对聚氨材料的反应性阻燃剂进行全面审查:当前的发展和未来的环境友好方向的机会
Paulina Parcheta-Szwindowska1, Julia Habaj1, Izabela Krzemińska1
1Department of Polymer Technology, Faculty of Chemistry, Gdańsk University of Technology, G. Narutowicza St. 11/12, 80-233 Gdańsk, Poland.
International journal of molecular sciences
|May 25, 2024
概括
这项研究比较了用于减少聚氨燃烧负载的反应性阻燃剂. 反应性阻燃剂提供优越的耐火性,没有迁移问题,与传统的添加剂不同.
科学领域:
- 聚合物科学 聚合物科学
- 材料科学 材料科学 材料科学
- 消防安全工程 消防安全工程
背景情况:
- 聚氨是建筑中的重要聚合物,需要增强的耐火性.
- 目前的阻燃剂方法包括添加剂和反应性阻燃剂.
- 添加剂阻燃剂可以迁移或挥发,损害材料性能.
研究的目的:
- 为了比较不同反应性阻燃剂在聚氨中的有效性.
- 分析这些阻燃剂对阻燃性和燃烧机制的影响.
- 评估使用反应性阻燃剂对环境的影响.
主要方法:
- 在聚氨加工过程中研究反应性阻燃剂.
- 通过燃烧试验分析阻燃性能.
- 评估环境影响和物质性质变化.
主要成果:
- 反应性阻燃剂与单体化学结合,防止迁移.
- 在具有反应性阻燃剂的聚氨中证明了提高阻燃性.
- 在减速剂中确定了燃烧机制和环境特征的差异.
结论:
- 反应性阻燃剂是提高聚氨消防安全的有希望的解决方案.
- 化学结合防止了添加物迁移,保持了材料的完整性和美学.
- 对特定反应性阻燃剂的进一步研究可以优化消防性能和环境可持续性.
相关概念视频
Types of Step-Growth Polymers: Polyesters
2.2K
The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
2.2K
Radical Chain-Growth Polymerization: Overview
2.4K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
2.4K
Polymer Classification: Architecture
2.7K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
2.7K
Step-Growth Polymerization: Overview
3.4K
Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
Many natural and synthetic polymers are produced by...
3.4K
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
Polymer Classification: Stereospecificity
2.4K
Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
2.4K


