New Approach for Macro Porous RB‐SiC Derived from SiC/Novolac‐type Phenolic Composite

A novel fabrication route to make macroporous silicon carbide (SiC) has been proposed in this study. The route is composed of the following two steps: the fabrication of porous α‐SiC/novolac‐type phenolic composite using hexamethylenetetramine (HMT) as a curing/blowing agent for the novolac monomer and a conventional reaction‐bonded (RB) sintering of the composite. The α‐SiC/novolac‐type phenolic composite was carbonized at 800°C for 2 h in N₂ gas and then reacted with the molten silicon at 1450°C for 30 min under vacuum, resulting in the macroporous RB‐SiC with an open porosity of 48% and relatively large pore size of ~110 μm. The compressive strength of the macroporous RB‐SiC was 113 MPa, which is relatively high compared to those reported for macroporous SiC of equivalent porosities and pore sizes.     

一种空空导弹复合制导交接班方案设计

首先分析空空复合制导交接班的特点以及交接时间点。然后结合具体的制导律,设计一种与不同的中段制导律、末段制导律匹配的空空复合制导交接班方案,实现中段制导和末段制导的平滑过渡,确定交接时间点。最后经理想制导系统仿真,验证了方案的有效性。     

Excess Solute Carbon and Retained Tetragonality in Tempered Fe-0.6C-1Mn Martensite and the Effect of Silicon Addition

The tetragonality and carbon distribution in tempered Fe-0.6C-1Mn martensite were investigated by X-ray diffraction and atom probe tomography to elucidate strain relaxation in the tetragonal lattice during tempering and its relationship with the solubility of excess carbon in martensite. Even though tetragonality (c/a) decreased with an increase in the tempering temperature, it persisted at low levels up to 400 °C. Si addition suppressed the decrease in tetragonality at 400 °C by inhibiting recovery in the dislocated matrix. Such persistence implies that dislocation migration is crucial for the complete release of tetragonal lattice strain at such a temperature, in addition to the decrease in the amount of solute carbon in martensite. A low level of tetragonality was observed for martensite containing carbon in the solid solution below the critical value of ~ 0.2 mass pct, at which a bcc structure was predicted. The amount of solute carbon after tempering was linearly correlated with tetragonality in the solute carbon content range of 0.07 to 0.6 mass pct, and the correlation coefficient was similar to those for as-quenched auto-tempered martensite and bainitic ferrite; these results indicate that the amount of excess carbon is simply determined by the amount of tetragonal lattice distortions remaining after carbide precipitation and recovery.

     

Nonsalt 1‐(arylmethyloxy)pyrene photoinitiators capable of initiating cationic polymerization

Analysis of photoproducts derived from 1‐(methoxynaphthalen‐1‐ylmethyloxy)pyrene initiators and polymer end groups demonstrated that methoxynaphthalen‐1‐ylmethyl carbocation is involved in the initiation steps for both styrene (St) and cyclohexene oxide (CHO) polymerization. Charge transfer from the pyrenyloxy oxygen atom to the methoxynaphthalen‐1‐ylmethyl chromophore in the singlet excited state is assumed to be responsible for the efficient generation of the carbocation species, which also initiates the copolymerization of St and CHO. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40510.     

Hydrogen‐bonding interaction between poly(ε‐caprolactone) and low‐molecular‐weight amino compounds

The specific interactions between several low‐molecular‐weight diamino compounds and poly(ε‐caprolactone) (PCL) have been investigated by FT‐IR. It was found that PCL and 3,3′‐diaminodiphenylmethane (3,3′‐DADPM) interact through strong intermolecular hydrogen bonds in the blend. Thermal and mechanical properties of PCL/3,3′‐DADPM blends were investigated by DSC and tensile measurements, respectively. The glass transition temperature of the blend increases while both the melting point and the elongation‐at‐break of the blend decrease with the increase of 3,3′‐DADPM content. Besides 3,3′‐DADPM, several other low‐molecular‐weight compounds containing two amino groups, such as o‐phenylenediamine or 1,6‐diaminohexane, were also added into PCL and the corresponding blend systems were investigated by FT‐IR and DSC. The effect of the chemical structure of the additives on the properties of PCL is discussed. © 2001 Society of Chemical Industry     

防爆技术在气动葫芦产品上的应用

气动葫芦等非电气设备应用在爆炸性环境时，在正常工作过程中会因机械摩擦和碰撞产生热表面、明火、灼热气体／液体、机械火花、绝热压缩、振动波、化学反应放热、铝热反应、粉尘自燃、电弧和静电放电等点燃源，形成爆炸危险。这些设备可以通过限制运行速度、润滑、限定材质、采用隔爆外壳等措施来达到防燃要求。     

Reaction joining of SiC ceramics using TiB2-based composites

SiC ceramics were reaction joined in the temperature range of 1450–1800 °C using TiB₂-based composites starting from four types of joining materials, namely Ti–BN, Ti–B₄C, Ti–BN–Al and Ti–B₄C–Si. XRD analysis and microstructure examination were carried out on SiC joints. It is found that the former two joining materials do not yield good bond for SiC ceramics at temperatures up to 1600 °C. However, Ti–BN–Al system results in the connection of SiC substrates at 1450 °C by the formation of TiB₂–AlN composite. Furthermore, nearly dense SiC joints with crack-free interface have been produced from Ti–BN–Al and Ti–B₄C–Si systems at 1800 °C, i.e. joints TBNA80 and TBCS80, whose average bending strengths are measured to be 65 MPa and 142 MPa, respectively. The joining mechanisms involved are also discussed.     

Effect of chloride ions on leaching rate of chalcopyrite

The effect of chloride on chalcopyrite leaching has been investigated by performing batch leaching tests with three kinds of leaching solutions and using Hiroyoshi’s model, which suggests that a zone of rapid leaching exists between the critical potential (E_c, equilibrium redox potential for the reduction of CuFeS₂ to Cu₂S) and the oxidation potential (E_ox, equilibrium redox potential for the oxidation of Cu₂S). The results of the leaching tests show that the leaching rate in hydrochloric acid solution is the fastest and that the relationship between the Cu leaching rate and oxidation–reduction potential (ORP) follows Hiroyoshi’s model. Thermodynamic calculations indicate that, with an increase in the chloride concentration, the concentration of cuprous ions increases as the chlorocuprate(I) complex ions are formed and the contribution of cuprous ions to the critical potential is greater than that of cupric ions, even though the concentration of cuprous ions is lower than that of cupric ions. This fact suggests that the formation of chlorocuprate(I) ions in a chloride solution may improve the chalcopyrite leaching rate by increasing the critical potential.