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wollastonite
CHIRALITY · 2026 ·Vol. 38 ·期 9 ·e70139 · IF 2.4

Prebiotic Absolute Asymmetric Synthesis of d‐Ribose on Wollastonite

Wendi Zhang,Yang Gao,Jiao Wang,Quanzheng Deng,Lu Han,Wanning Zhang,Yuxi Fang

ATP is the core substance of energy metabolism in all forms of life. The chirality of d ‐ribose is essential for ATP's function, ensuring efficient molecular recognition, metabolic stability, and co‐evolution with RNA in biological processes. However, origin of chirality of d ‐ribose is still unknown. Here, we demonstrate that wollastonite, an abundant Earth mineral, catalyzes the formose reaction between formaldehyde and glycolaldehyde and achieves high enantioselectivity (63.3%–91.3% ee ) toward d ‐ribose. The lower energy barrier for the transition state of d ‐glyceraldehyde compared to that of l ‐glyceraldehyde, which possesses a similar configuration to glyceraldehyde, results in the enantioselective synthesis of ribose. Experimental and computational studies reveal that the surface chirality of wollastonite, which is characterized by its wavy atomic arrangement, selectively reduces the adsorption energy of the d ‐glyceraldehyde intermediate compared to its l ‐enantiomer. This preferential adsorption kinetically promotes the d ‐glyceraldehyde pathway and steers the reaction toward d ‐ribose. Our work establishes wollastonite as an intrinsically enantioselective mineral catalyst, provides a mechanistic foundation for prebiotic chiral selection toward d ‐ribose, and highlights surface design principles for asymmetric synthesis. Wollastonite's inherent surface chirality lowers the energy barrier for d ‐glyceraldehyde, kinetically favoring its pathway over l ‐forms. This preferential adsorption steers the formose reaction toward d ‐ribose, offering a prebiotic mechanism for chiral selection.

✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF SEPARATION SCIENCE · 2011 ·Vol. 34 ·期 22 ·3287-3294 · IF 2.631

Selective recognition of sesamol using molecularly imprinted polymers containing magnetic wollastonite

Xue Wang,Jianming Pan,Wei Guan,Xiaohua Zou,Pengwei Huo,Yongsheng Yan,Wei Hu

The magnetic molecularly imprinted polymers (MMIPs) have been synthesized using piperonal molecules as dummy template and magnetic wollastonite composites as support. The resulting composites were applied to selective recognition of sesamol from aqueous solution. MMIPs were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) analysis, transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), thermogravimetric analysis (TGA), and vibrating sample magnetometer (VSM). MMIPs were demonstrated with an imprinted polymer film (90–100 nm) and exhibited magnetic property ( M s =8.60 emu/g) and thermal stability. The effective average diameter of the Fe 3 O 4 nanoparticles was about 10 nm and the thickness of magnetic film was about 160 nm. Batch mode adsorption studies were carried out to investigate the specific adsorption equilibrium, kinetics and selective recognition. The Langmuir isotherm model was fitted to the equilibrium data better than the Freundlich model, and the kinetic properties were well described by the pseudo-second-order equation. The value of E a in this study was 5.35 kJ/mol for MMIPs. In addition, the selective recognition experiments demonstrated that MMIPs have specific recognition ability toward sesamol.

CAS / MDL: 97-90-5 14024-18-1
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Progress in Natural Science-Materials International · 2025 · IF 7.1

The well-designed wollastonite-ZnIn2S4 composite photocatalysts for efficient hydrogen production

Jiangfeng Xu,Run Zhou,Yangzi Li,Yu Tu

A sustainable pathway to green hydrogen generation, the design and synthesis of targeted photocatalysts based on semiconductors or other organic/inorganic materials has emerged as a promising approach for efficient hydrogen production under light irradiation. In this paper, wollastonite-ZnIn 2 S 4 composite photocatalysts (ZIS-W) were successfully prepared by the chemical deposition method with wollastonite as the carrier. The hydrogen evolution reaction from water under simulated sunlight irradiation and the enhancement mechanism of ZIS-W were investigated. The results showed that ZIS-W exhibits favorable photocatalytic hydrogen evolution performance and stability, and the photocatalytic hydrogen evolution efficiency of ZIS-W was 4.94 ​mmol ​h −1  ​g −1 , which was 1.44 times higher than that of pure ZnIn 2 S 4 . The unique crystal structure of wollastonite provides favorable conditions for the growth of ZnIn 2 S 4 and effectively enhances the dispersion and stability of ZnIn 2 S 4 . The recombination of photogenerated electron-hole pairs was effectively suppressed while the specific surface area was increased. This study provided a facile synthesis method for preparing photocatalysts with highly efficient hydrogen generation.

CAS / MDL: 64-17-5 10025-82-8
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BRAZILIAN JOURNAL OF CHEMICAL ENGINEERING · 2022 ·Vol. 39 ·期 3 ·661-669 · IF 1.772

Preparation of precipitated calcium carbonate using wollastonite and CO2 from industrial exhaust

Jin Zhengwei,Yu Changjun,Wang Ruyang,Wei Wei,Jing Yunhuan,Wang Qi

The production of precipitated calcium carbonate (PCC) from carbonate-free minerals and CO 2 from industrial exhaust gas could lower energy consumption and promote CO 2 sequestration. The present study proposes a chemical looping process for the production of PCC from wollastonite (calcium silicate) and CO 2 from industrial exhaust using ammonium chloride as the looping medium; this study also included a pilot setup with a capacity of 3 kg of carbonate per hour to demonstrate the process. The process consisted of three phases: extraction of calcium from the wollastonite with hydrochloric acid; carbonation of the CO 2 in the extract solution in the presence of ammonia to produce calcium carbonate while generating ammonium chloride; and regeneration of hydrochloric acid and ammonia by the decomposition of ammonium chloride. A special air-lift reactor with an integrated settling vessel was designed for the carbonation reaction. The extraction and carbonation conditions were optimized, and fine calcium carbonate with a purity greater than 98% and a particle size of 2 μm was produced. The overall utilization of the calcium from wollastonite and the CO 2 reached 99 and 90%, respectively. This process avoids the high-temperature pyrolysis of limestone and thus consumes less energy. It also sequesters CO 2 from industrial exhaust and is a green and high-performing process for the production of PCC.

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CERAMICS INTERNATIONAL · 2020 · IF 3.83

Structural and electrochemical properties of Wollastonite-Based Chemically Bonded Phosphate Ceramic coatings

Ge Yan,Mingyang Wang,Tao Sun,Xinping Li,Fang Xu,Kun Tian,Weisong Yin

An inorganic anticorrosive coating, merging wollastonite into Chemically Bonded Phosphate Ceramic (CBPC) binders, was prepared to protect rebar from corrosion. In order to evaluate the corrosion resistance behavior of Wollastonite-based Chemically Bonded Phosphate Ceramic (WoCBPC) coatings, the electrochemical measurements were applied. The experiment results showed that the value of corrosion potential (E corr ) and polarization resistance (R p ) is the largest and the value of corrosion current density (I corr ) is the smallest among all WoCBPC coatings, when the content of wollastonite reaches 20% of the ceramic filler (WoCBPC20). Moreover, the resistance of WoCBPC20 coating (R c ) value was much higher than that of other WoCBPC coatings, which means the best anticorrosion properties. The structure formation of WoCBPC coatings was identified by using XRD as well as SEM/EDS techniques. The intensity of berlinite phase reaches the maximum with the introduction of wollastonite in WoCBPC20 coatings. Meanwhile, the fibrous wollastonite particles with high modulus can inhibit the spread of cracks in CBPC matrix. Therefore, the WoCBPC coatings show a barrier effect to prevent aggressive substances from contacting the rebar effectively.

✓ 已验证 DOI 高影响因子
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Journal of Building Engineering · 2022 · IF 7.144

Sulfate resistance and microstructure of metakaolin geopolymer reinforced by cellulose nanofiber and wollastonite

Ren Luo,Huai Liu,Ping Duan,Jiayuan Ye,Wei Chen,Zuhua Zhang,Aiguo Wang

As an alternative to the ordinary Portland cement (OPC), it is imperative to improve the performance of geopolymer under harsh conditions (such as sulfate/seawater attack). Sulfate attack is one of the reasons which cause deterioration and damages of geopolymer structures. Thus, the strategy of sulfate resistance attracts attention of researchers. As a reinforcement for geopolymer, the cellulose nanofiber (from waste bamboo powder) facilitates the utilization of waste bamboo powder. High-purity cellulose nanofiber (CNF) was obtained by using alkali, bleaching and acid hydrolysis treatments on waste bamboo powder. The purification effect and environmental impact of CNF were compared by different bleaching methods. The optimal conditions (containing 5 wt% H 2 O 2 , 0.04 wt% MgSO 4 and 0.05 wt% TAED) for CNF purification were determined. This work aims to investigate the effect of CNF and wollastonite (WS) on the sulfate resistance of metakaolin (MK) geopolymer. The deterioration mechanism of geopolymer reinforced by natural fiber (CNF and WS) exposed to sulfate environment was revealed by employing XRD , SEM and MIP . The influence of extreme sulfate environment on mechanical properties and microstructure was investigated. The analysis results of microstructure, mass loss rate and mechanical properties were also combined to evaluate the sulfate resistance. The outcomes show that the bleaching method of H 2 O 2 can effectively remove impurities and enhance the purification effect of CNF. The optimum mix proportion of MK geopolymer reinforced by natural fiber (formulated as 2% of CNF, 10% of WS and 88% of MK) is obtained. The compressive and flexural strengths are increased by up to 76.1% and 135.5% (compared to the control group), respectively. The deterioration of geopolymer is related to the concentration of Na 2 SO 4 and the immersion time. The degradation mechanism is attributed to the incomplete geopolymerization and the destruction of the pore structure due to sulfate attack exposure. The deterioration processes of geopolymer can be slowed down by introducing WS and CNF. It improves the sulfate resistance of the matrix from the structural aspect.

CAS / MDL: 7758-19-2
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POLYMER COMPOSITES · 2025 · IF 4.7

PP/wollastonite/bamboo flour ternary composite materials with improved thermal and mechanical properties

Jiawei Wei,Fang Wang,Ruru Liu,Xiangying Chen,Zhongjie Zhang

Based on the micro-structure of wollastonite (WS) and bamboo flour (BF), a series of PP/WS/BF ternary composite materials are prepared using blending, twin-screw melt extrusion, and injection molding processes. The experiment shows that the formulation and processing technology play a significant impact on the structure, thermal, and mechanical properties of the composites. BF has a significant impact on the nucleation and crystallization of PP, while WS has almost no effect on PP. BF improves tensile strength and enhances the strength of composites; WS improves the bending strength and flexural modulus and enhances the rigidity of composites. Taking the W-B-30-1:3 sample as an example, its tensile performance is the highest at 23.33 MPa, as well as bending strength and flexural modulus of 26.23 and 904.67 MPa, respectively. The combination of BF and WS leads to an increase in storage modulus, a decrease in loss modulus, a decrease in loss factor, an increase in glass transition temperature, and a decrease in bonding factor of ternary composite materials. This work can enrich the scope of PP composite materials, and the composite materials are expected to have potential applications in the fields of automotive interior parts with lightweight. Highlights Heterogeneous bonding among fillers enhances crystallization of composites. Wollastonite is more conducive to improving the thermal stability of composites. Adding fillers can more effectively enhance mechanical properties. The use of fillers increases interfacial compatibility and bonding performance.

CAS / MDL: 6683-19-8
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ACS Biomaterials Science & Engineering · 2017 · IF 3.234

Regeneration of the Osteochondral Defect by a Wollastonite and Macroporous Fibrin Biphasic Scaffold

Tao Shen,Yuankun Dai,Xuguang Li,Sanzhong Xu,Zhongru Gou,Changyou Gao

Osteochondral defect refers to the damage of cartilage as well as subchondral bone. Cartilage tissue engineering focusing on the regeneration of cartilage and disregarding the subchondral bone always leads to partial regeneration of the damage, resulting in poor mechanical and physiological properties. A scaffold suitable for in situ inductive regeneration of both types of tissues is urgently needed. In this study, a biphasic scaffold integrated by macro-porous fibrin and 3D-printed wollastonite (containing 8% MgSiO3 (CS-Mg8)) scaffolds, either preloaded with rabbit bone marrow mesenchymal stem cells (BMSCs) or not, were fabricated and used to repair osteochondral defects in vivo (full thickness osteochondral defects in rabbits, 4 mm in diameter and 4 mm in depth with bone marrow blood effusion). The fibrin scaffold had a pore size of 100–200 μm, and was degraded gradually and reached weight loss over 80% at 28 days. The presence of BMSCs could accelerate the degradation rate. BMSCs could well proliferate in the fibrin scaffold along with time prolongation. The CS-Mg8 scaffold possessed a regular structure of cross stacked CS-Mg8 rods, and was degraded rather slowly with a mass loss of 8.5% at 28 days. BMSCs adhered and showed well spreading on the CS-Mg8 scaffold, without apparent proliferation in vitro. In vivo transplantation of the biphasic scaffolds, either preloaded with BMSCs or not, could induce the regeneration of both cartilage and subchondral bone to a great extent. Loading of BMSCs enabled better regeneration of cartilage layer, leading to smoother macroscopic appearance, good integrity with surrounding tissue and tide mark formation. However, no significant difference in bone formation and in gene expression was found with and without BMSCs loading.

✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2026 · IF 3.1

Comodification of Polyethylene With EVA and Fibrous Wollastonite for Improved Thermal Cycling Crack Resistance

Yuhao Ma,Dingchen Yan,Juntao Xu,Jian Pan,Shanshan Xu,Hongsheng Tan

Polyethylene (PE) is widely used as a general-purpose plastic; however, its application in harsh environments is limited by poor resistance to thermal cycling crack resistance. In this study, a dual-modification strategy was developed to improve the thermal cycling crack resistance of PE by incorporating fibrous wollastonite (FW) and ethylene-vinyl acetate copolymer (EVA). FW acts as a rigid reinforcing phase that restricts polymer-chain mobility and helps suppress crack initiation. EVA serves as a flexible toughening phase and promotes energy dissipation during deformation. The combination of FW and EVA delays crack propagation and improves the crack resistance of PE. The combined use of FW and EVA produces a synergistic effect involving physical crack blocking and energy dissipation, thereby delaying crack propagation. Consequently, the modified PE demonstrates substantially enhanced resistance to thermal cycling cracking. The PE coating samples maintained structural integrity after cyclic exposure between −40°C and 60°C for 100 h. In addition, the tensile strength increased to 14.94 MPa, representing a 39% improvement compared with pristine PE (10.73 MPa). The combined FW-EVA system effectively improves PE's thermal cycling crack resistance, offering a feasible strategy for its high-demand applications.

✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2026 · IF 12.5

Towards negative-carbon biohydrogen: A dual-function wollastonite strategy for enhanced fermentation and CO2 sequestration

Weiming Li,Can Jin,Huida Duan,Fangcao Li,Zhangxun Huang,Haodong Zhao,Xiaoman Yu,Yimei Xi,Xiangfeng Zeng,Yongfeng Jia,Chi Cheng

Dark fermentation for biohydrogen requires continuous alkaline dosing to control process acidification and expensive separation units to remove co-produced CO 2 , resulting in high operational costs and energy consumption. Here, we introduce wollastonite as a dual-function agent to simultaneously enhance H 2 yield and capture CO 2 . An optimal dosage of 10 g/L was identified, which shortened the lag phase from 23.13 to 12.38 h and increased the hydrogen yield from 158.11 ± 3.44 mL/g glucose-consumed to 210.75 ± 15.87 mL/g glucose-consumed. Mechanistically, wollastonite buffered the system pH, steering metabolic flux away from lactate towards acetate synthesis by enriching Clostridium and suppressing Lactobacillus . Wollastonite also enabled in-situ CO 2 sequestration by precipitating it as CaCO 3 . However, maximal CO 2 capture was achieved at a higher dosage (≥15 g/L), which passively reached the required neutral pH but compromised the hydrogen yield. This created a conflict with the optimal 10 g/L dosage for hydrogenesis. To prioritize the primary goal of green hydrogen production, a two-stage strategy was developed. This approach first uses the optimal 10 g/L dosage for maximal fermentation, followed by a post-fermentation pH adjustment from 6.54 ± 0.18 to 7.0 to induce carbonation. The optimized process successfully sequestered 0.49 ± 0.05 of CO 2 per liter of medium, thereby increasing the H 2 content in the final biogas to a high of 58.2 ± 1.1%. Finally, a life cycle assessment (LCA) validated the environmental superiority of this strategy, confirming a significantly lower Global Warming Potential (GWP) for the entire process. This work thus provides a proof-of-concept for a pragmatic strategy that co-optimizes hydrogen production and carbon capture in a single, sustainable biorefinery process.

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Materials Today Sustainability · 2024 · IF 7.1

Preparation and characterization of a novel bifunctional heterogeneous Sr–La/wollastonite catalyst for biodiesel production

Jie Zhu,Tongxin Qu,Shengli Niu,Jisen Liu,Sitong Liu,Jie Geng,Zihao Yang,Abulikemu Abulizi

The development of reusable heterogeneous catalysts with acid-base bifunctions employing low-cost oil as a raw material is critical for optimizing the biodiesel synthesis process. In the present study, Sr–La/wollastonite bifunctional catalysts with the different Sr/La atomic ratios are synthesized using a straightforward impregnation technique. The results show that the Sr 7 La 3 /wollastonite catalyst establishes a biodiesel yield of 95.35% upon initial use and 85.14% after the fifth cycle of reuse, under the transesterification conditions of a catalyst content of 8 wt.%, methanol to oil molar ratio of 15, reaction duration of 3 h, and reaction temperature of 150 °C. The biodiesel yield of 91.62% is obtained even after the addition of 5 wt.% oleic acid, and the catalyst maintains a high biodiesel yield (>80%) for three reused cycles, which illustrates the good resistance to free fatty acids (FFAs). Meanwhile, the process parameters for transesterification are optimized utilizing Response Surface Methodology combined with Box-Behnken Design (RSM-BBD). With a methanol to oil molar ratio of 17.7 and a catalyst content of 6.4 wt.%, biodiesel yield is 96.08% at 149 °C for 3 h. This study revealed the enormous potential of the Sr–La/wollastonite bifunctional catalyst in biodiesel production.

CAS / MDL: 110-54-3
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MATERIALS & DESIGN · 2022 · IF 9.417

3D-printed magnesium-doped wollastonite/nano-hydroxyapatite bioceramic scaffolds with high strength and anti-tumor property

Huifeng Shao,Zhuoluo Jing,Pengcheng Xia,Tao Zhang,Zhiheng Nian,Wanshun Liu,Jiahua Zhu,Youping Gong,Rougang Zhou,Yong He,Qingqiang Yao

It is still a major challenge to remove tumor cells and fill bone defects after tumor resection. Combined with the 3D printing technology, the composite bioceramics scaffolds were fabricated with interconnected porous magnesium-doped wollastonite (CSi-Mg) scaffolds as the architecture and nano-hydroxyapatite ( n -HA) as the surface. The influence of manufacturing process on the n -HA layer thickness and degradation performance, biological performance and anti-tumor performance of the composite scaffolds were investigated. The n -HA surface layer could effectively retard the degradation rate of CSi-Mg scaffolds and maintain high mechanical strength (over 90 MPa) after immersion in simulated body fluid for 3 weeks. Meanwhile, CSi-Mg/n-HA3 scaffold induced about 50 % of cell death for human osteosarcoma cells (MG-63) in vitro. CSi-Mg/ n -HAx (x = 1, 3) scaffolds could improve the osteogenic performance of Rat BMSC. These findings demonstrate that the bioceramic composite scaffold with high strength, good osteogenic performance and anti-tumor performance is promising for the treatment of tissue injury after resection of osteosarcoma.

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