相关实验视频
Updated: Jun 23, 2025

08:13
Preparation of Biopolymer Aerogels Using Green Solvents
Published on: July 4, 2016
17.7K
从基极聚合物中获得的乙烯基聚合物的疏水性气凝:概念验证
Claudia Adolfs1, Razan Altarabeen2, Leon Kimmritz1
1TU Clausthal, Arnold-Sommerfeld-Str. 4, 38678, Clausthal-Zellerfeld, Germany.
Macromolecular rapid communications
|June 14, 2024
概括
研究人员通过修改甲基酸单体,开发出防水生物基气凝. 瓦尼林基组创造了疏水性气凝,克服了生物基材料的一个关键局限性.
科学领域:
- 材料科学 材料科学 材料科学
- 聚合物化学 聚合物化学
- 纳米技术 纳米技术
背景情况:
- 生物基气凝经常表现出水友性,限制了它们的应用.
- 开发疏水替代品对于扩大这些可持续材料的实用性至关重要.
研究的目的:
- 为了合成新型,防水,半孔生物基气凝.
- 研究甲基酸单体中不同非极性基对气凝性质的影响.
- 为了实现生物基气凝的内在疏水性.
主要方法:
- 通过甲基酸共聚合物合成交联的生物基共聚合物.
- 用于制造气凝的溶剂交换和超临界干燥.
- 纹理特性 (孔径,密度,表面积) 和水接触角度的表征.
主要成果:
- 气凝呈现出高孔隙度 (~96%) 和低密度 (0.07-0.11 g cm−3).
- 具体的表面积在120-240 m2 g-1之间,具有半孔网络.
- 含氨酸基组的气凝显示稳定的疏水接触角度 (~100°),而其他气凝则吸收水.
结论:
- 甲基酸乙烯基组的选择显著影响了气凝孔结构和疏水性.
- 建立了一条新的途径,使生物基气凝具有固有的疏水性.
- 单体结构量身定制使得生物基气凝特性能够针对特定应用进行优化.
相关概念视频
Free-Radical Chain Reaction and Polymerization of Alkenes
7.8K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
7.8K
Anionic Chain-Growth Polymerization: Overview
2.1K
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
2.1K
Radical Chain-Growth Polymerization: Mechanism
2.5K
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this...
2.5K
Ziegler–Natta Chain-Growth Polymerization: Overview
3.3K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.3K
Radical Chain-Growth Polymerization: Chain Branching
1.9K
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
1.9K
Anionic Chain-Growth Polymerization: Mechanism
2.0K
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
2.0K

