Academic literature on the topic 'Isopropyl compounds'

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Journal articles on the topic "Isopropyl compounds"

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Glamočlija, Una, Selma Špirtović-Halilović, Mirsada Salihović, et al. "Structure of Biologically Active Benzoxazoles: Crystallography and DFT Studies." Acta Chimica Slovenica 68, no. 1 (2021): 144–50. http://dx.doi.org/10.17344/acsi.2020.6237.

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Using X-ray single crystal diffraction, the crystal structures of biologically active benzoxazole derivatives were determined. DFT calculation was performed with standard 6-31G*(d), 6-31G** and 6-31+G* basis set to analyze the molecular geometry and compare with experimentally obtained X-ray crystal data of compounds. The calculated HOMO-LUMO energy gap in compound 2 (2-(2-hydroxynaphtalen-1-yl)-4-methyl-7-isopropyl-1,3-benzoxazol-5-ol) is 3.80 eV and this small gap value indicates that compound 2 is chemically more reactive compared to compounds 1 (4-methyl-2-phenyl-7-isopropyl-1,3-benzoxazol
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Tsuchiya, Y., M. F. Watanabe, and M. Watanabe. "Volatile Organic Sulfur Compounds Associated with Blue-Green Algae from Inland Waters of Japan." Water Science and Technology 25, no. 2 (1992): 123–30. http://dx.doi.org/10.2166/wst.1992.0043.

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Volatile organic sulfur compounds produced by Microcystis isolated from inland waters of Japan were identified. Compounds with an unpleasant smell have been detected from seven strains of Microcystis aeruginosa and three strains of M.wesenbergii. Isopropyl mercaptan was detected in all strains and isopropyl disulfide from five strains. Methyl isothiocyanate, isopropyl methyl sulfide, and isopropyl methyl disulfide were also found in some strains. Isopropyl mercaptan and isopropyl disulfide were decomposed by chlorination, with the formation of isopropyl sulfonyl chloride. A mutagenicity study
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JEON, JU-HYUN, SANG-GUEI LEE, and HOI-SEON LEE. "Isolation of Insecticidal Constituent from Ruta graveolens and Structure-Activity Relationship Studies against Stored-Food Pests (Coleoptera)." Journal of Food Protection 78, no. 8 (2015): 1536–40. http://dx.doi.org/10.4315/0362-028x.jfp-15-111.

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Isolates from essential oil extracted from the flowers and leaves of Ruta graveolens and commercial phenolic analogs were evaluated using fumigant and contact toxicity bioassays against adults of the stored-food pests Sitophilus zeamais, Sitophilus oryzae, and Lasioderma serricorne. The insecticidal activity of these compounds was then compared with that of the synthetic insecticide dichlorvos. To investigate the structure-activity relationships, the activity of 2-isopropyl-5-methylphenol and its analogs was examined against these stored-food pests. Based on the 50% lethal dose, the most toxic
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Jeffries, Benjamin, Zhong Wang, Robert I. Troup, et al. "Lipophilicity trends upon fluorination of isopropyl, cyclopropyl and 3-oxetanyl groups." Beilstein Journal of Organic Chemistry 16 (September 2, 2020): 2141–50. http://dx.doi.org/10.3762/bjoc.16.182.

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A systematic comparison of lipophilicity modulations upon fluorination of isopropyl, cyclopropyl and 3-oxetanyl substituents, at a single carbon atom, is provided using directly comparable, and easily accessible model compounds. In addition, comparison with relevant linear chain derivatives is provided, as well as lipophilicity changes occurring upon chain extension of acyclic precursors to give cyclopropyl containing compounds. For the compounds investigated, fluorination of the isopropyl substituent led to larger lipophilicity modulation compared to fluorination of the cyclopropyl substituen
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Barbosa-Cabrera, Elizabeth, Rosa Moo-Puc, Antonio Monge, Alma Delia Paz-González, Virgilio Bocanegra-García, and Gildardo Rivera. "In vitro and In Vivo Evaluation of Quinoxaline 1,4-di-N-oxide Against Giardia lamblia." Letters in Drug Design & Discovery 17, no. 4 (2020): 428–33. http://dx.doi.org/10.2174/1570180816666190618115854.

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Background: Giardiasis is an important public health problem. However, its pharmacological treatment is limited mainly to two drugs, metronidazole and nitazoxanide. Objectives: Screening four series of esters (methyl, ethyl, isopropyl and n-propyl) of quinoxaline-7- carboxylate 1,4-di-N-oxide in in vitro and in vivo models as antigiardiasis agents. Objectives: Screening four series of esters (methyl, ethyl, isopropyl and n-propyl) of quinoxaline-7- carboxylate 1,4-di-N-oxide in in vitro and in vivo models as antigiardiasis agents. Methods: Briefly, 4 × 104 trophozoites of G. lamblia were incub
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Lindsay, R. C., and T. P. Heil. "Flavor Tainting of Fish in the Upper Wisconsin River Caused by Alkyl- and Thiophenols." Water Science and Technology 25, no. 2 (1992): 35–40. http://dx.doi.org/10.2166/wst.1992.0032.

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Compounds responsible for pronounced off-flavors in Walleye pike (Stizostedion vitreum) and other sportfish in the Upper Wisconsin River were identified by gas chromatography-mass spectrometry and sensory techniques. Alkylphenols (2-isopropyl-, 3-isopropyl, 4-isopropyl-, 2,4-diisopropyl-, 2,5-diisopropyl-, 2,6-diisopropyl-, 3,5-diisopropyl-, 5-methyl-2-isopropyl-, and 2-methyl-5-isopropyl-) and thiophenol were found to be the principal contributors to flavor tainting in fish which was most pronounced in the spring. Data indicated that thiophenol entered the river sporadically through discharge
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Konieczny, Krzysztof, Arkadiusz Ciesielski, Julia Bąkowicz, Tomasz Galica, and Ilona Turowska-Tyrk. "Structural Transformations in Crystals Induced by Radiation and Pressure. Part 7. Molecular and Crystal Geometries as Factors Deciding about Photochemical Reactivity under Ambient and High Pressures." Crystals 8, no. 7 (2018): 299. http://dx.doi.org/10.3390/cryst8070299.

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We studied the photochemical reactivity of salts of 4-(2,4,6-triisopropylbenzoyl)benzoic acid with propane-1,2-diamine (1), methanamine (2), cyclohexanamine (3), and morpholine (4), for compounds (1), (3), and (4) at 0.1 MPa and for compounds (1) and (2) at 1.3 GPa and 1.0 GPa, respectively. The changes in the values of the unit cell parameters after UV irradiation and the values of the intramolecular geometrical parameters indicated the possibility of the occurrence of the Norrish–Yang reaction in the case of all the compounds. The analysis of the intramolecular geometry and free spaces revea
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Schiemenz, Günter Paulus, and Christian Näther. "peri-Interactions in Naphthalenes, 7 [1]. A Hetera-naphthalene as a Model Compound for 8-Dimethylaminonaphth- 1-yl Silicon and Phosphorus Compounds." Zeitschrift für Naturforschung B 57, no. 3 (2002): 309–18. http://dx.doi.org/10.1515/znb-2002-0309.

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AbstractIn a 4-isopropyl-1-oxa-3-oxonia-2-borata-naphthalene the isopropyl group exhibits the same conformational phenomena as the Me2N group in 8-dimethylamino-naphth-1-yl-silanes and related phosphorus compounds. Since the details can be fully rationalized on the basis of the steric situation and electronic factors are excluded, the common features cannot serve to infer dative interaction from nitrogen to silicon / phosphorus resulting in hypercoordination of the third period element atoms in the reference compounds.
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Hu, Yuan-bin, Jun-ying Sun, Tang-yun Yu, et al. "Proliferative Constituents from the Leaves of Micromelum integerrimum." Natural Product Communications 10, no. 10 (2015): 1934578X1501001. http://dx.doi.org/10.1177/1934578x1501001020.

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wo new compounds, 5- O-methyl-4-desmethyl-myricanol (1) and 6-formyl-5-isopropyl-3-hydroxymethyl-7-methyl-1H-indene (2), were isolated from the leaves of Micromelum integerrimum. Their structures were determined by spectroscopic methods. Additionally, compound 1 could stimulate the growth of NIH3T3 cells and promote cell migration. Compound 1 might exert its effects through increasing the protein expression of connective tissue growth factor.
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Oster, Ulrike, Martin Spraul, and Wolfhart Rüdiger. "Natural Inhibitors of Germination and Growth, V Possible Allelopathic Effects of Compounds from Thuja occidentalis." Zeitschrift für Naturforschung C 45, no. 7-8 (1990): 835–44. http://dx.doi.org/10.1515/znc-1990-7-815.

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Abstract Volatile compounds which are released from fresh leaves of Thuja occidentalis inhibited germination of seeds of Amaranthus caudatus and Lepidium sativum. The volatile compounds were obtained by a vacuum method applied to the leaves, by direct analysis of the content of secretory organs and by solvent extraction of leaves. The bioactive compounds proved to be monoterpenes. The highest bioactivity were found for alcoholic compounds followed by ketones, esters and finally hydrocarbons. Non-volatile germination inhibitors which were ex- tracted with hot water were abscisic acid (3-4 µg/g
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Dissertations / Theses on the topic "Isopropyl compounds"

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Alsoqyani, Faihan Saleh. "Supercritical water oxidation of nitrogen-containing organic compounds : process enhancement using isopropyl alcohol." Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7296/.

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The research in this thesis aimed to study efficiency and viability of supercritical water oxidation (SCWO) technology in treating diluted N,N-dimethylformamide (DMF), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) and ammonia containing model wastewaters that were selected due to their hazard, wide usage in industry and having different degrees of refractoriness. A lab-scale SCWO tubular reactor was operated to obtain necessary data to investigate the destruction of selected compounds at certain operating conditions in addition to studying the oxidation kinetics of DMF and DBU. Also, Isopropyl Alco
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Kane, Deborah M. "Evaluation of a sanitizing system using isopropyl alcohol quaternary ammonium formula and carbon dioxide for dry-processing environments." Thesis, Kansas State University, 2012. http://hdl.handle.net/2097/14175.

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Master of Science<br>Food Science<br>Kelly J. K. Getty<br>Dry-processing environments are particularly challenging to clean and sanitize because water introduced into systems not designed for wet cleaning can favor growth and establishment of pathogenic microorganisms such as Salmonella. The objective was to determine the efficacy of isopropyl alcohol quaternary ammonium (IPAQuat) formula and carbon dioxide (CO[subscript]2) sanitizer system for eliminating Enterococcus faecium and Salmonella on food contact surfaces. Coupons of stainless steel and conveyor belting material used in dry-proces
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COLTURATO, MARIA T. "Otimização das condições de marcação do cloridrato de N-isopropil-p-iodoanfetamina (IMP) com radioiodo. Estudos de distribuição biológica." reponame:Repositório Institucional do IPEN, 2000. http://repositorio.ipen.br:8080/xmlui/handle/123456789/9295.

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Made available in DSpace on 2014-10-09T12:25:49Z (GMT). No. of bitstreams: 0<br>Made available in DSpace on 2014-10-09T14:03:33Z (GMT). No. of bitstreams: 1 11316.pdf: 4559706 bytes, checksum: 49490bf32ac2f606f4a79e8d49abe990 (MD5)<br>Dissertacao (Mestrado)<br>IPEN/D<br>Intituto de Pesquisas Energeticas e Nucleares, IPEN/CNEN-SP
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Alvarez, Gonzalez Eleuterio. "Substitution d'ethers et d'alcools allyliques par differents nucleophiles en presence de complexes de nickel(0) : synthese stereoselective des dienes-1,4 a partir des sulfones dieniques avec le chlorure d'isopropylmagnesium en presence de sels de." Paris 6, 1987. http://www.theses.fr/1987PA066064.

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Dzedzevičiūtė, Rasa. "Propolio ekstrakcija nevandeniniais tirpikliais ir propolio fenolinių junginių atpalaidavimo iš modelinių sistemų tyrimas in vitro." Master's thesis, Lithuanian Academic Libraries Network (LABT), 2014. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2014~D_20140618_215743-13263.

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Darbo tikslas. Parinkti tinkamą nevandeninį tirpiklį propolio ekstrakcijai bei ekstrakcijos sąlygas; įvertinti propolio fenolinių junginių atpalaidavimą iš skystų modelinių sistemų biofarmaciniu tyrimu in vitro. Darbo uždaviniai. Parinkti nevandeninius propolio ekstrahentus bei įvertinti jų gebą ekstrahuoti polifenolinius propolio junginius. Nustatyti ekstraktų kokybę lemiančius fizikocheminius rodiklius. Parinkti technologinius parametrus ir ištirti jų įtaką propolio ekstraktų kokybei. Įvertinti ekstraktų su propoliu stabilumą. Atlikti biofarmacinį tyrimą in vitro, siekiant nustatyti propoli
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EL, JAZOULI MUSTAPHA. "Formation de liaisons carbone-carbone par l'intermediaire des imidothioesters : applications synthethiques." Caen, 1985. http://www.theses.fr/1985CAEN2016.

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Apres une etude de la metallation, suivie d'alkylation, de quelques imidothioesters satures, des reactions d'aldolisation dont la selectivite est examinee, sont realisees a partir d'un n-phenyl imidothioester. Les imidothioesters alpha -insatures dont la reactivite vis-a-vis de magnesiens et de lithiens est etudiee sont de bons accepteurs de michael. Par l'intermediaire des alkylthio-enaminates et d'une cetenimine issue de leur decomposition thermique, de nouvelles voies d'acces a des cetones dissymetriques, sont decrites a partir de n-phenyl imidothioesters satures et alpha -insatures. Synthe
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Baharmast, Bahman. "Monohalogénocyclopropanation de composés éthyléniques fonctionnalisés : réactions d'élimination sur les adduits." Grenoble 1, 1986. http://www.theses.fr/1986GRE10081.

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On etudie la stereoselectivite de la reaction de monohalogenocyclopropanation menee sur des alcools, esters. , cetones et acides alpha -ethyleniques, puis la methylmonohalogenocyclopropanation des cetones et alcools alpha -ethyleniques. Dans un dernier chapitre est abordee l'etude de la regioet de la stereo elimination sur les alcools halogeno- et methylhalogenocyclopropaniques apres etude prealable sur des composes halogenocyclopropaniques apres etude prealable sur des composes halogenocyclopropaniques non fonctionnalises
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Book chapters on the topic "Isopropyl compounds"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of titanium(III) complex supported by di(isopropyl) amide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_21.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of titanium(III) phenyl supported by di(isopropyl) amide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_22.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with N-isopropyl-5-bromo-1-hydroxy-2-phenylaldaminate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_415.

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Zlobin, Alexander, Valeriy Inozemcev, Sergey Komissarenko, et al. "Main steps of developing chemical organophosphorus agents abroad." In ORGANOPHOSPHORUS NEUROTOXINS. Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/11_017-034.

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Organophosphorus compounds (OPC) occupy a special place among chemical warfare agents (CWA). High level of toxicity, a wide range of physicochemical properties, polyapplication of action already in the 1930s attracted the close attention of foreign military experts. In 1936, the German chemist Gerhard Schrader for the first time synthesized O-ethyl-dimethylamidocyanophosphate, known today as a herd. By the beginning of the Second World War, the staff of his laboratory synthesized over two thousand new OPC. Some of these compounds were selected for further study as CW agents and subsequently were adopted as weapons by the German army. In 1938 the same Gerhard Schrader have synthesized the organophosphorus compound, closed to tabun, but more toxic: O-isopropyl methyl fluorophosphate, called sarin. In 1944 the German chemist, the 1938 Nobel laureate in chemistry Richard Kuhn synthesized soman and revealed the damaging effect of organophosphorus CWA’s. In 1941 the British chemist Bernard Saunders synthesized diisopropyl fluorophosphate. During World War II the industrial production of organophosphorus CWA’s was organized in Germany, Great Britain and in the USA. Germany produced tabun, sarin and soman, the western allies: diisopropyl fluorophosphate. Till the end of World War II the leadership in the sphere of the development of nerve agents belonged to Nazi Germany. After the end of the war the German scientists, many of whom were devoted Nazis, continued their work under the auspices of military departments of the USA and Great Britain. Subsequently phosphorylated thiocholine esters: V-series substances (VG, VM, VR, VX, EA 3148, EA3317 agents etc.) were synthesized with their participation. The wide range of organophosphorus compounds was tested on volunteers in Porton Down (Great Britain) and in the Edgewood arsenal (USA). But after the synthesis of V-series agents the work on organophosphorus CWA’s did not stop. In recent years there appeared the tendency of the transformation of real threats connected with the chemical weapons use, to propaganda sphere. In recent years, there has been a tendency toward the transformation of real threats associated with the use of chemical weapons into provocation and an advocacy field, but this does not mean that the search for new CWA in Western countries has been stopped.
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Zlobin, Alexander, Valeriy Inozemcev, Sergey Komissarenko, Igor Medveckiy, Igor Nelga, and Sergey Tretyakov. "Main steps of developing chemical organophosphorus agents abroad." In Organophosphorous Neurotoxins. Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/chapter_5e4132b5e7e856.69190447.

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Organophosphorus compounds (OPC) occupy a special place among chemical warfare agents (CWA). High level of toxicity, a wide range of physicochemical properties, polyapplication of action already in the 1930s attracted the close attention of foreign military experts. In 1936, the German chemist Gerhard Schrader for the first time synthesized O-ethyl-dimethylamidocyanophosphate, known today as a herd. By the beginning of the Second World War, the staff of his laboratory synthesized over two thousand new OPC. Some of these compounds were selected for further study as CW agents and subsequently were adopted as weapons by the German army. In 1938 the same Gerhard Schrader have synthesized the organophosphorus compound, closed to tabun, but more toxic: O-isopropyl methyl fluorophosphate, called sarin. In 1944 the German chemist, the 1938 Nobel laureate in chemistry Richard Kuhn synthesized soman and revealed the damaging effect of organophosphorus CWA’s. In 1941 the British chemist Bernard Saunders synthesized diisopropyl fluorophosphate. During World War II the industrial production of organophosphorus CWA’s was organized in Germany, Great Britain and in the USA. Germany produced tabun, sarin and soman, the western allies: diisopropyl fluorophosphate. Till the end of world war ii the leadership in the sphere of the development of nerve agents belonged to Nazi Germany. After the end of the war the German scientists, many of whom were devoted Nazis, continued their work under the auspices of military departments of the USA and Great Britain. Sub consequently phosphorylated thiocholine esters: V-series substances (VG, VM, VR, VX, EA 3148, EA3317 agents etc.) were synthesized with their participation. The wide range of organophosphorus compounds was tested on volunteers in Porton Down (Great Britain) and in the Edgewood arsenal (USA). But after the synthesis of V-series agents the work on organophosphorus CWA’s did not stop. In recent years there appeared the tendency of the transformation of real threats connected with the chemical weapons use, to propaganda sphere. In recent years, there has been a tendency toward the transformation of real threats associated with the use of chemical weapons into provocation and an advocacy field, but this does not mean that the search for new CWA in Western countries has been stopped.
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"23ξ-Isopropyl-24-methylcycloart-25-en-3β-ol." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0537-5_398.

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"23ξ-Isopropyl-24-methylcycloart-25-en-3β-yl Acetate." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0537-5_407.

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Oshima, K. "Synthesis of Isopropyl-, -Butyl-, and Cyclopropylmagnesium Halides." In Compounds of Groups 13 and 2 (Al, Ga, In, Tl, Be...Ba). Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-007-00547.

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"8β-Cinnamoyloxy-1β,10α;4β,5α-diepoxy-6α,7α(H)-germacran-6β-ol (8β-Cinnamoyl-epoxy-echinadiol; 4,5:8,9-Diepoxy-3-hydroxy-2-isopropyl-5,9-dimetyl-cyclodecyl Cinnamate)." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0539-9_635.

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"8β-Cinnamoyloxy-5β,6α,7α(H)-guai-10(14)-ene-4β,6β-diol (8β-Cinnamoyl-dihydroxynardol; 2,10-Dihydroxy-3-isopropyl-10-metyl-6-methylidenebicyclo[5.3.0]dec-4-yl Cinnamate)." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0539-9_1864.

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Conference papers on the topic "Isopropyl compounds"

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Zemba, Stephen G. "Do Odors at a Waste Management Facility Indicate a Risk to Health?" In 20th Annual North American Waste-to-Energy Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/nawtec20-7038.

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Odor control is a frequent issue at facilities that process municipal solid waste. Even waste-to-energy facilities, which are typically operated under “negative pressure,” may be less than 100% effective at preventing the occasional release of odorous emissions. When odors travel off-property to nearby residents and businesses, the tangible exposure often elicits concerns about the specific chemicals responsible for the odor and the potential for the emissions to affect public health. However, because the gaseous compounds that may lead to objectionable off-site odors are generally different t
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Budiarto. "The effect of antioxidant concentration of N-isopropyl-N-phenyl-p-phenylenediamine, and 2,2,4-trimethyl-1,2-dihydroquinoline and mixing time of physical properties, thermal properties, mechanical properties and microstructure on natural rubber compound." In PROCEEDINGS FROM THE 14TH INTERNATIONAL SYMPOSIUM ON THERAPEUTIC ULTRASOUND. Author(s), 2017. http://dx.doi.org/10.1063/1.4978141.

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