Synchrotron X-Ray Analysis and Morphology Evidence for Stereo-Assemblies of Periodic Aggregates in Poly(3-Hydroxybutyrate) with Unusual Photonic Iridescence

IF 4.3 3区 化学 Q2 POLYMER SCIENCE
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引用次数: 0

Abstract

Y.-H. Liao, S. Nagarajan, E. M. Woo, W.-T. Chuang, and Y.-W. Tsai, “Synchrotron X-Ray Analysis and Morphology Evidence for Stereo-Assemblies of Periodic Aggregates in Poly(3-Hydroxybutyrate) With Unusual Photonic Iridescence,” Macromolecular Rapid Communications 42, no. 14 (2021): 2100281, https://doi.org/10.1002/marc.202100281.

The authors would like to note that, in Figure 3b, the y-axis was mislabeled as “Band spacing” instead of the correct label, “Growth Rates (µm/min).”

We would like to clarify that Figure S3 (Supporting Information), which was published alongside the main paper as part of the Supporting Information, includes the same two panels: Figure S3a (Supporting Information) shows band spacing versus crystallization temperature (Tc), and Figure S3b (Supporting Information) presents growth rate versus Tc with the y-axis correctly labeled as “Growth rate (µm/s).” This figure covers data from PHB/PEO (75/25) blend spherulites crystallized at Tc = 30, 45, 50, 70, and 80 °C.

The updated Figure 3 is included as follows to ensure consistency with SI units and to replace the previously mislabeled version.

The authors would also like to introduce the following additional clarifications and corrections to the text:

Figures 1e and 4–Spiral spin direction: The direction of spiral band rotation (i.e., clockwise or counterclockwise) is not uniform across the sample but depends on the local nucleation site orientation and location of nucleation in the film layer. As a result, different spherulites—or even regions within the same spherulite—can exhibit varied spiral senses. This sample-dependent variability explains why Figures 1e and 4 show opposite spin directions; each image captures a different nucleus with its own local orientation.

Figure 3a–Band spacing maximum: The original text referred to 43 °C as the point of maximum band spacing. However, Figure 3a shows that the band spacing of the PHB/PTA (75/25) blend increases with increasing Tc, reaching a maximum of ≈45 µm at Tc ≈ 43–45 °C, but this point is hard to define precisely. Beyond this temperature—around Tc ≈ 45 °C—the bands broaden significantly and lose definition, appearing to ‘disappear’.

Figures 12b and 13–Labelling inconsistency: Figure 12b shows a scan across five points—Ridge (a), Valley (b), Ridge (c), Valley (d), Ridge (e). By contrast, Figure 13 presents a separate, shorter scan consisting of four points: Valley (a), Ridge (b), Valley (c), Ridge (d). The authors wish to note that this apparent inconsistency is due to the different scan ranges and point counts, not due to a conflict in the data.

We apologize for these errors.

异光子虹彩聚(3-羟基丁酸酯)周期性聚集体立体组装的同步加速器x射线分析和形态学证据。
中州。廖,S. Nagarajan, E. M. Woo, w . t。庄,和y - w。蔡,“异光子虹彩聚(3-羟基丁酸酯)周期性聚集体立体组装的同步加速器x射线分析和形态证据”,高分子快速通讯,42,no。14 (2021): 2100281, https://doi.org/10.1002/marc.202100281.The作者想指出,在图3b中,y轴被错误地标记为“频带间距”,而不是正确的标签“增长率(µm/min)”。我们想澄清的是,图S3(辅助信息)与主要论文一起发布,作为辅助信息的一部分,包括相同的两个面板:图S3a(辅助信息)显示带间距与结晶温度(Tc),图S3b(辅助信息)显示生长速率与Tc, y轴正确标记为“生长速率(µm/s)”。该图涵盖了PHB/PEO(75/25)混合球晶在Tc = 30、45、50、70和80℃时结晶的数据。更新后的图3如下所示,以确保与SI单位保持一致,并取代之前贴错标签的版本。图1e和图4 -螺旋自旋方向:螺旋带旋转的方向(即顺时针或逆时针)在整个样品中不是均匀的,而是取决于局部成核位点的方向和成核在膜层中的位置。因此,不同的球晶——甚至是同一球晶内的区域——可以表现出不同的螺旋感觉。这种样本相关的可变性解释了为什么图1e和图4显示相反的自旋方向;每张图像都捕捉到一个具有自己局部方向的不同核。图3a -最大带距:原文参考43°C作为最大带距点。然而,从图3a中可以看出,PHB/PTA(75/25)共混物的能带间距随着Tc的增加而增大,在Tc≈43-45℃时能带间距达到最大值≈45µm,但这一点很难精确定义。超过这个温度(约Tc≈45°c),波段显着变宽并失去清晰度,似乎“消失”。图12b和图13 -标记不一致:图12b显示了五个点的扫描-山脊(a),山谷(b),山脊(c),山谷(d),山脊(e)。相比之下,图13显示了一个独立的、较短的扫描,由四个点组成:谷(a)、岭(b)、谷(c)、岭(d)。作者希望指出,这种明显的不一致是由于不同的扫描范围和点计数,而不是由于数据中的冲突。我们为这些错误道歉。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
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