NEW JOURNAL OF CHEMISTRY
·
2024
·
IF 2.7
Yufen Wang,Yantao Wang,Yongqing Ma,Asma Mohmmad Elsharif,Chen Zhang,Weiran Yang,Christophe Len
A new transition-metal-free catalytic system which uses sodium iodide as the catalyst with formic acid as the hydrogen donor in a biphasic medium was reported for the reduction of the hydroxyl group and various unsaturated groups such as CC, CC, CN and CO. Using the same catalytic system, reductive N-formylation of nitroarenes with formic acid was explored to produce the corresponding amide in high selectivity. Moreover, the catalyst stability was evaluated and reaction mechanisms were studied and proposed for the three model reactions.
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MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Zhen Zhang,You Wang,Xueqi Li,Xinran Wu,Yunyi Hu,Rong An,Ling Xu,Xiangdong Qing
In the contribution, a novel chemometric coupling technique combined with high-performance liquid chromatography with diode array detector (HPLC-DAD) was developed for the rapid quantification and source apportionment of eight monoaromatic hydrocarbons (MACHs) in soil samples. The strategy was built on the three-dimensional calibration based on alternating trilinear decomposition coupling with the unsupervised classification using t-distributed stochastic neighbor embedding (named ATLD-t-SNE). Firstly, a validation set and a spiked soil set were used to investigate the quantitative performance of the developed method. The obtained average recoveries of eight MACHs in soil samples were between (95.0 ± 4.4)% and (111.9 ± 3.3)%, and the limits of detection ranged from 0.0041μg mL −1 to 1.85 μg mL −1 , which were better than the results of parallel factor analysis-alternating least squares (PARAFAC-ALS). Subsequently, the proposed approach was applied to analyze actual soil samples collected from tea plantations (7 samples) and industrial areas (60 samples), revealing the presence of ethylbenzene (EBZ) and (1,3,5)-trimethylbenzene (MTY) in both types of soil samples, could the absence of other six MACHs. Finally, ATLD-t-SNE was utilized to classify these soil samples and a comparison between the new strategy and ATLD combined with feature component analysis as well as principal component analysis (called ATLD-FCA and ATLD-PCA, respectively) was made. The finding indicated that ATLD-t-SNE provided better clustering than other two methods, indicating different sources of organic pollution of MACHs in soil samples.
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JOURNAL OF CHROMATOGRAPHY A
·
2024
·
IF 3.8
Hu Meng,Yuyu Wei,Liang Feng
In this work, a microchip gas chromatography (GC) column assembly utilizing a three-dimensional (3D) printed micro oven and a flexible stainless steel capillary column was developed. The assembly's performance and separation capabilities were characterized. The key components include a 3D printed aluminum plate (7.50 × 7.50 × 0.16 cm) with a 3-meter-long circular spiral channel, serving as the oven, and the column coiled on the channel with an inner diameter of 320 μm and a stationary phase of OV-1. A heating ceramic plate was affixed on the opposite side of the plate. The assembly weighed 40.3 g. The design allows for easy disassembly, or stacking of heating devices and columns, enabling flexibility in adjusting column length. When using n -C 13 as the test analyte at 140 °C, a retention factor ( k ) was 8.5, and 7797 plates (2599 plates/m) were obtained. The assembly, employing resistance heating, demonstrated effective separation performance for samples containing alkanes, aromatics, alcohols and ketones, with good reproducibility. The reduction in theoretical plates compared to oven heating was only 2.95 %. In the boiling point range of C 6 to C 18 , rapid temperature programming (120 °C/min) was achieved with a power consumption of 119.512 W. The assembly was successfully employed to separate benzene series compounds, gasoline and volatile organic compounds (VOCs), demonstrating excellent separation performance. This innovative design addresses the challenges of the complexity and low repeatability of the fabrication process and the high cost associated with microchip columns. Furthermore, its versatility makes it suitable for outdoor analysis applications.
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CRYSTAL GROWTH & DESIGN
·
2024
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IF 3.2
Liguo Gao,Ke Zeng,Ye Jia,Lingxue Kong,Anmin Liu,Tingli Ma,Junjiang Bao
The epitaxial growth of heterojunctions can reduce interface defects and enhance the stability of the crystal structures. However, a higher lattice mismatch can cause local lattice distortions at the interface, resulting in relaxed strains that eventually evolve into structural defects. Herein, a nearly zero-mismatch semicoherent interface was formed with a lattice mismatch (0.3%) by epitaxial growth CsPbBr3 on CdS quantum dots (QDs), leading to a strain-free semicoherent interface. Results demonstrated that CdS/CsPbBr3 heteronanocrystals (HNCs) had excellent stability and high photocatalytic performance compared with CsPbBr3. Theoretical calculations show that the Br–Cd bond forms strong electron coupling, which not only facilitates rapid electron transfer but also provides better structural stability. Compared to the individual CsPbBr3 nanocrystals (NCs), the CdS/CsPbBr3 HNCs exhibited higher stability and 2.1 times higher photocatalytic activity. It suggests that CdS/CsPbBr3 HNCs have potential application value in energy and environmental fields.
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CATALYSIS SURVEYS FROM ASIA
·
2024
·
IF 2.1
Zhou Hantao,Feng Shangzhen,Yang Jie,Jiang Huanjin,Zhang Xing,Chen Jixiang
Zeolites (Hβ, HZSM-5 and HM), TiO 2 and ZrO 2 supported NiCo alloy catalysts were tested for the hydrodeoxygenation of phenol in aqueous phase. It has been found that the catalyst acidity remarkably influences the catalyst activity and the product distribution. Zeolites supported catalysts give much higher yield of the deoxygenated products (mainly benzene and cyclohexane) than NiCo/TiO 2 and NiCo/ZrO 2 , where cyclohexanol and cyclohexanone are dominating. Associated with NH 3 -TPD, we suggest that the catalyst acidity promotes the hydrodeoxygenation. Hβ zeolite supported NiCo alloy is more active than others, attributed to its higher metal dispersion and more acid sites. Therein, the Hβ zeolite calcined at 750 o C has moderate acidity, and its supported NiCo alloy catalyst (NiCo/HB-750) shows the best performance. Under a suitable reaction condition, the phenol conversion and the total yield of deoxygenated products reaches 96.8% and 94.5% on NiCo/HB-750, respectively.
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TALANTA
·
2017
·
IF 4.162
Pingxiu Tang,Zilin Chen
Hypercrosslinked polymers (HCPs) are currently receiving great attention due to their unique characteristics and potential uses in diverse areas. However, the field of HCPs for open-tubular capillary electrochromatography (OT-CEC) separations has not been explored. Here, a knitted aromatic polymer (KAP) was in-situ grown on the inner wall of the capillary column for OT-CEC for the first time. The silylating reagent containing phenyl was served as monomer , immobilized on the inner wall of the capillary column, and then KAPs-modified capillary column was prepared through in-situ hypercrosslinking reaction. The surface structure and morphology of KAPs-modified capillary column was characterized by Fourier transform infrared spectra (FT-IR) and scanning electron microscopy (SEM). The prepared capillary columns showed good separation performance for neutral compounds, small biomolecules, such as nucleosides , amino acids , small peptides, and non-steroidal anti-inflammatory drugs, sulfa drugs. In addition, the KAPs-modified capillaries showed good reproducibility, with relative standard deviations for intra-day, inter-day and column-to-column runs less than 1.59%, 2.55%, and 5.19% respectively. The strategy of in-situ immobilization of KAPs provides a new approach for the application of the material in the analytical fields.
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JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY
·
2024
·Vol. 149
·期 10
·4491-4503
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IF 3
Chen Yongjia,Zhao Yilin,Hua Min,Pan Xuhai,Jiang Huichun,Jiang Juncheng
We investigated the inhibition of thermal runaway of styrene polymerization by DNPB. DNBP is an inhibitor in styrene polymerization reaction. Polymerization is one of eighteen hazardous processes. Styrene polymerization reaction is characterized by high heat production and fast reaction rate. Firstly, differential scanning calorimetry (DSC) and adiabatic calorimetry (ARC) were chosen to study the effect of different mass of DNBP on thermal behavior in non-isothermal and adiabatic environments. Secondly, exploring the inhibitory effect of DNBP at different runaway temperatures using an oil bath reactor. The results showed that when DNBP was at 0.80%, effective inhibition was obtained at different runaway temperatures. Finally, GC/MS and Gauss16 were used to infer the mechanism of inhibition in terms of macroscopic products and microscopic instabilities. The results showed that the products of the oil bath reactor experiments were related to the mass of DNBP, and when DNBP was 0.80%, the products increased and the main reaction was inhibited. Finally, it was deduced that the nitro group undergoes a possible path of direct addition reaction with the styrene radical before bond breaking.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
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IF 8.1
Yang Wang,Lina Zhou,Hui Li,Hailong Zhu,Teng Zhang,Menglun Yin,Qiuyue Xiang,Chen Hou
The photocatalytic (PC) degradation process of volatile organic compounds (VOCs) has been consistently restricted by the rapid recombination of photogenerated electrons and holes. To solve this problem, in this study, a novel photoelectrocatalytic (PEC) coupled system was constructed by integrating a single-chamber direct glucose fuel cell (SDGFC), which is capable of self-generating electricity, into the conventional PC system. The coupling system can inhibit the recombination of photogenerated electrons and holes by continuously generating a current without an applied power source. In addition, nitrogen-doped carbon quantum dots (N-CQDs) were prepared using biomass gelatin. This was employed as a PC material for the catalytic layer of the air cathode in the above coupling system, and the efficient degradation of benzene series (BTEX) was made easy by regulating the content of the N element. Notably, the N-CQDs under the optimal regulation ratio showed excellent optical properties and degradation performance, achieving an impressive PEC degradation rate of over 80 % for BTEX within 180 min. High-performance N-CQDs complement the novel PEC coupling system of self-generating electricity and provide robust support for BTEX degradation.
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ACS Applied Nano Materials
·
2024
·
IF 5.3
Qianchun Zhang,Yuxian Zhao,Zhaoru Ban,Li Jiang,Shan Tang
Cataluminescence (CTL) sensors are among the most simple, inexpensive, sensitive, and selective tools for gas sensing. This study presented a highly efficient and selective CTL sensor system based on mesoporous SiO2 nanomicrospheres for the quick and sensitive analysis of isobutyraldehyde. Furthermore, its response intensity was 12.7 times higher than that of a nonmesoporous SiO2-based sensor. The constructed CTL sensor exhibited a good linear range (R2 = 0.997) for detecting isobutyraldehyde, spanning 3.11–311 ppm, with a low detection limit of 1.1 ppm. This enabled successful analysis of trace isobutyraldehyde in real samples. Finally, the CTL mechanism of this sensor was further explored. This study presents an approach for the quality detection of an important volatile organic compound, isobutyraldehyde, by a mesoporous-based CTL sensor.
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JOURNAL OF CHROMATOGRAPHY A
·
2025
·
IF 4
Zhipeng Zhu,Min Zhang,Xiaohui Yan,Chenglong Shi,Bin Wang,Yanshuo Li,Dapeng Wu
A crosslinked polystyrene-divinylbenzene (PS-DVB) stationary phase was prepared onto silica gel with the pore size of 100 Å and 300 Å (SiL-PSD-10, SiL-PSD-30) by surface-initiated atom transfer radical polymerization (ATRP) for high performance liquid chromatography (HPLC) separation of alkylbenzenes, fullerites, and proteins, respectively. The SiL-PSD coating and the pore size distribution were characterized by FT-IR, TGA, and nitrogen adsorption-desorption isotherms. The crosslinking degree within stationary phase was determined in good consistency with the feeding ratio, as confirmed by RP-HPLC. It was found the SiL-PSD-10 particles could resist the harsh etching of 0.1 M NaOH for at least 6 h, while bare silica was totally dissolved and commercial C18 silica was partially dissolved under the same conditions. Under alkaline conditions (pH 11), the column bleeding rates of SiL-PSD-10 were reduced by 83 % and 96.0 % respectively compared to commercial C18 column and bare silica. Under accelerated aging conditions, SiL-PSD-10 maintained over 94 % of its initial column efficiency after exposure to 16,000 column volume of mobile phase. On SiL-PSD columns, alkylbenzenes could be separated in reversed-phase mode, and fullerite (C 60 /C 70 ) could be baseline resolved within 2 min with benzene as the mobile phase. During the continuous monitoring for 70 h, RSDs of the retention times of proteins were between 0.49 % and 1.19 %. Generally, SiL-PSD had been demonstrated to combine the excellent mechanical strength and uniform porosity of silica gel with the outstanding chemical resistance of PS-DVB, and could be used for HPLC separation across a wider pH.
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2025
·
IF 3.8
Yang Ruilin,Wang Ping,Guan Xinhui,Gu Xiaofei,Qiao Xiaoqiang
Phospholipids have been considered biomarkers for diagnosing many diseases in recent years. However, the isolation and analysis of phospholipids still face many difficulties. Styrene-maleic acid (SMA) copolymer is currently considered suitable for the separation and analysis of phospholipids due to its ability to enhance and improve the solubility of phospholipid bilayers on cell membranes. In this work, metal-free atom transfer radical polymerization was first exploited to graft SMA copolymer onto the surface of silica gel. With glycerol monolaurate (GML) as the derivatization reagent, Sil-SMA-GML polymer-brush silica-based stationary phase was first developed. The chromatographic retention mechanism revealed that the Sil-SMA-GML column is of hydrophilic/reversed-phase mixed-mode retention modes. The chromatographic separation performance evaluation indicated that the Sil-SMA-GML column had excellent separation capabilities for both hydrophilic and hydrophobic compounds. The maximum column efficiency was up to 78,600 N/m. The Sil-SMA-GML column could also achieve simultaneous separation and analysis of different phospholipid classes and species as well as complex phospholipid extracts from human serum and exosomal phospholipid extracts, demonstrating the good potential of the developed stationary phase. Graphical
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GREEN CHEMISTRY
·
2025
·
IF 9.2
Xinjun He,Mengqiao Gao,Fukun Li,Zhiyang Tang,Jie Qu,Jinxing Long,Qiang Zeng,Xuehui Li
Catalytic hydrogenolysis of lignin has attracted steady attentions in regard of producing high-value aromatic chemicals from the renewable resource and achieving the “carbon neutrality” goal. However, current techniques for lignin hydrogenolysis are highly challengeable due to the necessity of pure H2 and relatively low yields in monomers. In this work, a novel and efficient approach has been proposed for the conversion of lignin to monophenols under readily available and cost-effective syngas. The results demonstrated that CO has the dramatic promotion on the bagasse lignin hydrogenolysis over commercialized Pd/C at 230 °C for 4 h, the yield of monophenols reaches 357.2 mg/g at 3.0 MPa syngas (CO/H2=2/1), which is approximately 1.7 times of that under pure H2. As evidenced by quantitative 31P NMR analysis, the promoting effects of CO on lignin depolymerization are positively correlated with the content of side-chain hydroxyl groups in lignin. Further investigations on lignin model conversion reveal that CO suppresses the dehydroxylation at Cα-OH, with concomitant enhancement of Cβ-O bond cleavage (increasing from 10% in H₂ to 64% in syngas). This inhibitory effect on side-chain hydroxyls elimination directly correlates with the 1.7-fold increase of monophenol yields observed during catalytic depolymerization. Therefore, this work provides a new insight in lignin depolymerization using industrial catalyst of Pd/C and the cost-effective syngas.
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