The global production of plywood is constantly increasing as its application in the furniture and interior decoration industry becomes more widespread. An urgent issue is how to decrease the formaldehyde released from plywood, considering its carcinogenic effect on humans and harm to the environment. Reducing the free formaldehyde content of the urea formaldehyde (UF) adhesives used in the preparation process is considered an effective method. Therefore, it is necessary to identify a new type of formaldehyde scavengers. Here, the strongly reducing substance sodium borohydride was used to reduce and degrade the free formaldehyde in UF adhesives, and its effects on the properties of the UF adhesive and plywood were studied. When 0.7% sodium borohydride was added to the UF adhesive with a molar ratio of formaldehyde to urea of 1.4:1, the free formaldehyde content of the UF resin decreased to 0.21%, which is 53% lower than that of the untreated control. Moreover, the formaldehyde released from the plywood was reduced to 0.81 mg/L, ~45% lower than that from the group. The bonding strength of the treated samples could reach ~1.1 MPa, which was only reduced by ~4% compared to that of the control. This study of removing formaldehyde from UF adhesive by reduction could provide a new approach for suppressing formaldehyde release from the final products.

Sodium borohydride (NaBH4 ) has earned recognition as a promising hydrogen carrier, attributed to its exceptional hydrogen storage capacity, boasting a high theoretical storage capacity of 10.8 wt %. Nonetheless, the utilization of traditional pyrolysis and hydrolysis methods still presents a formidable challenge in achieving controlled hydrogen generation especially under ambient conditions. In this work, we report an innovative electrochemical strategy for production H2 by coupling NaBH4 electrooxidation reaction (BOR) at anode in alkaline media with hydrogen evolution reaction (HER) at cathode in acidic media. To implement this, we have developed a bifunctional electrocatalyst denoted as Pd-Mo2 C@CNTs, wherein Pd nanoparticles are grown in situ on Mo2 C embedded within N-doped carbon nanotubes. This electrocatalyst demonstrates exceptional performance in catalyzing both alkaline BOR and acidic HER. We have developed a hybrid acid/alkali cell, utilizing Pd/Mo2 C@CNTs as the anode and cathode electrocatalysts. This configuration showcases remarkable capabilities for self-sustained, precise, and uninterrupted indirect release of H2 stored in NaBH4 , even at high current densities of 100 mA cm-2 with a Faraday efficiency approaching 100 %. Additionally, this electrochemical device exhibits significant promise as a fuel cell, with the ability to deliver a maximum power density of 20 mW cm-2 .

Constructing a reliable and robust cobalt-based catalyst for hydrogen evolution via hydrolysis of sodium borohydride is appealing but challenging due to the deactivation caused by the metal leaching and re-oxidization of metallic cobalt. A unique core-shell-structured coronavirus-like Co@C microsphere was prepared via pyrolysis of Co-MOF. This special Co@C had a microporous carbon coating to retain the reduced state of cobalt and resist the metal leaching. Furthermore, several nano-bumps grown discretely on the surface afforded enriched active centers. Applied in the pyrolysis of NaBH4, the Co@C-650, carbonized at 650 °C, exhibited the best activity and reliable recyclability. This comparable performance is ascribed to the increased metallic active sites and robust stability.

As a promising hydrogen storage material, sodium borohydride (NaBH4) exhibits superior stability in alkaline solutions and delivers 10.8 wt.% theoretical hydrogen storage capacity. Nevertheless, its hydrolysis reaction at room temperature must be activated and accelerated by adding an effective catalyst. In this study, we synthesize Co nanoparticles supported on bagasse-derived porous carbon (Co@xPC) for catalytic hydrolytic dehydrogenation of NaBH4. According to the experimental results, Co nanoparticles with uniform particle size and high dispersion are successfully supported on porous carbon to achieve a Co@150PC catalyst. It exhibits particularly high activity of hydrogen generation with the optimal hydrogen production rate of 11086.4 mLH2∙min-1∙gCo-1 and low activation energy (Ea) of 31.25 kJ mol-1. The calculation results based on density functional theory (DFT) indicate that the Co@xPC structure is conducive to the dissociation of [BH4]-, which effectively enhances the hydrolysis efficiency of NaBH4. Moreover, Co@150PC presents an excellent durability, retaining 72.0% of the initial catalyst activity after 15 cycling tests. Moreover, we also explored the degradation mechanism of catalyst performance.

The design and construction of transition metal catalysts with high performance and low-cost characteristics are imperative for liquid hydrogen storage materials. In this study, we prepared ultrathin carbon-stabilized Co-doped CoxOy nanofilms (C-Co/CoxOy NFs) using an ionic liquid/water interface strategy for sodium borohydride (NaBH4) hydrolysis. Owing to its two-dimensional (2D) NF structure and the protective effects of the composite carbon, the C-Co/CoxOy NF catalyst exhibited remarkable activity and durability for hydrogen generation from NaBH4 hydrolysis. The hydrogen generation rate reached 8055 mL·min-1·gCo-1 (5106 mL·min-1·gCat-1) and the catalyst could be recycled more than 20 times, surpassing most reported metal-based catalysts under comparable conditions. In addition, the exceptional 2D Co-based NF structures, with numerous active sites, assisted in the activation of NaBH4 and water molecules, promoting hydrogen production. Thus, these results provided an in-depth understanding of hydrogen generation from NaBH4 hydrolysis, and an effective strategy for rationally designing highly active and durable 2D NF catalysts.

Previous researches suggested that polysaccharides from brown algae had anti-virus activity. We hypothesized that nature polysaccharide from marine plants might have the effect on anti-SARS-CoV-2 activity. By high throughput screening to target 3CLpro enzyme using polysaccharides library, we discover a crude polysaccharide 375 from seaweed Ecklonia kurome blocked 3CLpro enzymatic activity and shows good anti-SARS-CoV-2 infection activity in cell. Further, we show that homogeneous polysaccharide 37502 from the 375 may bind to 3CLpro well and disturb spike protein binding to ACE2 receptor. The structure characterization uncovers that 37502 is alginate. These results imply that the bioactivities of 375 on SARS-CoV-2 may target multiple key molecules implicated in the virus infection and replication. The above results suggest that 375 may be a potential drug candidate against SARS-CoV-2.

Silver nanoparticles (AgNPs) have stable reactivity and excellent optical absorption properties. They can be applied in various industries, such as environmental protection, biochemical engineering, and analyte monitoring. However, synthesizing AgNPs and determining their appropriate dosage as a coloring substance are difficult tasks. In this study, to optimize the process of AgNP synthesis and obtain a simple detection method for trace mercury in the environment, we evaluate several factors-including the reagent addition sequence, reaction temperature, reaction time, the pH of the solution, and reagent concentration-considering the color intensity and purity of AgNPs as the reaction optimization criteria. The optimal process for AgNP synthesis is as follows: Mix 10 mM of silver nitrate with trisodium citrate in a hot water bath for 10 min; then, add 10 mM of sodium borohydride to produce the AgNPs and keep stirring for 2 h; finally, adjust the pH to 12 to obtain the most stable products. For AgNP-based mercury detection, the calibration curve of mercury over the concentration range of 0.1-2 ppb exhibits good linearity (R2 > 0.99). This study provides a stable and excellent AgNP synthesis technique that can improve various applications involving AgNP-mediated reactions and has the potential to be developed as an alternative to using expensive detection equipment and to be applied for the detection of mercury in food.

Mechanochemistry has been proved to be an effective method to remediation of organic-contaminated sites. However, the high ball-to-powder mass ratio (CR) limits the large-scale application of mechanochemistry. In this study, co-milling additives were introduced to enhance the mechanochemical degradation of decabromodiphenyl ether (BDE209)-contaminated soil under the condition of low CR. Based on additive screening experiments, sodium borohydride was selected as the ideal additive to assist the mechanochemical degradation of BDE209, and the resulting removal efficiency was approximately 100% with 2 h of ball milling at a rotational speed of 550 rpm. The main degradation intermediates and degradation pathway of BDE209 were identified using gas chromatography-tandem mass spectrometry. It was proposed that the degradation of BDE209 by sodium borohydride-assisted mechanochemistry was a concurrent process of stepwise and multistage debromination. Meanwhile, the meta-bromine atom in BDE209 was more susceptible to debromination than those at the para and ortho positions. The evolution of the concentration of Br- was monitored by ion chromatography, which revealed that reduction and oxidation both occurred in the removal of BDE209. This paper provides a new perspective for reducing the CR in the mechanochemical remediation of BDE209-contaminated soil.

Catalytic hydrogen reduction has appeared as a promising strategy for chemical denitrification with advantages of high activity and simple operation. However, the risk and low utilization of H2 is the disadvantage of catalytic hydrogen reduction. In recent years, catalytic reduction reactions in the presence of sodium borohydride (NaBH4) have been extensively studied. NaBH4 can be used as an electron source to generate electrons on the surface of the catalyst and can catalyze the reduction of pollutants. But it makes commercialization costly and causes significant environmental pollution if widely use NaBH4. In this study, we prepared supported Pd/Sn bimetallic nanoparticles which could adsorb NaBH4 during the preparation of the Pd/Sn bimetallic catalyst as the prestoring reductant. No additional reducing agent is required during nitrate reduction process. The performance and mechanism for nitrate reduction by using Pd/Sn bimetallic nanoparticles were discussed. Moreover, the catalyst D-Pd1/Sn1 reached a complete nitrate removal in the municipal wastewater treatment plant effluent water within 3 h. The results provide a prospect for denitrification in biological wastewater treatment plants.

Catalytic hydrogen reduction appears to be a promising strategy for nitrate removal. However, the danger and low utilization of H2 are the disadvantages of catalytic hydrogen reduction. Sodium borohydride (NaBH4), considered a potential candidate for hydrogen storage, has been investigated as an electron source for the catalytic reduction of contaminants. However, extensive use of NaBH4 makes commercialization costly and causes environmental pollution. In this study, we prepared supported Cu/Pd bimetallic nanoparticles that could prestore hydrogen. No additional reducing agent was required during the nitrate reduction process. The performance and mechanism of Cu/Pd bimetallic nanoparticles for nitrate reduction are discussed. Good performance was obtained with high reactivity (99.04% nitrate removal efficiency) and high selectivity for N2 (94.71%). The Cu/Pd bimetallic catalyst could be recovered by NaBH4 for 5 cycles. Moreover, a 97.49% nitrate removal efficiency was obtained for actual wastewater, indicating good prospects for nitrate reduction applications.