Chemiluminescence in evaluating thermal oxidative stability of acrylonitrile-butadiene-styrene (ABS) copolymers. IV. Comparative study of various stabilizers in mass polymerization and emulsion resins

The thermal oxidative stability of ionic and emulsion ABS with various antioxidants and UV stabilizers was studied. It was found that Santonox R provides better protection than Irganox 1076 to both resins. It is also the case in formulations with Tinuvin 770 and Tinuvin 328.     

Chemiluminescence in evaluating the thermal oxidative stability of acrylonitrile-butadiene-styrene (ABS) copolymers. II. ABS/polycarbonate (PC) blends

The thermal oxidative stability of various ABS/PC compounds was studied by means of the chemiluminescence technique. Similarly to pure ABS, Irganox 1076 and Irganox MD 1024 perform as moderate antioxidants in ABS/PC and (ABS/PC + lubricant) blends. Neither Tinuvin 144, Irgaphos 168, nor their mixture affects the durability of the ABS/PC blend. At the same time, (Irgaphos 168 + Tinuvin 144) in combination with Irganoxes was found to provide a noticeable enhancement in durability to the (ABS/PC + lubricant) system. Titanium dioxide pigments by themselves have only a slight influence on the oxidative stability of the ABS/PC blend. Durability of the (ABS/PC + pigment) and (ABS/PC + lubricant) systems was found to be the same and the overall protective effect of Irganox 1076 was similar in both the (ABS/PC + lubricant) and the (ABS/PC + lubricant + pigment) systems. Certain modifiers significantly improve the durability of the ABS/PC compounds, although their function may differ in the systems with and without pigments.Guest Editor: Dr. Graham Swift, Rohm & Haas.     

Chemiluminescence in evaluating the thermal oxidative stability of acrylonitrile-butadiene-styrene (ABS) copolymers. 1. Influence of stabilizers and lubricants

The influence of lubricants, UV stabilizers, antioxidants, and metal deactivators on the resistance of ABS to thermal oxidation was studied by means of the chemiluminescence technique. Neither of the additives seems to affect significantly the induction period of oxidation. At the same time, the influence of various additives on the oxidation rate constant is remarkably different: the introduction of lubricants and UV stabilizers increases its value, while antioxidants and metal deactivators have the opposite effect. For the particular systems studied durability is decreased in samples containing the lubricant and UV stabilizers and increased in samples stabilized with the antioxidant and metal deactivator.     

Synergistic Effect of TNPP and Carbon Black in Weathered XLPE Materials

Carbon black is one of the most widely used and most effective ultraviolet (UV) light stabilizers for plastics applications. Several important segments of the plastics industry rely on carbon black for UV stabilization of weather-resistant products, including telecommunications, power cable jacketing, and plastic pipes. In this research work a combination of Trisnonylphospate (TNPP) antioxidant and different size carbon black were applied in crosslinked polyethylene (XLPE) to improve its wetherability. The primary reason for cross-linking polyethylene (PE) is to raise the thermal stability of the material under load. This substantially improves environmental stress crack resistance and resistance to slow crack growth. The results achieved of this additive package combination show a synergism effect and improved weatherability of electrical cable. Increased weathering lifetime was also achieved. Further, we were able to confirm in this work, that the size and quality of the carbon black dispersion in a XLPE samples is an important component of both the UV-resistance and mechanical properties of the finished plastic article. Incremental improvements of carbon black dispersion can positively influence the expected life of plastic articles. Mechanical testing and FTIR were used to detect degradation of the accelerated weathered XLPE samples. The morphological considerations of UV energy absorption and presents laboratory data demonstrating the link between dispersion and weatherability as well as between morphology and weatherability     

Effects of Saturated Acids on Physical Properties of UPE Resins Prepared from Recycled PET Products

In this study, effects of saturated acids on physical properties, including hardness, impact strength, flexural properties and thermal properties, of unsaturated polyester or UPE resins prepared from recycled PET bottles and fabrics were investigated. PET was depolymerized by glycolysis reaction with the excess propylene glycol in the presence of zinc acetate as a catalyst. UPE resins were then synthesized by polyesterification of these glycolyzed products with maleic anhydride as an unsaturated diacid as well as succinic acid and adipic acid as a saturated diacid. With the addition of styrene monomer, UPEs were subsequently casted into specimens by crosslinking reaction using methyl ethyl ketone peroxide and cobalt octoate as an initiator and a catalyst, respectively. Physical properties of the cured specimens were then studied. The results showed that, when a saturated acid was incorporated, the hardness of the cured UPE resins decreased due to the decreasing amount of crosslinks. The extended distance between crosslinking sites on molecular chains facilitated load distribution, resulting in the significant improvement of impact strength. The flexural strength was also improved when the small amount of saturated acid was used. The onset thermal degradation temperatures and the glass transition temperatures of the prepared UPE resins were almost unchanged.     

Alkyd-amino resins based on waste PET for coating applications

Waste polyethylene terephthalate (PET) flakes were depolymerized by using propylene glycol (PG) in the presence of zinc acetate as catalyst. Glycolysis reaction products of waste PET obtained by using PET/glycol molar ratio 1/2. Two short oil alkyd resins of high acid values (30-40mgKOH/g) were prepared from phthalic anhydride (PA), glycerin (G), coconut oil fatty acids (COFA) and glycolyzed products of waste PET (PET-based alkyd resins) or glycols (PG) (reference alkyd resins). These alkyd resins were blended with 30%, 40%, and 50% of a commercial urea-formaldehyde, melamine-formaldehyde and urea-formaldehyde/melamine-formaldehyde mixture (1/1 weight ratio) and heated at 140 degrees C. The physical and chemical properties such as drying time, hardness, abrasion resistance, adhesion strength, water resistance, alkaline resistance, acid resistance, gelation time, and thermal oxidative degradation resistance (with thermogravimetric analysis, TGA) of these alkyd-amino resins were investigated. The properties of the waste PET-based resins were found to be compatible with the properties of the reference resins.     

稳定化技术在铅砷复合污染土壤修复中的应用

以铅砷复合污染土壤为研究对象,采用硫酸亚铁和氧化钙作为稳定剂,通过正交实验得出各因素对土壤中铅的稳定率影响程度的大小顺序为:氧化钙添加量>硫酸亚铁添加量=养护周期>两种稳定剂的交互作用.最佳实验条件为硫酸亚铁添加量2 g/kg,氧化钙添加量10 g/kg,养护时间2 d.添加硫酸亚铁后,土壤pH对砷的稳定化效果影响不大...     

Infrared spectroscopy studies of the photooxidation of a polyethylene nonwoven fabric

The photooxidation of a nonwoven polyethylene fabric was investigated using Fourier transform infrared photoacoustic spectroscopy. The infrared spectroscopic data indicated that hydroperoxide, alcohol, aldehyde, ketone, carboxylic acid, and anhydride groups were formed as the products of the photooxidation of the polyethylene fabric and that the relative amount of carboxyl among all carbonyls increased as the photooxidation progressed. The distribution of the photooxidation products was inhomogeneous between the two surfaces of the fabric. The highest degree of photooxidation occurred on the surface of the fabric facing the UV radiation source, whereas the lowest degree of photooxidation was on the back surface of the fabric. We also found that the polyethylene nonwoven fabric showed a slower photooxidation rate than the polypropylene nonwoven fabric. The UV radiation at 254 nm caused photooxidation of polyethylene. No photooxidation was observed in the fabric exposed to the UV radiation at 350 nm under the same conditions.     

WEEE recycling: Pyrolysis of fire retardant model polymers

Pyrolysis treatments of model polymers were made with the aim of studying the recycling of wastes from electronic, electric equipment containing brominated flame retardants. Pyrolysis of flame retarded high impact polystyrene and epoxy resins were made both in flow and closed systems. Products of pyrolysis were analysed with FT-IR spectroscopy and GC-MS and the evolution of bromine was followed with a bromine ion specific electrode. The effect of alkali on pyrolysis was also studied demonstrating, as far epoxy resin is concerned, to be effective on decreasing bromine content in oil and volatile products leading to the recovery of bromine from the residue by washing. The alkali treatment was shown to be less effective in styrenic polymers containing brominated flame retardants.     

Biodegradability of Urea-Aldehyde Condensation Products

Condensation products of urea and different aldehydes (formaldehyde, isobutyraldehyde, crotonaldehyde) are used in large amounts (more than 300,000 tons per year) as resins, binders, and insulating materials for industrial applications, as well as in controlled-release nitrogen fertilizer for greens, lawns, or bioremediation processes. The biodegradability of these condensates and the enzymic mechanism of their degradation was studied in mircoorganisms isolated from soil, which were able to use these compounds as the sole source of nitrogen for growth. Different pure cultures of both gram-positive and gram-negative bacteria completely degraded methylenediurea, dimethylenetriurea, isobutylidenediurea, and crotonylidenediurea to urea, ammonia, and the corresponding aldehydes and carbon dioxide. Enzymes initiating this degradation were purified and characterized and turned out to be different with regard to their regulation of expression, their physicobiochemical properties, and their reaction mechanism.     

动态臭氧/紫外线法处理磺基水杨酸废水

研究了在有或无紫外线 (UV)照射的条件下臭氧 (O3 )对磺基水杨酸废水的处理效果。用O3 与UV协同处理磺基水杨酸废水比仅用O3 和仅用UV的处理效果好得多 ,其COD去除率大于后二者的COD去除率之和。试验选用的动态O3 /UV法处理磺基水杨酸废水的工艺条件为 :O3 发生器放电功率 90 %× 180W ,UV功率 14W ,废水循环流速 10 0mL/min ,处理时间 90min。在此条件下 ,废水COD去除率可达 80 %左右。在上述的O3 发生器放电功率、UV功率、废水循环流速条件下 ,处理 1min时废水变澄清     

Mechanism of Microbial Degradation of Slow-Release Fertilizers

Methyleneureas are condensation products of urea and formaldehyde of different molecular mass and solubility; they are used in large amounts both as resins, binders, and insulating materials for industrial applications, as well as a slow-release nitrogen fertilizer for greens, lawns, or in bioremediation processes. In the present study, the microbial breakdown of these products was investigated. The nitrogen was released as ammonia and urea, and the formaldehyde released immediately oxidized via formiate to carbon dioxide. The enzymatic mechanism of metabolization of methyleneureas was studied in microorganisms isolated from soil, which were able to use these compounds as the sole source of nitrogen for growth. A strain of the Gram-negative bacterium Ralstonia paucula (formerly Alcaligenes sp. CDC group IVc-2) completely degraded methylenediurea and dimethylenetriurea to urea, ammonia, formaldehyde, and carbon dioxide. The enzyme initiating this degradation (methylenediurease) was purified and turned out to be different from the previously described enzyme from Ochrobactrum anthropi with regard to its regulation of expression and physicobiochemical properties. Fungal degradation of methyleneureas may occur via the formation of organic acids, thus leading to a nonenzymatic degradation of methyleneureas, which are unstable under acidic conditions.     

Applying the Protective Role of Condensed Tannins to Acrylic-based Surface Coatings Exposed to Accelerated Weathering

Condensed tannins, extractable from tree bark have been assessed as functional additives to provide a protective role to acrylic-based coating resins. In addition to retaining high antioxidant capacity, the UV absorption properties of native and chemically modified tannins were found to be variously impacted by pH and degree of esterification or etherification. When added to acrylic-based coatings, these tannins were found to contribute colour to a white-base, but only small perceptive differences were found for clear coated wood using typical additive loadings of 0.1–0.4%. Integration of tannins in native or modified form to do not inhibit the cure of acrylic coatings or found to leach from cured coating films. Accelerated weathering was used to evaluate the photo-stability of tannin-modified acrylic and styrene-acrylic coatings. Native and modified tannins with maleate or methylcarboxylate groups retaining high antioxidant activity were associated with significantly greater coating longevity and performance than use of a synthetic photostabiliser. Moreover, esterified condensed tannins with a high degree of substitution also outperformed synthetic additives indicating the inherent UV absorption potential of these materials also contributed this efficacy within the acrylic and styrene-acrylic coating systems.     

A user evaluation of biodegradable cutlery

This paper summarizes a study evaluating the acceptance and perceived performance of disposable cutlery made from starch-based biodegradable resins relative to nondegradable polystyrene cutlery. Two hundred forty-three sailors onboard three U.S. Navy vessels ate their lunch using either biodegradable cutlery made with resins manufactured by one of two commercial companies or polystyrene cutlery. The cutlery was rated on several sensory and performance dimensions as well as for overall acceptability. Results indicated that sailors rated both the biodegradable and the polystyrene utensils as easy to hold. There were also no differences in the perceived ease of using each of the spoons. However, compared to the polystyrene utensils, both types of biodegradable utensils were viewed as less sturdy, as having a less attractive color, and as being less acceptable overall. The biodegradable forks and knives were also rated as more difficult to use for piercing and cutting food than the polystyrene ones. In addition, several significant differences emerged between the two types of biodegradable cutlery. The results are discussed in terms of the need for continued consumer testing of products developed from biodegradable polymeric materials.     

From Natural Oils to Epoxy Resins: A New Paradigm in Renewable Performance Materials

The direct conversion of natural products to useful engineering materials is desirable from both economic and environmental considerations. We describe the synthesis and properties of 100?% oil-based epoxy resins generated from three epoxidized oils. The catalyst, tris(pentafluorophenyl)borane (B(C₆F₅)₃) in toluene, allowed for controlled cationic polymerization at a very low concentration. Epoxidized oils (derived from triolein, soybean, and linseed oil) had varying epoxy content, rendering resins of different cross-link density. The polymerization was carried out at room temperature followed by post-curing at elevated temperature to speed up conversion. Epoxy resins were amorphous transparent glasses below glass transitions and hard rubbers above. Despite their high cross-link density, these materials show relatively low T_g’s reflecting the aliphatic nature of fatty acids and the presence of plasticizing “dangling” chains. The structure of the triglyceride starting oils influenced the properties of the resulting materials: the more regular structure of triolein compared to the very heterogeneous structures of soybean and linseed oils seemed to have enhanced some properties of the polymer networks. These epoxy polymers are potentially useful as encapsulating and potting compounds for electronic applications.

     

Synthesis of unsaturated polyester resin from glycolysed postconsumer PET wastes

The purpose of this study was to explore ways to extend the chemical recycling of poly(ethylene terephthalate) (PET) as a valuable feedstock for chemical processes. First, PET wastes were depolymerised using a glycolysis method in the presence of sodium carbonate, which is considered to be a less environmentally damaging option for a catalyst. Good yields of the monomer bis(2-hydroxyethyl) terephthalate (BHET) were obtained (80 %). Second, to develop an economically viable recycling programme for the reclaimed BHET, the conversion of purified BHET into unsaturated polyester resins (UPR) was studied. The recovered monomer was thus polyesterified with maleic anhydride and subsequently mixed with styrene monomer to prepare UPRs. The resins were casted by a crosslinking reaction using methyl ethyl ketone peroxide and cobalt 2-ethylhexanoate as the initiator and catalyst, respectively. The polyesterification reaction was followed by gel permeation chromatography. The curing process was studied by differential scanning calorimetry and infrared spectroscopy. The cured resin was subjected to various characterisation methods in order to determine its chemical, physical and mechanical properties. Resins with suitable properties for commercial application were obtained.     

Treatment of chromium plating process effluents with ion exchange resins.

The surface treatment industry deals with various heavy metals, including the elements Cr, Zn, Ni, Cd, and Cu. Conventional treatments of effluents generate class I solid residue. The aim of this investigation was to study the viability of ion exchange as an alternative process for treatment of rinse water and to determine the efficacy of two ion exchange systems, System 1: "strong" cationic resin-"strong" anionic resin and System 2: "strong" cationic resin-"weak" anionic resin. Commercial resins and solutions taken from rinse tanks of chromium plating companies were used in this investigation. A two-column system, one for the cationic resin and another for the anionic resin, both with 150 ml capacity was mounted. The solution was percolated at a rate of 10 ml/min. The following solutions were used for regeneration of the resins: 2% H2SO4 for the cationic and 4% NaOH for the anionic. The percolated solutions revealed chromium contents of less than 0.25 mg/l, independent of the system used. The "strong" cationic resin-"weak" anionic resin gave excellent regeneration results. The "strong" cationic-"strong" anionic resin presented problems during regeneration, and did not release the retained ions after percolation of 2000 ml of 4% NaOH solution. It is concluded that for this type of treatment, the system composed of "strong" cationic resin and "weak" anionic resin is more appropriate.     

再生聚丙烯的洁净化和高质化应用

聚丙烯以其优异的机械性能、高的性价比和多重改性方式成为重要的通用树脂之一,这些产品废弃后产生了种类繁多和数量巨大的再生聚丙烯.通过将再生聚丙烯根据性能和来源进行分类,然后分类阐述各再生聚丙烯物料特点,结合再生聚丙烯改性方式,为高质化应用提出方向.     

Using ultraviolet light to investigate petroleum-contaminated soil

Ultraviolet (UV) light can aid in the investigation of petroleum-contaminated soil and sediment. The visible fluorescence of many petroleum products under UV illumination often results in a striking contrast when compared with surrounding, uncontaminated media. This contrast can be used in a variety of applications, including delineating the extent of petroleum in excavations, locating seeps along shorelines, and selecting sample intervals in sediment cores. In another application, a field screening test using UV light combined with solvent extraction was developed to detect low levels of petroleum in soil. The test rapidly screens soil samples for the presence and relative concentration of petroleum hydrocarbons. The test was used to screen samples for laboratory analysis and identify residual petroleum product in boring samples.     

Reutilization of thermostable polyester wastes by means of agglomeration with phenolic resins

We report on the possibility of obtaining organic polymeric matrixes allowing the development of new high performance fire-resistant products by recycling downsized thermostable waste materials. Phenolic resins have been used as binders for recycled waste. Furthermore, considering that reinforced plastic triturations have superior properties (chemical, mechanical, water resistance, etc.) to wood agglomerates, significant advantages over conventional materials are anticipated. In summary, we propose a viable solution to some of the known problems caused by the consumption of wood and to the needs of strengthened plastic processing engineering. Using resins as a binder, several fire-resistant prototypes were prepared from polyester waste, and their mechanical properties, thermal stability, and fire-resistant properties were analyzed.