Optimization of Ti-PA efficiently catalytic the alcoholysis of waste PET using response surface methodology.

A new type of titanium phthalate (Ti-PA) catalyst was prepared by exchange method of phthalic acid and isopropyl titanate, which is never been reported before. The Ti-PA catalyst was characterized by FT-IR, TG, Uv-vis, BET, SEM, and EDS. The Ti-PA catalyst shows good catalytic activity in the alcoholysis reaction of polyethylene terephthalate (PET) and optimal experimental conditions for the alcoholysis process were optimized by response surface methodology; the Ti-PA catalyst provided a BHET yield of 81.98% for reaction lasting 3.98 h at 191 °C of 0.86% catalyst and 13.7 ml ethylene glycol; the model has good reliability. The kinetics and reaction mechanism of the process were explored and apparent activation energy is 75.52 kJ/mol. Finally, the good catalytic activity of Ti-PA was illustrated by comparing it with currently reported catalysts.

Ti-Si composite glycol salts: depolymerization and repolymerization studies of PET.

In this study, a Ti-Si-ethylene glycol salt (Ti/Si-EG) was synthesized and used as a catalyst for the depolymerization of PET-ethylene glycol to produce bis(hydroxyethyl)terephthalate (BHET), and the optimum conditions for the depolymerization were determined by response surface analysis: w(EG) : w(PET) was 4 : 1, the catalyst mass dosage was 0.56% (in terms of the mass of PET), the depolymerization temperature was 203 °C, the depolymerization time was 3.8 h, and the highest yield of the product (BHET) was 90.10%. Furthermore, the depolymerization product BHET was used as the raw material and Ti/Si-EG was used as the catalyst for the polycondensation reaction to synthesize PET, and the amount of the catalyst added was 0.015% by mass (in terms of BHET). The performance of the synthesized PET was tested to be the same as that of PET synthesized by the PTA method under the same conditions, thus achieving the resourceful treatment and high-value recycling of waste PET. The introduction of Si in the catalyst reduced the catalytic activity of Ti and avoided the problem of yellowing of polyester products, and the use of the glycol salt as a catalyst in the depolymerization and polycondensation reaction process did not introduce impurity groups.

Research progress of metal-organic framework-based material activation of persulfate to degrade organic pollutants in water.

The rapid development of industry in recent years has led to the introduction of serious pollutants into water bodies, and there is an urgent need for efficient organic degradation technologies. At present, selective peroxynitrite (PS) oxidation (SR-AOPs) is an effective way to treat pollutants in water bodies, and it is necessary to select a suitable material for the activation of peroxynitrite. Metal-organic frameworks (MOFs), with their tunable structure, large specific surface area, and tunable ligand molecules exhibit excellent reactivity and catalytic performance in the activation of persulfate. With MOF-based materials for PS activation as a novel advanced oxidation technology, this study reviews MOFs and their composites and derived materials. The current research status of activated persulfate for the treatment of organic pollutants in water, the influence of different systems on the degradation performance are discussed, and the activation and degradation mechanisms are discussed; the problems of the above materials in the degradation of organic pollutants are summarized, and research directions based on the coupled activated persulfate system of MOF materials are proposed.

Spatial and temporal differences in the response of water conservation and soil conservation to ecosystem fragmentation: evidence from Qilian Mountain National Park of China.

Using spatial autocorrelation methods, we explored the spatial and temporal differences in the response of soil conservation (SC) and water conservation (WC) to ecosystem fragmentation during 1990 to 2019 in Qilian Mountain National Park (QMNP) of China. We found that the degree of ecosystem fragmentation decreased over the past 30 years, improving the WC and SC capacity of the ecosystems. However, the relationship among them varied temporally and exhibited a variety of spatial patterns. The correlation between fragmentation and WC increases year by year, and the correlation with SC weakens. There is a mismatch between park-level and regional autocorrelation between fragmentation and WC and SC. The spatial relationships between fragmentation and WC and SC in the QMNP show "high-high" and "low-low" patterns in its eastern and western sections, respectively. This heterogeneity is related to the differences in ecosystem composition, especially in ecosystem WC and SC capacity, and the characteristics of ecosystem fragmentation in the east-west direction of the QMNP.

Optimization of Ti-BA efficiently for the catalytic alcoholysis of waste PET using response surface methodology.

A titanium benzoate (Ti-BA) catalyst was prepared by hydrothermal method, which has an ordered eight-face structure, and was used for polyethylene terephthalate (PET) depolymerization. With bis(2-hydroxyethyl)terephthalate (BHET) as the target molecule and ethylene glycol (EG) as the solvent, the best reaction conditions for catalytic alcoholysis via a PET alcoholic solution were investigated via response surface experiments and found to be a EG/PET mass ratio of 3.59, temperature of 217 °C and reaction time of 3.3 h. Under these conditions, the amount of the catalyst required was only 2% of the mass of the PET, and the yield of BHET reached 90.01% and under the same conditions, the yield of BHET could still reach 80.1%. Based on the experimental results, the mechanism of alcoholysis, Ti-BA catalyst activated ethylene glycol deprotonation to achieve the progressive degradation of polymers. This experiment provides a reference for the degradation of polymer waste and other transesterification reactions.

New Technology for the Synthesis of Glycerol Monooleate.

Herein, a new approach for glycerol monooleate (GMO) was developed. GMO was synthesized via the esterification method using self-made sodium oleate and 3-chloro-1,2-propanediol as reactants, tetrabutylammonium bromide as the catalyst, and toluene as the solvent. The effects of the reaction molar ratio, type and amount of catalyst, and reaction temperature and time on the yield were investigated. Results showed that the optimal process conditions for synthesizing GMO were as follows. The molar ratio of sodium oleate to 3-chloro-1,2-propanediol was 1:2, the reaction temperature was 115°C, the reaction time was 6 h, weight of toluene was 25 g, and the catalyst dosage was 3.5%. Under these conditions, high-purity GMO was synthesized with a yield of 89.02%.