颗粒煤的多扩散系数瓦斯解吸模型及扩散参数反演研究

为研究颗粒煤瓦斯解吸规律,基于Fick定律建立了颗粒煤的多扩散系数瓦斯解吸 模型,完成了颗粒煤瓦斯解吸模型的数值试验。引入了非负约束最小二乘法反演算法（ NNLS）,通过试验数据反演得出颗粒煤的扩散参数的B谱,从而确定出颗粒煤瓦斯扩散 系数D的准确范围。研究结果表明:颗粒煤瓦斯解吸符合Fick扩散定律,颗粒煤的多扩 散系数瓦斯解吸模型能很好地解决单一扩散系数模型的扩散系数随时间衰减的问题,准 确反映了颗粒煤瓦斯解吸规律,单一扩散系数瓦斯解吸模型只是多扩散系数瓦斯解吸模 型的一个特例;NNLS是一种有效的反演算法,利用NNLS方法可以准确反演出颗粒煤瓦斯 解吸过程中的扩散参数的B谱,通过B谱可方便计算出颗粒煤的瓦斯扩散系数。     

清水江水、鱼体和悬浮物中汞的特征及污染评价

为探明清水江水、鱼体和悬浮物中的汞污染情况,采用地质累积指数、单因子污染指数和潜在生态风险因子对清水江悬浮物进行了汞污染评价以及汞残留指数对清水江鱼体汞进行了污染评价。结果表明,清水江旁海段悬浮物汞污染程度高于清水江下司段,并已达到了重度潜在生态危害水平。然而,清水江水和鱼体未受到汞的污染,分析认为磷化工尾矿可能是加剧清水江悬浮物汞污染的原因之一。     

氧化·热化学脱硫研究

热化学脱硫法因铵盐回收率低、产物不稳定,无法解决实用化问题。氧化热化学法应用超强脉冲电场产生高浓度、高能量的活性粒子,使SO₂在氧化过程中生成H₂SO₄,与NH3进行热化学反应,生成稳定的固体微粒（NH₄）₂SO₄,用电收尘器加以回收。脱除率、回收率可达90％左右,脱除1m³烟气中SO₂耗能为4Wh,实现了干法高效脱硫。一次投资大幅度减少,回收铵盐基本上抵消了药品费和电费。     

应用模式生物检测饮用水源颗粒物的毒性效应

悬浮颗粒物在自然水体中广泛存在,大量小颗粒物(粒径<1μm)可吸附、聚集水中多种污染物,从而形成新的复合污染,影响水生生态系统。已有研究表明,颗粒物粒径越小,传统饮用水处理工艺越难以去除,因此,其表面吸附的污染物也会随之残留在水体中,对饮用水安全产生影响。本研究对南京某自来水厂进水和出水中的颗粒物进行了测定和对比,并选用3种不同种类的模式生物包括发光菌(Photobacterium phosphoreum)、纤细裸藻(Euglena gracilis)和蚕豆(Vicia faba L.),对饮用水源水中不同粒径颗粒物的毒性效应进行了测试。结果表明,传统水处理工艺对小颗粒物(粒径<1μm)的去除效果并不理想;经传统水处理工艺处理后,出水仍显著抑制发光菌发光强度以及纤细裸藻生长,对蚕豆的污染指数较高,可能存在一定健康隐患;进水中颗粒物粒径<1μm组对发光菌发光强度和纤细裸藻生长的抑制效应显著大于粒径≥1μm颗粒物组,蚕豆根尖的污染指数也更高,毒性更强。本研究结果可为饮用水的生物毒性检测和水处理工艺改良提供参考。     

西安城北地区秋季PM_(2.5)中的矿尘颗粒污染特征

采用单颗粒气溶胶飞行时间质谱仪(Single Particle Aerosol Mass Spectrometer,SPAMS)对西安市大气矿尘颗粒物进行连续12 d在线分析,共采集到107 425个同时含有正负质谱信息的矿尘颗粒,矿尘颗粒物占PM_(2.5)样本数的8.44%。结果表明,矿尘颗粒物的正离子碎片成分以Na~+、K~+、Al~+、Ca~+、CaO~+、Fe~+为主,同时还含有Pb~+等,负离子碎片成分以NO~-_2和NO~-_3为主,另外还含有HSO~-_4、SiO~-_3、HSiO~-_3、H(NO_3)~-_2等。在西安市大气细颗粒物中,矿尘颗粒物中贡献较大的几类(如含钙、含铁、铁氧颗粒物等)大多是老化的成分。将观测阶段采集到的矿尘颗粒纳入本地污染源谱进行来源分析,其主要来源为扬尘源、工业源、燃煤源和汽车尾气源等。     

大气细颗粒物水溶成分和非水溶成分的细胞毒性

为了研究细颗粒物不同成分细胞毒作用的差异,以细颗粒物水溶成分和非水溶成分对人肺癌上皮细胞株A549细胞染毒.结果表明,在染毒剂量为100 μg·mL-1、200 μg·mL-1和300 μg·mL-1的范围内,水溶成分的细胞毒性明显高于非水溶成分(P(0.05),表现为抑制细胞活性,导致细胞膜损伤增加.并且诱导细胞活性氧(ROS)的产生.使用N-乙酰半胱氨酸(NAC)和抗坏血酸(Vit C)阻断活性氧(ROS)产生的研究结果表明,与未加上述抗氧化剂的染毒组相比,加抗氧化剂的染毒组细胞的活性明显增强.因此,提示细颗粒物水溶成分是最主要的毒性成分之一,而氧化.应激损伤可能是细颗粒物细胞毒作用的重要机制之一.     

Atmospheric mineral particles collected at Qira in the Taklamakan Desert, China

Aerosol particles were collected in the situation of the widespread dust suspension on 21 February 1991 at Qira in the southern edge of the Taklamakan Desert, western China. The collected particles were examined by a transmission electron microscope equipped with an energy-dispersive X-ray (EDX) analyzer in order to obtain the size and elemental composition of individual mineral particles.On the basis of EDX analyses for 386 particles, mineral particles were present in high number fractions (>99%) of particles in the radius range of 0.1–4 μm. Particles mainly composed of silicates comprised 76% of mineral particles. “Ca-rich” particles were detected in 7% of all the particles. Ca in the particles would be present not only as CaCO₃ but also as an internal mixture of CaCO₃ and CaSO₄. Particles containing halite (NaCl) were detected in number proportions of about 10% and were mainly present in the radius range of 0.5 μm. Some halite particles would be modified by chemical reactions with sulfuric acid.     

Reconstructed mass-spectrometric pattern for characterization of carbon compounds in smoker's lung in situ

BACKGROUND: Cigarette smoke is a major anthropogenic pollutant and contributes to the permanent load of ambient particulate matter in the air, particularly indoors. It is the leading risk factor for premature loss of life due to chronic bronchitis, emphysema and lung cancer. Smoker's lung and graphite pneumoconiosis are pathological states characterized by the deposition of carbonaceous particles. METHODS: Mass spectrometry was used to evaluate unstained lung sections obtained in vivo from a heavy smoker and a patient with occupationally acquired graphite pneumoconiosis. RESULTS AND DISCUSSION: The composition of carbon compounds deposited in lung tissue samples is demonstrated here for the first time. Thirty carbonaceous-containing microareas from ten biopsies (three areas per biopsy) of lung tissues were analyzed mass-spectrometrically. In each case, the samples were taken from a smoker's lung or those demonstrating a graphite pneumoconiosis. The lung-tissue samples were selected by light microscopy before they were evaporated for mass spectrometry. First-order criteria were anionic and cationic mass peaks which occur within the mass patterns in lung tissues of smoker's lung, although not in graphite pneumoconiosis. Second-order criteria were mass peaks from smoker's lung with standard deviations SD < or = 14% of the mean value. First and second-order mass peaks matched the mass peaks of experimental cigarette-smoke condensate in 9 out of 11 peaks. A software program was developed that enabled fast, automated recognition of the typical mass peaks, and thereby confirmed the histological diagnosis of smoker's lung. CONCLUSIONS: The analysis of carbonaceous particles within lung biopsies from a heavy smoker corresponded to the spectra of tobacco condensate and not to the investigated biopsies of graphite peneumoconiosis. RECOMMENDATION AND OUTLOOK: The analyses were performed in order to find out whether mass-spectrometric criteria exist for the differentiation of carbonaceous lung-tissue deposits. Mass spectrometry may be a valuable tool in determining the composition of carbon compounds deposited in human lung tissue. So far, qualitative assessment of the composition of deposits in lung tissue is only possible after the patient is deceased (autopsy).     

超声波萃取—GC／MS测定大气颗粒物中的多环芳烃

采用超声波萃取大气颗粒物样品中的多环芳烃，样品不须纯化，直接可用于GC／MS分析，超声波萃取效率高，萃取时间短；采用MS的SIM方式对多环芳烃进行定性定量，回收率84.5%-108.5%，变异系数3.1%-14.5%。