Undecenoic Acid Research Articles

Microscopic, Micromeritic and Phytochemical Analysis of the Leaves of Pseuderanthemum maculatum (G. Lodd.) I. M. Turner, A Plant with Potential Pharmacognistic Uses

Background: Pseuderanthemum maculatum, Pseuderanthemum maculatum (G.Lodd.) I.M.Turner [previously Pseuderanthemum carruthersii (Seem.) Guillaumin var. carruthersii] is an ornamental plant with potential pharmacognostic uses in the management of hypertension and cancers. There hadn’t been much work done on this plant previously hence making the current research work very much significant. Methods: The leaves were collected, identified, air dried, pulverized, weighed and subjected to evaluation parameters using standard procedures. GC-MS analysis was also carried out on the dichloromethane extract of the leaf. Results: The results showed that the stomatal distribution was hypostomatic with diacytic stomatal type. Stomatal index was 23.12% and the stomatal number was 60 (69.9 ± 2.65)86. Flow rate of the leaf was poor with the bulk volume of 32.30 ± 1.04, tapped volume of 21.8 ± 0.76, bulk density of 0.32 ± 0.02, tapped density of 0.46 ± 0.02, angle of repose 42.65°, Carr's index of 31.06% and Hausner's ratio of 1.45 ± 0.03. The chemomicroscopy and fluorescence analyses revealed characteristic features for the drug. The water-soluble, methanol-soluble, ethanol-soluble extractive values were 20.67 %w/w, 11.67 %w/w and 11.33 %w/w respectively. The moisture content of the leaf powder was 9.84%w/w. The total ash, acid-insoluble and water-soluble ash values were 6.72%w/w, 1.34%w/w and 16.17%w/w respectively. The GC-MS analysis revealed the presence of 11 chemical constituents with phytochemicals such as hexanoic acid, benzoic acid, undecenoic acid, heptanoic acid and Eicosane which are of useful pharmaceutical importance. Conclusion: These data obtained from the pharmacognostic studies provides information about the identity, purity and quality of Pseuderanthemum maculatum.

Solvent-based synthesis, structural elucidation and thermal characterisation of free radical grafted PHBV

This study investigates the solvent-based free-radical graft copolymerization of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) with C11 (undecenoic acid, UDA), C12 (dodecene, DD), and C18 (octadecene, OD) alkene substrates using dicumyl peroxide as an initiator. Comprehensive Nuclear Magnetic Resonance (NMR) spectroscopy was employed to confirm and quantify grafting, which was achieved at up to 5.8 mol% of monomer units. Thermal analysis revealed a significant reduction in melting temperature for all modified PHBVs, ranging from 10-20°C decrease in comparison to virgin PHBV. A decrease in crystallisation temperature and a reduction in glass transition temperature was measured for the UDA and DD grafted PHBV. Additionally, molecular weight analysis showed a marked decrease in weight average molecular weight (M¯w) and number average molecular weight (M¯n) for PHBV grafted with UDA, which was attributed to the presence of carboxylic acid functionality, which accelerates chain scission. The molecular weight profiles of the dodecene and octadecene grafted PHBV were only marginally reduced (32% and 18% reductions in M¯w, respectively), which is a much less severe reduction than has been previously observed for similar chemistries. Overall, this work demonstrates that solvent-based free-radical graft copolymerization can reduce the melting temperature and disrupt the crystallinity of PHBV, hence improving its processability and progressing the field of PHA modification and application.

Enhancing Suppression of Chain Transfer via Installing Bulky N‐ortho‐Aryl Substituents into α‐Diimine Nickel System

AbstractRecently, the important role of sterically bulky aromatic substituents at the axial position of the metal center for synthesizing high‐performance catalysts were recognized. In this study, a series of α‐diimine nickel complexes with bulky N‐ortho‐aryl substituents were designed and synthesized. The as‐synthesized nickel complexes showed high activities (up to 2.3×107 g ⋅ mol−1 ⋅ h−1) and superior thermostability, giving access to moderately branched polyethylenes (35–86/1000 C) with high molecular weights (up to 197.5×104 g ⋅ mol−1). The polyethylene materials generated by these nickel complexes at 80 °C exhibited outstanding tensile mechanical. In addition, these nickel complexes could also catalyze the copolymerization of ethylene and polar monomer with modest activity (such as undecenoic acid, 10‐undecen‐1‐ol and 6‐chlorohex‐1‐ene), yielding functionalized polyolefin with adjustable molecular weights (6.8–222.9×104 g ⋅ mol−1) and incorporation ratios (0.2–4.3 mol %).

The synthesis of hyperbranched ethylene oligomers by nickel catalysts with oxazole structure

Since the discovery of Shell-Higher-Olefin-Process (SHOP), ethylene oligomerization has been one of the most significant processes of homogenous transition-metal catalysts. And the structure designing of catalysts is always the key issue for ethylene oligomerization. In this contribution, a series of oxazole-based nickel complexes were synthesized to prepare the hyperbranched ethylene oligomers. The catalytic performance could be modulated by adjusting the electronic and steric effects of the nickel catalysts. And DFT calculations were also performed to reveal the electronic and steric effects of the ligand structures. Specially, these nickel complexes could catalyze the copolymerization of ethylene and polar monomers (6-chlorohex-1-ene, undecenoic acid and 10-undecen-1-ol, etc.), generating polar hyperbranched oligomers. And the incorporation ratio of polar monomers could be adjusted by using different catalysts (0.1–1.0 mol%). The generated hyperbranched oligomer materials will exhibit some potential applications as lubricants or surface modifiers.

Porous silicon structures passivated with 10-undecenoic acid for possible ethanol sensing

Multifunctional sensing platforms are useful for classifying and quantifying different analytes. This work presents a simple optical sensor based on porous silicon film modified using open-air pyrolysis with 10-undecenoic acid. The fabricated structure was characterized using vis-NIR reflectance spectroscopy and the functional groups were identified using Fourier transform infrared spectroscopy. With respect to the control, the proposed undecenoic acid passivated porous silicon nanostructured film has been tested as reusable ethanol sensor in water.

The Role of Undecenoic Acid on the Preparation of Decorated MCM-41/Polyethylene Hybrids by In Situ Polymerization: Catalytic Aspects and Properties of the Resultant Materials

Functionalized polyethylene-based nanocomposites were prepared by in situ polymerization of ethylene with modified or neat MCM-41 nanoparticles (NMCM-41). Two different synthetic approaches were investigated to improve the compatibility between the hydrophobic HDPE matrix and the hydrophilic NMCM-41: (i) incorporation of UA into the polymeric matrix by copolymerization with ethylene, promoted by the zirconocene catalyst under homogeneous conditions, in the presence of pristine NMCM-41; (ii) use of undecenoic acid (UA) as an interfacial agent to obtain decorated NMCM-41 to be used as nanofiller for the in situ ethylene polymerization, catalyzed by Cp2ZrCl2/MAO under supported conditions. The strong polar character of the carboxylic group is expected to either increase the hydrophilicity of the HDPE chains (strategy i) or interact with the NMCM-41 surface and provide an additional link to the polymeric chains via copolymerization of the vinyl group under supported conditions (strategy ii). Although metallocene catalysts have been shown to copolymerize olefins with functional monomers, the presence of oxygen-containing compounds in the reaction media strongly affects the polymerization activity as a result of the interaction of functional groups with the electrophilic active center of the catalyst. Thus, UA was pre-contacted with tri(isobutyl)aluminum (TIBA) prior to its use in the polymerization to reduce the deactivating character of the carboxylic acid groups towards the zirconocene catalyst. The influence of the UA presence on the polymerization behavior of the protection step is discussed, and the polymerization activities observed for the different approaches are compared. In addition, the thermal behavior and structural details of the resulting materials have been characterized. The impact of using neat or functionalized NMCM-41 on the final dispersion within the polymeric matrix is also analyzed, which is correlated with the mechanical performance exhibited by these HDPE_UA_NMCM-41 nanocomposites.

Synthesis of lactones from fatty acids by ring-closing metathesis and their biological evaluation

The present study involves the synthesis of macrocyclic lactones by the esterification of unsaturated fatty acids (oleic acid, undecenoic acid, and erucic acid) with unsaturated alcohols (allyl alcohol, prop-2-ene-1-ol, oleyl alcohol, and undecenol) followed by a ring closing metathesis reaction employing Grubbs' second generation catalyst (1.0-1.5 mmol). The structure of the compounds was confirmed by 1H NMR, 13C NMR, FT-IR, and ESI-Mass spectral studies. The antibacterial activity of the synthesised lactones was evaluated. The larger ring-sized lactone, namely, erucic acid lactone, exhibited excellent antibacterial activity against three bacterial cell lines, namely, Staphylococcus aureus, Staphylococcus epidermidis, and Bacillus subtilis. Undecenoic acid-based lactones exhibited excellent antibacterial activity selectively against only Staphylococcus epidermidis. The assay of macrolactones for their in vitro anticancer activity was carried out by MTT for different cancer cell lines, namely, human prostate epithelial cancer cells (ATCC HTB-81), HepG2 derived from hepatic cancer cells (ATCC HB-8065), SKOV3 derived from human ovarian cancer cells (ATCC HTB-77), MDAMB-231 derived from human breast cancer cells (ATCC HTB-26) and Chinese hamster ovarian (CHO-K1) cell lines. The molecules selectively exhibited anticancer activity against Chinese hamster ovarian (CHO-K1) cell lines. Among macrolactones, (E)-oxacyclotridec-11-en-2-one (MALUN) was more active and its activity was much higher compared to others and on par with the reference standard Mitomycin C. This was followed by (E)-oxacyclotricos-14-en-2-one (MOLER) and (E)-oxacyclononadec-10-en-2-one (MOLOH). The fatty acid-based cyclic lactones with selective antibacterial and anticancer activities can be further explored for a variety of pharmaceutical formulations.

COSMO prediction of siloxane compounds absorption on type 3 and type 5 deep eutectic solvents

This study reports a Conductor-like Screening MOdel for Real Solvents (COSMO-RS) prediction for 151 type 3 (polar) and type 5 Deep Eutectic Solvents (DES, non-polar) for absorption of hexamethyldisiloxane, octamethyltrisiloxane, hexamethylcyclotrisiloxane, and octamethylcyclotetrasiloxane. Through the examination of generated sigma surfaces, sigma profiles, and sigma potentials, it was found that while the siloxane chains offer sufficiently strong hydrogen bond accepting sites, the steric hindrance of the methyl groups cause less polar solvents (type 5) to outperform the more polar ones (type 3). The thermodynamic study predicts thymol-based type 5 DES as significantly more affinitive for siloxane compounds than common conventional solvents (DEA, MEA, MDEA, menthol, and DPEG Blend) with lnγ activity coefficients reaching low as −0.64. Enthalpy of mixing study shows Vander Waals interactions dominate DES-siloxane compound interactions over hydrogen bonding by over 10x enthalpic release, clarifying discrepancy in literature on how siloxanes are solvated by DES. Thymol: Stearic acid (4:1) showed the lowest excess enthalpy of mixing at −10.4 kcal/mol. An environmental health and safety (EHS) study show the best performing DES components (camphor, capric acid, lauric acid, myristic acid, stearic acid, undecenoic acid, borneol, betaine, hexadecanoic acid, and thymol) are potentially environmentally benign and safe for operation procedures.

Experimental study on reactor scale-up for microwave-assisted pyrolysis of methyl ricinoleate

The microwave-assisted pyrolysis reactor with microwave absorbent bed can work continuously and efficiently to pyrolysis reactions, which makes it potential for reactor scale-up. In this paper, the scale-up of microwave-assisted pyrolysis reactor using silicon carbide (SiC) as microwave absorbent bed that was used for methyl ricinoleate (MR) pyrolysis was studied. The microwave power, SiC bed diameter and MR feed rate were enlarged from 1 kW, 126 mm and 0.9 kg/h for the lab-scale reactor to 7 kW, 580 mm and 7.0 kg/h for our self-designed scale-up reactor, respectively. The results show that temperature distribution of the scaled up SiC bed surface before feeding of MR was uniform and stable, which provides favorable conditions for efficient pyrolysis reaction on the bed surface. The selectivity and yield of the target product undecenoic acid methyl ester were 75.55% and 63.08%, respectively that reached the lab-scale test results. It needs to be emphasized that the scale-up process of microwave-assisted pyrolysis of MR has no obvious scale-up effect by using the microwave intensification heating and the microdroplet rapid heating technology. This study will provide guidance for the large-scale application of the microwave-assisted pyrolysis reactor in chemical industry.

Obtaining and Characterizing the Osmium Nanoparticles/n-Decanol Bulk Membrane Used for the p-Nitrophenol Reduction and Separation System.

Liquid membranes based on nanoparticles follow a continuous development, both from obtaining methods and characterization of techniques points of view. Lately, osmium nanoparticles have been deposited either on flat membranes, with the aim of initiating some reaction processes, or on hollow fiber membranes, with the aim of increasing the contact surface with the phases of the membrane system. This paper presents the obtainment and characterization of a liquid membrane based on osmium nanoparticles (Os–NP) dispersed in ndecanol (nDol) for the realization of a membrane system with a large contact surface between the phases, but without using a liquid membrane support. The dispersion of osmium nanoparticles in n-decanol is carried out by the method of reducing osmium tetroxide with 1–undecenoic acid (UDA). The resulting membrane was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive spectroscopy analysis (EDAX), thermoanalysis (TG, DSC), Fourier transform infra-red (FTIR) spectroscopy and dynamic light scattering (DLS). In order to increase the mass transfer surface, a design for the membrane system was realized with the dispersion of the membrane through the receiving phase and the dispersion of the source phase through the membrane (DBLM-dispersion bulk liquid membrane). The process performance was tested for the reduction of p–nitrophenol (pNP) from the source phase, using sodium tetra-borohydride (NaBH4), to p–aminophenol (pAP), which was transported and collected in the receiving phase. The obtained results show that membranes based on the dispersion of osmium nanoparticles in n–decanol can be used with an efficiency of over 90% for the reduction of p–nitrophenol and the separation of p–aminophenol.

Selective Electrochemical Oxidation of Alcohols Catalyzed by Partially Biobased TEMPO Analogs**

AbstractA new electrochemical catalyst has been synthesized from an analog of 2,2,6,6‐tetramethylpiperidine‐1‐oxyl (TEMPO) and the medium chain fatty acid, undecenoic acid. The electrochemical properties of the new material are shifted to more positive potential by ∼170 mV, typical for other substituted TEMPOs. The straightforward reaction gives a catalyst that has been tested in the oxidation of alcohols to aldehydes and ketones and gives reaction rates similar to TEMPOs when considered on a per nitroxyl basis. However, the new system gives an ∼ 3‐fold higher primary over secondary selectivity. This reaction shows promise as a versatile method in the potential to synthesize rationally designed electroactive materials with a high biobased content.

Simultaneous Release of Silver Ions and 10-Undecenoic Acid from Silver Iron-Oxide Nanoparticles Impregnated Membranes.

The bio-medical benefits of silver ions and 10–undecenoic acid in various chemical-pharmaceutical preparations are indisputable, thus justifying numerous research studies on delayed and/or controlled release. This paper presents the effect of the polymer matrix in the simultaneous release of silver ions and 10–undecenoic acid in an aqueous medium of controlled pH and ionic strength. The study took into consideration polymeric matrices consisting of cellulose acetate (CA) and polysulfone (PSf), which were impregnated with oxide nanoparticles containing silver and 10–undecenoic acid. The studied oxide nanoparticles are nanoparticles of iron and silver oxides obtained by an accessible electrochemical method. The obtained results show that silver can be released, simultaneously with 10–undecenoic acid, from an impregnated polymeric membrane, at concentrations that ensure the biocidal and fungicidal capacity. Concentrations of active substances can be controlled by choosing the polymer matrix or, in some cases, by changing the pH of the target medium. In the studied case, higher concentrations of silver ions are released from the polysulfone matrix, while higher concentrations of 10–undecenoic acid are released from the cellulose acetate matrix. The results of the study show that a correlation can be established between the two released target substances, which is dependent on the solubility of the organic compound in the aqueous medium and the interaction of this compound with the silver ions. The ability of 10–undecenoic acid to interact with the silver ion, both through the carboxyl and alkene groups, contributes to the increase in the content of the silver ions transported in the aqueous medium.

Operational Limits of the Bulk Hybrid Liquid Membranes Based on Dispersion Systems.

Liquid membranes usually have three main constructive variants: bulk liquid membranes (BLM), supported liquid membranes (SLM) and emulsion liquid membranes (ELM). Designing hybrid variants is very topical, with the main purpose of increasing the flow of substance through the membrane but also of improving the selectivity. This paper presents the operational limits of some kind of hybrid membrane constituted as a bulk liquid membrane (BLM), but which works by dispersing the aqueous source (SP) and receiving (RP) phases, with the membrane itself being a dispersion of nanoparticles in an organic solvent (NP–OSM). The approached operational parameters were the volume of phases of the hybrid membrane system, the thickness of the liquid membrane, the working temperature, the flow of aqueous phases, the droplet size of the aqueous phases dispersed across the membrane, the nature and concentration of nanoparticles in the membrane, the pH difference between the aqueous phases, the nature of the organic solvent, the salt concentration in the aqueous phases and the nature of transported chemical species. For this study, silver ion (SI) and p-nitrophenol (PNP) were chosen as transportable chemical species, the n-aliphatic alcohols (C6…C12) as membrane organic solvents, 10–undecenoic acid (UDAc) and 10-undecylenic alcohol (UDAl) as carriers and magnetic iron oxides as nanoparticles dispersed in the membrane phase. Under the experimentally established operating conditions, separation efficiencies of over 90% were obtained for both ionic and molecular chemical species (silver ions and p-nitrophenol). The results showed the possibility of increasing the flow of transported chemical species by almost 10 times for the silver ion and approximately 100 times for p-nitrophenol, through the appropriate choice of operational parameters, but they also exposed their limits in relation to the stability of the membrane system.

Osmium Recovery as Membrane Nanomaterials through 10-Undecenoic Acid Reduction Method.

The recovery of osmium from residual osmium tetroxide (OsO4) is a necessity imposed by its high toxicity, but also by the technical-economic value of metallic osmium. An elegant and extremely useful method is the recovery of osmium as a membrane catalytic material, in the form of nanoparticles obtained on a polymeric support. The subject of the present study is the realization of a composite membrane in which the polymeric matrix is the polypropylene hollow fiber, and the active component consists of the osmium nanoparticles obtained by reducing an alcoholic solution of osmium tetroxides directly on the polymeric support. The method of reducing osmium tetroxide on the polymeric support is based on the use of 10-undecenoic acid (10–undecylenic acid) (UDA) as a reducing agent. The osmium tetroxide was solubilized in t–butanol and the reducing agent, 10–undecenoic acid (UDA), in i–propanol, t–butanol or n–decanol solution. The membranes containing osmium nanoparticles (Os–NP) were characterized morphologically by the following: scanning electron microscopy (SEM), high-resolution SEM (HR–SEM), structurally: energy-dispersive spectroscopy analysis (EDAX), Fourier transform infrared (FTIR) spectroscopy. In terms of process performance, thermal gravimetric analysis was performed by differential scanning calorimetry (TGA, DSC) and in a redox reaction of an organic marker, p–nitrophenol (PNP) to p–aminophenol (PAP). The catalytic reduction reaction with sodium tetraborate solution of PNP to PAP yielded a constant catalytic rate between 2.04 × 10−4 mmol s−1 and 8.05 × 10−4 mmol s−1.

Transport and Separation of the Silver Ion with n-decanol Liquid Membranes Based on 10-undecylenic Acid, 10-undecen-1-ol and Magnetic Nanoparticles.

This paper presents a transport and recovery of silver ions through bulk liquid membranes based on n–decanol using as carriers 10–undecylenic acid and 10–undecylenyl alcohol. The transport of silver ions across membranes has been studied in the presence of two types of magnetic oxide nanoparticles obtained by the electrochemical method with iron electrodes in the electrolyte with and without silver ions, which act as promoters of turbulence in the membrane. Separation of silver ions by bulk liquid membranes using 10–undecylenic acid and 10–undecylenyl alcohol as carriers were performed by comparison with lead ions. The configuration of the separation module has been specially designed for the chosen separation process. Convective-generating magnetic nanoparticles were characterized in terms of the morphological and structural points of view: scanning electron microscopy (SEM), high-resolution SEM (HR–SEM), energy dispersive spectroscopy analysis (EDAX), Fourier Transform InfraRed (FTIR) spectroscopy, thermal gravimetric analysis (TGA), differential scanning calorimetry and magnetization. The process performance (flux and selectivity) was tested were tested for silver ion transport and separation through n–decanol liquid membranes with selected carriers. Under the conditions of the optimized experimental results (pH = 7 of the source phase, pH = 1 of the receiving phase, flow rate of 30 mL/min for the source phase and 9 mL/min for the receiving phase, 150 rot/min agitation of magnetic nanoparticles) separation efficiencies of silver ions of over 90% were obtained for the transport of undecenoic acid and about 80% for undecylenyl alcohol.

Amphiphilic and Perfluorinated Poly(3-Hydroxyalkanoate) Nanocapsules for 19F Magnetic Resonance Imaging.

Nanoparticles have recently emerged as valuable tools in biomedical imaging techniques. Here PEGylated and fluorinated nanocapsules based on poly(3-hydroxyalkanoate) containing a liquid core of perfluorooctyl bromide PFOB were formulated by an emulsion-evaporation process as potential 19F MRI imaging agents. Unsaturated poly(hydroxyalkanoate), PHAU, was produced by marine bacteria using coprah oil and undecenoic acid as substrates. PHA-g-(F; PEG) was prepared by two successive controlled thiol-ene reactions from PHAU with firstly three fluorinated thiols having from 3 up to 17 fluorine atoms and secondly with PEG-SH. The resulting PHA-g-(F; PEG)-based PFOB nanocapsules, with a diameter close to 250–300 nm, are shown to be visible in 19F MRI with an acquisition time of 15 min. The results showed that PFOB-nanocapsules based on PHA-g-(F; PEG) have the potential to be used as novel contrast agents for 19F MRI.

Onychomycosis Treatment with FotonaLaser

Onychomycosis is a fungal infection of the nails. It does not usually cause discomfort, but it alters the aesthetics of the affected nails and, if not treated in time, it can become chronic and spread. The cause of onychomycosis are fungi of the dermatophyte type. Onychomycosis is the disease that most frequently affects the nails of humans (50%), being responsible for more than half of the cases of nail alteration. Studies show prevalence figures between 2% - 18% of the population. It manifests in the form of onychodystrophy or alteration of the normal appearance of one or more fingernails or toenails. Toenails are affected more often than fingernails. It is very common to affect several nails at the same time. Clinically there may be onycholysis, subungual hyperkeratosis with desquamation, dyschromia ranging from yellowish or greenish to brown or black. The treatment of onychomycosis may require taking oral antifungal drugs (undecenoic acid, azoles and sometimes allylamines) combined with long-term treatment (2 to 18 months), they can cause liver damage, kidney failure, anemia, thrombocytopenia, neutropenia, gastrointestinal disorders and alopecia among other diseases. In addition, other treatments can be performed, ranging from surgery (laminectomy, matrixectomy), onychoabrasion, to the use of new therapies such as: photodynamic therapy, iontophoresis, and lasers today. The laser is a revolutionary treatment for Onychomycosis. It is a simple and effective procedure that uses Neodymium or Erbium: Yag laser to act to the depths of the damaged nail and the underlying skin, weakening and eliminating the fungus that has invaded the patient’s nail. The body’s natural defense process is stimulated to regenerate the nail in a normal way. Compared with traditional methods, the laser does not damage the tissue and is not limited to its chemical action like topical drugs, nor does it risk causing liver damage like oral medications. By applying the Fotona Laser with smoothmode technology throughout the nail plate, we achieve, through heat irradiation, eradicate any fungus or germ lodged in the nail. Without side effects, fast, simple and 100% safe.

Antibacterial, Compositional and Physicochemical Properties of Guizotia Scabra (Vis.) Chiov. Seed Oil Found on Jos-Plateau-Nigeria

The oil extract of G. scabra seeds was analyzed for its antibacterial, chemical and physical properties. Physical and chemical properties analyzed included moisture content (0.91%), acid value (13.65%), iodine value (132.27), peroxide value (18.58), saponification value (191.03), free fatty acids (6.86%) and density (0.87g/cm3). The oil was found to inhibit the growth of Staphylococcus aureus (SA), Escherichia coli (EC) and Salmonella typhi (ST) at an MIC of 50%. However, there was no effect on Shigella sonnei (SS). The fatty acid composition of the extracted oil was revealed using the Gas chromatography Mass spectrometry (GC-MS) method. A total of 18 components of the oil were identified. Oleic acid (27.07%), 10- undecenoic acid (19.99%), palmitic acid (10.56%) and stearic acid (6.22%) were detected as the dominant fatty acids in the G. scabra seed oil.

Program controlling the emission color of blend polymer phosphors containing Eu(III), Tb(III), Be(II) ions for WLEDs

Through of the technique route of pre-coordination and post-polymerization and final-blend by program controlling from vinyl-functionalized RGB complex monomers [Eu(TTA)3(UA)](TTA = 2-thenoyltrifluoroacetone, UAH= Undecenoic acid), [Tb(2-ABA)3(UA)](2-ABAH = 2-Aminobenzoic acid), [Be (BTZ) (MAA)](BTZ=Benzothiazole, MAA = Methylacrylic acid) with Methyl methacrylate(MMA) to synthesize the monochrome polymers poly(MMA-co-Eu(TTA)3(UA)) (abbr. PMEu), poly(MMA-co-Tb(2-ABA)3(UA)) (abbr. PMTb), poly(MMA-co- Be (BTZ) (MAA)) (abbr. PMBe), and finally obtain the white-light blend-polymer phosphors by program controlling. The monochrome polymers PMEu, PMTb, PMBe have 1.69, 11.53, 10.57 times of the luminescent intensity as RGB complex monomers. The serial blend polymer phosphors have the emission located in the white light region with the CIE coordinates close to the calculated ones running by the program. When the RGB ratio = 1:1.38:0.46, the experiment coordinates are situated at (0.32, 0.33), being close to the theoretical coordinates of (0.33, 0.33), proving that the program controlling can guide the tuning of the chromaticity of the emission color. The LED device was fabricated by the blend polymer phosphor with the RGB ratio of 1:1.38:0.46 matched with the chip of 365 nm wavelength, the color temperature is 6444 K, the color rendering index 84.2, and the luminance 12740 cd/m2 at 3.2 V. This research develops an approach of pre-coordination, post-polymerization and final-blend by program controlling that not only improves the luminescent intensity, but also suppresses the energy transfer, and more importantly achieves the precise adjustment to the white light.

Synthesis of telehelic oligodimethylsiloxanes with 4-carboxypyrrolidone fragments: rheological and thermal properties

Telehelic oligodimethylsiloxanes containing 4-carboxypyrrolidone fragments were synthesized by the reactions of oligodimethylsiloxanes bearing terminal 3-aminopropyl groups with itaconic acid. The thermal and rheological properties of the obtained polymers were studied. The activation energies of viscous flow of the oligomers obtained and the previously synthesized oligodimethylsiloxanes containing terminal fragments of undecenoic or benzoic acid are compared.