废旧电子材料回收利用现状及发展展望

随着科学技术的进步，各类电子产品已经成为人们生活中不可缺少的组成部分，而其发展和普及的背后，我们将面临越来越多淘汰的废旧电子产品对环境带来的压力。与此同时，各类资源的短缺也需要从这些富含众多金属元素的废旧电子材料中找出解决办法。从废旧电子材料回收的紧迫性和必要性出发，分别介绍了目前国内外回收技术的现状及发展方向，并介绍了模型在回收技术发展和实际应用中可以起到的辅助作用。     

高级氧化技术强化皮革废水生化处理效果初探

皮革废水中含大量难降解有机物,导致常规好氧生化处理速率低、效果差.实验考察了在Us(超声波)、UV(紫外光)、US/Fenton、UV/Fenton等高级氧化技术强化作用下的生化处理效果,结果表明,在相同水质和实验条件下,废水经Us、UV处理30min后可使后续生化反应速率显著提高,分别反应8h、24h后的COD去除率即可达到直接经微生物处理48h后达到的48%,但延长反应时间至48h对COD去除率没有明显提高;Fenton试剂强化US、UV的处理效果要高于单独Us、UV工艺,经30min预处理,随后在微生物作用下分别反应4h和8h即可达到45%和51%的COD去除率,同时延长反应时间也能使最终COD去除率明显提高,反应48h后,COD去除率可分别提高至64%和72%.     

混凝法在滇池蓝藻暴发期净水除藻的可行性研究

采用精制硫酸铝为混凝剂,L93^4正交法安排滇池蓝藻暴发期混凝沉降除藻除净水工艺实验。结果表明,混凝剂种类、水样pH值对蓝藻去除率有很大影响。研究确定了混凝剂除藻最佳操作条件,为混凝法去除蓝藻的工业化提供了理论和实际操作依据。     

Climate Change and Energy Technologies

The long time scale of the climate change problem and the inherent nature of the carbon cycle bring important implications for present technology development efforts. Even if major technology improvements are achieved for non-carbon-emitting technologies such as energy-intensity improvements, wind, solar, biomass, and nuclear over the course of the 21^st century, most examinations of potential future greenhouse emissions conclude that additional technology development will be required to stabilize greenhouse gas concentrations. The evelopment of an expanded suite of technologies including carbon capture and disposal, hydrogen systems and biotechnology hold the potential to dramatically reduce the cost of stabilizing greenhouse gas concentrations. This paper examines these technologies in the context of a global integrated assessment model of energy, agriculture, land-use, economics, and carbon cycle processes.     

炼油厂污水的综合治理

针对近年炼油厂高污染负荷污水增加问题,就采取预处理措施减少污染负荷及改进污水处理工艺提高污水处理能力进行了探讨,并提出污水综合治理方案.     

美国有害废弃物污染防治对策的动向

美国现有2.4亿人口,每年约产生2.5亿吨有害废弃物。近年来有害废气物产生量不断增加,所造成的危害成了重大的社会问题。为此,美国制定了资源保护再生法和风险基金法,依法进行管理和处理。在两法的基础上,美国环保局(EPA)实施了废弃物削减计划和风险基金技术评价(SITE)计划。下面就其主要内容加以介绍。 1 资源保护再生法资源保护再生法的最终目标是,保障人体健康和保护环境;减少废弃物量,合理使用能源和保护自然资源;削减有害废弃物的产生量。资源保护再生法所指的废弃物是,从家庭排出的厨房垃圾,商业和工业的碎屑,上下水处理设施和大气污染防治设施产生的污泥和其它废弃物。工业、商业、矿业、农业等产生的固体、液体和含有气体的废弃物。它不包括家庭污水和水质净化法控制的产业排水。有害废弃物是指具有易燃性、腐蚀性、反应性和浸出毒性较强的固体废弃物。     

A three-year follow-up on a child with low level trisomy 8 mosaicism which was diagnosed prenatally

We report on a case of trisomy 8 mosaicism detected prenatally in a single clone of amniotic fluid culture, and confirmed on fetal blood and on peripheral lymphocytes after birth. A follow-up was performed over 3 years, showing a clinically normal female with cognitive, neuropsychological, and linguistic development in a normal range.     

方头柱塞冷挤镦工艺及模具设计

分析了硬铝合金方头柱塞件的冷挤镦工艺 ,设计了方头柱塞冷挤镦件图 ,计算及选用了毛坯形状及尺寸 ,验算了许可变形程度 ,选择了冷成形用的设备 ,拟制了冷挤镦工艺前的毛坯处理并设计了方头柱塞冷挤镦模具结构。     

相对灰色关联度在城市污水处理工艺优选中的应用

通过对城市污水处理工艺评价指标的定量化处理，并根据奖优罚劣的原则对初始指标集进行[-1，1]区间线性规范化处理，确定理想最优方案（A^＊）和理想最劣方案（A-），以此计算出各待选方案与它们的相关系数（ζ）。采用变异系数法计算各指标权重（ω），并计算各候选方案相对最优方案的灰色关联度，进而确定最佳方案。     

Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by steroid analysis in the amniotic fluid of mid-pregnancy: Comparison with HLA typing in 17 pregnancies at risk for CAH

Amniotic fluid (AF) levels of 17-hydroxyprogesterone (17OHP) and testosterone (T) were determined at 16–17 weeks in 17 pregnancies at risk for CAH and results compared to 75 normal controls. The fetus was predicted to be unaffected in 12 cases on the findings of normal AF levels of both 17OHP and T and the latter allowed a correct prediction of fetal sex in all instances. HLA typing confirmed normality in 12 cases revealing 5 carriers, 5 homozygous normal and 2 indeterminate. Steroid levels of the 2 groups were similar. Three fetuses were predicted to be CAH affected on unambiguously high levels of 17OHP and T (in female only). HLA typing was in agreement, and the diagnosis was confirmed in 2 abortuses and a female newborn by physical and hormonal studies. In the last 2 cases AF levels of OHP and T were normal but HLA (A/B/C) genotypes were identical to the CAH affected siblings. Normal physical and hormonal findings in the 2 aborted fetuses would exclude the possibility of an in utero virilizing form of CAH. The discrepancy could be explained on the basis that the fetuses had an allelic form of 21-hydroxylase deficiency or on the basis of recombination (not fully tested). It is concluded that a fully informative prenatal diagnosis of CAH should not rely entirely on HLA typing but on hormonal studies.