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Synthesis and biological testing for pesticidal activity of 8-azasteroids 8-偶氮小行星的合成及杀虫活性的生物学检测
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-8-14
A. N. Pyrko
The aim of the present study is the synthesis and testing for pesticidal activities of 2,3-dimethoxy16,16-dimethyl-D-homo-8-azagona-1,3,5(10),13-tetraene-12,17а-one and 2,3-dimethoxy-16,16-dimethyl-dhomo-8-azagona-1,3,5(10),13-tetraene-12-imino-17а-one hydrochloride which could become the basis the basis of plant protection products. The first compound was obtained by condensation of 6,7-dimethoxy-2,3- dihydroisoquinoline with 2-acetyl-5,5-dimethylcyclohexane-1,3-dione. The second substance was synthesized by interaction of the first with ammonium chloride. 2-Acetyl-5,5-dimethylcyclohexane-1,3-dione was prepared by heating dimedone with acetic acid in polyphosphoric acid. 6,7-Dimethoxy-2,3-dihydroisoquinoline was synthesized in two steps. Boiling 2-(3,5-dimethoxyphenyl)ethylamine in formic acid gave the corresponding amide, which was cyclized in the presence of phosphorus oxychloride. The structure of the obtained compounds is confirmed by the data of IR, 1H NMR, UV spectra and elemental analysis. In the IR absorption spectra of 2,3-dimethoxy-16,16-dimethyl-D-homo-8-azagona-1,3,5(10),13-tetraene-12,17a-dione and 2,3-dimethoxy-16,16-dimethyl-D-homo-8-azagona-1,3,5(10),13-tetraen-12-imino-17a-one hydrochloride, enaminodiketone bands are present (1535, 1580, 1615, 1625, 1670 cm-1 ) and enimine ketone (1595, 1650, 3260 cm-1 ) groups, respectively. Their UV absorption spectra recorded in ethanol contain two absorption bands (265.303 and 268.317 nm) corresponding to ππ* transitions of the same molecular fragments. The mass spectra of the two obtained tetracycles contain peaks of molecular ions. 1H NMR spectra correspond to the structures of all obtained compounds The synthesized compounds were tested for certain types of insecticide (against Toxoptera graminum, Musca domestica, Meloidogyne incognita, Heliothis virescens, Diabrotica undecimpunctata howardi, Caenorhabditis elegans), fungicidal (against Drechslera, Erysiphe, Puccinia, Peronospora) and herbicidal (against Amaranthus retroflexus, Brassica rapa, Abutilon theophrasti, Alopecurus myosuroides, Avena fatua, Echinochloa crus galli) activities. Both synthesized compounds showed herbicidal activity against Amaranthus retroflexus, Brassica rapa, Abutilon theophrasti and insecticidal activity against Toxoptera graminum. Hydrochloride 2,3-dimethoxy-16,16-dimethyl-D-homo-8-azagon-1,3,5(10),13- tetraene-12-imino-17a-one showed insecticidal activity against Musca domestica and fungicidal activity against Drechslera.
本研究的目的是合成2,3-二甲氧基16,16-二甲基-d -同型-8-阿扎哥拿-1,3,5(10),13-四甲基-12,17 -1和2,3-二甲氧基-16,16-二甲基-多型-8-阿扎哥拿-1,3,5(10),13-四甲基-12-亚胺-17 -1盐化物,并进行杀虫活性测试,为植物保护产品的开发奠定基础。第一个化合物由6,7-二甲氧基-2,3-二氢异喹啉与2-乙酰-5,5-二甲基环己烷-1,3-二酮缩合而得。第二种物质是由第一种物质与氯化铵相互作用合成的。以二美酮为原料,在多磷酸中以乙酸加热制备了2-乙酰-5,5-二甲基环己烷-1,3-二酮。6,7-二甲氧基-2,3-二氢异喹啉分两步合成。在甲酸中煮沸2-(3,5-二甲氧基苯基)乙胺,得到相应的酰胺,在氯氧磷存在下环化。所得化合物的结构经红外光谱、核磁共振氢谱、紫外光谱和元素分析证实。在2,3-二甲氧基-16,16-二甲基-d -同-8-氮杂根-1,3,5(10),13-四烯-12,17a-二酮和2,3-二甲氧基-16,16-二甲基-d -同-8-氮杂根-1,3,5(10),13-四烯-12-亚胺-17a- 1盐酸的红外吸收光谱中,胺基二酮分别存在(1535,1580,1615,1625,1670 cm-1)和亚胺酮(1595,1650,3260 cm-1)基团。它们在乙醇中的紫外吸收光谱包含两个吸收带(265.303和268.317 nm),对应于同一分子片段的π*跃迁。得到的两个四环的质谱包含分子离子峰。合成的化合物对某些类型的杀虫剂(对禾形弓形虫、家蝇、黑线蛾、绿萝蛾、非impunctata howardi、秀丽隐隐线虫)、杀菌剂(对Drechslera、erysiphhe、Puccinia、Peronospora)和除草剂(对逆花苋、油菜、Abutilon theophrasti、Alopecurus myosuides、Avena fatua、棘爪动物活动。两种化合物均具有对逆转录苋、油菜、苘麻的除草活性和对禾状弓形虫的杀虫活性。盐酸2,3-二甲氧基-16,16-二甲基-d -同型-8-氮杂龙-1,3,5(10),13-四烯-12-亚胺-17a- 1对家蝇有杀虫活性,对锥虫有杀真菌活性。
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引用次数: 0
A technology for producing electrode materials for lithium-ion batteries from Kazakhstan spodumene raw materials 以哈萨克斯坦锂辉石为原料生产锂离子电池电极材料的技术
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-141-152
A. Zhanabayeva, G. Bishimbayeva, D. Zhumabayeva, A. Nalibayeva, Y. N. Abdikalykov
This study aims to develop a technology for producing innovative electrode materials for modern lithium batteries. An efficient technology for post-purifying of technical lithium carbonate to reach the level of battery quality (99.95%) was developed. This technology involves causticiziation of technical lithium carbonate, ultrafiltration and ion-exchange sorption of a lithium hydroxide solution, followed by precipitation of lithium carbonate with ammonium carbonate. Cation-exchange resins of the brands Purolite S930Plus, Purolite S940 and Purolite S950 were studied for sorption purification of lithium-containing solutions from calcium and magnesium impurities. Purolite S940 and Purolite S950 can be recommended as the most effective cation exchangers. The kinetic parameters of calcium and magnesium sorption were determined using a Purolite S940 cation exchanger. The bicarbonation mode was set at room temperature and a pressure of 0.3 atm. The synthesized samples of lithium-iron-phosphate studied by the sol-gel method. The structures of the obtained electrode materials corresponding to the standard profile of lithium-iron-phosphate were investigated by X-ray diffraction. The synthesized electrode materials in the structure of lithium half- and button cells confirmed their good electrochemical properties, stable operation of batteries and a high intercalation reversibility of lithium ions in the samples within the potential range of 2.5–4.3 V. The main research results are innovative cathode and anode materials of a new generation for modern lithium-ion batteries with significantly increased capacity and stability of operation, obtained from lithium precursors – battery grade lithium carbonate based on domestic mineral and technogenic raw materials.
本研究旨在开发一种用于现代锂电池的创新电极材料的生产技术。开发了一种高效的技术碳酸锂后净化工艺,使其达到电池质量水平(99.95%)。该技术包括技术碳酸锂的苛化,氢氧化锂溶液的超滤和离子交换吸附,然后用碳酸铵沉淀碳酸锂。研究了Purolite S930Plus、Purolite S940和Purolite S950阳离子交换树脂对含锂溶液中钙镁杂质的吸附净化作用。可推荐Purolite S940和Purolite S950作为最有效的阳离子交换剂。采用Purolite S940阳离子交换剂测定了钙镁吸附动力学参数。在室温和0.3 atm的压力下设置碳酸氢盐模式。采用溶胶-凝胶法对合成的磷酸铁锂样品进行了研究。用x射线衍射分析了所得电极材料与磷酸铁锂标准轮廓相对应的结构。在2.5 ~ 4.3 V电势范围内,合成的锂半扣电池结构电极材料具有良好的电化学性能,电池运行稳定,锂离子在样品中具有较高的嵌入可逆性。主要研究成果是利用锂前体——电池级碳酸锂,以国产矿物和技术原料为基础,获得容量显著提高、运行稳定的新一代现代锂离子电池创新正极材料和负极材料。
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引用次数: 0
Impurity-impurity interaction during the growth of UMG-Si-based mc-Si umg - si基mc-Si生长过程中杂质-杂质相互作用
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-15-29
R. V. Presnyakov, S. M. Peshcherova, A. G. Chueshova, V. Bychinskii, A. Nepomnyashchikh
This article investigates the relationship between the chemical composition and electrophysical properties of p- and n-type multicrystalline silicon ingots based on metallurgical silicon with a purity of 99.99 at.%. In particular, the role of impurity-impurity interactions in the production of multisilicon by the Bridgman vertical method is evaluated in order to identify approaches to controlling this process effectively. The phase equilibrium calculations in the “silicon–all impurities” and “silicon-impurity-oxygen” systems were carried out based on the Gibbs energy minimization in the Selector software package. The study investigates the rank correlations of the concentrations of various impurities with each other, as well as with the specified electrical resistivity (SER) and the lifetime of nonequilibrium charge carriers (NCC) in the direction of crystal growth. Pair correlations of the element distribution profiles were considered based on the role of the main factor represented by the ratio of individual impurity solubilities in solid or liquid silicon (k0), as well as from the standpoint of direct interaction between two elements. It was found that the k0 value for two individual impurities in silicon does not automatically lead to the pair correlation of their distribution profiles in the ingot. A significant effect on the distribution profiles of impurities in multisilicon with k0→0 has the factor of binding some part of the impurity into such a form that this impurity can be incorporated easily into a growing crystal. Binding may be induced by the interaction of the impurity in the melt with the oxygen background, its segregation at the grain boundaries, and its capture by the crystallization front in the composition of the liquid inclusion. Significant correlations of impurity distribution profiles in the ingot were demonstrated by the pairs whose elements interact without the formation of chemical compounds in the 25–1413 °C temperature range. The conducted phase equilibrium calculations for the “silicon–all impurities” system revealed the possibility of forming the VB2, TiB2, ZrB2, and MgTiO4 solid phases in the melt.
本文研究了纯度为99.99 at.%的冶金硅制备的p型和n型多晶硅锭的化学成分与电物理性能的关系。特别是,杂质-杂质相互作用的作用,在生产多晶硅的布里奇曼垂直方法进行了评估,以确定有效控制这一过程的方法。基于选择器软件包中的吉布斯能量最小化,进行了“全硅-杂质”和“硅-杂质-氧”体系的相平衡计算。研究了各种杂质浓度之间的等级相关性,以及与晶体生长方向上的规定电阻率(SER)和非平衡载流子(NCC)寿命的等级相关性。基于单个杂质在固硅或液态硅中的溶解度比(k0)所代表的主要因素的作用,以及两种元素之间直接相互作用的观点,考虑了元素分布曲线的对相关性。结果表明,硅中两种杂质的k0值并不会自动导致其在钢锭中的分布对相关性。当k0→0时,对多晶硅中杂质分布的显著影响是将杂质的某些部分结合成这样一种形式,使得该杂质可以很容易地结合到生长的晶体中。熔体中的杂质与氧背景的相互作用、其在晶界的偏析以及其在液体包裹体组成中的结晶锋的捕获可引起结合。在25-1413°C温度范围内,其元素相互作用而不形成化合物的对证明了铸锭中杂质分布曲线的显著相关性。对“全硅杂质”体系进行了相平衡计算,揭示了熔体中形成VB2、TiB2、ZrB2和MgTiO4固相的可能性。
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引用次数: 0
Thermochemical liquefaction of wheat straw in sub- and supercritical tetralin 麦秸在亚、超临界四氢萘中的热化学液化
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-160-166
S. N. Evstaf‘ev, E. S. Fomina, N. P. Tiguntceva
The present work investigates the thermochemical conversion of wheat straw biomass in a suband supercritical tetralin medium. The experiment was carried out in a batch reactor at 285, 330, 380, 420 and 460 °C for 10 minutes. The process of straw liquefaction in subcritical tetralin was characterised by relatively high efficiency. At 420 °C, the biomass conversion rate amounted to 98.2% a.d.m. The maximum yield of liquid products during liquefaction (81.6% a.d.m.) was obtained at 380 °C. The liquid products were fractionated by successive extraction with hexane, water and ethanol. According to GC-MS data, the liquefaction products soluble in hexane comprised a mixture of low-molecular weight degradation products of straw components and tetralin derivatives, including methyl esters of fatty acids, aromatic compounds, alkanes and minor alcohols and ketones. When the process temperature increased, the content of esters diminished, followed by an increment in the proportion of aromatic compounds up to 50% rel. No esters and phenolic compounds were present in the liquefaction products soluble in hexane obtained at 460 °C. Dehydrogenation, alkylation and isomerisation of tetralin with the formation of naphthalene, 1,4-dihydronaphthalene and alkyl derivatives of tetralin, naphthalene and indane occurred under the given conditions. The conducted comparative analysis of infrared spectra for straw and solid products of liquefaction suggested that, at temperatures of up to 330 °C, the process of polysaccharide fragmentation is more pronounced in the straw biomass, while, at higher temperatures, the process of lignin fragmentation prevails. As a result, the IR-spectrum of the solid product obtained at 380 °C revealed weakly pronounced absorption bands of alkylaromatic structural fragments. At the same time, only the absorption bands of mineral components in straw ash and adsorbed water were observed in the IR-spectrum of the solid product obtained at 420 °C.
本文研究了小麦秸秆生物质在亚超临界四氢萘介质中的热化学转化。实验在285、330、380、420和460℃的间歇式反应器中进行,时间为10分钟。在亚临界四氢萘条件下进行秸秆液化具有效率较高的特点。420℃时,生物质转化率达98.2% a.d.m, 380℃时液化液产率最高(81.6% a.d.m)。用正己烷、水和乙醇连续萃取,对液体产物进行分馏。GC-MS数据显示,可溶于己烷的液化产物由秸秆组分的低分子量降解产物和四氢化萘衍生物组成,包括脂肪酸甲酯、芳香族化合物、烷烃、少量醇类和酮类。当工艺温度升高时,酯类化合物含量降低,随后芳香族化合物的比例增加到50%,在460℃时获得的可溶于己烷的液化产物中不存在酯类和酚类化合物。在给定条件下,四氢萘发生脱氢、烷基化和异构化反应,生成萘、1,4-二氢萘以及四氢萘、萘和茚的烷基衍生物。通过对秸秆和固体液化产物红外光谱的对比分析发现,在330℃以下,秸秆生物质中多糖破碎化过程更为明显,而在更高温度下,木质素破碎化过程更为明显。结果表明,固体产物在380℃时的红外光谱显示出较弱的烷基芳体结构碎片吸收带。同时,在420℃下获得的固体产物的红外光谱中,只观察到秸秆灰和吸附水中矿物成分的吸收带。
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引用次数: 1
Synthesis of a graft copolymer of polybutyl acrylate on fish collagen substratum using the RbTe1.5W0.5O6 complex oxide photocatalyst RbTe1.5W0.5O6复合氧化物光催化剂在鱼胶原基质上合成聚丙烯酸丁酯接枝共聚物
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-97-108
L. Semenycheva, M. A. Uromicheva, V. Chasova, D. Fukina, A. Koryagin, N. Valetova, E. V. Suleimanov
In order to obtain a graft copolymer of polybutyl acrylate (PBA) on the substratum of emulsified fish collagen, RbTe1.5W0.5O6 complex oxide was used as a photocatalyst under visible light irradiation (λ = 400–700 nm). The emulsion was prepared by mixing the monomer and the aqueous collagen solution in a ratio of 1:2. Next, the catalyst was introduced into the resulting mixture, followed by stirring and ultrasound treatment. Before the reaction, the emulsion was bubbled with argon for 15 min. The reaction was carried out in an argon flow with continuous stirring. The radiation source was a 30 W visible light LED lamp placed at a distance of no more than 10 cm from the reaction mixture. At the end of the reaction, the emulsified organic phase was extracted with toluene, followed by phase isolation. In order to isolate the catalyst, the aqueous part of the solution was centrifuged for 30 min. Subsequently, the powder was repeatedly washed in distilled water at a temperature of 50 °C. The washed catalyst was dried, and the surface of the oxide after emulsion polymerization was examined using a scanning electron microscope. For the PBA–collagen graft copolymer emulsion isolated from the aqueous phase, molecular weight characteristics confirming the formation of a graft copolymer were obtained. It was established that the nitrogen content of amino acid residues in the PBA–collagen graft copolymer is significantly lower than in collagen, which indicates the formation of a graft copolymer. An analysis of films and sponges of PBA–collagen graft copolymer samples by scanning electron microscopy (SEM) showed a new structural-relief organization compared to collagen. A SEM analysis of the RbTe1.5W0.5O6 powder surface after the synthesis of the PBA–collagen graft copolymer detected fragments of polymer macromolecules on its surface. This can be explained by the fact that the catalyst used not only is a source of hydroxyl radicals, but сan also participate in the formation of a polymer on the powder surface due to the abstraction of a hydrogen atom from hydroxyl groups on its surface under the action of a hydroxyl radical.
在可见光(λ = 400-700 nm)照射下,以RbTe1.5W0.5O6配合物氧化物为光催化剂,制备聚丙烯酸丁酯(PBA)接枝共聚物。将单体与胶原水溶液按1:2的比例混合制备乳液。然后,将催化剂引入所得混合物中,然后进行搅拌和超声波处理。反应前用氩气吹泡15 min,反应在氩气流中连续搅拌进行。辐射源为30 W可见光LED灯,放置在距离反应混合物不超过10 cm的地方。在反应结束时,用甲苯提取乳化有机相,然后进行相分离。为了分离催化剂,将溶液的含水部分离心30min,然后将粉末在50℃的蒸馏水中反复洗涤。将洗涤后的催化剂干燥,用扫描电子显微镜观察乳液聚合后的氧化物表面。对于从水相分离得到的pba -胶原接枝共聚物乳液,得到了证实接枝共聚物形成的分子量特征。结果表明,pba -胶原接枝共聚物中氨基酸残基的氮含量明显低于胶原,表明接枝共聚物的形成。扫描电镜(SEM)对pba -胶原接枝共聚物样品的薄膜和海绵进行了分析,发现与胶原相比,pba -胶原接枝共聚物具有新的结构缓释组织。对合成pba -胶原接枝共聚物后的RbTe1.5W0.5O6粉末表面进行SEM分析,发现其表面存在高分子大分子碎片。这可以用这样的事实来解释:所使用的催化剂不仅是羟基自由基的来源,而且由于在羟基自由基的作用下,从其表面的羟基中抽出一个氢原子,因此不免会参与粉末表面聚合物的形成。
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引用次数: 0
Self-aggregating properties of inulin in a dilute solution 菊粉在稀溶液中的自聚集特性
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-38-49
A. Nasriddinov, A. Ashurov, S. Kholov, I. B. Ismoilov, S. Usmanova, Z. K. Mukhidinov
The creation of functional food products based on inulin-containing vegetable raw materials can provide the population with functional diabetic nutrition. In this regard, investigation of the technological parameters of obtaining inulin from Jerusalem artichoke tubers (Helianthus tuberosus L.) and determination of its quantitative characteristics seem highly relevant. This study aims to determine the qualitative characteristics of inulin obtained from Jerusalem artichoke tubers by both flash extraction and conventional methods. Jerusalem artichoke inulin samples were obtained by the flash extraction method at a high temperature of 105 °C during both shorter and longer periods of time and by the conventional method at a temperature of 75 °C in a neutral medium. The hydrodynamic properties and molecular weight of the samples demonstrated the self-aggregating properties of this biopolymer. Inulin obtained by the flash extraction method consists of two fractions: low-molecular weight inulin and high-molecular weight aggregate represented by a polysaccharide complex. These aggregates can be formed both by inter- and intramolecular interactions of various inulin fractions in the solution. As expected, their isolation using conventional methods appeared impossible: the method of concentration yielded a number of subfractions on the UV membrane and a large amount of aggregated water-insoluble microgel. At the same time, inulin obtained by the conventional method consists of one fraction, although having a high degree of polydispersity. In order to obtain high-quality inulin intended for nutritional and prophylactic purposes, it is preferable to use the flash extraction method over short periods of time.
以含菊粉的植物原料为原料研制功能性食品,可为糖尿病人群提供功能性营养。因此,研究从菊芋块茎中提取菊粉的工艺参数和测定菊粉的数量特征具有重要意义。以耶路撒冷洋蓟块茎为原料,采用闪蒸法和常规提取法对菊粉的质量特性进行了研究。用闪蒸法在105℃高温下、短时间和长时间下提取耶路撒冷洋蓟菊粉,用常规方法在75℃温度下在中性介质中提取菊芋菊粉。样品的水动力学性质和分子量证明了这种生物聚合物的自聚集特性。闪蒸法得到的菊粉由低分子量菊粉和以多糖配合物为代表的高分子量聚集体两部分组成。这些聚集体可以通过溶液中不同菊粉组分的分子间和分子内相互作用形成。正如预期的那样,用常规方法分离它们似乎是不可能的:浓度法在紫外膜上产生了许多亚组分和大量聚集的水不溶性微凝胶。同时,用常规方法得到的菊粉虽然具有高度的多分散性,但只有一个组分。为了获得具有营养和预防作用的高质量菊粉,最好采用短时间闪蒸提取法。
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引用次数: 2
Energy profile of formal 1,2-dyotropic rearrangement of diarylethenes 二芳烯正式1,2-各向异性重排的能量分布
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-153-159
E. K. Kouame, A. G. Lvov
Diarylethenes with thiophene substituents belong to photoswitchable compounds (photoswitches or photochromes). Upon UV irradiation, their colorless open-ring isomers (DAE-o) convert to the colored closed-ring isomers (DAE-c), while the back reaction is induced only by visible light irradiation. A multiple photoswitching of diarylethenes usually results in irreversible photorearrangement of DAE-c to the so-called annulated isomers DAE-a, that are stable thermally and photochemically. In the present communication, structures of a series of diarylethenes as well as their isomers were optimized on the B3LYP/6-31G(d) level of theory. It was disclosed for the first time, that DAE-a destabilized relatively DAE-c by 1.71–14.00 kcal/mol. These results are important for design of photocontrollable molecules and materials, operated in the oneway (permanent manner).
具有噻吩取代基的二亚乙烯属于光开关化合物(光开关或光致变色剂)。在紫外线照射下,它们的无色开环异构体(DAE-o)转化为有色闭环异构体(DAE-c),而反反应仅在可见光照射下发生。二乙烯的多次光开关通常导致DAE-c不可逆的光重排到所谓的环状异构体DAE-a,这是稳定的热和光化学。在本通讯中,一系列二乙烯及其异构体的结构在B3LYP/6-31G(d)理论水平上进行了优化。首次揭示了DAE-a相对于DAE-c的失稳量为1.71 ~ 14.00 kcal/mol。这些结果对单向(永久)操作的光可控分子和材料的设计具有重要意义。
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引用次数: 0
Feasibility study of using biodiesel fuels as a blendstock of commercial diesel fuels 使用生物柴油燃料作为商业柴油混合燃料的可行性研究
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-130-140
N. Belozertseva, O. M. Torchakova, I. Bogdanov, M. Kirgina
Reducing emissions associated with the combustion of hydrocarbon fuels and increasing the consumption of biofuels represents an urgent economic and environmental task. Biodiesel is an alternative to petroleum diesel fuel and is widely used as a commercial fuel blendstock. In this regard, it is important to study the feasibility of using biodiesel obtained from various raw materials as a blendstock of commercial diesel fuels, as well as to identify optimal ratios of biodiesel fuel/petroleum diesel fuel. The addition of even small amounts of biodiesel has a positive effect on the environmental properties of the fuel. In the present study, we synthesize biodiesel fuel from sunflower, corn, and rapeseed oils by the reaction of interesterification using ethyl alcohol as an interesterifying agent and sodium hydroxide as a catalyst. The composition and properties of the synthesized biodiesel fuels were determined. Blends of biodiesel/petroleum diesel fuel with 5, 10, 15, 20 vol.% biodiesel blend content were prepared followed by determination of their composition and properties. It was found that the addition of biodiesel fuel increases the density, viscosity, and self-ignition of the resulting fuel, at the same time as decreasing the sulfur content and making the fractional composition heavier. This effect is directly proportional to the concentration of biodiesel in the blend. The effect of reducing the limiting filterability temperature of the blend fuel by the addition of biodiesel was revealed, with its maximum achieved at different concentrations of biodiesel synthesized from sunflower, corn, and rapeseed oils. For the production of a summer commercial diesel fuel, we recommend blends of 10vol.% biodiesel fuel, derived from any of the vegetable oils under study, and 90vol.% petroleum diesel fuel.
减少与碳氢化合物燃料燃烧相关的排放和增加生物燃料的消费是一项紧迫的经济和环境任务。生物柴油是石油柴油的替代品,作为一种商业燃料混合物被广泛使用。在这方面,重要的是研究从各种原料中获得的生物柴油作为商业柴油混合燃料的可行性,以及确定生物柴油燃料/石油柴油燃料的最佳比例。添加少量的生物柴油对燃料的环境特性也有积极的影响。本研究以向日葵、玉米和菜籽油为原料,以乙醇为酯化剂,氢氧化钠为催化剂,通过酯化反应合成生物柴油燃料。测定了合成的生物柴油燃料的组成和性能。制备了生物柴油掺入量分别为5%、10%、15%和20%的生物柴油/石油柴油共混物,并测定了其组成和性能。研究发现,生物柴油燃料的加入增加了所得燃料的密度、粘度和自燃性,同时降低了硫含量,使分馏组分更重。这种效果与混合物中生物柴油的浓度成正比。结果表明,添加生物柴油对降低混合燃料的极限过滤温度有一定的影响,以葵花籽油、玉米油和菜籽油为原料合成的生物柴油在不同浓度下可达到最大过滤温度。对于夏季商用柴油燃料的生产,我们推荐10vol的混合物。从所研究的任何植物油中提取的%生物柴油燃料和90vol。%石油柴油燃料。
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引用次数: 0
Evaluation of the proteolytic activity of new cryoresistant lactobacillus strains 耐低温乳酸菌新菌株的蛋白水解活性评价
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-76-86
S. Kitaevskaya, V. Ponomarev, O. Reshetnik
The search for new functionally active strains of lactic acid bacteria, together with the development of domestic competitive starter cultures on their basis, are important directions of contemporary food biotechnology. Proteolytic activity represents one of the criteria for selecting lactic acid bacteria strains for their subsequent use in food production and largely determines the quality characteristics of the finished product. The present study aims to evaluate the proteolytic activity of 15 new cryoresistant strains of Lactobacillus genus lactic acid bacteria having a number of functional and technological properties. According to the results obtained, all strains demonstrated higher proteolytic activity in alkaline media and those close to neutral (pH = 6.5). In slightly acidic media, the strains under study showed minimal values of proteolytic activity, except for L. fermentum 12 and L. plantarum 21 strains. Strains L. casei 32, L. casei 36, L. fermentum 10, and L. acidophilum 9 (48.9–52.3 µg tyrosine/mL·min) showed the maximum proteolytic activity. The minimal proteolytic activity was characteristic of L. fermentum 12, L. fermentum 24, and L. plantarum 1 (27.7–28.9 µg tyrosine/mL·min). The studied paramenter depends on the conditions of proteolysis (substrate, medium pH) and represents an individual strain characteristic independent of the lactobacillus species membership. According to the results obtained, L. casei 32, L. casei 36, and L. fermentum 10 cryoresistant strains, manifesting high proteolytic activity and effectively affecting various protein substrates (casein, albumin, haemoglobin) in a wide range of medium pH values, can be recommended for inclusion in the composition of starter cultures for the production of fermented food products.
寻找具有功能活性的乳酸菌新菌株,并在此基础上开发具有竞争力的国产发酵剂,是当代食品生物技术发展的重要方向。蛋白水解活性是选择乳酸菌菌株用于食品生产的标准之一,在很大程度上决定了成品的质量特性。本研究旨在评价15株具有多种功能和工艺特性的乳酸菌属乳酸菌新品种的蛋白水解活性。结果表明,所有菌株在碱性培养基和接近中性(pH = 6.5)的培养基中均表现出较高的蛋白水解活性。在微酸性培养基中,除发酵乳杆菌12和植物乳杆菌21菌株外,其余菌株的蛋白水解活性均极低。菌株L. casei 32、L. casei 36、L. fermentum 10和L. acidophilum 9(48.9 ~ 52.3µg酪氨酸/mL·min)的蛋白水解活性最高。L. fermentum 12、L. fermentum 24和L. plantarum 1的蛋白水解活性最低(27.7 ~ 28.9µg酪氨酸/mL·min)。所研究的参数取决于蛋白质水解的条件(底物,培养基pH),并代表独立于乳酸菌种类成员的单个菌株特征。根据所获得的结果,干酪乳杆菌32、干酪乳杆菌36和发酵乳杆菌10耐低温菌株表现出高蛋白水解活性,并在广泛的培养基pH值范围内有效影响各种蛋白质底物(酪蛋白、白蛋白、血红蛋白),可以推荐用于发酵食品生产的发酵剂组成。
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引用次数: 2
Sorption of silver (I) ions from aqueous solutions using the synthetic sorbent 用合成吸附剂从水溶液中吸附银离子
Pub Date : 2022-04-01 DOI: 10.21285/2227-2925-2022-12-1-30-37
N. Afandiyeva, A. Maharramov, F. M. Chyragov
We study the sorption of silver ions from aqueous solutions by a synthetic chelating sorbent. In the presence of formaldehyde, a polymeric sorbent based on a copolymer of styrene with maleic anhydride, modified with N,N’-diphenylguanidine, was synthesized and further used for extracting Ag(I) ions. The composition and structure of the synthesized polymeric chelating sorbent were studied using IR and UV spectroscopy methods. A simple, inexpensive, and efficient method for extracting Ag(I) ions from aqueous solutions was used. The effect of various parameters on the sorption process was studied, including the acidity of the medium (pH), the initial concentration of the metal ion, the time required to establish complete sorption equilibrium, and ionic strength. The optimum pH value for the extraction of Ag(I) was found to be 6. The process is characterized by a high adsorption capacity reaching 547.2 mg/g. The research results showed that the time required to establish a complete sorption equilibrium for the sorbent modified with N,N’- diphenylguanidine is 60 min. Ag(I) adsorption increases up to the value of ionic strength of μ = 1, after which its intensity decreases. At the final stage, the process of desorption of absorbed silver ions was carried out. During desorption, the best eluting agent for the extraction of Ag(I) was determined to be 0.5 M HNO3. The sorbent can be re-used after regeneration. The copolymer of styrene and maleic anhydride modified with N,N’-diphenylguanidine has a high sorption capacity and, therefore, can be used as a potential adsorbent for the extraction of silver (I) from aqueous solutions.
研究了合成的螯合吸附剂对水溶液中银离子的吸附。在甲醛存在下,以苯乙烯-马来酸酐为共聚物,经N,N ' -二苯基胍改性,合成了一种高分子吸附剂,用于提取银离子。利用红外光谱和紫外光谱对合成的聚合物螯合吸附剂的组成和结构进行了研究。采用一种简单、廉价、高效的方法从水溶液中提取银离子。研究了介质酸度(pH)、金属离子初始浓度、建立完全吸附平衡所需时间、离子强度等参数对吸附过程的影响。发现银(I)的最佳提取pH值为6。该工艺的特点是吸附量高,达到547.2 mg/g。研究结果表明,N,N′-二苯胍修饰的吸附剂达到完全吸附平衡所需的时间为60 min,离子强度μ = 1时Ag(I)的吸附增大,离子强度μ = 1后吸附强度减小。最后对吸附银离子进行解吸。在解吸过程中,确定了提取Ag(I)的最佳洗脱剂为0.5 M HNO3。吸附剂再生后可重复使用。苯乙烯-马来酸酐共聚物经N,N ' -二苯基胍改性后具有较高的吸附能力,因此可作为一种潜在的吸附剂从水溶液中萃取银(I)。
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引用次数: 0
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