走出“描红”天地,构建创新课堂——高中数学教学反思与对策

创新教学是新课改的主要要求.文章针对目前高中数学教学中的＂描红＂式教学进行了反思,并提出针对性的两点对策——树立＂学生为主体＂的思想,给数学课堂增加＂多维营养＂,论述高中数学教学应改变落后教学态势,构建师生互动、发展创新能力为宗旨的课堂教学的几点体会.

让高中学生尽快走出“描红”天地

通过学习与反思，笔者对目前的数学教学提出对策，以帮助学生走出“描红”的误区。

歌剧舞美“描红”与灯光设计再度创作的实验教学

舞台灯光设计教学必须要建立在剧本、导演和舞台设计的基础上,才能完整地进行。文章阐述了舞台灯光设计“描红”式的教学改革,使学生在学习大师的舞台设计的同时,充分发挥自己的主观能动性,理解舞台美术的含义,从而深入地进行舞台灯光设计案头创作,最终呈现出优异的舞台效果。

Comparison of total splenic artery embolization and partial splenic embolization for hypersplenism

AIM:To evaluate whether total splenic artery embolization(TSAE) for patients with hypersplenism delivers better long-term outcomes than partial splenic embolization(PSE).METHODS:Sixty-one patients with hypersplenism eligible for TSAE(n = 27,group A) or PSE(n = 34,group B) were enrolled into the trial,which included clinical and computed tomography follow-up.Data on technical success,length of hospital stay,white blood cell(WBC) and platelet(PLT) counts,splenic volume and complications were collected at 2 wk,6 mo,and 1,2,3,4 years postoperatively.RESULTS:Both TSAE and PSE were technically successful in all patients.Complications were significantly fewer(P = 0.001),and hospital stay significantly shorter(P = 0.007),in group A than in group B.Postprocedure WBC and PLT counts in group A were significantly higher than those in group B from 6 mo to 4 years(P = 0.001),and post-procedure residual splenic volume in group A was significantly less than that observed in group B at 1,2,3 and 4 years post-procedure(P = 0.001).No significant differences were observed in red blood cell counts and liver function parameters between the two groups following the procedure.CONCLUSION:Our results indicate that TSAE for patients with hypersplenism not only delivers a better longterm outcome,but is also associated with lower complication rates and a shorter hospital stay than PSE.

Effect of a Novel Nucleating Agent on Isothermal Crystallization of Poly（L-lactic acid）

The effect of a novel active nucleating agent(TBC8-eb) on the isothermal crystallization of poly(L-lactic acid) (PLLA) was studied by differential scanning calorimetry(DSC) and Fourier transform infrared spectroscopy(FTIR) . The analysis on kinetics demonstrates that TBC8-eb can not only accelerate the crystallization rate but also transform most of the original spherulite crystals of PLLA into sheaf-like crystals. Furthermore,the free energy of folding(σe) of PLLA and PLLA with TBC8-eb is 0.15 and 0.06 J·m-2,respectively,which suggests that the addition of TBC8-eb favors the regular folding of molecule chains in the crystallization of PLLA,improv-ing its crystallization rate. The FTIR results show that TBC8-eb can accelerate the conformational ordering of PLLA in the isothermal crystallization. The conformational ordering of PLLA nucleated with TBC8-eb begins with the interchain interaction of CH3,and then a short helix emerges where a couple of CH3 groups interact.

Hydrothermal Synthesis of Rhombus-like SmCO3OH Microplates and Its Photoluminescence Property Doped with Eu^3＋

Rhombus-like SmCO3OH microplates with the edge lengths ranging from 5 μm to 10 μm and the thickness about 1.5 μm were synthesized through a simple hydrothermal method using urea as the precipitance. The structure and properties of the rhombus-like SmCO3OH microplates were characterized by X-ray diffraction, field-emission scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. The optical property of the rhombus-like SmCO3OH microplates doped with Eu^3＋ was investigated by photoluminescence. A broad and strong emission band at 677 nm was obtained, which can be contributed to producing light conversion film.

Investigation on specific heat capacity and thermal behavior of sodium hydroxyethyl sulfonate

The thermal decomposition process was studied by the TG–DTA analyzer. The results show that the decomposition process of sodium hydroxyethyl sulfonate consisted of three stages: the mass loss for the first, the second and third stages may be about the groups of CH_3CH_2OH, CH_3CHO and SO_2 volatilized, respectively. The decomposition residuum of three stages was analyzed by FT-IR, and the results of FT-IR agreed with the decomposition process predicted by theoretical weight loss. The specific heat capacity of sodium hydroxyethyl sulfonate was determined by differential scanning calorimetry(DSC). The melting temperature and melting enthalpy were obtained to be 465.41 K and 25.69 kJ·mol^(-1), respectively. The molar specific heat capacity of sodium hydroxyethyl sulfonate was determinated from 310.15 K to 365.15 K and expressed as a function of temperature.

Quantitative analysis of deformation in hollow cylinder tests on anisotropic clay formations

A series of triaxial laboratory experiments are performed on thick-walled hollow cylindrical samples of boom clay.The aim of this testing program is to better understand the anisotropic deformation during the excavation.The testing conditions are similar to those to be experienced by host rocks around disposal galleries for radioactive waste.X-ray computed tomography is performed at different steps for each test with the samples remaining inside the loading cell.Initial analysis of the tomography images allows of the observation of the deformation of the central hole.In addition,particles manual tracking and 3D volumetric digital image correlation processing methods are considered being used to analyze the particles displacements and the boundary deformation of the sample quantitatively.An unsymmetrical damaged zone is induced around the hole,with a reverse deformation trend being found at the boundary after unloading,which indicates that the significant anisotropic deformation of boom clay can be induced by mechanical unloading.

Microstructure and microwave dielectric properties of CaO-B_2O_3-SiO_2 glass ceramics with various B_2O_3 contents

The effects of B2O3 addition on both the sintering behavior and microwave dielectric properties of CaO-B2O3-SiO2 （CBS） glass ceramics were investigated by Fourier transform infrared spectroscopy （FTIR）, X-ray diffractometry （XRD） and scanning electron microscopy （SEM）. The results show that the increasing amount of B203 causes the increase of the contents of [BO3], [BO4] and [SiO4], which deduces the increase of CaB204 and a-SiO2 and the decrease of CaSiO3 correspondingly. No new phase is observed throughout the entire experiments. A bulk density of 2.54 g/cm3, a thermal expansion coefficient value of 11.95× 10-6 ℃-1 （20-500℃）, a dielectric constant er value of 6.42 and a dielectric loss tanδ value of 0.000 9 （measured at 9.7 GHz） are obtained for CBS glass ceramics containing 35%-B203 （mass fraction） sintered at 850 ℃ for 15 min.

Polyhydroxyl-aluminum pillaring improved adsorption capacities of Pb^(2+) and Cd^(2+) onto diatomite

In order to greatly improve adsorption capacity, the diatomite was pillared by polyhydroxyl-aluminum.A series of adsorption tests were conducted to obtain the optimum condition for pillared diatomite synthesis. The scanning electron microscopy （SEM）, Fourier transform infrared spectroscopy （FTIR）, surface area and porosity analyzer and micro-electrophoresis were used to determine pore structure and surface property.The pillared diatomite attaining the optimal adsorption densities （qe） of Pb^2＋ and Cd^2＋ was synthesized with the following conditions： Addition of pillaring solution containing Al3＋-oligomers with a concentration range of 0.1-0.2 mol/L to a suspension containing Na＋-diatomite to obtain the required Al/diatomite ratio of 10 mmol/g; synthesis temperature of 80 ℃ for 120 min; aging at a temperature of 105 ℃ for 16 h. The adsorption capacities of Pb^2＋ and Cd^2＋ on pillared diatomite increase by 23.79% and 27.36% compared with natural diatomite, respectively. The surface property of pillared diatomite is more favorable for ion adsorption than natural diatomite. The result suggests that diatomite can be modified by pillaring with polyhydroxyl-aluminum to improve its adsorption properties greatly.

In-situ Synthesis of ZSM-5 Zeolite from Metakaolin/Spinel and Its Catalytic Performance on Methanol Conversion

ZSM-5 zeolite was in-situ synthesized from metakaolin or s alumina sources, respectively. The ZSM-5 zeolite was characterized pinel by incorporating additional silica and by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, Fourier transform infrared （FT-IR） spectroscopy and N2 adsorption measurement. This supported zeolite was tested on the methanol to propylene （MTP） processes. Experimental results showed that the ZSM-5 zeolite exhibited high selectivity for propylene. The yield of propylene on ZSM-5 zeolite made from metakaolin was increased by 17.73%, while that on ZSM-5 zeolite made from spinel was raised by 9.90%, compared to that achieved with the commercial ZSM-5 zeolite. The significant increase in propylene production is probably due to the distinctive morphology of the ZSM-5 zeolite, which possessed a rough external surface covered with sphere-like particles and distribution of small crystals sized at around 400--500 nm. This morphology could help to generate more crystal defects so that more active centers could be exposed to the reaction mixture. In addition, the zeolite product had a gradient pore distribution and many medium Brǒnsted acid sites, both of which might also contribute to the increased propylene production.

A novel synthesis of LiFePO_4/C from Fe_2O_3 without extra carbon or carbon-containing reductant

A novel synthesis of LiFePO4/C from Fe2O3 with no extra carbon or carbon-containing reductant was introduced： Fe2O3 （＋NH4H2PO4）→Fe2P2O7（＋Li2CO3＋glucose）→LiFePO4/C. X-ray diffractometry （XRD）, Fourier transform infrared spectroscopy （FTIR） and scanning electron microscopy （SEM） were utilized to characterize relevant products obtained in the synthetic procedure. The reaction of Fe2P2O7 and Li2CO3 was investigated by thermo-gravimetric and differential thermal analysis （TGA-DTA）. Fe2O3 is completely reduced to Fe2P2O7 by NH4H2PO4 at 700 ℃ and Fe2P2O7 fully reacts with Li2CO3 to form LiFePO4 in the temperature range of 663.4-890 ℃. The primary particles of LiFePO4/C samples prepared at 670, 700 and 750 ℃ respectively exhibit uniform morphology and narrow size distribution, 0.5-3 μm for those obtained at 670 and 700 ℃ and 0.5-5 μm for those obtained at 750 ℃. LiFePO4/C （carbon content of 5.49%, mass fraction） made at 670 ℃ shows an appreciable average capacity of 153.2 mA·h/g at 0.1C in the first 50 cycles.

Structure-Property Relations in xWO3-0.31P2O5-0.31B2O3-（0.38-x）Cs2O （0.01 ≤ x ≤0.28） Glasses by IR, UV and EPR Spectroscopic Studies

Glasses in the series of xWO3-0.31P2O5-0.31B2O3-（0.38-x）Cs2O （0.01 ≤ x ≤0.28） （G1-G4： x= 0.01, 0.1, 0.19, 0.28） were prepared by sol-gel method. Glassy phase in the samples were ascertained by powder X-ray diffraction pattern. Differential scanning calorimetry （DSC） traces of the samples show glass transition temperature Tg, in the range 247-253 ℃. IR spectra at 300 K of G1-G4 show the presence of [WO6], [WO4], [PO4]^3-, [PO3]^2-, [BO4]^＋, [BO3] units in the glass matrix. Observed electron paramagnetic resonance （EPR） lineshapes show two signals with very different intensities which are associated with W^5＋ （5d^1） and Mo^5＋ （4d^1） （impurity） paramagnetic sites. Signal with values ofg factors in the range 1.68 〈 g⊥ 〈 1.72 and 1.58 〈 gⅡ 〈 1.62 are due to W^5＋ ions present in axially distorted octahedral symmetry. The optical absorption spectra show that the W^5＋ ions have pyramidal coordination, involving a tungstyl ion WO^3＋ （C4v symmetry）. EPR and optical studies suggest the existence of blocks of octahedra linked by tungsten clusters.

Adsorption of residual amine collector HAY from aqueous solution by refined carbon from coal fly ash and activated carbon

Refined carbon(RC) derived from coal fly ash(CFA) as well as powdered activated carbon(PAC) was investigated as adsorbent to remove residual amine collector HAY from aqueous solution.The RC and PAC were characterized by scanning electron microscopy(SEM),surface area measurement,Zeta potential measurement and Fourier transform infrared(FTIR) spectroscopy.The effect factors and mechanisms of HAY adsorption onto RC and PAC were studied in detail.The results show that the experimental kinetic data agree well with the pseudo second-order equation,and the Langmuir isotherm model is found to be more appropriate to explicate the experimental equilibrium isotherm results than the Freundlich model.The adsorption capacities of PAC and RC increase with pH.It is found that alkaline condition is conducive to the adsorption of HAY onto PAC and RC and the adsorption efficiency of RC is close to PAC at pH near 11.Zeta potential variation of adsorbents suggests that HAY generates electrostatic adsorption onto RC and PAC.FTIR analysis shows that the adsorption is dominantly of a physical process.The Box-Behnken design optimization conditions of process are RC 1 g/L,pH 11,temperature 302 K and initial HAY concentration 100 mg/L.Under these conditions,the measured adsorption ratio and adsorption capacity are 87.91%and 87.91 mg/g,respectively.Thus,the RC is considered to be a potential adsorbent for the removal of residual amine from aqueous solution.

Alginate-Casein Microspheres as Bioactive Vehicles for Nutrients

The aim of this work was to develop an alginate-casein composite microsphere as a bioaetive vehicle for oral administration of nutrients by a simple extrusion dripping method. Riboflavin was selected as a model drug, and the microencapsulation efficiency was raised to 97.94% after optimizing the preparation conditions by response surface methodology. In vitro release studies showed that riboflavin was released completely from alginate-casein microspheres in simulated intestinal fluids. Meanwhile, the morphology, structure and interaction between alginate and casein were characterized by scanning electron microscopy （SEM） and Fourier transform infrared （FTIR） spectra.

Soil Properties Degradation Assessment Using Infrared Scanning Technique of Soils （Case Study： Eastern of Congo）

Recently, near infrared reflectance （NIR） and mid-infrared （MIR） spectroscopy techniques are increasingly introduced as convenient and simple non-destructive techniques for quantifying several soil properties. This study uses MIR method to predict pH, soil organic C, total N, AI, Ca, Mg and K, CEC and soil texture for soil samples collected in Sud-Kivu, Congo. A total of 536 composite soil samples were taken from two locations （Burhale and Luhihi） at two depths （0-20 cm and 20-40 cm） using a spatially-stratified random sampling design within an area of 200 km2. Differences in characteristics were evaluated between the two locations, land use （cultivated vs. non-cultivated land） with soil depths. A random subset of the samples （10%） were analyzed using standard wet chemistry methods, and calibration models developed by MIR data to estimate soil properties for the full soil sample set. Partial least squares regression （PLS） method gave acceptable coefficients of determination between 0.71 and 0.93 for all parameters. Soil organic matter levels were higher in cultivated plots in Luhihi （3.9% C） than in Burhale （3.0% C）, suggesting lower levels of soil fertility in the later area. This indicates high levels of acidity, which are likely to limit crop production in the area. Phosphorus deficiency is acute in Burhale （2.4 mg P/kg） but less in Luhihi （5.4 mg P/kg）. In both locations, low levels of Ca and Mg indicate that soils may be susceptible to deficiencies in both elements.These findings provide new opportunities for monitoring soil quality in the region which can benefit multiple actors and scientists involved in the agricultural and environmental sectors.

Synthesis and characterization of MgSO_4·5Mg(OH)_2·2H_2O flake powders

Magnesium oxysulfate （MgSO4·5Mg（OH）2·2H2O） flake powders with an average diameter of 2 ~tm and a thickness of 0.052 μm were prepared using magnesium sulfate and sodium hydroxide as raw materials by hydrothermal synthesis process. The composition, morphology and structural features of the hydrothermal products were examined with X-ray powder diffraction （XRD）, scanning electron microscopy （SEM） and Fourier transform infrared spectroscopy （FTIR）. The experimental results indicate that in the conditions of n（NaOH）/n（MgSO4） of 1.25, the dosage of w（Na3PO4） crystal additives of 1.0% w（MgSO4）, stirring for 5 h at 180 ℃, the morphology of MgSO4·5Mg（OH）2·2H2O products is flaky and laminar, which is a kind of complex magnesium singlecrystal. The recycling of MgSO4 mother liquor was also investigated to make a full use of the materials and reduce disposal. The results prove that there is no adverse effect on the yield and purity of the products.

Rapid biosorption and reduction removal of Cr(Ⅵ) from aqueous solution by dried seaweeds

Four types of common seaweeds(Laminaria japonica,Undaria pinnatifida,Porphyra haitanensis,and Gracilaria lemaneiformis) were examined to remove Cr(Ⅵ) ions from aqueous solution.The experimental parameters that affected the biosorption process including pH,biomass dosage,contact time and temperature were investigated via batch experiments.The surface characteristics of seaweeds before and after Cr(Ⅵ) adsorption were studied with scanning electron microscopy and Fourier transform infrared spectroscopy.The results show that an initial solution with the pH of 1.0 is most favorable for Cr(Ⅵ) adsorption.Rapid adsorption is observed in the initial stage and adsorption equilibrium state is reached within 1 h.The adsorption efficiency by Porphyra haitanensis is the maximum among four types of seaweed powders,followed by Laminaria japonica and Undaria pinnatifida with biosorption efficiency up to 90%.The removal rate of Gracilaria lemaneiformis is less than 60%.The kinetic data obtained using the seaweeds are found to follow pseudo-second order kinetic model.Experimental sorption data adequately correlate with the Langmuir model.FTIR indicates that amino and carboxyl groups play an important role in the process of Cr(Ⅵ) adsorption and a large percentage of Cr(Ⅵ) ions are reduced by reductive groups on the surface of seaweeds.

Polymorph and morphology of CaCO_3 in relation to precipitation conditions in a bubbling system

Simulating the typical carbonation step in a mineral CO_2 sequestration, precipitated calcium carbonate(PCC) was prepared by bubbling CO_2 gas into a rich Ca solution. These carbonation reactions were conducted at three p H ranges, namely 10.0–9.0, 9.0–8.0, and 8.0–7.0, in which temperature and CO_2 flow rate are additional experimental variables. The PCC obtained in experiments was examined by Fourier transform infrared spectroscopy(FTIR)and X-ray diffraction(XRD). It was found that supersaturation determined by p H value and flow rate of CO_2 has significant influence on polymorph of PCC. Vaterite was preferably formed at high supersaturation, while dissolution of metastable vaterite and crystallization of calcite occurred at low supersaturation. High temperature is a critical factor for the formation of aragonite. At 70 °C, vaterite, calcite and aragonite were observed to coexist in PCC because transformation from vaterite to aragonite via calcite occurred at this temperature. Scanning electron microscopy(SEM) technology was performed on prepared PCC, and various morphologies consistent with polymorphs were observed.

Microstructure and microwave dielectric properties of lead borosilicate glass ceramics with Al_2O_3

The effects of Al2O3 addition on both the sintering behavior and microwave dielectric properties of PbO-B203-SiO2 glass ceramics were investigated by Fourier transform infrared spectroscope （FTIR）, differential thermal analysis （DTA）, X-ray diffraction （XRD） and scanning electron microscopy （SEM）. The results show that with the increase of Al2O3 content the bands assigned to [SiO4] nearly disappear. Aluminum replaces silicon in the glass network, which is helpful for the formation of boron-oxygen rings. The increase of the transition temperature Tg and softening temperature Tf of PbO-B2O3-SiO2 glass ceramics leads to the increase of liquid phase precipitation temperature and promotes the structure stability in the glasses, and consequently contributes to the decreasing trend of crystallization. Densification and dielectric constants increase with the increase of Al2O3 content, but the dielectric loss is worsened. By contrast, the 3% （mass fraction） Al2O3-doped glass ceramics sintered at 725℃ have better properties of density p=2.72 g/cm3, dielectric constant Er=6.78, dielectric loss tan8=2.6×10^-3 （measured at 9.8 GHz）, which suggest that the glass ceramics can be applied in multilayer microwave devices requiring low sintering temperatures.