马马崖一级水电站预可行性研究枢纽布置及特点

马马崖一级水电站于2005年11月完成预可行性研究报告,工程枢纽采用碾压混凝土重力坝、左岸地面厂房、右岸导流洞方案,具有淹没少、移民少、工期短及投资少等较优越的技术经济指标,且交通较方便。目前,该电站正在进行可行性研究阶段的勘测设计工作,并正在抓紧前期工程施工,力争2009年年底发电。     

影响带锯机锯切质量的原因及处理措施

通过对锯切装置的改进，提高了锯切性能，降低了锯条成本，保证了锯切质量，使设备更加高效、安全的工作。     

球墨铸铁材料对激光的吸收率

球墨铸铁因其优良性能而被广泛用作模具材料。对球墨铸铁冲压模具的激光表面处理已成为改善其耐磨性、提高使用寿命的重要方法。一定激光参量下吸收率的大小又直接影响到表面处理的质量。因此,确定球墨铸铁材料对激光的吸收率十分必要。通过热电偶测温,计算机数据采集系统进行定点温度采集,并结合数值模拟方法,对吸收率进行了标定,即首先根据预置的吸收率计算,预测被测点处的温度响应,并与实测响应比较,不断修正吸收率值,使预测温度响应和实验值吻合,由此获得吸收率。采用这种方法获得了球墨铸铁材料在大气条件下对激光的吸收率为23.3%。为激光处理球墨铸铁材料时工艺参量的选择和优化提供了一定参考。     

提供宽范围负载阻抗的有源可变电阻器

功率电阻、可变电阻和其他电子负载常常用于测试电源和电压调节器,如图1所示.虽然功能和机械电位器相同,但它基于有源器件,能够提供很宽的负载电阻范围,阻值调节分辨率高,发热比机械电位器少.     

Preparation and properties ofgem-dichlorocyclopropane derivatives of long-chain fatty esters

Methyl oleate (18∶1) and linoleate (18∶2) were readily transformed to the correspondinggem-dichlorocyclopropane derivatives in high yield, using triethylbenzylammonium chloride as the phase-transfer catalyst in the presence of aqueous NaOH and CHCl₃. Reaction of dichlorocarbene with methyl 12-hydroxystearate furnished methyl 12-chlorostearate (49%) and 12-O-formylstearate (19%). The hydroxy group in methyl ricinoleate was protected (O-tetrahydropyran-2′-yl) prior to dichlorocyclopropanation of the ethylenic bond. Removal of the protecting group allowed the hydroxy group to be converted to a chloride,O-acetyl, azido orO-formyl function. Treatment of methyl ricinoleate with thionyl chloride, followed by the reaction with dichlorocarbene gave the corresponding 12-chloro-dichlorocyclopropane derivative. The dichlorocyclopropane derivative of oleic acid was transformed to a C₁₉ allenic fatty acid when treated witht-butyl lithium. However, the remaining dichlorocyclopropane derivatives, containing an additional functional group in the alkyl chain, failed to yield the corresponding allenic derivatives. All derivatives were characterized by a combination of spectroscopic and chromatographic techniques, including infrared,¹H nuclear magnetic resonance (NMR), and¹³C NMR spectroscopy.     

Reducing energy-related CO2 emissions using accelerated weathering of limestone

The use and impacts of accelerated weathering of limestone (AWL; reaction: CO₂+H₂O+CaCO₃→Ca²⁺+2(HCO₃⁻) is explored as a CO₂ capture and sequestration method. It is shown that significant limestone resources are relatively close to a majority of CO₂-emitting power plants along the coastal US, a favored siting location for AWL. Waste fines, representing more than 20% of current US crushed limestone production (>10⁹ tonnes/yr), could provide an inexpensive or free source of AWL carbonate. With limestone transportation then as the dominant cost variable, CO₂ mitigation costs of $3-$4/tonne appear to be possible in certain locations. Perhaps 10–20% of US point–source CO₂ emissions could be mitigated in this fashion. It is experimentally shown that CO₂ sequestration rates of 10⁻⁶ to 10⁻⁵ moles/sec per m² of limestone surface area are achievable, with reaction densities on the order of 10⁻² tonnes CO₂ m⁻³day⁻¹, highly dependent on limestone particle size, solution turbulence and flow, and CO₂ concentration. Modeling shows that AWL would allow carbon storage in the ocean with significantly reduced impacts to seawater pH relative to direct CO₂ disposal into the atmosphere or sea. The addition of AWL-derived alkalinity to the ocean may itself be beneficial for marine biota.