scholarly journals Fabrication of Novel Ball-Like Polystyrene Films Containing Schiff Base Microspheres as Photostabilizers

Polymers ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1185 ◽  
Author(s):  
Emad Yousif ◽  
Dina Ahmed ◽  
Gamal El-Hiti ◽  
Mohammad Alotaibi ◽  
Hassan Hashim ◽  
...  

Polystyrene films containing a low concentration of three highly aromatic Schiff bases were prepared using the casting method. The polystyrene films were irradiated with ultraviolet light (300 h). The polystyrene infrared spectra, weight loss, molecular weight reduction and the surface morphology were examined upon irradiation. The Schiff bases acted as photostabilizers and reduced the photodegradation of polystyrene films to a significant level in comparison to the blank film. The images recorded of the surface of the miscible polystyrene/Schiff base blends showed novel ball-like microspheres with a diameter of 3.4–4.3 µm. The Schiff bases were able to endow excellent protection to polystyrene against ultraviolet irradiation.

Polymers ◽  
2021 ◽  
Vol 13 (17) ◽  
pp. 2982
Author(s):  
Anaheed A. Yaseen ◽  
Emaad T. B. Al‐Tikrity ◽  
Emad Yousif ◽  
Dina S. Ahmed ◽  
Benson M. Kariuki ◽  
...  

The scale of production of polystyrene has escalated in the recent past in order to meet growing demand. As a result, a large quantity of polystyrene waste continues to be generated along with associated health and environmental problems. One way to tackle such problems is to lengthen the lifetime of polystyrene, especially for outdoor applications. Our approach is the synthesis and application of new ultraviolet photostabilizers for polystyrene and this research is focused on four cephalexin Schiff bases. The reaction of cephalexin and 3-hydroxybenzaldehyde, 4-dimethylaminobenzaldehyde, 4-methoxybenzaldehyde, and 4-bromobanzaldehyde under acidic condition afforded the corresponding Schiff bases in high yields. The Schiff bases were characterized and their surfaces were examined. The Schiff bases were mixed with polystyrene to form homogenous blends and their effectiveness as photostabilizers was explored using different methods. The methods included monitoring the changes in the infrared spectra, weight loss, depression in molecular weight, and surface morphology on irradiation. In the presence of the Schiff bases, the formation of carbonyl group fragments, weight loss, and decrease in molecular weight of polystyrene were lower when compared with pure polystyrene. In addition, undesirable changes in the surface such as the appearance of dark spots, cracks, and roughness were minimal for irradiated polystyrene containing cephalexin Schiff bases. Mechanisms by which cephalexin Schiff bases stabilize polystyrene against photodegradation have also been suggested.


2019 ◽  
Vol 9 (3-4) ◽  
pp. 169-177 ◽  
Author(s):  
Ahmed A. Ahmed ◽  
Dina S. Ahmed ◽  
Gamal A. El-Hiti ◽  
Mohammad Hayal Alotaibi ◽  
Hassan Hashim ◽  
...  

Abstract A Schiff base containing the 1,2,4-triazole moiety was synthesized and added to polystyrene at low concentration for a homogenous blend. The polystyrene film was irradiated with ultraviolet light and the surface morphology was analyzed. Micrographs of the polystyrene/Schiff base blend after irradiation indicated the fabrication of a terrestrial crack-like material. This was ascribed to the presence of the Schiff base, relatively long irradiation time, and photostability induced by the base. After irradiation, the blank polystyrene film formed a cotton-like fibrous material.


1970 ◽  
Vol 25 (10) ◽  
pp. 1090-1094 ◽  
Author(s):  
S. R. Gupta ◽  
J. P. Tandon

Titanium (IV) complexes of monofunctional bidentate Schiff bases, such as salicylideneaniline, β-hydroxynaphthylideneaniline, benzylidene-o-aminophenol, benzylidene-2-hydroxyethylamine and benzylidene-2-hydroxy-n-propylamine have been prepared. The reactions between titanium isopropoxide and the Schiff bases in varying molar ratios resulted in the synthesis of several new derivatives of the general type, Ti (OPri)4-x (SB)x (where x = 1. 2. 3 or 4 and SB⊖ is the anion of the Schiff base SBH) in quantitative yields. The molecular weight determinations of some of the soluble derivatives indicate the possibility of coordination numbers five or seven for the central metal atom.


1971 ◽  
Vol 26 (1) ◽  
pp. 11-13 ◽  
Author(s):  
P. Prashar ◽  
J. P. Tandon

A number of new niobium (V) - Schiff base complexes of the type Nb (SB) x (OPri) 5 - 2x and Nb(SB)2(SBH) (where SB2⊖ and SBH⊖ are anions of the Schiff bases and x =1 or 2) have been synthesised by the interaction of niobium pentaisopropoxide with the Schiff bases in different stoichiometric ratios. The molecular weight determinations and IR studies of a few derivatives have also been carried out.Scanty references are available in the literature regarding the Schiff base complexes of niobium (V) and tantalum (V) 1, 2 and such derivatives have been prepared from the corresponding metal chlorides and the Schiff bases. In a series of papers published earlier 3, 4, a more convenient method, for the synthesis of such derivatives, by the interaction of metal alkoxides with the Schiff bases in anhydrous benzene medium, has been reported. The present paper describes the synthesis of several new niobium (V) derivatives with the Schiff bases derived from the condensation of salicylaldehyde or o-hydroxyacetophenone with n-hydroxyalkylamines.


1973 ◽  
Vol 28 (1-2) ◽  
pp. 63-68 ◽  
Author(s):  
J. P. Tandon ◽  
R. N. Prasad

The 1 : 1 and 2 : 3 interactions of aluminium isopropoxide with bifunctional tridentate Schiff bases, derived by the condensation of o-hydroxyacetophenone with hydroxyalkylamines [such as 2-hydroxyethylamine, 2-hydroxy-1-propylamine, 1-hydroxy-2-methyl-2-propylamine and 1-hydroxy-2-butylamine] have been investigated. The resulting derivatives of the types, Al(OPrt)(SB) and Al2(SB)3 (where SB2- is the anion of the corresponding Schiff base, SBH2) have been isolated in almost quantitative yields. The ebullioscopic determination of molecular weights in benzene has shown the isopropoxy derivatives to be dimers, whereas the dialuminium-tris-Schiff base derivatives to be monomers. The infrared spectra of these compounds have been recorded and plausible structures indicated.


Polymers ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1202
Author(s):  
Joanna Brzeska ◽  
Agnieszka Tercjak ◽  
Wanda Sikorska ◽  
Barbara Mendrek ◽  
Marek Kowalczuk ◽  
...  

One of the methods of making traditional polymers more environmentally friendly is to modify them with natural materials or their biodegradable, synthetic equivalents. It was assumed that blends with polylactide (PLA), polysaccharides: chitosan (Ch) and starch (St) of branched polyurethane (PUR) based on synthetic poly([R,S]-3-hydroxybutyrate) (R,S-PHB) would degrade faster in the processes of hydrolysis and oxidation than pure PUR. For the sake of simplicity in the publication, all three modifiers: commercial PLA, Ch created by chemical modification of chitin and St are called bioadditives. The samples were incubated in a hydrolytic and oxidizing environment for 36 weeks and 11 weeks, respectively. The degradation process was assessed by observation of the chemical structure as well as the change in the mass of the samples, their molecular weight, surface morphology and thermal properties. It was found that the PUR samples with the highest amount of R,S-PHB and the lowest amount of polycaprolactone triol (PCLtriol) were degraded the most. Moreover, blending with St had the greatest impact on the susceptibility to degradation of PUR. However, the rate of weight loss of the samples was low, and after 36 weeks of incubation in the hydrolytic solution, it did not exceed 7% by weight. The weight loss of Ch and PLA blends was even smaller. However, a significant reduction in molecular weight, changes in morphology and changes in thermal properties indicated that the degradation of the samples should occur quickly after this time. Therefore, when using these polyurethanes and their blends, it should be taken into account that they should decompose slowly in their initial life. In summary, this process can be modified by changing the amount of R,S-PHB, the degree of cross-linking, and the type and amount of second blend component added (bioadditives).


2019 ◽  
Vol 20 (4) ◽  
pp. 399-411 ◽  
Author(s):  
Shiqi Luo ◽  
George Binh Lenon ◽  
Harsharn Gill ◽  
Heidi Yuen ◽  
Angela Wei Hong Yang ◽  
...  

Background: Obesity has become a worldwide health concern. Pharmacotherapies are now being introduced because lifestyle modifications alone are insufficient for weight management. The treatment outcomes of current approved anti-obesity agents are not satisfying due to drug-related intolerances. And so natural therapies including herbal medicines are popular alternatives for weight reduction; however, there are limited studies about their mechanism of actions. Methods: Five databases (PubMed, Scopus, Google Scholar, Science Direct, Proquest) were searched to investigate the targets and safety profiles of the current and past anti-obesity drugs that have been approved by the Food and Drug Administration (FDA) or the European Medicines Agency (EMA) as well as the commonly used off-label agents. The targets for weight-loss natural products and their principle bioactive components have also been searched. Only articles in English were included. Results: The targets for current anti-obesity single agents include pancreatic lipase, Glucagon Like Peptide-1(GLP-1) receptor, and serotonin 2C (5-HT2C) receptor. Potential targets such as amylin, pancreatic alpha amylase, leptin receptor, melanocortin receptor 4 receptor (MC4R), Peroxisome Proliferator- Activated Receptors gamma (PPAR γ), endocannabinoid 1 (CB1) receptor and Adenosine Monophosphate (AMP)-Activated Protein Kinase (AMPK) were discussed in various studies. Natural compounds have been found to interact with targets like pancreatic lipase, pancreatic alpha amylase, AMPK and PPAR γ to achieve weight reduction. Conclusion: Current pharmacotherapies and natural chemical compounds do act on same targets. Further investigations on the interactions between herbal compounds and the above targets are essential for the development of novel weight-loss therapies.


Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1564
Author(s):  
Jong Tae Leem ◽  
Woong Cheol Seok ◽  
Ji Beom Yoo ◽  
Sangkug Lee ◽  
Ho Jun Song

EPOSS of polyhedral oligomeric silsesquioxanes (POSS) mixture structure and LPSQ of ladder-like polysilsesquioxane (LPSQ) structure were synthesized via sol–gel reaction. EPSQ had a high molecular weight due to polycondensation by potassium carbonate. The EPSQ film showed uniform surface morphology due to regular double-stranded structure. In contrast, the EPOSS-coated film showed nonuniform surface morphology due to strong aggregation. Due to the aggregation, the EPOSS film had shorter d-spacing (d1) than the EPSQ film in XRD analysis. In pencil hardness and nanoindentation analysis, EPSQ film showed higher hardness than the EPOSS film due to regular double-stranded structure. In addition, in the in-folding (r = 0.5 mm) and out-folding (r = 5 mm) tests, the EPSQ film did not crack unlike the EPOSS coated film.


Polymers ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 2018
Author(s):  
Muhammad Samsuri ◽  
Ihsan Iswaldi ◽  
Purba Purnama

Stereocomplexation is one of several approaches for improving polylactide (PLA) properties. The high molecular weight of poly L-lactide (PLLA) and poly D-lactide (PDLA) homopolymers are a constraint during the formation of stereocomplex PLAs (s-PLAs). The presence of s-PLA particles in PLA PLLA/PDLA blends can initiate the formation of s-PLA crystalline structures. We used the solution casting method to study the utilization of s-PLA materials from high molecular weight PLLA/PDLA blends for increasing s-PLA formation. The s-PLA particles initiated the formation of high molecular weight PLLA/PDLA blends, obtaining 49.13% s-PLA and 44.34% of the total crystalline fraction. In addition, the mechanical properties were enhanced through s-PLA crystalline formation and the increasing of total crystallinity of the PLLA/PDLA blends. The s-PLA particles supported initiation for s-PLA formation and acted as a nucleating agent for PLA homopolymers. These unique characteristics of s-PLA particles show potential to overcome the molecular weight limitation for stereocomplexation of PLLA/PDLA blends.


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