用超常的复性温度改善小麦RAPD分析的效果

用 38～ 6 6℃不同复性温度处理 ,比较了 18条随机引物的扩增结果。发现复性温度在 40～ 5 0℃之间均有数量不等的扩增产物 ,不同引物的最高复性温度不同 ,有些引物用 6 0℃以上的复性温度仍有扩增产物。一些在 35～38℃的复性温度下非特异性产物较多的引物 ,通过大幅度提高复性温度 ,能提高扩增产物的特异性 ,获得清晰的RAPD带型。

PCR温度特性实验研究与分析

目的:测量PCR温度的准确性和均一性。方法:PCR主程序:变性95℃,30 s,退火55℃,40 s,延伸72℃,50s,6个循环;热电偶分别放在孔内和管内。结果:每个循环以及每次测量的孔和管内的温度重复性很好;变性阶段,孔的温度和管内液体温度与程序温度偏差较大,温度准确性都较差,但所有孔的温度都达到通常需要的变性温度(变性90℃以上),但是44.4%的孔在90℃以上停留的时间不能达到设置的时间;变性阶段,11.1%管内液体不能达到所需的变性温度(90℃)。结论:这些缺陷可能导致扩增结果假阳性或假阴性。

Influence of pyrolysis temperature on structure and dielectric properties of polycarbosilane derived silicon carbide ceramic

β-SiC ceramic powders were obtained by pyrolyzing polycarbosilane in vacuum at 800-1200 °C. The β-SiC ceramic powders were characterized by TGA/DSC, XRD and Raman spectroscopy. The dielectric properties of β-SiC ceramic powders were investigated by measuring their complex permittivity by rectangle wave guide method in the frequency range of 8.2-18 GHz. The results show that both real part ε′ and imaginary part ε″ of complex permittivity increase with increasing pyrolysis temperature. The mechanism was proposed that order carbon formed at high temperature resulted in electron relaxation polarization and conductance loss, which contributes to the increase in complex permittivity.

Study on Preparation of Temperature-sensitive Injectable Hydrogel

To get a sort of new scaffold material for soft tissue reconstruction,we have prepared XLHA-PNIPAAm and XLHA-MC injectable hydrogels through blending crosslinked HA(XLHA) and two temperature-sensitive materials differed in degradation poly(N-isopropylacrylamide)(PNIPAAm) and methylcellulose(MC),respectively.We tested the injectablility,enzymatic biodegradability,temperature-sensitivity,structure cytotoxicity and hemolysis of the two injectable hydrogels.Our research has successfully obtained the preparation condition of XLHA-PNIPAAm injectable hydrogel,and verified that adding non-degradable material PNIPAAm can postpone the degradation of HA more effectively than degradable material MC.PNIPAAm prepared with 5 kGy dose radiation,MBAAm/NIPAAm(M/M)=0.015,monomer concentration=3% produced XLHA-PNIPAAm with slowest enzymatic biodegradability.DSC results showed that temperature-sensitivity of the XLHA-PNIPAAm was more stable than that of XLHA-MC.Two composite hydrogels were qualified in cytotoxicity and hemolysis tests and the biocompatibility of XLHA-PNIPAAm hydrogel showed better than XLHA-MC hydrogel.

Effect of pyrolysis temperature on properties of ACF/CNT composites

Activated carbon fiber/carbon nanotube(ACF/CNT) composites were fabricated by chemical vapor deposition(CVD) process.The effects of pyrolysis temperature on properties of ACF/CNT composites,including BET specific surface area,mass increment rate and adsorption efficiency for rhodamine B in solution,were investigated by scanning electron microscopy.The results show that the pyrolysis temperature is a key factor affecting the qualities of ACF/CNT composites.The mass increment rate and BET specific surface area sharply decrease with the increase of pyrolysis temperatures from 550 ℃ to 850 ℃ and the minimum diameter of CNTs appears at 750 ℃.The maximum adsorption efficiency of ACF/CNT composites for rhodamine B is obtained at 650 ℃.ACF/CNT composites are expected to be useful in adsorption field.

Effect of CaO composition on oxidation and burning behaviors of AM50 Mg alloy

Oxidation and burning behaviors were studied for CaO added AM50 Mg composites which were manufactured by conventional melting and casting processes without SF6 protective gas. CaO added AM50 Mg composites show the stable oxidation resistance, while AMS0 Mg alloys show the poor oxidation resistance. The effects of CaO addition on the burning resistance under ambient, nitrogen and dry air atmospheres were examined for CaO added AM50 Mg composites. With increasing CaO addition, the burning temperature increases under ambient, nitrogen and dry air atmospheres. The burning temperatures of small test specimen under all conditions greatly increase even by 0.3% CaO （mass fraction） addition into AM50 Mg alloys.

Temperature-resistant and flexible supercapacitors based on 10-inch wafer-scale nanocarbon films

Most of the supercapacitors reported in literatures showed little or no flexibility in the working temperature around 150℃. However, the supercapacitors are generally exposed under complex system or extreme temperature, such as electric vehicles and extremely cold area. Herein, we successfully fabricated a large-scale robust nanocarbon hybrid film consisting of reduced graphene oxide (rGO), carbon nanotubes (CNTs) and MnOx nano-flowers with the size up to 550 cm^2. The mechanical properties of the hybrid films depend on the ratio o f CNTs. The supercapacitors prepared with the hybrid films exhibit high flexibility and keep their performances in a temperature range from - 20 to 200℃. In addition, the devices display remarkable electrochemical and deformation stability at extrem e temperature. This strategy has a potential for the more efficient preparation of flexible electrode materials.

A robust self-healing polyurethane elastomer: From H-bonds and stacking interactions to well-defined microphase morphology

Self-healing materials have attracted considerable attention because of their improved safety, lifetime, energy efficiency and environmental impact. Supramolecular interactions have been extensively considered in the field of self-healing materials due to their excellent reversibility and sensitive responsiveness to environmental stimuli. However,development of a polymeric material with good mechanical performance as well as self-healing capacity is very challenging. In this study, we report a robust self-healing polyurethane(PU) elastomer polypropylene glycol-2-amino-5-(2-hydroxyethyl)-6-methylpyrimidin-4-ol(PPG-mUPy) by integrating ureidopyrimidone(UPy) motifs with a PPG segment with a well-defined architecture and microphase morphology.To balance the self-healing capacity and mechanical performance, a thermal-triggered switch of H-bonding is introduced. The quadruple H-bonded UPy dimeric moieties in the backbone induce phase separation to form a hard domain as well as enable further aggregation into microcrystals by virtue of the stacking interactions, which are stable in ambient temperature. This feature endows the PU with high mechanical strength. Meanwhile, a high healing efficiency can be realized, when the reversibility of the H-bond was unlocked from the stacking at higher temperature. An optimized sample PPG1000-mUPy50%with a good balance of mechanical performance(20.62 MPa of tensile strength) and healing efficiency(93% in tensile strength) was achieved. This strategy will provide a new idea for developing robust self-healing polymers.

Relative humidity and temperature dependence of mechanical degradation of natural fiber composites^(?)

In this paper,the mechanical degradation of natural fiber composites is studied with the consideration of the relative humidity and the temperature.A nonlinear constitutive model is established,which employs an internal variable to describe the mechanical degradation related to the energy dissipation during moisture absorption.The existing experimental researches demonstrated that the mechanical degradation is an irreversible thermodynamic process induced by the degradation of fibers and the damages of interfaces between fiber and matrix,both of which depend on the variation of the relative humidity or the temperature.The evolution of the mechanical degradation is obtained through the determination of dissipation rates as a function of the relative humidity and the temperature.The theoretically predicted mechanical degradations are compared with experimental results of sisal fiber reinforced composites subject to different relative humidity and temperatures,and a good agreement is found.

Structural and electrical properties of high Curie temperature Aurivillius phase composite ceramics with largely enhanced piezoelectricity

High performance piezoelectric ceramics with high Curie temperatures(TC) are the bottle necks of relevant high temperature devices. In this study, the electrical performance and microstructure of Li and Mn codoped Aurivillius-type composite ceramics with a composition Ca_(0.99-x_Bi_(6.99+x)(Li Mn)_(0.01) Nb Ti_5O_(24)(x = 0–0.8) were systematically investigated. The results indicated that uniform intergrowth structure with a lattice similar to that of the end member CBT could be formed at a low x value(x < 0.4). Phase separation occurred when more A-site Ca^(2+) ions were replaced by Bi^(3+) ions. Nevertheless, all composite samples showed d_(33) values about 2 to 3 times of that of the constituent phase Ca Bi_4Ti_4O_(15) and Bi_3 Ti NbO_9 with still a high depolarization temperature. The performance of the samples was found to be related to the density and larger lattice distortion along the polarization a axis. The results also demonstrated that formation of the compound system was an effective way in improving the performance of Aurivillius-type high TC piezoelectric ceramics.