Aminolysis ofO-alkylO-4-nitropyenyl chloromethylphosphonates in reverse micellar solutions of the nonionic surfactant

The reaction ofn-hexylamine withO-alkylO-4-nitrophenyl chloromethylphosphonates in toluene solutions of poly(ethylene glycol)-600 monolaurate (PM) has been studied by spectrophotometry. The reverse micelles of the nonionic surfactant increase more than tenfold the observed rate constant of aminolysis. The catalytic activity of the surfactant is practically independent of the alkyl radical length of phosphonate. An increase in the concentration of amine results in a decrease in the catalytic efficiency. The character of the dependence of the rate constant on the concentration of PM is affected by the alkyl chain length of the substrate. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1735–1738, September, 1998.     

Network structure consisting of chain-like arrays of gold nanoparticles and silica layer prepared using a nonionic reverse-micelle template

A nonionic reverse-micelle based approach is described for fabrication of a network structure consisting of chain-like arrays of gold nanoparticles, followed by coating process with a uniform silica layer using a sol-gel method. The hexadecyl-poly (ethylene oxide-15) ether (designated C₁₆E₁₅) is used as a template for this study. The effects of a water-to-surfactant molar ratio (w) as well as the concentration of tetraethyl orthosilicate ([TEOS]_oil) are investigated on the resulting organized structures.     

Small angle neutron scattering from micellar solutions of triton X-100

Micellar solutions of non-ionic surfactant triton X-100 (8% by weight) show phase separation at cloud pointT _cp ～ 335 K. This paper reports results of small angle neutron scattering (SANS) experiments from this solution as a function of temperature between 298 and 332 K. The range of wave-vector transferQ, covered in these experiments is from 0.02 to 0.15 Å^?1. It is seen that as one approachesT _cp, the neutron scattering cross section diverges in the region of lowQ (<0.06 Å^?1) while it is independent of temperature in region of largeQ(>0.06 Å^?1). We believe that the divergence of scattering at lowQ with an increase in temperature is because of changes in the structure factorS(Q) of the solution. The measured distributions have been analyzed using four different models for inter-micellar potential. The models used to calculate the structure factorS(Q) are (1) mean spherical approximation (MSA) with Yukawa tail for attractive potential, (2) MSA with an attractive square well potential, (3) random phase approximation (RPA) with an attractive square-well potential and (4) Sticky hard sphere model (attractive square-well potential with Percus-Yevick approximation). The strengths of the attractive potential required to fit the SANS data are (?6.6 to ? 14.4)/kt for model (1), (? 6.6 to ? 15.0)/kt for model (2), (? 3.8 to ? 7.3)/k _B T for model (3) and (?2 to ?2.7)/kt for model (4). On the basis of reasonableness of the derived strength of the potential near the phase separation temperature and its relative temperature dependence, it is concluded that present data favour the Sticky hard sphere model.     

Reaction of 2-alkylaminomethylphenols with 4-nitrophenyl-bis(chloromethyl)phosphinate in toluene micellar solutions of polyethylene glycol-600 monolaurate

The effect of polyethylene glycol-600 monolaurate (PEG-ML) reversed micelles on the reaction of 2-alkylaminomethylphenols (AMP) with 4-nitrophenyl-bis(chloromethyl) phosphinate in toluene has been investigated. PEG-ML increases the observed rate constant of the reaction by more than one order of magnitude. AMP concentration in solution affects the position of the maximum on the concentration dependence of the micellar-catalyzed-reaction rate constants. The reaction rate constant in the micellar phase and the binding constant of the substrate with micelles depend on the alkyl chain length and AMP concentration. Inhibition of the reaction studied is observed in the presence of high PEG-ML concentrations and low AMP concentrations.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2134–2138, December, 1994.     

Effect of addition of hydrophilic ionic liquid 3-methyl-1-pentylimidazolium tetrafluoroborate ([C5mim][BF4]) on an aqueous solution of triton X-100

The effect of addition of 3-methyl-1-pentylimidazolium tetrafluoroborate ([C₅mim][BF₄]) on the micellization of a nonionic surfactant, Triton X-100 (TX-100), has been investigated. The techniques employed to study the aggregation behavior are fluoremetry, dynamic light scattering (DLS), and transmission electron microscopy (TEM) and the concentration range covered is 0–2?wt% [C₅mim][BF₄]. The probes, viz. pyrene and pyrene-1-carboxaldehyde (PyCHO), have been used for fluorescence analysis. According to the findings, the addition of pentyl-chained ionic liquid (IL) to aqueous TX-100 results in a dramatic increase in critical micelle concentration (cmc) decrease in micellar size, and aggregation number pointing toward an overall “unfavorable” aggregation process.     

硅衬底CMP过程中抛光雾的控制

抛光雾(Haze)是硅晶圆精抛过程中表面质量评定的重要参数之一.主要研究了化学机械抛光(CMP)过程中抛光液磨料质量分数、pH值、FA/O型非离子表面活性剂和混合表面活性剂对Haze值的影响.实验结果显示,磨料质量分数为0.1％是影响Haze值变化的拐点.当磨料质量分数由2％降至0.1％时Haze值下降迅速;当磨料质量分数由0.1％降至0.01％乃至0％时Haze值稍有增加.抛光液pH值约为9.5时Haze值最低,硅片表面质量最好,在此基础上提高或降低pH值都会增加Haze值.随着非离子表面活性剂体积分数的增加,Haze值快速下降.渗透剂脂肪醇聚氧乙烯醚(JFC)和FA/O型非离子表面活性剂混合使用比单独使用其中任何一种更有利于降低Haze值,且当JFC与FA/O的体积比为3∶1时,Haze值降到0.034,满足了工业生产的要求.     

Complex formation between polyethylene oxide-containing nonionic surfactants and α- and β-cyclodextrins

The inclusion complexes based on polyethylene oxide (PEO)-containing nonionic surfactants and ()-cyclodextrins (CD) were synthesized. Their composition and crystal structure were studied. The inclusion complexes of the surfactants with -CD form a crystal structure similar to that of the -CD—PEO complex. The inclusion complexes of the nonionic surfactants with -CD form a structure similar to that of the -CD—PEO complex. The structural models of the crystalline complexes were proposed. The micelle-forming abilities of the surfactants in dilute solutions in the presence of CD were studied. The CD binding to a surfactant molecule in aqueous solutions begins from the PEO fragment. Possible reasons for the formation of inclusion complexes between noncomplementary surfactant and -CD molecules were discussed. The thermal stability was studied, and the possibility of thermal dissociation of the pseudo-complementary -CD—surfactant complexes was shown.     

Aqueous and nonaqueous microemulsions with high molecular weight alkanes

This study extends the existing phenomenological thermodynamic model of aqueous microemulsions to nonaqueous microemulsions and examines the phase patterns when the melting temperature of the alkane oil is in the range of other liquid-liquid transition temperatures. The liquid paraffins studied are the alkane oils of greater than 17 carbons and are solid at room temperature. Water, water and ethylene glycol (41 by wt.), propylene glycol and water (41 by wt.), and propylene glycol are the four non-oleic components examined. Homogeneous polyoxyethylene nonionic surfactants and the commercial surfactants of the Brij series, Neodol series, and the LP series were used. Small-angle x-ray scattering gives evidence for the presence of microstructures in these solutions and, thus these systems are true microemulsions at temperatures above the melting point of the alkane. Systematic paths to move from aqueous to nonaqueous microemulsions are outlined. These results are utilized in optimizing the performance requirements of an inkjet printing application.     

Aggregation of amphiphilic aminomethylated calix[4]resorcinarenes and the nonionic surfactant Triton-X-100 in organic solvents

Aggregation and intermolecular interactions of amphiphilic calix[4]resorcinarene (1), aminomethylated calix[4]resorcinarenes (AMC 2—7) with different structures of the upper rim (including the oxazine structure in 6 and 7) and hydrophobic substituents on the lower (2—5), upper (6), or both rims (7) in the absence and in the presence of the nonionic surfactant Triton-X-100 (8) and p-nitrophenol (9) in chloroform and 1,4-dioxane were studied by permittivity measurements and 2D ROESY ¹H NMR technique. The tendency of amphiphilic derivatives 1—7 toward self-aggregation and mixed aggregation with surfactant 8 primarily depends on the nature of both the solvent and the polar groups on the upper rim of calixarenes. In chloroform, AMC—8 aggregates show interactions of the methyl and methylene groups of the hydrophobic substituents of AMC with the ethyleneoxy fragments of surfactant 8, while in stable intermolecular complexes of 5 and 6 with compound 9, the methylene groups of the long-chain radicals of the AMC strongly interact with the aromatic protons ortho to the hydroxy group of 9. In 1,4-dioxane, calix[4]resorcinarenes 1 and 5 are bound in stable solvates, which prevents them from forming aggregates and mixed micelles.     

Spectrophotometric determination of cationic and anionic surfactants with anionic dyes in the presence of nonionic surfactants,part I: A general aspect

The behavior of color development of anionic azo dyes, methyl orange and its analogues, was examined in aqueous media by changing the microenvironment of the dyes. The addition of alcohols, organic onium ions, anionic surfactants and nonionic surfactants brought about a decrease of the band at wavelengths near 480 nm and an increase of the band at wavelengths near 420 nm. Such a shift toward the shorter wavelengths in spectra was attributed to the change of the micro-environment around the dyes from a polar field to a less polar field; that is, the shift is caused by the change of the contribution of the following resonance forms, On the basis of the color change phenomena, the spectrophotometric methods for the determination of organic onium ions and anionic surfactants were proposed.