离交过程微量谷氨酸快速测定的探讨

在味精生产中,冷冻等电提取谷氨酸晶体后的母液里,一般尚有谷氨酸含量1.30％～1.60％。早期作为废液被排放了,近几年来,随着科技的发展,各味精厂多用强酸性阳离子交换树脂进行吸附回收。由于技术水平的提高、吸附后排放液中谷氨酸含量逐步在下降,有的已下降到0.

Investigation of the Ion-Exchange Behavior of Zeolite Y in the Presence of Resin

Ion-exchange process of zeolite Y using ammonium-type resin as an exchange reagent was successfully carried out. The effect of temperature, space velocity and ion concentration on the breakthrough curves was carefully investigated. At the first exchange section, the maximum proportion of qualified zeolites(QR) was obtained at a temperature of 70 ℃, a weight hourly space velocity of 0.61 h-1, and an ion concentration of 197 mg/L. The minimum length of mass-transfer zone(MTZ) of the resin bed was achieved at a temperature of 70 ℃, a space velocity of 0.61 h-1, and an ion concentration of 423 mg/L. At the second exchange section, the length of MTZ of the resin bed was significantly increased, and the exchange of Na+ ions contained in zeolite Y was more difficult than that achieved at the first exchange section. In both the first and the second exchange sections, the zeolite Y subjected to ion exchange with the resin maintained the similar physical and chemical properties as compared to those exchanged by the conventional approaches, but the zeolite Y, which was obtained after ion exchange, contained a significantly lower content of Na2 O.

Effect of Mg^(2+) content in ion-exchanged Shengli lignite on its equilibrium adsorption water content and its mechanism

Mg ion-exchanged samples were prepared with acid-washed Shengli lignite.The chemical composition of the ash of the raw sample was determined by X-ray fluorescence.The equilibrium adsorption water contents of samples were determined in a range of relative humidity.The ion-exchange process was characterized by FT-IR,ash content,and p H value.A possible mechanism is proposed for equilibrium adsorption water of ion-exchanged samples at different humidities.The extent of ion-exchange reaction between Mg2+and lignite is controlled by the concentration of Mg2+in Mg SO4solution.The effect of Mg2+on equilibrium adsorption water content varies with relative humidity and content of Mg2+.The factor that controls equilibrium adsorption water content at low relative humidity is water interactions with sorption sites,which are Mg2+–carboxyl group complex.At middle relative humidity capillary force between Mg2+–water clusters Mg+(H2O)nand capillary is more important.At high relative humidity,free water–free water interactions are more significant.

17α-Ethinylestradiol removal from water by magnetic ion exchange resin

Magnetic ion exchange(MIEX) resins have received considerable attention in drinking water treatment due to their fast and efficient removal of dissolved organic carbon(DOC). Two types of mechanisms, i.e., ion exchange,reversible and irreversible adsorption, may occur during pollutants removal by MIEX. This work examined the removal mechanism of 17α-Ethinylestradiol(EE2) by MIEX. As one of typical estrogen micro-pollutants,EE2 existed as neutral molecule in natural water, and its charge density was close to zero [(0.00000219 ±0.00000015) meq·(μg EE2)^(-1)] based on the potentiometric titration method. However, the removal of EE2 by MIEX was much higher than that of other micro-pollutants previously reported. Multi-cycle adsorptionregeneration experiments and ion exchange stoichiometry analysis were conducted to elucidate the removal mechanism of EE2 by MIEX resin. The results suggested that the main removal mechanism of EE2 by MIEX was ion exchange instead of reversible micro-pore adsorption. The experimental analysis based on Donnan theory indicated that the internal micro-environment of resin beads was alkaline, in the alkaline environment EE2 would be ionized into negatively charged groups. As a result, ion exchange reaction occurred inside the pore of MIEX resin, and the removal process of EE2 by MIEX was dominated by the ion exchange reaction.

Technological Parameters for Preparation and Granulation of Ammonium Ion-Exchange Material

As a raw material,kaolin was modified to prepare a high-performance ammonium ion-exchange material.According to cation-exchange capacity (CEC) measurement,the prepared ammonium ion-exchange material has an ammonium ion-exchange capacity greater than 75mg/g and can be used to remove ammonia nitrogen in water treatment.A pharmaceutical extruder-rounder was used to study the effects of granulation process.Polyethylene glycol6000 (PEG-6000) was used as the pore-forming agent and calcining temperature of 650℃ was used as the optimal condition.NMR data indicate that 27 Al is mainly converted from hexa-coordinated Al to tetra-coordinated Al during the modification.Compared with 29 Si in the original kaolin,29 Si in the modified kaolin does not have an obvious change.A comparison of the data with Langmuir and Freundlich isotherm models shows a good correlation.The Freundlich model describes the process more accurately,and the adsorption process of ammonia nitrogen in water with the ammonium ion-exchange material closely matches the pseudo-second-order reaction.

Determination of rhenium and osmium by ICP-MS for galena and sphalerite

Digestion with aqua regia in a Carius tube and separation of Re with anion exchange resin is commonly employed for Re–Os dating of molybdenite and pyrite.However, the recovery of Re is extremely low when this routine anion exchange method is applied to galena,causing difficulty in Re–Os dating of galena. In this study,we investigated the mechanism of Re loss during sample preparation and tested a revised procedure for Re–Os dating of galena and sphalerite.

Tungsten removal from molybdate solutions using chelating ion-exchange resin:Equilibrium adsorption isotherm and kinetics

The equilibrium adsorption isotherm and kinetic of the sorption process for W and Mo on macro chelating resin D403 were investigated on single Na2 Mo O4 and Na2WO4 solutions.The sorption isotherm results show that the adsorption process of W obeys the Freundlich model very well whereas the exchange process with Mo approximately follows the Henry model.The kinetic experiments show that the intraparticle diffusion process was the rate-determining step for W sorption on the resin,and the corresponding activation energy is calculated to be 21.976 k J/mol.

Investigation of Improved Signal Process and Control Circuit for Color-PDP

We present an alternative current-plasma display panel (AC-PDP) signal process and control circuit that fulfills the signal process and transform function. We proposed a novel driving logical waveform generator based on the SCI interface, which can real-time adjust the parameters to optimize performance of the PDP and facilitate the research and test. The use of nesting state-machine and parameterized design not only improves the resource utilization, but also makes it efficient and readable. The design has been written in synthesizable Verilog and fully verified using Xilinx FPGA device and applied in 42-in AC-PDP module.

Unexpected luminescence enhancement of upconverting nanocrystals by cation exchange with well retained small particle size

Highly luminescent upconversion nanoparticles （UCNPs） with small sizes are highly desirable for bioapplications. A facile in situ cation exchange strategy has been developed to greatly enhance the UC luminescence of hexagonal phase NaYF4 NPs while maintaining their small particle size and shape. Via a cation exchange treatment by hot-injecting Gd3＋ precursors into the as-prepared NPs solution without pre-separation, the naked-eye visible UC emission of the NPs was enhanced about 29 times under 980 nm near infrared （NIR） excitation with unchanged particle size. The cation exchange process was further demonstrated for the case of NaYF4 nanorods （NRs）. After the cation exchange, the nanorod was broken into two NPs with stronger emission. The cation exchanged hydrophobic UCNPs were further encapSulated with poly（amino acid） and successfully applied for targeted cancer cell UC luminescence imaging.

Characterization of polyoxometalates by electrospray ionization mass spectrometry

The electrospray behaviors of saturated, substituted, and lacunary polyoxometalates （POMs） with classic Keggin and Dawson structures were investigated systematically by electrospray mass spectrometry （ESI-MS）. The anions included Keggin [SiW12O40]4-, [SiW11O39]8-, [SiW10O36]8 , [SiW9O34]10-, Dawson [P2W18O62]6-, [P2W17O61]10-, and metal-substituted Keggin derivatives such as [PW11MnO40]7-, [SiW10V2O40]6-, and [GeWgCu3O37]10-. Common species observed in the mass spectra arose from the protonation or cationization of either intact or dehydrated precursor ions. Compared to saturated and substituted POMs, lacunary POMs exhibited distinguished MS behaviors such as a much higher degree of cationization and dehydration of the bare polyoxoanions present in the mass spectra. In addition, some of these lacunary POMs were found to undergo subtle speciation change in solution. Freshly prepared solutions are suggested for synthetics for which lacunary POMs are starting materials. The advantages of the cation-exchange process which are prior to MS analysis are illustrated by an example.

Tuning Zn^(2+) coordination tunnel by hierarchical gel electrolyte for dendrite-free zinc anode

Aqueous zinc-ion batteries(ZIBs)are perceived as one of the most upcoming grid-scale storage systems.However,the issues of electrode dissolution,dendrite formation,and corrosion in traditional liquid electrolytes have plagued its progress.In this work,Zn dendrite growth and side reactions are effectively suppressed by a highly-confined tannic acid(TA)modified sodium alginate(SA)composite gel electrolyte(TA-SA).The ion-confinement effect is enhanced by divalent zinc ions coordinated with carboxyl groups and chelated with phenolic hydroxyl groups,thus guiding and regulating Zn deposition to achieve steady zinc plating/stripping behavior.As a consequence,the Zn/TA-SA/NH_(4)V_(4)O_(10) full cells deliver a high specific capacity of 238.6 mAh g^(-1) and maintain 94.51%over 900 cycles at 2 A g^(-1).Notably,after resting over 5 d,the capacity can be stabilized with a capacity retention of 97.25%after 200 cycles at 2 A g^(-1).This highlyconfined and hydrogen bond-strengthened gel electrolyte may provide an effective strategy for the future development of quasi-solid-state metal batteries.