The high conductivity of electrocatalyst can eliminate the Schottky energy barrier at the interface of heterogeneous phases during an electrocatalytic reaction and accelerate the rapid electron transfer to the catalyt...The high conductivity of electrocatalyst can eliminate the Schottky energy barrier at the interface of heterogeneous phases during an electrocatalytic reaction and accelerate the rapid electron transfer to the catalytic active center.Therefore,the electronic conductivity is a vital parameter for oxygen reduction reaction(ORR).Covalent triazine frameworks(CTFs)have shown great potential application as electrocatalysts in ORR with a merit of the diverse building blocks.However,the intrinsic low conductivity and high impedance of CTFs could be significant setbacks in electrocatalytic application.Herein,CTFs were constructed by introducing F and N co-modification for efficient 2e^(-)ORR.Compared with the pristine CTF,the co-presence of F,N could increase the conductivity obviously by 1000-fold.As a result,F-N-CTF exhibits enhanced catalytic performance of H_(2)O_(2)generation and selectivity towards reaction pathways.This work reveals the importance of conductivity optimization for CTFs and provides guidance for designing high conductivity non-metallic organic semiconductor catalysts for 2e^(-)ORR.展开更多
Photoinduced molecular oxygen activation is crucial for artificial photosynthesis.However,metal-free semiconductor photocatalysts with high activation efficiency are still lacking up to now.Herein,two isomorphic tris(...Photoinduced molecular oxygen activation is crucial for artificial photosynthesis.However,metal-free semiconductor photocatalysts with high activation efficiency are still lacking up to now.Herein,two isomorphic tris(triazolo)triazine-based covalent organic frameworks were successfully constructed under solvothermal conditions.And they possess high crystallinity,inherent porosity with large surface area and good stability.Strong electron donor-acceptor skeletons expand the visible light harvesting,also facilitate the charge separation and thus lead to their superior activity of photoinduced molecular oxygen activation including photosynthesis of tetrahydroquinolines and hydrogen peroxide.This work provides a way to improve the efficiency of molecular oxygen activation through the rational design of COFs,and also opens new avenues for the construction of highly active and metal-free photocatalysts toward sustainable solar-to-chemical energy conversion.展开更多
Converting CO_(2)and water into valuable chemicals like plant do is considered a promising approach to address both environmental and energy issues.Taking inspiration from the structures of natural leaves,we designed ...Converting CO_(2)and water into valuable chemicals like plant do is considered a promising approach to address both environmental and energy issues.Taking inspiration from the structures of natural leaves,we designed and synthesized a novel copper-coordinated covalent triazine framework(CuCTF)supported by silicon nanowire arrays on wafer chip.This marks the first-ever application of such a hybrid material in the photoelectrocatalytic reduction of CO_(2)under mild conditions.The Si@CuCTF6 heterojunction has exhibited exceptional selectivity of 95.6%towards multicarbon products(C_(2+))and apparent quantum efficiency(AQE)of 0.89%for carbon-based products.The active sites of the catalysts are derived from the nitrogen atoms of unique triazine ring structure in the ordered porous framework and the abundant Cu-N coordination sites with bipyridine units.Furthermore,through DFT calculations and operando FTIR spectra analysis,we proposed a comprehensive mechanism for the photoelectrocatalytic CO_(2)reduction,confirming the existence of key intermediate species such as*CO_(2)-,*=C=O,*CHO and*CO-CHO etc.This work not only provides a new way to mimic photosynthesis of plant leaves but also gives a new opportunity to enter this research field in the future.展开更多
Solar‐driven CO_(2)conversion to precious fossil fuels has been proved to become a potential way to decrease CO_(2)with producing renewable fuels,which mainly relies on photocatalysts with efficient charge separation...Solar‐driven CO_(2)conversion to precious fossil fuels has been proved to become a potential way to decrease CO_(2)with producing renewable fuels,which mainly relies on photocatalysts with efficient charge separation.In this work,a metal free heterostructure of covalent triazine framework(CTF)and graphite carbon nitride(g‐C_(3)N_(4),abbreviated as CN)is applied in the CO_(2)photoreduction for the first time.Detailed characterization methods such as photoluminescence(PL)and time‐resolved PL(TR‐PL)decay are utilized to reveal the photo‐induced carries separating process on g‐C_(3)N_(4)/CTF(CN/CTF)heterostructure.The introduced CTF demonstrated a great boosting photocatalytic activity for CN,bringing about the transform rates of CO_(2)to CO reaching 151.1μmol/(g·h)with a 30 h stabilization time,while negligible CH_(4)was detected.The optimal CN/CTF heterostructure could more efficiently separate charges with a lower probability of recombination under visible light irradiation,which made the photoreduction efficiency of CO_(2)to CO be 25.5 and 2.5 times higher than that of CTF and CN,respectively.This investigation is expected to offer a new thought for fabricating high‐efficiency photocatalyst without metal in solar‐energy‐driven CO_(2)reduction.展开更多
The photocatalytic production of syngas using a noble-metal-free catalytic system is a promising approach for renewable energy and environmental sustainability.In this study,we demonstrate an efficient catalytic syste...The photocatalytic production of syngas using a noble-metal-free catalytic system is a promising approach for renewable energy and environmental sustainability.In this study,we demonstrate an efficient catalytic system formed by integrating Co single sites,which act as the active sites,in covalent triazine frameworks(CTFs),which act as the photoabsorber,for the photocatalytic production of syngas from CO2 in aqueous solution.The enhanced light absorption of the CTFs,which contain intramolecular heterojunctions,in conjunction with 0.8 mmol L^‒1 of the Co complex enables excellent syngas production with a yield of 3303μmol g‒1(CO:H2=1.4:1)in 10 h,which is about three times greater than that achieved using CTF without a heterojunction.In the photocatalytic reaction,the coordinated single Co centers accept the photogenerated electrons from the CTF,and serve as active sites for CO2 conversion through an adsorption-activation-reaction mechanism.Theoretical calculations further reveal that the intramolecular heterojunctions highly promote photogenerated charge separation,thus boosting photocatalytic syngas production.This work reveals the promising potential of CTFs for single-metal-site-based photocatalysis.展开更多
Adsorption of atrazine, prometryne and prometon was determined on six soils with different physical and chemical properties. The adsorption isotherms of three herbicides could well fit Freundlich equation. On all of s...Adsorption of atrazine, prometryne and prometon was determined on six soils with different physical and chemical properties. The adsorption isotherms of three herbicides could well fit Freundlich equation. On all of six soils, adsorption of herbicides increased in the order: atrazine ≈prometon<prometryne. This order is quite the same to the calculation result of by means of excess thermodynamic properties of triazine. The Freundlich adsorption constants, K f, showed to have good correlation with organic matter(OM%) of soils for each of these herbicides, suggesting that OM is the main factor, which dominates in the adsorption process of these triazine herbicides.展开更多
A new method for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine (TAAT) is described. The key intermediate 4,4′,6,6′-tetra(azido)hydrazo-1,3,5-triazine (TAHT) was synthesized by nucleophilic substitution...A new method for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine (TAAT) is described. The key intermediate 4,4′,6,6′-tetra(azido)hydrazo-1,3,5-triazine (TAHT) was synthesized by nucleophilic substitution in the case of sodium azide as nucleophile. N-Bromosuccinide (NBS) was used as oxidant to oxidize TAHT by a tractable operation under mild reaction condition. The target compound TAAT was obtained with a facile process and high overall yield of 81%. The structures of TAAT and its intermediates were identified by spectroscopic methods.展开更多
Carbon super-heterostructures with high nitrogen contents from the covalent hybrid precursors of covalent triazine frameworks(CTFs)and zeolitic imidazolic frameworks(ZIFs)are scarcely explored because of CTF's ord...Carbon super-heterostructures with high nitrogen contents from the covalent hybrid precursors of covalent triazine frameworks(CTFs)and zeolitic imidazolic frameworks(ZIFs)are scarcely explored because of CTF's ordered structure and toxic superacid that dissolves or destabilizes the metal nodes.To solve this problem,herein,we report a straightforward two-step pathway for the covalent hybridization of disordered CTF(d–CTF)–ZIF composites via preincorporation of an imidazole(IM)linker into ordered CTFs,followed by the imidazole-site-specific covalent growth of ZIFs.Direct carbonization of these synthesized d–CTF−IM−ZIF hybrids results in unique hollow carbon super-heterostructures with ultrahigh nitrogen content(>18.6%),high specific surface area(1663m^(2)g^(−1)),and beneficial trace metal(Co/Zn NPs)contents for promoting the redox pseudocapacitance.As proof of concept,the obtained carbon super-heterostructure(Co–Zn–NC_(SNH)–800)is used as a positive electrode in an asymmetric supercapacitor,demonstrating a remarkable energy density of 61Wh kg^(−1)and extraordinary cyclic stability of 97%retention after 30,000 cycles at the cell level.Our presynthetic modifications of CTF and their covalent hybridization with ZIF crystals pave the way toward new design strategies for synthesizing functional porous carbon materials for promising energy applications.展开更多
Highly porous nitrogen-doped carbon materials were synthesized by the carbonization of a low-cost porous covalent triazine polymer, PCTP-3, which had been synthesized by the AlClcatalyzed FriedelCrafts reaction of rea...Highly porous nitrogen-doped carbon materials were synthesized by the carbonization of a low-cost porous covalent triazine polymer, PCTP-3, which had been synthesized by the AlClcatalyzed FriedelCrafts reaction of readily available monomers. The nature of the bond and structure of the resulting materials were confirmed using various spectroscopic methods, and the effects of KOH activation on the textural properties of the porous carbon materials were also examined. The KOH-activated porous carbon（aPCTP-3c） materials possessed a high surface area of 2271 mgand large micro/total pore volumes of 0.87/0.95 cmg, respectively, with narrower micropore size distributions than the porous carbon prepared without activation（PCTP-3c）. The aPCTP-3c exhibited the best COuptakes of 284.5 and 162.3 mg gand CHuptakes of 39.6 and 25.9 mg gat 273 and 298 K/1 bar, respectively, which are comparable to the performance of some benchmark carbon materials under the same conditions. The prepared materials exhibited high CO/Nselectivity and could be regenerated easily.展开更多
A new method for the determination of atrazine, simazine and prometryn in water samples by on-line sweeping concentration technique in micellar electrokinetic chromatography （MEKC） was developed. Various parameters ...A new method for the determination of atrazine, simazine and prometryn in water samples by on-line sweeping concentration technique in micellar electrokinetic chromatography （MEKC） was developed. Various parameters affecting sample enrichment and separation efficiency were systematically studied. Compared with the conventional MEKC method, up to 60-200-fold improvement in concentration sensitivity was achieved in terms of peak height by using this sweeping injection technique. The compound strychnine was used as the internal standard for the improvement of the experimental reproducibility. The limits of detection （S/ N = 3：1） for atrazine, simazine and prometryn were 9, 10 and 0.5 ng mL-1, respectively. This method has been successfully applied to the analysis of atrazine, simazine and prometryn in lake, steam and ground water.展开更多
Polymeric carbon nitride(PCN)has garnered increasing attention as a metal-free photocatalyst with a suitable band gap.In efforts to enhance its photocatalytic performance,researchers have examined various PCN material...Polymeric carbon nitride(PCN)has garnered increasing attention as a metal-free photocatalyst with a suitable band gap.In efforts to enhance its photocatalytic performance,researchers have examined various PCN materials,including poly(heptazine imide)(PHI)and poly(triazine imide)(PTI),two isomers within the PCN family that exhibit distinct and superior photocatalytic activity compared to other forms.The challenge,however,lies in the common practice among researchers to categorize PHI and PTI along with other PCN types under the overarching term“g-C_(3)N_(4),”which significantly impedes optimization efforts.The objective of this review is to provide comprehensive insights into the structural features,photoelectrochemical properties,and effective characterization methods employed for distinguishing between PHI and PTI materials.The review also summarizes various optimization strategies,such as crystallinity adjustments,defect engineering,morphology control,constructing heterojunction,and atomic-level metal loading dispersion,to elevate the photocatalytic activity of PHI and PTI,in addition to summarizing the history of carbon nitride development.Furthermore,this review highlights the primary applications of PHI and PTI,encompassing nitrogen fixation,biomass conversion,organic synthesis,CO_(2)reduction,pollutant degradation,H_(2)O_(2)production,and photocatalytic water splitting.Lastly,the prospects and challenges associated with further advancing PHI and PTI are thoroughly examined.展开更多
A temperature-controlled ionic liquid dispersive liquid-phase microextraction in combination with high performance liquid chromatography was developed for the enrichment and determination of triazine herbicides such a...A temperature-controlled ionic liquid dispersive liquid-phase microextraction in combination with high performance liquid chromatography was developed for the enrichment and determination of triazine herbicides such as cyanazine,simazine,and atrazine in water samples.1-Octyl-3-methylimidazolium hexafluorophosphate（[C8MIM][PF6]） was selected as the extraction solvent.Several experimental parameters were optimized.Under the optimal conditions,the linear range for cyanazine was in the concentration range of 0.5–80 mg/L and the linear range for simazine and atrazine was in the range of1.0–100 mg/L.The limit of detection（LOD,S/N = 3） was in the ranges of 0.05–0.06 mg/L,and the intra day and inter day precision（RSDs,n = 6） was in the ranges of 3.2%–6.6% and 4.8%–8.9%,respectively.Four real water samples were analyzed with the developed method,and the experimental results showed that the spiked recoveries were satisfactory.All these exhibited that the developed method was a valuable tool for monitoring such pollutants.展开更多
Based on a novel triazine compound,the properties of tanned leather and commercial feasibility in pilot scale have been investigated.Then this novel approach tanning was compared with conventional chrome tanning:in th...Based on a novel triazine compound,the properties of tanned leather and commercial feasibility in pilot scale have been investigated.Then this novel approach tanning was compared with conventional chrome tanning:in the condition of less-salt pickling and chrome free,the physicochemical properties including thermal stability and mechanical strength were analyzed.Meanwhile,the surface roughness and fiber dispersion were evaluated as well.The results show that the thermal stability and mechanical strength of the triazine compound tanned leather are similar to conventional chrome tanned leather,the fiber bundle is well-dispersed and much evener than that of chrome treating.The optimized tanning approach has obvious reduction in environmental impact and leads an excellent biodegradability of tanning liquor.In industrial application,the cost of materials and water treatment are reduced effectively.The production of chrome free leather can encourage the sustainable development of leather industry and protects ecological environment in some extent.展开更多
Effects of four kinds of triazine herbicides on the photodegradation of acetochlor were studied on glass surface and in aqueous solution under three kinds of light sources, i.e., xenon lamp, high pressure mercury lamp...Effects of four kinds of triazine herbicides on the photodegradation of acetochlor were studied on glass surface and in aqueous solution under three kinds of light sources, i.e., xenon lamp, high pressure mercury lamp and natural sunlight. The results indicated that atrazine, simetryne, prometryne and ametryne exhibited significant effects on the photoquenching degradation of acetochlor, and there was an obvious positive correlation between their effects and the dosage of four kinds of triazine herbicides.展开更多
Tirazine based microporous polymeric (TMP) network was found to be an efficient metal-free catalyst for the epoxidation of styrene. The reactions were performed in water as an environmentally benign medium using H2O2 ...Tirazine based microporous polymeric (TMP) network was found to be an efficient metal-free catalyst for the epoxidation of styrene. The reactions were performed in water as an environmentally benign medium using H2O2 as a green oxidant at ambient temperature. The reaction afforded higher yield with 90% conversion of styrene and 98% selectivity to styrene oxide in 6 h. The triazine based microporous polymeric network can be readily recovered and reused up to 4 cycles without significant loss in catalytic activity and selectivity.展开更多
An alternative and fast method for the analysis of a mixture of nine triazines herbicides in soil is presented. The method is based on MAE （microwave-assisted extraction） of herbicides using ethyl acetate as extract...An alternative and fast method for the analysis of a mixture of nine triazines herbicides in soil is presented. The method is based on MAE （microwave-assisted extraction） of herbicides using ethyl acetate as extractant. The economy in the use of solvents coupled with the decrease in extraction time and lower power consumption make MAE a technique that meets the principles of green chemistry. MAE operational parameters, extraction time, mass of the sample and extraction temperature, were optimized by RSM （response surface methodology）. Determination of analytes was completed using gas chromatograph coupled to mass spectrometry detection. The selected triazines could be efficiently extracted by the solvent at 80 ℃ for 10 min, with 80% output of maximum power. When the optimized method was applied to analysis samples, the recoveries of analytes ranged from 81.8 to 106.0% and relative standard deviations were lower than 8.41%. The method is stable and reasonable, which can be used for the determination of ninetriazine herbicides residues in soil.展开更多
In order to synthesize new polyamide（PA） 5 and copolyamides（Co PA） 7a-7d, a new-type of dicarboxylic acid containing triazine ring was successfully synthesized from 2,4-dichloro-6-methoxy-s-triazine 1 and 4-aminob...In order to synthesize new polyamide（PA） 5 and copolyamides（Co PA） 7a-7d, a new-type of dicarboxylic acid containing triazine ring was successfully synthesized from 2,4-dichloro-6-methoxy-s-triazine 1 and 4-aminobenzoic acid. New polyamide 5 containing triazine moiety was prepared from 4,4＇-（6-methoxy-1,3,5-triazine-2,4-diyl）bis（azanediyl）dibenzoic acid 3 and 4,4′-diaminodiphenylether by direct polycondensation reaction. Then new series thermally stable copolyamides 7a-7d with high solubility in common organic solvents were synthesized from the direct polycondensation reaction of diacid 3 as a first monomer, aliphatic-aromatic diacids 6a-6d as second diacids and 4,4′-diaminodiphenylether. All of the above polymers were fully characterized by 1H-NMR and FTIR spectroscopy, elemental analysis（CHN）, inherent viscosity, solubility tests, gel permeation chromatography（GPC）, differential scanning calorimetry（DSC） and thermogravimetric analysis（TGA）. The resulted Co PAs 7a-7d have shown good inherent viscosities, solubility and thermal properties.展开更多
A new environmentally friendly photo-acid generator（PAG）, 1-{4＇-[4,6-bis（trichloromethyl）-1,3,5-triazin- 2-yl] [ 1, 1＇-biphenyl]-4-yl}-O-acetyloxime ethanone（TZ4） consisting of both an oxime ester group and a ...A new environmentally friendly photo-acid generator（PAG）, 1-{4＇-[4,6-bis（trichloromethyl）-1,3,5-triazin- 2-yl] [ 1, 1＇-biphenyl]-4-yl}-O-acetyloxime ethanone（TZ4） consisting of both an oxime ester group and a triazine group was designed and synthesized. From the measurements of absorption, fluorescence and the photo-acid generation, it was found that the novel PAG has an excellent radical-generating efficiency. And the other three bis-（trichloromethyl） triazine derivatives 2-[2-（4-methoxyphenyl）ethenyl]-4,6-bis（trichloromethyl）-l,3,5-triazine（TZ1）, 2-[2-（3,4-dimethoxyphenyl）ethenyl]-4,6-bis（trichloromethyl）-1,3,5-triazine（TZ2） and 2-（1,3-benzodioxol-5-yl）-4,6-bis（trichloromethyl）-1,3,5-triazine（TZ3） were synthesized and studied in this work. In the acid measurement, the acid-forming performance of S-triazinyl derivatives was evaluated by the method ascertained in our laboratory. The results indicate that the novel triazine has the better acid-forming performance that subsequently catalyzes the deblocking of a protecting group in copolymers.展开更多
Porous polymer(pyrrolopyrrole)was successfully prepared via domino-ring-formation reaction.The chemical-physical properties of cyanided covalent triazine frameworks(CTF-CN)were characteriazed by fourier transform infr...Porous polymer(pyrrolopyrrole)was successfully prepared via domino-ring-formation reaction.The chemical-physical properties of cyanided covalent triazine frameworks(CTF-CN)were characteriazed by fourier transform infrared spectra(FT-IR),scanning electron microscopy(SEM),nuclear magnetic resonance(NMR),specific surface area analyzer(BET)and thermogravimetric analysis(TGA),respectively.The experimental results of adsorption of chloranil(TCBQ)in aqueous solution indicated that CTF-CN exhibited distinctive adsorption capacity toward TCBQ owing to its large specific surface area.Specifically,the adsorption equilibrium of as-prepared polymer was executed within 5 h and the calculated adsorption capacity was 499.76 mg/g.Furthermore,the adsorption kinetics could be well defined with the linear pseudo-second-order model,which implies that the chemical interaction are relative important in the course of TCBQ removal.Finally,the current studies verify that CTF-CN has unique rigid and nano-porous framework structure,which can be employed for the treatment of a series of harmful aromatic substances.展开更多
Photocatalysis using the abundant solar energy is an environmentally friendly and efficient way to degrade organic matter.Covalent triazine frameworks(CTFs),a new class of metal-free organic semiconductors responsive ...Photocatalysis using the abundant solar energy is an environmentally friendly and efficient way to degrade organic matter.Covalent triazine frameworks(CTFs),a new class of metal-free organic semiconductors responsive to visible light,are promising materials for water treatment.In this study,an original CTF,namely CTF-1,was modified by S-doping to form CTFSx,which were used as metal-free catalysts for degradation of methyl orange(MO)and bisphenol A(BPA).The outcomes demonstrated that the photocatalytic degradation of MO and BPA by CTFSxwas superior to that by CTF-1,with better stability and reusability.Within 6 h,53.2%MO and 84.7%BPA were degraded by CTFS5,and the degradation rate constants were 0.145 h-1and 0.29 h-1,respectively,which were 3.6 and 5.8 times higher than those of CTF-1.Further investigation revealed that enhanced visible light absorption,a reduced degree of free carrier recombination,rapid separation and transfer of photogenerated electrons and holes,and improved·OH oxidation capacity were important factors contributing to the significantly enhanced photocatalytic activity.The S-doping method effectively improved the light absorption performance,electronic structure,and modulation band structure of CTF-1.This work highlights the potential application of low-cost metal-free catalysts driven by visible light for the removal of organic pollutants from wastewater.展开更多
基金the financial support by the National Natural Science Foundation of China(Nos.22205124,52172206)Natural Science Foundation of Shandong province(Nos.ZR2021QB070,ZR2023QB110)+2 种基金Basic Research Projects for the Pilot Project of Integrating Science and Education and Industry of Qilu University of Technology(Shandong Academy of Sciences)(Nos.2023PY024,2023PX108)Special Fund for Taishan Scholars Projectthe Development Plan of Youth Innovation Team in Colleges and Universities of Shandong Province。
文摘The high conductivity of electrocatalyst can eliminate the Schottky energy barrier at the interface of heterogeneous phases during an electrocatalytic reaction and accelerate the rapid electron transfer to the catalytic active center.Therefore,the electronic conductivity is a vital parameter for oxygen reduction reaction(ORR).Covalent triazine frameworks(CTFs)have shown great potential application as electrocatalysts in ORR with a merit of the diverse building blocks.However,the intrinsic low conductivity and high impedance of CTFs could be significant setbacks in electrocatalytic application.Herein,CTFs were constructed by introducing F and N co-modification for efficient 2e^(-)ORR.Compared with the pristine CTF,the co-presence of F,N could increase the conductivity obviously by 1000-fold.As a result,F-N-CTF exhibits enhanced catalytic performance of H_(2)O_(2)generation and selectivity towards reaction pathways.This work reveals the importance of conductivity optimization for CTFs and provides guidance for designing high conductivity non-metallic organic semiconductor catalysts for 2e^(-)ORR.
文摘Photoinduced molecular oxygen activation is crucial for artificial photosynthesis.However,metal-free semiconductor photocatalysts with high activation efficiency are still lacking up to now.Herein,two isomorphic tris(triazolo)triazine-based covalent organic frameworks were successfully constructed under solvothermal conditions.And they possess high crystallinity,inherent porosity with large surface area and good stability.Strong electron donor-acceptor skeletons expand the visible light harvesting,also facilitate the charge separation and thus lead to their superior activity of photoinduced molecular oxygen activation including photosynthesis of tetrahydroquinolines and hydrogen peroxide.This work provides a way to improve the efficiency of molecular oxygen activation through the rational design of COFs,and also opens new avenues for the construction of highly active and metal-free photocatalysts toward sustainable solar-to-chemical energy conversion.
基金supported by Natural Science Foundation of Gansu Province(23JRRA745)the Fundamental Research Funds for the Central Universities(lzujbky2021-sp55).
文摘Converting CO_(2)and water into valuable chemicals like plant do is considered a promising approach to address both environmental and energy issues.Taking inspiration from the structures of natural leaves,we designed and synthesized a novel copper-coordinated covalent triazine framework(CuCTF)supported by silicon nanowire arrays on wafer chip.This marks the first-ever application of such a hybrid material in the photoelectrocatalytic reduction of CO_(2)under mild conditions.The Si@CuCTF6 heterojunction has exhibited exceptional selectivity of 95.6%towards multicarbon products(C_(2+))and apparent quantum efficiency(AQE)of 0.89%for carbon-based products.The active sites of the catalysts are derived from the nitrogen atoms of unique triazine ring structure in the ordered porous framework and the abundant Cu-N coordination sites with bipyridine units.Furthermore,through DFT calculations and operando FTIR spectra analysis,we proposed a comprehensive mechanism for the photoelectrocatalytic CO_(2)reduction,confirming the existence of key intermediate species such as*CO_(2)-,*=C=O,*CHO and*CO-CHO etc.This work not only provides a new way to mimic photosynthesis of plant leaves but also gives a new opportunity to enter this research field in the future.
文摘Solar‐driven CO_(2)conversion to precious fossil fuels has been proved to become a potential way to decrease CO_(2)with producing renewable fuels,which mainly relies on photocatalysts with efficient charge separation.In this work,a metal free heterostructure of covalent triazine framework(CTF)and graphite carbon nitride(g‐C_(3)N_(4),abbreviated as CN)is applied in the CO_(2)photoreduction for the first time.Detailed characterization methods such as photoluminescence(PL)and time‐resolved PL(TR‐PL)decay are utilized to reveal the photo‐induced carries separating process on g‐C_(3)N_(4)/CTF(CN/CTF)heterostructure.The introduced CTF demonstrated a great boosting photocatalytic activity for CN,bringing about the transform rates of CO_(2)to CO reaching 151.1μmol/(g·h)with a 30 h stabilization time,while negligible CH_(4)was detected.The optimal CN/CTF heterostructure could more efficiently separate charges with a lower probability of recombination under visible light irradiation,which made the photoreduction efficiency of CO_(2)to CO be 25.5 and 2.5 times higher than that of CTF and CN,respectively.This investigation is expected to offer a new thought for fabricating high‐efficiency photocatalyst without metal in solar‐energy‐driven CO_(2)reduction.
文摘The photocatalytic production of syngas using a noble-metal-free catalytic system is a promising approach for renewable energy and environmental sustainability.In this study,we demonstrate an efficient catalytic system formed by integrating Co single sites,which act as the active sites,in covalent triazine frameworks(CTFs),which act as the photoabsorber,for the photocatalytic production of syngas from CO2 in aqueous solution.The enhanced light absorption of the CTFs,which contain intramolecular heterojunctions,in conjunction with 0.8 mmol L^‒1 of the Co complex enables excellent syngas production with a yield of 3303μmol g‒1(CO:H2=1.4:1)in 10 h,which is about three times greater than that achieved using CTF without a heterojunction.In the photocatalytic reaction,the coordinated single Co centers accept the photogenerated electrons from the CTF,and serve as active sites for CO2 conversion through an adsorption-activation-reaction mechanism.Theoretical calculations further reveal that the intramolecular heterojunctions highly promote photogenerated charge separation,thus boosting photocatalytic syngas production.This work reveals the promising potential of CTFs for single-metal-site-based photocatalysis.
文摘Adsorption of atrazine, prometryne and prometon was determined on six soils with different physical and chemical properties. The adsorption isotherms of three herbicides could well fit Freundlich equation. On all of six soils, adsorption of herbicides increased in the order: atrazine ≈prometon<prometryne. This order is quite the same to the calculation result of by means of excess thermodynamic properties of triazine. The Freundlich adsorption constants, K f, showed to have good correlation with organic matter(OM%) of soils for each of these herbicides, suggesting that OM is the main factor, which dominates in the adsorption process of these triazine herbicides.
文摘A new method for the synthesis of 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine (TAAT) is described. The key intermediate 4,4′,6,6′-tetra(azido)hydrazo-1,3,5-triazine (TAHT) was synthesized by nucleophilic substitution in the case of sodium azide as nucleophile. N-Bromosuccinide (NBS) was used as oxidant to oxidize TAHT by a tractable operation under mild reaction condition. The target compound TAAT was obtained with a facile process and high overall yield of 81%. The structures of TAAT and its intermediates were identified by spectroscopic methods.
基金Ministry of Trade,Industry&Energy of Korea,Grant/Award Number:RS‐2022‐00155717National Research Foundation of Korea,Grant/Award Numbers:2020H1D3A1A04081472,2022M3J1A1054323。
文摘Carbon super-heterostructures with high nitrogen contents from the covalent hybrid precursors of covalent triazine frameworks(CTFs)and zeolitic imidazolic frameworks(ZIFs)are scarcely explored because of CTF's ordered structure and toxic superacid that dissolves or destabilizes the metal nodes.To solve this problem,herein,we report a straightforward two-step pathway for the covalent hybridization of disordered CTF(d–CTF)–ZIF composites via preincorporation of an imidazole(IM)linker into ordered CTFs,followed by the imidazole-site-specific covalent growth of ZIFs.Direct carbonization of these synthesized d–CTF−IM−ZIF hybrids results in unique hollow carbon super-heterostructures with ultrahigh nitrogen content(>18.6%),high specific surface area(1663m^(2)g^(−1)),and beneficial trace metal(Co/Zn NPs)contents for promoting the redox pseudocapacitance.As proof of concept,the obtained carbon super-heterostructure(Co–Zn–NC_(SNH)–800)is used as a positive electrode in an asymmetric supercapacitor,demonstrating a remarkable energy density of 61Wh kg^(−1)and extraordinary cyclic stability of 97%retention after 30,000 cycles at the cell level.Our presynthetic modifications of CTF and their covalent hybridization with ZIF crystals pave the way toward new design strategies for synthesizing functional porous carbon materials for promising energy applications.
基金supported by Basic Science Research Program through the National Research Foundation of Korea(NRF)funded by the Ministry of Education(grant number:2015042434)the support by the Korea Research Fellowship Program(grant number:2017H1D3A1A02013620)
文摘Highly porous nitrogen-doped carbon materials were synthesized by the carbonization of a low-cost porous covalent triazine polymer, PCTP-3, which had been synthesized by the AlClcatalyzed FriedelCrafts reaction of readily available monomers. The nature of the bond and structure of the resulting materials were confirmed using various spectroscopic methods, and the effects of KOH activation on the textural properties of the porous carbon materials were also examined. The KOH-activated porous carbon（aPCTP-3c） materials possessed a high surface area of 2271 mgand large micro/total pore volumes of 0.87/0.95 cmg, respectively, with narrower micropore size distributions than the porous carbon prepared without activation（PCTP-3c）. The aPCTP-3c exhibited the best COuptakes of 284.5 and 162.3 mg gand CHuptakes of 39.6 and 25.9 mg gat 273 and 298 K/1 bar, respectively, which are comparable to the performance of some benchmark carbon materials under the same conditions. The prepared materials exhibited high CO/Nselectivity and could be regenerated easily.
基金sponsored by the Natural Science Foundation of Hebei (Nos.B2006000413,B2008000210).
文摘A new method for the determination of atrazine, simazine and prometryn in water samples by on-line sweeping concentration technique in micellar electrokinetic chromatography （MEKC） was developed. Various parameters affecting sample enrichment and separation efficiency were systematically studied. Compared with the conventional MEKC method, up to 60-200-fold improvement in concentration sensitivity was achieved in terms of peak height by using this sweeping injection technique. The compound strychnine was used as the internal standard for the improvement of the experimental reproducibility. The limits of detection （S/ N = 3：1） for atrazine, simazine and prometryn were 9, 10 and 0.5 ng mL-1, respectively. This method has been successfully applied to the analysis of atrazine, simazine and prometryn in lake, steam and ground water.
基金supported by the National Natural Science Foundation of China(No.52273264)。
文摘Polymeric carbon nitride(PCN)has garnered increasing attention as a metal-free photocatalyst with a suitable band gap.In efforts to enhance its photocatalytic performance,researchers have examined various PCN materials,including poly(heptazine imide)(PHI)and poly(triazine imide)(PTI),two isomers within the PCN family that exhibit distinct and superior photocatalytic activity compared to other forms.The challenge,however,lies in the common practice among researchers to categorize PHI and PTI along with other PCN types under the overarching term“g-C_(3)N_(4),”which significantly impedes optimization efforts.The objective of this review is to provide comprehensive insights into the structural features,photoelectrochemical properties,and effective characterization methods employed for distinguishing between PHI and PTI materials.The review also summarizes various optimization strategies,such as crystallinity adjustments,defect engineering,morphology control,constructing heterojunction,and atomic-level metal loading dispersion,to elevate the photocatalytic activity of PHI and PTI,in addition to summarizing the history of carbon nitride development.Furthermore,this review highlights the primary applications of PHI and PTI,encompassing nitrogen fixation,biomass conversion,organic synthesis,CO_(2)reduction,pollutant degradation,H_(2)O_(2)production,and photocatalytic water splitting.Lastly,the prospects and challenges associated with further advancing PHI and PTI are thoroughly examined.
基金financially supported by the National Natural Science Foundation of China (No. 21377167)Program for New Century Excellent Talents in University (No. NCET-10-0813)
文摘A temperature-controlled ionic liquid dispersive liquid-phase microextraction in combination with high performance liquid chromatography was developed for the enrichment and determination of triazine herbicides such as cyanazine,simazine,and atrazine in water samples.1-Octyl-3-methylimidazolium hexafluorophosphate（[C8MIM][PF6]） was selected as the extraction solvent.Several experimental parameters were optimized.Under the optimal conditions,the linear range for cyanazine was in the concentration range of 0.5–80 mg/L and the linear range for simazine and atrazine was in the range of1.0–100 mg/L.The limit of detection（LOD,S/N = 3） was in the ranges of 0.05–0.06 mg/L,and the intra day and inter day precision（RSDs,n = 6） was in the ranges of 3.2%–6.6% and 4.8%–8.9%,respectively.Four real water samples were analyzed with the developed method,and the experimental results showed that the spiked recoveries were satisfactory.All these exhibited that the developed method was a valuable tool for monitoring such pollutants.
文摘Based on a novel triazine compound,the properties of tanned leather and commercial feasibility in pilot scale have been investigated.Then this novel approach tanning was compared with conventional chrome tanning:in the condition of less-salt pickling and chrome free,the physicochemical properties including thermal stability and mechanical strength were analyzed.Meanwhile,the surface roughness and fiber dispersion were evaluated as well.The results show that the thermal stability and mechanical strength of the triazine compound tanned leather are similar to conventional chrome tanned leather,the fiber bundle is well-dispersed and much evener than that of chrome treating.The optimized tanning approach has obvious reduction in environmental impact and leads an excellent biodegradability of tanning liquor.In industrial application,the cost of materials and water treatment are reduced effectively.The production of chrome free leather can encourage the sustainable development of leather industry and protects ecological environment in some extent.
文摘Effects of four kinds of triazine herbicides on the photodegradation of acetochlor were studied on glass surface and in aqueous solution under three kinds of light sources, i.e., xenon lamp, high pressure mercury lamp and natural sunlight. The results indicated that atrazine, simetryne, prometryne and ametryne exhibited significant effects on the photoquenching degradation of acetochlor, and there was an obvious positive correlation between their effects and the dosage of four kinds of triazine herbicides.
文摘Tirazine based microporous polymeric (TMP) network was found to be an efficient metal-free catalyst for the epoxidation of styrene. The reactions were performed in water as an environmentally benign medium using H2O2 as a green oxidant at ambient temperature. The reaction afforded higher yield with 90% conversion of styrene and 98% selectivity to styrene oxide in 6 h. The triazine based microporous polymeric network can be readily recovered and reused up to 4 cycles without significant loss in catalytic activity and selectivity.
文摘An alternative and fast method for the analysis of a mixture of nine triazines herbicides in soil is presented. The method is based on MAE （microwave-assisted extraction） of herbicides using ethyl acetate as extractant. The economy in the use of solvents coupled with the decrease in extraction time and lower power consumption make MAE a technique that meets the principles of green chemistry. MAE operational parameters, extraction time, mass of the sample and extraction temperature, were optimized by RSM （response surface methodology）. Determination of analytes was completed using gas chromatograph coupled to mass spectrometry detection. The selected triazines could be efficiently extracted by the solvent at 80 ℃ for 10 min, with 80% output of maximum power. When the optimized method was applied to analysis samples, the recoveries of analytes ranged from 81.8 to 106.0% and relative standard deviations were lower than 8.41%. The method is stable and reasonable, which can be used for the determination of ninetriazine herbicides residues in soil.
文摘In order to synthesize new polyamide（PA） 5 and copolyamides（Co PA） 7a-7d, a new-type of dicarboxylic acid containing triazine ring was successfully synthesized from 2,4-dichloro-6-methoxy-s-triazine 1 and 4-aminobenzoic acid. New polyamide 5 containing triazine moiety was prepared from 4,4＇-（6-methoxy-1,3,5-triazine-2,4-diyl）bis（azanediyl）dibenzoic acid 3 and 4,4′-diaminodiphenylether by direct polycondensation reaction. Then new series thermally stable copolyamides 7a-7d with high solubility in common organic solvents were synthesized from the direct polycondensation reaction of diacid 3 as a first monomer, aliphatic-aromatic diacids 6a-6d as second diacids and 4,4′-diaminodiphenylether. All of the above polymers were fully characterized by 1H-NMR and FTIR spectroscopy, elemental analysis（CHN）, inherent viscosity, solubility tests, gel permeation chromatography（GPC）, differential scanning calorimetry（DSC） and thermogravimetric analysis（TGA）. The resulted Co PAs 7a-7d have shown good inherent viscosities, solubility and thermal properties.
基金Supported by the National Natural Science Foundation of China(No.20876180)
文摘A new environmentally friendly photo-acid generator（PAG）, 1-{4＇-[4,6-bis（trichloromethyl）-1,3,5-triazin- 2-yl] [ 1, 1＇-biphenyl]-4-yl}-O-acetyloxime ethanone（TZ4） consisting of both an oxime ester group and a triazine group was designed and synthesized. From the measurements of absorption, fluorescence and the photo-acid generation, it was found that the novel PAG has an excellent radical-generating efficiency. And the other three bis-（trichloromethyl） triazine derivatives 2-[2-（4-methoxyphenyl）ethenyl]-4,6-bis（trichloromethyl）-l,3,5-triazine（TZ1）, 2-[2-（3,4-dimethoxyphenyl）ethenyl]-4,6-bis（trichloromethyl）-1,3,5-triazine（TZ2） and 2-（1,3-benzodioxol-5-yl）-4,6-bis（trichloromethyl）-1,3,5-triazine（TZ3） were synthesized and studied in this work. In the acid measurement, the acid-forming performance of S-triazinyl derivatives was evaluated by the method ascertained in our laboratory. The results indicate that the novel triazine has the better acid-forming performance that subsequently catalyzes the deblocking of a protecting group in copolymers.
基金the National Natural Science Foundation of China(Nos.21976069,21677062,21507155)。
文摘Porous polymer(pyrrolopyrrole)was successfully prepared via domino-ring-formation reaction.The chemical-physical properties of cyanided covalent triazine frameworks(CTF-CN)were characteriazed by fourier transform infrared spectra(FT-IR),scanning electron microscopy(SEM),nuclear magnetic resonance(NMR),specific surface area analyzer(BET)and thermogravimetric analysis(TGA),respectively.The experimental results of adsorption of chloranil(TCBQ)in aqueous solution indicated that CTF-CN exhibited distinctive adsorption capacity toward TCBQ owing to its large specific surface area.Specifically,the adsorption equilibrium of as-prepared polymer was executed within 5 h and the calculated adsorption capacity was 499.76 mg/g.Furthermore,the adsorption kinetics could be well defined with the linear pseudo-second-order model,which implies that the chemical interaction are relative important in the course of TCBQ removal.Finally,the current studies verify that CTF-CN has unique rigid and nano-porous framework structure,which can be employed for the treatment of a series of harmful aromatic substances.
基金supported by the National Natural Science Foundation of China(Nos.22006131 and 22276171)the Zhejiang Provincial Natural Science Foundation of China(No.LQ20B070010)+1 种基金the China Postdoctoral Science Foundation(Nos.2020T130598 and 2019M662106)the Fund of Zhuhai Science and Technology Bureau,China(No.ZH22017003210025PWC)。
文摘Photocatalysis using the abundant solar energy is an environmentally friendly and efficient way to degrade organic matter.Covalent triazine frameworks(CTFs),a new class of metal-free organic semiconductors responsive to visible light,are promising materials for water treatment.In this study,an original CTF,namely CTF-1,was modified by S-doping to form CTFSx,which were used as metal-free catalysts for degradation of methyl orange(MO)and bisphenol A(BPA).The outcomes demonstrated that the photocatalytic degradation of MO and BPA by CTFSxwas superior to that by CTF-1,with better stability and reusability.Within 6 h,53.2%MO and 84.7%BPA were degraded by CTFS5,and the degradation rate constants were 0.145 h-1and 0.29 h-1,respectively,which were 3.6 and 5.8 times higher than those of CTF-1.Further investigation revealed that enhanced visible light absorption,a reduced degree of free carrier recombination,rapid separation and transfer of photogenerated electrons and holes,and improved·OH oxidation capacity were important factors contributing to the significantly enhanced photocatalytic activity.The S-doping method effectively improved the light absorption performance,electronic structure,and modulation band structure of CTF-1.This work highlights the potential application of low-cost metal-free catalysts driven by visible light for the removal of organic pollutants from wastewater.
