SOME PHYSICAL PROPERTIES OF CHEMICAL STONEWARE BODIES1

Crushing, transverse and impact strength, thermal expansion, resistance to heat shock, and elasticity were determined for nine commercial chemical stoneware bodies. Although the thermal expansions were not widely different, great variations were obtained for the elasticity and crushing strength values of the various bodies. The elasticity and crushing strength of the more porous bodies were distinctly less than for the more vitreous bodies. The method of making and interpreting the impact test is discussed in detail.     

Some new relationships between temperature variations and sunspot cycles—2. Short-period variations

It is shown analytically that if f₀ represents the frequency of the 11-year sunspot cycle or that of the 22-year sunspot cycle or that of the 35- to 40-year sunspot cycle or that of the seasonal cycle, then large heat/temperature oscillations should exist in the surface–atmosphere system (SAS) at frequencies , , and 2f₀. Also if f₀ represents the frequency of the seasonal cycle alone, then large heat/temperature oscillations should exist in the SAS not only at the frequencies listed above but also at the additional frequencies and . Actual existence of heat/temperature oscillations in the SAS at the frequencies given above has been amply verified by means of past temperature records. Furthermore, we illustratively show that both the 11-year sunspot cycle and corresponding heat/temperature oscillations in the SAS at a period of 11 years maintain approximately stable phase relationships with each other as long as each of the latter oscillations steadily keeps to one amplitude–modulation state. The phase relationship may change if the heat/temperature oscillation involved switches into a different amplitude–modulation state. One of the spin-offs of the analysis reported herein is a realisation that the quasi-biennial oscillation is apparently composed of individual components at periods , 2 and 3 years.     

SOME PHYSICAL PROPERTIES OF ARTIFICIAL ALUMINOUS ABRASIVES1

Specimens representing six different bond compositions in soft, medium, and hard grades of artificial aluminous grinding wheels were tested for various physical properties such as hardness, elasticity, expansion, mechanical endurance, impact strength, etc. It was found that the expansion of present commercial grinding wheels and abrasive bonds is much less than that of artificial corundum. The strength of the wheels increases greatly with increasing percentages of bond. The methods of making the various physical determinations are given along with their interpretation.     

Synthesis and Biological Evaluation of Novel Epothilone B Side Chain Analogues

The design, synthesis, and biological evaluation of a series of epothilone analogues with novel side chains equipped with an amino group are described. Their design facilitates potential conjugation to selective drug delivery systems such as antibodies. Their synthesis proceeded efficiently via Stille coupling of a readily available vinyl iodide and heterocyclic stannanes. Cytotoxicity studies and tubulin binding assays revealed two of these analogues to be more potent than epothilones A–D and the anticancer agent ixabepilone, currently in clinical use.     

Fusion intermediates of HIV-1 gp41 as targets for antibody production: design, synthesis, and HR1-HR2 complex purification and characterization of generated antibodies

The objective of this project was to study the interaction between HR1 and HR2, the stability of the complex formed, and to characterize the antibodies produced against monomeric HR1 and HR2 peptides as well as the HR1-HR2 complex. In this work, HR1 was mimicked by peptide N36, and HR2 was mimicked by peptide C34L and its analogues C34M2, C34M3, and C34D. Whereas C34M2 and C34M3 are partially composed of D-amino acids, C34D has same sequence as C34L, but is assembled entirely of D-amino acids. Using CD analysis, SPR assays, and gel filtration chromatography, we demonstrate the physical interaction between N36 and C34L and its analogues C34M2 and C34M3, but not C34D. We show that the HR1-HR2 complex is formed rapidly (<1?min) and remains stable, as demonstrated by its inability, in contrast to each free peptide, to inhibit the formation of syncytia. To generate antibodies with predetermined specificity against the transiently exposed intermediate that corresponds to the six-helix bundle structure, purified preformed HR1-HR2 complex was used, in parallel with monomeric HR1 and HR2 peptides, as immunogens in mice. Although the produced antibodies recognize total HIV-1 envelope glycoproteins in ELISA, they are unable to neutralize HIV-1-mediated fusion at 37?°C. However, if the incubation with these antibodies is carried out at 27?°C, a temperature that allows stabilization of the transient intermediate complex, anti-peptide antibodies are able to bind their corresponding domains in HeLa cells expressing HIV-1 gp41 in co-culture with HeLa CD4-CCR5/CXCR4 during the dynamic mechanism of membrane fusion. In agreement with the latter results, these antibodies, if previously incubated for 2?h at 27?°C, are able to strongly neutralize HIV-1 entry by membrane fusion, as shown by their ability to block the formation of syncytia.     

The influence of oxidation reduction potential and water treatment processes on quartz lamp sleeve fouling in ultraviolet disinfection reactors

Ultraviolet (UV) disinfection systems are incorporated into drinking water production facilities because of their broad-spectrum antimicrobial capabilities, and the minimal disinfection by-product formation that generally accompanies their use. Selection of an optimal location for a UV system within a drinking water treatment facility depends on many factors; a potentially important consideration is the effect of system location on operation and maintenance issues, including the potential for fouling of quartz surfaces. To examine the effect of system location on fouling, experiments were conducted at a groundwater treatment facility, wherein aeration, chlorination, and sand filtration were applied sequentially for treatment. In this facility, access to the water stream was available prior to and following each of the treatment steps. Therefore, it was possible to examine the effects of each of these unit operations on fouling dynamics within a UV system. Results indicated zero-order formation kinetics for the fouling reactions at all locations. Increases in oxidation reduction potential, caused by water treatment steps such as aeration and chlorination, increased the rate of sleeve fouling and the rate of irradiance loss within the reactor. Analysis of metals in the sleeve foulant showed that calcium and iron predominate, and relative comparisons of foulant composition to water chemistry highlighted a high affinity for incorporation into the foulant matrix for both iron and manganese, particularly after oxidizing treatment steps. Fouling behavior was observed to be in qualitative agreement with representations of the degree of saturation, relative to the metal:ligand combinations that are believed to comprise a large fraction of the foulants that accumulate on the surfaces of quartz jackets in UV systems used to treat water.     

Synthesis of linear aliphatic polycarbonate macroglycols using dimethylcarbonate

A series of linear aliphatic polycarbonate polyols were synthesized using dimethylcarbonate and a linear alkane diol or specific combinations of linear alkane diols. Polyol synthesis was carried out in a two‐stage process using dimethylcarbonate and a linear alkane diol to prepare a series of homopolymer polycarbonate polyols. Polyol grades were characterized using Fourier transform infrared spectroscopy, gel permeation chromatography, and differential scanning calorimetery techniques. Suitable reaction conditions were developed to yield polycarbonate polyols of number average molecular weight between 700 and 1700. The crystallinity of the polycarbonate polyols was shown to reduce as the molecular weight of the alkane diols used in the polycarbonate synthesis was increased. These polymers offer the potential for use in the synthesis of ether free polyurethane elastomers for biomedical applications. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009