Lina Liu

Prof. Lina Liu


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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6 May 2019 in Polymers
Verified
Journal Article
Open access
PDF file
CZChencheng Zhao
Chencheng Zhao
XZXiaochun Zhang
Xiaochun Zhang
LLLina Liu
Lina Liu
YYYouming Yu
Youming Yu
WZWei Zheng
Wei Zheng
PSPinan Song
Pinan Song
Wooden structures in China’s ancient buildings hold highly historical and cultural values. There is an urgent need to repair and replace the damaged wooden structures after hundreds and thousands of years of exposure to weather. Unfortunately, to date there is still a lack of insightful understanding on how the chemical structure, composition, and micro-morphology evolve over the long-term natural aging before artificial ancient timbers can be developed. This work aims to systematically examine the outer surface, middle layer, and inner surface of the same piece of Chinese fir (Cunninghamia lanceolate) collected from an ancient Chinese building. Based on qualitative and quantitative analysis, both cellulose and hemicellulose in aged woods are found to experience significant degrees of degradation. The crystalline regions of cellulose are also determined to undergo moderate degradation as compared to the control fresh wood. In comparison, the lignin basically remains unchanged and its content in the inner layer slightly increases, as evidenced by more free phenol groups determined. Relative to the outer and inner layer, the middle layer of the ancient wood shows the lowest degree of degradation close to that of the fresh wood. This work offers guidelines for fabricating artificial ancient woods to repair the destroyed ones in China’s ancient architectures.

17 April 2025 in Forests
Verified
Journal Article
Open access
PDF file
YZYixuan Zheng
Yixuan Zheng
LLLina Liu
Lina Liu
MBMinzhen Bao
Minzhen Bao
FLFeng Lin
Feng Lin
XWXujun Wu
Xujun Wu
ZWZhang Weigang
Zhang Weigang
This study investigated the effects of thermal modification treatment on flattened bamboo lumber by using temperature (180 °C, 190 °C, 200 °C) and duration (2, 3, 4 h) as experimental variables. The physicochemical properties, crystallinity, bending deformation, chemical composition, and microstructural evolution of the material before and after treatment were systematically analyzed using universal mechanical testing, scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and nanoindentation. This comprehensive approach aimed to achieve high-performance flattened bamboo lumber. The results revealed that thermal modification significantly reduced the flexural modulus of elasticity and hardness of the flattened bamboo lumber, which reached their minimum values of 4479 MPa and 786.71 N, under the treatment at 190 °C/3 h. Conversely, it enhanced the longitudinal compressive strength of flattened bamboo lumber, achieving a maximum value of 57.28 MPa at 180 °C/2 h. At the microscale, the nanomechanical strength decreased under 190–200 °C treatments, accompanied by a tighter cell arrangement and evident shrinkage and deformation of the parenchyma cells. Dimensional stability tests combined with FTIR and crystallinity analyses demonstrated a reduction in the number of hydrophilic groups and improved dimensional stability after thermal modification. Notably, the material treated at 200 °C for 4 h retained its dimensional stability and exhibited no deformation.

18 December 2025 in Chinese Journal of Polymer Science
Verified
Journal Article
Closed access
PDF file
HHHang-Tian Hu
Hang-Tian Hu
DXDan Xie
Dan Xie
ZGZheng-Hong Guo
Zheng-Hong Guo
FCFeng-Qing Chen
Feng-Qing Chen
XHXing-Wei He
Xing-Wei He
LLLina Liu
Lina Liu

21 July 2026 in Molecules
Verified
Journal Article
Open access
PDF file
YFYuhao Fang
Yuhao Fang
GLGaobo Lou
Gaobo Lou
HYHongjiang Yu
Hongjiang Yu
LLLina Liu
Lina Liu
YCYifan Chen
Yifan Chen
In this study, novel and stable cellulose-based oleogels with tunable rheological properties were successfully developed for lubrication applications via cross-linking reactions of epoxidized soybean oil (ESO), microcrystalline cellulose (MCC), and isocyanate. This cross-linking strategy not only overcomes the incompatibility issue arising from the polarity difference between MCC and ESO but also enables precise control over the oleogels’ rheological behavior by tailoring the cross-linking density. The resulting oleogels exhibit excellent thermal stability, with an initial decomposition temperature (T5%) of approximately 300 °C. Furthermore, oxidation resistance is significantly enhanced with increasing cross-linking density, resulting in a substantial increase in the oxidation induction time (OIT) from 5 to 79 min at 210 °C. Rheological characterization reveals that the oleogels exhibit typical shear-thinning and thixotropic behavior. The plateau modulus (GN0) exhibits a positive correlation with cross-linking density, accompanied by a simultaneous improvement in structural recovery ability. Tribological tests show that the friction coefficient increases with the cross-linking degree, while four-ball tests indicate that the extreme-pressure load-carrying capacity is governed mainly by the nature of the base oil in addition to the cross-linking density of the gel network. This work provides a promising strategy for the development of high-performance and customizable bio-based lubricating materials.