FUEL
·
2022
·
IF 8.035
Xiaodong Wang,Xiaoran Li,Sen Liu,Haofei Zhou,Qiuye Li,Jianjun Yang
Cis-9-Octadecenylamine modified α-Fe 2 O 3 and Fe(OH) 3 nanoparticles were successfully synthesized by using a one-step synthetic method. XRD results revealed that lower ratio of oleylamine to Fe 3+ introduce forming hematite phase but higher ratio introduce forming Fe(OH) 3 phase. FTIR, TGA, contact angle, and XPS results indicated that olelyamine were modified on the surface of α-Fe 2 O 3 or Fe(OH) 3 . A larger amount of oleylamine modifier is conducive to the dispersion of the catalysts in heavy oil. Oleylamine modified Fe(OH) 3 can be transformed into α-Fe 2 O 3 in situ during the catalytic reaction and shows higher catalytic activity in the viscosity reduction of Shengli extra heavy crude oil.
研究领域:
化学工程
·
材料科学
·
石油工程
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产品关联
DOI
高影响因子
FUEL
·
2022
·
IF 8.035
Chenxi Lu,Yuanzhuo Zhou,Liangzhi Li,Hongwei Chen,Lishi Yan
Catalytic production of 5-hydroxymethylfurfural (5-HMF) from glucose is a promising routine for generation of varied value-added chemicals. Herein, Mixed-Metal metal–organic frameworks (MOFs)–Fe/MIL-101(Cr) and MIL-101(Cr, Fe) obtained from post-synthesis modification and one-pot synthesis approach respectively were applied for catalytic converting glucose to 5-HMF. The synthesized Mixed-Metal MOFs were characterized by PXRD, SEM, N 2 adsorption–desorption analysis, TGA, XPS and NH 3 -TPD. Cr-and Fe-containing Mixed-Metal MOFs Fe/MIL-101(Cr) and MIL-101(Cr, Fe) presented synergistic effect with enhanced catalytic ability for glucose transformation to 5-HMF compared with typical single-metal MOFs and sulfonic acid-functionalized MOFs. Moreover, these two Mixed-Metal MOFs also presented better thermal stability than single-metal MOFs like MIL-101(Cr). Fe/MIL-101(Cr) was found to possess higher catalytic performance than MIL-101(Cr, Fe). 55.8 % 5-HMF yield was obtained with Fe/MIL-101(Cr) at 170 °C for 2 h in DMSO/water system. In addition, Fe/MIL-101(Cr) demonstrated desired recyclability for five times without incredible loss in its activity. This study provides a Mixed-Metal strategy on MOFs for improving catalytic efficiency of glucose conversion to 5-HMF.
研究领域:
化学工程
·
材料科学
·
催化
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产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Jinshan Xie,Xiaoxiang He,Kexin Liu,Wulong Li,Zhanxiong Li
In this paper, carboxylated cotton fabric (CF-Ph-COOH) were obtained as active substrate by diazonium radical polymerization modification of cotton fibers. Then the MOF fabric composites were prepared by in situ growth of metal zirconium ions (Zr) and organic ligands on the surface of carboxylated cotton fabrics under carboxylic acid modifier. MOF fabric composites with controllable morphologies structures were achieved by regulating organic ligands, reaction time the type and dosage of regulator (formic acid and acetic acid). The prepared acetic acid regulated MOF fabric composites were designated as CF-HAc1-UiO-66, CF-HAc2-UiO-66, CF-HAc1-UiO-66-NH 2 , and CF-HAc2-UiO-66-NH 2 , respectively, and the formic acid regulated as CF-FA-UiO-66 and CF-FA-UiO-66-NH 2 . The fabricated carboxylic acid modulated MOF fabric composites were well characterized using SEM, TGA, XRD, FTIR, and XPS spectra. The adsorption experiment results show that carboxylic acid modulated Zr based MOF fabric composites can serve as adsorbent for effective removal of Cr(VI) from water, in which the CF-FA-UiO-66-NH 2 was prepared under the ratio of ZrCl 4 and BDC-NH 2 is 1.006 and with 5.47 M formic acid regulator exhibits that the optimal adsorption efficiency and the removal efficiency is 79.5 %. In addition, the adsorption of Cr(VI) in water by CFA-UiO-66-NH 2 showed a quasi-secondary kinetic model following the Langmuir adsorption model, showing a a typical of chemisorption. What’s more, the Cr(VI) removal efficiency and saturated adsorption capacity of CF-FA-UiO-66-NH 2 was up to 80 % and 318.85 mg/g, respectively. The prepared CF-FA-UiO-66-NH 2 MOF fabric composite was recyclable for removal of Cr(VI), and could be used as the potential adsorbent membrane for waste water treatment.
研究领域:
材料科学
·
环境工程
·
化学工程
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产品关联
DOI
高影响因子
RSC Advances
·
2016
·Vol. 6
·期 54
·48590-48598
·
IF 3.289
Yu Shang,Bo Jin,Rufang Peng,Zhicheng Guo,Qiangqiang Liu,Jun Zhao,Qingchun Zhang
A series of nitrogen-rich heterocyclic 1H,1′H-5,5′-bistetrazole-1,1′-diolate salts, namely, 1,2,4-triazolium (2), 3-amino-1,2,4-triazolium (3), 4-amino-1,2,4-triazolium (4), 3,5-diamino-1,2,4-triazolium (5), 2-methylimidazolium (6), imidazolium (7), pyrazolium (8), 3-amino-5-hydroxypyrazolium (9), dicyandiamidine (10), and 2,4-diamino-6-methyl-1,3,5-triazin (11), was synthesized with cations. These energetic salts were fully characterized through FT-IR, 1H NMR, 13C NMR, and elemental analysis. The structures of 2, 3·7H2O, 6·2H2O, 8, and 10·4H2O were further confirmed through single crystal X-ray diffraction. Their thermal stabilities were investigated through differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The results indicated that all of the salts possess excellent thermal stabilities with decomposition temperatures ranging from 225.7 °C to 314.0 °C. On the basis of the Kamlet–Jacobs formula, we carefully calculated their detonation velocities and detonation pressures. All of the salts, except 11, exhibit promising detonation performances with a detonation pressure of 20.23–28.69 GPa and a detonation velocity of 7050–8218 m s−1. These values are much higher than those of TNT. The impact sensitivities of the compounds were determined via a Fall hammer test. All of the compounds show excellent impact sensitivities of >50 J, and this finding is higher than that of TATB (50 J). Therefore, these ionic salts with excellent energetic properties could be applied as new energetic materials.
研究领域:
化学
·
材料科学
·
高能材料
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DOI
高影响因子
MOLECULES
·
2024
·Vol. 29
·期 22
·5378
·
IF 4.2
Qiaolin Zuo,Zhenzhong Fan,Qingwang Liu,Yuanfeng Fu,Luoqi Cui,Junfeng Yang
Aiming at the problem of excessive swelling of conventional microspheres for oilfield use, a novel amphiphilic polymerizable crosslinker (AE) was synthesized by quaternary ammonium modification of an unstable crosslinker (AE) using acrylamide, 2-acrylamido-2-methylpropanesulfonic acid as the monomers, N,N′-methylene bisacrylamide as the stabilizing crosslinker, ammonium peroxysulfate and sodium bisulfite as the initiator, and water as the solvent by using a reversed microemulsion method. Double-networked nanomicrospheres were prepared. The preparation conditions of the microspheres were optimized by the surface response method, focusing on the effects of the initiator addition and reaction temperature, and total crosslinker addition on the formation of nanomicrospheres. The samples were characterized by FTIR, TGA, laser particle sizer, and SEM to evaluate the retarded expansion performance and the modulation drive performance. The results showed that the optimal conditions for the preparation of microspheres were m(oil phase):m(water phase) = 3:2, stirring speed of 550 r/min, total crosslinking agent dosage of 0.6% (based on the total mass of monomers, hereinafter the same), initiator dosage of 0.30%, reaction temperature of 45 °C, and reaction time of 4 h. Compared with the conventional polymer microsphere PAM, PAE was slow-expanded for 45 d at 60 °C, and the expansion multiplier was about 16 times, with slow-expansion characteristics; the blocking rate of PAE reached 98.3%, the oil repulsion rate was 73.11%, and the increase in the recovery rate could be up to 11.23%. In this paper, a new type of nanomicrosphere material is investigated to realize the efficient implementation of oil field conditioning and driving.
研究领域:
材料科学
·
化学工程
·
石油工程
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产品关联
DOI
PubMed
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2021
·
IF 6.953
Yinchun Fang,Weihao Sun,Junwei Li,Hailong Liu,Xinhua Liu
Polyester/cotton blend fabrics are widely used in clothing and household textiles which combine the comfort of cotton and excellent mechanical strength of polyester. However, their high flammability due to the special “wick effect” resulting from the different thermal decomposition process of cotton and polyester causes greatly potential fire hazards. In this study, fully bio-based intumescent flame retardant (IFR) coating of chitosan/phytic acid (CS/PA) was layer-by-layer (LBL) assembly constructed on polyester/cotton blend fabrics. The LOI value of polyester/cotton blend fabric which was LBL assembly coated by 20 bilayers CS/PA reached 29.2%. And the dripping of coated fabric was eliminated. The results of cone calorimetry test confirmed CS/PA coating greatly improved the flame retardancy of polyester/cotton blend fabrics. Thermogravimetric analysis (TGA) results showed CS/PA coating changed the thermal decomposition process to promote the char formation of polyester/cotton blend fabrics. CS/PA coating on fabric could form the IFR system which acts through both condensed phase action by the catalysis dehydration reaction to forming stable char and gas phase action by the blowing effect. This research provides a new strategy to eco-friendly flame retardant and dripping-resistant for polyester/cotton blend fabrics by bio-based IFR system through facile LBL assembly method.
研究领域:
材料科学
·
纺织工程
·
消防安全
·
可持续化学
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产品关联
DOI
PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2013
·
IF 5.825
Xing Tang,Huawei Chen,Lei Hu,Weiwei Hao,Yong Sun,Xianhai Zeng,Lu Lin,Shijie Liu
A series of low-cost readily-assembled eco-friendly metal hydroxides were examined as catalysts in the synthesis of a novel platform molecule, γ-valerolactone (GVL), from biomass-derived ethyl levulinate (EL) via hydrogen transfer reaction. Among these catalysts, ZrO(OH) 2 · x H 2 O was found to be most active. EL conversion of 93.6% and GVL selectivity of 94.5% were achieved when 2-propanol was used as a hydrogen donor at 473 K with a reaction time of only 1 h. The complete reaction pathway and the probable main by-products for the conversion of EL to GVL were clearly deduced for the first time. The ZrO(OH) 2 · x H 2 O catalyst could be reused at least ten times without any significant loss of catalytic activity. Furthermore, characterizations were carried out on the fresh and spent ZrO(OH) 2 · x H 2 O catalysts with XRD, FT-IR, BET, TGA-DTA. Combined with the results of poisoning experiments, a plausible mechanism for catalytic transfer hydrogenation (CTH) of EL to GVL was proposed to be consisted of a catalytic cycle involving a six member ring transition state.
研究领域:
化学工程
·
催化
·
绿色化学
·
可再生能源
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产品关联
DOI
高影响因子
INDUSTRIAL CROPS AND PRODUCTS
·
2022
·
IF 6.449
Liangyun Sun,Juan Han,Jiacong Wu,Wenrui Huang,Yuanyuan Li,Yanli Mao,Lei Wang,Yun Wang
The special molecular structure and properties of cellulose restrict its resource utilization. In this work, two kinds of common inorganic salt hydrates (ZnBr 2 ·RH 2 O and FeCl 3 ·RH 2 O) were used to pretreat microcrystalline cellulose (MCC) by magnetic stirring method at temperatures below 80 °C. It was found that while high temperatures could shorten the dissolution time of MCC, while inorganic salt hydrates with either low water (ZnBr 2 ·3.5H 2 O and FeCl 3 ·5H 2 O) or high water (ZnBr 2 ·5H 2 O and FeCl 3 ·8H 2 O) content can prolong the dissolution time of MCC. The reactivity of regenerated cellulose (RC) after dissolution was evaluated by enzyme hydrolysis reaction. Moreover, ZnBr 2 ·4H 2 O and FeCl 3 ·6H 2 O have better pretreatment effect. The structure and surface morphology of MCC before and after pretreatment were investigated by XRD , FT-IR, SEM , AFM and TGA. The MCC was converted from cellulose Ⅰ to cellulose II through the pretreatment. With the extension of dissolution time, the strength of hydrogen bond and thermal stability of RC were both slightly weakened, Moreover, the crystallinity and degree of polymerization (DP) of RC decreased, and the surface morphology of RC was more rougher, more uneven and dispersed compared with the smooth and compact MCC. The adsorption rate curves showed that RC-ZnBr 2 ·4H 2 O was more conducive to the adsorption of cellulase , thereby accelerating the rate of RC hydrolysis. Furthermore, ZnBr 2 ·4H 2 O is a well reusable pretreatment solvent that can maintain a good pretreatment effect on cellulose after five cycles.
研究领域:
化学工程
·
材料科学
·
生物材料
·
生物技术
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产品关联
DOI
高影响因子
E-POLYMERS
·
2017
·Vol. 17
·期 6
·463-470
·
IF 0.949
Yongqian Nie,Xuanxi Leng,Yixue Jiang,Shigan Chai,Jinzhi Zhang,Qichao Zou
Unsaturated polyester resins (UPR) were prepared by the melt condensation method based on adipic acid, o-phthalic anhydride, maleic anhydride and ethylene glycol in the presence of PSS-(2,3-propanediol)propoxy-heptaisobutyl substituted (PSS-POSS) or/and 9 wt% [(6-oxide-6H-dibenz(c,e)(1,2)oxaphosphorin-6-yl)methyl]butanedioic (DDP). We synthesized UPR containing DDP (DDP-UPR) and UPR containing both DDP and PSS-POSS (DDP-PSS-POSS-UPR series). The chemical structures of the modified polyesters were characterized and confirmed by Fourier transform infrared (FTIR) and 31 P nuclear magnetic resonance ( 31 P NMR). The thermal stability and flammability behaviors of UPR were evaluated by thermogravimetric analysis (TGA) and limited oxygen index (LOI) and the vertical burning test. The morphology of residual char of UPR was shown by scanning electron microscopy (SEM). The results indicate that the incorporation of PSS-POSS has little influence on the thermal stability of DDP-UPR, but enhances the flame retardance of DDP-UPR, and when the PSS-POSS content reaches 10 wt%, the DDP-PSS-POSS-UPR has better flame retardance.
研究领域:
材料科学
·
聚合物化学
·
消防安全工程
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产品关联
DOI
高影响因子
POLYMER DEGRADATION AND STABILITY
·
2020
·
IF 4.032
Zhiyong Zhang,Dongsheng Li,Miaojun Xu,Bin Li
A novel phosphorus and nitrogen containing flame retardant named 1,4-bis(Diethyl methylenephosphonate) piperazine (BDEMPP) was synthesized. The chemical structures of BDEMPP were determined by Fourier transform infrared spectrum (FTIR), nuclear magnetic resonance (NMR) and gas chromatography-mass spectrometry (GC-MS). The flame retardant rigid polyurethane foams (FR-RPUFs) were prepared by one-pot and free foaming with incorporating BDEMPP/expanded graphite (EG) with polyether polyol and polymethylene polyphenyl isocyanate. The limit oxygen index (LOI), vertical burning (UL94) and cone calorimeter (CONE) test showed that the fire-retardant properties were improved due to the barrier effect of EG and residual char. With addition of 10 wt % EG and 15 wt % BDEMPP, RPUF/10EG/15BDEMPP passed UL94 V-0 with the LOI value of 25.7%. The thermogravimetric analysis (TGA) results revealed that the initial decompose temperature ( T 5% ) of RPUF/10EG/15BDEMPP was decreased compared with pure RPUF. However, the yield of residual char was increased from 0.35% for pure RPUF to 30.52% for RPUF/10EG/15BDEMPP at 800 °C. EG and BDEMPP had a slight influence on density and compression strength . The density and compression strength of pure RPUF was 45.42 kg m −3 and 213 kPa. As for RPUF/10EG/15BDEMPP, the density and compression strength was 44.18 kg m −3 and 180 kPa. The morphology and composition of residual char were investigated. The results demonstrated that the intact, compact and thick residual char with abundant of phosphorus and nitrogen was formed to enhance the flame retardancy and smoke suppression.
研究领域:
材料科学
·
高分子化学
·
消防安全工程
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DOI
高影响因子
JOURNAL OF POROUS MATERIALS
·
2021
·Vol. 28
·期 6
·1737-1747
·
IF 2.496
Jiang Haoxi,Zhao Yingying,Lin Jing,Chen Yifei,Wang Sheng
Highly dispersed palladium nanoparticles (NPs) supported on UiO-66 as catalyst for CO 2 methanation were prepared by supercritical fluid deposition (SFD). As a result, the most suitable Pd precursor salt and co-solvent are Na 2 PdCl 4 and ethanol/DMF, respectively. The best SFD process condition to deposit the Pd precursor on UiO-66 is 40 °C, 10 MPa and 2 h. Under the above condition, 4% Pd/UiO-66 exhibits the highest activity with 53% of CO 2 conversion and 95% of CH 4 selectivity while the turnover frequency (TOF) value is 3669.4 h −1 . The catalysts were characterized by XRD, BET, TEM, XPS, TGA, CO-DRIFTS and ICP-OES to investigate the structure–activity relationship. The 4% Pd/UiO-66 with the average size of 2.2 nm of Pd prepared in assistance of supercritical fluid behaved the similar activity as the 6%Pd/UiO-66 with average size of 9.7 nm of Pd prepared by sol–gel method. It is showed prospect of technique for reducing noble metal loading resulting from high dispersion effect.
研究领域:
催化
·
材料科学
·
化学工程
·
环境科学
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产品关联
DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2021
·
IF 7.46
Jia Ding,Fei Liu,Chunling Qi,Yunlei Zhou,Huanshun Yin,Shiyun Ai
A novel photoelectrochemical (PEC) biosensor was constructed for DNA hydroxymethylation detection based on Bi 4 NbO 8 Cl/PTC-NH 2 heterojunction and Fe-MIL-88NH 2 , where Bi 4 NbO 8 Cl/PTC-NH 2 was employed as photoactive material and Fe-MIL-88NH 2 was adopted as artificial hydrogen peroxide mimic enzyme. Based on the structure of hydroxymethylated cytosine in DNA sequence, 5-hydroxymethyl-2’-deoxycytidine (5hmdC) was employed as detected target molecule for the first time using PEC technique. After Bi 4 NbO 8 Cl/PTC-NH 2 heterojunction was modified on the substrate electrode, thioglycolic acid (TGA) was captured by forming amide bond, where the sulfhydryl group (-SH) of TGA was employed as the specific recognition of 5hmdC. Under M. HhaI catalysis, the −CH 2 OH of 5hmdC reacted selectively with the –SH. Finally, Fe-MIL-88NH 2 was modified on the electrode based on the crosslinker of 4-formylphenylboronic acid (FPBA), where FPBA possessed two active groups of formyl and boronic acid group, reacting with glycosyl of 5hmdC and amino of Fe-MIL-88NH 2 . Under the catalysis effect of Fe-MIL-88NH 2 , the insoluble substance was produced on the surface of electrodes, resulting in distinct lessening of PEC response. Under optimal conditions, the photocurrent shows a linear relationship with the logarithm value of 5hmdC concentration from 0.01-100 nM with a low detection limit of 6.48 pM. More importantly, this method can be applied to investigate the influence of exogenous phytohormone on 5hmdC content in the genomic DNA of rice seedling roots and leaves.
研究领域:
材料科学
·
分析化学
·
生物传感器
·
生物化学
·
纳米技术
·
电化学
·
基因组学
✓ 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）