Journal articles on the topic '4-Dichlorophenoxyacetic Acid (2'

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1

Rogers, Kim R., Alma B. Apostol, and William C. Brumley. "Capillary Electrophoresis Immunoassay for 2, 4-Dichlorophenoxyacetic Acid." Analytical Letters 33, no. 3 (January 2000): 443–53. http://dx.doi.org/10.1080/00032710008543064.

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2

Ghatbandhe, A. S., H. G. Jahagirdar, M. K. N. Yenkie, and S. D. Deosarkar. "Evaluation of Thermodynamic Parameters of 2, 4-Dichlorophenoxyacetic Acid (2, 4-D) Adsorption." Journal of Chemistry 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/519304.

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3

TAKANAMI, Ryohei, Yurika SAKAMOTO, Shogo TANIGUCHI, and Hiroaki OZAKI. "ADVANCED OXIDATION OF 2, 4- DICHLOROPHENOXYACETIC ACID AND DECOMPOSITION PRODUCTS." Journal of Japan Society of Civil Engineers, Ser. G (Environmental Research) 75, no. 7 (2019): III_11—III_17. http://dx.doi.org/10.2208/jscejer.75.7_iii_11.

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4

Trivedi, Nikhilesh S., and Sachin A. Mandavgane. "Fundamentals of 2, 4 Dichlorophenoxyacetic Acid Removal from Aqueous Solutions." Separation & Purification Reviews 47, no. 4 (March 19, 2018): 337–54. http://dx.doi.org/10.1080/15422119.2018.1450765.

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5

Balajee, S., and A. Mahadevan. "Biodegradation of 2, 4‐dichlorophenoxyacetic acid in soil byAzotobacter chroococcum." Toxicological & Environmental Chemistry 39, no. 3-4 (December 1993): 169–72. http://dx.doi.org/10.1080/02772249309357914.

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6

Jennifer A Sandberg Helen M Duhart. "DISTRIBUTION OF 2 4 DICHLOROPHENOXYACETIC ACID 2 4 D IN MATERNAL AND FETAL RABBITS." Journal of Toxicology and Environmental Health 49, no. 5 (November 20, 1996): 497–510. http://dx.doi.org/10.1080/009841096160718.

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7

Iken, I., A. Derkaoui, M. Malkki, A. Attari, S. Besri, A. Amarti, M. KHatouf, and S. Achour. "P50: Fatal poisoning by 2-4 dichlorophenoxyacetic acid: About two cases." Toxicologie Analytique et Clinique 26, no. 2 (June 2014): S50—S51. http://dx.doi.org/10.1016/s2352-0078(14)70111-8.

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8

Yu, Jicheng, Tingting Guo, Wei Zhang, Bailing Li, Litao Liu, and Ruinian Hua. "Green upconversion nanoparticles for 2, 4- dichlorophenoxyacetic acid and fenitrothion detection." Journal of Alloys and Compounds 771 (January 2019): 187–94. http://dx.doi.org/10.1016/j.jallcom.2018.08.202.

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9

Abd El-Fattah, Hanaa M., and Lamiaa A. A. Barakat. "Hepatoprotective Effect of Olive and Coconut oils against Oxidative Stress- Induced by 2, 4 Dichlorophenoxyacetic Acid." Indian Journal of Applied Research 3, no. 12 (October 1, 2011): 42–46. http://dx.doi.org/10.15373/2249555x/dec2013/11.

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10

MORITA, Hiroshi, Tomoko MAEHARA, and Masashi USHIYAMA. "Detection of 2, 4-Dichlorophenoxyacetic Acid in Lemons with an ELISA Kit." Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi) 34, no. 5 (1993): 411–14. http://dx.doi.org/10.3358/shokueishi.34.411.

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11

Kolberg, Jan, Kristen Helgeland, and Jon Jonsen. "The Herbicide 2, 4-Dichlorophenoxyacetic Acid II: Triglyceride Accumulation in L Cells." Acta Pharmacologica et Toxicologica 31, no. 5-7 (March 26, 2009): 481–87. http://dx.doi.org/10.1111/j.1600-0773.1972.tb03611.x.

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12

Moshiri, Mohammad, Seyed Reza Mousavi, and Leila Etemad. "Management of 2, 4- Dichlorophenoxyacetic Acid Intoxication by Hemodialysis: A Case Report." Iranian Journal of Toxicology 10, no. 1 (January 1, 2016): 53–55. http://dx.doi.org/10.32598/ijt.10.1.303.1.

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Background: The herbicide 2, 4-dichlorophenoxyacetic acid (2, 4-D) can cause moderate to lethal poisoning. Although urine alkalization has been recommended as the main treatment, hemodialysis (HD) may be more effective in severe cases. Case: On 24th June 2014, a 53- year-old man ingested a high amount of 40% 2, 4-D. He suffered from mouth and epigastric burning sensation, vomiting and nausea. He was treated, in Emam Reza’s Hospital of Mashhad University Of Medical Sciences, Mashhad , Iran, with maintenance daily fluid infusion plus 10 meq/L NaHCO3. Up to 9 hours after exposure, he became progressively stuporous. He developed diarrhea and hypotension, BP=100/60, unresponsive to volume replacement therapy. He received regular hemodialysis (HD) with bicarbonate for three hours. At the end of HD, his blood pressure rose to 110/70 and the level of consciousness began to improve. Four hours later, he was fully conscious with stable blood pressure (130/80 mmHg). Conclusion: HD may be an effective, safe and fast method for 2, 4-D high dose intoxication induced coma.
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13

Bazrafshan, Edris, Ferdos Kord Mostafapour, Hamed Faridi, Mahdi Farzadkia, Shahnaz Sargazi, and Ali Sohrabi. "Removal of 2, 4-Dichlorophenoxyacetic Acid (2, 4-D) From Aqueous Environments Using Single-Walled Carbon Nanotubes." Health Scope 2, no. 1 (May 11, 2013): 39–46. http://dx.doi.org/10.17795/jhealthscope-7710.

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14

Han, Sung Ok, and Peter B. New. "Effect of water availability on degradation of 2, 4-dichlorophenoxyacetic acid (2, 4-d) by soil microorganisms." Soil Biology and Biochemistry 26, no. 12 (December 1994): 1689–97. http://dx.doi.org/10.1016/0038-0717(94)90322-0.

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15

Jyothi. K., Bhagya Lakshmi. "Toxicity of Agricultural Herbicide 2, 4-Dichlorophenoxyacetic acid on growth, Photosynthesis and Respiration of Rice Field Cyanobacterium." International Journal of Scientific Research 2, no. 8 (June 1, 2012): 54–58. http://dx.doi.org/10.15373/22778179/aug2013/19.

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16

Pieper, Dietmar Helmut, Walter Reineke, Karl-Heinrich Engesser, and Hans-Joachim Knackmuss. "Metabolism of 2,4-dichlorophenoxyacetic acid, 4-chloro-2-methylphenoxyacetic acid and 2-methylphenoxyacetic acid by Alcaligenes eutrophus JMP 134." Archives of Microbiology 150, no. 1 (May 1988): 95–102. http://dx.doi.org/10.1007/bf00409724.

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17

G. Huitink, J. T. Walker, and T. L. Lavy. "Downwind Deposition Of 2, 4-Dichlorophenoxyacetic Acid Herbicide (2,4-D) In Invert Emulsion." Transactions of the ASAE 33, no. 4 (1990): 1051–56. http://dx.doi.org/10.13031/2013.31437.

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18

Oliveira, G. H., and J. Palermo-Neto. "Effects of 2, 4-Dichlorophenoxyacetic Acid (2, 4-D) on Open-Field Behaviour and Neurochemical Parameters of Rats." Pharmacology & Toxicology 73, no. 2 (August 1993): 79–85. http://dx.doi.org/10.1111/j.1600-0773.1993.tb01540.x.

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19

SCHULZE, GENE E., and JOHN A. DOUCHERTY. "Neurobehavioral Toxicity and Tolerance to the Herbicide 2, 4- Dichlorophenoxyacetic Acid-n-butyl Ester (2, 4-D Ester)." Toxicological Sciences 10, no. 3 (1988): 413–24. http://dx.doi.org/10.1093/toxsci/10.3.413.

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20

Domínguez May, Angel Virgilio, José Augusto Nah Hau, Israel García Sheseña, Sara Luz Nahuat Dzib, José Luis Giorgana Figueroa, Estefanía Escalante Zapata, José Efraín Ramírez Benítez, and Ana Paula Gamba Galeazzis. "6-BENZYLAMINOPURINE AND 2, 4-DICHLOROPHENOXYACETIC ACID EFFECT ON CALLUS GENESIS OF Brosimum alicastrum." Agrociencia 55, no. 2 (March 26, 2021): 133–44. http://dx.doi.org/10.47163/agrociencia.v55i2.2391.

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Brosimum alicastrum seeds contain a high percentage of protein and essential amino acids that contribute to a proper nutrition. This tree is an alternative in the so-called crusade against hunger and its management does not involve the use of agrochemicals. The objective of this research was to evaluate the morphogenic response of foliar explants with two growth regulators, 6-Benzylaminopurine (BAP) and 2,4-Dichlorophenoxyacetic Acid (2,4-D) in the induction of calli. Results demonstrated that the combination of 1.5 mg L-1 BAP and 1 mg L-1 2,4-D (TM) and 1.5 mg L-1 BAP with 2 mg L-1 2,4-D (TN) favored callus growth in 100% of foliar explants. Calli were grown in a period of 20 d, in a culture room at 25 ± 4 °C, with 16 h of illumination. Under these conditions, calli remained in slow growth for four weeks. Those explants that generated callus were sub-cultured in fresh medium without activated charcoal. In TM and TN treatments, the multiplication of the cell mass was favored; in TN globular structures were formed. However, explants the same treatments TM and TN with activated charcoal, and under ambient 29 ± 4 °C conditions increased callus growth, but became friable at two weeks. Thus, TM and TN were the better treatments, but activated charcoal was determined to have a negative effect on callus growth.
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21

Raskil’dina, Gul’nara Z., Evgeniya A. Yakovenko, Luisa M. M. Mryasova, and Simon S. Zlotskii. "SYNTHESIS AND HERBICID ACTIVITY OF ARYLOXYACETIC ACIDS AND AMIDES OF ARYLOXY ACETIC ACIDS CONTAINING CYCLOACETAL FRAGMENT." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 62, no. 1 (December 30, 2018): 91–97. http://dx.doi.org/10.6060/ivkkt.20196201.5753.

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The herbicidal activity of esters and amides based on commercially available phenoxy chlorides and 2,4-dichlorophenoxyacetic acids was studied. Esters of 2,2-methyl-4-hydroxymethyl-1,3-dioxolane, 5-ethyl-5-hydroxymethyl-1,3-dioxane and 1,3-dioxolan-4-ylmethanol and 1,3-dioxane-5 -ol (glycerin formulas), as well as amides containing gem-dichlorocyclopropane and 1,3-dioxolane fragments were obtained. The acid chlorides, 1,3-dioxacycloalkanes and secondary amines were prepared according to standard basic methods. Esters and amides were synthesized from these starting compounds in a short time and with a quantitative yield (more than 90%). As a result of the synthesis of a mixture of 1,3-dioxolan-4-ylmethyl phenylacetate and 1,3-dioxan-5-yl phenylacetate, the content of the 5-ring cyclic derivative over the 6-chain structure was predominant, which is obviously associated with greater activity in the esterification reaction of primary alcohol than secondary. The screening results showed that the activity relative to wheat of the 1,3-dioxalane ester of 2,4-dichlorophenoxyacetic acid is superior to the Octagon-Extra standard. With respect to peas, derivatives of 2,4-dichlorophenoxyacetic acid and 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane are close to the standard for inhibition of shoot mass. The results of N-benzyl-N-[(2,2-dichlorocyclopropyl) methyl] -2-phenoxyacetamide and N-[(2,2-dichlorocyclopropyl) methyl]-N-(1,3-dioxolan-4-ylmethyl)-2-phenoxyacetamide with respect to peas and wheat also showed a marked herbicidal effect, close in value to the reference one. The test results of synthesized benzamides on wheat showed that, at a concentration of 100 mg/l, the compounds act approximately the same as the reference preparation at a dose of 50 mg/l. The obtained results prove the prospects of creating herbicidal preparations based on phenoxy- chlorides and 2,4-dichlorophenoxyacetic acids containing 1,3-dioxacycloalkane fragments. Therefore, these objects are very attractive for further study and synthesis of biologically active compounds containing the above pharmacophore groups.
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22

Sieroń, Lesław, Joanna Kobyłecka, and Anna Turek. "Crystal Packing and Supramolecular Motifs in Four Phenoxyalkanoic Acid Herbicides—Low-Temperature Redeterminations." Organic Chemistry International 2011 (May 10, 2011): 1–5. http://dx.doi.org/10.1155/2011/608165.

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A low-temperature redetermination by X-ray crystallography of four phenoxyalkanoic acid herbicides, 4-chloro-2-methylphenoxyacetic acid (MCPA), rac-2-(4-chloro-2-methylphenoxy)propionic acid (MCPP), 2,4-dichlorophenoxyacetic acid (2,4-D), and 2,4-dichlorophenoxybutyric acid (2,4-DB), allowed the supramolecular structures of these compounds to be precisely described in terms of C⋯O/C–H⋯π interactions. The geometric parameters of the redetermined structures agree with those previously reported, but with improved precision.
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23

Trivedi, Nikhilesh S., Rhushikesh A. Kharkar, and Sachin A. Mandavgane. "Utilization of cotton plant ash and char for removal of 2, 4-dichlorophenoxyacetic acid." Resource-Efficient Technologies 2 (December 2016): S39—S46. http://dx.doi.org/10.1016/j.reffit.2016.11.001.

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24

Giri, R. R., H. Ozaki, S. Taniguchi, and R. Takanami. "Photocatalytic ozonation of 2, 4-dichlorophenoxyacetic acid in water with a new TiO2 fiber." International Journal of Environmental Science & Technology 5, no. 1 (December 26, 2007): 17–26. http://dx.doi.org/10.1007/bf03325993.

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25

SUN, YANLI. "Molecularly imprinted polymer for 2, 4-dichlorophenoxyacetic acid prepared by a sol-gel method." Journal of Chemical Sciences 126, no. 4 (July 2014): 1005–11. http://dx.doi.org/10.1007/s12039-014-0672-2.

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26

Chopra, RN, and BD Vashistha. "The Effect of Auxins and Antiauxins on Shoot-Bud Induction and Morphology in the Moss, Bryum atrovirens Will ex Brid." Australian Journal of Botany 38, no. 2 (1990): 177. http://dx.doi.org/10.1071/bt9900177.

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The protonema of the moss Bryum atrovirens remains bud-free under ordinary cultural conditions on Nitsch's basal medium. Exogenously applied auxins (Indole-3-acetic acid; 2-4-dichlorophenoxyacetic acid; α-naphthaleneacetic acid and β-naphthoxyacetic acid) induced buds on protonemata, whereas antiauxins (Maleic hydrazide and 2,3,5-triiodobenzoic acid) failed to do so. Morphology of the gametophores depended upon the concentration of auxin in the medium. In general, normal leafy gametophores resulted at lower concentrations, and at higher levels of auxins morphology was adversely affected. Simultaneous application of 6-benzylaminopurine and 2,4-dichlorophenoxyacetic acid advanced bud formation as well as increased bud number, but had no significant effect on the improvement of shoot morphology.
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27

Djebbar, K., A. Zertal, and T. Sehili. "Photocatalytic Degradation of 2,4-Dichlorophenoxyacetic Acid and 4-Chloro-2-Methylphenoxyacetic Acid in Water by using TiO2." Environmental Technology 27, no. 11 (November 2006): 1191–97. http://dx.doi.org/10.1080/09593332708618732.

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28

Tayyebi, Moslem, Yadollah Yamini, and Morteza Moradi. "Reverse micelle-mediated dispersive liquid-liquid microextraction of 2,4-dichlorophenoxyacetic acid and 4-chloro-2-methylphenoxyacetic acid." Journal of Separation Science 35, no. 18 (July 2, 2012): 2491–98. http://dx.doi.org/10.1002/jssc.201200150.

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29

McGhee, Ilona, and Richard G. Burns. "Biodegradation of 2,4-dichlorophenoxyacetic acid (2,4-D) and 2-methyl-4-chlorophenoxyacetic acid (MCPA) in contaminated soil." Applied Soil Ecology 2, no. 3 (September 1995): 143–54. http://dx.doi.org/10.1016/0929-1393(95)00056-q.

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30

Ishida, S., Y. Takahashi, and T. Nagata. "Isolation of cDNA of an auxin-regulated gene encoding a G protein beta subunit-like protein from tobacco BY-2 cells." Proceedings of the National Academy of Sciences 90, no. 23 (December 1, 1993): 11152–56. http://dx.doi.org/10.1073/pnas.90.23.11152.

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The addition of 2,4-dichlorophenoxyacetic acid to tobacco BY-2 cells that had been cultured in modified Linsmaier and Skoog medium deprived of auxin for 3 days induced cell division, whereas without 2,4-dichlorophenoxy-acetic acid application, no such induction of cell division was seen. When differential cDNA screening for auxin was done at 4 hr after the addition of 2,4-dichlorophenoxyacetic acid, the cDNA of an auxin-responsive gene designated arcA was isolated. The predicted gene product of arcA is a polypeptide with a M(r) of 35,825. arcA, thus, is a plant hormone-regulated gene that encodes a protein structurally related to the beta subunit of a guanine nucleotide-binding regulatory protein, which is composed of seven repetitive segments of Trp-Asp 40-aa repeats. The possibility that arcA gene products induce cell division is discussed.
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31

Hallberg, Kevin B., Martin P. Kelly, and Olli H. Tuovinen. "Simultaneous degradation of the herbicides 2,4-dichlorophenoxyacetic acid and 2-(2-methyl-4-chlorophenoxy)propionic acid by mixed bacterial cultures." Current Microbiology 23, no. 2 (August 1991): 65–69. http://dx.doi.org/10.1007/bf02092251.

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32

Hassan, Asaad F. "Enhanced adsorption of 2, 4-dichlorophenoxyacetic acid from aqueous medium by graphene oxide/alginate composites." DESALINATION AND WATER TREATMENT 141 (2019): 187–96. http://dx.doi.org/10.5004/dwt.2019.23523.

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33

Botrè, Claudio, Francesco Botrè, Franco Mazzei, and Elisabetta Podestà. "Inhibition-based biosensors for the detection of environmental contaminants: Determination of 2, 4-dichlorophenoxyacetic acid." Environmental Toxicology and Chemistry 19, no. 12 (December 2000): 2876–81. http://dx.doi.org/10.1002/etc.5620191204.

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34

Farhana, Lulu, and Peter B. New. "The 2, 4-dichlorophenol hydroxylase ofAlcaligenes eutrophusJMP134 is a homotetramer." Canadian Journal of Microbiology 43, no. 2 (February 1, 1997): 202–5. http://dx.doi.org/10.1139/m97-027.

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2, 4-Dichlorophenol hydroxylase (DCP-hydroxylase) is a key enzyme in the pathway for degradation of 2, 4-dichlorophenoxyacetic acid (2, 4-D) in many bacteria. In Alcaligenes eutrophus JMP134, DCP-hydroxylase was reported to consist of two dissimilar types of subunit of 66 and 45 kDa, a structure which is different from that in other bacteria. Using a different procedure involving affinity purification and ion-exchange chromatography, we have purified active enzyme from JMP134 and show that it has a native molecular mass of approximately 245 kDa and consists of a single type of subunit of 66 kDa, similar to all other flavoprotein monooxygenase enzymes. A 45-kDa polypeptide, found in partially purified enzyme preparations, was not required for enzyme activity but had some serologic and N-terminal amino acid sequence similarity to the 66-kDa enzyme subunit.Key words: 2, 4-dichlorophenol hydroxylase, Alcaligenes eutrophus, 2, 4-D biodegradation.
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35

Susarla, S., G. V. Bhaskar, and S. M. Rao Bhamidimarri. "Competitive Adsorption of Phenoxy Herbicide Chemicals in Soil." Water Science and Technology 26, no. 9-11 (November 1, 1992): 2121–24. http://dx.doi.org/10.2166/wst.1992.0676.

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A modified Freundlich-type bicomponent adsorption isotherm proposed by Sheindorf et al. (1981) was used to describe the competitive adsorption of 2,4-dichlorophenoxyacetic acid (2,4-D) and 2-methyl-4-chlorophenoxyacetic acid (MCPA) onto volcanic soil. The adsorption capacities of 2,4-D and MCPA reduced in presence of the other component compared to pure component adsorption capacities.
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36

Rodriguez-Mata, A. E., F. J. Tzompantzi, L. E. Amabilis-Sosa, I. Diaz-Peña, Y. Bustos-Terrones, and J. G. Rangel-Peraza. "Characterization of $$\text{SO}_{4}^{{2 - }}$$ /ZnO and Photodegradation Kinetics of 2,4-Dichlorophenoxyacetic Acid (2,4-D)." Kinetics and Catalysis 59, no. 6 (November 2018): 720–26. http://dx.doi.org/10.1134/s0023158418060125.

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37

Nethaji, S., and A. Sivasamy. "Graphene oxide coated with porous iron oxide ribbons for 2, 4-Dichlorophenoxyacetic acid (2,4-D) removal." Ecotoxicology and Environmental Safety 138 (April 2017): 292–97. http://dx.doi.org/10.1016/j.ecoenv.2017.01.001.

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38

de Duffard, Ana María Evangelista, Mirtha N. de Alderete, and Ricardo Duffard. "Changes in brain serotonin and 5-hydroxyindolacetic acid levels induced by 2, 4-dichlorophenoxyacetic butyl ester." Toxicology 64, no. 3 (December 1990): 265–70. http://dx.doi.org/10.1016/0300-483x(90)90119-2.

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39

Doczekalska, Beata, Krzysztof Kuśmierek, Andrzej Świątkowski, and Monika Bartkowiak. "Adsorption of 2,4-dichlorophenoxyacetic acid and 4-chloro-2-metylphenoxyacetic acid onto activated carbons derived from various lignocellulosic materials." Journal of Environmental Science and Health, Part B 53, no. 5 (January 16, 2018): 290–97. http://dx.doi.org/10.1080/03601234.2017.1421840.

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40

Kuhlmann, Birgit, and Barbara Kaczmarzcyk. "Biodegradation of the herbicides 2,4-dichlorophenoxyacetic acid, 2,4,5-trichlorophenoxyacetic acid, and 2-methyl-4-chlorophenoxyacetic acid in a sulfate-reducing aquifer." Environmental Toxicology & Water Quality 10, no. 2 (May 1995): 119–25. http://dx.doi.org/10.1002/tox.2530100206.

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41

Yang, Li Jiao, Feng Jie Zhang, Quan Sen Shao, Yun Na Wu, and Yu Ying Dong. "Effect of 2, 4-D on Adsorption of Copper onto the Black Soil." Advanced Materials Research 1051 (October 2014): 448–51. http://dx.doi.org/10.4028/www.scientific.net/amr.1051.448.

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Batch equilibrium adsorption was conducted to study the adsorption of copper in the black soil and the effect of 2, 4-dichlorophenoxyacetic acid (2, 4-D) on adsorption of copper was probed by soils. The results showed all of the adsorption isotherms of copper in the absence and presence of 2,4-D could be described by Freundlich equation (R2>0.99), the adsorption coefficients Kf increased with increasing concentration of 2,4-D.The In kinetic modeling, the pseudo-first order equation was considered as the most celebrated model. The pseudo-second order equation in copper was depressed in the presence of 2, 4-D. 2,4-D diminished the adsorption of copper on the black soil.
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42

Olejnik, A., I. Nowak, and G. Schroeder. "Functionalized polystyrene beads as carriers in release studies of two herbicides: 2,4-dichlorophenoxyacetic acid and 2-methyl-4-chlorophenoxyacetic acid." International Journal of Environmental Science and Technology 16, no. 10 (December 1, 2018): 5623–34. http://dx.doi.org/10.1007/s13762-018-2138-4.

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43

Rabhi, A. "EFFECT OF TEMPERATURE GIBBERELLIC ACID AND 2, 4-DICHLOROPHENOXYACETIC ACID ON VEGETATIVE INDUCTION IN CACTUS (OPUNTIA FICUS-INDICA (L.) MILLER.)." Acta Horticulturae, no. 811 (February 2009): 265–68. http://dx.doi.org/10.17660/actahortic.2009.811.34.

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44

Hoffmann, D., R. H. Müller, B. Kiesel, and W. Babel. "Isolation and characterization of an alkaliphilic bacterium capable of growing on 2,4-dichlorophenoxyacetic acid and 4-chloro-2-methylphenoxyacetic acid." Acta Biotechnologica 16, no. 2-3 (1996): 121–31. http://dx.doi.org/10.1002/abio.370160205.

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45

Hosseini Madani, Nasim Sadat, Seyed Pezhman Hosseini Shekarabi, Mehdi Shamsaie Mehrgan, and Nima Pourang. "Can 2, 4-dichlorophenoxyacetic acid alter growth performance, biochemical composition, and fatty acid profile of the marine microalga Isochrysis galbana?" Phycologia 59, no. 6 (October 26, 2020): 598–605. http://dx.doi.org/10.1080/00318884.2020.1827826.

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46

Premdas, Peter David, and Bryce Kendrick. "The Effects of 2, 4-Dichlorophenoxyacetic Acid, Pentachlorophenol and Mixtures of These on an Aero-aquatic Fungus." Journal of Freshwater Ecology 6, no. 2 (June 1991): 147–54. http://dx.doi.org/10.1080/02705060.1991.9665288.

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Goswami, Bhanita, and Debajyoti Mahanta. "Polyaniline-Fe3O4 and polypyrrole-Fe3O4 magnetic nanocomposites for removal of 2, 4-dichlorophenoxyacetic acid from aqueous medium." Journal of Environmental Chemical Engineering 8, no. 4 (August 2020): 103919. http://dx.doi.org/10.1016/j.jece.2020.103919.

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López-Granada, G., J. D. O. Barceinas-Sánchez, R. López, and R. Gómez. "High temperature stability of anatase in titania–alumina semiconductors with enhanced photodegradation of 2, 4-dichlorophenoxyacetic acid." Journal of Hazardous Materials 263 (December 2013): 84–92. http://dx.doi.org/10.1016/j.jhazmat.2013.07.060.

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49

Merkle, S. A., and A. T. Wiecko. "Regeneration of Robiniapseudoacacia via somatic embryogenesis." Canadian Journal of Forest Research 19, no. 2 (February 1, 1989): 285–88. http://dx.doi.org/10.1139/x89-043.

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Tissue cultures were initiated from developing seeds of black locust (Robiniapseudoacacia L.) collected from three trees at weekly intervals from 1 week following anthesis until early fruit maturity. Explants were cultured on media containing 0, 2, or 4 mg/L 2,4-dichlorophenoxyacetic acid and 0 or 0.25 mg/L 6-benzyladenine. Seeds explanted onto hormone-supplemented media remained on these media for 1 or 3 weeks before being placed on hormone-free media, or were maintained on hormone-supplemented media for the entire study. Direct somatic embryogenesis was observed in a single culture, initiated from a seed collected 4 weeks after anthesis and cultured for 1 week on a medium supplemented with 4 mg/L 2,4-dichlorophenoxyacetic acid and 0.25 mg/L 6-benzyladenine before transfer to basal medium. Although it could not be discerned from which part of the explant somatic embryos were derived, secondary embryogenesis continued from the radicles of cotyledonary-stage somatic embryos. Most somatic embryos were well formed, with two distinct cotyledons. Embryos germinated precociously, producing plantlets that were initially weak but later gained vigor and resembled seedlings.
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Ślusarkiewicz-Jarzina, Aurelia, Maciej Zenkteler, and Barbara Podlewska. "Regeneration of plants from leaves of Chrysanthemum morifolium Ram. cv. Bronze Bornholm in in vitro cultures." Acta Societatis Botanicorum Poloniae 51, no. 2 (2014): 173–78. http://dx.doi.org/10.5586/asbp.1982.015.

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Plants were obtained from cultured in vitro leaves of Chrysanthemum morifolium Ram. cv. Bronze Bornholm. The leaves were inoculated on Murashige and Skoog medium (MS) supplemented with cytokinins (kinetin - KIN, zeatin - ZEA, 6-benzyloaminopurine - BAP) and auxins (2,4-dichlorophenoxyacetic acid - 2,4-D, α-naphtaleneacetic acid - NAA, 3-indolilacetic acid - IAA, p-fluorophenylalanine - PFA) in various combinations and concentra-tions. The most suitable medium was that one which contained 4 mg/l KIN, 2 mg/l NAA and 50 mg/l PFA.
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