{"title":"Thickness and Compression Behavior of a Nonwoven Produced by Melt-Blowing a Polypropylene/Poly(ethylene terephthalate) Fiber Mix","authors":"Ren Tomisawa, Yutaka Ohkoshi, KyoungHou Kim","doi":"10.1007/s12221-024-00643-z","DOIUrl":null,"url":null,"abstract":"<div><p>In the present study, we fabricated nonwoven fabrics by melt-blowing (MB) with mixing polyethylene terephthalate (PET) and polypropylene (PP) fibers on a spinning line to improve the bulkiness and resistance under compression. That is, both PP and PET were simultaneously extruded from three nozzle holes laid down alternately, and they formed fiber state and then entangled each other during the whipping process. We investigated the effects of the MB manufacturing conditions, i.e., the hot air flow rate, the PET fiber fraction, and the presence or absence of annealing, on the compressibility of the obtained nonwovens. The fiber diameter histograms tended to split into two peaks as the PET fiber fraction increased. A larger PET fiber fraction produced a thicker nonwoven. Also, the compressibility increased, but the compression recovery rate did not. Annealing increased the thickness but decreased the compression recovery rate. Although thick fibers were increased by PET fiber mixing, they had insufficient rigid to resist compression. The decrease in the recovery rate can be explained by the brittleness of the PET fibers caused by crystallization of the non-oriented fibers during annealing.</p></div>","PeriodicalId":557,"journal":{"name":"Fibers and Polymers","volume":"25 9","pages":"3539 - 3548"},"PeriodicalIF":2.2000,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fibers and Polymers","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s12221-024-00643-z","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, TEXTILES","Score":null,"Total":0}
引用次数: 0
Abstract
In the present study, we fabricated nonwoven fabrics by melt-blowing (MB) with mixing polyethylene terephthalate (PET) and polypropylene (PP) fibers on a spinning line to improve the bulkiness and resistance under compression. That is, both PP and PET were simultaneously extruded from three nozzle holes laid down alternately, and they formed fiber state and then entangled each other during the whipping process. We investigated the effects of the MB manufacturing conditions, i.e., the hot air flow rate, the PET fiber fraction, and the presence or absence of annealing, on the compressibility of the obtained nonwovens. The fiber diameter histograms tended to split into two peaks as the PET fiber fraction increased. A larger PET fiber fraction produced a thicker nonwoven. Also, the compressibility increased, but the compression recovery rate did not. Annealing increased the thickness but decreased the compression recovery rate. Although thick fibers were increased by PET fiber mixing, they had insufficient rigid to resist compression. The decrease in the recovery rate can be explained by the brittleness of the PET fibers caused by crystallization of the non-oriented fibers during annealing.
在本研究中,我们采用熔喷法(MB)在纺丝生产线上混合聚对苯二甲酸乙二酯(PET)和聚丙烯(PP)纤维来制造无纺布,以改善其蓬松度和抗压性。也就是说,聚丙烯和聚对苯二甲酸乙二酯同时从交替铺设的三个喷嘴孔中挤出,并在鞭打过程中形成纤维状态,然后相互缠绕。我们研究了 MB 生产条件(即热空气流速、PET 纤维比例以及有无退火)对所得无纺布可压缩性的影响。随着 PET 纤维分量的增加,纤维直径直方图趋向于分成两个峰值。PET 纤维比例越大,无纺布越厚。此外,可压缩性增加,但压缩恢复率没有增加。退火增加了厚度,但降低了压缩恢复率。虽然通过混合 PET 纤维增加了纤维厚度,但它们的刚性不足以抵抗压缩。恢复率降低的原因可能是退火过程中无取向纤维结晶导致 PET 纤维变脆。
期刊介绍:
-Chemistry of Fiber Materials, Polymer Reactions and Synthesis-
Physical Properties of Fibers, Polymer Blends and Composites-
Fiber Spinning and Textile Processing, Polymer Physics, Morphology-
Colorants and Dyeing, Polymer Analysis and Characterization-
Chemical Aftertreatment of Textiles, Polymer Processing and Rheology-
Textile and Apparel Science, Functional Polymers