研究采用硫酸铵焙烧—水浸工艺提高菱镁矿的利用效率,结合XRD和TG-DTA分析以及对比硫酸铵焙烧MgO的物相变化得到焙烧过程中矿相的转化过程。实验结果表明,在菱镁矿粒度为~74μm、硫酸铵与菱镁矿物料摩尔比为1.6:1、焙烧温度为475℃和焙...研究采用硫酸铵焙烧—水浸工艺提高菱镁矿的利用效率,结合XRD和TG-DTA分析以及对比硫酸铵焙烧MgO的物相变化得到焙烧过程中矿相的转化过程。实验结果表明,在菱镁矿粒度为~74μm、硫酸铵与菱镁矿物料摩尔比为1.6:1、焙烧温度为475℃和焙烧时间为2 h的条件下,镁的提取率达到98.7%。反应中物相转化过程可以概括如下:MgCO_(3)先转变为(NH_(4))_(2)Mg_(2)(SO_(4))_(3),再分解得到MgSO_(4)。反应遵循化学反应和扩散混合控制机理,其表观活化能为33.02 k J/mol。展开更多
Be able to form large particles with protein via electrostatic force to enhance the intensity of resonance light scattering（RLS）,（NH4）2SO4 was used as a RLS probe to determine bovine serum albumin（BSA）,human ser...Be able to form large particles with protein via electrostatic force to enhance the intensity of resonance light scattering（RLS）,（NH4）2SO4 was used as a RLS probe to determine bovine serum albumin（BSA）,human serum albumin（HSA） and ovum albumin（OVA）.The experimental conditions were investigated,including the acidity and saturation degree of （NH4）2SO4.Under the optimum conditions,the enhanced RLS intensity is proportional to the concentration of BSA,HSA and OVA in the ranges of 5×10-8―1×10-6,2.5×10-8―8×10-7 and 5×10-8―1.5×10-6 mol/L,respectively.The detection limits for BSA,HAS and OVA are 6.6×10-9,3.8×10-9 and 7.4×10-9 mol/L,respectively.The effects of foreign substances were also examined.The practical and synthetic samples were analyzed with satisfactory results.展开更多
Initial atmospheric corrosion of zinc in the presence of Na2SO4 and (NH4)2SO4 was investigated via quartz crystal microbalance(QCM) in laboratory at relative humidity(RH) of 80% and 25 ℃. The results show that both N...Initial atmospheric corrosion of zinc in the presence of Na2SO4 and (NH4)2SO4 was investigated via quartz crystal microbalance(QCM) in laboratory at relative humidity(RH) of 80% and 25 ℃. The results show that both Na2SO4 and (NH4)2SO4 can accelerate the initial atmospheric corrosion of zinc. The combined effect of Na2SO4 and (NH4)2SO4 on the corrosion of zinc is greater than that caused by (NH4)2SO4 and less than that caused by Na2SO4. Fourier transform infrared spectroscopy(FTIR), X-ray diffractometry(XRD) and scanning electron microscopy(SEM) were used to characterize the corrosion products of zinc. (NH4)2Zn(SO4)2, Zn4SO4(OH)6·5H2O and ZnO present on zinc surface in the presence of (NH4)2SO4 while Zn4SO4(OH)6·5H2O and ZnO are the dominant corrosion products on Na2SO4-treated zinc surface. Probable mechanisms are presented to explain the experimental results.展开更多
Few studies are conducted to quantify the effects of enhanced N deposition on soil nitrous oxide （N2O） emission and methane （CH4） uptake in the meadow steppe of Inner Mongolia, China. A two-year field experiment w...Few studies are conducted to quantify the effects of enhanced N deposition on soil nitrous oxide （N2O） emission and methane （CH4） uptake in the meadow steppe of Inner Mongolia, China. A two-year field experiment was conducted to assess the effects of nitrogen （N） deposition rates （0, 10, and 20 kg N ha-1 year-1 as （NH4）2SO4） on soil N2O and CH4 fluxes. The seasonal and diurnal variations of soil N2O and CH4 fluxes were determined using the static chamber-gas chromatography method during the two growing seasons of 2008 and 2009. Soil temperature, moisture and mineral N （NH4＋-N and NO3-N） concentration were simultaneously measured. Results showed that low level of （NH4）2SO4 （10 kg N ha-1 year-1） did not significantly affect soil CH4 and N20 fluxes and other variables. High level of （NH4）2SO4 （20 kg N ha-1 year-1） significantly increased soil NO3-N concentration by 24.1% to 35.6%, decreased soil CH4 uptake by an average of 20.1%, and significantly promoted soil N2O emission by an average of 98.2%. Soil N2O emission responded more strongly to the added N compared to CH4 uptake. However, soil CH4 fluxes were mainly driven by soil moisture, followed by soil NO3--N concentration. Soil N2O fluxes were mainly driven by soil temperature, followed by soil moisture. Soil inorganic N availability was a key integrator of soil CH4 uptake and N2O emission. These results suggest that the changes of availability of inorganic N induced by the increased N deposition in soil may affect the CH4 and N2O fluxes in the cold semi-arid meadow steppe over the short term.展开更多
基金appreciate financial supports from the National Natural Science Foundation of China(Nos.51774070,52004165)the Science and Technology Project of Yunnan Province,China(No.202101AS070029)。
文摘研究采用硫酸铵焙烧—水浸工艺提高菱镁矿的利用效率,结合XRD和TG-DTA分析以及对比硫酸铵焙烧MgO的物相变化得到焙烧过程中矿相的转化过程。实验结果表明,在菱镁矿粒度为~74μm、硫酸铵与菱镁矿物料摩尔比为1.6:1、焙烧温度为475℃和焙烧时间为2 h的条件下,镁的提取率达到98.7%。反应中物相转化过程可以概括如下:MgCO_(3)先转变为(NH_(4))_(2)Mg_(2)(SO_(4))_(3),再分解得到MgSO_(4)。反应遵循化学反应和扩散混合控制机理,其表观活化能为33.02 k J/mol。
文摘Be able to form large particles with protein via electrostatic force to enhance the intensity of resonance light scattering（RLS）,（NH4）2SO4 was used as a RLS probe to determine bovine serum albumin（BSA）,human serum albumin（HSA） and ovum albumin（OVA）.The experimental conditions were investigated,including the acidity and saturation degree of （NH4）2SO4.Under the optimum conditions,the enhanced RLS intensity is proportional to the concentration of BSA,HSA and OVA in the ranges of 5×10-8―1×10-6,2.5×10-8―8×10-7 and 5×10-8―1.5×10-6 mol/L,respectively.The detection limits for BSA,HAS and OVA are 6.6×10-9,3.8×10-9 and 7.4×10-9 mol/L,respectively.The effects of foreign substances were also examined.The practical and synthetic samples were analyzed with satisfactory results.
基金Project(50261004) supported by the National Natural Science Foundation of China
文摘Initial atmospheric corrosion of zinc in the presence of Na2SO4 and (NH4)2SO4 was investigated via quartz crystal microbalance(QCM) in laboratory at relative humidity(RH) of 80% and 25 ℃. The results show that both Na2SO4 and (NH4)2SO4 can accelerate the initial atmospheric corrosion of zinc. The combined effect of Na2SO4 and (NH4)2SO4 on the corrosion of zinc is greater than that caused by (NH4)2SO4 and less than that caused by Na2SO4. Fourier transform infrared spectroscopy(FTIR), X-ray diffractometry(XRD) and scanning electron microscopy(SEM) were used to characterize the corrosion products of zinc. (NH4)2Zn(SO4)2, Zn4SO4(OH)6·5H2O and ZnO present on zinc surface in the presence of (NH4)2SO4 while Zn4SO4(OH)6·5H2O and ZnO are the dominant corrosion products on Na2SO4-treated zinc surface. Probable mechanisms are presented to explain the experimental results.
文摘利用NH3-(NH4)2SO4体系,对印刷电路板(printed circuit boards,PCB)生产过程中产生大量的含铜污泥中的铜进行浸析。对PCB污泥中重金属的质量分数进行了测定,其中铜在污泥中的质量分数为33.500%,其余金属质量分数较小。重点探讨了氨-硫酸铵浓度及pH、浸析时间、液固比、温度等条件对浸析率的影响。NH3-(NH4)2SO4体系对PCB污泥中铜浸析的最优条件为氨、硫酸铵浓度分别为3.0mol/L和1.5mol/L,液固比为20mL/g,浸析时间为180min,浸析温度为25℃。在最优条件下进行了浸析应用试验,结果表明铜的浸析率可达到97.5%,此方法的相对标准偏差(relative standard deviation,RSD)为0.63%。
基金supported by the National Natural Science Foundation of China (No. 31300375)the National Non-Profit Institute Research Grant of the Chinese Academy of Agricultural Sciences (No. BSRF201505)the Key Project of the National Scientific and Technical Support Program, China (No. 2013BAC03B03)
文摘Few studies are conducted to quantify the effects of enhanced N deposition on soil nitrous oxide （N2O） emission and methane （CH4） uptake in the meadow steppe of Inner Mongolia, China. A two-year field experiment was conducted to assess the effects of nitrogen （N） deposition rates （0, 10, and 20 kg N ha-1 year-1 as （NH4）2SO4） on soil N2O and CH4 fluxes. The seasonal and diurnal variations of soil N2O and CH4 fluxes were determined using the static chamber-gas chromatography method during the two growing seasons of 2008 and 2009. Soil temperature, moisture and mineral N （NH4＋-N and NO3-N） concentration were simultaneously measured. Results showed that low level of （NH4）2SO4 （10 kg N ha-1 year-1） did not significantly affect soil CH4 and N20 fluxes and other variables. High level of （NH4）2SO4 （20 kg N ha-1 year-1） significantly increased soil NO3-N concentration by 24.1% to 35.6%, decreased soil CH4 uptake by an average of 20.1%, and significantly promoted soil N2O emission by an average of 98.2%. Soil N2O emission responded more strongly to the added N compared to CH4 uptake. However, soil CH4 fluxes were mainly driven by soil moisture, followed by soil NO3--N concentration. Soil N2O fluxes were mainly driven by soil temperature, followed by soil moisture. Soil inorganic N availability was a key integrator of soil CH4 uptake and N2O emission. These results suggest that the changes of availability of inorganic N induced by the increased N deposition in soil may affect the CH4 and N2O fluxes in the cold semi-arid meadow steppe over the short term.
