Copolymerization of benzyl methacrylate and a methacrylate bearing benzophenoxy and hydroxyl side groups: Monomer reactivity ratios,thermal studies and dielectric measurements

Statistical copolymers of 2-hydroxy-3-benzophenoxy propyl methacrylate (HBPPMA) and benzyl methacrylate (BzMA) in different feed ratios were synthesized by free radical copolymerization method at 60 °C in presence of AIBN initiator. The compositions of copolymer were estimated from ¹H-NMR technique. The monomer reactivity ratios of HBPPMA and BzMA were calculated as r₁ (r_HBPPMA)=0.51±0.076 and r₂ (r_BzMA)=1.07±0.140 for Kelen-Tüdos method, and was estimated as r₁=0.37±0.0006 and r₂=0.64±0.0485 according to Fineman Ross equation. The average values estimated from the two methods showed that monomer reactivity ratio of benzyl methacrylate was a slightly high in comparison to HBPPMA. The copolymer system showed an azeotropic point, which is equal to M _BzMA =m _BzMA =0.43. DSC measurements showed that the T_g’s of poly(HBPPMA) and poly(BzMA) were 84 °C and 73 °C, respectively. The T_g in the copolymer system decreased with increase in benzyl methacrylate content. The decomposition temperature of poly(BzMA) and poly(HBPPMA) occurs in a single stage at about 207 °C and 260 °C, respectively. Those of HBPPMA-BzMA copolymer systems are between decomposition temperatures of two homopolymers. The dielectric constant, dielectric loss factor and electrical conductivity were investigated depend on the frequency of the copolymers. The highest dielectric constants depending on all the studied frequencies were recorded for the poly(HBPPMA) and the copolymer containing the highest HBPPMA unit. The dielectric constant for P(HBPPMA) and P(BzMA) at 1 kHz are 6.56 and 3.22, respectively. Also, those of copolymer systems were estimated between these two values. Similarly, poly(HBPPMA) and copolymers, which are prepared under the same conditions show the dissipation factor and conductivity as well.     

Enhancement of processability, stability and photoluminescence performance of poly(p-phenylene vinylene) containing diazine heterocycle unit

Two n-type conjugated polymers of pyrazine and quinoxaline containing poly(p-phenylene vinylene) (P-1) (P-2) have been synthesized through Wittig route. Formation of the polymers were confirmed by spectral (UV-Vis, PL, FT-IR and NMR), elemental and GPC analysis. These polymers were soluble in common organic solvents such as THF, CH₂Cl₂, CHCl₃ and CH₃CN. The resulting polymers have good thermal stability upto 308 and 361 °C with the 5 % weight loss. The absorption spectrum of the polymers displayed the maximum at 398 and 414 nm, corresponding to the ??-??* electronic transition of the conjugated polymer backbones. The optical band gap of these polymers found to have in the range of 2.5?C2.53 eV. The photoluminescence spectrum of the polymers was observed at 487 and 505 nm in CHCl₃ solution. AFM images depicted that the micrometer sized globular and triangular shaped particles can be seen from the polymer surfaces.     

Synthesis of chitosan 6-OH immobilized cyclodextrin derivates via click chemistry

The synthesis of chitosan 6-OH immobilized cyclodextrin (CTS-6-CD) via click chemistry was investigated. After protecting the 2-NH₂ group of chitosan by forming a Schiff base (BCTS) with benzaldehyde, the protected chitosan C₆-OH p-toluenesulfonate (BCTS-6-OTs) was generated by treating with p-toluenesulfonyl chloride. Afterwards, nucleophilic substitution of the sulfonate with NaN₃ furnished the Schiff base protected chitosan C₆-N₃ (BCTS-6-N₃). On the other hand, alkynylic β-cyclodextrin (CD-OPg) was obtained by alkynylation of β-cyclodextrin (β-CD). With these two substrates in hand, β-CD was immobilized at the Schiff base protected chitosan 6-OH position via click chemistry between CD-OPg and BCTS-6-N₃ to afford BCTS-6-CD, and then chitosan 6-OH immobilized cyclodextrin derivates (CTS-6-CD) was obtained by deprotecting the Schiff base of BCTS-6-CD. The structures of these products were characterized by FTIR, and their crystal properties and thermal stabilities were studied by XRD and TG respectively. By using UV spectroscopy to determine the immobilized amount, we also investigated the effect of the click reaction conditions on the immobilized loading of the synthesized BCTS-6-CD. It was found that the immobilized loading was 197.61 µmol·g^?1 in the BCTS-6-CD that was synthesized under the optimum conditions, and it went up to 223.17 µmol·g^?1 in CTS-6-CD by deprotecting the Schiff base group.     

Thermal degradation studies of poly(o-anisidine) doped with 5-sulfosalicylic acid

Thermal decomposition of the solid state of poly(o-anisidine) (POAN) base (POAN-EB) and salt [doped with 5-sulfosalicylic (SSA) acid] (SSA-doped POAN) forms has been studied by thermogravimetric analysis (TGA) and differential thermal analysis (DTA) under non-isothermal conditions. The potential (PE) and optimum molecular geometric (OMG) energies of the repeating unit (tetramer form) of investigated matrix were calculated using molecular mechanics (MM+) calculations. These calculations (PE= −3.48×10⁹ and OMG=−122.72 kJ mol⁻¹) indicate that the optimum molecular geometric structure of this matrix is highly stable. The empirical formula of the doped polymer is best represented by [POAN-2SSA.n/6H₂O] and substantiate by elemental analysis and MM+ calculations. The full polymer decomposition and degradation were found to occur in three stages during the temperature increase. The decomposition activation energy (E _d) of both POAN base (POAN-EB) and its doped (SSA-doped POAN) were calculated by employing different approximations. The heating rate of decomposition and the frequency factor (k _o ) as well as kinetic parameters were calculated for doped or base form of this matrix. A remarkable heating rate dependence of the decomposition rate of the SSA-doped POAN matrix was observed.     

Electro-optical and electrochemical properties of poly(1-hexyne)

Poly(1-hexyne) was prepared by the polymerization of 1-hexyne by using transition metal catalyst. The instrumental analysis data on the polymer structure revealed that the poly(1-hexyne) have the conjugated polyene backbone structure with n-butyl substituents. Poly(1-hexyne) showed UV-visible absorption band at 276 nm and PL spectrum at 415 nm, indicating relatively blue-shifted PL maximum value. From the relationship plot of the oxidation current density (log i _p,a) as a function of the scan rate (log v), it was found that the oxidation current of poly(1-hexyne) versus the scan rate is approximately linear relationship in the range of 30∼150 mV/sec and the exponent of scan rate, x value is found to be 0.424. It is explained by that the kinetics of the redox process are close to the diffusion-control process. The band gap energy of poly(1-hexyne) was estimated to be 2.98 eV and HOMO and LUMO level values of poly(1-hexyne) were 5.35 and 2.37 eV, respectively.     

Synthesis and electropolymerization of 9-(4-vinylbenzyl)-9H-carbazole on carbon fiber microelectrode: Capacitive behavior of poly(9-(4-vinylbenzyl)-9H-carbazole)

The synthesis of 9-(4-vinylbenzyl)-9H-carbazole (VBCz) monomer and surface characterizations of thin film coating of poly(9-(4-vinylbenzyl)-9H-carbazole), P(VBCz) homopolymer on carbon fiber microelectrode (CFME) was performed. Coatings of polymer thin films obtained, with different initial monomer concentrations, were characterized by cyclic voltammetry, scanning electron microscopy and Fourier transform infrared reflectance-attenuated total reflection spectroscopy. Different initial monomer concentrations (1, 3, 5, and 10 mM) were electrodeposited in 0.1 M lithium perchlorate/acetonitrile solution. The characterization of the thin polymer films was performed on the surface of carbon fiber, and composition of polymeric structure was proposed. Capacitor behavior of modified CFME was studied by electrochemical impedance spectroscopy. The deposition charge of polymer growth affected the redox parameters of resulting coated CFME.     

Synthesis of poly(norbornene ester)s by using (<Emphasis Type="Italic">η</Emphasis><Superscript>3</Superscript>-substituted allyl) palladium (NHC) complex as catalyst and investigation of their chemical structure - Glass transition temperature - Refractive index relationships

The synthesis of poly(norbornene ester)s by using a (η ³-substituted allyl) palladium (N-heterocyclic carbene (NHC)) complex as catalyst was performed and the relationship between chemical structure and glass transition temperature or refractive index of poly(norbornene ester)s was investigated. Norbornene ester monomers were synthesized via esterification of 5-norbornene-2-methyl alcohol and aromatic carboxylic acids. The polymerization catalyst, (η ³-substituted allyl) palladium (NHC) complex, was synthesized according to a published procedure. ¹H-NMR spectroscopy was performed to determine chemical structure of monomers and polymers. The molecular weight of the polymers was measured via gel permeation chromatography and the thermal properties were analyzed via thermogravimetric analysis and dynamic mechanical analysis. Refractive indices of polymer films were measured using a prism coupler. Polymers with the highest M _n (between 100 kg/mol and 300 kg/mol) were synthesized when the ratio of monomer to catalyst was 2000:1. The glass transition temperature of synthesized polymers was about 100 °C lower than that of conventional norbornene polymers. Among the six polymers of different chemical structures, four polymers exhibited a refractive index of 1.6 or more at a wavelength in the visible light region.     

Thermal degradation behaviors and fire retardant properties of poly(1,3,4-oxadiazole)s (POD) and poly(m-phenylene isophthalamide) (PMIA) fibers

Thermal degradation behaviors and fire retardant properties of poly(1,3,4-oxadiazole)s (POD) and poly(m-phenylene isophthalamide) (PMIA) fibers were investigated. The thermal gravimetric analysis (TGA) demonstrated that POD exhibited higher onset thermal degradation temperature (T_onset) than PMIA, exceeding nearly 80 °C. The thermal degradation kinetics, evaluated by the modified Coats-Redfern method, displayed that the apparent activation energy (E_a) of POD and PMIA fibers was similar when the conversion rate (α) ranges from 0.2 to 0.5, while with the α from 0.6 to 0.8, the E_a of POD was significantly lower than that of PMIA. The fire retardant performance of POD and PMIA fibers were evaluated by cone calorimeter under heat fluxes of 35, 50 and 75 kW/m², during which the temperature of the fibers were monitored by a thermocouple. Surprisingly, POD fibers showed inferior fire retardant performance in comparison with PMIA, with lower time to ignition (TTI) and higher peak heat release rate (PHRR). The origin of the different fire retardant properties of both fibers was revealed by analyzing the residual chars and gaseous products during thermal pyrolysis. The morphology confirmed that stable and compact chars can be formed in PMIA. In addition, the Fourier Transform Infrared Spectroscopy (FTIR) characterization of the residual char revealed that POD can form carbonaceous chars at the heat flux of 50 kW/m², while the heat flux of PMIA was 75 kW/m². The pyrolysis products characterized by pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS) indicated that POD can be pyrolyzed completely at 600 °C, while the temperature of PMIA was 700 °C.     

Mating disruption of the jasmine moth Palpita unionalis (Lepidoptera: Pyralidae) using a two pheromone component blend: A case study over three consecutive olive growing seasons in Egypt

Field studies were carried out from 2002 to 2004 in an olive grove near Cairo, Egypt, to evaluate the efficacy of the mating disruption to control the olive pest Palpita unionalis, during the 1st (May–June) or the 1st and the 2nd (September–November) distinct flight periods. The binary blend of the two pheromone components, E-11-hexadecenyl acetate and E-11-hexadecenal, at the ratio of 70:30 in hexane was dispensed from polyethylene (PE) vials or absorbed into montmorillonite and dispensed from PE bags at a dose of 80 g active ingredients per hectare. Efficacy was measured considering suppression of pheromone trap catches, reduction of the moth population and fruit damage during harvest in the pheromone treated compared to the control (CO) plots. Male captures in treated plots were reduced by 91.3% (2002), 91.8% (2003) and 80.6% (2004) during trapping periods of 8, 21 and 20 weeks, respectively. The number of eggs recorded and fruit damage were lower in the pheromone treated than in CO plot. The fruit infestation accounted to 13.6±2.7% vs. 37.8±3.9% in 2003, a low fruiting year and 9.7±0.75 vs. 34.8±2.8% in 2004, a high fruiting year in treated and CO plots, respectively. Capillary GC analysis indicated that the release rate of E-11-hexadecenyl acetate was effective for the testing period; whereas the release and degradation of E-11-hexadecenyl were high, the inclusion of a photostabilizer into the pheromone-clay complex during 2004 improved substantially the release rate and photooxidation of the aldehyde.     

Robust Water-Repellent Treatment of Cotton Fabrics with Polysiloxane Modified via Thiol-Ene Click Reaction

A facile and inexpensive way to prepare self-crosslinkable poly(dimethylsiloxane) (PDMS) for superhydrophobic treatment of cotton fabrics is reported in the study. Through thiol-ene click reaction between mercaptopropyltrimethoxysilane (MPTMOS) and vinyl-containing poly(dimethylsiloxane) (VPDMS), PDMS-g-TMOS can be simply and quickly synthesized. The trimethoxysilane group of PDMS-g-TMOS can react with hydroxyl group on cotton fabric and other -Si(OCH₃)₃ groups. The synthesized polysiloxane (PDMS-g-TMOS) was identified by FT-IR and ¹H-NMR. The morphology of the treated cotton fabric was observed by SEM and XPS was used to analyze the elemental composition on the surface of cotton fabric. The analysis results indicated that the surface was fully covered with PDMS. Due to the low surface energy of PDMS and the rough surfaces of cotton fabric, the optimized water contact angle (WCA) and sliding angle were respectively 154°±0.4° and 14°±0.5°, indicating superhydrophobicity. Moreover, water spray test (AATCC Test Method 22-2010) was also applied to evaluate the water repellency of treated cotton fabric and a score of 90 was assigned according to AATCC Test Method 22-2010. The durability of treated cotton fabric was tested by 50 laundering cycles. The resultant WCA barely decreased and the score of water spray test dropped from 90 to 80, showing the reasonable wash durability.     

Elasticity, microstructure and thermal stability of foliage and fruit fibres from four tropical crops

A comparative analysis of the elasticity, microstructure and thermal stability of fibres (thickness ranging from 43.4 to 189.4 µm) isolated from pineapple leaves (PALF), coconut coir (COIR), banana leaf-stem (BAN) and oil palm empty fruit bunch (OPEFB) reported in this study. Statistical analysis of the mechanical properties derived from tensile test to rupture reveals significant differences (P<0.05) in the fibre strength (σ), stiffness (E) and extensibility (parameterized by the strain to rupture, ?). It is observed that COIR fibres yield the smallest strength, σ (=99.8±22.5 MPa), and stiffness, E (= 0.5±0.1 GPa), while PALF fibres yield the largest σ (=639.5±301.6 MPa) and E (=7.1±3.1 GPa); PALF fibres exhibit the smallest ? (=0.11±0.03) but OPEFB fibres yield the largest ? (=2.0±1.3). From scanning electron micrographs, it is observed that cellulose fibril rupture predominates in OPEFB, COIR and BAN fibres; a large proportion of the cellulose fibrils fail by pullout in PALF fibres. Thermogravimetric analysis reveals that all fibres are thermally stable up to 250 °C; the fibre residue ranges from 30 to 80 wt% after heating to 500 °C. In particular, BAN experiences the highest weight loss and PALF experiences the lowest weight loss. The findings lend to a simple approach for determining the performance of the composites by assessing the type of natural fibres for reinforcing polymeric matrices.     

Sugars Profiles of Different Chestnut (Castanea sativa Mill.) and Almond (Prunus dulcis) Cultivars by HPLC-RI

Sugar profiles of different almond and chestnut cultivars were obtained by high-performance liquid chromatography (HPLC), by means of a refractive index (RI) detector. A solid-liquid extraction procedure was used in defatted and dried samples. The chromatographic separation was achieved using a Eurospher 100-5 NH₂ column using an isocratic elution with acetonitrile/water (70:30, v/v) at a flow rate of 1.0 ml/min. All the compounds were separated in 16 min. The method was optimized and proved to be reproducible and accurate. Generally, more than 95% of sugars were identified for both matrixes. Sugars profiles were quite homogeneous for almond cultivars; sucrose was the main sugar (11.46 ± 0.14 in Marcona to 22.23 ± 0.59 in Ferragnes g/100 g of dried weight), followed by raffinose (0.71 ± 0.05 in Ferraduel to 2.11 ± 0.29 in Duro Italiano), glucose (0.42 ± 0.12 in Pegarinhos two seeded to 1.47 ± 0.19 in Ferragnes) and fructose (0.11 ± 0.02 in Pegarinhos two seeded to 0.59 ± 0.05 in Gloriette). Commercial cultivars proved to have higher sucrose contents, except in the case of Marcona. Nevertheless, chestnut cultivars revealed a high heterogeneity. Sucrose was the main sugar in Aveleira (22.05 ± 1.48), Judia (23.30 ± 0.83) and Longal (9.56 ± 0.91), while glucose was slightly prevalent in Boa Ventura (6.63 ± 0.49). The observed variance could serve for inter-cultivar discrimination.     

Surface modification of poly(lactic acid) by UV/Ozone irradiation

Hydrophobic poly(lactic acid), PLA, was modified to give hydrophilicity and dyeability to cationic dyes via UV/O₃ irradiation. The UV irradiation treatment caused ester linkage of PLA surface to break down resulting in reduced molecular weight and generation of new photooxidized products as indicated in subtracted ATR spectra and ESCA analysis. It was found that water contact angle decreased from 61 ° to 39 ° and surface energy slightly increased with increasing UV energy, which was attributed to significant contribution of polar component rather than nonpolar component resulting from the surface photooxidation of PLA. Also the surface treatment increased dyeability of PLA to C.I. Basic Blue 41 in terms of both K/S and %E. The increased dyeability may be due to photochemically introduced anionic and dipolar dyeing sites which electrostatically interact with the cationic dye as ascertained by the decreased zeta potential and its pH dependence of the modified PLA.     

Synthesis and electropolymerization of 9-tosyl-9<Emphasis Type="Italic">H</Emphasis>-carbazole,electrochemical impedance spectroscopic study and circuit modelling

This work reports on the newly synthesized 9-tosyl-9H-carbazole (TsCz) monomer. Capacitive properties of the electrochemically grown homopolymer, poly(TsCz) film on carbon fibre microelectrode (CFME), are characterised by cyclic voltammetry (CV), Fourier transform infrared reflectance-attenuated total reflection spectroscopy (FTIR-ATR), scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). Different monomer concentrations (1, 3 and 10 mM) were used for electrodeposition in 0.1 M sodium perchlorate (NaClO₄)/acetonitrile (ACN) solution. The capacitive behaviour of modified CFMEs was defined via Nyquist, Bode-magnitude and Bode-phase plots. An equivalent electrical circuit R(CR)(QR)(CR) for different concentrations of poly(TsCz)/CFME was proposed and experimental data were simulated to obtain the numerical values of the circuit components. The Nyquist plot for poly(TsCz) shows the highest specific capacitance (50.0 mF cm⁻²) at frequency of 0.01 Hz in the initial monomer concentration of 10 mM.     

Radiation utilization efficiency,latent heat flux,and crop growth simulation in irrigated rice during post-flood period in east coast of India

To study the radiation utilization efficiency, latent heat flux, and simulate growth of rice during post-flood period in eastern coast of India, on-farm trial was conducted with three water regimes in main plots (W ₁ = continuous flooding of 5 cm, W ₂ = irrigation after 2 days of water disappearance, and W ₃ = irrigation after 5 days of water disappearance) and five nitrogen levels in subplots (N ₁ = 0 kg N ha^?1, N ₂ = 60 kg N ha^?1, N ₃ = 90 kg N ha^?1, N ₄ = 120 kg N ha^?1, and N ₅ = 150 kg N ha^?1) on a rice cultivar, ‘Lalat’. Average maximum radiation utilization efficiency (RUE) in terms of above ground dry biomass of 2.09 (±0.05), 2.10 (±0.02), and 1.9 (±0.08) g MJ^?1 were computed under W ₁, W ₂, and W ₃, respectively. Nitrogen increased the RUE significantly, mean RUE values were computed as 1.60 (±0.07), 1.78 (±0.02), 2.060 (±0.08), 2.30 (±0.07), and 2.34 (±0.08) g MJ^?1 when the crop was grown with 0, 60, 90, 120, and 150 kg ha^?1 nitrogen, respectively. Midday average latent heat flux (on clear days) varied from 7.4 to 14.9 and 8 to 13.6 MJ m^?2 day^?1 under W ₂ and W ₃ treatments, respectively, at different growth stages of the crop in different seasons. The DSSAT 4.5 model was used to simulate phenology, growth, and yield which predicted fairly well under higher dose of nitrogen (90 kg and above), but the model performance was found to be poor under low-nitrogen dose.     

Thermo-Mechanical Characterization of a Thermoplastic Copolyetherester (TPC): Experimental Investigation

In this article, the thermo-mechanical characterization of poly(butylene terephthalate)/poly(tetramethylene oxide) (PBT/PTMO) is studied by thermal analysis, dynamic mechanical analysis, and uniaxial tensile tests. The results of poly(ether esters) show that the melting temperature is equal to T _m =193 °C, which is 31 °C, lower than that of the melting temperature of poly(butylene terephthalate) (PBT). Its glass transition temperature, T _g is equal to -61 °C, determined by DMA. The melting and cooling temperatures (T _m , T _c ) after aging at T₀+48 h and T₀+week are virtually unchanged. Moreover, the results of the tensile tests show that the effect of the low deformation rate reduces the friction resulting from the sliding mechanisms between the amorphous and crystalline parts.     

Synthesis, characterization, and protonation of poly(2-N,N-dimethylamino-4,6-bis(2-furan)-pyrimidine)

A new monomer (2-N,N-dimethylamino-4,6-bis(2-furan)-pyrimidine) was synthesized and its homopolymer was successfully prepared by using ferric trichloride as an oxidant. The structure of monomer and polymer were fully characterized by ¹H-NMR, FT-IR, UV, fluorescent spectroscopy, and X-ray diffraction. The N,N-dimethylformamide solution of the polymer showed a UV-Vis peak at 387 nm and the PL spectrum gave a peak at 517 nm. We have observed that the polymer was sensitive to inorganic acids and the protonation behavior was investigated applying inorganic acids such as HCI and H₂SO₄. The corresponding UV-Vis peaks were observed at 464 and 357 nm, respectively. X-ray diffraction data shows that polymer had a certain crystalline region. The polymer exhibited an [η] value of 0.21 dl/g at 25 °C in H₂SO₄ (w=98 %).     

Radical Polymerization and Kinetics of N,N-diallyl-N,N-dimethylammonium Chloride and Vinyl Ether of Monoethanolamine

N,N-diallyl-N,N-dimethylammonium chloride (DADMAC) and vinyl ether of monoethanolamine copolymer (VEMEA) was synthesized by radical polymerization in aqueous media using ammonium persulfate as initiator. Copolymers synthesis was carried out by varying monomer composition at low conversion level. The viscosity of high molecular weight products was measured in aqueous 1 M NaCl solution and it was increased with increasing DADMAC amounts in the copolymer due to increasing positive charge. The structure of the product was identified by FTIR, ¹H, ¹³C-NMR spectroscopies and conductometric titration methods. We calculated monomer reactivity ratios with help of Finemann-Ross, Kelen-Tudos, and inverted Finemann-Ross methods. It was found that DADMAC is more reactive than VEMEA, therefore the amount of DADMAC in the copolymers always dominated regardless of the initial monomer ratio in solution and it was shown that the monomers are connected randomly in the polymer chain. The effect of various parameters such as monomer [M], initiator [I] concentrations, ratio of comonomers, etc. on polymerization was investigated systematically. So, the polymerization rate (R_p) equation was found to be R_p=k[M]^2.6[I]^0.6 where molar fractions of DADMAC and VEMEA was 90:10 and the temperature was 65 °C. Degree of polymerization was examined by using various monomers and initiator concentrations via the dilatometeric method. It was found that the polymerization rate increased directly with total monomer concentration and initiator content.     

Formaldehyde free cross-linking agents based on maleic anhydride copolymers

Low molecular weight copolymers of maleic anhydride and vinyl acetate were prepared to develop formaldehyde free cross-linking agents. Since lower molecular weight is favorable for efficient penetration of the finishing agent into the cotton fibers in the padding process, the concentration of the initiator, chain transfer agent and the monomer ratios were varied to obtain copolymers of low molecular weights. The prepared polymers were characterized by GPC,¹H-NMR, FTIR, DSC and TGA. Copolymers of molecular weights of 2 000 to 10 000 were obtained and it was found that the most efficient method of controlling the molecular weight was by varying the monomer ratios. Poly(maleic anhydride-co-vinyl acetate) did not dissolve in water, but the maleic anhydride residue hydrolyzed within a few minutes to form poly(maleic acid-co-vinyl acetate) and dissolved in water. However, the maleic acid units undergo dehydration to form anhydride groups on heating above 160 °C to some extent even in the absence of catalysts. The possibility of using the copolymers as durable press finishing agent for cotton fabric was investigated. Lower molecular weight poly(maleic anhydride-co-vinyl acetate) copolymers were more efficient in introducing crease resistance, which appears to be due to the more efficient penetration of the crosslinking agent into cotton fabrics. The wrinkle recovery angles of cotton fabrics treated with poly(maleic anhydride-co-vinyl acetate) copolymers were slightly lower than those treated with DMDHEU and were higher when higher curing temperatures or higher concentrations of copolymer were used, and when catalyst, NaH₂PO₂, was added. The strength retention of the poly(maleic anhydride-co-vinyl acetate) treated cotton fabrics was excellent.     

Alkylresorcinol composition allows the differentiation of Triticum spp. having different degrees of ploidy

Total alkylresorcinol (AR) content and homologue composition were assessed in whole grain flours of 15 varieties each of bread wheat, durum, spelt, emmer, and einkorn grown in four different environments. Bread wheat (761 ± 92 μg/g DM) and spelt (743 ± 57 μg/g) belonging to the hexaploid species showed higher AR concentrations than the tetraploid durum (654 ± 48 μg/g, p < 0.05), while the concentrations found in the diploid einkorn (737 ± 91 μg/g) and the tetraploid emmer (697 ± 94 μg/g) did not significantly differ from the other species. The AR content showed a remarkable heritability and, thus, seemed to be mainly determined by genetic factors. If ARs were assumed to be deposited within a specific AR-rich layer of the kernel, AR levels of all varieties would easily surpass their minimal inhibitory concentrations against fungal pathogens within this barrier layer. Although the AR carrying a C21:0 side chain was the main homologue in all species, the levels of all AR homologues and their relative composition significantly differed between hexaploid (bread wheat and spelt), tetraploid (durum and emmer) and diploid (einkorn) species. Consequently, a clear-cut differentiation of Triticum species and derived whole grain flours according to their degrees of ploidy was established based on concentrations of saturated C₁₇-, C₁₉-, C₂₁-, C₂₃-, and C₂₅-substituted ARs.