400 research outputs found

    Aqueous phase fly-ash catalyzed [4+2] Diels-Alder reaction of aryl enones and cyclopentadiene: Synthesis and insect antifeedant activities of aryl bicyclo [2.2.1] heptene-2-yl-methanones

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    A series containing ten aryl 3-(substituted phenyl) bicyclo [2.2.1] heptene-2-yl-methanone derivatives including 3- (substituted phenyl) bicyclo [2.2.1]hepten-2-yl-(pyren-1-yl)- methanones have been synthesized by aqueous phase fly-ash catalyzed [4+2] Diels-Alder cyclo addition reaction of cyclopentadiene and aryl chalcones. The yields of the methanones are more than 60%. The synthesized methanones are characterized by their physical constants and spectral data. The insect antifeedant activities of synthesized methanones have been studied using Dethler’s leaf-discs bioassay method

    Synthesis, spectral studies and insect antifeedant activities of some 4-substituted 1-naphthacyl bromide and its esters

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    About nine 4-substituted 1-naphthacyl bromides and its esters have been synthesized by greener synthetic method using fly-ash catalyzed water mediated reaction.  These acyl bromides and esters have been characterized by their physical constants, Mass, IR and NMR spectral data.  These carbonyl frequencies(cm-1) of existed rotomers of these compounds have been assigned and correlated with Hammett substituent constants, F, R and Swain-Lupton’s parameters.  The insect antifeedant activities of the synthesized acyl bromide and esters have been evaluated using 4th instar larvae Achoea Janatha L

    Hydroxyapatite Catalyzed Cyclization of Aryl Enones: Solvent-Free Efficient Synthesis of Some 4-Aryl-5,6-Dihydro-6-(Substituted Phenyl)-4H-1,3-Oxazine-2-Amines

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    Some 4-aryl-5,6-dihydro-6-(substituted phenyl)-4H-1,3-oxazine- 2-amine derivatives including 4-(4-methyl-1-naphthyl)-5,6- dihydro-6-(substituted phenyl)-4H-1,3-oxazine-2-amines have been synthesised by hydroxyapatite catalyzed solvent-free cyclization of aryl chalcones and urea using microwave irradiation under solventfree condition. The yields of the oxazines were more than 85%. The synthesised oxazine amines have been characterized by their physical constants, analytical and spectroscopic data

    NOWY, AUTOMATYCZNY SYSTEM KONTROLI OBCIĄŻENIA SŁONECZNEGO OPARTY NA SZTUCZNEJ INTELIGENCJI

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    In modern times, solar panels have become a common sight in many households as they provide electricity for various purposes. Typically, the solar panel's charges a battery, and any excess energy generated is usually wasted once the battery is fully charged. However, by utilizing this extra energy, heavy loads can be powered as well. This is where a solar power controller comes into play, which measures the parameters of the solar cell through multiple sensor and adjusts the load accordingly. When the power output of the PV cell is high, the load runs on solar power, and if the power is not sufficient, the load switches to the main supply. The load switches back to solar power when it becomes high again. Monitoring the solar cell parameters allows for real-time identification of the power produced by the solar panel.W dzisiejszych czasach panele słoneczne stały się powszechnym widokiem w wielu gospodarstwach domowych, ponieważ zapewniają energię elektryczną do różnych celów. Zazwyczaj panele słoneczne ładują akumulator, a nadmiar wytworzonej energii jest zwykle marnowany po pełnym naładowaniu akumulatora. Jednakże, wykorzystując tę dodatkową energię, można również zasilać duże obciążenia. W tym miejscu do gry wkracza kontroler energii słonecznej, który mierzy parametry ogniwa słonecznego za pomocą wielu czujników i odpowiednio dostosowuje obciążenie. Gdy moc wyjściowa ogniwa fotowoltaicznego jest wysoka, obciążenie jest zasilane energią słoneczną, a jeśli moc nie jest wystarczająca, obciążenie przełącza się na główne źródło zasilania. Obciążenie przełącza się z powrotem na zasilanie energią słoneczną, gdy jej moc ponownie staje się wysoka. Monitorowanie parametrów ogniwa fotowoltaicznego pozwala na identyfikację mocy wytwarzanej przez panel fotowoltaiczny w czasie rzeczywistym

    CHŁODZENIE PANELI FOTOWOLTAICZNYCH Z WYKORZYSTANIEM EFEKTU STOSU

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    Unsatisfactory feat of the photo-voltaic cell is solitary in every of the foremost issues among the promotion of PV technology. A vital strand changing cell performance is operative temperature of the cell. The voltage of the cell, declines near directly with a rise in the operative temperature of the photo-voltaic cell. The temperature condition on the in-operative surface of a photo-voltaic panel remains usually 22–30°C beyond the normal temperature conditions. Upon the premise concerning those issues, the potency of the photo-voltaic cell will be refined by sustaining their operative temperatures as low as possible. This paper portrays a technique of PV/solar panel cooling using convection generated by the chimney effect. This paper considers the diminution of warmth from the Photo-voltaic panel for both active and inactive conditions.Niezadowalająca wydajność ogniwa fotowoltaicznego jest jednym z najważniejszych problemów związanych z promocją technologii PV. Istotnym czynnikiem wpływającym na wydajność ogniwa jest jego temperatura robocza. Napięcie ogniwa spada niemal bezpośrednio wraz ze wzrostem temperatury roboczej ogniwa fotowoltaicznego. Temperatura na powierzchni działającego panelu fotowoltaicznego pozostaje zwykle o 22–30°C wyższa od normalnych warunków temperaturowych. Zgodnie z założeniami dotyczącymi tych kwestii, moc ogniwa fotowoltaicznego zostanie poprawiona poprzez utrzymanie ich temperatury roboczej na jak najniższym poziomie. Niniejszy artykuł przedstawia technikę chłodzenia paneli fotowoltaicznych/solarnych z wykorzystaniem konwekcji generowanej przez efekt kominowy. W artykule uwzględniono zmniejszenie ciepła z panelu fotowoltaicznego zarówno w warunkach aktywnych, jak i nieaktywnych

    A facile designed highly moderate craspedia flowerlike sulphated Bi2O3-fly ash catalyst: Green synthetic strategy for (6H-pyrido[3,2-b]carbazol-4-yl)aniline derivatives in water

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    AbstractThe air pollutant fly ash was facile designed as a green catalyst and practical to organic synthesis. We have designed sulfated Bi2O3-fly ash catalyst (12wt%) and it was characterized by Fourier transform infrared (FT-IR), confocal Raman, Powder X-ray diffraction (XRD), Field emission electron microscopy (FE-SEM), elemental color mapping, energy-dispersive X-ray spectroscopy (EDS), Transmission electron microscopy (TEM) and Brunauer–Emmett–Teller (BET) techniques. The sulfated Bi2O3-fly ash was found an excellent catalytic application for the synthesis of (6H-pyrido[3,2-b]carbazol-4-yl)aniline derivatives in water has been described. The synthesized (6H-pyrido[3,2-b]carbazol-4-yl)aniline derivatives were confirmed by spectral techniques Fourier transform infrared (FT-IR), Nuclear magnetic resonance (NMR) and Liquid chromatography–mass spectrometry (LC–MS). The significant catalytic role of Bi–N interaction was readily form adduct, moreover Bi–O bond was favorable for hydrogen abstraction, dehydration and aromatization. Due to the strong potential, the precise reaction time and high yield have been achieved, which is realized from hot filtration test. The sulfated Bi2O3-fly ash catalyst could be reused for five successive run, the resulting in no appreciable change in the catalytic activity. The crystal phase and surface morphology of fifth run catalyst were examined by powder XRD, FE-SEM, EDS and TEM techniques, and the results revealed no changes in catalyst nature. The sulfated Bi2O3-fly ash catalyst has high efficiency, reusability, good catalytic activity, environmentally harmless and notable potential in industrial applications

    Synthesis, assessment of substituent effect and antimicrobial activities of some substituted (E)-Nbenzylidene- 5-bromopyridin-2-amines

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    A series of substituted (E)-N-benzylidene-5-bromopyridin-2-amine compounds have been synthesized from 5-bromo-2-aminopyridine with different substituted benzaldehydes. The structure of the adducts was confirmed by their physical constants, UV, IR and NMR spectral data. The observed UV absorption maximum λmaxC=N(nm), IR frequencies νC=N(cm-1), The 1H and 13C NMR δ(ppm) chemical shifts values have been correlated with Hammett substituent constants and F and R parameters using single and multi-linear regression analysis. From the results of statistical analysis, the effect of substituents on the spectral data has been studied. The antimicrobial activities of all synthesized imines have been studied using Bauer-Kirby method

    Spectral LFER studies in some N-(substituted phenyl) formamides

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    A series of N-(substituted phenyl) formamides were synthesised by sulphated titania (TiO2-SO4 2-) catalyzed formylation of substituted anilines and formic acid in acetonitrile medium at room temperature. The synthesised formamide derivatives are characterized by their spectral data. The infrared νNH, CO (cm-1) stretches, chemical shifts(δ, ppm) of NH, COH and ipso carbons(Ar-C-NH) were assigned and correlated with Hammett substituent constants using single and multi-regression analysis. From the results of statistical analyses, the effect of substituents on the spectral data have been studied

    Synthesis of Schiff’s bases of 2-amino benzo[d]thiazole from higher hetero aldehydes and ketones using Mo-Al2O3 composite based organo catalyst

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    We have used a new metal supported organo catalyst successfully to carry out the high yield Schiff’s base reaction at ambient temperature. This methodology has the benefits of straightforward conditions, excellent yields, no work-up, environmental benign process and reusable solid catalyst. The catalyst speeds up the Schiff base reaction with less time and several Schiff bases were synthesised and given IR,1H,13C NMR characterisation
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