螯合纤维的合成及其吸附重金属离子的研究

研究了含有胺肟基和胺腙基功能纤维的合成、结构表征和螯合性能。新型合纤维对多种重金属离子具有良好的吸附性能，能从被污染的水体和土壤中去除重金属离子，经洗脱后可回收金属，螯合纤维能反复使用。     

离子色谱法在石化工业废水分析中的应用

用IC-6离子色谱分析仪，研究石化工业废水中阴离子的测定技术，并首次建立炼油、化肥外排废水中F^-、Cl^-、NO2^-、PO4^3-、NO3^-、SO4^2-等阴离子含量测定的岗位。以含0．0054mol／L碳酸氢钠和0．0050mol／L碳酸钠为淋洗液，在电流70mA、流速1．5mL／min、泵压0～42MPa的条件下，测得各阴离子的相关系数均大于0．995、相对标准偏差（RSD）〈5．00％、加标回收率为95％～116％。     

电极流动分析仪的研制和应用

采用固定电极测试状态的方法，将流动技术引入到离子电极直接电位分析法中，设计并试制了电极流动分析仪。配用市售硝酸根电极、钠电极、氟电极、氯电极和氨电极进行了环境样品的测定。结果表明，电极流动分析仪法的分析速度比直接电位法提高２－３倍，变异系数，２．９％－５．０％之间，回收率在９０％－１０５％之间；直接电位法变异系数在２．３％－６．７％之间，加收率在９０％－１０９％之间。     

色谱痕量分析中的非线性效应及影响

根据溶质在流动相与固定相中吸附平衡热力学的观点简要讨论了色谱分离中的非线性原理，及其在进行色谱痕量分析采用大进样量时对定性和定量的影响，并提出了改进方法。同时也探讨了非线性效应对样品前处理及未知物馏份制备分离的影响与应用。     

顶空气相色谱法测定食品中甜蜜素含量

采用顶空气相色谱法测定食品中甜蜜素含量,探讨了气液相平衡条件及色谱条件的选择,实验结果表明甜蜜素的标准溶液在0.1-0.4μg/l范围内具有良好的线性关系,回收率为87.5%-101.8%,相对标准偏差为2.6%.     

Effects of particle thermal characteristics on flame microstructures during dust explosions of three long-chain monobasic alcohols in a half-closed chamber

To reveal clearly the effects of particle thermal characteristics on flame microstructures during organic dust explosions, three long-chain monobasic alcohols, solid at room temperature and similar in physical-chemical properties, were chosen to conduct experiments in a half-closed chamber. In the experiments, the dust materials were dispersed into the chamber by air to form dust clouds and the hybrids were ignited by an electrical spark. A high-speed optical schlieren system was used to record the flame propagation behaviors. A fine thermocouple and an ion current probe were respectively used to measure the flame temperature profile and the reaction behaviors of the combustion zone. Based on the experimental results, combustion behaviors and flame microstructures in dust clouds with different thermal characteristics were analyzed in detail. As a result, it was found that the dust flame surfaces were completely covered by cellular structures that significantly increased the flame frontal areas. Flame propagated more quickly and the number of the cellular cells increased as increasing the volatility of the particles. On the contrary, maximum temperature and the thickness of the preheated zone decreased as increasing the volatility of the particles. According to the ion current profile, the particles in the preheat zone were pyrolyzed to intermediate radicals and the radicals' fraction in the higher volatile dust flame was higher than that in the lower volatile dust flame.     

Capability of cation exchange technology to remove proven N-nitrosodimethylamine precursors

N-nitrosodimethylamine(NDMA) precursors consist of a positively charged dimethylamine group and a non-polar moiety, which inspired us to develop a targeted cation exchange technology to remove NDMA precursors. In this study, we tested the removal of two representative NDMA precursors, dimethylamine(DMA) and ranitidine(RNTD), by strong acidic cation exchange resin. The results showed that pH greatly affected the exchange efficiency, with high removal(DMA 78% and RNTD 94%) observed at pH pk_a-1 when the molar ratio of exchange capacity to precursor was 4. The exchange order was obtained as follows: Ca~(2+) Mg~(2+) RNTD~+ K~+ DMA~+ NH_4~+ Na~+. The partition coefficient of DMA~+to Na~+was 1.41 ± 0.26, while that of RNTD~+to Na~+was 12.1 ± 1.9. The pseudo second-order equation fitted the cation exchange kinetics well. Bivalent inorganic cations such as Ca~(2+)were found to have a notable effect on NA precursor removal in softening column test. Besides DMA and RNTD, cation exchange process also worked well for removing other 7 model NDMA precursors. Overall, NDMA precursor removal can be an added benefit of making use of cation exchange water softening processes.     

Study of cyanide removal from contaminated water using zinc peroxide nanomaterial

The present study highlights the potential application of zinc peroxide(ZnO_2)nanomaterial as an efficient material for the decontamination of cyanide from contaminated water. A process patent for ZnO_2 synthesis has been granted in United States of America(US Patent number 8,715,612; May 2014),South Africa,Bangladesh,and India. The ZnO_2 nanomaterial was capped with polyvinylpyrrolidone(PVP)to control the particle size. The PVP capped ZnO_2nanomaterial(PVP-ZnO_2)before and after adsorption of cyanide was characterized by scanning electron microscope,transmission electron microscope,X-ray diffractometer,Fourier transform infrared spectroscopy and time of flight-secondary ion mass spectrometry. The remaining concentration of cyanide after adsorption by PVP-ZnO_2 was determined using ion chromatograph. The adsorption of cyanide over PVP-ZnO_2 was also studied as a function of p H,adsorbent dose,time and concentration of cyanide. The maximum removal of cyanide was observed in p H range 5.8–7.8 within 15 min. The adsorption data was fitted to Langmuir and Fruendlich isotherm and it has been observed that data follows both the isotherms and also follows second order kinetics.     

菌渣中阿维菌素残留检测方法及其无害化工艺研究

文章建立了简单、快速的阿维菌素菌渣中阿维菌素残留量高校液相色谱检测方法以及利用水热法处理阿维菌素菌渣。采用固相萃取-高效液相色谱检测方法测定阿维菌素菌渣中阿维菌素残留量,提取剂为乙腈/水=4/1(V/V),采用HLB固相萃取柱进行净化。加标回收率90.3%~107.3%,相对标准偏差(RSD)为3.00%~5.69%,阿维2菌素标准曲线线性相关系数R~2=0.999 6,线性范围为1.0~1 000 mg/L。利用正交实验,水热法处理阿维菌素菌渣,在190℃的温度下处理2 h后,菌渣中阿维菌素残留量由991.30降至0.84 mg/kg,去除率达99.92%。处理前后的菌渣与有机肥标准作对比,除含水率外其余检测指标均达到有机肥标准要求。该项研究为阿维菌素菌渣的资源化利用提供了理论依据。     

URG-9000型离子色谱仪常见问题及解决办法

介绍了URG-9000型离子色谱仪在运行中常见的问题,URG监测的离子数据部分或全部缺失、数据异常、偏低等情况。并对这些常见问题的出现原因进行了分析说明,通过做校准曲线,考虑背景电导等提出了相应的解决方法。为了提高仪器的运行稳定性保证数据的可靠、准确性,提出了仪器日常维护的一些注意事项。