A alumina-magnesium composite oxide catalyst (Al-Mg) was synthesized for catalytic degradation of poly vinyl chloride (PVC) containing polymer mixtures, i.e. polypropylene (PP)/PVC, low-density polyethylene (LDPE)/PVC, polystyrene (PS)/PVC, and LDPE/PP/PS/PVC. In the catalytic degradations the Al-Mg composite oxide catalyst accelerated the rate of polymer degradation and lowered the carbon distribution of liquid products. In addition, it showed good effect on the fixation of evolved HCl and greatly decreased the chlorine content in the oil. These results suggested that the Al-Mg composite oxide catalyst can be effectively used for catalytic degradation and dechlorination of PVC-containing mixed plastics. 相似文献
Catalytic coprocessing of low density polyethylene (LDPE) with coal and heavy petroleum resid was investigated using four different catalysts that included both hydrotreating and hydrocracking catalysts. Reaction systems that were evaluated included LDPE alone; LDPE with coal; and LDPE, coal, and resid. The catalysts used were NiMo/Al2O3, a hydrotreating catalyst with some hydrocracking activity, and the hydrocracking catalysts Zeolyst 753, NiMo/zeolite, and HZSM-5. These catalysts were reacted individually or in combinations of 10 wt.% of each hydrocracking catalyst in NiMo/Al2O3. The catalytic reactions were performed at two temperatures, 400 and 430°C, using 1 wt.% of each catalyst or a combination of catalysts on a total feed basis. The effects of the different catalysts on the reaction products were measured in terms of solvent fractionation and total boiling point distribution. Reactions at the higher reaction temperature of 430°C resulted in substantially higher conversion and production of lighter products than the reactions at 400°C. The LDPE reaction system was sensitive to the catalyst type, and yielded increased conversion and lighter products when Zeolyst 753 and NiMo/zeolite were used. By contrast, the conversion and product slate obtained from the LDPE and coal systems were low and showed no effect due to the different types of catalyst. Introduction of resid to the LDPE/coal system increased the reactivity of the system and allowed the catalysts to have a larger effect. The hydrocracking catalysts were the most active in producing more conversion and hexane soluble material. Comparison of the effect of increasing the reaction time up to 5 h with 1 wt.% catalyst loading to the effect of increasing the catalyst loading from 1 wt.% to 10 wt.% for a reaction time of 1 h showed that increased reaction time was much more effective than catalyst loading in converting the solid LDPE to liquid reaction products. 相似文献
The composition of oils derived from the on-line, low pressure zeolite upgrading of biomass pyrolysis oils from a fluidized bed pyrolysis unit have been investigated in relation to the regeneration of the zeolite catalyst. The catalyst used was H-ZSM-5 zeolite. The gases were analysed by packed column gas chromatography. The composition of the oils before catalysis and after catalyst upgrading were analysed by liquid chromatography fractionation, followed by coupled gas chromatography—mass spectrometry of each fraction. In particular, the aromatic and oxygenated aromatic species were identified and quantified. In addition, the oils were analysed for their elemental composition and molecular weight range using size exclusion chromatography. Before catalysis the biomass pyrolysis oil was highly oxygenated but after catalysis a highly aromatic oil was formed with high concentrations of monocyclic aromatic hydrocarbons. In addition, significant concentrations of polycyclic aromatic hydrocarbons (PAH) were formed. Regeneration of the zeolite catalyst showed that continued regeneration reduced the effectiveness of the catalyst in converting biomass pyrolysis oils to an aromatic product. Elemental analysis of the upgraded oils showed an increase in the oxygen content of the oil with increasing regeneration of the catalyst. The molecular weight range of the oils was found to decrease markedly after catalysis, but continued regeneration of the catalyst increased the molecular weight range of the upgraded oils. Detailed analysis of the uncatalysed oils showed they contained low concentrations of aromatic and PAH species which markedly increased in concentration after catalysis. The overall effect of increasing catalyst regeneration was a decrease in the concentration of aromatic hydrocarbons and PAH. Also as the catalyst was regenerated, the number of methyl groups on the parent single ring aromatic compound or PAH increased. The oxygenated aromatic species in the oil before catalysis were mainly, phenols and benzenediols and their alkylated homologues. After catalysis some of the oxygenated species were reduced and some increased in concentration. A dual mechanistic route is suggested for the formation of aromatics and PAH during the catalytic upgrading of biomass pyrolysis oils: (1) the formation of low-molecular-weight hydrocarbons on the catalyst which then undergo aromatization reactions to produce aromatic hydrocarbons and PAH; (2) deoxygenation of oxygenated compounds found in the non-phenolic fraction of the pyrolysis oils which directly form aromatic compounds. 相似文献
Conversion of vegetable oils predominantly composed of triglycerides using pyrolysis type reactions represents a promising option for the production of renewable fuels and chemicals. The purpose of this article was to compare catalytic cracking with thermal cracking on production of gaseous hydrocarbon and gasoline conversion by cottonseed oil, and to discuss the difference on composition of products from catalytic cracking and thermal cracking. Reaction products are heavily dependant on the catalyst type (catalyst activation) and reaction conditions. They can range from dry gas to light distillate, such as dry gas, liquefied petroleum gas and gasoline. When the temperature of catalytic cracking is over 460 °C, the effects of thermal cracking must be considerable. 相似文献
Effective treatment of residue generated from the pyrolysis of polystyrene wastes has been one of the important factors in
the recovery of styrene monomer and oil from polystyrene wastes. Depending on the experimental conditions, the yields of oil
and styrene monomer are considerably decreased in the presence of residue. Here the residue was decomposed effectively in
a catalytic fluidized-bed reactor. Nitrogen and silica sand were used as a fluidizing gas and a bed material, respectively.
Effects of catalyst, temperature and gas velocity on the characteristics of decomposition of the residue were examined. It
was found that the residue could be decomposed to oil or chemicals effectively by means of a catalytic fluidized-bed reacting
system. The yields of oil and individual chemicals and the composition of the products were dependent upon the operating variables
such as reaction temperature, catalyst and gas velocity. 相似文献
This paper investigates three aspects of linear-low-density polyethylene (LLDPE) rheological properties: shear viscosity variations with shear rate and temperature, tensile behavior determined with an extensiometer, and extrusion defects. The differences in shear viscosity variation with shear rate and temperature between LLDPE and LDPE (low-density polyethylene) are shown. These differences, attributed to wider molecular weight distribution and to long chain branching (LCB) in LDPE, involve different extrusion behaviors. The lack of LCB in LLDPE can be demonstrated by comparison of the measured Newtonian viscosity with the value of the same parameter calculated from molecular weight distribution and composition law of Newtonian viscosities. The lack of LCB leads to good melt extensibility, which is shown by tensile properties of polyethylene melts determined with a non-isothermal extensiometer. The melt fracture phenomenon is studied because it promotes surface defects on bubbles in film application. Extrudate distortions are examined at the laboratory extruder outlet. This test shows differences between LLDPE and LDPE, but also between some LLDPE samples. 相似文献
Summary: The rheological behavior of polyethylenes is mainly dominated by the molecular weight, the molecular weight distribution and by the type, the amount and the distribution of the chain branches. In this work a linear metallocene catalyzed polyethylene (m‐PE), a branched metallocene catalyzed polyethylene (m‐bPE), a conventional linear low density polyethylene (LLDPE) and a low density polyethylene (LDPE) have been investigated in order to compare their rheological behavior in shear and in elongational flow. The four samples have similar melt flow index and in particular a value typical of film blowing grade. The melt viscosity has been studied both in shear and in isothermal and non‐isothermal elongational flow. The most important features of the results are that in shear flow the m‐PE sample shows less pronounced non Newtonian behavior while in the elongational flow the behavior of m‐PE is very similar to that of the linear low density polyethylene: the narrower molecular weight distribution and the better homogeneity of the branching distribution are reasonably responsible for this behavior. Of course the most pronounced non‐linear behavior is shown, as expected, by the LDPE sample and by the branched metallocene sample. This similar behavior has to be attributed to the presence of branching. Similar comments hold in non‐isothermal elongational flow; the LDPE sample shows the highest values of the melt strength and the other two samples show very similar values. As for the breaking stretching ratio the opposite is true for LDPE while m‐PE and LLDPE show higher values. The transient isothermal elongational viscosity curves show that the branched samples show a strain hardening effect, while LLDPE and m‐PE samples present a linear behavior.
Dimensionless flow curves of different polyethylene samples. 相似文献