氢氧化钠滴定醋酸过程中溶液粒子浓度关系的讨论

通过氢氧化钠滴定醋酸实验的分析,阐述了“pH=7中性点”和“化学计量点”的区别以及滴定过程各阶段溶液中溶质的变化情况;运用“微粒观”、“平衡观”、“守恒观”、“辩证观”讨论溶液中的粒子关系,有利于学生掌握分析电离平衡和水解平衡同时存在时溶液酸碱性的判断方法,建立解决此类问题的化学思维模式.

低温燃烧合成法制备纳米NiFe_2O_4

以九水硝酸铁、六水硝酸镍、水溶性肼类燃料为原料,添加金属离子络合剂、分散剂等为辅助剂,利用溶液燃烧合成法制备了纳米NiFe2O4粉体。利用XRD、TEM、SEM等测试方法对产物进行了表征,并研究了不同燃料、络合剂用量、分散剂用量、煅烧温度对粉体粒径和形貌的影响。实验结果表明,在以水溶性肼为燃料、络合剂2g、分散剂2g、煅烧温度800℃、煅烧时间2h时,可获得粒径均匀的纳米NiFe2O4粉体。所得产物的粒径范围为40～80nm,结构膨松,分散性良好。

化学元素的形成和地球年龄——为侯德封先生百年诞辰而作

本文从宇宙的起源出发、用核化学的观点分析了太阳上发生的核反应 ,进而讨论了不同质量区内化学元素的形成过程。中等质量的核素成因有三 :核反应、核衰变和核裂变。对放射性核素的研究表明 :宇宙中存在的放射性核素起源于星子的内核。地核的组成是“粒子溶液” ,它是处在超高温度和压力环境中、无个性基本粒子密集体。现有的年龄测定方法 ,大多数都是以放射性衰变规律为基础、用两个特定时间所存在的原子数目来计算年龄 ,因此 ,要求选用作为时计的核素具有足够长的寿命 ,同时还要有明确的起始时刻和原子的数目。

骨组织工程多孔支架材料性质及制备技术

多孔性生物可降解支架的选择和制备是组织工程技术成功运用的关键。从骨架的材料要求、常用的骨架材料、骨架的制备技术等几个方面对组织工程和生物降解支架的研究进行了综述 。

KR过程铁水包底部倾斜对铁水混匀现象影响的水模型研究

以210 t铁水包为原型建立1∶7的水模型,研究底部倾斜对KR过程铁水混匀现象的影响。研究了铁水包底部倾斜时搅拌桨转速和浸入深度对混匀时间、漩涡、液相中粒子分散和扭矩的影响,并与平底铁水包进行了对比。结果发现,包底倾斜17.5°时,混匀时间较平底时减少30.6%。搅拌桨转速为110 r/min时,浸入深度增加会导致液相中粒子分散变差,倾底铁水包中粒子分散程度优于平底铁水包。搅拌桨转速为160 r/min时,平底铁水包中粒子分散程度优于倾底铁水包。将平底改为倾底后,同工况下扭矩大幅增加。

Diffusion of Nanoparticles in Semidilute Polymer Solutions： A Multiparticle Collision Dynamics Study

The diffusion of nanoparticles immersed in semidilute polymer solutions is investigated by a hybrid mesoscopic multiparticle collision dynamics method. Effects of polymer concentration and hydrodynamic interactions among polymer monomers are focused. Extensive simulations show that the dependence of diffusion coefficient D on the polymer concentration c agrees with Phillies equation D-exp （-αc^δ） with a scaling exponent δ≈0.97 which coincides with the experimental one in literature. For increasing nanoparticle size, the scaling prefactor α increases monotonically while the scaling exponent always keeps fixed. Moreover, we also study the diffusion of nanoparticle without hydrodynamic interactions and find that mobility of the nanoparticle slows down, and the scaling exponent is obviously different from the one in experiments, implying that hydrodynamic interactions play a crucial role in the diffusion of a nanoparticle in semidilute polymer solutions.

评价一次性使用输血器具用尼龙血液过滤网过滤性能的新方法

建立一种使用240μm和160μm的标准粒子溶液评价尼龙血液过滤网过滤性能新方法,代替传统人体血液的评价方法。并通过试验证实,用该方法评价过滤网的过滤性能具有良好的重复性,操作简便、试验材料可得性强、避免因使用血液带来的安全隐患等优点。可用于尼龙血液过滤网和输血器生产的过程控制。

Carotenoids Particle Formation by Supercritical Fluid Technologies

Based on the solubility in supercritical CO2,two strategies in which CO2 plays different roles are used to make quercetine and astaxanthin particles by supercritical fluid technologies.The experimental results showed that micronized quercetine particles with mean particle size of 1.0-1.5 μm can be made via solution enhanced dispersion by supercritical fluids(SEDS) process,in which CO2 worked as turbulent anti-solvent;while for astaxanthin,micronized particles with mean particle size of 0.3-0.8 μm were also made successfully by rapid expansion supercritical solution(RESS) process.

Research on the Critical Conditions for Clay Particle Release During Saline Aquifer Freshening Process

Water sensitivity phenomenon occurs during saline aquifer freshening process in seawater intrusion area, and clay particles released in the phenomenon can damage the infiltration capacity of the aquifer. In order to find out the factors and mechanisms for clay particle release, laboratory column infiltration experiments simulating saline aquifer freshening process were designed to measure the critical conditions(critical flow velocity, critical salt concentration and critical ionic strength) and force analysis for clay particle according to DLVO electric double layer theory was employed to illustrate the mechanisms for particle release. The research results showed that critical flow velocity for clay particle release is influenced by salt concentration of injecting solution. When salt concentration of injecting solution is very high, clay particles are not released, indicating that there does not exist a critical flow velocity in this situation. As salt concentration of injecting solution decreases, particles start to be released. The critical salt concentration for clay particle release is 0.052 mol L-1 in our work, which was determined by a constant-flux experiment for stepwise displacement of high concentration Na Cl solution. The critical ionic strength for clay particle release decreases as Ca2+ molar content percentage of the mixed solution of Na Cl and Ca Cl2 increases following the first-order exponential decay equation y = 0.0391e-0.266 x + 0.0015.

Static magnetic field-assisted synthesis of Fe3O4 nanoparticles and their adsorption of Mn(Ⅱ) in aqueous solution

A facile method for synthesis of the magnetic Fe_3O_4 nanoparticles was introduced.Magnetic nanoparticles were prepared via co-precipitation method with(PMF) and without(AMF) 0.15 T static magnetic field.The effects of magnetic field on the properties of magnetic nanoparticles were studied by XRD,TEM,SEM,VSM and BET.The results showed that the magnetic field in the co-precipitation reaction process did not result in the phase change of the Fe_3O_4 nanoparticles but improved the crystallinity.The morphology of Fe_3O_4 nanoparticles was varied from random spherical particles to rod-like cluster structure.The VSM results indicated that the saturation magnetization value of the Fe_3O_4 nanoparticles was significantly improved by the magnetic field.The BET of Fe_3O_4nanoparticles prepared with the magnetic field was larger than the control by 23.5%.The batch adsorption experiments of Mn(Ⅱ) on the PMF and AMF Fe_3O_4 nanoparticles showed that the Mn(II) equilibrium capacity was increased with the pH value increased.At pH 8,the Mn(Ⅱ) adsorption capacity for the PMF and AMF Fe_3O_4 was reached at 36.81 and 28.36 mg·g^(-1),respectively.The pseudo-second-order model fitted better the kinetic models and the Freundlich model fitted isotherm model well for both PMF and AMF Fe_3O_4.The results suggested that magnetic nanoparticles prepared by the magnetic field presented a fairly good potential as an adsorbent for an efficient removal of Mn(Ⅱ) from aqueous solution.

Effects of Humic Acid and Solution Ph on Dispersion of Na-and Ca-Soil Clays

Dispersed soil clays have a negative impact on soil structure and contribute to soil erosion and contaminant movement. In this study, two typical soils from the south of China were chosen for investigating roles of pH and humic acid (HA) on dispersion of soil clays. Critical flocculation concentration (CFC) of the soil clay suspension was determined by using light transmission at a wavelength of 600 um. The results indicated that effects of pH and HA on dispersion of the soil clays were closely related to the type of the major minerals making up the soil and to the valence of the exchangeable canons as well. At four rates of pH(4, 6, 8 and 10), the CFC for the Na-yellow-brown soil treated with H2O2 was increased from 0.32 to 0.56, 6.0 to 14.0,10.0 to 24.6 and 26.0 to 52.0 mmol L-1 NaCl, respectively when Na-HA was added at the rate of from 0 to 40 mg L-1. With the same Na-HA addition and three pH (6, 8 and 10) treatments, the CFC for the Na-red soil was increased from 0.5 to 20.0, 1.0 to 40.0 and 6.0 to 141.0 mmol L-1 NaCl, respectively. Obviously,pH and HA has greater effects on clay dispersion of the red soil(dominated by 1:1 minerals and oxides)than on that of the yellow-brown soil(dominated by 2: 1 minerals). However, at three rates of pH (6, 8 and 10) and with the addition of Ca-HA from 0 to 40 mg L-1, the CFC of the Ca-yellow-brown soil and Ca-red soil treated with H2O2 was increased from 0.55 to 0.81, 0.75 to 1.28, 0.55 to 1.45 and 0.038 to 0.266, 0.25 to 0.62, 0.7 to 1.6 mmol CaCl2 L-1, respectively. So, Na-soil clays are more sensitive to pH and HA than Ca-soil clays.

Selective removal of heavy metal ions from aqueous solutions with surface functionalized silica nanoparticles by different functional groups

The industrial silica fume pretreated by nitric acid at 80 °C was re-used in this work. Then, the obtained silica nanoparticles were surface functionalized by silane coupling agents, such as(3-Mercaptopropyl) triethoxysilane(MPTES) and(3-Amincpropyl) trithoxysilane(APTES). Some further modifications were studied by chloroaceetyl choride and 1,8-Diaminoaphalene for amino modified silica. The surface functionalized silica nanoparticles were characterized by Fourier transform infrared(FI-IR) and X-ray photoelectron spectroscopy(XPS). The prepared adsorbent of surface functionalized silica nanoparticles with differential function groups were investigated in the selective adsorption about Pb2+, Cu2+, Hg2+, Cd2+ and Zn2+ions in aqueous solutions. The results show that the(3-Mercaptopropyl) triethoxysilane functionalized silica nanoparticles(SiO2-MPTES) play an important role in the selective adsorption of Cu2+ and Hg2+, the(3-Amincpropyl) trithoxysilane(APTES) functionalized silica nanoparticles(SiO2-APTES) exhibited maximum removal efficiency towards Pb2+ and Hg2+, the 1,8-Diaminoaphalene functionalized silica nanoparticles was excellent for removal of Hg2+ at room temperature, respectively.

Obtaining Sulfur Nanoparticles from Sodium Polysulfide Aqueous Solution

This paper thoroughly studies the＇. process of obtaining sulfur nanoparticles in aqueous medium from sodium polysulfide. Nanosize sulfur particles with orthorhombic structure were obtained at room temperature by mixing sodium polysulfide aqueous solution with various inorganic and organic acids. Sulfur nanoparticles were characterized by laser particle-size analyzer, X-ray diffraction, electron probe microscopy. Size of sulfur nanoparticles in aqueous dispersion is affected ;trongly by acid concentration, as well as nature of alcohols, used as wetting agents when measuring sulfur particles size iin aqueous medium. Availability of obtaining sulfur nanoparticles of 22-25 nm average si;,e in aqueous medium was revealed. High biological activity of sulfur nanoparticles and ethylalcohol composition on wheat grain couching was established.

Influence factors on thermal conductivity of ammonia-water nanofluids

In order to investigate the mechanism of nanoparticles enhancing the heat and mass transfer of the ammonia-water absorption process,several types of binary nanofluids were prepared by mixing Al2O3 nanoparticles with polyacrylic acid(PAA),TiO2 with polyethylene glycol(PEG 1000),and TiN,SiC,hydroxyapatite(noodle-like) with PEG 10000 to ammonia-water solution,respectively.The thermal conductivities were measured by using a KD2 Pro thermal properties analyzer.The influences of surfactant and ammonia on the dispersion stabilities of the binary nanofluids were investigated by the light absorbency ratio index methods.The results show that the type,content and size of nanoparticles,the temperature as well as the dispersion stability are the key parameters that affect the thermal conductivity of nanofluids.For the given nanoparticle material and the base fluid,the thermal conductivity ratio of the nanofluid to the ammonia-water liquid increases as the nanoparticle content and the temperature are increased,and the diameter of nanoparticle is decreased.Furthermore,the thermal conductivity ratio increases significantly by improving the stabilities of nanofluids,which is achieved by adding surfactants or performing the proper ammonia content in the fluid.

Synthesis of magnetic core–shell structure Fe_3O_4@MCM-41 nanoparticle by vesicles in aqueous solutions

In this study, magnetic core–shell structure Fe3O4@MCM-41 nanoparticles were synthesized with vesicles as soft templates. In the preparation, Fe Cl2 and tetraethy orthosilicate(TEOS) were selected as Fe processor and Si precursor, respectively. Stable vesicles first formed in 0.03 mol·L-11:2 mixture of anionic surfactant sodium dodecyl sulfate and cationic surfactant cetyltrimethyl ammonium bromide. Then, TEOS was added in the vesicle aqueous solution, leading to a highly dispersed solution. After high-temperature calcination, Fe3O4@MCM-41 nanoparticles were obtained. Their structure and morphology were characterized by Saturn Digisizer, transmission electron microscope and vibrating sample magneto-meter. The results indicate that the vesicles are spherical and their size could be tuned between 20 and 50 nm. The average grain diameter of synthesize magnetic core–shell Fe3O4@MCM-41 particles is 100–150 nm and most of them are in elliptical shape. The dispersion of magnetic particles is very good and magnetization values are up to 33.44 emu·g-1, which are superior to that of other Fe3O4 materials reported.

SYNTHESIS OF BOWL-LIKE PARTICLES BY EMULSION POLYMERIZATION AND RELEASE BEHAVIOR OF SOLVENT FROM THE PARTICLES

Poly(styrene-glycidyl methacrylate) particles having bowl-shaped hollow structures were synthesized by swollen seed emulsion polymerization. The PS emulsion synthesized through soap-free emulsion polymerization was swollen by toluene, and then the mixture of second monomers was added under polymerization condition. So a thin shell of poly(styrene-glycidyl methacrylate) cross-linked by triethylene glycol diacrylate was formed around the swollen PS particle. The bowl-shaped particles were obtained after the collapsing of the thin shell when the toluene emanated from the particles, but the shapes were effected by the degrees of cross-linking. The shape of the particles was observed by SEM. The release behavior of solvent from the particles was examined by TG.

Au＋-cetyltrimethylammonium bromide solution： A novel precursor for seed-mediated growth of gold nanoparticles in aqueous solution

The appropriate choice of chemical composition of a metallic precursor, which produces the basic structure units in the growth process of nanocrystals, is a high priority in the synthesis of metal--especially Au--nanoparticles. In the present work, Au seeds （prepared by the reduction of Au3＋ solution with NaBI~ in the presence of cetyltrimethylammonium bromide （CTAB）） have been used to initiate the growth of Au nanoparticles from two different Au precursors. When an aqueous Au＋ solution prepared in the presence of CTAB micelles was treated with ascorbic acid in the presence of the gold seeds, a high yield （up to 92%） of gold nanoparticles was obtained. By varying the volume of the seed solution with a fixed amount of Au＋, we can effectively control the morphological transformation of the resulting Au nanoparticles from cubes to octahedra. When an aqueous Au3＋ solution was prepared in the presence of CTAB micelles and treated with ascorbic acid in the presence of the gold seeds, smaller yields of Au nanoparticles were obtained. A preliminary growth mechanism has been proposed based on the changes induced by varying the amount of ascorbic acid and the ratio of the concentration of Au＊ to the number of seeds.

Effects of nanoparticles on devitrification and recrystallization of aqueous glycerol and PEG-600 solutions

Nanoparticles in solution offer unique electrical, mechanical and thermal properties due to their physical presence and interac- tion with the state of dispersion. This work is aimed to study the effects of hydroxyapatite （HA） nanoparticles on the behavior of devitrification and recrystallization of glycerol （60% w/w） and PEG-600 （50% w/w） solutions during warming. HA nano- particles of different sizes （20, 40, 60 nm） and concentrations （0.1%, 0.5%, w/w） were incorporated into solutions, and were studied by calorimetric analysis coupled with cryomicroscopy. The presence of HA nanoparticles has little effect on the devit- rification end temperatures, but affects the devitrification onset temperatures of glycerol and PEG-600 solutions. The investi- gation with the cryomicroscope observed that the ice morphologies of glycerol and PEG-600 solutions are dendritic and spher- ic respectively. The ice fraction of glycerol solution containing 0.1% HA with the size of 60 nm decreased to 2/5 of that of the solution without nanoparticles at -45℃. The ice fractions of PEG-600 solutions increased signifcantly between -64℃ and -54℃, and the ice fraction of PEG-600 solution without nanoparticles increased by 92% within the temperature range. The findings have significant implications for biomaterial cryopreservation, cryosurgery, and food manufacturing. The complexity of ice crystal growth kinetics in nanoparticle-containing solutions awaits further study.