shear rate, was +20.2 kcal/mole. The direction and magnitude of this value are consistent with degradation induced through a mechanical reduced activation for thermal degradation.     

1-O-alkyl-2,3-diacylglycerols in the skin surface lipids of the hairless mouse

A neutral lipid class was isolated by thin-layer chromatography from the skin surface lipids of the hairless mouse. The fraction migrated faster than triglycerides and had a migration rate similar to that of diacyl alkanediols (diester wax). Upon deacylation, however, the long-chain diols were identified as 1-alkylglycerol ethers based on their chromatographic properties and on the mass spectra of their nicotinylidene derivatives. Thus, the skin lipid fraction was identified as 1-O-alkyl-diacylglycerol. The alkyl moieties were all saturated and even-numbered and ranged in chainlength from C₁₆ to C₂₂ with 1-O-hexadecylglycerol amounting to 34% of the total glycerol ether moieties. The fatty acids derived from this lipid fraction were mostly monoenoic with chainlengths ranging from C₁₆ to C₂₄. The major acyl component was eicosenoic acid (20∶1) representing 61% of the total fatty acids.     

Polymerization of 2-dibutylamino-1,3,5-triazine-4,6-dithiol on wire during friction process

2-Dibutylamino-1,3,5-triazine-4,6-dithiol (DB) and a mixture of DB and triallylisocyanurate (TAIC) were used as a lubricant during steel wire drawing due to a dry process. DB gave a polymer film with 180 nm in thickness to wire surfaces during the wire drawing. The polymer film had a disulfide structure on the backbone and contained a small amount of DB monomer and olygomer. Molecular weight and polymer weight increased with the drawing rate. The mixture of DB and TAIC gave mainly a three-dimensional polymer film with 225 nm in thickness to wire surfaces during drawing. The polymer film insoluble in THF had mono and disulfide structures and contained a small amount of linear polymer, DB, and TAIC. Such tribological polymerizations are estimated as follows: DB produces dithiyl radicals on a nascent surface formed during drawing and in the presence of oxygen and heat. The dithiyl radicals were polymerized by coupling with each other to give disulfide bonds or added to allyl groups in TAIC to give monosulfide bonds. It is concluded that this technique should be possible to use for unifying metal processing and surface treatment. © 1995 John Wiley & Sons, Inc.