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Characterization of micro fibrillation process of cellulose and mercerized cellulose pulp

机译:纤维素和丝光纤维素浆粕微原纤化过程的表征

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Here we detail the fibrillation process for cellulose and mercerized cellulose pulps. Native and mercerized cellulose showed a high degree of purity as indicated by alpha-cellulose content measurement and XRD analysis. Furthermore, a stark change in fiber morphology indicated aggregation of fibrils on the surface due to mercerization. Fibrillation of pulp was carried out in the following subsequent steps: Disintegration, PFI refining, microgrinding by 20 passes and 60 passes in a Super Mass Colloider respectively. Fiber samples were collected at every stage and highly uniform films were made by ultrafiltration and hot press method. The fibers and films made from fibers were then characterized by measuring physical properties, contact angle, thermal, mechanical, and SEM analysis. The main objective was to characterize the physical properties of the films made from different degrees of fibrillation. The films obtained were of fairly close grammage approximately 35 g m(-2). The target grammage was 40 g m(-2), and the slightly lower grammage indicated some fiber loss during the fabrication process. Additionally, it was observed that the density of the films increased with increasing degree of fibrillation from about 180 g m(-3) to 455 g m(-3) for cellulose I and 95 g m(-3) to 385 g m(-3) for cellulose II. Cellulose I films showed some contact angle to begin with which increased at every stage (14-64 degrees), whereas cellulose II films did not display a contact angle until the final stage of fibrillation. The films also showed increasing strength and an evolution of tensile strength from initially displaying a tear behavior indicating poor bonding to typical micro fibrillated cellulose films behavior as the fibers became increasingly fibrillated. The ultimate tensile strength for cellulose changed from tear behavior with no defined break to 134.5 MPa. While on the other hand, the same change for cellulose II was a maximum of 75.1 MPa from tear behavior. Increasing fibrillation of fibrils in both cases showed a decrease in fiber size, well differentiated for the two types of pulps at every stage.
机译:在这里,我们详细介绍了纤维素和丝光纤维素纸浆的原纤化过程。天然和丝光纤维素显示出高纯度,如α-纤维素含量测量和XRD分析所表明。此外,纤维形态的明显变化表明由于丝光作用,纤维在表面上聚集。在以下后续步骤中进行纸浆原纤化:分别在Super Mass Colloider中进行20遍和60遍的崩解,PFI精制,微粉碎。在每个阶段收集纤维样品,并通过超滤和热压法制成高度均匀的薄膜。然后通过测量物理性能,接触角,热,机械和SEM分析来表征纤维和由纤维制成的薄膜。主要目的是表征由不同程度的原纤化制成的薄膜的物理性能。获得的膜的克重相当接近,约为35 g m(-2)。目标克重为40 g m(-2),稍低的克重表示在制造过程中一些纤维损失。另外,观察到膜的密度随着纤丝​​化程度的增加而增加,从纤维素I的约180 gm(-3)增至455 gm(-3),纤维素I从95 gm(-3)增至385 gm(-3)。纤维素II。纤维素I薄膜开始出现一些接触角,并在每个阶段(14-64度)开始增加,而纤维素II薄膜直到原纤化的最后阶段才显示出接触角。膜还显示出增加的强度和从最初表现出的撕裂行为开始的抗张强度的演变,这表明随着纤维变得越来越原纤化而与典型的微原纤化纤维素膜的粘合性差。纤维素的极限拉伸强度从无断裂的撕裂行为变为134.5 MPa。另一方面,对于纤维素II,相同的变化是撕裂行为的最大值为75.1MPa。在两种情况下,原纤维的原纤化增加都显示出纤维尺寸的减小,这两种纤维在每个阶段均具有明显的区别。

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