Additional Functional Groups Research Articles

Gamma-ray irradiation to achieve high tensile performance of unidirectional CNT yarn laminates

Continuous carbon nanotube (CNT) yarn fabricated from a floating catalyst chemical vapor deposition (FCCVD) method is treated under gamma-ray irradiation to enhance the mechanical properties of the CNT yarn and its unidirectional composite laminates. Gammy-ray doses varying from 50 kGy to 1200 kGy are used to irradiate CNT yarns and their microstructures, tensile properties and surface characterizations are studied. The graphitic structure change is not clear from the transmission electron microscopy, however, the specific tensile strength and modulus of yarn vary slightly within 10 % as the dose increased. This modulus trend coincides with mesoscopic distinct element modeling (mDEM) simulation results. Surface characterization shows additional oxygen functional groups and smaller contact angles after irradiation. Interestingly, the specific tensile properties of composite laminates also increase relative to the yarns, and the unidirectional laminate from CNT yarn treated with the optimal dose of 700 kGy achieves specific strength and modulus as high as 1.89 GPa/gcm−3 and 258 GPa/gcm−3, respectively, which are 30.9 % and 37 % increases compared to the control laminate. The results indicate that radiation-induced crosslinking among the CNTs and the formation of surface-active sites leads to enhanced load transfer in the yarns and promote CNT/resin interfacial bonding.

Decarboxylation and Tandem Reduction/Decarboxylation Pathways to Substituted Phenols from Aromatic Carboxylic Acids Using Bimetallic Nanoparticles on Supported Ionic Liquid Phases as Multifunctional Catalysts.

Valuable substituted phenols are accessible via the selective decarboxylation of hydroxybenzoic acid derivatives using multifunctional catalysts composed of bimetallic iron-ruthenium nanoparticles immobilized on an amine-functionalized supported ionic liquid phase (Fe25Ru75@SILP+IL-NEt2). The individual components of the catalytic system are assembled using a molecular approach to bring metal and amine sites into close contact on the support material, providing high stability and high decarboxylation activity. Operating under a hydrogen atmosphere was found to be essential to achieve high selectivity and yields. As the catalyst materials enable also the selective hydrogenation and hydrodeoxygenation of various additional functional groups (i.e., formyl, acyl, and nitro substituents), direct access to the corresponding phenols can be achieved via integrated tandem reactions. The approach opens versatile synthetic pathways for the production of valuable phenols from a wide range of readily available substrates, including compounds derived from lignocellulosic biomass.

Assessment of the feed additive consisting of orthophosphoric acid for all animal species for the renewal of its authorisation (Prayon S.A.; Chemische Fabrik Budenheim KG; BK Giulini GmbH).

Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the application for renewal of orthophosphoric acid as a technological additive (functional group: preservatives) for all animal species. The applicant has provided evidence that the additive currently on the market complies with the existing conditions of authorisation. There is no evidence that would lead the FEEDAP Panel to reconsider its previous conclusions. Thus, the Panel concluded that the additive remains safe for all animal species provided that the optimal Ca:P ratio is maintained. Additionally, the FEEDAP Panel concluded that orthophosphoric acid remains safe for the consumer and the environment under the authorised conditions of use. Regarding the user safety, orthophosphoric acid is corrosive to the skin and eyes and should be considered as hazardous to the respiratory tract. There is no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.

Safety and efficacy of a feed additive consisting of Enterococcus faeciumDSM 33761, Pediococcus acidilacticiDSM 33758, Bifidobacterium animalisDSM 16284, Limosilactobacillus reuteriDSM 33751 and Ligilactobacillus salivariusDSM 16351 (Biomin® C5) for chickens for fattening, chickens reared for laying, turkeys for fattening, turkeys reared for breeding and minor poultry species for fattening and reared for laying/breeding (Biomin GmbH).

Following a request from the European Commission, the EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of a feed additive consisting of viable cells of Enterococcus faecium DSM 33761, Pediococcus acidilactici DSM 33758, Bifidobacterium animalis DSM 16284, Limosilactobacillus reuteri DSM 33751 and Ligilactobacillus salivarius DSM 16351 (Biomin® C5) as a zootechnical additive (functional group: gut flora stabiliser) for chickens for fattening, chickens reared for laying, turkeys for fattening, turkeys reared for breeding and minor poultry species for fattening and reared for laying/breeding. Biomin® C5 is marketed in two formulations: a coated and a non-coated formulation with a total minimum microbial count of 1 × 1011 and 4 × 1010 colony forming unit (CFU)/g product, respectively. The Panel considered that the use of Biomin® C5 in feed at the proposed conditions of use raises no risk for the target species, consumers and the environment. Both coated and non-coated formulations of Biomin® C5 are considered respiratory and skin sensitisers, but not skin irritants. The FEEDAP Panel was not in the position to conclude on the eye irritation potential of any formulation. Due to lack of sufficient data, the FEEDAP Panel could not conclude on the efficacy of the additive in the target species at the proposed conditions of use. Biomin® C5 is compatible with nicarbazin, diclazuril, decoquinate and halofuginone. No conclusions can be drawn on the compatibility of Biomin® C5 with monensin sodium, robenidine hydrochloride, maduramicin ammonium and lasalocid A sodium.

Complexity-Building ESIPT-Assisted Synthesis of Fused Polyheterocyclic Sulfonamides.

Excited State Intramolecular Proton Transfer (ESIPT), originally discovered and explored in depth in a number of extensive photophysical studies, is more recently rediscovered as a powerful synthetic tool, offering rapid access to complex polyheterocycles. In our prior work we have employed ESIPT in aromatic o-keto amines and amides, leading to diverse primary photoproducts-complex quinolinols or azacanes possessing a fused lactam moiety-which could additionally be modified in short, high-yielding postphotochemical reactions to further grow complexity of the heterocyclic core scaffold and/or to decorate it with additional functional groups. Given that sulfonamides are generally known as privileged substructures, in this study we pursued two goals: (i) To explore whether sulfonamides could behave as proton donors in the context of ESIPT-initiated photoinduced reactions; (ii) To assess the scope of subsequent complexity-building photochemical and postphotochemical steps, which give access to polyheterocyclic molecular cores with fused cyclic sulfonamide moieties. In this work we show that this is indeed the case. Simple sulfonamide-containing photoprecursors produced the sought-after heterocyclic products in experimentally simple photochemical reactions accompanied by significant step-normalized complexity increases as corroborated by the Böttcher complexity scores.

Linker-Functionalized Phosphinate Metal-Organic Frameworks: Adsorbents for the Removal of Emerging Pollutants.

Metal-organic frameworks (MOFs) are attracting increasing attention as adsorbents of contaminants of emerging concern that are difficult to remove by conventional processes. This paper examines how functional groups covering the pore walls of phosphinate-based MOFs affect the adsorption of specific pharmaceutical pollutants (diclofenac, cephalexin, and sulfamethoxazole) and their hydrolytic stability. New structures, isoreticular to the phosphinate MOF ICR-7, are presented. The phenyl ring facing the pore wall of the presented MOFs is modified with dimethylamino groups (ICR-8) and ethyl carboxylate groups (ICR-14). These functionalized MOFs were obtained from two newly synthesized phosphinate linkers containing the respective functional groups. The presence of additional functional groups resulted in higher affinity toward the tested pollutants compared to ICR-7 or activated carbon. However, this modification also comes with a reduced adsorption capacity. Importantly, the introduction of the functional groups enhanced the hydrolytic stability of the MOFs.

Design and Synthesis of a Polyketone Building Block with Vinyl Groups-9,10-Diethyl-9,10-ethenoanthracene-2,3,6,7(9H,10H)-tetraone-and a Preliminary Photoelectrical Property Study of Its Azaacene Derivatives.

Polyketone compounds are powerful building blocks to synthesize various organic functional materials. Despite that a great many number of planar and non-planar polyketone building blocks have been developed, one issue is that generally there are only ketone functional groups on the molecular skeleton, which will constrain their transformation and further limit the development of functional materials. In this work, we report the design and synthesis of a building block 9,10-diethyl-9,10-ethenoanthracene-2,3,6,7(9H,10H)-tetraone with additional vinyl functional groups. In addition, its azaacene derivatives were also synthesized, and their preliminary physicochemical properties were studied.

Effect of plasma treatment on electrochemical performance of lignin-based carbon fibers

The abundant and renewable nature of lignin obtained from wood renders it as a sustainable carbon resource for energy storage applications. However, their environmentally unfavorable processing conditions and limited energy storage performance prohibit the use of lignin-based carbon materials' use as supercapacitor electrodes. The material's properties require advancement to overcome the limitation of low specific capacitances. In this study, we report on the impact on the electrochemical performance of inherently hydrophobic lignin-based carbon fibers (LCF) by subjecting them to a mild plasma treatment. The electrode’s capacitance was thus increased by 20%, with better rate capability and energy-power performance (11 Wh/kg and 0.8 kW/kg) in the KOH electrolyte. The quantified improvements were attributed to the capacitive functional groups, and enhanced surface wettability, which increased ion accessibility to active surface area improving charge-transfer ability to the surface with more additional functional groups. Remarkably, the selected plasma conditions introduced mostly desirable functional groups that limited any parasitic faradaic reactions prone to affect the device's long-term cycling stability and self-discharge characteristics. Furthermore, the impact of different inherent and introduced oxygen surface functional groups, including COO−, COH, CO, and CO, on the capacitive performance of these fibers at different device conditions (such as cycling and electrochemical activation) was investigated in different aqueous electrolytes. To ensure environmental favorability, the electrospinning of lignin fibers was conducted using a high molecular fraction of lignin without the inclusion of any fossil-based co-spinning polymers.

Synthesis, Structure, Reactivity, and Intramolecular Donor-Acceptor Interactions in a Phosphinoferrocene Stibine and Its Corresponding Phosphine Chalcogenides and Stiboranes.

Ferrocene-based phosphines equipped with additional functional groups are versatile ligands for coordination chemistry and catalysis. This contribution describes a new compound of this type, combining phosphine and stibine groups at the ferrocene backbone, viz. 1-(diphenylphosphino)-1'-(diphenylstibino)ferrocene (1). Phosphinostibine 1 and the corresponding P-chalcogenide derivatives Ph2P(E)fcSbPh2 (1E, fc = ferrocene-1,1'-diyl, E = O, S, Se) were synthesized and further converted to the corresponding stiboranes Ph2P(E)fcSb(O2C6Cl4)Ph2 (6 and 6E) by oxidation with o-chloranil. All compounds were characterized by spectroscopic methods, X-ray diffraction analysis, cyclic voltammetry, and theoretical methods. Both NMR spectroscopy and DFT calculations confirmed the presence of P → Sb and P═O → Sb donor-acceptor interactions in 6 and 6O, triggered by the oxidation of the stibine moiety into Lewis acidic stiborane. The corresponding interactions in 6S and 6Se were of the same type but significantly weaker. A coordination study with AuCl as the model metal fragment revealed that the phosphine group acts as the "primary" coordination site, in line with its higher basicity. The obtained Au(I) complexes were applied as catalysts in the Au-catalyzed cyclization of N-propargylbenzamide and in the oxidative [2 + 2 + 1] cyclization of ethynylbenzene with acetonitrile and pyridine N-oxides. The catalytic results showed that the stibine complexes had worse catalytic performance than their phosphine counterparts, most likely due to the formation of weaker coordination bonds and hence poorer stabilization of the active metal species. Nevertheless, the stibine moiety could be used to fine-tune the properties of the ligated metal center by changing the oxidation state or substituents at the "remote" Sb atom.

Synthesis, crystal growth and supramolecular chemistry of 4-dimethylaminopyridinium salts of benzoates and a phenolate ion

Abstract Seven novel molecular salts were synthesized from the commonly available 4-dimethylaminopyridine organic base and benzoic acid derivatives contain additional functional groups. Benzoic acids with additional hydroxyl, nitro, amino, and bromo functional groups, were successfully employed and investigated their role in non-covalent interactions within the supramolecular chemistry of heterosynthons solid-state architecture. The collection of all 4-dimethylamopyrinium salts of benzoates and phenolate was accomplished through the utilization of conventional solvent evaporation technique. The resulting molecular salts were afforded by deprotonation of the acidic moiety such as COOH, or OH to the ring N of 4-dimethylaminopyridine, establishing a strong charged-assisted hydrogen bond between the deprotonated group (benzoate or phenolate) and protonated ring N. The structure of compounds was fully elucidated by single X-ray diffraction, powder X-ray diffraction, 1H NMR, FT-IR, and thermogravimetric analysis. The crystal packing is interpreted by the strong charge-assisted N–H⋯O hydrogen bond between the NH+ and the corresponding deprotonated group and O–H⋯O, N–H⋯N hydrogen bonding. The analysis concluded that C–H⋯O, CH3⋯O, C–H⋯π, CH3⋯π, π–π, C–H⋯Br, and CH3⋯Br contacts contribute significantly to stabilizing and expanding the high-dimensionality (2D–3D framework) of the structures. The structures were thoroughly explored for their various bonding and nonbonding interactions, as well as their supramolecular chemistry in detail. The antimicrobial activities of all compounds were evaluated using the Oxford cup method.

Assessment of the feed additive consisting of alpha-galactosidase produced by Saccharomyces cerevisiaeCBS 615.94 and endo-1,4-beta-glucanase produced by Aspergillus nigerCBS 120604 (Agal-Pro BL/BL-L®) for use in chickens for fattening, minor poultry species for fattening and chickens reared for laying for the renewal of its authorisation (Kerry Ingredients & Flavours Ltd.).

Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the assessment of the application for renewal of Agal-Pro BL/BL-L®. The additive is a preparation of alpha-galactosidase produced by a genetically modified strain of Saccharomyces cerevisiae (CBS 615.94) and endo-1,4-beta-glucanase produced by a non-genetically modified strain of Aspergillus niger (CBS 120604). It is intended to be used as a zootechnical additive (functional group: digestibility enhancers) in chickens for fattening in its solid and liquid forms (Agal-Pro BL® and Agal-Pro BL-L®), and in minor poultry species for fattening and chickens reared for laying only in its solid form (Agal-Pro BL®). The applicant has provided evidence that the additive currently on the market complies with the existing conditions of authorisation. There is no new evidence that would lead the FEEDAP Panel to reconsider its previous conclusions. Thus, the Panel concludes that the additive remains safe for the target animals, consumers and the environment under the authorised conditions of use. Regarding user safety, the additive is considered an irritant to the skin and eyes and a dermal sensitiser. Due to the proteinaceous nature of the active substances, it should be considered a respiratory sensitiser. There is no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.

Surface Heterogeneity Affects Adsorption Selectivity for CO2 Over CH4 in Bare Mesostructured Silica with 2D Hexagonal Symmetry and Different Pore Size

AbstractMesoporous silica‐based materials are used as sorbents and supports in many fields. The ordered pore architecture of MCM‐41, and the absence of interconnections, make it suitable as a model system. The surface is natively functionalized by many silanol groups, endowing the material with a polar surface to directly interact with the target species or to mount additional functional groups. Either bare or functionalized, surface silanol arrangement is crucial to material performance. In the case of CO2 capture with amine‐functionalized silica, silanol groups are responsible for fundamental H‐bonds during chemisorption, but they also modulate the effect and weight of humidity on the material performance. In addition, the silanol groups can also tune the weight of physisorption over chemisorption. The relationship between these aspects and the textural features of mesostructured silica has not been addressed in detail. In this study, computer models are employed to investigate the adsorption capacity and selectivity of bare mesostructured silica with three different pore sizes. Results are rationalized in terms of silanol surface density and pore curvature. The importance of the energetic inequivalence between Q3 and Q2 sites on the silica surface is emphasized, as this causes adsorption behavior to deviate from ideality.

Regio- and Enantioselective Catalytic δ-C-H Amidation of Dioxazolones Enabled by Open-Shell Copper-Nitrenoid Transfer.

Controlling regio- and enantioselectivity in C-H functionalization reactions is of paramount importance due to their versatile synthetic utilities. Herein, we describe a new approach for the asymmetric δ-C(sp3)-H amidation catalysis of dioxazolones using a Cu(I) precursor with a chiral bisoxazoline ligand to access six-membered lactams with high to excellent regio- and enantioselectivity (up to >19:1 rr and >99:1 er). Combined experimental and computational mechanistic studies unveiled that the open-shell character of the postulated Cu-nitrenoids enables the regioselective hydrogen atom abstraction and subsequent enantio-determining radical rebound of the resulting carbon radical intermediates. The synthetic utility of this asymmetric cyclization was demonstrated in the diastereoselective introduction of additional functional groups into the chiral δ-lactam skeleton as well as in the rapid access to biorelevant azacyclic compounds.

Multigram Synthesis of α‐ and γ‐((Hetera)cyclo)alkylpyridines through α‐Arylation of (Hetero)aliphatic Nitriles

AbstractA systematic study on the SnAr reaction of halogenated fluoropyridines and (hetero)aliphatic nitrile anions as an approach to the synthesis of functionalized pyridines bearing a (cyclo)alkyl or saturated heterocyclic substituent by is described. The scope of the method was demonstrated on a wide range of (hetero)aliphatic nitriles (including three‐ to six‐membered cycloalkane derivatives and N‐, O‐, S‐containing saturated heterocycles) and all isomeric halogenated 2‐and 4‐fluoropyridines. High chemo‐ and regioselectivity (i. e., exclusive substitution of the fluorine atom), as well as excellent scalability of the proposed reaction sequence were demonstrated (up to 450 g for the arylation step or up to 77 g of cycloalkylpyridine over two steps in a single run). The utility of the synthesized products was illustrated in the additional functional group transformations resulting in synthetically valuable pyridine‐containing building blocks.

Efficacy of a feed additive consisting of endo‐1,4‐beta‐xylanase produced by Komagataella phaffii ATCC PTA‐127053 (Xygest™ HT) for all poultry species (Kemin Europa N.V.)

Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the efficacy of endo-1,4-beta-xylanase produced by Komagataella phaffii ATCC PTA-127053 (Xygest™ HT) as a zootechnical feed additive (functional group: digestibility enhancers) for all poultry. In a previous opinion, the FEEDAP Panel concluded that Xygest™ HT is safe for all poultry, consumers, and the environment. The additive is not considered to be irritant to eyes and skin but a dermal and a respiratory sensitiser, although exposure by inhalation is unlikely. The Panel also concluded that the additive has the potential to be efficacious in laying hens at 45,000 U/kg complete feed and this conclusion was extrapolated to all laying poultry. However, the Panel could not conclude on the efficacy of the product in growing poultry at the proposed conditions of use. In the current application, the applicant provided an additional efficacy trial in chickens for fattening. The results showed a higher apparent metabolisable energy (nitrogen corrected) in chickens fed the additive at the minimum proposed level of 30,000 U/kg complete feed when compared to the control group. Considering the previously submitted studies in laying hens and chickens for fattening, and the newly submitted study in chickens for fattening, the Panel concluded that Xygest™ HT has the potential to be efficacious to enhance digestibility in all poultry at the corresponding proposed minimum levels in feed.

Safety and efficacy of a feed additive consisting of endo-1,4-beta-xylanase, endo-1,3(4)-beta-glucanase and endo-1,4-beta-glucanase produced by Trichoderma reeseiATCC 74444 (Ronozyme® Multigrain) for use in poultry for fattening, poultry for laying and piglets (weaned) (DSM Nutritional Products).

Ronozyme® Multigrain G/L is the trade name of the feed additive under assessment containing endo-1,4-beta-xylanase, endo-1,4-beta-glucanase and endo-1,3(4)-beta-glucanase produced by a non-genetically modified strain of Trichoderma reesei (ATCC 74444). It is authorised for use as a zootechnical additive (functional group: digestibility enhancer) in poultry for fattening, poultry for laying and weaned piglets. This scientific opinion concerns the request for the renewal of the authorisation of the additive for the species/categories for which there is an authorisation. The applicant provided evidence that the additive currently in the market complies with the conditions of the authorisation. There is no new evidence that would lead the EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) to reconsider previous conclusions that the additive is safe for the animal species/categories, the consumer and the environment under the authorised conditions of use. Regarding the safety for the user, the additive should be considered a potential respiratory sensitiser. In absence of data, the Panel could not conclude on the potential of the additive to cause skin and eye irritation or dermal sensitisation. There was no need for assessing the efficacy of the additive in the context of the renewal of the authorisation for poultry for fattening, poultry for laying and weaned piglets.

Safety and efficacy of a feed additive consisting of a preparation of essential oils of thyme and star anise, and quillaja bark powder (BIOSTRONG® 510 all natural) for all poultry species (Delacon Biotechnik GmbH).

Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the safety and efficacy of a preparation consisting of essential oils of thyme and star anise, and quillaja bark powder (BIOSTRONG® 510 all natural) as a zootechnical feed additive (functional groups: digestibility enhancer; other zootechnical additives) for all poultry species. BIOSTRONG® 510 all natural is a preparation of partially microencapsulated essential oils, quillaja bark powder, dried herbs and dried spices. The additive contains estragole (up to ■■■■■. For short-living animals, the EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) had no safety concerns when the additive is used at the recommended level of 150 mg/kg complete feed for chickens for fattening and other poultry species for fattening. For long-living animals, the use of the additive was considered of concern owing to the presence of estragole. No safety concern would be expected for the consumer and the environment from the use of the additive at the recommended use level in feed. The Panel concluded that the additive is corrosive to the eyes but not irritant to skin. It may be a respiratory irritant or dermal or respiratory sensitiser. When handling the additive, exposure of unprotected users to estragole ■■■■■ may occur. Therefore, to reduce the risk, the exposure of the users should be minimised. The additive BIOSTRONG® 510 all natural was considered efficacious for chickens for fattening at the use level 150 mg/kg complete feed. This conclusion was extrapolated to all poultry species for fattening or reared for laying/breeding. ■■■■■.

Safety and efficacy of a feed additive consisting of Macleaya cordata (Willd.) R. Br. extract and leaves (Sangrovit® extra) for all poultry species (excluding laying and breeding birds) (Phytobiotics Futterzusatzstoffe GmbH).

Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the safety and efficacy of Macleaya cordata (Willd.) R. Br. extract and leaves (Sangrovit® Extra) when used as a zootechnical feed additive (functional group: other zootechnical additives) for all poultry species (excluding laying and breeding birds). The additive is standardised to contain a concentration of the sum of the four alkaloids sanguinarine, chelerythrine, protopine and allocryptopine of 1.25%, with 0.5% sanguinarine. Owing to the presence of the DNA intercalators sanguinarine and chelerythrine, a concern for genotoxicity was identified. The EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) had no safety concerns when the additive is used at the recommended level of 150 mg/kg complete feed (corresponding to 0.750 mg sanguinarine/kg complete feed) for chickens for fattening and other poultry species for fattening. No conclusion can be drawn for poultry reared for laying/breeding. The use of Sangrovit® Extra in poultry species for fattening at the maximum recommended level was considered of low concern for consumers. The additive was shown to be irritant to the eyes but not irritant to skin or a skin sensitiser. The FEEDAP Panel could not exclude the potential of the additive to be a respiratory sensitiser. When handling the additive, exposure of unprotected users to sanguinarine and chelerythrine may occur. Therefore, to reduce the risk, the exposure of users should be reduced. The use of Sangrovit® Extra as a feed additive under the proposed conditions of use was considered safe for the environment. The additive Sangrovit® Extra had the potential to be efficacious in improving performance of chickens for fattening at 45 mg/kg complete feed. This conclusion was extended to chickens reared for laying/breeding and extrapolated to all poultry species for fattening or reared for laying/breeding.

Safety and efficacy of a feed additive consisting of Lentilactobacillus buchneriDSM 32650 as a feed additive for all animal species (BioCC OÜ).

Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the safety and efficacy of Lentilactobacillus buchneri DSM 32650 as a technological feed additive (functional group: silage additive) for all animal species. The additive is intended to improve the production of silage at a proposed application rate of 1 × 108 colony-forming units (CFU)/kg fresh material. The bacterial species L. buchneri is considered by the European Food Safety Authority to be suitable for the qualified presumption of safety (QPS) approach. As the identity of the strain has been established and no antimicrobial resistance determinants of concern were detected, the use of the strain as a silage additive is considered safe for the target species, consumers and the environment. In the absence of data, the FEEDAP Panel cannot conclude on the potential of the additive to be a skin/eye irritant or a skin sensitiser. Given the proteinaceous nature of the active agent, the additive should be considered a respiratory sensitiser. The FEEDAP Panel concluded that Lentilactobacillus buchneri DSM 32650 at a minimum concentration of 1 × 108 CFU/kg fresh material may extend the aerobic stability of silage from easy and moderately difficult to ensile fresh material with a dry matter content ranging from 28% to 45%.

Synthesizing sulfhydryl-functionalized biochar for effectively removing mercury ions from contaminated water.

Biochar is regarded as an effective adsorbent for heavy metal pollution treatment, and functional optimization is still needed to improve its performance. We created raw biochar (BC and BP) from corn straw and pine sawdust, which were modified to produce sulfhydryl-modified biochar (MBC and MBP). Isothermal adsorption experiments and adsorption kinetics experiments as well as the related model fitting were performed to evaluate the adsorption performance of biochar on Hg(II). According to the results of the Langmuir model fitting, the maximum adsorption capacities of sulfhydryl-modified biochar were 193.05mg/g (MBC) and 178.04mg/g (MBP), respectively, which were approximately 1.6 times higher than the raw biochar. The results showed that adding sulfhydryl groups to biochar can improve its adsorption performance. The prompt effect resulted from the sulfhydryl modification providing additional functional groups and enhanced chemisorption and physical adsorption properties.