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Publication DateContact Dermatitis, ISSN 0105-1873, 11/2018, Volume 79, Issue 5, pp. 288 - 294
Background: Allergic contact dermatitis caused by p-phenylenediamine (PPD) is a health concern for hair dye users. Because of its lower sensitization potency,...
contact allergy | allergic contact dermatitis | phenylenediamine | open use test | 2‐methoxymethyl | diagnostic patch tests | hair dyes | p-phenylenediamine | 2-methoxymethyl-p-phenylenediamine | ALLERGY | INDUCTION | DERMATOLOGY | Phenylenediamines - adverse effects | Dermatitis, Allergic Contact - immunology | Phenylenediamines - immunology | Hair Dyes - chemistry | Humans | Middle Aged | Male | Patch Tests - methods | Hair Dyes - adverse effects | Cross Reactions | Dose-Response Relationship, Drug | Young Adult | Dermatitis, Allergic Contact - diagnosis | Dermatitis, Allergic Contact - etiology | Adolescent | Adult | Female | Aged | Allergy | Hair dyes | Testing | Hair | Phenylenediamine | Dyes | Contact dermatitis | Hypersensitivity | Health risk assessment | Dermatitis | p‐phenylenediamine | 2‐methoxymethyl‐p‐phenylenediamine | Original
contact allergy | allergic contact dermatitis | phenylenediamine | open use test | 2‐methoxymethyl | diagnostic patch tests | hair dyes | p-phenylenediamine | 2-methoxymethyl-p-phenylenediamine | ALLERGY | INDUCTION | DERMATOLOGY | Phenylenediamines - adverse effects | Dermatitis, Allergic Contact - immunology | Phenylenediamines - immunology | Hair Dyes - chemistry | Humans | Middle Aged | Male | Patch Tests - methods | Hair Dyes - adverse effects | Cross Reactions | Dose-Response Relationship, Drug | Young Adult | Dermatitis, Allergic Contact - diagnosis | Dermatitis, Allergic Contact - etiology | Adolescent | Adult | Female | Aged | Allergy | Hair dyes | Testing | Hair | Phenylenediamine | Dyes | Contact dermatitis | Hypersensitivity | Health risk assessment | Dermatitis | p‐phenylenediamine | 2‐methoxymethyl‐p‐phenylenediamine | Original
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Loading RightsMaterials Chemistry and Physics, ISSN 0254-0584, 02/2018, Volume 205, pp. 423 - 435
Aim of this study is to bring systematic comparison of structure and properties of the redox-active oxidation products of various phenylenediamines prepared...
Poly(o-phenylenediamine) | Conducting polymers | Poly(p-phenylenediamine) | FTIR and Raman spectroscopies | Poly(m-phenylenediamine) | P-PHENYLENEDIAMINE | NITROGEN-CONTAINING CARBON | MATERIALS SCIENCE, MULTIDISCIPLINARY | RAMAN-SPECTROSCOPY | LARGE-SCALE SYNTHESIS | PALLADIUM NANOPARTICLES | EFFECTIVE ADSORPTION | ANILINE OLIGOMERS | POLY-O-PHENYLENEDIAMINE | THIN POLYANILINE FILMS | METAL-ION SORPTION
Poly(o-phenylenediamine) | Conducting polymers | Poly(p-phenylenediamine) | FTIR and Raman spectroscopies | Poly(m-phenylenediamine) | P-PHENYLENEDIAMINE | NITROGEN-CONTAINING CARBON | MATERIALS SCIENCE, MULTIDISCIPLINARY | RAMAN-SPECTROSCOPY | LARGE-SCALE SYNTHESIS | PALLADIUM NANOPARTICLES | EFFECTIVE ADSORPTION | ANILINE OLIGOMERS | POLY-O-PHENYLENEDIAMINE | THIN POLYANILINE FILMS | METAL-ION SORPTION
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Loading RightsJournal of Electroanalytical Chemistry, ISSN 1572-6657, 02/2019, Volume 834, pp. 206 - 215
To further improve the capacitive performances of reduced graphene oxide-based materials is still crucial although N-doped reduced graphene oxide hydrogels...
Supercapacitors | o-Phenylenediamine | N-doped graphene | Sulfuric acid | ELECTROCHEMISTRY | CHEMISTRY, ANALYTICAL | MESOPOROUS CARBON | ENERGY | BORON | HYDROXYLAMINE | P-PHENYLENEDIAMINE | ELECTRODE MATERIAL | POLY(O-PHENYLENEDIAMINE) | COMPOSITE | HYDROTHERMAL SYNTHESIS | CAPACITANCE | Phenylenediamine | Electrochemical analysis | Hydrogels | Flux density | Graphene | Capacitance | Nitrogen | Energy storage
Supercapacitors | o-Phenylenediamine | N-doped graphene | Sulfuric acid | ELECTROCHEMISTRY | CHEMISTRY, ANALYTICAL | MESOPOROUS CARBON | ENERGY | BORON | HYDROXYLAMINE | P-PHENYLENEDIAMINE | ELECTRODE MATERIAL | POLY(O-PHENYLENEDIAMINE) | COMPOSITE | HYDROTHERMAL SYNTHESIS | CAPACITANCE | Phenylenediamine | Electrochemical analysis | Hydrogels | Flux density | Graphene | Capacitance | Nitrogen | Energy storage
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Loading RightsCONTACT DERMATITIS, ISSN 0105-1873, 03/2016, Volume 74, Issue 3, pp. 152 - 158
Background. Penetration, autoxidation and N-acetylation of p-phenylenediamine (PPD) have been studied in vitro and ex vivo. However, a clear understanding of...
aman spectroscopy | skin | in vivo | phenylenediamine | PPD | penetration | in vivo | Raman spectroscopy | p -phenylenediamine (PPD) | IMMUNE-RESPONSE | N-ACETYLATION | KERATINOCYTES | MICROSPECTROSCOPY | CONTACT ALLERGY | DERMATOLOGY | p-phenylenediamine (PPD) | ELICITATION | ALLERGY | SENSITIZATION | ALLERGIC PATIENTS | EXPOSURE | BANDROWSKIS BASE | Coloring Agents - administration & dosage | Skin - metabolism | Humans | Half-Life | Male | Skin Absorption | Phenylenediamines - administration & dosage | Phenylenediamines - metabolism | Skin - chemistry | Phenylenediamines - pharmacokinetics | Coloring Agents - metabolism | Adult | Female | Spectrum Analysis, Raman | Coloring Agents - pharmacokinetics | Acetylation | Index Medicus
aman spectroscopy | skin | in vivo | phenylenediamine | PPD | penetration | in vivo | Raman spectroscopy | p -phenylenediamine (PPD) | IMMUNE-RESPONSE | N-ACETYLATION | KERATINOCYTES | MICROSPECTROSCOPY | CONTACT ALLERGY | DERMATOLOGY | p-phenylenediamine (PPD) | ELICITATION | ALLERGY | SENSITIZATION | ALLERGIC PATIENTS | EXPOSURE | BANDROWSKIS BASE | Coloring Agents - administration & dosage | Skin - metabolism | Humans | Half-Life | Male | Skin Absorption | Phenylenediamines - administration & dosage | Phenylenediamines - metabolism | Skin - chemistry | Phenylenediamines - pharmacokinetics | Coloring Agents - metabolism | Adult | Female | Spectrum Analysis, Raman | Coloring Agents - pharmacokinetics | Acetylation | Index Medicus
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Loading RightsScientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 1 - 17
In this paper, Co-Al layered double hydroxides (LDHs), Co-Al LDHs/poly(o-phenylenediamine) (PoPD) and Ag nanoparticles decorated Co-Al LDHs/PoPD (Ag@Co-Al...
Electrodes | Nanoparticles | Phenylenediamine | Uric acid | 2,4-Dinitrophenol | o-Phenylenediamine
Electrodes | Nanoparticles | Phenylenediamine | Uric acid | 2,4-Dinitrophenol | o-Phenylenediamine
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Loading RightsNatural Product Research, ISSN 1478-6419, 09/2006, Volume 20, Issue 11, pp. 1024 - 1030
The evaluation of the cytotoxic properties in vitro of three synthetic tripods containing pyrazole: N,N-bis[(3,5-dimethylpyrazol-1-yl)methyl]aniline (1);...
tdpmppd: N,N,N′,N′-tetrakis-[(1,5-dimethylpyrazol-3-yl)methyl]-para-phenylenediamine | bdpma: N,N-bis[(3,5-dimethylpyrazol-1-yl)methyl]aniline | Tripod | Anticancer activity | Cytotoxicity | tdpmpp: N,N,N′,N′-tetrakis[(3,5-dimethylpyrazol-1-yl)methyl]-para-phenylenediamine | In vitro | Pyrazole | tdpmppd: N,N,N′, N′-tetrakis-[(1,5- dimethylpyrazol-3-yl)methyl]-para-phenylenediamine | tdpmpp: N,N,N′, N′-tetrakis[(3,5-dimethylpyrazol-1-yl)methyl]-para- phenylenediamine | tripod | 5-dimethylpyrazol-1-yl)methyl]-para-phenylenediamine | tdpmpp : N,N,N ',N '-tetrakis | CHEMISTRY, MEDICINAL | in vitro | METAL-ION EXTRACTION | pyrazole | bdpma : N,N-bis[(3,5-dimethylpyrazol-1-yl)methyl]aniline | anticancer activity | CHEMISTRY, APPLIED | cytotoxicity | tdpmppd : N,N,N ',N '-tetrakis-[(1,5-dimethylpyrazol-3-yl)methyl]-para-phenylenediamine | Pyrazoles - chemistry | Aniline Compounds - pharmacology | Humans | Cell Line, Tumor | Phenylenediamines - pharmacology | Antineoplastic Agents - pharmacology | Molecular Structure | Aniline Compounds - chemistry | Antineoplastic Agents - chemistry | Phenylenediamines - chemistry | Pyrazoles - pharmacology
tdpmppd: N,N,N′,N′-tetrakis-[(1,5-dimethylpyrazol-3-yl)methyl]-para-phenylenediamine | bdpma: N,N-bis[(3,5-dimethylpyrazol-1-yl)methyl]aniline | Tripod | Anticancer activity | Cytotoxicity | tdpmpp: N,N,N′,N′-tetrakis[(3,5-dimethylpyrazol-1-yl)methyl]-para-phenylenediamine | In vitro | Pyrazole | tdpmppd: N,N,N′, N′-tetrakis-[(1,5- dimethylpyrazol-3-yl)methyl]-para-phenylenediamine | tdpmpp: N,N,N′, N′-tetrakis[(3,5-dimethylpyrazol-1-yl)methyl]-para- phenylenediamine | tripod | 5-dimethylpyrazol-1-yl)methyl]-para-phenylenediamine | tdpmpp : N,N,N ',N '-tetrakis | CHEMISTRY, MEDICINAL | in vitro | METAL-ION EXTRACTION | pyrazole | bdpma : N,N-bis[(3,5-dimethylpyrazol-1-yl)methyl]aniline | anticancer activity | CHEMISTRY, APPLIED | cytotoxicity | tdpmppd : N,N,N ',N '-tetrakis-[(1,5-dimethylpyrazol-3-yl)methyl]-para-phenylenediamine | Pyrazoles - chemistry | Aniline Compounds - pharmacology | Humans | Cell Line, Tumor | Phenylenediamines - pharmacology | Antineoplastic Agents - pharmacology | Molecular Structure | Aniline Compounds - chemistry | Antineoplastic Agents - chemistry | Phenylenediamines - chemistry | Pyrazoles - pharmacology
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Loading RightsChemical Communications : Chem Comm, ISSN 1359-7345, 01/2018, Volume 54, Issue 38, pp. 4862 - 4865
Ion-doped poly(p-phenylenediamine) (Fe-ppd) nanoparticles were prepared at room temperature by using FeCl3 as an oxidant. Fe-ppd exhibited high photothermal...
Nanoparticles | Therapy | Phenylenediamine | Photothermal conversion | Iron chlorides
Nanoparticles | Therapy | Phenylenediamine | Photothermal conversion | Iron chlorides
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Nature Communications, ISSN 2041-1723, 08/2015, Volume 6, Issue 1, p. 7992
Replacement of precious platinum with efficient and low-cost catalysts for electrocatalytic hydrogen evolution at low overpotentials holds tremendous promise...
Pyrolysis | Catalysts | Hydrogen | Colloids | Hydrogen evolution | Cobalt | Carbon | Silica | Silicon dioxide | Phenylenediamine | Platinum | o-Phenylenediamine | Evolution | Catalysis | Noble metals | Coordination compounds | Metal complexes | Clean energy | Hydrogen ion concentration
Pyrolysis | Catalysts | Hydrogen | Colloids | Hydrogen evolution | Cobalt | Carbon | Silica | Silicon dioxide | Phenylenediamine | Platinum | o-Phenylenediamine | Evolution | Catalysis | Noble metals | Coordination compounds | Metal complexes | Clean energy | Hydrogen ion concentration
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Loading RightsChemistry of Natural Compounds, ISSN 0009-3130, 1/2017, Volume 53, Issue 1, pp. 118 - 120
Heating an equimolar mixture of opianic acid and o-phenylenediamine in MeOH or EtOH produced 2-(2-carboxy-3,4-dimethoxyphenyl)benzimidazole, which was readily...
4,5-dichloro- o -phenylenediamine | Pharmacy | o -phenylenediamine | opianic acid | Plant Sciences | Organic Chemistry | benzimidazole derivatives | 4,5-dichloro-o-phenylenediamine | Opianic acid | Benzimidazole derivatives | O-phenylenediamine | CHEMISTRY, ORGANIC | CHEMISTRY, MEDICINAL | o-phenylenediamine
4,5-dichloro- o -phenylenediamine | Pharmacy | o -phenylenediamine | opianic acid | Plant Sciences | Organic Chemistry | benzimidazole derivatives | 4,5-dichloro-o-phenylenediamine | Opianic acid | Benzimidazole derivatives | O-phenylenediamine | CHEMISTRY, ORGANIC | CHEMISTRY, MEDICINAL | o-phenylenediamine
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Loading RightsJournal of Fluorescence, ISSN 1053-0509, 1/2018, Volume 28, Issue 1, pp. 359 - 372
Fluorescence investigations on interactions between 7,8-benzo-4-azidomethyl coumarin (7BAMC) and quenchers ortho-phenylenediamine (OPD) and...
Biomedicine, general | Biochemistry, general | Biotechnology | Analytical Chemistry | Biomedicine | Stern–Volmer plots | Binding constant | Ortho -phenylenediamine | Biological and Medical Physics, Biophysics | Sphere of action static quenching model | Para -phenylenediamine | Ortho-phenylenediamine | Para-phenylenediamine | Stern-Volmer plots | CHEMISTRY, ANALYTICAL | PROTEIN | BIOCHEMICAL RESEARCH METHODS | CHEMISTRY, PHYSICAL | PROBES | DYE | ACETONITRILE | BOVINE SERUM-ALBUMIN | Fluorescence | Electric properties
Biomedicine, general | Biochemistry, general | Biotechnology | Analytical Chemistry | Biomedicine | Stern–Volmer plots | Binding constant | Ortho -phenylenediamine | Biological and Medical Physics, Biophysics | Sphere of action static quenching model | Para -phenylenediamine | Ortho-phenylenediamine | Para-phenylenediamine | Stern-Volmer plots | CHEMISTRY, ANALYTICAL | PROTEIN | BIOCHEMICAL RESEARCH METHODS | CHEMISTRY, PHYSICAL | PROBES | DYE | ACETONITRILE | BOVINE SERUM-ALBUMIN | Fluorescence | Electric properties
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Loading RightsEuropean annals of allergy and clinical immunology, ISSN 1764-1489, 03/2019, Volume 51, Issue 2, pp. 62 - 67
Allergic contact dermatitis after exposure to p-phenylenediamine (PPD)-containing hair dye products is a common and important clinical problem. Because there...
2-methoxymethyl-p-phenylenediamine | allergic reaction | p-phenylenediamine
2-methoxymethyl-p-phenylenediamine | allergic reaction | p-phenylenediamine
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Loading RightsRegulatory Toxicology and Pharmacology, ISSN 0273-2300, 07/2014, Volume 69, Issue 2, pp. 263 - 272
Azo dyes in textiles may release aromatic amines after enzymatic cleavage by skin bacteria or after dermal absorption and metabolism in the human body. From...
Textile dyes | Carcinogenicity | Skin sensitization | Genotoxicity | MEDICINE, LEGAL | PHARMACOLOGY & PHARMACY | TOXICOLOGY | Amines - chemistry | Amines - toxicity | Azo Compounds - chemistry | Amines - analysis | Humans | Azo Compounds - adverse effects | Clothing - adverse effects | Coloring Agents - adverse effects | Molecular Structure | Toxicity Tests | Textiles - toxicity | Coloring Agents - chemistry | Textile fabrics | Textile industry | Aromatic amines | Index Medicus
Textile dyes | Carcinogenicity | Skin sensitization | Genotoxicity | MEDICINE, LEGAL | PHARMACOLOGY & PHARMACY | TOXICOLOGY | Amines - chemistry | Amines - toxicity | Azo Compounds - chemistry | Amines - analysis | Humans | Azo Compounds - adverse effects | Clothing - adverse effects | Coloring Agents - adverse effects | Molecular Structure | Toxicity Tests | Textiles - toxicity | Coloring Agents - chemistry | Textile fabrics | Textile industry | Aromatic amines | Index Medicus
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Loading RightsContact Dermatitis, ISSN 0105-1873, 08/2019, Volume 81, Issue 2, pp. 138 - 140
p‐Phenylenediamine (PPD) (1,4‐diaminobenzene; CAS no. 106‐50‐3) is well known as key allergen in hair dye‐related allergic contact dermatitis. PPD can be...
contact allergy | phenylenediamine (PPD) | case report | monoacetyl‐PPD (MAPPD) | diacetyl‐PPD (DAPPD) | acetyltransferase | diacetyl-PPD (DAPPD) | p-phenylenediamine (PPD) | ALLERGY | monoacetyl-PPD (MAPPD) | PARAPHENYLENEDIAMINE | N-acetyltransferase | DERMATOLOGY | Phenylenediamine | Acetyltransferase | Dyes | Contact dermatitis | Allergies | N‐acetyltransferase | p‐phenylenediamine (PPD) | Contact Point | Contact Points
contact allergy | phenylenediamine (PPD) | case report | monoacetyl‐PPD (MAPPD) | diacetyl‐PPD (DAPPD) | acetyltransferase | diacetyl-PPD (DAPPD) | p-phenylenediamine (PPD) | ALLERGY | monoacetyl-PPD (MAPPD) | PARAPHENYLENEDIAMINE | N-acetyltransferase | DERMATOLOGY | Phenylenediamine | Acetyltransferase | Dyes | Contact dermatitis | Allergies | N‐acetyltransferase | p‐phenylenediamine (PPD) | Contact Point | Contact Points
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Loading Rights1995, BUA report, ISBN 9783777606477, Volume 97., xxi, 259
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Talanta, ISSN 0039-9140, 01/2016, Volume 146, pp. 181 - 187
A novel electrochemical sensor based on a molecularly imprinted polymer, poly(o-phenylenediamine) (PoPD), has been developed for selective and sensitive...
Poly(o-phenylenediamine) | Gold electrode | Molecular imprinted polymer | Furosemide | Electropolymerization | CHEMISTRY, ANALYTICAL | LIQUID-CHROMATOGRAPHY | URINE | FLOW-INJECTION | ELECTRODE | POLY(O-PHENYLENEDIAMINE) MEMBRANES | Gold - chemistry | Phenylenediamines - chemical synthesis | Sodium Hydroxide - chemistry | Humans | Polymerization | Furosemide - chemistry | Molecular Imprinting | Electrodes | Time Factors | Surface Properties | Furosemide - urine | Electrochemistry - instrumentation | Phenylenediamines - chemistry | Furosemide - analysis | Hydrogen-Ion Concentration | Atomic force microscopy | Chemical properties | Polymer industry | Sensors | Electric properties
Poly(o-phenylenediamine) | Gold electrode | Molecular imprinted polymer | Furosemide | Electropolymerization | CHEMISTRY, ANALYTICAL | LIQUID-CHROMATOGRAPHY | URINE | FLOW-INJECTION | ELECTRODE | POLY(O-PHENYLENEDIAMINE) MEMBRANES | Gold - chemistry | Phenylenediamines - chemical synthesis | Sodium Hydroxide - chemistry | Humans | Polymerization | Furosemide - chemistry | Molecular Imprinting | Electrodes | Time Factors | Surface Properties | Furosemide - urine | Electrochemistry - instrumentation | Phenylenediamines - chemistry | Furosemide - analysis | Hydrogen-Ion Concentration | Atomic force microscopy | Chemical properties | Polymer industry | Sensors | Electric properties
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Loading RightsContact Dermatitis, ISSN 0105-1873, 07/2013, Volume 69, Issue 1, pp. 32 - 39
Background p-Phenylenediamine (PPD) is the primary patch test screening agent for hair dye contact allergy, and approximately 100 different hair dye chemicals...
toluenediamine | PPD | phenylenediamine | 3‐nitro | hydroxyethylaminophenol | hair dye allergy | aminophenol | toluene‐2,5‐diamine | methylaminophenol | 2‐amino‐3‐hydroxypyridine | p -methylaminophenol | p -aminophenol | p -phenylenediamine | 2-amino-3-hydroxypyridine | m -aminophenol | p -toluenediamine | toluene-2,5-diamine | 3-nitro- p -hydroxyethylaminophenol | m-aminophenol | p-phenylenediamine | DERMATITIS | 3-nitro-p-hydroxyethylaminophenol | RECOMMENDATION | DERMATOLOGY | p-methylaminophenol | toluene-2 | 5-diamine | p-toluenediamine | ALLERGY | SENSITIZATION | PRODUCTS | p-aminophenol | HAIRDRESSERS | Phenylenediamines - adverse effects | Coloring Agents - administration & dosage | Patch Tests - statistics & numerical data | Prevalence | Hair Dyes - chemistry | Humans | Risk Factors | Male | Phenylenediamines - administration & dosage | Dermatitis, Allergic Contact - epidemiology | Hair Dyes - adverse effects | Young Adult | Dermatitis, Allergic Contact - diagnosis | Denmark - epidemiology | Adult | Coloring Agents - adverse effects | Female | Administration, Topical | Aluminum compounds | Allergy | Toluene diamine | Hair dyes | Allergic reaction | Toluene | Medical research | Dyes | Medical and Health Sciences | Medicin och hälsovetenskap | Dermatologi och venereologi | Dermatology and Venereal Diseases | hair dye | allergy | Klinisk medicin | Clinical Medicine
toluenediamine | PPD | phenylenediamine | 3‐nitro | hydroxyethylaminophenol | hair dye allergy | aminophenol | toluene‐2,5‐diamine | methylaminophenol | 2‐amino‐3‐hydroxypyridine | p -methylaminophenol | p -aminophenol | p -phenylenediamine | 2-amino-3-hydroxypyridine | m -aminophenol | p -toluenediamine | toluene-2,5-diamine | 3-nitro- p -hydroxyethylaminophenol | m-aminophenol | p-phenylenediamine | DERMATITIS | 3-nitro-p-hydroxyethylaminophenol | RECOMMENDATION | DERMATOLOGY | p-methylaminophenol | toluene-2 | 5-diamine | p-toluenediamine | ALLERGY | SENSITIZATION | PRODUCTS | p-aminophenol | HAIRDRESSERS | Phenylenediamines - adverse effects | Coloring Agents - administration & dosage | Patch Tests - statistics & numerical data | Prevalence | Hair Dyes - chemistry | Humans | Risk Factors | Male | Phenylenediamines - administration & dosage | Dermatitis, Allergic Contact - epidemiology | Hair Dyes - adverse effects | Young Adult | Dermatitis, Allergic Contact - diagnosis | Denmark - epidemiology | Adult | Coloring Agents - adverse effects | Female | Administration, Topical | Aluminum compounds | Allergy | Toluene diamine | Hair dyes | Allergic reaction | Toluene | Medical research | Dyes | Medical and Health Sciences | Medicin och hälsovetenskap | Dermatologi och venereologi | Dermatology and Venereal Diseases | hair dye | allergy | Klinisk medicin | Clinical Medicine
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Loading RightsDermatitis, ISSN 1710-3568, 09/2018, Volume 29, Issue 5, pp. 285 - 286
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Loading RightsJournal of Luminescence, ISSN 0022-2313, 01/2016, Volume 169, pp. 186 - 190
In this paper, we demonstrated a fluorescent o-phenylenediamine–m-phenylenediamine copolymer sensing system, which was synthesized by a facile and one-step...
o-Phenylenediamine–m-phenylenediamine copolymer | Fluorescent sensoring | Chromium(VI) ion | o-Phenylenediamine-m-phenylenediamine copolymer | AQUEOUS-MEDIA | HEXAVALENT CHROMIUM | MERCURY IONS | NANOPARTICLES | REMOVAL | CR(VI) | SEMICONDUCTING POLYMER DOTS | GRAPHENE QUANTUM DOTS | GREEN SYNTHESIS | SILICA | OPTICS | Chromium | Chemical industry | Herbicides | Pesticides industry | Chelates | Detectors | Fluorescence | Chemical synthesis
o-Phenylenediamine–m-phenylenediamine copolymer | Fluorescent sensoring | Chromium(VI) ion | o-Phenylenediamine-m-phenylenediamine copolymer | AQUEOUS-MEDIA | HEXAVALENT CHROMIUM | MERCURY IONS | NANOPARTICLES | REMOVAL | CR(VI) | SEMICONDUCTING POLYMER DOTS | GRAPHENE QUANTUM DOTS | GREEN SYNTHESIS | SILICA | OPTICS | Chromium | Chemical industry | Herbicides | Pesticides industry | Chelates | Detectors | Fluorescence | Chemical synthesis
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