A solution of the DGLAP equation for gluon at low x

We obtain a solution of the DGLAP equation for the gluon at low x first by expanding the gluon in a Taylor series and then using the method of characteristics. We test its validity by comparing it with that of Glück, Reya and Vogt. The convergence criteria of the approximation used are also discussed. We also calculate εF ₂(x,Q)²/ε In Q ² using its approximate relations with the gluon distribution at low x. The predictions are then compared with the HERA data.     

Taylor-Galerkin algorithms for viscoelastic flow: Application to a model problem

Coupled and decoupled Taylor-Galerkin algorithms are considered for viscoelastic flow and a model problem—transient startup Poiseuille flow in a channel under a fixed pressure gradient. All algorithms reproduce the steady-state solutions and are stable at high elasticity numbers (E). For a fixed mesh, the coupled and decoupled versions (TGC and TGD) give exceptional time-accuracy at low elasticity numbers [to within O(1%) at E = 1] and reasonable accuracy at high elasticity numbers [to within O(10%) at E = 10, 100]. By definition, the decoupled false-transient scheme (TGF), which uses different time scales for velocity and stress time stepping, provides a poor transient history. Where the main requirement is to compute a steady-state algorithm efficiency is crucial. The TGF scheme attains a steady state between six to eight times faster than does the TGC scheme, and the latter is over twice as fast as the TGD form. © 1994 John Wiley & Sons, Inc.     

The polya-1 property for convex approximation

If f∈L_p[0, 1], let f_p be its best L_p-approximant by convex functions. It is shown that if exists uniformly on closed subintervals of (0,1). This research was partially supported by Grant No. 020-033-58 from the Faculty Research Committee, Idaho State University.     

The synthesis of imidazole-2-thione nucleosides

Ribosylation of the trimethylsilyl derivative ( 1b ) of imidazole-2-thione ( 1a ) using either stannic chloride or silver perchlorate as catalyst resulted in the formation of the acylated derivatives of 1-(β-D-ribofuranosyl)imidazole-2-thione ( 3c ) and 1,3-di-(β-D-ribofuranosyl)imidazole-2-thione ( 4c ) with the latter predominating ( 4c:3c , ca. 2:1 ). The diribosylated nucleoside 4c was shown to be the N,N-disubstituted product rather than the N,S-disubstituted product by ¹H nmr and ¹³C nmr spectroscopy. Employment of the iodine-catalyzed fusion procedure reversed the aforementioned product ratios and provided the monoriboside 3c in excellent yield. When the trimethylsilyl derivative ( 5b ) of 2-methylthioimidazole ( 5a ) was reacted with 2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide ( 2d ) in acetonitrile, the major product was 1,3-di-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-imidazole-2-thione ( 4b ). The formation of 4b in this reaction is thought to arise via the Hilbert-Johnson mechanism.     

Flow-injection determination of sulphite and assay of sulphite oxidase

Sulphite (1–80 × 10^?5 M) in formaldehyde-stabilized solutions is determined by injection into a flowing stream of pH 8.5 phosphate buffer, passing through a mini-column of sulphite oxidase immobilized on controlled-pore glass, with amperometric detection of the hydrogen peroxide produced. Sulphite oxidase (5–100 U l^?) is determined by injection into a flowing stream of formaldehyde-stabilized 2 × 10^?3 M sodium sulphite in pH 8.0 phosphate buffer; hydrogen peroxide is again monitored.