自控温加热带的研制

研究了炭黑含量、辐照剂量以及体系共结晶性对以高密度聚乙烯/乙烯 丙烯酸乙烯酯共聚物为基材的自控温加热带电阻率及电热稳定性能的影响,以及加工条件和后处理工艺对材料电性能的影响。结果表明,50～80kGy的辐照剂量为本体系提供优异的电热稳定性,适当的加工及后处理工艺能大大改善该体系的导电性。     

Eco‐friendly durable press finishing of cellulose‐containing fabrics

To impart easy‐care properties to cellulose‐containing fabrics along with avoiding any harmful effects of formaldehyde on both the health and the environment, attempts have been made to use citric acid (CA) as an ester crosslinking agent along with different catalytic systems in the absence and presence of certain additives. Further, fixation conditions, type of crosslinking agent, as well as type of substrate have been studied. Results revealed that the enhancement in carboxyl content, performance properties, and the decrease in tear strength (TS) as well as in whiteness indices (WI) of the finished fabric samples were increased by increasing CA concentration up to 80 g/L and by raising thermofixation temperature from 140 up to 180°C for 90 s. Inclusion of triethanolamine hydrochloride (TEA. HCl), decreased the carboxyl content, TS, color strength K/S, as well as oily stain release rating (SRR) of the finished fabric samples along with an increase in bound nitrogen (%N), wrinkle recovery angle WRA, and an improvement in WI without affecting the durable press rating (DP). Within the range examined (0–30 g/L), increasing PEG‐600 concentration improved the wet resiliency, TS, as well as WI properties of the finished samples. Increasing DMDHEU ratio in the CA/DMDHEU crosslinking system gave rise to an increase in %N, WRA (dry and wet), DP, as well as in free CH₂O of finished fabrics, along with a slight improvement in WI values. On the other hand, the TS, carboxyl content, K/S, SRR values of the finished fabric samples were lower at a higher DMDHEU ratio. Increase in carboxyl content, %N, WRA (dry and wet), DP and SRR, as well as extent of post dyeing (K/S) of the treated fabric samples upon using different ester crosslinking agents followed the descending order: citric acid > pyromellitic dianhydride. The opposite holds true for the TS, and WI values. Among the esterifying catalysts used, and for a given set of finishing conditions, NaH₂PO₂ · H₂O proved to be the most effective one, and the following order of effectiveness may be drawn: NaH₂PO₂ · H₂O > K₂HPO₄ > Na₃–citrate > Na₂–tartrate. Inclusion of silicone softener in the finishing formulation brought about an improvement in softeness degree, WRA, %N, DP, TS as well as K/S values along with a decrease in carboxyl content, SRR, and WI values of the treated fabric samples, regardless of the used silicone softener.The performance properties of the finished fabric samples were determined by the type and nature of the substrate. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2243–2253, 2002     

Curing of mixtures of epoxy resins and 4‐methyl‐1,3‐dioxolan‐2‐one with several initiators

Diglycidyl ether of bisphenol A or 3,4‐epoxycyclohexylmethyl 3,4‐epoxycyclohexane carboxylate were mixed with different proportions of 4‐methyl‐1,3‐dioxolan‐2‐one and cured using lanthanide triflates as initiators. In order to compare the materials obtained, conventional initiators such as boron trifluoride complexes and N,N‐dimethylaminopyridine were also tested. The curing process was followed by differential scanning calorimetry (DSC) and Fourier transform IR in attenuated total reflectance mode. This technique proved that the carbonate accelerates the curing process because it helps to form the active initiating species, although it was not chemically incorporated into the network and remained entrapped in the material. The DSC kinetic study was also reported. © 2006 Wiley Periodicals Inc. J Appl Polym Sci 102: 2086–2093, 2006     

Crosslinking of corn starch with sodium trimetaphosphate in solid state by microwave irradiation

Corn starch was crosslinked with sodium trimetaphosphate (STMP) in solid state under microwave irradiation to improve the degree of substitution (DS) and decrease the reaction time. The effects of modification factors on the crosslinking of starch were systematically studied. It was found that the microwave irradiation provided a convenient and efficient method to prepare crosslinked starch with sufficient DS. The DS value of crosslinked starches obtained by microwave irradiation was significantly improved and the reaction time was also dramatically decreased to achieve an appropriate DS value by microwave irradiation, when compared with using traditional method. The high microwave power provided faster reaction kinetics to obtain the desired DS value at an identical reaction condition. If the reaction temperature is lower than the decomposition temperature of crosslinked starch, the higher DS value can be achieved at the higher microwave power. It was detected that the DS data obtained by reacting intermittently was higher than those by reacting continuously. It was also noticed that DS data varied drastically with the increasing of the amount of STMP and sodium carbonate. The swelling ratio of crosslinked starch in water was lower than that of native starch because of the nongelatinization of highly crosslinked starch. SEM analysis indicated that the crosslinking of corn starch by microwave irradiation caused no significant changes in the microstructure of starch granules. Light microscope analysis also showed the uniformity of so‐prepared crosslinked corn starch applying microwave irradiation. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5854–5860, 2006     

Controlled release of insecticide carbaryl from sodium alginate,sodium alginate/gelatin,and sodium alginate/sodium carboxymethyl cellulose blend beads crosslinked with glutaraldehyde

Interpenetrating network polymeric beads of sodium alginate (NaAlg) and its blend with gelatin (gels) or sodium carboxymethyl cellulose (NaCMC) have been prepared by crosslinking with a common crosslinking agent, glutaraldehyde (GA), for the release of insecticide carbaryl (Carb). The prepared beads were characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. Scanning electron microscopy confirmed the spherical nature and surface morphology of the particles. Bead characteristics, such as carbaryl entrapment efficiency, particle size, equilibrium swelling degree, and carbaryl release kinetics, were determined. The effects of the preparation conditions, such as Carb/NaAlg ratio, time of exposure to GA, blend ratio, and temperature of release medium on the carbaryl release, were investigated for 25 days at 25°C. It was observed that the carbaryl release decreased with increase in crosslinking of network, while it increased with increase in Carb/NaAlg ratio and temperature. The release of carbaryl also increased with increase in Gel or NaCMC content in the blend beads. The highest carbaryl release was found to be 100%, for the beads that were prepared with 1 : 1 NaAlg/Gel at 16 days. The diffusion coefficients have been calculated for the transport of insecticide through the polymeric beads, using initial time approximation method. These values were also consistent with the carbaryl release data. The carbaryl release from most of the bead formulations followed the Fickian trend. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1310–1319, 2006     

Antimicrobial protection of cotton and cotton/polyester fabrics by radiation and thermal treatments. I. Effect of ZnO formulation on the mechanical and dyeing properties

Cotton and cotton/polyester fabrics were treated against microbial attack by applying a formulation based essentially on ZnO under high‐energy radiation and thermal curing. To achieve the homogeneity and the reactivity of the treating formulation, a binder (Impron MTP) and a dispersing agent (Setamol WS) were used with ZnO. The antimicrobial property of the fabrics was evaluated, in terms of mechanical properties, by a soil burial test. Moreover, the effect of antimicrobial finishing on the dyeing properties in terms of color strength was investigated. It was found that the best composition that affords the best antimicrobial protection to cotton fabrics contains 2% ZnO, 2% binder, and 1% dispersing agents. For the cotton/polyester blend, the best results were achieved at the same conditions except the ZnO was 1%. It was found that the treatment under the effect of electron‐beam irradiation is better than that of gamma irradiation and thermal curing. The results showed that when the finishing process was carried out before dyeing with a reactive dye, it affects the color strength rather than performing the finishing after the dyeing process. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1129–1137, 2003     

Novel pyridinium photoinitiators and their applications for the ultraviolet crosslinking of acrylic pressure‐sensitive adhesives

The demand for ultraviolet (UV)‐crosslinkable pressure‐sensitive adhesives (PSAs) has rapidly been increasing. A variety of different PSAs containing new photoreactive pyridinium derivatives have been evaluated for their effectiveness in improving adhesion and cohesion in UV‐crosslinkable PSAs. PSAs have been evaluated with respect to the tack, peel adhesion, and shear strength. This article summarizes the breakthrough technology used to achieve better performances in UV‐crosslinkable acrylic PSAs. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Effect of the nature and degree of crosslinking on the Rose Bengal uptake by DVB‐, NNMBA‐, HDODA‐, and TTEGDA‐crosslinked aminopolyacrylamides

Polyacrylamides with 2–20 mol % divinyl benzene (DVB), N,N′‐methylene‐bisacrylamide (NNMBA), 1,6‐hexanediol diacrylate (HDODA), and tetraethyleneglycol diacrylate (TTEGDA) crosslinking and without crosslinking were prepared by free radical solution polymerization. Amino functions were incorporated into these polymers by transamidation with excess ethylenediamine. The dye uptake of nonprotonated and protonated aminopolyacrylamides was followed by batch equilibration method towards Rose Bengal (RB), Methyl Orange (MO), Methyl Red (MR), and Methylene Blue (MB). RB uptake by the polyacrylamide‐supported systems is higher than other dyes. Generally the dye uptake by the protonated systems is higher than the nonprotonated systems. To optimize the conditions of dye uptake, the effect of the concentration of RB solutions, temperature, and pH were followed. Kinetic studies showed that the uptake of RB by both nonprotonated and protonated crosslinked aminopolyacrylamides is a phase boundary process followed by three‐dimensional diffusion. The extent of RB uptake by the various systems depends on the nature and degree of crosslinking, and the relative rigidity/flexibility ofthe polyacrylamide support. Thus, the dye uptake followed the order: linear > NNMBA‐ > DVB‐ > TTEGDA‐ > HDODA‐crosslinked system. The dye uptake followed the same trend as the variation of amino capacity with degree of crosslinking in the respective crosslinked system. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Ion‐exchange resins. II. Acrylamide crosslinked copolymers as precursors for some ion exchangers

Crosslinked copolymers of acrylamide (AA) and ethylacrylate and some ion exchangers derived from them containing either primary amine groups, obtained by the Hofmann degradation of the amide groups, or carboxylic groups, obtained by the alkaline hydrolysis of the ester groups, were studied. Divinylbenzene and N,N′‐methylenebisacrylamide were used as crosslinkers. The starting copolymers and the corresponding ion exchangers were characterized by IR spectroscopy, swelling behavior, and thermogravimetric analysis. The ion‐exchanger properties were correlated with the crosslinker nature and the chemical reactions performed on the AA copolymers. The average molecular weight between two crosslinks, determined from the swelling data in water, was compared with that calculated on the basis of the copolymerization stoichiometry only for the carboxylic cation exchangers. In this way, the preservation of the crosslink density after the hydrolysis was revealed. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2701–2707, 2003     

聚碳硅烷/聚硅氮烷先驱体体系的交联

考察了Si-C-N陶瓷的先驱体聚碳硅烷（PCS）/聚氮硅烷（PSZ）体系的交联条件。包括交联时间，温度，引发剂和催化剂的种类和用量对交联产物及陶瓷产率的影响。并采用热重分析（TG）法研究了PCS/PSZ体系的交联和裂解过程。结果表明，mpcs:mPSZ:mxylene:mDCP等于2：2：1：0.05，交联条件为温度120℃，压力2MPa。时间6h时，得到的交联产物外观较好。陶瓷产率较高。达到77.8%。