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表面活性剂溶液对光子晶体晶格周期的影响
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作者 褚明利 吕广超 +1 位作者 刘丽 吴广峰 《长春工业大学学报》 CAS 2020年第3期244-250,共7页
采用无皂乳液聚合方法制备了粒径为233 nm的阳离子型聚甲基丙烯酸甲酯纳米微球PMMA-co-P(MATMAC),微球具有良好的单分散性和较高的表面电荷密度(61.4μC·cm^-2),再由此阳离子纳米微球自组装成光子晶体,光子晶体的反射峰位置在510 n... 采用无皂乳液聚合方法制备了粒径为233 nm的阳离子型聚甲基丙烯酸甲酯纳米微球PMMA-co-P(MATMAC),微球具有良好的单分散性和较高的表面电荷密度(61.4μC·cm^-2),再由此阳离子纳米微球自组装成光子晶体,光子晶体的反射峰位置在510 nm处,采用扫描电镜(SEM)表征了光子晶体的周期性结构。 展开更多
关键词 阳离子纳米微球 光子晶体 表面活性剂吸附 反射光谱
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表面活性剂的吸附等温线与表面活性 被引量:1
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作者 王涛 刘云 《北京日化》 2006年第3期10-12,共3页
本文论述了表面活性剂的吸附等温线四个不同阶段,对各种参数,如分子结构、温度、盐的浓度对于表面活性剂吸附性的影响进行了介绍。
关键词 表面活性:吸附等温线 固液界面
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肺表面活性剂补充疗法的现状
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作者 李平 《国外医学情报》 1997年第10期3-3,共1页
用肺表面活性剂吸附肺泡气液界面、降低表面张力,可以防止肺泡萎陷和肺水肿。新生儿呼吸窘迫综合征就是由于表面活性物质缺乏引起的,经呼吸道补充肺表面活性剂(表面活性剂补充疗法)可以提高患儿存活率。因急性呼吸窘迫综合征(ARDS)有表... 用肺表面活性剂吸附肺泡气液界面、降低表面张力,可以防止肺泡萎陷和肺水肿。新生儿呼吸窘迫综合征就是由于表面活性物质缺乏引起的,经呼吸道补充肺表面活性剂(表面活性剂补充疗法)可以提高患儿存活率。因急性呼吸窘迫综合征(ARDS)有表面活性物质异常,所以可以预测出表面活性剂补充疗法的有效性。 展开更多
关键词 表面活性 合成表面活性 表面活性物质 补充疗法 加工型 气液界面 肺水肿 表面活性剂吸附 表面张力 肺泡
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复合驱油技术应用中推荐低浓度表活剂体系 被引量:2
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作者 戚连庆 朱洪庆 +3 位作者 孙艳萍 刘凤霞 宋志学 彭齐国 《大庆石油地质与开发》 CAS CSCD 北大核心 2010年第3期143-149,共7页
复合驱体系常使用相对高的表活剂浓度,但是最近的研究表明:过低的界面张力将使得驱油过程处于“第二类”驱动状况下,驱油效果相对降低,这就要求必须重新考虑体系的组成问题。通过油藏数值模拟方法,优化选择了低浓度表活剂体系,驱... 复合驱体系常使用相对高的表活剂浓度,但是最近的研究表明:过低的界面张力将使得驱油过程处于“第二类”驱动状况下,驱油效果相对降低,这就要求必须重新考虑体系的组成问题。通过油藏数值模拟方法,优化选择了低浓度表活剂体系,驱油实验验证低浓度体系驱油效果良好;又用数值模拟方法对表活剂吸附问题作了较深入的讨论,得出驱油过程处于“第一类”驱动状况下表活剂吸附不影响驱油效果;通过现场试验结果比较也看到低浓度体系驱油方案效果良好。因此在复合驱技术应用中推荐低表活剂浓度体系。 展开更多
关键词 三元复合驱 驱动状况 毛管数 表面活性剂吸附
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在用十二烷基硫酸盐捕收剂浮选天青石时碳酸根离子的作用 被引量:3
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作者 A.洛帕茨瓦尔维索 雷小双 肖力子 《国外金属矿选矿》 2002年第7期20-24,共5页
应用电动测量和微浮选法研究了在有和没有碳酸盐组分存在时阴离子捕收剂十二烷基硫酸钠对天青石的浮选。用电动测量、矿物溶解测定、红外光谱和矿物 /溶液平衡法研究了在碳酸盐水溶液中 ,天青石表面向碳酸锶的转变过程。在pH 3~ 11范围... 应用电动测量和微浮选法研究了在有和没有碳酸盐组分存在时阴离子捕收剂十二烷基硫酸钠对天青石的浮选。用电动测量、矿物溶解测定、红外光谱和矿物 /溶液平衡法研究了在碳酸盐水溶液中 ,天青石表面向碳酸锶的转变过程。在pH 3~ 11范围内 ,在没有碳酸盐的溶液中 ,十二烷基硫酸盐由于在天青石表面上化学吸附而有效地浮选天青石 ,此时它在天青石表面上形成了十二烷基硫酸锶。在 pH 7 8处 ,可溶的碳酸盐组分使天青石表面开始向碳酸锶转变 ,但此时不影响天青石的浮选。只在 pH高于 10时天青石浮选受到抑制 ,这是由于CO2 - 3 和HCO- 3 组分在天青石表面上特效吸附 ,阻止十二烷基硫酸盐在碳酸盐化的天青石表面上吸附。 展开更多
关键词 捕收 碳酸根离子 浮选 天青石 十二烷基硫酸钠 电动现象 表面活性剂吸附 工业矿物浮选 碳酸锶
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用选择性抑制剂浮选分离塑料
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《湖南有色金属》 CAS 1997年第5期5-5,共1页
关键词 浮选分离 选择性抑制 表面活性剂吸附 气溶胶OT 有机混合物 水性聚合物 木质磺酸盐 聚磷酸脂 聚乙缩醛 聚苯基醚
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Low-temperature collecting performance of a new combined collector on scheelite flotation
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作者 ZHANG Zheng-quan JIAO Fen +4 位作者 YANG Cong-ren QIN Wen-qing WEI Qian WANG Xu LI Wei 《Journal of Central South University》 SCIE EI CAS CSCD 2024年第10期3730-3740,共11页
The reduced ability of fatty acids to dissolve and disperse at low temperatures limits their effectiveness in winter applications.In this study,a green and environment-friendly reagent,polyethylene glycol 2000(PEG-200... The reduced ability of fatty acids to dissolve and disperse at low temperatures limits their effectiveness in winter applications.In this study,a green and environment-friendly reagent,polyethylene glycol 2000(PEG-2000),was used to evaluate its effect on the collecting performance of sodium oleate during scheelite flotation at low temperatures.The effect of PEG-2000 on the flotation of scheelite with the collector sodium oleate(NaOL)was studied by flotation tests,surface tension tests,infrared spectral analysis,and zeta potential measurements.Flotation tests showed that adding PEG-2000 can enhance the collecting ability of NaOL on scheelite at low temperature(5℃).The recovery of scheelite with the mixed collector of PEG-200 and NaOL is 4.39%higher than that with NaOL only.The surface tension tests,infrared spectral analysis and zeta potential measurements revealed that PEG-2000 and OL^(−)are co-adsorbed on the scheelite surface at low temperatures.The presence of PEG-2000 promoted the increase of the adsorption concentration of oleate ions(OL^(−))on the scheelite surface.The reason was that PEG-2000 has a shielding effect on the electrostatic repulsion between the OL^(−)groups,which changes the micellar configuration of OL^(−)in the solution system and makes the OL^(−)gather more tightly on the surface of scheelite,leading to the enhancement of its hydrophobicity.This discovery provides a reference for the development of collecting reagents for efficient flotation recovery of scheelite under low temperature environment. 展开更多
关键词 SCHEELITE FLOTATION low temperature nonionic surfactant polyethylene glycol ADSORPTION
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TMAH+Triton中Si湿法腐蚀机理研究现状 被引量:2
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作者 姚明秋 苏伟 +1 位作者 唐彬 王芳 《微纳电子技术》 CAS 北大核心 2014年第6期386-393,共8页
在微机电系统(MEMS)领域硅各向异性湿法腐蚀是制作许多元器件的一项重要技术,加入非离子型表面活性剂的腐蚀液可以在硅基片上制作出各种形状,但是对于真正的腐蚀机理还有待进一步研究。介绍了硅湿法腐蚀机理的研究现状,通过不同腐蚀条... 在微机电系统(MEMS)领域硅各向异性湿法腐蚀是制作许多元器件的一项重要技术,加入非离子型表面活性剂的腐蚀液可以在硅基片上制作出各种形状,但是对于真正的腐蚀机理还有待进一步研究。介绍了硅湿法腐蚀机理的研究现状,通过不同腐蚀条件下得出的不同腐蚀结果分析其腐蚀机理。介绍了当非离子型表面活性剂加入碱性溶液时固体表面的活性剂吸附层结构,重点介绍了表面活性剂Triton X-100加入各向异性碱性腐蚀剂四甲基氢氧化铵(TMAH)后对活性剂吸附状态和硅腐蚀速率产生影响的根本原因。不同晶向硅表面的H基和OH基数量会影响其表面活性剂的吸附能力,硅在纯TMAH腐蚀液和加入活性剂Triton后的TMAH腐蚀液中的腐蚀速率存在一定差异,高质量分数的TMAH下加入不同体积分数的Triton时,不同晶面在活性剂吸附和腐蚀速率上也存在不同,给出了出现这些现象的机理分析。研究硅腐蚀机理可以为器件设计提供有效的理论支持,有助于制作更多新的MEMS结构。 展开更多
关键词 各向异性湿法腐蚀 四甲基氢氧化铵(TMAH) TRITON X-100 表面活性剂吸附 腐蚀速率
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Comparative studies on flotation of aluminosilicate minerals with Gemini cationic surfactants BDDA and EDDA 被引量:8
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作者 黄志强 钟宏 +2 位作者 王帅 夏柳荫 刘广义 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2013年第10期3055-3062,共8页
Gemini quaternary ammonium salt surfactants, butane-a, co-bis(dimethyl dodeculammonium bromide) (BDDA) ethane-a, fl-bis(dimethyl dodeculammonium bromide) (EDDA) were adopted to comparatively study the flotatio... Gemini quaternary ammonium salt surfactants, butane-a, co-bis(dimethyl dodeculammonium bromide) (BDDA) ethane-a, fl-bis(dimethyl dodeculammonium bromide) (EDDA) were adopted to comparatively study the flotation behaviors of kaolinite, pyrophyllite and illite. It was found that three silicate minerals all exhibited good floatability with Gemini cationic surfactants as collectors over a wide pH range, while BDDA showed a stronger collecting power than EDDA. FTIR spectra and zeta potential analysis indicated that the mechanism of adsorption of Gemini collector molecules on three silicate minerals surfaces was almost identical for the electronic attraction and hydrogen bonds effect. The theoretically obtained results of density functional theory (DFT) at B3LYP/6-31G (d) level demonstrated the stronger collecting power of BDDA presented in the floatation test and zeta potential measurement. 展开更多
关键词 aluminosilicate minerals Gemini cationic surfactants reverse flotation adsorption mechanism
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有机化钙硅胶的制备和性质
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作者 沈钟 邵长生 +2 位作者 温劲松 陈丽特 孙载坚 《江苏化工》 1993年第2期10-13,共4页
通过阴离子表面活性剂(SAS、SDS和SDBS)在钙硅胶上的吸附研究了有机化钙硅胶的制备。测定了此硅胶的Zeta电位、差热分析,红外光谱、物理结构、润湿热、接触角、热稳定性和水解稳定性、并对实验结果进行了讨论。
关键词 有机化钙硅胶 表面活性吸附
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Modeling of mass transfer characteristics of bubble column reactor with surfactant present 被引量:10
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作者 赵伟荣 史惠祥 汪大翚 《Journal of Zhejiang University Science》 EI CSCD 2004年第6期714-720,共7页
Danckwert’s method was used to determine the specific interfacial area, a, and the individual mass transfer coefficient, kL, during absorption of CO2 in a bubble column with an anionic surfactant in the carbonate-bi... Danckwert’s method was used to determine the specific interfacial area, a, and the individual mass transfer coefficient, kL, during absorption of CO2 in a bubble column with an anionic surfactant in the carbonate-bicarbonate buffer solution and NaAsO2 as catalyst, the presence of which decreases the specific interfacial area and the individual mass transfer coefficient. The specific interfacial area and the individual mass transfer coefficient increase with increasing su- perficial gas velocity. The specific interfacial area decreases whereas the individual mass transfer coefficient increases with increasing temperature. The results of experiments were used to determine the dependence of a, kL, and kLa on the surface tension, the temperature of the absorption phase, and the superficial velocity of the gas. The calculated results from the correlation were found to be within 10% deviation from the actual experimental results. 展开更多
关键词 Mass transfer coefficient SURFACTANT Bubble column reactor Gas absorption
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Electrochemical study on adsorption behavior of surfactants at β-2CaO·SiO2/NaAlO2 interface 被引量:2
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作者 Hai-yan YU Bo WANG +2 位作者 Xiao-lin PAN Ting-ting DING Shi-wen BI 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2013年第8期2416-2421,共6页
β-2CaO'SiO2 was obtained with analytical grade reagents. Polyethylene glycol (PEG), sodium polyacrylate (PAAS) and their mixture were used to inhibit the decomposition of β-2CaO·SiO2 in sodium aluminate so... β-2CaO'SiO2 was obtained with analytical grade reagents. Polyethylene glycol (PEG), sodium polyacrylate (PAAS) and their mixture were used to inhibit the decomposition of β-2CaO·SiO2 in sodium aluminate solution. The potential of solid-liquid interface and the adsorption mechanism were studied by the methods of Zeta potential measurement and XPS. The results indicate that PEG and PAAS have synergistic effect on the inhibition of secondary reaction. The inhibitory effect is the best when the volume ratio of PAAS to PEG is 1:1 and the total concentration is 12.5 mg/L. PAAS adsorbs on the surface of β-2CaO-SiO2 by the formation of --COOCa coordinate bond, and the negative charge enters into Stem layer, which results in the decrease of particle potential and the obvious change of binding energy of Ca 2p, Si 2p and O Is. PEG only physically adsorbs on the surface ofβ-2CaO·SiO2, and had little effect on particle potential and binding energy of Ca 2p, Si 2p and O Is. 展开更多
关键词 sodium aluminate solution secondary reaction SURFACTANT (-potential interfacial adsorption electrochemicalperfon'nance
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Characteristics of Amine Surfactant Modified Peanut Shell and Its Sorption Property for Cr(VI) 被引量:7
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作者 岳敏 张猛 +4 位作者 刘斌 许醒 李小明 岳钦艳 马春元 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2013年第11期1260-1268,共9页
Modified peanut shell (MPS) was prepared by amination reaction with peanut shell (PS) as the starting material The sorption of Cr(VI) oxyanions on MPS in static and column tests were investigated. In addition, t... Modified peanut shell (MPS) was prepared by amination reaction with peanut shell (PS) as the starting material The sorption of Cr(VI) oxyanions on MPS in static and column tests were investigated. In addition, the sorption isotherm and kinetic models were applied to confirm the sorption capacity and the sorption mechanisms. BET surface area anysis showed the physicochemical characterist!cs of the samples. The results of zeta potential,Fourier transform infrared (FT-IR) and Raman spectra analysis illustrated that chemical adsorption and ion exi change are the potential sorption mechanism. The static sorption test showed that the maximum sorption capacity (qm) of MPS for Cr(VI) increased with temperature, which indicated that the Cr(VI) sorption rocess was endothermic. The saturated sorption capacity of Cr(VI) in the colunm sorption test was 138.34 mg.g-1, which accounted for 93.9% of the qmax at 25 ℃. The regeneration capacity of MPS was evaluated using HC1 solution as an eluent. The high regeneration efficiency (82.6%) validated the dominance of the ion exchange mechanism in the Cr(VI) sorption process with C1ions displacing Cr(VI) oxyanion on MPS. The Langmuir isotherm model showed a higher correlation coefficient than the other adsorption isotherm models. And in the kinetic study, a pseudo-second-order model fit the data best. 展开更多
关键词 modified peanut shell AMINATION Cr(VI) ADSORPTION MECHANISM
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Unsteady Motion of a Single Droplet in Surfactant Solutions 被引量:2
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作者 李晓锦 毛在砂 费维扬 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2003年第6期715-725,共11页
A numerical investigation of the unsteady motion of a deformed drop released freely in another quiescent liquid contaminated by surfactant is presented in this paper. The finite difference method was used to solve num... A numerical investigation of the unsteady motion of a deformed drop released freely in another quiescent liquid contaminated by surfactant is presented in this paper. The finite difference method was used to solve numerically the coupled time-dependent Navier-Stokes and convective-diffusion equations in a body-fitted orthogonal coordinate system. Numerical simulation was conducted on the experimental cases, in which MIBK drops with the size ranging from 1.24 mm to 1.97 mm rose and accelerated freely in pure water and in dilute sodium dodecyl sulphate (SDS) aqueous solution. The applicability of the numerical scheme was validated by the agreement between the simulation results and the experimental data. Both the numerical and experimental results showed that the velocitytime profile exhibited a maximum rising velocity for drops in SDS solutions, which was close to the terminal velocity in pure water, before it dropped down to a steady-state value. The effect of the sorption kinetics of surfactant on the accelerating motion was also evaluated. It is also suggested that introduction of virtual mass force into the formulation improved obviously the precision of numerical simulation of transient drop motion. 展开更多
关键词 SURFACTANT single drop unsteady motion sorption kinetics numerical simulation
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Photocatalytic Degradation of Diethyl Phthalate with Surfactant Addition
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作者 张天永 扈娟 +2 位作者 张友兰 李彬 费学宁 《Transactions of Tianjin University》 EI CAS 2006年第4期258-263,共6页
This paper studies the adsorption of diethyl phthalate (DEP,an environmental hormone) on the surface of nanoscale TiO2, effects of pH value of solutions, initial concentrations of DEP and additive surfactant on phot... This paper studies the adsorption of diethyl phthalate (DEP,an environmental hormone) on the surface of nanoscale TiO2, effects of pH value of solutions, initial concentrations of DEP and additive surfactant on photocatalytic degradation and dynamics of DEP. Under ultra violet illumination, the interaction between DEP and surfactants including DBS (sodium dodecylbenzenesulfonate), CTAB (cetyltrimethylammonium bromide), and OP-10 (nonylphenol polyoxyethylene ether) was exploited from the perspective of degradation speed calculated by the data of high pressure liquid chromatography (HPLC) and UV-Vis spectra, respectively. Photocatalytic degradation of DEP followed pseudo first-order reaction kinetics. DEP as substrate degraded fast when its initial concentration was 130 mg/L. TiO2 had certain adsorption ability of DEP. TiO2 could adsorb the most DEP at the approximately neutral pH of 6.91. Degradation of DEP was not affected obviously by additives OP-10 and DBS. Degradation rate of DEP was not enhanced greatly in the presence of surfactants, but degradation of DBS was sped up. Degradation rate of DEP was depressed in the presence of additive CTAB. The more CTAB was added, the less DEP was degraded. Degradation rate of CTAB became slow with the increase of initial CTAB concentration. The possible adsorption models among TiO2, DEP and surfactants were given. 展开更多
关键词 diethyl phthalate SURFACTANT ADSORPTION dynamics PHOTOCATALYSIS DEGRADATION
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State of Pepsin and Acidic Protease in Solid Phase System and the Factors Increasing Their Destabilization
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作者 H. T. Hasanov A. H. Boboev +1 位作者 A. H. Hasanov M. M. Rahimov 《Journal of Food Science and Engineering》 2011年第4期303-312,共10页
The adsorption state and catalytic properties of pepsin and acidic protease from microorganisms Asp. awamori and Asp. oryzae were studied in solid phase system (in presence of sorsilen, DEAE- and CM-cellulose). Acco... The adsorption state and catalytic properties of pepsin and acidic protease from microorganisms Asp. awamori and Asp. oryzae were studied in solid phase system (in presence of sorsilen, DEAE- and CM-cellulose). According to the results, adsorption capacity and catalytic activity of enzymes depend on the physical nature of surface groups of the solid phase. Changing the stability of enzymes in the system with solid phase is observed even the adsorption bond is less stable (in the case of DEAE- and CM-cellulose in acidic media). Injection to the medium ethanol, surfactants, sodium chloride and changing the temperature of the incubation medium could prevent the negative effects of the solid phases. When sorsilen is used as solid phase, pepsin and acidic protease from Asp. awamori suffer from high surface inactivation. Various surfactants influence adsorption state of enzymes differently. Non-ionic surfactants (Triton X-100) prevent adsorption and restore catalytic properties of enzymes. 展开更多
关键词 PEPSIN acid proteinase Asp. awamori Asp. oryzae sorsilen adsorption state inactivation regulation.
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Enhanced degradation of carbon tetrachloride by surfactant-modified zero-valent iron
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作者 MENG Ya-feng GUAN Bao-hong WU Zhong-biao WANG Da-hui 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2006年第9期702-707,共6页
Sorption of carbon tetrachloride (CT) by zero-valent iron (ZVI) is the rate-limiting step in the degradation of CT, so the sorption capacity of ZVl is of great importance. This experiment was aimed at enhancing th... Sorption of carbon tetrachloride (CT) by zero-valent iron (ZVI) is the rate-limiting step in the degradation of CT, so the sorption capacity of ZVl is of great importance. This experiment was aimed at enhancing the sorption of CT by ZVI and the degradation rate of CT by modification of surfactants. This study showed that ZVI modified by cationic surfactants has favorable synergistic effect on the degradation of CT. The CT degradation rate of ZVI modified by cetyl pyridinium bromide (CPB) was higher than that of the unmodified ZVI by 130%, and the CT degradation rate of ZVI modified by cetyl trimethyl ammonium bromide (CTAB) was higher than that of the unmodified ZVI by 81%. This study also showed that the best degradation effect is obtained at the near critical micelle concentrations (CMC) and that high loaded cationic surfactant does not have good synergistic effect on the degradation due to its hydrophilicity and the block in surface reduction sites. Furthermore degradation of CT by ZVI modified by nonionic surfactant has not positive effect on the degradation as the ionic surfactant and the ZVI modified by anionic surfactant has hardly any obvious effects on the degradation. 展开更多
关键词 Enhanced degradation SORPTION SURFACTANTS Synergistic effect Zero-valent iron (ZVI)
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