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1.
The formation of gold nanoparticles and clusters in solutions of reverse micelles formed by Tritons X-45, X-114, and X-100 (polyoxyethylene isooctylphenyl ethers with degrees of polymerization n = 5, 7–8 and 9–10, respectively) in the presence of sodium sulfite is studied. The stability of these particles is shown to depend on the length of ethylene oxide chains in surfactant molecules, water content in micelles, and the presence of special additives. It is found that, on one hand, L-ascorbic acid favors a reduction of HAuCl4 and, on the other hand, affects the stability of resultant particles.  相似文献   

2.
表面活性剂在非水溶剂中聚集态的研究所见的报导与水体系相比要少得多.然而近年来对非水体系的研究日益增多.这是因为表面活性剂在非水溶剂中的应用日趋增加,但与水体系相反,对非水体系的性质了解甚少.对表面活性剂非水体系的研究还有助于对其聚集体的共溶剂效应有更深的认识.TritonX-100(以下简写为TX-100)是典型的非离子表面活性剂,在工业上有着广泛的应用.乙二醇在多醇中与水的化学结构最相近问,然而它却是水结构的破坏剂,加入少量的乙二醇会使水的冰点急剧下降.乙二醇又是蛋白质的变性溶剂.表面活性剂在乙二醇中的胶…  相似文献   

3.
The adsorption isotherms of nonionic surfactants Triton X-100 and Triton X-305 from water and cyclohexane on carbon black have been determined at 15 and 30°C. The Langmuir-type and BET-type isotherms are obtained for adsorption of Triton X-100 and Triton X-305 from water and cyclohexane respectively. Both the contact angles of water for graphite/water/air and graphite/water/cyclohexane decrease monotonously with increasing surfactant concentration. From these results, it is proposed that the adsorption of Triton X-100 and Triton X-305 on carbon black or graphite from water is monolayer. For the adsorption from cyclohexane solutions, the ethyleneoxide group of the surfactant molecules may be adsorbed onto the polar spot at the surface of carbon black, and the hydrophobic group of adsorbed molecules may direct toward the liquid phase or attaches to the nonpolar surface region around the polar spot. As the concentration increases, the ethylene oxide groups of the adsorbed molecules can be aggregated with each other via polar interactions to form hemi-reversed micelle.  相似文献   

4.
Dessent CE  Kim J  Johnson MA 《Faraday discussions》2000,(115):395-406; discussion 407-29
We report the observation of resonance structure in the absorption and X-/NO2- photofragment action spectra of the X-.CH3NO2 (X- = I- and Br-) complexes in the region above the electron detachment threshold. The resonance structure corresponds to peaks which appear at the onsets for vibrational excitation of the -NO2 wag, scissors, and stretch modes of neutral CH3NO2, the modes which most strongly distort upon electron capture into its pi* lowest unoccupied molecular orbital. We attribute the peaks to excitation of vibrational Feshbach resonances of the CH3NO2- transient negative ion, where near-threshold excitation of X-.CH3NO2 spectroscopically accesses states of the free electron-CH3NO2 system.  相似文献   

5.
The spectral (both absorption and fluorescence) and photoelectrochemical studies of a few selective dyes, namely, anionic erythrosin B, neutral riboflavin and cationic safranin O have been carried out in aqueous solution of triton X-100, a neutral surfactant. The results show that the ionic dyes, erythrosin B and safranin O form 1:1 electron donor-acceptor (EDA) or charge-transfer (CT) complexes with triton X-100 both in the ground and excited states, whereas neutral dye riboflavin in its excited state forms 1:1 complex with triton X-100. In these complexes, the dyes act as electron acceptors whereas triton X-100 acts as an electron donor. The fluorescence spectra of erythrosin B and safranin O in presence of triton X-100 show enhancement of fluorescence intensity with red and blue shifts respectively while riboflavin shows normal quenching of fluorescence. A good correlation has been found among photovoltage generation of the systems consisting of these dyes and triton X-100, spectral shift due to complex formation and thermodynamic properties of these complexes.  相似文献   

6.
The influence of UV-irradiation on the interaction of hemoglobin (Hb) with Triton X-100 is investigated by UV–Vis absorption spectroscopy, fluorescence spectroscopy and freeze-fractured transmission electron microscopy. It is found that in Triton X-100/H2O systems Hb can convert to hemichrome but heme is not present, whereas in Triton X-100/n-C5H11OH/H2O microemulsion Hb can convert to hemichrome and then induce the heme monomer to leave the hydrophobic cavity of Hb. UV-irradiation can also convert Hb to hemichrome, and subsequently make heme to be photodegraded, in which the conversion rate depends on the structure of the surfactant aggregates. Furthermore, in order to understand the mechanism of photostabilization of Hb in Triton X-100 systems, the photostabilization of heme in the Triton X-100 aqueous solutions and Triton X-100/n-C5H11OH/H2O microemulsions has been studied.  相似文献   

7.
Cloud point of nonionic surfactant Triton X-45 in aqueous solution   总被引:1,自引:0,他引:1  
Triton X-45, a nonionic surfactant with a low hydrophile-lypophile balance value and dispersible in aqueous solution at room temperature, has a Krafft point above the room temperature. The cloud point of Triton X-45 in an aqueous solution is different from the conventional aqueous nonionic surfactant micelle solution. It was further confirmed by a determination of the effect of additives on the phase behavior of aqueous solutions containing Triton X-45. The experimental fact eliminates the prevalent concept that the cloud point of Triton X-45 is below room temperature, which is helpful to exploit a biocompatible medium for a microbial growth and then for whole cell microbial transformation in a nonaqueous medium.  相似文献   

8.
X射线荧光光谱分析   总被引:9,自引:0,他引:9  
陶光仪 《分析试验室》1995,14(3):92-100
本文是“分析试验室”定期评述中“X射线荧光光谱分析”学科的第五篇评述。它收集了国内学者1992年7月到1994年6月期间发表在国内外刊物上的171篇文章,并对此期间我国X射线荧光光谱分析的概况和发展进行评述。内容包括XRF仪器,同步辐射XRF,全反射XRF,粒子激发X线发射光谱,定量分析方法,制样技术,以及在各个科学烽戒严领域中的应用。  相似文献   

9.
有机酸对非离子型表面活性剂浊点的影响   总被引:1,自引:0,他引:1  
有机酸对非离子表面活性剂TritonX-100浊点的影响与酸的亲水性能、空间效应及其在胶束中的增溶位置有关。直链一元酸的加入均使浊点下降,且酸的碳链越长影响越大。直链二元酸对TritonX-100浊点下降的影响小于直链一元酸,且碳原子数nc<6时,使得浊点略有升高;nc≥6时,使得浊点下降。由于空间位阻作用,支链酸和取代酸使TritonX-100浊点降低幅度较小。  相似文献   

10.
ABSTRACT

The diffusion coefficient of the micelle, the first CMC and the second CMC of Triton X-100 are determined by cyclic voltammetry without any probe. The first CMC and the second CMC of Triton X-100 are 3.1x lO?1 and 1.3× 10?1 respectively. The viscosity of the micelle solution, the micellar aggregation number and the micellar size increase but the diffusion coefficient decreases with Triton X-100 concentration increasing. The mechanism of the electrochemical reaction of Triton X-100 at platinum electrode is deduced by measurements of conductivity, pH and cyclic voltammetry.  相似文献   

11.
研究了用5-Br-PADCAP-Triton X-100作为络合滴定指示剂测定铜的方法。在pH 4.5的乙酸-乙酸钠介质中,采用5-Br-PADCAP为指示剂,以Triton X-100增敏、增稳,用EDTA为络合剂滴定铜。结果表明,用5-Br-PADCAP-Triton X-100作金属指示剂,能改善反应条件,提高变色灵敏度,优于用PAN和PAN-S作金属指示剂。  相似文献   

12.
Experiments with Triton X-100 as a model surfactant were performed under steadystate conditions, using deoxygenated solutions as well as those saturated with N2O, O2 or N2O/O2 mixtures. The Triton X-100 decomposition yield was dependent on the O2 content of the irradiated system. Oxygen promoted surfactant decomposition in aqueous solution containing only Triton X-100.  相似文献   

13.
Three polymeric adsorbents with hydrogen bonding acceptors, methylamine,N-methyl-acetamide and aminotri(hydroxymethyl)methane modified resins are synthesized fromchloromethylated X-5 resin. Adsorption isotherms of phenol and theophylline onto the three modifiedresins and the original X-5 resin from aqueous solution are measured. The results show thatadsorption of compounds with hydrogen bonding donor onto methylamine and N-methylacetamidemodified resins is enhanced as compared with that onto X-5 resin, and adsorption mechanismbetween the adsorbents and the adsorbates is mainly based on hydrogen bonding and hydrophobicinteraction. While adsorption of compounds with hydrogen bonding donor ontoaminotri(hydroxymethyl)methane modified resin is lowered as compared with that onto X-5 resin, andadsorption mechanism between the adsorbent and the adsorbates is mainly based on hydrophobicinteraction.  相似文献   

14.
1. INTRODUCTION Adsorption capacity and selectivity are improved when some ion exchange groups or hydrogen bonding acceptor or/and donors are introduced into common polymeric adsorbents [1~5]. R. F. Shi et al have synthesized a series of bifunctional ads…  相似文献   

15.
参照文献方法合成了BSA保护的水溶性发光金纳米粒子, 并考察了此探针在非离子表面活性剂曲通X-100中的发光行为.根据观察到的发光增强效应, 建立了一种简单的测定曲通X-100的方法.考察了发光金纳米粒子的浓度、体系酸度、反应时间及共存物质对测定的影响.在最佳条件下, 发光强度与曲通X-100的浓度分别在0~150 μmol/L和150~600 μmol/L范围内分段成正比关系.两条工作曲线的交点所对应的浓度与曲通X-100的临界胶束浓度十分吻合, 为胶束形成过程提供了直接的指示.作为一种生物相容性探针, 发光金纳米粒子被用于生物学样品中曲通X-100的分析测定, 结果令人满意.  相似文献   

16.
Fluorescence enhancement of Tb3+ has been studied, using substituted benzoic acids as ligands. These ligands enhance the fluorescence of Tb3+ by about three orders of magnitude. The enhancement is observed due to ligand sensitized fluorescence. The fluorescence of Tb3+ in these complexes is synergistically enhanced by the addition of trioctylphosphine oxide (TOPO) in Triton X-100. The synergism displayed by TOPO was observed only when Triton X-100 micellar medium was used. TOPO dissolved in SDS/DTAB micellar medium did not result in synergistic fluorescence enhancement of Tb3+. These observations are discussed in detail and the synergism displayed by TOPO is rationalized on the basis of the structure of the surfactants.  相似文献   

17.
采用无水相体系的胶体通过丝网印刷工艺制备TiO2薄膜电极,研究发现曲拉通(TritonX-100)可以明显改变TiO2电极显微结构,且对染料敏化太阳电池的性能影响显著.过少或过多的曲拉通都将导致开路电压、短路电流、填充因子以及效率的降低.由3gP25粉末配制的胶体中,曲拉通适宜的加入量约为0.8mL.  相似文献   

18.
The hydrolysis of cephanone in Triton X-100 micelle and Triton X-100/n-C5H11OH/H2O(O/W) microemulsion were studied by means of UV-Vis absorption spectroscopy. The results show that compared with water, Triton X-100 micelle and Triton X-100/n-C5H11OH/H2O (O/W) microemulsion can inhibit the hydrolysis of cephanone. The inhibition effects of Triton X-100 micelle and Triton X-100/n-C5H11OH/H2O (O/W) microemulsion on the hydrolysis of cephanone are related to the location of cephanone in the interphases of Triton X-100 miceUes and Triton X-100/n-C5H11OH/H2O(O/W) microemulsion droplets.  相似文献   

19.
As a key part of Hard Disc(HDI),the thin film of lube is possibly degraded and destroyed by the interaction between the magnetic head and disk during the hard disk working. Both TGA and FTIR are used to study lubes failure mechanism of HDI and investigate the function of X-1P as an additive in HDI lube. TGA experiment results show that the sample PFPE / X-1P / Al2O3 is much more stable than the sample PFPE / Al2O3 just as sample PFPE,and the sample PFPE / Al2O3 will degrade with high speed at enough high temperature. FTIR experiments present the results similar to that of TGA experiments. From IR sorption spectra at different heating times for the three samples,it can be found that the sample PFPE & the sample PFPE / X-1P / Al2O3 are similarly stable,but different from the sample PFPE / Al2O3 for which new CF = O absorption peak appeared after heated for 15 min and became stronger with the extending for heating time. FTIR experiment results further verifies that alumina is a catalyst for PFPE degradation reaction and X-1P can effectively passivate the catalyst and stabilize PFPE. In order to investigate X-1P's role to mechanical & tribological performances of HDI,the CSS experiment is also performed and the experiment results tell that the presence of X-1P dip-coated on the magnetic head can greatly reduce the friction between head and disk and improve CSS performance of HDI. In addition,the failure mechanism of HDI lube and X-1P's working principle as a HDI lube additive are analyzed and discussed respectively. The aluminum atom of alumina has empty orbits which can accept isolated electron pairs,and is a kind of Lewis acid with stronger electrophilic trend. Oxygen atom of PFPE has isolated electron pairs and shows nucleophilic trend. When the magnetic head contacts with the HDI lube,it is possible for alumina to induce PFPE to disproportionally degrade first from the ether bonding at enough high moment temperature. For X-1P,owing to its special molecule structure,not only has a good chemical stability but also shows stronger nucleophilic trend. When alumina contacts with the compounds of X-1P and PFPE,X-1P can be absorbed on the alumina surface prior to PFPE and keeps PFPE out of contact with alumina,and as such to protect PFPE out of degradation.  相似文献   

20.
活性艳红X-3B水溶液的光化学与光催化协同脱色反应   总被引:30,自引:0,他引:30  
 对影响活性艳红X-3B水溶液光化学与光催化协同脱色反应的各种条件(如溶液的pH值,紫外光照强度,空气流量,催化剂用量及溶液的初始浓度等)进行了考察.结果表明,降解率随着紫外光照强度的增强而加快,随着X-3B初始浓度的增大而减慢;催化剂最佳用量为4g/L,空气最佳流量为4.3L/h.在X-3B水溶液的光催化脱色过程中,存在有光解反应,但它远不如光催化反应重要.因此,活性艳红X-3B水溶液的降解是光化学与光催化的协同脱色反应.  相似文献   

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