MACROMOLECULES
·
2015
·
IF 5.8
Zefeng Song,Ke Wang,Chengqiang Gao,Shuang Wang,Wangqing Zhang
A new multi-stimuli-responsive homopolymer of poly[N-[2-(diethylamino)ethyl]acrylamide] (PDEAEAM), which combines the thermoresponsive and pH/CO2-responsive moieties of the diethylamino and acrylamide groups, was proposed and synthesized by RAFT polymerization. Well-defined PDEAEAM was synthesized by solution RAFT polymerization as indicated by the linear increase in the polymer molecular weight with the monomer conversion and the narrow molecular weight distribution. The appending diethylamino group in the polymer backbone was found to be crucial to determine the thermoresponse of PDEAEAM in water. The parameters including the polymerization degree, the polymer concentration, the deuterated solvent, the terminal attached on the polymer backbone, the additives of salt and urea, and pH and bubbling CO2 affecting the thermoresponse of PDEAEAM in aqueous solution at the lower critical solution temperature (LCST) were investigated. The temperature-variable 1H NMR analysis suggests that the dehydration of PDEAEAM at temperature above LCST is ascribed to the weakened hydrogen bonding between the CONHCH2 and/or (CH2N(CH2CH3)2) moieties with the solvent of water. The proposed multi-stimuli-responsive homopolymer of PDEAEAM has two advantages of (1) the convenient and controllable RAFT synthesis and (2) the pH/CO2 tunable LCST at ∼36 °C being very close to body temperature.
研究领域:
高分子化学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Nano Materials
·
2024
·
IF 5.3
Hairong Wu,Kunpeng Hou,Guorui Xu,Genglin Li,Jiawei Chang,Tianfang Luan,Wenhao Shao,Jirui Hou
The CO2-responsive Pickering emulsions employed have garnered considerable attention across enhanced oil recovery agents, delivery of crude, and oilfield-produced fluid treatment. This study focuses on the design of an innovative type of Janus nanoparticle (JNP) and its application in the construction of CO2 stimuli-responsive Pickering emulsions. The emulsion stabilized by JNPs demonstrates swift phase separation subsequent to the injection of CO2. Furthermore, the mechanism of the CO2-stimulated responsiveness enabled by the JNPs was proposed. Based on the Schiff reaction, the synthesis of JNPs was achieved successfully via the Pickering emulsion template method. The properties of the JNPs were studied using various analytical techniques such as Fourier transform infrared, thermogravimetric analysis, scanning electron microscopy, transmission electron microscopy, etc. The developed responsive system, composed of JNPs and sodium oleate surfactant, showed high interfacial activity at the oil/water interface. The study revealed that the responsive system-stabilized Pickering emulsions could remain stable at 70 °C and room temperature for 24 and 120 h, respectively. Furthermore, the introduction of CO2 for 1.5 min resulted in phase separation because the nanoparticles lost the amphiphilic nature, triggering a significant decrease in interfacial activity and the protonation of sodium oleate surfactant inactivation. Then, the particles started to desorb from the interface. This study proposes a convenient, simple, and cost-effective approach for preparing fast CO2-responsive Pickering emulsions. It provides novel insights into the advancement of oilfield-produced fluid treatment, transportation of crude oil, and enhanced oil recovery.
研究领域:
化学工程
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材料科学
·
石油工程
✓ 已验证
产品关联
DOI
高影响因子
LANGMUIR
·
2024
·
IF 3.7
Zhuoxue Li,Yunlei Shi,Yimian Ding,Dazhen Xiong,Zhiyong Li,Huiyong Wang,Jikuan Qiu,Xiaopeng Xuan,Jianji Wang
A Pickering emulsion is a natural microreactor for interfacial catalysis in which an emulsifier is critical. Recently, a metal–organic framework (MOF) has attracted attention to emulsify water–organic mixtures for constructing a Pickering emulsion. However, a few stimuli-responsive Pickering emulsions based on MOFs have been reported, and the MOF emulsifiers cannot be regenerated at room temperature. Herein, the Zr-MOF with a rodlike morphology is synthesized using ionic liquid as a modulator and then modified with n-(trimethoxysilylpropyl)imidazole (C3im) to prepare a series of functionalized Zr-MOFs (MOF-C3im). It is found that MOF-C3im is an excellent emulsifier to construct stable and CO2-responsive Pickering emulsions even at low content (>0.20 wt %). Notably, the emulsification and demulsification of the emulsions can be easily and reversibly switched by bubbling of CO2 and N2 alternatively at room temperature because CO2 and imidazole molecules anchored on the Zr-MOF underwent a reversible acid–base reaction, resulting in an obvious change in the wettability of the emulsifier. As a proof of concept, the reduction reactions of nitrobenzene have been successfully carried out in these Pickering emulsions, demonstrating the efficient integration as a microreactor for chemical reaction, product separation, and emulsifier recycling under ambient conditions. This strategy provides an innovative option to develop stimulus-responsive Pickering emulsions for sustainable chemical processes.
研究领域:
材料科学
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化学工程
·
催化反应
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Nanoscale
·
2015
·Vol. 8
·期 2
·1140-1146
·
IF 7.394
Chunmei Gao,Shaoyu Lü,Mingzhu Liu,Can Wu,Yun Xiong
The synthesis and properties of CO2 responsive and fluorescent dendritic polymers, poly(amido amine)/Pluronic F127 (PAMAM/F127), are reported in this paper. The morphologies and sizes of PAMAM/F127 dendritic polymers were investigated by dynamic light scattering (DLS) and transmission electron microscopy (TEM). PAMAM/F127 dendritic polymers showed unimolecular micelle morphologies at low concentrations, and changed to multimolecular micelles at higher concentrations. Additionally, fluorescence spectra and confocal laser scanning microscopy images showed that PAMAM/F127 dendritic polymers exhibited a fluorescent enhancement response to the presence of CO2. Apart from that, the release behavior of PAMAM/F127 gels under simulated body fluids was investigated by choosing curcumin as the hydrophobic drug. The results indicated that PAMAM/F127 dendritic polymers can be used to improve the solubility of curcumin, and the drug released faster in the presence of CO2. Such CO2 responsive fluorescent dendritic polymers are potentially applicable in cellular imaging or drug controlled release.
研究领域:
材料科学
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生物医学工程
·
药学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2019
·Vol. 136
·期 18
·47439
·
IF 2.188
Shanshan Guo,Yangbufan Lv,Yangwei Chen,Shaojun Cai
Global decrease in crude oil resources and frequent crude oil leaks cause the energy crisis and ecological pollution. The absorption and release of leaked crude oil through absorption materials are a necessary process for environmental protection and recycling. In this article, a CO 2 -responsive olefin copolymer was obtained by copolymerization of styrene and an amine-containing olefin monomer. The structure of resultant copolymer was characterized by FTIR; thermal properties and CO 2 -responsive morphology changes were determined by DSC/TGA and SEM, respectively. Copolymers had certain absorption capacity for toluene with absorption rate up to 180.0%. The absorbed toluene could be released upon CO 2 stimulation with desorption rate up to 84.6%. The CO 2 -responsive copolymer could be regenerated through a simple heating process and showed stable absorption–desorption performance even after being recycled for 4 times. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 47439.
研究领域:
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2021
·
IF 6.707
Xiaohan Yang,Hanbin Liu,Liwei Qian,Qingjun Meng,Haiwei Wu,Zhijian Li,Hongwei Zhou
The remediation of water that polluted by organic dyes and nanoparticles (NPs) remains a great challenge. However, second pollution of solid waste may produce if the adsorbents are not degradable or recyclable. The stimuli-responsive materials were regarded to be able to resolve this problem by reversible adsorption-desorption under stimuli. Here in this work, the surface of cellulose fibers was modified with CO 2 -responsive molecules through a simple esterification followed by an aza-Michael addition reaction. The chemical structure was confirmed with Fourier transform infrared spectra (FT-IR), X-ray photoelectron spectroscopy (XPS), x-ray diffractometer (XRD) and thermal analysis. The gas-responsiveness was demonstrated by monitoring of the pH, conductivity and surface zeta potential. Anionic dyes and negative charged NPs in water can be selectively and reversibly captured by the CO 2 -responsive surface on cellulose fibers, suggesting the inexpensive, readily available and smart cellulose fibers may find great potential in water remediation.
研究领域:
材料科学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2025
·
IF 8.5
Zhonghai Tang,Yunlan Chen,Changyong Cai,Shaoping Ma,Zhijian Tan
The extraction of Rosa roxburghii polysaccharides using conventional methods suffers from low extraction efficiency and poor selectivity. Recently, green and efficient methods of polysaccharide extraction have received increasing attention. In this study, a CO 2 -responsive ionic liquid (IL) was developed for the extraction of Rosa roxburghii polysaccharides. This IL can achieve efficient extraction, and can be recycled, and reused in the extraction process. The maximum polysaccharide extraction yield of the IL was 253 mg/g under optimal single-factor experiment conditions. Three fractionated polysaccharides, RTFP-1, RTFP-2, and RTFP-3, were obtained by further purification, and their preliminary structures were characterized. RTFP-2 and RTFP-3 showed higher antioxidant and hypoglycemic activities than RTFP-1. This IL maintains high extraction efficiency after 5 cycles and reuse. This extraction method based on a CO 2 -responsive IL provides an efficient and sustainable method for polysaccharide extraction.
研究领域:
植物学
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生物化学
·
绿色化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ENERGY & FUELS
·
2024
·
IF 5.2
Yue Gu,Hongjun Tu,Ming Zhou
In this paper, a biobased ternary composite microgel (CS-DP-AA) was designed and prepared, which was based on chitosan and had a reversible response to CO2. The synthesis of CS-DP-AA microgel was proved by infrared spectroscopy, chromatography–mass spectrometry, X-ray photoelectron spectroscopy, and Raman spectroscopy. The structure and properties of CS-DP-AA microgel before and after CO2 response were characterized by scanning electron microscope, transmission electron microscope, ultraviolet visible spectrophotometer, laser particle size analyzer, zeta potentiometer, and other instruments, and the CO2 response mechanism was explored. The results show that CS-DP-AA microgel had great CO2 response performance and stability, and the UV transmittance could still reach 90.01% (relative) at 268.98 h after CO2 response. Subsequently, the rheological properties of CS-DP-AA microgel were evaluated by a rotary rheometer, which shows that CS-DP-AA microgel after the CO2 response had obvious viscoelasticity. Although shear thinning appeared with the increase in shear rate, the CS-DP-AA microgel after the CO2 response still had good viscosity under high temperature, high pressure, and high shear rate, which proves that it had great rheological properties. On the other hand, the ability of CS-DP-AA microgel to plug gas channeling in reservoirs was evaluated by a dual-core parallel-core physical simulation experimental device. The results show that the CS-DP-AA microgel injected into the core can indeed react with the CO2 adsorbed in the pores of the porous core and plug the larger pores. After the response, the resistance coefficient of the system increased significantly, reaching 80 times that of the previous value. It has been shown that CS-DP-AA microgel can indeed block gas channeling in oil reservoirs, expand the sweep efficiency and swept volume of the CO2 gas drive, contribute to the recovery rate of oil reservoirs, and ensure the smooth development of oil reservoirs, which has a good application prospect in plugging gas channeling in oil reservoirs.
研究领域:
材料科学
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石油工程
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY
·
2021
·
IF 2.262
Yi Zhao,Yangchuan Ke,Xu Hu,Fangfang Peng,Chengcheng Yu,Liang Xing
A new kind of CO2 responsive polymeric surfactant (named DEA-SSS) was synthesized by using 2-(diethylamino)ethyl methacrylate (DEA) and sodium styrene sulfonate (SSS) via radical polymerization. The structure and composition of the copolymer were characterized by FT-IR spectrometer, 1HNMR, and elemental analyzer. It was found that the surface and interfacial tension would be much reduced by adding the synthesized surfactant at low concentration. The amphiphilic copolymer could be dispersed in water after bubbling CO2 and precipitated out upon N2 injection. The variation of copolymer solution with and without CO2 adding was also characterized by electric conductivity meter and transmission electron microscopy (TEM). Pickering emulsion of liquid paraffin in water was prepared using the copolymer as the sole emulsifier with high speed stirring. It was demulsified after purging with CO2 and emulsified again by removal of CO2. The nano-emulsion was made using method of phase inversion composition at elevated temperature through mixing the surfactant with Brij30. When the CO2/N2 were bubbled circularly, the size distribution of nano-emulsions would change reversibly.
研究领域:
材料科学
·
化学工程
·
界面化学
✓ 已验证
产品关联
DOI
高影响因子
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
·
2018
·Vol. 20
·期 16
·11285-11295
·
IF 3.906
Shanshan Dai,Yuxin Suo,Dongfang Liu,Peiyao Zhu,Jihe Zhao,Jiang Tan,Hongsheng Lu
A series of CO2-responsive oil-in-water (O/W) emulsions were prepared by introducing hydrophobic tertiary amines (TAs) with varying alkane carbon numbers (ACNs) into the emulsion stabilized by sodium dodecyl benzene sulfonate (SDBS). TAs are converted to bicarbonate salts upon bubbling of CO2, which can form ion pairs with SDBS via electrostatic interaction, and then disrupt the stability of the emulsion. The reversible switch can be triggered by the removal of CO2. The ACN of TA, the concentration of SDBS/TA, the bubbling time of CO2, and the number of cycles are taken into account in order to study the controllable mechanism of these CO2-responsive emulsions. Because of the improved miscibility with oil, the ion pairs with TAs of larger ACNs can much more easily adhere to the oil phase, and then speed up the rupture rate of the oil droplets. The corresponding demulsification process is tracked by studying the interfacial tension, the zeta potential of the droplets, and microscope snapshots of all the systems. The UV-vis spectrophotometer analysis of the water phase and the 1H-nuclear magnetic resonance (1H NMR) test are further designed to comprehend the significance of ACNs and the solubility product of the formed ion pairs.
研究领域:
化学工程
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材料科学
·
界面化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
EUROPEAN POLYMER JOURNAL
·
2021
·
IF 4.598
Zhanfeng He,Qiang Chen,Yuanyuan Luo,Yuan He,Yinshan Zhang,Tong Liu,Wenyuan Xu,Jiali Zhang,Yongxin Liu,Leyan Xiong,Shaohui Wang,Zanru Guo
Adsorbent with high and recyclable adsorption for pollutants without secondary pollution is one of great potential in water treatment. Here, degradable CO 2 -responsive microgels with big size and wrinkled porous structure were prepared. The microgels underwent reversible volume phase changes upon alternative stimulus of CO 2 and N 2 , and thereby exhibited a switchable, selective, and recyclable adsorption for anionic dyes and metalloids (Cr(VI) and As(V)). The adsorption performance was improved due to the wrinkled porous structure, and the maximum adsorption capacity was up to 1537 mg g −1 for metanil yellow (MY). The competitive adsorption in binary and ternary system revealed that the affinity was in the order of MY > ponceau S (PS) > Cr(VI). Besides, the adsorbates could be desorbed by heating or treating with solution of pH 12. Microgels regenerated with CO 2 trigger exhibited high adsorption ability after ten consecutive recycling trials, and could be applied to fixed-bed adsorption/desorption system. Moreover, microgels could be degraded. Thus, this kind of degradable microgels have potential applications in the treatment of complex industrial wastewaters and avoid the additional pollution caused by the accumulation of waste adsorbents.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY
·
2023
·
IF 2.2
Azizullah Shaikh,Caili Dai,Yongpeng Sun,Varel Foutou,Mingwei Zhao,Qing You,Guang Zhao,Xin Sun,Xingxing Ding,Allah Bakhsh,Jiawei Liu
In recent years, a polymer-free fracturing fluid is under research to minimize the conductivity damage in formation and fracture during and after fracturing. Through extensive experiments, we prepared CO2-sensitive wormlike micelles (WLMs) based fracturing fluid system using anionic surfactant NaOA (Sodium Oleate-C18H33NaO2) and TMTAD (2,6,10-trimethyl-2,6,10-triazaundecane-C11H27N3). Rheological results from viscosity variation with steady shear rate using CO2/pH/time-response after CO2 bubbling confirm that the 3NaOA-TMTAD (3:1) was found as the best one in the properties of WLMs structure and the intermolecular interactions when comparing to 1NaOA-TMTAD and 2NaOA-TMTAD. Further, the surface tension after CO2 bubbling shows a good capability to decrease about 27.01 mN·m−1 at a CMC of 0.543 mM. The cryo-TEM test justifies the occurrence of spherical and WLMs in the fluid, before and after CO2 injection. The fluid system presents an outstanding sand suspension and gel breaking property, which are the positive features during the fracturing and flow back period; respectively. Good response with the alternative changes in CO2 pressures possesses an effective influence on shear viscosity using different temperatures (25 and 85 °C) and shear rates (20, 170, and 200 s−1). Also, the results of a linear relationship and low filtration coefficients verify that the fluid system has good filtration property. Such an easy and environmentally benign fluid system may be involved as a potential candidate in fracturing in unconventional hydrocarbon reservoirs, to reduce the formation damage which is usually very common in the polymer-based fracturing fluid.
研究领域:
石油工程
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材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）