New family of high-resolution ion exchangers for protein and nucleic acid purifications from laboratory to process scales

A new family of polymer-based ion exchangers was tested for the purification of acidic and basic proteins on both the analytical and preparative scales. Protein-Pak HR series packings are available as strong cation (SP) and weak anion (DEAE) exchangers, allowing the development of a purification method regardless of the isoelectric point of protein. Three particle sizes, 8, 15 and 40 microns, are offered in scalable Advanced Purification (AP) glass columns or as bulk packings. The lower back pressures of the 15- and 40-microns packings compared to that of the 8-microns material allow rapid throughput of large volumes without exceeding the pressure limitations of the resin or the column. The capacity of the AP1 (100 mm x 10 mm) glass columns, containing these ion-exchange packings, is comparable to other ion-exchange columns. The resolution of mouse serum, plasmids, and a standard protein mixture was demonstrated and compared with the results obtained with other resin-based ion exchangers of similar particle size. Proteins were purified without significant loss of biological activity or mass.     

Dead Ends and Detours En Route to Total Syntheses of the 1990s A list of abbreviations can be found at the end of the article

From the very beginning organic chemistry and total synthesis have been intimately joined. In fact, one of the first things that freshmen in organic chemistry learn is how to join two molecules together to obtain a more complex one. Of course they still have a long way to go to become fully mature synthetic chemists, but they must have the primary instinct to build molecules, as synthesis is the essence of organic chemistry. With the different points of view that actually coexist in the chemical community about the maturity of the science (art, or both) of organic synthesis, it is clear that nowadays we know how to make almost all of the most complex molecules ever isolated. The primary question is how easy is it to accomplish? For the readers of papers describing the total synthesis of either simple or complex molecules, it appears that the routes followed are, most of the time, smooth and free of troubles. The synthetic scheme written on paper is, apparently, done in the laboratory with few, if any, modifications and these, essentially, seem to be based on finding the optimal experimental conditions to effect the desired reaction. Failures in the planned synthetic scheme to achieve the goal, detours imposed by unexpected reactivity, or the absence of reactivity are almost never discussed, since they may diminish the value of the work reported. This review attempts to look at total synthesis from a different side; it will focus on troubles found during the synthetic work that cause detours from the original synthetic plan, or on the dead ends that eventually may force redesign. From there, the evolution from the original route to the final successful one that achieves the synthetic target will be presented. The syntheses discussed in this paper have been selected because they contain explicit information about the failures of the original synthetic plan, together with the evolution of the final route to the target molecule. Therefore, they contain a lot of useful negative information that may otherwise be lost.     

The application of a252Cf neutron multiplier for routine instrumental neutron activation analysis

The successful application of instrumental neutron activation analysis for routine determinations depends on the ability to produce accurate and precise analytical results in a relatively short time. An important factor in obtaining the desired speed has been the availability of a low-cost, moderate-flux neutron source for on-site use. The²⁵²Cf neutron multiplier (CFX), designed and constructed by Intelcom Rad Tech Corporation of San Diego, California, is a subcritical assembly capable of continuous, stable operation and has provided us with the ability to determine more than 35 elements as major and minor components. The CFX produces a thermal neutron flux of ∼2×10³ n/cm²-sec by a 100-fold multiplication of the neutrons emitted from a 1 mg²⁵²Cf source. Of particular importance in its application at Kodak has been the determination of the halogens Cl, Br, and I, both singly and simultaneously, in various matrices including photographic materials.     

l1 solution of linear inequalities

The numerical solution of a possible inconsistent system oflinear inequalities in the l₁ sense is considered. The non-differentiablel₁ norm minimization problem is approximated by a piecewisequadratic Huber smooth function. A continuation algorithm isdesigned to find an l₁ solution of the inequality system. Inthe case where the linear inequality system is consistent, asolution is obtained by solving any smoothed problem. Otherwise,the algorithm is shown to terminate in a finite number of iterations.We also consider an alternative smoothing scheme which sharessimilar properties with the first one, but results in an improvedcomputational performance of the continuation algorithm on inconsistentsystems. Numerical experiments are conducted to test the efficiencyof the algorithm.