Nitrogen Research Articles

Detecting and sourcing GHGs and atmospheric trace gases in a municipal waste treatment plant using coupled chemistry and isotope compositions

Landfill operations and waste processing facilities are important and highly heterogeneous sources of both greenhouse gases (GHGs) and non-GHG air pollutants in the atmosphere. This arises the need for detailed apportionment of waste sources in order to locate and subsequently reduce emissions from landfills. Here, a time series of in situ measurements of atmospheric trace gases and spatial allocation of specific emission source types under different processing phases and environmental conditions were conducted in and in the surroundings of a Municipal Solid Waste Treatment Plant (MSWTP) in south-western Poland. Results revealed that several individual GHG sources dominated across the waste processing facility and that GHGs concentrations displayed spatial seasonality. An increase in the ground-level CH4 concentrations, from ∼ 30.3 to 56.3 ppmv, was observed close (∼5 – 10 m) to the major emission sources within the MSWTP. While hotspot areas generally yielded elevated CH4 concentrations near the soil surface, these were relatively low (2.4 to 8.9 ppmv) along the facility’s fence line. The study of the corresponding δ13C delineated the extent of dispersion plumes downwind emission hotspots, characterized by a 13C depletion (around 4.0 ‰) in the atmospheric CH4 and CO2. For CH4, emissions were isotopically discriminated between the extraction wells at active quarters/cells (δ13C = –58.3 ± 1.1 ‰) and biogas produced in the biological waste treatment installation (δ13C = –62.7 ± 0.7 ‰). Most of the trace compounds (non-methane hydrocarbons, halocarbons, oxygen-bearing organic gases, ketones, nitrogenous and sulphurous gases, and other admixture compounds) detected at the ground surface were linked to the CH4- and CO2-rich spots. Despite the relatively high variability in the concentrations of organic and inorganic compounds observed at the MSWTP active zones, our results suggest that they do not have a meaningful impact on the surrounding air quality.

Assessment of carbon efficiency in wastewater treatment plants through Stochastic non-parametric data envelopment analysis (StoNED): Insights from Spanish facilities

Evaluating the carbon efficiency (CE) of wastewater treatment plants (WWTPs) is crucial for guiding these facilities towards carbon neutrality. Nevertheless, enhancing carbon performance ought not to be pursued to the detriment of pollutant removal efficiency. In this study, the CE of WWTPs is calculated as a composite index that integrates carbon emissions with the volume of pollutants removed from wastewater, including organic matter, suspended solids, nitrogen, and phosphorus. To achieve this, the Stochastic Non-parametric Envelopment of Data (StoNED) method is employed. This approach, distinct from the commonly used Data Envelopment Analysis (DEA), accounts for both empirical data and random variations in the estimation of CE, thereby enhancing the reliability of the CE evaluation. The study assesses the CE of 109 Spanish WWTPs, finding that none of them are fully carbon efficient. This involves that all plants have potential to reduce greenhouse gas emissions without sacrificing pollutant removal efficiency. The average CE of the WWTPs is 0.529, indicating a possible reduction in carbon emissions by approximately 0.076 kg of CO2 equivalent per cubic meter of wastewater treated. The analysis also reveals that neither the volume of wastewater treated nor the type of reactor used for secondary treatment has a significant impact on the CE of the facilities. The CE metric proposed in this study serves as an important decision-support tool for advancing towards the carbon neutrality of wastewater treatment processes. By providing a more comprehensive understanding of the environmental performance of WWTPs, it helps identifying areas for improvement and guiding policy and operational decisions.

Application of enaminone ruthenium(II) complexes as catalysts in the transfer hydrogenation of ketones

This study reported the synthesis of two new ligands (1,2) and their Ru(II)-enaminone complexes (3,4). The Ru(II) complexes were obtained from the reaction of the [RuCl2(p-cymene)]2 dimers with the new enaminone derivative ligands (1,2). The use of standard spectroscopy techniques entirely characterized the compounds. Single crystal studies investigated the crystal structure of ligand (1) and complexes (3,4). X-ray diffraction data analysis was used to confirm the enaminone form of 1. Also, 3 and 4 exhibited the classical three-legged piano stool structure with Ru(II) coordinated by the nitrogen and oxygen atoms of 1 and a chloride ligand as the legs and the η6-π-bound p-cymene ligand occupies the seat of the piano stool. The Ru(II) complexes have been studied as catalysts in the transfer hydrogenation of acetophenone and other various ketones in the presence of KOtBu. The catalytic conditions were optimized using different substrate/catalyst and base/catalyst ratios. We found that the complexes show good activities and up to 100 % selectivity. The best turnover frequency (1667 h−1) was found for 3 when using acetophenone as the substrate.

Understanding the interaction between soil ORP and enzyme activity: How does wetland type affect constructed wetland performance for the advanced treatment of swine wastewater?

Constructed wetlands (CWs) are widely used for the advanced treatment of swine wastewater. Wetland type is the most critical parameter for engineering applications; therefore, the performance of horizontal/vertical subsurface flow CWs (HSFCWs and VSFCWs) was explored over one year of operation. The effects of five antibiotics (40 μg/L each), copper (Cu, 1.0 mg/L), and their combination on CW performance and soil oxidation–reduction potential (ORP) and enzyme activity were investigated. The annual removal efficiencies of HSFCWs and VSFCWs for total organic carbon (TOC), nitrogen, and phosphorus were 72.03 %–84.49 % and 87.15 %–90.72 %, for antibiotics were 91.35 %–99.52 % and 87.33 %–99.57 %, and for Cu were 97.37 %–97.44 % and 95.52 %–96.85 %, respectively. The CWs removed antibiotics through substrate adsorption, plant absorption, and biodegradation. Total antibiotic residues in HSFCW and VSFCW soils ranged from 6.29 to 17.31 and 24.57 to 589.07 μg/kg, respectively, and enrofloxacin and roxithromycin posed medium and high risks in VSFCW non-rhizosphere soil. The amount of residual antibiotics in Phragmites australis parts was in the order of fibrous roots > rhizomes > aboveground. ORP and enzyme activities were greater in rhizosphere soil than in non-rhizosphere soil and greater in the VSFCWs than in the HSFCWs. CW performance and soil enzyme activities decreased under the stress of antibiotics and coexistence of antibiotics and Cu. These findings advance our knowledge of CW design, elucidate the unique advantages of CWs, and offer efficient operation strategies for swine wastewater advanced treatment, helping researchers recognize the adverse effects of antibiotics on CWs.

Temperature sensitivity of soil respiration declines with climate warming in subalpine and alpine grassland soils

AbstractWarming as a climate change phenomenon affects soil organic matter dynamics, especially in high elevation ecosystems. However, our understanding of the controls of soil organic matter mineralization and dynamics remains limited, particularly in alpine (above treeline) and subalpine (below treeline) grassland ecosystems. Here, we investigated how downslope (warming) and upslope (cooling) translocations, in a 5-years reciprocal transplanting experiment, affects soil respiration and its temperature sensitivity (Q10), soil aggregation, and soil organic matter carbon (C) and nitrogen (N) composition (C/N ratio). Downslope translocation of the alpine (2440 m a.s.l.) and subalpine (1850 m a.s.l.) to the lowland site (350 m a.s.l.) resulted in a temperature change during the growing seasons of + 4.4K and + 3.3K, respectively. Warming of alpine soils (+ 4.4K) reduced soil organic carbon (SOC) content by 32%, which was accompanied by a significant decrease of soil macroaggregates. Macroaggregate breakdown induced an increased respiration quotient (qCO2) by 27% following warming of alpine soils. The increase in qCO2 respiration was associated with a significant decrease (from 2.84 ± 0.05 to 2.46 ± 0.05) in Q10, and a change in soil organic matter composition (lower C/N ratios). Cooling did not show the opposite patterns to warming, implying that other mechanisms, such as plant and microbial community shifts and adaptation, were involved. This study highlights the important role of SOC degradability in regulating the temperature response of soil organic matter mineralization. To predict the adverse effect of warming on soil CO2 release and, consequently, its negative feedback on climate change, a comprehensive understanding of the mechanisms of C storage and turnover is needed, especially at high elevations in the Alps that are particularly affected by rising temperatures.

Electrolyte-triggered in-situ polymerization of multi-site organic cathodes for superior-longevity cation-anion co-storage secondary batteries

Organic electrodes are promising as next-generation energy storage materials owing to their diverse structures, low mass, and environmental friendliness. Nevertheless, the dissolution and degradation of organic active species in electrolytes are remaining obstacles to their authentic commercialization. Herein, we report an instantaneous in-situ upgrading strategy to convert multi-site organic cathode materials, e.g., 1-aminoanthraquinone (1-AAQ) and 1,5-diaminoanthraquinone (1,5-DAAQ), into poly(1-aminoanthraquinone) (PAAQ) and poly(1,5-diaminoanthraquinone) (PDAAQ) simply by dropping the electrolyte during battery assembly without extra operations. The remarkable chemistry is essentially a chemical polymerization process of redox-active organic monomers triggered by the electrolyte containing magnesium bis(hexamethyldisilazide) (Mg(HMDS)2) as an initiator. Notably, due to the π-conjugated polymer chain with inhibited dissolution, high conductivity, and improved stability, the as-obtained PDAAQ cathode delivered a high specific capacity (254 mAh/g at 100 mA/g), superior rate performance (83 mAh/g at 2000 mA/g), and excellent cycling stability for over 8000 cycles accompanied by an average capacity decay of only 0.0026 % per cycle. Detailed characterizations further explore the kinetic behaviors and verify a reversible hybrid cation–anion co-redox mechanism of PDDAQ cathode, which involves reversible Mg2+ cation insertion/extraction on AQ units and anion doping/de-doping reactions on the PANI backbones. Density functional theory (DFT) computations demonstrate the optimized structure of the discharged products and indicate that Mg2+ preferably interact with two carbonyls oxygen atoms and nitrogen atom for both PAAQ and PDAAQ. This study demonstrates an intriguing in-situ chemical-polymerization synthetic approach for preparing multi-site organic electrode materials that compromise structure optimization and synthetic efforts, offering great promise for high-performance and sustainable secondary batteries.

Sustainable ammonia and amines from chitin

Efforts are underway to explore alternative methods to the Haber-Bosch process for sustainable ammonia production, while the potential for ammonia extraction from natural nitrogenous biomass is under-exploited. Here, a synergistic catalytic strategy involving acid and modified Ru-based catalysts is communicated for the direct production of amines and ammonia from chitin. Phosphoric acid promotes the cleavage of ether bonds in biomass polymers and also serves to protect amino groups from being removed. Selective hydrogenation, deoxygenation, and amination can be achieved by controllably adjusting the ratio of Ru0/Run+. The utilization of nitrogen atoms in chitin can reach up to 95 % (21 % amines, 74 % ammonium), and the catalytic process is applicable to waste shrimp shells. This study demonstrates the possibility of efficient production of nitrogen-containing compounds from abundant biopolymers.

Computational screening of single-atom transition metals on boron-rich boron nitride nanosheets for efficient hydrogen evolution catalysis in all pH range.

Low-cost and high-efficiency catalysts are of crucial importance for the electrocatalytic hydrogen evolution reaction (HER). Two-dimensional (2D) boron nitride (B-N) compounds formed by the combination of boron and nitrogen atoms of group III and V elements are promising candidates for electrocatalytic HER due to their significant electronic properties. Hence, an electrocatalyst is computer-aided designed with isolated single atoms of 3d, 4d, and 5d transition metals supported on 2D B-N (B2N, B5N3, and B7N5) monolayers to fabricate single-atom catalysts (SACs) with an excellent HER performance. Moreover, pH modulations are considered to improve the HER activity theoretically based on first-principles calculation. Our results indicate that B-N compounds surface doping with transition metal atoms can effectively enhance the HER catalytic performance over a wide range of pH. Among all SACs studied, Co-, Ti-, V-, Nb-, Ru-, Tc-, Zr-, and Os-embedded B2N, Sc-, Cr-, Mn-, Ti-, and Y-embedded B5N3, and Sc- and Mn-embedded B7N5 have excellent catalytic activity under acidic conditions, while Mo-, Ir-, Re-, Ta-, and W-embedded B2N and Ti- and Fe-embedded B7N5 show high catalytic activity under alkaline conditions. Interestingly, Hf@B2N and V@B5N3 systems exhibit promising catalytic activity under acidic, neutral, and alkaline conditions. Our work offers cost-effective candidates with a wide pH range HER performance for exploring ideal electrocatalysts.

Influence of Acetylene Concentration on N2O and N2 Emissions from an Intensive Vegetable Soil under Anoxic and Oxic Conditions

Acetylene (C2H2) is often employed to assess soil total denitrification (N2O + N2) due to its ease of implementation. However, this technique underestimates soil denitrification in soils with low nutrient contents, particularly those supporting grain yields. To our knowledge, there are limited studies that have specifically investigated the impact of C2H2 on nutrient-rich vegetable soils, especially concerning the emissions of N2 and N2O and the nitrogenous gas product ratio (i.e., N2O/(N2O + N2)). In this study, we conducted both anoxic and oxic incubations at various C2H2 concentrations (0%, 0.01%, and 10%, v/v) and utilized a robotized sampling and analysis system to quantify soil N2, N2O, and CO2 emissions. Our findings revealed that the cumulative N2O production in soil treated with 10%C2H2 was significantly lower than that in soil treated with 0.01%C2H2 and soil without C2H2. Contrarily, high concentrations of C2H2 (10%, v/v) led to increased N2 production. Similar trends were observed under oxic conditions, where 10%C2H2 concentration did not enhance N2O production but markedly increased N2 and CO2 emissions. Moreover, the N2O/(N2O + N2) product ratio was notably higher in soils treated with 0%C2H2 compared to the 10%C2H2 treatment under anoxic conditions. These findings indicate that high concentrations of acetylene could facilitate the reduction of N2O to N2 and lead to underestimated soil total denitrification in vegetable soil, regardless of anoxic or oxic conditions. This discovery underscores the drawbacks when employing high concentrations of acetylene to evaluate actual total denitrification in intensive greenhouse vegetable soils, highlighting the necessity for further investigation into alternative methodologies.

Distribution and Mineralization of Organic Nitrogen in Fluvo-Aquic Soils with Varying Textures

Distribution and Mineralization of Organic Nitrogen in Fluvo-Aquic Soils with Varying Textures

Sequence-sensitivity in functional synthetic polymer properties.

Recently, a new class of synthetic methyl methacrylate-based random heteropolymers (MMA-based RHPs) has displayed protein-like properties. Their function appears to be insensitive to the precise sequence. Here, through atomistic molecular dynamics simulation, we show that there are universal protein-like features of MMA-based RHPs that are insensitive to the sequence, and mostly depend on the overall composition. In particular, we find that MMA-based RHPs ``fold'' into globules with heterogeneous hydration patterns. However, the insensitivity to sequence identity observed in MMA-based RHPs dramatically changes when we substitute the backbone architecture with acrylate or replace the oxygen atom in the side chain with a nitrogen atom (methacrylamide or acrylamide). Using principal component analysis and an intersection-over-union based index, we demonstrate that different sequences may not overlap in the property space, meaning that their properties are controlled by the sequence rather than fixed composition. We further investigate the sequence-insensitive capability of the MMA-based RHPs as previously reported on bacterial phospholipase OmpLA stabilization through heterodimerization. As experimentally observed, such polymers enhance the stability of OmpLA as reliably as its native bilayer environment. The design of such MMA-based RHPs provides a sequence-insensitive alternative to protein-mimetic biomaterials that is orthogonal to the sequence-structure-function paradigm of proteins.

Crystal structure of a hydrogen-bonded 2:1 co-crystal of 4-nitrophenol and 4,4′-bipyridine

In the title compound, C10H8N2·2C6H5NO3, 4-nitrophenol and 4,4′-bipyridine crystallized together in a 2:1 ratio in the space group P21/n. There is a hydrogen-bonding interaction between the nitrogen atoms on the 4,4′-bipyridine molecule and the hydrogen atom on the hydroxyl group on the 4-nitrophenol, resulting in trimolecular units. This structure is a polymorph of a previously reported structure [Nayak & Pedireddi (2016). Cryst. Growth Des. 16, 5966–5975], which differs mainly due to a twist in the 4,4′-bipyridine molecule.

Sequence‐sensitivity in functional synthetic polymer properties

Recently, a new class of synthetic methyl methacrylate‐based random heteropolymers (MMA‐based RHPs) has displayed protein‐like properties. Their function appears to be insensitive to the precise sequence. Here, through atomistic molecular dynamics simulation, we show that there are universal protein‐like features of MMA‐based RHPs that are insensitive to the sequence, and mostly depend on the overall composition. In particular, we find that MMA‐based RHPs ``fold'' into globules with heterogeneous hydration patterns. However, the insensitivity to sequence identity observed in MMA‐based RHPs dramatically changes when we substitute the backbone architecture with acrylate or replace the oxygen atom in the side chain with a nitrogen atom (methacrylamide or acrylamide). Using principal component analysis and an intersection‐over‐union based index, we demonstrate that different sequences may not overlap in the property space, meaning that their properties are controlled by the sequence rather than fixed composition. We further investigate the sequence‐insensitive capability of the MMA‐based RHPs as previously reported on bacterial phospholipase OmpLA stabilization through heterodimerization. As experimentally observed, such polymers enhance the stability of OmpLA as reliably as its native bilayer environment. The design of such MMA‐based RHPs provides a sequence‐insensitive alternative to protein‐mimetic biomaterials that is orthogonal to the sequence‐structure‐function paradigm of proteins.

N-qubit universal quantum logic with a photonic qudit and O(N) linear optics elements

High-dimensional quantum units of information, or qudits, can carry more than one quantum bit of information in a single degree of freedom and can, therefore, be used to boost the performance of quantum communication and quantum computation protocols. A photon in a superposition of 2N time bins—a time-bin qudit—contains as much information as N qubits. Here, we show that N-qubit states encoded in a single time-bin qudit can be arbitrarily and deterministically generated, manipulated, and measured using a number of linear optics elements that scale linearly with N, as opposed to prior proposals of single-qudit implementation of N-qubit logic, which typically requires O(2N) elements. The simple and cost-effective implementation we propose can be used as a small-scale quantum processor. We then demonstrate a path toward scalability by interfacing distinct qudit processors to a matter qubit (atom or quantum dot spin) in an optical resonator. Such a cavity quantum electrodynamics system allows for more advanced functionalities, such as single-qubit nondemolition measurement and two-qubit gates between distinct qudits. It could also enable quantum interfaces with other matter quantum nodes in the context of quantum networks and distributed quantum computing.

Synthesis of N2-Substituted 1,2,3-Triazoles.

We present a novel synthetic approach for the synthesis of the 1,2,3-triazole core, with a particular focus on the direct and regioselective synthesis of the synthetically more challenging triazoles having additional substituents at the N2 nitrogen atom. Through treatment of readily accessible geminal diazides with organic hydrazines under mild thermolysis conditions, a broad spectrum of N2-alkyl- and N2-aryl-1,2,3-triazoles are easily generated. For example, geminal diazides derived from ketoesters, ketoamides, and ketones were converted under the reaction conditions. The product structures were confirmed via NMR as well as single-crystal structure analysis.

Investigation of the Synthesis and Energetic Properties of an ANTA-Based Energetic Plasticizer.

Energetic plasticizers are being sought for their use in energetic formulations when combined with explosives. An energetic plasticizer based on the insensitive highly explosive 3-amino-5-nitro-l,2,4-triazole (ANTA) was synthesized and characterized by spectroscopy, X-ray crystallography, thermal analyses, and safety testing. Lastly, density functional theory calculations were employed to examine the observed selectivity among the three nucleophilic ring nitrogen atoms of ANTA toward electrophiles such as ANTA acrylate; this selectivity was found to be a combination of steric, electronic, and hydrogen bonding effects.

Molecular Docking of Natural Alkaloids with Bcl-xL Protein in The Apoptosis Process

Background: The anti-apoptotic protein Bcl-xL is a viable target for cancer therapy due to its critical role in cancer formation and resistance to chemotherapy. Insights into Bcl-xL’s role have spurred the development of a new category of cancer drugs called Bcl-xL inhibitors, which mimic the BH3-only protein to cause apoptosis. It could be initiated using alkaloids, owing to their remarkable biological characteristics. Alkaloids, among the biggest obtainable from plants, possess a distinctive structure characterized by the presence of a nitrogen atom in various positions within the molecule. Objective: In the current study, the potential of various alkaloids as Bcl-xL inhibitors was investigated through a molecular docking study. Methods: AutoDock Vina software was used to perform docking simulations of the alkaloids. Results: Ten alkaloids/Bcl-xL protein complexes demonstrated strong binding affinities less than -8.0 kcal/mol-1. These complexes include phaenthine (26), 4,5-Dioxoaporphine (1), anonaine (2), atherospermidine (4), limacine (14), liriodenine (16), monomargine (18), ouregidione (24), oxostephanine (25), and taliscanine (29) as the ligand of Bcl-xL protein. Notably, the complexes of Bcl-xL/dicentrinone (10), ouregidione (24), stepharine (28), and taliscanine (29) displayed three to four hydrogen bonds along with hydrophobic contacts. Conclusion: These results suggest that certain alkaloids could act as potential Bcl-xL inhibitors, mimicking BH3-only proteins and thereby potentially triggering apoptosis during cancer treatment.

Synthesis and characterization of Mn(II),Co(II), Ni(II),Cu(II) ,Ca(II) complexes with the ligand derived from indomethacin

The 2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)-N'-(4-methylbenzylidene)acetohydrazide ( (IB) was synthesized through the condensation of hydrazide derived from indomethacin with 4-methyl benzaldehyde. Additionally, the complexes obtained from the ligand were characterized by infrared, UV-visible, 1H, 13C NMR spectroscopy, elemental analysis, atomic absorption, molar conductance, and magnetic susceptibility. Measurements have shown that the ligand behaves as a bidentated ligand and is coordinated to the central metal ion through the oxygen atom for the carbonyl group and the nitrogen atom for the azomethine group. The structure of the ligand and complexes was confirmed. With the exception of the copper complex, which has an octahedral geometry, all of the complexes have adopted a tetrahedral geometry.

Differences in Nitrogen Sources and Contributions in Shallow Groundwater in Plateau Lake Area with Different Climate Types

Clarifying the concentration, major sources, and contribution differences of nitrogen in shallow groundwater in plateau lake areas with different climate types can provide a novel direction for the control of nitrate （NO3-） pollution in regional groundwater. Taking the shallow groundwater around Erhai Lake in the subtropical monsoon climate zone and Chenghai Lake in the dry-hot valley area of the Jinsha River as the research objects, using hydrochemical indexes and multi-isotope techniques （δ15N-NO3-, δ18O-NO3-, δ18O-H2O, and δ2H-H2O） combined with the stable isotope （SIAR） model； the differences in nitrogen concentration in shallow groundwater around Erhai Lake and Chenghai Lake were analyzed, the sources of NO3- were identified, and the contribution rates of each pollution source were calculated. The results showed that water quality of more than 33% and 5% of shallow groundwater sampling points around Erhai Lake and Chenghai Lake was worse than the groundwater Class Ⅲ quality requirements （GB/T 14848） of 20 mg·L-1 for nitrate nitrogen （NO3--N）, respectively. The δ18O-H2O and δ2H-H2O in shallow groundwater around Erhai Lake and Chenghai Lake were parallel to the global and Chinese atmospheric precipitation lines, and a large intercept was present, indicating that atmospheric precipitation was not the major recharge source of groundwater in the two regions. The contribution rate of different NO3- sources in shallow groundwater around Erhai Lake was the highest for soil organic nitrogen （53.77%）, followed by nitrogen fertilizer （21.75%） and manure and sewage （21.55%）, and atmospheric deposition nitrogen （2.93%） was the lowest. Denitrification occurred in the transformation process of nitrogen in groundwater. The contribution rate of different NO3- sources in shallow groundwater around Chenghai Lake was manure and sewage （44.88%） > soil organic nitrogen （37.03%） > nitrogen fertilizer （16.17%） > atmospheric deposition nitrogen （1.92%）, and nitrification occurred in the transformation process of nitrogen in groundwater. The climate type significantly affected the shallow groundwater level, altering the migration and transformation process of nitrogen, thereby affecting the nitrogen concentration in groundwater and the contribution of NO3- as the chief source. However, the major source of NO3- was not affected by the climate type； however was more affected by land use, agricultural activities, and manure treatment methods.

Synthesis and Polymerization of Poly Acryl Imide and One of Their Derivatives Then Curing the Product with Alkyl Halide

The present work involved four steps: First step include reaction of acrylamide ,N-?-Methylen-bis(acryl amide) and N-tert Butyl acryl amide with poly acryloyl chloride in the presence of triethyl amine (Et3N) as catalyst, the second step include homopolymerization of all products of the first step by using benzoyl peroxide(BPO) as initiator in (80-90)Co in the presence of Nitrogen gas(N2). In the third step the poly acrylimide which prepare in second step was convert into potassium salt by using alcoholic potassium hydroxide solution. Fourth step include Alkylation of the prepared polymeric salts in third step by react it with different alkyl halides(benzyl chloride, allylbromide , methyl iodide) by using DMF as solvent for(10-12) hours. Structure Confirmation of all prepared polymers were proved using FT-IR, 1H-NMR and C13-NMR spectroscopy for some polymers. Other physical properties including softening and melting points of the polymers were also measured.