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JOURNAL OF MOLECULAR LIQUIDS · 2016 · IF 2.74

Enhanced methane hydrate formation with SDS-coated Fe3O4 nanoparticles as promoters

Guo-Qiang Liu,Fei Wang,Sheng-Jun Luo,Dong-Yan Xu,Rong-Bo Guo

Nano metal fluids have been applied to promote the formation of natural gas hydrates . In this work, the sol of SDS@Fe 3 O 4 (named as SDS@Fe 3 O 4 ) were prepared and used as promoters in methane hydrate formation. Compared with SDS , SDS@Fe 3 O 4 produced much better promotion and the main superiority was that SDS@Fe 3 O 4 could significantly shorten the induction periods of hydrate formation. When SDS was used, the induction periods lasted about 40–60   min, while when SDS@Fe 3 O 4 was used at the same concentrations, hydrates nucleated within 10   min, especially, even no obvious induction periods were observed when SDS@Fe 3 O 4 was used in some experiments. Particle size showed significant influences on the promotion of SDS@Fe 3 O 4 to methane hydrate formation and smaller particles resulted in rapider hydrate formation. In addition, SDS@Fe 3 O 4 showed excellent repeatability during the hydrate formation-dissociation cycles.

研究领域: 化学工程 · 材料科学
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CHEMICAL ENGINEERING SCIENCE · 2023 · IF 4.7

SDS-promoted methane hydrate growth in presence of a superhydrophobic substrate

Xiaolai Zhang,Jiatao Zhao,Chen Chen,Haoyu Yuan,Yonghao Zhang,Yan He,Fei Wang

As one of the most efficient promoters for methane hydrate formation, SDS (sodium dodecyl sulfate) works mainly by causing the hydrates to grow upwards along the reactor sidewall. In this work, super-hydrophobic surface was constructed and adopted for methane hydrate formation, in the aim of revealing the promotion mechanism of SDS. Morphological observations showed that SDS led to violent fluctuation at the gas/liquid interface, which represented the unstable state of the gas/liquid interface during the initial hydrate growth process and reached stable via morphology transformation, either upward growth or outward diffusion, leading to the surface growth of methane hydrates. In-situ Raman Spectra revealed that the fluctuation structure was the combination of water, hydrate mass with cages minorly occupied by methane molecules, and methane hydrates; and with the continuation of the fluctuation phenomenon, the water percentage decreased, the hydrate mass increased and then transformed to methane hydrates gradually.

研究领域: 化学工程 · 材料科学
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CORROSION SCIENCE · 2022 · IF 7.72

Microstructure and corrosion behavior of PEO-LDHs-SDS superhydrophobic composite film on magnesium alloy

Haiyang Wang,Yulai Song,Xuegang Chen,Guodong Tong,Linyang Zhang

The MgAl-LDHs film was in situ grown on the PEO film of magnesium alloy by hydrothermal growth method, and the PEO-LDHs-SDS composite film modified by sodium dodecyl sulfate (SDS) was further prepared. The results show that compared with the single-layer PEO film, the PEO-LDHs-SDS composite film exhibits excellent short-term and long-term protection performance, which can be attributed to the blocking effect of the superhydrophobic surface of the composite film, the sealing effect of LDHs on the micropores of the PEO film, and the readsorption and corrosion inhibition of SDS anions.

研究领域: 材料科学 · 腐蚀工程 · 表面工程
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Selective ammonia recovery from wastewater by SDS-AC based microfiltration membrane flow electrode capacitor deionization

Chengsi Hou,Shuai Peng,Zhengwei Zhou,Longqian Xu,Yue Wang,Jianfeng Zhu,Pan Zhang,Zuofeng Chen,Zhendong Lei,Deli Wu

Flow Electrode Capacitance Deionization (FCDI) has been frequently used for NH 4 + recovery from wastewater as a low-energy, high-efficiency electrochemical technique. However, issues such as high cost (mainly due to the use of ion-exchange membranes) and weak selectivity have limited the expansion of their applications. In this study, SDS-AC was prepared and applied in microfiltration membrane FCDI (MFFCDI) to recover ammonia (NH 4 + ). The material characterization results showed that the surfactant was stably loaded on the AC surface, and the adsorption capacity of modified AC for NH 4 + was greatly enhanced. During the recovery process, NH 4 + migrated to the electrode chamber and immobilized on the SDS-AC, while Na + migrated to the electrode chamber and then released to the desalination chamber due to co-ion repulsion. Based on this principle, selective recovery of NH 4 + was achieved (selectivity = 3.51). At the end of the recovery, more than 70 % of the NH 4 + was immobilized on the SDS-AC and the NH 4 + could be desorbed with NaOH. The results of the recycling experiments showed good stability of the SDS-AC-based MFFCDI system, and the recovery of food waste fermentation liquor demonstrated that the system could realize the selective recovery of NH 4 + from complex feed water. In summary, the SDS-AC-based MFFCDI technology has great potential for the application of NH 4 + recovery from wastewater. Although the scale of this study was limited to the laboratory stage, it still shows potential for application in engineering. In the future, larger scale applications in engineering will be carried out and the environmental and economic benefits of the technology will be assessed through a full life cycle analysis.

CAS / MDL: 12125-02-9 7647-14-5
研究领域: 环境科学 · 电化学工程
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ACS Omega · 2023 · IF 4.1

Synthesis of Calcium Carbonate Hollow Microspheres and the Pelletization Mechanism by Electrostatic Attraction of PEG–SDS

Lei Wang,Zeen Yv,Licheng Ma,Qi Zheng,Tong Wang,Xiaokui Che,Xinglan Cui,Hongxia Li,Shenyv Wei,Xinyue Shi

Calcium carbonate is a common natural mineral with a wide range of applications. In this study, hollow calcite microspheres were successfully synthesized by using calcium chloride and sodium carbonate as raw materials in an SDS–PEG system. The results suggested that the appropriate concentration of SDS is necessary during the spherical crystallization of calcium carbonate. It was found that the crystals started to aggregate under the effect of SDS, and aggregation was enhanced with an increase in SDS concentration, leading to the transformation from hollow to solid microspheres. However, high temperatures will lead to the transformation from calcite to aragonite, resulting in the collapse of the formed spherical structure. Infrared spectroscopy and conductivity analysis suggested that when the concentration of SDS reached 0.3 g/L in the PEG–SDS system, SDS and PEG formed a spherical supramolecular structure. This structure could act as a template, leading to the aggregation of calcite through electrostatic attraction and finally to the formation of a hollow spherical structure.

CAS / MDL: 25322-68-3
研究领域: 材料科学 · 化学工程
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Materials Research Express · 2020 ·Vol. 7 ·期 8 ·085005 · IF 1.929

Effect of surfactant SDS on the morphology and photocatalytic performance of Zn2GeO4 nanorods

Jun Li,Xuemei Diao,Yumin Xiao,Lizhao Qin,Hua Lin,Qing Li,Bin Liao

The continuous discharge of organic dye effluents from textile industries causes severe global water pollution. A sustainable and effective route needs to be developed for the treatment of textile effluent in order to enable environmental protection and water recycling. In particular, the nanomaterials-based photocatalytic degradation of organic compounds is a promising approach to minimize water pollution. Herein, a facile hydrothermal method was reported for the preparation of Zn2GeO4 nanorods (NDs) with unique size, shape, and surface chemistry using sodium lauryl sulfate (SDS) as the surfactant. The crystal structure, size, and shape of the synthesized NDs were characterized by x-ray diffraction pattern (XRD) and field-emission scanning electron microscopy (FESEM). Initially, the XRD pattern revealed that SDS plays a crucial role in the formation of highly pure Zn2GeO4 NDs with rhombohedral crystalline nature. It was clearly noticed that increasing SDS concentration results in the formation of Zn2GeO4 NDs with decreased size ranges (100 nm). Conversely, the size of Zn2GeO4 NDs increased at higher SDS concentrations. The photocatalytic activity of Zn2GeO4 NDs was evaluated by the degradation of methyl orange (MO) in aqueous solution. Under light irradiation, the Zn2GeO4 NDs prepared by using different concentrations of SDS exhibited varied photocatalytic performance. Among the tested samples, Zn2GeO4 NDs prepared with 0.1 g of SDS showed the best photocatalytic activity with a MO decomposition rate of 94.6% within 60 min. This study suggests that SDS can be used to modulate the morphology and photocatalytic performance of Zn2GeO4 NDs, and the resultant Zn2GeO4 NDs can serve as a photocatalyst in wastewater treatment.

研究领域: 材料科学 · 环境科学
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Recyclable and high-efficiency methane hydrate formation promoter based on SDS-coated superparamagnetic nano-Fe3O4

Chen Chen,Haoyu Yuan,Xiaoming Wang,Yan Lin,Yan He,Fei Wang

Gas hydrate has been proposed as an effective medium for gas separation, desalination, gas storage and so on, yet the low reaction rate has been hindering the industrialization of hydrate-based technology . Hence various kinds of promoters, especially nano particles , have been introduced and investigated to increase the rate of hydrate formation. However, the recyclability of these promoters has not been given sufficient attention from an environmental friendly and economic point of view. In this study, a recyclable magnetic Fe 3 O 4 nanoparticle coated with SDS (SDS-coated Fe 3 O 4 ) was synthesized and successfully used for hydrate formation promotion as well as cycle experiments. The results showed that SDS-coated Fe 3 O 4 exhibited more efficient promotion for hydrate formation than bare Fe 3 O 4 in the studied concentration range. Especially, the induction time and reaction time can be significantly reduced to 77.6 ± 24.1 and 36 ± 3 min, respectively, and the methane storage capacity can be maintained up to 130 ± 5.9 v/v with the concentration of 20 g/L SDS-coated Fe 3 O 4 . Further comparison of bare Fe 3 O 4 and SDS-coated Fe 3 O 4 during cycle experiments showed that after 5 cycles, the methane storage capacity and reaction time in presence of SDS-coated Fe 3 O 4 can still be maintained as 119.5 ± 8 v/v and 110 ± 10 min, which were even better than the performance of bare Fe 3 O 4 just after two cycles. To sum up, SDS-coated Fe 3 O 4 can be recycled and reused many times for the hydrate formation, indicating that the SDS-coated Fe 3 O 4 has a potential to increase the recyclability and its economy for promoters in the hydrate-based technology.

研究领域: 化学工程 · 环境科学 · 材料科学
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Polymers · 2025 ·Vol. 17 ·期 7 ·994 · IF 4.9

One-Step Synergistic SDS-H2O2 Process for High-Purity Chitin Extraction from Fly Larvae

Yuhuan Qiu,Zhongtao Zhao,Feng Hu,Mengyi Liu,Xiaowen Shi

This study develops an efficient method for chitin extraction from fly larvae using a synergistic sodium dodecyl sulfate (SDS)-hydrogen peroxide (H2O2) system. Through a three-factor orthogonal experimental design, the optimal conditions were determined as 7% H2O2, 80 °C, and 15% SDS, achieving 97.93% deproteinization and 95.66% lipid removal efficiencies. Comparative analyses revealed that the SDS-H2O2system outperformed traditional alkaline and deep eutectic solvent treatments in both purification performance and structural preservation. Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) confirmed the high purity and crystallinity of the extracted chitin. Chitin prepared by this method demonstrated good Pb2+adsorption (99.91%), highlighting its potential for targeted heavy metal remediation.

CAS / MDL: 304-59-6
研究领域: 生物化学 · 环境科学
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CHEMICAL PHYSICS LETTERS · 2022 · IF 2.719

Foam optimization evaluation for enhanced oil recovery based on hydrophilic SiO2/SDS dispersions

Hui Xu,Yan Chen,Nannan Liu,Xinglong Chen,Dan Wu,Binshan Ju,Minglu Shao

The foam instability is still a question to enhance oil recovery. In this work, the modification process of the SiO 2 nanoparticles by kH-570 was described and the models of SDS and SiO 2 nanoparticles at the gas–liquid interface established were aimed to verify the mechanism of SiO 2 nanoparticles on foam stability. The results showed that the foam performance of the hydrophilic SiO 2 /SDS dispersion was better than that of SiO 2 /SDS dispersion depending on desorption energy and maximum capillary pressure of SiO 2 nanoparticles at the gas–liquid interface.   Finally, the oil recovery (45.25%) by using hydrophilic SiO 2 /SDS dispersion at 2.0% modified SiO 2  + 0.4% SDS.

研究领域: 石油工程 · 材料科学
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JOURNAL OF MOLECULAR LIQUIDS · 2024 · IF 5.3

Influence of IDS and SDS compound ratio on pore structure and wettability of bituminous coal and anthracite: Experimental and simulation discussion

Xiao-Han Wang,Bingyou Jiang,Chunshan Zheng,Gaochao Pan,Shiju Wang,Yi Zhang,Ben Ji

The pore and wetting characteristics of bituminous coal and anthracite treated with different proportions of tetrasodium iminodisuccinate (IDS) and sodium dodecyl sulfate (SDS) were measured. The pore structure characteristics of the coal were studied via low-temperature nitrogen adsorption analysis and the Frenkel-Halsey-Hill fractal theory. Zeta potential measurements were conducted to quantitatively analyze the degree of aggregation or dispersion of coal particles dissolved in solution. Changes in the coal surface morphology were observed and analyzed by scanning electron microscopy (SEM). The results show that when the ratio of IDS:SDS is 1:3, the specific surface area (SSA) values of bituminous coal and anthracite are the lowest. The composite reagent has a greater effect on improving the pore structure of anthracite than bituminous coal. Compared with bituminous coal, anthracite has better pore connectivity and a wider pore network. The absolute zeta potentials of bituminous coal and anthracite reach the maximum at an IDS:SDS ratio of 1:3, with values of 91.08 mV and 91.35 mV, respectively. The electrostatic potential distributions of the molecules show that the advantages of the electrostatic potential difference with water molecules enable IDS and SDS molecules to effectively attract water molecules and form hydrogen bonds, thus revealing the optimization mechanism of coal wettability .

CAS / MDL: 151-21-3 144538-83-0
研究领域: 矿物学 · 表面化学
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Comparison of SDS and L-Methionine in promoting CO2 hydrate kinetics: Implication for hydrate-based CO2 storage

Xuejian Liu,Junjie Ren,Daoyi Chen,Zhenyuan Yin

The continuously increasing CO 2 emissions since industrialization has sparked widespread concerns on environmental and climate change issues. Carbon sequestration and storage technologies (e.g., hydrate-based CO 2 sequestration) present promising potential for the disposing of excessive CO 2 in geological media. High gas uptake capacity and rapid CO 2 hydrate formation kinetics are required for the application of such a technology. In this study, we compared the kinetic promotion effects of sodium dodecyl sulfate (SDS) and L -methionine ( L -Met) on CO 2 hydrate with the objective of identification of an effective and eco-friendly CO 2 hydrate kinetic promoter. The experimental results suggested that L -Met (0.1 wt%) promotes CO 2 hydrates formation significantly with a gas uptake in CO 2 hydrate five times more than SDS at the same concentration. The hydrate morphology observations indicated that the wall-climbing hydrates associated with the addition of L -Met induced by the capillary driving force offer a possible explanation for the difference in the observed kinetics. A novel calculation method was developed to quantify the partition of CO 2 in gas, liquid and hydrate phases. Increasing the initial gas–liquid ratio promotes CO 2 stored in the hydrate phase as solid rather than in the liquid phase as dissolution. We further demonstrated the reusability of L -Met in five consecutive cycles of CO 2 hydrate formation and dissociation. It was assessed that L -Met as a CO 2 hydrate kinetic promoter is superior to SDS and can be employed as an efficient, reliable and eco-friendly kinetic promoter for the hydrate-based CO 2 sequestration technology.

CAS / MDL: 63-68-3 151-21-3
研究领域: 环境科学 · 化学工程
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ANALYTICAL BIOCHEMISTRY · 2024 · IF 2.6

LC-MS characterization of N/O-glycans of α- and β-subunits of chicken ovomucin separated by SDS-PAGE

Cheng Li,Qinghui Chen,Jinqiao Rong,Houde He,Yu Lu,Yuxia Liu,Zhongfu Wang

As the main active glycoprotein of egg white, the biological functions of chicken ovomucin α- and β-subunit are closely related to the structure of glycans. However, the exact composition and structure of the subunit glycans are still unknown. We obtained highly pure chicken ovomucin α-subunit and β-subunit protein bands by the strategy combined with two-step isoelectric precipitation and SDS-PAGE gel electrophoresis. The ammonia-catalyzed one-pot procedure was then used to release and capture α-and β-subunit protein glycans with 1-phenyl- 3-Methyl-5-pyrazolone (PMP). The N / O -glycans of bis-PMP derivatives were purified and analyzed by LC-MS. More importantly, an effective dual modification was performed to accurately quantify neutral and sialylated O -glycans through methylamidation of sialic acid residues and simultaneously through carbonyl condensation reactions of reducing ends with PMP. We first showed that the α-subunit protein has only N -glycosylation modification, and the β-subunit only O -glycosylation, a total of 22  N -glycans and 20 O -glycans were identified in the α- and β-subunit, respectively. In addition, the complex N -glycan (47 %) and the sialylated O -glycan (77 %) are each major types of the above subunits. Such findings in this study provide a basis for studying the functional and biological activities of chicken ovomucin glycans.

研究领域: 生物化学 · 糖生物学 · 蛋白质组学
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