纺织学报 ›› 2026, Vol. 47 ›› Issue (03): 225-232.doi: 10.13475/j.fzxb.20251004201

• 功能性纺织品 • 上一篇    下一篇

竹浆纤维的抑菌性及其抑菌成分研究

田俊莹1,2, 程有旗1, 何天虹1,2(), 姚金波1, 李振峰3, 武松亮3   

  1. 1 天津工业大学 纺织科学与工程学院, 天津 300387
    2 天津工业大学 先进纺织复合材料教育部重点实验室, 天津 300387
    3 河北吉藁化纤有限责任公司, 河北 石家庄 052160
  • 收稿日期:2025-10-21 修回日期:2026-01-28 出版日期:2026-03-15 发布日期:2026-03-15
  • 通讯作者: 何天虹(1973—),女,副教授,博士。主要研究方向为功能服装材料。E-mail:hetianhong@tiangong.edu.cn
  • 作者简介:田俊莹(1968—),女,副教授,博士。主要研究方向为绿色染整技术及功能纺织品。

Study on antibacterial properties and antibacterial components of bamboo pulp fibers

TIAN Junying1,2, CHENG Youqi1, HE Tianhong1,2(), YAO Jinbo1, LI Zhenfeng3, WU Songliang3   

  1. 1 School of Textile Science and Engineering, Tiangong University, Tianjin 300387, China
    2 Key Laboratory for Advanced Textile Composite Materials (Ministry of Education), Tiangong University,, Tianjin 300387, China
    3 Hebei Jigao Chemical Fiber Co., Ltd., Shijiazhuang, Hebei 052160, China
  • Received:2025-10-21 Revised:2026-01-28 Published:2026-03-15 Online:2026-03-15

摘要:

竹浆纤维具有天然抑菌性,但其抑菌成分至今尚不明确,为揭示竹浆纤维的抑菌性来源,测试分析了竹浆纤维的形态结构、元素和化学基团组成,并尝试采用溶剂萃取、溶解法提取竹浆纤维中的抑菌成分;为更有效地分离竹浆纤维中的抑菌成分,通过硫酸水解的方法将竹浆纤维降解成低分子物质,结合气相色谱-质谱联用技术分离、分析降解产物。结果表明,经溶剂萃取后,竹浆纤维仍保持较好的抑菌性;采用N-甲基吗啉-N-氧化物与碱/尿素体系溶解竹浆纤维,再于非溶剂中沉淀析出再生纤维素,对该再生纤维素进行抑菌性能测试时其菌落生长数量仍低于对照棉,证明部分抑菌成分与纤维素结合紧密;气相色谱-质谱联用分析表明,竹浆纤维水解产物中含有醛类、酚类、酮类等27种化合物,其中糠醇、糠醛、2-十一酮、麦芽酚、2-羟基-4-甲氧基苯甲醛5种化学成分,在相关研究中被证实具有抑菌活性,是竹浆纤维中的主要抑菌成分。

关键词: 竹浆纤维, 抑菌性, 酸水解法, 抑菌成分, 纤维素纤维, 再生纤维素, 气相色谱-质谱联用

Abstract:

Objective Bamboo pulp fibers are a type of regenerated cellulose fiber, produced from bamboo pulp by wet spinning method, and the bamboo pulp is cellulose substance extracted from natural bamboo through a series of chemical processes. Bamboo pulp fibers have excellent properties such as moisture absorption, permeable properties, and good antibacterial properties. However, the antibacterial mechanism of bamboo pulp fibers has not been fully elucidated yet. The objective of this study is to explore the antibacterial activity and functional components of bamboo pulp fibers, thereby establishing a theoretical foundation for the development and practical application of related products.

Method The shaking flask method was employed to determine the antibacterial rate of bamboo pulp fibers. The morphological structure, elemental composition, and chemical group composition of fibers were tested by scanning electron microscopy (SEM), organic elemental analysis and infrared spectroscopy. In order to further seperate antibacterial components in the bamboo pulp fibers, the method of dissolving bamboo pulp fibers with N-methylmorpholine-N-oxide (NMMO) and alkali/urea were used, then cellulose was precipitated in a non-solvent. Finally, the bamboo pulp fibers were degraded by sulfuric acid hydrolysis. A two-step sulfuric acid degradation method was adopted, and bamboo fibers were degraded with a concentrated sulfuric acid solution at low temperature, followed by dilute acid at an elevated temperature. Gas chromatography-mass spectrometry (GC-MS) was adopted to separate and analyze the components in the bamboo pulp fibers.

Results The SEM results showed that uneven grooves and cracks appeared in the surface of bamboo pulp fibers, making the fibers dry, which is unfavorable for bacterial survival and reproduction. Organic elemental analysis results indicated that bamboo pulp fibers are mainly composed of carbon, hydrogen, and oxygen elements, together with 0.20% nitrogen element. The infrared spectroscopy results indicated that bamboo pulp fibers have the characteristic absorption peaks of cellulose. After extraction with solvents such as methanol, ethanol and ethyl acetate, the antibacterial rate of bamboo pulp fibers decreased slightly but remained 70% or above, indicating that the antibacterial components in bamboo pulp fibers were not effectively separated. The regenerated cellulose from bamboo pulp fibers dissolved by NMMO had an antibacterial rate of 48.20% against Escherichia coli, while that dissolved by the alkali/urea system had an antibacterial rate of 67.60% against Escherichia coli, indicating that the antibacterial components in bamboo pulp fibers were not completely isolated, which proved that some antibacterial components were tightly bound to cellulose. The experiments on degradation of bamboo pulp fibers demonstrated that the sugar yield was the highest when the sulfuric acid concentration was 53%. Barium salt was added to remove sulfate ions from the bamboo fiber degradation solution. The GC-MS results analysis indicated that the hydrolysate of bamboo pulp fibers contained 27 compounds including carbohydrates, aldehydes, phenols, ketones and other substances. Among them, 5 chemical components, namely furfuryl alcohol, furfural, 2-undecan-one, maltol, and 2-hydroxy-4-methoxybenzaldehyde, had been confirmed to possess antibacterial activity and are the main antibacterial components in bamboo pulp fibers.

Conclusion The study on the antibacterial activity and antibacterial components of bamboo pulp fibers demonstrated that bamboo pulp fibers exert a stable inhibitory effect on Escherichia coli. The antibacterial activity of bamboo pulp fibers originates from the synergistic effect of multiple antibacterial components and the micromorphological structure. The study on the antibacterial activity and antibacterial components of bamboo pulp fibers provides a theoretical basis for the development of bamboo pulp fiber products.

Key words: bamboo pulp fiber, antibacterial property, sulfuric acid hydrolysis method, antibacterial component, cellulosic fiber, regenerated cellulose, gas chromatography-mass spectrometry

中图分类号: 

  • TS 102.2

图1

溶剂萃取流程图"

图2

棉、竹浆纤维与未接触对照菌落生长情况"

图3

竹浆纤维微观形貌"

图4

竹浆纤维红外光谱图"

表1

不同溶剂提取后竹浆纤维的抑菌率"

编号 溶剂/提取方法 抑菌率/%
1 水/索式提取 71.3
2 无水乙醇/浸提 73.0
3 75%乙醇/索式提取 75.4
4 75%乙醇/混合提取 75.3
5 无水甲醇/浸提 68.7
6 水/超声波提取 80.3

图5

再生纤维素菌落生长情况"

图6

葡萄糖标准曲线"

图7

不同质量分数硫酸水解产物紫外光吸收光谱图"

图8

硫酸质量分数与得糖量关系"

图9

水解产物气质联用总离子流图"

表2

竹浆纤维水解产物的气相色谱-质谱联用分析结果"

序号 保留时间/min 化合物名称 CAS号 分子式 成分类型
1 1.599 N-甲基酪胺 370-98-9 C9H13NO 生物碱
2 1.867 丙酮醛 78-98-8 C3H4O2
3 3.075 N,N-二甲基甲酰胺 68-12-2 C3H7NO 溶剂残留
4 4.916 巴豆醛 123-73-9 C4H6O
5 4.954 2-羟基-2-环戊烯-1-酮 10493-98-8 C5H6O2
6 4.981 糠醛 98-01-1 C5H4O2
7 5.099 糠醇 98-00-0 C5H6O2
8 5.374 2H-吡喃-2-酮 504-31-4 C5H4O2
9 5.734 2(5H)-呋喃酮 497-23-4 C4H4O2 呋喃衍生物
10 5.931 环己酮 108-94-1 C6H10O
11 6.463 5-甲基糠醛 620-02-0 C6H6O2
12 6.565 4-甲氧基-3-丁烯-2-酮 4652-27-1 C5H8O2
13 6.840 2-十一酮 112-12-9 C11H22O
14 7.112 2H-吡喃-2,6(3H)-二酮 5926-95-4 C5H4O3
15 7.692 甲基环戊烯醇酮 80-71-7 C6H8O2
16 8.407 2-羟基吡啶 142-08-5 C5H5NO 吡啶衍生物
17 8.852 2-糠酸甲酯 611-13-2 C6H6O3
18 9.422 麦芽酚 118-71-8 C6H6O3
19 10.168 2,3-二氢-3,5二羟基-6-甲基-4(H)-吡喃-4-酮 28564-83-2 C6H8O4
20 10.591 3-氨基苯酚 591-27-5 C6H7NO
21 10.729 5-甲基-2-乙酰基呋喃 1193-79-9 C7H8O2 呋喃衍生物
22 10.959 (+/-)-β-羟基-γ-丁内酯 5469-16-9 C4H6O3 内酯
23 11.558 5-乙酰氧基甲基-2-呋喃醛 10551-58-3 C8H8O4
24 11.917 5-羟甲基糠醛 67-47-0 C6H6O3
25 14.159 甲基2-脱氧-BETA-D-赤式-吡喃戊糖苷 17676-20-9 C6H12O4 糖苷
26 15.576 2-羟基-4-甲氧基苯甲醛 673-22-3 C8H8O3
27 18.903 1,6-脱水-Β-D-呋喃葡萄糖 7425-74-3 C6H10O5 糖苷
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