Towards garden city wonderlands: new town planning in 1950s Taiwan

This article explores the historical context, process and result of introducing and implementing ‘new’ town planning in early post‐war Taiwan. The two so‐called ‘garden cities’ are examined: Jhong‐Sing New Village and Yonghe City, both of which were formulated in the mid‐1950s by the same group of local planners. It reveals that the assumed necessity of importing Western planning paradigms arose from the abrupt escalation of urban concentration caused by the late 1940s mass migrations from China. To cope with this unprecedented population growth, planning profession was swiftly established. The novice planners, in search of a reference for developing ‘new’ towns to decentralise excessive urbanisation, modelled their ‘new’ town planning on English suburban morphology. In the absence of an input of external expertise, the planners appeared to mistake aesthetic order and pastoral imagery of low‐density residential development in England as practically viable solutions to the pressing urban problems in Taiwan. In a false hope that adopting Western ideas and practices would quickly lead the island to a better world, Taiwan initiated the importation of planning paradigms. This planning transfer not only evidently manifests a mode of ‘borrowing’ in post‐colonial countries in international diffusion but also re‐articulates the disseminating nature of modern planning and the existence of one‐direction flows characterising the global dynamics of diffusion in the twentieth century.     

An Engineered Cholesterol Oxidase Catalyses Enantioselective Oxidation of Non-steroidal Secondary Alcohols

The enantioselective oxidation of 2° alcohols to ketones is an important reaction in synthetic chemistry, especially if it can be achieved using O₂-driven alcohol oxidases under mild reaction conditions. However to date, oxidation of secondary alcohols using alcohol oxidases has focused on activated benzylic or allylic substrates, with unactivated secondary alcohols showing poor activity. Here we show that cholesterol oxidase (EC 1.1.3.6) could be engineered for activity towards a range of aliphatic, cyclic, acyclic, allylic and benzylic secondary alcohols. Additionally, since the variants demonstrated high (S)-selectivity, deracemisation reactions were performed in the presence of ammonia borane to obtain enantiopure (R)-alcohols.     

Impact of culture source and linoleic acid (C18:2) on biohydrogen production from glucose under mesophilic conditions

Genomic and statistical methods were used to demonstrate the effects of linoleic acid (LA) on hydrogen (H₂) production in mixed anaerobic cultures from two sources (designated as A and B). The microbial composition of the control cultures CA and CB were statistically different. Bacteroidaceae (26%) and Clostridiaceae (10%) dominated CA whereas Clostridiaceae (33%) and Bacteroidaceae (10%) dominated CB. Homoacetogens directed 42% of the electron equivalents to acetate production and decreased the H₂ yield by 50% in CA compared to CB. The maximum H₂ yields (3.11 ± 0.02 and 3.11 ± 0.07 mol H₂ mol⁻¹ glucose in LA-treated cultures ALA and BLA, respectively) were statistically the same. Cultures ALA and BLA followed the acetate-butyrate pathway while CA and CB followed propionate and homoacetogenic pathways. LA-treated and control cultures were statistically different based on the type and quantity of metabolites; the differences were also confirmed by principal component analysis (PCA).     

Ammonia synthesis enhanced by magnesium chloride absorption

Conversion to ammonia with Haber–Bosch catalysts can be increased above 95% by selective absorption of ammonia by MgCl₂. The maximum conversion depends on reaction and absorption equilibria. At very short times, the measured conversion rate is the same with and without absorption by the MgCl₂ salt; the overall rate constants are comparable to those in the literature. At larger times, conversion to ammonia can be over seven times greater with MgCl₂ than without. However, the overall rate constants can be over 10 times slower because they are controlled by ammonia diffusion in the solid salt. An approximate, pseudosteady state theory consistent with these results provides a strategy for improving the overall rate while keeping the conversion over 90%. For example, the absorption rates might be increased using smaller particles of absorbent on a porous inert absorbent support. The results provide part of the basis for designing small scale ammonia plants. © 2015 American Institute of Chemical Engineers AIChE J, 61: 1364–1371, 2015     

Capsosomes with Multilayered Subcompartments: Assembly and Loading with Hydrophobic Cargo

Therapeutic artificial cells or organelles are nanoengineered vehicles that are expected to substitute for missing or lost cellular function. The creation of capsosomes, polymer carrier capsules containing liposomal subcompartments, is a promising approach towards constructing such therapeutic devices using the layer‐by‐layer assembly method. Herein, the assembly of intact, nonaggregated capsosomes containing multiple liposome layers is reported. It is also further demonstrated that thiocoraline, a hydrophobic model peptide with antitumor activity, can be efficiently loaded into the membrane of the liposomal subcompartments of the capsosomes. Cell viability assays verify the activity of the trapped antitumor cargo. It is also shown that pristine capsosomes do not display inherent cytotoxic effects. The ability to tune the number of liposome layers and hence the drug loading in capsosomes as well as their noncytotoxicity provide new opportunities for the creation of therapeutic artificial cells and organelles.     

Thermodynamic consistency of the multi-scale Gibbs–Helmholtz constrained equation of state

The multi-scale Gibbs–Helmholtz constrained (GHC) equation is a new predictive cubic equation of state that constrains the energy parameter in the SRK equation to satisfy the Gibbs–Helmholtz equation. It makes use of internal energies of departure calculated from NTP Monte Carlo simulations at the molecular length scale and a novel up-scaling expression to determine the energy parameter at the bulk phase length scale.