Series of TiO 2-ZnO heterojunction composite films with different n(Zn)/n(Ti) ratios were prepared by UDP450 magnetron sputter ion plating equipment, and the mole ratio of Zn to Ti was controlled by adjusting the ...Series of TiO 2-ZnO heterojunction composite films with different n(Zn)/n(Ti) ratios were prepared by UDP450 magnetron sputter ion plating equipment, and the mole ratio of Zn to Ti was controlled by adjusting the current values of sputtering target. The effects of n(Zn)/n(Ti) on the microstructures of TiO2-ZnO films were investigated by SEM, AFM, Raman and XPS, and their photocatalytic decomposition of methyl orange solutions was evaluated. The results show that an increase in n(Zn)/n(Ti) typically results in a decrease in the grain size of composite films firstly and then an increase of grain size, while an increase in n(Zn)/n(Ti) leads to an increase in film roughness firstly and then a decrease in film roughness. Both grain size and roughness of TiO2-ZnO films reach the maximum and minimum at n(Zn)/n(Ti) of 1/9.3, respectively. The n(Zn)/n(Ti) shows little effect on the valences of Zn and Ti elements, which mainly exist in the form of TiO2 and ZnO phases. The n(Zn)/n(Ti) has influence on the amount of anatase/rutile TiO2 heterojunction in the film. With increase of the n(Zn)/n(Ti), the absorption intensity of the composite film increases and the absorption region extends to 450 nm, which is redshifted as much as 150 nm in comparison with the pure TiO2 films. However, the photocatalytic abilities of heterogeneous composite films do not depend on the n(Zn)/n(Ti) but rather on the microstructures of the TiO2-ZnO composite films. Degradation rate of the film reaches the maximum and the photocatalytic decomposition of pollutants works best when n(Zn)/n(Ti)=1:9.3.展开更多
In order to produceα-calcium sulfate hemihydrate(α-CaSO4·0.5H2O)whiskers with high aspect ratios,a minor amount of CuCl2·2H2O was used as the modifying agent in the process of hydrothermal treatment of cal...In order to produceα-calcium sulfate hemihydrate(α-CaSO4·0.5H2O)whiskers with high aspect ratios,a minor amount of CuCl2·2H2O was used as the modifying agent in the process of hydrothermal treatment of calcium sulfate dihydrate(CaSO4·2H2O)precursor.The presence of 2.60×10–3 mol/L CuCl2·2H2O resulted in the increase of the aspect ratios ofα-CaSO4·0.5H2O whiskers from 81 to 253.The preferential adsorption of Cu2+on the negative{110}and{100}facets ofα-CaSO4·0.5H2O crystal structures was confirmed by EDS and XPS.And ATR-FTIR demonstrated the ligand adsorption of Cu2+on the surface ofα-CaSO4·0.5H2O whiskers.The experimental results reveal that the whiskers with high aspect ratios are attributed to the adsorption of Cu2+,which promotes the 1-D growth ofα-CaSO4·0.5H2O whiskers along the c axis.展开更多
The microstructure of aqueous CuCl2 has been studied through lots of technologies for many years; however, it remains a controversial subject. In this study, a new spectroscopic method has been proposed to analyze the...The microstructure of aqueous CuCl2 has been studied through lots of technologies for many years; however, it remains a controversial subject. In this study, a new spectroscopic method has been proposed to analyze the UV-visible spectra of thin fihn of CuCl2/H2O solutions at different concentrations. This method is the combination of ratio spectra, difference spectra and second order difference spectra. By using this method, two new bands at -230 and -380 nm are obviously observed. The bands are assigned as the contacted ion pairs [CuCl3(H2O)n]- or [CuCl4(H2O)n]2-, which demonstrates that ion pairs exist in the CuCl2/H2O solution. Such finding agrees with the recent theoretical spectra obtained by time-dependent density functional theory. Furthermore, the populations of the contacted ion pairs are discussed. This study not only offers the direct spectroscopic evidence of [CuCl3(H2O)n]- or [CuCl4(H2O)n]2- in aqueous CuCl2, but also suggests that the spec- troscopic analysis method is powerful to extract the weak bands in a strong overlapping spectrum.展开更多
The potential energy surface of O(^1D)+C2H5Cl reaction was studied using QCISD(T)/6- 311++G(d,p)//MP2/6-31G(d,p) method. The calculations reveal an insertion-elimination mechanism. The insertion reaction o...The potential energy surface of O(^1D)+C2H5Cl reaction was studied using QCISD(T)/6- 311++G(d,p)//MP2/6-31G(d,p) method. The calculations reveal an insertion-elimination mechanism. The insertion reaction of O(^1D) and C2H5Cl produces two energy-rich intermediates, IM1 and IM2, which subsequently decompose into various products. The calculations of the branching ratios of various products formed through the two intermediates were carried out using RRKM (Rice-Ramsperger-Kassel-Marcus) theory at the collision energies of 0, 20.9, 41.8, 62.7, 83.6, 104.5, and 125.4 kJ/mol. HCl is the main decomposition product for IM1; CH2OH is the main decomposition product for IM2. Since IM1 is more stable than IM2, HCl is probably the main product of the O(^1D)+C2H5Cl reaction.展开更多
目的探讨糖尿病视网膜病变(DR)患者餐后2 h血糖(2 h PG)升高对眼底图像中动静脉宽度比(AVR)的影响。方法选取DR患者316例,均行标准75 g口服葡萄糖耐量试验(OGTT)检测空腹血糖(FPG)和餐后2 h PG,根据餐后血糖变化幅度(2 h PG-FPG)将所有...目的探讨糖尿病视网膜病变(DR)患者餐后2 h血糖(2 h PG)升高对眼底图像中动静脉宽度比(AVR)的影响。方法选取DR患者316例,均行标准75 g口服葡萄糖耐量试验(OGTT)检测空腹血糖(FPG)和餐后2 h PG,根据餐后血糖变化幅度(2 h PG-FPG)将所有研究对象按三分位分为3组,低分位组(G1)104例、中分位组(G2)108例及高分位组(G3)104例。测量各组眼底图像中AVR水平,采用Pearson相关性分析和多元线性回归分析DR患者AVR的影响因素。结果 (1)G3组和G2组餐后2 h PG、空腹胰岛素(FIns)、糖化血红蛋白(Hb A1c)及稳态模型评估-胰岛素抵抗指数(HOMA-IR)均高于G1组,且G3组餐后2 h PG和Hb A1c高于G2组;G3组和G2组2 h AVR较G1组降低,G3组较G2组降低(P<0.05),而各组间空腹AVR比较,差异无统计学意义(P>0.05);(2)Pearson相关分析显示,AVR与FPG、餐后2 h PG、Hb A1c、收缩压(SBP)及舒张压(DBP)均呈负相关(P<0.05);(3)多元线性回归分析显示,餐后2 h PG为DR患者AVR的影响因素(P<0.05)。结论餐后2 h PG升高可能会导致AVR降低,对DR患者应动态观察AVR的变化,对判断DR的严重程度具有意义。展开更多
The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its per...The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its performance.However,its mechanism and active sites remain unclear and need to be further elucidated.Here,the noble‐metal‐free In_(x)‐Co_(y) oxides catalysts were prepared.Much‐improved performance and obvious product selectivity shift were observed.The optimized catalyst(In_(1)‐Co_(4))(9.7 mmol g_(cat)^(–1) h^(–1))showed five times methanol yields than pure In_(2)O_(3)(2.2 mmol g_(cat)^(–1) h^(–1))(P=4.0 MPa,T=300°C,GHSV=24000 cm^(3)_(STP) g_(cat)^(–1) h^(–1),H_(2):CO_(2)=3).And the cobalt‐catalyzed CO_(2) methanation activity was suppressed,although cobalt was most of the metal element.To unravel this selectivity shift,detailed catalysts performance evaluation,together with several in‐situ and ex‐situ characterizations,were employed on cobalt and In‐Co for comparative study.The results indicated CO_(2) hydrogenation on cobalt and In‐Co catalyst both followed the formate pathway,and In‐Co reconstructed and generated a surface In_(2)O_(3)‐enriched core‐shell‐like structure under a reductive atmosphere.The enriched In_(2)O_(3) at the surface significantly enhanced CO_(2) adsorption capacity and well stabilized the intermediates of CO_(2) hydrogenation.CO_(2) and carbon‐containing intermediates adsorbed much stronger on In‐Co than cobalt led to a feasible surface C/H ratio,thus allowing the*CH_(3)O to desorb to produce CH_(3)OH instead of being over‐hydrogenated to CH_(4).展开更多
Molybdenum disulfide(MoS_(2)) films are widely deployed in industrial applications owing to their inherent interlayer slip characteristics, offering energy consumption savings and prolonged mechanical part performance...Molybdenum disulfide(MoS_(2)) films are widely deployed in industrial applications owing to their inherent interlayer slip characteristics, offering energy consumption savings and prolonged mechanical part performance. Nevertheless, their practical utility is limited by environmental constraints and the limitations of preparation techniques, which hinder the attainment of robust superlubricity(friction coefficient < 0.01). Herein, through magnetron sputtering technology, we synthesize a core-shell-like nanocomposite composed of MoS_(2)nanosheets encapsulating B_(4)C. The core-shell-like structure enables the resulting films to preferentially grow crystalline MoS_(2), providing them with outstanding mechanical properties and efficient lubrication over a wide range of temperatures. Remarkably, such film achieves robust macroscale superlubricity and an ultralow wear rate(1.7 ×10^(-8)mm^(3)N-1m^(-1)) under high contact stress in a mild vacuum environment. This noteworthy outcome is primarily attributable to the self-segmentation of the macroscale contact interface during the friction process, involving:(1) a large amount of wear debris is embedded into the wear track to create extensive micro-sized asperities;(2) a nanolayer of amorphous carbon enriched with oxide nanoparticles is formed on the uppermost part of these asperities;(3) numerous incommensurate nanocontacts comprising nanoparticles and highly oriented MoS_(2)nanosheets are established, culminating in the achievement of robust superlubricity. Our pioneering design, coupled with the elucidation of the underlying superlubricity mechanism, holds significant promise for advancing the development of robust and high-performance lubricants.展开更多
目的通过分析血清胱抑素C(Cys-C)、β2微球蛋白(β2-MG)、尿酸(UA)等联合项目与糖尿病肾病(DN)的相关性,从而找出准确诊断DN的相关因素。方法选取259名糖尿病(DM)患者,收集Cys-C、β2-MG、UA等相关项目指标,运用相应的统计学方法分析相...目的通过分析血清胱抑素C(Cys-C)、β2微球蛋白(β2-MG)、尿酸(UA)等联合项目与糖尿病肾病(DN)的相关性,从而找出准确诊断DN的相关因素。方法选取259名糖尿病(DM)患者,收集Cys-C、β2-MG、UA等相关项目指标,运用相应的统计学方法分析相关项目与尿白蛋白/肌酐比值(UACR)的关系。结果UACR≥30 mg/g作为DN的诊断临界点时,显示Cys-C、β2-MG、UA、收缩压(SBP)、餐后2 h血糖(2 h PG)、病程等6个项目是UACR的独立危险因素,当某一DM患者Cys-C≥1.435 mg/L、β2-MG≥2.055 mg/L、UA≥320μmol/L、SBP≥145 mmHg、2 h PG≥8.5 mmol/L、病程≥4.5年时,患者发展成早期DN的风险较大,相对应的临界值患病概率为81.5%。结论联合检测Cys-C、β2-MG、UA、SBP、2 h PG、病程等6个项目可以较好预测DN的发生。展开更多
Methane (CH4) plasma was used to produce amorphous hydrogenated carbon (a- C:H) films by a single capacitively coupled radio frequency (RF) powered plasma system. The system consists of two parallel electrodes...Methane (CH4) plasma was used to produce amorphous hydrogenated carbon (a- C:H) films by a single capacitively coupled radio frequency (RF) powered plasma system. The system consists of two parallel electrodes: the upper electrode is connected to 13.56 MHz RF power and the lower one is connected to the ground. Thin films were deposited on glass slides with different sizes and on silicon wafers. The influence of the plasma species on film characteristics was studied by changing the plasma parameters. The changes of plasma species during the deposition were investigated by optical emission spectroscopy (OES). The structural and optical properties were analyzed via Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and UV-visible spectroscopy, and the thicknesses of the samples were measured by a profilometer. The sp3/sp2 ratio and the existing H atoms play a significant role in the determination of the chemical properties of thin films in the plasma. The film quality and deposition rate were both increased by raising the power and the flow rate.展开更多
The catalytic pyrolyses of rayon have been studied respectively by thermo-gravimetric analysis (TGA) when rayon was treated with phosphoric acid (PA), three ammonium phosphate salts and ammonium sulfate (AS). The air ...The catalytic pyrolyses of rayon have been studied respectively by thermo-gravimetric analysis (TGA) when rayon was treated with phosphoric acid (PA), three ammonium phosphate salts and ammonium sulfate (AS). The air is favorable to the catalysis of dibasic ammonium phosphate (DAP), but not to those of ADP, PA, AP, and AS obviously. It is put forward that a peak’s shape character can be described with the ratio of height to half-height-width (H/W /2) of the peak on a differential thermo-gravimetric (DTG) curve. A flat cracking peak, presenting a more moderate dehydration reaction, has a smaller ratio and could lead to higher carbonization and activation yields. The experimental results prove this view. According to expectation, the order of catalysis is: DAP≥ADP>PA> APAS no catalyst.展开更多
Aqueous E pH Diagram is an essential tool for analyzing hydrometallurgical and corrosion processes. Due to the requirements for environmental protection and energy saving in recent years, waste water processing a...Aqueous E pH Diagram is an essential tool for analyzing hydrometallurgical and corrosion processes. Due to the requirements for environmental protection and energy saving in recent years, waste water processing and hydrometallurgical process of concentrate have been greatly developed. The construction of E pH diagrams has turned to multi component systems. However, there are some limits in plotting such diagrams. There is only one diagram for one multi component system, which can not reflect the truth of the aqueous reaction. In the paper, a new computation method is proposed to construct E pH diagrams. Component activity term is used to determine the boundary of stable areas. For the multi component systems, different atom ratios of elements have been taken into account. M S H 2O system is chosen to study since it is of importance in metallurgical solution. Compared with conventional methods, the algorithm is simple and conforms to real conditions.展开更多
基金Project (2010JQ6008) supported by the Natural Science Foundation of Shaanxi Province,China
文摘Series of TiO 2-ZnO heterojunction composite films with different n(Zn)/n(Ti) ratios were prepared by UDP450 magnetron sputter ion plating equipment, and the mole ratio of Zn to Ti was controlled by adjusting the current values of sputtering target. The effects of n(Zn)/n(Ti) on the microstructures of TiO2-ZnO films were investigated by SEM, AFM, Raman and XPS, and their photocatalytic decomposition of methyl orange solutions was evaluated. The results show that an increase in n(Zn)/n(Ti) typically results in a decrease in the grain size of composite films firstly and then an increase of grain size, while an increase in n(Zn)/n(Ti) leads to an increase in film roughness firstly and then a decrease in film roughness. Both grain size and roughness of TiO2-ZnO films reach the maximum and minimum at n(Zn)/n(Ti) of 1/9.3, respectively. The n(Zn)/n(Ti) shows little effect on the valences of Zn and Ti elements, which mainly exist in the form of TiO2 and ZnO phases. The n(Zn)/n(Ti) has influence on the amount of anatase/rutile TiO2 heterojunction in the film. With increase of the n(Zn)/n(Ti), the absorption intensity of the composite film increases and the absorption region extends to 450 nm, which is redshifted as much as 150 nm in comparison with the pure TiO2 films. However, the photocatalytic abilities of heterogeneous composite films do not depend on the n(Zn)/n(Ti) but rather on the microstructures of the TiO2-ZnO composite films. Degradation rate of the film reaches the maximum and the photocatalytic decomposition of pollutants works best when n(Zn)/n(Ti)=1:9.3.
基金Project(B14034)supported by the National 111 Project,ChinaProject(2015CX005)supported by the Innovation Driven Plan of Central South University,ChinaProject(2016zzts104)supported by the Fundamental Research Funds for the Central Universities,China
文摘In order to produceα-calcium sulfate hemihydrate(α-CaSO4·0.5H2O)whiskers with high aspect ratios,a minor amount of CuCl2·2H2O was used as the modifying agent in the process of hydrothermal treatment of calcium sulfate dihydrate(CaSO4·2H2O)precursor.The presence of 2.60×10–3 mol/L CuCl2·2H2O resulted in the increase of the aspect ratios ofα-CaSO4·0.5H2O whiskers from 81 to 253.The preferential adsorption of Cu2+on the negative{110}and{100}facets ofα-CaSO4·0.5H2O crystal structures was confirmed by EDS and XPS.And ATR-FTIR demonstrated the ligand adsorption of Cu2+on the surface ofα-CaSO4·0.5H2O whiskers.The experimental results reveal that the whiskers with high aspect ratios are attributed to the adsorption of Cu2+,which promotes the 1-D growth ofα-CaSO4·0.5H2O whiskers along the c axis.
文摘The microstructure of aqueous CuCl2 has been studied through lots of technologies for many years; however, it remains a controversial subject. In this study, a new spectroscopic method has been proposed to analyze the UV-visible spectra of thin fihn of CuCl2/H2O solutions at different concentrations. This method is the combination of ratio spectra, difference spectra and second order difference spectra. By using this method, two new bands at -230 and -380 nm are obviously observed. The bands are assigned as the contacted ion pairs [CuCl3(H2O)n]- or [CuCl4(H2O)n]2-, which demonstrates that ion pairs exist in the CuCl2/H2O solution. Such finding agrees with the recent theoretical spectra obtained by time-dependent density functional theory. Furthermore, the populations of the contacted ion pairs are discussed. This study not only offers the direct spectroscopic evidence of [CuCl3(H2O)n]- or [CuCl4(H2O)n]2- in aqueous CuCl2, but also suggests that the spec- troscopic analysis method is powerful to extract the weak bands in a strong overlapping spectrum.
基金ACKNOWLEDGMENT This work was supported Science Foundation of China by the National Natural (No.50772107).
文摘The potential energy surface of O(^1D)+C2H5Cl reaction was studied using QCISD(T)/6- 311++G(d,p)//MP2/6-31G(d,p) method. The calculations reveal an insertion-elimination mechanism. The insertion reaction of O(^1D) and C2H5Cl produces two energy-rich intermediates, IM1 and IM2, which subsequently decompose into various products. The calculations of the branching ratios of various products formed through the two intermediates were carried out using RRKM (Rice-Ramsperger-Kassel-Marcus) theory at the collision energies of 0, 20.9, 41.8, 62.7, 83.6, 104.5, and 125.4 kJ/mol. HCl is the main decomposition product for IM1; CH2OH is the main decomposition product for IM2. Since IM1 is more stable than IM2, HCl is probably the main product of the O(^1D)+C2H5Cl reaction.
文摘目的探讨糖尿病视网膜病变(DR)患者餐后2 h血糖(2 h PG)升高对眼底图像中动静脉宽度比(AVR)的影响。方法选取DR患者316例,均行标准75 g口服葡萄糖耐量试验(OGTT)检测空腹血糖(FPG)和餐后2 h PG,根据餐后血糖变化幅度(2 h PG-FPG)将所有研究对象按三分位分为3组,低分位组(G1)104例、中分位组(G2)108例及高分位组(G3)104例。测量各组眼底图像中AVR水平,采用Pearson相关性分析和多元线性回归分析DR患者AVR的影响因素。结果 (1)G3组和G2组餐后2 h PG、空腹胰岛素(FIns)、糖化血红蛋白(Hb A1c)及稳态模型评估-胰岛素抵抗指数(HOMA-IR)均高于G1组,且G3组餐后2 h PG和Hb A1c高于G2组;G3组和G2组2 h AVR较G1组降低,G3组较G2组降低(P<0.05),而各组间空腹AVR比较,差异无统计学意义(P>0.05);(2)Pearson相关分析显示,AVR与FPG、餐后2 h PG、Hb A1c、收缩压(SBP)及舒张压(DBP)均呈负相关(P<0.05);(3)多元线性回归分析显示,餐后2 h PG为DR患者AVR的影响因素(P<0.05)。结论餐后2 h PG升高可能会导致AVR降低,对DR患者应动态观察AVR的变化,对判断DR的严重程度具有意义。
文摘The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its performance.However,its mechanism and active sites remain unclear and need to be further elucidated.Here,the noble‐metal‐free In_(x)‐Co_(y) oxides catalysts were prepared.Much‐improved performance and obvious product selectivity shift were observed.The optimized catalyst(In_(1)‐Co_(4))(9.7 mmol g_(cat)^(–1) h^(–1))showed five times methanol yields than pure In_(2)O_(3)(2.2 mmol g_(cat)^(–1) h^(–1))(P=4.0 MPa,T=300°C,GHSV=24000 cm^(3)_(STP) g_(cat)^(–1) h^(–1),H_(2):CO_(2)=3).And the cobalt‐catalyzed CO_(2) methanation activity was suppressed,although cobalt was most of the metal element.To unravel this selectivity shift,detailed catalysts performance evaluation,together with several in‐situ and ex‐situ characterizations,were employed on cobalt and In‐Co for comparative study.The results indicated CO_(2) hydrogenation on cobalt and In‐Co catalyst both followed the formate pathway,and In‐Co reconstructed and generated a surface In_(2)O_(3)‐enriched core‐shell‐like structure under a reductive atmosphere.The enriched In_(2)O_(3) at the surface significantly enhanced CO_(2) adsorption capacity and well stabilized the intermediates of CO_(2) hydrogenation.CO_(2) and carbon‐containing intermediates adsorbed much stronger on In‐Co than cobalt led to a feasible surface C/H ratio,thus allowing the*CH_(3)O to desorb to produce CH_(3)OH instead of being over‐hydrogenated to CH_(4).
基金supported by the National Natural Science Foundation of China (Grant Nos. U21A20127, 52375220)the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDB 0470302)the Natural Science Foundation of Ningbo (Grant No. 2022J300)。
文摘Molybdenum disulfide(MoS_(2)) films are widely deployed in industrial applications owing to their inherent interlayer slip characteristics, offering energy consumption savings and prolonged mechanical part performance. Nevertheless, their practical utility is limited by environmental constraints and the limitations of preparation techniques, which hinder the attainment of robust superlubricity(friction coefficient < 0.01). Herein, through magnetron sputtering technology, we synthesize a core-shell-like nanocomposite composed of MoS_(2)nanosheets encapsulating B_(4)C. The core-shell-like structure enables the resulting films to preferentially grow crystalline MoS_(2), providing them with outstanding mechanical properties and efficient lubrication over a wide range of temperatures. Remarkably, such film achieves robust macroscale superlubricity and an ultralow wear rate(1.7 ×10^(-8)mm^(3)N-1m^(-1)) under high contact stress in a mild vacuum environment. This noteworthy outcome is primarily attributable to the self-segmentation of the macroscale contact interface during the friction process, involving:(1) a large amount of wear debris is embedded into the wear track to create extensive micro-sized asperities;(2) a nanolayer of amorphous carbon enriched with oxide nanoparticles is formed on the uppermost part of these asperities;(3) numerous incommensurate nanocontacts comprising nanoparticles and highly oriented MoS_(2)nanosheets are established, culminating in the achievement of robust superlubricity. Our pioneering design, coupled with the elucidation of the underlying superlubricity mechanism, holds significant promise for advancing the development of robust and high-performance lubricants.
文摘目的通过分析血清胱抑素C(Cys-C)、β2微球蛋白(β2-MG)、尿酸(UA)等联合项目与糖尿病肾病(DN)的相关性,从而找出准确诊断DN的相关因素。方法选取259名糖尿病(DM)患者,收集Cys-C、β2-MG、UA等相关项目指标,运用相应的统计学方法分析相关项目与尿白蛋白/肌酐比值(UACR)的关系。结果UACR≥30 mg/g作为DN的诊断临界点时,显示Cys-C、β2-MG、UA、收缩压(SBP)、餐后2 h血糖(2 h PG)、病程等6个项目是UACR的独立危险因素,当某一DM患者Cys-C≥1.435 mg/L、β2-MG≥2.055 mg/L、UA≥320μmol/L、SBP≥145 mmHg、2 h PG≥8.5 mmol/L、病程≥4.5年时,患者发展成早期DN的风险较大,相对应的临界值患病概率为81.5%。结论联合检测Cys-C、β2-MG、UA、SBP、2 h PG、病程等6个项目可以较好预测DN的发生。
基金supported by the Scientific Research Project Fund of Duzce University under the projectnumber 2013.05.02.195
文摘Methane (CH4) plasma was used to produce amorphous hydrogenated carbon (a- C:H) films by a single capacitively coupled radio frequency (RF) powered plasma system. The system consists of two parallel electrodes: the upper electrode is connected to 13.56 MHz RF power and the lower one is connected to the ground. Thin films were deposited on glass slides with different sizes and on silicon wafers. The influence of the plasma species on film characteristics was studied by changing the plasma parameters. The changes of plasma species during the deposition were investigated by optical emission spectroscopy (OES). The structural and optical properties were analyzed via Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and UV-visible spectroscopy, and the thicknesses of the samples were measured by a profilometer. The sp3/sp2 ratio and the existing H atoms play a significant role in the determination of the chemical properties of thin films in the plasma. The film quality and deposition rate were both increased by raising the power and the flow rate.
文摘The catalytic pyrolyses of rayon have been studied respectively by thermo-gravimetric analysis (TGA) when rayon was treated with phosphoric acid (PA), three ammonium phosphate salts and ammonium sulfate (AS). The air is favorable to the catalysis of dibasic ammonium phosphate (DAP), but not to those of ADP, PA, AP, and AS obviously. It is put forward that a peak’s shape character can be described with the ratio of height to half-height-width (H/W /2) of the peak on a differential thermo-gravimetric (DTG) curve. A flat cracking peak, presenting a more moderate dehydration reaction, has a smaller ratio and could lead to higher carbonization and activation yields. The experimental results prove this view. According to expectation, the order of catalysis is: DAP≥ADP>PA> APAS no catalyst.
文摘Aqueous E pH Diagram is an essential tool for analyzing hydrometallurgical and corrosion processes. Due to the requirements for environmental protection and energy saving in recent years, waste water processing and hydrometallurgical process of concentrate have been greatly developed. The construction of E pH diagrams has turned to multi component systems. However, there are some limits in plotting such diagrams. There is only one diagram for one multi component system, which can not reflect the truth of the aqueous reaction. In the paper, a new computation method is proposed to construct E pH diagrams. Component activity term is used to determine the boundary of stable areas. For the multi component systems, different atom ratios of elements have been taken into account. M S H 2O system is chosen to study since it is of importance in metallurgical solution. Compared with conventional methods, the algorithm is simple and conforms to real conditions.