Analysis of disulfoton sulfoxide in chingentsuai by pulsed splitless mass spectrometry using programmed temperature vaporization (PTV) inlet

A peak considered to be due to disulfoton sulfoxide as a metabolite of disulfoton was detected in the analysis of the chingentsuai extraction solution of vegetables by GC-FPD. In the analysis by GC/MS for identification, though the retention time and the mass spectrum were the same as those of the standard, the spectrum was different from MS library data. It appeared that decomposition of disulfoton sulfoxide occurred at the inlet. Therefore, we used a programmed temperature vaporization (PTV) inlet in the pulsed splitless mode to achieve a low inlet temperature and high injection pressure. As a result, the expected mass spectrum of disulfoton sulfoxide was obtained. Under this condition, the peak obtained from chingentsuai was identified as disulfoton sulfoxide. Disulfoton sulfoxide was detected from 2 of 25 chingentsuai samples, at concentrations of 0.66 microg/g and 0.14 microg/g.     

Studies on syntheses and permeabilities of special polymer membranes

Summary An active transport of alkali metal ion through cation exchange membranes was studied under various conditions. This active transport was facilitated by using a greater anion species on an acidic side in a diaphragm cell, in which one side of the solution was adjusted to be acidic and the other side alkaline across the membrane. An active transport fraction of alkali metal ion was in order poly(styrenesulfonate)>benzenesulfonate>Cl^– >I^–>Br^– of anion species on the acidic side. A rate, fraction and period of the active transport of metal ion were significantly influenced by an electric potential gradient in the membrane.     

Transformation of Yttria-Doped Tetragonal ZrO2 Poly crystals by Annealing under Controlled Humidity Conditions

Phase changes on the surface resulting from low-temperature annealing of yttria-doped tetragonal ZrO₂ polycrystals under controlled humidity conditions were investigated at 0.1 to 7350 Pa of water vapor pressure and 100° to 600°C for 1 to 50 h. The tetragonal-to-monoclinic phase transformation was greatly accelerated by increasing water vapor pressure; the transformation rate was first order with respect to the concentration of tetragonal ZrO₂ on the surface of the sample.     

Studies on the ATP3 gene of Saccharomyces cerevisiae: presence of two closely linked copies,ATP3a and ATP3b,on the right arm of chromosome II

In this paper, we present evidence that there are two closely linked copies of the ATP3 gene coding for the gamma subunit of the F(1)F(0)-ATPase complex (EC3.6.1.34) in four laboratory strains of Saccharomyces cerevisiae, even though the yeast genome project has reported that ATP3 is a single-copy gene on chromosome II. We previously reported that the gene dosage (three copies) of ATP1 and ATP2 is coincident with the subunit number of F(1)-alpha and F(1)-beta, but that the gene dosage of ATP3 was not consistent with the subunit stoichiometry of F(1)F(0)-ATPase. By applying long PCR and gene walking analyses, we estimated that the two copies of ATP3 were approximately 20 kb apart, and we designated that which is proximal to the centromere ATP3a, while we named that which is distal ATP3b. The nucleotide sequences of the two copies of ATP3 were identical to the reported sequence in the W303-1A, W303-1B and LL20 strains, while only the DC5 strain had a single base substitution in its ATP3a. With the exception of this substitution, the other nucleotide sequences were identical to the upstream 860 bp and the downstream 150 bp. The differences between ATP3 with the single base substitution (Ser(308) to Phe) and ATP3 without the substitution on the complementation of the ATP3 disruptant and on the maintenance of the mitochondrial DNA were observed, suggesting that Atp3ap and Atp3bp in the DC5 strain might have different functions. However, it should not always be necessary for yeast cells to carry different types of ATP3 because the other three strains carry the same type of ATP3. It was also demonstrated that the disruption of the ATP3 genes basically leads to a loss of wild-type mtDNA, but the stability of the mtDNA is not dependent on the ATP3 alone.     

Impact ionization and Auger recombination at high carrier temperature

We have calculated impact ionization (II) and Auger recombination (AR) lifetimes in hot carrier solar cells (HC-SCs) in operation, and found that these lifetimes are much longer than the average retention times of photo-generated carriers in the cells at an appropriate range of applied voltage, under practical conditions of 500–1000 times-concentrated solar irradiation and carrier thermalization times of several hundred picoseconds. This means that the particle conservation (PC) model, in which II and AR are completely excluded, can be applied to predict the conversion efficiency. In contrast, the PC model does not stand under the ideal condition of the maximally concentrated irradiation and no thermalization of carriers, as previously pointed out.