石墨炉原子吸收光谱法测定海河下游水中痕量镉

原子吸收光谱法直接测定高盐水中痕量镉时,有很大背景吸收和误差。本文采用络合—萃取技术使共存元素与待测元素分离,既消除了基体干扰,又达到了富集作用,使测定结果准确可靠。     

Highly active mixed-phase TiO2 photocatalysts fabricated at low temperature and the correlation between phase composition and photocatalytic activity

The idea of varying volume ratio of water to ethanol in solvent was firstly employed to yield phase composition controllable mixedphase titanium dioxide (TiO2) photocatalysts via a low temperature solvothermal route at 353 K. It was found that anatase contents increase from 0 to 100% with increase of ethanol contents in solvent. The mixed-phase TiO2 with 60% anatase content exhibited the best photocatalytic activity in photodecomposing formaldehyde (FAD) under UV light irradiation, which increases by about ...     

铅锌冶炼废水处理后沉渣重金属元素特征与环境活性研究

通过扫描电子显微镜与X射线衍射仪分析、BCR法三步连续提取及元素化学分析,对铅锌冶炼废水处理后沉渣中重金属的赋存状态、环境活性进行研究。结果表明,沉渣中主要毒害元素为Zn、Pb、Mn、Cd和Cu,且以非晶态存在,其含量分别为62350、29530、7650、4530和830 mg/kg。渣中Zn和Cd酸可提取态所占比例较大,分别为37.72%和34.44%; Mn的可还原态相对含量很高,达到49.67%;Zn和Pb的可氧化态含量较高,分别占全量的34.16%、34.68%;Pb和Cu的残渣态含量较高,分别占全量的39.72%和61.69%。     

邕江流域有机氯农药残留问题的初步研究

采用固相萃取和GC-ECD对邕江流域水体中17种痕量有机氯农药的残留状况进行分析测定,检测结果表明,邕江干流均检出硫酸硫丹,但有机氯农药浓度较低,均未超过现有相关标准。城市内河残留的有机氯农药以六六六为主,主要来自于长期的历史残留,而硫酸硫丹除朝阳溪和相思湖丰水期未检测到外,均普遍检出。方法检出限为1~5ng/L,替代物加标回收率为103.5%~112.0%。     

A miniature stainless steel net dumbbell-shaped stir-bar for the extraction of phthalate esters in instant noodle and rice soup samples

Abstract

This work reports the development of a very-simple-to-construct stir-bar extraction device so called “a dumbbell-shaped stainless steel stir-bar.” The extraction device was assembled from a rolled up stainless steel net filled with an XAD-2 sorbent and a metal rod to allow the use of a magnetic stirrer during extraction. The dumbbell-shaped stainless steel stir-bar was used to extract diethyl phthalate (DEP), dibutyl phthalate (DBP), and di(2-ethylhexyl) phthalate (DEHP) before analysis by a gas chromatograph equipped with an electron capture detector (GD-ECD). Under the optimal conditions, the developed method provided a good linearity from 10.0 to 1,000.0?ng mL^?1 for all three compounds. Limits of detection and limits of quantification were 9.37?±?0.29?ng mL^?1 and 31.22?±?0.95?ng mL^?1 for DEP, 5.73?±?0.31?ng mL^?1 and 19.1?±?1.0?ng mL^?1 for DBP and 3.30?±?0.06?ng mL^?1 and 11.0?±?0.19?ng mL^?1 for DEHP, respectively. Good recoveries in the range of 81.89?±?0.17 to 109.5?±?2.0% were achieved when the method was used to extract phthalate esters in five instant noodle and two rice soup samples.     

Performance of a large-scale greenhouse solar dryer integrated with phase change material thermal storage system for drying of chili

ABSTRACT

Large-scale greenhouse solar dryers have been used for drying various products and this type of dryer is usually equipped with LPG burner as auxiliary heater, which creates more operating cost. To overcome this problem, phase change material (PCM) thermal storage was proposed to substitute for the LPG burner. In this work, the performance of a large-scale greenhouse solar dryer integrated with a PCM as a latent heat storage for drying of chili was investigated. Experimental studies were conducted to compare the performance of this dryer with that of another large-scale greenhouse solar dryer without the PCM thermal storage and open sun drying. Chili with an initial moisture content of 74.7% (w.b.) was dried to a final moisture content of 10.0% (w.b.) in 2.5 days, 3.5 days, and 11 days using the solar dryer integrated with the PCM thermal storage, the solar dryer without the PCM thermal storage and the open sun drying, respectively. The performance of the solar dryer integrated with the PCM thermal storage was also evaluated using exergy analysis. The exergy efficiency of the drying room of the solar dryer integrated with the PCM thermal storage and the solar dryer without the PCM thermal storage for drying of chili was found to be 13.1% and 11.4%, respectively and the thermal storage helps to dry chili during adverse weather conditions. The results of exergy analysis implied that the exergy losses from the dryer with the PCM should be reduced.     

金黄色葡萄球菌的演相培养及A蛋白的提取

对金黄色葡萄球菌（Ｓｔａｐｈｙｌｏｃｏｃｃｕｓａｕｒｅｕｓ）ＣｏｗａｎⅠ的培养及Ａ蛋白提取工艺进行了优化研究．结果表明：在培养基中分别增加牛肉膏和蛋白陈的含量，有利于提高菌体生物量及Ａ蛋白的得率；少量酵母浸膏及葡萄糖对生物量及Ａ蛋白得率有促进作用，但当达到一定浓度时则会产生基质抑制作用；恒定培养过程的ｐＨ值有利于Ａ蛋白得率的增加，０．０３（）／ｍｉｎ通气量、搅拌速度２００ｒ／ｍｉｎ是能满足菌体生长的条件．根据Ａ蛋白耐热性强这一特性，采用加热法除去大部分杂质，然后用ＩｇＧ－琼脂糖凝胶亲和层析实现了Ａ蛋白的提纯．     

Variation in some chemical parameters and organic matter in soils regenerated by the addition of municipal solid waste

The organic fraction of a municipal solid waste was added in different doses to an eroded soil formed of loam and with no vegetal cover. After three years, the changes in macronutrient content and the chemical-structural composition of its organic matter were studied. The addition of the organic fraction from a municipal solid waste had a positive effect on soil regeneration, the treated soils being covered with spontaneous vegetation from 1 yr onwards. An increase in electrical conductivity and a fall in pH were noted in the treated soils as were increases in macronutrients, particularly N and available P and the different carbon fractions. Optical density measurements of the organic matter extracted with sodium pyrophosphate showed that the treated soils contained an organic matter with less condensed compounds and with a greater tendency to evolve than the control. A pyrolysis-gas chromatography study of the organic matter extracted with pyrophosphate showed large quantities of benzene both in the treated soils and control; pyrrole was also relatively abundant, although this fragment decreased as the dose rose. Xylenes and pyridine were present in greater quantities in the control and furfural in the treated soils. Three years after addition to the soil, the organic matter had a higher proportion of fragments derived from aromatic compounds and a smaller proportion derived from hydrocarbons. Similarity indices showed that, although the added and newly formed organic matter 3 yr after addition continued to differ from that of the original soil and to be more mineralizable, the transformations it has undergone made it more similar to the original organic matter of the soil than it was at the moment of being added.     

固体可燃物易点燃性标准的探讨

可燃性固体的引燃和熄灭与辐射到其表面的临界热能量和产生挥发分所必需的表面温度有关。探讨固体可燃物易点燃性标准,燃怀标准,对防火和灭火在理论上有一定的指导意义。本文在理论分析的基础上,提出了一种用固体挥发分的临界质量通量量化解释引燃和熄灭条件的方法,给出了易点燃性的标准。     

Determination of particulate polycyclic aromatic hydrocarbons in ambient air by gas chromatography-mass spectrometry after molecularly imprinted polymer extraction

A solid phase extraction procedure (SPE) is described for the quantitative analysis of polycyclic aromatic hydrocarbons (PAHs) in atmospheric particulate matter (PM), as ubiquitous environmental pollutants routinely measured in air quality monitoring. A SPE cartridge was used based on a molecular imprinted polymer (MIP-SPE) properly tailored for selective retention of PAHs with 4 and more benzene fused rings. The performance of the clean-up procedure was evaluated with the specific concern of selective purification towards saturated hydrocarbons, which are the PM components mostly interfering GC analysis of target PAHs. Under optimized operative conditions, the MIP-SPE provided analyte recovery close to 95% for heavier PAHs, from benzo(α)pyrene to benzo(ghi)perylene, and close to 90% for four benzene rings PAHs, with good reproducibility (RSDs: 2.5%-5.9%). Otherwise, C₁₇-C₃₂ n-alkanes were nearly completely removed. The proposed method was critically compared with Solid Phase Micro Extraction (SPME) using a polyacrylate fiber. Both methods were successfully applied to the analysis of ambient PM_2.5 samples collected at an urban polluted site. Between the two procedures, the MIP-SPE provided the highest recovery (R% ≥ 93%) for PAHs with 5 and more benzene rings, but lower for lighter PAHs. In contrast, SPME showed a mean acceptable R% value (∼ 80%) for all the investigated PAHs, except for the heaviest PAHs in the most polluted samples (R%: 110%-138%), suggesting an incomplete purification from the interfering n-hydrocarbons.