乳化酸+硝酸粉末酸压技术在泥灰岩储层中的应用

华北油田泥灰岩储层曾进行多种类型的酸化增产改造工艺,但均未取得理想效果。经过对泥灰岩地层进行大量的油藏地质、室内试验研究以及工程、地质技术人员的反复论证,优选出一种切实可行的酸压改造措施——前置液+高温乳化酸+固体硝酸酸压工艺。经过现场应用,收到了较好的增产效果,为华北油田泥灰岩储层改造措施找到了突破口。     

一种制备磁性粉末的新技术--均匀颗粒成型法

采用均匀颗粒成型法（Uniform Dropler Spray-UDS）制备Fe基合金粉末，该方法制备的颗粒粒度分布均匀，性能一致，大大优于传统的粉末制备方法（如破碎法、气雾化），具有广阔的应用前景。本文分析了粉末制备过程中颗粒尺寸的影响因素，结果表明：颗粒的大小主要取决于坩埚底部小孔、坩埚内外气体压强差以及振荡频率三个独立变量。     

DT型粉状炸药专用蜡的研制

以多种含蜡馏分为基础原料，添加适量DT复合添加剂研制的DT型粉状炸药专用蜡具有优异的分散性和抗水性，可满足各种低梯粉状炸药要求，简化炸药配方，方便操作及其质量控制，以其生产的炸药爆速高，贮存期长，各项性能满足GB12437－2000标准要求。     

Influence of Ti Powder Characteristics on Combustion Synthesis of Porous NiTi Alloy

Porous NiTi shape memory alloy (SMA) is a novel biomedical material used for human hard tissue implant .The influence of elemental titanium powder characteristics such as powder morphology, particle size and specific surface area( SSA) on the minimal ignition temperature ,combustion temperature and final product of porous Ni-Ti SMA fabricated by combustion synthesis method was investigated in this paper by scanning electron microscopy (SEM) and laser diffraction.The preliminary data indicated that the titanium powder characteristics had a strong effect on combustion synthesis of porous NiTi SMA.     

硅粉/酚醛制备低成本碳化硅陶瓷复合材料

以低成本的硅粉和酚醛为原料 ,采用浆料浸渍 热压成型 反应烧结法制备了Cf SiC单向板 ,并对工艺条件进行了探讨。制备得到的单向板的弯曲强度达到 45 6 .8MPa ,断裂韧性达到 7.94MPa·m1 2 。     

纳米NiO粉体的制备及其表征

采用溶胶转化－凝胶法制备了纳米级NiO粉体。Ni(OH)2粉体的TG－DSC分析表明：在升温速率为10℃/min的条件下，粉体在489K时开始显著分解，626K时分解完毕。X－射线衍射分析表明：分解产物为纯净的NiO2。NiO粉体的化学成分分析表明：其纯度高于国家标准。TEM电镜分析表明：NiO粉体呈单分散的球形或棒状颗粒。对NiO粉体的热敏性能有待进一步研究。     

Oxidation of porous nanocrystalline titanium nitride. II. Scale structure and composition

We have used x-ray phase analysis to study the composition of the products of reaction between oxygen and nanocrystalline powders with particle sizes 15, 40, 55, and 80 nm, and also specimens pressed (and sintered) from them. The powders were oxidized in air at 100°C (400 h) to 500°C (5 min), while the sintered specimens were oxidized at 600–900°C for 15, 120, and 240 min. In all cases, in the initial oxidation step the oxynitride Ti(O_xN_y) is formed, which over time is oxidized to TiO, Ti₂O₃, Ti₃O₅, TiO₂ (anatase) and TiO₂ (rutile). In the range 600–800°C, formation of a continuous oxide layer and conversion of anatase to rutile slows down diffusion of oxygen in the scale. We have established that at 900°C, the growth rate of the scale thickness increases and so the reflections from the oxynitride are barely noticeable on the diffraction patterns taken from the surface of the oxidized specimen. In these diffraction patterns, along with strong reflections from the rutile, we also observed weak reflections from lower oxides and anatase, which may be due to reaction between oxygen and the titanium ions diffused to the scale surface. We have concluded that at T > 850°C, the mechanism for oxidation of TiN changes. This is due to superposition of counterdiffusion of titanium ions on the diffusion of oxygen. __________ Translated from Poroshkovaya Metallurgiya, Nos. 3–4(448), pp. 72–78, March–April, 2006.     

钛铁矿流态化氧化机理研究

对低品位钛铁矿进行预氧化、预还原等预处理后可满足硫酸法生产钛白粉工艺所需高品位钛铁矿的要求。本试验采用流态化预氧化方法处理风化程度低、含硫较高的钛铁矿。结果表明 :流态化氧化可大幅度地降低钛铁矿中硫含量 ;钛铁矿流态化氧化的适宜温度为 :80 0～ 90 0℃ ,且在此温度范围内 ,随温度的升高 ,钛铁矿的氧化速度增加 ,在 90 0℃时 ,5 0min钛铁矿基本能完成氧化     

单壁纳米碳管/纳米铝基复合材料的增强效果

用半连续氢电弧法和活性氢等离子蒸发法分别制备出单壁纳米碳管(SWNTs)和纳米A1粉体，然后用提纯后的SWNTs和纳米A1粉体制备出SWNTs含量(质量分数)分别为0、2．5％、5．0％、7．5％和10.0％的单壁纳米碳管／纳米铝基块体复合材料．SWNTs对高强度纳米A1基体具有显著的增强作用，当SWNTs含量小于5．0％时，材料的硬度随着SWNTs含量的提高线性上升．其中5％SWNTs和纳米A1的复合增强效果最好，其硬度可达2.89GPa，大约是粗晶A1(0．15GPa)的20倍．当SWNTs含量超过5．0％时，增强效果开始缓慢的下降．讨论了单壁纳米碳管增强纳米铝基复合材料的强化机制．     

Preparation of Compound Ultrafine CeO2 by Wet-Solid-Phase Mechanochemical Modification

To satisfy practical requirements from industrial applications, an alternate route for synthesis compound ultrafine CeO2 powders by wet-solid-phase mechanochemical modification using industrial grade hydrated cerium carbonate as raw material was proposed.The effect of modifier reaction percentage, reaction time, calcining temperature and modifier amount on particle size, density, suspensibility, and hardness of compound CeO2 powder was investigated.The phase evolutions of preparation process were characterized by XRD.SEM micrograph of the final product shows that compound CeO2 powders obtained are well-dispersed, spherically-shaped, uniformly-sized and submicron-sized particles.The method is readily available in raw material, low in cost, simple in process, and has great potential for industrialization.The compound CeO2 powders of different physical properties can be synthesized by controlling the above-mentioned influence factors in preparation process.