395 resultados para green house gas


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Section taken through new bath house.

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New bath house (centre), with existing buildings to either side.

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Timber framing to new bath house (centre), with existing buildings to either side.

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Timber framing to new bath house, as seen from beachfront.

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Timber framing to new bath house (centre), with existing buildings to either side.

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Timber framing to new bath house, as seen looking towards water from deck area (to be constructed).

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Timber framing to new bath house (centre), with existing buildings to either side.

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As seen looking towards water from deck area.

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New bath house (centre), with existing buildings to either side during sunset.

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New bath house (centre), with existing buildings to either side.

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Existing boat house undergoing renovations.

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Existing boat house undergoing renovation. Existing cottage on left. Bath house to be constructed.

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New bath house (centre), with existing buildings to either side.

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Hand-drawn floor plan.

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Hydrogen is being seen as an alternative energy carrier to conventional hydrocarbons to reduce greenhouse gas emissions. High efficiency separation technologies to remove hydrogen from the greenhouse gas, carbon dioxide, are therefore in growing demand. Traditional thermodynamic separation systems utilise distillation, absorption and adsorption, but are limited in efficiency at compact scales. Molecular sieve silica (MSS) membranes can perform this separation as they have high permselectivity of hydrogen to carbon dioxide, but their stability under thermal cycling is not well reported. In this work we exposed a standard MSS membrane and a carbonised template MSS (CTMSS) membrane to thermal cycling from 100 to 450°C. The standard MSS and carbonised template CTMSS membranes both showed permselectivity of helium to nitrogen dropping from around 10 to 6 in the first set of cycles, remaining stable until the last test. The permselectivity drop was due to small micropore collapse, which occurred via structure movement during cycling. Simulating single stage membrane separation with a 50:50 molar feed of H2:CO2, H2 exiting the permeate stream would start at 79% and stabilise at 67%. Higher selectivity membranes showed less of a purity drop, indicating the margin at which to design a stable membrane separation unit for CO2 capture.