JOURNAL OF MATERIALS IN CIVIL ENGINEERING
·
2024
·Vol. 36
·期 9
·04024251
·
IF 3.1
Cuizhen Zhang,Xinde Tang,Xiaodong Chen,Haichao Guo,Xuefan Li,Laixue Pang,Yong Yang,Fuying Dong
Polycarboxylate superplasticizers (PCEs) have been extensively used in the areas of construction and building; however, the application limitation of PCEs has emerged owing to their sensitivity to clay. In this work, three anticlay PCEs were synthesized by introducing acrylamide (AM), methacryloxyethyltrimethyl ammonium chloride (DMC), or 3-[2-(methacryloyloxy) ethyl] dimethylammonio-propane-1-sulfonate (DMAPS) into the polycarboxylate copolymer of ethylene glycol monovinyl polyethylene glycol ether (EPEG) and acrylic acid (AA), denoted as A-PCE, D-PCE, and S-PCE, respectively. The structures of these superplasticizers were characterized by gel permeation chromatography (GPC) and Fourier-transform infrared spectroscopy (FTIR). Compared with the common polycarboxylate superplasticizers (O-PCEs), the resultant anticlay PCEs showed better dispersion as far as the fluidity of cement paste and mortar were concerned. With the content of 0.5% per weight sodium bentonite in place of cement, these anticlay PCEs exhibited better clay resistance than O-PCE. In addition, the compressive strengths of mortar and concrete by the addition of A-PCE, D-PCE, or S-PCE were slightly higher than those of O-PCE. Total organic carbon (TOC) revealed that the sensitivity of A-PCE, D-PCE, and S-PCE to clay was lower than that of O-PCE. X-ray diffraction (XRD) proved that the layer spacing of clay increased after treatment with superplasticizer. In combination of adsorption determination with XRD analysis, a possible mechanism was proposed. Unlike the PEG side chains inserting into the clay layers for O-PCE, the cations in functional groups entered the clay layers through cation exchange for anticlay PCEs preferentially.
研究领域:
建筑材料
·
化学工程
·
土木工程
✓ 已验证
DOI
高影响因子
PROGRESS IN ORGANIC COATINGS
·
2017
·
IF 2.858
Xian-Wei Cheng,Jin-Ping Guan,Xu-Hong Yang,Ren-Cheng Tang
This research work reported a novel approach to develop flame retardant silk fabric using naturally occurring phytic acid (PA) rich in phosphorus and TiO 2 nanoparticles through a pad-dry-cure technique. A polycarboxylic acid [1,2,3,4–butanetetracarboxylic acid (BTCA)] was employed to stabilize and improve the adhesion of TiO 2 on silk surface. The flame retardancy of the treated silk fabric was determined in terms of limiting oxygen index, vertical burning, and pyrolysis combustion flow calorimetry, and the durability of flame retardancy to washing was discussed. PA and TiO 2 were found to have a joint flame retardant effect. The combination of PA, TiO 2 and BTCA was able to endow silk fabric with excellent flame retardancy, and the good flame retardant ability was kept even after 25 times of washing. The reasons for the good washing durability of the treated silk fabric were discussed. Finally, a significant condensed-phase flame retardant mechanism of the silk fabric treated with the PA/TiO 2 /BTCA system was revealed by the analyses of thermogravimetry and pyrolysis combustion flow calorimetry.
研究领域:
纺织科学
·
材料科学
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2024
·
IF 7.7
Huiyu Jiang,Yanlong Bu,Geao Liu,Wen Zhang,Xian-Wei Cheng
For protein fibers, polycarboxylic acids represent a green strategy to enhance durability without using formaldehyde. This study evaluated the physical and flame retardant properties of silk fabrics treated with three formaldehyde-free crosslinkers : citric acid (CA), 1,2,3,4-butanetetracarboxylic acid (BTCA), and 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTCA). Results showed that these acids bond with silk protein through esterification and amidation , improving washing durability. Particularly, PBTCA integrates phosphorus into silk, boosting flame retardancy. While BTCA led to the highest weight gain and improved wrinkle recovery, it negatively impacted the tensile strength and softness of silk fabrics. Conversely, PBTCA adeptly balanced enhanced wrinkle resistance with minimal effects on tensile strength and softness, and least affected the silk fabrics' whiteness, thus preserving its aesthetic appeal. All crosslinkers improved flame retardancy, but PBTCA displayed superior performance, achieving a limiting oxygen index of 32.4 % at an 80 g/L concentration. In vertical burning tests, PBTCA treated silk fabrics showed reductions in damage length and demonstrated self-extinguishing properties, qualifying them for a higher flame retardant grade. Phosphorus in PBTCA promotes char formation during combustion, essential for effective flame retardation and smoke reduction. This research highlights the exceptional potential of silk treated with PBTCA, showcasing its suitability for demanding applications.
研究领域:
纺织科学
·
材料科学
✓ 已验证
DOI
PubMed
高影响因子
Materials
·
2019
·Vol. 12
·期 7
·1132
·
IF 2.972
Kuangyi Hu,Zhenping Sun
Influence of polycarboxylate superplasticizers (PCs) with different functional units on the hydration heat and hydration products of C3A-gypsum was investigated. Three kinds of PCs with different monomers were discussed. It was seen that PCs mainly shortened the induction stage of C3A-gypsum hydration, and the amount of remaining gypsum was related to the duration of the induction stage. The second heat flow peak of the sample with PCs was higher than that of the blank. Moreover, PC intercalation occurred during the hydration.Keywords:polycarboxylate superplasticizers;C3A-gypsum;functional units;hydration
研究领域:
建筑材料学
·
化学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
RSC Advances
·
2016
·Vol. 6
·期 95
·92943-92952
·
IF 3.289
Henghui Huang,Qi Yao,Hualin Chen,Bailing Liu
In order to improve the scale inhibition efficiency of existing scale inhibitors for industrial water and to reduce the phosphorus pollution of water bodies, a new type of scale inhibitor with a hyper-branched structure has been developed in this study. First, an AB′ type of functional monomer (AMA) was synthesized from maleic anhydride (MAH) and propylene glycol, then copolymerized with monomer B (MAH) through radical polymerization, resulting in a hyper-branched polycarboxylic acid. The synthesis conditions, such as reaction temperature and time, monomer ratio and initiator dosage, have been investigated for obtaining the expected hyper-branched polymer with good scale inhibition performance. The scale inhibition efficiency of the obtained products was determined according to their resistance to the crystallization of calcium sulfate and calcium carbonate under the optimal application conditions. The experimental results show that the hyper-branched polycarboxylic acid provides a scale inhibiting efficiency for CaCO3 and CaSO4 as high as 95.2% and 92.3%, respectively. In addition, XRD analysis showed that the good scale inhibition of the hyper-branched polycarboxylic acid is attributed to its ability to inhibit and destroy the formation of crystals, changing the crystal forms of the calcium scale. This conclusion indicates that the prepared hyper-branched polycarboxylic acid has great application potential in the treatment of industrial water.
研究领域:
材料科学
·
环境科学
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2018
·Vol. 135
·期 32
·46572
·
IF 1.901
Hongwei Zhao,Bing Liao,Fuwei Nian,Kun Wang,Ying Guo,Hao Pang
In this work, three kinds of HPEG-type polycarboxylate superplasticizers (PCs) were synthesized with three kinds of typical functional monomers: [diallyl dimethyl ammonium chloride (DMDAAC), 2-hydroxyethyl methacrylate (HEMA), and 2-(dimethylamino) ethyl methacrylate (DMAM), respectively. The effects of montmorillonite clay on the fluidity of cement/PC pastes were investigated. It was found that the fluidity was negatively affected by the clays in the order: DMAM-PC < HEMA-PC < conventional PC (CPC) < DMDAAC-PC. The DMAM-PC was found to disperse cement well even in presence of montmorillonite clay. The dispersion performance of DMDAAC-PC was much more effectively affected by clay due to the reaction between ammonium and montmorillonite. More study including mortar fluidity, adsorption behavior and morphology of the cement samples were investigated in details. Thermogravimetric analysis and X-ray diffraction experiments allowed us to observe the influence of PCs on the hydrated products. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 46572.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF WUHAN UNIVERSITY OF TECHNOLOGY-MATERIALS SCIENCE EDITION
·
2018
·Vol. 33
·期 1
·226-232
·
IF 0.524
Chen Gang,Lei Jiaheng,Du Yong,Chen Xuebing
The dispersion ability of polycarboxylate superplasticizer (PCE) in fresh concrete was much impeded by clay impurities. To improve the dispersion of PCE in the clay-contained concrete, a novel PCE with carboxyl as a specific branched chain terminal group was synthesized, using modified polyether as the raw material which was prepared through esterification between hexahydrophthalic anhydride (HHPA) and isobutenyl polyoxyethylene ether (IPEG) with hydroxy as the terminal group. The esterification product and PCE molecular structure were characterized by infrared spectroscopy and 1HNMR resonance. The results confirmed that the product molecular structure was a comb-type copolymer with long-chain terminal carboxyl group and PEO attached directly to the backbone chain. The as-synthesized PCEs had favorable dispersibility in cement than conventional PCE in the presence of montmorillonite (Mmt) clay. This can be attributed to the introduction of electronegative carboxyl to PCE long-chain terminal group, which reduces the adsorption of PCE on Mmt, and thus improves the tolerance of PCE to the Mmt.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING RESEARCH & DESIGN
·
2018
·
IF 2.795
Qingwu Long,Jiaqi Huang,Shu Xiong,Liang Shen,Yan Wang
FO technology has attracted growing attention in water treatment and desalination applications recently. The development of a suitable draw solute with high performance and low cost is therefore in high demand to facilitate practical FO applications. In this study, two oligomeric carboxylates — poly maleic acid sodium (PMAS) and poly(itaconate-co-acrylate) sodium [P(IA-co-AA)] with controllable molecular weights of 400–1000 Da, are synthesized via one-step polymerization and employed as novel draw solutes for FO applications. The successful synthesis is confirmed via by various characterization techniques. The osmotic pressure, relative viscosity and FO performance of PMAS and P(IA-co-AA) draw solutions with different concentrations are studied systematically. Two types of FO membranes are employed, and their performance is compared using PMAS draw solution. With 0.5 mol/kg PMAS draw solution and DI water feed solution, high water fluxes of 30.6 and 62.4 LMH can be achieved using HTI-TFC and homemade PSf-TFC membrane in the FO tests, respectively. 0.5 mol/kg PMAS draw solution is further studied for the desalination of 0.6 mol/kg NaCl solution via FO, with a water flux of 6.63 LMH obtained. The diluted PMAS solution after FO test can be recovered by nanofiltration with a high rejection rate. The excellent performance and available recovery route of the developed oligomeric carboxylates imply their great potential as promising draw solutes for FO applications.
研究领域:
水处理
·
材料科学
·
环境工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF WUHAN UNIVERSITY OF TECHNOLOGY-MATERIALS SCIENCE EDITION
·
2021
·Vol. 36
·期 3
·446-455
·
IF 0.957
Zhang Ying,Wang Pengshuo,Sun Guowen,Yang Jianming,Gao Rui
A low adsorption clay-resistant polycarboxylate superplasticizer (KN-PC) was synthesized using acrylic acid and isopentenol polyoxyethylene ether as the main reaction materials. The structural characterization and clay-resistant mechanism of the KN-PC were explored using Fourier transform infrared spectroscopy and X-ray diffraction, and the effect of the KN-PC on the performance of composite paste with various montmorillonite (MMT) contents was analyzed. Compared with ordinary polycarboxylate superplasticizer (PC), the KN-PC has a low sensitivity to the MMT. By the action of the MMT, the adsorption dosage of the KN-PC on the MMT is much smaller than that of the PC.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
Polymers
·
2022
·Vol. 14
·期 16
·3367
·
IF 4.967
Junqi Wang,Ruiqing Liu,Yiwen Tang,Junfeng Zhu,Yonghui Sun,Guanghua Zhang
Since there are not many studies on the application of polymeric surfactants in viscosity reduction emulsification of heavy oil, a series of polyether carboxylic acid–sulfonate polymeric surfactants were synthesized. The viscosity reduction performance and the effect of different chain lengths on the viscosity reduction effect were also investigated. The viscosity reduction, emulsification, wetting, and foaming performance tests showed that the viscosity reduction performance of this series of polymeric surfactants was excellent, with the viscosity reduction rate exceeding 95%, and the viscosity was reduced to 97 mPa·s by the polymeric surfactant with a molecular weight of 600 polyethers. It was also concluded that among the three surfactants with different side chains, the polymeric surfactant with a polyether molecular weight of 600, which is the medium side-chain length, had the best viscosity reduction performance. The study showed that the polyether carboxylic acid–sulfonate polymer surfactant had a promising application in the viscosity reduction of heavy oil.Keywords:polyether-type polycarboxylic acid;viscosity reduction;viscosity reducer;heavy oil
研究领域:
石油工程
·
化学工程
✓ 已验证
DOI
高影响因子
CONSTRUCTION AND BUILDING MATERIALS
·
2019
·
IF 4.046
Baoguo Ma,Chunbao Li,Yang Lv,Hongbo Tan,Hui Wang,Huahui Qi,Xiaohai Liu,Qi Yang,Pian Chen
The problem of bleeding and segregation in high fluidity concrete can be eliminated by the addition of viscosity-enhancing agents (VEA). However, the dispersion capacity of PCE would be perturbed by the addition of VEA. In most cases, this negative impact was due to competitive adsorption between VEA and PCE. In order to mitigate the negative impact, ester groups were introduced to reduce the adsorption capacity, and one new kind of viscosity-enhancing agents was designed; the polymers were copolymerized of acrylic acid (AA) and 2-hydroxyethyl acrylate (HEA), with 1:1 and 1:8 M ratios of AA and HEA. And then, the effect of these two VEAs on rheology of cement paste plasticized by PCE at 5 min and 30 min were studied. Adsorption behavior was analyzed by total organic carbon (TOC), and the zeta potential was also measured. The conformation of the polymers in liquid phase were analyzed by dynamic light scattering (DLS). And the decomposition of ester group under alkaline condition was verified by FTIR and 1 HNMR. The results indicated that the synthesized VEA could plasticize cement paste, and the reason was that VEA could be adsorbed by cement grains and act as the same role as the first-generation superplasticizer. The plasticizing capacity was increased over time, because the adsorption capacity was enhanced due to the released carboxyl groups from the decomposition of ester groups. Furthermore, from 5 min to 30 min, the decomposition of ester group could increase the conformation size of VEA by producing crosslinking in the presence of Ca 2+ , and the crosslinking act as positive role in increasing viscosity and resist the bleeding and segregation. Moreover, it was observed that VEA had negative impact on dispersion capacity of PCE, and the higher density of ester group resulted in lower negative impact at the beginning; one reason for this was because the higher density of ester group showed lower competitive adsorption capacity. Such results offered one new type of VEA available for superplasticizer system.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2019
·Vol. 137
·期 4
·48316
·
IF 2.188
Ruijun Gao,Yan Yao,Ling Wang,Hao Wu
Graphene oxide (GO) was modified by in situ esterification reaction with isopentenol polyoxyethylene ether (IPEG) to obtain GO precursor (GO-IPEG) with some polymerization activity. GO-modified polycarboxylic (GO-PCE) was prepared by GO-IPEG and acrylic acid (AA) using the method of in situ polymerization. The molecular structure of GO-IPEG and GO-PCE was characterized by Fourier transform infrared spectroscopy (FTIR), Raman spectra, and nuclear magnetic resonance (NMR). The dispersion properties and dispersion stability of GO-IPEG and GO-PCE in water solution were studied by ultraviolet–visible (UV–vis) absorption spectra, zeta potential, and atomic force microscope. The results of FTIR, Raman, 1 H-NMR, and 13 C-NMR indicate that IPEG was successfully grafted onto the surface of GO and then fabricated with AA by in situ free-radical polymerization. The results of UV–vis and zeta potential show that GO nanosheets have a better dispersion in GO-IPEG or GO-PCE system when the reaction time of GO and IPEG is 1 h, and the dispersion stability can reach up to 1 month. The better dispersion and application property are confirmed by atomic force microscopy image and cement fluidity, water reducing rate, and compression strength. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 48316.
研究领域:
材料科学
·
化学工程
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）