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101.
甲烷直接氧化制甲醇Ⅲ.反应气吹扫催化膜反应器(RSCMR) 总被引:2,自引:0,他引:2
用溶胶-凝胶法制备了“SiO_2/陶瓷”非对称无机膜,并用该膜制备了反应气吹扫催化膜反应器(RSCMR)装置。在RSCMR上考察了甲烷一步催化氧化制甲醇反应。结果表明,在研究的范围内,增加氧气或甲烷的浓度和吹扫气的流速(即总的反应气流量)有利于提高甲醇的收率;甲醇在反应条件下的热不稳定性是影响目标反应选择性的重要原因。RSCMR较膜反应器(CMR)系统能更有效地抑制甲醇的热分解,因而可得到较CMR更高的甲醇收率。当反应温度为700℃时,甲醇的收率在CMR中为0.5g/m ̄2h,在RSCMR中可达0.9g/m ̄2h。 相似文献
102.
103.
An automated sample pretreatment of human blood plasma for liquid chromatographic determination of three antidepressant drugs, dibenzepine; a tricyclic antidepressant (TCA), reboxetine; a selective noradrenaline reuptake inhibitor (SNRI) and fluvoxamine; a selective serotonin reuptake inhibitor (SSRI), based on supported liquid membrane (SLM) for unsurpassed sample clean-up and analyte enrichment, has been developed. The chromatograms after enrichment of plasma blank and aqueous blank are virtually indistinguishable. The entire analytical procedure revealed good linearity and low detection limits of 5, 15 and 20 ng mL–1 for dibenzepine, reboxetine and fluvoxamine, respectively. No carry-over effects were noted. The repeatability of extraction at three concentrations in the range 40–150 ng mL–1 for the three drugs was between ca. 3% and 7% as relative standard deviation. The reproducibility relative standard deviation during three different days (replacing the membrane each day) was not significantly higher. 相似文献
104.
105.
Páez-Hernández ME Aguilar-Arteaga K Valiente M Ramírez-Silva MT Romero-Romo M Palomar-Pardavé M 《Analytical and bioanalytical chemistry》2004,380(4):690-697
The results presented in this work deal with the prime application of activated composite membranes (ACMs) for the transport of Hg(II) ions in a continuous extraction–re-extraction system using di-(2-ethylhexyl)dithiophosphoric acid (DTPA) as carrier. The effects of variables such as the pH, the nature of the acid and the concentration of the casting solutions on the transport of Hg(II) are also investigated. When the ACM was prepared with a 0.5 M DTPA solution and when the feed solution contained 2.5×10–4 M Hg(II) in 0.1 M HCl, the amount of mercury extracted was greater than 76%. The re-extracted mercury was subsequently recovered by means of a stripping phase comprising 0.3 M thiourea solution in 2 M H2SO4, yielding 54% of the initial amount of mercury after transport had taken place for 180 min. 相似文献
106.
壳聚糖/聚丙烯酸聚电解质复合物膜对水/有机液体系的渗透汽化性能 总被引:8,自引:0,他引:8
以壳聚糖和聚丙烯酸为原料制备了聚电解质复合物膜,并对其分离水/乙醇体系的渗透汽化特性和浓度,温度,化学组成等因素的影响进行了研究,发现后处理方法对复合物膜的分离性能影响很大。同时对其它水/有机液体系,该膜也具备优异的分离性能。 相似文献
107.
Rong-Qiang Fu Tong-Wen Xu Yi-Yun Cheng Wei-Hua Yang Zhong-Xiao Pan 《Journal of membrane science》2004,240(1-2):141-147
Starburst dendrimer polyamidoamine (PAMAM) with ellipsoidal or spheroidal shape is structure-regular and has much more amino groups than conventional polymers. This paper investigates the possibility of these amino groups on water dissociation in a bipolar membrane interface. To do this, a bipolar membrane is prepared by casting the solution of sulfonated poly(phenylene oxide) (SPPO) in dimethyl formamide (DMF) on a commercial anion exchange membrane that is immersed in PAMAM aqueous solution in advance. The existence of PAMAM adsorbed on the membrane is proved by X-ray photoelectron spectroscopy (XPS), and the adsorption amount is evaluated by weighting method. The junction thickness of the prepared bipolar membrane is determined by electrochemical impedance spectroscopy (EIS), and the performance is evaluated by current–voltage curves. The experiments show that both the generation and concentration of PAMAM would strongly affect the characteristics of the bipolar membranes. There exists a transitional concentration for various generations PAMAMs to catalyze effectively the water dissociation, and above or below the transitional concentration the performance of bipolar membranes is decreasing. The higher the generation, the lower the concentration. Moreover, at a fixed solution concentration, there is not the simple relation of monotone decreasing or increasing between the performance of bipolar membranes and the generations of PAMAMs. All these can be explained according to the characteristics of PAMAMs combined with available water dissociation theory. 相似文献
108.
Moon Hwan Cho Seung Chang Yang Nam Keun Yang Yongjin Kang Jaejung Ko 《Journal of inclusion phenomena and macrocyclic chemistry》1998,30(4):279-287
The thermodynamic parameters for the interaction of Cu2+, Ni2+, Co2+, Cd2+, andAg+ with the new title ligand have been determined by titration calorimetry in 50% THF–methanol (V/V) at 25 °C.Ag+ exhibited remarkably higher complexation selectivity.Ag+ and several transition metal ions have been transportedusing this ligand as carrier in a bulk liquid membrane. CompetitiveAg+–M2+ transport studies have also beencarried out for the same system. In this membrane transport study, high transport of Ag+ was observed in both single and competitiveAg+–M2+ transport studies. The complexformation of N,N-bis[o-(diphenylphosphino)benzylidene]ethylenediamine (P2N2) with silver,[Ag(P2N2)] (NO3), (1) is reported. Complex 1 has been characterized by X-ray crystallography. 1 ismonoclinic, space group P21/n (No. 14), with cell dimensionsa = 13.398(4) , b=12.577(5) , c = 21.521(4) , =100.14(2) , V = 3570(2) 3 and Z = 4. 相似文献
109.
Sodium-dicyclohexyl- 18-crown-6 complex cation was used as carrier for the uphill transport of zinc as Zn(SCN)42? complex anion. By using L-cysteine as a metal ion acceptor in the receiving phase at the optimized pH of 7.6, the amount of zinc transport through the liquid membrane after 90 min was 97.2 ± 1.0%. The selectivity and efficiency of zinc transport from aqueous solutions containing equimolar mixtures of Ag+, Cd2+ Co2+, Cu2+, Fe2+, Ni2+, Pb2+, Pd2+, Sr2+, Bi3+, Cr3+ and Fe3+ ions was investigated. In the presence of NH2OH.HCl as a suitable masking agent in the source phase, the interfering effect of Cu2+ and Pb2+ ions was diminished drastically. 相似文献
110.
A comparison is made between the distribution of residue preferences, three dimensional nearest neighbour contacts, preferred rotamers, helix-helix crossover angles and peptide bond angles in three sets of proteins: a non-redundant set of accurately determined globular protein structures, a set of four-helix bundle structures and a set of membrane protein structures. Residue preferences for the latter two sets may reflect overall helix stabilising propensities but may also highlight differences arising out of the contrasting nature of the solvent environments in these two cases. The results bear out the expectation that there may be differences between residue type preferences in membrane proteins and in water soluble globular proteins. For example, the -branched residue types valine and isoleucine are considerably more frequently encountered in membrane helices. Likewise, glycine and proline, residue types normally associated with `helix-breaking' propensity are found to be relatively more common in membrane helices. Three dimensional nearest neighbour contacts along the helix, preferred rotamers, and peptide bond angles are very similar in the three sets of proteins as far as can be ascertained within the limits of the relatively low resolution of the membrane proteins dataset. Crossing angles for helices in the membrane protein set resemble the four helix bundle set more than the general non-redundant set, but in contrast to both sets they have smaller crossing angles consistent with the dual requirements for the helices to form a compact structure while having to span the membrane. In addition to the pairwise packing of helices we investigate their global packing and consider the question of helix supercoiling in helix bundle proteins. 相似文献