ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2023
·Vol. 30
·期 16
·47025-47037
·
IF 5.8
Wang Tianyu,Yang Lang,Rao Feng,Jiang Kaixi,Byrynnai Choduraa
Adding organics in the process of geopolymer synthesis can combine the functional groups of organics with the three-dimensional structure of geopolymer, thus changing the properties of geopolymer such as compressive strength, flexural strength, and acid resistance. In this work, excellent mechanical properties and acid resistance of metakaolin-blast furnance slag (Mk-BFS)-based geopolymer were synthesized by the incorporation of chitosan. The formation of sodium-alumino-silicate-hydrate (N-A-S–H) gel and calium-alumino-silicate-hydrate (C-A-S–H) gel in geopolymerization were characterized by 29 Si nuclear magnetic resonance (NMR). At 5% of chitosan, the compressive strength of Mk-BFS-based geopolymer could reach to 33.7 MPa. The results could be ascribed to that chitosan reacts with geopolymer to generate new C-O-Si structure meanwhile adhesion produced by the combination of positively charged cations and negatively charged ions makes the structure of geopolymer denser. After 7 days of sulfuric acid immersion, the reduction of compressive strength is less than 3 MPa, demonstrating its great acid resistance. The acid resistance of Mk-BFS-based geopolymer could attribute to that the free amino groups in chitosan preferentially react with acid solution and weakened the erosion of sulfuric acid. This study optimizes the compressive strength and acid resistance of geopolymer by adding appropriate amount of chitosan.
研究领域:
材料科学
·
硅酸盐化学
·
无机非金属材料
·
功能复合材料
·
建筑材料
✓ 已验证
DOI
高影响因子
POLYMERS FOR ADVANCED TECHNOLOGIES
·
2017
·Vol. 28
·期 11
·1438-1447
·
IF 1.907
Xin Liu,Xuewen Guo,Yunfei Zhi,Shaoyun Shan,Yonghao Ni,Qingming Jia
The recent development of sulfur dioxide (SO 2 ) polymerization has seen a renaissance in its chemistry, especially poly(olefin sulfone)s from the copolymerization of SO 2 , and unsaturated hydrocarbons can be found to have many applications, including transient electronic packaging, drug delivery, and electron beam-resistant materials. In this work, a type of functional poly(norbornene sulfone) was synthesized via two different polymerization methods. Aiming to understanding the effects of different polymerization methods on poly(olefin sulfone)s and gain further understanding on the kinetics of poly(olefin sulfone)s's thermal instability, we investigated their detailed thermal degradation behaviors using thermogravimetry and analyzed the resultant kinetics in accordance with three kinetic models. The results supported the conclusion that although the poly(norbornene sulfone)s obtained have different activation energy, the thermal degradation kinetics are the same and also obey the D n type. Copyright © 2017 John Wiley & Sons, Ltd.
研究领域:
高分子化学
·
材料科学
·
热分析
·
功能高分子
·
可控降解材料
✓ 已验证
DOI
高影响因子
MATERIALS & DESIGN
·
2015
·
IF 3.501
Heng Zhang,Libo Wang,Qiang Chen,Ping Li,Aiguo Zhou,Xinxin Cao,Qianku Hu
In this study, a Ti 3 C 2 nanomaterial and Ti 3 C 2 /UHMWPE (ultrahigh molecular weight polyethylene) nanocomposites were prepared. The morphology, structure and properties of the Ti 3 C 2 /UHMWPE nanocomposites were investigated. The results indicate that Ti 3 C 2 nanoparticle can improve the thermal and mechanical properties of UHMWPE . The crystallinity and hardness of the Ti 3 C 2 /UHMWPE nanocomposite increase with the content of Ti 3 C 2 . The tensile and breaking strengths of the nanocomposites are enhanced with increasing Ti 3 C 2 content and reach maximum values at a mass fraction of 0.75 wt.%. The creep performance is enhanced after the addition of Ti 3 C 2 to the matrix. The frictional properties of the Ti 3 C 2 /UHMWPE composites were investigated using a pin-on-disc tester. The Ti 3 C 2 /UHMWPE composites exhibited a better friction-reducing performance compared with pure UHMWPE . The addition of Ti 3 C 2 can reduce the adhesive wear and plow friction, which results in the worn surfaces of the Ti 3 C 2 /UHMWPE composite being smoother than those of pure UHMWPE.
研究领域:
材料科学
·
高分子材料
·
摩擦学
·
纳米复合材料
·
机械工程
✓ 已验证
DOI
高影响因子
COLLOID AND POLYMER SCIENCE
·
2014
·Vol. 292
·期 10
·2633-2645
·
IF 2.41
Cong Houluo,Zheng Sixun
In this contribution, we reported the synthesis of poly( N -isopropylacrylamide)- block -poly(acrylic acid) (PNIPAAm- b -PAA) copolymer networks via sequential reversible addition-fragmentation chain transfer (RAFT) polymerization. The PNIPAAm- b -PAA block copolymer networks were characterized by means of Fourier transform infrared spectroscopy (FTIR) and small angle X-ray scattering (SAXS). The volume phase transition (VPT) temperatures of the PNIPAAm- b -PAA hydrogels were measured by means of micro-differential scanning calorimetry (micro-DSC). It was found that the block copolymer hydrogels displayed the VPT temperatures lower than the control PNIPAAm hydrogel. Compared to the control PNIPAAm hydrogel, the deswelling and reswelling properties of the block copolymer hydrogels were significantly improved. The improved thermoresponsive properties of the PNIPAAm- b -PAA hydrogels have been interpreted on the basis of the formation of the architecture of the block copolymer networks.
研究领域:
高分子化学
·
生物材料
·
药物递送
·
组织工程
·
智能响应材料
✓ 已验证
DOI
高影响因子
JOURNAL OF MOLECULAR LIQUIDS
·
2020
·
IF 5.065
Yawei Song,Kuanjun Fang,Mohd Nadeem Bukhari,Kun Zhang,Zhiyuan Tang
Inkjet printability of dye-based inks including stability, jetting morphology, and color performance is difficult to maintain due to the strong dye molecular interaction. Herein, carboxyl-rich polymer nanospheres were introduced to the dye-based inks, forming a novel kind of multilayer dye/polymer nanospheres to enhance the inkjet printability. Disperse dyes were firstly loaded into poly (styrene-butyl acrylate-methacrylate) nanospheres at 95 °C, and then encapsulated by poly (styrene-methacrylate) polymer layer through seed polymerization to form multilayer structure. The results showed that hydrogen bonds were formed between disperse dyes and nanospheres, and the interaction was enhanced when more carboxyl groups were polymerized on nanosphere surface. Moreover, due to the high surface carboxyl group content, the stability was significantly improved in comparison with disperse dye suspension. After inkjet printing , the dye/nanosphere dispersion showed more stable droplet formation and higher color depth. Besides, because of the self-curing ability of polymer nanospheres, satisfactory fastness was obtained for practical application. The results from this study can promote the optimization of dye-based ink formulations, and show great potential in obtaining high quality inkjet printing products.
研究领域:
材料科学
·
高分子化学
·
表面化学
·
印刷电子学
·
功能材料
✓ 已验证
DOI
高影响因子
Energy & Environmental Materials
·
2022
·Vol. 6
·期 4
·e12568
·
IF 13.443
Kai Chen,Yuxue Sun,Xiaorong Zhang,Jun Liu,Haiming Xie
The self-healing solid polymer electrolytes (SHSPEs) can spontaneously eliminate mechanical damages or micro-cracks generated during the assembly or operation of lithium-ion batteries (LIBs), significantly improving cycling performance and extending service life of LIBs. Here, we report a novel cross-linked network SHSPE (PDDP) containing hydrogen bonds and dynamic disulfide bonds with excellent self-healing properties and non-flammability. The combination of hydrogen bonding between urea groups and the metathesis reaction of dynamic disulfide bonds endows PDDP with rapid self-healing capacity at 28 °C without external stimulation. Furthermore, the addition of 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIMTFSI) improves the ionic conductivity (1.13 × 10 −4 S cm −1 at 28 °C) and non-flammability of PDDP. The assembled Li/PDDP/LiFePO 4 cell exhibits excellent cycling performance with a discharge capacity of 137 mA h g −1 after 300 cycles at 0.2 C. More importantly, the self-healed PDDP can recover almost the same ionic conductivity and cycling performance as the original PDDP.
研究领域:
材料科学
·
高分子化学
·
电化学
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2017
·Vol. 52
·期 19
·11701-11714
·
IF 2.599
Wei Xiuzhen,Hong Jialiang,Zhu Shuangshuang,Chen Jinyuan,Lv Bosheng
Polyethyleneimine (PEI) of various molecular weights and trimesoyl chloride (TMC) were utilized to prepare composite nanofiltration (NF) membranes via interfacial polymerization. The changes in the surface structure and chemical composition of the prepared membranes were evaluated using SEM, ATR-FTIR, XPS and surface potential measurements. The pure-water flux and rejection rates of the inorganic salts (MgCl 2 , MgSO 4 , Na 2 SO 4 and NaCl) through the resultant NF membranes were also investigated. The results showed that the performance of the composite NF membranes was significantly affected by the molecular weight of the PEI. Notably, the permeate flux and rejection rate of the NF membranes increased with the PEI molecular weight. In addition, when the NF membranes were used to treat actual wastewater from the electroplating industry, the NF membranes presented high-efficiency separation properties for heavy metal ions. The rejection rates of the NF membranes at 0.4 MPa for chromium, nickel, zinc and copper ions reached 92.6, 89.6, 89.2 and 86.3%, respectively.
研究领域:
材料科学
·
膜分离技术
·
环境工程
·
高分子化学
·
水处理
✓ 已验证
DOI
高影响因子
Defence Technology
·
2023
·
IF 5.1
Weitao Yang,Yuchen Gao,Rui Hu,Manman Li,Fengqi Zhao,He Jiang,Xuan Zhang
Smart materials, which exhibit shape memory behavior in response to external stimuli, have shown great potential for use in biomedical applications. In this study, an energetic composite was fabricated using a UV-assisted DIW 3D printing technique and a shape memory material (SMP) as the binder. This composite has the ability to reduce the impact of external factors and adjust gun propellant combustion behavior. The composition and 3D printing process were delineated, while the internal structure and shape memory performance of the composite material were studied. The energetic SMP composite exhibits an angle of reversal of 18 s at 70°, with a maximum elongation typically reaching up to 280% of the original length and a recovery length of approximately 105% during ten cycles. Additionally, thermal decomposition and combustion behavior were also demonstrated for the energetic SMP composite.
研究领域:
材料科学
·
高分子化学
·
推进剂技术
·
智能响应材料
·
增材制造
✓ 已验证
DOI
高影响因子
JOURNAL OF MOLECULAR STRUCTURE
·
2022
·
IF 3.841
Qi Wang,Shaopeng Fu,Xingyao Yang,Qinghao Sun,Junwei Zhang,Yichun Peng,Rongling Zhang,Zezhou Liang,Jianfeng Li
An organic nitrogen/oxygen-rich polymer (PFN-NDIN) was prepared via Suzuki reaction between 2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-bis(3-N,N- dimethylaminopropyl)-9H-fluorene (FNB) and 4,9-dibromo-2,7-bis(3-(dimethyl-amino)propyl)naphthalenediimide (NDINBr 2 ) and utilized as a new inhibitor for HRB400 steels corrosion in alkaline medium of simulated concrete pore solution. The inhibition efficiency of this inhibitor was evaluated by electrochemical techniques. The electrochemical impedance spectroscopy (EIS) results showed that the protective capacity of PFN-NDIN on HRB400 steel increased with increasing concentration to attain 92.85% efficacy with 400 ppm at 288 K. Potentiodynamic polarization (PDP) plots indicated that PFN-NDIN is effective and acts as a hybrid inhibitor. The adsorption behavior of PFN-NDIN was fitted and found to follow the Langmuir isothermal adsorption line, with discussion of the relevant thermodynamic parameters. The effect of temperature on this inhibitor's the rust-inhibiting effect was investigated. The surface was then studied, showing that the interfacial corrosion of HRB400 steel was inhibited by PFN-NDIN molecules. The relationship between PFN-NDIN molecules’ structure and the inhibition efficiency was investigated by quantum chemical calculations. Several parameters were calculated, the findings revealed that the prepared materials correlated well with their electronic contribution capability.
研究领域:
材料腐蚀与防护
·
高分子化学
·
电化学
·
建筑材料科学
·
表面科学
·
量子化学
✓ 已验证
DOI
高影响因子
POLYMERS FOR ADVANCED TECHNOLOGIES
·
2017
·Vol. 29
·期 2
·982-988
·
IF 1.907
Jiayu Xian,Jieting Geng,Yan Wang,Lin Xia
Shape-memory polymers are important smart materials with potential applications in smart textiles, medical devices, and sensors. We prepared trans-1,4-polyisoprene, low-density polyethylene (LDPE), and high-density polyethylene (HDPE) shape-memory composites using a simple mechanical blend method. The mechanical, thermal, and shape-memory properties of the composites were studied. Our results showed that the shape-memory composites could memorize 3 temporary shapes, as revealed by the presence of broad melting transition peaks in the differential scanning calorimetry curves. In the trans-1,4-polyisoprene/LDPE/HDPE composites, the cross-linked network and the crystallization of the LDPE and HDPE portions can serve as fixed domains, and all crystallizations can act as reversible domains. We proposed a schematic diagram to explain the vital role of the cross-linked network and the crystallization in the shape-memory process.
研究领域:
高分子材料科学
·
生物医学工程
·
智能材料
·
功能高分子
·
热响应材料
✓ 已验证
DOI
高影响因子
INDUSTRIAL CROPS AND PRODUCTS
·
2017
·
IF 3.181
Xinyan Yan,Zhaolan Zhai,Zhanqian Song,Shibin Shang,Xiaoping Rao
A series of polymeric surfactants , poly acrylic acid rosin polyethylene glycol esters (P-AAR-PEG), have been synthesized from natural diterpenic rosin. Their structures were characterized by Fourier Transform Infrared Spectrometer (FTIR) and their molecular weights were characterized by Gel Permeation Chromatography (GPC). Their critical micelle concentration (CMC), surface tension (γ CMC ), foaming property (FP), and hydrophile-lipophile balance (HLB) value were evaluated. Their thermal properties were measured by Thermal Gravimetric Analyzer (TGA) and fluid behaviors were studied by Rotational Rheometer. The influence of concentration on the properties of oil-in-water emulsions was examined and contrasted the stability of emulsion by the mean droplet size between day1 and day7. The weight-average molecular weight of P-AAR-PEG ranged from 1770 to 5071. CMC values of P-AAR-PEG were ranged from 0.33 to 0.87 g/L and the corresponding γ CMC values were ranged from 37.8 to 39.1 mN/m respectively. Their CMC and γ CMC values decreased and then increased with the increment of molecular weight of hydrophile group. Rheological measurements indicated that the P-AAR-PEG solutions changed from pseudoplastic property to Newtonian with increasing shear rate. P-AAR-PEG1000 had good emulsion ability to turpentine in water. When the concentration of P-AAR-PEG1000 was 8 wt%, the emulsion remained stable for more than 7 days.
研究领域:
高分子化学
·
表面与界面化学
·
材料科学
·
胶体化学
·
应用化学
✓ 已验证
DOI
高影响因子
EUROPEAN POLYMER JOURNAL
·
2013
·Vol. 49
·期 6
·1731-1741
·
IF 2.562
Wenwen Yu,Dezhi Zhang,Miao Du,Qiang Zheng
A series of novel polyurethane (PU)/epoxy resin (EP) graft interpenetrating polymer network (IPN) composites with graded length side chains were prepared from toluene diisocyanate (TDI), polytetrahydrofuran glycol (PTMG), EP, trimethylolpropane (TMP), and diol chain extenders. The effects of the side chain lengths, content, and groups on the damping properties and mechanical properties were investigated. Two damping peaks were observed in the PU/EP IPN system, indicating that the peak damping factor (tan δ ) increased with increased side chain length at low temperatures. The introduction of an apolar side chain slightly narrowed the damping range. However, the side chain carrying polar groups broadened the damping temperature range. The strong H-bond interaction between the ester group of side chain and the N H of hard segments in PU was believed to favor microphase separation to form a larger-sized domain and induce the appearance of the relaxation peak at high temperatures. Consequently, the effective damping temperature range was broadened. The side chain content tethered in the hard segment remarkably influenced the damping properties of PU/EP IPNs both at low and high temperatures. The width and intensity of the tan δ peaks of PU/EP IPNs increased with increased side chain content. The mechanical properties (tensile strength and elongation at break) were significantly affected by the side chain content. Thus, an important method of improving the mechanical damping of elastomers by controlling the side chain molecular structure was established.
研究领域:
高分子材料科学
·
功能高分子
·
阻尼材料
·
复合材料
·
聚合物共混物
·
材料力学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）