文献检索

查找使用阿拉丁产品的科研文献

检索与阿拉丁产品相关的同行评审论文、DOI、PubMed 编号、期刊、作者、CAS 号及研究领域。

科研影响力快照

与阿拉丁产品相关的已发表科研成果

在搜索之前,这些指标可帮助访客快速了解产品关联科研的规模与质量。

346,364+ SCI 论文 与阿拉丁产品引用相关
2,295,288.15 总影响因子 匹配文献记录中影响因子的总和
81.20 最高期刊影响因子 匹配期刊中的最高 IF
6.63 平均期刊影响因子 匹配文献的平均 IF

参考指标 指标基于阿拉丁文献引用数据库及期刊影响因子记录。文献关联仅供科研参考,请以原始文献为准。

热门产品

视图 列表 网格

显示第13至21个,产品总数21个

设置提升方向
Raney Ni
CATALYSIS COMMUNICATIONS · 2016 · IF 3.389

Effect of zeolite solid acids on the in situ hydrogenation of bio-derived phenol

Yanhong Huang,Shuqian Xia,Peisheng Ma

The effect of zeolite solid acids on the in situ hydrogenation of bio-derived phenol over Raney Ni was investigated, which indicated that the conversion of phenol increased with the addition of zeolite solid acids and Hbeta (Si/Al   =   60) showed the best performance of high phenol conversion and selectivity towards the desired products and low carbon loss. In addition, the quantity of Hbeta (Si/Al   =   60) and Raney Ni had marked impact on the carbon loss, but little effect on both the conversion and the products distribution. And the mixed catalysts of Raney Ni and Hbeta (Si/Al   =   60) exhibited excellent stability.

研究领域: 化学工程 · 催化反应
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Advanced Science · 2025 · IF 14.1

Tunable Transfer-Hydrodeoxygenated Upgrading of Lignin-Derived Propylphenols to Versatile Value-Added Alkane-Based Chemicals

Yanyan Yu,Yilin Li,Yuhan Lou,Mengyuan Chen,Yongzhuang Liu,Haipeng Yu

Catalytic refining of lignin holds promise for producing sustainable platform chemicals. In this work, a gaseous hydrogen-free catalytic hydrodeoxygenation system is developed for upgrading lignin-derived phenols to alkane chemicals. Commercially available Raney Ni and HZSM-5 are used as a combinational catalyst, with isopropanol serving as the hydrogen-donating solvent. By modifying the temperature and the ratio of Raney Ni to HZSM-5, the reaction pathways for hydrogenation and deoxygenation can be tailored to specific requirements. As a result, a 97.1% yield of alkane fuels is achieved, with 64.4% propylcyclohexane and 32.7% propylbenzene obtained in one-pot reaction from the hydrodeoxygenation of 2-methoxy-4-propylphenol using a 3:1 mass ratio of Ni to HZSM-5, further increasing the ratio of HZSM-5 leads to a selectively production of propylbenzene in 62.0% yield. Through careful regulation of the catalytic system and the design of hydrogenation–deoxygenation pathways, excellent yields of 4-propylcyclohexanol (92.2%), propylcyclohexene (93.3%), and propylcyclohexane (93.2%) are directionally achieved. The catalyst maintained a conversion rate of over 99% after five cycles, demonstrating excellent robustness. This study offers a strategic system that expedites the selective upgrading of lignin-derived chemicals, heralding a pathway toward sustainable fuels and chemicals.

研究领域: 化学工程 · 可再生能源 · 催化科学
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS · 2016 · IF 3.652

Structural characterization and pyrolysis behavior of holocellulose obtained from lignin-first biorefinery

Yalun Hu,Isaac Nartey Oduro,Yong Huang,Yunming Fang

The structural characteristics and pyrolysis behaviors of two holocelluloses obtained from lignin-first biorefinery with Ru/C or Raney Ni as catalysts were studied in this paper. The infrared spectra of the remaining solid from the lignin-first biorefinery show that both lignin and a portion of hemicellulose were decomposed. Compared with Ru/C, Raney Ni was more effective for delignification and gave a holocellulose with higher degree of crystallinity, based on both the ratio of infrared bands (1372   cm −1 /2900   cm −1 ) and XRD analysis. The pyrolyses of holocelluloses were performed in fixed-bed and free-falling reactors, and the resulting char yields from both reactors were significantly higher than those of the parent biomass and commercial cellulose. This resulted from the cleavage of cellulose chain during the lignin-first biorefinery. Raney Ni related biorefinery cleaved cellulose chain to a higher degree.

研究领域: 生物化学 · 能源科学 · 材料科学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
AICHE JOURNAL · 2023 ·Vol. 69 ·期 7 ·e18056 · IF 3.7

Maltose hydrogenation to maltitol over industrial Raney Ni catalyst: Kinetics and mechanism

Haoan Fan,Bolong Li,Xuezhi Zhao,Zhecheng Fang,Chao Chen,Wenhua Zhou,Wulong Yang,Mian Li,Xiuyang Lu,Jie Fu

The kinetics and mechanisms of selective maltose hydrogenation over Raney Ni remain poorly understood, which hinders the industrial advancement of maltitol production for biorefining. Herein, the impact of hydrogenation conditions and in-depth mechanistic characterizations were carefully investigated in this research. Optimization of reaction conditions illustrated that maltitol formation was favored by moderate reaction temperatures (≤130°C), high hydrogen pressures (>7 MPa), and near-neutral sodium phosphate buffer (pH = 6.47). Kinetic studies demonstrated the E a of 45.5 kJ/mol for the hydrogenation of maltose. The in situ IR revealed that the hydrogenation of maltose over Raney Ni occurs in the order of ring opening and adsorption via CO of the aldose form followed by hydrogenation. The UV–vis spectra demonstrated the near-neutral setting (pH = 6.47) promoted the production of open-chain aldose conformation and selective CO hydrogenation to the corresponding alcohols. The present study on concentrated-maltose hydrogenation paves the way for the industrial development of maltitol manufacturing.

研究领域: 化学工程 · 催化 · 生物化工
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Green Processing and Synthesis · 2017 ·Vol. 6 ·期 4 ·363-370 · IF 0.782

Two-step hydrogen transfer catalysis conversion of lignin to valuable small molecular compounds

Zhihao Li,Zhihao Bi,Lifeng Yan

As the major composite of biomass, lignin can be utilized as feedstock for valuable chemicals, especially phenols. Catalysis hydrogenation of lignin is an attractive route for the conversion. However, most of them require hydrogen gas under high pressure which is dangerous. Hydrogen transfer reaction provides an alternative route to degrade and hydrogenate lignin or its units to small molecular compounds. Here, a two-step method has been employed using Raney Ni and Pd/C catalysts consecutively for hydrogen transfer catalysis for lignin. The results reveal that lignin can be degraded efficiently about 90% during conversion, and the major products are phenols with ~30% in yield. It provides a new green method for converting natural lignin to valuable chemicals.

研究领域: 生物质化学 · 催化化学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
CHEMICAL COMMUNICATIONS · 2013 ·Vol. 49 ·期 46 ·5328-5330 · IF 6.378

RANEY® Ni catalyzed transfer hydrogenation of levulinate esters to γ-valerolactone at room temperature

Zhen Yang,Yao-Bing Huang,Qing-Xiang Guo,Yao Fu

A catalytic transfer hydrogenation process was developed for the production of γ-valerolactone (GVL) from ethyl levulinate (EL) and a H-donor at room temperature. Ethyl levulinate was almost quantitatively converted to γ-valerolactone. Further, a two step process for producing GVL from biomass derived platform molecules was also reported.

研究领域: 化学工程 · 可再生能源
✓ 已验证 DOI PubMed 高影响因子
查看原文 查看 PubMed
JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

An efficient reduction of unsaturated bonds and halogen-containing groups by nascent hydrogen over Raney Ni catalyst

Weilai Wang,Junfeng Niu,Zhifeng Yang

Presence of unsaturated bonds and halogen-containing groups is the most common characteristic of toxic and harmful environmental pollutants. Herein, catalytic hydrogenation was chosen as a water quality control method for such contaminants. Considering the safety, availability and activity of the hydrogen source, electrochemical in situ hydrogen generation was introduced. Under the combined action of Raney Ni (R-Ni) and nascent hydrogen (Nas-H 2 ), three compounds (50 mg L −1 , 90 ml), i.e., acrylamide, 2, 6-dibromo-4-nitrophenol and 2-chloro-4-fluorobenzonitrile achieved complete hydrogenation reduction in a short time. The improved system realized the quantitative consumption of hydrogen source and the efficient operation of hydrogenation reaction under mild conditions. Additionally, the alkaline environment formed by hydrogen evolution reaction (HER) avoided secondary pollution caused by catalyst dissolution. Atomic hydrogen (H·) produced from R-Ni and Nas-H 2 was the active free radical of the reaction. The hydrogenation activities of different functional groups were obtained according to the following order: Ph-NO 2 > -C = C- > Ph-C≡N > Ph-Br > Ph-Cl > Ph-F. This work indicates that the catalytic hydrogenation system consisting of R-Ni and Nas-H 2 is a promising technology to reduce unsaturated bonds and halogen-containing groups.

CAS / MDL: 64-18-6
研究领域: 环境科学 · 化学工程 · 催化 · 水处理
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
ACS Sustainable Chemistry & Engineering · 2023 · IF 8.4

Highly Efficient Alkaline Water Electrolysis Using Alkanolamine-Functionalized Zirconia-Blended Separators

Xiaomei Yuan,Tao Yan,Zhikun Liu,Peng Kang

Alkaline water electrolysis is one of the most promising technologies for green hydrogen production. Here, we synthesized a series of alkanolamine-modified zirconia particles by a one-pot method to construct zirconia-based composite membranes for alkaline water electrolysis. Among these membranes, the diethanolamine (DEA)-functionalized zirconia separator exhibits superior hydrophilicity with a low water contact angle of 44° and low area resistance of 0.12 Ω·cm2, which were 47 and 60%, respectively, less than that of the commercial Zirfon PERL UTP 500 separator. Conceivably, the DEA-functionalized zirconia separator presents high electrochemical performance with a current density of 1114 mA cm–2 at 2.0 V with Raney Ni as the cathode catalyst and CoMnO@CoFe layered double hydroxide (LDH) as the anode catalyst at 80 °C, closing the gap with proton exchange membrane electrolysis. In addition, the DEA-modified separator exhibits high stability for over 150 h at a high current density of 500 mA cm–2 and stable cell voltages in 30 wt % KOH at 80 °C.

研究领域: 材料科学 · 电化学 · 可再生能源
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Green Energy & Environment · 2024 · IF 10.7

Atmospheric reductive catalytic fractionation of lignocellulose integrated with one-pot catalytic conversion of carbohydrate yielding valuable lignin monomers and platform chemicals from corn straw

Meng-Ying Liu,Zhe-Hui Zhang,Xue-Qi Wang,Qian Sun,Chen Zhang,Yu Li,Zhuohua Sun,Katalin Barta,Feng Peng,Tong-Qi Yuan

Developing a cost-effective and environmentally friendly process for the production of valuable chemicals from abundant herbal biomass receives great attentions in recent years. Herein, taking advantage of the “lignin first” strategy, corn straw is converted to valuable chemicals including lignin monomers, furfural and 5-methoxymethylfurfural via a two steps process. The key of this research lies in the development of a green and low-cost catalytic process utilizing magnetic Raney Ni catalyst and high boiling point ethylene glycol. The utilization of neat ethylene glycol as the sole slovent under atmospheric conditions obviates the need for additional additives, thereby facilitating the entire process to be conducted in glass flasks and rendering it highly convenient for scaling up. In the initial step, depolymerization of corn straw lignin resulted in a monomer yield of 18.1 wt%. Subsequently, in a dimethyl carbonate system, the carbohydrate component underwent complete conversion in a one-pot process, yielding furfural and 5-methoxymethylfurfural as the primary products with an impressive yield of 47.7 %.

研究领域: 化学工程 · 生物质转化 · 催化 · 可再生能源
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
已复制

文献关联基于可获得的产品、CAS、DOI 及引用记录。收录不代表作者或出版方对阿拉丁产品的背书,请以原始文献为准。