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THE FUTURE, - Solvay

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Performance<br />

improvement<br />

34<br />

Performance improvement > INNOVATIONS 09<br />

209784 209805 209806<br />

NEW EFFICIENT CROSS-FLOW FILTRATION<br />

PROJECT<br />

Two-in-one wash<br />

<strong>THE</strong> PROJECT. A key phase in the<br />

hydrogenation stage of the hydrogen peroxide<br />

manufacturing process is the separation of the<br />

catalyst from the reaction mixture.<br />

The system currently in use, consisting of direct<br />

fi ltration and then washing the fi lter cake with a<br />

reverse fl ow, dates from the 50s and the many<br />

improvements made over time have reached their<br />

limits in terms of effi ciency. This system is not<br />

feasible in the giant installations of the future<br />

(beyond the current 330 Ktons). Effi ciency is lost<br />

due to the mechanical wear of the catalyst, and<br />

power consumption is much too high due to the<br />

reverse fl ow.<br />

In the new cross-fl ow system, through the use of<br />

tangential forces the catalyst is washed<br />

simultaneously with the fi ltration operation, and<br />

then returned to the reactor.<br />

This idea from the 90s has been developed only<br />

recently. A pilot plant built in Povoa (Portugal) in<br />

2008 has enabled us to test and optimize the<br />

operating parameters for a larger installation. These<br />

were then applied at Curitiba (Brazil) over an<br />

11 month period in order to carefully study all the<br />

hydrodynamic phenomena and defi ne the<br />

parameters for a 160 Ktons/year unit.<br />

This original process has shown its full savings<br />

potential in terms of energy, materials (less catalyst<br />

losses from wear), labour and maintenance.<br />

It is also opening the way to even larger units<br />

than the biggest ones built until now, i.e. above<br />

400 Ktons/year.<br />

SBU PEROXIDES/BELGIUM<br />

> Jal Dadabhoy; Pedro Borges; Patrick Dhaese;<br />

Massimo Fedeli; Cesar Muller; Gustavo Nakamura.<br />

RECRUIT & REWARD<br />

Looking for our future<br />

colleagues<br />

<strong>THE</strong> PROJECT. To continue the growth of<br />

<strong>Solvay</strong> Biologicals BV in the Netherlands in a very<br />

diffi cult employment market, the company needed<br />

to fi nd creative and innovative ways to fi ll its<br />

vacant positions.<br />

To address the problem, we recognized and made<br />

use of the fact that by far the best ambassadors<br />

<strong>Solvay</strong> has are its own employees.<br />

We introduced a pioneering scheme whereby we<br />

asked our employees to actively introduce us to<br />

possible new colleagues. If they introduced a<br />

candidate who successfully fi lled an open<br />

vacancy, they would receive a EUR 1 500 reward.<br />

This strategy could easily be replicated at other<br />

<strong>Solvay</strong> sites.<br />

PHARMACEUTICALS SECTOR<br />

> Françoise Jeuken; Marvin Beusekamp;<br />

Hannelore Kornet; Judith Kruit; Anja Oudshoorn.<br />

CLINICAL TRIAL SUPPLY: COMPUTER<br />

SIMULATIONS REDUCE WASTE AND SAVE<br />

MILLIONS<br />

Stop over-production!<br />

<strong>THE</strong> PROJECT. Until recently, to avoid<br />

interruption of clinical trials due to depleted study<br />

medication stocks, over-production of trial<br />

supplies was normal. This represented not only<br />

a waste of compound, but a waste of time in<br />

production of the active pharmaceutical<br />

ingredient, formulation, packaging, storage,<br />

distribution and at the end of the study<br />

reconciliation and destruction of unused<br />

medication supplies, all of which had a signifi cant<br />

impact on environment, budget and resources.<br />

Now for each trial different computer simulations<br />

are used to calculate the safe minimum amount<br />

of compound required, integrating a level of<br />

acceptable risk which reduces the overage<br />

(excess) of compound produced for each study.<br />

Proven advantages in terms of clinical trials<br />

include shorter lead times, quicker<br />

commencement of clinical trials, and increased<br />

satisfaction at clinical trial sites.<br />

PHARMACEUTICALS SECTOR<br />

> Geurt-Paul Koning; Marina Romay;<br />

Henk Teunissen; Ad Theeuwes; Philippa Tibbits;<br />

Serge VandeWitte; Erik Vanleeuwen; Isabel White.

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