离子选择电极测氟的二次标准加入法计算机程序的改进

在离子选择电极直接电位法中应用二次标准加入法,需要用计算机编制程序用迭代法计算结果。我们所见到的文献所述的计算公式及计算机程序均较繁杂,且对测定过程要求较高。本文在用离子选择电极二次标准加入法测定水及土壤中氟离子时,对计算机程序做了改进,简化了计算公式,缩短了运算时间,测定结果可靠。

地尔硫离子选择性电极的研制

以四苯硼纳和地尔硫形成的离子缔合物为电活性物质,研制成的地尔硫PVC膜离子选择性电极,其Nernst响应范围为10^(-2)～10^(-4)mol/L,用直接电位法测定盐酸地尔硫(艹卓)的含量,并用分别溶液法测定了10种物质的选择系数,表明该电极具有操作简便、响应迅速、选择性好、准确性高、性能稳定等优点.

Adsorption of Potassium and Calcium Ions by Variable Charge Soils

Interactions of potassium and calcium ions with four typical variable charge soils in South China were examined by measuring pK-0.5pCa value with a potassium ion-selective electrode and a calcium ion-selective electrode,and pK value with a potassium ion-selective electrode.The results showed that adsorption of potassium and calcium ions increased with soil suspension pH,and the tendency of the pK-0.5pCa value changing with pH differed with respect to pH range and potassium to calcium ratio.Adsorption of equal amount of calcium and potassium ions led to release of an identical number of protons,suggesting similar adsorption characteristics of these two ions when adsorbed by variable charge soils.Compared with red soil,latosol and lateritic red soil had higher adsorption selectivities for calcium ion.The red soil had a greater affinity for potassium ion than that for calcium ion at low concentration,which seems to result from its possession of 2:1 type minerals,such as vermiculite and mica with a high affinity for potassium ion.The results indicated that adsorption of potassium and calcium ions by the variable charge soils was chiefly caused by the electrostatic attraction between the cations and the soil surfaces.Moreover,it was found that sulfate could affect the adsorption by changing soil surface properties and by forming ion-pair.

Adsorption Kinetics of Pb^(2+) and Cu^(2+) on Variable Charge Soils and Minerals:Ⅰ.Technique

A new technique for studying the adsorption kinetics of heavy metals,Pb^2+ and Cu^2+,on variable charge surfaces was established with two selective electrodes and microcomputer control system.Feasibility of the technique,including interference of other ions (mainly Fe^3+ and Al^3+),response time of electrodes,and the pH range of testing,was studied.Comparision with the most widely used miscible displacement technique,which was considered insufficient in studying 30-minute rapid reactions,at present time showed that the new technique was more advantageous in testing in situ,easy to operate,and economic.

Adsorption Kinetics of Pb^(2+) and Cu^(2+) on Variable Charge Soils and Minerals: Ⅲ. Adsorption Kinetics of Pb^(2+) Within 30 Minutes

The adsorption kinetics of Pb^2+ on different soils and minerals with variable charges was studied by the two ion-selective electrode technique at different pH and concentrations.The results showed that more than 95% of adsorption on all the samples occurred during the first 5 minutes.All adsorption time-dependent data could fit the surface second-order equation very well.The values of Xm were goethite>kaolinite,and latosol>red soil at the same initial reaction concentration.The values of k were kaolinite>>goethite,and latosol>red soil at the same reaction pH and initial concentration.The higher the suspension pH,the faster the adsorption occurred.The meaning of Xm got by the two ion-selective electrode technique(one kind of batch technique) was different from that by the miscible displacement technique in that the former was only the equilibrium adsorption amount at a definite concentration and pH,but the latter was almost equal to the adsorption capacity at a definite pH with much less influence of concentration.One Pb^2+ was supposed to occupy two adsorption sites as the adsorption mechanism is concerned.

Kinetic Characteristics of Nitrate Uptake by Wheat and Rape and Their Determination

15-day old seedlings of wheat and rape were grown in a series of solutions with different concentrations of KNO3 for a definite period of time. The changes in NO3- concentration of the solutions were determined by the double ion-selective electrode method, and then the amount of NO3- taken up by the plants was estimated and values of Km and Imax of the Michealis-Menten equation were calculated. Results show that both the method and conditions of determination affected the values of Km and Imax. For example, the Km value was appreciably reduced when the volume of culture solution was increased or when the duration of nutrient uptake was shortened; the Km value obtained with short-term depletion method was higher than that obtained with long-term one. Similar Variations were found for the values of Imax. There was a considerable difference in the characteristics of uptake kinetics between wheat and rape when determined under the same conditions of determination. The isotherm of NO3- uptake by wheat could be separated into saturated and unsaturated parts, and when the concentration of NO3- exceeded 180 uuuuuuuuuuuuM, the relationship between the rate of NO3- uptake and NO3- concentration tended to be linear. However, the isotherm of NO3- uptake by rape was found to fit the Michealis-Menten equation and no linear relationship could be found.

Direct Determination of Potassium-Sodium Activity Ratio in Soil Suspension with Two Ion-Selective Electrodes

A K+-selective electrode and a Na+-selective electrode were used to construct a measuring cell without liquid-junction for the determination of the ion activity ratio of K+ to Na+ in soil suspensions. The measured cell potential was not affected by the total electrolyte concentration when the total cation concentration was 10-1-10-3 mol L-1 and the concentration ratio CK+ / CNa+. was 10:1 to 1:50. When the concentration ratios were equal to 1and the total electrolyte concentrations were 10-2 and 10-3 mol L-1, the ion activity ratio measurement would not be affected by pH in the pH range of 3.5 to 11.5 and 4.4 to 11 respectively. Ions other than H+ have no remarkable influence on the measurement. The ion activity ratio of K+ to Na+ measured directly in soil suspension agree well with those in centrifuged supernant solution. The relative deviation was within 4%. From the measured ion activity ratio, the difference of the bonding energies of K+ and Na+ ions was calculated.

Determination of Boron Trifluoride in Boron Trifluoride Complex by Fluoride Ion Selective Electrode

A method was proposed to determine boron trifluoride in boron trifluoride complex using fluoride ion selective electrode(ISE). Hydroxide was chosen to mask aluminum for the determination of 0.01—0.1 mol/L of fluoride. The simulation indicated that the permissible aluminum masked at a certain p H value was limited and hardly related to F-concentration and boric acid. It is better to control p H value below 11.5 and the aluminum concentration within 0.025 mol/L to minimize the interference of hydroxide to the fluoride ISE. The decomposition conditions of boron trifluoride by aluminum chloride were investigated. It is found that the F-detection ratio will approach 1.0 if the Al/F molar ratio is 0.3—0.7 and aluminum concentration is no more than 0.02 mol/L when heated at 80 ℃ for 10 min. In one word, hydroxide is quite fit to mask aluminum for samples which contain high content of fluoride and aluminum and the BF3 content can be successfully determined by this method.

Dolomite apatite separation by amphoteric collector in presence of bacteria

Bioflotation represents one of the growing trends to enhance the selectivity of conventional flotation processes. It utilizes the micro-organisms to replace or to interact with the chemical reagents to increase the gap between surface properties of similar minerals and to enhance the separation selectivity. In this work, dolomite-phosphate separation was investigated using amphoteric collector （dodecyl-N-carboxyethyl-N-hyroxyethyl-imidazoline） in presence of bacteria. Two types of bacteria, Corynebacterium- diphtheriae-intermedius （CDI）, and Pseudomonas aeruginosa （PA）, were used. The collector-bacteria interaction was characterized by Fourier transform infra-red （FTIR）, frothing height and Zeta potential. The results show that the collector-bacteria interaction improves the flotation selectivity. Although, the PA positively affects the separation results, the CDI cannot lower the MgO to less than 1%. A phosphate content of 0.7% MgO and 31.77% P205 with a recovery of 68% at pH 11, 3.0 kg/t amphoteric collector, 4× 10^7 cells of PA is obtained.

Research on Fluorine release of coal and clay used by residents in Zhaotong Fluorosis areas,Yunnan Province

The Fluorine release rate of coal, clay of different Fluorine content, and coal mixed with clay used by resident households were studied by using the ion selective electrode （ISE） and solidoid balance methods, and the degree of influence on Fluorine pollu- tion generated by coal and clay was analyzed according to the proportion characteristics of coal used by resident households. The results show that the Fluorine release rate of coal is more than 95% during combustion; The Fluorine release rate of clay is more than 99%; The Fluorine release rate of coal mixed with clay is between 56.44% and 96.64%, and the average value is 76.68%. The clay as a binder for fine coal is one important source of Fluorine pollution caused by coal-combustion in Zhaotong, Yunnan Province. When the Fluorine content of coal is less than 80 mg/kg, the F[uodne amount released from clay （in which Fluorine content is more than 530 mg/kg） is more than 50% of the total Fluorine amount released from coal and clay during coal-combustion. The Fluorine amount released from clay （in which Fluorine content is more than 1 000 mg/kg） is more than 70% of total Fluorine amount released from coal and clay during coal-combustion.

Development of Chloride Electrode Coated Wire and Composite Systems for Determination Chloride Ion in Gunungkidul Spring Water

The purpose of this research was to fmd out effectiveness of chloride solid membrane electrode of coated wire system compared to solid membrane electrode of composite system, the Nernstian response and character＇s potential response （detection limit, selectivity and response time）. The chloride ISEs （ion selective electrodes） in this research were the solid membrane chloride ISEs based AgC1. There were two types of chloride ISEs that were developed, namely the chloride ISEs of coated wire and composite systems. Both types of electrodes were characterized. The selectivity was done by comparing Esel of the chloride standard solutions and Esel of the interference ions （Br- and I-）. The measurement of chloride ions in water samples was done by using the coated wire chloride ISE, the composite chloride ISE and the Mohr method. We compared the result of the two chloride ISE methods to that of standard method for chloride determination （Mohr） by using F-test and Post Hoc Test LSD （least significant difference） and Duncan. Analysis by using F-test and Post Hoc Test （LSD and Duncan） and characterization results of both the methods showed that coated wire chloride ISE was more effective compared to composite chloride ISE. Nemstian response was 59.83 mV/decade, linier range measurement was 10-1-10-5 M, limit detection was 1.23 × 10-5 M, response time along was 25 s and interfering ion was 10-4 M Br-.

Dechlorination of zinc dross by microwave roasting

Traditional treatments of zinc dross have many disadvantages,such as complicated recovering process and serious environmental pollution.In this work,a new process of chlorine removal from zinc dross by microwave was proposed for solving problem of recycling the zinc dross.With better ability of absorbing the microwave than zinc oxide,the main material in zinc dross,chlorides,can be heated and evaporated rapidly during microwave roasting.Various parameters including roasting temperature,duration time and stirring speed were optimized.The microstructure of roasted materials was characterized by X-ray diffraction(XRD) and scanning electron microscope(SEM).The content of the chloride was analyzed by the method of chlorine ion selective electrode.The experiments indicate that the best duration time is 60 min with a stirring speed of 15 r/min during the microwave roasting process.The dechlorination rate reaches peak value of 88% at 700 ℃.The chlorine is removed as HCl gas when water vapor is used as activating agent,which means that it can be recovered into hydrochloride acid.

Long-term follow-up of right ventricular outflow tract septal pacing

Objective Right ventricular outflow tract septum has become widely used us an electrode placement site. However, data concerning lead performances and complications for lead repositioning with this technique were scant. The purpose of this study was to observe long- term lead performances and complications of right ventricular outflow tract septal pacing and provide evidences for choosing an optimal electrode implantation site. Methods Thirty-six patients with septal active electrode implantation and 39 with apical passive electrode implantation were enrolled in this study. Pacing threshold, R-wave sensing, lead impedance, pacing QRS width and pacing-related compli- cations for two groups at implantation and follow-up were compared. Results There were higher pacing threshold and shorter pacing QRS width at implantation in the septal group compared with the apical group. There were no differences between the septal and the apical groups in pacing threshold, R-wave sensitivity, lead impedance and pace-related complication during a follow-up. Conclusions Right ventricular outflow tract septum could be used as a first choice for implantation site because it had long-term stable lead performances and no serious complications compared with the traditional apical site.

PVC Membrane Selective Electrode for Determination of Cadmium(Ⅱ) Ion in Chocolate Samples

Benzil bis(carbohydrazone)(BBC) is prepared and explored as new N N Schiff's base, which plays the role of an excellent ion carrier in the construction of a Cd(II) ion membrane sensor. The tris(2-ethylhexyl) phosphate best performance corresponds to a membrane composition of 30% poly(vinyl chloride), 65%(TEHP), 3.5% BBC and 1.5% tetradodecyl-ammoniumtetrakis(4-chlorophenyl) borate(ETH 500). This sensor shows very good selectivity and sensitivity towards cadmium ion over a wide variety of cations, including alkali, alkaline earth, transition and heavy metal ions. The effect of membrane composition, selectivity, pH and influence of additive on the response properties of electrode were investigated. The response mechanism was discussed in the view of UV-spectroscopy. The electrode exhibits a Nernstian behavior(with slope of 29.7 mV per decade) over a very wide concentration range from 1.0×10?1 to 1.0×10?8 mol·L?1 with a detection limit of 3.2×10?8 mol·L?1. It shows rela-tively fast response time in whole concentration range(<8 s) and can be used for at least 10 weeks in the pH range of 2.0-9.0. The proposed sensor is successfully used for the determination of cadmium in different chocolate sam-ples and as indicator electrode in titration with ethylene diamine tetraacetate(EDTA).

Design of Fe （Ⅲ） and Hg （Ⅱ） Ion Selective Electrodes

Principally the basis of ISE is selecting of a support solid matrix and a nonsoluble compound or complexes of insighted cation, mixed with this solid. For preparing the ISE membranes there are some materials such PVC, PE, organic polyelectrolytes, conducting polymers and inorganic compounds. The black white microscope photos are included, too. Detailed schemes and pictures of the electrodes and correlations were shown in the following article. Results are seen compatible for construction of the versatile ISE electrodes.

A natural chemical technology for reducing fluoridation through chloride contents in muscles of fish

Accumulation trend of fluoride ion was carried out in 25 fish species, collected randomly from fresh water and marine water, Sindh, Pakistan to ensure the level of chloride contents by Selective Ion Electrode （SIE） method. Results showed an inverse relation in between chloride and fluoride concentration in muscles of fish under investigation, It was observed that chloride ions contents of marine water fish were significantly higher as compared with fresh water fish. This may be related with the habitat of marine water fish while no appreciable divergence in fluoride concentration in both regions was observed. This indicated that the deliberation of fluoride is the phenomena of nature of fish and self-determining. Highest concentration of fluoride ion in fresh water fish and marine water fish showed an inverse level of chloride ion in it, reflects water body conditions of both resources. A probable mechanism of accumulation of fluoride with respect to essential chloride ion which may be related with the size of ionic radii of both halides ion is described in relevant section of this article. Where a larger ionic radii of chloride ion believed to play an imperative role in reducing fluoridation in fishes. This may be regarded as natural chemical technology for reducing fluoride in muscle （edible part） of fish of both regions.

Non-equilibrium thermodynamics analysis and its application in interfacial mass transfer

Interfacial transfer plays an important role in multi-phase chemical processes. However, it is difficult to describe the complex interfacial transport behavior by the traditional mass transfer model. In this paper, we describe an interfacial mass transfer model based on linear non-equilibrium thermodynamics for the analysis of the rate of interfacial transport. The interfacial transfer process rate J depends on the interface mass transfer coefficient K, interfacial area A and chemical potential gradient at the interface. Potassium compounds were selected as model systems. A model based on linear non-equilibrium thermo-dynamics was established in order to describe and predict the transport rate at the solid-solution interface. Together with accurate experimental kinetic data for potassium ions obtained using ion-selective electrodes, a general model which can be used to describe the dissolution rate was established and used to analyze ways of improving the process rate.

Metal sulfide quantum dots-aggregated PAMAM dendrimer for cadmium ion-selective electrode-based immunoassay of alpha-fetoprotein

An ion-selective electrode(ISE)-based immunoassay has been innovatively designed for the sensitive detection of liver cancer biomarker(alpha-fetoprotein,AFP),using metal sulfide quantum dot(QD)-based nano labels.Cd S QDs-aggregated PAMAM dendrimer(QD-DE)was first synthesized and functionalized with polyclonal rabbit anti-human AFP antibodies.Thereafter,a sandwich immunoreaction was implemented on monoclonal mouse anti-human AFP antibody-coated microplate by using antibody-functionalized QD-DE as the secondary antibody.Accompanying the immunocomplex,subsequent potentiometric detection of cadmium ion dissolved from the QD-DE under acidic condition was conducted on a portable cadmium ion-selective electrode(Cd-ISE).Results revealed that the electrode potential of the Cd-ISE increased with the increment of AFP concentration from 0.1 to 100 ng m L^(-1)at a detection limit(LOD)of 68 pg m L^(-1).The relative standard deviations(RSD)were below9.09%and 10.54%for the intra-and inter-assay,respectively.Additionally,six human serum specimens were determined on CdISE-based immunosensor by using commercial human AFP ELISA kit as the reference,and gave good relationship between two methods.Importantly,Cd-ISE-based immunoassay offers the promise for simple and cost-effective screening of disease-related biomarkers.

Selectively constructing sandwich-like heterostructure of CdS/PbTiO_(3)/TiO_(2)to improve visible-light photocatalytic H_(2)evolution

Fast migration and efficient spatial separation of photogenerated charges in photocatalytic materials are indispensable to efficient solar water splitting reactions.Here,we construct a three-phase heterostructure of CdS/PbTiO_(3)/TiO_(2)by selectively depositing CdS and TiO_(2)at oppositely poled crystal facets of PbTiO_(3)using single-domain ferroelectric PbTiO_(3).The heterostructure has matching band edge alignments and strong interfacial connections at different moieties.The heterostructure combines the interfacial electrical and ferroelectric fields because of their peculiar microstructures,which provide a strong driving force throughout the whole bulk to separate photogenerated charges.Almost two orders of magnitude improvement of visible-light-driven photocatalytic H_(2) production has been realized in CdS/PbTiO_(3)/TiO_(2)compared with bare PbTiO_(3)/TiO_(2),showing the efficiency of charge separation in the heterostructure.The idea of combining ferroelectrics with potential light capture semiconductor provides a paradigm to accurately design charge migration pathways,bringing a step closer to efficient solar water splitting.