Study on effect of crosslink structure on decomposition of epoxy resins in nitric acid

One chemical approach using nitric acid as the solvent to decompose thermosetting epoxy resin was discussed. The samples were prepared by using different kinds of curing agents, namely polyamide (PA651), isophorone diamine (IPDA), 4,4'-diaminodiphenylmethane (DDM) and 2-ethyl-4-methy-imidazole (EMI-2,4) and different kinds of epoxy resins, namely bisphenol-A epoxy resin(E-44), bisphenol-A epoxy resin(E-51), N,N,N',N' teraglycidy 4,4' diaminodiphenyl methane (AG-80) and diglycidyl-4,5-epoxycyclohexane-1,2-dicarboxylate (TDE-85). Their effects on decomposition rate were investigated and the decomposition products were analyzed by Infra-red (IR) spectra, and Gas Chromatography-Mass Spectrometry (GC-MS). Based on conclusions drawn from experiments, the mechanism of degrading thermosetting epoxy resin with nitric acid was envisaged tentatively.

Catalytic Decomposition of Nitric Oxide by LaCoO3 Nano-particles Prepared by Rotary CVD

Catalytic direct decomposition of NO by perovskite-type catalysts has attracted much attention for the various possible components and the unique structure. LaCoO_3 nanoparticles were precipitated on a-Al_2O_3 micro powders by rotary chemical vapor deposition（rotary CVD） and its catalytic performance for the decomposition of NO was investigated. LaCoO_3 nano-particles with 100 nm in average diameter and 1.5% in mass were uniformly dispersed on a-Al_2O_3 powder. The conversion of NO increased with increasing temperature from 400 to 950 ℃, and reached 28.7% at 950 ℃. The gas velocity of transformed NO on LaCoO_3 nano-particles catalyst per mass unit was 7.7 mL/（g min）, showing a good catalytic activity over the calculated results of pure catalysts. After five times of aging performance experiments, the NO conversion kept the same value, showing a good aging performance and thermal stability.

The production of carbon nanotubes from carbon dioxide:challenges and opportunities

Recent advances in the production of carbon nanotubes （CNTs） are reviewed with an emphasis on the use of carbon dioxide （CO2） as a sole source of carbon. Compared to the most widely used carbon precursors such as graphite, methane, acetylene, ethanol, ethylene, and coal-derived hydrocarbons, CO2 is competitively cheaper with relatively high carbon yield content. However, CNT synthesis from CO2 is a newly emerging technology, and hence it needs to be ex- plored further. A theoretical and analytical comparison of the cur- rently existing CNT-CO2 synthesis techniques is given including a review of some of the process parameters （i.e., temperature, pres- sure, catalyst, etc.） that affect the CO2 reduction rate. Such analysis indicates that there is still a fundamental need to further explore the following aspects so as to realize the full potential of CO2 based CNT technology： （1） the CNT-CO2 synthesis and formation mechanism, （2） catalytic effects of transitional metals and mechanisms, （3） uti- lization of metallocenes in the CNT-CO2 reactions, （4） applicability of ferrite-organometallic compounds in the CNT-CO2 synthesis reactions, and （5） the effects of process parameters such as temperature, etc.