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11.
Crosslinked poly(N-isopropylacrylamide) gel was tested on the feasibility for a preparative electrophoretic matrix. Horse heart myoglobin and bovine hemoglobin were well separated on the gel matrix electrophoretically by molecular sieving effect of the gel network. Relative mobilities of those proteins in the gel were larger than those in a crosslinked polyacrylamide gel of the same polymer concentration. After the separation, the protein-containing portion of the gel underwent swelling at 4°C and deswelling at 37°C, alternatively. As a result of the deswelling, each protein was recovered in a discharged solution out of the gel at almost 100% yield. 相似文献
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13.
Masato Matsugi Masakazu Hasegawa Sachina Okamoto Yoshimi Ikeya Yuji Mori 《Tetrahedron letters》2007,48(23):4147-4150
A modified light-fluorous Mukaiyama reagent bearing a C8F17 tag was prepared and examined in ester and amide forming condensation reactions. Following the reactions, the desired product was effectively separated from the fluorous pyridone by-product using a simple fluorous solid phase extraction. 相似文献
14.
Hisatoyo Morinaga Bungo Ochiai Hideharu Mori Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2006,44(12):3778-3786
Natural human hair was modified by the graft polymerization of propylene sulfide in an aqueous medium. The amount of the polymer grafted onto the reduced hair was 0.15–0.19 g on 1.0 g of hair. The grafted polymer was isolated by the hydrolysis of the hair in the polymer‐grafted hair under basic conditions and was confirmed to be poly(propylene sulfide) by 1H NMR, 13C NMR, and Fourier transform infrared spectra. The number‐average molecular weights of the isolated polymers from the grafted products were 10,000–12,000. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3778–3786, 2006 相似文献
15.
Mikaru Ikedo Masanobu Mori Kazumasa Kurachi Wenzhi Hu Kazuhiko Tanaka 《Analytical sciences》2006,22(1):117-121
The selective and simultaneous ion-exclusion chromatography (IEC) with UV-detection on a weakly acidic cation-exchange resin column in the H+ -form (TSKgel Super IC-A/C) was developed and applied for the simultaneous determination of phosphate and silicate ions as the water quality parameters required for optimizing the water-leaching process for ceramics glaze raw materials of natural origin including feldspar, woods-ash, and straw-ash. Phosphate and silicate ions in these water-leaching process water samples were separated selectively from the coexisting anions such as sulfate, chloride, nitrate and carbonate ions, based on the ion-exclusion separation mechanism. They were detected selectively and simultaneously by a postcolumn derivatization with molybdenum-yellow using the UV-detector. Under the optimized separation and detection conditions (eluent, 0-1 mM sulfuric acid; reactant, 10 mM sodium molybdate-25 mM sulfuric acid; detector, UV at 370 nm; temperature, 45 degrees C), the linearity of calibration was in the range 0.1 - 10 ppm for both phosphate and silicate ions, and the detection limits at S/N = 3 were 2.58 ppb for silicate ions and 4.75 ppb for phosphate ions. The effectiveness of this method was demonstrated in practical applications to the water-leaching process for some ceramics glaze raw materials. 相似文献
16.
A wetting/dewetting process was utilized to prepare self-organized organic dye particles of micrometer and submicrometer size.
Near-field scanning optical microscopy successfully identified near-field excited near-field fluorescence from single particles.
The majority of the small particles with diameters around 2 mm or less, however, did not show fluorescence under near-field
observation. In contrast, far-field fluorescence, when excited by a polarized evanescent field, was observed, with the intensity
depending on the excitation polarization, indicating that molecules' transition moment within dye particles was oriented parallel
to the substrate surface. Single particle fluorescence spectrum consistently showed an identical sharp peak with a large redshift,
indicating that the particles were composed of identical dye aggregates similar to J-aggregates. These observations suggest
that the near-field at the probe tip was polarized parallel to the probe axis. Another observation, that molecules were oriented
in a similar direction among adjacent particles, suggests that the dewetting process contributed to the alignment of the molecular
direction among adjacent particles, which further proves that the present specimen was formed by a self-organizing mechanism. 相似文献
17.
Kumita T Sagawa H Auchincloss P Blanis D Bodek A Budd H Eno S Fry CA Harada H Ho YH Kim YK Mori T Olsen SL Shaw NM Sill A Thorndike EH Ueno K Zheng HW Abe K Fujii Y Higashi Y Kim SK Kurihara Y Maki A Nozaki T Omori T Sakai Y Sugimoto Y Takaiwa Y Terada S Walker R Imlay R Kirk P Lim J McNeil RR Metcalf W Myung SS Cheng CP Gu P Li J Li YK Ye MH Zhu YC Abashian A Gotow K Hu KP Low EH Mattson ME Piilonen L Sterner KL Lusin S Rosenfeld C Wang AT Wilson S Frautschi M Kagan H Kass R Trahern CG 《Physical review D: Particles and fields》1990,42(5):1339-1349
18.
Bond IA Budding E Conway MJ Fenton KB Fujii H Fujii Z Fujimoto M Hasegawa H Hayashida N Honda M Hotta N Humble JE Kabe S Kasahara K Kifune T Masaike A Matsubara Y Mitsui K Miura Y Mori M Murakami K Muraki Y Nagano M Nakamura K Nakamura T Norris PM Ohashi Y Okada A Saito T Sakata M Sato H Shibata S Shima M Storey JR Tanimori T Teshima M Torii S Uchino K Watase Y Woodhams MD Yamamoto Y Yock PC Yuda T 《Physical review letters》1988,61(20):2292-2295
19.
20.
The colour development between 4-(2-pyridylazo)-resorcinol(PAR) and osmium(VIII) in the presence of cationic and nonionic surfactants in a weakly acidic medium was more stable and reproducible than in the absence of surfactant (PAR-alone method). An improved spectrophotometric determination of osmium(VIII) with PAR was investigated in the presence of mixed surfactants of N-hexadecyltrimethylammonium chloride (HTAC) and Brij 58 [poly(oxyethylene)lauryl ether] as cationic and nonionic surfactants at pH 6.0-7.2. The calibration graph was linear in the range 0-110 microg/10 ml osmium(VIII), and the apparent molar absorptivity was 2.4 x 10(4) l.mole(-1).cm(-1) with a Sandell sensitivity of 0.0079 microg/cm(2) osmium(VIII). 相似文献