Category: 826-36-8

Wang, Yi; Ji, Qingjie; Xu, Jixiang; Wan, Jun; Wang, Lei published their research in Separation and Purification Technology on December 1 ,2021. The article was titled 《Activation of peroxydisulfate using N-doped carbon-encapsulated Ni species for efficient degradation of tetracycline》.Quality Control of Triacetonamine The article contains the following contents:

In this study, N-doped porous carbon materials embedded with NiNx species (Ni@NC) were fabricated via the pyrolysis of Ni-doped zeolitic imidazolate frameworks-8 (ZIF-8) at the temperature of 900°C. The obtained Ni@NC-1 catalyst exhibited excellent activity in activating the peroxydisulfate (PDS) that was used for removing tetracycline (TC). The catalytic system exhibited good stability, wide pH adaptation, and high resistance to the operational environment. It was supposed that NiNx species could attach to PDS and act as electron acceptors to receive the electrons for activating the PDS, thus generating highly reactive superoxide radicals (·O-2) and singlet oxygen (1O2) species for rapid degradation of TC. The electron transfer and dissolved oxygen-derived ·O-2 were also responsible for the degradation of TC. In addition, the Ni@NC-1/PDS system exhibited high efficiency for removing oxytetracycline, ciprofloxacin, or levofloxacin. The results of this study would promote the design of other MOFs-derived carbon-encapsulated metal species for efficiently activating persulfate to remove antibiotics from the wastewater. In the experiment, the researchers used Triacetonamine(cas: 826-36-8Quality Control of Triacetonamine)

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine-containing compounds are also frequently employed in synthesis as ligands or auxiliaries. Accordingly, many efforts have been devoted to the development of novel methods for the synthesis of these compounds over the years.Quality Control of Triacetonamine

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

Liang, Dongmin; Hu, Yongyou; Xiao, Chun; Wang, Guobin; Xie, Jieyun; Zhu, Xiaoqiang published their research in Science of the Total Environment on August 15 ,2022. The article was titled 《Highly efficient catalytic ozonation for ammonium in water upon γ-Al2O3@Fe/Mg with acidic-basic sites and oxygen vacancies》.Electric Literature of C9H17NO The article contains the following contents:

Catalytic ozonation has prospects in the advanced treatment of nitrogen removal, and solid base MgO can efficiently catalyze the ozonation of ammonium nitrogen. However, it is necessary to improve the problem of easy loss, difficult recovery, and low percentage of gaseous products. Here, MgO, amorphous Fe2O3,and γ-Al2O3 were selected as dopingcomponents and supports, resp., to prepare γ-Al2O3@Fe/Mg composite catalysts with abundant acidic-basicsites and oxygen vacancies. The results show that γ-Al2O3@Fe/Mg5 can efficiently catalyze the ozonation of ammonium nitrogen (98.73%) with 67.82% gaseous product selectivity under the conditions of initial pH = 7, catalyst dosage of 112.88 g/L, and ozone dosage of 2.4 mg/min. The doping of Fe2O3 and MgO with a weaker lattice oxygen binding energy improves the gaseous product selectivity. The mechanism of ammonium nitrogen removal for γ-Al2O3@Fe/Mg5 is revealed, especially the intrinsic contribution of acidic-basic sites and oxygen vacancies. The pH and active sites play different roles in ozone decomposition for NH4+ removal. Surface hydroxyl protonation on basic sites and oxygen vacancies and electron transfer on acidic sites are responsible for ozone decomposition to hydroxyl radicals. Moreover, γ-Al2O3@Fe/Mg5 exhibits good stability, few leaching ions, and can be settled in waterfor easy recovery. This study suggests that γ-Al2O3@Fe/Mg5 is a good candidate for the catalytic ozonation of ammonium nitrogen. After reading the article, we found that the author used Triacetonamine(cas: 826-36-8Electric Literature of C9H17NO)

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine-containing compounds are also frequently employed in synthesis as ligands or auxiliaries. Accordingly, many efforts have been devoted to the development of novel methods for the synthesis of these compounds over the years.Electric Literature of C9H17NO

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

Reference of TriacetonamineOn May 18, 2021 ,《Interface-Promoted Direct Oxidation of p-Arsanilic Acid and Removal of Total Arsenic by the Coupling of Peroxymonosulfate and Mn-Fe-Mixed Oxide》 appeared in Environmental Science & Technology. The author of the article were Ke, Ming-Kun; Huang, Gui-Xiang; Mei, Shu-Chuan; Wang, Zhao-Hua; Zhang, Ying-Jie; Hua, Tian-Wei; Zheng, Li-Rong; Yu, Han-Qing. The article conveys some information:

As one of the extensively used feed additives in livestock and poultry breeding, p-arsanilic acid (p-ASA) has become an organoarsenic pollutant with great concern. For the efficient removal of p-ASA from water, the combination of chem. oxidation and adsorption is recognized as a promising process. Herein, hollow/porous Mn-Fe-mixed oxide (MnFeO) nanocubes were synthesized and used in coupling with peroxymonosulfate (PMS) to oxidize p-ASA and remove the total arsenic (As). Under acidic conditions, both p-ASA and total As could be completely removed in the PMS/MnFeO process and the overall performance was substantially better than that of the Mn/Fe monometallic system. More importantly, an interface-promoted direct oxidation mechanism was found in the p-ASA-involved PMS/MnFeO system. Rather than activate PMS to generate reactive oxygen species (i.e., SO4·-, ·OH, and 1O2), the MnFeO nanocubes first adsorbed p-ASA to form a ligand-oxide interface, which improved the oxidation of the adsorbed p-ASA by PMS and ultimately enhanced the removal of the total As. Such a direct oxidation process achieved selective oxidation of p-ASA and avoidance of severe interference from the commonly present constituents in real water samples. After facile elution with dilute alkali solution, the used MnFeO nanocubes exhibited superior recyclability in the repeated p-ASA removal experiments Therefore, this work provides a promising approach for efficient abatement of phenylarsenical-caused water pollution based on the PMS/MnFeO oxidation process.Triacetonamine(cas: 826-36-8Reference of Triacetonamine) was used in this study.

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine-containing compounds are also frequently employed in synthesis as ligands or auxiliaries. Accordingly, many efforts have been devoted to the development of novel methods for the synthesis of these compounds over the years.Reference of Triacetonamine

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

《Correlation Study Between Biochemical and Molecular Pathways of Trichoderma harzianum Recombinant Strains on Plant Growth and Health》 was written by Eslahi, Negin; Kowsari, Mojegan; Zamani, Mohammad Reza; Motallebi, Mostafa. Application In Synthesis of Triacetonamine And the article was included in Journal of Plant Growth Regulation on April 30 ,2022. The article conveys some information:

The genus of Trichoderma are mostly found in soil. Trichoderma species are known as probiotic with biocontrol and biofertilizer activity. They are producers of secondary metabolites like volatile organic compounds (VOCs) with antifungal, antibacterial, and growth promoter properties. Trichoderma VOCs can induce resistance to plant pathogens leading to improved plant growth and health. In this study, we compared the performance of Trichoderma harzianum recombinant strains (T13 and T15), containing chimeric chit42 with Chitin Binding Domain (ChBD) and wild-type (Tw) strain on plant growth promotion. To achieve this goal, the ability of strains in plant growth-promoting (production of IAA and siderophore) and fungal gene expression involved in biocontrol and biofertilizer activity, as well as, VOCs from T. harzianum strains (wild-type and recombinants) by headspace gas chromatog.-mass spectrometry (GC-SPME) have been investigated. In addition, bean seeds were exposed to the T. harzianum strains in a shared atm. In addition to growth indexes (root fresh and dry weight, root length, and lateral root number), expression of root growth-related genes was measured by qTR-PCR. The results showed that recombinant strains had increased ability to produce IAA and siderophore. In addition, T. harzianum genes expression anal. demonstrated an upregulation in biocontrol and biofertilizer-associated genes in T13 and T15 strains. VOCs profile of strains revealed a total of 11, 57, and 29 metabolites from the Tw, T15, and T13, resp. Most of the VOCs produced from T13 and T15 had growth enhancement and biocontrol activity, resp., on the plant. The diversity of VOCs from T. harzianum recombinant strains (T13 and T15) involved in growth-promoting and biocontrol activity, was higher than the Tw strain. These compounds might work synergistically to promote growth, and enhance biocontrol and antifungal activity, and thus, recombinant strains with higher diversity of VOCs might be more effective than Tw. Plant phenotypic characterization and root genes expression showed that the recombinant strains, T13 particularly, were effective in growth-promoting compared to the Tw strain. In this study, we observed a pos. correlation among the production of secondary metabolite and mol. pathways of recombinant strains on plant growth activity. This finding can create a link between basic and applied studies in agriculture. The experimental process involved the reaction of Triacetonamine(cas: 826-36-8Application In Synthesis of Triacetonamine)

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine is a key saturated heterocyclic scaffold found in several of the top-selling small molecule pharmaceuticals and natural alkaloids, with a diverse range of biological activities. Hence, continuous efforts have been made to develop convenient methods to prepare piperidine derivatives.Application In Synthesis of Triacetonamine

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

Peng, Yanhua; Xie, Guansheng; Shao, Penghui; Ren, Wei; Li, Mengling; Hu, Yufeng; Yang, Liming; Shi, Hui; Luo, Xubiao published their research in Applied Catalysis, B: Environmental on August 5 ,2022. The article was titled 《A comparison of SMX degradation by persulfate activated with different nanocarbons: Kinetics, transformation pathways, and toxicity》.Safety of Triacetonamine The article contains the following contents:

Nanocarbon-based advanced oxidation processes (AOPs) are widely used in wastewater purification However, the properties of different carbon catalysts lead to differences in the organic degradation mechanism and toxicity of wastewater treatment. Herein, this study provides insight into the differences between the oxidation of sulfamethoxazole (SMX) by carbon nanotube (CNT)/peroxymonosulfate (PMS), nanodiamond (ND)/PMS and PMS-alone systems. The pseudo-first-order reaction constant of the reaction of the SO4·–dominated CNT/PMS system with SMX is 19-fold and 30-fold higher than those of the 1O2-dominated ND/PMS system and PMS direct oxidation system at pH= 7, resp. In addition, d. functional theory (DFT) calculations and product anal. show that SO4·- mainly attacks the aniline and sulfonyl groups, while oxidation of the aniline group is the dominant mode of PMS direct oxidation and 1O2 reactivity. The formation of nitro and nitroso byproducts after SMX degradation determines the toxicity difference, and the CNT/PMS system is even more advantageous. In the experiment, the researchers used Triacetonamine(cas: 826-36-8Safety of Triacetonamine)

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine is a key saturated heterocyclic scaffold found in several of the top-selling small molecule pharmaceuticals and natural alkaloids, with a diverse range of biological activities. Hence, continuous efforts have been made to develop convenient methods to prepare piperidine derivatives.Safety of Triacetonamine

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

Zhou, Chan; Zhu, Lei; Deng, Lin; Zhang, Haojie; Zeng, Hanxuan; Shi, Zhou published their research in Separation and Purification Technology on December 1 ,2021. The article was titled 《Efficient activation of peroxymonosulfate on CuS@MIL-101(Fe) spheres featured with abundant sulfur vacancies for coumarin degradation: Performance and mechanisms》.Quality Control of Triacetonamine The article contains the following contents:

For improving the catalytic activity and recyclability of CuS in Fenton-like reaction processes, novel sulfur vacancies-enriched CuS@MIL-101(Fe) was constructed, characterized, and examined as heterogeneous catalysts for activating peroxymonosulfate (PMS) to degrade coumarin (COU). Thanks to the redox pairs of Fe3+/Fe2+, Cu+/Cu2+, S2-/S2-2/S0/sulfate species, copper-iron synergistic effect and sulfur vacancies, the CuS@MIL-101(Fe) realized a complete removal of COU (30μM) in 10 min with reaction rate constant of 0.577 min-1, which was 11.1 and 17.0 times of CuS and MIL-101(Fe), resp. The effect of various exptl. conditions (i.e., initial pH, CuS@MIL-101(Fe) dosage, PMS concentration, and background anions) on COU degradation was discussed, and the stability and versatility of CuS@MIL-101(Fe) was studied as well. Radical scavenging experiments and ESR (EPR) spectroscopy identified ·OH and 1O2 as the main reactive oxygen species (ROS). Finally, the possible mechanism of higher COU degradation efficiency in the CuS@MIL-101(Fe) activated PMS system and the degradation pathways were also deeply explored. Consequently, this work provided a novel insight into construction of sulfur vacancies-enriched heterogeneous catalysts for efficiently activating PMS for refractory organic pollutants elimination.Triacetonamine(cas: 826-36-8Quality Control of Triacetonamine) was used in this study.

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine-containing compounds are also frequently employed in synthesis as ligands or auxiliaries. Accordingly, many efforts have been devoted to the development of novel methods for the synthesis of these compounds over the years.Quality Control of Triacetonamine

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

Takajo, Tokuko; Kurihara, Yoshinori; Iwase, Kodai; Miyake, Daiki; Tsuchida, Kazunori; Anzai, Kazunori published their research in Chemical & Pharmaceutical Bulletin on February 29 ,2020. The article was titled 《Basic investigations of singlet oxygen detection systems with ESR for the measurement of singlet oxygen quenching activities》.Reference of Triacetonamine The article contains the following contents:

Singlet oxygen (1O2) is highly oxidative and exerts strong cytotoxic effects. We tried to establish the best combination of a singlet oxygen generation system and a detection method with ESR, for measurement of the quenching activities of various substances. The photosensitizing reaction of rose bengal or thermal decomposition of 4-methyl-1,4-etheno-2,3-benzodioxin-1(4H)-propanoic acid (endoperoxide, EP) was used for the generation of 1O2, and a sterically hindered secondary amine, 2,2,6,6-tetramethyl-4-piperidone (TEMPD) or 2,2,6,6-tetramethyl-4-piperidinol (TEMP-OH), was used as the 1O2 detection probe. These secondary amines were oxidized by 1O2 to form stable nitroxide radicals, which were detectable by ESR. TEMPD was found to be readily oxidized by air, causing large background signals in comparison with TEMP-OH. The ESR signal obtained by the irradiation of rose bengal with visible light in the presence of TEMP-OH consisted of two kinds of nitroxide radical overlapping. In contrast, only a single nitroxide signal was observed when TEMP-OH was reacted with 1O2 generated from EP. Therefore, the best combination should be EP as the 1O2 generator and TEMP-OH as the detection probe. When using this combination, we found that the concentrations of some organic solvents such as DMSO and acetonitrile should be kept constant for reliable quantification, because the concentrations of organic solvents affect the ESR signal intensity. The results came from multiple reactions, including the reaction of Triacetonamine(cas: 826-36-8Reference of Triacetonamine)

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine is a key saturated heterocyclic scaffold found in several of the top-selling small molecule pharmaceuticals and natural alkaloids, with a diverse range of biological activities. Hence, continuous efforts have been made to develop convenient methods to prepare piperidine derivatives.Reference of Triacetonamine

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

Recommanded Product: TriacetonamineOn September 5, 2020 ,《Diatomite supported hierarchical 2D CoNi3O4 nanoribbons as highly efficient peroxymonosulfate catalyst for atrazine degradation》 was published in Applied Catalysis, B: Environmental. The article was written by Dong, Xiongbo; Ren, Bangxing; Zhang, Xiangwei; Liu, Xiaorui; Sun, Zhiming; Li, Chunquan; Tan, Ye; Yang, Shanshan; Zheng, Shuilin; Dionysiou, Dionysios D.. The article contains the following contents:

Reactive oxygen radicals generated by peroxymonosulfate (PMS) activation exhibit great potential to treat refractory pollutants of emerging concern; however, mass production of efficient, cost-effective catalysts for PMS activation is a long-term goal for its widespread practical application. A CoNi3O4/diatomite hybrid was prepared via vertically oriented growth of two dimensional (2D) CoNi3O4 nanoribbons of at. layer-thickness on a cost-effective diatomite template. Distinct from stacked CoNi3O4, the CoNi3O4/diatomite composite has abundant exposed edges, sharp corners, and open diffusion channels. Abundant exposed edges and sharp corners create more open space and active sites for PMS activation. Open diffusion channels accelerate PMS and pollutants migration. Such properties provide CoNi3O4/diatomite hybrid excellent PMS activation efficiency. Sulfate radical played the dominant role in atrazine degradation, and superoxide radical contributed to reversible redox cycle of Co2+/Co3+ and Ni2+/Ni3+. This work provided a strategy for cost-effective mass production of Fenton-like 2D catalysts. In the experiment, the researchers used Triacetonamine(cas: 826-36-8Recommanded Product: Triacetonamine)

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine is ubiquitous structural motif widely occurred in diverse synthetically and naturally occurring bioactive molecules. Piperidines are an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.Recommanded Product: Triacetonamine

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

HPLC of Formula: 826-36-8On March 15, 2021, Ye, Jian; Dai, Jiangdong; Wang, Lulu; Li, Chunxiang; Yan, Yongsheng; Yang, Guoyu published an article in Journal of Colloid and Interface Science. The article was 《Investigation of catalytic self-cleaning process of multiple active species decorated macroporous PVDF membranes through peroxymonosulfate activation》. The article mentions the following:

Currently, carbon-based catalysts integrated with macroporous catalytic membrane have aroused considerable attention for environmental remediation because of its practicability and high efficiency. Herein, nitrogen doped carbon nanotube hybrids (Fe-Co@NC-CNTs) decorated with multiple active species (Fe3Co7/CoFe2O4@Fe/Co-N-C) were designed through N-mol. assisted pyrolysis of bimetallic (Fe/Co) metal-organic frameworks, and then immobilized on poly(vinylidene fluoride) (PVDF) membrane to construct macroporous Fe-Co@NC-CNTs/PVDF catalytic membrane via directional freezing technique, where active sites were efficiently exposed for oxidants and target pollutants. As expected, Fe-Co@NC-CNTs/PVDF membrane successfully achieved almost 100% bisphenol A (BPA) degradation after 40 min via PMS activation, which was significantly overperformed the majority of conventional carbon-based catalysts. Besides, we found that Fe-Co@NC-CNTs/PVDF membrane not only exhibited ideal catalytic and self-cleaning property in humic acid (HA)-BPA coexistence system, but also maintained the excellent reusability and ultrahigh water flux (10464.45 L m-2 h-1) even after 5 cycles. Notably, in EPR anal. and quenching experiments, it was found that sulfate radicals (SO4·- and ·OH) and singlet oxygen (1O2) participated the degradation process while 1O2 made a major contribution. More significantly, this study is very meaningful for the development of novel catalytic self-cleaning membranes with PMS activation. The experimental part of the paper was very detailed, including the reaction process of Triacetonamine(cas: 826-36-8HPLC of Formula: 826-36-8)

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine is a key saturated heterocyclic scaffold found in several of the top-selling small molecule pharmaceuticals and natural alkaloids, with a diverse range of biological activities. Hence, continuous efforts have been made to develop convenient methods to prepare piperidine derivatives.HPLC of Formula: 826-36-8

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

Zhao, Zhendong; Zhou, Wenjun; Lin, Daohui; Zhu, Lizhong; Xing, Baoshan; Liu, Zhiqi published an article in Applied Catalysis, B: Environmental. The title of the article was 《Construction of dual active sites on diatomic metal (FeCo-N/C-x) catalysts for enhanced Fenton-like catalysis》.Name: Triacetonamine The author mentioned the following in the article:

High metal loading of single-atom catalysts enables excellent catalytic activity, but possibly causes serious aggregation problem. Herein, a series of diat. FeCo-N/C-x (x represents metal content) were skillfully designed and applied to improve the catalytic activity for peroxymonosulfate (PMS) activation toward degrading organic micropollutants. The unprecedented dual active sites, referring to Fe(N3)-Co(N3) moiety and FeCo alloy, are constructed on the obtained FeCo-N/C-x, thereby exhibiting significantly greater performance toward degrading aqueous phenol (e.g., 0.316 min-1 for FeCo-N/C-3) via PMS activation, compared with those of traditional single-atom Co-N/C (0.011 min-1) and Fe-N/C (0.018 min-1). Combined exptl. and theor. calculations demonstrate the independent functions of dual active sites, in which Fe(N3)-Co(N3) and FeCo alloy can decrease the energy barrier of O-O bond cleaving resulting in the formation of high-valent FeCo=O reactive species and singlet oxygen, resp. This study opens up a new platform toward constructing dual active sites for enhanced Fenton-like catalytic activity. In the experiment, the researchers used Triacetonamine(cas: 826-36-8Name: Triacetonamine)

Triacetonamine(cas: 826-36-8) is a member of piperidine. Piperidine is ubiquitous structural motif widely occurred in diverse synthetically and naturally occurring bioactive molecules. Piperidines are an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.Name: Triacetonamine

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem