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31.
O. F. Shlensky 《Journal of Thermal Analysis and Calorimetry》1993,40(3):941-947
New modifications of a contact heater are suggested for investigating thermal decomposition processes, as well as for determining
kinetic characteristics of substances under conditions of intense heating to a fixed constant temperature.
Zusammenfassung Zur Untersuchung von thermischen Zersetzungsprozessen und der Bestimmung der Reaktionskinetik von Substanzen bei intensivem Erhitzen auf vorgegebene konstante Temperaturen wird eine neue Abart von Kontakterhitzern beschrieben.相似文献
32.
V. Yu. Filinovskii 《Russian Journal of Electrochemistry》2006,42(12):1319-1324
Identity of mathematical problems concerning calculation of the distribution of reactants’ concentrations and the current near the surface of a nonuniform (strip) electrode and distribution of displacements and forces in the case of an elastic layer “antiplane” deformation caused by the punch action. Formulas for calculating the current at a strip electrode are derived for various ratios between the electrode width and the diffusion layer thickness by means of asymptotic methods designed for calculating problems of mechanical contact interactions. It is noted that calculations of the diffusion current for involved activity distributions at the electrode surface may benefit from asymptotic methods of mechanics of contact interactions. 相似文献
33.
Thomas R. Gengenbach Zoran R. Vasic Sheng Li Ronald C. Chatelier Hans J. Griesser 《Plasmas and Polymers》1997,2(2):91-114
The properties and composition of plasma polymer surfaces stored in air can change considerably over time, especially as a
result of oxidative reactions. When plasma polymers contain an element other than O, it is possible to probe for mechanisms
in addition to oxidation that contribute to the aging of the surface. Plasma polymers containing N were fabricated from either
1,3-diaminopropane (DAP),n-heptylamine (nHA), or allylamine (AA), and studied by X-ray photo-electron spectroscopy (XPS) and air/water contact angles
(CA). For each of the plasma polymers, a multiexponential increase in the O/C ratio was observed over time using XPS. The
N/C ratios remained constant (AA) or decreased somewhat (nHA and DAP). In contrast, the trends in CA values differed, declining
for the nHA surfaces, rising for the AA, and changing little for the DAP. Surface roughness, assessed by scanning tunnelling
or atomic force microscopy, did not change over time. The diverse adjustments in the polarity of each surface and the similar
compositional changes between them are reconcilable if the aging of the plasma polymer surface is a manifestation of the superposition
of concurrent oxidative reactions and partial surface reorientation; the former introduce polar groups and the latter transports
then from the surface to deeper regions beyond the CA probe depth but within the XPS analysis depth. These processes vary
between different plasma polymers. Data for the alkylamine plasma polymers is also compared with that for two plasma polymers
fabricated from methanol. The change in composition, but not polarity, of the DAP surface after 4 days of storage demonstrates
the importance of using multiple techniques to characterize the aging of plasma polymer surfaces. 相似文献
34.
The development of all-solid-state potentiometric ion selective electrodes for monitoring of ascorbic acid, by using a screen-printed compatible solid contact is described. The applied methodology is based on the use of PVC membrane modified with some firstly-tested ionophores (triphenyltin(IV)chloride, triphenyltin(IV)hydroxide and palmitoyl-l-ascorbic acid) and a novel one synthesized in our laboratory (dibutyltin(IV) diascorbate). Synthesis protocol and some preliminary identification studies are given. A conductive graphite-based polymer thick film ink was used as an internal solid contact between the graphite electrode and the PVC membrane. The presence and the nature of the solid contact (plain or doped with lanthanum 2,6-dichlorophenolindophenol (DCPI)) seem to enhance the analytical performance of the electrodes in terms of sensitivity, dynamic range, and response time. The analytical performance of the constructed electrodes was evaluated with potentiometry, constant-current chronopotentiometry and electrochemical impedance spectroscopy (EIS). The interference effect of various compounds was also tested. The potential response of the optimized Ph3SnCl-based electrode was linear against ascorbic acid concentration range 0.005-5.0 mM. The applicability of the proposed sensors in real samples was also tested. The detection limit was 0.002 mM ascorbic acid (50 mM phosphate, pH 5 in 50 mM KCl). The slope of the electrodes was super-Nernstian and pH dependent, indicating a mechanism involving a combination of charge transfer and ion exchange processes. Fabrication of screen-printed ascorbate ISEs has also been demonstrated. 相似文献
35.
Electrospraying/electrospinning of poly(γ-stearyl-L-glutamate) (PSLG) was investigated on a series solutions with different concentrations in chloroform. Field emission scanning electron microscopy (FESEM) and attenuated total reflectance Fourier transform infrared spectroscopy (FT-IR/ATR) were used to characterize the morphology and structure of the electrosprayed/electrospun polypeptide mats. It was found that electrospraying of PSLG with concentrations lower than 16 wt% afforded beads, while microfibers could be electrospun at the concentration of 22 wt%. The hydrophobicity of the electrosprayed/electrospun PSLG mats was investigated with static water contact angle (WCA) and tilt angle measurements. It was demonstrated that the superhydrophobic surfaces of PSLG with WCAs and tilt angles in the ranges of 150°-170° and 16.5°-4.2°, respectively, were obtained through electrospraying/electrospinning process. 相似文献
36.
触头用银合金粉末的氧化性能和氧化后的组织结构 总被引:1,自引:0,他引:1
通过热重实验和扫描电子显微等方法,研究了4种触头用银合金粉末的氧化性能及氧化后的组织结构。发现Ag-Sn-RE合金粉末氧化以后,在粉末表层形成一层纯银层,其组织结构理想;它的氧化性能最好,适于制备触头材料。Ag-Sn-RE合金粉末的优良氧化性能与其氧化后理想的组织结构有关。稀土元素可以降低合金粉末的氧化温度,其它影响作用有待于进一步研究。 相似文献
37.
《Surface and interface analysis : SIA》2003,35(8):667-672
The individual and combined adsorption behavior of polyamides and two different silanes to multicomponent glass surfaces was probed with a combination of x‐ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and static contact angle measurements. Samples were analyzed with and without solvent rinsing to separate the weakly bound (physisorbed) and more strongly bound (chemisorbed) species. High‐resolution XPS on N 1s revealed that the polyamides adsorb to the glass surfaces via protonated amine species at the acidic (OH) sites on the glass surface. Angle‐resolved XPS confirmed this by showing that the alkyl portion of the polymer is oriented away from the glass interface. In competitive coadsorption studies it was found that amino‐terminated silanes preferentially adsorb to the glass surface, relegating the polyamide to a physisorbed outer layer. When mercaptoterminated silanes were competitively coadsorbed the polyamide was preferentially adsorbed even when present at a concentration twenty times less than that of the silane. Altogether, this work reveals the strong interaction between surface silanols and amino‐functionalized organics. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
38.
Jin Ho Lee Heoung Woo Kim Pyong Ki Pak Hai Bang Lee 《Journal of polymer science. Part A, Polymer chemistry》1994,32(8):1569-1579
Functional group gradient surfaces where the density of functional groups changes gradually along the sample length were prepared. The functional group (? COOH, ? CONH2, and ? OH group) gradient surfaces were produced by the treatment of low-density PE sheets using a corona with gradually increasing power, followed by the graft copolymerization of acrylic acid and subsequent substitution reaction of carboxylic acid groups to amide or hydroxyl groups. The prepared gradient surfaces were characterized by the measurement of water contact angle, FTIR-ATR, and ESCA. The gradient surfaces prepared can be used to systematically investigate the interactions of biological or other species in terms of the surface functional groups and their density of polymeric materials. © 1994 John Wiley & Sons, Inc. 相似文献
39.
The viscosity of PEG-modified urethane acrylate (PMUA) showed peculiar behavior in the course of soap-free emulsification. Moreover, the viscosity change with added amounts of water was influenced by the reaction molar ratio of polyethylene glycol (PEG). The rate of increase in viscosity slowed and the ratio of increase in viscosity increased as the reaction molar ratio of PEG increased. This peculiar viscosity behavior was due to the microphase separation between hydrophilic and hydrophobic segments of PMUA, and the orientation of polyoxyethylene groups at O/W interface which influenced droplet size of the soap-free PMUA emulsion. The location of polyoxyethylene groups of this resin at O/W interface was confirmed using the adsorption isotherm measurement of PMUA molecules containing polyoxyethylene groups at water/benzene interface. The microphase separation behavior of PMUA between hydrophilic and hydrophobic segments could apply to the preparation of the PMUA gels containing peculiar structure. PMUA gels were prepared using dioxane (UAG) and the swelling behavior of these gels were compared to that of gels prepared using water (UAHG) in the same medium. In the same medium, the swelling behavior of UAHG gels differed from that of UAG gels because of the difference in the microstructure of gel due to the microphase separation between hydrophilic and hydrophobic segments. This phase separation in the course of gelation in water could be confirmed using contact angle measurement. 相似文献
40.
建立了一种同时检测塑料食品接触材料中13种紫外吸收剂的超高效合相色谱法。以甲醇为溶剂对塑料食品接触材料样品进行超声提取,经C18固相萃取柱净化,过0.22 μm有机滤膜,采用超高效合相色谱仪分析。选择ACQUTY UPC2 HSS C18 SB色谱柱(150 mm×3.0 mm,1.8 μm),以超临界二氧化碳为流动相,异丙醇为改性剂进行梯度洗脱,在最优色谱条件下,13种紫外吸收剂能够在4 min内实现有效分离。结果表明,在各自线性范围内,13种紫外吸收剂的线性关系良好,标准曲线相关系数不低于0.9985,检出限(S/N=3)为0.05~0.15 mg/kg,加标回收率为86.8%~115.7%,相对标准偏差为0.73%~5.61%。该方法快速简便,准确可靠,同时大大减少了有机溶剂的消耗,可用于塑料食品接触材料中13种紫外吸收剂的快速检测。 相似文献