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Synthesis and characterization of castor oil-based polymeric surfactants

Xujuan HUANG,He LIU,Shibin SHANG,Zhaosheng CAI,Jie SONG,Zhanqian SONG

《农业科学与工程前沿（英文）》 2016年 第3卷 第1期   页码 46-54 doi: 10.15302/J-FASE-2016083

摘要： Dehydrated castor oil was epoxidized using phosphoric acid as a catalyst and acetic acid peroxide as an oxidant to produce epoxidized castor oil (ECO). Ring-opening polymerization with stannic chloride was used to produce polymerized ECO (PECO), and sodium hydroxide used to give hydrolyzed PECO (HPECO). The HPECO was characterized by Fourier transform infrared, H and C nuclear magnetic resonance spectroscopies, gel permeation chromatography, and differential scanning calorimetry. The weight-average molecular weight of soluble PECO and HPECO were 5026 and 2274 g·mol , respectively. PECO and HPECO exhibited glass transition. Through neutralizing the carboxylic acid of HPECO with different counterions, castor oil-based polymeric surfactants (HPECO-M, where M= Na , K or triethanolamine ion) exhibited high efficiency to reduce the surface tension of water. The critical micelle concentration (CMC) values of HPECO-M ranged from 0.042 to 0.098 g·L and the minimum equilibrium surface tensions at CMC ( ) of HPECO-M ranged from 25.6 to 30.0 mN·m . The water-hexadecane interfacial energy was calculated from measured surface tension using harmonic and geometric mean methods. Measured values of water-hexadecane interfacial tension agreed well with those calculated using the harmonic and geometric mean methods.

关键词： epoxidized vegetable oil     ring-opening polymerization     interfacial tension     polymeric surfactant    

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Influences of spinel type and polymeric surfactants on the size evolution of colloidal magnetic nanocrystals

Tahereh R. BASTAMI,Mohammad H. ENTEZARI,Chiwai KWONG,Shizhang QIAO

《化学科学与工程前沿（英文）》 2014年 第8卷 第3期   页码 378-385 doi: 10.1007/s11705-014-1441-y

摘要： Two types of polymeric surfactants, PEG and PVP , were used for the preparation of magnetic ferrite MFe O (M= Mn, Fe) colloidal nanocrystals using a solvothermal reaction method. The effect of spinel type effect on the size evolution of various nanoparticles was investigated. It was found that Fe O nanoparticles exhibited higher crystalinity and size evolution than MnFe O nanoparticles with use of the two surfactants. It is proposed that this observation is due to fewer tendencies of surfactants on the surface of Fe O building blocks nanoparticles than MnFe O . Less amounts of surfactant or capping agent on the surface of nanoparticles lead to the higher crystalibity and larger size. It is also suggested that the type of spinel (normal or inverted spinel) plays a key role on the affinity of the polymeric surfactant on the surface of building blocks.

关键词： spinel type     polymeric surfactant     size evolution     mangnetic ferrite nanoparticle    

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Biosorption of Cu(II) to extracellular polymeric substances (EPS) from

Xiangliang PAN, Jing LIU, Wenjuan SONG, Daoyong ZHANG

《环境科学与工程前沿（英文）》 2012年 第6卷 第4期   页码 493-497 doi: 10.1007/s11783-012-0416-9

摘要： Biosorption of extracellular polymeric substances (EPS) from sp. (cyanobacterium) with Cu(II) was investigated using fluorescence spectroscopy. Three fluorescence peaks were found in the excitation-emission matrix (EEM) fluorescence spectra of EPS. Fluorescence of peak A (Ex/Em= 275/452 nm) and peak C (Ex/Em= 350/452 nm) were originated from humic-like substances and fluorescence of peak B (Ex/Em= 275/338 nm) was attributed to protein-like substances. Fluorescence of peaks A, B, and C could be quenched by Cu(II). The effective quenching constants (lg K ) were 2.8–5.84 for peak A, 6.4–9.24 for peak B, and 3.48–6.68 for peak C, respectively. The values of lg K showed a decreasing trend with increasing temperature, indicating that the quenching processes were static in nature. The binding constants (lg K ) followed the order of peak A>peak B>peak C, implying that the humic-like substances in EPS have greater Cu(II) binding capacity than the protein-like substances. The binding site number, , in EPS-Cu(II) complexes for peaks A, B, and C was less than 1. This suggests the negative cooperativity between multiple binding sites and the presence of more than one Cu binding site.

关键词： biosorption     conditional binding constant     extracellular polymeric substances (EPS)     fluorescence quenching    

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Influence of extracellular polymeric substances from activated sludge on the aggregation kinetics of

《环境科学与工程前沿（英文）》 2022年 第16卷 第2期 doi: 10.1007/s11783-021-1450-2

摘要：

• The NPs aggregation in the electrolyte solution is consistent with the DLVO theory.

关键词： Silver nanoparticles     Silver sulfide nanoparticles     Extracellular polymeric substances     Aggregation kinetics     Influence mechanisms    

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Comparison of CNT-PVA membrane and commercial polymeric membranes in treatment of emulsified oily wastewater

Gang Yi, Xinfei Fan, Xie Quan, Shuo Chen, Hongtao Yu

《环境科学与工程前沿（英文）》 2019年 第13卷 第2期 doi: 10.1007/s11783-019-1103-x

摘要：

CNT-PVA membrane was fabricated and compared with polymeric membranes.

The separation performance was evaluated by homemade and cutting fluid emulsions.

The three membranes show similar oil retention rates.

CNT-PVA membranes have higher permeation fluxes compared with polymeric membranes.

CNT-PVA membrane shows higher fouling resistance.

关键词： Oily wastewater     Microfiltration     Carbon nanotube membrane     Commercial polymeric membrane    

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The construction of pseudo-Janus silica/surfactant assembly and their application to stabilize Pickering

《化学科学与工程前沿（英文）》 2022年 第16卷 第7期   页码 1101-1113 doi: 10.1007/s11705-021-2095-1

摘要： Nanoparticles with high surface energy and chemical activity have drawn substantial attention in petroleum industry. Recently, Janus nanoparticles exhibited tremendous potential in enhanced oil recovery (EOR) due to their asymmetric structures and properties. In this study, a series of amphiphilic pseudo-Janus@OTAB (PJ@C18) nanoparticles with different concentrations of stearyltrimethylammoium bromide (OTAB) were successfully fabricated. The structures and properties of PJ@C18 were characterized by Fourier transform infrared spectroscopy and ζ-potential measurements. Based on the emulsification experimental results, the interaction models and the self-assembly behavior between hydrophilic nanoparticles (SiO2@NH2) and OTAB molecules at the oil/water interface were proposed, which was further confirmed via the measurements of the contact angle and dynamic interfacial tension. Interestingly, it was found that the change of pH value from 7.5 to 4.0 caused the type reversal of the PJ@C18-1000 stabilized Pickering emulsions. Furthermore, the PJ@C18-1000 stabilized Pickering emulsion system with excellent salt and temperature tolerances (10000 mg∙L–1, 90 °C) significantly improved the oil recovery in the single-tube (more than 17%) and double-tube (more than 25%) sand pack model flooding tests. The findings of this study could help to better understand the construction mechanism of pseudo-Janus silica/surfactant assembly and the potential application of PJ@C18-1000 stabilized Pickering emulsions for EOR.

关键词： Janus nanoparticles     surfactant     double phase inversion     self-assembly     enhanced oil recovery    

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Progress in use of surfactant in nearly static conditions in natural gas hydrate formation

Zhen PAN, Yi WU, Liyan SHANG, Li ZHOU, Zhien ZHANG

《能源前沿（英文）》 2020年 第14卷 第3期   页码 463-481 doi: 10.1007/s11708-020-0675-2

摘要： Natural gas hydrate is an alternative energy source with a great potential for development. The addition of surfactants has been found to have practical implications on the acceleration of hydrate formation in the industrial sector. In this paper, the mechanisms of different surfactants that have been reported to promote hydrate formation are summarized. Besides, the factors influencing surfactant-promoted hydrate formation, including the type, concentration, and structure of the surfactant, are also described. Moreover, the effects of surfactants on the formation of hydrate in pure water, brine, porous media, and systems containing multiple surfactants are discussed. The synergistic or inhibitory effects of the combinations of these additives are also analyzed. Furthermore, the process of establishing kinetic and thermodynamic models to simulate the factors affecting the formation of hydrate in surfactant-containing solutions is illustrated and summarized.

关键词： gas hydrate     kinetic hydrate promoter     compounding     model     surfactant     mechanism    

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The prediction of adsorption isotherms of ester vapors on hypercrosslinked polymeric adsorbent

Liuyan WU,Lijuan JIA,Xiaohan LIU,Chao LONG

《环境科学与工程前沿（英文）》 2016年 第10卷 第3期   页码 482-490 doi: 10.1007/s11783-015-0826-6

摘要： Adsorption isotherms of methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate and ethyl propionate on hypercrosslinked polymeric resin (ND-100) were measured at 303K, 318K and 333K,respectively, and well fitted by Dubinin–Astakhov (DA) equation. The plots of the adsorbed volume ( ) versus the adsorption potential ( ) at three different temperatures all fell basically onto one single curve for every ester. A predicted model based on DA equation was obtained on the basis of adsorption equilibrium data of methyl acetate, ethyl acetate and ethyl propionate at 318K. The model equation successfully predicted the adsorption isotherms of methyl acetate, ethyl acetate and ethyl propionate on ND-100 at 303K, and 333K, and also gave accurate predictive results for adsorption isotherms of the other two ester compounds (propyl acetate and isopropyl acetate) on ND-100 at 303K, 318K and 333K. The results proved the effectiveness of DA model for predicting the adsorption isotherms of ester compounds onto ND-100. In addition, the relationship between physico-chemical properties of adsorbates and their adsorption properties was also investigated. The results showed that molecular weight, molar volume and molar polarizability had good linear correlations with the parameter (which represents adsorption characteristic energy) of DA equation.

关键词： hypercrosslinked polymeric adsorbent     adsorption isotherm     ester     prediction    

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Adsorption selectivity of salicylic acid and 5-sulfosalicylic acid onto hypercrosslinked polymeric adsorbents

LIU Fuqiang, CHEN Jinlong, LI Aimin, XIA Mingfang, FEI Zhenghao

《环境科学与工程前沿（英文）》 2007年 第1卷 第1期   页码 73-78 doi: 10.1007/s11783-007-0014-4

摘要： Both bottle-point and column-feeding experiments involving different solutes and sorbents were carried out to investigate the adsorption selectivity and separation performance of salicylic acid and 5-sulfosalicylic acid. Their adsorption isotherms onto such hypercrosslinked polymeric adsorbents as NDA-100 and NDA-99 could be well described by the Freundlich equations whose characteristics describe extrathermic and favorable adsorption processes. The adsorption towards NDA-100 mainly depended on the π-π interaction, while that towards NDA-99 was extremely influenced by the static-electric interaction. Additionally, the adsorptive capacity of salicylic acid on NDA-99 decreased while it increased on NDA-100 with the presence of 5-sulfosalicylic acid in the adsorptive environment as the competitive component. Comparatively, the adsorption capacity of 5-sulfosalicylic acid decreased on both resins with salicylic acid as the competitive component. In fact, the difference in the interaction between adsorbent and adsorbate resulted in the straight antagonism on the effective adsorption sites on the adsorbent. In conclusion, the adsorption selectivity of salicylic acid onto NDA-100 was obviously larger than that onto NDA-99 with the existence of 5-sulfosalicylic acid in the adsorptive environment. A satisfactory separation and recovery of tested solutes in aqueous phase could be foreseeably achieved by the sequencing adsorption technique involving NDA-100 as well as NDA-99.

关键词： 5-sulfosalicylic     bottle-point     hypercrosslinked polymeric     satisfactory separation     NDA-100    

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Stability of three-dimensional printable foam concrete as function of surfactant characteristics

《结构与土木工程前沿（英文）》   页码 935-947 doi: 10.1007/s11709-023-0964-z

摘要： Extrudability is one of the most critical factors when designing three-dimensional printable foam concrete. The extrusion process likely affects the foam stability which necessitates the investigation into surfactant properties particularly for concrete mixes with high foam contents. Although many studies have been conducted on traditional foam concrete in this context, studies on three-dimensional printed foam concrete are scarce. To address this research gap, the effects of surfactant characteristics on the stability, extrudability, and buildability of three-dimensional printed foam concrete mixes with two design densities (1000 and 1300 kg/m3) using two different surfactants and stabilizers (synthetic-based sodium lauryl sulfate stabilized with carboxymethyl cellulose sodium salt, and natural-based hingot surfactant stabilized with xanthan gum) were investigated in this study. Fresh density tests were conducted before and after the extrusion to determine stability of the foam concrete. The results were then correlated with surfactant qualities, such as viscosity and surface tension, to understand the importance of key parameters in three-dimensional printing of foam concrete. Based on the experimental results, surfactant solu1tion with viscosity exceeding 5 mPa·s and surface tension lower than 31 mN/m was recommended to yield stable three-dimensional printable foam concrete mixes. Nevertheless, the volume of foam in the mix significantly affected the printability characteristics. Unlike traditional foam concrete, the variation in the stabilizer concentration and density of concrete were found to have insignificant effect on the fresh-state-characteristics (slump, slump flow, and static yield stress) and air void microstructure of the stable mixes.

关键词： foam concrete     3D printable concrete     stability     rheology     air void microstructure    

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Adsorption of 1,3-propanediol from synthetic mixture using polymeric resin as adsorbents

W. LUERRUK, A. SHOTIPRUK, V. TANTAYAKOM, P. PRASITCHOKE, C. MUANGNAPOH

《化学科学与工程前沿（英文）》 2009年 第3卷 第1期   页码 52-57 doi: 10.1007/s11705-009-0087-7

摘要： The aim of this work was to separate 1,3-PDO from a synthetic mixture using polymeric resins, Amberlite XAD-7 and XAD-16 resins. The equilibrium adsorption of 1,3-PDO onto two polymeric resins were investigated in binary and tertiary systems. Experimental results of binary component adsorption equilibrium indicated that the adsorption capacity ( ) of 1,3-PDO at 160 g/L onto XAD-7 and XAD-16 was 835.96 and 584.61 mg 1,3-PDO/g dry resin, respectively. The adsorption isotherms were closely predicted by the Langmuir-Freundlich model among the two isotherm model tested. The value of n of 1,3-PDO adsorbed on XAD-7 are much higher than those on XAD-16. This result suggested that XAD-7 resin has a higher affinity for the 1,3-PDO adsorption than XAD-16 resin. Moreover, the value of adsorption capacity of 1,3-PDO in the binary and tertiary component were compared at the same conditions. In the tertiary system, although the selectivity of 1,3-PDO from XAD-7 was approximately six times higher than XAD-16, the adsorption capacity of 1,3-PDO at 160 g/L onto XAD-16 was higher than XAD-7. Interestingly, the reusability of XAD-7 and XAD-16 resins in the three cycle times shows a slight loss of adsorption capacity. Furthermore, the investigation about desorption by an ethanol/water mixture at 50% ( / ) indicated that the desorption yield of 1,3-PDO from XAD-7 was lower than XAD-16 resin for both the binary and tertiary component. This was due to the more favorable adsorption characteristics of XAD-7 resin than XAD-16 resin.

关键词： adsorption     1     3-propanediol     glycerol     polymeric resin     adsorption isotherm    

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Contributions of adsorption, bioreduction and desorption to uranium immobilization by extracellular polymeric

《环境科学与工程前沿（英文）》 2023年 第17卷 第9期 doi: 10.1007/s11783-023-1707-z

摘要：

● EPS immobilizes U(VI) via adsorption, bioreduction and desorption.

关键词： Adsorption     Bioreduction     Desorption     Kinetics     Isotherm     Uranium    

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Multiphase surfactant-assisted reaction-separation system in a microchannel reactor

Salah ALJBOUR, Tomohiko TAGAWA, Mohammad MATOUQ, Hiroshi YAMADA

《化学科学与工程前沿（英文）》 2009年 第3卷 第1期   页码 33-38 doi: 10.1007/s11705-009-0108-6

摘要： The Lewis acid-catalyzed addition of trimethylsilyl cyanide to -chlorobenzaldehyde in a microchannel reactor was investigated. The microchannel was integrated to promote both reaction and separation of the biphase system. FeF and Cu(triflate) were used as water-stable Lewis acid catalysts. Sodium dodecyl sulfate was incorporated in the organic-aqueous system to enhance the reactivity and to manipulate the multiphase flow inside the microchannel. It was found that the dynamics and the kinetics of the multiphase reaction were affected by the new micellar system. Parallel multiphase flow inside the microchannel was obtained, allowing for continuous and acceptable phase separation. Enhanced selectivity was achieved by operating at lower conversion values.

关键词： Lewis acid catalysis     multiphase reactions     process intensification     microchannel reactor     green engineering    

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Formation of microporous polymeric membranes via thermally induced phase separation: A review

Min Liu,Shenghui Liu,Zhenliang Xu,Yongming Wei,Hu Yang

《化学科学与工程前沿（英文）》 2016年 第10卷 第1期   页码 57-75 doi: 10.1007/s11705-016-1561-7

摘要： A review of recent research related to microporous polymeric membranes formed via thermally induced phase separation (TIPS) and the morphologies of these membranes is presented. A summary of polymers and suitable diluents that can be used to prepare these microporous membranes via TIPS are summarized. The effects of different kinds of polymer materials, diluent types, cooling conditions, extractants and additive agents on the morphology and performance of TIPS membranes are also discussed. Finally new developments in TIPS technology are summarized.

关键词： polymer     microporous membrane     thermally induced phase separation    

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Preparation and sedimentation behavior of conductive polymeric nanoparticles

WANG Jixiao, LIU Rui, ZHANG Xiaoyan, ZHOU Zhibin, WANG Zhi, WANG Shichang

《化学科学与工程前沿（英文）》 2008年 第2卷 第3期   页码 231-235 doi: 10.1007/s11705-008-0055-7

摘要： A facile route to prepare FeO/polypyrrole (PPY) core-shell magnetic nanoparticles was developed. FeO nanoparticles were first prepared by a chemical co-precipitation method, and then FeO/PPY core-shell magnetic composite nanoparticles were prepared by in-situ polymerization of pyrrole in the presence of FeO nanoparticles. The obtained nanoparticles were characterized by scanning electronic microscopy (SEM), transmission electronic microscopy (TEM) and laser particle size analyzer. The images indicate that the size of FeO particles is about 10 nanometers, and the particles are completely covered by PPY. The FeO/PPY core-shell magnetic composite nanoparticles are about 100 nanometers and there are several FeO particles in one composite nanoparticle. The yield of the composite nanoparticles was about 50%. The sedimentation behavior of FeO/PPY core-shell magnetic nanoparticles in electrolyte and soluble polymer solutions was characterized. The experimental results indicate that the sedimentation of particles can be controlled by adjusting electrolyte concentration, solvable polymers and by applying a foreign field. This result is useful in preparing gradient materials and improving the stability of suspensions.
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标题 作者 时间 类型 操作

Synthesis and characterization of castor oil-based polymeric surfactants

Xujuan HUANG,He LIU,Shibin SHANG,Zhaosheng CAI,Jie SONG,Zhanqian SONG

期刊论文

Influences of spinel type and polymeric surfactants on the size evolution of colloidal magnetic nanocrystals

Tahereh R. BASTAMI,Mohammad H. ENTEZARI,Chiwai KWONG,Shizhang QIAO

期刊论文

Biosorption of Cu(II) to extracellular polymeric substances (EPS) from

Xiangliang PAN, Jing LIU, Wenjuan SONG, Daoyong ZHANG

期刊论文

Influence of extracellular polymeric substances from activated sludge on the aggregation kinetics of

期刊论文

Comparison of CNT-PVA membrane and commercial polymeric membranes in treatment of emulsified oily wastewater

Gang Yi, Xinfei Fan, Xie Quan, Shuo Chen, Hongtao Yu

期刊论文

The construction of pseudo-Janus silica/surfactant assembly and their application to stabilize Pickering

期刊论文

Progress in use of surfactant in nearly static conditions in natural gas hydrate formation

Zhen PAN, Yi WU, Liyan SHANG, Li ZHOU, Zhien ZHANG

期刊论文

The prediction of adsorption isotherms of ester vapors on hypercrosslinked polymeric adsorbent

Liuyan WU,Lijuan JIA,Xiaohan LIU,Chao LONG

期刊论文

Adsorption selectivity of salicylic acid and 5-sulfosalicylic acid onto hypercrosslinked polymeric adsorbents

LIU Fuqiang, CHEN Jinlong, LI Aimin, XIA Mingfang, FEI Zhenghao

期刊论文

Stability of three-dimensional printable foam concrete as function of surfactant characteristics

期刊论文

Adsorption of 1,3-propanediol from synthetic mixture using polymeric resin as adsorbents

W. LUERRUK, A. SHOTIPRUK, V. TANTAYAKOM, P. PRASITCHOKE, C. MUANGNAPOH

期刊论文

Contributions of adsorption, bioreduction and desorption to uranium immobilization by extracellular polymeric

期刊论文

Multiphase surfactant-assisted reaction-separation system in a microchannel reactor

Salah ALJBOUR, Tomohiko TAGAWA, Mohammad MATOUQ, Hiroshi YAMADA

期刊论文

Formation of microporous polymeric membranes via thermally induced phase separation: A review

Min Liu,Shenghui Liu,Zhenliang Xu,Yongming Wei,Hu Yang

期刊论文

Preparation and sedimentation behavior of conductive polymeric nanoparticles

WANG Jixiao, LIU Rui, ZHANG Xiaoyan, ZHOU Zhibin, WANG Zhi, WANG Shichang

期刊论文