Molecules

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20 pages, 32731 KiB

Open AccessArticle

Elucidation of the Structure of Lignin–Carbohydrate Complexes in Ginkgo CW-DHP by ¹³C-²H Dual Isotope Tracer

by Kai Zhang, Yanchao Liu, Sheng Cui and Yimin Xie

Molecules 2021, 26(19), 5740; https://doi.org/10.3390/molecules26195740 - 22 Sep 2021

Cited by 5 | Viewed by 1878

To elucidate the chemical linkages between lignin and carbohydrates in ginkgo cell walls, ¹³C-²H-enriched cell wall-dehydrogenation polymers (CW-DHP) were selectively prepared with cambial tissue from Ginkgo biloba L. by feeding D-glucose-[6-²H₂], coniferin-[α-¹³C], and phenylalanine [...] Read more.

To elucidate the chemical linkages between lignin and carbohydrates in ginkgo cell walls, ¹³C-²H-enriched cell wall-dehydrogenation polymers (CW-DHP) were selectively prepared with cambial tissue from Ginkgo biloba L. by feeding D-glucose-[6-²H₂], coniferin-[α-¹³C], and phenylalanine ammonia-lyase (PAL) inhibitor. The abundant detection of ¹³C and ²H confirmed that D-glucose-[6-²H₂] and coniferin-[α-¹³C] were involved in the normal metabolism of ginkgo cambial cells that had been effectively labelled with dual isotopes. In the ginkgo CW-DHP, ketal and ether linkages were formed between the C-α of lignin side chains and carbohydrates, as revealed by solid state CP/MAS ¹³C-NMR differential spectroscopy. Furthermore, the DMSO/TBAH ionic liquids system was used to fractionate the ball-milled CW-DHP into three lignin-carbohydrate complex (LCC) fractions: glucan–lignin complex (GL), glucomannan–lignin complex (GML), and xylan–lignin complex (XL). The XRD determination indicated that the cellulose type I of the GL was converted into cellulose type II during the separation process. The molecular weight was in the order of Ac-GL > Ac-GML > XL. The ¹³C-NMR and ¹H-NMR differential spectroscopy of ¹³C-²H-enriched GL fraction indicated that lignin was linked with cellulose C-6 by benzyl ether linkages. It was also found that there were benzyl ether linkages between the lignin side chain C-α and glucomannan C-6 in the ¹³C-²H-enriched GML fraction. The formation of ketal linkages between the C-α of lignin and xylan was confirmed in the ¹³C-²H-enriched XL fraction. Full article

(This article belongs to the Special Issue Functional Biomass Derived Materials)

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14 pages, 3900 KiB

Open AccessArticle

Rational Design of Cellulose Nanofibrils Separator for Sodium-Ion Batteries

by Hongyang Zhou, Jin Gu, Weiwei Zhang, Chuanshuang Hu and Xiuyi Lin

Molecules 2021, 26(18), 5539; https://doi.org/10.3390/molecules26185539 - 12 Sep 2021

Cited by 9 | Viewed by 2903

Abstract

Cellulose nanofibrils (CNF) with high thermal stability and excellent electrolyte wettability attracted tremendous attention as a promising separator for the emerging sodium-ion batteries. The pore structure of the separator plays a vital role in electrochemical performance. CNF separators are assembled using the bottom-up [...] Read more.

Cellulose nanofibrils (CNF) with high thermal stability and excellent electrolyte wettability attracted tremendous attention as a promising separator for the emerging sodium-ion batteries. The pore structure of the separator plays a vital role in electrochemical performance. CNF separators are assembled using the bottom-up approach in this study, and the pore structure is carefully controlled through film-forming techniques. The acid-treated separators prepared from the solvent exchange and freeze-drying demonstrated an optimal pore structure with a high electrolyte uptake rate (978.8%) and Na⁺ transference number (0.88). Consequently, the obtained separator showed a reversible specific capacity of 320 mAh/g and enhanced cycling performance at high rates compared to the commercial glass fiber separator (290 mAh/g). The results highlight that CNF separators with an optimized pore structure are advisable for sodium-ion batteries. Full article

(This article belongs to the Special Issue Functional Biomass Derived Materials)

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15 pages, 3612 KiB

Open AccessArticle

Rubber Seed Oil-Based UV-Curable Polyurethane Acrylate Resins for Digital Light Processing (DLP) 3D Printing

by Yun Hu, Guoqiang Zhu, Jinshuai Zhang, Jia Huang, Xixi Yu, Qianqian Shang, Rongrong An, Chengguo Liu, Lihong Hu and Yonghong Zhou

Molecules 2021, 26(18), 5455; https://doi.org/10.3390/molecules26185455 - 8 Sep 2021

Cited by 17 | Viewed by 3503

Abstract

Novel UV-curable polyurethane acrylate (PUA) resins were developed from rubber seed oil (RSO). Firstly, hydroxylated rubber seed oil (HRSO) was prepared via an alcoholysis reaction of RSO with glycerol, and then HRSO was reacted with isophorone diisocyanate (IPDI) and hydroxyethyl acrylate (HEA) to [...] Read more.

Novel UV-curable polyurethane acrylate (PUA) resins were developed from rubber seed oil (RSO). Firstly, hydroxylated rubber seed oil (HRSO) was prepared via an alcoholysis reaction of RSO with glycerol, and then HRSO was reacted with isophorone diisocyanate (IPDI) and hydroxyethyl acrylate (HEA) to produce the RSO-based PUA (RSO-PUA) oligomer. FT-IR and ¹H NMR spectra collectively revealed that the obtained RSO-PUA was successfully synthesized, and the calculated C=C functionality of oligomer was 2.27 per fatty acid. Subsequently, a series of UV-curable resins were prepared and their ultimate properties, as well as UV-curing kinetics, were investigated. Notably, the UV-cured materials with 40% trimethylolpropane triacrylate (TMPTA) displayed a tensile strength of 11.7 MPa, an adhesion of 2 grade, a pencil hardness of 3H, a flexibility of 2 mm, and a glass transition temperature up to 109.4 °C. Finally, the optimal resin was used for digital light processing (DLP) 3D printing. The critical exposure energy of RSO-PUA (15.20 mJ/cm²) was lower than a commercial resin. In general, this work offered a simple method to prepare woody plant oil-based high-performance PUA resins that could be applied in the 3D printing industry. Full article

(This article belongs to the Special Issue Functional Biomass Derived Materials)

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13 pages, 19857 KiB

Open AccessArticle

Ultralight, High Capacitance, Mechanically Strong Graphene-Cellulose Aerogels

by Xiuya Wang, Ke Wan, Pengbo Xie, Yuanyuan Miao and Zhenbo Liu

Molecules 2021, 26(16), 4891; https://doi.org/10.3390/molecules26164891 - 12 Aug 2021

Cited by 11 | Viewed by 2538

Abstract

With increasing energy demand driving the need for eco-friendly and efficient energy storage technology, supercapacitors are becoming increasingly prevalent in wearable devices because of their portability and stability. The performance of these supercapacitors is highly dependent on the choice of electrode material. The [...] Read more.

With increasing energy demand driving the need for eco-friendly and efficient energy storage technology, supercapacitors are becoming increasingly prevalent in wearable devices because of their portability and stability. The performance of these supercapacitors is highly dependent on the choice of electrode material. The high capacitance and mechanical properties needed for these materials can be achieved by combining graphene’s stable electrical properties with renewable cellulose’s excellent mechanical properties into porous aerogels. In this study, graphene-cellulose hydrogels were prepared by a one-step hydrothermal method, with porous, ultra-light, and mechanically strong graphene-cellulose aerogels then prepared by freeze-drying. These composite aerogels possess excellent mechanical strength and high specific capacitance, capable of bearing about 1095 times the pressure of their own weight. Electrochemical tests show the specific capacitance of these composite aerogels can reach 202 F/g at a scanning rate of 5 mA/cm². In view of their high surface area and fast charge transport provided by their 3D porous structure, graphene-cellulose aerogels have great potential as sustainable supercapacitor electrodes. Full article

(This article belongs to the Special Issue Functional Biomass Derived Materials)

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14 pages, 4478 KiB

Open AccessArticle

HTO/Cellulose Aerogel for Rapid and Highly Selective Li⁺ Recovery from Seawater

by Hongbo Qian, Shaodong Huang, Zhichen Ba, Wenxuan Wang, Feihan Yu, Daxin Liang, Yanjun Xie, Yonggui Wang and Yan Wang

Molecules 2021, 26(13), 4054; https://doi.org/10.3390/molecules26134054 - 2 Jul 2021

Cited by 14 | Viewed by 3853

Abstract

To achieve rapid and highly efficient recovery of Li⁺ from seawater, a series of H₂TiO₃/cellulose aerogels (HTO/CA) with a porous network were prepared by a simple and effective method. The as-prepared HTO/CA were characterized and their Li⁺ [...] Read more.

To achieve rapid and highly efficient recovery of Li⁺ from seawater, a series of H₂TiO₃/cellulose aerogels (HTO/CA) with a porous network were prepared by a simple and effective method. The as-prepared HTO/CA were characterized and their Li⁺ adsorption performance was evaluated. The obtained results revealed that the maximum capacity of HTO/CA to adsorb Li⁺ was 28.58 ± 0.71 mg g⁻¹. The dynamic k₂ value indicated that the Li⁺ adsorption rate of HTO/CA was nearly five times that of HTO powder. Furthermore, the aerogel retained extremely high Li⁺ selectivity compared with Mg²⁺, Ca²⁺, K⁺, and Na⁺. After regeneration for five cycles, the HTO/CA retained a Li⁺ adsorption capacity of 22.95 mg g⁻¹. Moreover, the HTO/CA showed an excellent adsorption efficiency of 69.93% ± 0.04% and high selectivity to Li⁺ in actual seawater. These findings confirm its potential as an adsorbent for recovering Li⁺ from seawater. Full article

(This article belongs to the Special Issue Functional Biomass Derived Materials)

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12 pages, 3609 KiB

Open AccessArticle

Preparation of Lignin-Based High-Ortho Thermoplastic Phenolic Resins and Fibers

by Yu Ren, Jin Xie, Xiahong He, Rui Shi and Can Liu

Molecules 2021, 26(13), 3993; https://doi.org/10.3390/molecules26133993 - 30 Jun 2021

Cited by 7 | Viewed by 2024

Abstract

Surplus lignin, which is inefficiently used, is generated in the forestry industry. Currently, most studies use lignin instead of phenol to synthesize thermosetting resins which cannot be reprocessed, thus affecting its application field. Thermoplastic phenolic resin has an orderly structure and excellent molding [...] Read more.

Surplus lignin, which is inefficiently used, is generated in the forestry industry. Currently, most studies use lignin instead of phenol to synthesize thermosetting resins which cannot be reprocessed, thus affecting its application field. Thermoplastic phenolic resin has an orderly structure and excellent molding performance, which can greatly improve its application field and economic value. Herein, phenol was partially replaced with enzymolysis lignin (without treatment), generating lignin-based high-ortho thermoplastic phenolic resins (LPRs), and then lignin-based phenolic fibers (LPFs) were prepared by melt spinning. FTIR, ¹³C-NMR and GPC were used to characterize the ortho–para position ratio (O/P value), molecular weight and its distribution (PDI), and rheological properties of the resin. TG, XRD, SEM and tensile property studies were used to determine the thermal stability, orientation, and surface morphology of the fiber. Lignin addition resulted in the decline of the O/P value and molecular weight of the resin. For the 10% LPR, the O/P value, Mw, and PDI were 1.28, 4263, and 2.74, respectively, with the fiber exhibiting relatively good spinnability. The tensile strength and elongation at break of the 10% LPF were 160.9 MPa and 1.9%, respectively. The addition of lignin effectively improved the thermal properties of the fiber, and the carbon yields of 20% LPF before and after curing were 39.7% and 53.6%, respectively, which were 22.2% and 13.7% higher than that of the unmodified fiber, respectively. Full article

(This article belongs to the Special Issue Functional Biomass Derived Materials)

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13 pages, 2418 KiB

Open AccessArticle

Viscoelasticity and Solution Stability of Cyanoethylcellulose with Different Molecular Weights in Aqueous Solution

by Qian Li, Yuehu Li, Zehua Jin, Yujie Li, Yifan Chen and Jinping Zhou

Molecules 2021, 26(11), 3201; https://doi.org/10.3390/molecules26113201 - 27 May 2021

Cited by 2 | Viewed by 2053

Abstract

Water-soluble cellulose ethers are widely used as stabilizers, thickeners, and viscosity modifiers in many industries. Understanding rheological behavior of the polymers is of great significance to the effective control of their applications. In this work, a series of cyanoethylcellulose (CEC) samples with different [...] Read more.

Water-soluble cellulose ethers are widely used as stabilizers, thickeners, and viscosity modifiers in many industries. Understanding rheological behavior of the polymers is of great significance to the effective control of their applications. In this work, a series of cyanoethylcellulose (CEC) samples with different molecular weights were prepared with cellulose and acrylonitrile in NaOH/urea aqueous solution under the homogeneous reaction. The rheological properties of water-soluble CECs as a function of concentration and molecular weight were investigated using shear viscosity and dynamic rheological measurements. Viscoelastic behaviors have been successfully described by the Carreau model, the Ostwald-de-Waele equation, and the Cox–Merz rule. The entanglement concentrations were determined to be 0.6, 0.85, and 1.5 wt% for CEC-11, CEC-7, and CEC-3, respectively. All of the solutions exhibited viscous behavior rather than a clear sol-gel transition in all tested concentrations. The heterogeneous nature of CEC in an aqueous solution was determined from the Cox–Merz rule due to the coexistence of single chain complexes and aggregates. In addition, the CEC aqueous solutions showed good thermal and time stability, and the transition with temperature was reversible. Full article

(This article belongs to the Special Issue Functional Biomass Derived Materials)

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12 pages, 6707 KiB

Open AccessFeature PaperArticle

Investigating Lignin-Derived Monomers and Oligomers in Low-Molecular-Weight Fractions Separated from Depolymerized Black Liquor Retentate by Membrane Filtration

by Kena Li, Jens Prothmann, Margareta Sandahl, Sara Blomberg, Charlotta Turner and Christian Hulteberg

Molecules 2021, 26(10), 2887; https://doi.org/10.3390/molecules26102887 - 13 May 2021

Cited by 3 | Viewed by 2235

Abstract

Base-catalyzed depolymerization of black liquor retentate (BLR) from the kraft pulping process, followed by ultrafiltration, has been suggested as a means of obtaining low-molecular-weight (LMW) compounds. The chemical complexity of BLR, which consists of a mixture of softwood and hardwood lignin that has [...] Read more.

Base-catalyzed depolymerization of black liquor retentate (BLR) from the kraft pulping process, followed by ultrafiltration, has been suggested as a means of obtaining low-molecular-weight (LMW) compounds. The chemical complexity of BLR, which consists of a mixture of softwood and hardwood lignin that has undergone several kinds of treatment, leads to a complex mixture of LMW compounds, making the separation of components for the formation of value-added chemicals more difficult. Identifying the phenolic compounds in the LMW fractions obtained under different depolymerization conditions is essential for the upgrading process. In this study, a state-of-the-art nontargeted analysis method using ultra-high-performance supercritical fluid chromatography coupled to high-resolution multiple-stage tandem mass spectrometry (UHPSFC/HRMSⁿ) combined with a Kendrick mass defect-based classification model was applied to analyze the monomers and oligomers in the LMW fractions separated from BLR samples depolymerized at 170–210 °C. The most common phenolic compound types were dimers, followed by monomers. A second round of depolymerization yielded low amounts of monomers and dimers, while a high number of trimers were formed, thought to be the result of repolymerization. Full article

(This article belongs to the Special Issue Functional Biomass Derived Materials)

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