Determination of bithionol, bromophen, nitroxynil, oxyclozanide, and tribromsalan in milk with liquid chromatography coupled with tandem mass spectrometry

LC/MS/MS was developed to determine the residues of bithionol (BTN), bromofen (BMF), nitroxynil (NTX), oxyclozanide (OCZ), and tribromsalan (TBS) in milk. Samples were extracted with ethyl acetate and cleaned up by liquid-liquid separation with acetonitrile and n-hexane. The compounds were determined by RP-LC using a C18 column with 0.1% formic acid-methanol. Mass spectral acquisition was performed in the negative mode by applying selected-reaction monitoring. The method was validated in milk spiked with these compounds at 5-600 microg/kg; average recoveries were in the range 83.8-97.1%, with RSD values of 1.4-8.0%. The interassay RSDs were less than 11%. The LODs of these compounds in milk were 0.1 microg/kg. The method was applied to 24 raw milk samples. The concentration of these compounds in all samples was lower than the Japanese maximum residue limits. The method is rapid, sensitive, and specific for monitoring residues of BTN, BMF, NTX, OCZ, and TBS in milk.     

A comparative study on acute toxicity of methylarsonic acid,dimethylarsinic acid and trimethylarsine oxide in mice

The acute toxicity of methylarsonic acid, CH₃AsO(OH)₂ (MAA), dimethylarsininc acid, (CH₃)₂AsO(OH) (DMAA), and trimethylarsine oxide, (CH₃)₃AsO (TMAO), were examined in mice with oral administration. The LD₅₀ values of MAA, DMAA and TMAO were 1.8, 1.2 and 10.6 g kg^?1 respectively. The toxicity of MAA and DMAA was very much lower than that for inorganic arsenic compounds. It was shown that TMAO has a similar acute toxicity to arsenobetaine. On the other hand, when the mice were administered 14.4 g kg^?1 of TMAO once only orally, a garlic-like odor (trimethylarsine, (CH₃)₃As) was definitely detectable in the exhalation of the animals by the human olfactory sense within about a few minutes.     

Velocity field after wave breaking

The velocity field in breaking water waves is considered in this paper. A numerical simulation describes in detail the transition from a primary overturning and consequent rebounding jets into a bore front, where the vorticity in the coherent large‐scale eddy structures devolves into turbulence. Spatial changes in the frequency spectra of the kinetic energy and the enstrophy are associated with the production, transport and dissipation of the Reynolds stress and the various wave and turbulent mixing length scales. Mean velocity fields and the wave and kinetic energy in a surf zone are evaluated. Fourier and wavelet spectral analysis is applied to study both the surface elevation and energy changes, and the distinction that must be made between spilling and plunging breakers is clarified in this paper. Copyright © 2002 John Wiley & Sons, Ltd.     

Mechanism of crystallization of enzyme protein thermolysin

The mechanism of crystallization of enzyme protein thermolysin was investigated. The size distribution of thermolysin precipitates was measured by dynamic light scattering during precipitation, and the surface and cross section of the finally obtained precipitate were observed by scanning electron microscopy. The thermolysin precipitates obtained at the initial supersaturation ratio of 8.9 to 164 and pH 7.0 were hexagonal rods having an average size of 9.2×1.5 μm, and were composed of a number of small particles of 15 to 200 nm in diameter. The average size of the small particles was 60 nm in diameter, and the formation of the particles was found to be completed in the early stage of precipitation. Observation of the finally recovered thermolysin precipitate by polarizing microscopy revealed that the precipitate is a crystalline solid. From these data, a possible mechanism of thermolysin crystallization was proposed. The crystallization proceeds through two steps: the first step is the formation of primary particles, and the second step is crystal growth by highly ordered aggregation of the primary particles.     

Overwrite recording on different recording media

A contact printing model is introduced to explain the re-recording dip in overwrite recording. The first signal on a recording medium is transferred to the medium surface, where the second signal increases the susceptibility to transfer the S-1 signal magnetically with opposite phase. The output signal of S-1 will be compensated by the transferred signal, and will be zero, which is supposed to be the re-recording dip. The contact printing model is confirmed by experiments.     

Reflecting a triangle in the plane

We prove that if the three angles of a triangleT in the plane are different from (60°, 60°, 60°), (30°, 30°, 120°), (45°,45°,90°),(30°,60°,90°), then the set of vertices of those triangles which are obtained fromT by repeating ‘edge-reflection’ is everywhere dense in the plane.     

Arranging Solid Balls to Represent a Graph

 By solid balls, we mean a set of balls in R ³ no two of which can penetrate each other. Every finite graph G can be represented by arranging solid balls in the following way: Put red balls in R ³, one for each vertex of G, and connect two red balls by a chain when they correspond to a pair of adjacent vertices of G, where a chain means a finite sequence of blue solid balls in which each consecutive balls are tangent. (We may omit the chain if the two red balls are already tangent.) The ball number b(G) of G is the minimum number of balls (red and blue) necessary to represent G. If we put the balls and chains on a table so that all balls sit on the table, then the minimum number of balls for G is denoted by b _T (G). Among other things, we prove that b(K ₆)=8,b(K ₇)=13 and b _T (K ₅)=8,b _T (K ₆)=14. We also prove that c ₁ n ³<b(K _n )<c ₂ n ³ log n, c ₃ n ⁴ log n<b _T (K _n )<c ₄ n ⁴. Received: March 29, 1999 Final version received: January 17, 2000     

Rh-catalyzed π-facial selective intermolecular hydroacylation of norbornenes

Rh-catalyzed π-facial selective intermolecular hydroacylations of norbornenes with salicylaldehyde have been attained. In the reaction with norbornylene, the exo-hydroacylated product was produced because of steric hindrance. In the case of norbornadiene, the endo-product was obtained because of chelation effect. Lastly, because of chelation and remote substituent effects, the product formed in the reaction of 7-tert-butoxynorbornadiene was the endo,syn-product. Deuterium-labeling experiments revealed that the hydroacylation stereoselectively proceeded via endo- and exo-intermediates.