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981.
Temperature coefficients (Deltadelta/DeltaT) of amide chemical shifts of N-acetylglucosamine residues have been measured in a range of oligosaccharides of the important vertebrate polysaccharide hyaluronan. Odd- and even-numbered oligosaccharides with glucuronic acid, Delta-4,5-unsaturated glucuronic acid and N-acetylglucosamine at the termini were investigated. All amide proton temperature coefficients were only slightly less negative (-6.9 to - 9.1 ppb/ degrees C) than those of amide protons in free exchange with water (approximately equal to -11 ppb/ degrees C), indicating an absence of persistent intramolecular hydrogen bonds. With the exception of amide groups in reducing-terminal N-acetylglucosamine rings, all amide proton environments have the same temperature coefficient (-6.9 ppb/ degrees C), irrespective of differences in amide group chemical shifts and (3)J(HH) coupling constants, i.e. they do not sense subtle differences in orientation of the amide group. Amide nitrogen temperature coefficients report the same phenomena but with greater sensitivity. These data provide a set of reference values for temperature coefficients measured in other carbohydrates with acetamido sugars. 相似文献
982.
In this study, a 38 mL monolith with homogeneous porous structure was produced by a single polymerization from glycidyl methacrylate (GMA) and ethylene dimethacrylate (EDMA) in the presence of porogens and an initiator. The uniform temperature distribution within the reaction system was achieved by adding reactant mixture continuously and enhancing the heat transfer ability of the polymerization system. Homogeneous porous structure in the monolith was proved by SEM and the pore size distribution profiles measured by mercury intrusion porosimetry. Experimental results from proteins separation indicated that the dynamic capacity and resolution of radial flow monolithic column were independent of flow rates. Furthermore, the pressure drop on the column was linearly dependent on the flow rate and did not exceed 1.7 MPa even at a flow rate of 50 mL/min, which proved that the prepared monolith could be used in the quick separation and preparation of biopolymers. 相似文献
983.
Interface Engineering of a CoOx/Ta3N5 Photocatalyst for Unprecedented Water Oxidation Performance under Visible‐Light‐Irradiation 下载免费PDF全文
Shanshan Chen Dr. Shuai Shen Guiji Liu Yu Qi Prof. Fuxiang Zhang Prof. Can Li 《Angewandte Chemie (International ed. in English)》2015,54(10):3047-3051
Cocatalysts have been extensively used to promote water oxidation efficiency in solar‐to‐chemical energy conversion, but the influence of interface compatibility between semiconductor and cocatalyst has been rarely addressed. Here we demonstrate a feasible strategy of interface wettability modification to enhance water oxidation efficiency of the state‐of‐the‐art CoOx/Ta3N5 system. When the hydrophobic feature of a Ta3N5 semiconductor was modulated to a hydrophilic one by in situ or ex situ surface coating with a magnesia nanolayer (2–5 nm), the interfacial contact between the hydrophilic CoOx cocatalyst and the modified hydrophilic Ta3N5 semiconductor was greatly improved. Consequently, the visible‐light‐driven photocatalytic oxygen evolution rate of the resulting CoOx/MgO(in)–Ta3N5 photocatalyst is ca. 23 times that of the pristine Ta3N5 sample, with a new record (11.3 %) of apparent quantum efficiency (AQE) under 500–600 nm illumination. 相似文献
984.
对氨基苯亚甲基硫代若丹宁固相萃取分离光度法测定环境水和食品样品中的铅 总被引:5,自引:0,他引:5
合成了新试剂对氨基苯亚甲基硫代若丹宁(ABTR),并用红外光谱、核磁共振氢谱和元素分析鉴定其结构。研究了ABTR与铅的显色反应,在pH3.8的HAc NaAc缓冲介质中,吐温80存在下,ABTR与铅反应生成2∶1稳定络合物,该络合物可被WatersSep PakC18小柱固相萃取,小柱上富集的络合物用乙醇洗脱后富集倍数可达50倍,在乙醇介质中,λmax=545nm,体系摩尔吸光系数ε=1.09×105L·mol-1·cm-1。铅量在0.05~4.0μg/mL内符合比尔定律,本法可用于环境水和食品样品中铅的测定。 相似文献
985.
Ju Yong Lee Hye Kyeong Min Donghoon Choi Myeong Hee Moon 《Journal of chromatography. A》2010,1217(10):1660-1666
This study describes a coupled analytical method to carry out the systematic profiling of phospholipids (PLs) in high-density lipoproteins (HDL) and low-density lipoproteins (LDL) from human blood plasma. HDL and LDL of healthy human plasma samples were separated by size and collected on a semi-preparative scale using multiplexed hollow fiber flow field-flow fractionation (MxHF5). Phospholipid mixtures contained in the resulting HDL and LDL fractions were analyzed by shotgun nanoflow liquid chromatography–tandem mass spectrometry (nLC–ESI-MS–MS). We utilized a dual scan method for the separation and simultaneous characterization of complicated PL mixtures by nLC–ESI-MS–MS, such that phosphatidylcholine (PC) and phosphatidylethanolamine (PE) molecules were detected in positive ion mode in a first LC run. In a second LC run, phosphatidylinositol (PI), phosphatidylglycerol (PG), and phosphatidic acid (PA) were detected in negative ion mode. In this study, a total of 56 PLs from HDL and 52 PLs from LDL particles were characterized by their molecular structures from data dependent collision-induced dissociation (CID) experiments, and their relative abundances were compared. 相似文献
986.
Heqing Jiang Dr. Fangyi Liang Oliver Czuprat Konstantin Efimov Armin Feldhoff Dr. Steffen Schirrmeister Dr. Thomas Schiestel Dr. Haihui Wang Prof. Jürgen Caro Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(26):7898-7903
A porous perovskite BaCoxFeyZr0.9?x?yPd0.1O3?δ (BCFZ‐Pd) coating was deposited onto the outer surface of a BaCoxFeyZr1?x?yO3?δ (BCFZ) perovskite hollow‐fiber membrane. The surface morphology of the modified BCFZ fiber was characterized by scanning electron microscopy (SEM), indicating the formation of a BCFZ‐Pd porous layer on the outer surface of a dense BCFZ hollow‐fiber membrane. The oxygen permeation flux of the BCFZ membrane with a BCFZ‐Pd porous layer increased 3.5 times more than that of the blank BCFZ membrane when feeding reactive CH4 onto the permeation side of the membrane. The blank BCFZ membrane and surface‐modified BCFZ membrane were used as reactors to shift the equilibrium of thermal water dissociation for hydrogen production because they allow the selective removal of the produced oxygen from the water dissociation system. It was found that the hydrogen production rate increased from 0.7 to 2.1 mL H2 min?1 cm?2 at 950 °C after depositing a BCFZ‐Pd porous layer onto the BCFZ membrane. 相似文献
987.
An experimental circulating water loop has been constructed to study the deposition of hematite particles of average diameter 320 nm on polypropylene pipe walls in the ranges pH 4–11, Re 3300–17,700 at 25 °C. Real-time turbidimetric measurements were used to measure the deposited concentrations. Results showed that the deposition rate increased when pH decreased and when the flow rate increased. Adhesion was observed even under repulsive electrostatic conditions (pH > 7), where the surfaces of hematite and polypropylene were both negative, indicating that the kinetic energy of at least a part of the particles surpassed the electrostatic repulsive potentials. The experimental curves were fitted by a model assuming simultaneous adhesion and removal of particles, leading to adhesion and removal rate constants, whose values depend on pH and flow rate. Removal is negligible below pH 9. 相似文献
988.
989.
自来水的生产工艺在教科书中仅以图片形式出现, 将其改进为模拟实验, 可以在一个素材中学习沉降、过滤、吸附等多种净化水的方法, 同时了解每种方法的净化程度和顺序的选择。 相似文献
990.
Zhao RS Cheng CG Yuan JP Jiang T Wang X Lin JM 《Analytical and bioanalytical chemistry》2007,387(2):687-694
A novel purge-and-trap method coupled with gas chromatography-mass spectrometry (GC-MS) is developed for the analysis of trace
and ultratrace phenols based on their derivatization with acetic anhydride. Parameters affecting the extraction efficiency,
such as purge temperature, concentration of sodium chloride, purge time, and volume of derivatization reagent, were investigated.
The optimized conditions were addition of 150 μL acetic anhydride, purge time of 25 min at the purge temperature of 60 °C
with 30% NaCl. The linear range was 0.2–100 μg L−1 for phenols. The limits of detection (LODs) ranged from 0.08 to 0.15 μg L−1 and the relative standard deviations (RSDs) for most of the phenols at the 10 μg L−1level were below 10%. Natural water samples collected from a pool were successfully analyzed using the proposed method. The
recovery of spiked water samples was 72.9–84.2%. 相似文献