基于酸和烯酸聚合物的水凝对胀性质的结构影响
Grzegorz Kowalski1, Mariusz Witczak1, Łukasz Kuterasiński2
1Department of Engineering and Machinery for Food Industry, Faculty of Food Technology, University of Agriculture in Kraków, ul. Balicka 122, 30-149 Kraków, Poland.
Molecules (Basel, Switzerland)
|May 11, 2024
概括
这项研究开发了具有高吸水能力的耐用基酸盐 (SA) 水凝. 这些基于SA的水凝表现出与合成聚合物相当的性能,提供了一个有前途的生物材料替代品.
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
- 生物材料工程 生物材料工程
背景情况:
- 水凝在各种应用中至关重要,但通常依赖于合成聚合物.
- 从天然生物聚合物,如藻酸盐 (SA) 开发水凝,提供生物相容性和可持续性.
- 研究基于SA的水凝的合成和特性对于推进生物材料应用至关重要.
研究的目的:
- 使用藻酸盐 (SA) 和部分中和的聚烯酸合成和表征新型水凝.
- 调查交叉链接剂 (N,N'-甲基二甲胺,MBA) 和SA度对水凝特性的影响.
- 评估开发的基于SA的水凝的吸水能力和结构完整性.
主要方法:
- 使用激素聚合来合成水凝,与N,N'-甲基二甲胺 (MBA) 进行交叉链接.
- 里埃变换红外光谱 (FTIR) 证实了成功的合成和化学结合.
- 不同扫描热量计 (DSC) 分析了由于交叉连接而产生的热性质和结构变化.
主要成果:
- FTIR证实了SA.上聚酸的有效合成和化学接种.
- DSC的分析表明,在交叉连接后,水凝网络的结构修改.
- 含有高SA含量的水凝 (高达33%重量) 具有出色的耐用性,稳定性和高吸水率 (350g·g-1),与合成水凝相比.
- 随着MBA度的增加,水的膨胀能力下降,但随着SA含量增加,水的膨胀率仍然很高.
结论:
- 该研究成功合成了具有显著吸水能力的基于SA的强大的水凝.
- 这些发现突出了使用高度的SA来制造稳定,高性能水凝的潜力.
- 这些基于SA的水凝为各种应用提供了与纯合成水凝的可行,可能更可持续的替代方案.
相关概念视频
Acid Strength and Molecular Structure
Binary Acids and Bases
In the absence of any leveling effect, the acid strength of binary compounds of hydrogen with nonmetals (A) increases as the H-A bond strength decreases down a group in the periodic table. For group 17, the order of increasing acidity is HF < HCl < HBr < HI. Likewise, for group 16, the order of increasing acid strength is H2O < H2S < H2Se < H2Te. Across a row in the periodic table, the acid strength of binary hydrogen compounds increases with increasing...
In the absence of any leveling effect, the acid strength of binary compounds of hydrogen with nonmetals (A) increases as the H-A bond strength decreases down a group in the periodic table. For group 17, the order of increasing acidity is HF < HCl < HBr < HI. Likewise, for group 16, the order of increasing acid strength is H2O < H2S < H2Se < H2Te. Across a row in the periodic table, the acid strength of binary hydrogen compounds increases with increasing...
Molecular Structure and Acidity
An acid can be deprotonated to form a conjugate base or an anion. If the produced anion is more stable, then the acid is stronger. On the contrary, if the anion is unstable, then the acid is weaker. Hence, to determine the acidity of the compound, the stability of its conjugate base is studied using various factors.
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
Leveling Effect and Non-Aqueous Acid-Base Solutions
This lesson defines the leveling effect in acidic and basic solutions and its role in aqueous and non-aqueous solutions. It is essential to understand the competing nature of various species in a chemical system.
The Leveling Effect of a Solvent
A generic acid (HA) reacts with the generic base (B-) to yield the corresponding conjugate base (A-) and conjugate acid (HB):
The Leveling Effect of a Solvent
A generic acid (HA) reacts with the generic base (B-) to yield the corresponding conjugate base (A-) and conjugate acid (HB):
Structures of Carboxylic Acid Derivatives
Structure of Carboxylic Acid Derivatives
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the unhybridized p...
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the unhybridized p...
Basicity of Aliphatic Amines
Amines can behave as Brønsted–Lowry bases by accepting a proton from the acid to form corresponding conjugate acids. Due to a lone pair of nonbonding electrons, aliphatic amines can also act as Lewis bases by forming a covalent bond with an electrophile.
To measure the basicity of amines, two conventions are generally used. The first defines Kb as the basicity constant for the deprotonation reaction of water by the amine, as presented in Figure 1. Conventionally, lower Kb indicates higher...
To measure the basicity of amines, two conventions are generally used. The first defines Kb as the basicity constant for the deprotonation reaction of water by the amine, as presented in Figure 1. Conventionally, lower Kb indicates higher...
Physical Properties of Carboxylic Acids
Carboxylic acids with lower molecular weight exhibit a sharp and unpleasant odor. They also have higher boiling and melting points than analogous compounds, such as aldehydes, ketones, and alcohols.


